AnnotationDbi/DESCRIPTION0000644000175200017520000000427114710267466016054 0ustar00biocbuildbiocbuildPackage: AnnotationDbi Title: Manipulation of SQLite-based annotations in Bioconductor Description: Implements a user-friendly interface for querying SQLite-based annotation data packages. biocViews: Annotation, Microarray, Sequencing, GenomeAnnotation URL: https://bioconductor.org/packages/AnnotationDbi Video: https://www.youtube.com/watch?v=8qvGNTVz3Ik BugReports: https://github.com/Bioconductor/AnnotationDbi/issues Version: 1.68.0 License: Artistic-2.0 Encoding: UTF-8 Author: Hervé Pagès, Marc Carlson, Seth Falcon, Nianhua Li Maintainer: Bioconductor Package Maintainer Depends: R (>= 2.7.0), methods, stats4, BiocGenerics (>= 0.29.2), Biobase (>= 1.17.0), IRanges Imports: DBI, RSQLite, S4Vectors (>= 0.9.25), stats, KEGGREST Suggests: utils, hgu95av2.db, GO.db, org.Sc.sgd.db, org.At.tair.db, RUnit, TxDb.Hsapiens.UCSC.hg19.knownGene, org.Hs.eg.db, reactome.db, AnnotationForge, graph, 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4aa40297bfed905a09402a948b048860 *vignettes/databaseTypes.pdf AnnotationDbi/NAMESPACE0000644000175200017520000000712514710217313015550 0ustar00biocbuildbiocbuildimport(methods) importFrom(stats, setNames) importFrom(stats4, summary) import(DBI) import(RSQLite) import(BiocGenerics) import(Biobase) import(S4Vectors) import(IRanges) importFrom(KEGGREST, keggList) exportClasses( ## from R/AllClasses.R "Bimap", "FlatBimap", "AnnObj", "AnnDbObj", #"AnnDbTable", "L2Rlink", "AnnDbBimap", "GoAnnDbBimap", "Go3AnnDbBimap", "GOTermsAnnDbBimap", "AnnDbMap", "IpiAnnDbMap", "AgiAnnDbMap", "ProbeAnnDbBimap", "ProbeAnnDbMap", "ProbeIpiAnnDbMap", "ProbeGo3AnnDbBimap", ## Virtual mother-class for all Annoations "AnnotationDb", "OrgDb", "ChipDb", "GODb", "ReactomeDb", ## ## Class for faux-bimaps (select based bimaps) ## "AnnotationDbMap", ## from R/GOTerms.R "GOTerms", ## Special Frame objects "GOFrame", "GOAllFrame", "KEGGFrame" ) exportMethods( ## from R/AnnDbObj-lowAPI.R "dbconn", "dbfile", "taxonomyId", "dbmeta", "dbschema", "dbInfo", #"Ltablename", "Rtablename", #"Lfilter", "Rfilter", #"flatten", ## from R/Bimap.R (the Bimap interface) "direction", "direction<-", "revmap", "colnames", "colmetanames", "Lkeyname", "Rkeyname", "keyname", "tagname", "Rattribnames", "Rattribnames<-", "Lkeys", "Rkeys", "keys", "Lkeys<-", "Rkeys<-", "keys<-", "subset", "[", "Llength", "Rlength", "length", "isNA", "mappedLkeys", "mappedRkeys", "mappedkeys", "count.mappedLkeys", "count.mappedRkeys", "count.mappedkeys", "show", "summary", "toTable","as.data.frame", "head", "tail", "nrow", "links", "count.links", "nhit", "ncol", "dim", "toggleProbes", "hasMultiProbes","hasSingleProbes", "getBimapFilters", ## from R/GOTerms.R "GOID", "Term", "Ontology", "Synonym", "Secondary", "Definition", ## Special Frame Methods "GOFrame", "GOAllFrame", "getGOFrameData", "KEGGFrame", "getKEGGFrameData", ## from R/BimapFormatting.R "as.list", #"toLList", "toRList", "toList", "as.character", ## from R/Bimap-envirAPI.R "ls", "mget", "eapply", "get", "exists", "[[", "$", "contents", "sample", ## more... "initialize", ##Methods for AnnotationDb "saveDb", "species", "columns", "keytypes", "select", "mapIds", "orgPackageName" ) export( unlist2, ## from R/AnnDbObj-lowAPI.R showQCData, ## from R/SQL.R debugSQL, dbGetTable, ## from R/GOTerms.R GOTerms, makeGOGraph, ## from R/AnnDbPkg-templates-common.R dbFileConnect, dbFileDisconnect, #addToNamespaceAndExport, mergeToNamespaceAndExport, ## from methods-geneCentricDbs getOrgPkgForSchema, chooseCentralOrgPkgSymbol, mapIds_base, resort_base, testForValidKeytype, testSelectArgs, ## from R/loadDb.R loadDb, ## from the R/createAnnObjs.*_DB.R files createAnnObjs.SchemaChoice, NCBICHIP_DB_SeedGenerator, filterSeeds, ## from R/AnnDbPkg-checker.R #checkProperty0, checkMAPCOUNTS, ## helpers for map creation, temporary ## until pluggable maps come online make_eg_to_go_map, make_go_to_eg_map, toSQLStringSet, organismKEGGFrame, #Convenience function to allow automatic mapping of IDs: inpIDMapper, intraIDMapper, idConverter, ## AnnotationDb metadata, createSimpleBimap, ## S3 methods as.list.Bimap, as.data.frame.Bimap ) S3method(as.list, Bimap) S3method(as.data.frame, Bimap) AnnotationDbi/NEWS0000644000175200017520000002616014710217313015030 0ustar00biocbuildbiocbuildCHANGES IN VERSION 1.54.0 ------------------------- NEW FEATURES o There is a new replacement package for the Inparanoid orthology packages, called Orthology.eg.db o This package uses NCBI orthology data to map NCBI Gene IDs between species using the usual select() interface MODIFICATIONS o UniGene data have been removed from OrgDb and ChipDb packages o Gene type data have been added to OrgDb and ChipDb packages CHANGES IN VERSION 1.53.0 ------------------------- NEW FEATURES o organismKEGGFrame() provides a data.frame of species names and KEGG orgs MODIFICATIONS o Conversion from KEGG.db (which was deprecated) to KEGGREST - This involved changing how KEGG Ids checked when creating a KEGGFrame object. o Removal of any use of Inparanoid data/structures since the hom.*.inp.db packages have been removed. The data is extremely outdated and there is no replacement for it. - Removed the InparanoidDb object and all of the methods CHANGES IN VERSION 1.36.0 ------------------------- BUG FIXES o fix bug in dbschema method for DBIConnection objects o keys() no longer fails when global variable 'y' exists CHANGES IN VERSION 1.34.0 ------------------------- NEW FEATURES o export ALIAS2EG symbol in NAMESPACE for frog, mosquito, chimp and rhesus OrgDbs o add how to use EnsDb section to vignette MODIFICATIONS o work on code base and exported functions - break up code in geneCentricDbs file - re-name and export functions used by select() in AnnotationForge and GenomicFeatures - re-name and export functions used by annotation package builders in AnnotationForge o remove library(RSQLite) from dbFileConnect() o modify unit tests for new PFAM identifiers in Bioconductor 3.3 o use elementNROWS() instead of elementLengths() o modify mapIds() to preserve data type returned from select() o reduce time of AnnDbPkg-checker.Rd example BUG FIXES o bugfix for select() and mapIds() when there are many:many mappings o bugfix in test_generateExtraRows unit test. CHANGES IN VERSION 1.32.0 ------------------------- BUG FIXES o maps between chip and org packages work with loaded but not attached packages. CHANGES IN VERSION 1.31.0 ------------------------- NEW FEATURES and API changes o columns() and keytypes() sort their return values. o ls() on a Bimap option returns keys in sort()ed order, by default CHANGES IN VERSION 1.30.0 ------------------------- NEW FEATURES and API changes o Adds mapIds() which allows users who miss mget() to extract data from AnnnotationDb objects: but without the dangers of using mget() (which fails if you pass in a bad key) o Adds dbconn() and dbfile() methods to the list of things that AnnotationDb derived objects shoould always be expected to support BUG FIXES AND CODE MAINTENANCE o loadDb() now is smarter about whether or not it attaches a supporting package CHANGES IN VERSION 1.24.0 ------------------------- NEW FEATURES and API changes o keys method now has new arguments to allow for more sophisticated filtering. o cols method is now the columns method to make for a more constistent interface. o cols argument is now the columns argument (for select) to also make the interface consistent across all use cases BUG FIXES AND CODE MAINTENANCE o better argument checking for select and related methods o keys that end with ' will no longer cause grief except to hapless life scientists who will still have to wonder who in their right mind thinks it's a good idea for a gene symbol to be the same except end with a 'prime'. CHANGES IN VERSION 1.22.0 ------------------------- NEW FEATURES o There is now a convenience function for extracting data from the GO.db package as a graph object. The function is called: makeGOGraph. o Adds supportedSeqnameMappings() and findSequenceRenamingMaps() utilities. o Improved vignette for new users BUG FIXES AND CODE MAINTENANCE o Fixes a bug in select for users accessing reactome.db o Fixes a bug in select for users requesting via a PROBEID o Fixes a bug in select for users using rat chip packages o Fixes a bug in mget, for Bimap objects (when ifnotfound=NA) ************************************************** * * * 1.20.x SERIES NEWS * * * ************************************************** CHANGES IN AnnotationDbi VERSION 1.20.x NEW FEATURES o There is a new introductory vignette for AnnotationDbi. It explains how to use the new simplified select method interface and also describes how developers can implement their own select interfaces for exposing new annotation resources. o select support has been added for both the inparanoid and reactome.db packages. These are in addition to existing support for all ChipDb, OrgDb, and TranscriptDb packages. GO.db also has a select interface. o Code has been added to enhance backwards compatibility between select and bimaps. The aim here is that old code that uses bimaps should still work with packages that have the same kind of data exposed using only a select() interface. SIGNIFICANT USER-VISIBLE CHANGES o AnnotationDbi has been split up and simplified. All code needed for building and supporting new packages has been moved to a new package called AnnotationForge. The remaining code is what is needed to support day-to-day interaction with the Annotation interface. BUG FIXES AND CODE MAINTENANCE o The code for generating bimaps has been simplified and overhauled. o The code for making manual pages in annotation packages has been simplified so that there will be far less redundancy o The select(), cols, keys, and keytypes methods saw several bug fixes and a code overhaul to enhance both speed and reliablity. ************************************************** * * * 1.16.x SERIES NEWS * * * ************************************************** CHANGES IN AnnotationDbi VERSION 1.16 NEW FEATURES o New Object types: Org.Db, ChipDb, GODb. These are loaded when an Annotation package is loaded. o select method for these new objects to extract data.frames of available annotations. Users can specify keys, along with the keytype, and the columns of data that they want extracted from the annotation package. o keys now will operate on new objects to expose most ID types as keys o keytypes will show which kinds of IDs can be used as a key by select o cols will display the kinds of data that can be extracted by select o Users who need organism packages for organisms that are annotated at NCBI can now use makeOrgPackageFromNCBI() to generate a basic organism package on the fly SIGNIFICANT USER-VISIBLE CHANGES o New objects are always named after the package that loaded them. So if you just loaded the hgu95av2.db package, your ChipDb object will be called hgu95av2.db o new fields are now required in the metadata table of annotation packages to allow the on-the-fly creation of these new objects. If you are constructing a custom package and want to extend this infrastructure, you may need to add some fields to the metadata table. BUG FIXES o makeProbePackage, and other generated Annotation packages have had templates modified so that packages can load and also to enable loading of new objects to allow new features in this release. o updated GOFrame constructor to allow use of new types of evidence codes. o generated packages will create databases with the appropiate metadata entries for the new objects. ************************************************** * * * 1.9.x SERIES NEWS * * * ************************************************** CHANGES IN AnnotationDbi VERSION 1.9.5 NEW FEATURES o An organism package has been added for Streptomyces coelicolor o extensive overhaul of inparanoid packages means that inparanoid packages now match to 100 different organisms o Extended support for ensembl mappings to yeast and flies. NOTEWORTHY CHANGES BETWEEN THIS version and 1.3.11 o All chip packages now depend on org packages. This simplifies the schema and also allows for more convenient updating of these packages and smaller downloads for users. o chip package mappings that contain probes which map to multiple targets are now hidden by default, with the ability to be exposed when required. See the use of the new toggleProbes() method. ************************************************** * * * 1.3.11 SERIES NEWS * * * ************************************************** CHANGES IN AnnotationDbi VERSION 1.3.11 NEW FEATURES o Support has been added for 3 more organisms, this means that the current list of supported organisms as of 1.3.11 is the following: Arabidopsis thaliana Bos taurus Caenorhabditis elegans Canis familiaris Drosophila melanogaster Danio rerio Escherichia coli K12 Strain Escherichia coli Sakai Strain Gallus gallus Homo sapiens Mus musculus Plasmodium falciparum Rattus norvegicus Saccharomyces cerevisiae Sus scrofa o Added support for GO to canine and pig packages by using BLAST2GO (this data was not available from NCBI for these organisms). o ZFIN IDs are supported for Zebrafish packages. o Wormbase IDs are supported for C. elegans packages. o Uniprot IDs have been added to almost all package types. o CHRLOCEND mapping has been added which give gene end positions for almost all packages and compliments the CHRLOC mapping which already provides the start positions. ************************************************** * * * 1.3.9 SERIES NEWS * * * ************************************************** CHANGES IN AnnotationDbi VERSION 1.3.9 NEW FEATURES o Support added for Malaria, Zebrafish, two strains of E coli, bovine and canine. ************************************************** * * * 1.1.7 SERIES NEWS * * * ************************************************** CHANGES IN AnnotationDbi VERSION 1.1.7 NEW FEATURES o Annotation packages now have a function to display basic quality control information. o 5 Inparanoid packages have been added for use in studies involving homology. o Ensembl gene ID maps have been added to all mammalian packages. o MGI IDs maps have been added for all Mouse packages. o Protein to gene mappings have been added to appropriate organism based packages so that it will be possible to get from the IDs in the inparanoid packages to a gene based ID for the 5 main organism types (ie. Human, Mouse, Rat, Fly, Yeast). o Support has been added for PFAM so that there can now be a PFAM.db package. o AnnotationDbi is now compliant with the 1.0 schema definition. AnnotationDbi/R/0000755000175200017520000000000014710217313014525 5ustar00biocbuildbiocbuildAnnotationDbi/R/00RTobjs.R0000644000175200017520000000013614710217313016213 0ustar00biocbuildbiocbuild### Environment for storing run-time objects RTobjs <- new.env(hash=TRUE, parent=emptyenv()) AnnotationDbi/R/AllClasses.R0000644000175200017520000001770214710217313016705 0ustar00biocbuildbiocbuild### ========================================================================= ### The Bimap interface and the FlatBimap class. ### ------------------------------------------------------------------------- ### This is just an interface i.e. a virtual class with no slot (a kind of ### Java "interface"). setClass("Bimap", representation( "VIRTUAL", ifnotfound="list" ), prototype( ifnotfound=list() # empty list => raise an error on first key not found ) ) setClass("FlatBimap", contains="Bimap", representation( colmetanames="character", # must have a length <= ncol of data slot direction="integer", data="data.frame", Lkeys="character", Rkeys="character" ), prototype( direction=1L, # left-to-right by default Lkeys=as.character(NA), Rkeys=as.character(NA) ) ) ### ========================================================================= ### Containers for SQLite-based annotation data. ### ------------------------------------------------------------------------- ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "AnnObj" class. ### setClass("AnnObj", representation( "VIRTUAL", objName="character", objTarget="character" # "chip hgu95av2" or "YEAST" or... ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "AnnDbObj" class. ### setClass("AnnDbObj", contains="AnnObj", representation( "VIRTUAL", ## Used to define objects like "dbconn" or "dbfile" that are shared ## by all the AnnDbObj objects defined on top of the same database ## (like all the AnnDbObj objects in a given ann db package). datacache="environment" ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "AnnDbTable" class. ### ### WARNING: THIS CLASS IS CURRENTLY BROKEN! ### setClass("AnnDbTable", contains="AnnDbObj", representation( leftTable="character", leftCol="character", from="character", showCols="character" # cols to show in addition to the left col ) ) ### ========================================================================= ### Containers for SQLite-based annotation maps. ### ------------------------------------------------------------------------- setClass("L2Rlink", representation( tablename="character", # length 1 Lcolname="character", # left col (length 1) tagname="character", # tag col (length 1 + name) Rcolname="character", # right col (length 1) Rattribnames="character", # right attrib cols (length n + names) Rattrib_join="character", # right attrib join (length 1, SQL string) filter="character", # filter (length 1, SQL string) altDB="character" # optional alternate DB (string of DB name) ), prototype( tagname=as.character(NA), Rattrib_join=as.character(NA), filter="1" ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "AnnDbBimap" class and subclasses. ### ### An AnnDbBimap object is a directed mapping between left values and ### right values. The direction of the mapping is "left-to-right" or ### "right-to-left". ### If the mapping is "left-to-right", the left values are the keys of the ### map and are retrieved with the "keys" or "ls" methods. The type, format ### and location in the DB of the right values depend on the particular ### subclass of the AnnDbBimap object. ### setClass("AnnDbBimap", contains=c("Bimap", "AnnDbObj"), representation( L2Rchain="list", # list of L2Rlink objects direction="integer", # 1L for left-to-right, -1L for right-to-left # and 0L for undirected Lkeys="character", Rkeys="character" ), prototype( direction=1L, # left-to-right by default Lkeys=as.character(NA), Rkeys=as.character(NA) ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### GO-related bimaps. ### ### For a GoAnnDbBimap object, the right values are named lists of GO nodes, ### each GO node being represented as a 3-element list of the form ### list(GOID="GO:0006470" , Evidence="IEA" , Ontology="BP") setClass("GoAnnDbBimap", contains="AnnDbBimap") ### Like "GoAnnDbBimap" but the right table is splitted in 3 parts. setClass("Go3AnnDbBimap", contains="GoAnnDbBimap", representation( rightTables="character" ) ) ### For a GOTermsAnnDbBimap object, the right values are GONode objects. setClass("GOTermsAnnDbBimap", contains="AnnDbBimap") ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Non reversible bimaps (hence we can just call them "maps"). ### setClass("AnnDbMap", contains="AnnDbBimap", representation( rightColType="character" ) ) setClass("IpiAnnDbMap", contains="AnnDbMap") ### We need 2 additional slots ('replace.single' and 'replace.multiple') to ### deal with silly maps ACCNUM/ENTREZID/MULTIHIT in the ### ARABIDOPSISCHIP_DB schema. These maps are complementary maps that both ### map probeset ids to AGI locus ids (note that the name of the maps doesn't ### help): in the ENTREZID map, probeset ids that have multiple matches are ### mapped to "multiple", and in the MULTIHIT map, probeset ids that have <= 1 ### match are mapped to NAs. Sooooo: ### - for ENTREZID: don't set replace.single (default is character(0)), ### use replace.multiple="multiple", ### - for MULTIHIT: use replace.single=NA, ### don't set replace.multiple (default is character(0)), setClass("AgiAnnDbMap", contains="AnnDbMap", representation( replace.single="character", replace.multiple="character" ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### probe Bimaps ### ### These classes is are needed so that we can more cleanly separate the probe ### mappings along with their more unusual Lkeys and Rkeys methods... setClass("ProbeAnnDbBimap", contains="AnnDbBimap") setClass("ProbeAnnDbMap", contains="AnnDbMap") setClass("ProbeIpiAnnDbMap", contains="IpiAnnDbMap") setClass("ProbeGo3AnnDbBimap", contains="Go3AnnDbBimap") ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### GoFrames ### ### for people who cannot have bimaps but need a way to pass around their data ### setClass("AnnotFrame", representation("VIRTUAL") ) ## For standard GO mappings. setClass("GOFrame", contains="AnnotFrame", representation(data="data.frame", organism="character"), prototype=prototype(organism="")) ## For 'GO 2 ALL' style mappings setClass("GOAllFrame", contains="GOFrame") ## For standard KEGG mappings. setClass("KEGGFrame", contains="AnnotFrame", representation(data="data.frame", organism="character"), prototype=prototype(organism="")) ############################################################################## ## Annotations will be the base virtual class for all the annotation packages ## in the project. .AnnotationDb <- setRefClass( "AnnotationDb", fields=list( conn="SQLiteConnection", packageName="character" ), methods = list(finalize = function() { if (RSQLite::dbIsValid(.self$conn)) RSQLite::dbDisconnect(.self$conn) }) ) .OrgDb <- setRefClass("OrgDb", contains="AnnotationDb") .ChipDb <- setRefClass("ChipDb", contains="AnnotationDb") .GODb <- setRefClass("GODb", contains="AnnotationDb") .ReactomeDb <- setRefClass("ReactomeDb", contains="AnnotationDb") .OrthologyDb <- setRefClass("OrthologyDb", contains = "AnnotationDb") AnnotationDbi/R/AllGenerics.R0000644000175200017520000001141114710217313017036 0ustar00biocbuildbiocbuild### Bimap interface ### (Please don't sort this section in alphabetical order) setGeneric("direction", function(x) standardGeneric("direction")) setGeneric("direction<-", signature="x", function(x, value) standardGeneric("direction<-")) setGeneric("revmap", function(x, ...) standardGeneric("revmap")) setGeneric("colmetanames", function(x) standardGeneric("colmetanames")) setGeneric("Lkeyname", function(x) standardGeneric("Lkeyname")) setGeneric("Rkeyname", function(x) standardGeneric("Rkeyname")) setGeneric("keyname", function(x) standardGeneric("keyname")) setGeneric("tagname", function(x) standardGeneric("tagname")) setGeneric("Rattribnames", function(x) standardGeneric("Rattribnames")) setGeneric("Rattribnames<-", signature="x", function(x, value) standardGeneric("Rattribnames<-")) setGeneric("Lkeys", function(x) standardGeneric("Lkeys")) setGeneric("Rkeys", function(x) standardGeneric("Rkeys")) setGeneric("keys", signature="x", function(x, keytype, ...) standardGeneric("keys")) setGeneric("Lkeys<-", signature="x", function(x, value) standardGeneric("Lkeys<-")) setGeneric("Rkeys<-", signature="x", function(x, value) standardGeneric("Rkeys<-")) setGeneric("keys<-", signature="x", function(x, value) standardGeneric("keys<-")) setGeneric("Llength", function(x) standardGeneric("Llength")) setGeneric("Rlength", function(x) standardGeneric("Rlength")) setGeneric("isNA", function(x) standardGeneric("isNA")) setGeneric("mappedLkeys", function(x) standardGeneric("mappedLkeys")) setGeneric("mappedRkeys", function(x) standardGeneric("mappedRkeys")) setGeneric("mappedkeys", function(x) standardGeneric("mappedkeys")) setGeneric("count.mappedLkeys", function(x) standardGeneric("count.mappedLkeys")) setGeneric("count.mappedRkeys", function(x) standardGeneric("count.mappedRkeys")) setGeneric("count.mappedkeys", function(x) standardGeneric("count.mappedkeys")) setGeneric("links", function(x) standardGeneric("links")) setGeneric("count.links", function(x) standardGeneric("count.links")) setGeneric("nhit", function(x) standardGeneric("nhit")) setGeneric("toggleProbes", signature="x", function(x, value) standardGeneric("toggleProbes")) setGeneric("hasMultiProbes", function(x) standardGeneric("hasMultiProbes")) setGeneric("hasSingleProbes", function(x) standardGeneric("hasSingleProbes")) setGeneric("getBimapFilters", function(x) standardGeneric("getBimapFilters")) setGeneric("toLList", function(x) standardGeneric("toLList")) setGeneric("toRList", function(x) standardGeneric("toRList")) setGeneric("toList", function(x) standardGeneric("toList")) setGeneric("GOFrame", function(x, organism) standardGeneric("GOFrame")) setGeneric("GOAllFrame", function(x) standardGeneric("GOAllFrame")) setGeneric("getGOFrameData", function(x) standardGeneric("getGOFrameData")) setGeneric("KEGGFrame", function(x, organism) standardGeneric("KEGGFrame")) setGeneric("getKEGGFrameData", function(x) standardGeneric("getKEGGFrameData")) setGeneric("GOID", function(object) standardGeneric("GOID")) setGeneric("Term", function(object) standardGeneric("Term")) setGeneric("Definition", function(object) standardGeneric("Definition")) setGeneric("Synonym", function(object) standardGeneric("Synonym")) setGeneric("Secondary", function(object) standardGeneric("Secondary")) ### Others (do whatever you want with them ;-) setGeneric("taxonomyId", function(x) standardGeneric("taxonomyId")) setGeneric("dbmeta", signature="x", function(x, name) standardGeneric("dbmeta")) setGeneric("dbschema", signature="x", function(x, file="", show.indices=FALSE) standardGeneric("dbschema")) setGeneric("dbInfo", function(x) standardGeneric("dbInfo")) setGeneric("Ltablename", function(x) standardGeneric("Ltablename")) setGeneric("Rtablename", function(x) standardGeneric("Rtablename")) setGeneric("Lfilter", function(x) standardGeneric("Lfilter")) setGeneric("Rfilter", function(x) standardGeneric("Rfilter")) setGeneric("flatten", function(x, ...) standardGeneric("flatten")) setGeneric("orgPackageName", function(x, ...) standardGeneric("orgPackageName")) ## AnnotationDb setGeneric("saveDb", signature="x", function(x, file) standardGeneric("saveDb")) ## Don't do this. There is already a dbconn() method. So use that one. ##setGeneric("dbConn", function(x) standardGeneric("dbConn")) setGeneric("packageName", function(x) standardGeneric("packageName")) setGeneric("columns", signature="x", function(x) { value <- standardGeneric("columns") sort(value) }) setGeneric("keytypes", signature="x", function(x) { value <- standardGeneric("keytypes") sort(value) }) setGeneric("select", signature="x", function(x, keys, columns, keytype, ...) standardGeneric("select")) setGeneric("mapIds", signature="x", function(x, keys, column, keytype, ..., multiVals) standardGeneric("mapIds")) AnnotationDbi/R/AnnDbObj-lowAPI.R0000644000175200017520000002516114710217313017423 0ustar00biocbuildbiocbuild### ========================================================================= ### Low-level API for AnnDbObj objects ### ---------------------------------- ### ### The "AnnDbObj" class is a general purpose container for SQLite-based ### annotation data (refer to AllClasses.R for the definition of the "AnnDbObj" ### class and its derived classes). ### ### This file defines and implements the low-level API for AnnDbObj objects. ### This API has the following regular function: ### showQCData ### This API consists of the following set of generics: ### dbconn, ### dbfile, ### dbmeta, ### dbschema, ### dbInfo, ### Ltablename, Rtablename, ### Lfilter, Rfilter, ### flatten, ### show ### ### The environment-like API for Bimap objects (ls, mget, etc...) is defined ### in the Bimap-envirAPI.R file. ### ### ------------------------------------------------------------------------- ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "showQCData" function. ### ## I need this function to see what mappings exist and only report if ## they DO exist. But I DO want to use the mappings in addition to ## the map_counts table (because otherwise I have not verified that ## they exist and only looked that the map_counts expect them to ## exist). showQCData <- function(prefix, datacache){ cat(paste0("Quality control information for ", prefix, ":\n\n\n")) map_counts <- createMAPCOUNTS(dbconn(datacache), prefix) map_counts <- map_counts[!grepl('PFAM$', names(map_counts)) & !grepl('PROSITE$', names(map_counts))] cat("This package has the following mappings:\n\n") for(i in seq_len(length(map_counts))){ mapname <- names(map_counts)[i] map <- mget(mapname,inherits=TRUE,ifnotfound=NA) if(!is.na(map)[[1]]){ cat(mapname, "has", map_counts[i], "mapped keys (of", length(map[[1]]), "keys)\n") } } cat("\n\nAdditional Information about this package:\n\n") cat(paste0("DB schema: ",dbmeta(datacache, 'DBSCHEMA'), "\n")) cat(paste0("DB schema version: ",dbmeta(datacache, 'DBSCHEMAVERSION'), "\n")) ## Things to check for (may or may not be in some packages) meta = list( "ORGANISM" = "Organism: ", "EGSOURCEDATE" ="Date for NCBI data: ", "GOSOURCEDATE" = "Date for GO data: ", "KEGGSOURCEDATE" = "Date for KEGG data: ", "GPSOURCEDATE" = "Date for Golden Path data: ", ## "IPISOURCEDATE" = "Date for IPI data: ", "TAIRSOURCEDATE" = "Data for TAIR data: ", "YGSOURCEDATE" = "Date for SGD data: ", "FBSOURCEDATE" = "Date for Flybase data: ", "ENSOURCEDATE" = "Date for Ensembl data: " ) for(i in 1:length(meta)){ test = 0 test = try( dbmeta(datacache, names(meta)[i]),silent=TRUE ) if(inherits(test,"try-error")){ test = 0 } if(test != 0){ cat(meta[[i]], dbmeta(datacache, names(meta)[i]), "\n", sep="") } } } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "dbconn" methods. ### setMethod("dbconn", "environment", function(x) get("dbconn", envir=x)) setMethod("dbconn", "AnnDbObj", function(x) dbconn(x@datacache)) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "dbfile" methods. ### setMethod("dbfile", "environment", function(x) get("dbfile", envir=x)) setMethod("dbfile", "AnnDbObj", function(x) dbfile(dbconn(x))) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "dbmeta" methods. ### setMethod("dbmeta", "DBIConnection", function(x, name) { if (!is.character(name) || length(name) != 1 || is.na(name)) stop("'name' must be a non-NA character string") name <- toSQLStringSet(name) SQL <- paste0("SELECT value FROM metadata WHERE name=", name) value <- dbQuery(x, SQL, 1) if (length(value) == 0) stop("meta ", name, " not found") if (length(value) != 1) stop("more than 1 meta found for ", name, " in metadata table (bad table)") value } ) setMethod("dbmeta", "environment", function(x, name) dbmeta(dbconn(x), name)) setMethod("dbmeta", "AnnDbObj", function(x, name) dbmeta(x@datacahe, name)) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "dbschema" methods. ### setMethod("dbschema", "DBIConnection", function(x, file="", show.indices=FALSE) { schema <- dbmeta(x, "DBSCHEMA") version <- dbmeta(x, "DBSCHEMAVERSION") file <- system.file("DBschemas", paste0("schemas_", version), paste0(schema, ".sql"), package="AnnotationDbi") lines <- readLines(file) if (!show.indices) { ## Remove the CREATE INDEX lines createIndexStart <- "CREATE INDEX" createIndexEnd <- ";" ii <- which(substr(lines, 1, nchar(createIndexStart)) == createIndexStart & substr(lines, nchar(lines)-nchar(createIndexEnd)+1, nchar(lines)) == createIndexEnd) ii <- setdiff(ii, grep(createIndexEnd, substr(lines, 1, nchar(lines)-nchar(createIndexEnd)), fixed=TRUE)) ## Remove comments preceding the CREATE INDEX blocks beforeLastBlock <- function(ii, i) { while ((i >= 1) && !(i %in% ii)) i <- i - 1 while ((i >= 1) && (i %in% ii)) i <- i - 1 i } i <- max(ii) while (i >= 1) { i <- beforeLastBlock(ii, i) while (i >= 1) { if (substr(lines[i], 1, 2) != "--") break ii <- c(i, ii) i <- i - 1 } } lines <- lines[-ii] } ## ## Remove empty trailing lines ## ii <- integer(0) ## i <- length(lines) ## while ((i >= 1) && (lines[i] == "")) { ## ii <- c(i, ii) ## i <- i - 1 ## } ## lines <- lines[-ii] cat(lines, sep="\n") } ) setMethod("dbschema", "environment", function(x, file="", show.indices=FALSE) dbschema(dbconn(x), file=file, show.indices=show.indices)) setMethod("dbschema", "AnnDbObj", function(x, file="", show.indices=FALSE) dbschema(x@datacache, file=file, show.indices=show.indices)) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "dbInfo" methods. ### setMethod("dbInfo", "DBIConnection", function(x) { dbGetTable(x, "metadata") } ) setMethod("dbInfo", "environment", function(x) dbInfo(dbconn(x))) setMethod("dbInfo", "AnnDbObj", function(x) dbInfo(x@datacache)) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "Ltablename", "Rtablename", "Lfilter" and "Rfilter" methods. ### ### They do NOT access the database! ### setMethod("Ltablename", "AnnDbBimap", function(x) L2Rchain.Ltablename(x@L2Rchain)) setMethod("Rtablename", "AnnDbBimap", function(x) L2Rchain.Rtablename(x@L2Rchain)) setMethod("Rtablename", "Go3AnnDbBimap", function(x) x@rightTables) setMethod("Lfilter", "AnnDbBimap", function(x) L2Rchain.Lfilter(x@L2Rchain)) setMethod("Rfilter", "AnnDbBimap", function(x) L2Rchain.Rfilter(x@L2Rchain)) ### ========================================================================= ### The "flatten" methods ### --------------------- ### ### Note that because we use the same JOIN for a map and its corresponding ### "reverse" map (this is made possible thanks to the use of INNER joins), ### then the result returned by "flatten" or "nrow" does not depend on the ### direction (direct/reverse) of the map which is a nice property ### (e.g. 'nrow(map) == nrow(revmap(map))'). ### ### The 'Lkeys' and 'Rkeys' args can be one of the following: ### - NULL: the arg is ignored. ### - A NA-free character vector: only the rows with a "left key" (1st ### field) matching one of the keys in 'Lkeys' and a "right key" ### (2nd field) matching one of the keys in 'Rkeys' are ### retrieved. ### Note that the 'Lkeys' and 'Rkeys' args are _not_ checked i.e. ### only NULL and NA-free character vectors are guaranted to work properly. ### ### CURRENTLY BROKEN! #setMethod("flatten", "AnnDbTable", # function(x) # { # dbRawAnnDbMapToTable(dbconn(x), Ltablename(x), Lkeyname(x), Lkeys, # NULL, NULL, NULL, # x@showCols, x@from) # } #) setMethod("flatten", "AnnDbBimap", function(x, fromKeys.only=FALSE) { data0 <- dbSelectFromL2Rchain(dbconn(x), x@L2Rchain, x@Lkeys, x@Rkeys) Lkeys <- Rkeys <- as.character(NA) if (!fromKeys.only || direction(x) == 1) Lkeys <- Lkeys(x) if (!fromKeys.only || direction(x) == -1) Rkeys <- Rkeys(x) new("FlatBimap", colmetanames=colmetanames(x), direction=direction(x), data=data0, Lkeys=Lkeys, Rkeys=Rkeys) } ) ### This method needs to retrieve and bind data from the 3 GO tables. ### Binding the results of the 3 SELECTs can be done early in SQLite with ### a UNION: ### dbGetQuery("query1 UNION query2 UNION query3") ### or later in R with rbind(): ### rbind(dbGetQuery("query1"), dbGetQuery("query2"), dbGetQuery("query3")) ### Surprisingly the latter is almost twice faster than the former! setMethod("flatten", "Go3AnnDbBimap", function(x, fromKeys.only=FALSE) { getPartialSubmap <- function(ontology) { tablename <- Rtablename(x)[ontology] L2Rchain <- makeGo3L2Rchain(x@L2Rchain, tablename, ontology) dbSelectFromL2Rchain(dbconn(x), L2Rchain, x@Lkeys, x@Rkeys) } data0 <- rbind(getPartialSubmap("BP"), getPartialSubmap("CC"), getPartialSubmap("MF")) Lkeys <- Rkeys <- as.character(NA) if (!fromKeys.only || direction(x) == 1) Lkeys <- Lkeys(x) if (!fromKeys.only || direction(x) == -1) Rkeys <- Rkeys(x) new("FlatBimap", colmetanames=colmetanames(x), direction=direction(x), data=data0, Lkeys=Lkeys, Rkeys=Rkeys) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "show" method. ### setMethod("show", "AnnDbTable", function(object) { cat(object@objName, " table for ", object@objTarget, " (object of class \"", class(object), "\")\n", sep="") } ) AnnotationDbi/R/AnnDbPkg-checker.R0000644000175200017520000002722014710217313017701 0ustar00biocbuildbiocbuild### ========================================================================= ### AnnDbPkg checking functions ### --------------------------- ### ### Some functions for checking SQLite-based ann packages. ### ### ------------------------------------------------------------------------- ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "checkProperty0" function. ### ### Check that Property0 is satisfied on a given package (see FlatBimap.R ### file for more info). ### checkProperty0 <- function(pkgname) { mths <- Bimap_methods ## Temporary remove these 2 methods, they are not yet implemented ## for AnnDbBimap objects mths <- mths[!(mths %in% c("links", "count.links"))] # temporary removal ## First we check that there is a generic for all the expected Bimap ## methods and that this generic has indeed a corresponding method for ## Bimap objects. for (FUN in mths) { if (!isGeneric(FUN)) stop("AnnotationDbi problem: \"", FUN, "\" should be a generic") fdef <- getGeneric(FUN) classes <- ls(get(".MTable", envir = environment(fdef)), all.names=TRUE) if (!any(sapply(classes, function(class) extends(class, "Bimap")))) stop("AnnotationDbi problem: can't find a \"", FUN, "\" method for Bimap objects") } ## Then we check #pkgenv <- asNamespace(pkgname) # so it works also if the pkg has no NAMESPACE pkgenv <- as.environment(paste("package", pkgname, sep=":")) for (objname in ls(pkgenv)) { x <- pkgenv[[objname]] if (!is(x, "AnnDbBimap")) next cat("Testing Bimap methods on object '", objname, "':\n", sep="") for (FUN in mths) { cat(" - method: \"", FUN, "\"... ", sep="") fdef <- get(FUN) y1 <- fdef(x) y2 <- fdef(flatten(x)) if (!identical(y1, y2)) stop(FUN, "(x) and ", FUN, "(flatten(x)) are not identical") cat("OK\n") } } } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "checkMAPCOUNTS" function. ### ### Typical use: ### > checkMAPCOUNTS("hgu95av2.db") ### checkMAPCOUNTS <- function(pkgname) { require(pkgname, character.only=TRUE) || stop(pkgname, " package needed") if (substr(pkgname, nchar(pkgname) - 2, nchar(pkgname)) != ".db") stop(pkgname, " doesn't look like the name of an SQLite-based annotation package") prefix <- substr(pkgname, 1, nchar(pkgname) - 3) getMap <- function(mapname) get(mapname, envir=asNamespace(pkgname)) MAPCOUNTS <- getMap(paste0(prefix, "MAPCOUNTS")) ## remove defunct MAPCOUNTS MAPCOUNTS <- MAPCOUNTS[!grepl('PFAM$', names(MAPCOUNTS)) & !grepl('PROSITE$', names(MAPCOUNTS))] ## Then continue for (mapname in names(MAPCOUNTS)) { cat("Counting mapped keys for map ", mapname, ":\n", sep="") map <- getMap(mapname) map_length <- length(map) cat(" - length(map) = ", map_length, "\n", sep="") ## count0 count0 <- MAPCOUNTS[mapname] cat(" - MAPCOUNTS[\"", mapname, "\"] = ", count0, "\n", sep="") if (is(map, "AgiAnnDbMap") && mappedLkeysIsNotAvailable(map)) { ## count.mappedkeys and mappedkeys are not available for silly map MULTIHIT cat(" - count1 = not available for this map ==> SKIPPED!\n") cat(" - count2 = not available for this map ==> SKIPPED!\n") } else { ## count1 if (is.vector(map) && is.null(names(map))) # to deal with the REJECTORF case t1 <- system.time(count1 <- sum(!is.na(map))) else t1 <- system.time(count1 <- count.mappedkeys(map)) cat(" - count1 = ", count1, " (", t1[3], " s)\n", sep="") if (count1 != count0) stop("count1 and count0 differ") if (is.vector(map) && is.null(names(map))) next ## count2 t2 <- system.time(count2 <- length(mappedkeys(map))) cat(" - count2 = ", count2, " (", t2[3], " s)\n", sep="") if (count2 != count0) stop("count2 and count0 differ") if (is(map, "IpiAnnDbMap") || is(map, "GOTermsAnnDbBimap")) next } ## count3 if(map_length == 0){ count3 <- 0 t3 <- 0 }else{ t3 <- system.time(count3 <- sum(sapply(as.list(map), function(x) length(x)!=1 || !is.na(x)))) } cat(" - count3 = ", count3, " (", t3[3], " s)\n", sep="") if (count3 != count0) stop("count3 and count0 differ") } } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "compareAnnDataIn2Pkgs" function. ### ### The identical.uulists function is a replacement for setequal when ### used on "uulists". ### Conceptually, a "uulist" is an unordered, unamed list. 2 uulists ### are identical if they contain the same elements, possibly in ### different orders, with different outer names and with different number ### of occurences for any given element. 2 elements are considered to be ### the same if they are strictly identical (identical(e1, e2) is TRUE). ### setequal(x, y) checks that all elts in x are also in y and that all ### elts in y are also in x. It works for atomic vectors and lists. ### For example, setequal is TRUE for: ### x <- list(a=2:3, 5) ### y <- list(c(b='5'), 2:3, 2:3) ### But the comparison between elements ignore their types, their outer names ### ("a" in x) and their inner names ("b" in y)! ### With identical.uulists: ### x <- list(a=2:3, 5, 5) # setequal(x, y) identical.uulists(x, y) ### y <- list(5, 2:3, 2:3) # TRUE TRUE ### y <- list(c(b=5), 2:3, 2:3) # TRUE FALSE ### y <- list(5, 2:3, c(2,3)) # TRUE FALSE identical.uulists <- function(x, y) { ## Quick and dirty implementation (inefficient) XeltsAreInY <- function(x, y) { all(sapply(x, function(ex) any(sapply(y, function(ey) identical(ex, ey))))) } XeltsAreInY(x, y) && XeltsAreInY(y, x) } ### x and y must be collections. ### A collection can be a NULL, an unamed atomic vectors, ### a named atomic vectors, an unamed lists or a named list. ### Will ignore duplicated elements in the collections. identical.collections <- function(x, y) { ## If x and y have different types _and_ at least one of them is not a ## single NA then we return FALSE. if (typeof(x) != typeof(y) && (length(x) != 1 || !is.na(x) || length(y) != 1 || !is.na(y))) return(FALSE) ## Now we can assume that x and y have the same type _except_ if ## they are both NAs (and in this case we can't just return TRUE ## because we need to compare the names too). nmx <- names(x) nmy <- names(y) if (is.null(nmx) != is.null(nmy)) return(FALSE) if (is.null(nmx)) { if (is.list(x)) return(identical.uulists(x, y)) else return(setequal(x, y)) } if (!setequal(nmx, nmy)) return(FALSE) nm0 <- unique(nmx) for (nm in nm0) { x1 <- x[nmx %in% nm] y1 <- y[nmy %in% nm] if (is.list(x1)) { if (!identical.uulists(x1, y1)) return(FALSE) } else { if (!setequal(x1, y1)) return(FALSE) } } return(TRUE) } ### "compareAnnDataIn2Pkgs" compares the annotation data between 2 packages. ### We use it to validate our SQLite-based ann packages by comparing each of ### them to its envir-based sibling package e.g.: ### > library(AnnotationDbi) ### > AnnotationDbi:::compareAnnDataIn2Pkgs("hgu95av2", "hgu95av2.db", "hgu95av2") ### compareAnnDataIn2Pkgs <- function(pkgname1, pkgname2, prefix, quick=FALSE, verbose=FALSE) { require(pkgname1, character.only=TRUE) || stop(pkgname1, " package needed") require(pkgname2, character.only=TRUE) || stop(pkgname2, " package needed") getMap <- function(pkgname, mapname) { get(mapname, envir=as.environment(paste("package", pkgname, sep=":")), inherits=FALSE) } maps1 <- names(getMap(pkgname1, paste0(prefix, "MAPCOUNTS"))) maps2 <- names(getMap(pkgname2, paste0(prefix, "MAPCOUNTS"))) notin2 <- setdiff(maps1, maps2) if (length(notin2) != 0) { cat("Maps in ", pkgname1, "::", prefix, "MAPCOUNTS", " not in ", pkgname2, "::", prefix, "MAPCOUNTS:\n", sep="") cat(" ", paste(notin2, collapse=", "), "\n\n", sep="") } notin1 <- setdiff(maps2, maps1) if (length(notin1) != 0) { cat("Maps in ", pkgname2, "::", prefix, "MAPCOUNTS", " not in ", pkgname1, "::", prefix, "MAPCOUNTS:\n", sep="") cat(" ", paste(notin1, collapse=", "), "\n\n", sep="") } maps <- intersect(maps1, maps2) mismatch_summary <- list() for (mapname in maps) { cat("*** Comparing ", mapname, " maps:\n", sep="") map1 <- getMap(pkgname1, mapname) cat("*** map1 is ", mapname, " from package ", pkgname1, "\n", sep="") map2 <- getMap(pkgname2, mapname) cat("*** map2 is ", mapname, " from package ", pkgname2, "\n", sep="") ## Compare lengths length1 <- length(map1) mapped_keys1 <- mappedkeys(map1) count1 <- length(mapped_keys1) cat("*** length(map1) = ", length1, " (", count1, " mapped keys)\n", sep="") length2 <- length(map2) mapped_keys2 <- mappedkeys(map2) count2 <- length(mapped_keys2) cat("*** length(map2) = ", length2, " (", count2, " mapped keys)\n", sep="") common_keys <- intersect(ls(map1), ls(map2)) common_mapped_keys <- intersect(mapped_keys1, mapped_keys2) count3 <- length(common_mapped_keys) cat("*** nb of common keys = ", length(common_keys), " (", count3, " common mapped keys)\n", sep="") if (count3 == 0) { cat("*** ==> NOTHING WORTH COMPARING!\n") mismatch_summary[[mapname]] <- NA next } if (quick) { ## Quick test (on a sample of 50 common mapped keys) size <- 50L if (size > count3) size <- count3 random_keys <- sample(common_mapped_keys, size) submap1 <- mget(random_keys, envir=map1) if (!identical(names(submap1), random_keys)) stop("mget() didn't return the expected keys on map1") submap2 <- mget(random_keys, envir=map2) if (!identical(names(submap2), random_keys)) stop("mget() didn't return the expected keys on map2") OK <- sapply(random_keys, function(key) identical.collections(map1[[key]], map2[[key]])) nmis <- sum(!OK) cat("*** nb of mismatches (on a sample of ", size, " keys) = ", nmis, "\n", sep="") } else { ## Full test (on all common keys) OK <- sapply(common_keys, function(key) identical.collections(map1[[key]], map2[[key]])) nmis <- sum(!OK) cat("*** nb of mismatches = ", nmis, "\n", sep="") } mismatch_summary[[mapname]] <- nmis } mismatch_summary <- unlist(mismatch_summary) nb_PASSED <- sum(mismatch_summary == 0, na.rm=TRUE) nb_FAILED <- length(mismatch_summary) - nb_PASSED cat("SUMMARY OF MISMATCHES:\n") show(mismatch_summary) cat(" - nb of map comparisons = ", length(mismatch_summary), "\n", sep="") cat(" - nb of PASSED maps = ", nb_PASSED, "\n", sep="") cat(" - nb of FAILED maps = ", nb_FAILED, "\n", sep="") mismatch_summary } AnnotationDbi/R/AnnDbPkg-templates-common.R0000644000175200017520000000631714710217313021565 0ustar00biocbuildbiocbuild### The functions below are shared across all SQLite-based ann data packages. ### They're centralized here and used in the templates of the ann data ### packages instead of being redefined over and over in every templates. ### Used at load time (in .onLoad) by the SQLite-based ann data package to ### dynamically add exported symbols to its namespace environment. .kosherPkg <- function(pkgname){ if(pkgname %in% c('PFAM.db','mpedbarray.db','pedbarrayv9.db', 'pedbarrayv10.db','humanCHRLOC','mouseCHRLOC', 'ratCHRLOC')){ return(FALSE) }else{ return(TRUE) } } addToNamespaceAndExport <- function(x, value, pkgname) { prefix <- sub('.db','',pkgname) dc <- eval(parse(text=paste0(pkgname,":::datacache"))) warnIfDep <- function(){ if(grepl("CHR$",x)){ bimapName <- paste0(prefix,"CHR") }else if(grepl("CHRLENGTHS$",x)){ bimapName <- paste0(prefix,"CHRLENGTHS") }else if(grepl("CHRLOC$",x)){ bimapName <- paste0(prefix,"CHRLOC") }else if(grepl("CHRLOCEND$",x)){ bimapName <- paste0(prefix,"CHRLOCEND") } x <- dc[[bimapName]] x } warnIfDef <- function(){ if(grepl("PFAM",x)){ bimapName <- paste0(prefix,"PFAM") }else{ bimapName <- paste0(prefix,"PROSITE") } x <- dc[[bimapName]] msg = wmsg(paste0(bimapName, " is defunct. ", "Please use select() if you need access to PFAM or PROSITE accessions. \n")) if(interactive()){ stop(msg) } } ns <- asNamespace(pkgname) ## Uncomment after the release if(grepl("CHR",x) && .kosherPkg(pkgname)){ assign(x, value, envir=dc) ## stash it, for later retrieval makeActiveBinding(sym=x, fun=warnIfDep, env=ns) }else if(any(grepl("PFAM",x), grepl("PROSITE",x)) && .kosherPkg(pkgname)){ assign(x, value, envir=dc) ## stash it makeActiveBinding(sym=x, fun=warnIfDef, env=ns) }else{ assign(x, value, envir=ns) ## Older way of doing this. } namespaceExport(ns, x) } mergeToNamespaceAndExport <- function(envir, pkgname) { keys <- ls(envir, all.names=TRUE) for (key in keys) addToNamespaceAndExport(key, envir[[key]], pkgname) } ## debug(AnnotationDbi:::mergeToNamespaceAndExport); ## debug(AnnotationDbi:::addToNamespaceAndExport); ## library(org.Hs.eg.db) ## I am stuck on how to use makeActiveBinding() correctly ## It's clear I need to use it INSTEAD of assign(). But the problem ## is that x is currently pointing to a character vector and no value is available for ## So basically, I think that warnIf needs to re-run the code that ## produces the symbols (so as to re-create them on the fly). BUT: I ## can't do that without a mountain of refactoring (templating system ## is in way). ## SO: I need a way to stash the initial envs so that I can read them ## in later on... (Save the initial env as well as the key names). ## BUT: if I have to do that, how can I hide the envir with the ## goodies in it? Anonymous env? ## new.env(parent=emptyenv()) ## Hervé reminded me that we have this datacache env already. So I will just use that... ## AnnotationDbi/R/Bimap-envirAPI.R0000644000175200017520000001614514710217313017362 0ustar00biocbuildbiocbuild### ========================================================================= ### Environment-like API for AnnDbBimap objects ### ------------------------------------------- ### ### This file defines an environment-like API for the AnnDbBimap objects (ls, ### mget, eapply, get, exists, [[ and $) for backward compatibility with the ### classic envir-based annotation maps. ### This environment-like API is defined on top of the low-level API for ### AnnDbObj objects (refer to AnnDbObj-lowAPI.R for the definition of this ### low-level API). ### ### Notes: ### - The "length" method is not redefined here since it is considered to ### belong to the low-level API. ### - The "sample" method is not part of the "real" environment API. ### ### ------------------------------------------------------------------------- ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "ls" new generic. ### .ls <- function(name, pattern, sorted){ keys <- keys(name) if (!missing(pattern)) keys <- keys[grep(pattern, keys)] if (sorted) keys <- sort(keys) keys } setMethod("ls", signature(name="Bimap"), function(name, pos=-1L, envir=as.environment(pos), all.names=FALSE, pattern, sorted=TRUE){ if (!missing(pos)) warning("ignoring 'pos' argument") if (!missing(envir)) warning("ignoring 'envir' argument") if (!missing(all.names)) warning("ignoring 'all.names' argument") .ls(name, pattern, sorted) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### "mget" methods. ### ### 'mget(x, map)' vs 'as.list(map)': ### 1. mget checks its 'x' arg. and gracefully fails if it's not of ### the expected type (i.e. NULL or NA-free character vector), ### 2. 'mget(keys(map), map)' is identical to 'as.list(map)'. ### Note that for a real "environment", 'as.list(envir)' is not identical ### to 'mget(ls(envir), envir)': the 2 lists have the same elements but ### not necesarily in the same order! setMethod("mget", signature(x="ANY", envir="Bimap"), function(x, envir, mode, ifnotfound, inherits) { if (missing(ifnotfound)) { ifnotfound <- list() } else { if (!is.vector(ifnotfound) || length(ifnotfound) != 1 || !is.na(ifnotfound)) stop("only NA is currently supported for 'ifnotfound'") ifnotfound <- as.list(ifnotfound) } keys0 <- keys(envir) envir@ifnotfound <- ifnotfound keys(envir) <- x ans <- as.list(envir) if (length(ifnotfound) == 0) return(ans) ans[!(names(ans) %in% keys0)] <- ifnotfound ans } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "eapply" new generic. ### setMethod("eapply", signature(env="Bimap"), function(env, FUN, ..., all.names = FALSE, USE.NAMES = TRUE) { lapply(as.list(env), FUN, ...) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### "get" methods. ### ### We want this: ### get("1027_at", envir=hgu95av2GO) ### and this ### get("1027_at", hgu95av2GO) ### to work so we need to dispatch on the 'pos' arg too. ### .get <- function(what, map) mget(what[1], map)[[1]] setMethod("get", signature(x="ANY", pos="ANY", envir="Bimap"), function(x, pos, envir, mode, inherits) { .get(x, envir) } ) setMethod("get", signature(x="ANY", pos="Bimap", envir="missing"), function(x, pos, envir, mode, inherits) { .get(x, pos) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "exists" new generic. ### ### We want this: ### exists("1027_at", envir=hgu95av2GO) ### and this ### exists("1027_at", hgu95av2GO) ### to work so we need to dispatch on the 'where' arg too. ### ### Like the original "exists" function for environment objects, our "exists" ### methods only use the first element of 'x'. But unlike the original, our ### methods will raise an error if this first element is a character NA. ### .exists <- function(x, map) { if (!is.character(x) || length(x) == 0 || x[1] %in% c(NA, "")) stop("invalid first argument") x[1] %in% keys(map) } setMethod("exists", signature(x="ANY", where="ANY", envir="Bimap"), function(x, where, envir, frame, mode, inherits) { .exists(x, envir) } ) setMethod("exists", signature(x="ANY", where="Bimap", envir="missing"), function(x, where, envir, frame, mode, inherits) { .exists(x, where) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "[[" and "$" generics. ### .doubleBracketSub <- function(x, i, j, ...) { subscripts <- list(...) if (!missing(i)) subscripts$i <- i if (!missing(j)) subscripts$j <- j # At this point, 'subscripts' should be guaranteed # to be of length <= 1 if (length(subscripts) == 0) stop("no index specified") i <- subscripts[[1]] if (length(i) < 1) stop("attempt to select less than one element") if (length(i) > 1) stop("attempt to select more than one element") if (!is.character(i) || is.na(i)) stop("wrong argument for subsetting an object of class ", sQuote(class(x))) val <- mget(i, envir=x, ifnotfound=NA)[[1]] # We could just do '!(i %in% keys(x))' but checking 'identical(val, NA)' # first is very cheap and will fail most of the time thus preventing # evaluation of '!(i %in% keys(x))' which is a lot more expensive. if (identical(val, NA) && !(i %in% keys(x))) val <- NULL val } setMethod("[[", "Bimap", function(x, i, j, ...){ # 'x' is guaranteed to be a "Bimap" object (if it's not, then the # method dispatch algo will not call this method in the first place), # so nargs() is guaranteed to be >= 1 if (nargs() >= 3) stop("too many subscripts") .doubleBracketSub(x, i, j, ...) } ) setMethod("$", "Bimap", function(x, name) x[[name]]) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### "contents" methods. ### ### The "contents" method for environment objects is defined in Biobase. ### setMethod("contents", "Bimap", function(object, all.names) { msg <- c("The contents() method for Bimap objects is deprecated. ", "Please use as.list() instead.") .Deprecated(msg=c(" ", wmsg(msg))) if (!missing(all.names)) warning("ignoring 'all.names' argument") as.list(object) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "sample" new generic. ### .sample <- function(x, size, replace, prob) { keys <- ls(x) keys <- keys[sample(length(keys), size, replace, prob)] mget(keys, x) } setMethod("sample", "Bimap", function(x, size, replace=FALSE, prob=NULL) .sample(x, size, replace, prob) ) setMethod("sample", "environment", function(x, size, replace=FALSE, prob=NULL) .sample(x, size, replace, prob) ) AnnotationDbi/R/Bimap.R0000644000175200017520000011760514710217313015712 0ustar00biocbuildbiocbuild### ========================================================================= ### The bimap concept and the Bimap interface ### ----------------------------------------- ### The bimap concept ### ----------------- ### ### A bimap is made of: ### ### - 2 sets of objects: the left objects and the right objects. All the ### objects have a name and this name is unique in each set (i.e. in the ### left set and in the right set). The names of the left (resp. right) ### objects are called the left (resp. right) keys or the Lkeys (resp. the ### Rkeys). ### ### - Any number of links (edges) between the left and right objects. Note ### that the links can be tagged. In our model, for a given bimap, either ### none or all the links are tagged. ### ### In other words, a bimap is a bipartite graph. ### ### Here are some examples: ### ### 1. bimap B1: ### ### 4 left objects (Lkeys): "a", "b", "c", "d" ### 3 objects on the right (Rkeys): "A", "B", "C" ### ### Links (edges): ### "a" <--> "A" ### "a" <--> "B" ### "b" <--> "A" ### "d" <--> "C" ### ### Note that: ### - There can be any number of links starting from or ending at a ### given object. ### - The links in this example are untagged. ### ### 2. bimap B2: ### ### 4 left objects (Lkeys): "a", "b", "c", "d" ### 3 objects on the right (Rkeys): "A", "B", "C" ### ### Tagged links (edges): ### "a" <-"x"-> "A" ### "a" <-"y"-> "B" ### "b" <-"x"-> "A" ### "d" <-"x"-> "C" ### "d" <-"y"-> "C" ### ### Note that there are 2 links between objects "d" and "C": ### 1 with tag "x" and 1 with tag "y". ### ### ### Flat representation of a bimap ### ------------------------------ ### ### The flat representation of a bimap is a data frame. For example, ### for B1, it is: ### ### left right ### a A ### a B ### b A ### d C ### ### If in addition the right objects have 1 multi-valued attribute, for ### example, a numeric vector: ### ### A <-- c(1.2, 0.9) ### B <-- character(0) ### C <-- -1:1 ### ### then the flat representation of B1 becomes: ### ### left right Rattrib1 ### a A 1.2 ### a A 0.9 ### a B NA ### b A 1.2 ### b A 0.9 ### d C -1 ### d C 0 ### d C 1 ### ### Note that now the number of rows is greater than the number of links! ### ### ### The Bimap interface in AnnotationDbi ### ------------------------------------ ### ### AnnDbBimap and FlatBimap objects: ### ### A AnnDbBimap object is a bimap whose data are stored in a data base. ### A FlatBimap object is a bimap whose data (left keys, right keys and ### links) are stored in memory (in a data frame for the links). ### Conceptually, AnnDbBimap and FlatBimap objects are the same (only ### their internal representation differ) so it's natural to try to define ### a set of methods that make sense for both (so they can be manipulated ### in a similar way). This common interface is the Bimap interface. ### ### The "flatten" generic: ### ### flatten(x) converts AnnDbBimap object x into FlatBimap object y ### with no loss of information ### ### Note that a FlatBimap object can't be converted into an AnnDbBimap ### object (well, in theory maybe it could be, but for now the data bases ### we use to store the data of the AnnDbBimap objects are treated as ### read-only). This conversion from AnnDbBimap to FlatBimap is performed ### by the "flatten" generic function (with methods for AnnDbBimap objects ### only). ### ### Property0: ### ### The "flatten" generic plays a very useful role when we need to ### understand or explain exactly what a given Bimap method f will do when ### applied to an AnnDbBimap object. It's generally easier to explain what ### it does on a FlatBimap object and then to just say "and it does the ### same thing on a AnnDbBimap object". This is exactly what Property0 ### says: ### ### for any AnnDbBimap object x, f(x) is expected to be indentical ### to f(flatten(x)) ### ### Of course, this implies that the f method for AnnDbBimap objects ### return the same type of object than the f method for FlatBimap objects. ### In this sense, the "revmap" and "subset" Bimap methods are particular ### because they are expected to return an object of the same class as ### their argument x, so f(x) can't be identical to f(flatten(x)). For ### these methods, Property0 says: ### ### for any AnnDbBimap object x, flatten(f(x)) is expected to ### be identical to f(flatten(x)) ### ### The checkProperty0() function (AnnDbPkg-checker.R file) checks that ### Property0 is satisfied on all the AnnDbBimap objects defined in a given ### package (FIXME: checkProperty0 is currently broken). ### ### Finally, note that both AnnDbBimap and FlatBimap objects have a read-only ### semantic: the user can subset them but cannot change their data. ### ### ------------------------------------------------------------------------- ### KEEP THIS IN SYNC WITH THE STATE OF AFFAIRS! Only methods of the first and ### second group go here. Bimap_methods <- c( ## GROUP 1: 15 methods that _must_ be defined for FlatBimap objects ## _and_ AnnDbBimap objects "colnames", "colmetanames", "Rattribnames<-", "direction", "direction<-", "Lkeys", "Rkeys", "Lkeys<-", "Rkeys<-", "subset", "mappedLkeys", "mappedRkeys", "nrow", "links", "toLList", "toRList", ## GROUP 2: Methods for which a default is provided (in this file) but ## some of them are redefined for AnnDbBimap objects to obtain better ## performance "Lkeyname", "Rkeyname", "tagname", "Rattribnames", "revmap", "Llength", "Rlength", "count.mappedLkeys", "count.mappedRkeys", "count.links", ## GROUP 3: Directed methods (i.e. what they return depends on the ## direction of the map). All what they do is to dispatch on the ## corresponding undirected method according to the value of direction(x) "keyname", "keys", "length", "mappedkeys", "count.mappedkeys", "toList", "isNA" ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "direction" and "direction<-" methods. ### .DIRECTION_STR2INT <- c("L --> R"=1L, "L <-- R"=-1L, "undirected"=0L) .normalize.direction <- function(direction) { if ((!is.numeric(direction) && !is.character(direction)) || length(direction) != 1 || is.na(direction)) stop("'direction' must be a single (non-NA) integer or string") if (is.character(direction)) { direction <- match.arg(tolower(direction), names(.DIRECTION_STR2INT)) return(do.call(switch, c(EXPR=direction, as.list(.DIRECTION_STR2INT)))) } if (!(direction %in% .DIRECTION_STR2INT)) stop("when a numeric value, 'direction' should be one of 1, -1 or 0") as.integer(direction) } setMethod("direction", "FlatBimap", function(x) x@direction) setMethod("direction", "AnnDbBimap", function(x) x@direction) setReplaceMethod("direction", "FlatBimap", function(x, value) { x@direction <- .normalize.direction(value) x } ) setReplaceMethod("direction", "AnnDbBimap", function(x, value) { direction <- .normalize.direction(value) if (direction == 0) stop("undirected AnnDbBimap objects are not supported") if (direction != x@direction) { x@objName <- paste0("revmap(", x@objName, ")") x@direction <- direction } x } ) setReplaceMethod("direction", "AnnDbMap", function(x, value) { stop("changing the direction of an \"", class(x), "\" object is not supported") } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "revmap" methods. ### ### Conceptual definition: ### revmap(x) is the reverse of map x i.e. the map that provides the ### reverse lookup (or mapping) ### ### I would have liked to use "reverse" instead of "revmap" but "reverse" is ### already defined as a generic in Biostrings and it seems that the second ### of the 2 packages to be loaded breaks the generic and attached methods ### defined in the first. Don't know how to deal with this situation :-/ ### ### The "rev" generic defined in package:base can't be used neither because ### it doesn't allow passing additional arguments to or from methods (i.e. it ### has no '...' arg) and we want to be able to pass the 'objName' arg. ### Other generics defined in package:base where having a '...' arg could be ### useful: "unlist", "t" and "scale" (just in case someone feels brave enough ### to request this on R-devel). ### ### Note that "revmap" for "AnnDbBimap" objects does _not_ query the database! ### setMethod("revmap", "Bimap", function(x) { direction(x) <- - direction(x); x } ) setMethod("revmap", "AnnDbBimap", function(x, objName=NULL) { x <- callNextMethod(x) # calls "revmap" method for "Bimap" objects if (!is.null(objName)) x@objName <- toString(objName) x } ) setMethod("revmap", "environment", function(x) list2env(reverseSplit(as.list(x))) ) setMethod("revmap", "list", function(x) reverseSplit(x) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "colnames" and "colmetanames" methods. ### setMethod("colnames", "FlatBimap", function(x, do.NULL=TRUE, prefix="col") colnames(x@data) ) setMethod("colnames", "AnnDbBimap", function(x, do.NULL=TRUE, prefix="col") L2Rchain.colnames(x@L2Rchain) ) setMethod("colmetanames", "FlatBimap", function(x) x@colmetanames ) setMethod("colmetanames", "AnnDbBimap", function(x) L2Rchain.colmetanames(x@L2Rchain) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "Lkeyname", "Rkeyname" and "keyname" methods. ### setMethod("Lkeyname", "Bimap", function(x) { colnames <- colnames(x) names(colnames) <- colmetanames(x) colnames["Lkeyname"] } ) setMethod("Lkeyname", "AnnDbBimap", function(x) L2Rchain.Lkeyname(x@L2Rchain)) setMethod("Rkeyname", "Bimap", function(x) { colnames <- colnames(x) names(colnames) <- colmetanames(x) colnames["Rkeyname"] } ) setMethod("Rkeyname", "AnnDbBimap", function(x) L2Rchain.Rkeyname(x@L2Rchain)) setMethod("keyname", "Bimap", function(x) switch(as.character(direction(x)), "1"=Lkeyname(x), "-1"=Rkeyname(x), stop("keyname() is undefined for an undirected bimap")) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "tagname" methods. ### setMethod("tagname", "Bimap", function(x) { colnames <- colnames(x) names(colnames) <- colmetanames(x) colnames["tagname"] } ) setMethod("tagname", "AnnDbBimap", function(x) L2Rchain.tagname(x@L2Rchain)) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "Rattribnames" and "Rattribnames<-" methods. ### setMethod("Rattribnames", "Bimap", function(x) { colnames(x)[-seq_along(colmetanames(x))] } ) setMethod("Rattribnames", "AnnDbBimap", function(x) L2Rchain.Rattribnames(x@L2Rchain)) setReplaceMethod("Rattribnames", "FlatBimap", function(x, value) { colnames0 <- colnames(x@data) if (!is.null(value) && !is.character(value)) stop("Rattrib names must be a character vector or NULL") if (!all(value %in% Rattribnames(x))) stop("invalid Rattrib names") if (any(duplicated(value))) stop("can't assign duplicated Rattrib names") ii <- c(seq_along(colmetanames(x)), match(value, colnames0)) x@data <- x@data[ii] if (length(ii) < length(colnames0)) x@data <- unique(x@data) ## Needed because subsetting a data frame can change the names ## of its cols (for the duplicated names) colnames(x@data) <- colnames0[ii] x } ) setReplaceMethod("Rattribnames", "AnnDbBimap", function(x, value) { Rattribnames0 <- Rattribnames(x) L2Rchain.Rattribnames(x@L2Rchain) <- value if (length(Rattribnames(x)) < length(Rattribnames0)) x <- as(x, Class="AnnDbBimap", strict=TRUE) x } ) setReplaceMethod("Rattribnames", "Go3AnnDbBimap", function(x, value) { stop("can't modify the Rattrib names of a ", class(x), " object") } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "Lkeys", "Rkeys" and "keys" methods. ### setMethod("Lkeys", "FlatBimap", function(x) { if (length(x@Lkeys) == 1 && is.na(x@Lkeys)) return(mappedLkeys(x)) x@Lkeys } ) .inslot.Lkeys <- function(x) { length(x@Lkeys) != 1 || !is.na(x@Lkeys) } setMethod("Lkeys", "AnnDbBimap", function(x) { if (.inslot.Lkeys(x)) return(x@Lkeys) dbUniqueVals(dbconn(x), Ltablename(x), Lkeyname(x), Lfilter(x), x@datacache) } ) setMethod("Rkeys", "FlatBimap", function(x) { if (length(x@Rkeys) == 1 && is.na(x@Rkeys)) return(mappedRkeys(x)) x@Rkeys } ) .inslot.Rkeys <- function(x) { length(x@Rkeys) != 1 || !is.na(x@Rkeys) } setMethod("Rkeys", "AnnDbBimap", function(x) { if (.inslot.Rkeys(x)) return(x@Rkeys) dbUniqueVals(dbconn(x), Rtablename(x), Rkeyname(x), Rfilter(x), x@datacache) } ) setMethod("Rkeys", "Go3AnnDbBimap", function(x) { if (.inslot.Rkeys(x)) return(x@Rkeys) getNames <- function(ontology) { tablename <- Rtablename(x)[ontology] dbUniqueVals(dbconn(x), tablename, "go_id", Rfilter(x), x@datacache) } ## Because a given go_id can only belong to 1 of the 3 ontologies... ## (if not, then apply unique to this result) c(getNames("BP"), getNames("CC"), getNames("MF")) } ) setMethod("Rkeys", "AnnDbMap", function(x) { stop("Rkeys() is not supported for an \"", class(x), "\" object") } ) setMethod("keys", "Bimap", function(x) switch(as.character(direction(x)), "1"=Lkeys(x), "-1"=Rkeys(x), stop("keys() is undefined for an undirected bimap")) ) ## - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ## For the Probe mappings, I need to be able to ## just gets the Lkeys() with NO FILTERING. .GetUniqueLKeys = function(x){ if (.inslot.Lkeys(x)) return(x@Lkeys) dbUniqueVals(dbconn(x), Ltablename(x), Lkeyname(x), "1", x@datacache) } setMethod("Lkeys", "ProbeAnnDbBimap",function(x){.GetUniqueLKeys(x)}) setMethod("Lkeys", "ProbeAnnDbMap",function(x){.GetUniqueLKeys(x)}) setMethod("Lkeys", "ProbeIpiAnnDbMap",function(x){.GetUniqueLKeys(x)}) setMethod("Lkeys", "ProbeGo3AnnDbBimap",function(x){.GetUniqueLKeys(x)}) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "Lkeys<-", "Rkeys<-" and "keys<-" replacement methods. ### .checkKeysAreWellFormed <- function(keys) if (!is.null(keys) && (!is.character(keys) || any(is.na(keys)))) stop("keys must be supplied in a character vector with no NAs") .checkKeys <- function(keys, valid.keys, ifnotfound) { .checkKeysAreWellFormed(keys) if (length(ifnotfound) == 0) { not_found <- which(!(keys %in% valid.keys)) if (length(not_found) != 0) stop("value for \"", keys[not_found[1]], "\" not found") } } setReplaceMethod("Lkeys", "FlatBimap", function(x, value) { if (!is.null(value)) { .checkKeys(value, Lkeys(x), x@ifnotfound) if (!is.null(names(value))) names(value) <- NULL x@Lkeys <- value ii <- which(x@data[[1]] %in% value) cn <- colnames(x@data) x@data <- x@data[ii, ] colnames(x@data) <- cn } x } ) setReplaceMethod("Lkeys", "AnnDbBimap", function(x, value) { if (!is.null(value)) { .checkKeys(value, Lkeys(x), x@ifnotfound) if (!is.null(names(value))) names(value) <- NULL x@Lkeys <- value } x } ) setReplaceMethod("Rkeys", "FlatBimap", function(x, value) { if (!is.null(value)) { .checkKeys(value, Rkeys(x), x@ifnotfound) if (!is.null(names(value))) names(value) <- NULL x@Rkeys <- value ii <- which(x@data[[2]] %in% value) cn <- colnames(x@data) x@data <- x@data[ii, ] colnames(x@data) <- cn } x } ) setReplaceMethod("Rkeys", "AnnDbBimap", function(x, value) { if (!is.null(value)) { .checkKeys(value, Rkeys(x), x@ifnotfound) if (!is.null(names(value))) names(value) <- NULL x@Rkeys <- value } x } ) setReplaceMethod("keys", "Bimap", function(x, value) { switch(as.character(direction(x)), "1"=`Lkeys<-`(x, value), "-1"=`Rkeys<-`(x, value), stop("keys<- is undefined for an undirected bimap")) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "subset" methods. ### setMethod("subset", "Bimap", function(x, Lkeys=NULL, Rkeys=NULL, drop.invalid.keys=FALSE) { if (drop.invalid.keys) { .checkKeysAreWellFormed(Lkeys) .checkKeysAreWellFormed(Rkeys) Lkeys <- Lkeys[Lkeys %in% Lkeys(x)] Rkeys <- Rkeys[Rkeys %in% Rkeys(x)] } Lkeys(x) <- Lkeys Rkeys(x) <- Rkeys x } ) setMethod("subset", "AnnDbBimap", function(x, Lkeys=NULL, Rkeys=NULL, drop.invalid.keys=FALSE, objName=NULL) { ## Call "subset" method for "Bimap" objects x <- callNextMethod(x, Lkeys=Lkeys, Rkeys=Rkeys, drop.invalid.keys=drop.invalid.keys) if (!is.null(objName)) x@objName <- toString(objName) x } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "[" methods. ### ### Supported 'i' types: character vector, numeric vector, logical vector, ### NULL and missing. setMethod("[", "Bimap", function(x, i, j, ..., drop) { if (!missing(j) || length(list(...)) > 0) stop("invalid subsetting") if (missing(i)) return(x) keys <- keys(x) if (is.character(i)) { keys(x) <- i } else { keys(x) <- keys[i] } x } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "Llength", "Rlength" and "length" methods. ### setMethod("Llength", "Bimap", function(x) length(Lkeys(x))) setMethod("Llength", "AnnDbBimap", function(x) { if (.inslot.Lkeys(x)) return(length(x@Lkeys)) dbCountUniqueVals(dbconn(x), Ltablename(x), Lkeyname(x), Lfilter(x), x@datacache) } ) setMethod("Rlength", "Bimap", function(x) length(Rkeys(x))) setMethod("Rlength", "AnnDbBimap", function(x) { if (.inslot.Rkeys(x)) return(length(x@Rkeys)) dbCountUniqueVals(dbconn(x), Rtablename(x), Rkeyname(x), Rfilter(x), x@datacache) } ) setMethod("Rlength", "Go3AnnDbBimap", function(x) { if (.inslot.Rkeys(x)) return(length(x@Rkeys)) countNames <- function(ontology) { tablename <- Rtablename(x)[ontology] dbCountUniqueVals(dbconn(x), tablename, "go_id", Rfilter(x), x@datacache) } ## Because a given go_id can only belong to 1 of the 3 ontologies... countNames("BP") + countNames("CC") + countNames("MF") } ) setMethod("Rlength", "AnnDbMap", function(x) { stop("Rlength() is not supported for an \"", class(x), "\" object") } ) setMethod("length", "Bimap", function(x) switch(as.character(direction(x)), "1"=Llength(x), "-1"=Rlength(x), stop("length() is undefined for an undirected bimap")) ) ## - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ## For the Probe mappings, I need to be get length ## of the Lkeys() with NO FILTERING. .GetLKeyLength = function(x){ if (.inslot.Lkeys(x)) return(length(x@Lkeys)) dbCountUniqueVals(dbconn(x), Ltablename(x), Lkeyname(x), "1", x@datacache) } setMethod("Llength", "ProbeAnnDbBimap",function(x){.GetLKeyLength(x)}) setMethod("Llength", "ProbeAnnDbMap",function(x){.GetLKeyLength(x)}) setMethod("Llength", "ProbeIpiAnnDbMap",function(x){.GetLKeyLength(x)}) setMethod("Llength", "ProbeGo3AnnDbBimap",function(x){.GetLKeyLength(x)}) ##library(ALL);library(hgu95av2.db);library(genefilter);data(ALL);nsFilter(ALL) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "isNA" methods. ### ### Like "is.na", "isNA" returns a named logical vector that associates each ### key in the map with TRUE except for those keys that are actually mapped ### to something (other than an NA). setMethod("isNA", "Bimap", function(x) { mapped_keys <- mappedkeys(x) keys <- keys(x) ans <- !(keys %in% mapped_keys) names(ans) <- keys ans } ) ### "is.na" on environments has a silly semantic but since it is sealed then ### it can't be redefined. setMethod("isNA", "environment", function(x) is.na(as.list(x, all.names=TRUE)) ) ### And for ANY other vector-like object for which an "is.na" ### method is defined (e.g. an environment or a list) setMethod("isNA", "ANY", function(x) is.na(x)) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "mappedLkeys", "mappedRkeys" and "mappedkeys" methods. ### ### Note that for the maps in DB schemas like HUMANCHIP_DB, all the "right ### keys" are expected to be mapped to at least one "left key" hence ### mappedRkeys(x) should be the same as Rkeys(x) for those maps (maybe ### something worth checking in a test unit). ### setMethod("mappedLkeys", "FlatBimap", function(x) unique(x@data[[match("Lkeyname", x@colmetanames)]]) ) setMethod("mappedLkeys", "AnnDbBimap", function(x) { dbUniqueMappedKeys(dbconn(x), x@L2Rchain, x@Lkeys, x@Rkeys, 1, x@datacache) } ) setMethod("mappedLkeys", "Go3AnnDbBimap", function(x) { getMappedKeys <- function(ontology) { tablename <- Rtablename(x)[ontology] L2Rchain <- makeGo3L2Rchain(x@L2Rchain, tablename, ontology) dbUniqueMappedKeys(dbconn(x), L2Rchain, x@Lkeys, x@Rkeys, 1, x@datacache) } keys1 <- getMappedKeys("BP") keys2 <- getMappedKeys("CC") keys3 <- getMappedKeys("MF") unique(c(keys1, keys2, keys3)) } ) ### For an AgiAnnDbMap object (like silly maps ACCNUM and MULTIHIT in ### ARABIDOPSISCHIP_DB), the "mappedLkeys" method for AnnDbBimap objects ### would ignore the x@replace.single and x@replace.multiple slots leading ### to a wrong result when one of those slots is NA. ### But who cares, those maps are silly anyway... mappedLkeysIsNotAvailable <- function(x) { (length(x@replace.single) == 1 && is.na(x@replace.single)) || (length(x@replace.multiple) == 1 && is.na(x@replace.multiple)) } setMethod("mappedLkeys", "AgiAnnDbMap", function(x) { if (mappedLkeysIsNotAvailable(x)) stop("mappedLkeys() is not available for map ", x@objName) callNextMethod(x) } ) setMethod("mappedRkeys", "FlatBimap", function(x) unique(x@data[[match("Rkeyname", x@colmetanames)]]) ) setMethod("mappedRkeys", "AnnDbBimap", function(x) { dbUniqueMappedKeys(dbconn(x), x@L2Rchain, x@Lkeys, x@Rkeys, -1, x@datacache) } ) setMethod("mappedRkeys", "Go3AnnDbBimap", function(x) { getMappedKeys <- function(ontology) { tablename <- Rtablename(x)[ontology] L2Rchain <- x@L2Rchain L2Rchain[[length(L2Rchain)]]@tablename <- tablename dbUniqueMappedKeys(dbconn(x), L2Rchain, x@Lkeys, x@Rkeys, -1, x@datacache) } keys1 <- getMappedKeys("BP") keys2 <- getMappedKeys("CC") keys3 <- getMappedKeys("MF") ## Because a given go_id can only belong to 1 of the 3 ontologies... ## (if not, then apply unique to this result) c(keys1, keys2, keys3) } ) setMethod("mappedRkeys", "AnnDbMap", function(x) { stop("mappedRkeys() is not supported for an \"", class(x), "\" object") } ) setMethod("mappedkeys", "Bimap", function(x) switch(as.character(direction(x)), "1"=mappedLkeys(x), "-1"=mappedRkeys(x), stop("mappedkeys() is undefined for an undirected bimap")) ) setMethod("mappedkeys", "environment", function(x) { ## This is needed because the ! operator loses the "names" attributes ## when applied on a named vector of length 0 if (length(x) == 0) return(character(0)) notNA <- !isNA(x) names(notNA)[notNA] } ) setMethod("mappedkeys", "vector", function(x) { if (is.null(names(x))) stop("mappedkeys() is not defined on an unnamed vector") ## This is needed because the ! operator loses the "names" attributes ## when applied on a named vector of length 0 if (length(x) == 0) return(character(0)) notNA <- !isNA(x) names(notNA)[notNA] } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "count.mappedLkeys", "count.mappedRkeys" and "count.mappedkeys" methods. ### setMethod("count.mappedLkeys", "Bimap", function(x) length(mappedLkeys(x))) setMethod("count.mappedLkeys", "AnnDbBimap", function(x) { dbCountUniqueMappedKeys(dbconn(x), x@L2Rchain, x@Lkeys, x@Rkeys, 1, x@datacache) } ) setMethod("count.mappedLkeys", "Go3AnnDbBimap", function(x) length(mappedLkeys(x)) ) setMethod("count.mappedLkeys", "AgiAnnDbMap", function(x) { if (mappedLkeysIsNotAvailable(x)) stop("count.mappedLkeys() is not available for map ", x@objName) callNextMethod(x) } ) setMethod("count.mappedRkeys", "Bimap", function(x) length(mappedRkeys(x))) setMethod("count.mappedRkeys", "AnnDbBimap", function(x) { dbCountUniqueMappedKeys(dbconn(x), x@L2Rchain, x@Lkeys, x@Rkeys, -1, x@datacache) } ) setMethod("count.mappedRkeys", "Go3AnnDbBimap", function(x) { countMappedNames <- function(ontology) { tablename <- Rtablename(x)[ontology] L2Rchain <- makeGo3L2Rchain(x@L2Rchain, tablename, ontology) dbCountUniqueMappedKeys(dbconn(x), L2Rchain, x@Lkeys, x@Rkeys, -1, x@datacache) } ## Because a given go_id can only belong to 1 of the 3 ontologies... countMappedNames("BP") + countMappedNames("CC") + countMappedNames("MF") } ) setMethod("count.mappedRkeys", "AnnDbMap", function(x) { stop("count.mappedRkeys() is not supported for an \"", class(x), "\" object") } ) setMethod("count.mappedkeys", "Bimap", function(x) switch(as.character(direction(x)), "1"=count.mappedLkeys(x), "-1"=count.mappedRkeys(x), stop("count.mappedkeys() is undefined for an undirected bimap")) ) setMethod("count.mappedkeys", "ANY", function(x) length(mappedkeys(x))) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "show" and "summary" methods. ### .key.summary <- function(keys, nmapped) { len0 <- length(keys) if (len0 == 0) return("") if (len0 > 2) keys <- keys[1:2] string <- paste0("\"", keys, "\"", collapse=", ") if (len0 > 2) string <- paste0(string, ", ...") paste0(string, " (total=", len0, "/mapped=", nmapped, ")") } .Bimap.summary <- function(x) { ## Left keys cat("| Lkeyname: ", Lkeyname(x), sep="") if (is(x, "AnnDbBimap")) cat(" (Ltablename: ", Ltablename(x), ")", sep="") cat("\n") tmp <- mappedLkeys(x) # just to put them in the cache cat("| Lkeys: ", .key.summary(Lkeys(x), count.mappedLkeys(x)), "\n", sep="") cat("|\n") if (!is(x, "AnnDbMap")) { ## Right keys cat("| Rkeyname: ", Rkeyname(x), sep="") if (is(x, "AnnDbBimap")) cat(" (Rtablename: ", Rtablename(x), ")", sep="") cat("\n") tmp <- mappedRkeys(x) # just to put them in the cache cat("| Rkeys: ", .key.summary(Rkeys(x), count.mappedRkeys(x)), "\n", sep="") cat("|\n") } ## Tag if (!is.na(tagname(x))) cat("| tagname: ", tagname(x), "\n|\n", sep="") ## direction direction <- names(.DIRECTION_STR2INT)[.DIRECTION_STR2INT == direction(x)] cat("| direction: ", direction, "\n", sep="") } .is.submap <- function(x) { .inslot.Lkeys(x) || .inslot.Rkeys(x) } setMethod("show", "FlatBimap", function(object) { cat("\"", class(object), "\" object:\n", sep="") cat("|\n") .Bimap.summary(object) cat("\ndata:\n") if (nrow(object) <= 20) { show(object@data) } else { show(head(object, n=10)) cat("...\n") cat("(", nrow(object), " rows)\n", sep="") } } ) setMethod("show", "AnnDbBimap", function(object) { map <- "map" if (.is.submap(object)) map <- "submap" cat(object@objName, " ", map, " for ", object@objTarget, " (object of class \"", class(object), "\")\n", sep="") } ) setMethod("summary", "Bimap", function(object) show(object)) setMethod("summary", "AnnDbBimap", function(object) { show(object) cat("|\n") .Bimap.summary(object) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "toTable" methods. ### setMethod("toTable", "FlatBimap", function(x) { x@data } ) setMethod("toTable", "Bimap", function(x) { toTable(flatten(x, fromKeys.only=TRUE)) } ) as.data.frame.Bimap <- function(x, row.names=NULL, optional=FALSE, ...) { if (!is.null(row.names)) warning(wmsg("the \"as.data.frame\" method for Bimap objects ", "ignores the 'row.names' argument")) if (!identical(optional, FALSE)) warning(wmsg("the \"as.data.frame\" method for Bimap objects ", "ignores the 'optional' argument")) if (length(list(...)) != 0L) stop(wmsg("the \"as.data.frame\" method for Bimap objects ", "doesn't take any extra argument")) toTable(x) } setMethod("as.data.frame", "Bimap", as.data.frame.Bimap) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "head" and "tail" methods. ### ### TODO: Define these methods to AnnDbBimap objects. ### setMethod("head", "FlatBimap", function(x, ...) { c <- colnames(x) y <- head(x@data, ...) if (!identical(colnames(y), c)) colnames(y) <- c y } ) setMethod("tail", "FlatBimap", function(x, ...) { c <- colnames(x) y <- tail(x@data, ...) if (!identical(colnames(y), c)) colnames(y) <- c y } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "nrow" methods. ### setMethod("nrow", "Bimap", function(x) nrow(toTable(x))) setMethod("nrow", "FlatBimap", function(x) nrow(x@data) ) ### CURRENTLY BROKEN! setMethod("nrow", "AnnDbTable", function(x) { dbCountRawAnnDbMapRows(dbconn(x), Ltablename(x), Lkeyname(x), NULL, NULL, x@from) } ) setMethod("nrow", "AnnDbBimap", function(x) { dbCountRowsFromL2Rchain(dbconn(x), x@L2Rchain, x@Lkeys, x@Rkeys) } ) setMethod("nrow", "Go3AnnDbBimap", function(x) { countRows <- function(ontology) { tablename <- Rtablename(x)[ontology] L2Rchain <- makeGo3L2Rchain(x@L2Rchain, tablename, ontology) dbCountRowsFromL2Rchain(dbconn(x), L2Rchain, x@Lkeys, x@Rkeys) } countRows("BP") + countRows("CC") + countRows("MF") } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "links" methods. ### setMethod("links", "FlatBimap", function(x) { Rattribnames(x) <- NULL x@data } ) setMethod("links", "Bimap", function(x) { Rattribnames(x) <- NULL links(flatten(x, fromKeys.only=TRUE)) } ) setMethod("links", "Go3AnnDbBimap", function(x) links(flatten(x, fromKeys.only=TRUE))) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "count.links" methods. ### setMethod("count.links", "Bimap", function(x) { Rattribnames(x) <- NULL nrow(x) } ) setMethod("count.links", "Go3AnnDbBimap", function(x) nrow(x)) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "nhit" methods. ### ### TODO: maybe it could be optimized for AnnDbBimap objects with a fast (and ### smart) SQL query (involving COUNT, HAVING or/and GROUP?) that retrieves ### only the strictly necessary stuff. ### Something that would be worth testing (e.g. with unit testing): ### y <- nhit(x) # y is a named integer vector ### names(y) should be identical to names(x) ### sum(y) should be equal to count.links(x) ### setMethod("nhit", "list", function(x) { sapply(x, function(xx) if (length(xx) == 1L && is.na(xx)) 0L else length(xx) ) } ) setMethod("nhit", "Bimap", function(x) nhit(as.list(x))) setMethod("nhit", "environment", function(x) { #nhit(as.list(x, all.names=TRUE)) ## Using eapply should be faster than the above (not tested, I'm just ## assuming). unlist( eapply(x, function(xx) if (length(xx) == 1 && is.na(xx)) 0L else length(xx), all.names=TRUE ), recursive=FALSE ) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "ncol" and "dim" methods. ### setMethod("ncol", "Bimap", function(x) length(colnames(x))) setMethod("dim", "Bimap", function(x) c(nrow(x), ncol(x))) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Method to remove the multiple mapping filter from AnnDbBimaps that have a probe mapping in them. ### .toggleFilter = function(x, value = c("all","single","multiple")){ type <- match.arg(value) ans <- x if(ans@L2Rchain[[1]]@tablename!="probes"){ stop("This method can only be used on mappings where the Lkeys are probes.") } switch(type, "all" = ans@L2Rchain[[1]]@filter <- "{is_multiple} IN ('1','0')", "single" = ans@L2Rchain[[1]]@filter <- "{is_multiple}='0'", "multiple" = ans@L2Rchain[[1]]@filter <- "{is_multiple}='1'" ) return(ans) } setMethod("toggleProbes", "ProbeAnnDbBimap", function(x, value){.toggleFilter(x, value)}) setMethod("toggleProbes", "ProbeAnnDbMap", function(x, value){.toggleFilter(x, value)}) setMethod("toggleProbes", "ProbeIpiAnnDbMap", function(x, value){.toggleFilter(x, value)}) setMethod("toggleProbes", "ProbeGo3AnnDbBimap", function(x, value){.toggleFilter(x, value)}) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Methods to indicate the mask setting of the probes ### .hasMultiProbes = function(x){ f <- x@L2Rchain[[1]]@filter if((f=="{is_multiple}='1'" || f=="{is_multiple} IN ('1','0')") && x@L2Rchain[[1]]@tablename=="probes"){ ans <- TRUE }else{ ans <- FALSE } return(ans) } setMethod("hasMultiProbes", "ProbeAnnDbBimap",function(x){.hasMultiProbes(x)}) setMethod("hasMultiProbes", "ProbeAnnDbMap",function(x){.hasMultiProbes(x)}) setMethod("hasMultiProbes", "ProbeIpiAnnDbMap",function(x){.hasMultiProbes(x)}) setMethod("hasMultiProbes", "ProbeGo3AnnDbBimap",function(x){.hasMultiProbes(x)}) .hasSingleProbes = function(x){ f <- x@L2Rchain[[1]]@filter if((f=="{is_multiple}='0'" || f=="{is_multiple} IN ('1','0')") && x@L2Rchain[[1]]@tablename=="probes"){ ans <- TRUE }else{ ans <- FALSE } ans } setMethod("hasSingleProbes", "ProbeAnnDbBimap",function(x){.hasSingleProbes(x)}) setMethod("hasSingleProbes", "ProbeAnnDbMap",function(x){.hasSingleProbes(x)}) setMethod("hasSingleProbes", "ProbeIpiAnnDbMap",function(x){.hasSingleProbes(x)}) setMethod("hasSingleProbes", "ProbeGo3AnnDbBimap",function(x){.hasSingleProbes(x)}) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The BimapFilter methods. ### ##usage: getBimapFilter(myBiMap) ##returns the filter that is on there for any Bimap setMethod("getBimapFilters", "AnnDbBimap", ## function(x){L2Rchain.bimapFilter(x@L2Rchain)}) function(x) { L2Rchain <- x@L2Rchain filter <- sapply(L2Rchain, function(x){x@filter}) filter <- filter[!is.na(filter)] return(filter) }) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Method for making a FlatBimap by using the select method. ### ## This method takes x, which is an AnnotationDb object, and also a SINGLE ## cols value. It is not exported, and is used only for testing the backwards ## compatibility provided by getAnnMap() in the annotate package. ## I need to check with Hervé if my assumptions here are correct that I ## Don't want any NAs in @data OR in @Rkeys and @Lkeys??? ## Maybe I don't want NAs in only one or the other? ## And maybe the answer is in how mappedLkeys and mappedRkeys work? makeFlatBimapUsingSelect <- function(x, col){ suppressWarnings(tab <- select(x, keys=keys(x), columns=col)) ## tab cannot contain ANY NA values??? - seems like a dicey idea... ## what about keys that are unmapped but still valid? idx = apply(tab, MARGIN=1, function(x){!any(is.na(x))}) tab <- tab[idx,] ## keys have to be unique as well lkys <- unique(tab[,1]) rkys <- unique(tab[,2]) new("FlatBimap", colmetanames=c("Lkeyname", "Rkeyname"), direction=1, data=tab, Lkeys=lkys, Rkeys=rkys) } ## Hervé says that I in fact want to have no NAs (and be unique) in the Rkey and Lkeys, and that I ALSO do not want ANY NAs in either column of @data. So I have modified this function accordingly ## OLD method for making bimaps (probably should deprecate this after the release) ##Makes a simpleBimap for tables that are added outside of standard AnnotationForge Schemas. ##This function requires that the bimap map from a single table in the DB. createSimpleBimap <- function(tablename, Lcolname, Rcolname, datacache, objName=as.character(NA), objTarget=as.character(NA)) { seed <- list( objName=objName, objTarget=objTarget, Class="AnnDbBimap", L2Rchain=list( list( tablename=tablename, Lcolname=Lcolname, Rcolname=Rcolname ) ), datacache=datacache ) createAnnDbBimap(seed, list()) } AnnotationDbi/R/BimapFormatting.R0000644000175200017520000003411514710217313017737 0ustar00biocbuildbiocbuild### ========================================================================= ### Formatting a Bimap as a list or character vector ### ------------------------------------------------ ### ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Convenience functions used in this file only (not exported) ### ### The ".fromCol", ".toCol" and ".tagCol" functions. ### 'x' must be a Bimap object. ### ### Note that we must use 'x@data[[2]]' instead of 'x@data[[Rkeyname(x)]]' ### because 'x' colnames are not necessarily unique e.g.: ### > head(flatten(subset(GOBPPARENTS, "GO:0000001")), 2) ### go_id go_id Evidence ### 1 GO:0000001 GO:0048308 isa ### 2 GO:0000001 GO:0048311 isa ### ### TODO: Make these methods use colmetanames(x) to find the positions of the ### left, right and tag cols in x@data instead of hardcoding this with ### x@data[[1]], x@data[[2]] and x@data[[3]]. ### .fromCol <- function(x) { if (direction(x) == 1) x@data[[1]] else x@data[[2]] } .toCol <- function(x) { if (direction(x) == 1) x@data[[2]] else x@data[[1]] } .tagCol <- function(x) { if (is.na(tagname(x))) return(NULL) x@data[[3]] } ### The ".formatList" function. ### 'x' must be a list with unique names. ### ### .formatList() will re-order the elements in 'x' based on the names passed ### in the 'names' arg (a character vector): ### ### > x <- list(aa=1, b=2:-1, c=3) ### > names <- c("a", "c", "d", "c") ### > AnnotationDbi:::.formatList(x, names) ### $a ### [1] NA ### ### $c ### [1] 3 ### ### $d ### [1] NA ### ### $c ### [1] 3 ### ### Note that the returned list must always have exactly: ### - the length of the 'names' arg ### - the names passed in the 'names' arg and in the same order ### ### In addition, .formatList() allows to replace some values in the original ### list by a value specified by the caller: ### ### > names <- c("d", "b", "aa", "b") ### > AnnotationDbi:::.formatList(x, names, replace.multiple="multiple") ### $d ### [1] NA ### ### $b ### [1] "multiple" ### ### $aa ### [1] 1 ### ### $b ### [1] "multiple" .formatList <- function(x, names, replace.single=NULL, replace.multiple=NULL) { if (length(x) != 0) x <- list2env(x) doReplaceSingle <- length(replace.single) != 0L doReplaceMultiple <- length(replace.multiple) != 0L formatVal <- function(key) { val <- x[[key]] lval <- length(val) if (lval == 1L) { if (doReplaceSingle) return(replace.single) } else if (lval > 1L) { if (doReplaceMultiple) return(replace.multiple) } else { # lval == 0 val <- NA } val } names(names) <- names lapply(names, formatVal) } ### The ".from.colpos" and ".to.colpos" functions. ### 'x' must be a Bimap object. .from.colpos <- function(x) { if (direction(x) == 1) side = "Lkeyname" else side = "Rkeyname" match(side, colmetanames(x)) } .to.colpos <- function(x) { .from.colpos(revmap(x)) } ### The ".toListOfLists" function. ### ### This function converts FlatBimap object 'x' to a list of right objects ### if is 'x' a mono-valued (many-to-one) map, or to a list of lists of right ### objects if 'x' is a multi-valued map. ### By default (if arg 'FUN' is omitted), each right object itself is stored ### in a named list. ### ### Back to the bimap B1 given in the Bimap.R file: ### ### A natural way of representing objects A, B, C in R is to use lists: ### - object A: list("A", c(1.2, 0.9)) ### - object B: list("B", character(0)) ### - object C: list("C", -1:1) ### ### And a natural way for representing map B1 in R is to use a named list ### of 4 elements (one for each left object) where: ### - the "a" element is a named list of 2 elements, one named "A" and ### containing the representation of A, and one named "B" and ### containing the representation of B, ### - the "b" element is a named list of 1 element, named "A" and ### containing the representation of A, ### - the "c" element is NA ### - the "d" element is a named list of 1 element, named "C" and ### containing the representation of C. ### ### .toListOfLists() does this conversion from "flat" to "list". ### ### Arguments: ### ### 'x': a Bimap object. ### ### 'mode': 3 modes are supported: ### mode 1: mono-valued map ### mode 2: multi-valued map containing 1 right object per row (i.e. ### all right objects are stored in a single row, this can only be ### known in advance if we know that their tags are mono-valued) ### mode 3: multi-valued map where more than 1 row can be needed to ### store a given right object (this can happen only if at least ### one of the tags are multi-valued) ### In our example above, bimap B1 is of mode 3. ### ### 'FUN': a formatting function applied on-the-fly on each object during ### the "folding" process. If 'FUN' is omitted then ### 'function(...) list(...)' is used so no information is lost and ### the formatting can always be done later with: ### ### > y <- .toListOfLists(x) ### > y <- lapply(y, function(val) ### lapply(val, function(x) do.call(myfun, x))) ### ### The result will be the same as with just: ### ### > y <- .toListOfLists(x, FUN=myfun) ### ### but the latter will be faster. ### ### TODO: make it work for "L <- R" maps ### .toListOfLists <- function(x, mode, FUN) { keys <- keys(x) ans <- as.list(rep.int(as.character(NA), length(keys))) names(ans) <- keys if (nrow(x) == 0) return(ans) if (direction(x) == -1) stop("right-to-left folding not yet ready, sorry") if (missing(FUN)) FUN <- function(...) list(...) ## First slicing (top level) slicer1 <- .from.colpos(x) slicer2 <- .to.colpos(x) if (slicer2 > slicer1) slicer2 <- slicer2 - 1 keepcols <- seq_len(length(x@data))[- slicer1] slicing_one <- lapply(keepcols, function(j) split(x@data[[j]], x@data[[slicer1]])) names(slicing_one) <- names(x@data)[- slicer1] found_keys <- names(slicing_one[[1]]) ii <- match(keys, found_keys) for (i1 in seq_len(length(keys))) { i2 <- ii[i1] if (is.na(i2)) next slice_one <- lapply(slicing_one, function(col) col[[i2]]) if (mode == 1) { ans[[i1]] <- do.call(FUN, slice_one) next } if (mode == 2 || !any(duplicated(slice_one[[1]]))) { ans[[i1]] <- do.call(mapply, c(FUN=FUN, slice_one, SIMPLIFY=FALSE)) next } ## Sub-slicing keepcols <- seq_len(length(slice_one))[- slicer2] slicing_two <- lapply(keepcols, function(j) split(slice_one[[j]], slice_one[[slicer2]])) slicing_two <- c(list(names(slicing_two[[1]])), slicing_two) names(slicing_two) <- c(names(slice_one)[slicer2], names(slice_one)[- slicer2]) ans[[i1]] <- do.call(mapply, c(FUN=FUN, slicing_two, SIMPLIFY=FALSE)) } ans } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "as.list" methods. ### as.list.Bimap <- function(x, ...) as.list(x) setMethod("as.list", "FlatBimap", function(x, ...) { Rattribnames(x) <- NULL toCol <- .toCol(x) names(toCol) <- .tagCol(x) y <- split(toCol, .fromCol(x)) .formatList(y, keys(x)) } ) setMethod("as.list", "Bimap", function(x, ...) { Rattribnames(x) <- NULL y <- flatten(x, fromKeys.only=TRUE) as.list(y) } ) ### Needed to deal with the PFAM and PROSITE maps. ### Their colnames are: ### PFAM: "probe_id", "ipi_id", "PfamId" ### PROSITE: "probe_id", "ipi_id", "PrositeId" setMethod("as.list", "IpiAnnDbMap", function(x, ...) { y <- flatten(x, fromKeys.only=TRUE) toCol <- y@data[[3]] names(toCol) <- .toCol(y) z <- split(toCol, .fromCol(y)) .formatList(z, keys(y)) } ) setMethod("as.list", "AgiAnnDbMap", function(x, ...) { y <- flatten(x, fromKeys.only=TRUE) z <- split(.toCol(y), .fromCol(y)) .formatList(z, keys(y), x@replace.single, x@replace.multiple) } ) setMethod("as.list", "GoAnnDbBimap", function(x, ...) { y <- flatten(x, fromKeys.only=TRUE) if (direction(y) == -1) return(as.list(y)) keys <- keys(y) ann_list <- as.list(rep.int(as.character(NA), length(keys))) names(ann_list) <- keys if (nrow(y@data) != 0) { makeGOList <- function(GOIDs, Evidences, Ontologies) { mapply(function(gid, evi, ont) list(GOID=gid, Evidence=evi, Ontology=ont), GOIDs, Evidences, Ontologies, SIMPLIFY=FALSE) } fromCol <- .fromCol(y) GOIDs <- split(y@data[["go_id"]], fromCol) Evidences <- split(y@data[["Evidence"]], fromCol) Ontologies <- split(y@data[["Ontology"]], fromCol) ## The 'GOIDs', 'Evidences' and 'Ontologies' lists have the same ## names in the same order. found_keys <- names(GOIDs) # same as 'names(Evidences)' and 'names(Ontologies)' ii <- match(keys, found_keys) for (i1 in seq_len(length(keys))) { i2 <- ii[i1] if (is.na(i2)) next ann_list[[i1]] <- makeGOList(GOIDs[[i2]], Evidences[[i2]], Ontologies[[i2]]) } } ann_list } ) ### Formatting the right objects with 'makeGONode' instead of just using the ### default formatting provided by .toListOfLists() (the default is to create ### a list for each object) makes things _much_ slower: ### > x <- flatten(GOTERM) ### > system.time(y <- .toListOfLists(x, "Lkeyname", mode=1)) ### user system elapsed ### 1.888 0.016 1.905 ### > system.time(y <- .toListOfLists(x, "Lkeyname", mode=1, FUN=makeGONode)) ### user system elapsed ### 20.893 0.072 21.066 ### Why is the S4 initialization mechanism so slow? setMethod("as.list", "GOTermsAnnDbBimap", function(x, ...) { y <- flatten(x, fromKeys.only=TRUE) makeGONode <- function(go_id, Term, Ontology, Definition, ...) { new("GOTerms", GOID=go_id[1], Term=Term[1], Ontology=Ontology[1], Definition=Definition[1], ...) } .toListOfLists(y, mode=1, makeGONode) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "toLList", "toRList" and "toList" methods. ### ### NOTE: These methods are not exported yet (will be soon). ### TODO: Define these methods for FlatBimap objects. ### .alignAnnList <- function(ann_list, keys) { y <- list2env(ann_list) key2val <- function(key) { val <- y[[key]] if (is.null(val)) { val <- NA } else { if (class(val) == "data.frame") row.names(val) <- NULL } val } names(keys) <- keys lapply(keys, key2val) } setMethod("toLList", "FlatBimap", function(x) { if (nrow(x@data) == 0) ann_list <- list() else ann_list <- split(x@data[ , -1], x@data[[1]]) .alignAnnList(ann_list, Lkeys(x)) } ) setMethod("toLList", "AnnDbBimap", function(x) { toLList(flatten(x, fromKeys.only=TRUE)) } ) setMethod("toLList", "AnnDbMap", function(x) { y <- flatten(x, fromKeys.only=TRUE) if (length(x@rightColType) == 1 && typeof(y@data[[2]]) != x@rightColType) { converter <- get(paste0("as.", x@rightColType)) y@data[[2]] <- converter(y@data[[2]]) } toLList(y) } ) setMethod("toRList", "FlatBimap", function(x) { if (nrow(x@data) == 0) ann_list <- list() else ann_list <- split(x@data[ , -2], x@data[[2]]) .alignAnnList(ann_list, Rkeys(x)) } ) setMethod("toRList", "AnnDbBimap", function(x) { toRList(flatten(x, fromKeys.only=TRUE)) } ) setMethod("toRList", "AnnDbMap", function(x) { stop("toRList() is not supported for an \"", class(x), "\" object") } ) setMethod("toList", "Bimap", function(x) switch(as.character(direction(x)), "1"=toLList(x), "-1"=toRList(x), stop("toList() is undefined for an undirected bimap")) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "as.character" methods. ### ### Only defined for untagged AnnDbBimap objects for now. ### ### TODO: Extend to FlatBimap objects. ### ### R doesn't let me add a 'keys' arg here: ### Error in rematchDefinition(definition, fdef, mnames, fnames, signature) : ### methods can add arguments to the generic only if '...' is an argument to the generic setMethod("as.character", "AnnDbBimap", function(x) { if (!is.na(tagname(x))) stop("AnnDbBimap object with tags cannot be coerced to a character vector") Rattribnames(x) <- NULL y <- flatten(x, fromKeys.only=TRUE) ans <- .toCol(y) if (!is.character(ans)) ans <- as.character(ans) names(ans) <- .fromCol(y) if (any(duplicated(names(ans)))) warning("returned vector has duplicated names") ans } ) setMethod("as.character", "FlatBimap", function(x) { res <- x@data if(x@direction==1){ ans <- as.character(res[,2]) names(ans) <- as.character(res[,1]) }else{ ans <- as.character(res[,1]) names(ans) <- as.character(res[,2]) } if (any(duplicated(names(ans)))) warning("returned vector has duplicated names") ans ans } ) AnnotationDbi/R/FlatBimap.R0000644000175200017520000000215014710217313016505 0ustar00biocbuildbiocbuild### ========================================================================= ### FlatBimap objects ### ----------------- ### ### Possible col metanames are: "Lkeyname", "Rkeyname" and "tagname" ### There must be exactly 1 "Lkeyname" and 1 "Rkeyname" col. ### There can be 0 or 1 "tagname" col. setMethod("initialize", "FlatBimap", function(.Object, colmetanames, direction, data, Lkeys, Rkeys) { if (!is.character(colmetanames) || any(duplicated(colmetanames)) || !all(colmetanames %in% c("Lkeyname", "Rkeyname", "tagname")) || !all(c("Lkeyname", "Rkeyname") %in% colmetanames)) stop("invalid col metanames") if (ncol(data) < length(colmetanames)) stop("FlatBimap object has not enough columns") .Object@colmetanames <- colmetanames if (!missing(direction)) .Object@direction <- .normalize.direction(direction) .Object@data <- data .Object@Lkeys <- Lkeys .Object@Rkeys <- Rkeys if (any(duplicated(Rattribnames(.Object)))) stop("duplicated Rattrib names") .Object } ) AnnotationDbi/R/GOTerms.R0000644000175200017520000003043114710217313016171 0ustar00biocbuildbiocbuildsetClass("GOTerms", representation( GOID="character", # a single string (mono-valued) Term="character", # a single string (mono-valued) Ontology="character", # a single string (mono-valued) Definition="character", # a single string (mono-valued) Synonym="character", # any length including 0 (multi-valued) Secondary="character" # any length including 0 (multi-valued) ) ) ### The mono-valued slots are also the mandatory slots. .GONODE_MONOVALUED_SLOTS <- c("GOID", "Term", "Ontology", "Definition") ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Initialization. ### setMethod("initialize", "GOTerms", function(.Object, ...) { args <- list(...) argnames <- names(args) if (is.null(argnames) || any(argnames == "")) stop("all arguments must be named") argnames <- match.arg(argnames, slotNames(.Object), several.ok=TRUE) if (!(all(.GONODE_MONOVALUED_SLOTS %in% argnames))) { s <- paste(.GONODE_MONOVALUED_SLOTS, collapse=", ") stop("arguments ", s, " are mandatory") } for (i in seq_len(length(args))) { argname <- argnames[i] value <- args[[i]] if ((argname %in% .GONODE_MONOVALUED_SLOTS)) { if (length(value) != 1) stop("can't assign ", length(value), " values to mono-valued slot ", argname) } else { value <- value[!(value %in% c(NA, ""))] } slot(.Object, argname) <- value } .Object } ) GOTerms <- function(GOId, term, ontology, synonym = "", secondary = "", definition = ""){ return(new("GOTerms", GOID = GOId, Term = term, Synonym = synonym, Secondary = secondary, Definition = definition, Ontology = ontology)) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "GOID", "Term", "Ontology", "Definition", "Synonym" and "Secondary" ### generics (accessor methods). ### setMethod("GOID", "GOTerms", function(object) object@GOID) setMethod("Term", "GOTerms", function(object) object@Term) setMethod("Ontology", "GOTerms", function(object) object@Ontology) setMethod("Definition", "GOTerms", function(object) object@Definition) setMethod("Synonym", "GOTerms", function(object) object@Synonym) setMethod("Secondary", "GOTerms", function(object) object@Secondary) ##.GOid2go_termField() retrieves ids of type field from go_term .GOid2go_termField <- function(ids, field){ ## message(cat("Before SQL \n")) ##test sql <- sprintf("SELECT go_id, %s FROM go_term WHERE go_id IN ('%s')", field, paste(ids, collapse="','")) res <- dbGetQuery(GO.db::GO_dbconn(), sql) if(dim(res)[1]==0 && dim(res)[2]==0){ stop("None of your IDs match IDs from GO. Are you sure you have valid IDs?") }else{ ans <- res[[2]] names(ans) <- res[[1]] return(ans[ids]) ##This only works because each GO ID is unique (and therefore a decent index ID) } } setMethod("GOID", "GOTermsAnnDbBimap",function(object) .GOid2go_termField(keys(object),"go_id") ) setMethod("GOID", "character",function(object) .GOid2go_termField(object,"go_id") ) setMethod("Term", "GOTermsAnnDbBimap",function(object) .GOid2go_termField(keys(object),"term") ) setMethod("Term", "character",function(object) .GOid2go_termField(object,"term") ) setMethod("Ontology", "GOTermsAnnDbBimap",function(object) .GOid2go_termField(keys(object),"ontology") ) setMethod("Ontology", "character",function(object) .GOid2go_termField(object,"ontology") ) setMethod("Definition", "GOTermsAnnDbBimap",function(object) .GOid2go_termField(keys(object),"definition") ) setMethod("Definition", "character",function(object) .GOid2go_termField(object,"definition") ) ##.GOid2go_synonymField() retrieves ids of type field from go_synonym .GOid2go_synonymField <- function(ids, field){ sql <- paste0("SELECT gt.go_id, gs.",field," FROM go_term AS gt, go_synonym AS gs WHERE gt._id=gs._id AND go_id IN ('",paste(ids, collapse="','"),"')") res <- dbGetQuery(GO.db::GO_dbconn(), sql) if(dim(res)[1]==0 && dim(res)[2]==0){ stop("None of your IDs match IDs from GO. Are you sure you have valid IDs?") }else{ ans = split(res[,2],res[,1]) return(ans[ids])##once again (this time in list context), we are indexing with unique IDs. } } setMethod("Synonym", "GOTermsAnnDbBimap",function(object) .GOid2go_synonymField(keys(object),"synonym") ) setMethod("Synonym", "character",function(object) .GOid2go_synonymField(object,"synonym") ) setMethod("Secondary", "GOTermsAnnDbBimap",function(object) .GOid2go_synonymField(keys(object),"secondary") ) setMethod("Secondary", "character",function(object) .GOid2go_synonymField(object,"secondary") ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "show" methods. ### setMethod("show", "GOTerms", function(object) { s <- character(0) for (slotname in slotNames(object)) { x <- slot(object, slotname) if ((slotname %in% .GONODE_MONOVALUED_SLOTS) && length(x) != 1) { warning("mono-valued slot ", slotname, " contains ", length(x), " values") } else { if (length(x) == 0) next } s <- c(s, paste0(slotname, ": ", x)) } cat(strwrap(s, exdent=4), sep="\n") } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The methods to construct a GOFrame or a GOAllFrame ### .attachGO <- function(con){ requireNamespace("GO.db") GOLoc = system.file("extdata", "GO.sqlite", package="GO.db") attachSQL = paste0("ATTACH '", GOLoc, "' AS go;") dbAttach(con, attachSQL) } .testGOFrame <- function(x, organism=""){ drv <- dbDriver("SQLite") con <- dbConnect(drv) ##Test that some GOIDs are real and that the evidence codes are legit. .attachGO(con) GOIDs = x[,1] eviCodes = x[,2] realGOIDs = as.character(dbGetQuery(con, "SELECT go_id FROM go_term;")[,1]) ##Test that the data.frame has some rows of data in it if(!dim(x)[1]>0){ stop("There are no rows of data in the data.frame supplied to make a GOFrame.") } ## TODO, Add evidence codes to GO.sqlite so that we can test this properly ## without any hard coding realEviCodes = c( "EXP", "IDA", "IPI", "IMP", "IGI", "IEP", "HTP", "HDA", "HMP", "HGI", "HEP", "ISS", "ISO", "ISA", "ISM", "IGC", "IBA", "IBD", "IKR", "IRD", "RCA", "TAS", "NAS", "IC", "ND", "IEA" ) if(is.na(table(GOIDs %in% realGOIDs)["TRUE"])){ stop("None of elements in the 1st column of your data.frame object are legitimate GO IDs.") } if (any(bad <- !eviCodes %in% realEviCodes)) { msg <- sprintf("invalid GO Evidence codes: '%s'", paste(unique(eviCodes[bad]), collapse="' '")) stop(msg) } if(length(x[,1]) != length(x[,2]) || length(x[,1]) != length(x[,3])){ stop("You need to have evidence codes and genes for all your GO IDs.") } if(organism!=""){ new("GOFrame", data = x, organism = organism) }else{new("GOFrame", data = x)} } setMethod("GOFrame", signature=signature(x="data.frame", organism="character"), function(x, organism){.testGOFrame(x, organism)}) setMethod("GOFrame", signature=signature(x="data.frame", organism="missing"), function(x){.testGOFrame(x)}) ## Helper method for converting GOFrame type data.frames into GOAllFrame objects .convertGOtoGO2ALL = function(frame, type = c("BP","CC","MF")){ drv <- dbDriver("SQLite") con <- dbConnect(drv) ##require type to be legit type <- match.arg(type) ##Now Make a table dbExecute(con, "CREATE TABLE data (go_id VARCHAR(10), evidence VARCHAR(3), gene_id INTEGER)") ##populate it with the stuff in frame: clnVals = frame sqlIns <- "INSERT INTO data (go_id, evidence, gene_id) VALUES (?,?,?)" dbBegin(con) res <- dbSendQuery(con,sqlIns, params=unclass(unname(clnVals))) dbClearResult(res) dbCommit(con) ##Now I have to make a 'go_data' table from 'data' that to INSURE that all ##the GO IDs are also in GO.db... .attachGO(con) go_dataSQL = paste0( "CREATE TABLE go_data as SELECT t.go_id AS go_id, g.evidence as evidence, g.gene_id AS gene_id FROM data AS g, go.go_term AS t WHERE g.go_id=t.go_id AND t.ontology='",toupper(type),"'") dbExecute(con,go_dataSQL) dbExecute(con,"CREATE INDEX gdgo on go_data(go_id)") ##Now I have to make the literal table from GO offspringSQL <- paste0("CREATE TABLE go_offspring_literal as SELECT t1.go_id AS go_id, t2.go_id AS offspring_id FROM go.go_",tolower(type),"_offspring as o, go.go_term as t1, go.go_term as t2 WHERE o._id = t1._id AND o._offspring_id = t2._id") dbExecute(con, offspringSQL) dbExecute(con,"CREATE INDEX literalo on go_offspring_literal(offspring_id)") dbExecute(con,"CREATE INDEX literalgo on go_offspring_literal(go_id)") ##Now I need to make the final table: finalSQL = paste0("CREATE TABLE go_all_data as SELECT t.go_id as go_id, g.evidence AS evidence, g.gene_id as gene_id FROM go_data as g CROSS JOIN go_offspring_literal as o CROSS JOIN go.go_term as t WHERE o.go_id=t.go_id and o.offspring_id=g.go_id and t.ontology='",toupper(type),"' UNION SELECT go_id, evidence, gene_id FROM go_data") dbExecute(con,finalSQL) ##And return res = dbGetQuery(con, "SELECT * FROM go_all_data") dbDisconnect(con) return(res) } ## Method to make GOAllFrame objects from GOFrame objects setMethod("GOAllFrame", "GOFrame", function(x){ bp = .convertGOtoGO2ALL(x@data,"BP") mf = .convertGOtoGO2ALL(x@data,"MF") cc = .convertGOtoGO2ALL(x@data,"CC") res = rbind(bp,mf,cc) new("GOAllFrame", data = res, organism = x@organism) }) ## Method to access the data in a GOFrame object setMethod("getGOFrameData", "GOFrame", function(x){x@data}) setMethod("getGOFrameData", "GOAllFrame", function(x){x@data}) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Methods to construct a KEGGFrame ### .testKEGGFrame <- function(x, organism=""){ ##Test that some KEGGIDs are real and that the evidence codes are legit. KEGGIDs <- x[,1] kegg_query <- data.frame(keggList("pathway")) ids <- rownames(kegg_query) realKEGGIDs <- substr(ids, 4, nchar(ids)) ##Test that the data.frame has some rows of data in it if(!dim(x)[1]>0){ stop("There are no rows of data in the data.frame supplied to make a KEGGFrame.") } if(!any(KEGGIDs %in% realKEGGIDs)){ stop("None of elements in the 1st column of your data.frame object are legitimate KEGG IDs.") } if(length(x[,1]) != length(x[,2])){ ## TODO, I don't think that this is going to test this effectively... I probbaly need a different test. stop("You need to have genes for all your KEGG IDs.") } if(organism!=""){ new("KEGGFrame", data = x, organism = organism) }else{new("KEGGFrame", data = x)} } setMethod("KEGGFrame", c(x="data.frame", organism="character"), .testKEGGFrame) setMethod("KEGGFrame", c(x="data.frame", organism="missing"), .testKEGGFrame) ## Method to access the data in a KEGGFrame object setMethod("getKEGGFrameData", "KEGGFrame", function(x){x@data}) organismKEGGFrame <- function() { org <- data.frame(keggList("organism")[,c("species", "organism")]) org$species <- gsub("\\s*\\([^\\)]+\\)", "", org$species) org } ####################################################################### ## Now add a convenience method to just represent the GO as a graph. ## This method should take arg for which ontology the user wants, and ## return a graph. ## users who want less can just use subgraph. ## weight of graph edges will always be 1 for each edge makeGOGraph <- function(ont = c("bp","mf","cc")){ match.arg(ont) df <- switch(ont, "bp"= toTable(GO.db::GOBPPARENTS), "mf"= toTable(GO.db::GOMFPARENTS), "cc"= toTable(GO.db::GOCCPARENTS) ) graph::ftM2graphNEL(as.matrix(df[, 1:2]), W=rep(1,dim(df)[1])) } ## f = makeGOGraph("bp") AnnotationDbi/R/SQL.R0000644000175200017520000005454614710217313015325 0ustar00biocbuildbiocbuild### ========================================================================= ### SQL functions ### ------------- ### ### ------------------------------------------------------------------------- assign("debugSQL", FALSE, envir=RTobjs) debugSQL <- function() { debugSQL <- !get("debugSQL", envir=RTobjs) assign("debugSQL", debugSQL, envir=RTobjs) debugSQL } ## Needed to deal properly with "NULL data frames with 0 rows" returned ## by RSQLite when the result of a SELECT query has 0 row .make0rowDataFrame <- function(colnames) { args <- sapply(colnames, function(col) character(0)) args <- c(args, list(check.names=FALSE, stringsAsFactors=FALSE)) do.call(data.frame, args) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Generate SQL code. ### ### Some string constants .SINGLE_QUOTE <- '\'' .TWO_SINGLE_QUOTE <- paste0(.SINGLE_QUOTE, .SINGLE_QUOTE) .LBRACE_REGX <- '\\{' .RBRACE_REGX <- '\\}' .OUTOFCONTEXT_COLNAME_REGX <- paste0( .LBRACE_REGX, "([^{}", .SINGLE_QUOTE, "]*)", .RBRACE_REGX) ### Replace out-of-context SQL colnames by their "contextualized" versions. ### Example: ### > .contextualizeColnames("{aa} < {bb}", "SOMECONTEXT") ### [1] "SOMECONTEXT.aa < SOMECONTEXT.bb" ### ### 'template': a character vector where elements are out-of-context SQL code. ### 'context': a single string providing the "context" i.e. a table name ### or table alias. .contextualizeColnames <- function(template, context) { replacement <- "\\1" if (!missing(context) && !is.na(context) && context != "") replacement <- paste(context, replacement, sep=".") gsub(.OUTOFCONTEXT_COLNAME_REGX, replacement, template) } .toSQLStringSet <- function(names) { if (length(names) == 0) return("") names <- gsub(.SINGLE_QUOTE, .TWO_SINGLE_QUOTE, names, fixed=TRUE) paste0(.SINGLE_QUOTE, names, .SINGLE_QUOTE, collapse=",") } toSQLStringSet <- .toSQLStringSet # an alias for export .toSQLWhere <- function(colname, names) { if (length(names) == 1 && is.na(names)) paste(colname, "IS NOT NULL") else paste0(colname, " IN (", .toSQLStringSet(names), ")") } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### L2Rlink/L2Rchain manipulation. ### ### AnnDbBimap objects have an L2Rchain slot which must be a non-empty list of ### L2Rlink objects. ### ### Unlike the default "initialize" method, ours allows partial matching. setMethod("initialize", "L2Rlink", function(.Object, ...) { args <- list(...) if (length(args) != 0) { argnames <- names(args) if (is.null(argnames) || any(argnames == "")) stop("all arguments must be named") argnames <- match.arg(argnames, slotNames(.Object), several.ok=TRUE) for (i in seq_len(length(args))) slot(.Object, argnames[i]) <- args[[i]] } .Object } ) L2Rlink <- function(...) new("L2Rlink", ...) setMethod("toString", "L2Rlink", function(x) { paste0("{", x@Lcolname, "}", x@tablename, "{", x@Rcolname, "}") } ) setMethod("show", "L2Rlink", function(object) { callNextMethod() return(invisible(NULL)) ## FIXME: code below is broken s <- paste("{Lcolname}table{Rcolname}:", toString(object)) extracols <- c( if (!is.na(L2Rlink@tagname)) L2Rlink@tagname, L2Rlink@Rattribnames ) if (length(extracols) != 0) { if (!is.null(names(extracols))) extracols <- paste(extracols, "AS", names(extracols)) extracols <- paste(extracols, collapse=", ") s <- c(s, paste("extracols:", extracols)) } if (!is.na(object@Rattrib_join[1])) s <- c(s, paste("Rattrib_join:", object@Rattrib_join)) s <- c(s, paste("filter:", object@filter)) cat(strwrap(s, exdent=4), sep="\n") } ) setMethod("rev", "L2Rlink", function(x) { tmp <- x@Lcolname x@Lcolname <- x@Rcolname x@Rcolname <- tmp x } ) L2Rchain.rev <- function(L2Rchain) rev(lapply(L2Rchain, rev)) .L2Rchain.toString <- function(L2Rchain) paste(sapply(L2Rchain, toString), collapse="-") L2Rchain.Ltablename <- function(L2Rchain) L2Rchain[[1]]@tablename L2Rchain.Rtablename <- function(L2Rchain) L2Rchain[[length(L2Rchain)]]@tablename L2Rchain.Lfilter <- function(L2Rchain) { filter <- L2Rchain[[1]]@filter if (filter == "1") return(filter) paste0("(", .contextualizeColnames(filter), ")") } L2Rchain.Rfilter <- function(L2Rchain) { filter <- L2Rchain[[length(L2Rchain)]]@filter if (filter == "1") return(filter) paste0("(", .contextualizeColnames(filter), ")") } L2Rchain.Lkeyname <- function(L2Rchain) L2Rchain[[1]]@Lcolname L2Rchain.Rkeyname <- function(L2Rchain) L2Rchain[[length(L2Rchain)]]@Rcolname ### Return the first tag colname found (from left to right) or NA if the ### L2Rchain chain has no tag. L2Rchain.tagname <- function(L2Rchain) { tagname <- sapply(L2Rchain, function(L2Rlink) L2Rlink@tagname) tagname <- tagname[!is.na(tagname)][1] if (is.na(tagname)) return(tagname) if (!is.null(names(tagname))) return(names(tagname)) .contextualizeColnames(tagname) } L2Rchain.Rattribnames <- function(L2Rchain) { Rattribnames0 <- L2Rchain[[length(L2Rchain)]]@Rattribnames if (length(Rattribnames0) == 0) return(character(0)) names(Rattribnames0) } `L2Rchain.Rattribnames<-` <- function(L2Rchain, value) { if (is.null(value)) { L2Rchain[[length(L2Rchain)]]@Rattribnames <- character(0) L2Rchain[[length(L2Rchain)]]@Rattrib_join <- as.character(NA) return(L2Rchain) } if (!is.character(value)) stop("Rattrib names must be a character vector or NULL") Rattribnames0 <- L2Rchain[[length(L2Rchain)]]@Rattribnames if (!all(value %in% names(Rattribnames0))) stop("invalid Rattrib names") if (any(duplicated(value))) stop("can't assign duplicated Rattrib names") L2Rchain[[length(L2Rchain)]]@Rattribnames <- Rattribnames0[value] L2Rchain } ### THIS IS THE CURRENT DESIGN: the left col is the 1st col, the right col is ### the 2nd col and the (optional) tag is the 3rd col, IT MUST BE KEPT ### CONSISTENT THROUGH ALL THE REST OF THIS FILE... FOR NOW. L2Rchain.colmetanames <- function(L2Rchain) { tagname <- L2Rchain.tagname(L2Rchain) c( "Lkeyname", "Rkeyname", if (!is.na(tagname)) "tagname" ) } L2Rchain.colnames <- function(L2Rchain) { tagname <- L2Rchain.tagname(L2Rchain) c( L2Rchain.Lkeyname(L2Rchain), L2Rchain.Rkeyname(L2Rchain), if (!is.na(tagname)) tagname, L2Rchain.Rattribnames(L2Rchain) ) } ### Return a named list of 6 elements. Those elements are pieces of a SQL ### SELECT statement used by some of the DB functions in this file to build ### appropriate ( and hopefully valid ;-) ) full SELECT statements. ### Those code chunks correspond to the following parts of the SELECT ### statement: ### SELECT what FROM from WHERE where ### hence the 6 elements returned by .makeSQLchunks() are divided in ### 3 groups: ### 1) The "what" group: ### - what_Lkey: single string containing the "contextualized" name of ### the leftmost col of 'L2Rchain'. ### - what_Rkey: same but for the rightmost col. ### - what_tag: same for the tag col (character(0) if no tag) which in ### addition is right-pasted with " AS ". ### - what_Rattribs: character vector (can be of length 0) where each ### element is the "contextualized" name of a right attribute ### right-pasted with " AS ". ### 2) The "from" group: ### - from: single string containing the "from" part of the SELECT. ### - this will have to append the altDB IF it is something other than the default DB ### 3) The "where" group: ### - where: single string obtained by "contextualizing" all filters ### contained in 'L2Rchain', putting them in parenthezis and pasting ### them together with the " AND " separator. ### If 'L2Rchain' contains no filters then 'where' is the string "1". ###I need things to be pretty general here because I want to loop through and attach all needed databases, and then at the end, after we have made all the objects, I need to detach all the databases Right now, this assumes that there will not need to be more than about 16 different databases attached for a single session, but I think this is a safe assumption, and also, if we attached and detached them ALL then we would be possibly inviting bad performance to the party. So this seems like an ok compromise for now... ### Need to swap periods for underscores, because periods have a special meaning in SQLite statements. .mangleDBName <- function(name){ gsub("\\.","_",name) } .getaltDBs <- function(map){ .getDB <- function(link){ if(length(link@altDB)>0){ return(link@altDB) } } unique(unlist(lapply(map@L2Rchain, .getDB))) } .attachDBs <- function(dbconn, dbList){ dbListLen = length(dbList) for(i in seq_len(dbListLen)){ altDB = dbList[i] altDBFile = system.file("extdata", paste0(altDB,".sqlite"), package=paste0(altDB,".db")) SQL <- paste0("ATTACH DATABASE '",altDBFile,"' AS ", .mangleDBName(altDB),";") dbAttach(dbconn, SQL) } } attachDBs <- function(dbconn, ann_objs){ lengthObjs = length(ann_objs) allAltDBs = unique(unlist(lapply(ann_objs,.getaltDBs))) .attachDBs(dbconn, allAltDBs) } .makeSQLchunks <- function(L2Rchain) { what_tag <- what_Rattribs <- where <- character(0) chainlen <- length(L2Rchain) for (i in seq_len(chainlen)) { L2Rlink <- L2Rchain[[i]] tablename <- L2Rlink@tablename Lcolname <- L2Rlink@Lcolname Rcolname <- L2Rlink@Rcolname ##This should define the tablename to be prefixed ONLY when it matters if(length(L2Rlink@altDB)>0){ ##Then just append the name onto the table tablename = paste0(.mangleDBName(L2Rlink@altDB),".",tablename) } if (chainlen == 1) { context <- from <- tablename what_Lkey <- paste(context, Lcolname, sep=".") what_Rkey <- paste(context, Rcolname, sep=".") } else { if (i == 1) { context <- "_L" what_Lkey <- paste(context, Lcolname, sep=".") from <- paste(tablename, "AS", context) } else { if (i == chainlen) { context <- "_R" what_Rkey <- paste(context, Rcolname, sep=".") } else { context <- paste0("_", i) } on <- paste0(prev_context, ".", prev_Rcolname, "=", context, ".", Lcolname) from <- paste(from, "INNER JOIN", tablename, "AS", context, "ON", on) } prev_context <- context prev_Rcolname <- Rcolname } if (!is.na(L2Rlink@tagname)) { if (length(what_tag) != 0) stop("'L2Rchain' has more than one tag") tagname <- L2Rlink@tagname what_tag <- .contextualizeColnames(tagname, context) if (!is.null(names(tagname))) what_tag <- paste(what_tag, "AS", names(tagname)) } if (i == chainlen && length(L2Rlink@Rattribnames) != 0) { Rattribnames <- L2Rlink@Rattribnames what_Rattribs <- .contextualizeColnames(Rattribnames, context) if (is.null(names(Rattribnames))) stop("Rattribnames in 'L2Rchain' must be a named character vector") what_Rattribs <- paste(what_Rattribs, "AS", names(Rattribnames)) Rattrib_join <- L2Rlink@Rattrib_join if (!is.na(Rattrib_join)) from <- paste(from, .contextualizeColnames(Rattrib_join, context)) } filter <- L2Rlink@filter if (filter != "1") where <- c(where, .contextualizeColnames(filter, context)) } if (length(where) == 0) where <- "1" else where <- paste0("(", where, ")", collapse=" AND ") SQLchunks <- list( what_Lkey=what_Lkey, what_Rkey=what_Rkey, what_tag=what_tag, what_Rattribs=what_Rattribs, from=from, where=where ) #if (get("debugSQL", envir=RTobjs)) { # cat("SQLchunks:\n") # cat(" what_Lkey: ", SQLchunks$what_Lkey, "\n", sep="") # cat(" what_Rkey: ", SQLchunks$what_Rkey, "\n", sep="") # cat(" what_tag: ", SQLchunks$what_tag, "\n", sep="") # cat(" what_Rattribs:\n") # show(SQLchunks$what_Rattribs) # cat(" from: ", SQLchunks$from, "\n", sep="") # cat(" where:\n") # show(SQLchunks$where) #} SQLchunks } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### DB functions. ### ### Use dbQuery(conn, SQL, 1) instead of dbQuery(conn, SQL)[[1]], ### it's much safer! dbQuery <- function(conn, SQL, j0=NA) { if (get("debugSQL", envir=RTobjs)) { if (!is.character(SQL) || length(SQL) != 1 || is.na(SQL)) stop("[debugSQL] 'SQL' must be a single string") cat("[debugSQL] SQL query: ", SQL, "\n", sep="") st <- system.time(data0 <- dbGetQuery(conn, SQL)) cat("[debugSQL] time: ", st["user.self"], " seconds\n", sep="") } else { data0 <- dbGetQuery(conn, SQL) } if (is.na(j0)) return(data0) ## Needed to deal properly with data frame with 0 column ("NULL data ## frames with 0 rows") returned by RSQLite when the result of a SELECT ## query has 0 row if (nrow(data0) == 0) character(0) else data0[[j0]] } dbAttach <- function(conn, SQL){ obj <- dbSendStatement(conn, SQL) dbClearResult(obj) } dbGetTable <- function(conn, tablename, extra.SQL=NULL) { SQL <- paste0("SELECT * FROM ", tablename) if (!is.null(extra.SQL)) SQL <- paste(SQL, extra.SQL) dbQuery(conn, SQL) } ### CURRENTLY BROKEN! dbRawAnnDbMapToTable <- function(conn, Ltablename, Lkeyname, Lkeys, Rtablename, Rkeyname, Rkeys, show.colnames, from) { # if (!is.null(Rtablename)) # Rkeyname <- paste(Rtablename, Rkeyname, sep=".") # Lkeyname <- paste(Ltablename, Lkeyname, sep=".") SQL <- paste("SELECT", paste(show.colnames, collapse=","), "FROM", from) SQL <- paste(SQL, "WHERE", .toSQLWhere(Lkeyname, Lkeys)) if (!is.null(Rtablename)) SQL <- paste(SQL, "AND", .toSQLWhere(Rkeyname, Rkeys)) dbQuery(conn, SQL) } ### CURRENTLY BROKEN! dbCountRawAnnDbMapRows <- function(conn, Ltablename, Lkeyname, Rtablename, Rkeyname, from) { SQL <- paste("SELECT COUNT(*) FROM", from) SQL <- paste(SQL, "WHERE", .toSQLWhere(Lkeyname, NA)) if (!is.null(Rtablename)) SQL <- paste(SQL, "AND", .toSQLWhere(Rkeyname, NA)) dbQuery(conn, SQL, 1) } .makeSQL <- function(SQLchunks, SQLwhat, Lkeys, Rkeys) { where <- c( .toSQLWhere(SQLchunks$what_Lkey, Lkeys), SQLchunks$where, .toSQLWhere(SQLchunks$what_Rkey, Rkeys) ) where <- paste(where, collapse=" AND ") paste("SELECT", SQLwhat, "FROM", SQLchunks$from, "WHERE", where) } dbSelectFromL2Rchain <- function(conn, L2Rchain, Lkeys, Rkeys) { SQLchunks <- .makeSQLchunks(L2Rchain) cols <- c( SQLchunks$what_Lkey, SQLchunks$what_Rkey, SQLchunks$what_tag, SQLchunks$what_Rattribs ) SQLwhat <- paste(cols, collapse=",") SQL <- .makeSQL(SQLchunks, SQLwhat, Lkeys, Rkeys) data0 <- dbQuery(conn, SQL) colnames(data0) <- L2Rchain.colnames(L2Rchain) if (nrow(data0) != 0) return(data0) .make0rowDataFrame(L2Rchain.colnames(L2Rchain)) } dbCountRowsFromL2Rchain <- function(conn, L2Rchain, Lkeys, Rkeys) { SQLchunks <- .makeSQLchunks(L2Rchain) SQLwhat <- "COUNT(*)" SQL <- .makeSQL(SQLchunks, SQLwhat, Lkeys, Rkeys) dbQuery(conn, SQL, 1) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### dbUniqueVals() and dbCountUniqueVals() ### .dbUniqueVals.SQLresultname <- function(datacache, tablename, colname, filter) { if (is.null(datacache) || filter != "1") return(NULL) full.colname <- paste(tablename, colname, sep=".") paste("dbUniqueVals", full.colname, sep="-") } dbUniqueVals <- function(conn, tablename, colname, filter, datacache=NULL) { SQLresultname <- .dbUniqueVals.SQLresultname(datacache, tablename, colname, filter) if (!is.null(SQLresultname)) { if (exists(SQLresultname, envir=datacache, inherits=FALSE)) { SQLresult <- get(SQLresultname, envir=datacache) if (get("debugSQL", envir=RTobjs)) cat("[debugSQL] Using cached result from SQL query: ", SQLresult$SQL, "\n", sep="") return(SQLresult$result) } } what <- paste("DISTINCT", colname) where <- .toSQLWhere(colname, NA) SQL <- paste("SELECT", what, "FROM", tablename, "WHERE", where) if (filter != "1") SQL <- paste(SQL, "AND", filter) vals <- dbQuery(conn, SQL, 1) if (!is.character(vals)) vals <- as.character(vals) if (!is.null(SQLresultname)) { if (get("debugSQL", envir=RTobjs)) cat("[debugSQL] Putting last SQL query and result in cache\n") SQLresult <- list(SQL=SQL, result=vals) assign(SQLresultname, SQLresult, envir=datacache) } vals } ### Read-only caching! dbCountUniqueVals <- function(conn, tablename, colname, filter, datacache=NULL) { SQLresultname <- .dbUniqueVals.SQLresultname(datacache, tablename, colname, filter) if (!is.null(SQLresultname)) { if (exists(SQLresultname, envir=datacache, inherits=FALSE)) { SQLresult <- get(SQLresultname, envir=datacache) if (get("debugSQL", envir=RTobjs)) cat("[debugSQL] Using cached result from SQL query: ", SQLresult$SQL, "\n", sep="") return(length(SQLresult$result)) } } what <- paste0("COUNT(DISTINCT ", colname, ")") SQL <- paste("SELECT", what, "FROM", tablename) if (filter != "1") SQL <- paste(SQL, "WHERE", filter) dbQuery(conn, SQL, 1) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### dbUniqueMappedKeys() and dbCountUniqueMappedKeys() ### ### IMPORTANT: Use shared cached symbols! ### .dbUniqueMappedKeys.SQLresultname <- function(datacache, L2Rchain, Lkeys, Rkeys, where, direction) { if (is.null(datacache) || length(Lkeys) != 1 || !is.na(Lkeys) || length(Rkeys) != 1 || !is.na(Rkeys) || where != "1") return(NULL) if (direction == 1) symbol <- "uniqueLeftMappedKeys" else symbol <- "uniqueRightMappedKeys" paste(symbol, .L2Rchain.toString(L2Rchain), sep="-") } dbUniqueMappedKeys <- function(conn, L2Rchain, Lkeys, Rkeys, direction, datacache=NULL) { SQLchunks <- .makeSQLchunks(L2Rchain) SQLresultname <- .dbUniqueMappedKeys.SQLresultname(datacache, L2Rchain, Lkeys, Rkeys, SQLchunks$where, direction) if (!is.null(SQLresultname)) { if (exists(SQLresultname, envir=datacache, inherits=FALSE)) { SQLresult <- get(SQLresultname, envir=datacache) if (get("debugSQL", envir=RTobjs)) cat("[debugSQL] Using cached result from SQL query: ", SQLresult$SQL, "\n", sep="") return(SQLresult$result) } } what_Lkey <- SQLchunks$what_Lkey what_Rkey <- SQLchunks$what_Rkey if (direction == 1) distinct_col <- what_Lkey else distinct_col <- what_Rkey what <- paste("DISTINCT", distinct_col) SQL <- .makeSQL(SQLchunks, what, Lkeys, Rkeys) vals <- dbQuery(conn, SQL, 1) if (!is.null(SQLresultname)) { if (get("debugSQL", envir=RTobjs)) cat("[debugSQL] Putting last SQL query and result in cache\n") SQLresult <- list(SQL=SQL, result=vals) assign(SQLresultname, SQLresult, envir=datacache) } vals } ### Read-only caching! dbCountUniqueMappedKeys <- function(conn, L2Rchain, Lkeys, Rkeys, direction, datacache=NULL) { SQLchunks <- .makeSQLchunks(L2Rchain) SQLresultname <- .dbUniqueMappedKeys.SQLresultname(datacache, L2Rchain, Lkeys, Rkeys, SQLchunks$where, direction) if (!is.null(SQLresultname)) { if (exists(SQLresultname, envir=datacache, inherits=FALSE)) { SQLresult <- get(SQLresultname, envir=datacache) if (get("debugSQL", envir=RTobjs)) cat("[debugSQL] Using cached result from SQL query: ", SQLresult$SQL, "\n", sep="") return(length(SQLresult$result)) } } what_Lkey <- SQLchunks$what_Lkey what_Rkey <- SQLchunks$what_Rkey if (direction == 1) distinct_col <- what_Lkey else distinct_col <- what_Rkey SQLwhat <- paste0("COUNT(DISTINCT ", distinct_col, ")") SQL <- .makeSQL(SQLchunks, SQLwhat, Lkeys, Rkeys) dbQuery(conn, SQL, 1) } ## ### Bimap filter function ## L2Rchain.bimapFilter <- function(L2Rchain){ ## filter <- sapply(L2Rchain, function(x){x@filter}) ## filter <- filter[!is.na(filter)] ## return(filter) ## } ## ### BimapFilterReplace function ## L2Rchain.bimapFilterReplace <- function(L2Rchain, value){ ## ori_filt_1 <- L2Rchain[[1]]@filter ## ori_filt_2 <- L2Rchain[[2]]@filter ## message(ori_filt_1) ## message(ori_filt_2) ## species_filt_1 <- gsub("{seed_status}=.+AND","", ori_filt_1, perl=TRUE) ## species_filt_2 <- gsub("{seed_status}=.+AND","", ori_filt_2, perl=TRUE) ## new_filt_1 <- as.character(paste0("{seed_status}='",value,"' AND",species_filt_1)) ## new_filt_2 <- as.character(paste0("{seed_status}='",value,"' AND",species_filt_2)) ## message(new_filt_1) ## message(new_filt_2) ## L2Rchain[[1]]@filter <- new_filt_1 ## L2Rchain[[2]]@filter <- new_filt_2 ## ##output ## ## filter <- sapply(L2Rchain, function(x){x@filter}) ## ## filter <- filter[!is.na(filter)][1] ## ## message(cat("the new filter is:",filter)) ## } AnnotationDbi/R/createAnnObjs-utils.R0000644000175200017520000003210614710217313020526 0ustar00biocbuildbiocbuild### All the createAnnObjs.*_DB() functions currently support the same DB ### schema version (of course, each function support its own schema). DBSCHEMAVERSION <- "2.1" checkDBSCHEMA <- function(dbconn, DBSCHEMA) { schema <- dbmeta(dbconn, "DBSCHEMA") if (schema != DBSCHEMA) stop("invalid DB schema (found ", schema, ", expected ", DBSCHEMA, ")") version <- dbmeta(dbconn, "DBSCHEMAVERSION") if (version != DBSCHEMAVERSION) stop("invalid DB schema version (found ", version, ", expected ", DBSCHEMAVERSION, ")") } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### ### Go3tablenames <- function(all=FALSE) { tablenames <- c("go_bp", "go_cc", "go_mf") if (all) tablenames <- paste0(tablenames, "_all") names(tablenames) <- c("BP", "CC", "MF") tablenames } makeGo3L2Rchain <- function(L2Rchain, tablename, ontology) { chainlen <- length(L2Rchain) L2Rchain[[chainlen]]@tablename <- tablename L2Rchain[[chainlen]]@Rattribnames["Ontology"] <- paste0("'", ontology, "'") L2Rchain } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### ### ### If 'envir' is not NULL then the created objects are assigned to it. ### TODO: The function should check for name clashes createAnnObjs <- function(class, seeds, seed0, envir=NULL) { if (is.null(envir)) envir <- new.env(hash=TRUE, parent=emptyenv()) for (seed in seeds) { seed$Class <- class for (slot in names(seed0)) { if (is.null(seed[slot][[1]])) seed[[slot]] <- seed0[[slot]] } envir[[seed$objName]] <- do.call(new, seed) } envir } ## Function to get all these create statements out of the namespace. createAnnObjs.SchemaChoice = function(schema, prefix, target, dbconn, datacache){ FUN <- get(paste0("createAnnObjs.", schema)) FUN(prefix, target, dbconn, datacache) } createAnnDbBimap <- function(seed, seed0) { for (slot in names(seed0)) { if (is.null(seed[slot][[1]])) seed[[slot]] <- seed0[[slot]] } L2Rchain <- seed$L2Rchain seed$L2Rchain <- lapply(L2Rchain, function(L2Rlink) do.call("L2Rlink", L2Rlink)) do.call(new, seed) } createAnnDbBimaps <- function(seeds, seed0, envir=NULL) { if (is.null(envir)) envir <- new.env(hash=TRUE, parent=emptyenv()) for (seed in seeds) envir[[seed$objName]] <- createAnnDbBimap(seed, seed0) envir } ### 3 special maps that are not AnnDbBimap objects (just named vectors). createCHRLENGTHS <- function(dbconn, dbname="") { if(dbname==""){ ##The usual case data <- dbGetTable(dbconn, "chrlengths") }else{ ##For when people are doing a "CROSS" joined package, we want data from the "org" DB data <- dbGetTable(dbconn, paste0(.mangleDBName(dbname),".chrlengths")) } CHRLENGTHS <- data[["length"]] names(CHRLENGTHS) <- data[["chromosome"]] CHRLENGTHS } createREJECTORF <- function(dbconn) { data <- dbGetTable(dbconn, "reject_orf") data[["systematic_name"]] } createMAPCOUNTS <- function(dbconn, prefix) { data <- dbGetTable(dbconn, "map_counts", "WHERE map_name != 'TOTAL' ORDER BY map_name") if(dim(data)[1]!=0){ MAPCOUNTS <- data[["count"]] names(MAPCOUNTS) <- paste0(prefix, data[["map_name"]]) return(MAPCOUNTS) }else{ return(integer()) } } ### Rename all objects in the 'envir' environment by prefixing them ### with 'prefix'. The function is dumb i.e. it doesn't check for (neither ### doesn't try to avoid) possible name clashes. Note that those issues ### could be easily avoided by assigning the renamed objects to a separate ### environment but... prefixAnnObjNames <- function(envir, prefix) { keys <- ls(envir, all.names=TRUE) for (key in keys) { new_key <- paste0(prefix, key) envir[[new_key]] <- envir[[key]] } remove(list=keys, envir=envir) # remove old keys envir } ##################################################################### ## Below are helper functions to define helpful startup messages for ## especially ornery packages: ## TODO: for these organsism add a waring about Blast2GO (being stale) ## taxIDList = c("Canis_familiaris"="9615", ## "Sus_Scrofa"="9823", ## "Anopheles_gambiae"="180454", ## "Xenopus_laevis"="8355", ## "Macaca_mulatta"="9544", ## "Pan_troglodytes"="9598") ## ## "Escherichia_coli_K12"="511145") ## The above has been fixed, so we removed the warning for Bioc 3.13 choosePackage <- function(pkgType){ ## defines a blackList to choose the type of message based on the pkg name. ## If you are not in the blackList, then we don't need a message. ## Default fallthrough message means there is no message. type <- switch(EXPR = pkgType, "ecoli2.db" = "partial", "hugene10stprobeset.db" = "exon_probeset", #"hugene10stv1cdf" = "unsupported", ## not AnnotationDbi "hugene11stprobeset.db" = "exon_probeset", "lumiHumanAll.db" = "lumi", "lumiHumanIDMapping.db" = "lumi", "lumiMouseAll.db" = "lumi", "lumiMouseIDMapping.db" = "lumi", "lumiRatAll.db" = "lumi", "lumiRatIDMapping.db" = "lumi", "mogene10stprobeset.db" = "exon_probeset", "mogene11stprobeset.db" = "exon_probeset", "ragene10stprobeset.db" = "exon_probeset", "ragene11stprobeset.db" = "exon_probeset", "HuExExonProbesetLocation" = "hg19", "GGHumanMethCancerPanelv1.db" = "deprecated", "HuExExonProbesetLocationHg18" = "deprecatedRaffaeleCalogero", "HuExExonProbesetLocationHg19" = "deprecatedRaffaeleCalogero", "illuminaHumanv1BeadID.db" = "deprecatedMarkDunning", "illuminaHumanv2BeadID.db" = "deprecatedMarkDunning", "illuminaHumanv3BeadID.db" = "deprecatedMarkDunning", "illuminaHumanv4BeadID.db" = "deprecatedMarkDunning", "illuminaMousev1BeadID.db" = "deprecatedMarkDunning", "illuminaMousev1p1BeadID.db" = "deprecatedMarkDunning", "illuminaMousev2BeadID.db" = "deprecatedMarkDunning", "illuminaRatv1BeadID.db" = "deprecatedMarkDunning", ## Simon, Ferrari and Favero can get a pass till next time ## Pass given on 11/8/10 ## "hs25kresogen.db" = "deprecatedSimonDeBernard", ## "mm24kresogen.db" = "deprecatedSimonDeBernard", ## "org.Cf.eg" = "B2GOstale", ## "org.Ss.eg" = "B2GOstale", ## "org.Ag.eg" = "B2GOstale", ## "org.Xl.eg" = "B2GOstale", ## "org.Mmu.eg" = "B2GOstale", ## "org.Pt.eg" = "B2GOstale", ## "canine.db" = "B2GOstale", ## "canine2.db" = "B2GOstale", ## "xlaevis.db" = "B2GOstale", ## End of the B2GO warnings (remove once problem is resolved) "org.Sco.eg.db" = "deprecated", "KEGG.db" = "keggstale", ## deprecation of inparanoid and plasmo packages "hom.Hs.inp.db" = "inparanoid", "hom.Mm.inp.db" = "inparanoid", "hom.Rn.inp.db" = "inparanoid", "hom.Dm.inp.db" = "inparanoid", "hom.Sc.inp.db" = "inparanoid", "hom.At.inp.db" = "inparanoid", "hom.Ce.inp.db" = "inparanoid", "hom.Dr.inp.db" = "inparanoid", "org.Pf.plasmo.db" = "plasmo", "NO_MESSAGE_TYPE" ) } ## This function defines stock messages that can be associated with certain ## packages. ## It can also be called directly by people who are outside of the system but ## want a stock message annotMessage <- function(msgType, pkgType){ msg <- switch(EXPR = msgType, "deprecated" = paste("\n",pkgType,"is an older package, and", "the package contributor no longer supports it. Please", "be advised that this package is now out of date and should", "not occur in future bioconductor releases."), "deprecatedSimonDeBernard" = paste("\n",pkgType,"is", "an older package, and the package contributor no", "longer supports it. Please be advised that this", "package is now out of date and should not occur in", "future bioconductor releases."), "deprecatedRaffaeleCalogero" = paste("\n",pkgType,"is", "an older package, and the package contributor no", "longer supports it. Please be advised that this", "package is now out of date and should not occur in", "future bioconductor releases. For a more current", "package containing the same kind of data, please use", "the HuExExonProbesetLocation package instead"), "deprecatedMarkDunning" = paste("\n",pkgType,"is an", "older package, and the package contributor no longer", "supports it. Please be advised that this package is", "now out of date and should not occur in future", "bioconductor releases. For a more current package", "containing the same kind of data, please use the", "appropriate illumina_XXX_.db packages instead of the", "illumina_XXX_BeadID.db packages and make use of the new", "illumina_XXX_ARRAYADDRESS mapping to convert between", "BeadIDs and Illumina IDs. \n\n *_XXX_ here refers to the", "species and version for this platform"), "keggstale" = paste("\n",pkgType,"contains mappings based on", " older", "data because the original resource was removed from the", "the public domain before the most recent update was", "produced. This package should now be considered deprecated", "and future versions of Bioconductor may not have it", "available. Users who want more current data are encouraged", "to look at the KEGGREST or reactome.db packages"), "B2GOstale" = paste("\n",pkgType,"contains GO mappings based", "on older data", "because the Blast2GO data resource was removed from", "the public domain just before the most recent update was", "produced. We are working on an alternative means to get", "this kind of data before the next release."), "exon_probeset" = paste("\n",pkgType,"is based on exon", "probesets. For a more gene-centric view, use the", "transcriptcluster version of this package."), "unsupported" = paste("\n The data", "in this package are based on mapping files labeled as", "'unsupported' by their source."), "lumi" = paste("\n",pkgType,"is using or is likely to", "need access to special nuID identifiers. Users can learn", "about these identifiers from vignette documentation", "provided with the lumi package."), "partial" = paste("\n",pkgType,"is providing annotations", "for only one of the species that are supported by this", "platform. You may want to get other annotations from other", "sources/packages in order to cover all the species that", "are represented by probes on this platform."), "hg19" = paste("\n The",pkgType,"package was build to match", "the HG19 build."), "inparanoid" = paste("\n", pkgType, "is based on old data", "that are no longer updated and will be", "deprecated. Please use the orthology.eg.db", "package instead."), "plasmo" = paste("\n", pkgType, "is based on old data that are", "no longer updated.", pkgType, "is deprecated", "and will be removed from Bioconductor version", "3.15."), "NO_MESSAGE_TYPE" = "" ) if(msg != ""){ msg <- paste0("\n", paste(strwrap(msg, exdent=2), collapse="\n"), "\n") } } annoStartupMessages <- function(pkgType){ msgType <- choosePackage(pkgType) annotMessage(msgType, pkgType) } ## function for name-mangling (or not name-mangling depending on how people ## want their DB objects named). Basically this code exists so that I can ## change this without having to alter a ton of files whenever someone decides ## that they don't like our name convention. dbObjectName <- function(pkgname, dbType){ ## if(dbType=="ChipDb"){ ## names <- strsplit(pkgname, split="\\.") ## newName <- paste(paste(unlist(names)[1],collapse="_"), ## dbType,sep="_") ## }else{ ## names <- strsplit(pkgname, split="\\.") ## newName <- paste(paste(unlist(names)[c(2,3)],collapse="_"), ## dbType,sep="_") ## } ## newName ## For now we will just use the package name pkgname } AnnotationDbi/R/createAnnObjs.ARABIDOPSISCHIP_DB.R0000644000175200017520000001735614710217313022152 0ustar00biocbuildbiocbuild### ========================================================================= ### An SQLite-based ann data package (AnnDbPkg) provides a set of pre-defined ### AnnObj objects that are created at load-time. This set depends only on ### the underlying db schema i.e. all the SQLite-based ann data packages that ### share the same underlying db schema will provide the same set of AnnObj ### objects. ### ### This file describes the set of AnnObj objects provided by any ### ARABIDOPSISCHIP_DB-based package i.e. any SQLite-based ann data package based ### on the ARABIDOPSISCHIP_DB schema. ### The createAnnObjs.ARABIDOPSISCHIP_DB() function is the main entry point for ### this file: it is called by any ARABIDOPSISCHIP_DB-based package at load-time. ### ------------------------------------------------------------------------- orgPkg = "org.At.tair" ARABIDOPSISCHIP_DB_L2Rlink1 <- list(tablename="probes", Lcolname="probe_id", Rcolname="gene_id", filter="{is_multiple}='0'") ARABIDOPSISCHIP_DB_L2Rlink2 <- list(tablename="genes", Lcolname="gene_id", Rcolname="_id", altDB=orgPkg) ### Mandatory fields: objName, Class and L2Rchain ARABIDOPSISCHIP_DB_AnnDbBimap_seeds <- list( list( objName="ACCNUM", Class="ProbeAnnDbBimap", L2Rchain=list( ARABIDOPSISCHIP_DB_L2Rlink1, ARABIDOPSISCHIP_DB_L2Rlink2, list( tablename="genes", Lcolname="_id", Rcolname="gene_id" ) )##, ## replace.multiple="multiple" ), list( objName="ARACYC", Class="ProbeAnnDbBimap", L2Rchain=list( ARABIDOPSISCHIP_DB_L2Rlink1, ARABIDOPSISCHIP_DB_L2Rlink2, list( tablename="aracyc", Lcolname="_id", Rcolname="pathway_name", altDB=orgPkg ) ) ), list( objName="CHR", Class="ProbeAnnDbBimap", L2Rchain=list( ARABIDOPSISCHIP_DB_L2Rlink1, ARABIDOPSISCHIP_DB_L2Rlink2, list( tablename="gene_info", Lcolname="_id", Rcolname="chromosome", altDB=orgPkg ) ) ), list( objName="ENZYME", Class="ProbeAnnDbBimap", L2Rchain=list( ARABIDOPSISCHIP_DB_L2Rlink1, ARABIDOPSISCHIP_DB_L2Rlink2, list( tablename="ec", Lcolname="_id", Rcolname="ec_number", altDB=orgPkg ) ) ), list( objName="ARACYCENZYME", Class="ProbeAnnDbBimap", L2Rchain=list( ARABIDOPSISCHIP_DB_L2Rlink1, ARABIDOPSISCHIP_DB_L2Rlink2, list( tablename="enzyme", Lcolname="_id", Rcolname="ec_name", altDB=orgPkg ) ) ), list( objName="GENENAME", Class="ProbeAnnDbBimap", L2Rchain=list( ARABIDOPSISCHIP_DB_L2Rlink1, ARABIDOPSISCHIP_DB_L2Rlink2, list( tablename="gene_info", Lcolname="_id", Rcolname="gene_name", altDB=orgPkg ) ) ), list( objName="ENTREZID", Class="ProbeAnnDbBimap", L2Rchain=list( ARABIDOPSISCHIP_DB_L2Rlink1, ARABIDOPSISCHIP_DB_L2Rlink2, list( tablename="entrez_genes", Lcolname="_id", Rcolname="gene_id" ) ) ), ## list( ## objName="MULTIHIT", ## Class="ProbeAgiAnnDbMap", ## L2Rchain=list( ## ARABIDOPSISCHIP_DB_L2Rlink1, ## ARABIDOPSISCHIP_DB_L2Rlink2, ## list( ## tablename="genes", ## Lcolname="_id", ## Rcolname="gene_id", ## altDB=orgPkg ## ) ## ), ## replace.single=as.character(NA) ## ), list( objName="PATH", Class="ProbeAnnDbBimap", L2Rchain=list( ARABIDOPSISCHIP_DB_L2Rlink1, ARABIDOPSISCHIP_DB_L2Rlink2, list( tablename="kegg", Lcolname="_id", Rcolname="path_id", altDB=orgPkg ) ) ), list( objName="PMID", Class="ProbeAnnDbBimap", L2Rchain=list( ARABIDOPSISCHIP_DB_L2Rlink1, ARABIDOPSISCHIP_DB_L2Rlink2, list( tablename="pubmed", Lcolname="_id", Rcolname="pubmed_id", altDB=orgPkg ) ) ), list( objName="SYMBOL", Class="ProbeAnnDbBimap", L2Rchain=list( ARABIDOPSISCHIP_DB_L2Rlink1, ARABIDOPSISCHIP_DB_L2Rlink2, list( tablename="gene_info", Lcolname="_id", Rcolname="symbol", altDB=orgPkg ) ) ), list( objName="CHRLOC", Class="ProbeAnnDbMap", L2Rchain=list( ARABIDOPSISCHIP_DB_L2Rlink1, ARABIDOPSISCHIP_DB_L2Rlink2, list( tablename="chromosome_locations", Lcolname="_id", tagname=c(Chromosome="{seqname}"), Rcolname="start_location", altDB=orgPkg ) ), rightColType="integer" ), list( objName="CHRLOCEND", Class="ProbeAnnDbMap", L2Rchain=list( ARABIDOPSISCHIP_DB_L2Rlink1, ARABIDOPSISCHIP_DB_L2Rlink2, list( tablename="chromosome_locations", Lcolname="_id", tagname=c(Chromosome="{seqname}"), Rcolname="end_location", altDB=orgPkg ) ), rightColType="integer" ), list( objName="GO", Class="ProbeGo3AnnDbBimap", L2Rchain=list( ARABIDOPSISCHIP_DB_L2Rlink1, ARABIDOPSISCHIP_DB_L2Rlink2, list( #tablename="go_term", # no rightmost table for a Go3AnnDbBimap Lcolname="_id", tagname=c(Evidence="{evidence}"), Rcolname="go_id", Rattribnames=c(Ontology="NULL"), altDB=orgPkg ) ), rightTables=Go3tablenames() ) ) createAnnObjs.ARABIDOPSISCHIP_DB <- function(prefix, objTarget, dbconn, datacache) { checkDBSCHEMA(dbconn, "ARABIDOPSISCHIP_DB") ## AnnDbBimap objects seed0 <- list( objTarget=objTarget, datacache=datacache ) ann_objs <- createAnnDbBimaps(ARABIDOPSISCHIP_DB_AnnDbBimap_seeds, seed0) attachDBs(dbconn, ann_objs) ## Reverse maps ann_objs$ENZYME2PROBE <- revmap(ann_objs$ENZYME, objName="ENZYME2PROBE") ann_objs$PATH2PROBE <- revmap(ann_objs$PATH, objName="PATH2PROBE") ann_objs$PMID2PROBE <- revmap(ann_objs$PMID, objName="PMID2PROBE") ann_objs$GO2PROBE <- revmap(ann_objs$GO, objName="GO2PROBE") map <- ann_objs$GO2PROBE map@rightTables <- Go3tablenames(all=TRUE) map@objName <- "GO2ALLPROBES" ann_objs$GO2ALLPROBES <- map ## 2 special map that is not an AnnDbBimap object (just a named integer vector) ann_objs$CHRLENGTHS <- createCHRLENGTHS(dbconn, dbname="org.At.tair") ann_objs$MAPCOUNTS <- createMAPCOUNTS(dbconn, prefix) ## 1 special string to let us know who the supporting org package is. ann_objs$ORGPKG <- "org.At.tair" ## Some pre-caching Lkeys(ann_objs$GO) prefixAnnObjNames(ann_objs, prefix) } AnnotationDbi/R/createAnnObjs.ARABIDOPSIS_DB.R0000644000175200017520000001460314710217313021476 0ustar00biocbuildbiocbuild### ========================================================================= ### An SQLite-based ann data package (AnnDbPkg) provides a set of pre-defined ### AnnObj objects that are created at load-time. This set depends only on ### the underlying db schema i.e. all the SQLite-based ann data packages that ### share the same underlying db schema will provide the same set of AnnObj ### objects. ### ### This file describes the set of AnnObj objects provided by any ### ARABIDOPSIS_DB-based package i.e. any SQLite-based ann data package based ### on the ARABIDOPSIS_DB schema. ### The createAnnObjs.ARABIDOPSIS_DB() function is the main entry point for ### this file: it is called by any ARABIDOPSIS_DB-based package at load-time. ### ------------------------------------------------------------------------- ARABIDOPSIS_DB_L2Rlink1 <- list(tablename="genes", Lcolname="gene_id", Rcolname="_id") ### Mandatory fields: objName, Class and L2Rchain ARABIDOPSIS_DB_AnnDbBimap_seeds <- list( list( objName="ARACYC", Class="AnnDbBimap", L2Rchain=list( ARABIDOPSIS_DB_L2Rlink1, list( tablename="aracyc", Lcolname="_id", Rcolname="pathway_name" ) ), direction=-1L ), list( objName="CHR", Class="AnnDbBimap", L2Rchain=list( ARABIDOPSIS_DB_L2Rlink1, list( tablename="gene_info", Lcolname="_id", Rcolname="chromosome" ) ) ), list( objName="ENZYME", Class="AnnDbBimap", L2Rchain=list( ARABIDOPSIS_DB_L2Rlink1, list( tablename="ec", Lcolname="_id", Rcolname="ec_number" ) ) ), list( objName="ARACYCENZYME", Class="AnnDbBimap", L2Rchain=list( ARABIDOPSIS_DB_L2Rlink1, list( tablename="enzyme", Lcolname="_id", Rcolname="ec_name" ) ) ), list( objName="GENENAME", Class="AnnDbBimap", L2Rchain=list( ARABIDOPSIS_DB_L2Rlink1, list( tablename="gene_info", Lcolname="_id", Rcolname="gene_name" ) ) ), list( objName="PATH", Class="AnnDbBimap", L2Rchain=list( ARABIDOPSIS_DB_L2Rlink1, list( tablename="kegg", Lcolname="_id", Rcolname="path_id" ) ) ), list( objName="PMID", Class="AnnDbBimap", L2Rchain=list( ARABIDOPSIS_DB_L2Rlink1, list( tablename="pubmed", Lcolname="_id", Rcolname="pubmed_id" ) ) ), list( objName="SYMBOL", Class="AnnDbBimap", L2Rchain=list( ARABIDOPSIS_DB_L2Rlink1, list( tablename="gene_info", Lcolname="_id", Rcolname="symbol" ) ) ), list( objName="CHRLOC", Class="AnnDbMap", L2Rchain=list( ARABIDOPSIS_DB_L2Rlink1, list( tablename="chromosome_locations", Lcolname="_id", tagname=c(Chromosome="{seqname}"), Rcolname="start_location" ) ), rightColType="integer" ), list( objName="CHRLOCEND", Class="AnnDbMap", L2Rchain=list( ARABIDOPSIS_DB_L2Rlink1, list( tablename="chromosome_locations", Lcolname="_id", tagname=c(Chromosome="{seqname}"), Rcolname="end_location" ) ), rightColType="integer" ), list( objName="REFSEQ", Class="AnnDbBimap", L2Rchain=list( ARABIDOPSIS_DB_L2Rlink1, list( tablename="refseq", Lcolname="_id", Rcolname="accession" ) ) ), list( objName="ENTREZID", Class="AnnDbBimap", L2Rchain=list( ARABIDOPSIS_DB_L2Rlink1, list( tablename="entrez_genes", Lcolname="_id", Rcolname="gene_id" ) ) ), ## list( ## objName="UNIPROT", ## Class="AnnDbBimap", ## L2Rchain=list( ## ARABIDOPSIS_DB_L2Rlink1, ## list( ## tablename="uniprot", ## Lcolname="_id", ## Rcolname="uniprot_id" ## ) ## ) ## ), list( objName="GO", Class="Go3AnnDbBimap", L2Rchain=list( ARABIDOPSIS_DB_L2Rlink1, list( #tablename="go_term", # no rightmost table for a Go3AnnDbBimap Lcolname="_id", tagname=c(Evidence="{evidence}"), Rcolname="go_id", Rattribnames=c(Ontology="NULL") ) ), rightTables=Go3tablenames() ) ) createAnnObjs.ARABIDOPSIS_DB <- function(prefix, objTarget, dbconn, datacache) { checkDBSCHEMA(dbconn, "ARABIDOPSIS_DB") ## AnnDbBimap objects seed0 <- list( objTarget=objTarget, datacache=datacache ) ann_objs <- createAnnDbBimaps(ARABIDOPSIS_DB_AnnDbBimap_seeds, seed0) ## Reverse maps ann_objs$ENZYME2TAIR <- revmap(ann_objs$ENZYME, objName="ENZYME2TAIR") ann_objs$PATH2TAIR <- revmap(ann_objs$PATH, objName="PATH2TAIR") ann_objs$PMID2TAIR <- revmap(ann_objs$PMID, objName="PMID2TAIR") ann_objs$GO2TAIR <- revmap(ann_objs$GO, objName="GO2TAIR") ann_objs$REFSEQ2TAIR <- revmap(ann_objs$REFSEQ, objName="REFSEQ2TAIR") map <- ann_objs$GO2TAIR map@rightTables <- Go3tablenames(all=TRUE) map@objName <- "GO2ALLTAIRS" ann_objs$GO2ALLTAIRS <- map ## 2 special maps that are not AnnDbBimap objects (just named integer vectors) ann_objs$CHRLENGTHS <- createCHRLENGTHS(dbconn) ann_objs$MAPCOUNTS <- createMAPCOUNTS(dbconn, prefix) ## Some pre-caching Lkeys(ann_objs$GO) #mappedLkeys(ann_objs$GO) #Rkeys(ann_objs$GO2TAIR) #mappedRkeys(ann_objs$GO2TAIR) prefixAnnObjNames(ann_objs, prefix) } AnnotationDbi/R/createAnnObjs.COELICOLOR_DB.R0000644000175200017520000001453314710217313021372 0ustar00biocbuildbiocbuild### ========================================================================= ### An SQLite-based ann data package (AnnDbPkg) provides a set of pre-defined ### AnnObj objects that are created at load-time. This set depends only on ### the underlying db schema i.e. all the SQLite-based ann data packages that ### share the same underlying db schema will provide the same set of AnnObj ### objects. ### ### This file describes the set of AnnObj objects provided by any ### COELICOLOR_DB-based package i.e. any SQLite-based ann data package based ### on the COELICOLOR_DB schema. ### The createAnnObjs.COELICOLOR_DB() function is the main entry point for ### this file: it is called by any COELICOLOR_DB-based package at load-time. ### ------------------------------------------------------------------------- COELICOLOR_DB_L2Rlink1 <- list(tablename="genes", Lcolname="gene_id", Rcolname="_id") ### Mandatory fields: objName, Class and L2Rchain COELICOLOR_DB_AnnDbBimap_seeds <- list( list( objName="ACCNUM", Class="AnnDbBimap", L2Rchain=list( COELICOLOR_DB_L2Rlink1, list( tablename="accessions", Lcolname="_id", Rcolname="accession" ) ) ), list( objName="ALIAS2EG", Class="AnnDbBimap", L2Rchain=list( COELICOLOR_DB_L2Rlink1, list( tablename="alias", Lcolname="_id", Rcolname="alias_symbol" ) ), direction=-1L ), list( objName="CHR", Class="AnnDbBimap", L2Rchain=list( COELICOLOR_DB_L2Rlink1, list( tablename="chromosomes", Lcolname="_id", Rcolname="chromosome" ) ) ), list( objName="ENZYME", Class="AnnDbBimap", L2Rchain=list( COELICOLOR_DB_L2Rlink1, list( tablename="ec", Lcolname="_id", Rcolname="ec_number" ) ) ), list( objName="GENENAME", Class="AnnDbBimap", L2Rchain=list( COELICOLOR_DB_L2Rlink1, list( tablename="gene_info", Lcolname="_id", Rcolname="gene_name" ) ) ), list( objName="PATH", Class="AnnDbBimap", L2Rchain=list( COELICOLOR_DB_L2Rlink1, list( tablename="kegg", Lcolname="_id", Rcolname="path_id" ) ) ), list( objName="PMID", Class="AnnDbBimap", L2Rchain=list( COELICOLOR_DB_L2Rlink1, list( tablename="pubmed", Lcolname="_id", Rcolname="pubmed_id" ) ) ), list( objName="REFSEQ", Class="AnnDbBimap", L2Rchain=list( COELICOLOR_DB_L2Rlink1, list( tablename="refseq", Lcolname="_id", Rcolname="accession" ) ) ), list( objName="LOCUSTAG", Class="AnnDbBimap", L2Rchain=list( COELICOLOR_DB_L2Rlink1, list( tablename="locus", Lcolname="_id", Rcolname="locus_tag" ) ) ), list( objName="PROTEINGI", Class="AnnDbBimap", L2Rchain=list( COELICOLOR_DB_L2Rlink1, list( tablename="protein", Lcolname="_id", Rcolname="protein_gi" ) ) ), list( objName="SYMBOL", Class="AnnDbBimap", L2Rchain=list( COELICOLOR_DB_L2Rlink1, list( tablename="symbol", Lcolname="_id", Rcolname="symbol" ) ) ), list( objName="CHRLOC", Class="AnnDbMap", L2Rchain=list( COELICOLOR_DB_L2Rlink1, list( tablename="chromosome_locations", Lcolname="_id", tagname=c(Chromosome="{seqname}"), Rcolname="start_location" ) ), rightColType="integer" ), list( objName="CHRLOCEND", Class="AnnDbMap", L2Rchain=list( COELICOLOR_DB_L2Rlink1, list( tablename="chromosome_locations", Lcolname="_id", tagname=c(Chromosome="{seqname}"), Rcolname="end_location" ) ), rightColType="integer" ), list( objName="GO", Class="Go3AnnDbBimap", L2Rchain=list( COELICOLOR_DB_L2Rlink1, list( #tablename="go_term", # no rightmost table for a Go3AnnDbBimap Lcolname="_id", tagname=c(Evidence="{evidence}"), Rcolname="go_id", Rattribnames=c(Ontology="NULL") ) ), rightTables=Go3tablenames() ) ) createAnnObjs.COELICOLOR_DB <- function(prefix, objTarget, dbconn, datacache) { checkDBSCHEMA(dbconn, "COELICOLOR_DB") ## AnnDbBimap objects seed0 <- list( objTarget=objTarget, datacache=datacache ) ann_objs <- createAnnDbBimaps(COELICOLOR_DB_AnnDbBimap_seeds, seed0) ## Reverse maps ann_objs$ACCNUM2EG <- revmap(ann_objs$ACCNUM, objName="ACCNUM2EG") ann_objs$ENZYME2EG <- revmap(ann_objs$ENZYME, objName="ENZYME2EG") ann_objs$PATH2EG <- revmap(ann_objs$PATH, objName="PATH2EG") ann_objs$PMID2EG <- revmap(ann_objs$PMID, objName="PMID2EG") ann_objs$REFSEQ2EG <- revmap(ann_objs$REFSEQ, objName="REFSEQ2EG") ann_objs$SYMBOL2EG <- revmap(ann_objs$SYMBOL, objName="SYMBOL2EG") ann_objs$GO2EG <- revmap(ann_objs$GO, objName="GO2EG") map <- ann_objs$GO2EG map@rightTables <- Go3tablenames(all=TRUE) map@objName <- "GO2ALLEGS" ann_objs$GO2ALLEGS <- map ## 2 special maps that are not AnnDbBimap objects (just named integer vectors) ann_objs$CHRLENGTHS <- createCHRLENGTHS(dbconn) ann_objs$MAPCOUNTS <- createMAPCOUNTS(dbconn, prefix) ## Some pre-caching Lkeys(ann_objs$GO) prefixAnnObjNames(ann_objs, prefix) } AnnotationDbi/R/createAnnObjs.GO_DB.R0000644000175200017520000002224114710217313020240 0ustar00biocbuildbiocbuild### ========================================================================= ### An SQLite-based ann data package (AnnDbPkg) provides a set of pre-defined ### AnnObj objects that are created at load-time. This set depends only on ### the underlying db schema i.e. all the SQLite-based ann data packages that ### share the same underlying db schema will provide the same set of AnnObj ### objects. ### ### This file describes the set of AnnObj objects provided by any ### GO_DB-based package i.e. any SQLite-based ann data package based ### on the GO_DB schema. ### The createAnnObjs.GO_DB() function is the main entry point for ### this file: it is called by any GO_DB-based package at load-time. ### ------------------------------------------------------------------------- ### Mandatory fields: objName, Class and L2Rchain GO_DB_AnnDbBimap_seeds <- list( # list( # objName="ENTREZID2GO", # Class="GoAnnDbBimap", # L2Rchain=list( # list( # tablename="go_gene", # Lcolname="gene_id", # tagname=c(Relationship_type="{relationship_type}"), # Rcolname="_id" # ), # list( # tablename="go_term", # Lcolname="_id", # Rcolname="go_id", # Rattribnames=c(Ontology="{ontology}") # ) # ) # ), # ## TODO: Try to define the ENTREZID map as the reverse of ENTREZID2GO # list( # objName="ENTREZID", # Class="AnnDbBimap", # L2Rchain=list( # list( # tablename="go_term", # Lcolname="go_id", # Rcolname="_id" # ), # list( # tablename="go_gene", # Lcolname="_id", # tagname=c(Relationship_type="{relationship_type}"), # Rcolname="gene_id" # ) # ) # ), # list( # objName="ALLENTREZID", # Class="AnnDbBimap", # L2Rchain=list( # list( # tablename="go_term", # Lcolname="go_id", # Rcolname="_id" # ), # list( # tablename="go_all_gene", # Lcolname="_id", # tagname=c(Relationship_type="{relationship_type}"), # Rcolname="gene_id" # ) # ) # ), list( objName="BPPARENTS", Class="AnnDbBimap", L2Rchain=list( list( tablename="go_term", Lcolname="go_id", Rcolname="_id", filter="{ontology}='BP'" ), list( tablename="go_bp_parents", Lcolname="_id", tagname=c(RelationshipType="{relationship_type}"), Rcolname="_parent_id" ), list( tablename="go_term", Lcolname="_id", Rcolname="go_id" ) ) ), list( objName="CCPARENTS", Class="AnnDbBimap", L2Rchain=list( list( tablename="go_term", Lcolname="go_id", Rcolname="_id", filter="{ontology}='CC'" ), list( tablename="go_cc_parents", Lcolname="_id", tagname=c(RelationshipType="{relationship_type}"), Rcolname="_parent_id" ), list( tablename="go_term", Lcolname="_id", Rcolname="go_id" ) ) ), list( objName="MFPARENTS", Class="AnnDbBimap", L2Rchain=list( list( tablename="go_term", Lcolname="go_id", Rcolname="_id", filter="{ontology}='MF'" ), list( tablename="go_mf_parents", Lcolname="_id", tagname=c(RelationshipType="{relationship_type}"), Rcolname="_parent_id" ), list( tablename="go_term", Lcolname="_id", Rcolname="go_id" ) ) ), list( objName="BPANCESTOR", Class="AnnDbBimap", L2Rchain=list( list( tablename="go_term", Lcolname="go_id", Rcolname="_id", filter="{ontology}='BP'" ), list( tablename="go_bp_offspring", Lcolname="_offspring_id", Rcolname="_id" ), list( tablename="go_term", Lcolname="_id", Rcolname="go_id" ) ) ), list( objName="CCANCESTOR", Class="AnnDbBimap", L2Rchain=list( list( tablename="go_term", Lcolname="go_id", Rcolname="_id", filter="{ontology}='CC'" ), list( tablename="go_cc_offspring", Lcolname="_offspring_id", Rcolname="_id" ), list( tablename="go_term", Lcolname="_id", Rcolname="go_id" ) ) ), list( objName="MFANCESTOR", Class="AnnDbBimap", L2Rchain=list( list( tablename="go_term", Lcolname="go_id", Rcolname="_id", filter="{ontology}='MF'" ), list( tablename="go_mf_offspring", Lcolname="_offspring_id", Rcolname="_id" ), list( tablename="go_term", Lcolname="_id", Rcolname="go_id" ) ) ), list( objName="TERM", Class="GOTermsAnnDbBimap", L2Rchain=list( list( tablename="go_term", Lcolname="go_id", Rcolname="go_id", Rattribnames=c( Term="{term}", Ontology="{ontology}", Definition="{definition}", Synonym="go_synonym.synonym", Secondary="go_synonym.secondary" ), Rattrib_join="LEFT JOIN go_synonym ON {_id}=go_synonym._id" ) ) ), list( objName="OBSOLETE", Class="GOTermsAnnDbBimap", L2Rchain=list( list( tablename="go_obsolete", Lcolname="go_id", Rcolname="go_id", Rattribnames=c( Term="{term}", Ontology="{ontology}", Definition="{definition}", ## The RSQLite driver crashes on queries like ## SELECT NULL, ... FROM ... ## so a temporary workaround is to use ## SELECT '', ... FROM ... #Synonym="NULL", #Secondary="NULL" Synonym="''", Secondary="''" ) ) ) ), list( objName="SYNONYM", Class="GOTermsAnnDbBimap", L2Rchain=list( list( tablename="go_synonym", Lcolname="synonym", Rcolname="_id", filter="{like_go_id}=1" ), list( tablename="go_term", Lcolname="_id", Rcolname="go_id", Rattribnames=c( Term="{term}", Ontology="{ontology}", Definition="{definition}", Synonym="go_synonym.synonym", Secondary="go_synonym.secondary" ), Rattrib_join="LEFT JOIN go_synonym ON {_id}=go_synonym._id" ) ) ) ) createAnnObjs.GO_DB <- function(prefix, objTarget, dbconn, datacache) { checkDBSCHEMA(dbconn, "GO_DB") ## AnnDbBimap objects seed0 <- list( objTarget=objTarget, datacache=datacache ) ann_objs <- createAnnDbBimaps(GO_DB_AnnDbBimap_seeds, seed0) ## Reverse maps revmap2 <- function(from, to) { map <- revmap(ann_objs[[from]], objName=to) L2Rchain <- map@L2Rchain tmp <- L2Rchain[[1]]@filter L2Rchain[[1]]@filter <- L2Rchain[[length(L2Rchain)]]@filter L2Rchain[[length(L2Rchain)]]@filter <- tmp map@L2Rchain <- L2Rchain map } ann_objs$BPCHILDREN <- revmap2("BPPARENTS", "BPCHILDREN") ann_objs$CCCHILDREN <- revmap2("CCPARENTS", "CCCHILDREN") ann_objs$MFCHILDREN <- revmap2("MFPARENTS", "MFCHILDREN") ann_objs$BPOFFSPRING <- revmap2("BPANCESTOR", "BPOFFSPRING") ann_objs$CCOFFSPRING <- revmap2("CCANCESTOR", "CCOFFSPRING") ann_objs$MFOFFSPRING <- revmap2("MFANCESTOR", "MFOFFSPRING") ## 1 special map that is not an AnnDbBimap object (just a named integer vector) ann_objs$MAPCOUNTS <- createMAPCOUNTS(dbconn, prefix) prefixAnnObjNames(ann_objs, prefix) } AnnotationDbi/R/createAnnObjs.KEGG_DB.R0000644000175200017520000000450614710217313020454 0ustar00biocbuildbiocbuild### ========================================================================= ### An SQLite-based ann data package (AnnDbPkg) provides a set of pre-defined ### AnnObj objects that are created at load-time. This set depends only on ### the underlying db schema i.e. all the SQLite-based ann data packages that ### share the same underlying db schema will provide the same set of AnnObj ### objects. ### ### This file describes the set of AnnObj objects provided by any ### KEGG_DB-based package i.e. any SQLite-based ann data package based ### on the KEGG_DB schema. ### The createAnnObjs.KEGG_DB() function is the main entry point for ### this file: it is called by any KEGG_DB-based package at load-time. ### ------------------------------------------------------------------------- ### Mandatory fields: objName, Class and L2Rchain KEGG_DB_AnnDbBimap_seeds <- list( list( objName="PATHID2NAME", Class="AnnDbBimap", L2Rchain=list( list( tablename="pathway2name", Lcolname="path_id", Rcolname="path_name" ) ) ), list( objName="PATHID2EXTID", Class="AnnDbBimap", L2Rchain=list( list( tablename="pathway2gene", Lcolname="pathway_id", Rcolname="gene_or_orf_id" ) ) ), list( objName="ENZYMEID2GO", Class="AnnDbBimap", L2Rchain=list( list( tablename="ec2go", Lcolname="ec_no", Rcolname="go_id" ) ) ) ) createAnnObjs.KEGG_DB <- function(prefix, objTarget, dbconn, datacache) { checkDBSCHEMA(dbconn, "KEGG_DB") ## AnnDbBimap objects seed0 <- list( objTarget=objTarget, datacache=datacache ) ann_objs <- createAnnDbBimaps(KEGG_DB_AnnDbBimap_seeds, seed0) ## Reverse maps ann_objs$PATHNAME2ID <- revmap(ann_objs$PATHID2NAME, objName="PATHNAME2ID") ann_objs$EXTID2PATHID <- revmap(ann_objs$PATHID2EXTID, objName="EXTID2PATHID") ann_objs$GO2ENZYMEID <- revmap(ann_objs$ENZYMEID2GO, objName="GO2ENZYMEID") ## 1 special map that is not an AnnDbBimap object (just a named integer vector) ann_objs$MAPCOUNTS <- createMAPCOUNTS(dbconn, prefix) prefixAnnObjNames(ann_objs, prefix) } AnnotationDbi/R/createAnnObjs.MALARIA_DB.R0000644000175200017520000000743314710217313021007 0ustar00biocbuildbiocbuild### ========================================================================= ### An SQLite-based ann data package (AnnDbPkg) provides a set of pre-defined ### AnnObj objects that are created at load-time. This set depends only on ### the underlying db schema i.e. all the SQLite-based ann data packages that ### share the same underlying db schema will provide the same set of AnnObj ### objects. ### ### This file describes the set of AnnObj objects provided by any ### MALARIA_DB-based package i.e. any SQLite-based ann data package based ### on the MALARIA_DB schema. ### The createAnnObjs.MALARIA_DB() function is the main entry point for ### this file: it is called by any MALARIA_DB-based package at load-time. ### ------------------------------------------------------------------------- MALARIA_DB_L2Rlink1 <- list(tablename="genes", Lcolname="gene_id", Rcolname="_id") ### Mandatory fields: objName, Class and L2Rchain MALARIA_DB_AnnDbBimap_seeds <- list( list( objName="ALIAS2ORF", Class="AnnDbBimap", L2Rchain=list( MALARIA_DB_L2Rlink1, list( tablename="alias", Lcolname="_id", Rcolname="alias_symbol" ) ), direction=-1L ), list( objName="ENZYME", Class="AnnDbBimap", L2Rchain=list( MALARIA_DB_L2Rlink1, list( tablename="ec", Lcolname="_id", Rcolname="ec_number" ) ) ), list( objName="GENENAME", Class="AnnDbBimap", L2Rchain=list( MALARIA_DB_L2Rlink1, list( tablename="gene_info", Lcolname="_id", Rcolname="gene_name" ) ) ), list( objName="PATH", Class="AnnDbBimap", L2Rchain=list( MALARIA_DB_L2Rlink1, list( tablename="kegg", Lcolname="_id", Rcolname="path_id" ) ) ), list( objName="SYMBOL", Class="AnnDbBimap", L2Rchain=list( MALARIA_DB_L2Rlink1, list( tablename="gene_info", Lcolname="_id", Rcolname="symbol" ) ) ), list( objName="GO", Class="Go3AnnDbBimap", L2Rchain=list( MALARIA_DB_L2Rlink1, list( #tablename="go_term", # no rightmost table for a Go3AnnDbBimap Lcolname="_id", tagname=c(Evidence="{evidence}"), Rcolname="go_id", Rattribnames=c(Ontology="NULL") ) ), rightTables=Go3tablenames() ) ) createAnnObjs.MALARIA_DB <- function(prefix, objTarget, dbconn, datacache) { checkDBSCHEMA(dbconn, "MALARIA_DB") ## AnnDbBimap objects seed0 <- list( objTarget=objTarget, datacache=datacache ) ann_objs <- createAnnDbBimaps(MALARIA_DB_AnnDbBimap_seeds, seed0) ## Reverse maps ann_objs$ENZYME2ORF <- revmap(ann_objs$ENZYME, objName="ENZYME2ORF") ann_objs$PATH2ORF <- revmap(ann_objs$PATH, objName="PATH2ORF") ann_objs$SYMBOL2ORF <- revmap(ann_objs$SYMBOL, objName="SYMBOL2ORF") ann_objs$GO2ORF <- revmap(ann_objs$GO, objName="GO2ORF") map <- ann_objs$GO2ORF map@rightTables <- Go3tablenames(all=TRUE) map@objName <- "GO2ALLORFS" ann_objs$GO2ALLORFS <- map ## 2 special maps that are not AnnDbBimap objects (just named integer vectors) ann_objs$MAPCOUNTS <- createMAPCOUNTS(dbconn, prefix) ## Some pre-caching Lkeys(ann_objs$GO) #mappedLkeys(ann_objs$GO) #Rkeys(ann_objs$GO2ORF) #mappedRkeys(ann_objs$GO2ORF) prefixAnnObjNames(ann_objs, prefix) } AnnotationDbi/R/createAnnObjs.NCBICHIP_DBs.R0000644000175200017520000003770114710217313021304 0ustar00biocbuildbiocbuild## Generic code to createAnnObjs for bimaps of NCBICHIP packages ## 1st the big list: NCBICHIP_DB_SeedGenerator <- function(orgPkg){ #orgPkg = "org.Hs.eg" ## Oh crap NCBICHIP_DB_L2Rlink1 <- list(tablename="probes", Lcolname="probe_id", Rcolname="gene_id", filter="{is_multiple}='0'") NCBICHIP_DB_L2Rlink2 <- list(tablename="genes", Lcolname="gene_id", Rcolname="_id", altDB=orgPkg) ### Mandatory fields: objName, Class and L2Rchain NCBICHIP_DB_AnnDbBimap_seeds <- list( list( objName="ACCNUM", Class="ProbeAnnDbBimap", L2Rchain=list( list( tablename="accessions", Lcolname="probe_id", Rcolname="accession" ) ) ), list( objName="ALIAS2PROBE", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="alias", Lcolname="_id", Rcolname="alias_symbol" ) ), direction=-1L ), list( objName="CHR", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="chromosomes", Lcolname="_id", Rcolname="chromosome", altDB=orgPkg ) ) ), list( objName="ENTREZID", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="genes", Lcolname="_id", Rcolname="gene_id", altDB=orgPkg ) ) ), list( objName="ENZYME", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="ec", Lcolname="_id", Rcolname="ec_number", altDB=orgPkg ) ) ), list( objName="GENENAME", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="gene_info", Lcolname="_id", Rcolname="gene_name", altDB=orgPkg ) ) ), list( objName="MAP", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="cytogenetic_locations", Lcolname="_id", Rcolname="cytogenetic_location", altDB=orgPkg ) ) ), list( objName="OMIM", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="omim", Lcolname="_id", Rcolname="omim_id", altDB=orgPkg ) ) ), list( objName="PATH", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="kegg", Lcolname="_id", Rcolname="path_id", altDB=orgPkg ) ) ), list( objName="PMID", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="pubmed", Lcolname="_id", Rcolname="pubmed_id", altDB=orgPkg ) ) ), list( objName="REFSEQ", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="refseq", Lcolname="_id", Rcolname="accession", altDB=orgPkg ) ) ), list( objName="SYMBOL", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="gene_info", Lcolname="_id", Rcolname="symbol", altDB=orgPkg ) ) ), ## removed UniGene in Bioc 3.13 ## list( ## objName="UNIGENE", ## Class="ProbeAnnDbBimap", ## L2Rchain=list( ## NCBICHIP_DB_L2Rlink1, ## NCBICHIP_DB_L2Rlink2, ## list( ## tablename="unigene", ## Lcolname="_id", ## Rcolname="unigene_id", ## altDB=orgPkg ## ) ## ) ## ), list( objName="CHRLOC", Class="ProbeAnnDbMap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="chromosome_locations", Lcolname="_id", tagname=c(Chromosome="{seqname}"), Rcolname="start_location", altDB=orgPkg ) ), rightColType="integer" ), list( objName="CHRLOCEND", Class="ProbeAnnDbMap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="chromosome_locations", Lcolname="_id", tagname=c(Chromosome="{seqname}"), Rcolname="end_location", altDB=orgPkg ) ), rightColType="integer" ), list( objName="PFAM", Class="ProbeIpiAnnDbMap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="pfam", Lcolname="_id", Rcolname="ipi_id", Rattribnames=c(PfamId="{pfam_id}"), altDB=orgPkg ) ) ), list( objName="PROSITE", Class="ProbeIpiAnnDbMap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="prosite", Lcolname="_id", Rcolname="ipi_id", Rattribnames=c(PrositeId="{prosite_id}"), altDB=orgPkg ) ) ), list( objName="ENSEMBL", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="ensembl", Lcolname="_id", Rcolname="ensembl_id", altDB=orgPkg ) ) ), list( objName="UNIPROT", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="uniprot", Lcolname="_id", Rcolname="uniprot_id", altDB=orgPkg ) ) ), list( objName="FLYBASE", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="flybase", Lcolname="_id", Rcolname="flybase_id", altDB=orgPkg ) ) ), list( objName="FLYBASECG", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="flybase_cg", Lcolname="_id", Rcolname="flybase_cg_id", altDB=orgPkg ) ) ), list( objName="MGI", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="mgi", Lcolname="_id", Rcolname="mgi_id", altDB=orgPkg ) ) ), list( objName="WORMBASE", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="wormbase", Lcolname="_id", Rcolname="wormbase_id", altDB=orgPkg ) ) ), list( objName="ZFIN", Class="ProbeAnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( tablename="zfin", Lcolname="_id", Rcolname="zfin_id", altDB=orgPkg ) ) ), list( objName="GO", Class="ProbeGo3AnnDbBimap", L2Rchain=list( NCBICHIP_DB_L2Rlink1, NCBICHIP_DB_L2Rlink2, list( Lcolname="_id", tagname=c(Evidence="{evidence}"), Rcolname="go_id", Rattribnames=c(Ontology="NULL"), altDB=orgPkg ) ), rightTables=Go3tablenames() ) ) ## return this NCBICHIP_DB_AnnDbBimap_seeds } ## Then we need to define our specific functions. createAnnObjs.BOVINECHIP_DB <- function(prefix, objTarget, dbconn, datacache, schema="BOVINECHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.CANINECHIP_DB <- function(prefix, objTarget, dbconn, datacache, schema="CANINECHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.CHICKENCHIP_DB <- function(prefix, objTarget, dbconn, datacache, schema="CHICKENCHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.ECOLICHIP_DB <- function(prefix, objTarget, dbconn, datacache, schema="ECOLICHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.FLYCHIP_DB <- function(prefix, objTarget, dbconn, datacache, schema="FLYCHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.HUMANCHIP_DB <- function(prefix, objTarget, dbconn, datacache, schema="HUMANCHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.MOUSECHIP_DB <- function(prefix, objTarget, dbconn, datacache, schema="MOUSECHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.PIGCHIP_DB <- function(prefix, objTarget, dbconn, datacache, schema="PIGCHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.RATCHIP_DB <- function(prefix, objTarget, dbconn, datacache, schema="RATCHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.RHESUSCHIP_DB <- function(prefix, objTarget, dbconn, datacache, schema="RHESUSCHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.WORMCHIP_DB <- function(prefix, objTarget, dbconn, datacache, schema="WORMCHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.XENOPUSCHIP_DB <- function(prefix, objTarget, dbconn, datacache, schema="XENOPUSCHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.ZEBRAFISHCHIP_DB<- function(prefix, objTarget, dbconn, datacache, schema="ZEBRAFISHCHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } ## Added for better B/C support: createAnnObjs.ANOPHELESCHIP_DB<- function(prefix, objTarget, dbconn, datacache, schema="ANOPHELESCHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.CHIMPCHIP_DB<- function(prefix, objTarget, dbconn, datacache, schema="CHIP_DB", class="CHIMPChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.COELICOLORCHIP_DB<- function(prefix, objTarget, dbconn, datacache, schema="COELICOLORCHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.MALARIACHIP_DB<- function(prefix, objTarget, dbconn, datacache, schema="MALARIACHIP_DB", class="ChipDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } AnnotationDbi/R/createAnnObjs.NCBIORG_DBs.R0000644000175200017520000005336714710217313021216 0ustar00biocbuildbiocbuild## Generic code to createAnnObjs for bimaps of NCBIORG packages ## This file will define what it means to be MOUSE_DB or HUMAN_DB etc. as a ## series of functions named like createAnnObjs.MOUSE_DB() etc. ## Start with a huge named list of all the possible mappings. NCBIORG_DB_SeedGenerator <- function(orgPkg){ NCBIORG_DB_L2Rlink1 <- list(tablename="genes", Lcolname="gene_id", Rcolname="_id") NCBIORG_DB_AnnDbBimap_seeds <- list( list( objName="ACCNUM", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="accessions", Lcolname="_id", Rcolname="accession" ) ) ), list( objName="ALIAS2EG", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="alias", Lcolname="_id", Rcolname="alias_symbol" ) ), direction=-1L ), list( objName="CHR", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="chromosomes", Lcolname="_id", Rcolname="chromosome" ) ) ), list( objName="ENZYME", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="ec", Lcolname="_id", Rcolname="ec_number" ) ) ), list( objName="GENENAME", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="gene_info", Lcolname="_id", Rcolname="gene_name" ) ) ), list( objName="MAP", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="cytogenetic_locations", Lcolname="_id", Rcolname="cytogenetic_location" ) ) ), list( objName="OMIM", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="omim", Lcolname="_id", Rcolname="omim_id" ) ) ), list( objName="PATH", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="kegg", Lcolname="_id", Rcolname="path_id" ) ) ), list( objName="PMID", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="pubmed", Lcolname="_id", Rcolname="pubmed_id" ) ) ), list( objName="REFSEQ", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="refseq", Lcolname="_id", Rcolname="accession" ) ) ), list( objName="SYMBOL", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="gene_info", Lcolname="_id", Rcolname="symbol" ) ) ), ## removed UniGene in Bioc 3.13 ## list( ## objName="UNIGENE", ## Class="AnnDbBimap", ## L2Rchain=list( ## NCBIORG_DB_L2Rlink1, ## list( ## tablename="unigene", ## Lcolname="_id", ## Rcolname="unigene_id" ## ) ## ) ## ), ## Added Gene type in Bioc 3.13 list( objName="GENETYPE", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="genetype", Lcolname="_id", Rcolname="gene_type" ) ) ), list( objName="CHRLOC", Class="AnnDbMap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="chromosome_locations", Lcolname="_id", tagname=c(Chromosome="{seqname}"), Rcolname="start_location" ) ), rightColType="integer" ), list( objName="CHRLOCEND", Class="AnnDbMap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="chromosome_locations", Lcolname="_id", tagname=c(Chromosome="{seqname}"), Rcolname="end_location" ) ), rightColType="integer" ), list( objName="PFAM", Class="IpiAnnDbMap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="pfam", Lcolname="_id", Rcolname="ipi_id", Rattribnames=c(PfamId="{pfam_id}") ) ) ), list( objName="PROSITE", Class="IpiAnnDbMap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="prosite", Lcolname="_id", Rcolname="ipi_id", Rattribnames=c(PrositeId="{prosite_id}") ) ) ), list( objName="ENSEMBL", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="ensembl", Lcolname="_id", Rcolname="ensembl_id" ) ) ), list( objName="ENSEMBLPROT", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="ensembl_prot", Lcolname="_id", Rcolname="prot_id" ) ) ), list( objName="ENSEMBLTRANS", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="ensembl_trans", Lcolname="_id", Rcolname="trans_id" ) ) ), list( objName="UNIPROT", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="uniprot", Lcolname="_id", Rcolname="uniprot_id" ) ) ), list( objName="UCSCKG", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="ucsc", Lcolname="_id", Rcolname="ucsc_id" ) ) ), list( objName="FLYBASE", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="flybase", Lcolname="_id", Rcolname="flybase_id" ) ) ), list( objName="FLYBASECG", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="flybase_cg", Lcolname="_id", Rcolname="flybase_cg_id" ) ) ), list( objName="FLYBASEPROT", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="flybase_prot", Lcolname="_id", Rcolname="prot_id" ) ) ), list( objName="MGI", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="mgi", Lcolname="_id", Rcolname="mgi_id" ) ) ), list( objName="WORMBASE", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="wormbase", Lcolname="_id", Rcolname="wormbase_id" ) ) ), list( objName="ZFIN", Class="AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( tablename="zfin", Lcolname="_id", Rcolname="zfin_id" ) ) ), list( objName="GO", Class="Go3AnnDbBimap", L2Rchain=list( NCBIORG_DB_L2Rlink1, list( #tablename="go_term", # no rightmost table for a Go3AnnDbBimap Lcolname="_id", tagname=c(Evidence="{evidence}"), Rcolname="go_id", Rattribnames=c(Ontology="NULL") ) ), rightTables=Go3tablenames() ) ) ## return this NCBIORG_DB_AnnDbBimap_seeds } ## Then some helper functions to take a list of arguments and convert them into the ann_objs object that is returned by each function ## helper to make MOUSE_DB_AnnDbBimap_seeds from the big list and a list of mappings that are needed ## helper to translate schema to species name getSpeciesFromSchema <- function(schema){ species <- switch(EXPR = schema, "ANOPHELES_DB"="Anopheles gambiae", "ARABIDOPSISCHIP_DB"="Arabidopsis thaliana", "ARABIDOPSIS_DB"="Arabidopsis thaliana", "BOVINECHIP_DB"="Bos taurus", "BOVINE_DB"="Bos taurus", "CANINECHIP_DB"="Canis familiaris", "CANINE_DB"="Canis familiaris", "CHICKENCHIP_DB"="Gallus gallus", "CHICKEN_DB"="Gallus gallus", "CHIMP_DB"="Pan troglodytes", "COELICOLOR_DB"="Streptomyces coelicolor", "ECOLICHIP_DB"="Escherichia coli", "ECOLI_DB"="Escherichia coli", "FLYCHIP_DB"="Drosophila melanogaster", "FLY_DB"="Drosophila melanogaster", "GO_DB"=NA, "HUMANCHIP_DB"="Homo sapiens", "HUMAN_DB"="Homo sapiens", "KEGG_DB"=NA, "MALARIA_DB"="Plasmodium falciparum", "MOUSECHIP_DB"="Mus musculus", "MOUSE_DB"="Mus musculus", "ORGANISM_DB"=NA, "PFAM_DB"=NA, "PIGCHIP_DB"="Sus scrofa", "PIG_DB"="Sus scrofa", "RATCHIP_DB"="Rattus norvegicus", "RAT_DB"="Rattus norvegicus", "RHESUSCHIP_DB"="Macaca mulatta", "RHESUS_DB"="Macaca mulatta", "WORMCHIP_DB"="Caenorhabditis elegans", "WORM_DB"="Caenorhabditis elegans", "XENOPUSCHIP_DB"="Xenopus laevis", "XENOPUS_DB"="Xenopus laevis", "YEASTCHIP_DB"="Saccharomyces cerevisiae", "YEAST_DB"="Saccharomyces cerevisiae", "YEASTNCBI_DB"="Saccharomyces cerevisiae", "ZEBRAFISHCHIP_DB"="Danio rerio", "ZEBRAFISH_DB"="Danio rerio") species } ## helper to translate schema to assoicated org package getOrgPkgForSchema <- function(schema){ species <- switch(EXPR = schema, "ANOPHELESCHIP_DB" = "org.Ag.eg.db", "ARABIDOPSISCHIP_DB"="org.At.tair", "BOVINECHIP_DB"="org.Bt.eg", "CANINECHIP_DB"="org.Cf.eg", "CHICKENCHIP_DB"="org.Gg.eg", "CHIMPCHIP_DB" = "org.Pt.eg.db", "COELICOLORCHIP_DB" = "org.Sco.eg.db", "ECOLICHIP_DB"="org.EcK12.eg", "FLYCHIP_DB"="org.Dm.eg", "HUMANCHIP_DB"="org.Hs.eg", "MALARIACHIP_DB" = "org.Pf.plasmo.db", "MOUSECHIP_DB"="org.Mm.eg", "PIGCHIP_DB"="org.Ss.eg", "RATCHIP_DB"="org.Rn.eg", "RHESUSCHIP_DB"="org.Mmu.eg", "WORMCHIP_DB"="org.Ce.eg", "XENOPUSCHIP_DB"="org.Xl.eg", "YEASTCHIP_DB"="org.Sc.sgd", "ZEBRAFISHCHIP_DB"="org.Dr.eg") species } ## helper to filter seeds above based on the schema filterSeeds <- function(allSeeds, schema, class){ ## logic to decide what to leave and what to keep: ## 1st get the schema name species <- getSpeciesFromSchema(schema) ## then call .definePossibleTables to get detailed schema info. schemaDet <- .definePossibleTables(class, species) classNames <- names(schemaDet) names <- sapply(allSeeds, function(x){x$objName}) ## if you are in both lists, then we want you as a seed idx <- match(classNames,names) idx <- idx[!is.na(idx)] seeds <- allSeeds[idx] names(seeds) <- NULL ## clean out names ## return filtered seeds seeds } .revmapper <-function(name, ann_objs, class){ if(class=="OrgDb"){ name2<- paste0(name,"2EG") }else if (class=="ChipDb"){ name2<- paste0(name,"2PROBE") } ann_objs[[name2]] <- revmap(ann_objs[[name]], objName=name2) } ## helper to add the revmaps (based on that same list and the maps that are ## sometimes reversed) and also to put things together. .addRevMapSeeds <- function(ann_objs, class){ ## We have a list of things we would like to add revmaps for, but we can ## only do that if they exist. if(class=="OrgDb"){ revMapables <- c("ACCNUM","ENZYME","MAP","OMIM","PATH","PMID","REFSEQ", "SYMBOL","ENSEMBL","ENSEMBLPROT", "ENSEMBLTRANS", "MGI","FLYBASE","FLYBASECG","FLYBASEPROT","GO") }else if (class=="ChipDb"){ revMapables <- c("ENZYME","PATH","PMID","ENSEMBL","MGI","FLYBASE", "FLYBASECG","GO") } ## now filter so that rMapNames is only the names that we actually have mapNames <- ls(ann_objs) idx <- match(revMapables, mapNames) idx <- idx[!is.na(idx)] rMapNames <- mapNames[idx] ## then loop through the rMapNames to call revmap and assign values in. lapply(rMapNames, .revmapper, ann_objs, class) ## After we make our revmaps, we need to do some special work for GO (always) ## BUT the following still has to be customized for either 2EG or 2PROBE... if(class=="OrgDb"){ map <- ann_objs$GO2EG map@rightTables <- Go3tablenames(all=TRUE) map@objName <- "GO2ALLEGS" ann_objs$GO2ALLEGS <- map }else if (class=="ChipDb"){ map <- ann_objs$GO2PROBE map@rightTables <- Go3tablenames(all=TRUE) map@objName <- "GO2ALLPROBES" ann_objs$GO2ALLPROBES <- map } ## return the objects ann_objs } ## 1st three arguments for this are all hard coded below for each case createAnnObjs.NCBI_DB <- function(prefix, objTarget, dbconn, datacache, schema, class){ checkDBSCHEMA(dbconn, schema) ## AnnDbBimap objects seed0 <- list( objTarget=objTarget, datacache=datacache ) ## Get allSeeds if(class=="OrgDb"){ allSeeds <- NCBIORG_DB_SeedGenerator() }else if (class=="ChipDb"){ dbname <- getOrgPkgForSchema(schema) allSeeds <- NCBICHIP_DB_SeedGenerator(dbname) } else { ## for Orthology.eg.db we just want to return return(NULL) } ## filter the seeds to match the schema seeds <- filterSeeds(allSeeds, schema, class) ## now make the bimaps ann_objs <- createAnnDbBimaps(seeds, seed0) ## Then add reversemaps ann_objs <- .addRevMapSeeds(ann_objs, class) ## 2 special maps that are not AnnDbBimap objects (just named integer vectors) if(class=="OrgDb"){ if(!any(c("ECOLI_DB","XENOPUS_DB","PIG_DB") %in% schema)){ ## CHRLENGTHS exceptions. ann_objs$CHRLENGTHS <- createCHRLENGTHS(dbconn) } }else if (class=="ChipDb"){ attachDBs(dbconn, ann_objs) if(!any(c("ECOLICHIP_DB","XENOPUSCHIP_DB","PIGCHIP_DB") %in% schema)){ ## more exceptions ann_objs$CHRLENGTHS <- createCHRLENGTHS(dbconn, dbname="") } ann_objs$ORGPKG <- dbname } ann_objs$MAPCOUNTS <- createMAPCOUNTS(dbconn, prefix) ## Some pre-caching Lkeys(ann_objs$GO) prefixAnnObjNames(ann_objs, prefix) } ## Then define each function briefly like this: createAnnObjs.ANOPHELES_DB <- function(prefix, objTarget, dbconn, datacache, schema="ANOPHELES_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.BOVINE_DB <- function(prefix, objTarget, dbconn, datacache, schema="BOVINE_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.CANINE_DB <- function(prefix, objTarget, dbconn, datacache, schema="CANINE_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.CHICKEN_DB <- function(prefix, objTarget, dbconn, datacache, schema="CHICKEN_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.CHIMP_DB <- function(prefix, objTarget, dbconn, datacache, schema="CHIMP_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.ECOLI_DB <- function(prefix, objTarget, dbconn, datacache, schema="ECOLI_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.FLY_DB <- function(prefix, objTarget, dbconn, datacache, schema="FLY_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.HUMAN_DB <- function(prefix, objTarget, dbconn, datacache, schema="HUMAN_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.MOUSE_DB <- function(prefix, objTarget, dbconn, datacache, schema="MOUSE_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.PIG_DB <- function(prefix, objTarget, dbconn, datacache, schema="PIG_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.RAT_DB <- function(prefix, objTarget, dbconn, datacache, schema="RAT_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.RHESUS_DB <- function(prefix, objTarget, dbconn, datacache, schema="RHESUS_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.WORM_DB <- function(prefix, objTarget, dbconn, datacache, schema="WORM_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.XENOPUS_DB <- function(prefix, objTarget, dbconn, datacache, schema="XENOPUS_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } createAnnObjs.ZEBRAFISH_DB <- function(prefix, objTarget, dbconn, datacache, schema="ZEBRAFISH_DB", class="OrgDb"){ createAnnObjs.NCBI_DB(prefix,objTarget,dbconn,datacache,schema,class) } AnnotationDbi/R/createAnnObjs.ORGANISM_DB.R0000644000175200017520000001517014710217313021155 0ustar00biocbuildbiocbuild### ========================================================================= ### An SQLite-based ann data package (AnnDbPkg) provides a set of pre-defined ### AnnObj objects that are created at load-time. This is a more dynamic set ### of mappings that will vary with the schema that is available. ### ### This file describes the set of AnnObj objects provided by any ### ORGANISM_DB-based package i.e. any SQLite-based ann data package based ### on the ORGANISM_DB schema. ### The createAnnObjs.ORGANISM_DB() function is the main entry point for ### this file: it is called by any ORGANISM_DB-based package at load-time. ### ------------------------------------------------------------------------- ORGANISM_DB_L2Rlink1 <- list(tablename="genes", Lcolname="gene_id", Rcolname="_id") makeAnnDbBiMapSeed <- function(objName,tablename,Rcolname){ list( objName=objName, Class="AnnDbBimap", L2Rchain=list( ORGANISM_DB_L2Rlink1, list( tablename=tablename, Lcolname="_id", Rcolname=Rcolname ) ) ) } makeGo3AnnDbBiMapSeed <- function(){ list( list( objName="GO", Class="Go3AnnDbBimap", L2Rchain=list( ORGANISM_DB_L2Rlink1, list( #tablename="go_term", # no rightmost table for a Go3AnnDbBimap Lcolname="_id", tagname=c(Evidence="{evidence}"), Rcolname="go_id", Rattribnames=c(Ontology="NULL") ) ), rightTables=Go3tablenames() ) ) } ## ## for now, there are only two like this, and they are both from an odd table ## ## this may go away in time, so fine for this to be an exception ## makeAnnDbMapSeeds <- function(){ ## list( ## list( ## objName="CHRLOC", ## Class="AnnDbMap", ## L2Rchain=list( ## ORGANISM_DB_L2Rlink1, ## list( ## tablename="chromosome_locations", ## Lcolname="_id", ## tagname=c(Chromosome="{seqname}"), ## Rcolname="start_location" ## ) ## ), ## rightColType="integer" ## ), ## list( ## objName="CHRLOCEND", ## Class="AnnDbMap", ## L2Rchain=list( ## ORGANISM_DB_L2Rlink1, ## list( ## tablename="chromosome_locations", ## Lcolname="_id", ## tagname=c(Chromosome="{seqname}"), ## Rcolname="end_location" ## ) ## ), ## rightColType="integer" ## ) ## ) ## } ## for future expansion (assuming we ever get access to these) ## makeIpiAnnDbBiMapSeed <- function(objName,tablename,Rcolname){ ## } getDBMaps <- function(dbconn){ ## Get into the DB and list the tables rawtabs <- dbListTables(dbconn) ## drop unsupported (sqlite_stat1) and specialized (go, and chrloc) tables idx <- grep(paste0("sqlite_stat1|map_counts|metadata|map_metadata|genes", "|^go_|prosite|pfam|chrlengths", "|chromosome_locations"), rawtabs, invert=TRUE) tabs <- rawtabs[idx] ## I require a reference frame objNames = c("ACCNUM", "ALIAS2EG", "CHR", "ENZYME", "GENENAME", "MAP", "OMIM", "PATH", "PMID", "REFSEQ", "SYMBOL", "GENETYPE", "ENSEMBL", "ENSEMBLPROT", "ENSEMBLTRANS", "UNIPROT") tables = c("accessions","alias", "chromosomes","ec", "gene_info", "cytogenetic_locations", "omim", "kegg", "pubmed", "refseq", "gene_info", "genetype", "ensembl", "ensembl_prot", "ensembl_trans", "uniprot") fields = c("accession", "alias_symbol", "chromosome", "ec_number", "gene_name", "cytogenetic_location", "omim_id","path_id", "pubmed_id", "accession", "symbol", "gene_type", "ensembl_id", "prot_id", "trans_id", "uniprot_id") possibleMaps <- data.frame(objName=objNames, tables=tables, fields=fields, stringsAsFactors=FALSE) ## subset to just ones that we see tables for possibleMaps[as.vector(t(possibleMaps["tables"]))%in% tabs,] } ## Used to create the seeds: createORGANISMSeeds <- function(maps, dbconn){ ## 1st lets loop and make the regular ones seeds <- list() for(i in seq_len(dim(maps)[1])){ seeds[[i]] <- makeAnnDbBiMapSeed(objName = maps[i,"objName"], tablename = maps[i,"tables"], Rcolname = maps[i,"fields"]) } ## Then we have to append a couple of exceptions. ## And, we have to test for these separately in here. if(length(grep("go_bp", dbListTables(dbconn)))>0 && length(grep("go_cc", dbListTables(dbconn)))>0 && length(grep("go_mf", dbListTables(dbconn)))>0 && length(grep("go_bp_all", dbListTables(dbconn)))>0 && length(grep("go_cc_all", dbListTables(dbconn)))>0 && length(grep("go_mf_all", dbListTables(dbconn)))>0 ){ seeds <- c(seeds, makeGo3AnnDbBiMapSeed()) } if(length(grep("chromosome_locations", dbListTables(dbconn)))>0){ seeds <- c(seeds, makeAnnDbMapSeeds()) } seeds } createAnnObjs.ORGANISM_DB <- function(prefix, objTarget, dbconn, datacache) { checkDBSCHEMA(dbconn, "ORGANISM_DB") ## AnnDbBimap objects seed0 <- list( objTarget=objTarget, datacache=datacache ) ## troll the DB and set up the Mapping "seeds" maps <- getDBMaps(dbconn) ORGANISM_DB_AnnDbBimap_seeds <- createORGANISMSeeds(maps, dbconn) ann_objs <- createAnnDbBimaps(ORGANISM_DB_AnnDbBimap_seeds, seed0) ## GO2ALL mapping requires GO mappings. if(length(grep("go_bp", dbListTables(dbconn)))>0 && length(grep("go_cc", dbListTables(dbconn)))>0 && length(grep("go_mf", dbListTables(dbconn)))>0 && length(grep("go_bp_all", dbListTables(dbconn)))>0 && length(grep("go_cc_all", dbListTables(dbconn)))>0 && length(grep("go_mf_all", dbListTables(dbconn)))>0 ){ ann_objs$GO2EG <- revmap(ann_objs$GO, objName="GO2EG") map <- ann_objs$GO2EG map@rightTables <- Go3tablenames(all=TRUE) map@objName <- "GO2ALLEGS" ann_objs$GO2ALLEGS <- map ## Some pre-caching Lkeys(ann_objs$GO) } ## 2 special maps that are not AnnDbBimap objects (named int vectors) if(length(grep("chrlengths", dbListTables(dbconn)))>0){ ann_objs$CHRLENGTHS <- createCHRLENGTHS(dbconn) } if(length(grep("map_counts", dbListTables(dbconn)))>0){ ann_objs$MAPCOUNTS <- createMAPCOUNTS(dbconn, prefix) } prefixAnnObjNames(ann_objs, prefix) } AnnotationDbi/R/createAnnObjs.PFAM_DB.R0000644000175200017520000002032414710217313020456 0ustar00biocbuildbiocbuild### ========================================================================= ### An SQLite-based ann data package (AnnDbPkg) provides a set of pre-defined ### AnnObj objects that are created at load-time. This set depends only on ### the underlying db schema i.e. all the SQLite-based ann data packages that ### share the same underlying db schema will provide the same set of AnnObj ### objects. ### ### This file describes the set of AnnObj objects provided by any ### PFAM_DB-based package i.e. any SQLite-based ann data package based ### on the PFAM_DB schema. ### The createAnnObjs.PFAM_DB() function is the main entry point for ### this file: it is called by any PFAM_DB-based package at load-time. ### ------------------------------------------------------------------------- PFAM_DB_L2Rlink1 <- list(tablename="probes", Lcolname="probe_id", Rcolname="_id") ### Mandatory fields: objName, Class and L2Rchain PFAM_DB_AnnDbBimap_seeds <- list( list( objName="CAZY", Class="AnnDbBimap", L2Rchain=list( list( tablename="cazy", Lcolname="ac", Rcolname="cazy" ) ) ), list( objName="DE", Class="AnnDbBimap", L2Rchain=list( list( tablename="de", Lcolname="ac", Rcolname="de" ) ) ), list( objName="HOMSTRAD", Class="AnnDbBimap", L2Rchain=list( list( tablename="homstrad", Lcolname="ac", Rcolname="homstrad" ) ) ), list( objName="ID", Class="AnnDbBimap", L2Rchain=list( list( tablename="id", Lcolname="ac", Rcolname="id" ) ) ), list( objName="INTERPRO", Class="AnnDbBimap", L2Rchain=list( list( tablename="interpro", Lcolname="ac", Rcolname="interpro" ) ) ), list( objName="LOAD", Class="AnnDbBimap", L2Rchain=list( list( tablename="load", Lcolname="ac", Rcolname="load" ) ) ), list( objName="MEROPS", Class="AnnDbBimap", L2Rchain=list( list( tablename="merops", Lcolname="ac", Rcolname="merops" ) ) ), list( objName="MIM", Class="AnnDbBimap", L2Rchain=list( list( tablename="mim", Lcolname="ac", Rcolname="mim" ) ) ), ###THIS ONE HAS MORE STUFF to display list( objName="PDB", Class="AnnDbBimap", L2Rchain=list( list( tablename="pdb", Lcolname="ac", Rcolname="pdb", Rattribnames=c(StartPoint="{start_point}",EndPoint="{end_point}" ) ) ) ), ## list( ## objName="PFAMB", ## Class="AnnDbBimap", ## L2Rchain=list( ## list( ## tablename="pfamb", ## Lcolname="ac", ## Rcolname="pfamb" ## ) ## ) ## ), list( objName="PRINTS", Class="AnnDbBimap", L2Rchain=list( list( tablename="prints", Lcolname="ac", Rcolname="prints" ) ) ), list( objName="PROSITE", Class="AnnDbBimap", L2Rchain=list( list( tablename="prosite", Lcolname="ac", Rcolname="prosite" ) ) ), list( objName="PROSITEPROFILE", Class="AnnDbBimap", L2Rchain=list( list( tablename="prosite_profile", Lcolname="ac", Rcolname="prosite_profile" ) ) ), list( objName="RM", Class="AnnDbBimap", L2Rchain=list( list( tablename="rm", Lcolname="ac", Rcolname="rm" ) ) ), ### Use an R attrib for this one. list( objName="SCOP", Class="AnnDbBimap", L2Rchain=list( list( tablename="scop", Lcolname="ac", Rcolname="scop", Rattribnames=c(Placement="{placement}") ) ) ), list( objName="SMART", Class="AnnDbBimap", L2Rchain=list( list( tablename="smart", Lcolname="ac", Rcolname="smart" ) ) ), list( objName="TC", Class="AnnDbBimap", L2Rchain=list( list( tablename="tc", Lcolname="ac", Rcolname="tc" ) ) ), list( objName="TP", Class="AnnDbBimap", L2Rchain=list( list( tablename="tp", Lcolname="ac", Rcolname="tp" ) ) ), list( objName="URL", Class="AnnDbBimap", L2Rchain=list( list( tablename="url", Lcolname="ac", Rcolname="url" ) ) ) ) createAnnObjs.PFAM_DB <- function(prefix, objTarget, dbconn, datacache) { checkDBSCHEMA(dbconn, "PFAM_DB") ## AnnDbBimap objects seed0 <- list( objTarget=objTarget, datacache=datacache ) ann_objs <- createAnnDbBimaps(PFAM_DB_AnnDbBimap_seeds, seed0) ## Reverse maps ## ann_objs$ENZYME2PROBE <- revmap(ann_objs$ENZYME, objName="ENZYME2PROBE") ## ann_objs$PATH2PROBE <- revmap(ann_objs$PATH, objName="PATH2PROBE") ## ann_objs$PMID2PROBE <- revmap(ann_objs$PMID, objName="PMID2PROBE") ## ann_objs$GO2PROBE <- revmap(ann_objs$GO, objName="GO2PROBE") ## ann_objs$ENSEMBL2PROBE <- revmap(ann_objs$ENSEMBL, objName="ENSEMBL2PROBE") ## map <- ann_objs$GO2PROBE ## map@rightTables <- Go3tablenames(all=TRUE) ## map@objName <- "GO2ALLPROBES" ## ann_objs$GO2ALLPROBES <- map ann_objs$CAZY2AC <- revmap(ann_objs$CAZY, objName="CAZY2AC") ann_objs$DE2AC <- revmap(ann_objs$DE, objName="DE2AC") ann_objs$HOMSTRAD2AC <- revmap(ann_objs$HOMSTRAD, objName="HOMSTRAD2AC") ann_objs$ID2AC <- revmap(ann_objs$ID, objName="ID2AC") ann_objs$INTERPRO2AC <- revmap(ann_objs$INTERPRO, objName="INTERPRO2AC") ann_objs$LOAD2AC <- revmap(ann_objs$LOAD, objName="LOAD2AC") ann_objs$MEROPS2AC <- revmap(ann_objs$MEROPS, objName="MEROPS2AC") ann_objs$MIM2AC <- revmap(ann_objs$MIM, objName="MIM2AC") ann_objs$PDB2AC <- revmap(ann_objs$PDB, objName="PDB2AC") ## ann_objs$PFAMB2AC <- revmap(ann_objs$PFAMB, objName="PFAMB2AC") ann_objs$PRINTS2AC <- revmap(ann_objs$PRINTS, objName="PRINTS2AC") ann_objs$PROSITE2AC <- revmap(ann_objs$PROSITE, objName="PROSITE2AC") ann_objs$PROSITEPROFILE2AC <- revmap(ann_objs$PROSITEPROFILE, objName="PROSITEPROFILE2AC") ann_objs$RM2AC <- revmap(ann_objs$RM, objName="RM2AC") ann_objs$SCOP2AC <- revmap(ann_objs$SCOP, objName="SCOP2AC") ann_objs$SMART2AC <- revmap(ann_objs$SMART, objName="SMART2AC") # ann_objs$TC2AC <- revmap(ann_objs$TC, objName="TC2AC") ann_objs$TP2AC <- revmap(ann_objs$TP, objName="TP2AC") ann_objs$URL2AC <- revmap(ann_objs$URL, objName="URL2AC") ## 2 special maps that are not AnnDbBimap objects (just named integer vectors) ## ann_objs$CHRLENGTHS <- createCHRLENGTHS(dbconn) ann_objs$MAPCOUNTS <- createMAPCOUNTS(dbconn, prefix) ## Some pre-caching # Lkeys(ann_objs$GO) #mappedLkeys(ann_objs$GO) #Rkeys(ann_objs$GO2PROBE) #mappedRkeys(ann_objs$GO2PROBE) #Rkeys(ann_objs$GO2ALLPROBES) #mappedRkeys(ann_objs$GO2ALLPROBES) prefixAnnObjNames(ann_objs, prefix) } AnnotationDbi/R/createAnnObjs.YEASTCHIP_DB.R0000644000175200017520000001575014710217313021273 0ustar00biocbuildbiocbuild### ========================================================================= ### An SQLite-based ann data package (AnnDbPkg) provides a set of pre-defined ### AnnObj objects that are created at load-time. This set depends only on ### the underlying db schema i.e. all the SQLite-based ann data packages that ### share the same underlying db schema will provide the same set of AnnObj ### objects. ### ### This file describes the set of AnnObj objects provided by any ### YEASTCHIP_DB-based package i.e. any SQLite-based ann data package based ### on the YEASTCHIP_DB schema. ### The createAnnObjs.YEASTCHIP_DB() function is the main entry point for ### this file: it is called by any YEASTCHIP_DB-based package at load-time. ### ------------------------------------------------------------------------- orgPkg = "org.Sc.sgd" ## YEASTCHIP_DB_L2Rlink1 <- list(tablename="probes", Lcolname="probe_id", Rcolname="_id") YEASTCHIP_DB_L2Rlink1 <- list(tablename="probes", Lcolname="probe_id", Rcolname="systematic_name", filter="{is_multiple}='0'") YEASTCHIP_DB_L2Rlink2 <- list(tablename="sgd", Lcolname="systematic_name", Rcolname="_id", altDB=orgPkg) ### Mandatory fields: objName, Class and L2Rchain YEASTCHIP_DB_AnnDbBimap_seeds <- list( list( objName="ALIAS", Class="ProbeAnnDbBimap", L2Rchain=list( YEASTCHIP_DB_L2Rlink1, YEASTCHIP_DB_L2Rlink2, list( tablename="gene2alias", Lcolname="_id", Rcolname="alias", altDB=orgPkg ) ) ), list( objName="CHR", Class="ProbeAnnDbBimap", L2Rchain=list( YEASTCHIP_DB_L2Rlink1, YEASTCHIP_DB_L2Rlink2, list( tablename="chromosome_features", Lcolname="_id", Rcolname="chromosome", altDB=orgPkg ) ) ), list( objName="CHRLOC", Class="ProbeAnnDbMap", L2Rchain=list( YEASTCHIP_DB_L2Rlink1, YEASTCHIP_DB_L2Rlink2, list( tablename="chromosome_features", Lcolname="_id", tagname=c(Chromosome="{chromosome}"), Rcolname="start", altDB=orgPkg ) ), rightColType="integer" ), list( objName="CHRLOCEND", Class="ProbeAnnDbMap", L2Rchain=list( YEASTCHIP_DB_L2Rlink1, YEASTCHIP_DB_L2Rlink2, list( tablename="chromosome_features", Lcolname="_id", tagname=c(Chromosome="{chromosome}"), Rcolname="stop", altDB=orgPkg ) ), rightColType="integer" ), list( objName="DESCRIPTION", Class="ProbeAnnDbBimap", L2Rchain=list( YEASTCHIP_DB_L2Rlink1, YEASTCHIP_DB_L2Rlink2, list( tablename="chromosome_features", Lcolname="_id", Rcolname="feature_description", altDB=orgPkg ) ) ), list( objName="ENZYME", Class="ProbeAnnDbBimap", L2Rchain=list( YEASTCHIP_DB_L2Rlink1, YEASTCHIP_DB_L2Rlink2, list( tablename="ec", Lcolname="_id", Rcolname="ec_number", altDB=orgPkg ) ) ), list( objName="GENENAME", Class="ProbeAnnDbBimap", L2Rchain=list( YEASTCHIP_DB_L2Rlink1, YEASTCHIP_DB_L2Rlink2, list( tablename="sgd", Lcolname="_id", Rcolname="gene_name", altDB=orgPkg ) ) ), list( objName="PATH", Class="ProbeAnnDbBimap", L2Rchain=list( YEASTCHIP_DB_L2Rlink1, YEASTCHIP_DB_L2Rlink2, list( tablename="kegg", Lcolname="_id", Rcolname="path_id", altDB=orgPkg ) ) ), list( objName="PMID", Class="ProbeAnnDbBimap", L2Rchain=list( YEASTCHIP_DB_L2Rlink1, YEASTCHIP_DB_L2Rlink2, list( tablename="pubmed", Lcolname="_id", Rcolname="pubmed_id", altDB=orgPkg ) ) ), list( objName="GO", Class="ProbeGo3AnnDbBimap", L2Rchain=list( YEASTCHIP_DB_L2Rlink1, YEASTCHIP_DB_L2Rlink2, list( #tablename="go_term", # no rightmost table for a Go3AnnDbBimap Lcolname="_id", tagname=c(Evidence="{evidence}"), Rcolname="go_id", Rattribnames=c(Ontology="NULL"), altDB=orgPkg ) ), rightTables=Go3tablenames() ), list( objName="ENSEMBL", Class="ProbeAnnDbBimap", L2Rchain=list( YEASTCHIP_DB_L2Rlink1, YEASTCHIP_DB_L2Rlink2, list( tablename="ensembl", Lcolname="_id", Rcolname="ensembl_id", altDB=orgPkg ) ) ), list( objName="ORF", Class="ProbeAnnDbBimap", L2Rchain=list( YEASTCHIP_DB_L2Rlink1, YEASTCHIP_DB_L2Rlink2, list( tablename="sgd", Lcolname="_id", Rcolname="systematic_name", altDB=orgPkg ) ) ) ) createAnnObjs.YEASTCHIP_DB <- function(prefix, objTarget, dbconn, datacache) { checkDBSCHEMA(dbconn, "YEASTCHIP_DB") ## AnnDbBimap objects seed0 <- list( objTarget=objTarget, datacache=datacache ) ann_objs <- createAnnDbBimaps(YEASTCHIP_DB_AnnDbBimap_seeds, seed0) attachDBs(dbconn, ann_objs) ## Reverse maps ann_objs$ENZYME2PROBE <- revmap(ann_objs$ENZYME, objName="ENZYME2PROBE") ann_objs$PATH2PROBE <- revmap(ann_objs$PATH, objName="PATH2PROBE") ann_objs$PMID2PROBE <- revmap(ann_objs$PMID, objName="PMID2PROBE") ann_objs$ALIAS2PROBE <- revmap(ann_objs$ALIAS, objName="ALIAS2PROBE") ann_objs$ENSEMBL2PROBE <- revmap(ann_objs$ENSEMBL, objName="ENSEMBL2PROBE") ann_objs$GO2PROBE <- revmap(ann_objs$GO, objName="GO2PROBE") map <- ann_objs$GO2PROBE map@rightTables <- Go3tablenames(all=TRUE) map@objName <- "GO2ALLPROBES" ann_objs$GO2ALLPROBES <- map ## 2 special maps that are not AnnDbBimap objects (just named integer vectors) ann_objs$CHRLENGTHS <- createCHRLENGTHS(dbconn, dbname="org.Sc.sgd") ann_objs$MAPCOUNTS <- createMAPCOUNTS(dbconn, prefix) ## 1 special string to let us know who the supporting org package is. ann_objs$ORGPKG <- "org.Sc.sgd" ## Some pre-caching Lkeys(ann_objs$GO) prefixAnnObjNames(ann_objs, prefix) } AnnotationDbi/R/createAnnObjs.YEASTNCBI_DB.R0000644000175200017520000001647314710217313021266 0ustar00biocbuildbiocbuild### ========================================================================= ### An SQLite-based ann data package (AnnDbPkg) provides a set of pre-defined ### AnnObj objects that are created at load-time. This set depends only on ### the underlying db schema i.e. all the SQLite-based ann data packages that ### share the same underlying db schema will provide the same set of AnnObj ### objects. ### ### This file describes the set of AnnObj objects provided by any ### YEASTNCBI_DB-based package i.e. any SQLite-based ann data package based ### on the YEASTNCBI_DB schema. ### The createAnnObjs.YEASTNCBI_DB() function is the main entry point for ### this file: it is called by any YEASTNCBI_DB-based package at load-time. ### ------------------------------------------------------------------------- YEASTNCBI_DB_L2Rlink1 <- list(tablename="genes", Lcolname="gene_id", Rcolname="_id") ### Mandatory fields: objName, Class and L2Rchain YEASTNCBI_DB_AnnDbBimap_seeds <- list( list( objName="ACCNUM", Class="AnnDbBimap", L2Rchain=list( YEASTNCBI_DB_L2Rlink1, list( tablename="accessions", Lcolname="_id", Rcolname="accession" ) ) ), list( objName="ALIAS2EG", Class="AnnDbBimap", L2Rchain=list( YEASTNCBI_DB_L2Rlink1, list( tablename="alias", Lcolname="_id", Rcolname="alias_symbol" ) ), direction=-1L ), list( objName="CHR", Class="AnnDbBimap", L2Rchain=list( YEASTNCBI_DB_L2Rlink1, list( tablename="chromosomes", Lcolname="_id", Rcolname="chromosome" ) ) ), list( objName="ENZYME", Class="AnnDbBimap", L2Rchain=list( YEASTNCBI_DB_L2Rlink1, list( tablename="ec", Lcolname="_id", Rcolname="ec_number" ) ) ), list( objName="GENENAME", Class="AnnDbBimap", L2Rchain=list( YEASTNCBI_DB_L2Rlink1, list( tablename="gene_info", Lcolname="_id", Rcolname="gene_name" ) ) ), list( objName="PATH", Class="AnnDbBimap", L2Rchain=list( YEASTNCBI_DB_L2Rlink1, list( tablename="kegg", Lcolname="_id", Rcolname="path_id" ) ) ), list( objName="PMID", Class="AnnDbBimap", L2Rchain=list( YEASTNCBI_DB_L2Rlink1, list( tablename="pubmed", Lcolname="_id", Rcolname="pubmed_id" ) ) ), list( objName="REFSEQ", Class="AnnDbBimap", L2Rchain=list( YEASTNCBI_DB_L2Rlink1, list( tablename="refseq", Lcolname="_id", Rcolname="accession" ) ) ), list( objName="SYMBOL", Class="AnnDbBimap", L2Rchain=list( YEASTNCBI_DB_L2Rlink1, list( tablename="gene_info", Lcolname="_id", Rcolname="symbol" ) ) ), ## list( ## objName="ENSEMBL", ## Class="AnnDbBimap", ## L2Rchain=list( ## YEASTNCBI_DB_L2Rlink1, ## list( ## tablename="ensembl", ## Lcolname="_id", ## Rcolname="ensembl_id" ## ) ## ) ## ), ## list( ## objName="ENSEMBLPROT", ## Class="AnnDbBimap", ## L2Rchain=list( ## YEASTNCBI_DB_L2Rlink1, ## list( ## tablename="ensembl_prot", ## Lcolname="_id", ## Rcolname="prot_id" ## ) ## ) ## ), ## list( ## objName="ENSEMBLTRANS", ## Class="AnnDbBimap", ## L2Rchain=list( ## YEASTNCBI_DB_L2Rlink1, ## list( ## tablename="ensembl_trans", ## Lcolname="_id", ## Rcolname="trans_id" ## ) ## ) ## ), list( objName="UNIPROT", Class="AnnDbBimap", L2Rchain=list( YEASTNCBI_DB_L2Rlink1, list( tablename="uniprot", Lcolname="_id", Rcolname="uniprot_id" ) ) ), list( objName="SGD", Class="AnnDbBimap", L2Rchain=list( YEASTNCBI_DB_L2Rlink1, list( tablename="sgd", Lcolname="_id", Rcolname="sgd_id" ) ) ), list( objName="ORF", Class="AnnDbBimap", L2Rchain=list( YEASTNCBI_DB_L2Rlink1, list( tablename="locus_tag", Lcolname="_id", Rcolname="locus_tag" ) ) ), list( objName="GO", Class="Go3AnnDbBimap", L2Rchain=list( YEASTNCBI_DB_L2Rlink1, list( #tablename="go_term", # no rightmost table for a Go3AnnDbBimap Lcolname="_id", tagname=c(Evidence="{evidence}"), Rcolname="go_id", Rattribnames=c(Ontology="NULL") ) ), rightTables=Go3tablenames() ) ) createAnnObjs.YEASTNCBI_DB <- function(prefix, objTarget, dbconn, datacache) { checkDBSCHEMA(dbconn, "YEASTNCBI_DB") ## AnnDbBimap objects seed0 <- list( objTarget=objTarget, datacache=datacache ) ann_objs <- createAnnDbBimaps(YEASTNCBI_DB_AnnDbBimap_seeds, seed0) ## Reverse maps ann_objs$ACCNUM2EG <- revmap(ann_objs$ACCNUM, objName="ACCNUM2EG") ann_objs$ENZYME2EG <- revmap(ann_objs$ENZYME, objName="ENZYME2EG") ## ann_objs$MAP2EG <- revmap(ann_objs$MAP, objName="MAP2EG") ann_objs$PATH2EG <- revmap(ann_objs$PATH, objName="PATH2EG") ann_objs$PMID2EG <- revmap(ann_objs$PMID, objName="PMID2EG") ann_objs$REFSEQ2EG <- revmap(ann_objs$REFSEQ, objName="REFSEQ2EG") ann_objs$SYMBOL2EG <- revmap(ann_objs$SYMBOL, objName="SYMBOL2EG") ann_objs$ORF2EG <- revmap(ann_objs$ORF, objName="ORF2EG") ann_objs$SGD2EG <- revmap(ann_objs$SGD, objName="SGD2EG") ## ann_objs$ENSEMBL2EG <- revmap(ann_objs$ENSEMBL, objName="ENSEMBL2EG") ## ann_objs$ENSEMBLPROT2EG <- revmap(ann_objs$ENSEMBLPROT, objName="ENSEMBLPROT2EG") ## ann_objs$ENSEMBLTRANS2EG <- revmap(ann_objs$ENSEMBLTRANS, objName="ENSEMBLTRANS2EG") ann_objs$GO2EG <- revmap(ann_objs$GO, objName="GO2EG") map <- ann_objs$GO2EG map@rightTables <- Go3tablenames(all=TRUE) map@objName <- "GO2ALLEGS" ann_objs$GO2ALLEGS <- map ## 2 special maps that are not AnnDbBimap objects (just named integer vectors) ann_objs$CHRLENGTHS <- createCHRLENGTHS(dbconn) ann_objs$MAPCOUNTS <- createMAPCOUNTS(dbconn, prefix) ## Some pre-caching Lkeys(ann_objs$GO) #mappedLkeys(ann_objs$GO) #Rkeys(ann_objs$GO2EG) #mappedRkeys(ann_objs$GO2EG) prefixAnnObjNames(ann_objs, prefix) } AnnotationDbi/R/createAnnObjs.YEAST_DB.R0000644000175200017520000002037114710217313020622 0ustar00biocbuildbiocbuild### ========================================================================= ### An SQLite-based ann data package (AnnDbPkg) provides a set of pre-defined ### AnnObj objects that are created at load-time. This set depends only on ### the underlying db schema i.e. all the SQLite-based ann data packages that ### share the same underlying db schema will provide the same set of AnnObj ### objects. ### ### This file describes the set of AnnObj objects provided by any ### YEAST_DB-based package i.e. any SQLite-based ann data package based ### on the YEAST_DB schema. ### The createAnnObjs.YEAST_DB() function is the main entry point for ### this file: it is called by any YEAST_DB-based package at load-time. ### ------------------------------------------------------------------------- YEAST_DB_L2Rlink1 <- list(tablename="sgd", Lcolname="systematic_name", Rcolname="_id") ### Mandatory fields: objName, Class and L2Rchain YEAST_DB_AnnDbBimap_seeds <- list( list( objName="ALIAS", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="gene2alias", Lcolname="_id", Rcolname="alias" ) ) ), list( objName="CHR", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="chromosome_features", Lcolname="_id", Rcolname="chromosome" ) ) ), list( objName="CHRLOC", Class="AnnDbMap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="chromosome_features", Lcolname="_id", tagname=c(Chromosome="{chromosome}"), Rcolname="start" ) ), rightColType="integer" ), list( objName="CHRLOCEND", Class="AnnDbMap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="chromosome_features", Lcolname="_id", tagname=c(Chromosome="{chromosome}"), Rcolname="stop" ) ), rightColType="integer" ), list( objName="DESCRIPTION", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="chromosome_features", Lcolname="_id", Rcolname="feature_description" ) ) ), list( objName="ENZYME", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="ec", Lcolname="_id", Rcolname="ec_number" ) ) ), list( objName="GENENAME", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="sgd", Lcolname="_id", Rcolname="gene_name" ) ) ), list( objName="PATH", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="kegg", Lcolname="_id", Rcolname="path_id" ) ) ), list( objName="PMID", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="pubmed", Lcolname="_id", Rcolname="pubmed_id" ) ) ), list( objName="GO", Class="Go3AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( #tablename="go_term", # no rightmost table for a Go3AnnDbBimap Lcolname="_id", tagname=c(Evidence="{evidence}"), Rcolname="go_id", Rattribnames=c(Ontology="NULL") ) ), rightTables=Go3tablenames() ), list( objName="COMMON2ORF", Class="AnnDbBimap", L2Rchain=list( list( tablename="gene2systematic", Lcolname="gene_name", Rcolname="systematic_name" ) ) ), list( objName="INTERPRO", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="interpro", Lcolname="_id", Rcolname="interpro_id" ) ) ), list( objName="PFAM", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="pfam", Lcolname="_id", Rcolname="pfam_id" ) ) ), list( objName="SMART", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="smart", Lcolname="_id", Rcolname="smart_id" ) ) ), list( objName="SGD", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="sgd", Lcolname="_id", Rcolname="sgd_id" ) ) ), list( objName="ENTREZID", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="genes", Lcolname="_id", Rcolname="gene_id" ) ) ), list( objName="REFSEQ", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="refseq", Lcolname="_id", Rcolname="accession" ) ) ), list( objName="ENSEMBL", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="ensembl", Lcolname="_id", Rcolname="ensembl_id" ) ) ), list( objName="ENSEMBLPROT", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="ensembl_prot", Lcolname="_id", Rcolname="prot_id" ) ) ), list( objName="ENSEMBLTRANS", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="ensembl_trans", Lcolname="_id", Rcolname="trans_id" ) ) ), list( objName="UNIPROT", Class="AnnDbBimap", L2Rchain=list( YEAST_DB_L2Rlink1, list( tablename="uniprot", Lcolname="_id", Rcolname="uniprot_id" ) ) ) ) createAnnObjs.YEAST_DB <- function(prefix, objTarget, dbconn, datacache) { checkDBSCHEMA(dbconn, "YEAST_DB") ## AnnDbBimap objects seed0 <- list( objTarget=objTarget, datacache=datacache ) ann_objs <- createAnnDbBimaps(YEAST_DB_AnnDbBimap_seeds, seed0) ## Reverse maps ann_objs$ENZYME2ORF <- revmap(ann_objs$ENZYME, objName="ENZYME2ORF") ann_objs$PATH2ORF <- revmap(ann_objs$PATH, objName="PATH2ORF") ann_objs$PMID2ORF <- revmap(ann_objs$PMID, objName="PMID2ORF") ann_objs$ALIAS2ORF <- revmap(ann_objs$ALIAS, objName="ALIAS2ORF") ann_objs$ENSEMBL2ORF <- revmap(ann_objs$ENSEMBL, objName="ENSEMBL2ORF") ann_objs$ENSEMBLPROT2ORF <- revmap(ann_objs$ENSEMBLPROT, objName="ENSEMBLPROT2ORF") ann_objs$ENSEMBLTRANS2ORF <- revmap(ann_objs$ENSEMBLTRANS, objName="ENSEMBLTRANS2ORF") ann_objs$GO2ORF <- revmap(ann_objs$GO, objName="GO2ORF") map <- ann_objs$GO2ORF map@rightTables <- Go3tablenames(all=TRUE) map@objName <- "GO2ALLORFS" ann_objs$GO2ALLORFS <- map ## 3 special maps that are not AnnDbBimap objects (just named vectors) ann_objs$CHRLENGTHS <- createCHRLENGTHS(dbconn) ann_objs$REJECTORF <- createREJECTORF(dbconn) ann_objs$MAPCOUNTS <- createMAPCOUNTS(dbconn, prefix) ## Some pre-caching Lkeys(ann_objs$GO) prefixAnnObjNames(ann_objs, prefix) } AnnotationDbi/R/flatten.R0000644000175200017520000001073614710217313016314 0ustar00biocbuildbiocbuild### ### Flattening different kinds of environments and maps ### ### A toCV. function takes a vector (or a single NA) and returns ### a character vector of the same length (or NULL). ### A _CVL object is a list of character vector or NULL elements. ### ### Flatten the GO envir found in HUMANCHIP, MOUSECHIP and RATCHIP packages. flatten.GOenvir <- function(env) { ## 'x' is a named list of "GO triplets". The names are the GO ids. ## A "GO triplet" is itself a list with 3 elements (GOID, Evidence, ## Ontology). toCV.go_id <- function(x) { if (!is.list(x)) { if (!isTRUE(is.na(x))) warning("right value in GO map is neither a list or a single NA") return(NULL) } names(x) } toCV.Evidence <- function(x) { if (!is.list(x)) { if (!isTRUE(is.na(x))) warning("right value in GO map is neither a list or a single NA") return(NULL) } sapply(x, function(goelt) goelt$Evidence, USE.NAMES=FALSE) } toCV.Ontology <- function(x) { if (!is.list(x)) { if (!isTRUE(is.na(x))) warning("right value in GO map is neither a list or a single NA") return(NULL) } sapply(x, function(goelt) goelt$Ontology, USE.NAMES=FALSE) } go_id_CVL <- eapply(env, toCV.go_id, all.names=TRUE) Evidence_CVL <- eapply(env, toCV.Evidence, all.names=TRUE) Ontology_CVL <- eapply(env, toCV.Ontology, all.names=TRUE) lens <- sapply(go_id_CVL, length) probe_id <- rep.int(names(go_id_CVL), lens) go_id <- unlist(go_id_CVL, recursive=FALSE, use.names=FALSE) Evidence <- unlist(Evidence_CVL, recursive=FALSE, use.names=FALSE) Ontology <- unlist(Ontology_CVL, recursive=FALSE, use.names=FALSE) data.frame(probe_id=probe_id, Evidence=Evidence, go_id=go_id, Ontology=Ontology, stringsAsFactors=FALSE) } ### Flatten the GO2PROBE and GO2ALLPROBES envir found in HUMANCHIP, ### MOUSECHIP and RATCHIP packages. flatten.GO2PROBEenvir <- function(env) { ## 'x' is a named character vector of probe ids. The names are the ## Evidence codes. toCV.probe_id <- function(x) { if (any(is.na(x))) warning("left value in GO2PROBE map contains NAs") x } toCV.Evidence <- function(x) { Evidence <- names(x) if (any(is.na(Evidence))) warning("left value in GO2PROBE map contains NAs") Evidence } probe_id_CVL <- eapply(env, toCV.probe_id, all.names=TRUE) Evidence_CVL <- eapply(env, toCV.Evidence, all.names=TRUE) lens <- sapply(probe_id_CVL, length) go_id <- rep.int(names(probe_id_CVL), lens) probe_id <- unlist(probe_id_CVL, recursive=FALSE, use.names=FALSE) Evidence <- unlist(Evidence_CVL, recursive=FALSE, use.names=FALSE) data.frame(probe_id=probe_id, Evidence=Evidence, go_id=go_id, stringsAsFactors=FALSE) } ### Some sanity checking checkPROBE2GOmappings <- function(GO, GO2PROBE, GO2ALLPROBES) { cat("Checking PROBE2GO mappings:\n") is_mapped <- eapply(GO, function(x) !(is.atomic(x) && is.vector(x) && isTRUE(is.na(x))), all.names=TRUE) is_mapped <- unlist(is_mapped, recursive=FALSE, use.names=TRUE) mapped_probe_id <- sort(names(is_mapped)[is_mapped]) cat(length(mapped_probe_id), " probe ids are mapped to at least 1 GO id\n", sep="") GOflat <- flatten.GOenvir(GO) ii <- order(GOflat$probe_id, GOflat$go_id, GOflat$Evidence) GOflat <- GOflat[ii, ] if (!identical(unique(GOflat$probe_id), mapped_probe_id)) stop("unexpected or missing probe ids in flat representation of GO") GO2PROBEflat <- flatten.GO2PROBEenvir(GO2PROBE) ii <- order(GO2PROBEflat$probe_id, GO2PROBEflat$go_id, GO2PROBEflat$Evidence) GO2PROBEflat <- GO2PROBEflat[ii, ] if (!identical(unique(GO2PROBEflat$probe_id), mapped_probe_id)) stop("unexpected or missing probe ids in flat representation of GO2PROBE") if (!all(GOflat[ , c("probe_id", "Evidence", "go_id")] == GO2PROBEflat)) stop("flat representations of GO and GO2PROBE differ") GO2ALLPROBESflat <- flatten.GO2PROBEenvir(GO2ALLPROBES) ii <- order(GO2ALLPROBESflat$probe_id, GO2ALLPROBESflat$go_id, GO2ALLPROBESflat$Evidence) GO2ALLPROBESflat <- GO2ALLPROBESflat[ii, ] if (!identical(unique(GO2ALLPROBESflat$probe_id), mapped_probe_id)) stop("unexpected or missing probe ids in flat representation of GO2ALLPROBESflat") } AnnotationDbi/R/inpIDMapper.R0000644000175200017520000003117514710217313017027 0ustar00biocbuildbiocbuild##inpMap is a map between an entrez gene and whatever thing inparanoid uses. ##You must ALWAYS have one of these for this function to work. .getMappingData = function(species){ switch(species, "HOMSA" = {srcSpcAb<-"Hs"; srcDBAb<-"eg"; require(paste0("org.",srcSpcAb,".",srcDBAb,".db"),character.only=TRUE); inpMap <- "org.Hs.egENSEMBLPROT"; centralID <- "EG"}, "MUSMU" = {srcSpcAb<-"Mm"; srcDBAb<-"eg"; require(paste0("org.",srcSpcAb,".",srcDBAb,".db"),character.only=TRUE); inpMap = "org.Mm.egENSEMBLPROT"; centralID <- "EG"}, "DROME" = {srcSpcAb<-"Dm"; srcDBAb<-"eg"; require(paste0("org.",srcSpcAb,".",srcDBAb,".db"),character.only=TRUE); inpMap = "org.Dm.egFLYBASEPROT"; centralID <- "EG"}, "RATNO" = {srcSpcAb<-"Rn"; srcDBAb<-"eg"; require(paste0("org.",srcSpcAb,".",srcDBAb,".db"),character.only=TRUE); inpMap = "org.Rn.egENSEMBLPROT"; centralID <- "EG"}, "CAEEL" = {srcSpcAb<-"Ce"; srcDBAb<-"eg"; require(paste0("org.",srcSpcAb,".",srcDBAb,".db"),character.only=TRUE); inpMap = "org.Ce.egWORMBASE"; centralID <- "EG"}, "ARATH" = {srcSpcAb<-"At"; ##Won't work till we ltrim off the decimals off the TAIR IDs in the inp pkgs srcDBAb<-"eg"; require(paste0("org.",srcSpcAb,".",srcDBAb,".db"),character.only=TRUE); ##inpMap = NA; ##Should not be needed since this one should be like yeast centralID <- "TAIR"}, "DANRE" = {srcSpcAb<-"Dr"; srcDBAb<-"eg"; require(paste0("org.",srcSpcAb,".",srcDBAb,".db"),character.only=TRUE); inpMap = "org.Dr.egZFIN"; centralID <- "EG"}, "SACCE" = {srcSpcAb<-"Sc"; srcDBAb<-"sgd"; require(paste0("org.",srcSpcAb,".",srcDBAb,".db"),character.only=TRUE); inpMap = NA; ##Not needed for yeast (uses the same ID in inparanoid as the central ID in the org package) centralID <- "ORF"} ) return(c(srcSpcAb, srcDBAb, inpMap, centralID)) } ##helper function to remove NAs and drop any duplicates that may emerge from mapping. ##a fair amount of this is needed since if you have any NAs that you feed into mget, you can end up matching EVERYTHING. .cleanup = function(ids){ ids = ids[!is.na(ids)] dupIndex = duplicated(ids) ids = ids[!dupIndex] } ##helper function to rename things .reLabel = function(srcIDs, destIDs, renameString){ if(length(destIDs)==length(srcIDs)){ names(destIDs) = names(srcIDs) }else{ stop("Cannot rename ", renameString) } return(destIDs) } ##helper function to decide what to do with multiple values. .handleMultipleMatches = function(ids, keepMultiples){ if(keepMultiples==FALSE){ ids = lapply(ids, function(x){if(length(x)>1) x=NA else x=x}) }else{ ids = lapply(ids, function(x){if(length(x)>1) x=as.character(x)[1] #return the 1st thing else if(length(x)<1) x=NA else if(length(x)==1) x=as.character(x) }) } return(ids) } ##TODO: rename the internal variables. They should be named better. inpIDMapper = function(ids, srcSpecies, destSpecies, srcIDType="UNIPROT", destIDType="EG", keepMultGeneMatches=FALSE, keepMultProtMatches=FALSE, keepMultDestIDMatches=TRUE){ ##Argument checking if(srcSpecies==destSpecies){stop("The srcSpecies and destSpecies should be different. 'No matter where you go, there you are.' - Bucakaroo Banzai")} if(srcIDType=="SYMBOL"){stop("I refuse to attempt this on the grounds that SYMBOLS are nearly worthless as IDs, and it would be irresponsible to proceed. If you must use symbols, you will have to process them one step at a time and double check your work, because they cannot be relied upon to be uniquely mapped onto a single gene.")} ##I need to set up the right thing based on what the package is setupVals = .getMappingData(srcSpecies) srcSpcAbrv = setupVals[1] srcDBAbrv = setupVals[2] if(!is.na(setupVals[3])){protMap = get(setupVals[3])} centralID1 = setupVals[4] #require the hom package and map require(paste0("hom.",srcSpcAbrv,".inp.db"),character.only=TRUE) homMap = get(paste0("hom.",srcSpcAbrv,".inp",destSpecies)) if(srcIDType!=centralID1){toSrcEGMap = get(paste0("org.",srcSpcAbrv,".",srcDBAbrv,srcIDType))} ##more info to map back out to an entrez gene ID at the end. mapBackVals = .getMappingData(destSpecies) destSpcAbrv = mapBackVals[1] destDBAbrv = mapBackVals[2] centralID2 = mapBackVals[4] if(!is.na(mapBackVals[3])){geneMap = get(mapBackVals[3])} ###MGET#1 Get mapped into the initial EGs if(srcIDType==centralID1){ genes = ids names(genes) = ids }else{ ids = .cleanup(ids) genes = mget(as.character(ids), revmap(toSrcEGMap), ifnotfound=NA) genes = .cleanup(genes) } ##Before the 2nd mgt, we need to have ONLY ONE answer for each element. genes = .handleMultipleMatches(genes, keepMultGeneMatches) genes = .cleanup(genes) ###MGET#2 map to the ID type used by inparanoid. if(exists("protMap", inherits=FALSE)){ inpIDs = mget(as.character(genes), protMap, ifnotfound=NA) ##Carry the names for the uniprot IDs over... inpIDs = .reLabel(genes, inpIDs, "inpIDs") inpIDs = .cleanup(inpIDs) }else{ inpIDs = genes } ###MGET#3 map across species with inparanoid ##I have to check each one of these possible mappings for a match... destList = lapply(inpIDs, function(x){mget(as.character(x), homMap, ifnotfound=NA)}) ##and then drop the NA elements of each of those sub-lists destIDs = lapply(destList, function(x){x = x[!is.na(x)]}) ##after the "tricks" to map the inparanoid mappings, the IDs list is double "nested" so we have to clean that up here... destIDs = lapply(destIDs, unlist) ##quick?? hack to make this work: dindex = vector() for(i in seq_len(length(destIDs))){ dindex = c(dindex, !is.null(destIDs[[i]]) ) } dnames = names(destList)[dindex] destIDs = destIDs[dindex] ##I have to (MUST!) drop the extras at this stage for this to work... destIDs = .handleMultipleMatches(destIDs, keepMultProtMatches) destIDs = unlist(destIDs) if(length(destIDs)==length(dnames)){names(destIDs)=dnames}else{stop("Names are not congruent")} ##Before the 4th mgt, we need to be down to ONLY ONE answer per element again. ##The hacking above probably makes this step unecessary at this point finIDs = .handleMultipleMatches(destIDs, keepMultProtMatches) uniqIDs = .cleanup(finIDs) ###MGET#4 dest species EG don't do this if we are already "there" if(exists("geneMap", inherits=FALSE)){ EGIDs = mget(as.character(uniqIDs), revmap(geneMap), ifnotfound=NA) EGIDs = .reLabel(uniqIDs, EGIDs, "EGIDs") EGIDs = .cleanup(EGIDs) #do before the rename, because there may be duplicates) }else{ EGIDs = uniqIDs } ###MGET#5 final mapping (may not be needed if they wanted EGs) ##Finally give the user the ID type that they asked for (ORF, EntrezID = (which is the default), UNIPROT etc.). if(destIDType != centralID2 && toupper(destDBAbrv)!=destIDType){ ##We will need a special case here if we decide to unify the eg IDs into the SGD org DB... resultMap = get(paste0("org.",destSpcAbrv,".",destDBAbrv,destIDType)) resultIDs = mget(as.character(EGIDs), resultMap, ifnotfound=NA) }else{resultIDs = EGIDs} resultIDs = .reLabel(EGIDs, resultIDs, "resultIDs") if(keepMultDestIDMatches==FALSE){resultIDs = .handleMultipleMatches(resultIDs, keepMultiples=TRUE)} resultIDs = .cleanup(resultIDs) resultIDs } ####################################################################################################### ## Here we need to define a function to remap things for us ## (assemble package names, load them etc. ## This might really be useful to someone who does not want to use the mappings. ###################################################################################################### intraIDMapper = function(ids, species, srcIDType="UNIPROT", destIDType="EG", keepMultGeneMatches=FALSE){ ##Argument checking if(srcIDType==destIDType){stop("The SrcIDType and destIDType should be different. 'No matter where you go, there you are.' - Bucakaroo Banzai")} if(srcIDType=="SYMBOL"){stop("I refuse to attempt this on the grounds that SYMBOLS are nearly worthless as IDs, and it would be irresponsible to proceed. If you must use symbols, you will have to use them one step at a time and double check your work, because they cannot be relied upon to be uniquely mapped onto a single gene.")} ##Need to set things up and invoke the library etc. setupVals = .getMappingData(species) srcSpcAbrv = setupVals[1] srcDBAbrv = setupVals[2] centralID = setupVals[4] ##cleanup the source IDs in case there are missing values. ids = .cleanup(ids) if(srcIDType==centralID){##srcIDType is a central ID (EG, ORF etc.) map = get(paste0("org.",srcSpcAbrv,".",srcDBAbrv,destIDType)) ##eg. org.Hs.eg.UNIPROT and we have an "EG" ##Get the new names resultIDs <- unlist2(mget(as.character(ids), map, ifnotfound=NA)) } else if(destIDType==centralID){##destIDType is a central ID (EG, ORF etc.) map = get(paste0("org.",srcSpcAbrv,".",srcDBAbrv,srcIDType)) ##eg. org.Hs.eg.UNIPROT and we have an "UNIPROT" map = revmap(map) ##So In this case it has to be revmapped ##Get the new names resultIDs <- unlist2(mget(as.character(ids), map, ifnotfound=NA)) } else if(srcIDType!=centralID && destIDType!=centralID){ ##Get the central IDs map1 = get(paste0("org.",srcSpcAbrv,".",srcDBAbrv,srcIDType)) ##This one will be the map that goes TO the central ID map1 = revmap(map1) ##Therefore this one has to be reversed resultIDs1 = unlist2(mget(as.character(ids), map1, ifnotfound=NA)) ##Before the 2nd mget, we need to have ONLY ONE answer for each element. resultIDs1 = .handleMultipleMatches(resultIDs1, keepMultGeneMatches) resultIDs1 = .cleanup(resultIDs1) ##in case there are NAs ##Then get the dest IDs. map2 = get(paste0("org.",srcSpcAbrv,".",srcDBAbrv,destIDType)) resultIDs = unlist2(mget(as.character(resultIDs1), map2, ifnotfound=NA)) resultIDs = .handleMultipleMatches(resultIDs, keepMultGeneMatches) resultIDs = .reLabel(resultIDs1, resultIDs, "resultIDs") ##two mappings so we want to keep initial names } resultIDs = .cleanup(resultIDs) resultIDs } ####################################################################################################### ## Finally lets just make a wrapper function to tie it all together. ## The purpose of this is really just for programmatic access. ## That is, it's just to allow people to set things up generically ## when then need a conversion to be done elsewhere ####################################################################################################### idConverter = function(ids, srcSpecies, destSpecies, srcIDType = "UNIPROT", destIDType = "EG", keepMultGeneMatches=FALSE, keepMultProtMatches=FALSE, keepMultDestIDMatches=TRUE){ if(srcSpecies != destSpecies){ inpIDMapper(ids=ids, srcSpecies=srcSpecies, destSpecies=destSpecies, srcIDType=srcIDType, destIDType=destIDType, keepMultGeneMatches=keepMultGeneMatches, keepMultProtMatches=keepMultProtMatches, keepMultDestIDMatches=keepMultDestIDMatches) }else{##else it's 'intra' intraIDMapper(ids=ids, species = srcSpecies, srcIDType=srcIDType, destIDType=destIDType, keepMultGeneMatches=keepMultGeneMatches) } } AnnotationDbi/R/loadDb.R0000644000175200017520000001173614710217313016045 0ustar00biocbuildbiocbuild############################################################################### ## loadDb is for loading a database from a string (path) to that .sqlite file. ## Helper makes queries more compact and allows debug. dbEasyQuery <- function(conn, SQL, j0=NA) { ## if (get("debugSQL", envir=RTobjs)) { ## if (!is.character(SQL) || length(SQL) != 1L || is.na(SQL)) ## stop("[debugSQL] 'SQL' must be a single string") ## cat("[debugSQL] SQL query: ", SQL, "\n", sep="") ## st <- system.time(data0 <- dbGetQuery(conn, SQL)) ## cat("[debugSQL] time: ", st["user.self"], " seconds\n", sep="") ## } else { data0 <- dbGetQuery(conn, SQL) ## } if (is.na(j0)) return(data0) ## Needed to deal properly with data frame with 0 column ("NULL data ## frames with 0 rows") returned by RSQLite when the result of a SELECT ## query has 0 row if (nrow(data0) == 0L) character(0) else data0[[j0]] } ## gets field from metadata .getMetaValue <- function(conn, name) { colnames <- c("name", "value") msg <- .valid.table.colnames(conn, "metadata", colnames) if (!is.null(msg)) stop(msg) sql <- paste0("SELECT * FROM metadata", " WHERE name = '", name, "'") data <- dbEasyQuery(conn, sql) if (nrow(data) != 1L) { msg <- paste0("The metadata table in the DB has 0 or more ", "than 1 '", name, "' entries") stop(msg) } data$value } .valid.colnames <- function(conn, tablename, colnames) { sql0 <- paste0("SELECT * FROM ", tablename, " LIMIT 0") data0 <- dbEasyQuery(conn, sql0) colnames0 <- colnames(data0) if (!all(colnames %in% colnames0)) { msg <- paste0("the ", tablename, " table in the DB doesn't have ", "all the expected columns (", paste0("\"", colnames, "\"", collapse=", "), ")") return(msg) } NULL } .valid.table.colnames <- function(conn, tablename, colnames) { tmp <- try(dbExistsTable(conn, tablename), silent=TRUE) if (is(tmp, "try-error")) return("invalid DB file") if (!tmp) return(paste0("the DB has no ", tablename, " table")) .valid.colnames(conn, tablename, colnames) } .valid.metadata.table <- function(conn, name, value) { colnames <- c("name", "value") msg <- .valid.table.colnames(conn, "metadata", colnames) if (!is.null(msg)) return(msg) db_value <- try(.getMetaValue(conn, name), silent = TRUE) if(is(db_value, "try-error")) return(db_value[1]) if (is.na(db_value) || db_value != value) { return(paste0("'", name, "' is not '", value, "'")) } NULL } .attach_supporting_pkg <- function(conn, db_type) { supporting_pkg <- try(.getMetaValue(conn, "Supporting package"), silent=TRUE) if (is(supporting_pkg, "try-error")) { if (is.null(getClassDef(db_type))) stop("this db is of type ", db_type, " but this is not ", "a defined class") } else { if (!suppressWarnings(require(supporting_pkg, character.only=TRUE))) stop("this db is of type ", db_type, " and requires the ", supporting_pkg, " package before it can be loaded") } } ### We distinguish 2 uses of loadDb(): ### 1. By the end-user for loading a standalone .sqlite file. In that case ### 'packageName' should NOT be specified. ### 2. By the .onLoad() hook of an annotation package. In that case ### 'packageName' must be specified and indicate the name of the ### annotation package. loadDb <- function(file, packageName=NA) { conn <- dbFileConnect(file) stopifnot(dbExistsTable(conn, "metadata")) db_type <- .getMetaValue(conn, "Db type") ## TEMP: On 07/25/2014 TranscriptDb was renamed TxDb so we need to ## replace with TxDb until there are no more SQLite db files around ## that have 'Db type' set to 'TranscriptDb' (will take a couple of ## years). if (db_type == "TranscriptDb") db_type <- "TxDb" if (identical(packageName, NA)) { ## loadDb() was called by the end-user. ## The user doesn't necessarily have the supporting package in his/her ## search path so we try to attach it for him/her in order to get ## access to the definition of the class specified in 'db_type'. .attach_supporting_pkg(conn, db_type) packageName <- character(0) } else { ## loadDb() was called by the .onLoad() hook of package 'packageName'. ## This package *should* import the supporting package so we should ## already have access to the definition of the class specified in ## 'db_type'. There is no need to import the namespace of the ## supporting package. if (!(isSingleString(packageName) && packageName != "")) stop("'packageName' must be NA or a single non-empty string") } new(db_type, conn=conn, packageName=packageName) } AnnotationDbi/R/makeMap.R0000644000175200017520000000306714710217313016231 0ustar00biocbuildbiocbuildmake_eg_to_go_map <- function(chip) { if (length(grep("\\.db$", chip))) chip <- substr(chip, 1, nchar(chip) - 3) chipNS <- getNamespace(paste0(chip, ".db")) chip2GO <- get(paste0(chip, "GO"), chipNS) chipGO2PROBE <- get(paste0(chip, "GO2PROBE"), chipNS) L2Rchain <- list(new("L2Rlink", tablename="probes", Lcolname="gene_id", Rcolname="gene_id"), chip2GO@L2Rchain[[2]], chip2GO@L2Rchain[[3]]) eg2go.map <- new("Go3AnnDbBimap", rightTables=chipGO2PROBE@rightTables, L2Rchain=L2Rchain, datacache=chipGO2PROBE@datacache, objName="ENTREZID2GO", objTarget=paste("chip", chip)) eg2go.map } make_go_to_eg_map <- function(chip) { map <- make_eg_to_go_map(chip) revmap(map) } ## Notes by Hervé: ## 1) First define the left-to-right path that you need to take to go from ## the ENZYME space to the ENTREZID space. You can look at the ## hgu95av2ENZYME2PROBE/hgu95av2ENTREZID slots for this or consult ## the schemas definitions in AnnotationDbi: ## L2Rchain <- list( ## new("L2Rlink", tablename="ec", Lcolname="ec_number", Rcolname="_id"), ## new("L2Rlink", tablename="genes", Lcolname="_id", Rcolname="gene_id") ## ) ## 2) Create a new AnnDbBimap instance: ## hgu95av2ENZYME2ENTREZID <- new("AnnDbBimap", ## L2Rchain=L2Rchain, ## datacache=hgu95av2ENZYME@datacache, ## objName="ENZYME2ENTREZID", ## objTarget="chip hgu95av2" ## ) AnnotationDbi/R/methods-AnnotationDb.R0000644000175200017520000000767414710217313020707 0ustar00biocbuildbiocbuildAnnotationDb <- function(conn, ...) { .AnnotationDb$new(conn=conn, ...) } ## setMethod(show, "AnnotationDb", ## function(object) ## { ## cat("class:", class(object), "\n") ## }) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Low-level accessor (not exported). ### ## These two things should just go away and be replaced with:x$conn ## .getConn <- function(envir) get("conn", envir=envir, inherits=FALSE) ## txdbConn <- function(txdb) .getConn(txdb@envir) # ## On the fence about whether or not to export dbconn(), it could be useful, # ## but it is also quite similar to say: org.Hs.eg_dbconn(), so if we export # ## it, it will have to deprecate the older ways. For now, I will just call it # ## using AnnotationDbi:::dbconn(db), Also AnnDbBiMaps have something called # ## dbconn() (lowercase "c") - blergh... # setMethod("dbconn", "AnnotationDb", # function(x) x$conn # ) ## Accesor for packageName setMethod("packageName", "AnnotationDb", function(x) x$packageName ) ## Overload metadata for AnnotationDb setMethod("metadata", "AnnotationDb", function(x) dbReadTable(dbconn(x), "metadata") ) ## Get the species AnnotationDb setMethod("species", "AnnotationDb", function(object){ res <- as.character(dbEasyQuery(dbconn(object), "SELECT value FROM metadata WHERE name='ORGANISM'")) if(res == "character(0)"){ ## then try again. res <- as.character(dbEasyQuery(dbconn(object), "SELECT value FROM metadata WHERE name='Organism'")) } if(res == "character(0)"){ ## then try again. res <- as.character(dbEasyQuery(dbconn(object), "SELECT value FROM metadata WHERE name='Genus and Species'")) } res } ) ## Try to make this generic setMethod("show", "AnnotationDb", function(object) { cat(class(object), "object:\n") metadata <- metadata(object) for (i in seq_len(nrow(metadata))) { cat("| ", metadata[i, "name"], ": ", metadata[i, "value"], "\n", sep="") } message("\n","Please see: help('select') for usage information", sep="") } ) setMethod("saveDb", "AnnotationDb", function(x, file) { if (!isSingleString(file)) stop("'file' must be a single string") sqliteCopyDatabase(dbconn(x), file) return(x) ## return the thing you just saved. } ) setMethod("columns", "AnnotationDb", function(x) { tables <- dbListTables(x$conn) sapply(tables, dbListFields, conn=x$conn) } ) cols <- function(x) .Deprecated("columns") .selectWarnReact <- function(x, keys, columns, keytype, ...){ extraArgs <- list(...) if(missing(keytype)){ .selectReact(x, keys, columns, keytype=extraArgs[["kt"]]) }else{ .selectReact(x, keys, columns, keytype) } } ## library(AnnotationDbi) ## library(RSQLite) ## library(GenomicFeatures); fl = system.file("extdata", "UCSC_knownGene_sample.sqlite", package="GenomicFeatures") ## conn = dbConnect(SQLite(), fl) ## loadDb(fl) ## bug ## loadFeatures(fl) ## other bug ## GenomicFeatures:::TxDb(conn) ## bug ## AnnotationDbi:::loadDb(fl) ## other bug ## TODO: add option to replace multi-matches with NAs or to just remove them. ## To cleanly handle having 'multiVals' being EITHER a FUN or something else: ## DO like: if(is.function(multiVals)){}else{match.arg(multiVals)} ############################################################################### ## New method just to make it easier to access the sqlite file (and thus make ## it easier to make use of great new stuff like dplyr) ## Basically I want this thing to return the sqlite file name path as a string ## make dbconn() and dbfile() methods for AnnotationDb objects (and export it) setMethod("dbconn", "AnnotationDb", function(x) x$conn) setMethod("dbfile", "AnnotationDb", function(x) dbfile(dbconn(x))) AnnotationDbi/R/methods-OrthologyDb.R0000644000175200017520000000620314710217313020546 0ustar00biocbuildbiocbuild## Code specifically for the Orthology.eg.db package ## the underlying DB only has two tables, one that has ## species -> taxonid mappings, and another that has ## taxon/gene -> othertaxon/gene orthology mappings ## we have to map the column and keytype to taxon ID ## and then make the query between taxa .keyColMapper <- function(x, colOrKey){ colOrKey <- toupper(sub("\\.", "_", colOrKey)) taxonid <- dbGetQuery(dbconn(x), paste0("select taxid from names where name='", colOrKey, "';")) taxonid } ## This part refactored in 11/2022. ## the genes table in the underlying DB was converted to have ## each row duplicated in reverse order, which makes lookups easier ## e.g., its now like this where the second row is the reverse map of the first ## ## taxid gene_id other_taxid other_gene_id ## 9606 100 10090 12345 ## 10090 12345 9606 100 ## ## What this gains us is quicker direct lookups ## e.g., we can get from human to mouse and vice versa ## by just doing a query on gene_id -> other_gene_id ## ## Also, there are any number of mappings that are like this: ## taxid gene_id other_taxid other_gene_id ## 8030 100136351 9606 5894 ## 9606 5894 7955 557109 ## Where there isn't a direct mapping from 8030 -> 7955, ## but there is an implicit mapping from 8030 -> 9606 -> 7955 ## By duplicating the rows we can make a performant lookup that ## includes any mapping via a single extra species .straightQuery <- function(x, fromTax, toTax, keys){ sql <- paste0("SELECT gene_id, other_gene_id FROM genes WHERE ", "taxid = '", fromTax, "' AND other_taxid='", toTax, "' AND ", "gene_id IN ('", paste(keys, collapse = "','"), "');") res <- dbGetQuery(dbconn(x), sql) res } .doubleQuery <- function(x, fromTax, toTax, keys){ sql <- paste0("SELECT G1.gene_id, G2.other_gene_id FROM genes ", "AS G1 INNER JOIN genes AS G2 ON G1.other_gene_id=G2.gene_id ", "WHERE G1.taxid='", fromTax, "' AND G2.other_taxid='", toTax, "' AND G1.gene_id IN ('", paste(keys, collapse = "','"), "');") res <- dbGetQuery(dbconn(x), sql) res } ## select function for Ontology.eg.db package .selectOnto <- function(x, keys, columns, keytype, ...){ fromTax <- .keyColMapper(x, keytype) toTax <- .keyColMapper(x, columns) res <- rbind(.straightQuery(x, fromTax, toTax, keys), .doubleQuery(x, fromTax, toTax, keys)) out <- data.frame(keys, rep(NA, length(keys))) names(out) <- c(keytype, columns) out[,2] <- res[match(out[,1], res[,1]),2] out } .ontoKeys <- function(x, keytype) { tax <- .keyColMapper(x, keytype) sql <- paste0("SELECT gene_id FROM genes WHERE taxid='", tax, "' UNION SELECT other_gene_id FROM ", "genes WHERE other_taxid='", tax, "';") res <- dbGetQuery(dbconn(x), sql)[,1] res } .justFirstUpper <- function(string){ stringlst <- strsplit(string, "") gsub("_", ".", do.call(c, lapply(stringlst, function(x) paste(c(x[1], tolower(x[-1])), collapse = "")))) } AnnotationDbi/R/methods-ReactomeDb.R0000644000175200017520000003465214710217313020330 0ustar00biocbuildbiocbuild## 1st the legacy stuff: ### Mandatory fields: objName, Class and L2Rchain reactome_AnnDbBimap_seeds <- list( list( objName="PATHID2NAME", Class="AnnDbBimap", L2Rchain=list( list( tablename="pathway2name", Lcolname="DB_ID", Rcolname="path_name" ) ) ), list( objName="PATHID2EXTID", Class="AnnDbBimap", L2Rchain=list( list( tablename="pathway2gene", Lcolname="DB_ID", Rcolname="gene_id" ) ) ), list( objName="REACTOMEID2GO", Class="AnnDbBimap", L2Rchain=list( list( tablename="reactome2go", Lcolname="DB_ID", Rcolname="go_id" ) ) ) ) createAnnObjs.reactome <- function(prefix, objTarget, dbconn, datacache) { ##checkDBSCHEMA(dbconn, "reactome") ## AnnDbBimap objects seed0 <- list( objTarget=objTarget, datacache=datacache ) ann_objs <- createAnnDbBimaps(reactome_AnnDbBimap_seeds, seed0) ## Reverse maps ann_objs$PATHNAME2ID <- revmap(ann_objs$PATHID2NAME, objName="PATHNAME2ID") ann_objs$EXTID2PATHID <- revmap(ann_objs$PATHID2EXTID, objName="EXTID2PATHID") ann_objs$GO2REACTOMEID <- revmap(ann_objs$REACTOMEID2GO, objName="GO2REACTOMEID") ## 1 special map that is not an AnnDbBimap object (just a named integer vector) ann_objs$MAPCOUNTS <- createMAPCOUNTS(dbconn, prefix) prefixAnnObjNames(ann_objs, prefix) } ## newer select methods: setMethod("keytypes", "ReactomeDb", function(x) c("ENTREZID","GO","PATHNAME","PATHID","REACTOMEID") ) setMethod("columns", "ReactomeDb", function(x) c("ENTREZID","GO","PATHNAME","PATHID","REACTOMEID") ) .keysReact <- function(x, keytype){ ## argument checking testForValidKeytype(x, keytype) sql <- switch(keytype, "ENTREZID" = "SELECT gene_id FROM pathway2gene", "GO" = "SELECT go_id FROM reactome2go", "PATHNAME" = "SELECT path_name FROM pathway2name", "PATHID" = paste0("SELECT DB_ID FROM pathway2name UNION ", "SELECT DB_ID FROM pathway2gene"), ## need proper reactome tables for this one: "REACTOMEID" = "SELECT DB_ID FROM DatabaseObject", stop("No keytype specified for .keys")) as.character(unique(dbQuery(dbconn(x), sql, 1L))) } setMethod("keys", "ReactomeDb", function(x, keytype, ...){ if(missing(keytype)) keytype <- "ENTREZID" #.keysReact(x, keytype) smartKeys(x=x, keytype=keytype, ..., FUN=.keysReact) } ) ## I think the way to go is to generate the SQL based on table associations. ## pathways_ids are DB_IDs (a subset) ## DatabaseObject and all standard reactome tables also have DB_IDs as keys... ## So to get stuff, I just need to make an outer join across all affected tables, joining on DB_IDs etc as appropriate. Then at the end, I need to go to uppercase, and drop any unwanted columns. While we are in here, I should probably clean up the schema a bit (change reactome_id over to DB_ID on the supplemental tables - DONE) ## This could all get really complicated if we start to expand this a lot... ## match a col value to appropriate table ## Can ALSO match to a subquery (when appropriate) ## every thing that this function returns must contain the central ID. ## TODO: this needs to actually match up with TWO things (more complex): ## 1) the table/query (done). ## 2) the colnames .getTable <- function(col, retVal="table"){ res <- switch(col, "ENTREZID" = c("pathway2gene","gene_id"), "GO" = c("reactome2go","go_id"), "PATHNAME" = c("pathway2name","path_name"), "PATHID" = c("pathway2name","DB_ID"), ## need proper reactome tables "REACTOMEID" = c("DatabaseObject","DB_ID"), stop("No col specified for .keys")) ## Then test and return appropriate records. if(retVal=="table"){ res <- res[[1]] }else if(retVal=="colname"){ res <- res[[2]] } res } ## match all cols .getTables <- function(cols, retVal="table"){ res <- character(length(cols)) for(i in seq_len(length(cols))){ res[i] <- .getTable(cols[i], retVal=retVal) } names(res) <- cols unique(res) } ## ## FUTURE TODO: if we have more than one table per type (and we will), then we ## ## need to have a way to get all those together and do that join as a ## ## subquery, but then treat it as a single table for the rest of the way... ## ## match a pair of things to a join ## .makeJoinWhereClause <- function(table1, table2){ ## joins <- character() ## if(!missing(table1) && !missing(table2)){ ## ## Two tables that need to be joined. ## joins <- paste(c(paste0(table1,".DB_ID"), ## paste0(table2,".DB_ID")), ## collapse="=") ## }else{ ## ## Then there is only one table involved (no join needed) ## } ## joins ## } ## ## .makeJoinWhereClause("pathway2gene","pathway2name") ## ## match a pair of things to a join ## .makeJoinRelationship <- function(table1, table2){ ## joins <- character() ## if(!missing(table1) && !missing(table2)){ ## ## Two tables that need to be joined. ## joins <- paste(table1,"LEFT OUTER JOIN",table2, "ON") ## }else{ ## ## Then there is only one table involved (no join needed) ## } ## joins ## } ## ## .makeJoinRelationship("pathway2gene","pathway2name") ## ## match all pairs for a given vector. ## ## Initially I thought to make use of this to solve the problem. ## ## combn(LETTERS[1:4], 2L) ## ## But no, because that it way too many joins. All I really need is one join ## ## for each link in the chain. So if I have a, b, c. I just need a-b and ## ## b-c. I don't care about a-c etc. Number of links will always be n-1 ## ## (where n is the number of types. what I really need to use here is ## ## split... n <- length(types) - 1 a b c a b b c So remove 1st and last, Then ## ## rep(middleVals, each=2) then append 1st and last back on. Then split by 2s ## ## needed to properly rep the tables vector. ## .stutter <- function(tables){ ## if(length(tables>2)){ ## start <- tables[1] ## n <- length(tables) ## end <- tables[n] ## tablesTrunc <- tables[2:(n-1)] ## tablesReps <- rep(tablesTrunc, each=2) ## res <- c(start, tablesReps, end) ## }else{ ## stop("To stutter you need at least 3 tables") ## } ## split(repTables, rep(1:(n-1), each=2)) ## } ## ## Needed to process all the joins ## .makeJoins <- function(tables){ ## n <- length(tables) ## res <- character() ## if(length(tables)==2){ ## res[1] <- paste(.makeJoinRelationship(tables[1],tables[2]), ## .makeJoinWhereClause(tables[1],tables[2]), "UNION", ## .makeJoinRelationship(tables[2],tables[1]), ## .makeJoinWhereClause(tables[2],tables[1])) ## }else{ ## repChunks <- .stutter(tables) ## ## Then ## for(i in seq_len(length(repChunks))){ ## res[i] <-paste(.makeJoinRelationship(repChunks[[i]][1],repChunks[[i]][2]), ## .makeJoinWhereClause(repChunks[[i]][1],repChunks[[i]][2]), ## "UNION", ## .makeJoinRelationship(repChunks[[i]][2],repChunks[[i]][1]), ## .makeJoinWhereClause(repChunks[[i]][2],repChunks[[i]][1])) ## } ## } ## unique(res) ## } ## types = c("ENTREZID", "PATHNAME") ## types = c("ENTREZID", "PATHNAME", "GO") ## tables = .getTables(types) ## .makeJoins(tables) ## This is for making simple queries .extractWithSimpleQuery <- function(x, table, colType, keys){ ## generate a simple query for each table sql <- paste("SELECT * FROM", table, "WHERE", colType,"IN", paste0('("',paste(keys, collapse='","'),'")') ) ## then extract it dbQuery(dbconn(x), sql) } ## this calls .extractWithSimpleQuery for each table and merges results .collateQueryResults <- function(x, tables, colType, keys, mergeID="DB_ID"){ res <- data.frame() mergeKeys <- character() for(i in seq_len(length(tables))){ if(i==1){ res <- .extractWithSimpleQuery(x, tables[i], colType, keys) }else{ if(i==2){ mergeKeys <- res[[mergeID]] } ## cond. for speed res <- merge(res, .extractWithSimpleQuery(x, tables[i], colType=mergeID, keys=mergeKeys), by.x=mergeID, by.y=mergeID, all.x=TRUE, all.y=TRUE) } } res } ## function for making select happen .selectReact <- function(x, keys, cols, keytype){ ## Some argument checking testSelectArgs(x, keys=keys, cols=cols, keytype=keytype) ## filter out keys that are not legit (just from the DB query) ktKeys = keys(x, keytype=keytype) qkeys <- keys[keys %in% ktKeys] ## collate possible types (type must ALWAYS be in front) types <-unique(c(keytype,cols)) ## this was not enough ## translate to relevant "tables" (some virtual) that I need stuff from tables <- .getTables(types) ## need to know the colType that goes with the INITIAL keytype.. colType <- .getTable(keytype, retVal="colname") ## now I need to go through each table, and for each I want to extract the ## missing piece with a SIMPLE query (basically get ONE thing), and then ## append it onto the results res <- .collateQueryResults(x, tables, colType, qkeys, mergeID="DB_ID") ## resort_base just needs: ## the results, ## ALL of the keys, ## the colname that matches the keys (jointype or colType) and ## the reqCols (which means the column names expected to be in the results ## at this point, ## primary object (i.e., TxDb, OrgDb etc.)) reqCols <- .getTables(types, retVal="colname") ## now drop any unrequested cols res <- res[,reqCols,drop=FALSE] ## And then resort/tidy etc. res <- resort_base(res, keys, jointype=colType, reqCols=reqCols) ## Capture relationship between uc and lc names names(reqCols) <- types ## Then match to the colnames colnames(res) <- names(reqCols)[match(colnames(res),reqCols)] ## OLDE (delete later): ## joins <- .makeJoins(tables) ## create a join for these tables. ## TODO: add keys to this query. ## sql <- paste("SELECT * FROM",joins, collapse=" UNION ") ## res <- dbQuery(dbconn(x), sql, 1L) ## TODO: sort the results res } ## select method setMethod("select", "ReactomeDb", function(x, keys, columns, keytype, ...){ ## if (missing(keytype)) keytype <- "ENTREZID" kt <- "ENTREZID" .selectWarnReact(x, keys, columns, keytype, kt=kt, ...) ## .selectReact(x, keys, columns, keytype) } ) ## usage: ## head(keys(reactome.db)) ## head(keys(reactome.db, keytype="PATHNAME")) ## head(keys(reactome.db, keytype="PATHNAME", pattern="Homo.sapiens")) ## k = head(keys(reactome.db, keytype="ENTREZID", pattern="Homo.sapiens", column="PATHNAME")) ### Works, but this shows how sometimes we can only enrich by doing this... and this can be tricky! ## select(reactome.db, k, cols=c("ENTREZID","PATHNAME"), keytype="ENTREZID") ### The following works (but is probably too slow for a unit test) ## length(keys(reactome.db, keytype="ENTREZID", column="GO")) ## length(keys(reactome.db, keytype="ENTREZID")) ## TODO: ## Change this to be either full outer joins, or devise a new strategy??? ## Remove repeated cols? (maybe done for me by resort_base?) ## resort_base() ## translate names (needs some new functions. ## Add a WHERE IN clause to the end for filtering out the keys... ## Full outer joins are just not going to work. I need a different approach. ## I need instead to just write a nibbler. Something that will just nibble at ## the SQL DB as needed and get just what is needed one slice at a time (just ## not practical to generate big ass queries all the time). ## The code will know ## 1) what tables have the data for each cols value ## 2) for each nibble (bite) it can call a simpler select function that just ## "knows" how to make VERY simple SQL queries based on the .getTables ## function idea (including the original keys). For more hopeless queries, ## subqueries can be placed in this function, but the point is that this ## function will only know how to get one kind of thing at a time. ## 3) then the results of each nibble can be merged into place in R ## This above part is mostly "done" (except I have to pass keys in!) ## Next comes the part where I remap col names and re-order/resort the results. ## 4) Use our method (resort_base) to clean up ## 5) rename the columns (this should be mapped up near where we specify what tables/queries are needed to extract based on COLs) ## WHY DO IT THIS WAY? Because if I write/generate a SQL query I end up ## pulling WAY more stuff back than I will ever need. This is slow and ## painful and the queries are all going to have to start as full outer joins, ## and I don't even know a priori what order they should be put in... In ## actual fact, I only want the records that go with my keys. So I will look ## up matches one tiny query at a time, and then merge the results together ## for a hybrid approach that I hope will be more performant. ## So to pull this off, I will need to deal with the fact that sometimes the ## keys I need will change mid-job. So I may start with GO IDs, so fine, I ## look up the reactome IDs (easy), but then I also need Entrez IDs, my code ## needs to be smart enough to use reactome IDs next after it fails to be able ## to nibble out the Entrez IDs using just the GO IDs. And it needs to have a ## logical set of fall back keys to use... ## TODO: ## 1) make this work when the initial keys don't all match. - filtering these in .reactSelect before calling to the DB is probably sufficient.... - DONE ## 2) find an example where the dim(res) is not the same number every time. IOW, verify that merge nibbling is not the equivalent of an inner join... - hint: just test with other IDs like DB_IDs - DONE ## 3) implement filtering and column renaming. - almost done, still have to do renaming and vectorize the colnames identifing (this latter step should take care of #4 below) - DONE ## 4) remove columns that are not requested from the results - DONE ## Bugs: ## 6) Do I have a resort_base bug with keys becoming duplicated??? - fixed? ## 7) Add documentation aliases ## 5) Finish up unit tests. (all here - but they get their own page) AnnotationDbi/R/methods-SQLiteConnection.R0000644000175200017520000000016614710217313021475 0ustar00biocbuildbiocbuildsetMethod("dbconn", "SQLiteConnection", function(x) x) setMethod("dbfile", "SQLiteConnection", function(x) x@dbname) AnnotationDbi/R/methods-geneCentricDbs-keys.R0000644000175200017520000005001214710217313022137 0ustar00biocbuildbiocbuild### ========================================================================= ### keys() and keytype() - related functions for gene-centric Dbs ### ------------------------------------------------------------------------- ## Three helpers for deprecating keytypes ## One to just list the bum keytypes .listDeprecatedKeytypes <- function(){ c('CHR','CHRLOC','CHRLOCEND') ## Uncomment after the release } ## Another for keytypes to remove unwanted keytypes .filterDeprecatedKeytypes <- function(keytypes){ keytypes[!(keytypes %in% .listDeprecatedKeytypes())] } ## this is a 'standard' warning for people who try to use keys or cols ## that are no longer valid due to being deprecated .deprecatedColsMessage <- function(){ depCols <- paste(.listDeprecatedKeytypes(), collapse="','") warning(wmsg(paste0("Accessing gene location information via '", depCols,"' is deprecated. Please use a range ", "based accessor like genes(), or select() with ", "columns values like TXCHROM and TXSTART ", "on a TxDb or OrganismDb object instead.\n"))) } ## And one for keys and select to warn if the user tries to use them .checkForDeprecatedKeytype <- function(keytype){ if(any(.listDeprecatedKeytypes() %in% keytype )){ .deprecatedColsMessage() } } ## Need an accessor for getting the central ID for a DB (when appropriate) .getCentralID <- function(x){ as.character(dbQuery(dbconn(x), "SELECT value FROM metadata WHERE name='CENTRALID'")) } ## Sometimes we need to translate a centralID into a central keytype. chooseCentralOrgPkgSymbol <- function(x){ centralID <- .getCentralID(x) keytype <- switch(EXPR = centralID, "EG" = "ENTREZID", "TAIR" = "TAIR", "ORF" = "ORF", "GID" = "GID") keytype } ## keys methods return the possible primary keys. So for EG based packages, ## this will be the viable entrez gene IDs. ## Must use SELECT DISTINCT for now because some packages like ag.db ## (Arabidopsis) have repeated probe ids in the probes table (those are the ## probe ids that hit multiple genes). ## TODO: When 'x' has the new slot containing the package name, use ## dbUniqueVals() (defined in SQL.R) and pass pkgname:::datacache to it. ## dbUniqueVals() is what's used behind the scene by the Lkeys/Rkeys/keys ## methods for AnnDbBimap objects so the "keys" methods below will give a ## consistent answer (and will take advantage of the cache). ## helper to get keys .queryForKeys <- function(x, keytype){ if(class(x)=="ChipDb"){ x <- .getOrgPkg(x) } table <- .getDBLocs(x, keytype) field <- .getDBLocs(x, keytype, value="field") sql <- paste("SELECT DISTINCT",field,"FROM",table) res <- dbQuery(dbconn(x), sql) t(res) } .legacyKeys <- function(x, keytype){ ## have to swap keytype ## keytype <- .swapSymbolExceptions(x, keytype) keytype <- .simplifyCols(x, keytype) ## Some org packages may have entrez genes in weird places... centralID <- .getCentralID(x) EGgeneTable <- character() if(centralID == "EG" || centralID == "ORF"){ EGgeneTable <- "genes" }else if(centralID == "TAIR"){ EGgeneTable <- "entrez_genes" } ## now decide if(class(x) == "OrgDb" && species(x) != "Plasmodium falciparum"){ res <- switch(EXPR = keytype, "ENTREZID" = dbQuery(dbconn(x), paste("SELECT gene_id FROM", EGgeneTable), 1L), "TAIR" = dbQuery(dbconn(x), "SELECT gene_id FROM genes", 1L), "ORF" = dbQuery(dbconn(x), "SELECT systematic_name FROM sgd", 1L), "PROBEID" = stop("PROBEID is not supported for Organism packages"), .queryForKeys(x, keytype)) } if(class(x) == "OrgDb" && species(x) == "Plasmodium falciparum"){ res <- switch(EXPR = keytype, "ORF" = dbQuery(dbconn(x), paste("SELECT gene_id FROM", EGgeneTable), 1L), .queryForKeys(x, keytype)) } if(class(x) == "ChipDb"){ res <- switch(EXPR = keytype, "ENTREZID" = dbQuery(dbconn(x), "SELECT gene_id FROM probes", 1L), "PROBEID" = dbQuery(dbconn(x), "SELECT DISTINCT probe_id FROM probes", 1L), .queryForKeys(x, keytype)) } if(class(x) == "GODb"){ res <- switch(EXPR = keytype, "GOID" = dbQuery(dbconn(x), "SELECT DISTINCT go_id FROM go_term", 1L), .queryForKeys(x, keytype)) } as.character(res[!is.na(res)]) } ## special functions for newer NOSCHEMA_DB's .deriveTableNameFromField <- function(field, x){ if(class(x)=="ChipDb"){ y <- x ## Switcheroo x <- .getOrgPkg(x) try(.attachDB(x,y), silent=TRUE) ## not a disaster if we fail } con <- dbconn(x) tables <- .getDataTables(con) if(exists("y", inherits=FALSE)){ tables <- c("c.probes", tables) } colTabs <- sapply(tables, FUN=dbListFields, con=con, simplify = FALSE) colTabs <- colTabs[grep("go_[mcb].+", names(colTabs), invert = TRUE)] m <- unlist2(sapply(colTabs, match, field, simplify = FALSE)) ## cannot ever be repeated tab <- names(m)[!is.na(m)] if(length(tab)!=1){stop("Two fields in the source DB have the same name.")} tab } .noSchemaKeys <- function(x, keytype){ tab <- .deriveTableNameFromField(field=keytype, x) ## So now we know table name (tab) and field (keytype) if(class(x)=="ChipDb"){ y <- x ## Switcheroo x <- .getOrgPkg(x) try(.attachDB(x,y), silent=TRUE) ## not a disaster if we fail } sql <- paste("SELECT",keytype,"FROM",tab) res <- dbQuery(dbconn(x), sql, 1L) as.character(res[!is.na(res)]) } ## general keys function .keys <- function(x, keytype){ .checkForDeprecatedKeytype(keytype) testForValidKeytype(x, keytype) schema <- metadata(x)[metadata(x)$name=="DBSCHEMA",]$value if(schema=="NOSCHEMA_DB" || schema=="NOCHIPSCHEMA_DB"){ .noSchemaKeys(x, keytype) }else{ .legacyKeys(x, keytype) } } #################################################################### ## So the new idea is that each place where I want to "enhance" keys, ## I should just be able to use a helper to wrap up the actual keys ## method... ## And we need a master helper to tie it all together smartKeys <- function(x, keytype, ..., pattern, column, fuzzy=FALSE, FUN) { ## check args, then... ## FUN is the base keys method .keys <- FUN ## So 1st we need helpers for other "keys" situations ## keys0 is for when we have a pattern we want to match in the keys .keys0 <- function(x, keytype, ..., pattern, fuzzy=FALSE) { ## assumes 'pattern' present FUN <- if (fuzzy) agrep else grep FUN(pattern, .keys(x, keytype), value=TRUE, ...) } ## keys1 is for when we have a column but no pattern ## so we want to filter by column .keys1 <- function(x, keytype, ..., column) { ## column acts as filter k <- suppressWarnings(select(x, as.character(.keys(x, keytype)), column, keytype)) k[[keytype]][ !is.na(k[[column]]) ] } ## keys2 is for when we have a column, and a pattern to match on that ## column, and we want all the keys of a particular keytype that match ## that column. .keys2 <- function(x, keytype, ..., pattern, column, fuzzy=FALSE) { ## assumes 'pattern', 'column' present FUN <- if (fuzzy) agrep else grep k <- suppressWarnings(select(x, as.character(.keys(x, keytype)), column, keytype)) k[[keytype]][ FUN(pattern, k[[column]], ...) ] } ## Now decide which function to call... if (missing(pattern) && missing(column)) k <- .keys(x, keytype) else if (missing(column)) k <- .keys0(x, keytype, ..., pattern=pattern, fuzzy=fuzzy) else if (missing(pattern)) k <- .keys1(x, keytype, ..., column=column) else k <- .keys2(x, keytype, ..., pattern=pattern, column=column, fuzzy=fuzzy) unique(k) } ## TODO: don't fail to document all the new arguments (pattern, column and fuzzy) setMethod("keys", "OrgDb", function(x, keytype, ...){ if(missing(keytype)){ keytype <- chooseCentralOrgPkgSymbol(x) } smartKeys(x=x, keytype=keytype, ..., FUN=.keys) } ) setMethod("keys", "ChipDb", function(x, keytype, ...){ if(missing(keytype)) keytype <- "PROBEID" smartKeys(x=x, keytype=keytype, ..., FUN=.keys) } ) setMethod("keys", "GODb", function(x, keytype, ...){ if(missing(keytype)) keytype <- "GOID" smartKeys(x=x, keytype=keytype, ..., FUN=.keys) } ) setMethod("keys", "OrthologyDb", function(x, keytype, ...) .ontoKeys(x, keytype, ...) ) ## new uses for keys: ## now TERM is a real key? (TODO: someone tell the keytypes) ## head(keys(GO.db, keytype="TERM")) ## get TERM keys that match a particular pattern ## head(keys(GO.db, keytype="TERM", pattern="mitochondrion")) ## get GOIDs where a TERM exists. ## head(keys(GO.db, keytype="GOID", column="TERM")) ## get keys of type GOID that go with a pattern match in TERM ## head(keys(GO.db, keytype="GOID", pattern="mitochondrion", column="TERM")) ## select(GO.db, keys =head(keys(GO.db, keytype="GOID", pattern="mitochondrion", column="TERM")), cols=c("GOID","TERM")) ## do the above but use fuzzy matching ## head(keys(GO.db, keytype="GOID", pattern="mitochondrion", column="TERM", fuzzy=TRUE)) ## select(GO.db, keys = head(keys(GO.db, keytype="GOID", pattern="mitochondrion", column="TERM", fuzzy=TRUE)), cols=c("GOID","TERM")) ## Can just get keys (straight up) ## head(keys(org.Hs.eg.db, keytype="SYMBOL")) ## keys1 situation works fine (and smartKeys is called twice.) ## Can filter by column (only return keys where there is a value for "PATH" ## length(keys(org.Hs.eg.db, keytype="ENTREZID", column="PATH")) ## is shorter than: ## length(keys(org.Hs.eg.db, keytype="ENTREZID")) ## debug(AnnotationDbi:::smartKeys) ## Can just get keys that match a pattern ## keys(org.Hs.eg.db, keytype="SYMBOL", pattern="BRCA") ## Can get a key that matches a pattern on some other column ## head(keys(org.Hs.eg.db,keytype="ENTREZID",pattern="MSX",column="SYMBOL")) ## keytypes method is to allow the user to specify what kind of keytype is ## passed in to either keys or the select methods. ## temporarily:this method will be VERY unsophisticated. ## TODO: would like to find a way to restore these blacklisted types to being ## able to be used, but I need a way around the lack of an Rkeys() method etc. ## keytypesBlackList <- c("CHRLOCEND","CHRLOC","PFAM","PROSITE", ## "DESCRIPTION", "GENENAME") ## .filterKeytypes <- function(x, baseType, keytypesBlackList){ ## res <- .cols(x, baseType=baseType) ## res <- res[!res %in% keytypesBlackList] ## ## append the centralID (if not already present) ## centralID <- .getCentralID(x) ## if(centralID == "EG"){ centralID <- "ENTREZID" } ## res <- c(res, centralID) ## unique(res) ## } setMethod("keytypes", "OrgDb", ## function(x) .filterKeytypes(x, baseType="ENTREZID", keytypesBlackList) function(x){ kts <- .cols(x, baseType="ENTREZID") .filterDeprecatedKeytypes(kts) } ) setMethod("keytypes", "ChipDb", ## function(x) .filterKeytypes(x, baseType="PROBEID", keytypesBlackList) function(x){ kts <- .cols(x, baseType="ENTREZID") .filterDeprecatedKeytypes(kts) } ) setMethod("keytypes", "GODb", function(x) return(c("GOID","TERM","ONTOLOGY","DEFINITION")) ## only one type makes sense ) setMethod("keytypes", "OrthologyDb", function(x) .justFirstUpper(dbGetQuery(dbconn(x), "select name from names;")[,1]) ) ## Marc's TODO: ##X .5) make keytype so that it uses the mapping names instead of internal stuff ##X 1) make keytypes so that it returns all possible keytypes ##X 2) make keys() so that it gets correct keys for correct keytypes ##X 3) make select() so that it is more efficient (pre-filter) ##X 4) make select() so that it uses keytypes to initially map in to the correct thing and then call internal funcs. ## 4.5) Make sure this thing is sorting correctly! ## 5) document all this stuff. ############################# ## TEST CODE: ## library(org.Hs.eg.db) ## ls(2) ## con = AnnotationDbi:::dbconn(org.Hs.eg.db) ## keys = head(keys(org.Hs.egCHR)) ## debug(AnnotationDbi:::.queryForKeys) ## debug(AnnotationDbi:::.keys) ## example of keys that uses keytype ## keys = keys(org.Hs.eg.db, keytype="ALIAS2EG")[1:4] ## example of keys that does not use keytype ## keys = keys(org.Hs.eg.db)[1:5] ## default keytype example ## keys = keys(org.Hs.eg.db)[1:5] ## cols = c("SYMBOL", "UNIPROT") ## select(org.Hs.eg.db, keys, cols) ## idType = "gene_id" ## debug(AnnotationDbi:::resort_base) ## debug(AnnotationDbi:::.mergeBimaps) ## debug(AnnotationDbi:::.select) ############################# ## keytype example ## library(hgu95av2.db); columns(hgu95av2.db); columns(org.Hs.eg.db); head(keys(org.Hs.eg.db, "ALIAS")); keys(org.Hs.eg.db, keytype="PROBEID")## should be an error ## library(org.Hs.eg.db); keys2 = head(keys(org.Hs.eg.db, "ALIAS"));cols = c("SYMBOL", "GO");res <- select(org.Hs.eg.db, keys2, cols, keytype="ALIAS"); head(res); dim(res) ## debug(AnnotationDbi:::.select) ## library(hgu95av2.db); keys2 = head(keys(hgu95av2.db, "ALIAS"));cols = c("SYMBOL", "GO");res <- select(hgu95av2.db, keys2, cols, keytype="ALIAS"); head(res); dim(res) ## works now ## library(org.Hs.eg.db);keys2 = head(Rkeys(org.Hs.egALIAS2EG));cols = c("SYMBOL","ENTREZID", "GO");res <- select(org.Hs.eg.db, keys2, cols, keytype="ALIAS") ## works now ## keys = head(keys(org.Hs.eg.db)); cols = c("SYMBOL","ENTREZID", "GO");res <- select(org.Hs.eg.db, keys, cols, keytype="ENTREZID") ## also works now ## library(hgu95av2.db); keys = head(keys(hgu95av2.db)); cols = c("SYMBOL","ENTREZID", "GO", "PROBEID"); res <- select(hgu95av2.db, keys, cols, keytype="PROBEID"); head(res) ## This shouldn't work - wrong keytype): ## keys = head(keys(hgu95av2.db)); cols = c("SYMBOL","ENTREZID", "GO"); res <- select(hgu95av2.db, keys, cols, keytype="ENTREZID") ## This does work (and should): ## library(hgu95av2.db); keys = head(keys(hgu95av2.db)); cols = c("SYMBOL","ENTREZID", "GO"); res <- select(hgu95av2.db, keys, cols, keytype="PROBEID"); head(res) ## library(GO.db); select(GO.db, keys(GO.db)[1:4], c("TERM","SYNONYM")) ## library(hgu95av2.db); okeys = keys(hgu95av2.db,keytype="OMIM")[1:4]; cols = c("SYMBOL", "UNIPROT", "PATH"); select(hgu95av2.db, okeys, cols, keytype="OMIM") ## TODO Bugs/refinements: ## TODO: this one should produce an output... - FIXED ## keys = head(keys(hgu95av2.db, "ENTREZID")); cols = c("PROBEID","SYMBOL","ENTREZID", "GO"); res <- select(hgu95av2.db, keys, cols, keytype="ENTREZID"); head(res) ## 3) Add a NEWS page with info. about these changes. ## strange bug: - killed ## 4) Putting "ENTREZID" in for keytype and then giving probe IDs as keys should NOT work for hgu95av2.db: but it does... (it only seems to allow this with the one kind of key) ## also need to roll back the removal of the keytype from the columns. ## library(org.Hs.eg.db);keys2 = head(Rkeys(org.Hs.egALIAS2EG));cols = c("SYMBOL","ENTREZID", "GO");res <- select(org.Hs.eg.db, keys2, cols, keytype="ALIAS"); ## Strange bug: ## the following all work: ## foo = select(org.Hs.eg.db, keys=head(keys(org.Hs.eg.db),n=2),cols="REFSEQ"); head(foo) ## foo = select(org.Hs.eg.db, keys=head(keys(org.Hs.eg.db),n=2),cols=c("REFSEQ","ACCNUM")); head(foo) ## foo = select(org.Hs.eg.db, keys=head(keys(org.Hs.eg.db),n=2),cols=c("ACCNUM")); head(foo) ## But this does NOT work (fixed): ## foo = select(org.Hs.eg.db, keys=head(keys(org.Hs.eg.db),n=2),cols=head(columns(org.Hs.eg.db))); head(foo); head(columns(org.Hs.eg.db)) ## debug(AnnotationDbi:::.nameExceptions) ## debug(AnnotationDbi:::.addNAsInPlace) ## Requirements for having a select method that works and plays well with ## others: ## 1) Use the same arguments for the method (obvious) ## 2) remove dulicated columns. ## Martins slow select example. It takes advantage of the fact that for ## simple cases, like the one below, our select method has to gather each ## piece and then merge them together which costs a lot of time (both to merge ## and also because we don't pre-subset). ## Also our code is doing more post-processing (returning prettier results in ## particular order etc.) ## Also because our code is blind to what the user wants out, we move ALL of ## each bimap through memory and don't pare them down till we merge them ## together and this is ultimately inefficient. ## If the code knew (as Martin did in this case) the relationships between ## these different elements (perhaps it could learn that graph from the DB), ## then it could make smarter decisions about how to query. ## library(org.Hs.eg.db) ## sym <- "ITGA7" ## system.time(res0 <- toTable(org.Hs.egPFAM[ org.Hs.egALIAS2EG[[sym]] ])) ## system.time(res1 <- select(org.Hs.eg.db, sym, "PFAM", "ALIAS")) ## system.time(res3 <- toTable(org.Hs.egGO[ org.Hs.egALIAS2EG[[sym]] ])) ## system.time(res4 <- select(org.Hs.eg.db, sym, "GO", "ALIAS")) ## ALSO: there is something to be said for the notion that we need a general ## solution to this problem that does NOT involve a Bimap. Bimaps are nice, ## but we don't normally have them for a new resource and we might want a ## faster way to handle these sorts of manipulations when we don't have them. ## Basically, I think that I want to use a graph here, but not require one ## from the user, I need to 1) be able to infer the graph from SQL, 2) be able ## to path-find through the graph such that all the keys requested are ## hit. and 3) be able to construct a sensible query from that graph. Tall ## order, but a fun problem. ## Reasons for generalizing this: 1) I need to be able to do this in ALL ## databases (not just bimap ones). and 2) We are moving away from bimaps and ## 3) I want to be able to add mappings to existing bimap based data resources ## that are actually not available as a bimap (reactome) and 4) I would really ## like to be able to transparently pull data from another resource and just ## have it appear to be in one place. Sort of like we currently do for ## microRNAs with TxDbs ## Really radical thoughts: ## What if discovery functions just reported based on which databases were ## installed (instead of just what was in a package?). ## What if select searched across all of these databases to make joins on the ## fly as appropriate by already knowing how to connect the dots? ## What if we could have select work out how things connect based on the type ## of package, and some internal information about how those would be joined? ## THE R CMD build bug: ## For AnnotationDbi: ## R --vanilla ## utils::Sweave("IntroToAnnotationPackages.Rnw") ## runs no problem ## BUT: ## R --vanilla ## utils::Sweave("AnnotationDbi.Rnw") ## utils::Sweave("IntroToAnnotationPackages.Rnw") ## FAILBOAT ## This failure is happening because the values that are left littered in the ## global namespace are allowed to leak down into the scope of the functions ## being called... ## Bug was able to happen this way: ## y = "foo" ## source("AnnotationDbi/inst/doc/IntroToAnnotationPackages.R") ## was caused by overly grabby exists() calls combined with the sloppy way ## that R CMD check leaves variables all over the place when it runs R CMD ## check. exists() calls are no longer grabby. ## ALSO, lexical scoping meant that the exists() call being falsely tripped ## led to a call of species(y) actually being executed when I should never ## have been ## fieldNames <- c("gene_id","accession","accession") ## expectedCols <- c("ENTREZID","ACCNUM","REFSEQ") ## type <- ## the na bug ## sym <- "ITGA7" ## select(org.Hs.eg.db,sym,"PFAM",keytype="ALIAS"); ## Problem: our code that filters rows needs to drop the keytype column before filtering NAs AnnotationDbi/R/methods-geneCentricDbs.R0000644000175200017520000013546614710217313021207 0ustar00biocbuildbiocbuild### ========================================================================= ### Methods form mapping keys to table and fields, select() and ### column() methods for gene-centric Dbs ### ------------------------------------------------------------------------- ## For GO, I should just define a whole distinct set. ## For Chip packages, they should be nearly the same, but we either have to do ## some extra complexity to join across DBs OR I can just do one final merge ## in R. I may want my own .generateQuery() function for chip packages, or I ## may just want my own .extractData() function(), and to point to a different ## "x" when using chip packages. ## ALSO: I will need a way to deduce the org package that goes with each chip ## package. hgu95av2ORGPKG will (for example) get you this. DONE: .getOrgPkg <- function(x){ pkgname <- packageName(x) orgsymbol <- sub(".db$","ORGPKG", pkgname) orgroot <- get(orgsymbol, getNamespace(pkgname)) orgpkgname <- paste0(orgroot, ".db") get(orgpkgname, loadNamespace(orgpkgname)) } ## This gets the exact path to the chip DB. .getChipDbFile <- function(x){ pkgname <- packageName(x) pkgroot <- sub(".db$","", pkgname) filesymbol <- paste0(pkgroot, "_dbfile") get(filesymbol, loadNamespace(pkgname))() } ## Limitation: I can only have ONE table and ONE field for each list name. ## So if we have fields like GO that should pull back multiple things, then we ## have to expand those ahead of time. .expandCols <- function(x, cols){ ## known expansions for cols: if("CHRLOC" %in% cols){ after <- match("CHRLOC", cols) cols <- append(cols, c("CHRLOCCHR"),after) } if("GO" %in% cols){ after <- match("GO", cols) cols <- append(cols, c("EVIDENCE","ONTOLOGY"),after) } if("GOALL" %in% cols){ after <- match("GOALL", cols) cols <- append(cols, c("EVIDENCEALL","ONTOLOGYALL"),after) } if("ORF" %in% cols && species(x)=="Saccharomyces cerevisiae"){ after <- match("ORF", cols) cols <- append(cols, c("SGD"),after) } if("COMMON" %in% cols){ after <- match("COMMON", cols) cols <- append(cols, c("SGD"),after) } ## special case: if PROBEIDS are requested, they MUST be in front! if("PROBEID" %in% cols){ cols <- append("PROBEID", setdiff(cols, "PROBEID")) } unique(cols) } ## ORG PKGS CHECKLIST: ## org.Ag.eg.sqlite ## done ## org.At.tair.sqlite ## done ## org.Bt.eg.sqlite ## done ## org.Ce.eg.sqlite ## done ## org.Cf.eg.sqlite ## done ## org.Dm.eg.sqlite ## done ## org.Dr.eg.sqlite ## done ## org.EcK12.eg.sqlite ## done ## org.EcSakai.eg.sqlite ## done ## org.Gg.eg.sqlite ## done ## org.Hs.eg.sqlite ## done ## org.Mm.eg.sqlite ## done ## org.Mmu.eg.sqlite ## done ## org.Pf.plasmo.sqlite ## done ## org.Pt.eg.sqlite ## done ## org.Rn.eg.sqlite ## done ## org.Sc.sgd.sqlite ## done ## org.Ss.eg.sqlite ## done ## org.Xl.eg.sqlite ## done ## none of the above.. ## done .defineTables <- function(x){ class <- class(x) species <- species(x) .definePossibleTables(class, species) } .definePossibleTables <- function(class, species){ ## 1st the generic/universal things .defTables <- list("ENTREZID" = c("genes","gene_id"), "PFAM" = c("pfam","pfam_id"), "IPI" = c("pfam","ipi_id"), "PROSITE" = c("prosite","prosite_id"), "ACCNUM" = c("accessions","accession"), "ALIAS" = c("alias","alias_symbol"), "ALIAS2EG" = c("alias","alias_symbol"), "ALIAS2PROBE" = c("alias","alias_symbol"), "CHR" = c("chromosomes","chromosome"), "CHRLOCCHR" = c("chromosome_locations","seqname"), "CHRLOC" = c("chromosome_locations","start_location"), "CHRLOCEND" = c("chromosome_locations","end_location"), "ENZYME" = c("ec","ec_number"), "MAP" = c("cytogenetic_locations","cytogenetic_location"), "PATH" = c("kegg","path_id"), "PMID" = c("pubmed","pubmed_id"), "REFSEQ" = c("refseq","accession"), "SYMBOL" = c("gene_info","symbol"), "GENETYPE" = c("genetype","gene_type"), "ENSEMBL" = c("ensembl","ensembl_id"), "ENSEMBLPROT" = c("ensembl_prot","prot_id"), "ENSEMBLTRANS" = c("ensembl_trans","trans_id"), "GENENAME" = c("gene_info","gene_name"), "UNIPROT" = c("uniprot","uniprot_id"), "GO" = c("go","go_id"), "EVIDENCE" = c("go","evidence"), "ONTOLOGY" = c("go","ontology"), "GOALL" = c("go_all","go_id"), "EVIDENCEALL" = c("go_all","evidence"), "ONTOLOGYALL" = c("go_all","ontology") ) ## exceptions for ALL OrgDbs if(class=="OrgDb"){ ## I should probably remove ucsckg from select... #.defTables <- c(.defTables, list("UCSCKG" = c("ucsc","ucsc_id")) ) .defTables <- .defTables[!(names(.defTables) %in% c("ALIAS2PROBE"))] } ## exceptions for ALL ChipDbs if(class=="ChipDb"){ .defTables <- c(.defTables, list("PROBEID" = c("c.probes","probe_id")) ) } ## species specific exceptions if(species=="Anopheles gambiae"){ ## drop unsupported mappings .defTables <- .defTables[!(names(.defTables) %in% c("ALIAS", "ALIAS2PROBE", "MAP", "CHRLOC", "CHRLOCEND", "GENETYPE", "CHRLOCCHR", "PFAM", "IPI", "PROSITE") )] } if(species=="Arabidopsis thaliana"){ ## add these .defTables <- c(.defTables, list("TAIR" = c("genes","gene_id"), "ARACYC" = c("aracyc","pathway_name"), "ARACYCENZYME" = c("enzyme","ec_name"))) ## remove these: .defTables <- .defTables[!(names(.defTables) %in% c("ACCNUM", "ALIAS", "ALIAS2EG", "ALIAS2PROBE", "MAP", "GENETYPE", "PFAM", "IPI", "PROSITE", "ENSEMBL", "ENSEMBLPROT", "ENSEMBLTRANS", "UNIPROT", "ENTREZID", "CHR") )] ## "re-add" these (redefine, so must have been removed in prior step) .defTables <- c(.defTables, list("ENTREZID" = c("entrez_genes","gene_id"), "CHR"=c("gene_info","chromosome") )) } if(species=="Bos taurus"){ .defTables <- .defTables[!(names(.defTables) %in% c("MAP") )] } if(species=="Caenorhabditis elegans"){ .defTables <- c(.defTables, list("WORMBASE" = c("wormbase","wormbase_id"))) .defTables <- .defTables[!(names(.defTables) %in% c("MAP", "PFAM", "GENETYPE", "IPI", "PROSITE") )] } if(species=="Canis familiaris"){ .defTables <- .defTables[!(names(.defTables) %in% c("MAP", "PFAM", "IPI", "PROSITE") )] } if(species=="Drosophila melanogaster"){ .defTables <- c(.defTables, list("FLYBASE" = c("flybase","flybase_id"), "FLYBASECG" = c("flybase_cg","flybase_cg_id"), "FLYBASEPROT" = c("flybase_prot","prot_id"))) .defTables <- .defTables[!(names(.defTables) %in% c("PFAM", "IPI", "PROSITE") )] } if(species=="Danio rerio"){ .defTables <- c(.defTables, list("ZFIN" = c("zfin","zfin_id"))) .defTables <- .defTables[!(names(.defTables) %in% c("MAP","GENETYPE"))] } if(species=="Escherichia coli"){ .defTables <- .defTables[!(names(.defTables) %in% c("CHR", "MAP", "GENETYPE", "CHRLOC", "CHRLOCEND", "CHRLOCCHR", "PFAM", "IPI", "PROSITE", "ENSEMBL", "ENSEMBLPROT", "ENSEMBLTRANS", "UNIPROT"))] } if(species=="Gallus gallus"){ .defTables <- .defTables[!(names(.defTables) %in% c("MAP"))] } if(species=="Homo sapiens"){ .defTables <- c(.defTables, list("OMIM" = c("omim","omim_id"), "UCSCKG" = c("ucsc","ucsc_id")) ) } if(species=="Mus musculus"){ .defTables <- c(.defTables, list("MGI" = c("mgi","mgi_id")) )#, # "UCSCKG" = c("ucsc","ucsc_id")) ) .defTables <- .defTables[!(names(.defTables) %in% c("MAP") )] } if(species=="Macaca mulatta"){ .defTables <- .defTables[!(names(.defTables) %in% c("ALIAS", "ALIAS2PROBE", "MAP", "PFAM", "IPI", "PROSITE"))] } if(species=="Plasmodium falciparum"){ .defTables <- c(.defTables, list( "ORF" = c("genes","gene_id") )) .defTables <- .defTables[!(names(.defTables) %in% c("ENTREZID", "ACCNUM", "ALIAS", "ALIAS2PROBE", "ALIAS2EG", "CHR", "CHRLOC", "CHRLOCEND", "CHRLOCCHR", "GENETYPE", "MAP", "PMID", "REFSEQ", "GENETYPE", "PFAM", "IPI", "PROSITE", "ENSEMBL", "ENSEMBLPROT", "ENSEMBLTRANS", "UNIPROT") )] .defTables <- c(.defTables, list("ALIAS" = c("alias","alias_symbol") )) } if(species=="Pan troglodytes"){ .defTables <- .defTables[!(names(.defTables) %in% c("ALIAS", "ALIAS2PROBE", "MAP", "GENETYPE", "PFAM", "IPI", "PROSITE") )] } if(species=="Rattus norvegicus"){ #.defTables <- .defTables ## no changes (for now) .defTables <- .defTables[!(names(.defTables) %in% c("MAP") )] } if(species=="Saccharomyces cerevisiae"){ .defTables <- c(.defTables, list( "ORF" = c("gene2systematic","systematic_name"), "DESCRIPTION" = c("chromosome_features","feature_description"), "COMMON" = c("gene2systematic","gene_name"), "INTERPRO" = c("interpro","interpro_id"), "SMART" = c("smart","smart_id"), "SGD" = c("sgd","sgd_id") )) .defTables <- .defTables[!(names(.defTables) %in% c("ACCNUM", "MAP", "SYMBOL", "GENETYPE", "PROSITE", "ALIAS", "ALIAS2EG", "ALIAS2PROBE", "CHRLOC", "CHRLOCEND", "CHRLOCCHR", "GENENAME", "IPI", "CHR") )] .defTables <- c(.defTables, list("ALIAS" = c("gene2alias","alias"), "CHRLOC" = c("chromosome_features","start"), "CHRLOCEND" = c("chromosome_features","stop"), "CHRLOCCHR" = c("chromosome_features","chromosome"), "GENENAME" = c("sgd","gene_name"), "CHR" = c("chromosome_features","chromosome") )) } if(species=="Sus scrofa"){ .defTables <- .defTables[!(names(.defTables) %in% c("MAP", "CHRLOC", "CHRLOCEND", "CHRLOCCHR", "PFAM", "IPI", "PROSITE", "ENSEMBL", "ENSEMBLPROT", "ENSEMBLTRANS") )] } if(species=="Xenopus laevis"){ .defTables <- .defTables[!(names(.defTables) %in% c("ALIAS", "ALIAS2PROBE", "MAP", "CHRLOC", "CHRLOCEND", "CHRLOCCHR", "PFAM", "IPI", "PROSITE", "ENSEMBL", "ENSEMBLPROT", "ENSEMBLTRANS") )] } stockSpecies <- c("Anopheles gambiae", "Arabidopsis thaliana", "Bos taurus", "Caenorhabditis elegans", "Canis familiaris", "Drosophila melanogaster", "Danio rerio", "Escherichia coli", "Gallus gallus", "Homo sapiens", "Mus musculus", "Macaca mulatta", "Plasmodium falciparum", "Pan troglodytes", "Rattus norvegicus", "Saccharomyces cerevisiae", "Sus scrofa", "Xenopus laevis") if(!(species %in% stockSpecies)){ ## What follows is a very optimistic list! .defTables <- list("ENTREZID" = c("genes","gene_id"), "ACCNUM" = c("accessions","accession"), "ALIAS" = c("alias","alias_symbol"), "ALIAS2EG" = c("alias","alias_symbol"), "ALIAS2PROBE" = c("alias","alias_symbol"), "CHR" = c("chromosomes","chromosome"), "PMID" = c("pubmed","pubmed_id"), "REFSEQ" = c("refseq","accession"), "SYMBOL" = c("gene_info","symbol"), "GENETYPE" = c("genetype","gene_type"), "GENENAME" = c("gene_info","gene_name"), "GO" = c("go","go_id"), "EVIDENCE" = c("go","evidence"), "ONTOLOGY" = c("go","ontology") ) } ## ultimately I think I need GO.db to have it's OWN select methods. ## it's just too many responsibilities for this select to also handle the ## somewhat obscure GO database schema. So many things will not really work ## untill I do that change (ancestors etc.) if(class=="GODb"){ .defTables <- list("GOID" = c("go_term","go_id"), "TERM" = c("go_term","term"), "ONTOLOGY" = c("go_term","ontology"), "DEFINITION" = c("go_term","definition") ## "BPPARENTS" = c("go_bp_parents","_parent_id"), ## "CCPARENTS" = c("go_cc_parents","_parent_id"), ## "MFPARENTS" = c("go_mf_parents","_parent_id"), ## "BPANCESTOR" = c("",""), ## "CCANCESTOR" = c("",""), ## "MFANCESTOR" = c("",""), ## "OBSOLETE" = c("",""), ## "SYNONYM" = c("go_synonym","synonym"), ## "BPCHILDREN" = c("",""), ## "CCCHILDREN" = c("",""), ## "MFCHILDREN" = c("",""), ## "BPOFFSPRING" = c("go_bp_offspring","_offspring_id"), ## "CCOFFSPRING" = c("go_cc_offspring","_offspring_id"), ## "MFOFFSPRING" = c("go_mf_offspring","_offspring_id") ) } ## then return with this result .defTables } ## helper for getting out the table OR the field from .defineTables .getDBLoc <- function(x, col, value="table"){ res <- .defineTables(x) if(col %in% names(res)){ res <- res[[col]] } else { stop("'col' value '", col, "' is not defined") } ## Then test and return appropriate records. if(value=="table"){ res <- res[1] }else if(value=="field"){ res <- res[2] }else if(value=="full.field"){ res <- paste(res[1],res[2],sep=".") } res } ## vectorized version of .getDBLoc .getDBLocs <- function(x, cols, value="table"){ res <- character(length(cols)) for(i in seq_len(length(cols))){ res[i] <- .getDBLoc(x, cols[i], value=value) } names(res) <- cols unique(res) } ## .getFullyQualifiedDBLocs <- function(x, cols){ ## tables <- .getDBLocs(x, cols, value="table") ## fields <- .getDBLocs(x, cols, value="field") ## paste(tables, fields, sep=".") ## } ## x is the org package object, y is the chip package object. .attachDB <- function(x,y){ chipDb <- .getChipDbFile(y) chipSQL <- paste0("ATTACH '",chipDb,"' AS c") #message(chipSQL) dbAttach(dbconn(x), chipSQL) } .generateQuery <- function(x, cols, keytype, keys){ ## If it is a chip package, get the org package instead if(class(x)=="ChipDb"){ y <- x ## then flip to using the org package, and actually attach to that. x <- .getOrgPkg(x) try(.attachDB(x,y), silent=TRUE) ## not really a disaster if we fail here ## because we have a "y" defined, we have to define the dblocs this way: dblocs <- .getDBLocs(y, cols) ## Fully qualified keytype and species are set up like this ## fullKeytype <- .getFullyQualifiedDBLocs(y, keytype) fullKeytype <- .getDBLocs(y, keytype, value = "full.field") species <- species(x) ## if we have c.probes in dblocs, then we MUST join to genes table if("c.probes" %in% dblocs && species(x)!="Saccharomyces cerevisiae"){ dblocs <- unique(append(dblocs, c("genes"), match("c.probes", dblocs))) } if("c.probes" %in% dblocs && species(x)=="Saccharomyces cerevisiae"){ dblocs <- unique(append(dblocs, c("sgd"), match("c.probes", dblocs))) } }else{ ## this means there is only an org pkg... dblocs <- .getDBLocs(x, cols) ## fullKeytype <- .getFullyQualifiedDBLocs(x, keytype) fullKeytype <- .getDBLocs(x, keytype, value = "full.field") species <- species(x) } ## Get fields if(exists("y", inherits=FALSE)){ ## IOW if it was a chip package at the top... fields <- .getDBLocs(y,cols,value="full.field") fields <- paste(paste(fields,paste0(fields,"'"),sep=" AS '"), collapse=",") }else{ fields <- .getDBLocs(x,cols,value="full.field") fields <- paste(paste(fields,paste0(fields,"'"),sep=" AS '"), collapse=",") } #message(paste(dblocs,collapse=",")) ## then make the 1st part of the query. for(i in seq_len(length(dblocs))){ if(i==1){ res <- paste("SELECT ",fields," FROM",dblocs[i]) }else{ ## if(species=="Saccharomyces cerevisiae" && ## (dblocs[i]=="gene2systematic" || dblocs[i-1]=="gene2systematic")){ ## join <- "systematic_name" ## }else if(dblocs[i]=="c.probes" || dblocs[i-1]=="c.probes"){ ## IOW if joining to OR from c.probes we want "gene_id" if(species=="Saccharomyces cerevisiae"){ join <- "systematic_name" }else{ join <- "gene_id" } }else{ join <- "_id" } res <- c(res, paste("LEFT JOIN ",dblocs[i],"USING (",join,")")) } } res <- paste(res, collapse=" ") ## then use the keytype and keys to append the WHERE clause strKeys <- paste0('"',keys,'"',collapse=",") where <- paste("WHERE ",fullKeytype,"in (",strKeys,")" ) paste(res, where) } ## usage: ## library(org.Hs.eg.db) ## cols = c("ENTREZID","SYMBOL","PFAM") ## keytype = "ALIAS" ## keys = "ITGA7" ## x = org.Hs.eg.db ## AnnotationDbi:::.generateQuery(x, cols, keytype, keys) ## cols = c("ENTREZID","SYMBOL","PFAM") ## keytype = "ENTREZID"; keys = head(keys(org.Hs.eg.db)); x = org.Hs.eg.db ## AnnotationDbi:::.generateQuery(x, cols, keytype, keys) ## AnnotationDbi:::.extractData(x, cols, keytype, keys) ## select(org.Hs.eg.db,keys, cols, "ENTREZID") ## library(hgu95av2.db); x = hgu95av2.db;cols = c("ENTREZID","SYMBOL","PFAM") ## keytype = "PROBEID"; keys = head(keys(hgu95av2.db)) ## AnnotationDbi:::.generateQuery(x, cols, keytype, keys) ## OK ## AnnotationDbi:::.extractData(x, cols, keytype, keys) ## select(hgu95av2.db,keys, cols, keytype) ## cols = c("ENTREZID", "SYMBOL", "CHRLOC") ## AnnotationDbi:::.extractData(x, cols, keytype, keys) ## select(hgu95av2.db,keys, cols, keytype) ## cols = c("ENTREZID", "SYMBOL", "GO") ## AnnotationDbi:::.extractData(x, cols, keytype, keys) ## select(hgu95av2.db,keys, cols, keytype) ## GO.db example attempt: ## library(GO.db);x<- GO.db;keys<-head(keys(GO.db)); cols = c("ONTOLOGY", "DEFINITION", "TERM"); keytype="GOID" ## AnnotationDbi:::.extractData(x, cols, keytype, keys) ## select(hgu95av2.db,keys, cols, keytype) ## I also need a method to call my generated sql and get the data. ## NOTE: the order that cols come back in is determined by the DB. ## Some resorting is done downstream. .extractData <- function(x, cols, keytype, keys){ ## Take the cols, append the keytype to FRONT cols <- unique(c(keytype, cols)) ## do any necessary col expansion: cols <- unique(.expandCols(x, cols)) ## generate the query sql <- .generateQuery(x, cols, keytype, keys) #message(sql) ## get field names for relevant cols cols <- unique(c(keytype, cols)) headerTables <- .getDBLocs(x, cols, value="full.field") if(class(x)=="ChipDb"){ y <- x ## save for test below x <- .getOrgPkg(x) ## then flip to using the org package } res <- dbQuery(dbconn(x), sql) ## then cleanup by doing a detach: if(exists("y", inherits=FALSE)){ ## I should not have to use inherits=FALSE? dbAttach(dbconn(x), "DETACH DATABASE c") } ## then subset to only relevant cols res[,(colnames(res) %in% headerTables)] } ## usage: ## .extractData(x, cols, keytype, keys) ## helper used for dropping out ugly redundant col names. ## (BIMAP FREE!) .simplifyCols <- function(x, cols){ blackList <- c(ALIAS="ALIAS2PROBE", ALIAS="ALIAS2EG", CHR="CHRLOCCHR") ## CHR="CHRLOC", ## Don't put cols here till removal is FINAL.. ## CHR="CHRLOCEND", ## CHR="CHR") idx <- !(cols %in% blackList) unique(cols[idx]) } .filterSuffixes <- function(tab){ ## clean up .x and .y extensions? colnames(tab) <- gsub("\\.x","",colnames(tab)) colnames(tab) <- gsub("\\.y","",colnames(tab)) ## clean up .1's colnames(tab) <- gsub("\\.1","",colnames(tab)) tab } ############################################################################### ## Helpers for tidying up the final table. ## resort_base drops unwanted rows, rearanges cols and puts things ## into order that the keys were initially ## drop rows that don't match .dropUnwantedRows <- function(tab, keys, jointype) { ## drop duplicated or 'all NA' (other than jointype) rows ntest <- ncol(tab) - sum(colnames(tab) == jointype) idx <- duplicated(tab) | (rowSums(is.na(tab)) == ntest) tab <- tab[!idx,, drop=FALSE] ## add back rows for keys that were completely removed noMatchKeys <- unique(keys[!keys %in% tab[[jointype]]]) if (n <- length(noMatchKeys)) { ridx <- nrow(tab) + seq.int(n) cidx <- colnames(tab) %in% jointype tab[ridx, cidx] <- noMatchKeys } ## place rows in order of first appearance of key idx <- order(match(tab[[jointype]], keys)) tab <- tab[idx,, drop=FALSE] rownames(tab) <- NULL tab } ## resort the Column Names .resortColumns <- function(tab, jointype, reqCols) { tab <- .filterSuffixes(tab) ## Removes duplicate suffixes if (!all(colnames(tab) %in% reqCols)) stop("[internal] some of 'reqCols' are not in 'tab'") cnames <- c(jointype, reqCols[!reqCols %in% jointype]) tab[, cnames, drop=FALSE] } ## Create extra rows .generateExtraRows <- function(tab, keys, jointype) { ## 4 possibilities ## if there are not dups, then we skip this function. ## if(any(duplicated(keys)) ## expand the keys ## if(any(duplicated(tab[[jointype]]))) ## some messages may apply ## AND if they are BOTH redundant how do I decide which row to expand? ## I think that I have to throw a warning and NOT do this step in that case? keyTest <- any(duplicated(keys)) rowTest <- any(duplicated(tab[[jointype]])) if (keyTest && !rowTest){ ind = match(keys, tab[[jointype]]) tab <- tab[ind,,drop=FALSE] rownames(tab) <- NULL } else if (keyTest && rowTest) { indlst <- split(row.names(tab), tab[[jointype]]) ind <- unlist(indlst[keys]) tab <- tab[ind,] } ## We now just always give (terse) messages about relationship of ## data to columns returned. if(!keyTest && !rowTest) { txt <- "'select()' returned 1:1 mapping between keys and columns" } else if (!keyTest && rowTest) { txt <- "'select()' returned 1:many mapping between keys and columns" } else if (keyTest && !rowTest) { txt <- "'select()' returned many:1 mapping between keys and columns" } else if (keyTest && rowTest) { ## User will get data "as is" txt <- "'select()' returned many:many mapping between keys and columns" } message(paste(strwrap(txt), collapse="\n")) tab } ## select() returned 1:1 mapping between keys and columns ## select() returned 1:many mapping between keys and columns ## select() returned many:1 mapping between keys and columns ## Also will want mesage for many:many ## .resort() was renamed resort_base() ## resort_base() is the main function for cleaning up a table so that ## results look formatted the way we want them to. resort_base <- function(tab, keys, jointype, reqCols) { if (jointype %in% colnames(tab)) { tab <- .dropUnwantedRows(tab, keys, jointype) ## rearrange to make sure cols are in correct order tab <- .resortColumns(tab, jointype, reqCols) } ## Duplicate any rows as appropriate (based on those keys) .generateExtraRows(tab, keys, jointype) } ## helper so that we can be ready for when there are multiple things getting ## duplicated... ## The current version of these helper functions are not "smart", but it could ## be made so if needed. The reason why not smart is because it will be a lot ## faster if we can get away with it being "dumb" and not looking up the types ## of values from the DB for each type. .replaceValues <- function(dups, fieldNames, expectedCols){ newVals <- expectedCols[fieldNames %in% dups] after <- match(dups, fieldNames) - 1 ## -1 b/c we aim to replac: not follow cols <- append(fieldNames, newVals, after) ## then remove the dups values cols[!(cols %in% dups)] } ## helper for ambiguous/duplicated columns .adjustForDupColNames <- function(res, expectedCols){ fieldNames <- colnames(res) ## get duplicated vals dups <- fieldNames[duplicated(fieldNames)] ## for each value of dups, we want to call .replaceValues for(i in seq_len(length(dups))){ if(i==1){ cols <- .replaceValues(dups[i], fieldNames, expectedCols) }else{ cols <- .replaceValues(dups[i], cols, expectedCols) } } cols } ## helper looks at cols and trys to warn users about many:1 relationships .warnAboutManyToOneRelationships <- function(cols){ file=system.file("extdata","manyToOneBlackList.Rda",package="AnnotationDbi") blackList <- get(load(file)) problemCols <- cols[cols %in% blackList] ## give message if there are more than 4 (for now) if(length(problemCols) > 4){ msg = paste("You have selected the following columns that can have a many to one relationship with the primary key: ", paste(problemCols,collapse=", "),". Because you have selected more than a few such columns there is a risk that this selection may balloon up into a very large result as the number of rows returned multiplies accordingly. To experience smaller/more manageable results and faster retrieval times, you might want to consider selecting these columns separately.") warning(paste(strwrap(msg, exdent=2), collapse="\n"), immediate.=TRUE, call.=FALSE) } } ## the core of the select method for GO org and chip packages. .legacySelect <- function(x, keys=NULL, cols=NULL, keytype, jointype) { ## IF CHR, CHR or CHRLOC are requested then you must deny the ## request as these are now deprecated if(any(.listDeprecatedKeytypes() %in% cols)){ .deprecatedColsMessage() } ## if asked for what they have, just return that. if(all(cols %in% keytype) && length(cols)==1){ res <- data.frame(keys=keys) colnames(res) <- cols return(res) } if(is.null(keys)) keys <- keys(x) ## if no keys provided: use them all if(is.null(cols)) cols <- columns(x) ## if no cols provided: use them all ## call .simplifyCols to ensure we use same colnames as columns() cols <- .simplifyCols(x, cols) ## keytype <- .swapSymbolExceptions(x, keytype) keytype <- .simplifyCols(x, keytype) ## oriCols is a snapshot of col requests needed for column filter below oriCols <- unique(c(keytype, cols)) ## Check if the user is selecting too many cols with many:1 relationships .warnAboutManyToOneRelationships(cols) ## Generate query and extract the data res <- .extractData(x, cols=cols, keytype=keytype, keys=keys) ## these are the colnames we need to have gotten back from the DB expectedCols <- .expandCols(x, oriCols) oriTabCols <- .getDBLocs(x, expectedCols, value="full.field") ## I need to know the jointype... jointype <- .getDBLocs(x, keytype, value="full.field") ## Remove suffixes in case there were dups res <- .filterSuffixes(res) ## If we can, then we should re-arrange to make sure cols come back in same ## order as they asked for initially. Expanded cols cannot be re-arranged. if(all(expectedCols %in% oriCols) && any(oriCols != expectedCols) ){ ## We need to make it so that oriTabCols is in the SAME order as oriCols oriTabCols <- .getDBLocs(x, oriCols, value="full.field") ## then we need to make expectedCols to match oriCols expectedCols <- oriCols } ## Then if any suffixes were actually removed, it means there were duplicated ## cols. Duplicated cols means I have to do some label swapping. if( length(oriTabCols) < length(colnames(res))){ oriTabCols <- .adjustForDupColNames(res, expectedCols) ## BADNESS! colnames(res) <- .adjustForDupColNames(res, expectedCols) } ## resort_base will resort the rows relative to the jointype etc. if(dim(res)[1]>0){ res <- resort_base(res, keys, jointype, oriTabCols) } colnames(res) <- expectedCols[match(colnames(res), oriTabCols)] rownames(res) <- NULL res } ## This just needs to generate a simple query and then return the ## results with no _id's ## A simple strategy will work EXCEPT for the weird case where I need ## to pull out multiple fields at once. (like GO) ## Do I need to pay attention to the order??? - it seems that I don't... .appendGenesToTabs <- function(tabs){ names <- names(tabs) tabs <- c("genes",tabs) names(tabs) <- c("GID", names) tabs } .noSchemaSelect <- function(x, keys=NULL, cols=NULL, keytype){ ## 1st pool all the fields we need to extract fields <- unique(c(cols, keytype)) ## Then get the tables to go with each one. tabs <- sapply(fields, .deriveTableNameFromField, x=x) ## make fully qualified fields of these tabs (the ones we want to extract) f.fields <- paste(tabs, fields, sep=".") ## if it's a Chip package, attach and point to org package for x if(class(x)=="ChipDb"){ y <- x ## then flip to using the org package, and actually attach to that. x <- .getOrgPkg(x) try(.attachDB(x,y), silent=TRUE) ## not a disaster if we fail ## Also make sure we include the genes table (only needed for the join) if(!("genes" %in% tabs)) tabs <- .appendGenesToTabs(tabs) } ## Make non-redundant list of tables to visit nrTabs <- unique(tabs) ## Now join to each table for(i in seq_along(nrTabs)){ if(i==1){ sql <- paste("SELECT ",paste(f.fields, collapse=","), " FROM",tabs[1]) }else{ ## IF we see c.probes in nrTabs[i], it means we have to ## use gene_id instead. if("c.probes" %in% nrTabs[i]){ sql <- c(sql, paste("LEFT JOIN ",nrTabs[i],"USING (GID)")) }else{ sql <- c(sql, paste("LEFT JOIN ",nrTabs[i],"USING (_id)")) } } } sql <- paste(sql, collapse=" ") ## add the where clause strKeys <- paste0('"',keys,'"',collapse=",") fullKeytype <- tabs[names(tabs)==keytype] fullKeytype <- paste(fullKeytype, names(fullKeytype), sep=".") where <- paste("WHERE ",fullKeytype,"in (",strKeys,")" ) sql <- paste(sql, where) ## then call that res <- dbQuery(dbconn(x), sql) ## cleanup and re-organize resort_base(res, keys, jointype=keytype, fields) } ############################################################################### ## HELPERS for argument validation {in select() and keys()} .isSingleString <- function(x){ is.atomic(x) && length(x) == 1L && is.character(x) } testForValidKeytype <- function(x, keytype){ if(!.isSingleString(keytype)){ stop("'keytype' must be a a single string") } ## deprecated keytypes are still technically 'valid' pkts <- c(keytypes(x), .listDeprecatedKeytypes()) if(!(keytype %in% pkts)){ msg <- paste0("Invalid keytype: ",keytype,". Please use the keytypes method to see a listing of valid arguments.") stop(msg) } } .testForValidCols <- function(x, cols){ if (!is.character(cols)){ stop("'columns' must be a character vector") } pcols <- c(columns(x), .listDeprecatedKeytypes()) if(!all(cols %in% pcols) && !is.null(cols)){ badCols <- cols[!(cols %in% pcols)] msg <- paste0("Invalid columns: ",paste(badCols, collapse=","),". Please use the columns method to see a listing of valid arguments.") stop(msg) } } ## fks is an alternate vector of keys to consult for validity. ## Normally this will be NULL and the test function should consult ## keys for the supplied keytype .testForValidKeys <- function(x, keys, keytype, fks=NULL){ if (!is.character(keys)){ stop("'keys' must be a character vector") } if (length(keys) == 0L) { return() } if(is.null(fks)){ ## Normally, fks is just NULL and so we will call keys() ktKeys <- keys(x, keytype) }else{ ## This lets the caller say wait: use these keys instead ktKeys <- fks } if(!(any(ktKeys %in% keys))){ msg <- paste0("None of the keys entered are valid keys for '",keytype, "'. Please use the keys method to see a listing of valid arguments.") stop(msg) ## later when things are better, demote this to a warning() } } testSelectArgs <- function(x, keys, cols, keytype, fks=NULL, skipValidKeysTest=FALSE){ testForValidKeytype(x, keytype) .testForValidCols(x, cols) ## I may need for this test to sometimes not happen... if(skipValidKeysTest==FALSE){ .testForValidKeys(x, keys, keytype, fks) } } ## library(Homo.sapiens); select(Homo.sapiens, c('11'), 'SYMBOL', 'GENEID') ## general select function .select <- function(x, keys=NULL, cols=NULL, keytype, jointype, ...){ ## Some argument handling and checking extraArgs <- list(...) if('fks' %in% names(extraArgs)){fks<-extraArgs[["fks"]]}else{fks<-NULL} if('skipValidKeysTest' %in% names(extraArgs)){ skipValidKeysTest<-extraArgs[["skipValidKeysTest"]]}else{ skipValidKeysTest<-FALSE} testSelectArgs(x, keys=keys, cols=cols, keytype=keytype, fks=fks, skipValidKeysTest=skipValidKeysTest) ## Now get the schema and call select schema <- metadata(x)[metadata(x)$name=="DBSCHEMA",]$value if(schema=="NOSCHEMA_DB" || schema=="NOCHIPSCHEMA_DB"){ .noSchemaSelect(x, keys, cols, keytype) }else{ .legacySelect(x, keys, cols, keytype, jointype) } } ## Helper for setting the jointype to an appropriate default .chooseJoinType <- function(x){ if(.getCentralID(x) == "ORF" && species(x) == "Saccharomyces cerevisiae"){ jointype <- "gene2systematic.systematic_name" }else{ jointype <- "genes.gene_id" } jointype } ####################################################################### ## So an issue was that keytype was not defined carefully enough and ## was getting substituted when cols arg was used in conjunction with ## no keytype specified... So when there is not keytype, the user ## must tell us which one it is OR we have to somehow "know" ## TO FIX: I need to guess the keytype and pass it along as some other ## name into ... ## Hack: I will pass it in as kt ## And halfway through this hack, it seems that if there is an ## argument passed in AFTER your other ones that the problem I was ## having magically clears up??? WTH? setMethod("select", "OrgDb", function(x, keys, columns, keytype, ...) { if (missing(keytype)) keytype <- chooseCentralOrgPkgSymbol(x) jointype <- .chooseJoinType(x) .select(x, keys, columns, keytype, jointype=jointype, ...) ## .selectWarnJT(x, keys, columns, keytype, jointype=jointype, ## kt=kt, ...) } ) setMethod("select", "ChipDb", function(x, keys, columns, keytype, ...){ if (missing(keytype)) keytype <- "PROBEID" .select(x, keys, columns, keytype, jointype="probes.probe_id", ...) ## .selectWarnJT(x, keys, columns, keytype, jointype="probes.probe_id", ## kt=kt, ...) } ) setMethod("select", "GODb", function(x, keys, columns, keytype, ...){ if (missing(keytype)) keytype <- "GOID" .select(x, keys, columns, keytype, jointype="go_term.go_id", ...) ## .selectWarnJT(x, keys, columns, keytype, jointype="go_term.go_id", ## ...) } ) setMethod("select", "OrthologyDb", function(x, keys, columns, keytype, ...){ if(length(columns) > 1L){ warning(paste("The columns argument was", length(columns), "long. Only using the first item", columns[1]), call. = FALSE) columns <- columns[1] } if (missing(keytype)){ warning("Default mapping from Homo sapiens is being made.", call. = FALSE) keytype <- "Homo.sapiens" } .selectOnto(x, keys, columns, keytype, ...) } ) ############################# ## Internally we want to reconstruct these guys so we can merge() on them ## c <- columns(GO.db)[7] ## prefix = "GO" ## foo = paste0(prefix,c) ## bar = eval(parse(text=foo)) ############################################################################## ## cols methods return the list of things that users can ask for. This can be ## just the table names, or it might be a list of mappings .legacyCols <- function(x, baseType){ ## cols <- .makeColAbbrs(x) cols <- names(.defineTables(x)) if(!missing(baseType)){ cols <- c(baseType, cols) } ## translate relevant short bimap names to "cute" names cols <- .simplifyCols(x, cols) ## filter out columns that have been deprecated here hideCols <- .listDeprecatedKeytypes() cols <- cols[!(cols %in% hideCols)] ## .cols does not care about your names names(cols) <- NULL unique(cols) } ## These helpers will go into the DB and extract col values for newer ## NOSCHEMA_DB's .getDataTables <- function(con){ tables <- dbListTables(con) tables[!tables %in% c("metadata","map_metadata","map_counts")] } .noSchemaCols <- function(x){ if(class(x)=="ChipDb"){ y <- x ## The old switcheroo x <- .getOrgPkg(x) } con <- dbconn(x) tables <- .getDataTables(con) cols <- unique(unlist(sapply(tables, FUN=dbListFields, con=con))) cols <- cols[!cols %in% "_id"] if(exists('y', inherits=FALSE)){cols <- c("PROBEID", cols)} cols } ## general .cols function .cols <- function(x, baseType){ schema <- metadata(x)[metadata(x)$name=="DBSCHEMA",]$value if(schema=="NOSCHEMA_DB" || schema=="NOCHIPSCHEMA_DB"){ .noSchemaCols(x) }else{ .legacyCols(x, baseType) } } setMethod("columns", "OrgDb", function(x){ baseType <- chooseCentralOrgPkgSymbol(x) .cols(x, baseType) } ) setMethod("columns", "ChipDb", function(x) .cols(x, baseType="PROBEID") ) setMethod("columns", "GODb", function(x) .cols(x) ## does not have a missing baseType ) ## for the OrthologyDb package, the columns and keytypes are the same thing - the species names setMethod("columns", "OrthologyDb", function(x) .justFirstUpper(dbGetQuery(dbconn(x), "select name from names;")[,1]) ) ####################################################################### ## Some testing of my deprecation: ## library(org.Hs.eg.db); k = head(keys(org.Hs.eg.db, 'ENTREZID')); k; ## head(keys(org.Hs.eg.db, 'CHR')); ## select(org.Hs.eg.db, k, 'SYMBOL', 'ENTREZID'); ## head(select(org.Hs.eg.db, k[1], 'SYMBOL', 'CHR')); ## This method will just get all data for one column, one keytype ## and one set of keys. Then it will return either the 1st match for each, ## filter out based on a rule OR return a CharacterList mapIds_base <- function(x, keys, column, keytype, ..., multiVals=c("filter", "asNA", "first","list","CharacterList")) { if (missing(multiVals)) multiVals <- 'first' if (!is.function(multiVals)) match.arg(multiVals) if (length(keys) < 1) stop(wmsg("mapIds must have at least one key to match against.")) if (length(column) > 1) stop(wmsg("mapIds can only use one column.")) if (length(keytype) >1 ) stop(wmsg("mapIds can only use one keytype.")) ## select, split and sort by keys res <- select(x, keys=unique(keys), columns=column, keytype=keytype) res <- split(res[[column]], f=res[[keytype]])[keys] ## handle multiple matches .filter <- function(data) { idx <- elementNROWS(data) == 1 nms <- names(data)[idx] data <- as.character(unlist(data[idx])) setNames(data, nms) } .asNA <- function(data) { idx <- elementNROWS(data) > 1 data[idx] <- NA_character_ unlist(data) } if (is.function(multiVals)) { sapply(res, FUN=multiVals) } else { switch(multiVals, "list" = res, "filter" = .filter(res), "asNA" = .asNA(res), "CharacterList" = as(res, 'CharacterList'), "first" = sapply(res, FUN=function(x) {x[[1]]}) ) } } setMethod("mapIds", "AnnotationDb", function(x, keys, column, keytype, ..., multiVals) mapIds_base(x, keys, column, keytype, ..., multiVals=multiVals) ) ## TODO: add option to replace multi-matches with NAs or to just remove them. ## To cleanly handle having 'multiVals' being EITHER a FUN or something else: ## DO like: if(is.function(multiVals)){}else{match.arg(multiVals)} ## trace(mapIds, browser(), signature='AnnotationDb') ## library(org.Hs.eg.db); mapIds(org.Hs.eg.db, c('1','10'), 'ENTREZID', 'ENTREZID') .taxonomyId <- function(x){ conn <- dbconn(x) res <- dbGetQuery(conn, 'SELECT value from metadata where name like "TAXID" or name like "Taxonomy ID"') as.integer(res) } setMethod("taxonomyId", "AnnotationDb", function(x){.taxonomyId(x)}) AnnotationDbi/R/print.probetable.R0000644000175200017520000000040414710217313020120 0ustar00biocbuildbiocbuildprint.probetable = function(x, maxrows = 3, ...) { nr = nrow(x) np = min(nr, maxrows) cat("Object of class", class(x), "with", nr, "rows and", ncol(x), "columns.\n") if(nr>maxrows) cat("First", np, "rows are:\n") print.data.frame(x[seq_len(np), ]) } AnnotationDbi/R/test_AnnotationDbi_package.R0000644000175200017520000000036514710217313022117 0ustar00biocbuildbiocbuild## if(!suppressWarnings(library('org.testing.db',logical.return=TRUE))){ ## install.packages(system.file('extdata','org.testing.db', package='AnnotationDbi'), repos=NULL) ## } .test <- function() BiocGenerics:::testPackage("AnnotationDbi") AnnotationDbi/R/unlist2.R0000644000175200017520000000314514710217313016253 0ustar00biocbuildbiocbuild### ========================================================================= ### unlist2(): A replacement for base::unlist() that does not mangle the ### names. ### ------------------------------------------------------------------------- make.name.tree <- function(x, recursive, what.names) { if (!is.character(what.names) || length(what.names) != 1) stop("'what.names' must be a single string") what.names <- match.arg(what.names, c("inherited" , "full")) .make.name.tree.rec <- function(x, parent_name, depth) { if (length(x) == 0) return(character(0)) x_names <- names(x) if (is.null(x_names)) x_names <- rep.int(parent_name, length(x)) else if (what.names == "full") x_names <- paste0(parent_name, x_names) else x_names[x_names == ""] <- parent_name if (!is.list(x) || (!recursive && depth >= 1L)) return(x_names) if (what.names == "full") x_names <- paste0(x_names, ".") lapply(seq_len(length(x)), function(i) .make.name.tree.rec(x[[i]], x_names[i], depth + 1L)) } .make.name.tree.rec(x, "", 0L) } unlist2 <- function(x, recursive=TRUE, use.names=TRUE, what.names="inherited") { ans <- unlist(x, recursive, FALSE) if (!use.names) return(ans) if (!is.character(what.names) || length(what.names) != 1) stop("'what.names' must be a single string") what.names <- match.arg(what.names, c("inherited" , "full")) names(ans) <- unlist(make.name.tree(x, recursive, what.names), recursive, FALSE) ans } AnnotationDbi/R/utils.R0000644000175200017520000000345114710217313016013 0ustar00biocbuildbiocbuild### ========================================================================= ### Miscellaneous low-level utils ### ------------------------------------------------------------------------- ### ### Used at load time (in .onLoad) by all SQLite-based ann data packages. dbFileConnect <- function(dbfile) { ## This is a protection against dbConnect() working even with non-existing ## files (for our use case, the .sqlite file _must_ exist): if (!file.exists(dbfile)) stop("DB file '", dbfile, "' not found") ## Use of 'vsf="unix-none"' added on 01/11/2017 to avoid the infamous "da- ## tabase is locked" error that some users have reported on a few occasions ## in the past 10 years (and that we were never able to reproduce). Last ## time it was reported was on 01/11/2017 by Rob Bradley at Fred Hutch. ## Rob was trying to access TxDb.Hsapiens.UCSC.hg19.knownGene from multiple ## nodes on the Hutch cluster where TxDb.Hsapiens.UCSC.hg19.knownGene is ## installed on an NFS file system. Many thanks to Ben McGough, System ## Administrator at the Hutch, for investigating this and suggesting the ## 'vsf="unix-none"' solution. ## See ?`dbConnect,SQLiteDriver-method` and http://www.sqlite.org/vfs.html ## for more information about the the SQLite OS Interface or "VFS". if (.Platform$OS.type == "unix") { dbConnect(SQLite(), dbname=dbfile, cache_size=64000L, synchronous="off", flags=SQLITE_RO, vfs="unix-none") } else { ## Use default 'vfs' on Windows. dbConnect(SQLite(), dbname=dbfile, cache_size=64000L, synchronous="off", flags=SQLITE_RO) } } ### Used at unload time (in .onUnload) by all SQLite-based ann data packages. dbFileDisconnect <- function(dbconn) { dbDisconnect(dbconn) } AnnotationDbi/README.md0000644000175200017520000000072714710217313015611 0ustar00biocbuildbiocbuild[](https://bioconductor.org/) **AnnotationDbi** is an R/Bioconductor package that implements a user-friendly interface for querying SQLite-based annotation data packages. See https://bioconductor.org/packages/AnnotationDbi for more information including how to install the release version of the package (please refrain from installing directly from GitHub). AnnotationDbi/build/0000755000175200017520000000000014710267466015441 5ustar00biocbuildbiocbuildAnnotationDbi/build/vignette.rds0000644000175200017520000000056714710267466020010 0ustar00biocbuildbiocbuildRO0l I夗&`Lx!:V-maz/^~,*ZSuwĭ=0|akOȓUF.M8 A$ȏ'$ha䐢"+Yh]u(N=hKJMeI*';Ş(+, 0ȬZה# L[bWޗ+$1et;x5x eϔQxfnǁ饶F*!'')ntUbd}YN7{%/]-Q'CYhnJS*.TbS8b1u0 XWU4#$AnnotationDbi/inst/0000755000175200017520000000000014710267466015317 5ustar00biocbuildbiocbuildAnnotationDbi/inst/DBschemas/0000755000175200017520000000000014710217313017132 5ustar00biocbuildbiocbuildAnnotationDbi/inst/DBschemas/SchemaGuidelines.txt0000644000175200017520000000502114710217313023102 0ustar00biocbuildbiocbuildSchemaGuidelines ================ We want our schemas to be as portable as possible. In particular they should be compatible with SQLite, MySQL, PostgreSQL and Oracle. All the current schemas (i.e. the *_DB.sql files in schemas_0.9/ and schemas_1.0/) have been successfully tested (i.e. imported) with SQLite (3.4.1), MySQL+InnoDB (5.0.26) and PostgreSQL (8.1.9) on a 64-bit openSUSE 10.2 system. They have not been tested on Oracle yet. o All of the *_DB.sql files must define a "metadata" table (with cols "name" and "value") and all the *.sqlite files using one of these schemas must have a 'DBSCHEMA' and a 'DBSCHEMAVERSION' entry in their "metadata" table. o Make explicit use of the NULL or NOT NULL constraint on every column (except on PRIMARY KEY cols that are implicitly NOT NULL). o Centralize all the data type definitions in the DataTypes.txt file and use them consistently across all the *_DB.sql files. o Use preferably CHAR(n) or VARCHAR(n) types instead of non-standard TEXT type for character columns. Note that n must be <= 255 for compatibility with MySQL. Don't define an INDEX (or try to put a UNIQUE constraint, which implicitly creates an INDEX) on a TEXT column since this is not portable. Also don't define an INDEX on a CHAR(n) or VARCHAR(n) column where n is large (i.e. > 80) since this is not portable either. Doing so when n <= 80 should be safe though. o Always use a character type for "external" (aka "real world") ids even for ids like Entrez Gene IDs, PubMed IDs or OMIM IDs that are in fact integers. o Put PRIMARY KEY and UNIQUE definitions "in line" at the end of the column definition (after the SQL type and the NULL/NOT NULL constraint for UNIQUE). o Make the PRIMARY KEY column the first column in the CREATE TABLE statement. o Put "regular" (i.e. non PRIMARY KEY, non UNIQUE) INDEX definitions all together at the end of the *_DB.sql file. o Make sure that referenced tables are created before referencing tables. o Make the FOREIGN KEYs portable. This means that: - Use portable syntax. Putting FOREIGN KEY (col) REFERENCES table (col) inside the CREATE TABLE statement but at the end of it (after all the column definitions) is compatible with SQLite (which will just ignore it), MySQL+InnoDB and PostgreSQL. - There must be NOT NULL and UNIQUE constraints on the referenced column (typically a PRIMARY KEY). - The referencing and referenced columns must have the same type. o Prefix with an underscore the column names that store "internal" ids. AnnotationDbi/inst/DBschemas/schemas_0.9/0000755000175200017520000000000014710217313021143 5ustar00biocbuildbiocbuildAnnotationDbi/inst/DBschemas/schemas_0.9/00README.TXT0000644000175200017520000000125614710217313022645 0ustar00biocbuildbiocbuildThis directory contains version 0.9 of the full set of schemas used in the sqlite-based annotation data packages. Version 0.9 is our target for the BioC 2.1 release i.e. it is the version that we plan to use in the data packages that will be released with Bioconductor 2.1 (AnnotationDbi 1.0.0). Version 0.9 has been successfully tested (i.e. imported) with SQLite (3.4.1), MySQL+InnoDB (5.0.26) and PostgreSQL (8.1.9) on a 64-bit openSUSE 10.2 system. It has not been tested on Oracle yet. All the *.sqlite files using one of the 0.9 schemas must set DBSCHEMAVERSION to 0.9 in their "metadata" table. See the DataTypes.txt file for all the data types used across the 0.9 schemas. AnnotationDbi/inst/DBschemas/schemas_0.9/ARABIDOPSISCHIP_DB.sql0000644000175200017520000001201514710217313024434 0ustar00biocbuildbiocbuild-- -- ARABIDOPSISCHIP_DB schema -- ========================= -- -- The "genes" table is the central table. CREATE TABLE genes ( id INTEGER PRIMARY KEY, gene_id CHAR(9) NOT NULL UNIQUE -- AGI locus ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( id INTEGER NULL, -- REFERENCES genes probe_id VARCHAR(80) NOT NULL, -- manufacturer ID is_multiple SMALLINT NOT NULL, -- a silly and useless field FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE aracyc ( id INTEGER NOT NULL, -- REFERENCES genes pathway_name VARCHAR(255) NOT NULL, -- AraCyc pathway name FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE chromosome_locations ( id INTEGER NOT NULL, -- REFERENCES genes chromosome CHAR(1) NOT NULL, -- Arabidopsis chromosome start_location INTEGER NOT NULL, FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE ec ( -- Table id INTEGER NOT NULL, -- ec_number VARCHAR(13) NOT NULL, -- NOT FOREIGN KEY (id) REFERENCES genes (id) -- ); -- used! CREATE TABLE enzyme ( id INTEGER NOT NULL, -- REFERENCES genes ec_name VARCHAR(255) NOT NULL, -- EC name FOREIGN KEY (id) REFERENCES genes (id) ); -- Note that the "gene_info" table differs from other schemas: -- o no UNIQUE constraint on col "id" -- o no NOT NULL constraints on cols "gene_name" and "symbol" -- o one additional col "chromosome" CREATE TABLE gene_info ( id INTEGER NOT NULL, -- REFERENCES genes gene_name VARCHAR(255) NULL, -- gene name symbol VARCHAR(80) NULL, -- gene symbol chromosome CHAR(1) NULL, -- Arabidopsis chromosome FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_bp ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_bp_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_cc ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_cc_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_mf ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_mf_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE kegg ( id INTEGER NOT NULL, -- REFERENCES genes kegg_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE pubmed ( id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (id) REFERENCES genes (id) ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE qcdata ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (id); CREATE INDEX Faracyc ON aracyc (id); CREATE INDEX Fchromosome_locations ON chromosome_locations (id); CREATE INDEX Fec ON ec (id); CREATE INDEX Fenzyme ON enzyme (id); CREATE INDEX Fgene_info ON gene_info (id); CREATE INDEX Fgo_bp ON go_bp (id); CREATE INDEX Fgo_bp_all ON go_bp_all (id); CREATE INDEX Fgo_cc ON go_cc (id); CREATE INDEX Fgo_cc_all ON go_cc_all (id); CREATE INDEX Fgo_mf ON go_mf (id); CREATE INDEX Fgo_mf_all ON go_mf_all (id); CREATE INDEX Fkegg ON kegg (id); CREATE INDEX Fpubmed ON pubmed (id); -- Other indexes. CREATE INDEX Lprobes ON probes (probe_id); AnnotationDbi/inst/DBschemas/schemas_0.9/DataTypes.txt0000644000175200017520000001536014710217313023607 0ustar00biocbuildbiocbuildEntrez Gene ID -------------- SQL type: VARCHAR(10) Examples: '10251', '283297', '100113407' Note: highest value observed so far is 100113407 manufacturer ID --------------- SQL type: VARCHAR(80) Examples: '1000_at', '1002_f_at', 'AFFX-HUMISGF3A/M97935_MA_at' GenBank accession number ------------------------ SQL type: VARCHAR(20) Examples: 'X60188', 'NR_003589', 'HG3432-HT3618' Note: the maximum length observed so far is 13 but using VARCHAR(20) is a safety precaution for longer accession numbers that could appear in the future gene symbol or alias -------------------- SQL type: VARCHAR(80) Examples: 'NPEPPS', 'myr4', 'DKFZp434G0625PRO34003' Note: the maximum length observed so far is 21 but using VARCHAR(80) is a safety precaution for longer aliases that could appear in the future sequence name ------------- SQL type: VARCHAR(20) Examples: '1', '22', 'X', 'Y', '6_cox_hap1', '22_random' chromosome name --------------- SQL type: VARCHAR(2) Examples: '1', '22', 'X', 'Y', 'M', 'MT', 'Un' Note: a chromosome name is a particular sequence name cytoband location ----------------- SQL type: VARCHAR(20) Examples: '1p34.2', 'Yp11.32', '19q13.11-q13.12' Note: the maximum length observed so far is 15 but using VARCHAR(20) is a safety precaution for longer cytoband locations that could appear in the future EC number (no "EC:" prefix) --------------------------- SQL type: VARCHAR(13) Examples: '1.1.4.1', '3.2.1.14', '1.14.99.36' Note: the maximum length observed so far is 10 but using VARCHAR(13) is a safety precaution for longer EC numbers that could appear in the future EC number (with "EC:" prefix) ----------------------------- SQL type: VARCHAR(16) Examples: 'EC:1.1.4.1', 'EC:3.2.1.14', 'EC:1.14.99.36' EC name ------- SQL type: VARCHAR(255) Examples: 'lipase', 'photosystem I', '6-phosphofructokinase' Note: the maximum length observed so far is 99 gene name --------- SQL type: VARCHAR(255) Examples: 'deoxyribonuclease I-like 1', 'vitrin' Note: the maximum length observed so far is 251 OMIM ID ------- SQL type: CHAR(6) Examples: '231550', '601421', '611258' Note: highest value observed so far is 611258 IPI accession number -------------------- SQL type: CHAR(11) Examples: 'IPI00328276', 'IPI00789644' Pfam ID ------- SQL type: CHAR(7) Examples: 'PF00069', 'PF08266' PROSITE ID ---------- SQL type: CHAR(7) Examples: 'PS00107', 'PS00657' PubMed ID --------- SQL type: VARCHAR(10) Examples: '2437', '2583089', '17652175' Note: highest value observed so far is 17652175 RefSeq accession number ----------------------- SQL type: VARCHAR(20) Examples: 'NM_018009', 'NP_001035700' Note: RefSeq accession numbers seem to be valid GenBank accession numbers UniGene ID ---------- SQL type: VARCHAR(10) Examples: 'Hs.2', 'Hs.511848', 'Hs.695912' Note: highest value observed so far for Human is Hs.695912 FlyBase ID ---------- SQL type: CHAR(11) Examples: 'FBgn0001942', 'FBgn0030936', 'FBgn0051992' Yeast ORF ID ------------ SQL type: VARCHAR(14) Examples: 'YPL141C', 'YGRWsigma7', 'YPRWdelta14' Note: the maximum length observed so far is 11 but using VARCHAR(14) is a safety precaution for longer Yeast ORF IDs that could appear in the future Yeast gene name --------------- SQL type: VARCHAR(14) Examples: 'ADK2', 'TMA23', '21S_RRNA_4', 'MF(ALPHA)1' Note: the maximum length observed so far is 10 but using VARCHAR(14) is a safety precaution for longer Yeast gene names that could appear in the future SGD ID ------ SQL type: CHAR(10) Examples: 'S000004794', 'S000037040', 'S000123281' Note: highest value observed so far is S000123281 Yeast feature description ------------------------- SQL type: TEXT Note: this can be a text of any length Yeast gene alias ---------------- SQL type: VARCHAR(13) Examples: 'CDH1', 'DNA33', 'EF-1 alpha', 'ATPEPSILON' Note: the maximum length observed so far is 10 but using VARCHAR(13) is a safety precaution for longer Yeast gene aliases that could appear in the future InterPro ID ----------- SQL type: CHAR(9) Examples: 'IPR001440', 'IPR008688', 'IPR015809' Note: highest value observed so far is IPR015809 SMART ID -------- SQL type: CHAR(7) Examples: 'SM00055', 'SM00220', 'SM00717' AGI locus ID ------------ SQL type: CHAR(9) Examples: 'AT1G01010', 'ATCG00830', 'ATMG01410' AraCyc pathway name ------------------- SQL type: VARCHAR(255) Examples: 'SAM cycle', 'trans,trans-farnesyl diphosphate biosynthesis' Note: the maximum length observed so far is 77 but using VARCHAR(255) is a safety precaution for longer AraCyc pathways that could appear in the future Arabidopsis chromosome ---------------------- SQL type: CHAR(1) 7 possible values: '1', '2', '3', '4', '5', 'C', 'M' GO ontology (short label) ------------------------- SQL type: VARCHAR(9) 4 possible values: 'universal', 'BP', 'CC', 'MF' GO ontology (full label) ------------------------ SQL type: VARCHAR(18) 4 possible values: 'universal', 'biological_process', 'cellular_component', 'molecular_function' GO ID ----- SQL type: CHAR(10) Examples: 'all', 'GO:0000001', 'GO:0016491' Note: except for 'all' they are all of the form 'GO:1234567' textual label for the GO term ----------------------------- SQL type: VARCHAR(255) Examples: 'larval fat body development', 'age-dependent response to reactive oxygen species during chronological cell aging' Note: the maximum length observed so far is 193 textual definition for the GO term ---------------------------------- SQL type: TEXT Note: this can be a text of any length type of GO child-parent relationship ------------------------------------ SQL type: VARCHAR(7) 2 possible values: 'isa', 'part_of' GO evidence code ---------------- SQL type: CHAR(3) 14 possible values: 'IC', 'IDA', 'IEA', 'IEP', 'IGC', 'IGI', 'IMP', 'IPI', 'ISS', 'NAS', 'ND', 'RCA', 'TAS', 'NR' Note: see http://www.geneontology.org/GO.evidence.shtml for the meaning of the GO evidence codes KEGG pathway short ID --------------------- SQL type: CHAR(5) Examples: '00100', '05223', '07218' Note: highest value observed so far is 07218 KEGG pathway long ID -------------------- SQL type: CHAR(8) Examples: 'hsa00680', 'rno05220', 'ath00120', 'dme00910' KEGG pathway name ----------------- SQL type: VARCHAR(80) Examples: 'Butanoate metabolism', '3-Chloroacrylic acid degradation' Note: the maximum length observed so far is 63 Entrez Gene or ORF ID --------------------- SQL type: VARCHAR(20) Examples: 'YDR156W', 'AT4G15280', 'Dmel_CG10045' or an Entrez Gene ID Note: the maximum length observed so far is 12 AnnotationDbi/inst/DBschemas/schemas_0.9/FLYCHIP_DB.sql0000644000175200017520000001330114710217313023325 0ustar00biocbuildbiocbuild-- -- FLYCHIP_DB schema -- ================= -- -- The "genes" table is the central table. CREATE TABLE genes ( id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( id INTEGER NULL, -- REFERENCES genes probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE alias ( id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE chromosomes ( id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE chromosome_locations ( id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE cytogenetic_locations ( id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE ec ( id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE gene_info ( id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_bp ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_bp_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_cc ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_cc_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_mf ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_mf_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE kegg ( id INTEGER NOT NULL, -- REFERENCES genes kegg_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE flybase ( id INTEGER NOT NULL, -- REFERENCES genes flybase_id CHAR(11) NOT NULL, -- FlyBase ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE pubmed ( id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE refseq ( id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE unigene ( id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (id) REFERENCES genes (id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chr VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE qcdata ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (id); CREATE INDEX Falias ON alias (id); CREATE INDEX Fchromosomes ON chromosomes (id); CREATE INDEX Fchromosome_locations ON chromosome_locations (id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (id); CREATE INDEX Fec ON ec (id); CREATE INDEX Fgo_bp ON go_bp (id); CREATE INDEX Fgo_bp_all ON go_bp_all (id); CREATE INDEX Fgo_cc ON go_cc (id); CREATE INDEX Fgo_cc_all ON go_cc_all (id); CREATE INDEX Fgo_mf ON go_mf (id); CREATE INDEX Fgo_mf_all ON go_mf_all (id); CREATE INDEX Fkegg ON kegg (id); CREATE INDEX Fflybase ON flybase (id); CREATE INDEX Fpubmed ON pubmed (id); CREATE INDEX Frefseq ON refseq (id); CREATE INDEX Funigene ON unigene (id); AnnotationDbi/inst/DBschemas/schemas_0.9/FLY_DB.sql0000644000175200017520000001320214710217313022661 0ustar00biocbuildbiocbuild-- -- FLY_DB schema -- ============= -- -- The "genes" table is the central table. CREATE TABLE genes ( id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE accessions ( id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE alias ( id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE chromosomes ( id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE chromosome_locations ( id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE cytogenetic_locations ( id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE ec ( id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE gene_info ( id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_bp ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_bp_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_cc ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_cc_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_mf ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_mf_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE kegg ( id INTEGER NOT NULL, -- REFERENCES genes kegg_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE flybase ( id INTEGER NOT NULL, -- REFERENCES genes flybase_id CHAR(11) NOT NULL, -- FlyBase ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE pubmed ( id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE refseq ( id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE unigene ( id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (id) REFERENCES genes (id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chr VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE qcdata ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (id); CREATE INDEX Falias ON alias (id); CREATE INDEX Fchromosomes ON chromosomes (id); CREATE INDEX Fchromosome_locations ON chromosome_locations (id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (id); CREATE INDEX Fec ON ec (id); CREATE INDEX Fgo_bp ON go_bp (id); CREATE INDEX Fgo_bp_all ON go_bp_all (id); CREATE INDEX Fgo_cc ON go_cc (id); CREATE INDEX Fgo_cc_all ON go_cc_all (id); CREATE INDEX Fgo_mf ON go_mf (id); CREATE INDEX Fgo_mf_all ON go_mf_all (id); CREATE INDEX Fkegg ON kegg (id); CREATE INDEX Fflybase ON flybase (id); CREATE INDEX Fpubmed ON pubmed (id); CREATE INDEX Frefseq ON refseq (id); CREATE INDEX Funigene ON unigene (id); AnnotationDbi/inst/DBschemas/schemas_0.9/GO_DB.sql0000644000175200017520000001163114710217313022540 0ustar00biocbuildbiocbuild-- -- GO_DB schema -- ============ -- CREATE TABLE go_ontology ( term_type VARCHAR(18) NOT NULL UNIQUE, -- GO ontology (full label) ontology VARCHAR(9) PRIMARY KEY -- GO ontology (short label) ); CREATE TABLE go_obsolete ( go_id CHAR(10) PRIMARY KEY, -- GO ID term VARCHAR(255) NOT NULL, -- textual label for the GO term ontology VARCHAR(9) NOT NULL, -- REFERENCES go_ontology definition TEXT NULL, -- textual definition for the GO term FOREIGN KEY (ontology) REFERENCES go_ontology (ontology) ); -- The "go_term" table is the central table. CREATE TABLE go_term ( term_id INTEGER PRIMARY KEY, go_id CHAR(10) NOT NULL UNIQUE, -- GO ID term VARCHAR(255) NOT NULL, -- textual label for the GO term ontology VARCHAR(9) NOT NULL, -- REFERENCES go_ontology definition TEXT NULL, -- textual definition for the GO term FOREIGN KEY (ontology) REFERENCES go_ontology (ontology) ); -- Data linked to the "go_term" table. CREATE TABLE go_synonym ( term_id INTEGER NOT NULL, -- REFERENCES go_term synonym VARCHAR(255) NOT NULL, -- label or GO ID secondary CHAR(10) NULL, -- GO ID like_go_id SMALLINT, -- boolean (1 or 0) FOREIGN KEY (term_id) REFERENCES go_term (term_id) ); -- child-parent relationship. CREATE TABLE go_bp_parents ( term_id INTEGER NOT NULL, -- REFERENCES go_term parent_id INTEGER NOT NULL, -- REFERENCES go_term evidence VARCHAR(7) NOT NULL, -- type of GO child-parent relationship FOREIGN KEY (term_id) REFERENCES go_term (term_id), FOREIGN KEY (parent_id) REFERENCES go_term (term_id) ); CREATE TABLE go_cc_parents ( term_id INTEGER NOT NULL, -- REFERENCES go_term parent_id INTEGER NOT NULL, -- REFERENCES go_term evidence VARCHAR(7) NOT NULL, -- type of GO child-parent relationship FOREIGN KEY (term_id) REFERENCES go_term (term_id), FOREIGN KEY (parent_id) REFERENCES go_term (term_id) ); CREATE TABLE go_mf_parents ( term_id INTEGER NOT NULL, -- REFERENCES go_term parent_id INTEGER NOT NULL, -- REFERENCES go_term evidence VARCHAR(7) NOT NULL, -- type of GO child-parent relationship FOREIGN KEY (term_id) REFERENCES go_term (term_id), FOREIGN KEY (parent_id) REFERENCES go_term (term_id) ); -- parent-offspring relationship. CREATE TABLE go_bp_offspring ( term_id INTEGER NOT NULL, -- REFERENCES go_term offspring_id INTEGER NOT NULL, -- REFERENCES go_term FOREIGN KEY (term_id) REFERENCES go_term (term_id), FOREIGN KEY (offspring_id) REFERENCES go_term (term_id) ); CREATE TABLE go_cc_offspring ( term_id INTEGER NOT NULL, -- REFERENCES go_term offspring_id INTEGER NOT NULL, -- REFERENCES go_term FOREIGN KEY (term_id) REFERENCES go_term (term_id), FOREIGN KEY (offspring_id) REFERENCES go_term (term_id) ); CREATE TABLE go_mf_offspring ( term_id INTEGER NOT NULL, -- REFERENCES go_term offspring_id INTEGER NOT NULL, -- REFERENCES go_term FOREIGN KEY (term_id) REFERENCES go_term (term_id), FOREIGN KEY (offspring_id) REFERENCES go_term (term_id) ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE qcdata ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- A useless table that needs to be removed (or fixed). CREATE TABLE gene2go_evidence ( evidence_code TEXT ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgo_term ON go_term (ontology); CREATE INDEX Fgo_synonym ON go_synonym (term_id); CREATE INDEX Fgo_obsolete ON go_obsolete (ontology); CREATE INDEX F1go_bp_parents ON go_bp_parents (term_id); CREATE INDEX F2go_bp_parents ON go_bp_parents (parent_id); CREATE INDEX F1go_cc_parents ON go_cc_parents (term_id); CREATE INDEX F2go_cc_parents ON go_cc_parents (parent_id); CREATE INDEX F1go_mf_parents ON go_mf_parents (term_id); CREATE INDEX F2go_mf_parents ON go_mf_parents (parent_id); CREATE INDEX F1go_bp_offspring ON go_bp_offspring (term_id); CREATE INDEX F2go_bp_offspring ON go_bp_offspring (offspring_id); CREATE INDEX F1go_cc_offspring ON go_cc_offspring (term_id); CREATE INDEX F2go_cc_offspring ON go_cc_offspring (offspring_id); CREATE INDEX F1go_mf_offspring ON go_mf_offspring (term_id); CREATE INDEX F2go_mf_offspring ON go_mf_offspring (offspring_id); AnnotationDbi/inst/DBschemas/schemas_0.9/HUMANCHIP_DB.sql0000644000175200017520000001442514710217313023553 0ustar00biocbuildbiocbuild-- -- HUMANCHIP_DB schema -- =================== -- -- The "genes" table is the central table. CREATE TABLE genes ( id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( id INTEGER NULL, -- REFERENCES genes probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE alias ( id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE chromosomes ( id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE chromosome_locations ( id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE cytogenetic_locations ( id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE ec ( id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE gene_info ( id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_bp ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_bp_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_cc ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_cc_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_mf ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_mf_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE kegg ( id INTEGER NOT NULL, -- REFERENCES genes kegg_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE omim ( id INTEGER NOT NULL, -- REFERENCES genes omim_id CHAR(6) NOT NULL, -- OMIM ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE pfam ( id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE prosite ( id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE pubmed ( id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE refseq ( id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE unigene ( id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (id) REFERENCES genes (id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chr VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE qcdata ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (id); CREATE INDEX Falias ON alias (id); CREATE INDEX Fchromosomes ON chromosomes (id); CREATE INDEX Fchromosome_locations ON chromosome_locations (id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (id); CREATE INDEX Fec ON ec (id); CREATE INDEX Fgo_bp ON go_bp (id); CREATE INDEX Fgo_bp_all ON go_bp_all (id); CREATE INDEX Fgo_cc ON go_cc (id); CREATE INDEX Fgo_cc_all ON go_cc_all (id); CREATE INDEX Fgo_mf ON go_mf (id); CREATE INDEX Fgo_mf_all ON go_mf_all (id); CREATE INDEX Fkegg ON kegg (id); CREATE INDEX Fomim ON omim (id); CREATE INDEX Fpfam ON pfam (id); CREATE INDEX Fprosite ON prosite (id); CREATE INDEX Fpubmed ON pubmed (id); CREATE INDEX Frefseq ON refseq (id); CREATE INDEX Funigene ON unigene (id); AnnotationDbi/inst/DBschemas/schemas_0.9/HUMAN_DB.sql0000644000175200017520000001432614710217313023107 0ustar00biocbuildbiocbuild-- -- HUMAN_DB schema -- =============== -- -- The "genes" table is the central table. CREATE TABLE genes ( id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE accessions ( id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE alias ( id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE chromosomes ( id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE chromosome_locations ( id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE cytogenetic_locations ( id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE ec ( id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE gene_info ( id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_bp ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_bp_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_cc ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_cc_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_mf ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_mf_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE kegg ( id INTEGER NOT NULL, -- REFERENCES genes kegg_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE omim ( id INTEGER NOT NULL, -- REFERENCES genes omim_id CHAR(6) NOT NULL, -- OMIM ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE pfam ( id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE prosite ( id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE pubmed ( id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE refseq ( id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE unigene ( id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (id) REFERENCES genes (id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chr VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE qcdata ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (id); CREATE INDEX Falias ON alias (id); CREATE INDEX Fchromosomes ON chromosomes (id); CREATE INDEX Fchromosome_locations ON chromosome_locations (id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (id); CREATE INDEX Fec ON ec (id); CREATE INDEX Fgo_bp ON go_bp (id); CREATE INDEX Fgo_bp_all ON go_bp_all (id); CREATE INDEX Fgo_cc ON go_cc (id); CREATE INDEX Fgo_cc_all ON go_cc_all (id); CREATE INDEX Fgo_mf ON go_mf (id); CREATE INDEX Fgo_mf_all ON go_mf_all (id); CREATE INDEX Fkegg ON kegg (id); CREATE INDEX Fomim ON omim (id); CREATE INDEX Fpfam ON pfam (id); CREATE INDEX Fprosite ON prosite (id); CREATE INDEX Fpubmed ON pubmed (id); CREATE INDEX Frefseq ON refseq (id); CREATE INDEX Funigene ON unigene (id); AnnotationDbi/inst/DBschemas/schemas_0.9/KEGG_DB.sql0000644000175200017520000000172514710217313022753 0ustar00biocbuildbiocbuild-- -- KEGG_DB schema -- ============== -- CREATE TABLE ec2go ( ec_no VARCHAR(16) NOT NULL, -- EC number (with "EC:" prefix) go_id CHAR(10) NOT NULL -- GO ID ); CREATE TABLE pathway2gene ( pathway_id CHAR(8) NOT NULL, -- KEGG pathway long ID gene_id VARCHAR(20) NOT NULL -- Entrez Gene or ORF ID ); CREATE TABLE pathway2name ( path_id CHAR(5) NOT NULL UNIQUE, -- KEGG pathway short ID path_name VARCHAR(80) NOT NULL UNIQUE -- KEGG pathway name ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE qcdata ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Indexes. CREATE INDEX Ipathway2gene ON pathway2gene (gene_id); AnnotationDbi/inst/DBschemas/schemas_0.9/RODENTCHIP_DB.sql0000644000175200017520000001406714710217313023700 0ustar00biocbuildbiocbuild-- -- RODENTCHIP_DB schema -- ==================== -- -- The "genes" table is the central table. CREATE TABLE genes ( id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( id INTEGER NULL, -- REFERENCES genes probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE alias ( id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE chromosomes ( id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE chromosome_locations ( id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE cytogenetic_locations ( id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE ec ( id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE gene_info ( id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_bp ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_bp_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_cc ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_cc_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_mf ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_mf_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE kegg ( id INTEGER NOT NULL, -- REFERENCES genes kegg_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE pfam ( id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE prosite ( id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE pubmed ( id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE refseq ( id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE unigene ( id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (id) REFERENCES genes (id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chr VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE qcdata ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (id); CREATE INDEX Falias ON alias (id); CREATE INDEX Fchromosomes ON chromosomes (id); CREATE INDEX Fchromosome_locations ON chromosome_locations (id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (id); CREATE INDEX Fec ON ec (id); CREATE INDEX Fgo_bp ON go_bp (id); CREATE INDEX Fgo_bp_all ON go_bp_all (id); CREATE INDEX Fgo_cc ON go_cc (id); CREATE INDEX Fgo_cc_all ON go_cc_all (id); CREATE INDEX Fgo_mf ON go_mf (id); CREATE INDEX Fgo_mf_all ON go_mf_all (id); CREATE INDEX Fkegg ON kegg (id); CREATE INDEX Fpfam ON pfam (id); CREATE INDEX Fprosite ON prosite (id); CREATE INDEX Fpubmed ON pubmed (id); CREATE INDEX Frefseq ON refseq (id); CREATE INDEX Funigene ON unigene (id); AnnotationDbi/inst/DBschemas/schemas_0.9/RODENT_DB.sql0000644000175200017520000001377014710217313023234 0ustar00biocbuildbiocbuild-- -- RODENT_DB schema -- ================ -- -- The "genes" table is the central table. CREATE TABLE genes ( id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE accessions ( id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE alias ( id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE chromosomes ( id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE chromosome_locations ( id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE cytogenetic_locations ( id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE ec ( id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE gene_info ( id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_bp ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_bp_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_cc ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_cc_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_mf ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE go_mf_all ( id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE kegg ( id INTEGER NOT NULL, -- REFERENCES genes kegg_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE pfam ( id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE prosite ( id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE pubmed ( id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE refseq ( id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (id) REFERENCES genes (id) ); CREATE TABLE unigene ( id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (id) REFERENCES genes (id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chr VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE qcdata ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (id); CREATE INDEX Falias ON alias (id); CREATE INDEX Fchromosomes ON chromosomes (id); CREATE INDEX Fchromosome_locations ON chromosome_locations (id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (id); CREATE INDEX Fec ON ec (id); CREATE INDEX Fgo_bp ON go_bp (id); CREATE INDEX Fgo_bp_all ON go_bp_all (id); CREATE INDEX Fgo_cc ON go_cc (id); CREATE INDEX Fgo_cc_all ON go_cc_all (id); CREATE INDEX Fgo_mf ON go_mf (id); CREATE INDEX Fgo_mf_all ON go_mf_all (id); CREATE INDEX Fkegg ON kegg (id); CREATE INDEX Fpfam ON pfam (id); CREATE INDEX Fprosite ON prosite (id); CREATE INDEX Fpubmed ON pubmed (id); CREATE INDEX Frefseq ON refseq (id); CREATE INDEX Funigene ON unigene (id); AnnotationDbi/inst/DBschemas/schemas_0.9/YEASTCHIP_DB.sql0000644000175200017520000001043314710217313023563 0ustar00biocbuildbiocbuild-- -- YEASTCHIP_DB schema -- =================== -- -- The "sgd" table is the central table. CREATE TABLE sgd ( id INTEGER PRIMARY KEY, systematic_name VARCHAR(14) NULL UNIQUE, -- Yeast ORF ID gene_name VARCHAR(14) NULL UNIQUE, -- Yeast gene name sgd_id CHAR(10) NOT NULL UNIQUE -- SGD ID ); -- Data linked to the "sgd" table. CREATE TABLE probes ( id INTEGER NULL, -- REFERENCES sgd probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE chromosome_features ( id INTEGER NOT NULL, -- REFERENCES sgd chromosome VARCHAR(2) NULL, -- chromosome name start INTEGER NULL, feature_description TEXT NULL, -- Yeast feature description FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE ec ( id INTEGER NOT NULL, -- REFERENCES sgd ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE gene2alias ( id INTEGER NOT NULL, -- REFERENCES sgd alias VARCHAR(13) NOT NULL, -- Yeast gene alias FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE go_bp ( id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE go_bp_all ( id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE go_cc ( id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE go_cc_all ( id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE go_mf ( id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE go_mf_all ( id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE kegg ( id INTEGER NOT NULL, -- REFERENCES sgd kegg_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE pubmed ( id INTEGER NOT NULL, -- REFERENCES sgd pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (id) REFERENCES sgd (id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chr VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE qcdata ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (id); CREATE INDEX Fchromosome_features ON chromosome_features (id); CREATE INDEX Fec ON ec (id); CREATE INDEX Fgene2alias ON gene2alias (id); CREATE INDEX Fgo_bp ON go_bp (id); CREATE INDEX Fgo_bp_all ON go_bp_all (id); CREATE INDEX Fgo_cc ON go_cc (id); CREATE INDEX Fgo_cc_all ON go_cc_all (id); CREATE INDEX Fgo_mf ON go_mf (id); CREATE INDEX Fgo_mf_all ON go_mf_all (id); CREATE INDEX Fkegg ON kegg (id); CREATE INDEX Fpubmed ON pubmed (id); AnnotationDbi/inst/DBschemas/schemas_0.9/YEAST_DB.sql0000644000175200017520000001172314710217313023122 0ustar00biocbuildbiocbuild-- -- YEAST_DB schema -- =============== -- -- The "sgd" table is the central table. CREATE TABLE sgd ( id INTEGER PRIMARY KEY, systematic_name VARCHAR(14) NULL UNIQUE, -- Yeast ORF ID gene_name VARCHAR(14) NULL UNIQUE, -- Yeast gene name sgd_id CHAR(10) NOT NULL UNIQUE -- SGD ID ); -- Data linked to the "sgd" table. CREATE TABLE chromosome_features ( id INTEGER NOT NULL, -- REFERENCES sgd chromosome VARCHAR(2) NULL, -- chromosome name start INTEGER NULL, feature_description TEXT NULL, -- Yeast feature description FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE ec ( id INTEGER NOT NULL, -- REFERENCES sgd ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE gene2alias ( id INTEGER NOT NULL, -- REFERENCES sgd alias VARCHAR(13) NOT NULL, -- Yeast gene alias FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE go_bp ( id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE go_bp_all ( id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE go_cc ( id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE go_cc_all ( id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE go_mf ( id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE go_mf_all ( id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE interpro ( id INTEGER NOT NULL, -- REFERENCES sgd interpro_id CHAR(9) NOT NULL, -- InterPro ID FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE kegg ( id INTEGER NOT NULL, -- REFERENCES sgd kegg_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE pfam ( id INTEGER NOT NULL, -- REFERENCES sgd pfam_id CHAR(7) NOT NULL, -- Pfam ID FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE pubmed ( id INTEGER NOT NULL, -- REFERENCES sgd pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (id) REFERENCES sgd (id) ); CREATE TABLE smart ( id INTEGER NOT NULL, -- REFERENCES sgd smart_id CHAR(7) NOT NULL, -- SMART ID FOREIGN KEY (id) REFERENCES sgd (id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chr VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE gene2systematic ( gene_name VARCHAR(14) NULL, -- Yeast gene name systematic_name VARCHAR(14) NULL -- Yeast ORF ID ); CREATE TABLE reject_orf ( systematic_name VARCHAR(14) PRIMARY KEY -- Yeast ORF ID ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE qcdata ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosome_features ON chromosome_features (id); CREATE INDEX Fec ON ec (id); CREATE INDEX Fgene2alias ON gene2alias (id); CREATE INDEX Fgo_bp ON go_bp (id); CREATE INDEX Fgo_bp_all ON go_bp_all (id); CREATE INDEX Fgo_cc ON go_cc (id); CREATE INDEX Fgo_cc_all ON go_cc_all (id); CREATE INDEX Fgo_mf ON go_mf (id); CREATE INDEX Fgo_mf_all ON go_mf_all (id); CREATE INDEX Finterpro ON interpro (id); CREATE INDEX Fkegg ON kegg (id); CREATE INDEX Fpfam ON pfam (id); CREATE INDEX Fpubmed ON pubmed (id); CREATE INDEX Fsmart ON smart (id); AnnotationDbi/inst/DBschemas/schemas_1.0/0000755000175200017520000000000014710217313021133 5ustar00biocbuildbiocbuildAnnotationDbi/inst/DBschemas/schemas_1.0/00README.TXT0000644000175200017520000000471714710217313022642 0ustar00biocbuildbiocbuildThis directory contains version 1.0 of the full set of schemas used in the sqlite-based annotation data packages. Version 1.0 is our target for the BioC 2.2 release. Version 1.0 has been successfully tested (i.e. imported) with SQLite (3.4.1), MySQL+InnoDB (5.0.26) and PostgreSQL (8.1.9) on a 64-bit openSUSE 10.2 system. It has not been tested on Oracle yet. All the *.sqlite files using one of the 1.0 schemas must set DBSCHEMAVERSION to 1.0 in their "metadata" table. See the DataTypes.txt file for all the data types used across the 1.0 schemas. SUMMARY OF CHANGES SINCE VERSION 0.9 ------------------------------------ Note that those changes are disruptive (i.e. they potentially break the SQL queries written for version 0.9). New schemas: o replaced RODENT_DB schema by MOUSE_DB and RAT_DB schemas o replaced RODENTCHIP_DB schema by MOUSECHIP_DB and RATCHIP_DB schemas o added the Inparanoid schemas: INPARANOIDHOMSA_DB, INPARANOIDMUSMU_DB, INPARANOIDRATNO_DB, INPARANOIDDROME_DB and INPARANOIDSACCE_DB o added the PFAM_DB schema All schemas: o renamed "qcdata" table -> "map_counts" All probe-based and org-based schemas: o renamed internal id "id" -> "_id" o renamed chromosome_locations.chromosome -> chromosome_locations.seqname o renamed kegg.kegg_id col -> kegg.path_id o renamed chrlengths.chr col -> chrlengths.chromosome All probe-based schemas: o moved "_id" col to last position in "probes" table o removed the "accessions" table Schemas for Human, Mouse and Rat: o added "ensembl" table HUMAN_DB and RAT_DB schemas: o added "ensembl_prot" table MOUSE_DB and MOUSECHIP_DB schemas: o added "mgi" table FLY_DB and FLYCHIP_DB schemas: o added "flybase_cg" table FLY_DB schema: o added "flybase_prot" table GO_DB schema: o renamed "term_id" cols -> "_id" o renamed "offspring_id" cols -> "_offspring_id" o renamed "parent_id" cols -> "_parent_id" o renamed "evidence" cols -> "relationship_type" o removed "gene2go_evidence" table o moved "ontology" col to 1st position in "go_ontology" table o removed go_obsolete.term_id column and made go_obsolete.go_id the new PRIMARY KEY Note that, ideally, we could add UNIQUE constraints on (_id, _parent_id) in the go_[bp|cc|mf]_parents tables and on (_id, _offspring_id) in the go_[bp|cc|mf]_offspring tables but the cost of doing this is high (+5M for the size of GO.sqlite: 37M instead of 32M). KEGG_DB schema: o renamed "gene_id" col -> "gene_or_orf_id" AnnotationDbi/inst/DBschemas/schemas_1.0/ARABIDOPSISCHIP_DB.sql0000644000175200017520000001213714710217313024431 0ustar00biocbuildbiocbuild-- -- ARABIDOPSISCHIP_DB schema -- ========================= -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id CHAR(9) NOT NULL UNIQUE -- AGI locus ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( probe_id VARCHAR(80) NOT NULL, -- manufacturer ID is_multiple SMALLINT NOT NULL, -- a silly and useless field _id INTEGER NULL, -- REFERENCES genes FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE aracyc ( _id INTEGER NOT NULL, -- REFERENCES genes pathway_name VARCHAR(255) NOT NULL, -- AraCyc pathway name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname CHAR(1) NOT NULL, -- Arabidopsis chromosome start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( -- Table _id INTEGER NOT NULL, -- ec_number VARCHAR(13) NOT NULL, -- NOT FOREIGN KEY (_id) REFERENCES genes (_id) -- ); -- used! CREATE TABLE enzyme ( _id INTEGER NOT NULL, -- REFERENCES genes ec_name VARCHAR(255) NOT NULL, -- EC name FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Note that the "gene_info" table differs from other schemas: -- o no UNIQUE constraint on col "id" -- o no NOT NULL constraints on cols "gene_name" and "symbol" -- o one additional col "chromosome" CREATE TABLE gene_info ( _id INTEGER NOT NULL, -- REFERENCES genes gene_name VARCHAR(255) NULL, -- gene name symbol VARCHAR(80) NULL, -- gene symbol chromosome CHAR(1) NULL, -- Arabidopsis chromosome FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (_id); CREATE INDEX Faracyc ON aracyc (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fenzyme ON enzyme (_id); CREATE INDEX Fgene_info ON gene_info (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpubmed ON pubmed (_id); -- Other indexes. CREATE INDEX Lprobes ON probes (probe_id); AnnotationDbi/inst/DBschemas/schemas_1.0/BOVINECHIP_DB.sql0000644000175200017520000001352314710217313023653 0ustar00biocbuildbiocbuild-- -- BOVINECHIP_DB schema -- =================== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number _id INTEGER NULL, -- REFERENCES genes FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/BOVINE_DB.sql0000644000175200017520000001342414710217313023207 0ustar00biocbuildbiocbuild-- -- BOVINE_DB schema -- =============== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/CANINECHIP_DB.sql0000644000175200017520000000673514710217313023635 0ustar00biocbuildbiocbuild-- -- CANINECHIP_DB schema -- =================== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number _id INTEGER NULL, -- REFERENCES genes FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/CANINE_DB.sql0000644000175200017520000000663614710217313023171 0ustar00biocbuildbiocbuild-- -- CANINE_DB schema -- =============== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/CHICKENCHIP_DB.sql0000644000175200017520000001411014710217313023726 0ustar00biocbuildbiocbuild-- -- CHICKENCHIP_DB schema -- =================== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number _id INTEGER NULL, -- REFERENCES genes FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- Ensembl Gene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fensembl ON ensembl (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/CHICKEN_DB.sql0000644000175200017520000001441214710217313023267 0ustar00biocbuildbiocbuild-- -- CHICKEN_DB schema -- =============== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- Ensembl Gene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes(_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/DataTypes.txt0000644000175200017520000002701614710217313023600 0ustar00biocbuildbiocbuildAC ID -------------- SQL type: VARCHAR(12) Examples: 'PF00389.21', 'PF02826.10', 'P63103.1' Note: max length appears to be about 10 This seems to be the central ID for all things PFAM. CAZY ID -------------- SQL type: VARCHAR(6) Examples: 'GT_57', 'GH_29', 'CBM_19' Note: max length seems to be 6 HOMSTRAD ID -------------- SQL type: VARCHAR(20) Examples: 'Dala_Dala_ligas_N', 'A2M_B', 'Haloperoxidase' Note: max length seems to be less than 20 INTERPRO ID -------------- SQL type: VARCHAR(9) Examples: 'IPR003391', 'IPR002612', 'IPR005830' Note: max length seems to be 9 LOAD ID -------------- SQL type: VARCHAR(15) Examples: 'Adrenomedullin', 'Adeno_PIX', 'BCMA-Tall_bind' Note: max length seems to be less than 15 MEROPS ID -------------- SQL type: VARCHAR(3) Examples: 'S10', 'M55', 'T1' Note: max length seems to be 3 MIM ID -------------- SQL type: VARCHAR(6) Examples: '104311', '128230', '222600' Note: max length seems to be 6 PDB ID -------------- SQL type: VARCHAR(6) Examples: '1u69 B', '1odn A', '2kfn A' Note: max length seems to be 6 start of alignment -------------- SQL type: INTEGER Examples: '3', '180', '256' Note: just an int end of alignment -------------- SQL type: INTEGER Examples: '288', '224', '334' Note: always just an int PFAMB ID -------------- SQL type: VARCHAR(8) Examples: 'PB012689', 'PB177858', 'PB176422' Note: max length seems to be 8, these are the machine called PFAM IDs. PRINTS ID -------------- SQL type: VARCHAR(7) Examples: 'PR00178', 'PR01233', 'PR00543' Note: max length seems to be 7 PROSITE ID -------------- SQL type: VARCHAR(9) Examples: 'PDOC00403', 'PDOC00174', 'PDOC00578' Note: max length seems to be 9 PROSITE_PROFILE ID -------------- SQL type: VARCHAR(7) Examples: 'PS50032', 'PS50203', 'PS50119' Note: max length seems to be 7 RM ID -------------- SQL type: VARCHAR(8) Examples: '11011151', '2254264', '15531590' Note: max length seems to be 8 SCOP ID -------------- SQL type: VARCHAR(4) Examples: '1rla', '1by6', '3gcc' Note: max length seems to be 4 SCOP placement -------------- SQL type: VARCHAR(2) Examples: 'fa', 'fa', 'sf' Note: max length seems to be 2. I only ever see the values fa and sf. SMART ID -------------- SQL type: VARCHAR(9) Examples: 'ZnF_UBR1', 'RasGEFN', 'PLDc' Note: max length seems to be about 9 TC ID -------------- SQL type: VARCHAR(6) Examples: '3.A.15', '9.B.33', '2.A.27' Note: max length seems to be PFAM ID ID -------------- SQL type: VARCHAR(15) Examples: 'ADP_ribosyl_GH', 'Adeno_E1B_55K_N', 'AfaD' Note: max length seems to be 15 DE ID -------------- SQL type: VARCHAR(80) Examples: 'Adenovirus GP19K', 'ADP-specific Phosphofructokinase/Glucokinase conserved region' Note: A description field. This one can be very big TP ID -------------- SQL type: VARCHAR(6) Examples: 'Repeat', 'Family', 'Domain', 'Motif' Note: max length is 6. This is only ever one of the above 4 values. URL ID -------------- SQL type: VARCHAR(80) Examples: 'http://bioinformatics.weizmann.ac.il/hotmolecbase/entries/ps1.htm' Note: max length is unknown. These can obviously get pretty big. Inparanoid ID -------------- SQL type: VARCHAR(30) Examples: 'ENSP00000351750', 'FBpp0073215', 'MGI:1274784' Note: character string that corresponds to a gene OR protein ID. IDs from one species are all of the same type, but what type will be used for a species can vary... Inparanoid Cluster ID -------------- SQL type: INTEGER Examples: '1', '2', '34' Note: These are integers which indicate the groupings assigned by inparanoids algorithm. Inparanoid Species ID -------------- SQL type: VARCHAR(15) Examples: 'ensHOMSA.fa', 'modMUSMU.fa', 'modDROME.fa' Note: These indicate the species, the type of ID used by Inparanoid ID and finally the kind of table these data were extracted from Inparanoid Score -------------- SQL type: VARCHAR(20) Examples: '1.0', '0.1513', '0.3578' Note: The score indicates the degree to which this protein is considered to belong to the Inparanoid grouping Inparanoid Seed Status -------------- SQL type: VARCHAR(4) Examples: '100%', '', '99%' Note: 0 to 100%. 100% indicates a true "seed" paralog. Entrez Gene ID -------------- SQL type: VARCHAR(10) Examples: '10251', '283297', '100113407' Note: highest value observed so far is 100113407 Ensembl Gene ID -------------- SQL type: VARCHAR(20) Examples: 'ENSRNOG00000016924', 'ENSMUSG00000028125', 'ENSG00000127837' Note: highest value observed so far is 18 characters long Ensembl Protein ID -------------- SQL type: VARCHAR(20) Examples: 'ENSP00000370606', 'ENSRNOP00000027' Note: Ensembl protein IDs, one peptide per ID. manufacturer ID --------------- SQL type: VARCHAR(80) Examples: '1000_at', '1002_f_at', 'AFFX-HUMISGF3A/M97935_MA_at' GenBank accession number ------------------------ SQL type: VARCHAR(20) Examples: 'X60188', 'NR_003589', 'HG3432-HT3618' Note: the maximum length observed so far is 13 but using VARCHAR(20) is a safety precaution for longer accession numbers that could appear in the future gene symbol or alias -------------------- SQL type: VARCHAR(80) Examples: 'NPEPPS', 'myr4', 'DKFZp434G0625PRO34003' Note: the maximum length observed so far is 21 but using VARCHAR(80) is a safety precaution for longer aliases that could appear in the future sequence name ------------- SQL type: VARCHAR(20) Examples: '1', '22', 'X', 'Y', '6_cox_hap1', '22_random' chromosome name --------------- SQL type: VARCHAR(2) Examples: '1', '22', 'X', 'Y', 'M', 'MT', 'Un' Note: a chromosome name is a particular sequence name cytoband location ----------------- SQL type: VARCHAR(20) Examples: '1p34.2', 'Yp11.32', '19q13.11-q13.12' Note: the maximum length observed so far is 15 but using VARCHAR(20) is a safety precaution for longer cytoband locations that could appear in the future EC number (no "EC:" prefix) --------------------------- SQL type: VARCHAR(13) Examples: '1.1.4.1', '3.2.1.14', '1.14.99.36' Note: the maximum length observed so far is 10 but using VARCHAR(13) is a safety precaution for longer EC numbers that could appear in the future EC number (with "EC:" prefix) ----------------------------- SQL type: VARCHAR(16) Examples: 'EC:1.1.4.1', 'EC:3.2.1.14', 'EC:1.14.99.36' EC name ------- SQL type: VARCHAR(255) Examples: 'lipase', 'photosystem I', '6-phosphofructokinase' Note: the maximum length observed so far is 99 gene name --------- SQL type: VARCHAR(255) Examples: 'deoxyribonuclease I-like 1', 'vitrin' Note: the maximum length observed so far is 251 OMIM ID ------- SQL type: CHAR(6) Examples: '231550', '601421', '611258' Note: highest value observed so far is 611258 IPI accession number -------------------- SQL type: CHAR(11) Examples: 'IPI00328276', 'IPI00789644' Pfam ID ------- SQL type: CHAR(7) Examples: 'PF00069', 'PF08266' PROSITE ID ---------- SQL type: CHAR(7) Examples: 'PS00107', 'PS00657' PubMed ID --------- SQL type: VARCHAR(10) Examples: '2437', '2583089', '17652175' Note: highest value observed so far is 17652175 RefSeq accession number ----------------------- SQL type: VARCHAR(20) Examples: 'NM_018009', 'NP_001035700' Note: RefSeq accession numbers seem to be valid GenBank accession numbers UniGene ID ---------- SQL type: VARCHAR(10) Examples: 'Hs.2', 'Hs.511848', 'Hs.695912' Note: highest value observed so far for Human is Hs.695912 FlyBase ID ---------- SQL type: CHAR(11) Examples: 'FBgn0001942', 'FBgn0030936', 'FBgn0051992' FlyBase CG ID ---------- SQL type: CHAR(10) Examples: 'CG3038', 'CG13377', 'CG2945' Flybase Protein ID -------------- SQL type: VARCHAR(20) Examples: 'FBpp0073215', 'FBpp0110310', 'FBpp0071474' Note: Flybase protein IDs, one peptide per ID. Yeast ORF ID ------------ SQL type: VARCHAR(14) Examples: 'YPL141C', 'YGRWsigma7', 'YPRWdelta14' Note: the maximum length observed so far is 11 but using VARCHAR(14) is a safety precaution for longer Yeast ORF IDs that could appear in the future Yeast gene name --------------- SQL type: VARCHAR(14) Examples: 'ADK2', 'TMA23', '21S_RRNA_4', 'MF(ALPHA)1' Note: the maximum length observed so far is 10 but using VARCHAR(14) is a safety precaution for longer Yeast gene names that could appear in the future SGD ID ------ SQL type: CHAR(10) Examples: 'S000004794', 'S000037040', 'S000123281' Note: highest value observed so far is S000123281 Yeast feature description ------------------------- SQL type: TEXT Note: this can be a text of any length Yeast gene alias ---------------- SQL type: VARCHAR(13) Examples: 'CDH1', 'DNA33', 'EF-1 alpha', 'ATPEPSILON' Note: the maximum length observed so far is 10 but using VARCHAR(13) is a safety precaution for longer Yeast gene aliases that could appear in the future InterPro ID ----------- SQL type: CHAR(9) Examples: 'IPR001440', 'IPR008688', 'IPR015809' Note: highest value observed so far is IPR015809 SMART ID -------- SQL type: CHAR(7) Examples: 'SM00055', 'SM00220', 'SM00717' AGI locus ID ------------ SQL type: CHAR(9) Examples: 'AT1G01010', 'ATCG00830', 'ATMG01410' AraCyc pathway name ------------------- SQL type: VARCHAR(255) Examples: 'SAM cycle', 'trans,trans-farnesyl diphosphate biosynthesis' Note: the maximum length observed so far is 77 but using VARCHAR(255) is a safety precaution for longer AraCyc pathways that could appear in the future Arabidopsis chromosome ---------------------- SQL type: CHAR(1) 7 possible values: '1', '2', '3', '4', '5', 'C', 'M' GO ontology (short label) ------------------------- SQL type: VARCHAR(9) 4 possible values: 'universal', 'BP', 'CC', 'MF' GO ontology (full label) ------------------------ SQL type: VARCHAR(18) 4 possible values: 'universal', 'biological_process', 'cellular_component', 'molecular_function' GO ID ----- SQL type: CHAR(10) Examples: 'all', 'GO:0000001', 'GO:0016491' Note: except for 'all' they are all of the form 'GO:1234567' textual label for the GO term ----------------------------- SQL type: VARCHAR(255) Examples: 'larval fat body development', 'age-dependent response to reactive oxygen species during chronological cell aging' Note: the maximum length observed so far is 193 textual definition for the GO term ---------------------------------- SQL type: TEXT Note: this can be a text of any length type of GO child-parent relationship ------------------------------------ SQL type: VARCHAR(7) 2 possible values: 'isa', 'part_of' GO evidence code ---------------- SQL type: CHAR(3) 14 possible values: 'IC', 'IDA', 'IEA', 'IEP', 'IGC', 'IGI', 'IMP', 'IPI', 'ISS', 'NAS', 'ND', 'RCA', 'TAS', 'NR' Note: see http://www.geneontology.org/GO.evidence.shtml for the meaning of the GO evidence codes KEGG pathway short ID --------------------- SQL type: CHAR(5) Examples: '00100', '05223', '07218' Note: highest value observed so far is 07218 KEGG pathway long ID -------------------- SQL type: CHAR(8) Examples: 'hsa00680', 'rno05220', 'ath00120', 'dme00910' KEGG pathway name ----------------- SQL type: VARCHAR(80) Examples: 'Butanoate metabolism', '3-Chloroacrylic acid degradation' Note: the maximum length observed so far is 63 Entrez Gene or ORF ID --------------------- SQL type: VARCHAR(20) Examples: 'YDR156W', 'AT4G15280', 'Dmel_CG10045' or an Entrez Gene ID Note: the maximum length observed so far is 12 AnnotationDbi/inst/DBschemas/schemas_1.0/ECOLICHIP_DB.sql0000644000175200017520000001045714710217313023527 0ustar00biocbuildbiocbuild-- -- ECOLICHIP_DB schema -- =================== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number _id INTEGER NULL, -- REFERENCES genes FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/ECOLI_DB.sql0000644000175200017520000001036114710217313023055 0ustar00biocbuildbiocbuild-- -- ECOLI_DB schema -- =============== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/FLYCHIP_DB.sql0000644000175200017520000001403514710217313023322 0ustar00biocbuildbiocbuild-- -- FLYCHIP_DB schema -- ================= -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number _id INTEGER NULL, -- REFERENCES genes FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE flybase ( _id INTEGER NOT NULL, -- REFERENCES genes flybase_id CHAR(11) NOT NULL, -- FlyBase ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE flybase_cg ( id INTEGER NOT NULL, -- REFERENCES genes flybase_cg_id VARCHAR(10) NOT NULL, -- FlyBase CG ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fflybase ON flybase (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fflybase ON flybase (_id); CREATE INDEX Fflybasecg ON flybase_cg (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/FLY_DB.sql0000644000175200017520000001433714710217313022663 0ustar00biocbuildbiocbuild-- -- FLY_DB schema -- ============= -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE flybase ( _id INTEGER NOT NULL, -- REFERENCES genes flybase_id CHAR(11) NOT NULL, -- FlyBase ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE flybase_cg ( _id INTEGER NOT NULL, -- REFERENCES genes flybase_cg_id VARCHAR(10) NOT NULL, -- FlyBase CG ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE flybase_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Flybase Protein ID FOREIGN KEY (_id) REFERENCES genes(_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fflybase ON flybase (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fflybase ON flybase (_id); CREATE INDEX Fflybasecg ON flybase_cg (_id); CREATE INDEX Fflybasep ON flybase_prot (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/GO_DB.sql0000644000175200017520000001131014710217313022522 0ustar00biocbuildbiocbuild-- -- GO_DB schema -- ============ -- CREATE TABLE go_ontology ( ontology VARCHAR(9) PRIMARY KEY, -- GO ontology (short label) term_type VARCHAR(18) NOT NULL UNIQUE -- GO ontology (full label) ); CREATE TABLE go_obsolete ( go_id CHAR(10) PRIMARY KEY, -- GO ID term VARCHAR(255) NOT NULL, -- textual label for the GO term ontology VARCHAR(9) NOT NULL, -- REFERENCES go_ontology definition TEXT NULL, -- textual definition for the GO term FOREIGN KEY (ontology) REFERENCES go_ontology (ontology) ); -- The "go_term" table is the central table. CREATE TABLE go_term ( _id INTEGER PRIMARY KEY, go_id CHAR(10) NOT NULL UNIQUE, -- GO ID term VARCHAR(255) NOT NULL, -- textual label for the GO term ontology VARCHAR(9) NOT NULL, -- REFERENCES go_ontology definition TEXT NULL, -- textual definition for the GO term FOREIGN KEY (ontology) REFERENCES go_ontology (ontology) ); -- Data linked to the "go_term" table. CREATE TABLE go_synonym ( _id INTEGER NOT NULL, -- REFERENCES go_term synonym VARCHAR(255) NOT NULL, -- label or GO ID secondary CHAR(10) NULL, -- GO ID like_go_id SMALLINT, -- boolean (1 or 0) FOREIGN KEY (_id) REFERENCES go_term (_id) ); -- child-parent relationship. CREATE TABLE go_bp_parents ( _id INTEGER NOT NULL, -- REFERENCES go_term _parent_id INTEGER NOT NULL, -- REFERENCES go_term relationship_type VARCHAR(7) NOT NULL, -- type of GO child-parent relationship FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_parent_id) REFERENCES go_term (_id) ); CREATE TABLE go_cc_parents ( _id INTEGER NOT NULL, -- REFERENCES go_term _parent_id INTEGER NOT NULL, -- REFERENCES go_term relationship_type VARCHAR(7) NOT NULL, -- type of GO child-parent relationship FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_parent_id) REFERENCES go_term (_id) ); CREATE TABLE go_mf_parents ( _id INTEGER NOT NULL, -- REFERENCES go_term _parent_id INTEGER NOT NULL, -- REFERENCES go_term relationship_type VARCHAR(7) NOT NULL, -- type of GO child-parent relationship FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_parent_id) REFERENCES go_term (_id) ); -- parent-offspring relationship. CREATE TABLE go_bp_offspring ( _id INTEGER NOT NULL, -- REFERENCES go_term _offspring_id INTEGER NOT NULL, -- REFERENCES go_term FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_offspring_id) REFERENCES go_term (_id) ); CREATE TABLE go_cc_offspring ( _id INTEGER NOT NULL, -- REFERENCES go_term _offspring_id INTEGER NOT NULL, -- REFERENCES go_term FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_offspring_id) REFERENCES go_term (_id) ); CREATE TABLE go_mf_offspring ( _id INTEGER NOT NULL, -- REFERENCES go_term _offspring_id INTEGER NOT NULL, -- REFERENCES go_term FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_offspring_id) REFERENCES go_term (_id) ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgo_term ON go_term (ontology); CREATE INDEX Fgo_synonym ON go_synonym (_id); CREATE INDEX Fgo_obsolete ON go_obsolete (ontology); CREATE INDEX F1go_bp_parents ON go_bp_parents (_id); CREATE INDEX F2go_bp_parents ON go_bp_parents (_parent_id); CREATE INDEX F1go_cc_parents ON go_cc_parents (_id); CREATE INDEX F2go_cc_parents ON go_cc_parents (_parent_id); CREATE INDEX F1go_mf_parents ON go_mf_parents (_id); CREATE INDEX F2go_mf_parents ON go_mf_parents (_parent_id); CREATE INDEX F1go_bp_offspring ON go_bp_offspring (_id); CREATE INDEX F2go_bp_offspring ON go_bp_offspring (_offspring_id); CREATE INDEX F1go_cc_offspring ON go_cc_offspring (_id); CREATE INDEX F2go_cc_offspring ON go_cc_offspring (_offspring_id); CREATE INDEX F1go_mf_offspring ON go_mf_offspring (_id); CREATE INDEX F2go_mf_offspring ON go_mf_offspring (_offspring_id); AnnotationDbi/inst/DBschemas/schemas_1.0/HUMANCHIP_DB.sql0000644000175200017520000001511114710217313023534 0ustar00biocbuildbiocbuild-- -- HUMANCHIP_DB schema -- =================== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number _id INTEGER NULL, -- REFERENCES genes FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- Ensembl Gene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE omim ( _id INTEGER NOT NULL, -- REFERENCES genes omim_id CHAR(6) NOT NULL, -- OMIM ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fomim ON omim (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fensembl ON ensembl (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/HUMANCROSSCHIP_DB.sql0000644000175200017520000001511114710217313024346 0ustar00biocbuildbiocbuild-- -- HUMANCHIP_DB schema -- =================== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number _id INTEGER NULL, -- REFERENCES genes FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- Ensembl Gene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE omim ( _id INTEGER NOT NULL, -- REFERENCES genes omim_id CHAR(6) NOT NULL, -- OMIM ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fomim ON omim (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fensembl ON ensembl (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/HUMAN_DB.sql0000644000175200017520000001541314710217313023075 0ustar00biocbuildbiocbuild-- -- HUMAN_DB schema -- =============== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- Ensembl Gene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes(_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE omim ( _id INTEGER NOT NULL, -- REFERENCES genes omim_id CHAR(6) NOT NULL, -- OMIM ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fomim ON omim (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/INPARANOIDDROME_DB.sql0000644000175200017520000003355314710217313024445 0ustar00biocbuildbiocbuild-- -- INPARANOID_DB schema -- ============= -- CREATE TABLE aedes_aegypti ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE anopheles_gambiae ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE apis_mellifera ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE arabidopsis_thaliana ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE bos_taurus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_briggsae ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_elegans ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_remanei ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE candida_glabrata ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE canis_familiaris ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE ciona_intestinalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE cryptococcus_neoformans ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE danio_rerio ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE debaryomyces_hanseneii ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE dictyostelium_discoideum ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE homo_sapiens ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE drosophila_pseudoobscura ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE entamoeba_histolytica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE escherichia_coliK12 ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE gallus_gallus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE gasterosteus_aculeatus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE kluyveromyces_lactis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE macaca_mulatta ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE monodelphis_domestica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE mus_musculus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE oryza_sativa ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE pan_troglodytes ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE rattus_norvegicus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE saccharomyces_cerevisiae ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE schizosaccharomyces_pombe ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE takifugu_rubripes ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE tetraodon_nigroviridis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE xenopus_tropicalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE yarrowia_lipolytica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX aedae_c ON aedes_aegypti(clust_id); CREATE INDEX aedae_s ON aedes_aegypti(species); CREATE INDEX anoga_c ON anopheles_gambiae(clust_id); CREATE INDEX anoga_s ON anopheles_gambiae(species); CREATE INDEX apime_c ON apis_mellifera(clust_id); CREATE INDEX apime_s ON apis_mellifera(species); CREATE INDEX arath_c ON arabidopsis_thaliana(clust_id); CREATE INDEX arath_s ON arabidopsis_thaliana(species); CREATE INDEX bosta_c ON bos_taurus(clust_id); CREATE INDEX bosta_s ON bos_taurus(species); CREATE INDEX caebr_c ON caenorhabditis_briggsae(clust_id); CREATE INDEX caebr_s ON caenorhabditis_briggsae(species); CREATE INDEX caeel_c ON caenorhabditis_elegans(clust_id); CREATE INDEX caeel_s ON caenorhabditis_elegans(species); CREATE INDEX caere_c ON caenorhabditis_remanei(clust_id); CREATE INDEX caere_s ON caenorhabditis_remanei(species); CREATE INDEX cangl_c ON candida_glabrata(clust_id); CREATE INDEX cangl_s ON candida_glabrata(species); CREATE INDEX canfa_c ON canis_familiaris(clust_id); CREATE INDEX canfa_s ON canis_familiaris(species); CREATE INDEX cioin_c ON ciona_intestinalis(clust_id); CREATE INDEX cioin_s ON ciona_intestinalis(species); CREATE INDEX cryne_c ON cryptococcus_neoformans(clust_id); CREATE INDEX cryne_s ON cryptococcus_neoformans(species); CREATE INDEX danre_c ON danio_rerio(clust_id); CREATE INDEX danre_s ON danio_rerio(species); CREATE INDEX debha_c ON debaryomyces_hanseneii(clust_id); CREATE INDEX debha_s ON debaryomyces_hanseneii(species); CREATE INDEX dicdi_c ON dictyostelium_discoideum(clust_id); CREATE INDEX dicdi_s ON dictyostelium_discoideum(species); CREATE INDEX homsa_c ON drosophila_melanogaster(clust_id); CREATE INDEX homsa_s ON drosophila_melanogaster(species); CREATE INDEX drops_c ON drosophila_pseudoobscura(clust_id); CREATE INDEX drops_s ON drosophila_pseudoobscura(species); CREATE INDEX enthi_c ON entamoeba_histolytica(clust_id); CREATE INDEX enthi_s ON entamoeba_histolytica(species); CREATE INDEX escco_c ON escherichia_coliK12(clust_id); CREATE INDEX escco_s ON escherichia_coliK12(species); CREATE INDEX galga_c ON gallus_gallus(clust_id); CREATE INDEX galga_s ON gallus_gallus(species); CREATE INDEX gasac_c ON gasterosteus_aculeatus(clust_id); CREATE INDEX gasac_s ON gasterosteus_aculeatus(species); CREATE INDEX klula_c ON kluyveromyces_lactis(clust_id); CREATE INDEX klula_s ON kluyveromyces_lactis(species); CREATE INDEX macmu_c ON macaca_mulatta(clust_id); CREATE INDEX macmu_s ON macaca_mulatta(species); CREATE INDEX mondo_c ON monodelphis_domestica(clust_id); CREATE INDEX mondo_s ON monodelphis_domestica(species); CREATE INDEX musmu_c ON mus_musculus(clust_id); CREATE INDEX musmu_s ON mus_musculus(species); CREATE INDEX orysa_c ON oryza_sativa(clust_id); CREATE INDEX orysa_s ON oryza_sativa(species); CREATE INDEX pantr_c ON pan_troglodytes(clust_id); CREATE INDEX pantr_s ON pan_troglodytes(species); CREATE INDEX ratno_c ON rattus_norvegicus(clust_id); CREATE INDEX ratno_s ON rattus_norvegicus(species); CREATE INDEX sacce_c ON saccharomyces_cerevisiae(clust_id); CREATE INDEX sacce_s ON saccharomyces_cerevisiae(species); CREATE INDEX schpo_c ON schizosaccharomyces_pombe(clust_id); CREATE INDEX schpo_s ON schizosaccharomyces_pombe(species); CREATE INDEX fugru_c ON takifugu_rubripes(clust_id); CREATE INDEX fugru_s ON takifugu_rubripes(species); CREATE INDEX tetni_c ON tetraodon_nigroviridis(clust_id); CREATE INDEX tetni_s ON tetraodon_nigroviridis(species); CREATE INDEX xentr_c ON xenopus_tropicalis(clust_id); CREATE INDEX xentr_s ON xenopus_tropicalis(species); CREATE INDEX yarli_c ON yarrowia_lipolytica(clust_id); CREATE INDEX yarli_s ON yarrowia_lipolytica(species); AnnotationDbi/inst/DBschemas/schemas_1.0/INPARANOIDHOMSA_DB.sql0000644000175200017520000003356614710217313024452 0ustar00biocbuildbiocbuild-- -- INPARANOID_DB schema -- ============= -- CREATE TABLE aedes_aegypti ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE anopheles_gambiae ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE apis_mellifera ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE arabidopsis_thaliana ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE bos_taurus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_briggsae ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_elegans ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_remanei ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE candida_glabrata ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE canis_familiaris ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE ciona_intestinalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE cryptococcus_neoformans ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE danio_rerio ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE debaryomyces_hanseneii ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE dictyostelium_discoideum ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE drosophila_melanogaster ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE drosophila_pseudoobscura ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE entamoeba_histolytica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE escherichia_coliK12 ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE gallus_gallus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE gasterosteus_aculeatus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE kluyveromyces_lactis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE macaca_mulatta ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE monodelphis_domestica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE mus_musculus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE oryza_sativa ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE pan_troglodytes ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE rattus_norvegicus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE saccharomyces_cerevisiae ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE schizosaccharomyces_pombe ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE takifugu_rubripes ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE tetraodon_nigroviridis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE xenopus_tropicalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE yarrowia_lipolytica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX aedae_c ON aedes_aegypti(clust_id); CREATE INDEX aedae_s ON aedes_aegypti(species); CREATE INDEX anoga_c ON anopheles_gambiae(clust_id); CREATE INDEX anoga_s ON anopheles_gambiae(species); CREATE INDEX apime_c ON apis_mellifera(clust_id); CREATE INDEX apime_s ON apis_mellifera(species); CREATE INDEX arath_c ON arabidopsis_thaliana(clust_id); CREATE INDEX arath_s ON arabidopsis_thaliana(species); CREATE INDEX bosta_c ON bos_taurus(clust_id); CREATE INDEX bosta_s ON bos_taurus(species); CREATE INDEX caebr_c ON caenorhabditis_briggsae(clust_id); CREATE INDEX caebr_s ON caenorhabditis_briggsae(species); CREATE INDEX caeel_c ON caenorhabditis_elegans(clust_id); CREATE INDEX caeel_s ON caenorhabditis_elegans(species); CREATE INDEX caere_c ON caenorhabditis_remanei(clust_id); CREATE INDEX caere_s ON caenorhabditis_remanei(species); CREATE INDEX cangl_c ON candida_glabrata(clust_id); CREATE INDEX cangl_s ON candida_glabrata(species); CREATE INDEX canfa_c ON canis_familiaris(clust_id); CREATE INDEX canfa_s ON canis_familiaris(species); CREATE INDEX cioin_c ON ciona_intestinalis(clust_id); CREATE INDEX cioin_s ON ciona_intestinalis(species); CREATE INDEX cryne_c ON cryptococcus_neoformans(clust_id); CREATE INDEX cryne_s ON cryptococcus_neoformans(species); CREATE INDEX danre_c ON danio_rerio(clust_id); CREATE INDEX danre_s ON danio_rerio(species); CREATE INDEX debha_c ON debaryomyces_hanseneii(clust_id); CREATE INDEX debha_s ON debaryomyces_hanseneii(species); CREATE INDEX dicdi_c ON dictyostelium_discoideum(clust_id); CREATE INDEX dicdi_s ON dictyostelium_discoideum(species); CREATE INDEX drome_c ON drosophila_melanogaster(clust_id); CREATE INDEX drome_s ON drosophila_melanogaster(species); CREATE INDEX drops_c ON drosophila_pseudoobscura(clust_id); CREATE INDEX drops_s ON drosophila_pseudoobscura(species); CREATE INDEX enthi_c ON entamoeba_histolytica(clust_id); CREATE INDEX enthi_s ON entamoeba_histolytica(species); CREATE INDEX escco_c ON escherichia_coliK12(clust_id); CREATE INDEX escco_s ON escherichia_coliK12(species); CREATE INDEX galga_c ON gallus_gallus(clust_id); CREATE INDEX galga_s ON gallus_gallus(species); CREATE INDEX gasac_c ON gasterosteus_aculeatus(clust_id); CREATE INDEX gasac_s ON gasterosteus_aculeatus(species); CREATE INDEX klula_c ON kluyveromyces_lactis(clust_id); CREATE INDEX klula_s ON kluyveromyces_lactis(species); CREATE INDEX macmu_c ON macaca_mulatta(clust_id); CREATE INDEX macmu_s ON macaca_mulatta(species); CREATE INDEX mondo_c ON monodelphis_domestica(clust_id); CREATE INDEX mondo_s ON monodelphis_domestica(species); CREATE INDEX musmu_c ON mus_musculus(clust_id); CREATE INDEX musmu_s ON mus_musculus(species); CREATE INDEX orysa_c ON oryza_sativa(clust_id); CREATE INDEX orysa_s ON oryza_sativa(species); CREATE INDEX pantr_c ON pan_troglodytes(clust_id); CREATE INDEX pantr_s ON pan_troglodytes(species); CREATE INDEX ratno_c ON rattus_norvegicus(clust_id); CREATE INDEX ratno_s ON rattus_norvegicus(species); CREATE INDEX sacce_c ON saccharomyces_cerevisiae(clust_id); CREATE INDEX sacce_s ON saccharomyces_cerevisiae(species); CREATE INDEX schpo_c ON schizosaccharomyces_pombe(clust_id); CREATE INDEX schpo_s ON schizosaccharomyces_pombe(species); CREATE INDEX fugru_c ON takifugu_rubripes(clust_id); CREATE INDEX fugru_s ON takifugu_rubripes(species); CREATE INDEX tetni_c ON tetraodon_nigroviridis(clust_id); CREATE INDEX tetni_s ON tetraodon_nigroviridis(species); CREATE INDEX xentr_c ON xenopus_tropicalis(clust_id); CREATE INDEX xentr_s ON xenopus_tropicalis(species); CREATE INDEX yarli_c ON yarrowia_lipolytica(clust_id); CREATE INDEX yarli_s ON yarrowia_lipolytica(species); AnnotationDbi/inst/DBschemas/schemas_1.0/INPARANOIDMUSMU_DB.sql0000644000175200017520000003356614710217313024511 0ustar00biocbuildbiocbuild-- -- INPARANOID_DB schema -- ============= -- CREATE TABLE aedes_aegypti ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE anopheles_gambiae ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE apis_mellifera ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE arabidopsis_thaliana ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE bos_taurus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_briggsae ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_elegans ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_remanei ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE candida_glabrata ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE canis_familiaris ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE ciona_intestinalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE cryptococcus_neoformans ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE danio_rerio ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE debaryomyces_hanseneii ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE dictyostelium_discoideum ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE drosophila_melanogaster ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE drosophila_pseudoobscura ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE entamoeba_histolytica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE escherichia_coliK12 ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE gallus_gallus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE gasterosteus_aculeatus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE kluyveromyces_lactis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE macaca_mulatta ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE monodelphis_domestica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE homo_sapiens ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE oryza_sativa ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE pan_troglodytes ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE rattus_norvegicus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE saccharomyces_cerevisiae ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE schizosaccharomyces_pombe ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE takifugu_rubripes ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE tetraodon_nigroviridis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE xenopus_tropicalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE yarrowia_lipolytica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX aedae_c ON aedes_aegypti(clust_id); CREATE INDEX aedae_s ON aedes_aegypti(species); CREATE INDEX anoga_c ON anopheles_gambiae(clust_id); CREATE INDEX anoga_s ON anopheles_gambiae(species); CREATE INDEX apime_c ON apis_mellifera(clust_id); CREATE INDEX apime_s ON apis_mellifera(species); CREATE INDEX arath_c ON arabidopsis_thaliana(clust_id); CREATE INDEX arath_s ON arabidopsis_thaliana(species); CREATE INDEX bosta_c ON bos_taurus(clust_id); CREATE INDEX bosta_s ON bos_taurus(species); CREATE INDEX caebr_c ON caenorhabditis_briggsae(clust_id); CREATE INDEX caebr_s ON caenorhabditis_briggsae(species); CREATE INDEX caeel_c ON caenorhabditis_elegans(clust_id); CREATE INDEX caeel_s ON caenorhabditis_elegans(species); CREATE INDEX caere_c ON caenorhabditis_remanei(clust_id); CREATE INDEX caere_s ON caenorhabditis_remanei(species); CREATE INDEX cangl_c ON candida_glabrata(clust_id); CREATE INDEX cangl_s ON candida_glabrata(species); CREATE INDEX canfa_c ON canis_familiaris(clust_id); CREATE INDEX canfa_s ON canis_familiaris(species); CREATE INDEX cioin_c ON ciona_intestinalis(clust_id); CREATE INDEX cioin_s ON ciona_intestinalis(species); CREATE INDEX cryne_c ON cryptococcus_neoformans(clust_id); CREATE INDEX cryne_s ON cryptococcus_neoformans(species); CREATE INDEX danre_c ON danio_rerio(clust_id); CREATE INDEX danre_s ON danio_rerio(species); CREATE INDEX debha_c ON debaryomyces_hanseneii(clust_id); CREATE INDEX debha_s ON debaryomyces_hanseneii(species); CREATE INDEX dicdi_c ON dictyostelium_discoideum(clust_id); CREATE INDEX dicdi_s ON dictyostelium_discoideum(species); CREATE INDEX drome_c ON drosophila_melanogaster(clust_id); CREATE INDEX drome_s ON drosophila_melanogaster(species); CREATE INDEX drops_c ON drosophila_pseudoobscura(clust_id); CREATE INDEX drops_s ON drosophila_pseudoobscura(species); CREATE INDEX enthi_c ON entamoeba_histolytica(clust_id); CREATE INDEX enthi_s ON entamoeba_histolytica(species); CREATE INDEX escco_c ON escherichia_coliK12(clust_id); CREATE INDEX escco_s ON escherichia_coliK12(species); CREATE INDEX galga_c ON gallus_gallus(clust_id); CREATE INDEX galga_s ON gallus_gallus(species); CREATE INDEX gasac_c ON gasterosteus_aculeatus(clust_id); CREATE INDEX gasac_s ON gasterosteus_aculeatus(species); CREATE INDEX klula_c ON kluyveromyces_lactis(clust_id); CREATE INDEX klula_s ON kluyveromyces_lactis(species); CREATE INDEX macmu_c ON macaca_mulatta(clust_id); CREATE INDEX macmu_s ON macaca_mulatta(species); CREATE INDEX mondo_c ON monodelphis_domestica(clust_id); CREATE INDEX mondo_s ON monodelphis_domestica(species); CREATE INDEX homsa_c ON mus_musculus(clust_id); CREATE INDEX homsa_s ON mus_musculus(species); CREATE INDEX orysa_c ON oryza_sativa(clust_id); CREATE INDEX orysa_s ON oryza_sativa(species); CREATE INDEX pantr_c ON pan_troglodytes(clust_id); CREATE INDEX pantr_s ON pan_troglodytes(species); CREATE INDEX ratno_c ON rattus_norvegicus(clust_id); CREATE INDEX ratno_s ON rattus_norvegicus(species); CREATE INDEX sacce_c ON saccharomyces_cerevisiae(clust_id); CREATE INDEX sacce_s ON saccharomyces_cerevisiae(species); CREATE INDEX schpo_c ON schizosaccharomyces_pombe(clust_id); CREATE INDEX schpo_s ON schizosaccharomyces_pombe(species); CREATE INDEX fugru_c ON takifugu_rubripes(clust_id); CREATE INDEX fugru_s ON takifugu_rubripes(species); CREATE INDEX tetni_c ON tetraodon_nigroviridis(clust_id); CREATE INDEX tetni_s ON tetraodon_nigroviridis(species); CREATE INDEX xentr_c ON xenopus_tropicalis(clust_id); CREATE INDEX xentr_s ON xenopus_tropicalis(species); CREATE INDEX yarli_c ON yarrowia_lipolytica(clust_id); CREATE INDEX yarli_s ON yarrowia_lipolytica(species); AnnotationDbi/inst/DBschemas/schemas_1.0/INPARANOIDRATNO_DB.sql0000644000175200017520000003356114710217313024461 0ustar00biocbuildbiocbuild-- -- INPARANOID_DB schema -- ============= -- CREATE TABLE aedes_aegypti ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE anopheles_gambiae ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE apis_mellifera ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE arabidopsis_thaliana ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE bos_taurus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_briggsae ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_elegans ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_remanei ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE candida_glabrata ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE canis_familiaris ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE ciona_intestinalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE cryptococcus_neoformans ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE danio_rerio ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE debaryomyces_hanseneii ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE dictyostelium_discoideum ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE drosophila_melanogaster ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE drosophila_pseudoobscura ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE entamoeba_histolytica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE escherichia_coliK12 ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE gallus_gallus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE gasterosteus_aculeatus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE kluyveromyces_lactis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE macaca_mulatta ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE monodelphis_domestica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE mus_musculus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE oryza_sativa ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE pan_troglodytes ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE homo_sapiens ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE saccharomyces_cerevisiae ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE schizosaccharomyces_pombe ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE takifugu_rubripes ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE tetraodon_nigroviridis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE xenopus_tropicalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE yarrowia_lipolytica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX aedae_c ON aedes_aegypti(clust_id); CREATE INDEX aedae_s ON aedes_aegypti(species); CREATE INDEX anoga_c ON anopheles_gambiae(clust_id); CREATE INDEX anoga_s ON anopheles_gambiae(species); CREATE INDEX apime_c ON apis_mellifera(clust_id); CREATE INDEX apime_s ON apis_mellifera(species); CREATE INDEX arath_c ON arabidopsis_thaliana(clust_id); CREATE INDEX arath_s ON arabidopsis_thaliana(species); CREATE INDEX bosta_c ON bos_taurus(clust_id); CREATE INDEX bosta_s ON bos_taurus(species); CREATE INDEX caebr_c ON caenorhabditis_briggsae(clust_id); CREATE INDEX caebr_s ON caenorhabditis_briggsae(species); CREATE INDEX caeel_c ON caenorhabditis_elegans(clust_id); CREATE INDEX caeel_s ON caenorhabditis_elegans(species); CREATE INDEX caere_c ON caenorhabditis_remanei(clust_id); CREATE INDEX caere_s ON caenorhabditis_remanei(species); CREATE INDEX cangl_c ON candida_glabrata(clust_id); CREATE INDEX cangl_s ON candida_glabrata(species); CREATE INDEX canfa_c ON canis_familiaris(clust_id); CREATE INDEX canfa_s ON canis_familiaris(species); CREATE INDEX cioin_c ON ciona_intestinalis(clust_id); CREATE INDEX cioin_s ON ciona_intestinalis(species); CREATE INDEX cryne_c ON cryptococcus_neoformans(clust_id); CREATE INDEX cryne_s ON cryptococcus_neoformans(species); CREATE INDEX danre_c ON danio_rerio(clust_id); CREATE INDEX danre_s ON danio_rerio(species); CREATE INDEX debha_c ON debaryomyces_hanseneii(clust_id); CREATE INDEX debha_s ON debaryomyces_hanseneii(species); CREATE INDEX dicdi_c ON dictyostelium_discoideum(clust_id); CREATE INDEX dicdi_s ON dictyostelium_discoideum(species); CREATE INDEX drome_c ON drosophila_melanogaster(clust_id); CREATE INDEX drome_s ON drosophila_melanogaster(species); CREATE INDEX drops_c ON drosophila_pseudoobscura(clust_id); CREATE INDEX drops_s ON drosophila_pseudoobscura(species); CREATE INDEX enthi_c ON entamoeba_histolytica(clust_id); CREATE INDEX enthi_s ON entamoeba_histolytica(species); CREATE INDEX escco_c ON escherichia_coliK12(clust_id); CREATE INDEX escco_s ON escherichia_coliK12(species); CREATE INDEX galga_c ON gallus_gallus(clust_id); CREATE INDEX galga_s ON gallus_gallus(species); CREATE INDEX gasac_c ON gasterosteus_aculeatus(clust_id); CREATE INDEX gasac_s ON gasterosteus_aculeatus(species); CREATE INDEX klula_c ON kluyveromyces_lactis(clust_id); CREATE INDEX klula_s ON kluyveromyces_lactis(species); CREATE INDEX macmu_c ON macaca_mulatta(clust_id); CREATE INDEX macmu_s ON macaca_mulatta(species); CREATE INDEX mondo_c ON monodelphis_domestica(clust_id); CREATE INDEX mondo_s ON monodelphis_domestica(species); CREATE INDEX musmu_c ON mus_musculus(clust_id); CREATE INDEX musmu_s ON mus_musculus(species); CREATE INDEX orysa_c ON oryza_sativa(clust_id); CREATE INDEX orysa_s ON oryza_sativa(species); CREATE INDEX pantr_c ON pan_troglodytes(clust_id); CREATE INDEX pantr_s ON pan_troglodytes(species); CREATE INDEX homsa_c ON rattus_norvegicus(clust_id); CREATE INDEX homsa_s ON rattus_norvegicus(species); CREATE INDEX sacce_c ON saccharomyces_cerevisiae(clust_id); CREATE INDEX sacce_s ON saccharomyces_cerevisiae(species); CREATE INDEX schpo_c ON schizosaccharomyces_pombe(clust_id); CREATE INDEX schpo_s ON schizosaccharomyces_pombe(species); CREATE INDEX fugru_c ON takifugu_rubripes(clust_id); CREATE INDEX fugru_s ON takifugu_rubripes(species); CREATE INDEX tetni_c ON tetraodon_nigroviridis(clust_id); CREATE INDEX tetni_s ON tetraodon_nigroviridis(species); CREATE INDEX xentr_c ON xenopus_tropicalis(clust_id); CREATE INDEX xentr_s ON xenopus_tropicalis(species); CREATE INDEX yarli_c ON yarrowia_lipolytica(clust_id); CREATE INDEX yarli_s ON yarrowia_lipolytica(species); AnnotationDbi/inst/DBschemas/schemas_1.0/INPARANOIDSACCE_DB.sql0000644000175200017520000003355214710217313024414 0ustar00biocbuildbiocbuild-- -- INPARANOID_DB schema -- ============= -- CREATE TABLE aedes_aegypti ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE anopheles_gambiae ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE apis_mellifera ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE arabidopsis_thaliana ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE bos_taurus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_briggsae ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_elegans ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE caenorhabditis_remanei ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE candida_glabrata ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE canis_familiaris ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE ciona_intestinalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE cryptococcus_neoformans ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE danio_rerio ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE debaryomyces_hanseneii ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE dictyostelium_discoideum ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE drosophila_melanogaster ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE drosophila_pseudoobscura ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE entamoeba_histolytica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE escherichia_coliK12 ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE gallus_gallus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE gasterosteus_aculeatus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE kluyveromyces_lactis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE macaca_mulatta ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE monodelphis_domestica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE mus_musculus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE oryza_sativa ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE pan_troglodytes ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE rattus_norvegicus ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE homo_sapiens ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE schizosaccharomyces_pombe ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE takifugu_rubripes ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE tetraodon_nigroviridis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE xenopus_tropicalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE yarrowia_lipolytica ( inp_id VARCHAR(30) UNIQUE NOT NULL, --Inparanoid ID clust_id INTEGER NOT NULL, --Inparanoid Cluster ID species CHAR(5) NOT NULL, --Inparanoid Species ID score VARCHAR(6) NOT NULL, --Inparanoid Score seed_status CHAR(4) --Inparanoid Seed Status ); CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX aedae_c ON aedes_aegypti(clust_id); CREATE INDEX aedae_s ON aedes_aegypti(species); CREATE INDEX anoga_c ON anopheles_gambiae(clust_id); CREATE INDEX anoga_s ON anopheles_gambiae(species); CREATE INDEX apime_c ON apis_mellifera(clust_id); CREATE INDEX apime_s ON apis_mellifera(species); CREATE INDEX arath_c ON arabidopsis_thaliana(clust_id); CREATE INDEX arath_s ON arabidopsis_thaliana(species); CREATE INDEX bosta_c ON bos_taurus(clust_id); CREATE INDEX bosta_s ON bos_taurus(species); CREATE INDEX caebr_c ON caenorhabditis_briggsae(clust_id); CREATE INDEX caebr_s ON caenorhabditis_briggsae(species); CREATE INDEX caeel_c ON caenorhabditis_elegans(clust_id); CREATE INDEX caeel_s ON caenorhabditis_elegans(species); CREATE INDEX caere_c ON caenorhabditis_remanei(clust_id); CREATE INDEX caere_s ON caenorhabditis_remanei(species); CREATE INDEX cangl_c ON candida_glabrata(clust_id); CREATE INDEX cangl_s ON candida_glabrata(species); CREATE INDEX canfa_c ON canis_familiaris(clust_id); CREATE INDEX canfa_s ON canis_familiaris(species); CREATE INDEX cioin_c ON ciona_intestinalis(clust_id); CREATE INDEX cioin_s ON ciona_intestinalis(species); CREATE INDEX cryne_c ON cryptococcus_neoformans(clust_id); CREATE INDEX cryne_s ON cryptococcus_neoformans(species); CREATE INDEX danre_c ON danio_rerio(clust_id); CREATE INDEX danre_s ON danio_rerio(species); CREATE INDEX debha_c ON debaryomyces_hanseneii(clust_id); CREATE INDEX debha_s ON debaryomyces_hanseneii(species); CREATE INDEX dicdi_c ON dictyostelium_discoideum(clust_id); CREATE INDEX dicdi_s ON dictyostelium_discoideum(species); CREATE INDEX drome_c ON drosophila_melanogaster(clust_id); CREATE INDEX drome_s ON drosophila_melanogaster(species); CREATE INDEX drops_c ON drosophila_pseudoobscura(clust_id); CREATE INDEX drops_s ON drosophila_pseudoobscura(species); CREATE INDEX enthi_c ON entamoeba_histolytica(clust_id); CREATE INDEX enthi_s ON entamoeba_histolytica(species); CREATE INDEX escco_c ON escherichia_coliK12(clust_id); CREATE INDEX escco_s ON escherichia_coliK12(species); CREATE INDEX galga_c ON gallus_gallus(clust_id); CREATE INDEX galga_s ON gallus_gallus(species); CREATE INDEX gasac_c ON gasterosteus_aculeatus(clust_id); CREATE INDEX gasac_s ON gasterosteus_aculeatus(species); CREATE INDEX klula_c ON kluyveromyces_lactis(clust_id); CREATE INDEX klula_s ON kluyveromyces_lactis(species); CREATE INDEX macmu_c ON macaca_mulatta(clust_id); CREATE INDEX macmu_s ON macaca_mulatta(species); CREATE INDEX mondo_c ON monodelphis_domestica(clust_id); CREATE INDEX mondo_s ON monodelphis_domestica(species); CREATE INDEX musmu_c ON mus_musculus(clust_id); CREATE INDEX musmu_s ON mus_musculus(species); CREATE INDEX orysa_c ON oryza_sativa(clust_id); CREATE INDEX orysa_s ON oryza_sativa(species); CREATE INDEX pantr_c ON pan_troglodytes(clust_id); CREATE INDEX pantr_s ON pan_troglodytes(species); CREATE INDEX ratno_c ON rattus_norvegicus(clust_id); CREATE INDEX ratno_s ON rattus_norvegicus(species); CREATE INDEX homsa_c ON saccharomyces_cerevisiae(clust_id); CREATE INDEX homsa_s ON saccharomyces_cerevisiae(species); CREATE INDEX schpo_c ON schizosaccharomyces_pombe(clust_id); CREATE INDEX schpo_s ON schizosaccharomyces_pombe(species); CREATE INDEX fugru_c ON takifugu_rubripes(clust_id); CREATE INDEX fugru_s ON takifugu_rubripes(species); CREATE INDEX tetni_c ON tetraodon_nigroviridis(clust_id); CREATE INDEX tetni_s ON tetraodon_nigroviridis(species); CREATE INDEX xentr_c ON xenopus_tropicalis(clust_id); CREATE INDEX xentr_s ON xenopus_tropicalis(species); CREATE INDEX yarli_c ON yarrowia_lipolytica(clust_id); CREATE INDEX yarli_s ON yarrowia_lipolytica(species); AnnotationDbi/inst/DBschemas/schemas_1.0/KEGG_DB.sql0000644000175200017520000000173114710217313022740 0ustar00biocbuildbiocbuild-- -- KEGG_DB schema -- ============== -- CREATE TABLE ec2go ( ec_no VARCHAR(16) NOT NULL, -- EC number (with "EC:" prefix) go_id CHAR(10) NOT NULL -- GO ID ); CREATE TABLE pathway2gene ( pathway_id CHAR(8) NOT NULL, -- KEGG pathway long ID gene_or_orf_id VARCHAR(20) NOT NULL -- Entrez Gene or ORF ID ); CREATE TABLE pathway2name ( path_id CHAR(5) NOT NULL UNIQUE, -- KEGG pathway short ID path_name VARCHAR(80) NOT NULL UNIQUE -- KEGG pathway name ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Indexes. CREATE INDEX Ipathway2gene ON pathway2gene (gene_id); AnnotationDbi/inst/DBschemas/schemas_1.0/MALARIA_DB.sql0000644000175200017520000000674314710217313023301 0ustar00biocbuildbiocbuild-- -- MALARIA_DB schema -- =============== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Falias ON alias (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/MOUSECHIP_DB.sql0000644000175200017520000001511614710217313023561 0ustar00biocbuildbiocbuild-- -- MOUSECHIP_DB schema -- =================== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number _id INTEGER NULL, -- REFERENCES genes FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- Ensembl Gene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE mgi ( _id INTEGER NOT NULL, -- REFERENCES genes mgi_id VARCHAR(20) NOT NULL, -- Ensembl Gene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fmgi ON mgi (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/MOUSE_DB.sql0000644000175200017520000001501714710217313023115 0ustar00biocbuildbiocbuild-- -- MOUSE_DB schema -- =============== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- Ensembl Gene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE mgi ( _id INTEGER NOT NULL, -- REFERENCES genes mgi_id VARCHAR(20) NOT NULL, -- Ensembl Gene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fmgi ON mgi (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/PFAM_DB.sql0000644000175200017520000000671414710217313022754 0ustar00biocbuildbiocbuildCREATE TABLE metadata ( name TEXT, value TEXT ); CREATE TABLE cazy ( ac VARCHAR(12) NOT NULL, --AC ID cazy VARCHAR(6) NOT NULL --CAZY ID ); CREATE TABLE homstrad ( ac VARCHAR(12) NOT NULL, --AC ID homstrad VARCHAR(20) NOT NULL --HOMSTRAD ID ); CREATE TABLE interpro ( ac VARCHAR(12) NOT NULL, --AC ID interpro VARCHAR(9) NOT NULL --INTERPRO ID ); CREATE TABLE load ( ac VARCHAR(12) NOT NULL, --AC ID load VARCHAR(15) NOT NULL --LOAD ID ); CREATE TABLE merops ( ac VARCHAR(12) NOT NULL, --AC ID merops VARCHAR(3) NOT NULL --MEROPS ID ); CREATE TABLE mim ( ac VARCHAR(12) NOT NULL, --AC ID mim VARCHAR(6) NOT NULL --MIM ID ); CREATE TABLE pdb ( ac VARCHAR(12) NOT NULL, --AC ID pdb VARCHAR(6) NOT NULL, --PDB ID start_point INTEGER, --start of alignment end_point INTEGER --end of alignment ); CREATE TABLE pfamb ( ac VARCHAR(12) NOT NULL, --AC ID pfamb VARCHAR(8) NOT NULL --PFAMB ID ); CREATE TABLE prints ( ac VARCHAR(12) NOT NULL, --AC ID prints VARCHAR(7) NOT NULL --PRINTS ID ); CREATE TABLE prosite ( ac VARCHAR(12) NOT NULL, --AC ID prosite VARCHAR(9) NOT NULL --PROSITE ID ); CREATE TABLE prosite_profile ( ac VARCHAR(12) NOT NULL, --AC ID prosite_profile VARCHAR(7) NOT NULL --PROSITE_PROFILE ID ); CREATE TABLE rm ( ac VARCHAR(12) NOT NULL, --AC ID rm VARCHAR(8) NOT NULL --RM ID ); CREATE TABLE scop ( ac VARCHAR(12) NOT NULL, --AC ID scop VARCHAR(4) NOT NULL, --SCOP ID placement VARCHAR(2) NOT NULL --SCOP placement ); CREATE TABLE smart ( ac VARCHAR(12) NOT NULL, --AC ID smart VARCHAR(9) NOT NULL --SMART ID ); CREATE TABLE tc ( ac VARCHAR(12) NOT NULL, --AC ID tc VARCHAR(6) NOT NULL --TC ID ); CREATE TABLE url ( ac VARCHAR(12) NOT NULL, --AC ID url VARCHAR(80) NOT NULL --URL ID ); CREATE TABLE id ( ac VARCHAR(12) NOT NULL, --AC ID id VARCHAR(15) NOT NULL --PFAM ID ID ); CREATE TABLE de ( ac VARCHAR(12) NOT NULL, --AC ID de VARCHAR(80) NOT NULL --DE ID ); CREATE TABLE tp ( ac VARCHAR(12) NOT NULL, --AC ID tp VARCHAR(6) NOT NULL --TP ID ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX cazy_ac ON cazy(ac); CREATE INDEX homstrad_ac ON homstrad(ac); CREATE INDEX interpro_ac ON interpro(ac); CREATE INDEX load_ac ON load(ac); CREATE INDEX merops_ac ON merops(ac); CREATE INDEX mim_ac ON mim(ac); CREATE INDEX pdb_ac ON pdb(ac); CREATE INDEX pfamb_ac ON pfamb(ac); CREATE INDEX prints_ac ON prints(ac); CREATE INDEX prosite_ac ON prosite(ac); CREATE INDEX prosite_profile_ac ON prosite_profile(ac); CREATE INDEX rm_ac ON rm(ac); CREATE INDEX scop_ac ON scop(ac); CREATE INDEX smart_ac ON smart(ac); CREATE INDEX tc_ac ON tc(ac); CREATE INDEX url_ac ON url(ac) CREATE INDEX id_ac ON id(ac); CREATE INDEX de_ac ON de(ac); CREATE INDEX tp_ac ON tp(ac); AnnotationDbi/inst/DBschemas/schemas_1.0/PIGCHIP_DB.sql0000644000175200017520000000673214710217313023314 0ustar00biocbuildbiocbuild-- -- PIGCHIP_DB schema -- =================== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number _id INTEGER NULL, -- REFERENCES genes FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/PIG_DB.sql0000644000175200017520000000663314710217313022650 0ustar00biocbuildbiocbuild-- -- PIG_DB schema -- =============== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/RATCHIP_DB.sql0000644000175200017520000001454214710217313023321 0ustar00biocbuildbiocbuild-- -- RATCHIP_DB schema -- ================= -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number _id INTEGER NULL, -- REFERENCES genes FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- Ensembl Gene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fensembl ON ensembl (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/RAT_DB.sql0000644000175200017520000001504414710217313022653 0ustar00biocbuildbiocbuild-- -- RAT_DB schema -- ============= -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- Ensembl Gene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes(_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/WORMCHIP_DB.sql0000644000175200017520000001235714710217313023461 0ustar00biocbuildbiocbuild-- -- WORMCHIP_DB schema -- =================== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number _id INTEGER NULL, -- REFERENCES genes FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/WORM_DB.sql0000644000175200017520000001226014710217313023006 0ustar00biocbuildbiocbuild-- -- WORM_DB schema -- =============== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/YEASTCHIP_DB.sql0000644000175200017520000001050414710217313023552 0ustar00biocbuildbiocbuild-- -- YEASTCHIP_DB schema -- =================== -- -- The "sgd" table is the central table. CREATE TABLE sgd ( _id INTEGER PRIMARY KEY, systematic_name VARCHAR(14) NULL UNIQUE, -- Yeast ORF ID gene_name VARCHAR(14) NULL UNIQUE, -- Yeast gene name sgd_id CHAR(10) NOT NULL UNIQUE -- SGD ID ); -- Data linked to the "sgd" table. CREATE TABLE probes ( probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID _id INTEGER NULL, -- REFERENCES sgd FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE chromosome_features ( _id INTEGER NOT NULL, -- REFERENCES sgd chromosome VARCHAR(2) NULL, -- chromosome name start INTEGER NULL, feature_description TEXT NULL, -- Yeast feature description FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES sgd ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE gene2alias ( _id INTEGER NOT NULL, -- REFERENCES sgd alias VARCHAR(13) NOT NULL, -- Yeast gene alias FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES sgd path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES sgd pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES sgd (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (_id); CREATE INDEX Fchromosome_features ON chromosome_features (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgene2alias ON gene2alias (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpubmed ON pubmed (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/YEAST_DB.sql0000644000175200017520000001200214710217313023101 0ustar00biocbuildbiocbuild-- -- YEAST_DB schema -- =============== -- -- The "sgd" table is the central table. CREATE TABLE sgd ( _id INTEGER PRIMARY KEY, systematic_name VARCHAR(14) NULL UNIQUE, -- Yeast ORF ID gene_name VARCHAR(14) NULL UNIQUE, -- Yeast gene name sgd_id CHAR(10) NOT NULL UNIQUE -- SGD ID ); -- Data linked to the "sgd" table. CREATE TABLE chromosome_features ( _id INTEGER NOT NULL, -- REFERENCES sgd chromosome VARCHAR(2) NULL, -- chromosome name start INTEGER NULL, feature_description TEXT NULL, -- Yeast feature description FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES sgd ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE gene2alias ( _id INTEGER NOT NULL, -- REFERENCES sgd alias VARCHAR(13) NOT NULL, -- Yeast gene alias FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE interpro ( _id INTEGER NOT NULL, -- REFERENCES sgd interpro_id CHAR(9) NOT NULL, -- InterPro ID FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES sgd path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES sgd pfam_id CHAR(7) NOT NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES sgd pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE smart ( _id INTEGER NOT NULL, -- REFERENCES sgd smart_id CHAR(7) NOT NULL, -- SMART ID FOREIGN KEY (_id) REFERENCES sgd (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE gene2systematic ( gene_name VARCHAR(14) NULL, -- Yeast gene name systematic_name VARCHAR(14) NULL -- Yeast ORF ID ); CREATE TABLE reject_orf ( systematic_name VARCHAR(14) PRIMARY KEY -- Yeast ORF ID ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosome_features ON chromosome_features (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgene2alias ON gene2alias (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Finterpro ON interpro (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Fsmart ON smart (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/ZEBRAFISHCHIP_DB.sql0000644000175200017520000001411214710217313024201 0ustar00biocbuildbiocbuild-- -- ZEBRAFISHCHIP_DB schema -- =================== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE probes ( probe_id VARCHAR(80) PRIMARY KEY, -- manufacturer ID accession VARCHAR(20) NULL, -- GenBank accession number _id INTEGER NULL, -- REFERENCES genes FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- Ensembl Gene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fensembl ON ensembl (_id); AnnotationDbi/inst/DBschemas/schemas_1.0/ZEBRAFISH_DB.sql0000644000175200017520000001441414710217313023542 0ustar00biocbuildbiocbuild-- -- ZEBRAFISH_DB schema -- =============== -- -- The "genes" table is the central table. CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); -- Data linked to the "genes" table. CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- Ensembl Gene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes(_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number (no "EC:" prefix) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Standalone data tables. CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); -- Metadata tables. CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/0000755000175200017520000000000014710217313021134 5ustar00biocbuildbiocbuildAnnotationDbi/inst/DBschemas/schemas_2.0/00README.TXT0000644000175200017520000000156314710217313022637 0ustar00biocbuildbiocbuildThis directory contains version 2.0 of the full set of schemas used in the sqlite-based annotation data packages. Version 2.0 is our target for the BioC 2.5 release. All the *.sqlite files using one of the 2.0 schemas must set DBSCHEMAVERSION to 2.0 in their "metadata" table. See the DataTypes.txt file for all the data types used across the 2.0 schemas. SUMMARY OF CHANGES SINCE VERSION 1.0 ------------------------------------ Note that some of these changes are disruptive (i.e. they potentially break the SQL queries written for version 1.0). All probe-based schemas: o dropped all tables except the following: genbank, map_counts, map_metadata, metadata, probes o _id in the probes table is now replaced by a gene_id which is a foreign key to a matching org package o accessions table has been added to hold accessions associated with probes by the manufacturer AnnotationDbi/inst/DBschemas/schemas_2.0/ANOPHELES_DB.sql0000644000175200017520000001533014710217313023542 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/ARABIDOPSISCHIP_DB.sql0000644000175200017520000000142314710217313024426 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE probes (probe_id VARCHAR(80) NOT NULL, is_multiple SMALLINT NOT NULL, gene_id VARCHAR(10) NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.0/ARABIDOPSIS_DB.sql0000644000175200017520000001275714710217313023776 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id CHAR(9) NOT NULL UNIQUE -- AGI locus ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE entrez_genes ( _id INTEGER PRIMARY KEY, gene_id CHAR(9) NOT NULL UNIQUE -- AGI locus ID ); CREATE TABLE gene_info ( _id INTEGER NOT NULL, -- REFERENCES genes gene_name VARCHAR(255) NULL, -- gene name symbol VARCHAR(80) NULL, -- gene symbol chromosome CHAR(1) NULL, -- Arabidopsis chromosome FOREIGN KEY (_id) REFERENCES genes (_id)); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE aracyc ( _id INTEGER NOT NULL, -- REFERENCES genes pathway_name VARCHAR(255) NOT NULL, -- AraCyc pathway name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE enzyme ( _id INTEGER NOT NULL, -- REFERENCES genes ec_name VARCHAR(255) NOT NULL, -- EC name FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fentrez_genes ON entrez_genes(gene_id); CREATE INDEX Fgene_info ON gene_info (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Faracyc ON aracyc (_id); CREATE INDEX Fenzyme ON enzyme (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/BOVINECHIP_DB.sql0000644000175200017520000000160114710217313023646 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.0/BOVINE_DB.sql0000644000175200017520000001774414710217313023221 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/CANINECHIP_DB.sql0000644000175200017520000000160114710217313023621 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.0/CANINE_DB.sql0000644000175200017520000001652214710217313023165 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/CHICKENCHIP_DB.sql0000644000175200017520000000160114710217313023730 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.0/CHICKEN_DB.sql0000644000175200017520000001774414710217313023303 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/CHIMP_DB.sql0000644000175200017520000001551014710217313023064 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/DataTypes.txt0000644000175200017520000002701614710217313023601 0ustar00biocbuildbiocbuildAC ID -------------- SQL type: VARCHAR(12) Examples: 'PF00389.21', 'PF02826.10', 'P63103.1' Note: max length appears to be about 10 This seems to be the central ID for all things PFAM. CAZY ID -------------- SQL type: VARCHAR(6) Examples: 'GT_57', 'GH_29', 'CBM_19' Note: max length seems to be 6 HOMSTRAD ID -------------- SQL type: VARCHAR(20) Examples: 'Dala_Dala_ligas_N', 'A2M_B', 'Haloperoxidase' Note: max length seems to be less than 20 INTERPRO ID -------------- SQL type: VARCHAR(9) Examples: 'IPR003391', 'IPR002612', 'IPR005830' Note: max length seems to be 9 LOAD ID -------------- SQL type: VARCHAR(15) Examples: 'Adrenomedullin', 'Adeno_PIX', 'BCMA-Tall_bind' Note: max length seems to be less than 15 MEROPS ID -------------- SQL type: VARCHAR(3) Examples: 'S10', 'M55', 'T1' Note: max length seems to be 3 MIM ID -------------- SQL type: VARCHAR(6) Examples: '104311', '128230', '222600' Note: max length seems to be 6 PDB ID -------------- SQL type: VARCHAR(6) Examples: '1u69 B', '1odn A', '2kfn A' Note: max length seems to be 6 start of alignment -------------- SQL type: INTEGER Examples: '3', '180', '256' Note: just an int end of alignment -------------- SQL type: INTEGER Examples: '288', '224', '334' Note: always just an int PFAMB ID -------------- SQL type: VARCHAR(8) Examples: 'PB012689', 'PB177858', 'PB176422' Note: max length seems to be 8, these are the machine called PFAM IDs. PRINTS ID -------------- SQL type: VARCHAR(7) Examples: 'PR00178', 'PR01233', 'PR00543' Note: max length seems to be 7 PROSITE ID -------------- SQL type: VARCHAR(9) Examples: 'PDOC00403', 'PDOC00174', 'PDOC00578' Note: max length seems to be 9 PROSITE_PROFILE ID -------------- SQL type: VARCHAR(7) Examples: 'PS50032', 'PS50203', 'PS50119' Note: max length seems to be 7 RM ID -------------- SQL type: VARCHAR(8) Examples: '11011151', '2254264', '15531590' Note: max length seems to be 8 SCOP ID -------------- SQL type: VARCHAR(4) Examples: '1rla', '1by6', '3gcc' Note: max length seems to be 4 SCOP placement -------------- SQL type: VARCHAR(2) Examples: 'fa', 'fa', 'sf' Note: max length seems to be 2. I only ever see the values fa and sf. SMART ID -------------- SQL type: VARCHAR(9) Examples: 'ZnF_UBR1', 'RasGEFN', 'PLDc' Note: max length seems to be about 9 TC ID -------------- SQL type: VARCHAR(6) Examples: '3.A.15', '9.B.33', '2.A.27' Note: max length seems to be PFAM ID ID -------------- SQL type: VARCHAR(15) Examples: 'ADP_ribosyl_GH', 'Adeno_E1B_55K_N', 'AfaD' Note: max length seems to be 15 DE ID -------------- SQL type: VARCHAR(80) Examples: 'Adenovirus GP19K', 'ADP-specific Phosphofructokinase/Glucokinase conserved region' Note: A description field. This one can be very big TP ID -------------- SQL type: VARCHAR(6) Examples: 'Repeat', 'Family', 'Domain', 'Motif' Note: max length is 6. This is only ever one of the above 4 values. URL ID -------------- SQL type: VARCHAR(80) Examples: 'http://bioinformatics.weizmann.ac.il/hotmolecbase/entries/ps1.htm' Note: max length is unknown. These can obviously get pretty big. Inparanoid ID -------------- SQL type: VARCHAR(30) Examples: 'ENSP00000351750', 'FBpp0073215', 'MGI:1274784' Note: character string that corresponds to a gene OR protein ID. IDs from one species are all of the same type, but what type will be used for a species can vary... Inparanoid Cluster ID -------------- SQL type: INTEGER Examples: '1', '2', '34' Note: These are integers which indicate the groupings assigned by inparanoids algorithm. Inparanoid Species ID -------------- SQL type: VARCHAR(15) Examples: 'ensHOMSA.fa', 'modMUSMU.fa', 'modDROME.fa' Note: These indicate the species, the type of ID used by Inparanoid ID and finally the kind of table these data were extracted from Inparanoid Score -------------- SQL type: VARCHAR(20) Examples: '1.0', '0.1513', '0.3578' Note: The score indicates the degree to which this protein is considered to belong to the Inparanoid grouping Inparanoid Seed Status -------------- SQL type: VARCHAR(4) Examples: '100%', '', '99%' Note: 0 to 100%. 100% indicates a true "seed" paralog. Entrez Gene ID -------------- SQL type: VARCHAR(10) Examples: '10251', '283297', '100113407' Note: highest value observed so far is 100113407 Ensembl Gene ID -------------- SQL type: VARCHAR(20) Examples: 'ENSRNOG00000016924', 'ENSMUSG00000028125', 'ENSG00000127837' Note: highest value observed so far is 18 characters long Ensembl Protein ID -------------- SQL type: VARCHAR(20) Examples: 'ENSP00000370606', 'ENSRNOP00000027' Note: Ensembl protein IDs, one peptide per ID. manufacturer ID --------------- SQL type: VARCHAR(80) Examples: '1000_at', '1002_f_at', 'AFFX-HUMISGF3A/M97935_MA_at' GenBank accession number ------------------------ SQL type: VARCHAR(20) Examples: 'X60188', 'NR_003589', 'HG3432-HT3618' Note: the maximum length observed so far is 13 but using VARCHAR(20) is a safety precaution for longer accession numbers that could appear in the future gene symbol or alias -------------------- SQL type: VARCHAR(80) Examples: 'NPEPPS', 'myr4', 'DKFZp434G0625PRO34003' Note: the maximum length observed so far is 21 but using VARCHAR(80) is a safety precaution for longer aliases that could appear in the future sequence name ------------- SQL type: VARCHAR(20) Examples: '1', '22', 'X', 'Y', '6_cox_hap1', '22_random' chromosome name --------------- SQL type: VARCHAR(2) Examples: '1', '22', 'X', 'Y', 'M', 'MT', 'Un' Note: a chromosome name is a particular sequence name cytoband location ----------------- SQL type: VARCHAR(20) Examples: '1p34.2', 'Yp11.32', '19q13.11-q13.12' Note: the maximum length observed so far is 15 but using VARCHAR(20) is a safety precaution for longer cytoband locations that could appear in the future EC number (no "EC:" prefix) --------------------------- SQL type: VARCHAR(13) Examples: '1.1.4.1', '3.2.1.14', '1.14.99.36' Note: the maximum length observed so far is 10 but using VARCHAR(13) is a safety precaution for longer EC numbers that could appear in the future EC number (with "EC:" prefix) ----------------------------- SQL type: VARCHAR(16) Examples: 'EC:1.1.4.1', 'EC:3.2.1.14', 'EC:1.14.99.36' EC name ------- SQL type: VARCHAR(255) Examples: 'lipase', 'photosystem I', '6-phosphofructokinase' Note: the maximum length observed so far is 99 gene name --------- SQL type: VARCHAR(255) Examples: 'deoxyribonuclease I-like 1', 'vitrin' Note: the maximum length observed so far is 251 OMIM ID ------- SQL type: CHAR(6) Examples: '231550', '601421', '611258' Note: highest value observed so far is 611258 IPI accession number -------------------- SQL type: CHAR(11) Examples: 'IPI00328276', 'IPI00789644' Pfam ID ------- SQL type: CHAR(7) Examples: 'PF00069', 'PF08266' PROSITE ID ---------- SQL type: CHAR(7) Examples: 'PS00107', 'PS00657' PubMed ID --------- SQL type: VARCHAR(10) Examples: '2437', '2583089', '17652175' Note: highest value observed so far is 17652175 RefSeq accession number ----------------------- SQL type: VARCHAR(20) Examples: 'NM_018009', 'NP_001035700' Note: RefSeq accession numbers seem to be valid GenBank accession numbers UniGene ID ---------- SQL type: VARCHAR(10) Examples: 'Hs.2', 'Hs.511848', 'Hs.695912' Note: highest value observed so far for Human is Hs.695912 FlyBase ID ---------- SQL type: CHAR(11) Examples: 'FBgn0001942', 'FBgn0030936', 'FBgn0051992' FlyBase CG ID ---------- SQL type: CHAR(10) Examples: 'CG3038', 'CG13377', 'CG2945' Flybase Protein ID -------------- SQL type: VARCHAR(20) Examples: 'FBpp0073215', 'FBpp0110310', 'FBpp0071474' Note: Flybase protein IDs, one peptide per ID. Yeast ORF ID ------------ SQL type: VARCHAR(14) Examples: 'YPL141C', 'YGRWsigma7', 'YPRWdelta14' Note: the maximum length observed so far is 11 but using VARCHAR(14) is a safety precaution for longer Yeast ORF IDs that could appear in the future Yeast gene name --------------- SQL type: VARCHAR(14) Examples: 'ADK2', 'TMA23', '21S_RRNA_4', 'MF(ALPHA)1' Note: the maximum length observed so far is 10 but using VARCHAR(14) is a safety precaution for longer Yeast gene names that could appear in the future SGD ID ------ SQL type: CHAR(10) Examples: 'S000004794', 'S000037040', 'S000123281' Note: highest value observed so far is S000123281 Yeast feature description ------------------------- SQL type: TEXT Note: this can be a text of any length Yeast gene alias ---------------- SQL type: VARCHAR(13) Examples: 'CDH1', 'DNA33', 'EF-1 alpha', 'ATPEPSILON' Note: the maximum length observed so far is 10 but using VARCHAR(13) is a safety precaution for longer Yeast gene aliases that could appear in the future InterPro ID ----------- SQL type: CHAR(9) Examples: 'IPR001440', 'IPR008688', 'IPR015809' Note: highest value observed so far is IPR015809 SMART ID -------- SQL type: CHAR(7) Examples: 'SM00055', 'SM00220', 'SM00717' AGI locus ID ------------ SQL type: CHAR(9) Examples: 'AT1G01010', 'ATCG00830', 'ATMG01410' AraCyc pathway name ------------------- SQL type: VARCHAR(255) Examples: 'SAM cycle', 'trans,trans-farnesyl diphosphate biosynthesis' Note: the maximum length observed so far is 77 but using VARCHAR(255) is a safety precaution for longer AraCyc pathways that could appear in the future Arabidopsis chromosome ---------------------- SQL type: CHAR(1) 7 possible values: '1', '2', '3', '4', '5', 'C', 'M' GO ontology (short label) ------------------------- SQL type: VARCHAR(9) 4 possible values: 'universal', 'BP', 'CC', 'MF' GO ontology (full label) ------------------------ SQL type: VARCHAR(18) 4 possible values: 'universal', 'biological_process', 'cellular_component', 'molecular_function' GO ID ----- SQL type: CHAR(10) Examples: 'all', 'GO:0000001', 'GO:0016491' Note: except for 'all' they are all of the form 'GO:1234567' textual label for the GO term ----------------------------- SQL type: VARCHAR(255) Examples: 'larval fat body development', 'age-dependent response to reactive oxygen species during chronological cell aging' Note: the maximum length observed so far is 193 textual definition for the GO term ---------------------------------- SQL type: TEXT Note: this can be a text of any length type of GO child-parent relationship ------------------------------------ SQL type: VARCHAR(7) 2 possible values: 'isa', 'part_of' GO evidence code ---------------- SQL type: CHAR(3) 14 possible values: 'IC', 'IDA', 'IEA', 'IEP', 'IGC', 'IGI', 'IMP', 'IPI', 'ISS', 'NAS', 'ND', 'RCA', 'TAS', 'NR' Note: see http://www.geneontology.org/GO.evidence.shtml for the meaning of the GO evidence codes KEGG pathway short ID --------------------- SQL type: CHAR(5) Examples: '00100', '05223', '07218' Note: highest value observed so far is 07218 KEGG pathway long ID -------------------- SQL type: CHAR(8) Examples: 'hsa00680', 'rno05220', 'ath00120', 'dme00910' KEGG pathway name ----------------- SQL type: VARCHAR(80) Examples: 'Butanoate metabolism', '3-Chloroacrylic acid degradation' Note: the maximum length observed so far is 63 Entrez Gene or ORF ID --------------------- SQL type: VARCHAR(20) Examples: 'YDR156W', 'AT4G15280', 'Dmel_CG10045' or an Entrez Gene ID Note: the maximum length observed so far is 12 AnnotationDbi/inst/DBschemas/schemas_2.0/ECOLI_DB.sql0000644000175200017520000001133314710217313023056 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Falias ON alias (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/FLYCHIP_DB.sql0000644000175200017520000000160114710217313023316 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.0/FLY_DB.sql0000644000175200017520000001612314710217313022657 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE flybase ( _id INTEGER NOT NULL, -- REFERENCES genes flybase_id VARCHAR(80) NOT NULL, -- FlyBase ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE flybase_cg ( _id INTEGER NOT NULL, -- REFERENCES genes flybase_cg_id VARCHAR(10) NOT NULL, -- FlyBase CG ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE flybase_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Flybase Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Funiprot ON uniprot (_id); CREATE INDEX Fflybase ON flybase (_id); CREATE INDEX Fflybasecg ON flybase_cg (_id); CREATE INDEX Fflybasep ON flybase_prot (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/GO_DB.sql0000644000175200017520000001233514710217313022533 0ustar00biocbuildbiocbuildCREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE go_ontology ( ontology VARCHAR(9) PRIMARY KEY, -- GO ontology (short label) term_type VARCHAR(18) NOT NULL UNIQUE -- GO ontology (full label) ); CREATE TABLE go_term ( _id INTEGER PRIMARY KEY, go_id CHAR(10) NOT NULL UNIQUE, -- GO ID term VARCHAR(255) NOT NULL, -- textual label for the GO term ontology VARCHAR(9) NOT NULL, -- REFERENCES go_ontology definition TEXT NULL, -- textual definition for the GO term FOREIGN KEY (ontology) REFERENCES go_ontology (ontology) ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE go_obsolete ( go_id CHAR(10) PRIMARY KEY, -- GO ID term VARCHAR(255) NOT NULL, -- textual label for the GO term ontology VARCHAR(9) NOT NULL, -- REFERENCES go_ontology definition TEXT NULL, -- textual definition for the GO term FOREIGN KEY (ontology) REFERENCES go_ontology (ontology) ); CREATE TABLE go_synonym ( _id INTEGER NOT NULL, -- REFERENCES go_term synonym VARCHAR(255) NOT NULL, -- label or GO ID secondary CHAR(10) NULL, -- GO ID like_go_id SMALLINT, -- boolean (1 or 0) FOREIGN KEY (_id) REFERENCES go_term (_id) ); CREATE TABLE go_bp_offspring ( _id INTEGER NOT NULL, -- REFERENCES go_term _offspring_id INTEGER NOT NULL, -- REFERENCES go_term FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_offspring_id) REFERENCES go_term (_id) ); CREATE TABLE go_mf_offspring ( _id INTEGER NOT NULL, -- REFERENCES go_term _offspring_id INTEGER NOT NULL, -- REFERENCES go_term FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_offspring_id) REFERENCES go_term (_id) ); CREATE TABLE go_cc_offspring ( _id INTEGER NOT NULL, -- REFERENCES go_term _offspring_id INTEGER NOT NULL, -- REFERENCES go_term FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_offspring_id) REFERENCES go_term (_id) ); CREATE TABLE go_bp_parents ( _id INTEGER NOT NULL, -- REFERENCES go_term _parent_id INTEGER NOT NULL, -- REFERENCES go_term relationship_type VARCHAR(7) NOT NULL, -- type of GO child-parent relationship FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_parent_id) REFERENCES go_term (_id) ); CREATE TABLE go_mf_parents ( _id INTEGER NOT NULL, -- REFERENCES go_term _parent_id INTEGER NOT NULL, -- REFERENCES go_term relationship_type VARCHAR(7) NOT NULL, -- type of GO child-parent relationship FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_parent_id) REFERENCES go_term (_id) ); CREATE TABLE go_cc_parents ( _id INTEGER NOT NULL, -- REFERENCES go_term _parent_id INTEGER NOT NULL, -- REFERENCES go_term relationship_type VARCHAR(7) NOT NULL, -- type of GO child-parent relationship FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_parent_id) REFERENCES go_term (_id) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgo_term ON go_term (ontology); CREATE INDEX Fgo_obsolete ON go_obsolete (ontology); CREATE INDEX gs2 on go_synonym(synonym); CREATE INDEX Fgo_synonym ON go_synonym (_id); CREATE INDEX of1 on go_bp_offspring(_id, _offspring_id); CREATE INDEX of2 on go_bp_offspring(_offspring_id, _id); CREATE INDEX F1go_bp_offspring ON go_bp_offspring (_id); CREATE INDEX F2go_bp_offspring ON go_bp_offspring (_offspring_id); CREATE INDEX of3 on go_mf_offspring(_id, _offspring_id); CREATE INDEX of4 on go_mf_offspring(_offspring_id, _id); CREATE INDEX F1go_mf_offspring ON go_mf_offspring (_id); CREATE INDEX F2go_mf_offspring ON go_mf_offspring (_offspring_id); CREATE INDEX of5 on go_cc_offspring(_id, _offspring_id); CREATE INDEX of6 on go_cc_offspring(_offspring_id, _id); CREATE INDEX F1go_cc_offspring ON go_cc_offspring (_id); CREATE INDEX F2go_cc_offspring ON go_cc_offspring (_offspring_id); CREATE INDEX pa1 on go_bp_parents(_id, _parent_id); CREATE INDEX pa2 on go_bp_parents(_parent_id, _id); CREATE INDEX F1go_bp_parents ON go_bp_parents (_id); CREATE INDEX F2go_bp_parents ON go_bp_parents (_parent_id); CREATE INDEX pa3 on go_mf_parents(_id, _parent_id); CREATE INDEX pa4 on go_mf_parents(_parent_id, _id); CREATE INDEX F1go_mf_parents ON go_mf_parents (_id); CREATE INDEX F2go_mf_parents ON go_mf_parents (_parent_id); CREATE INDEX pa5 on go_cc_parents(_id, _parent_id); CREATE INDEX pa6 on go_cc_parents(_parent_id, _id); CREATE INDEX F1go_cc_parents ON go_cc_parents (_id); CREATE INDEX F2go_cc_parents ON go_cc_parents (_parent_id); AnnotationDbi/inst/DBschemas/schemas_2.0/HUMANCHIP_DB.sql0000644000175200017520000000160114710217313023534 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.0/HUMAN_DB.sql0000644000175200017520000002140614710217313023075 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE omim ( _id INTEGER NOT NULL, -- REFERENCES genes omim_id CHAR(6) NOT NULL, -- OMIM ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ucsc ( _id INTEGER NOT NULL, -- REFERENCES genes ucsc_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Fomim ON omim (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); CREATE INDEX Fucsc ON ucsc (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/INPARANOID_DB.sql0000644000175200017520000002627314710217313023660 0ustar00biocbuildbiocbuildCREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255)); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL); CREATE TABLE aedes_aegypti ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE anopheles_gambiae ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE apis_mellifera ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE bos_taurus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE caenorhabditis_briggsae ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE canis_familiaris ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE ciona_intestinalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE gallus_gallus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE gasterosteus_aculeatus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE arabidopsis_thaliana ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE caenorhabditis_elegans ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE caenorhabditis_remanei ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE candida_glabrata ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE cryptococcus_neoformans ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE danio_rerio ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE debaryomyces_hanseneii ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE dictyostelium_discoideum ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE drosophila_melanogaster ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE drosophila_pseudoobscura ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE entamoeba_histolytica ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE escherichia_coliK12 ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE takifugu_rubripes ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE kluyveromyces_lactis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE macaca_mulatta ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE monodelphis_domestica ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE mus_musculus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE oryza_sativa ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE pan_troglodytes ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE rattus_norvegicus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE saccharomyces_cerevisiae ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE schizosaccharomyces_pombe ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE tetraodon_nigroviridis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE xenopus_tropicalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE yarrowia_lipolytica ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX aedae_c ON aedes_aegypti(clust_id); CREATE INDEX aedae_s ON aedes_aegypti(species); CREATE INDEX anoga_c ON anopheles_gambiae(clust_id); CREATE INDEX anoga_s ON anopheles_gambiae(species); CREATE INDEX apime_c ON apis_mellifera(clust_id); CREATE INDEX apime_s ON apis_mellifera(species); CREATE INDEX bosta_c ON bos_taurus(clust_id); CREATE INDEX bosta_s ON bos_taurus(species); CREATE INDEX caebr_c ON caenorhabditis_briggsae(clust_id); CREATE INDEX caebr_s ON caenorhabditis_briggsae(species); CREATE INDEX canfa_c ON canis_familiaris(clust_id); CREATE INDEX canfa_s ON canis_familiaris(species); CREATE INDEX cioin_c ON ciona_intestinalis(clust_id); CREATE INDEX cioin_s ON ciona_intestinalis(species); CREATE INDEX galga_c ON gallus_gallus(clust_id); CREATE INDEX galga_s ON gallus_gallus(species); CREATE INDEX gasac_c ON gasterosteus_aculeatus(clust_id); CREATE INDEX gasac_s ON gasterosteus_aculeatus(species); CREATE INDEX arath_c ON arabidopsis_thaliana(clust_id); CREATE INDEX arath_s ON arabidopsis_thaliana(species); CREATE INDEX caeel_c ON caenorhabditis_elegans(clust_id); CREATE INDEX caeel_s ON caenorhabditis_elegans(species); CREATE INDEX caere_c ON caenorhabditis_remanei(clust_id); CREATE INDEX caere_s ON caenorhabditis_remanei(species); CREATE INDEX cangl_c ON candida_glabrata(clust_id); CREATE INDEX cangl_s ON candida_glabrata(species); CREATE INDEX cryne_c ON cryptococcus_neoformans(clust_id); CREATE INDEX cryne_s ON cryptococcus_neoformans(species); CREATE INDEX danre_c ON danio_rerio(clust_id); CREATE INDEX danre_s ON danio_rerio(species); CREATE INDEX debha_c ON debaryomyces_hanseneii(clust_id); CREATE INDEX debha_s ON debaryomyces_hanseneii(species); CREATE INDEX dicdi_c ON dictyostelium_discoideum(clust_id); CREATE INDEX dicdi_s ON dictyostelium_discoideum(species); CREATE INDEX drome_c ON drosophila_melanogaster(clust_id); CREATE INDEX drome_s ON drosophila_melanogaster(species); CREATE INDEX drops_c ON drosophila_pseudoobscura(clust_id); CREATE INDEX drops_s ON drosophila_pseudoobscura(species); CREATE INDEX enthi_c ON entamoeba_histolytica(clust_id); CREATE INDEX enthi_s ON entamoeba_histolytica(species); CREATE INDEX escco_c ON escherichia_coliK12(clust_id); CREATE INDEX escco_s ON escherichia_coliK12(species); CREATE INDEX fugru_c ON takifugu_rubripes(clust_id); CREATE INDEX fugru_s ON takifugu_rubripes(species); CREATE INDEX klula_c ON kluyveromyces_lactis(clust_id); CREATE INDEX klula_s ON kluyveromyces_lactis(species); CREATE INDEX macmu_c ON macaca_mulatta(clust_id); CREATE INDEX macmu_s ON macaca_mulatta(species); CREATE INDEX mondo_c ON monodelphis_domestica(clust_id); CREATE INDEX mondo_s ON monodelphis_domestica(species); CREATE INDEX musmu_c ON mus_musculus(clust_id); CREATE INDEX musmu_s ON mus_musculus(species); CREATE INDEX orysa_c ON oryza_sativa(clust_id); CREATE INDEX orysa_s ON oryza_sativa(species); CREATE INDEX pantr_c ON pan_troglodytes(clust_id); CREATE INDEX pantr_s ON pan_troglodytes(species); CREATE INDEX ratno_c ON rattus_norvegicus(clust_id); CREATE INDEX ratno_s ON rattus_norvegicus(species); CREATE INDEX sacce_c ON saccharomyces_cerevisiae(clust_id); CREATE INDEX sacce_s ON saccharomyces_cerevisiae(species); CREATE INDEX schpo_c ON schizosaccharomyces_pombe(clust_id); CREATE INDEX schpo_s ON schizosaccharomyces_pombe(species); CREATE INDEX tetni_c ON tetraodon_nigroviridis(clust_id); CREATE INDEX tetni_s ON tetraodon_nigroviridis(species); CREATE INDEX xentr_c ON xenopus_tropicalis(clust_id); CREATE INDEX xentr_s ON xenopus_tropicalis(species); CREATE INDEX yarli_c ON yarrowia_lipolytica(clust_id); CREATE INDEX yarli_s ON yarrowia_lipolytica(species); AnnotationDbi/inst/DBschemas/schemas_2.0/KEGG_DB.sql0000644000175200017520000000236414710217313022744 0ustar00biocbuildbiocbuildCREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE pathway2name ( path_id CHAR(5) NOT NULL UNIQUE, -- KEGG pathway short ID path_name VARCHAR(100) NOT NULL UNIQUE -- KEGG pathway name ); CREATE TABLE pathway2gene ( pathway_id CHAR(8) NOT NULL, -- KEGG pathway long ID gene_or_orf_id VARCHAR(20) NOT NULL -- Entrez Gene or ORF ID ); CREATE TABLE ath_NCBI_pathway2gene ( pathway_id CHAR(8) NOT NULL, -- KEGG pathway long ID gene_or_orf_id VARCHAR(20) NOT NULL -- Entrez Gene or ORF ID ); CREATE TABLE ec2go(ec_no VARCHAR(16),go_id CHAR(10)); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Ipathway2gene ON pathway2gene (gene_or_orf_id); CREATE INDEX ath_NCBI_Ipathway2gene ON ath_NCBI_pathway2gene (gene_or_orf_id); AnnotationDbi/inst/DBschemas/schemas_2.0/MALARIA_DB.sql0000644000175200017520000000766514710217313023306 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Falias ON alias (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/MOUSECHIP_DB.sql0000644000175200017520000000160114710217313023554 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.0/MOUSE_DB.sql0000644000175200017520000002137614710217313023123 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ucsc ( _id INTEGER NOT NULL, -- REFERENCES genes ucsc_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE mgi ( _id INTEGER NOT NULL, -- REFERENCES genes mgi_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); CREATE INDEX Fucsc ON ucsc (_id); CREATE INDEX Fmgi ON mgi (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/PFAM_DB.sql0000644000175200017520000000633514710217313022754 0ustar00biocbuildbiocbuildCREATE TABLE metadata ( name TEXT, value TEXT ); CREATE TABLE cazy ( ac VARCHAR(12) NOT NULL, --AC ID cazy VARCHAR(6) NOT NULL --CAZY ID ); CREATE TABLE homstrad ( ac VARCHAR(12) NOT NULL, --AC ID homstrad VARCHAR(20) NOT NULL --HOMSTRAD ID ); CREATE TABLE interpro ( ac VARCHAR(12) NOT NULL, --AC ID interpro VARCHAR(9) NOT NULL --INTERPRO ID ); CREATE TABLE load ( ac VARCHAR(12) NOT NULL, --AC ID load VARCHAR(15) NOT NULL --LOAD ID ); CREATE TABLE merops ( ac VARCHAR(12) NOT NULL, --AC ID merops VARCHAR(3) NOT NULL --MEROPS ID ); CREATE TABLE mim ( ac VARCHAR(12) NOT NULL, --AC ID mim VARCHAR(6) NOT NULL --MIM ID ); CREATE TABLE pdb ( ac VARCHAR(12) NOT NULL, --AC ID pdb VARCHAR(6) NOT NULL, --PDB ID start_point INTEGER, --start of alignment end_point INTEGER --end of alignment ); CREATE TABLE prints ( ac VARCHAR(12) NOT NULL, --AC ID prints VARCHAR(7) NOT NULL --PRINTS ID ); CREATE TABLE prosite ( ac VARCHAR(12) NOT NULL, --AC ID prosite VARCHAR(9) NOT NULL --PROSITE ID ); CREATE TABLE prosite_profile ( ac VARCHAR(12) NOT NULL, --AC ID prosite_profile VARCHAR(7) NOT NULL --PROSITE_PROFILE ID ); CREATE TABLE rm ( ac VARCHAR(12) NOT NULL, --AC ID rm VARCHAR(8) NOT NULL --RM ID ); CREATE TABLE scop ( ac VARCHAR(12) NOT NULL, --AC ID scop VARCHAR(4) NOT NULL, --SCOP ID placement VARCHAR(2) NOT NULL --SCOP placement ); CREATE TABLE smart ( ac VARCHAR(12) NOT NULL, --AC ID smart VARCHAR(9) NOT NULL --SMART ID ); CREATE TABLE tc ( ac VARCHAR(12) NOT NULL, --AC ID tc VARCHAR(6) NOT NULL --TC ID ); CREATE TABLE url ( ac VARCHAR(12) NOT NULL, --AC ID url VARCHAR(80) NOT NULL --URL ID ); CREATE TABLE id ( ac VARCHAR(12) NOT NULL, --AC ID id VARCHAR(15) NOT NULL --ID ID ); CREATE TABLE de ( ac VARCHAR(12) NOT NULL, --AC ID de VARCHAR(80) NOT NULL --DE ID ); CREATE TABLE tp ( ac VARCHAR(12) NOT NULL, --AC ID tp VARCHAR(6) NOT NULL --TP ID ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX cazy_ac ON cazy(ac); CREATE INDEX homstrad_ac ON homstrad(ac); CREATE INDEX interpro_ac ON interpro(ac); CREATE INDEX load_ac ON load(ac); CREATE INDEX merops_ac ON merops(ac); CREATE INDEX mim_ac ON mim(ac); CREATE INDEX pdb_ac ON pdb(ac); CREATE INDEX prints_ac ON prints(ac); CREATE INDEX prosite_ac ON prosite(ac); CREATE INDEX prosite_profile_ac ON prosite_profile(ac); CREATE INDEX rm_ac ON rm(ac); CREATE INDEX scop_ac ON scop(ac); CREATE INDEX smart_ac ON smart(ac); CREATE INDEX tc_ac ON tc(ac); CREATE INDEX url_ac ON url(ac); CREATE INDEX id_ac ON id(ac); CREATE INDEX de_ac ON de(ac); CREATE INDEX tp_ac ON tp(ac); AnnotationDbi/inst/DBschemas/schemas_2.0/PIG_DB.sql0000644000175200017520000001276514710217313022654 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/RATCHIP_DB.sql0000644000175200017520000000160114710217313023312 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.0/RAT_DB.sql0000644000175200017520000002043014710217313022647 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/RHESUS_DB.sql0000644000175200017520000001551014710217313023235 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/WORMCHIP_DB.sql0000644000175200017520000000160114710217313023450 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.0/WORM_DB.sql0000644000175200017520000001606514710217313023016 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE wormbase ( _id INTEGER NOT NULL, -- REFERENCES genes wormbase_id VARCHAR(20) NOT NULL, -- wormbase id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); CREATE INDEX Fwormbase ON wormbase (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/XENOPUSCHIP_DB.sql0000644000175200017520000000160114710217313024025 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.0/XENOPUS_DB.sql0000644000175200017520000001235614710217313023372 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/YEASTCHIP_DB.sql0000644000175200017520000000151414710217313023554 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE probes (probe_id VARCHAR(80), systematic_name VARCHAR(14) NULL, gene_name VARCHAR(14) NULL, sgd_id CHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (systematic_name); AnnotationDbi/inst/DBschemas/schemas_2.0/YEAST_DB.sql0000644000175200017520000001475614710217313023124 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sgd ( _id INTEGER PRIMARY KEY, systematic_name VARCHAR(14) NULL UNIQUE, -- Yeast gene systematic name gene_name VARCHAR(14) NULL UNIQUE, -- Yeast gene name sgd_id CHAR(10) NOT NULL UNIQUE -- SGD ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE chromosome_features ( _id INTEGER NOT NULL, -- REFERENCES sgd chromosome VARCHAR(2) NULL, -- chromosome name start INTEGER NULL, stop INTEGER NULL, feature_description TEXT NULL, -- Yeast feature description FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE gene2alias ( _id INTEGER NOT NULL, -- REFERENCES sgd alias VARCHAR(13) NOT NULL, -- Yeast gene alias FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES sgd pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES sgd path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES sgd ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES sgd pfam_id CHAR(7) NOT NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES sgd (_id)); CREATE TABLE smart ( _id INTEGER NOT NULL, -- REFERENCES sgd smart_id CHAR(7) NOT NULL, -- SMART ID FOREIGN KEY (_id) REFERENCES sgd (_id)); CREATE TABLE interpro ( _id INTEGER NOT NULL, -- REFERENCES sgd interpro_id CHAR(9) NOT NULL, -- InterPro ID FOREIGN KEY (_id) REFERENCES sgd (_id)); CREATE TABLE reject_orf ( systematic_name VARCHAR(14) PRIMARY KEY); CREATE TABLE gene2systematic ( gene_name VARCHAR(14) NULL, -- Yeast gene name systematic_name VARCHAR(14) NULL); CREATE TABLE genes ( _id INTEGER NOT NULL, -- REFERENCES sgd gene_id VARCHAR(20) NOT NULL, -- gene id FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES sgd ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES sgd uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES sgd accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES sgd (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosome_features ON chromosome_features (_id); CREATE INDEX Fgene2alias ON gene2alias(_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fsmart ON smart (_id); CREATE INDEX Finterpro ON interpro (_id); CREATE INDEX Fgene ON genes(_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Funiprot ON uniprot (_id); CREATE INDEX Frefseq ON refseq (_id); AnnotationDbi/inst/DBschemas/schemas_2.0/ZEBRAFISHCHIP_DB.sql0000644000175200017520000000160114710217313024201 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.0/ZEBRAFISH_DB.sql0000644000175200017520000002033314710217313023540 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE zfin ( _id INTEGER NOT NULL, -- REFERENCES genes zfin_id VARCHAR(20) NOT NULL, -- zfin id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); CREATE INDEX Fzfin ON zfin (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/0000755000175200017520000000000014710217313021135 5ustar00biocbuildbiocbuildAnnotationDbi/inst/DBschemas/schemas_2.1/00README.TXT0000644000175200017520000000156314710217313022640 0ustar00biocbuildbiocbuildThis directory contains version 2.0 of the full set of schemas used in the sqlite-based annotation data packages. Version 2.0 is our target for the BioC 2.5 release. All the *.sqlite files using one of the 2.0 schemas must set DBSCHEMAVERSION to 2.0 in their "metadata" table. See the DataTypes.txt file for all the data types used across the 2.0 schemas. SUMMARY OF CHANGES SINCE VERSION 1.0 ------------------------------------ Note that some of these changes are disruptive (i.e. they potentially break the SQL queries written for version 1.0). All probe-based schemas: o dropped all tables except the following: genbank, map_counts, map_metadata, metadata, probes o _id in the probes table is now replaced by a gene_id which is a foreign key to a matching org package o accessions table has been added to hold accessions associated with probes by the manufacturer AnnotationDbi/inst/DBschemas/schemas_2.1/ANOPHELES_DB.sql0000644000175200017520000001533014710217313023543 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/ARABIDOPSISCHIP_DB.sql0000644000175200017520000000142314710217313024427 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE probes (probe_id VARCHAR(80) NOT NULL, is_multiple SMALLINT NOT NULL, gene_id VARCHAR(10) NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.1/ARABIDOPSIS_DB.sql0000644000175200017520000001275714710217313023777 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id CHAR(9) NOT NULL UNIQUE -- AGI locus ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE entrez_genes ( _id INTEGER PRIMARY KEY, gene_id CHAR(9) NOT NULL UNIQUE -- AGI locus ID ); CREATE TABLE gene_info ( _id INTEGER NOT NULL, -- REFERENCES genes gene_name VARCHAR(255) NULL, -- gene name symbol VARCHAR(80) NULL, -- gene symbol chromosome CHAR(1) NULL, -- Arabidopsis chromosome FOREIGN KEY (_id) REFERENCES genes (_id)); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE aracyc ( _id INTEGER NOT NULL, -- REFERENCES genes pathway_name VARCHAR(255) NOT NULL, -- AraCyc pathway name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE enzyme ( _id INTEGER NOT NULL, -- REFERENCES genes ec_name VARCHAR(255) NOT NULL, -- EC name FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fentrez_genes ON entrez_genes(gene_id); CREATE INDEX Fgene_info ON gene_info (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Faracyc ON aracyc (_id); CREATE INDEX Fenzyme ON enzyme (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/BOVINECHIP_DB.sql0000644000175200017520000000160114710217313023647 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.1/BOVINE_DB.sql0000644000175200017520000001774414710217313023222 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/CANINECHIP_DB.sql0000644000175200017520000000160114710217313023622 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.1/CANINE_DB.sql0000644000175200017520000001652214710217313023166 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/CHICKENCHIP_DB.sql0000644000175200017520000000160114710217313023731 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.1/CHICKEN_DB.sql0000644000175200017520000001774414710217313023304 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/CHIMP_DB.sql0000644000175200017520000001551014710217313023065 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/COELICOLOR_DB.sql0000644000175200017520000000710414710217313023657 0ustar00biocbuildbiocbuildCREATE TABLE gene_info ( _id INTEGER REFERENCES genes(_id), gene_name TEXT, symbol TEXT ); CREATE TABLE refseq ( _id INTEGER REFERENCES genes(_id), accession TEXT ); CREATE TABLE ec ( _id INTEGER REFERENCES genes(_id), ec_number TEXT ); CREATE TABLE kegg ( _id INTEGER REFERENCES genes(_id), path_id TEXT ); CREATE TABLE map_metadata ( map_name TEXT, source_name TEXT, source_url TEXT, source_date TEXT ); CREATE TABLE pubmed ( _id INTEGER REFERENCES genes(_id), pubmed_id TEXT ); CREATE TABLE locus ( _id INTEGER REFERENCES genes(_id), locus_tag TEXT -- SCO IDs ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id TEXT -- Entrez_Gene IDs ); CREATE TABLE accessions ( _id INTEGER NOT NULL, accession TEXT, -- RefSeq accessions FOREIGN KEY (_id) REFERENCES genes(_id) ); CREATE TABLE protein ( _id INTEGER REFERENCES genes(_id), protein_gi TEXT ); CREATE TABLE chrlengths ( chromosome VARCHAR(1) PRIMARY KEY, -- chromosome name [0: chromosome, 1: plasmid SCP1, 2: plasmid SCP2] length INTEGER NOT NULL ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(1), -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias (synonyms) FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE go_bp ( _id INTEGER REFERENCES genes(_id), go_id TEXT, evidence TEXT ); CREATE TABLE go_cc ( _id INTEGER REFERENCES genes(_id), go_id TEXT, evidence TEXT ); CREATE TABLE go_mf ( _id INTEGER REFERENCES genes(_id), go_id TEXT, evidence TEXT ); CREATE TABLE go_bp_all (_id INTEGER REFERENCES genes(_id),go_id TEXT,evidence TEXT); CREATE TABLE go_cc_all (_id INTEGER REFERENCES genes(_id),go_id TEXT,evidence TEXT); CREATE TABLE go_mf_all (_id INTEGER REFERENCES genes(_id),go_id TEXT,evidence TEXT); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- chromosome name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE symbol ( _id INTEGER REFERENCES genes(_id), symbol TEXT ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX en1 ON ec(_id); CREATE INDEX gi1 ON gene_info(_id); CREATE INDEX k1 ON kegg(_id); CREATE INDEX pu1 ON pubmed(_id); CREATE INDEX rs1 on refseq(_id); CREATE INDEX lt1 ON locus(_id); CREATE INDEX lt2 ON locus(locus_tag); CREATE INDEX ge2 ON genes(gene_id); CREATE INDEX ge1 on genes(_id); CREATE INDEX ac1 ON accessions(_id); CREATE INDEX ac2 ON accessions(accession); CREATE INDEX pr1 ON protein(_id); CREATE INDEX al1 ON alias(_id); CREATE INDEX ch ON chromosomes (_id); CREATE INDEX go1 ON go_bp(_id); CREATE INDEX go2 ON go_mf(_id); CREATE INDEX go3 ON go_cc(_id); CREATE INDEX go4 ON go_bp(go_id); CREATE INDEX go5 ON go_mf(go_id); CREATE INDEX go6 ON go_cc(go_id); CREATE INDEX chl ON chromosome_locations (_id); CREATE INDEX gisymbol ON symbol(_id); AnnotationDbi/inst/DBschemas/schemas_2.1/DataTypes.txt0000644000175200017520000002701614710217313023602 0ustar00biocbuildbiocbuildAC ID -------------- SQL type: VARCHAR(12) Examples: 'PF00389.21', 'PF02826.10', 'P63103.1' Note: max length appears to be about 10 This seems to be the central ID for all things PFAM. CAZY ID -------------- SQL type: VARCHAR(6) Examples: 'GT_57', 'GH_29', 'CBM_19' Note: max length seems to be 6 HOMSTRAD ID -------------- SQL type: VARCHAR(20) Examples: 'Dala_Dala_ligas_N', 'A2M_B', 'Haloperoxidase' Note: max length seems to be less than 20 INTERPRO ID -------------- SQL type: VARCHAR(9) Examples: 'IPR003391', 'IPR002612', 'IPR005830' Note: max length seems to be 9 LOAD ID -------------- SQL type: VARCHAR(15) Examples: 'Adrenomedullin', 'Adeno_PIX', 'BCMA-Tall_bind' Note: max length seems to be less than 15 MEROPS ID -------------- SQL type: VARCHAR(3) Examples: 'S10', 'M55', 'T1' Note: max length seems to be 3 MIM ID -------------- SQL type: VARCHAR(6) Examples: '104311', '128230', '222600' Note: max length seems to be 6 PDB ID -------------- SQL type: VARCHAR(6) Examples: '1u69 B', '1odn A', '2kfn A' Note: max length seems to be 6 start of alignment -------------- SQL type: INTEGER Examples: '3', '180', '256' Note: just an int end of alignment -------------- SQL type: INTEGER Examples: '288', '224', '334' Note: always just an int PFAMB ID -------------- SQL type: VARCHAR(8) Examples: 'PB012689', 'PB177858', 'PB176422' Note: max length seems to be 8, these are the machine called PFAM IDs. PRINTS ID -------------- SQL type: VARCHAR(7) Examples: 'PR00178', 'PR01233', 'PR00543' Note: max length seems to be 7 PROSITE ID -------------- SQL type: VARCHAR(9) Examples: 'PDOC00403', 'PDOC00174', 'PDOC00578' Note: max length seems to be 9 PROSITE_PROFILE ID -------------- SQL type: VARCHAR(7) Examples: 'PS50032', 'PS50203', 'PS50119' Note: max length seems to be 7 RM ID -------------- SQL type: VARCHAR(8) Examples: '11011151', '2254264', '15531590' Note: max length seems to be 8 SCOP ID -------------- SQL type: VARCHAR(4) Examples: '1rla', '1by6', '3gcc' Note: max length seems to be 4 SCOP placement -------------- SQL type: VARCHAR(2) Examples: 'fa', 'fa', 'sf' Note: max length seems to be 2. I only ever see the values fa and sf. SMART ID -------------- SQL type: VARCHAR(9) Examples: 'ZnF_UBR1', 'RasGEFN', 'PLDc' Note: max length seems to be about 9 TC ID -------------- SQL type: VARCHAR(6) Examples: '3.A.15', '9.B.33', '2.A.27' Note: max length seems to be PFAM ID ID -------------- SQL type: VARCHAR(15) Examples: 'ADP_ribosyl_GH', 'Adeno_E1B_55K_N', 'AfaD' Note: max length seems to be 15 DE ID -------------- SQL type: VARCHAR(80) Examples: 'Adenovirus GP19K', 'ADP-specific Phosphofructokinase/Glucokinase conserved region' Note: A description field. This one can be very big TP ID -------------- SQL type: VARCHAR(6) Examples: 'Repeat', 'Family', 'Domain', 'Motif' Note: max length is 6. This is only ever one of the above 4 values. URL ID -------------- SQL type: VARCHAR(80) Examples: 'http://bioinformatics.weizmann.ac.il/hotmolecbase/entries/ps1.htm' Note: max length is unknown. These can obviously get pretty big. Inparanoid ID -------------- SQL type: VARCHAR(30) Examples: 'ENSP00000351750', 'FBpp0073215', 'MGI:1274784' Note: character string that corresponds to a gene OR protein ID. IDs from one species are all of the same type, but what type will be used for a species can vary... Inparanoid Cluster ID -------------- SQL type: INTEGER Examples: '1', '2', '34' Note: These are integers which indicate the groupings assigned by inparanoids algorithm. Inparanoid Species ID -------------- SQL type: VARCHAR(15) Examples: 'ensHOMSA.fa', 'modMUSMU.fa', 'modDROME.fa' Note: These indicate the species, the type of ID used by Inparanoid ID and finally the kind of table these data were extracted from Inparanoid Score -------------- SQL type: VARCHAR(20) Examples: '1.0', '0.1513', '0.3578' Note: The score indicates the degree to which this protein is considered to belong to the Inparanoid grouping Inparanoid Seed Status -------------- SQL type: VARCHAR(4) Examples: '100%', '', '99%' Note: 0 to 100%. 100% indicates a true "seed" paralog. Entrez Gene ID -------------- SQL type: VARCHAR(10) Examples: '10251', '283297', '100113407' Note: highest value observed so far is 100113407 Ensembl Gene ID -------------- SQL type: VARCHAR(20) Examples: 'ENSRNOG00000016924', 'ENSMUSG00000028125', 'ENSG00000127837' Note: highest value observed so far is 18 characters long Ensembl Protein ID -------------- SQL type: VARCHAR(20) Examples: 'ENSP00000370606', 'ENSRNOP00000027' Note: Ensembl protein IDs, one peptide per ID. manufacturer ID --------------- SQL type: VARCHAR(80) Examples: '1000_at', '1002_f_at', 'AFFX-HUMISGF3A/M97935_MA_at' GenBank accession number ------------------------ SQL type: VARCHAR(20) Examples: 'X60188', 'NR_003589', 'HG3432-HT3618' Note: the maximum length observed so far is 13 but using VARCHAR(20) is a safety precaution for longer accession numbers that could appear in the future gene symbol or alias -------------------- SQL type: VARCHAR(80) Examples: 'NPEPPS', 'myr4', 'DKFZp434G0625PRO34003' Note: the maximum length observed so far is 21 but using VARCHAR(80) is a safety precaution for longer aliases that could appear in the future sequence name ------------- SQL type: VARCHAR(20) Examples: '1', '22', 'X', 'Y', '6_cox_hap1', '22_random' chromosome name --------------- SQL type: VARCHAR(2) Examples: '1', '22', 'X', 'Y', 'M', 'MT', 'Un' Note: a chromosome name is a particular sequence name cytoband location ----------------- SQL type: VARCHAR(20) Examples: '1p34.2', 'Yp11.32', '19q13.11-q13.12' Note: the maximum length observed so far is 15 but using VARCHAR(20) is a safety precaution for longer cytoband locations that could appear in the future EC number (no "EC:" prefix) --------------------------- SQL type: VARCHAR(13) Examples: '1.1.4.1', '3.2.1.14', '1.14.99.36' Note: the maximum length observed so far is 10 but using VARCHAR(13) is a safety precaution for longer EC numbers that could appear in the future EC number (with "EC:" prefix) ----------------------------- SQL type: VARCHAR(16) Examples: 'EC:1.1.4.1', 'EC:3.2.1.14', 'EC:1.14.99.36' EC name ------- SQL type: VARCHAR(255) Examples: 'lipase', 'photosystem I', '6-phosphofructokinase' Note: the maximum length observed so far is 99 gene name --------- SQL type: VARCHAR(255) Examples: 'deoxyribonuclease I-like 1', 'vitrin' Note: the maximum length observed so far is 251 OMIM ID ------- SQL type: CHAR(6) Examples: '231550', '601421', '611258' Note: highest value observed so far is 611258 IPI accession number -------------------- SQL type: CHAR(11) Examples: 'IPI00328276', 'IPI00789644' Pfam ID ------- SQL type: CHAR(7) Examples: 'PF00069', 'PF08266' PROSITE ID ---------- SQL type: CHAR(7) Examples: 'PS00107', 'PS00657' PubMed ID --------- SQL type: VARCHAR(10) Examples: '2437', '2583089', '17652175' Note: highest value observed so far is 17652175 RefSeq accession number ----------------------- SQL type: VARCHAR(20) Examples: 'NM_018009', 'NP_001035700' Note: RefSeq accession numbers seem to be valid GenBank accession numbers UniGene ID ---------- SQL type: VARCHAR(10) Examples: 'Hs.2', 'Hs.511848', 'Hs.695912' Note: highest value observed so far for Human is Hs.695912 FlyBase ID ---------- SQL type: CHAR(11) Examples: 'FBgn0001942', 'FBgn0030936', 'FBgn0051992' FlyBase CG ID ---------- SQL type: CHAR(10) Examples: 'CG3038', 'CG13377', 'CG2945' Flybase Protein ID -------------- SQL type: VARCHAR(20) Examples: 'FBpp0073215', 'FBpp0110310', 'FBpp0071474' Note: Flybase protein IDs, one peptide per ID. Yeast ORF ID ------------ SQL type: VARCHAR(14) Examples: 'YPL141C', 'YGRWsigma7', 'YPRWdelta14' Note: the maximum length observed so far is 11 but using VARCHAR(14) is a safety precaution for longer Yeast ORF IDs that could appear in the future Yeast gene name --------------- SQL type: VARCHAR(14) Examples: 'ADK2', 'TMA23', '21S_RRNA_4', 'MF(ALPHA)1' Note: the maximum length observed so far is 10 but using VARCHAR(14) is a safety precaution for longer Yeast gene names that could appear in the future SGD ID ------ SQL type: CHAR(10) Examples: 'S000004794', 'S000037040', 'S000123281' Note: highest value observed so far is S000123281 Yeast feature description ------------------------- SQL type: TEXT Note: this can be a text of any length Yeast gene alias ---------------- SQL type: VARCHAR(13) Examples: 'CDH1', 'DNA33', 'EF-1 alpha', 'ATPEPSILON' Note: the maximum length observed so far is 10 but using VARCHAR(13) is a safety precaution for longer Yeast gene aliases that could appear in the future InterPro ID ----------- SQL type: CHAR(9) Examples: 'IPR001440', 'IPR008688', 'IPR015809' Note: highest value observed so far is IPR015809 SMART ID -------- SQL type: CHAR(7) Examples: 'SM00055', 'SM00220', 'SM00717' AGI locus ID ------------ SQL type: CHAR(9) Examples: 'AT1G01010', 'ATCG00830', 'ATMG01410' AraCyc pathway name ------------------- SQL type: VARCHAR(255) Examples: 'SAM cycle', 'trans,trans-farnesyl diphosphate biosynthesis' Note: the maximum length observed so far is 77 but using VARCHAR(255) is a safety precaution for longer AraCyc pathways that could appear in the future Arabidopsis chromosome ---------------------- SQL type: CHAR(1) 7 possible values: '1', '2', '3', '4', '5', 'C', 'M' GO ontology (short label) ------------------------- SQL type: VARCHAR(9) 4 possible values: 'universal', 'BP', 'CC', 'MF' GO ontology (full label) ------------------------ SQL type: VARCHAR(18) 4 possible values: 'universal', 'biological_process', 'cellular_component', 'molecular_function' GO ID ----- SQL type: CHAR(10) Examples: 'all', 'GO:0000001', 'GO:0016491' Note: except for 'all' they are all of the form 'GO:1234567' textual label for the GO term ----------------------------- SQL type: VARCHAR(255) Examples: 'larval fat body development', 'age-dependent response to reactive oxygen species during chronological cell aging' Note: the maximum length observed so far is 193 textual definition for the GO term ---------------------------------- SQL type: TEXT Note: this can be a text of any length type of GO child-parent relationship ------------------------------------ SQL type: VARCHAR(7) 2 possible values: 'isa', 'part_of' GO evidence code ---------------- SQL type: CHAR(3) 14 possible values: 'IC', 'IDA', 'IEA', 'IEP', 'IGC', 'IGI', 'IMP', 'IPI', 'ISS', 'NAS', 'ND', 'RCA', 'TAS', 'NR' Note: see http://www.geneontology.org/GO.evidence.shtml for the meaning of the GO evidence codes KEGG pathway short ID --------------------- SQL type: CHAR(5) Examples: '00100', '05223', '07218' Note: highest value observed so far is 07218 KEGG pathway long ID -------------------- SQL type: CHAR(8) Examples: 'hsa00680', 'rno05220', 'ath00120', 'dme00910' KEGG pathway name ----------------- SQL type: VARCHAR(80) Examples: 'Butanoate metabolism', '3-Chloroacrylic acid degradation' Note: the maximum length observed so far is 63 Entrez Gene or ORF ID --------------------- SQL type: VARCHAR(20) Examples: 'YDR156W', 'AT4G15280', 'Dmel_CG10045' or an Entrez Gene ID Note: the maximum length observed so far is 12 AnnotationDbi/inst/DBschemas/schemas_2.1/ECOLI_DB.sql0000644000175200017520000001133314710217313023057 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Falias ON alias (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/FLYCHIP_DB.sql0000644000175200017520000000160114710217313023317 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.1/FLY_DB.sql0000644000175200017520000001761414710217313022666 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE flybase ( _id INTEGER NOT NULL, -- REFERENCES genes flybase_id VARCHAR(80) NOT NULL, -- FlyBase ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE flybase_cg ( _id INTEGER NOT NULL, -- REFERENCES genes flybase_cg_id VARCHAR(10) NOT NULL, -- FlyBase CG ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE flybase_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Flybase Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); CREATE INDEX Fflybase ON flybase (_id); CREATE INDEX Fflybasecg ON flybase_cg (_id); CREATE INDEX Fflybasep ON flybase_prot (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/GO_DB.sql0000644000175200017520000001233514710217313022534 0ustar00biocbuildbiocbuildCREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE go_ontology ( ontology VARCHAR(9) PRIMARY KEY, -- GO ontology (short label) term_type VARCHAR(18) NOT NULL UNIQUE -- GO ontology (full label) ); CREATE TABLE go_term ( _id INTEGER PRIMARY KEY, go_id CHAR(10) NOT NULL UNIQUE, -- GO ID term VARCHAR(255) NOT NULL, -- textual label for the GO term ontology VARCHAR(9) NOT NULL, -- REFERENCES go_ontology definition TEXT NULL, -- textual definition for the GO term FOREIGN KEY (ontology) REFERENCES go_ontology (ontology) ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE go_obsolete ( go_id CHAR(10) PRIMARY KEY, -- GO ID term VARCHAR(255) NOT NULL, -- textual label for the GO term ontology VARCHAR(9) NOT NULL, -- REFERENCES go_ontology definition TEXT NULL, -- textual definition for the GO term FOREIGN KEY (ontology) REFERENCES go_ontology (ontology) ); CREATE TABLE go_synonym ( _id INTEGER NOT NULL, -- REFERENCES go_term synonym VARCHAR(255) NOT NULL, -- label or GO ID secondary CHAR(10) NULL, -- GO ID like_go_id SMALLINT, -- boolean (1 or 0) FOREIGN KEY (_id) REFERENCES go_term (_id) ); CREATE TABLE go_bp_offspring ( _id INTEGER NOT NULL, -- REFERENCES go_term _offspring_id INTEGER NOT NULL, -- REFERENCES go_term FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_offspring_id) REFERENCES go_term (_id) ); CREATE TABLE go_mf_offspring ( _id INTEGER NOT NULL, -- REFERENCES go_term _offspring_id INTEGER NOT NULL, -- REFERENCES go_term FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_offspring_id) REFERENCES go_term (_id) ); CREATE TABLE go_cc_offspring ( _id INTEGER NOT NULL, -- REFERENCES go_term _offspring_id INTEGER NOT NULL, -- REFERENCES go_term FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_offspring_id) REFERENCES go_term (_id) ); CREATE TABLE go_bp_parents ( _id INTEGER NOT NULL, -- REFERENCES go_term _parent_id INTEGER NOT NULL, -- REFERENCES go_term relationship_type VARCHAR(7) NOT NULL, -- type of GO child-parent relationship FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_parent_id) REFERENCES go_term (_id) ); CREATE TABLE go_mf_parents ( _id INTEGER NOT NULL, -- REFERENCES go_term _parent_id INTEGER NOT NULL, -- REFERENCES go_term relationship_type VARCHAR(7) NOT NULL, -- type of GO child-parent relationship FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_parent_id) REFERENCES go_term (_id) ); CREATE TABLE go_cc_parents ( _id INTEGER NOT NULL, -- REFERENCES go_term _parent_id INTEGER NOT NULL, -- REFERENCES go_term relationship_type VARCHAR(7) NOT NULL, -- type of GO child-parent relationship FOREIGN KEY (_id) REFERENCES go_term (_id), FOREIGN KEY (_parent_id) REFERENCES go_term (_id) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgo_term ON go_term (ontology); CREATE INDEX Fgo_obsolete ON go_obsolete (ontology); CREATE INDEX gs2 on go_synonym(synonym); CREATE INDEX Fgo_synonym ON go_synonym (_id); CREATE INDEX of1 on go_bp_offspring(_id, _offspring_id); CREATE INDEX of2 on go_bp_offspring(_offspring_id, _id); CREATE INDEX F1go_bp_offspring ON go_bp_offspring (_id); CREATE INDEX F2go_bp_offspring ON go_bp_offspring (_offspring_id); CREATE INDEX of3 on go_mf_offspring(_id, _offspring_id); CREATE INDEX of4 on go_mf_offspring(_offspring_id, _id); CREATE INDEX F1go_mf_offspring ON go_mf_offspring (_id); CREATE INDEX F2go_mf_offspring ON go_mf_offspring (_offspring_id); CREATE INDEX of5 on go_cc_offspring(_id, _offspring_id); CREATE INDEX of6 on go_cc_offspring(_offspring_id, _id); CREATE INDEX F1go_cc_offspring ON go_cc_offspring (_id); CREATE INDEX F2go_cc_offspring ON go_cc_offspring (_offspring_id); CREATE INDEX pa1 on go_bp_parents(_id, _parent_id); CREATE INDEX pa2 on go_bp_parents(_parent_id, _id); CREATE INDEX F1go_bp_parents ON go_bp_parents (_id); CREATE INDEX F2go_bp_parents ON go_bp_parents (_parent_id); CREATE INDEX pa3 on go_mf_parents(_id, _parent_id); CREATE INDEX pa4 on go_mf_parents(_parent_id, _id); CREATE INDEX F1go_mf_parents ON go_mf_parents (_id); CREATE INDEX F2go_mf_parents ON go_mf_parents (_parent_id); CREATE INDEX pa5 on go_cc_parents(_id, _parent_id); CREATE INDEX pa6 on go_cc_parents(_parent_id, _id); CREATE INDEX F1go_cc_parents ON go_cc_parents (_id); CREATE INDEX F2go_cc_parents ON go_cc_parents (_parent_id); AnnotationDbi/inst/DBschemas/schemas_2.1/HUMANCHIP_DB.sql0000644000175200017520000000160114710217313023535 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.1/HUMAN_DB.sql0000644000175200017520000002140614710217313023076 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE omim ( _id INTEGER NOT NULL, -- REFERENCES genes omim_id CHAR(6) NOT NULL, -- OMIM ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ucsc ( _id INTEGER NOT NULL, -- REFERENCES genes ucsc_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Fomim ON omim (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); CREATE INDEX Fucsc ON ucsc (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/INPARANOID_DB.sql0000644000175200017520000007714114710217313023661 0ustar00biocbuildbiocbuildCREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255)); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL); CREATE TABLE Acyrthosiphon_pisum ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Aedes_aegypti ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Anopheles_gambiae ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Apis_mellifera ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Arabidopsis_thaliana ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Aspergillus_fumigatus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Batrachochytrium_dendrobatidis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Bombyx_mori ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Bos_taurus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Branchiostoma_floridae ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Brugia_malayi ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Caenorhabditis_brenneri ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Caenorhabditis_briggsae ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Caenorhabditis_elegans ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Caenorhabditis_japonica ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Caenorhabditis_remanei ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Candida_albicans ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Candida_glabrata ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Canis_familiaris ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Capitella_spI ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Cavia_porcellus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Chlamydomonas_reinhardtii ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Ciona_intestinalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Ciona_savignyi ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Coccidioides_immitis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Coprinopsis_cinereus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Cryptococcus_neoformans ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Cryptosporidium_hominis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Cryptosporidium_parvum ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Culex_pipiens ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Cyanidioschyzon_merolae ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Danio_rerio ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Daphnia_pulex ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Debaryomyces_hansenii ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Dictyostelium_discoideum ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Drosophila_ananassae ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Drosophila_grimshawi ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Drosophila_melanogaster ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Drosophila_mojavensis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Drosophila_pseudoobscura ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Drosophila_virilis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Drosophila_willistoni ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Entamoeba_histolytica ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Equus_caballus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Escherichia_coliK12 ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Fusarium_graminearum ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Gallus_gallus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Gasterosteus_aculeatus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Giardia_lamblia ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Helobdella_robusta ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Ixodes_scapularis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Kluyveromyces_lactis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Leishmania_major ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Lottia_gigantea ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Macaca_mulatta ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Magnaporthe_grisea ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Monodelphis_domestica ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Monosiga_brevicollis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Mus_musculus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Nasonia_vitripennis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Nematostella_vectensis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Neurospora_crassa ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Ornithorhynchus_anatinus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Oryza_sativa ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Oryzias_latipes ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Ostreococcus_tauri ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Pan_troglodytes ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Pediculus_humanus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Physcomitrella_patens ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Phytophthora_ramorum ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Phytophthora_sojae ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Plasmodium_falciparum ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Plasmodium_vivax ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Pongo_pygmaeus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Populus_trichocarpa ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Pristionchus_pacificus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Puccinia_graminis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Rattus_norvegicus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Rhizopus_oryzae ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Saccharomyces_cerevisiae ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Schistosoma_mansoni ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Schizosaccharomyces_pombe ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Sclerotinia_sclerotiorum ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Sorghum_bicolor ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Stagonospora_nodorum ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Strongylocentrotus_purpuratus ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Takifugu_rubripes ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Tetrahymena_thermophila ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Tetraodon_nigroviridis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Thalassiosira_pseudonana ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Theileria_annulata ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Theileria_parva ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Tribolium_castaneum ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Trichomonas_vaginalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Trichoplax_adhaerens ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Trypanosoma_cruzi ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Ustilago_maydis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Xenopus_tropicalis ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); CREATE TABLE Yarrowia_lipolytica ( inp_id VARCHAR(30) UNIQUE NOT NULL, clust_id INTEGER NOT NULL, species CHAR(5) NOT NULL, score VARCHAR(6) NOT NULL, seed_status CHAR(4)); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX ACYPI_c ON Acyrthosiphon_pisum(clust_id); CREATE INDEX ACYPI_s ON Acyrthosiphon_pisum(species); CREATE INDEX AEDAE_c ON Aedes_aegypti(clust_id); CREATE INDEX AEDAE_s ON Aedes_aegypti(species); CREATE INDEX ANOGA_c ON Anopheles_gambiae(clust_id); CREATE INDEX ANOGA_s ON Anopheles_gambiae(species); CREATE INDEX APIME_c ON Apis_mellifera(clust_id); CREATE INDEX APIME_s ON Apis_mellifera(species); CREATE INDEX ARATH_c ON Arabidopsis_thaliana(clust_id); CREATE INDEX ARATH_s ON Arabidopsis_thaliana(species); CREATE INDEX ASPFU_c ON Aspergillus_fumigatus(clust_id); CREATE INDEX ASPFU_s ON Aspergillus_fumigatus(species); CREATE INDEX BATDE_c ON Batrachochytrium_dendrobatidis(clust_id); CREATE INDEX BATDE_s ON Batrachochytrium_dendrobatidis(species); CREATE INDEX BOMMO_c ON Bombyx_mori(clust_id); CREATE INDEX BOMMO_s ON Bombyx_mori(species); CREATE INDEX BOSTA_c ON Bos_taurus(clust_id); CREATE INDEX BOSTA_s ON Bos_taurus(species); CREATE INDEX BRAFL_c ON Branchiostoma_floridae(clust_id); CREATE INDEX BRAFL_s ON Branchiostoma_floridae(species); CREATE INDEX BRUMA_c ON Brugia_malayi(clust_id); CREATE INDEX BRUMA_s ON Brugia_malayi(species); CREATE INDEX CAEBRE_c ON Caenorhabditis_brenneri(clust_id); CREATE INDEX CAEBRE_s ON Caenorhabditis_brenneri(species); CREATE INDEX CAEBR_c ON Caenorhabditis_briggsae(clust_id); CREATE INDEX CAEBR_s ON Caenorhabditis_briggsae(species); CREATE INDEX CAEEL_c ON Caenorhabditis_elegans(clust_id); CREATE INDEX CAEEL_s ON Caenorhabditis_elegans(species); CREATE INDEX CAEJA_c ON Caenorhabditis_japonica(clust_id); CREATE INDEX CAEJA_s ON Caenorhabditis_japonica(species); CREATE INDEX CAERE_c ON Caenorhabditis_remanei(clust_id); CREATE INDEX CAERE_s ON Caenorhabditis_remanei(species); CREATE INDEX CANAL_c ON Candida_albicans(clust_id); CREATE INDEX CANAL_s ON Candida_albicans(species); CREATE INDEX CANGL_c ON Candida_glabrata(clust_id); CREATE INDEX CANGL_s ON Candida_glabrata(species); CREATE INDEX CANFA_c ON Canis_familiaris(clust_id); CREATE INDEX CANFA_s ON Canis_familiaris(species); CREATE INDEX CAPSP_c ON Capitella_spI(clust_id); CREATE INDEX CAPSP_s ON Capitella_spI(species); CREATE INDEX CAVPO_c ON Cavia_porcellus(clust_id); CREATE INDEX CAVPO_s ON Cavia_porcellus(species); CREATE INDEX CHLRE_c ON Chlamydomonas_reinhardtii(clust_id); CREATE INDEX CHLRE_s ON Chlamydomonas_reinhardtii(species); CREATE INDEX CIOIN_c ON Ciona_intestinalis(clust_id); CREATE INDEX CIOIN_s ON Ciona_intestinalis(species); CREATE INDEX CIOSA_c ON Ciona_savignyi(clust_id); CREATE INDEX CIOSA_s ON Ciona_savignyi(species); CREATE INDEX COCIM_c ON Coccidioides_immitis(clust_id); CREATE INDEX COCIM_s ON Coccidioides_immitis(species); CREATE INDEX COPCI_c ON Coprinopsis_cinereus(clust_id); CREATE INDEX COPCI_s ON Coprinopsis_cinereus(species); CREATE INDEX CRYNE_c ON Cryptococcus_neoformans(clust_id); CREATE INDEX CRYNE_s ON Cryptococcus_neoformans(species); CREATE INDEX CRYHO_c ON Cryptosporidium_hominis(clust_id); CREATE INDEX CRYHO_s ON Cryptosporidium_hominis(species); CREATE INDEX CRYPA_c ON Cryptosporidium_parvum(clust_id); CREATE INDEX CRYPA_s ON Cryptosporidium_parvum(species); CREATE INDEX CULPI_c ON Culex_pipiens(clust_id); CREATE INDEX CULPI_s ON Culex_pipiens(species); CREATE INDEX CYAME_c ON Cyanidioschyzon_merolae(clust_id); CREATE INDEX CYAME_s ON Cyanidioschyzon_merolae(species); CREATE INDEX DANRE_c ON Danio_rerio(clust_id); CREATE INDEX DANRE_s ON Danio_rerio(species); CREATE INDEX DAPPU_c ON Daphnia_pulex(clust_id); CREATE INDEX DAPPU_s ON Daphnia_pulex(species); CREATE INDEX DEBHA_c ON Debaryomyces_hansenii(clust_id); CREATE INDEX DEBHA_s ON Debaryomyces_hansenii(species); CREATE INDEX DICDI_c ON Dictyostelium_discoideum(clust_id); CREATE INDEX DICDI_s ON Dictyostelium_discoideum(species); CREATE INDEX DROAN_c ON Drosophila_ananassae(clust_id); CREATE INDEX DROAN_s ON Drosophila_ananassae(species); CREATE INDEX DROGR_c ON Drosophila_grimshawi(clust_id); CREATE INDEX DROGR_s ON Drosophila_grimshawi(species); CREATE INDEX DROME_c ON Drosophila_melanogaster(clust_id); CREATE INDEX DROME_s ON Drosophila_melanogaster(species); CREATE INDEX DROMO_c ON Drosophila_mojavensis(clust_id); CREATE INDEX DROMO_s ON Drosophila_mojavensis(species); CREATE INDEX DROPS_c ON Drosophila_pseudoobscura(clust_id); CREATE INDEX DROPS_s ON Drosophila_pseudoobscura(species); CREATE INDEX DROVI_c ON Drosophila_virilis(clust_id); CREATE INDEX DROVI_s ON Drosophila_virilis(species); CREATE INDEX DROWI_c ON Drosophila_willistoni(clust_id); CREATE INDEX DROWI_s ON Drosophila_willistoni(species); CREATE INDEX ENTHI_c ON Entamoeba_histolytica(clust_id); CREATE INDEX ENTHI_s ON Entamoeba_histolytica(species); CREATE INDEX EQUCA_c ON Equus_caballus(clust_id); CREATE INDEX EQUCA_s ON Equus_caballus(species); CREATE INDEX ESCCO_c ON Escherichia_coliK12(clust_id); CREATE INDEX ESCCO_s ON Escherichia_coliK12(species); CREATE INDEX FUSGR_c ON Fusarium_graminearum(clust_id); CREATE INDEX FUSGR_s ON Fusarium_graminearum(species); CREATE INDEX GALGA_c ON Gallus_gallus(clust_id); CREATE INDEX GALGA_s ON Gallus_gallus(species); CREATE INDEX GASAC_c ON Gasterosteus_aculeatus(clust_id); CREATE INDEX GASAC_s ON Gasterosteus_aculeatus(species); CREATE INDEX GIALA_c ON Giardia_lamblia(clust_id); CREATE INDEX GIALA_s ON Giardia_lamblia(species); CREATE INDEX HELRO_c ON Helobdella_robusta(clust_id); CREATE INDEX HELRO_s ON Helobdella_robusta(species); CREATE INDEX IXOSC_c ON Ixodes_scapularis(clust_id); CREATE INDEX IXOSC_s ON Ixodes_scapularis(species); CREATE INDEX KLULA_c ON Kluyveromyces_lactis(clust_id); CREATE INDEX KLULA_s ON Kluyveromyces_lactis(species); CREATE INDEX LEIMA_c ON Leishmania_major(clust_id); CREATE INDEX LEIMA_s ON Leishmania_major(species); CREATE INDEX LOTGI_c ON Lottia_gigantea(clust_id); CREATE INDEX LOTGI_s ON Lottia_gigantea(species); CREATE INDEX MACMU_c ON Macaca_mulatta(clust_id); CREATE INDEX MACMU_s ON Macaca_mulatta(species); CREATE INDEX MAGGR_c ON Magnaporthe_grisea(clust_id); CREATE INDEX MAGGR_s ON Magnaporthe_grisea(species); CREATE INDEX MONDO_c ON Monodelphis_domestica(clust_id); CREATE INDEX MONDO_s ON Monodelphis_domestica(species); CREATE INDEX MONBR_c ON Monosiga_brevicollis(clust_id); CREATE INDEX MONBR_s ON Monosiga_brevicollis(species); CREATE INDEX MUSMU_c ON Mus_musculus(clust_id); CREATE INDEX MUSMU_s ON Mus_musculus(species); CREATE INDEX NASVI_c ON Nasonia_vitripennis(clust_id); CREATE INDEX NASVI_s ON Nasonia_vitripennis(species); CREATE INDEX NEMVE_c ON Nematostella_vectensis(clust_id); CREATE INDEX NEMVE_s ON Nematostella_vectensis(species); CREATE INDEX NEUCR_c ON Neurospora_crassa(clust_id); CREATE INDEX NEUCR_s ON Neurospora_crassa(species); CREATE INDEX ORNAN_c ON Ornithorhynchus_anatinus(clust_id); CREATE INDEX ORNAN_s ON Ornithorhynchus_anatinus(species); CREATE INDEX ORYSA_c ON Oryza_sativa(clust_id); CREATE INDEX ORYSA_s ON Oryza_sativa(species); CREATE INDEX ORYLA_c ON Oryzias_latipes(clust_id); CREATE INDEX ORYLA_s ON Oryzias_latipes(species); CREATE INDEX OSTTA_c ON Ostreococcus_tauri(clust_id); CREATE INDEX OSTTA_s ON Ostreococcus_tauri(species); CREATE INDEX PANTR_c ON Pan_troglodytes(clust_id); CREATE INDEX PANTR_s ON Pan_troglodytes(species); CREATE INDEX PEDPA_c ON Pediculus_humanus(clust_id); CREATE INDEX PEDPA_s ON Pediculus_humanus(species); CREATE INDEX PHYPA_c ON Physcomitrella_patens(clust_id); CREATE INDEX PHYPA_s ON Physcomitrella_patens(species); CREATE INDEX PHYRA_c ON Phytophthora_ramorum(clust_id); CREATE INDEX PHYRA_s ON Phytophthora_ramorum(species); CREATE INDEX PHYSO_c ON Phytophthora_sojae(clust_id); CREATE INDEX PHYSO_s ON Phytophthora_sojae(species); CREATE INDEX PLAFA_c ON Plasmodium_falciparum(clust_id); CREATE INDEX PLAFA_s ON Plasmodium_falciparum(species); CREATE INDEX PLAVI_c ON Plasmodium_vivax(clust_id); CREATE INDEX PLAVI_s ON Plasmodium_vivax(species); CREATE INDEX PONPY_c ON Pongo_pygmaeus(clust_id); CREATE INDEX PONPY_s ON Pongo_pygmaeus(species); CREATE INDEX POPTR_c ON Populus_trichocarpa(clust_id); CREATE INDEX POPTR_s ON Populus_trichocarpa(species); CREATE INDEX PRIPA_c ON Pristionchus_pacificus(clust_id); CREATE INDEX PRIPA_s ON Pristionchus_pacificus(species); CREATE INDEX PUCGR_c ON Puccinia_graminis(clust_id); CREATE INDEX PUCGR_s ON Puccinia_graminis(species); CREATE INDEX RATNO_c ON Rattus_norvegicus(clust_id); CREATE INDEX RATNO_s ON Rattus_norvegicus(species); CREATE INDEX RHIOR_c ON Rhizopus_oryzae(clust_id); CREATE INDEX RHIOR_s ON Rhizopus_oryzae(species); CREATE INDEX SACCE_c ON Saccharomyces_cerevisiae(clust_id); CREATE INDEX SACCE_s ON Saccharomyces_cerevisiae(species); CREATE INDEX SCHMA_c ON Schistosoma_mansoni(clust_id); CREATE INDEX SCHMA_s ON Schistosoma_mansoni(species); CREATE INDEX SCHPO_c ON Schizosaccharomyces_pombe(clust_id); CREATE INDEX SCHPO_s ON Schizosaccharomyces_pombe(species); CREATE INDEX SCLSC_c ON Sclerotinia_sclerotiorum(clust_id); CREATE INDEX SCLSC_s ON Sclerotinia_sclerotiorum(species); CREATE INDEX SORBI_c ON Sorghum_bicolor(clust_id); CREATE INDEX SORBI_s ON Sorghum_bicolor(species); CREATE INDEX STANO_c ON Stagonospora_nodorum(clust_id); CREATE INDEX STANO_s ON Stagonospora_nodorum(species); CREATE INDEX STRPU_c ON Strongylocentrotus_purpuratus(clust_id); CREATE INDEX STRPU_s ON Strongylocentrotus_purpuratus(species); CREATE INDEX TAKRU_c ON Takifugu_rubripes(clust_id); CREATE INDEX TAKRU_s ON Takifugu_rubripes(species); CREATE INDEX TETTH_c ON Tetrahymena_thermophila(clust_id); CREATE INDEX TETTH_s ON Tetrahymena_thermophila(species); CREATE INDEX TETNI_c ON Tetraodon_nigroviridis(clust_id); CREATE INDEX TETNI_s ON Tetraodon_nigroviridis(species); CREATE INDEX THAPS_c ON Thalassiosira_pseudonana(clust_id); CREATE INDEX THAPS_s ON Thalassiosira_pseudonana(species); CREATE INDEX THEAN_c ON Theileria_annulata(clust_id); CREATE INDEX THEAN_s ON Theileria_annulata(species); CREATE INDEX THEPA_c ON Theileria_parva(clust_id); CREATE INDEX THEPA_s ON Theileria_parva(species); CREATE INDEX TRICA_c ON Tribolium_castaneum(clust_id); CREATE INDEX TRICA_s ON Tribolium_castaneum(species); CREATE INDEX TRIVA_c ON Trichomonas_vaginalis(clust_id); CREATE INDEX TRIVA_s ON Trichomonas_vaginalis(species); CREATE INDEX TRIAD_c ON Trichoplax_adhaerens(clust_id); CREATE INDEX TRIAD_s ON Trichoplax_adhaerens(species); CREATE INDEX TRYCR_c ON Trypanosoma_cruzi(clust_id); CREATE INDEX TRYCR_s ON Trypanosoma_cruzi(species); CREATE INDEX USTMA_c ON Ustilago_maydis(clust_id); CREATE INDEX USTMA_s ON Ustilago_maydis(species); CREATE INDEX XENTR_c ON Xenopus_tropicalis(clust_id); CREATE INDEX XENTR_s ON Xenopus_tropicalis(species); CREATE INDEX YARLI_c ON Yarrowia_lipolytica(clust_id); CREATE INDEX YARLI_s ON Yarrowia_lipolytica(species); AnnotationDbi/inst/DBschemas/schemas_2.1/KEGG_DB.sql0000644000175200017520000000236414710217313022745 0ustar00biocbuildbiocbuildCREATE TABLE metadata ( name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE pathway2name ( path_id CHAR(5) NOT NULL UNIQUE, -- KEGG pathway short ID path_name VARCHAR(100) NOT NULL UNIQUE -- KEGG pathway name ); CREATE TABLE pathway2gene ( pathway_id CHAR(8) NOT NULL, -- KEGG pathway long ID gene_or_orf_id VARCHAR(20) NOT NULL -- Entrez Gene or ORF ID ); CREATE TABLE ath_NCBI_pathway2gene ( pathway_id CHAR(8) NOT NULL, -- KEGG pathway long ID gene_or_orf_id VARCHAR(20) NOT NULL -- Entrez Gene or ORF ID ); CREATE TABLE ec2go(ec_no VARCHAR(16),go_id CHAR(10)); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Ipathway2gene ON pathway2gene (gene_or_orf_id); CREATE INDEX ath_NCBI_Ipathway2gene ON ath_NCBI_pathway2gene (gene_or_orf_id); AnnotationDbi/inst/DBschemas/schemas_2.1/MALARIA_DB.sql0000644000175200017520000000766514710217313023307 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Falias ON alias (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/MOUSECHIP_DB.sql0000644000175200017520000000160114710217313023555 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.1/MOUSE_DB.sql0000644000175200017520000002137614710217313023124 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ucsc ( _id INTEGER NOT NULL, -- REFERENCES genes ucsc_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE mgi ( _id INTEGER NOT NULL, -- REFERENCES genes mgi_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); CREATE INDEX Fucsc ON ucsc (_id); CREATE INDEX Fmgi ON mgi (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/PFAM_DB.sql0000644000175200017520000000633514710217313022755 0ustar00biocbuildbiocbuildCREATE TABLE metadata ( name TEXT, value TEXT ); CREATE TABLE cazy ( ac VARCHAR(12) NOT NULL, --AC ID cazy VARCHAR(6) NOT NULL --CAZY ID ); CREATE TABLE homstrad ( ac VARCHAR(12) NOT NULL, --AC ID homstrad VARCHAR(20) NOT NULL --HOMSTRAD ID ); CREATE TABLE interpro ( ac VARCHAR(12) NOT NULL, --AC ID interpro VARCHAR(9) NOT NULL --INTERPRO ID ); CREATE TABLE load ( ac VARCHAR(12) NOT NULL, --AC ID load VARCHAR(15) NOT NULL --LOAD ID ); CREATE TABLE merops ( ac VARCHAR(12) NOT NULL, --AC ID merops VARCHAR(3) NOT NULL --MEROPS ID ); CREATE TABLE mim ( ac VARCHAR(12) NOT NULL, --AC ID mim VARCHAR(6) NOT NULL --MIM ID ); CREATE TABLE pdb ( ac VARCHAR(12) NOT NULL, --AC ID pdb VARCHAR(6) NOT NULL, --PDB ID start_point INTEGER, --start of alignment end_point INTEGER --end of alignment ); CREATE TABLE prints ( ac VARCHAR(12) NOT NULL, --AC ID prints VARCHAR(7) NOT NULL --PRINTS ID ); CREATE TABLE prosite ( ac VARCHAR(12) NOT NULL, --AC ID prosite VARCHAR(9) NOT NULL --PROSITE ID ); CREATE TABLE prosite_profile ( ac VARCHAR(12) NOT NULL, --AC ID prosite_profile VARCHAR(7) NOT NULL --PROSITE_PROFILE ID ); CREATE TABLE rm ( ac VARCHAR(12) NOT NULL, --AC ID rm VARCHAR(8) NOT NULL --RM ID ); CREATE TABLE scop ( ac VARCHAR(12) NOT NULL, --AC ID scop VARCHAR(4) NOT NULL, --SCOP ID placement VARCHAR(2) NOT NULL --SCOP placement ); CREATE TABLE smart ( ac VARCHAR(12) NOT NULL, --AC ID smart VARCHAR(9) NOT NULL --SMART ID ); CREATE TABLE tc ( ac VARCHAR(12) NOT NULL, --AC ID tc VARCHAR(6) NOT NULL --TC ID ); CREATE TABLE url ( ac VARCHAR(12) NOT NULL, --AC ID url VARCHAR(80) NOT NULL --URL ID ); CREATE TABLE id ( ac VARCHAR(12) NOT NULL, --AC ID id VARCHAR(15) NOT NULL --ID ID ); CREATE TABLE de ( ac VARCHAR(12) NOT NULL, --AC ID de VARCHAR(80) NOT NULL --DE ID ); CREATE TABLE tp ( ac VARCHAR(12) NOT NULL, --AC ID tp VARCHAR(6) NOT NULL --TP ID ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX cazy_ac ON cazy(ac); CREATE INDEX homstrad_ac ON homstrad(ac); CREATE INDEX interpro_ac ON interpro(ac); CREATE INDEX load_ac ON load(ac); CREATE INDEX merops_ac ON merops(ac); CREATE INDEX mim_ac ON mim(ac); CREATE INDEX pdb_ac ON pdb(ac); CREATE INDEX prints_ac ON prints(ac); CREATE INDEX prosite_ac ON prosite(ac); CREATE INDEX prosite_profile_ac ON prosite_profile(ac); CREATE INDEX rm_ac ON rm(ac); CREATE INDEX scop_ac ON scop(ac); CREATE INDEX smart_ac ON smart(ac); CREATE INDEX tc_ac ON tc(ac); CREATE INDEX url_ac ON url(ac); CREATE INDEX id_ac ON id(ac); CREATE INDEX de_ac ON de(ac); CREATE INDEX tp_ac ON tp(ac); AnnotationDbi/inst/DBschemas/schemas_2.1/PIG_DB.sql0000644000175200017520000001276514710217313022655 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/RATCHIP_DB.sql0000644000175200017520000000160114710217313023313 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.1/RAT_DB.sql0000644000175200017520000002043014710217313022650 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE cytogenetic_locations ( _id INTEGER NOT NULL, -- REFERENCES genes cytogenetic_location VARCHAR(20) NOT NULL, -- cytoband location FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Fcytogenetic_locations ON cytogenetic_locations (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/RHESUS_DB.sql0000644000175200017520000001551014710217313023236 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/WORMCHIP_DB.sql0000644000175200017520000000160114710217313023451 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.1/WORM_DB.sql0000644000175200017520000001606514710217313023017 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE wormbase ( _id INTEGER NOT NULL, -- REFERENCES genes wormbase_id VARCHAR(20) NOT NULL, -- wormbase id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); CREATE INDEX Fwormbase ON wormbase (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/XENOPUSCHIP_DB.sql0000644000175200017520000000160114710217313024026 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.1/XENOPUS_DB.sql0000644000175200017520000001235614710217313023373 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Funiprot ON uniprot (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/YEASTCHIP_DB.sql0000644000175200017520000000151414710217313023555 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE probes (probe_id VARCHAR(80), systematic_name VARCHAR(14) NULL, gene_name VARCHAR(14) NULL, sgd_id CHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (systematic_name); AnnotationDbi/inst/DBschemas/schemas_2.1/YEAST_DB.sql0000644000175200017520000001707014710217313023115 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sgd ( _id INTEGER PRIMARY KEY, systematic_name VARCHAR(14) NULL UNIQUE, -- Yeast gene systematic name gene_name VARCHAR(14) NULL UNIQUE, -- Yeast gene name sgd_id CHAR(10) NOT NULL UNIQUE -- SGD ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE chromosome_features ( _id INTEGER NOT NULL, -- REFERENCES sgd chromosome VARCHAR(2) NULL, -- chromosome name start INTEGER NULL, stop INTEGER NULL, feature_description TEXT NULL, -- Yeast feature description FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE gene2alias ( _id INTEGER NOT NULL, -- REFERENCES sgd alias VARCHAR(13) NOT NULL, -- Yeast gene alias FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES sgd pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES sgd go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES sgd path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES sgd ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES sgd pfam_id CHAR(7) NOT NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES sgd (_id)); CREATE TABLE smart ( _id INTEGER NOT NULL, -- REFERENCES sgd smart_id CHAR(7) NOT NULL, -- SMART ID FOREIGN KEY (_id) REFERENCES sgd (_id)); CREATE TABLE interpro ( _id INTEGER NOT NULL, -- REFERENCES sgd interpro_id CHAR(9) NOT NULL, -- InterPro ID FOREIGN KEY (_id) REFERENCES sgd (_id)); CREATE TABLE reject_orf ( systematic_name VARCHAR(14) PRIMARY KEY); CREATE TABLE gene2systematic ( gene_name VARCHAR(14) NULL, -- Yeast gene name systematic_name VARCHAR(14) NULL); CREATE TABLE genes ( _id INTEGER NOT NULL, -- REFERENCES sgd gene_id VARCHAR(20) NOT NULL, -- gene id FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES sgd ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES sgd ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES sgd ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES sgd prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES sgd trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES sgd uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES sgd (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES sgd accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES sgd (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosome_features ON chromosome_features (_id); CREATE INDEX Fgene2alias ON gene2alias(_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fsmart ON smart (_id); CREATE INDEX Finterpro ON interpro (_id); CREATE INDEX Fgene ON genes(_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); CREATE INDEX Frefseq ON refseq (_id); AnnotationDbi/inst/DBschemas/schemas_2.1/ZEBRAFISHCHIP_DB.sql0000644000175200017520000000160114710217313024202 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE accessions (probe_id VARCHAR(80),accession VARCHAR(20)); CREATE TABLE probes (probe_id VARCHAR(80), gene_id VARCHAR(10) NULL, is_multiple SMALLINT NOT NULL); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fgbprobes ON accessions (probe_id); CREATE INDEX Fprobes ON probes (probe_id); CREATE INDEX Fgenes ON probes (gene_id); AnnotationDbi/inst/DBschemas/schemas_2.1/ZEBRAFISH_DB.sql0000644000175200017520000002033314710217313023541 0ustar00biocbuildbiocbuildCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY, value VARCHAR(255) ); CREATE TABLE map_metadata ( map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL ); CREATE TABLE map_counts ( map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL ); CREATE TABLE genes ( _id INTEGER PRIMARY KEY, gene_id VARCHAR(10) NOT NULL UNIQUE -- Entrez Gene ID ); CREATE TABLE sqlite_stat1(tbl,idx,stat); CREATE TABLE gene_info ( _id INTEGER NOT NULL UNIQUE, -- REFERENCES genes gene_name VARCHAR(255) NOT NULL, -- gene name symbol VARCHAR(80) NOT NULL, -- gene symbol FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosomes ( _id INTEGER NOT NULL, -- REFERENCES genes chromosome VARCHAR(2) NOT NULL, -- chromosome name FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE accessions ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- GenBank accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE refseq ( _id INTEGER NOT NULL, -- REFERENCES genes accession VARCHAR(20) NOT NULL, -- RefSeq accession number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pubmed ( _id INTEGER NOT NULL, -- REFERENCES genes pubmed_id VARCHAR(10) NOT NULL, -- PubMed ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE unigene ( _id INTEGER NOT NULL, -- REFERENCES genes unigene_id VARCHAR(10) NOT NULL, -- UniGene ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chrlengths ( chromosome VARCHAR(2) PRIMARY KEY, -- chromosome name length INTEGER NOT NULL ); CREATE TABLE go_bp ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_bp_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_mf_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE go_cc_all ( _id INTEGER NOT NULL, -- REFERENCES genes go_id CHAR(10) NOT NULL, -- GO ID evidence CHAR(3) NOT NULL, -- GO evidence code FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE kegg ( _id INTEGER NOT NULL, -- REFERENCES genes path_id CHAR(5) NOT NULL, -- KEGG pathway short ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ec ( _id INTEGER NOT NULL, -- REFERENCES genes ec_number VARCHAR(13) NOT NULL, -- EC number FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE chromosome_locations ( _id INTEGER NOT NULL, -- REFERENCES genes seqname VARCHAR(20) NOT NULL, -- sequence name start_location INTEGER NOT NULL, end_location INTEGER NOT NULL, FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE pfam ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number pfam_id CHAR(7) NULL, -- Pfam ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE prosite ( _id INTEGER NOT NULL, -- REFERENCES genes ipi_id CHAR(11) NOT NULL, -- IPI accession number prosite_id CHAR(7) NULL, -- PROSITE ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE alias ( _id INTEGER NOT NULL, -- REFERENCES genes alias_symbol VARCHAR(80) NOT NULL, -- gene symbol or alias FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl2ncbi ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ncbi2ensembl ( _id INTEGER NOT NULL, -- REFERENCES genes ensembl_id VARCHAR(20) NOT NULL, -- ensembl id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_prot ( _id INTEGER NOT NULL, -- REFERENCES genes prot_id VARCHAR(20) NOT NULL, -- Ensembl Protein ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE ensembl_trans ( _id INTEGER NOT NULL, -- REFERENCES genes trans_id VARCHAR(20) NOT NULL, -- Ensembl Transcript ID FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE uniprot ( _id INTEGER NOT NULL, -- REFERENCES genes uniprot_id VARCHAR(20) NOT NULL, -- uniprot id FOREIGN KEY (_id) REFERENCES genes (_id) ); CREATE TABLE zfin ( _id INTEGER NOT NULL, -- REFERENCES genes zfin_id VARCHAR(20) NOT NULL, -- zfin id FOREIGN KEY (_id) REFERENCES genes (_id) ); -- Explicit index creation on the referencing column of all the foreign keys. -- Note that this is only needed for SQLite: PostgreSQL and MySQL create those -- indexes automatically. CREATE INDEX Fchromosomes ON chromosomes (_id); CREATE INDEX Faccessions ON accessions (_id); CREATE INDEX Frefseq ON refseq (_id); CREATE INDEX Fpubmed ON pubmed (_id); CREATE INDEX Funigene ON unigene (_id); CREATE INDEX Fgo_bp ON go_bp (_id); CREATE INDEX Fgo_bp_go_id ON go_bp (go_id); CREATE INDEX Fgo_mf ON go_mf (_id); CREATE INDEX Fgo_mf_go_id ON go_mf (go_id); CREATE INDEX Fgo_cc ON go_cc (_id); CREATE INDEX Fgo_cc_go_id ON go_cc (go_id); CREATE INDEX Fgo_bp_all ON go_bp_all (_id); CREATE INDEX Fgo_bp_all_go_id ON go_bp_all (go_id); CREATE INDEX Fgo_mf_all ON go_mf_all (_id); CREATE INDEX Fgo_mf_all_go_id ON go_mf_all (go_id); CREATE INDEX Fgo_cc_all ON go_cc_all (_id); CREATE INDEX Fgo_cc_all_go_id ON go_cc_all (go_id); CREATE INDEX Fkegg ON kegg (_id); CREATE INDEX Fec ON ec (_id); CREATE INDEX Fchromosome_locations ON chromosome_locations (_id); CREATE INDEX Fpfam ON pfam (_id); CREATE INDEX Fprosite ON prosite (_id); CREATE INDEX Falias ON alias (_id); CREATE INDEX Fensembl ON ensembl (_id); CREATE INDEX Fensembl2ncbi ON ensembl2ncbi (_id); CREATE INDEX Fncbi2ensembl ON ncbi2ensembl (_id); CREATE INDEX Fensemblp ON ensembl_prot (_id); CREATE INDEX Fensemblt ON ensembl_trans (_id); CREATE INDEX Funiprot ON uniprot (_id); CREATE INDEX Fzfin ON zfin (_id); AnnotationDbi/inst/NOTES-Herve0000644000175200017520000000460414710217313017167 0ustar00biocbuildbiocbuild- Fix this problem: library("org.Mm.eg.db") x <- org.Mm.egREFSEQ2EG mapped_seqs <- mappedkeys(x) y <- x[mapped_seqs] as.list(y) It occurs because the SQL statement is too long (the max length supported by SQLite seems to be 1000000 characters). For example, this will work: zz <- as.list(x[mapped_seqs[1:77403]]) but not this zz <- as.list(x[mapped_seqs[1:77404]]) nchar(toSQLStringSet(mapped_seqs[1:77404])) is 999869! - fix dbInfo() - in addition to dbschema(), provide a way to retrieve a high-level description of a given schema (UML? XML? via some S4 classes?) - add AnnotationDbi.Rnw vignette (main vignette) with more focus on the Bimap interface - fix the current INDEX mess (mix of old and new CREATE INDEX statements that lead to duplicated indices and an sqlite file bigger in size), I think all the old CREATE INDEX statements can be removed (they are the same as the new ones) except in GO_DB where some useful indices are missing in 0.9 - try adding a "go" (or "go_all") VIEW in the schema that contains the UNION of the go_[bp|cc|mf] (or go_[bp|cc|mf]_all) tables. 2 things to check carefully: the impact on the size of the SQLite file and the impact on the speed of the GO, GO2PROBES and GO2ALLPROBES maps (their definitions would first need to be modified to make them GoAnnDbBimap instances and have them use this new view as the right table instead of the 3 original tables). - look at subListExtract in Biobase and see where it can be used to improve speed in AnnotationDbi - pluggable maps -------------- If [to.tablename(x1),to.colname(x1)] (the right table/colname for a direct map, the left table/colname for a reverse map) is the same as [from.tablename(x2)|from.colname(x2)] (the left table/colname for a direct map, the right/colname table for a reverse map), and if inslot.to.keys(x1) and inslot.from.keys(x2) are both NAs, then x1 and x2 are "pluggable". x <- plugmaps(x1, x2), the result of the "plug" operation, is a map that goes from [from.tablename(x1),from.colname(x1)] to [to.tablename(x2)|to.colname(x2)]. Of course, only maps that belong to the same package will be pluggable this way (e.g. hgu95av2PATH2PROBE and hgu95av2ACCNUM, x1 is a reverse map and x2 a direct map). So, in fact, something else to check before to decide whether x1 and x2 are pluggable is that dbfile(x1) == dbfile(x2). AnnotationDbi/inst/TODO0000644000175200017520000000063414710217313015774 0ustar00biocbuildbiocbuildSome TODOs: 1) (from Marc) Add a function to the templates for all the classes to make the datacache available do this before we push out new devel packages in January. So near to where you see: @ANNOBJPREFIX@_dbInfo <- function() dbInfo(datacache) Add something that will produce: hgu95av2_datacache(), once it has been called. 2) Defunct CHR* family and PFAM and PROSITE. Coordinate with AnnotationForge. AnnotationDbi/inst/doc/0000755000175200017520000000000014710267466016064 5ustar00biocbuildbiocbuildAnnotationDbi/inst/doc/AnnotationDbi.R0000644000175200017520000002354414710267447020747 0ustar00biocbuildbiocbuild## ----style, eval=TRUE, echo=FALSE, results='asis'-------------------------- BiocStyle::latex() ## ----include=FALSE--------------------------------------------------------- library(knitr) opts_chunk$set(tidy=FALSE) ## ---- 0] # wantedp <- unique(unlist(wantedp)) # ans <- unlist(mget(wantedp, hgu95av2SYMBOL)) # }) # length(ans) # ans[1:10] ## ----schema, results='hide'------------------------------------------- hgu95av2_dbschema() ## ----schema2, results='hide'------------------------------------------ hgu95av2ORGPKG ## ----schema3, results='hide'------------------------------------------ org.Hs.eg_dbschema() ## ----hgu95av2_org_join, tidy=FALSE------------------------------------ orgDBLoc = system.file("extdata", "org.Hs.eg.sqlite", package="org.Hs.eg.db") attachSQL = paste("ATTACH '", orgDBLoc, "' AS orgDB;", sep = "") dbGetQuery(hgu95av2_dbconn(), attachSQL) ## ----complexDb-------------------------------------------------------- system.time({ SQL <- "SELECT DISTINCT probe_id,symbol FROM probes, orgDB.gene_info AS gi, orgDB.genes AS g, orgDB.go_bp AS bp WHERE bp._id=g._id AND gi._id=g._id AND probes.gene_id=g.gene_id AND bp.evidence IN ('IPI', 'IDA', 'IMP', 'IGI')" zz <- dbGetQuery(hgu95av2_dbconn(), SQL) }) #its a good idea to always DETACH your database when you are finished... dbGetQuery(hgu95av2_dbconn(), "DETACH orgDB" ) ## ----Question #6, echo=FALSE, results='hide'-------------------------- sql <- "SELECT gene_id, start_location, end_location, cytogenetic_location FROM genes AS g, chromosome_locations AS c, cytogenetic_locations AS cy WHERE g._id=c._id AND g._id=cy._id" dbGetQuery(org.Hs.eg_dbconn(),sql)[1:10,] ## ----Question #7, echo=FALSE, results='hide'-------------------------- orgDBLoc = system.file("extdata", "org.Hs.eg.sqlite", package="org.Hs.eg.db") attachSQL = paste("ATTACH '", orgDBLoc, "' AS orgDB;", sep = "") dbGetQuery(hgu95av2_dbconn(), attachSQL) goDBLoc = system.file("extdata", "GO.sqlite", package="GO.db") attachSQL = paste("ATTACH '", goDBLoc, "' AS goDB;", sep = "") dbGetQuery(hgu95av2_dbconn(), attachSQL) SQL <- "SELECT DISTINCT p.probe_id, gi.symbol, gt.go_id, gt.definition FROM probes AS p, orgDB.gene_info AS gi, orgDB.genes AS g, orgDB.go_bp AS bp, goDB.go_term AS gt WHERE bp._id=g._id AND gi._id=g._id AND p.gene_id=g.gene_id AND bp.evidence IN ('IPI', 'IDA', 'IMP', 'IGI') AND gt.go_id=bp.go_id" zz <- dbGetQuery(hgu95av2_dbconn(), SQL) dbGetQuery(hgu95av2_dbconn(), "DETACH orgDB") dbGetQuery(hgu95av2_dbconn(), "DETACH goDB") ## ----SessionInfo, echo=FALSE------------------------------------------ sessionInfo() AnnotationDbi/inst/doc/AnnotationDbi.Rnw0000644000175200017520000006654114710217313021303 0ustar00biocbuildbiocbuild%\VignetteIndexEntry{2. (Deprecated) How to use bimaps from the ".db" annotation packages} %\VignetteDepends{hgu95av2.db} %\VignetteKeywords{annotation, database} %\VignettePackage{AnnotationDbi} %\VignetteEngine{knitr::knitr} \documentclass[11pt]{article} <>= BiocStyle::latex() @ %% Excercises and Questions \usepackage{theorem} \theoremstyle{break} \newtheorem{Ex}{Exercise} \theoremstyle{break} \newtheorem{Q}{Question} %% And solution or answer \newenvironment{solution}{\color{blue}}{\bigskip} \title{How to use bimaps from the ".db" annotation packages} \author{Marc Carlson, Hervé Pagès, Seth Falcon, Nianhua Li} <>= library(knitr) opts_chunk$set(tidy=FALSE) @ \begin{document} \maketitle \textbf{NOTE} The `bimap' interface to annotation resources is not recommend; instead, use the approach in the vignette \href{http://bioconductor.org/packages/release/bioc/vignettes/AnnotationDbi/inst/doc/IntroToAnnotationPackages.pdf}{Introduction To Bioconductor Annotation Packages}. \section{Introduction} \subsubsection{Purpose} AnnotationDbi is used primarily to create mapping objects that allow easy access from R to underlying annotation databases. As such, it acts as the R interface for all the standard annotation packages. Underlying each AnnotationDbi supported annotation package is at least one (and often two) annotation databases. AnnotationDbi also provides schemas for theses databases. For each supported model organism, a standard gene centric database is maintained from public sources and is packaged up as an appropriate organism or "org" package. \subsubsection{Database Schemas} For developers, a lot of the benefits of having the information loaded into a real database will require some knowledge about the database schema. For this reason the schemas that were used in the creation of each database type are included in AnnotationDbi. The currently supported schemas are listed in the DBschemas directory of AnnotationDbi. But it is also possible to simply print out the schema that a package is currently using by using its "\_dbschema" method. There is one schema/database in each kind of package. These schemas specify which tables and indices will be present for each package of that type. The schema that a particular package is using is also listed when you type the name of the package as a function to obtain quality control information. The code to make most kinds of the new database packages is also included in AnnotationDbi. Please see the vignette on SQLForge for more details on how to make additional database packages. \subsubsection{Internal schema Design of org packages} The current design of the organism packages is deliberately simple and gene centric. Each table in the database contains a unique kind of information and also an internal identifier called \_id. The internal \_id has no meaning outside of the context of a single database. But \_id does connect all the data within a single database. As an example if we wanted to connect the values in the genes table with the values in the kegg table, we could simply join the two tables using the internal \_id column. It is very important to note however that \_id does not have any absolute significance. That is, it has no meaning outside of the context of the database where it is used. It is tempting to think that an \_id could have such significance because within a single database, it looks and behaves similarly to an entrez gene ID. But \_id is definitely NOT an entrez gene ID. The entrez gene IDs are in another table entirely, and can be connected to using the internal \_id just like all the other meaningful information inside these databases. Each organism package is centered around one type of gene identifier. This identifier is found as the gene\_id field in the genes table and is both the central ID for the database as well as the foreign key that chip packages should join to. The chip packages are 'lightweight', and only contain information about the basic probe to gene mapping. You might wonder how such packages can provide access to all the other information that they do. This is possible because all the other data provided by chip packages comes from joins that are performed by AnnotationDbi behind the scenes at run time. All chip packages have a dependency on at least one organism package. The name of the organism package being depended on can be found by looking at its "ORGPKG" value. To learn about the schema from the appropriate organism package, you will need to look at the "\_dbschema" method for that package. In the case of the chip packages, the gene\_id that in these packages is mapped to the probe\_ids, is used as a foreign key to the appropriate organism package. Specialized packages like the packages for GO and KEGG, will have their own schemas but will also adhere to the use of an internal \_id for joins between their tables. As with the organism packages, this \_id is not suitable for use as a foreign key. For a complete listing of the different schemas used by various packages, users can use the \Rfunction{available.dbschemas} function. This list will also tell you which model organisms are supported. <<>= library(DBI) library(org.Hs.eg.db) library(AnnotationForge) available.dbschemas() @ \section{Examples} \subsubsection{Basic information} The \Rpackage{AnnotationDbi} package provides an interface to SQLite-based annotation packages. Each SQLite-based annotation package (identified by a ``.db'' suffix in the package name) contains a number of \Rclass{AnnDbBimap} objects in place of the \Rclass{environment} objects found in the old-style environment-based annotation packages. The API provided by \Rpackage{AnnotationDbi} allows you to treat the \Rclass{AnnDbBimap} objects like \Rclass{environment} instances. For example, the functions \verb+[[+, \Rfunction{get}, \Rfunction{mget}, and \Rfunction{ls} all behave the same as they did with the older environment based annotation packages. In addition, new methods like \Rfunction{[}, \Rfunction{toTable}, \Rfunction{subset} and others provide some additional flexibility in accessing the annotation data. <>= options(continue=" ", prompt="R> ", width=72L) @ <>= library(hgu95av2.db) @ The same basic set of objects is provided with the db packages: <>= ls("package:hgu95av2.db") @ \begin{Ex} Start an R session and use the \Rfunction{library} function to load the \Rpackage{hgu95av2.db} software package. Use search() to see that an organism package was also loaded and then use the approriate "\_dbschema" methods to the schema for the \Rpackage{hgu95av2.db} and \Rpackage{org.Hs.eg.db} packages. <>= library(hgu95av2.db) search() hgu95av2_dbschema() org.Hs.eg_dbschema() @ \end{Ex} It is possible to call the package name as a function to get some QC information about it. <>= qcdata = capture.output(hgu95av2()) head(qcdata, 20) @ Alternatively, you can get similar information on how many items are in each of the provided maps by looking at the MAPCOUNTs: <>= hgu95av2MAPCOUNTS @ To demonstrate the \Rclass{environment} API, we'll start with a random sample of probe set IDs. <>= all_probes <- ls(hgu95av2ENTREZID) length(all_probes) set.seed(0xa1beef) probes <- sample(all_probes, 5) probes @ The usual ways of accessing annotation data are also available. <>= hgu95av2ENTREZID[[probes[1]]] hgu95av2ENTREZID$"31882_at" syms <- unlist(mget(probes, hgu95av2SYMBOL)) syms @ The annotation packages provide a huge variety of information in each package. Some common types of information include gene symbols (SYMBOL), GO terms (GO), KEGG pathway IDs (KEGG), ENSEMBL IDs (ENSEMBL) and chromosome start and stop locations (CHRLOC and CHRLOCEND). Each mapping will have a manual page that you can read to describe the data in the mapping and where it came from. <>= ?hgu95av2CHRLOC @ \begin{Ex} For the probes in 'probes' above, use the annotation mappings to find the chromosome start locations. <>= mget(probes, hgu95av2CHRLOC, ifnotfound=NA)[1:2] @ \end{Ex} \subsubsection{Manipulating Bimap Objects} Many filtering operations on the annotation \Rclass{Bimap} objects require conversion of the \Rclass{AnnDbBimap} into a \Rclass{list}. In general, converting to lists will not be the most efficient way to filter the annotation data when using a SQLite-based package. Compare the following two examples for how you could get the 1st ten elements of the hgu95av2SYMBOL mapping. In the 1st case we have to get the entire mapping into list form, but in the second case we first subset the mapping object itself and this allows us to only convert the ten elements that we care about. <>= system.time(as.list(hgu95av2SYMBOL)[1:10]) ## vs: system.time(as.list(hgu95av2SYMBOL[1:10])) @ There are many different kinds of \Rclass{Bimap} objects in AnnotationDbi, but most of them are of class \Rclass{AnnDbBimap}. All /Rclass{Bimap} objects represent data as a set of left and right keys. The typical usage of these mappings is to search for right keys that match a set of left keys that have been supplied by the user. But sometimes it is also convenient to go in the opposite direction. The annotation packages provide many reverse maps as objects in the package name space for backwards compatibility, but the reverse mappings of almost any map is also available using \Rfunction{revmap}. Since the data are stored as tables, no extra disk space is needed to provide reverse mappings. <>= unlist(mget(syms, revmap(hgu95av2SYMBOL))) @ So now that you know about the \Rfunction{revmap} function you might try something like this: <>= as.list(revmap(hgu95av2PATH)["00300"]) @ Note that in the case of the PATH map, we don't need to use revmap(x) because hgu95av2.db already provides the PATH2PROBE map: <>= x <- hgu95av2PATH ## except for the name, this is exactly revmap(x) revx <- hgu95av2PATH2PROBE revx2 <- revmap(x, objName="PATH2PROBE") revx2 identical(revx, revx2) as.list(revx["00300"]) @ Note that most maps are reversible with \Rfunction{revmap}, but some (such as the more complex GO mappings), are not. Why is this? Because to reverse a mapping means that there has to be a "value" that will always become the "key" on the newly reversed map. And GO mappings have several distinct possibilities to choose from (GO ID, Evidence code or Ontology). In non-reversible cases like this, AnnotationDbi will usually provide a pre-defined reverse map. That way, you will always know what you are getting when you call \Rfunction{revmap} While we are on the subject of GO and GO mappings, there are a series of special methods for GO mappings that can be called to find out details about these IDs. \Rfunction{Term},\Rfunction{GOID}, \Rfunction{Ontology}, \Rfunction{Definition},\Rfunction{Synonym}, and \Rfunction{Secondary} are all useful ways of getting additional information about a particular GO ID. For example: <>= Term("GO:0000018") Definition("GO:0000018") @ \begin{Ex} Given the following set of RefSeq IDs: c("NG\_005114","NG\_007432","NG\_008063"), Find the Entrez Gene IDs that would correspond to those. Then find the GO terms that are associated with those entrez gene IDs. \Rpackage{org.Hs.eg.db} packages. <>= rs = ls(revmap(org.Hs.egREFSEQ))[4:6] EGs = mget(rs, revmap(org.Hs.egREFSEQ), ifnotfound=NA) ##Then get the GO terms. GOs = mget(unlist(EGs), org.Hs.egGO, ifnotfound=NA) GOs ##Extract the GOIDs from this list: GOIDs = as.character(unique(sapply(GOs, names))) ##Then look up what these terms are: Term(GOIDs) @ \end{Ex} \subsubsection{The Contents and Structure of Bimap Objects} Sometimes you may want to display or subset elements from an individual map. A \Rclass{Bimap} interface is available to access the data in table (\Rclass{data.frame}) format using \Rfunction{[} and \Rfunction{toTable}. <>= head(toTable(hgu95av2GO[probes])) @ The \Rfunction{toTable} function will display all of the information in a \Rclass{Bimap}. This includes both the left and right values along with any other attributes that might be attached to those values. The left and right keys of the \Rclass{Bimap} can be extracted using \Rfunction{Lkeys} and \Rfunction{Rkeys}. If is is necessary to only display information that is directly associated with the left to right links in a \Rclass{Bimap}, then the \Rfunction{links} function can be used. The \Rfunction{links} returns a data frame with one row for each link in the bimap that it is applied to. It only reports the left and right keys along with any attributes that are attached to the edge between these two values. Note that the order of the cols returned by \Rfunction{toTable} does not depend on the direction of the map. We refer to it as an 'undirected method': <>= toTable(x)[1:6, ] toTable(revx)[1:6, ] @ Notice however that the Lkeys are always on the left (1st col), the Rkeys always in the 2nd col For length() and keys(), the result does depend on the direction, hence we refer to these as 'directed methods': <>= length(x) length(revx) allProbeSetIds <- keys(x) allKEGGIds <- keys(revx) @ There are more 'undirected' methods listed below: <>= junk <- Lkeys(x) # same for all maps in hgu95av2.db (except pseudo-map # MAPCOUNTS) Llength(x) # nb of Lkeys junk <- Rkeys(x) # KEGG ids for PATH/PATH2PROBE maps, GO ids for # GO/GO2PROBE/GO2ALLPROBES maps, etc... Rlength(x) # nb of Rkeys @ Notice how they give the same result for x and revmap(x) You might be tempted to think that \Rfunction{Lkeys} and \Rfunction{Llength} will tell you all that you want to know about the left keys. But things are more complex than this, because not all keys are mapped. Often, you will only want to know about the keys that are mapped (ie. the ones that have a corresponding Rkey). To learn this you want to use the \Rfunction{mappedkeys} or the undirected variants \Rfunction{mappedLkeys} and \Rfunction{mappedRkeys}. Similarily, the \Rfunction{count.mappedkeys}, \Rfunction{count.mappedLkeys} and \Rfunction{count.mappedRkeys} methods are very fast ways to determine how many keys are mapped. Accessing keys like this is usually very fast and so it can be a decent strategy to subset the mapping by 1st using the mapped keys that you want to find. <>= x = hgu95av2ENTREZID[1:10] ## Directed methods mappedkeys(x) # mapped keys count.mappedkeys(x) # nb of mapped keys ## Undirected methods mappedLkeys(x) # mapped left keys count.mappedLkeys(x) # nb of mapped Lkeys @ If you want to find keys that are not mapped to anything, you might want to use \Rfunction{isNA}. <>= y = hgu95av2ENTREZID[isNA(hgu95av2ENTREZID)] # usage like is.na() Lkeys(y)[1:4] @ \begin{Ex} How many probesets do not have a GO mapping for the \Rpackage{hgu95av2.db} package? How many have no mapping? Find a probeset that has a GO mapping. Now look at the GO mappings for this probeset in table form. <>= count.mappedLkeys(hgu95av2GO) Llength(hgu95av2GO) - count.mappedLkeys(hgu95av2GO) mappedLkeys(hgu95av2GO)[1] toTable(hgu95av2GO["1000_at"]) @ \end{Ex} \subsubsection{Some specific examples} Lets use what we have learned to get information about the probes that are are not assigned to a chromosome: <>= x <- hgu95av2CHR Rkeys(x) chroms <- Rkeys(x)[23:24] chroms Rkeys(x) <- chroms toTable(x) @ To get this in the classic named-list format: <>= z <- as.list(revmap(x)[chroms]) names(z) z[["Y"]] @ Many of the common methods for accessing \Rclass{Bimap} objects return things in list format. This can be convenient. But you have to be careful about this if you want to use unlist(). For example the following will return multiple probes for each chromosome: <>= chrs = c("12","6") mget(chrs, revmap(hgu95av2CHR[1:30]), ifnotfound=NA) @ But look what happens here if we try to unlist that: <>= unlist(mget(chrs, revmap(hgu95av2CHR[1:30]), ifnotfound=NA)) @ Yuck! One trick that will sometimes help is to use Rfunction{unlist2}. But be careful here too. Depending on what step comes next, Rfunction{unlist2} may not really help you... <>= unlist2(mget(chrs, revmap(hgu95av2CHR[1:30]), ifnotfound=NA)) @ Lets ask if the probes in 'pbids' mapped to cytogenetic location "18q11.2"? <>= x <- hgu95av2MAP pbids <- c("38912_at", "41654_at", "907_at", "2053_at", "2054_g_at", "40781_at") x <- subset(x, Lkeys=pbids, Rkeys="18q11.2") toTable(x) @ To coerce this map to a named vector: <>= pb2cyto <- as.character(x) pb2cyto[pbids] @ The coercion of the reverse map works too but issues a warning because of the duplicated names for the reasons stated above: <>= cyto2pb <- as.character(revmap(x)) @ \subsubsection{Accessing probes that map to multiple targets} In many probe packages, some probes are known to map to multiple genes. The reasons for this can be biological as happens in the arabidopsis packages, but usually it is due to the fact that the genome builds that chip platforms were based on were less stable than desired. Thus what may have originally been a probe designed to measure one thing can end up measuring many things. Usually you don't want to use probes like this, because if they manufacturer doesn't know what they map to then their usefullness is definitely suspect. For this reason, by default all chip packages will normally hide such probes in the standard mappings. But sometimes you may want access to the answers that the manufacturer says such a probe will map to. In such cases, you will want to use the \Rfunction{toggleProbes} method. To use this method, just call it on a standard mapping and copy the result into a new mapping (you cannot alter the original mapping). Then treat the new mapping as you would any other mapping. <>= ## How many probes? dim(hgu95av2ENTREZID) ## Make a mapping with multiple probes exposed multi <- toggleProbes(hgu95av2ENTREZID, "all") ## How many probes? dim(multi) @ If you then decide that you want to make a mapping that has only multiple mappings or you wish to revert one of your maps back to the default state of only showing the single mappings then you can use \Rfunction{toggleProbes} to switch back and forth. <>= ## Make a mapping with ONLY multiple probes exposed multiOnly <- toggleProbes(multi, "multiple") ## How many probes? dim(multiOnly) ## Then make a mapping with ONLY single mapping probes singleOnly <- toggleProbes(multiOnly, "single") ## How many probes? dim(singleOnly) @ Finally, there are also a pair of test methods \Rfunction{hasMultiProbes} and \Rfunction{hasSingleProbes} that can be used to see what methods a mapping presently has exposed. <>= ## Test the multiOnly mapping hasMultiProbes(multiOnly) hasSingleProbes(multiOnly) ## Test the singleOnly mapping hasMultiProbes(singleOnly) hasSingleProbes(singleOnly) @ \subsubsection{Using SQL to access things directly} While the mapping objects provide a lot of convenience, sometimes there are definite benefits to writing a simple SQL query. But in order to do this, it is necessary to know a few things. The 1st thing you will need to know is some SQL. Fortunately, it is quite easy to learn enough basic SQL to get stuff out of a database. Here are 4 basic SQL things that you may find handy: First, you need to know about SELECT statements. A simple example would look something like this: SELECT * FROM genes; Which would select everything from the genes table. SELECT gene\_id FROM genes; Will select only the gene\_id field from the genes table. Second you need to know about WHERE clauses: SELECT gene\_id,\_id FROM genes WHERE gene\_id=1; Will only get records from the genes table where the gene\_id is = 1. Thirdly, you will want to know about an inner join: SELECT * FROM genes,chromosomes WHERE genes.\_id=chromosomes.\_id; This is only slightly more complicated to understand. Here we want to get all the records that are in both the 'genes' and 'chromosomes' tables, but we only want ones where the '\_id' field is identical. This is known as an inner join because we only want the elements that are in both of these tables with respect to '\_id'. There are other kinds of joins that are worth learning about, but most of the time, this is all you will need to do. Finally, it is worthwhile to learn about the AS keyword which is useful for making long queries easier to read. For the previous example, we could have written it this way to save space: SELECT * FROM genes AS g,chromosomes AS c WHERE g.\_id=c.\_id; In a simple example like this you might not see a lot of savings from using AS, so lets consider what happens when we want to also specify which fields we want: SELECT g.gene\_id,c.chromosome FROM genes AS g,chromosomes AS c WHERE g.\_id=c.\_id; Now you are most of the way there to being able to query the databases directly. The only other thing you need to know is a little bit about how to access these databases from R. With each package, you will also get a method that will print the schema for its database, you can view this to see what sorts of tables are present etc. <>= org.Hs.eg_dbschema() @ To access the data in a database, you will need to connect to it. Fortunately, each package will automatically give you a connection object to that database when it loads. <>= org.Hs.eg_dbconn() @ You can use this connection object like this: <>= query <- "SELECT gene_id FROM genes LIMIT 10;" result = dbGetQuery(org.Hs.eg_dbconn(), query) result @ \begin{Ex} Retrieve the entrez gene ID and chromosome by using a database query. Show how you could do the same thing by using \Rfunction{toTable} <>= sql <- "SELECT gene_id, chromosome FROM genes AS g, chromosomes AS c WHERE g._id=c._id;" dbGetQuery(org.Hs.eg_dbconn(),sql)[1:10,] ##OR toTable(org.Hs.egCHR)[1:10,] @ \end{Ex} \subsubsection{Combining data from multiple annotation packages at the SQL level} For a more complex example, consider the task of obtaining all gene symbols which are probed on a chip that have at least one GO BP ID annotation with evidence code IMP, IGI, IPI, or IDA. Here is one way to extract this using the environment-based packages: <>= ## Obtain SYMBOLS with at least one GO BP ## annotation with evidence IMP, IGI, IPI, or IDA. system.time({ bpids <- eapply(hgu95av2GO, function(x) { if (length(x) == 1 && is.na(x)) NA else { sapply(x, function(z) { if (z$Ontology == "BP") z$GOID else NA }) } }) bpids <- unlist(bpids) bpids <- unique(bpids[!is.na(bpids)]) g2p <- mget(bpids, hgu95av2GO2PROBE) wantedp <- lapply(g2p, function(x) { x[names(x) %in% c("IMP", "IGI", "IPI", "IDA")] }) wantedp <- wantedp[sapply(wantedp, length) > 0] wantedp <- unique(unlist(wantedp)) ans <- unlist(mget(wantedp, hgu95av2SYMBOL)) }) length(ans) ans[1:10] @ All of the above code could have been reduced to a single SQL query with the SQLite-based packages. But to put together this query, you would need to look 1st at the schema to know what tables are present: <>= hgu95av2_dbschema() @ This function will give you an output of all the create table statements that were used to generate the hgu95av2 database. In this case, this is a chip package, so you will also need to see the schema for the organism package that it depends on. To learn what package it depends on, look at the ORGPKG value: <>= hgu95av2ORGPKG @ Then you can see that schema by looking at its schema method: <>= org.Hs.eg_dbschema() @ So now we can see that we want to connect the data in the go\_bp, and symbol tables from the org.Hs.eg.sqlite database along with the probes data in the hgu95av2.sqlite database. How can we do that? It turns out that one of the great conveniences of SQLite is that it allows other databases to be `ATTACHed'. Thus, we can keep our data in many differnt databases, and then 'ATTACH' them to each other in a modular fashion. The databases for a given build have been built together and frozen into a single version specifically to allow this sort of behavoir. To use this feature, the SQLite ATTACH command requires the filename for the database file on your filesystem. Fortunately, R provides a nice system independent way of getting that information. Note that the name of the database is always the same as the name of the package, with the suffix '.sqlite'.: <>= orgDBLoc = system.file("extdata", "org.Hs.eg.sqlite", package="org.Hs.eg.db") attachSQL = paste("ATTACH '", orgDBLoc, "' AS orgDB;", sep = "") dbGetQuery(hgu95av2_dbconn(), attachSQL) @ Finally, you can assemble a cross-db sql query and use the helper function as follows. Note that when we want to refer to tables in the attached database, we have to use the 'orgDB' prefix that we specified in the 'ATTACH' query above.: <>= system.time({ SQL <- "SELECT DISTINCT probe_id,symbol FROM probes, orgDB.gene_info AS gi, orgDB.genes AS g, orgDB.go_bp AS bp WHERE bp._id=g._id AND gi._id=g._id AND probes.gene_id=g.gene_id AND bp.evidence IN ('IPI', 'IDA', 'IMP', 'IGI')" zz <- dbGetQuery(hgu95av2_dbconn(), SQL) }) #its a good idea to always DETACH your database when you are finished... dbGetQuery(hgu95av2_dbconn(), "DETACH orgDB" ) @ \begin{Ex} Retrieve the entrez gene ID, chromosome location information and cytoband infomration by using a single database query. <>= sql <- "SELECT gene_id, start_location, end_location, cytogenetic_location FROM genes AS g, chromosome_locations AS c, cytogenetic_locations AS cy WHERE g._id=c._id AND g._id=cy._id" dbGetQuery(org.Hs.eg_dbconn(),sql)[1:10,] @ \end{Ex} \begin{Ex} Expand on the example in the text above to combine data from the \Rpackage{hgu95av2.db} and \Rpackage{org.Hs.eg.db} with the \Rpackage{GO.db} package so as to include the GO ID, and term definition in the output. <>= orgDBLoc = system.file("extdata", "org.Hs.eg.sqlite", package="org.Hs.eg.db") attachSQL = paste("ATTACH '", orgDBLoc, "' AS orgDB;", sep = "") dbGetQuery(hgu95av2_dbconn(), attachSQL) goDBLoc = system.file("extdata", "GO.sqlite", package="GO.db") attachSQL = paste("ATTACH '", goDBLoc, "' AS goDB;", sep = "") dbGetQuery(hgu95av2_dbconn(), attachSQL) SQL <- "SELECT DISTINCT p.probe_id, gi.symbol, gt.go_id, gt.definition FROM probes AS p, orgDB.gene_info AS gi, orgDB.genes AS g, orgDB.go_bp AS bp, goDB.go_term AS gt WHERE bp._id=g._id AND gi._id=g._id AND p.gene_id=g.gene_id AND bp.evidence IN ('IPI', 'IDA', 'IMP', 'IGI') AND gt.go_id=bp.go_id" zz <- dbGetQuery(hgu95av2_dbconn(), SQL) dbGetQuery(hgu95av2_dbconn(), "DETACH orgDB") dbGetQuery(hgu95av2_dbconn(), "DETACH goDB") @ \end{Ex} The version number of R and packages loaded for generating the vignette were: <>= sessionInfo() @ \end{document} AnnotationDbi/inst/doc/AnnotationDbi.pdf0000644000175200017520000065365514710267451021326 0ustar00biocbuildbiocbuild%PDF-1.5 % 54 0 obj << /Length 1867 /Filter /FlateDecode >> stream xڵXK4p傦qlK~$*@ )I̘?vk=^$v%ZV?nM*xh>OV*~g88~qv f c1%4OG2ݹ,vvP^ЏYcdL$(&!> /icpOQ`Z݌DA:g4V$Cʃ,ߤ^3d):lg*I-sY1%yl0?Ç/ ߣ8 TKV)ylCX偍)g}`x,E^%[ВpӮHc`ׁ\ $.}5ІI\Kpq̰WPя/9ɃHE.Bծv@/Jt[?LTT3Dg/\!Y+Cf8Kk|E{GNX^XF0~Be^Gx#c\ 8f=3.CF~%QK) ^l-5tS,B+b s G&O "/o s #_cZʑX؅> stream xڽk6 a2U%zݷI{-.mnC!KF=6-V$m ,h8Ҿu|w/ |/8數rx ]nuZǾCMRu'(^i4mx} M |wU?|a8z~ȏ$`[oQ>EB|Fg^F,Z^7ra5CՁ5K|^f+Jh72v3lϔ0K+Q`5%ֺGAcUR9`1ەJn73iezK6k0u.j!7%OUc&:Sx(?Hg싼!A`&_# Fi@nNm4= v7@()FlXƽu=buʬr ,1F Yy]W(v[;1wyϐe4[IC$*a`>VdIEO}6 geC $ :<9{g 9B`k~ *8nB)yYDFz[lx|ff4QS C^aMVG@e*6IPTVgwbe(ڱ.ga$!{{Ao@ivFR"ssQ~*#}w6g*N݇{@4`RAڡŮ=r[=3b'u yia?T9 Nuأ0Q8ySTBөXh?q8 }SbB8 +&{uPZ ɼU3>WXCM!K;T \j{4o$k&0؏ivNI/1!6ӔNtӾyͥ&kvN 4L7u!":ͱT=x& _V(qc]^^2a<A0^Q( 4(ނu (S CEơ>-YB yY4YI'hS `sMCԐڼE@Y8 Jbl3֖iy^F*+ej]ǰ#'p笧сix,#6'% Ⱥm쑸x8OK:'}\~AǪPcsT|Xǵ,y&T67ŏJ5Mmv hI57q{ΣX ф:uk"!`]s#!Uq G^H:C>vY ؕJJvPj?8H }[Ζb`WBijE@:@,E4WEJEpMA"BS,t`B9Kc`w@?#QH mSږmXd&\iJ&~яAeHcS6 $~L/P=)@{#NQ 'F؃ \֔`p.S*ڽn: =FG!cI ?uSax~6;Pr"Xnl0=^HOQ])A3 έa@Y ]M9=~+"cQBkdÐnoRH6e@$ӈ nF - 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Ƹb> endobj 255 0 obj << /Type /ObjStm /N 9 /First 70 /Length 381 /Filter /FlateDecode >> stream xڍTn0s,{(Rܺ˩ʁ&VCc0SpT 4y36.s$[⒬ @͠@NaTLNy-IXmWrkg"%Y ܜE0) ;.IfdվjÎC*Y,ƒTJ#T}_6wPu[Շ &Ph$hHہ<}g̘#c9$$(bIw߁t"R$x)ʥE K,tr<˔ITwՆ({[Vx+\׶j'n'WڃsoVjvIEmwboG mٖzdϤj-'өU.RBEzc;Mݺn?: endstream endobj 265 0 obj << /Type /XRef /Index [0 266] /Size 266 /W [1 3 1] /Root 263 0 R /Info 264 0 R /ID [<5905C0B30F9995B3496A2E52874321DF> <5905C0B30F9995B3496A2E52874321DF>] /Length 692 /Filter /FlateDecode >> stream x%Oaǯy)"BDQQ֛~"M)%a6[ٲ9Pl3f 8đ͉CGuuq?~,2wjk0I .P2PA6AdT`Mv{ƨVBH6JvsT` 8B6B0\ngn !S͠ pb}r}ݠ`.PZqcT[ @[iZ&R@[ŴAhpz 8Z@[O58`nEu3 tf5A[_UF,:bQ*5,m2nc5@t MP4Ц.~W&]L+iFݮ~T&_$۵'t" ]nͨq>d=Xیp< ps} Ɔs@P6EA1gal@PХ ;]p25t@bne2;_<ԀjՑ΀um:4tz%n۷Y%qwFUڽmq1}BUƣ̨6^jh陪7:>= BiocStyle::latex() @ %% Question, Exercise, Solution \usepackage{theorem} \theoremstyle{break} \newtheorem{Ext}{Exercise} \newtheorem{Question}{Question} \newenvironment{Exercise}{ \renewcommand{\labelenumi}{\alph{enumi}.}\begin{Ext}% }{\end{Ext}} \newenvironment{Solution}{% \noindent\textbf{Solution:}\renewcommand{\labelenumi}{\alph{enumi}.}% }{\bigskip} \title{AnnotationDbi: Introduction To Bioconductor Annotation Packages} \author{Marc Carlson} <>= library(knitr) opts_chunk$set(tidy=FALSE) @ \begin{document} \maketitle \begin{figure}[ht] \centering \includegraphics[width=.6\textwidth]{databaseTypes.pdf} \caption{Annotation Packages: the big picture} \label{fig:dbtypes} \end{figure} \Bioconductor{} provides extensive annotation resources. These can be \emph{gene centric}, or \emph{genome centric}. Annotations can be provided in packages curated by \Bioconductor, or obtained from web-based resources. This vignette is primarily concerned with describing the annotation resources that are available as packages. More advanced users who wish to learn about how to make new annotation packages should see the vignette titled "Creating select Interfaces for custom Annotation resources" from the \Rpackage{AnnotationForge} package. Gene centric \Rpackage{AnnotationDbi} packages include: \begin{itemize} \item Organism level: e.g. \Rpackage{org.Mm.eg.db}. \item Platform level: e.g. \Rpackage{hgu133plus2.db}, \Rpackage{hgu133plus2.probes}, \Rpackage{hgu133plus2.cdf}. \item System-biology level: \Rpackage{GO.db} \end{itemize} Genome centric \Rpackage{GenomicFeatures} packages include \begin{itemize} \item Transcriptome level: e.g. \Rpackage{TxDb.Hsapiens.UCSC.hg19.knownGene}, \Rpackage{EnsDb.Hsapiens.v75}. \item Generic genome features: Can generate via \Rpackage{GenomicFeatures} \end{itemize} One web-based resource accesses \href{http://www.biomart.org/}{biomart}, via the \Rpackage{biomaRt} package: \begin{itemize} \item Query web-based `biomart' resource for genes, sequence, SNPs, and etc. \end{itemize} The most popular annotation packages have been modified so that they can make use of a new set of methods to more easily access their contents. These four methods are named: \Rfunction{columns}, \Rfunction{keytypes}, \Rfunction{keys} and \Rfunction{select}. And they are described in this vignette. They can currently be used with all chip, organism, and \Rclass{TxDb} packages along with the popular GO.db package. For the older less popular packages, there are still conventient ways to retrieve the data. The \emph{How to use bimaps from the ".db" annotation packages} vignette in the \Rpackage{AnnotationDbi} package is a key reference for learnign about how to use bimap objects. Finally, all of the `.db' (and most other \Bioconductor{} annotation packages) are updated every 6 months corresponding to each release of \Bioconductor{}. Exceptions are made for packages where the actual resources that the packages are based on have not themselves been updated. \section{AnnotationDb objects and the select method} As previously mentioned, a new set of methods have been added that allow a simpler way of extracting identifier based annotations. All the annotation packages that support these new methods expose an object named exactly the same as the package itself. These objects are collectively called \Rclass{AnntoationDb} objects for the class that they all inherit from. The more specific classes (the ones that you will actually see in the wild) have names like \Rclass{OrgDb}, \Rclass{ChipDb} or \Rclass{TxDb} objects. These names correspond to the kind of package (and underlying schema) being represented. The methods that can be applied to all of these objects are \Rfunction{columns}, \Rfunction{keys}, \Rfunction{keytypes} and \Rfunction{select}. In addition, another accessor has recently been added which allows extraction of one column at at time. the \Rfunction{mapIds} method allows users to extract data into either a named character vector, a list or even a SimpleCharacterList. This method should work with all the different kinds of \Rclass{AnntoationDb} objects described below. \section{ChipDb objects and the select method} An extremely common kind of Annotation package is the so called platform based or chip based package type. This package is intended to make the manufacturer labels for a series of probes or probesets to a wide range of gene-based features. A package of this kind will load an \Rclass{ChipDb} object. Below is a set of examples to show how you might use the standard 4 methods to interact with an object of this type. First we need to load the package: <>= suppressPackageStartupMessages({ library(hgu95av2.db) }) @ If we list the contents of this package, we can see that one of the many things loaded is an object named after the package "hgu95av2.db": <>= ls("package:hgu95av2.db") @ We can look at this object to learn more about it: <>= hgu95av2.db @ If we want to know what kinds of data are retriveable via \Rfunction{select}, then we should use the \Rfunction{columns} method like this: <>= columns(hgu95av2.db) @ If we are further curious to know more about those values for columns, we can consult the help pages. Asking about any of these values will pull up a manual page describing the different fields and what they mean. <>= help("SYMBOL") @ If we are curious about what kinds of fields we could potentiall use as keys to query the database, we can use the \Rfunction{keytypes} method. In a perfect world, this method will return values very similar to what was returned by \Rfunction{columns}, but in reality, some kinds of values make poor keys and so this list is often shorter. <>= keytypes(hgu95av2.db) @ If we want to extract some sample keys of a particular type, we can use the \Rfunction{keys} method. <>= head(keys(hgu95av2.db, keytype="SYMBOL")) @ And finally, if we have some keys, we can use \Rfunction{select} to extract them. By simply using appropriate argument values with select we can specify what keys we want to look up values for (keys), what we want returned back (columns) and the type of keys that we are passing in (keytype) <>= #1st get some example keys k <- head(keys(hgu95av2.db,keytype="PROBEID")) # then call select select(hgu95av2.db, keys=k, columns=c("SYMBOL","GENENAME"), keytype="PROBEID") @ And as you can see, when you call the code above, select will try to return a data.frame with all the things you asked for matched up to each other. Finally if you wanted to extract only one column of data you could instead use the mapIds method like this: <>= #1st get some example keys k <- head(keys(hgu95av2.db,keytype="PROBEID")) # then call mapIds mapIds(hgu95av2.db, keys=k, column=c("GENENAME"), keytype="PROBEID") @ \section{OrgDb objects and the select method} An organism level package (an `org' package) uses a central gene identifier (e.g. Entrez Gene id) and contains mappings between this identifier and other kinds of identifiers (e.g. GenBank or Uniprot accession number, RefSeq id, etc.). The name of an org package is always of the form \emph{org...db} (e.g. \Rpackage{org.Sc.sgd.db}) where \emph{} is a 2-letter abbreviation of the organism (e.g. \Rpackage{Sc} for \emph{Saccharomyces cerevisiae}) and \emph{} is an abbreviation (in lower-case) describing the type of central identifier (e.g. \Rpackage{sgd} for gene identifiers assigned by the Saccharomyces Genome Database, or \Rpackage{eg} for Entrez Gene ids). Just as the chip packages load a \Rclass{ChipDb} object, the org packages will load a \Rclass{OrgDb} object. The following exercise should acquaint you with the use of these methods in the context of an organism package. %% select exercise \begin{Exercise} Display the \Rclass{OrgDb} object for the \Biocpkg{org.Hs.eg.db} package. Use the \Rfunction{columns} method to discover which sorts of annotations can be extracted from it. Is this the same as the result from the \Rfunction{keytypes} method? Use the \Rfunction{keytypes} method to find out. Finally, use the \Rfunction{keys} method to extract UNIPROT identifiers and then pass those keys in to the \Rfunction{select} method in such a way that you extract the gene symbol and KEGG pathway information for each. Use the help system as needed to learn which values to pass in to columns in order to achieve this. \end{Exercise} \begin{Solution} <>= library(org.Hs.eg.db) columns(org.Hs.eg.db) @ <>= help("SYMBOL") ## for explanation of these columns and keytypes values @ <>= keytypes(org.Hs.eg.db) uniKeys <- head(keys(org.Hs.eg.db, keytype="UNIPROT")) cols <- c("SYMBOL", "PATH") select(org.Hs.eg.db, keys=uniKeys, columns=cols, keytype="UNIPROT") @ \end{Solution} So how could you use select to annotate your results? This next exercise should hlep you to understand how that should generally work. \begin{Exercise} Please run the following code snippet (which will load a fake data result that I have provided for the purposes of illustration): <>= load(system.file("extdata", "resultTable.Rda", package="AnnotationDbi")) head(resultTable) @ The rownames of this table happen to provide entrez gene identifiers for each row (for human). Find the gene symbol and gene name for each of the rows in resultTable and then use the merge method to attach those annotations to it. \end{Exercise} \begin{Solution} <>= annots <- select(org.Hs.eg.db, keys=rownames(resultTable), columns=c("SYMBOL","GENENAME"), keytype="ENTREZID") resultTable <- merge(resultTable, annots, by.x=0, by.y="ENTREZID") head(resultTable) @ \end{Solution} \section{Using select with GO.db} When you load the GO.db package, a \Rclass{GODb} object is also loaded. This allows you to use the \Rfunction{columns}, \Rfunction{keys}, \Rfunction{keytypes} and \Rfunction{select} methods on the contents of the GO ontology. So if for example, you had a few GO IDs and wanted to know more about it, you could do it like this: <>= library(GO.db) GOIDs <- c("GO:0042254","GO:0044183") select(GO.db, keys=GOIDs, columns="DEFINITION", keytype="GOID") @ \section{Using select with TxDb packages} A \Rclass{TxDb} package (a 'TxDb' package) connects a set of genomic coordinates to various transcript oriented features. The package can also contain Identifiers to features such as genes and transcripts, and the internal schema describes the relationships between these different elements. All TxDb containing packages follow a specific naming scheme that tells where the data came from as well as which build of the genome it comes from. %% select exercise TxDb \begin{Exercise} Display the \Rclass{TxDb} object for the \Biocpkg{TxDb.Hsapiens.UCSC.hg19.knownGene} package. As before, use the \Rfunction{columns} and \Rfunction{keytypes} methods to discover which sorts of annotations can be extracted from it. Use the \Rfunction{keys} method to extract just a few gene identifiers and then pass those keys in to the \Rfunction{select} method in such a way that you extract the transcript ids and transcript starts for each. \end{Exercise} \begin{Solution} <>= library(TxDb.Hsapiens.UCSC.hg19.knownGene) txdb <- TxDb.Hsapiens.UCSC.hg19.knownGene txdb columns(txdb) keytypes(txdb) keys <- head(keys(txdb, keytype="GENEID")) cols <- c("TXID", "TXSTART") select(txdb, keys=keys, columns=cols, keytype="GENEID") @ \end{Solution} As is widely known, in addition to providing access via the \Rfunction{select} method, \Rclass{TxDb} objects also provide access via the more familiar \Rfunction{transcripts}, \Rfunction{exons}, \Rfunction{cds}, \Rfunction{transcriptsBy}, \Rfunction{exonsBy} and \Rfunction{cdsBy} methods. For those who do not yet know about these other methods, more can be learned by seeing the vignette called: \emph{Making and Utilizing TxDb Objects} in the \Rpackage{GenomicFeatures} package. \section{Using select with EnsDb packages} Similar to the \Rclass{TxDb} objects/packages discussed in the previous section, \Rclass{EnsDb} objects/packages provide genomic coordinates of gene models along with additional annotations (e.g. gene names, biotypes etc) but are tailored to annotations provided by Ensembl. The central methods \Rfunction{columns}, \Rfunction{keys}, \Rfunction{keytypes} and \Rfunction{select} are all implemented for \Rclass{EnsDb} objects. In addition, these methods allow also the use of the \Rclass{EnsDb} specific filtering framework to retrieve only selected information from the database (see vignette of the \Rpackage{ensembldb} package for more information). In the example below we first evaluate which columns, keys and keytypes are available for \Rclass{EnsDb} objects and fetch then the transcript ids, genomic start coordinate and transcript biotype for some genes. <>= library(EnsDb.Hsapiens.v75) edb <- EnsDb.Hsapiens.v75 edb ## List all columns columns(edb) ## List all keytypes keytypes(edb) ## Get the first keys <- head(keys(edb, keytype="GENEID")) ## Get the data select(edb, keys=keys, columns=c("TXID", "TXSEQSTART", "TXBIOTYPE"), keytype="GENEID") @ We can modify the queries above to retrieve only genes encoded on chromosome Y. To this end we use filter objects available for \Rclass{EnsDb} objects and its methods. <>= ## Retrieve all gene IDs of all lincRNAs encoded on chromosome Y linkY <- keys(edb, filter=list(GeneBiotypeFilter("lincRNA"), SeqNameFilter("Y"))) length(linkY) ## We get now all transcripts for these genes. txs <- select(edb, keys=linkY, columns=c("TXID", "TXSEQSTART", "TXBIOTYPE"), keytype="GENEID") nrow(txs) ## Alternatively, we could specify/pass the filters with the keys argument. txs <- select(edb, keys=list(GeneBiotypeFilter("lincRNA"), SeqNameFilter("Y")), columns=c("TXID", "TXSEQSTART", "TXBIOTYPE")) nrow(txs) @ The version number of R and packages loaded for generating the vignette were: <>= sessionInfo() @ \end{document} AnnotationDbi/inst/doc/IntroToAnnotationPackages.pdf0000644000175200017520000057113114710267466023657 0ustar00biocbuildbiocbuild%PDF-1.5 % 31 0 obj << /Length 1453 /Filter /FlateDecode >> stream xڵW[o6~2X^Eokt0Ze!J-rf Dw.yp$.֮3U yf4*B l$X.Jq%H,LBCm5uleɐ;(Q7 2& 2Gk&ՐNaYINٵO=MS4lYlLRiQ2vQooIfʞ@#H*zd " €e}r Eir''wn{e ڌMG&F.X"&y0ED*Z:/Q y]W[w~gi2Zꦿf@9d@8}mO,Voqȯ^+M,M|l$$yEe=n=aˢz>F믪j 0oט +b>voJwfl5ء^י.f.5Ơ MbDk#tE&CdbA-9 i Tvں~"H^&n]Cπ"娉0S;ߦf><-qzbOx02ɓ}Ӛm̫G=_ [D&]`|`ǔ]V st$)"q`yPI"XX>mPU,Qg#I?.aE]|@(tSv5{Wv~H"m@:<*fi/ŔT?3ciba٥O6H۵OA/;ͺ>דaR DbfCȟO&SۈFM(o$h~zmG_#Vu#=3P!Q;_)$',sy&'yygqwojSy֍30x׏.W̴)bM|V endstream endobj 28 0 obj << /Type /XObject /Subtype /Form /FormType 1 /PTEX.FileName (/home/biocbuild/bbs-3.20-bioc/tmpdir/RtmpVLHFpa/Rbuild361a08f7074d3/AnnotationDbi/vignettes/databaseTypes.pdf) /PTEX.PageNumber 1 /PTEX.InfoDict 43 0 R /BBox [0 0 792 612] /Resources << /ProcSet [ /PDF /Text ] /Font << /F0 44 0 R>> >> /Length 1560 /Filter /FlateDecode >> stream xڵn7 st֥(6^)qf%z]MYsVߐ%QMfxcϏ\۾M,\#O^ďv+(VknG`j:p#`lv?%iv)el ڣeCghX@) gFhi0arhLAj=#YEO`fiode&"u*Z0-MȊ, wtD!Ά.)өlۮ?S_u1cU>Gu}γ{ %ʽrkvz,r&L~{wp~9Tt/{gĦ#mu`+7ucb.pD::ޓNk78*K'?^= sivOpApV߾E##hx=W>s +]9ݑ.`LȧKq»VqEB V'uP~ޛ}8k\8'8 *[}%}t'\pnvq,*7 #ݑ"4ZGKr7q_'ҕ@t&H~VSlp<5v]ZpX`^@j58!5g$*) w,y=AnI1J'{K`tf+{wFb@d9K >) F]]RsT鉈xyυ苍I+w,pϭdSŘwI'nnTC1%x h>*N xSVk-Fntb*7p]6ک; =8ZSj֛$w]hc3O/'$b> 'mZY<.Nٛ|X:?,.@}w* +7= PV7I)2Ca&kdEJI$)NVTbi%GO%q;Ck m[l@݉\OJ 9DCҜ5K9/h*xqrUpތUn W~]`zo%oL6BVӧN?2"anT idaJRR$JNH&_"s1(iwRw&I aMlbcHC;c endstream endobj 47 0 obj << /Length 3171 /Filter /FlateDecode >> stream xZYs~ׯ`K8U;4q8lWRFrBrU5;Aq4hw7W__}u=Y ֋ MhH^ޏgMP͗7է 8eI_oRyچێ)yF~i~_BOVtZ: 4^K)vOSoP蘚OWi;05d]ԋP`bra[þ|b.w#{bo=%m[ D:-k9~S>r/.p?H/z - i%SˍɄW{+Xgq4m*ٗr۞l5%+k-䇲1ȴ^hIt89LGL] ('"2"v+jPI Reuw{ߴ4sabAFi#S ʬ0vm}:4*bo#^$aeVq&eJͅu2oو"a܈;!~1 Ow.G#Q AdyEpUDqD7GV&$nieC :šnCG1Q" V*M 8uuضwոQ{TX:t8.95XYGlvLNIMuȏ=o`` }ŴiPJMӳ|E tKp*de[%@rY2A'BpRθ9W9}JWq=}4*uɧ`v[i{'^x/xƥgjp/6vƊCXڃ2'n)B9sM"AٖKX+b%7щXड़/*9Q"IZԏr@ueohC"Ah|gJW͑&KY !_"Hd4ZfWow呤3Ks׻Z0 byA2QQYPw) ڹzs24k3gcy}Y?  |1̼jp0QAFi$bXRDX gn$嵉9q+2ga{bPa&-->g@t^)V+І ؽGi"L^i u9SP0).m2p?T(hjPXς V P P bDpJ.j!k̔(IȄ/!nfp8l ʹԧ,f~ۡ3sR53B-UA3PJGP&j( je`އΗZ~V.W:Zf$N{f_K[ق6< |kr_<3:ISMmE y֕WBT1o ɶ_Jhܵ5]d ZPVNAl-nк[f7xcƢƑy;=0lAvqtMQ \X~Pʝѱ ЇYhi&'M ]6+^Kb}R2Fv]+6,췩foePկ' w Id2S3Fr_ Ad{띺ʦJZ,T`!&f-" D|l'ZXţ}eGUe _2vT95T'R;ύ]i-wkFn`w63l乒uee rԊVzQ|E5c=r:Gs:L_,Xfk/AD" e)I4X|X<&S\phmgOTb*fP)j4 to?(2fNLX > stream xXߓ6~_\^dI 1ǹ=mf:>rgp1Nzbu V]x̖G]t`u~#AA B!PU, ‡$iquO鎓*(2TA:LN 6Fc%B ۋikT*IOe>.t4Qe%Ă YtI2F|3B`]?,|~~Wÿ( o=!~@{qUOT V"DIaLfv9$ MXu&ED*Tcƭ`;sbAi:$*Rbs2#nĜx={@S| ~\)h;ry! 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taxID inparanoidSpecies fives shortInpName Acromyrmex_echinatior Acromyrmex echinatior 103372 A.echinatior NA A.echinatior Acyrthosiphon_pisum Acyrthosiphon pisum 7029 A.pisum ACYPI A.pisum Aedes_aegypti Aedes aegypti 7159 A.aegypti AEDAE A.aegypti Agaricus_bisporus Agaricus bisporus 597362 A.bisporus NA A.bisporus Ailuropoda_melanoleuca Ailuropoda melanoleuca 9646 A.melanoleuca NA A.melanoleuca Ajellomyces_capsulata Ajellomyces capsulata 447093 A.capsulata NA A.capsulata Amphimedon_queenslandica Amphimedon queenslandica 400682 A.queenslandica NA A.queenslandica Anolis_carolinensis Anolis carolinensis 28377 A.carolinensis NA A.carolinensis Anopheles_darlingi Anopheles darlingi 43151 A.darlingi NA A.darlingi Anopheles_gambiae Anopheles gambiae 7165 A.gambiae ANOGA A.gambiae Apis_mellifera Apis mellifera 7460 A.mellifera APIME A.mellifera Aquifex_aeolicus Aquifex aeolicus 224324 A.aeolicus NA A.aeolicus Arabidopsis_thaliana Arabidopsis thaliana 3702 A.thaliana ARATH A.thaliana Arthrobotrys_oligospora Arthrobotrys oligospora 756982 A.oligospora NA A.oligospora Arthroderma_gypseum Arthroderma gypseum 535722 A.gypseum NA A.gypseum Ashbya_gossypii Ashbya gossypii 284811 A.gossypii NA A.gossypii Aspergillus_kawachii Aspergillus kawachii 1033177 A.kawachii NA A.kawachii Atta_cephalotes Atta cephalotes 12957 A.cephalotes NA A.cephalotes Aureococcus_anophagefferens Aureococcus anophagefferens 44056 A.anophagefferens NA A.anophagefferens Auricularia_delicata Auricularia delicata 717982 A.delicata NA A.delicata Babesia_bovis Babesia bovis 5865 B.bovis NA B.bovis Bacillus_subtilis Bacillus subtilis 224308 B.subtilis NA B.subtilis Bacteroides_thetaiotaomicron Bacteroides thetaiotaomicron 226186 B.thetaiotaomicron NA B.thetaiotaomicron Batrachochytrium_dendrobatidis Batrachochytrium dendrobatidis 684364 B.dendrobatidis BATDE B.dendrobatidis Beauveria_bassiana Beauveria bassiana 655819 B.bassiana NA B.bassiana Blastocystis_hominis Blastocystis hominis 12968 B.hominis NA B.hominis Bombyx_mori Bombyx mori 7091 B.mori BOMMO B.mori Bos_taurus Bos taurus 9913 B.taurus BOSTA B.taurus Botryotinia_fuckeliana Botryotinia fuckeliana 999810 B.fuckeliana NA B.fuckeliana Brachypodium_distachyon Brachypodium distachyon 15368 B.distachyon NA B.distachyon Bradyrhizobium_japonicum Bradyrhizobium japonicum 224911 B.japonicum NA B.japonicum Branchiostoma_floridae Branchiostoma floridae 7739 B.floridae BRAFL B.floridae Brassica_rapa Brassica rapa 51351 B.rapa NA B.rapa Brugia_malayi Brugia malayi 6279 B.malayi BRUMA B.malayi Caenorhabditis_brenneri Caenorhabditis brenneri 135651 C.brenneri CAEBRE C.brenneri Caenorhabditis_briggsae Caenorhabditis briggsae 6238 C.briggsae CAEBR C.briggsae Caenorhabditis_elegans Caenorhabditis elegans 6239 C.elegans CAEEL C.elegans Caenorhabditis_japonica Caenorhabditis japonica 281687 C.japonica CAEJA C.japonica Caenorhabditis_remanei Caenorhabditis remanei 31234 C.remanei CAERE C.remanei Callithrix_jacchus Callithrix jacchus 9483 C.jacchus NA C.jacchus Camponotus_floridanus Camponotus floridanus 104421 C.floridanus NA C.floridanus Candida_albicans Candida albicans 237561 C.albicans CANAL C.albicans Candida_glabrata Candida glabrata 284593 C.glabrata CANGL C.glabrata Canis_familiaris Canis familiaris 9615 C.familiaris CANFA C.familiaris Capsaspora_owczarzaki Capsaspora owczarzaki 595528 C.owczarzaki NA C.owczarzaki Cavia_porcellus Cavia porcellus 10141 C.porcellus CAVPO C.porcellus Chaetomium_globosum Chaetomium globosum 306901 C.globosum NA C.globosum Chlamydia_trachomatis Chlamydia trachomatis 272561 C.trachomatis NA C.trachomatis Chlamydomonas_reinhardtii Chlamydomonas reinhardtii 3055 C.reinhardtii CHLRE C.reinhardtii Chlorella_variabilis Chlorella variabilis 554065 C.variabilis NA C.variabilis Chloroflexus_aurantiacus Chloroflexus aurantiacus 324602 C.aurantiacus NA C.aurantiacus Ciona_intestinalis Ciona intestinalis 7719 C.intestinalis CIOIN C.intestinalis Ciona_savignyi Ciona savignyi 51511 C.savignyi CIOSA C.savignyi Clavispora_lusitaniae Clavispora lusitaniae 306902 C.lusitaniae NA C.lusitaniae Clonorchis_sinensis Clonorchis sinensis 79923 C.sinensis NA C.sinensis Coccidioides_immitis Coccidioides immitis 246410 C.immitis COCIM C.immitis Colletotrichum_gloeosporioides Colletotrichum gloeosporioides 1213859 C.gloeosporioides NA C.gloeosporioides Coprinopsis_cinerea Coprinopsis cinerea 240176 C.cinerea COPCI C.cinerea Cordyceps_militaris Cordyceps militaris 983644 C.militaris NA C.militaris Crassostrea_gigas Crassostrea gigas 29159 C.gigas NA C.gigas Cricetulus_griseus Cricetulus griseus 10029 C.griseus NA C.griseus Cryptococcus_neoformans Cryptococcus neoformans 214684 C.neoformans CRYNE C.neoformans Cryptosporidium_hominis Cryptosporidium hominis 237895 C.hominis CRYHO C.hominis Cryptosporidium_parvum Cryptosporidium parvum 353152 C.parvum CRYPA C.parvum Culex_quinquefasciatus Culex quinquefasciatus 7176 C.quinquefasciatus CULPI C.quinquefasciatus Danaus_plexippus Danaus plexippus 13037 D.plexippus NA D.plexippus Danio_rerio Danio rerio 7955 D.rerio DANRE D.rerio Daphnia_pulex Daphnia pulex 6669 D.pulex DAPPU D.pulex Debaryomyces_hansenii Debaryomyces hansenii 284592 D.hansenii DEBHA D.hansenii Deinococcus_radiodurans Deinococcus radiodurans 243230 D.radiodurans NA D.radiodurans Dictyoglomus_turgidum Dictyoglomus turgidum 515635 D.turgidum NA D.turgidum Dictyostelium_discoideum Dictyostelium discoideum 44689 D.discoideum DICDI D.discoideum Dictyostelium_purpureum Dictyostelium purpureum 5786 D.purpureum NA D.purpureum Drosophila_ananassae Drosophila ananassae 7217 D.ananassae DROAN D.ananassae Drosophila_grimshawi Drosophila grimshawi 7222 D.grimshawi DROGR D.grimshawi Drosophila_melanogaster Drosophila melanogaster 7227 D.melanogaster DROME D.melanogaster Drosophila_mojavensis Drosophila mojavensis 7230 D.mojavensis DROMO D.mojavensis Drosophila_pseudoobscura_pseudoobscura Drosophila pseudoobscura pseudoobscura 46245 D.pseudoobscura DROPS D.pseudoobscura Drosophila_virilis Drosophila virilis 7244 D.virilis DROVI D.virilis Drosophila_willistoni Drosophila willistoni 7260 D.willistoni DROWI D.willistoni Ectocarpus_siliculosus Ectocarpus siliculosus 2880 E.siliculosus NA E.siliculosus Edhazardia_aedis Edhazardia aedis 1003232 E.aedis NA E.aedis Emericella_nidulans Emericella nidulans 227321 E.nidulans NA E.nidulans Encephalitozoon_cuniculi Encephalitozoon cuniculi 284813 E.cuniculi NA E.cuniculi Entamoeba_histolytica Entamoeba histolytica 5759 E.histolytica ENTHI E.histolytica Enterocytozoon_bieneusi Enterocytozoon bieneusi 481877 E.bieneusi NA E.bieneusi Equus_caballus Equus caballus 9796 E.caballus EQUCA E.caballus Eremothecium_cymbalariae Eremothecium cymbalariae 931890 E.cymbalariae NA E.cymbalariae Escherichia_coli Escherichia coli 83333 E.coli ESCCO E.coli Exophiala_dermatitidis Exophiala dermatitidis 858893 E.dermatitidis NA E.dermatitidis Felis_catus Felis catus 9685 F.catus NA F.catus Fibroporia_radiculosa Fibroporia radiculosa 1078123 F.radiculosa NA F.radiculosa Fusarium_pseudograminearum Fusarium pseudograminearum 1028729 F.pseudograminearum NA F.pseudograminearum Fusobacterium_nucleatum Fusobacterium nucleatum 190304 F.nucleatum NA F.nucleatum Gaeumannomyces_graminis Gaeumannomyces graminis 644352 G.graminis NA G.graminis Gallus_gallus Gallus gallus 9031 G.gallus GALGA G.gallus Gasterosteus_aculeatus Gasterosteus aculeatus 69293 G.aculeatus GASAC G.aculeatus Geobacter_sulfurreducens Geobacter sulfurreducens 243231 G.sulfurreducens NA G.sulfurreducens Giardia_intestinalis Giardia intestinalis 184922 G.intestinalis GIALA G.intestinalis Gibberella_zeae Gibberella zeae 229533 G.zeae NA G.zeae Glarea_lozoyensis Glarea lozoyensis 1104152 G.lozoyensis NA G.lozoyensis Gloeobacter_violaceus Gloeobacter violaceus 251221 G.violaceus NA G.violaceus Glycine_max Glycine max 3847 G.max NA G.max Gorilla_gorilla_gorilla Gorilla gorilla gorilla 9595 G.gorilla NA G.gorilla Grosmannia_clavigera Grosmannia clavigera 655863 G.clavigera NA G.clavigera Halobacterium_salinarum Halobacterium salinarum 64091 H.salinarum NA H.salinarum Harpegnathos_saltator Harpegnathos saltator 610380 H.saltator NA H.saltator Heterocephalus_glaber Heterocephalus glaber 10181 H.glaber NA H.glaber Homo_sapiens Homo sapiens 9606 H.sapiens HOMSA H.sapiens Hordeum_vulgare Hordeum vulgare 112509 H.vulgare NA H.vulgare Hyaloperonospora_arabidopsidis Hyaloperonospora arabidopsidis 559515 H.arabidopsidis NA H.arabidopsidis Hypocrea_virens Hypocrea virens 413071 H.virens NA H.virens Ichthyophthirius_multifiliis Ichthyophthirius multifiliis 857967 I.multifiliis NA I.multifiliis Ixodes_scapularis Ixodes scapularis 6945 I.scapularis IXOSC I.scapularis Kazachstania_africana Kazachstania africana 1071382 K.africana NA K.africana Kluyveromyces_lactis Kluyveromyces lactis 284590 K.lactis KLULA K.lactis Korarchaeum_cryptofilum Korarchaeum cryptofilum 374847 K.cryptofilum NA K.cryptofilum Laccaria_bicolor Laccaria bicolor 486041 L.bicolor NA L.bicolor Lachancea_thermotolerans Lachancea thermotolerans 559295 L.thermotolerans NA L.thermotolerans Latimeria_chalumnae Latimeria chalumnae 7897 L.chalumnae NA L.chalumnae Leishmania_braziliensis Leishmania braziliensis 5660 L.braziliensis NA L.braziliensis Leishmania_infantum Leishmania infantum 5671 L.infantum NA L.infantum Leishmania_major Leishmania major 5664 L.major LEIMA L.major Leptosphaeria_maculans Leptosphaeria maculans 985895 L.maculans NA L.maculans Leptospira_interrogans Leptospira interrogans 189518 L.interrogans NA L.interrogans Loa_loa Loa loa 7209 L.loa NA L.loa Lodderomyces_elongisporus Lodderomyces elongisporus 379508 L.elongisporus NA L.elongisporus Loxodonta_africana Loxodonta africana 9785 L.africana NA L.africana Macaca_mulatta Macaca mulatta 9544 M.mulatta MACMU M.mulatta Macrophomina_phaseolina Macrophomina phaseolina 1126212 M.phaseolina NA M.phaseolina Magnaporthe_oryzae Magnaporthe oryzae 242507 M.oryzae NA M.oryzae Malassezia_globosa Malassezia globosa 425265 M.globosa NA M.globosa Marssonina_brunnea Marssonina brunnea 1072389 M.brunnea NA M.brunnea Melampsora_larici_populina Melampsora larici-populina 747676 M.larici-populina NA M.larici-populina Meleagris_gallopavo Meleagris gallopavo 9103 M.gallopavo NA M.gallopavo Metarhizium_acridum Metarhizium acridum 655827 M.acridum NA M.acridum Methanocaldococcus_jannaschii Methanocaldococcus jannaschii 243232 M.jannaschii NA M.jannaschii Methanosarcina_acetivorans Methanosarcina acetivorans 188937 M.acetivorans NA M.acetivorans Meyerozyma_guilliermondii Meyerozyma guilliermondii 294746 M.guilliermondii NA M.guilliermondii Micromonas_sp Micromonas sp. 296587 Micromonas.sp. NA Micromonas.sp. Mixia_osmundae Mixia osmundae 764103 M.osmundae NA M.osmundae Moniliophthora_perniciosa Moniliophthora perniciosa 554373 M.perniciosa NA M.perniciosa Monodelphis_domestica Monodelphis domestica 13616 M.domestica MONDO M.domestica Monosiga_brevicollis Monosiga brevicollis 81824 M.brevicollis MONBR M.brevicollis Mus_musculus Mus musculus 10090 M.musculus MUSMU M.musculus Mustela_putorius_furo Mustela putorius furo 9669 M.putorius NA M.putorius Mycobacterium_tuberculosis Mycobacterium tuberculosis 1773 M.tuberculosis NA M.tuberculosis Mycosphaerella_graminicola Mycosphaerella graminicola 336722 M.graminicola NA M.graminicola Myotis_lucifugus Myotis lucifugus 59463 M.lucifugus NA M.lucifugus Naegleria_gruberi Naegleria gruberi 5762 N.gruberi NA N.gruberi Nasonia_vitripennis Nasonia vitripennis 7425 N.vitripennis NASVI N.vitripennis Naumovozyma_castellii Naumovozyma castellii 1064592 N.castellii NA N.castellii Nectria_haematococca Nectria haematococca 660122 N.haematococca NA N.haematococca Nematocida_parisii Nematocida parisii 881290 N.parisii NA N.parisii Nematostella_vectensis Nematostella vectensis 45351 N.vectensis NEMVE N.vectensis Neosartorya_fumigata Neosartorya fumigata 330879 N.fumigata ASPFU N.fumigata Neospora_caninum Neospora caninum 572307 N.caninum NA N.caninum Neurospora_crassa Neurospora crassa 367110 N.crassa NEUCR N.crassa Nomascus_leucogenys Nomascus leucogenys 61853 N.leucogenys NA N.leucogenys Nosema_ceranae Nosema ceranae 578460 N.ceranae NA N.ceranae Oikopleura_dioica Oikopleura dioica 34765 O.dioica NA O.dioica Oreochromis_niloticus Oreochromis niloticus 8128 O.niloticus NA O.niloticus Ornithorhynchus_anatinus Ornithorhynchus anatinus 9258 O.anatinus ORNAN O.anatinus Oryctolagus_cuniculus Oryctolagus cuniculus 9986 O.cuniculus NA O.cuniculus Oryza_sativa Oryza sativa 39947 O.sativa ORYSA O.sativa Oryzias_latipes Oryzias latipes 8090 O.latipes ORYLA O.latipes Ostreococcus_tauri Ostreococcus tauri 70448 O.tauri OSTTA O.tauri Otolemur_garnettii Otolemur garnettii 30611 O.garnettii NA O.garnettii Pan_troglodytes Pan troglodytes 9598 P.troglodytes PANTR P.troglodytes Paracoccidioides_brasiliensis Paracoccidioides brasiliensis 482561 P.brasiliensis NA P.brasiliensis Paramecium_tetraurelia Paramecium tetraurelia 5888 P.tetraurelia NA P.tetraurelia Pediculus_humanus Pediculus humanus 121224 P.humanus PEDPA P.humanus Penicillium_digitatum Penicillium digitatum 1170229 P.digitatum NA P.digitatum Perkinsus_marinus Perkinsus marinus 423536 P.marinus NA P.marinus Phaeodactylum_tricornutum Phaeodactylum tricornutum 556484 P.tricornutum NA P.tricornutum Phaeosphaeria_nodorum Phaeosphaeria nodorum 321614 P.nodorum STANO P.nodorum Phanerochaete_carnosa Phanerochaete carnosa 650164 P.carnosa NA P.carnosa Physcomitrella_patens Physcomitrella patens 145481 P.patens PHYPA P.patens Phytophthora_infestans Phytophthora infestans 403677 P.infestans NA P.infestans Phytophthora_ramorum Phytophthora ramorum 164328 P.ramorum PHYRA P.ramorum Phytophthora_sojae Phytophthora sojae 1094619 P.sojae PHYSO P.sojae Pichia_pastoris Pichia pastoris 644223 K.pastoris NA K.pastoris Pichia_sorbitophila Pichia sorbitophila 559304 P.sorbitophila NA P.sorbitophila Piriformospora_indica Piriformospora indica 1109443 P.indica NA P.indica Plasmodium_berghei Plasmodium berghei 5823 P.berghei NA P.berghei Plasmodium_chabaudi Plasmodium chabaudi 5825 P.chabaudi NA P.chabaudi Plasmodium_falciparum Plasmodium falciparum 36329 P.falciparum PLAFA P.falciparum Plasmodium_knowlesi Plasmodium knowlesi 5851 P.knowlesi NA P.knowlesi Plasmodium_vivax Plasmodium vivax 126793 P.vivax PLAVI P.vivax Plasmodium_yoelii_yoelii Plasmodium yoelii yoelii 73239 P.yoelii NA P.yoelii Pneumocystis_jirovecii Pneumocystis jirovecii 1209962 P.jiroveci NA P.jiroveci Polysphondylium_pallidum Polysphondylium pallidum 13642 P.pallidum NA P.pallidum Pongo_abelii Pongo abelii 9601 P.abelii NA P.abelii Populus_trichocarpa Populus trichocarpa 3694 P.trichocarpa POPTR P.trichocarpa Postia_placenta Postia placenta 561896 P.placenta NA P.placenta Pristionchus_pacificus Pristionchus pacificus 54126 P.pacificus PRIPA P.pacificus Pseudogymnoascus_destructans Pseudogymnoascus destructans 658429 G.destructans NA G.destructans Pseudomonas_aeruginosa Pseudomonas aeruginosa 208964 P.aeruginosa NA P.aeruginosa Pteropus_alecto Pteropus alecto 9402 P.alecto NA P.alecto Puccinia_graminis Puccinia graminis 418459 P.graminis PUCGR P.graminis Pyrenophora_tritici_repentis Pyrenophora tritici-repentis 426418 P.tritici-repentis NA P.tritici-repentis Pyrobaculum_aerophilum Pyrobaculum aerophilum 178306 P.aerophilum NA P.aerophilum Pyrococcus_kodakaraensis Pyrococcus kodakaraensis 69014 P.kodakaraensis NA P.kodakaraensis Pythium_ultimum Pythium ultimum 65071 P.ultimum NA P.ultimum Rattus_norvegicus Rattus norvegicus 10116 R.norvegicus RATNO R.norvegicus Rhizopus_delemar Rhizopus delemar 246409 R.delemar RHIOR R.delemar Rhodopirellula_baltica Rhodopirellula baltica 243090 R.baltica NA R.baltica Rhodotorula_glutinis Rhodotorula glutinis 1001064 R.glutinis NA R.glutinis Ricinus_communis Ricinus communis 3988 R.communis NA R.communis Saccharomyces_cerevisiae Saccharomyces cerevisiae 559292 S.cerevisiae SACCE S.cerevisiae Salpingoeca_sp Salpingoeca sp. 946362 Salpingoeca.sp. NA Salpingoeca.sp. Sarcophilus_harrisii Sarcophilus harrisii 9305 S.harrisii NA S.harrisii Scheffersomyces_stipitis Scheffersomyces stipitis 322104 S.stipitis NA S.stipitis Schistosoma_mansoni Schistosoma mansoni 6183 S.mansoni SCHMA S.mansoni Schizophyllum_commune Schizophyllum commune 578458 S.commune NA S.commune Schizosaccharomyces_pombe Schizosaccharomyces pombe 284812 S.pombe SCHPO S.pombe Sclerotinia_sclerotiorum Sclerotinia sclerotiorum 665079 S.sclerotiorum SCLSC S.sclerotiorum Selaginella_moellendorffii Selaginella moellendorffii 88036 S.moellendorffii NA S.moellendorffii Serpula_lacrymans Serpula lacrymans 578457 S.lacrymans NA S.lacrymans Setaria_italica Setaria italica 4555 S.italica NA S.italica Solanum_lycopersicum Solanum lycopersicum 4081 S.lycopersicum NA S.lycopersicum Solanum_tuberosum Solanum tuberosum 4113 S.tuberosum NA S.tuberosum Solenopsis_invicta Solenopsis invicta 13686 S.invicta NA S.invicta Sordaria_macrospora Sordaria macrospora 771870 S.macrospora NA S.macrospora Sorghum_bicolor Sorghum bicolor 4558 S.bicolor SORBI S.bicolor Spathaspora_passalidarum Spathaspora passalidarum 619300 S.passalidarum NA S.passalidarum Spermophilus_tridecemlineatus Spermophilus tridecemlineatus 43179 S.tridecemlineatus NA S.tridecemlineatus Sporisorium_reilianum Sporisorium reilianum 999809 S.reilianum NA S.reilianum Streptomyces_coelicolor Streptomyces coelicolor 100226 S.coelicolor NA S.coelicolor Strongylocentrotus_purpuratus Strongylocentrotus purpuratus 7668 S.purpuratus STRPU S.purpuratus Sulfolobus_solfataricus Sulfolobus solfataricus 273057 S.solfataricus NA S.solfataricus Sus_scrofa Sus scrofa 9823 S.scrofa NA S.scrofa Synechocystis_sp Synechocystis sp. 1111708 Synechocystis.sp. NA Synechocystis.sp. Taeniopygia_guttata Taeniopygia guttata 59729 T.guttata NA T.guttata Takifugu_rubripes Takifugu rubripes 31033 T.rubripes TAKRU T.rubripes Talaromyces_stipitatus Talaromyces stipitatus 441959 T.stipitatus NA T.stipitatus Tetrahymena_thermophila Tetrahymena thermophila 312017 T.thermophila TETTH T.thermophila Tetraodon_nigroviridis Tetraodon nigroviridis 99883 T.nigroviridis TETNI T.nigroviridis Tetrapisispora_blattae Tetrapisispora blattae 1071380 T.blattae NA T.blattae Thalassiosira_pseudonana Thalassiosira pseudonana 35128 T.pseudonana THAPS T.pseudonana Theileria_annulata Theileria annulata 5874 T.annulata THEAN T.annulata Theileria_parva Theileria parva 5875 T.parva THEPA T.parva Thermodesulfovibrio_yellowstonii Thermodesulfovibrio yellowstonii 289376 T.yellowstonii NA T.yellowstonii Thermotoga_maritima Thermotoga maritima 243274 T.maritima NA T.maritima Thielavia_heterothallica Thielavia heterothallica 573729 T.heterothallica NA T.heterothallica Torulaspora_delbrueckii Torulaspora delbrueckii 1076872 T.delbrueckii NA T.delbrueckii Toxoplasma_gondii Toxoplasma gondii 5811 T.gondii NA T.gondii Trachipleistophora_hominis Trachipleistophora hominis 72359 T.hominis NA T.hominis Tribolium_castaneum Tribolium castaneum 7070 T.castaneum TRICA T.castaneum Trichinella_spiralis Trichinella spiralis 6334 T.spiralis NA T.spiralis Trichomonas_vaginalis Trichomonas vaginalis 5722 T.vaginalis TRIVA T.vaginalis Trichophyton_rubrum Trichophyton rubrum 559305 T.rubrum NA T.rubrum Trichoplax_adhaerens Trichoplax adhaerens 10228 T.adhaerens TRIAD T.adhaerens Trichosporon_asahii Trichosporon asahii 1186058 T.asahii NA T.asahii Trypanosoma_brucei_brucei Trypanosoma brucei brucei 999953 T.brucei NA T.brucei Trypanosoma_cruzi Trypanosoma cruzi 5693 T.cruzi TRYCR T.cruzi Tuber_melanosporum Tuber melanosporum 656061 T.melanosporum NA T.melanosporum Tupaia_chinensis Tupaia chinensis 246437 T.chinensis NA T.chinensis Uncinocarpus_reesii Uncinocarpus reesii 336963 U.reesii NA U.reesii Ustilago_maydis Ustilago maydis 237631 U.maydis USTMA U.maydis Vanderwaltozyma_polyspora Vanderwaltozyma polyspora 436907 V.polyspora NA V.polyspora Vavraia_culicis Vavraia culicis 948595 V.culicis NA V.culicis Verticillium_dahliae Verticillium dahliae 498257 V.dahliae NA V.dahliae Vitis_vinifera Vitis vinifera 29760 V.vinifera NA V.vinifera Vittaforma_corneae Vittaforma corneae 993615 V.corneae NA V.corneae Volvox_carteri Volvox carteri 3067 V.carteri NA V.carteri Wallemia_sebi Wallemia sebi 671144 W.sebi NA W.sebi Wickerhamomyces_ciferrii Wickerhamomyces ciferrii 1206466 W.ciferrii NA W.ciferrii Wuchereria_bancrofti Wuchereria bancrofti 6293 W.bancrofti NA W.bancrofti Xenopus_tropicalis Xenopus tropicalis 8364 X.tropicalis XENTR X.tropicalis Xiphophorus_maculatus Xiphophorus maculatus 8083 X.maculatus NA X.maculatus Yarrowia_lipolytica Yarrowia lipolytica 284591 Y.lipolytica YARLI Y.lipolytica Zygosaccharomyces_rouxii Zygosaccharomyces rouxii 559307 Z.rouxii NA Z.rouxii AnnotationDbi/inst/extdata/hcg110_ID0000644000175200017520000010144214710217313020217 0ustar00biocbuildbiocbuild1000_at X60188 1001_at X60957 1002_f_at X65962 1003_s_at X68149 1004_at X68149 1005_at X68277 1006_at X07820 1007_s_at U48705 1008_f_at U50648 1009_at U51004 100_g_at Y08200 1010_at U53442 1011_s_at U54778 1012_at U57317 1013_at U59913 1014_at U60325 1015_s_at U62293 1016_s_at U70981 1017_at U73737 1018_at U81787 1019_g_at U81787 101_at Y09305 1020_s_at U85611 1021_at J00219 1022_f_at V00542 1023_at X02158 1024_at X02612 1025_g_at X02612 1026_s_at U41068 1027_at U41068 1028_at U43431 1029_s_at U07794 102_at Y09306 1030_s_at U07806 1031_at U09564 1032_at U11872 1033_g_at U11872 1034_at U14394 1035_g_at U14394 1036_at U14407 1037_at U19180 1038_s_at U19247 1039_s_at U22431 103_at Z19585 1040_s_at U23435 1041_at U26403 1042_at U27185 1043_s_at U27516 1044_s_at U31556 1045_s_at U33838 1046_at U34605 1047_s_at U37055 1048_at U38480 1049_g_at U38480 104_at Z21966 1050_at U06452 1051_g_at U06452 1052_s_at M83667 1053_at M87338 1054_at M87339 1055_g_at M87339 1056_s_at M90391 1057_at M97815 1058_at S69790 1059_at S76475 105_at Z30425 1060_g_at S76475 1061_at U00672 1062_g_at U00672 1063_s_at U02566 1064_at U02680 1065_at U02687 1066_at U03187 1067_at U03858 1068_g_at U03858 1069_at U04636 106_at Z35278 1070_at M76766 1071_at M77810 1072_g_at M77810 1073_at M81601 1074_at M28209 1075_f_at M28585 1076_at M28983 1077_at M29474 1078_at M31661 1079_g_at M31661 107_at Z95624 1080_s_at M31667 1081_at M33764 1082_at M34667 1083_s_at M35093 1084_at M35296 1085_s_at M37238 1086_at M59941 1087_at M60459 1088_at M61176 1089_i_at M64936 108_g_at Z95624 1090_f_at M64936 1091_at M65066 1092_at M65199 1093_at M65254 1094_g_at M65254 1095_s_at M73239 1096_g_at M28170 1097_s_at L31584 1098_at L36051 1099_s_at L38503 109_at Z97074 1100_at L76191 1101_at L77864 1102_s_at M10901 1103_at M11567 1104_s_at M11717 1105_s_at M12886 1106_s_at M12959 1107_s_at M13755 1108_s_at M18391 1109_s_at M19989 110_at X96753 1110_at M21624 1111_at M22092 1112_g_at M22092 1113_at M22489 1114_at M22490 1115_at M25897 1116_at M28170 1117_at L27943 1118_at L28175 1119_at J05249 111_at Y08200 1120_at J05459 1121_g_at J05459 1122_f_at K03183 1123_at L01406 1124_at L04731 1125_s_at L05424 1126_s_at L05424 1127_at L07597 1128_s_at L09230 1129_at L11239 112_g_at X07024 1130_at L11284 1131_at L11285 1132_s_at L12060 1133_at L12701 1134_at L13738 1135_at L15388 1136_at L16991 1137_at L20852 1138_at L20859 1139_at L22075 113_i_at X14474 1140_at L25851 1141_at L27080 1142_at HG3432-HT3618 1143_s_at HG3432-HT3620 1144_at HG3432-HT3621 1145_g_at HG3432-HT3621 1146_at HG3477-HT3670 1147_at HG3510-HT3704 1148_s_at HG4704-HT5146 1149_at HG4740-HT5187 114_r_at X14474 1150_at HG620-HT620 1151_at HG662-HT662 1152_i_at J00117 1153_f_at J00117 1154_at J02645 1155_at J03069 1156_at J03133 1157_s_at J03171 1158_s_at J04046 1159_at J04156 115_at X14787 1160_at J04444 1161_at J04988 1162_g_at HG3227-HT3404 1163_at HG3254-HT3431 1164_at HG3344-HT3521 1165_at D49950 1166_at D78151 1167_s_at D86331 1168_at D88797 1169_at D88799 116_at X14968 1170_at HG1155-HT4822 1171_s_at HG1471-HT3923 1172_at HG172-HT3924 1173_g_at HG172-HT3924 1174_at HG1733-HT1748 1175_s_at HG1827-HT1856 1176_at HG2320-HT2416 1177_at HG2465-HT4871 1178_at HG2846-HT2983 1179_at HG2855-HT2995 117_at X51757 1180_g_at HG2855-HT2995 1181_at HG3227-HT3404 1182_at D42108 1183_at D43767 1184_at D45248 1185_at D49410 1186_at D49493 1187_at X84740 1188_g_at X84740 1189_at X85753 118_at X54938 1190_at Z48541 1191_s_at AB003102 1192_at AB003103 1193_at AF002224 1194_g_at AF002224 1195_s_at AF012024 1196_at D00591 1197_at D00654 1198_at D13168 1199_at D13748 119_at X63629 1200_at D14827 1201_at D14889 1202_g_at D14889 1203_at D17357 1204_at D26135 1205_at D26528 1206_at X66364 1207_at X66365 1208_at X78549 1209_at U78798 120_at X68742 1210_s_at U83600 1211_s_at U84388 1212_at U86529 1213_at U88666 1214_s_at V00535 1215_at X06562 1216_at X07109 1217_g_at X07109 1218_at X12794 1219_at X15949 121_at X69699 1220_g_at X15949 1221_at X54871 1222_at X66360 1223_at X66362 1224_at X66363 1225_g_at X66363 1226_at U69611 1227_g_at U69611 1228_s_at U73682 1229_at U78556 122_at X74331 1230_g_at U78556 1231_at M74525 1232_s_at M74587 1233_s_at M76125 1234_at M83941 1235_at M86400 1236_s_at M89914 1237_at S81914 1238_at U09759 1239_s_at U13021 123_at X75756 1240_at U13022 1241_at U14603 1242_at U15655 1243_at U18300 1244_at U18671 1245_i_at U25975 1246_at U35234 1247_g_at U35234 1248_at U37689 1249_at U43885 124_i_at X78342 1250_at U47077 1251_g_at M64788 1252_at M73547 1253_at L33801 1254_at L36861 1255_g_at L36861 1256_at L38929 1257_s_at L42379 1258_s_at L76568 1259_at L76568 125_r_at X78342 1260_s_at M16594 1261_i_at M16594 1262_s_at M19154 1263_at M20137 1264_at M25393 1265_g_at M25393 1266_s_at M26692 1267_at M55284 1268_at M58028 1269_at M61906 126_s_at X79200 1270_at M64788 1271_g_at L19067 1272_at L19161 1273_r_at L22005 1274_s_at L22005 1275_at L25441 1276_g_at D84110 1277_at D89016 1278_at HG162-HT3165 1279_s_at HG2649-HT2745 127_at X79568 1280_i_at HG2702-HT2798 1281_f_at HG2702-HT2798 1282_s_at HG2705-HT2801 1283_at HG2706-HT2802 1284_at HG2707-HT2803 1285_at HG2709-HT2805 1286_s_at HG429-HT429 1287_at J03473 1288_s_at J04617 1289_at L02321 128_at X82153 1290_g_at L02321 1291_s_at L03840 1292_at L11329 1293_s_at L11701 1294_at L13852 1295_at L19067 1296_at D83542 1297_at D84110 1298_at X86816 1299_at X93512 129_g_at X82153 1300_at Y08837 1301_s_at Z48481 1302_s_at Z48482 1303_at AB000462 1304_at AJ001487 1305_s_at D12620 1306_at D12686 1307_at D14533 1308_g_at D14533 1309_at D26598 130_s_at X82850 1310_at D26599 1311_at D26600 1312_at D38047 1313_at D38048 1314_at D44466 1315_at D78361 1316_at X55005 1317_at X70040 1318_at X74262 1319_at X74764 131_at X83928 1320_at X79510 1321_s_at U43916 1322_at U47677 1323_at X04803 1324_at U53174 1325_at U59423 1326_at U60519 1327_s_at U67156 1328_at U69108 1329_s_at U74382 132_at X85545 1330_at U78876 1331_s_at U83598 1332_f_at V00520 1333_f_at X02596 1334_s_at X03656 1335_at X04434 1336_s_at X06318 1337_s_at X06614 1338_s_at X13930 1339_s_at X14675 133_at X87212 1340_s_at X16323 1341_at X52056 1342_g_at U40705 1343_s_at S66896 1344_at S69369 1345_s_at S69370 1346_at S72043 1347_at S78187 1348_s_at S79219 1349_at S81294 134_at X95632 1350_at U02388 1351_at U07695 1352_at U11870 1353_g_at U11870 1354_at U12140 1355_g_at U12140 1356_at U18321 1357_at U20657 1358_s_at U22970 1359_at U32659 135_g_at X95632 1360_at U40622 1361_at U40705 1362_s_at M84820 1363_at M87770 1364_at M93426 1365_at M26062 1366_i_at M26880 1367_f_at M26880 1368_at M27492 1369_s_at M28130 136_at U65402 1370_at M29696 1371_s_at M29874 1372_at M31165 1373_at M31523 1374_g_at M31523 1375_s_at M32304 1376_at M36067 1377_at M58603 1378_g_at M58603 1379_at M59371 137_at U65404 1380_at M60828 1381_at M62303 1382_at M63488 1383_at M64929 1384_at M64930 1385_at M77349 1386_at M83738 1387_at M22005 1388_g_at J03258 1389_at J03779 138_at U66464 1390_s_at L00137 1391_s_at L04751 1392_at L16862 1393_at L20348 1394_at L25080 1395_at L25081 1396_at L27560 1397_at L32976 1398_g_at L32976 1399_at L34587 139_at U67988 1400_at M13207 1401_g_at M13207 1402_at M16038 1403_s_at M21121 1404_r_at M21121 1405_i_at M21121 1406_at M21985 1407_g_at M21985 1408_at J02986 1409_at J03161 140_s_at U68063 1410_at J03258 1411_at D16154 1412_g_at D16154 1413_at D26561 1414_at D26561 1415_at D26561 1416_g_at D26561 1417_at D26561 1418_at D29675 1419_g_at D29675 141_s_at U75276 1420_s_at D30655 1421_at D30742 1422_g_at D30742 1423_at D78514 1424_s_at D78577 1425_at D88795 1426_at D89077 1427_g_at D89077 1428_at HG3313-HT3490 1429_at J00268 142_at U75308 1430_at J00306 1431_at J02843 1432_s_at D16105 1433_g_at U68019 1434_at U92436 1435_f_at V00540 1436_at X16866 1437_at X52479 1438_at X75208 1439_s_at X75346 143_s_at U75309 1440_s_at X83490 1441_s_at X83492 1442_at X99101 1443_at Y08302 1444_at AB003177 1445_at AF014958 1446_at D00760 1447_at D00761 1448_at D00762 1449_at D00763 144_at U80628 1450_g_at D00763 1451_s_at D13666 1452_at U24576 1453_at U68018 1454_at U68019 1455_f_at M61855 1456_s_at M63838 1457_at M64174 1458_at M64572 1459_at M68941 145_s_at U80987 1460_g_at M68941 1461_at M69043 1462_s_at M80397 1463_at M93425 1464_at S73149 1465_s_at S75881 1466_s_at S81661 1467_at U12535 1468_at U12595 1469_at U12779 146_at U81802 1470_at U21090 1471_at U22376 1472_g_at U22376 1473_s_at U22376 1474_s_at U22376 1475_s_at U22376 1476_s_at U22376 1477_s_at M61853 1478_at L10717 1479_g_at L10717 147_at U82130 1480_at L12723 1481_at L23808 1482_g_at L23808 1483_at L34059 1484_at L34060 1485_at L36642 1486_at L37127 1487_at L38487 1488_at L77886 1489_s_at M19720 148_at U88629 1490_at M19720 1491_at M31166 1492_f_at M33317 1493_r_at M33318 1494_f_at M33318 1495_at M34057 1496_at M34668 1497_at L04270 1498_at L05148 1499_at L10413 149_at U90426 1500_at X51630 1501_at X57025 1502_s_at X66087 1503_at X95152 1504_s_at Z70276 1505_at D00596 1506_at D11086 1507_s_at D11151 1508_at D25303 1509_at D83646 150_at U96115 1510_g_at D83646 1511_at D84361 1512_at D86550 1513_at HG2261-HT2352 1514_g_at HG2261-HT2352 1515_at HG4074-HT4344 1516_g_at HG4074-HT4344 1517_at J02906 1518_at J04101 1519_at J04102 151_s_at V00599 1520_s_at X04500 1521_at X17620 1522_at U43408 1523_g_at U43408 1524_at U46194 1525_s_at U47011 1526_i_at U47011 1527_s_at U50527 1528_at U50531 1529_at U50534 152_f_at X00038 1530_g_at U50534 1531_at U50535 1532_g_at U50535 1533_at U63139 1534_at U64198 1535_at U68723 1536_at U77949 1537_at X00588 1538_s_at X00695 1539_at X02751 153_f_at X00088 1540_f_at X02956 1541_f_at X02958 1542_at X04571 1543_at U39657 1544_at U39817 1545_g_at S77812 1546_at U03056 1547_at U09607 1548_s_at U16720 1549_s_at U19557 154_at X07024 1550_at U19796 1551_g_at U19796 1552_i_at U22028 1553_r_at U22028 1554_f_at U22028 1555_f_at U22029 1556_at U23946 1557_at U24152 1558_g_at U24152 1559_at U24153 155_s_at U61397 1560_g_at U24153 1561_at U27193 1562_g_at U27193 1563_s_at M58286 1564_at M63167 1565_s_at M96995 1566_at S71824 1567_at S77812 1568_s_at L42243 1569_r_at L42243 156_s_at U64871 1570_f_at L49219 1571_f_at L49229 1572_s_at M10051 1573_at M12783 1574_s_at M13982 1575_at M14758 1576_g_at M14758 1577_at M23263 1578_g_at M23263 1579_at M27288 157_at U65011 1580_f_at M27318 1581_s_at M27504 1582_at M29540 1583_at M32315 1584_at M34065 1585_at M34309 1586_at M35878 1587_at M38258 1588_at L42243 1589_s_at L42243 158_at U40992 1590_s_at J00277 1591_s_at J03242 1592_at J04088 1593_at J04513 1594_at J05448 1595_at L06139 1596_g_at L06139 1597_at L13720 1598_g_at L13720 1599_at L25876 159_at U43142 1600_at L27071 1601_s_at L27559 1602_at L33881 1603_g_at L33881 1604_at L36644 1605_g_at L36644 1606_at L36645 1607_at L36844 1608_at HG4272-HT4542 1609_g_at HG4272-HT4542 160_at U43899 1610_s_at J00139 1611_s_at J00219 1612_s_at X56681 1613_s_at X63546 1614_s_at X63546 1615_at Z23115 1616_at D14838 1617_at D21205 1618_at D21241 1619_g_at D21241 161_at U44105 1620_at D31784 1621_at D85423 1622_at D87116 1623_s_at HG1761-HT1778 1624_at HG2036-HT2090 1625_at HG2309-HT2405 1626_at HG2714-HT2810 1627_at HG2715-HT2811 1628_at HG3175-HT3352 1629_s_at HG3187-HT3366 162_at U44839 1630_s_at HG3730-HT4000 1631_at HG3942-HT4212 1632_at HG3999-HT4269 1633_g_at U77735 1634_s_at X05839 1635_at U07563 1636_g_at U07563 1637_at U09578 1638_at U11732 1639_s_at U15642 163_at U46461 1640_at U17714 1641_s_at U32986 1642_at U35113 1643_g_at U35113 1644_at U36764 1645_at U43527 1646_at U45880 1647_at U51903 1648_at U60805 1649_at U61836 164_at U47931 1650_g_at U61836 1651_at U73379 1652_at U77735 1653_at M84711 1654_at M95712 1655_s_at S76978 1656_s_at U07563 1657_at D64053 1658_g_at D64053 1659_s_at D78132 165_g_at U47931 1660_at D83004 1661_i_at HG2261-HT2351 1662_r_at HG2261-HT2351 1663_at HG2325-HT2421 1664_at HG3543-HT3739 1665_s_at HG544-HT544 1666_at J00210 1667_s_at J02871 1668_s_at L15409 1669_at L20861 166_at U48405 1670_at L23959 1671_s_at L35253 1672_f_at L41913 1673_at M14764 1674_at M15990 1675_at M23379 1676_s_at M55409 1677_at M65062 1678_g_at M65062 1679_at D38503 167_at U49436 1680_at D43772 1681_at X03635 1682_s_at X58723 1683_at X69950 1684_s_at X69950 1685_at X82554 1686_g_at X82554 1687_s_at X84213 1688_s_at X87843 1689_at AB000895 168_at U50196 1690_at AB000896 1691_at AB000897 1692_s_at AF002700 1693_s_at D11139 1694_s_at D13413 1695_at D23662 1696_at D29013 1697_s_at D37781 1698_g_at U71087 1699_at U71088 169_at U51095 1700_at U82987 1701_at U86136 1702_at X01057 1703_g_at S75174 1704_at S76992 1705_s_at S82362 1706_at U01337 1707_g_at U01337 1708_at U07620 1709_g_at U07620 170_at U51096 1710_s_at U07804 1711_at U09477 1712_s_at U17743 1713_s_at U26727 1714_at U26914 1715_at U37518 1716_at U43586 1717_s_at U45878 1718_at U50523 1719_at U61981 171_at U56833 1720_at U65410 1721_g_at U65410 1722_at U71087 1723_g_at S61953 1724_at S75174 1725_s_at HG884-HT884 1726_at HG919-HT919 1727_at L07868 1728_at L13689 1729_at L41690 172_at U57650 1730_s_at M17446 1731_at M21574 1732_at M37825 1733_at M60315 1734_at M60556 1735_g_at M60556 1736_at M62402 1737_s_at M62403 1738_at M81933 1739_at M99487 173_at U59325 1740_g_at M99487 1741_s_at S37730 1742_at S61953 1743_s_at HG2007-HT2056 1744_at HG4433-HT4703 1745_at HG4679-HT5104 1746_s_at HG4683-HT5108 1747_at AD000092 1748_s_at AD000092 1749_at AD000092 174_s_at U61167 1750_at AD000092 1751_g_at AD000092 1752_at AD000092 1753_s_at AD000092 1754_at AF006041 1755_i_at D00003 1756_f_at D00003 1757_i_at D00408 1758_r_at D00408 1759_f_at D00408 175_s_at U33053 1760_s_at D11327 1761_at D37965 1762_at D38500 1763_at D38502 1764_s_at D85131 1765_at U86214 1766_g_at U86214 1767_s_at X14885 1768_s_at X59932 1769_at AD000092 176_at U37352 1770_at J00207 1771_s_at J03278 1772_s_at L00634 1773_at L00635 1774_at L06895 1775_at L24559 1776_at L24564 1777_at L36463 1778_g_at L36463 1779_s_at M16750 177_at U38545 1780_at M19722 1781_at M25269 1782_s_at M31303 1783_at M37190 1784_s_at S66427 1785_at S66431 1786_at U08023 1787_at U22398 1788_s_at U48807 1789_at U65928 178_f_at U38964 1790_s_at HG3914-HT4184 1791_s_at J00207 1792_g_at M68520 1793_at M80629 1794_at M92287 1795_g_at M92287 1796_s_at U05681 1797_at U40343 1798_at U41060 1799_at U64315 179_at U38980 1800_g_at U64315 1801_at U76638 1802_s_at X03363 1803_at X05360 1804_at X07730 1805_g_at X07730 1806_at X12556 1807_g_at X12556 1808_s_at X89101 1809_at AB003698 180_at S82470 1810_s_at D10495 1811_at D15049 1812_s_at HG1747-HT1764 1813_at HG363-HT363 1814_at D50683 1815_g_at D50683 1816_at D78156 1817_at D89667 1818_at HG1879-HT1919 1819_at HG1996-HT2044 181_g_at S82470 1820_g_at HG1996-HT2044 1821_at HG2600-HT2696 1822_at HG4677-HT5102 1823_g_at HG4677-HT5102 1824_s_at J05614 1825_at L33075 1826_at M12174 1827_s_at M13929 1828_s_at M27968 1829_at M36089 182_at U01062 1830_s_at M38449 1831_at M60314 1832_at M62397 1833_at M68520 1834_at D38449 1836_at D50310 1837_at HG1111-HT1111 1838_g_at HG1111-HT1111 1839_at HG1112-HT1112 183_at U01828 1840_g_at HG1112-HT1112 1841_s_at HG2723-HT2819 1842_at HG2724-HT2820 1843_at HG2825-HT2949 1844_s_at L05624 1845_at L36870 1846_at L78132 1847_s_at M13994 1848_at M22995 1849_s_at S57153 184_at U03642 1850_at U07418 1851_s_at U11821 1852_at X02910 1853_at X03072 1854_at X13293 1855_at X14445 1856_at X75042 1857_at AF010193 1858_at D38122 1859_s_at U33203 185_at U04840 1860_at U58334 1861_at U66879 1862_at U67092 1863_s_at U67092 1864_at X03663 1865_at X15217 1866_g_at X15217 1867_at AF005775 1868_g_at AF005775 1869_at AF015950 186_at U06454 1870_at D13540 1871_g_at D13540 1872_at D14134 1873_at D21089 1874_at D21090 1875_f_at D38498 1876_at HG1103-HT1103 1877_g_at HG1103-HT1103 1878_g_at M13194 1879_at M14949 187_at U07349 1880_at M92424 1881_at HG4058-HT4328 1882_g_at HG4058-HT4328 1883_s_at HG4757-HT5207 1884_s_at M15796 1885_at M31899 1886_at U53476 1887_g_at U53476 1888_s_at X06182 1889_s_at X12949 188_at U09303 1890_at AB000584 1891_at D14497 1892_s_at HG1437-HT1437 1893_s_at HG3125-HT3301 1894_f_at HG3236-HT3413 1895_at J04111 1896_s_at L05628 1897_at L07594 1898_at L24203 1899_s_at L33262 189_s_at U09937 1900_at L41870 1901_s_at M12036 1902_at M13194 1903_at HG3521-HT3715 1904_at D50692 1905_s_at HG2441-HT2537 1906_at HG511-HT511 1907_at L14812 1908_at L16464 1909_at M14745 190_at U12767 1910_s_at M14745 1911_s_at M60974 1912_s_at M74088 1913_at U47414 1914_at U66838 1915_s_at V01512 1916_s_at V01512 1917_at X03484 1918_at X15218 1919_at X16316 191_at U14383 1920_s_at X77794 1921_at HG2510-HT2606 1922_g_at HG2510-HT2606 1923_at M74091 1924_at U11791 1925_at Z36714 1926_at U48801 1927_s_at U77713 1928_s_at U78733 1929_at U83508 192_at U18062 1930_at U83659 1931_at U83660 1932_at U83661 1933_g_at U83661 1934_s_at X94216 1935_at AF007111 1936_s_at HG3523-HT4899 1937_at HG4036-HT4306 1938_at K03218 1939_at M22898 193_at U21858 1940_at M54968 1941_at U33761 1942_s_at U37022 1943_at X51688 1944_f_at AF001359 1945_at M25753 1946_at M60614 1947_g_at M60614 1948_f_at U31511 1949_at AA903299 194_at U25433 1950_s_at AB004922 1951_at AF004327 1952_s_at AF010607 1953_at AF024710 1954_at AF035121 1955_s_at AF035528 1956_s_at AF049656 1957_s_at AF054598 1958_at AJ000185 1959_at D88674 195_s_at U28014 1960_at L22967 1961_f_at L23210 1962_at M14502 1963_at U01134 1964_g_at U01134 1965_s_at U17326 1966_i_at U18334 1967_f_at U18334 1968_g_at X76079 1969_s_at X77743 196_s_at U28015 1970_s_at Z71929 1971_g_at U46922 1972_s_at U89330 1973_s_at V00568 1974_s_at X02469 1975_s_at X03563 1976_s_at X06292 1977_s_at X14798 1978_at X17033 1979_s_at X55504 197_at U29656 1980_s_at X58965 1981_s_at X60287 1982_s_at X66893 1983_at X68452 1984_s_at X69549 1985_s_at X73066 1986_at X74594 1987_at X76079 1988_at X76079 1989_at U43746 198_g_at U29656 1990_g_at U43746 1991_s_at U43784 1992_at U46922 1993_s_at U14680 1994_at U16028 1995_at U16815 1996_s_at U17105 1997_s_at U19599 1998_i_at U19599 1999_s_at U19775 199_s_at U33052 2000_at U26455 2001_g_at U26455 2002_s_at U27467 2003_s_at U28946 2004_at U29671 2005_s_at U31317 2006_at U31601 2007_g_at U31601 2008_s_at U33199 2009_at U33284 200_at S81957 2010_at U33760 2011_s_at U34584 2012_s_at U34994 2013_at U35117 2014_s_at U39064 2015_s_at U14658 2016_s_at M64241 2017_s_at M64349 2018_at M65188 2019_s_at M68892 201_s_at S82297 2020_at M73554 2021_s_at M73812 2022_at M77198 2023_g_at M77198 2024_s_at M79321 2025_s_at M80261 2026_at M83215 2027_at M87068 2028_s_at M96577 2029_at N36267 202_at M65217 2030_at N95031 2031_s_at U03106 2032_s_at U07375 2033_s_at U10564 2034_s_at U10906 2035_s_at M55914 2036_s_at M59040 2037_s_at M60725 2038_g_at M13995 2039_s_at M14333 203_at M68891 2040_s_at M14752 2041_i_at M14752 2042_s_at M15024 2043_s_at M15025 2044_s_at M15400 2045_s_at M16592 2046_at M21536 2047_s_at M23410 2048_s_at M26747 2049_s_at M29039 204_at M74297 2050_s_at M29870 2051_at M31767 2052_g_at M31767 2053_at M34064 2054_g_at M34064 2055_s_at M34189 2056_at M34641 2057_g_at M34641 2058_s_at M35011 2059_s_at M36881 205_g_at M74297 2060_at M13995 2061_at L12002 2062_at L19182 2063_at L20046 2064_g_at L20046 2065_s_at L22473 2066_at L22474 2067_f_at L22475 2068_s_at L22846 2069_s_at L23805 206_at M84424 2070_i_at L26318 2071_s_at L26318 2072_at L34057 2073_s_at L34058 2074_at L34954 2075_s_at L36719 2076_s_at L37361 2077_at L40385 2078_s_at M13228 2079_s_at M13970 207_at M86752 2080_s_at L04791 2081_s_at L07032 2082_s_at L08599 2083_at L10822 2084_s_at D12765 2085_s_at D14705 2086_s_at D17517 2087_s_at D21254 2088_s_at D31661 2089_s_at H06628 208_at M94151 2090_i_at H12458 2091_at H23429 2092_s_at J04765 2093_s_at J04977 2094_s_at K00650 209_at M94167 210_at M95678 211_at M97388 212_at M97639 213_at M97675 214_at M97676 215_g_at M97676 216_at M98539 217_at S39329 218_at S74221 219_i_at S76756 220_r_at S76756 221_s_at S78467 222_at S79639 223_at S81003 224_at S81439 225_at M31328 226_at M33336 227_g_at M33336 228_at M35416 229_at M37197 230_s_at M54914 231_at M55153 232_at M55210 233_s_at M55682 234_s_at M57399 235_at M59488 236_at M60165 237_s_at M60483 238_at M60724 239_at M63138 240_at M64231 241_g_at M64231 242_at M64571 243_g_at M64571 244_at M64673 245_at M25280 246_at M25629 247_s_at M26856 248_at L40388 249_at L41066 250_at L41067 251_at L41816 252_at L42324 253_g_at L42324 254_at M11353 255_s_at M13981 256_s_at M14199 257_at M14648 258_at M16441 259_s_at M16441 260_at M16447 261_s_at M19828 262_at M21154 263_g_at M21154 264_at M23533 265_s_at M24736 266_s_at L33930 267_at L34075 268_at L34657 269_at L40387 270_at J04449 271_s_at J05036 272_at K02054 273_g_at K02054 274_at L04282 275_at L05147 276_at L08069 277_at L08246 278_at L13436 279_at L13740 280_g_at L13740 281_s_at L14778 282_at L16782 283_at L16842 284_at L19778 285_g_at L19778 286_at L19779 287_at L19871 288_s_at L25931 289_at L29277 290_s_at L32831 291_s_at J04152 292_s_at HG3484-HT3678 293_at HG3884-HT4154 294_s_at HG4120-HT4392 295_s_at HG4318-HT4588 296_at HG4322-HT4592 297_g_at HG4322-HT4592 298_at HG4411-HT4681 299_i_at HG4518-HT4921 300_f_at HG4518-HT4921 301_at HG881-HT881 302_at HG896-HT896 303_at HG960-HT960 304_at HG961-HT961 305_g_at HG961-HT961 306_s_at J02621 307_at J03600 308_f_at J03756 309_f_at J03756 310_s_at J03778 311_s_at HG3044-HT3742 312_s_at HG3075-HT3236 313_at HG3162-HT3339 314_at D42138 315_at D45132 316_g_at D45132 317_at D55696 318_at D64142 319_g_at D64142 320_at D83703 321_at D88460 322_at D88532 323_at HG1019-HT1019 324_f_at HG1515-HT1515 325_s_at HG1763-HT1780 326_i_at HG1800-HT1823 327_f_at HG1800-HT1823 328_at HG2152-HT2222 329_s_at HG2238-HT2321 330_s_at HG2259-HT2348 331_at HG2566-HT4867 332_at HG2573-HT2669 333_s_at HG2639-HT2735 334_s_at HG2987-HT3136 335_r_at HG3033-HT3194 336_at D38081 337_at AF005043 338_at AF005887 339_at AF035752 340_at AJ001047 341_at D10202 342_at D12485 343_s_at D12485 344_s_at D13146 345_at D13789 346_s_at D13814 347_s_at D14530 348_at D14678 349_g_at D14678 350_at D28118 351_f_at D28423 352_at D30036 353_at D30037 354_s_at D37984 355_s_at D38037 356_at AB017430 357_at AF000430 358_at AF000545 359_at Y10659 360_at Y11999 361_at Y13620 362_at Z15108 363_at Z15114 364_s_at Z16411 365_at Z22780 366_s_at Z29066 367_at Z29067 368_at Z29083 369_s_at Z29331 370_at Z35102 371_at Z56281 372_f_at Z84718 373_at Z84718 374_f_at Z84718 375_at Z84718 376_at AB000220 377_g_at AB000220 378_s_at AB000381 379_at AB006679 380_at Y09445 381_s_at Y10055 382_at X70218 383_at X70340 384_at X71874 385_at X71874 386_g_at X71874 387_at X80230 388_at X80907 389_s_at X82279 390_at X85740 391_at X89416 392_g_at X89416 393_s_at X90976 394_at X92106 395_at X94629 396_f_at X97671 397_at X98311 398_at X98743 399_at X99325 400_at X99894 401_s_at X68985 402_s_at X69819 403_s_at X69878 404_at X52425 405_at X52773 406_at X53587 407_at X54131 408_at X54489 409_at X56468 410_s_at X57152 411_i_at X57351 412_s_at X58431 413_at X59372 414_at X59373 415_at X59656 416_s_at X61755 417_at X65293 418_at X65550 419_at X65550 420_at X65633 421_at X66397 422_s_at X66867 423_at X66899 424_s_at X66945 425_at X67325 426_at X51730 427_f_at V00551 428_s_at V00567 429_f_at X00734 430_at X00737 431_at X02530 432_s_at X02883 433_at X02883 434_at X03473 435_g_at X03473 436_at X04688 437_at X05232 438_at X07767 439_at X07876 440_at X12492 441_s_at X13967 442_at X15187 443_at X17360 444_g_at X17360 445_at U80669 446_at U89896 447_g_at U89896 448_s_at U93237 449_at U66469 450_g_at U66469 451_at U66559 452_at U66615 453_at U66616 454_at U66617 455_at U66618 456_at U66619 457_s_at U67122 458_at U68030 459_s_at U68485 460_at U68727 461_at U70063 462_at U70862 463_g_at U70862 464_s_at U72882 465_at U74667 466_at U77948 467_at U63717 468_at U66198 469_at U66406 470_at U66468 471_f_at U47634 472_at U48730 473_g_at U48730 474_at U49379 475_at U50062 476_s_at U50079 477_at U51127 478_g_at U51127 479_at U53446 480_at U56816 481_at U57452 482_at U59289 483_g_at U59289 484_at U59302 485_at U59748 486_at U60521 487_g_at U60521 488_at U61166 489_at U63329 490_g_at U63329 491_at U46116 492_g_at U46116 493_at U29171 494_at U31120 495_at U31628 496_s_at U32324 497_at U32680 498_at U33821 499_at U33822 500_at U37143 501_g_at U37143 502_s_at U37431 503_at U37690 504_at U39318 505_at U43077 506_s_at U43185 507_s_at U43189 508_at U43923 509_at U44378 510_g_at U44378 511_s_at U22322 512_at U22662 513_at U25265 514_at U26710 515_s_at U26712 517_at U07000 518_at U07132 519_g_at U07132 520_at U07358 521_at U07807 522_s_at U08471 523_s_at U13061 524_at U13695 525_g_at U13695 526_s_at U13696 527_at U14518 528_at U15590 529_at U15932 530_at U16258 531_at U16307 532_at U17418 533_g_at U17418 534_s_at U20391 535_s_at U20816 537_f_at U07000 538_at S53911 539_at S59184 540_at S67070 541_g_at S67070 542_at S74445 543_g_at S74445 544_at S76638 545_g_at S76638 546_at S76965 547_s_at S77154 548_s_at S80267 549_at S80343 550_at S82075 551_at U01877 552_at U02570 553_g_at U02570 554_at U03634 555_at U05227 556_s_at M96233 557_s_at M96738 558_at M98776 559_s_at S38742 560_s_at M63589 561_at M65085 562_g_at M65085 563_at M65290 564_at M69013 565_at M74047 566_at M79462 567_s_at M79463 568_at M80335 569_g_at M80335 570_at M83221 571_at M86667 572_at M86699 573_at M86826 574_s_at M87507 575_s_at M93036 576_at M93718 577_at M94250 578_at M94633 579_at M95724 580_at M60748 581_at M61916 582_g_at M29960 583_s_at M30257 584_s_at M30938 585_at M30938 586_s_at M31153 587_at M31210 588_at M31724 589_at M32313 590_at M32334 591_s_at M33684 592_at M34079 593_s_at M34353 594_s_at M55265 595_at M59465 596_s_at M59820 597_at M59964 598_at M60299 599_at M60721 600_at M28215 601_s_at M28439 602_s_at M29037 603_at M29960 604_at L78833 605_at L78833 606_at L78833 607_s_at M10321 608_at M12529 609_f_at M13485 610_at M15169 611_at M18185 612_s_at M19650 613_at M21389 614_at M22430 615_s_at M24351 616_s_at M24748 617_at M24902 618_at M26167 619_s_at M27394 620_at M28210 621_at M28211 622_at M28212 623_s_at M28213 624_at M28214 625_at L78833 626_s_at L78833 627_g_at L37112 628_at L37882 629_at L39064 630_at L39874 631_g_at L39874 632_at L40027 633_s_at L40386 634_at L41351 635_s_at L42374 636_at L43338 637_at L43366 638_at L46353 639_s_at L47345 640_at L48211 641_at L76517 642_s_at L76528 643_at L76571 644_at L78833 645_at L26336 646_s_at L29218 647_at L35545 648_at L37112 649_s_at L06797 650_s_at L07044 651_at L07493 652_g_at L07493 653_at L07540 654_at L07648 655_at L07949 656_at L08488 657_at L11373 658_at L12350 659_g_at L12350 660_at L13286 661_at L13698 662_at L13848 663_at L18960 664_at L19593 665_at L20321 666_at L20965 667_at L22206 668_s_at L22524 669_s_at L05072 670_s_at L05515 671_at J03040 672_at J03764 673_at J04031 674_g_at J04031 675_at J04164 676_g_at J04164 677_s_at J04430 678_at J04948 679_at J04990 680_s_at J05253 681_at J05556 682_at K01900 683_at K02100 684_at K02215 685_f_at K03460 686_s_at K03498 687_at K03498 688_at L02426 689_at L02867 690_s_at L04947 691_g_at J02783 692_s_at J02947 693_g_at HG2530-HT2626 694_at HG2689-HT2785 695_at HG331-HT331 696_at HG3502-HT3696 697_f_at HG3527-HT3721 698_f_at HG3635-HT3845 699_s_at HG371-HT1063 700_s_at HG371-HT26388 701_s_at HG3725-HT3981 702_f_at HG3729-HT3999 703_at HG3731-HT4001 704_at HG4167-HT4437 705_at HG4234-HT4504 706_at HG4582-HT4987 707_s_at HG880-HT880 708_at J00301 709_at J00314 710_at J02783 711_at HG2339-HT2435 712_s_at HG2379-HT3997 713_at HG2525-HT2621 714_at HG2530-HT2626 715_s_at D87002 716_at D87002 717_at D87119 718_at D87258 719_g_at D87258 720_at D87673 721_g_at D87673 722_at D87957 723_s_at HG1322-HT5143 724_at HG1604-HT1604 725_i_at HG1751-HT1768 726_f_at HG1751-HT1768 727_at HG1804-HT1829 728_at HG2028-HT2082 729_i_at HG2147-HT2217 730_r_at HG2147-HT2217 731_f_at HG2147-HT2217 732_f_at HG2148-HT2218 733_at HG2149-HT2219 734_at HG2157-HT2227 735_s_at HG2167-HT2237 736_f_at D87002 737_at D87002 738_at D38524 739_at D42072 740_at D49394 741_g_at D49394 742_at D49742 743_at D50370 744_at D50487 745_at D50495 746_at D50640 747_at D63134 748_s_at D63940 749_at D78586 750_at D85376 751_at D85418 752_s_at D85429 753_at D86425 754_s_at D87002 755_at D26070 756_at D26350 757_at D28364 758_at D38128 759_at D38145 760_at Y09216 761_g_at Y09216 762_f_at AB000905 763_at AB001106 764_s_at AB005535 765_s_at AB006781 766_at AB006782 767_at AF001548 768_at AF005361 769_s_at D00017 770_at D00632 771_s_at D00749 772_at D10656 773_at D10667 774_g_at D10667 775_at D10995 776_at D13435 777_at D13988 778_s_at D16827 779_at D21337 780_at X90978 781_at X98001 782_at U93867 783_at U96113 784_g_at U96113 785_at U96114 786_at X06745 787_at X51417 788_s_at X52001 789_at X52541 790_at X52599 791_g_at X52599 792_s_at X52611 793_at X54936 794_at X62055 795_s_at X66358 796_i_at X66358 797_at X68264 798_at X74330 799_at X80343 800_g_at X80343 801_at X82676 802_at X84002 803_at X84003 804_s_at X86371 805_at U52518 806_at U56998 807_at U57092 808_at U57093 809_at U57094 810_at U64105 811_at U64444 812_at U68111 813_at U68133 814_s_at U68135 815_at U70987 816_g_at U70987 817_at U72209 818_s_at U72936 819_at U76456 820_at U77604 821_s_at U78793 822_s_at U79115 823_at U84487 824_at U90313 825_at U48736 826_at U50553 827_s_at U52373 828_at U19487 829_s_at U21689 830_at U25801 831_at U28042 832_at U39317 833_at U40279 834_at U40462 835_at U41745 836_at U43148 837_s_at U43944 838_s_at U45328 839_at U46499 840_at U47742 841_at U48250 842_at U48251 843_at U48296 844_at U48707 845_at U16031 846_s_at U16811 847_at U17969 848_at U19261 849_g_at U19261 850_r_at S62539 851_s_at S62539 852_at S70348 853_at S74017 854_at S76617 855_at S78085 856_at S79267 857_at S87759 858_at S90469 859_at U03688 860_at U03911 861_g_at U03911 862_at U04313 863_g_at U04313 864_at U07664 865_at U08316 866_at U12471 867_s_at U12471 868_at U13991 869_at U14193 870_f_at M93311 871_s_at M95585 872_i_at S62539 873_at M26679 874_at M26683 875_g_at M26683 876_at M27543 877_at M27691 878_s_at M29386 879_at M30818 880_at M34539 881_at M35198 882_at M37435 883_s_at M54915 884_at M59911 885_g_at M59911 886_at M60527 887_at M62302 888_s_at M62302 889_at M73780 890_at M74524 891_at M77698 892_at M90657 893_at M91670 894_g_at M91670 895_at L19686 896_at L21998 897_at L33243 898_s_at L37360 899_at L38517 900_at L41349 901_g_at L41349 902_at L41939 903_at L42373 904_s_at L47276 905_at L76200 906_at L78440 907_at M13792 908_at M14660 909_g_at M14660 910_at M15205 911_s_at M19311 912_s_at M21056 913_at M21535 914_g_at M21535 915_at M24594 916_at L18983 917_g_at L18983 918_at HG4724-HT5166 919_at HG825-HT825 920_at HG846-HT846 921_s_at HG921-HT3995 922_at J02902 923_at J03589 924_s_at J03805 925_at J03909 926_at J03910 927_s_at J05582 928_at L02785 929_at L02932 930_at L07590 931_at L08177 932_i_at L11672 933_f_at L11672 934_at L11702 935_at L12168 936_s_at HG3570-HT3773 937_at HG3934-HT4204 938_at HG3936-HT4206 939_at HG406-HT406 940_g_at D12625 941_at D29012 942_at D31815 943_at D43968 944_s_at D49354 945_at D50063 946_at D50663 947_at D55716 948_s_at D63861 949_s_at D78275 950_at D87127 951_at D88378 952_at HG1139-HT4910 953_g_at HG1139-HT4910 954_s_at HG1614-HT1614 955_at HG1862-HT1897 956_at HG1980-HT2023 957_at HG2059-HT2114 958_s_at HG2274-HT2370 959_at HG2463-HT2559 960_g_at HG2463-HT2559 961_at D12625 962_at X83107 963_at X83441 964_at X95715 965_at X97630 966_at X97795 967_g_at X97795 968_i_at X98296 969_s_at X98296 970_r_at X98296 971_s_at Y00083 972_s_at Y00285 973_at Y10032 974_at Y10256 975_at Y13115 976_s_at Z11695 977_s_at Z35402 978_at Z79581 979_g_at Z79581 980_at AF002020 981_at X74794 982_at X74795 983_at X79483 984_g_at X79483 985_s_at X12830 986_at X13589 987_g_at X13589 988_at X16354 989_at X17576 990_at X51602 991_g_at X51602 992_at X52221 993_at X54637 994_at X58288 995_g_at X58288 996_at X59065 997_at X59727 998_s_at X59770 999_at X59812 AFFX-BioB-3_at J04423 AFFX-BioB-3_st J04423 AFFX-BioB-5_at J04423 AFFX-BioB-5_st J04423 AFFX-BioB-M_at J04423 AFFX-BioB-M_st J04423 AFFX-BioC-3_at J04423 AFFX-BioC-3_st J04423 AFFX-BioC-5_at J04423 AFFX-BioC-5_st J04423 AFFX-BioDn-3_at J04423 AFFX-BioDn-3_st J04423 AFFX-BioDn-5_at J04423 AFFX-BioDn-5_st J04423 AFFX-CreX-3_at X03453 AFFX-CreX-3_st X03453 AFFX-CreX-5_at X03453 AFFX-CreX-5_st X03453 AFFX-DapX-3_at L38424 AFFX-DapX-5_at L38424 AFFX-DapX-M_at L38424 AFFX-HSAC07/X00351_3_at X00351 AFFX-HSAC07/X00351_3_st X00351 AFFX-HSAC07/X00351_5_at X00351 AFFX-HSAC07/X00351_5_st X00351 AFFX-HSAC07/X00351_M_at X00351 AFFX-HSAC07/X00351_M_st X00351 AFFX-HUMGAPDH/M33197_3_at M33197 AFFX-HUMGAPDH/M33197_3_st M33197 AFFX-HUMGAPDH/M33197_5_at M33197 AFFX-HUMGAPDH/M33197_5_st M33197 AFFX-HUMGAPDH/M33197_M_at M33197 AFFX-HUMGAPDH/M33197_M_st M33197 AFFX-HUMISGF3A/M97935_3_at M97935 AFFX-HUMISGF3A/M97935_5_at M97935 AFFX-HUMISGF3A/M97935_MA_at M97935 AFFX-HUMISGF3A/M97935_MB_at M97935 AFFX-HUMRGE/M10098_3_at M10098 AFFX-HUMRGE/M10098_5_at M10098 AFFX-HUMRGE/M10098_M_at M10098 AFFX-HUMTFRR/M11507_3_at M11507 AFFX-HUMTFRR/M11507_5_at M11507 AFFX-HUMTFRR/M11507_M_at M11507 AFFX-LysX-3_at X17013 AFFX-LysX-5_at X17013 AFFX-LysX-M_at X17013 AFFX-M27830_3_at M27830 AFFX-M27830_5_at M27830 AFFX-M27830_M_at M27830 AFFX-MurFAS_at M83649 AFFX-MurIL10_at M37897 AFFX-MurIL2_at M16762 AFFX-MurIL4_at M25892 AFFX-PheX-3_at M24537 AFFX-PheX-5_at M24537 AFFX-PheX-M_at M24537 AFFX-ThrX-3_at X04603 AFFX-ThrX-5_at X04603 AFFX-ThrX-M_at X04603 AFFX-TrpnX-3_at K01391 AFFX-TrpnX-5_at K01391 AFFX-TrpnX-M_at K01391 AFFX-YEL002c/WBP1_at X61388 AFFX-YEL018w/_at U18530 AFFX-YEL021w/URA3_at K02207 AFFX-YEL024w/RIP1_at M23316 hum_alu_at U14573 AnnotationDbi/inst/extdata/hgu95av2_ID0000644000175200017520000064253114710217313020617 0ustar00biocbuildbiocbuild32739_at AA001791 41306_at AA004795 34862_at AA005018 40943_at AA009569 34027_f_at AA010078 38608_at AA010777 40608_at AA013087 38440_s_at AA015605 32876_s_at AA017195 35861_at AA018440 32875_at AA019845 41270_at AA019936 33662_at AA021140 41588_at AA022949 33394_at AA034074 41062_at AA037278 41063_g_at AA037278 38807_at AA043348 40907_at AA043502 40550_at AA044758 41360_at AA044787 39830_at AA044823 39502_at AA044910 32733_at AA045160 34889_at AA056747 32781_f_at AA058762 32782_r_at AA058762 40986_s_at AA058852 38676_at AA059408 32396_f_at AA079018 32397_r_at AA079018 32564_at AA083129 35235_at AA099265 35236_g_at AA099265 37398_at AA100961 32101_at AA112483 36633_at AA114830 38674_at AA115140 36846_s_at AA121509 36847_r_at AA121509 41289_at AA126505 41172_at AA126515 33865_at AA127624 38430_at AA128249 41548_at AA128314 40197_at AA129726 33144_at AA129777 34319_at AA131149 33541_s_at AA133246 32606_at AA135683 33399_at AA142942 41601_at AA142964 39289_at AA143021 33430_at AA143321 32251_at AA149307 32789_at AA149428 41837_at AA149431 40427_at AA149486 32555_at AA149637 32526_at AA149644 40168_at AA150110 32720_at AA151716 32721_at AA151922 34703_f_at AA151971 34704_r_at AA151971 32222_at AA152202 39031_at AA152406 33175_at AA156237 40079_at AA156240 39162_at AA156987 33409_at AA158243 40937_at AA160056 32203_at AA160708 33844_at AA160724 40819_at AA161065 35889_at AA165410 32566_at AA165701 40590_at AA166687 40911_at AA167197 41674_at AA169447 34340_at AA173896 40485_at AA176780 40486_g_at AA176780 37965_at AA181053 35972_at AA181196 37966_at AA187563 38667_at AA189161 39546_s_at AA191426 35813_at AA192359 41282_s_at AA194159 34805_at AA195301 41748_at AA196476 37612_at AA203126 33445_at AA203138 38305_at AA203187 38432_at AA203213 37314_at AA203214 41821_at AA203246 38695_at AA203303 41121_at AA203345 38981_at AA203354 40412_at AA203476 33390_at AA203487 32213_at AA203527 41810_at AA203545 41186_at AA203703 37102_at AA203717 40150_at AA205857 33198_at AA206524 39819_at AA213789 41847_at AA214546 32163_f_at AA216639 33647_s_at AA224768 39120_at AA224832 34980_at AA232316 39969_at AA255502 40952_at AA257983 35413_s_at AA258092 35451_s_at AA280726 40772_at AA284298 33049_at AA287446 40923_at AA290994 37368_at AA292277 40495_at AA306076 41732_at AA310786 34083_at AA311181 31798_at AA314825 40628_at AA322648 31958_i_at AA347932 41334_r_at AA398463 36406_at AA401397 39887_at AA401754 39905_i_at AA402332 39906_r_at AA402332 40261_at AA402524 39811_at AA402538 34778_at AA418080 34246_at AA418437 35470_at AA418537 35471_g_at AA418537 36027_at AA418779 41770_at AA420624 41771_g_at AA420624 35914_r_at AA424600 39538_at AA426361 38751_i_at AA426364 38752_r_at AA426364 38531_at AA428150 40722_at AA431822 41559_at AA434319 34947_at AA442560 40868_at AA442799 35805_at AA447263 31954_f_at AA447559 33832_at AA448478 32831_at AA453183 41315_at AA456343 39512_s_at AA457029 39513_r_at AA457029 39271_at AA461365 39272_g_at AA461365 38776_at AA464312 40287_s_at AA471042 40288_r_at AA471042 38306_at AA477576 39828_at AA477714 41300_s_at AA477898 34216_at AA478904 40273_at AA485440 38761_s_at AA487755 33081_at AA492299 33309_at AA521060 36547_r_at AA521233 33246_at AA521481 39827_at AA522530 39367_at AA522537 40112_at AA522698 40432_at AA522891 33582_s_at AA523313 33583_r_at AA523313 34359_at AA524058 40605_at AA524345 32109_at AA524547 32877_i_at AA524802 32878_f_at AA524802 31937_at AA526011 31938_g_at AA526011 36104_at AA526497 36647_at AA526812 35773_i_at AA527880 35774_r_at AA527880 41321_s_at AA528077 39862_at AA528252 41135_at AA530959 32149_at AA532495 33287_at AA533071 35003_at AA534868 37889_at AA535376 33608_at AA535815 35243_at AA535884 33953_at AA551201 38706_at AA552140 37290_at AA552988 40925_at AA554945 34963_at AA557228 39581_at AA570193 41646_at AA576724 33638_at AA584202 33639_g_at AA584202 34059_at AA586695 34060_g_at AA586695 34458_at AA586894 33782_r_at AA587372 34757_at AA595596 33075_at AA604464 33846_at AA620377 37928_at AA621555 38828_s_at AA628946 38829_r_at AA628946 33354_at AA630312 40561_at AA631074 34352_at AA631698 39119_s_at AA631972 35477_at AA635153 40801_at AA643063 38084_at AA648295 39526_at AA648931 37476_at AA650210 41721_at AA658877 39910_at AA663800 36553_at AA669799 37507_i_at AA675900 37508_f_at AA675900 34124_at AA676496 34711_at AA683055 39395_at AA704137 34119_at AA704268 40761_at AA705628 40762_g_at AA705628 35091_at AA706226 33210_at AA709159 38493_at AA714670 32835_at AA725102 38678_at AA733050 38679_g_at AA733050 37244_at AA746355 38485_at AA760866 35446_at AA767013 38846_at AA768912 39086_g_at AA768912 33177_at AA772106 41240_at AA772359 40615_at AA780049 38926_at AA780435 38309_r_at AA805659 33613_at AA806239 37940_f_at AA806768 38287_at AA808961 40707_at AA810792 36841_at AA811338 33686_at AA812696 32958_at AA812755 41340_at AA827795 33272_at AA829286 36400_at AA831707 38883_at AA843545 40534_at AA843737 32339_at AA844998 37348_s_at AA845349 36107_at AA845575 37923_at AA846749 37924_g_at AA846749 40574_at AA868268 32773_at AA868382 41621_i_at AA868898 41622_r_at AA868898 41571_at AA872560 36720_at AA873266 36347_f_at AA873858 36348_r_at AA873858 35916_s_at AA877215 41593_at AA877218 33854_at AA877795 39815_at AA883101 39816_g_at AA883101 40505_at AA883502 33347_at AA883868 36657_at AA883870 41844_at AA884494 34896_at AA884713 41351_at AA885106 41327_at AA887477 33234_at AA887480 38619_at AA888001 41598_at AA890010 39388_at AA902713 1949_at AA903299 38554_at AA903720 40987_at AA904259 37086_at AA904395 35598_at AA904505 38620_at AA905543 41274_at AA908993 40347_at AA913812 35514_at AA916905 38693_at AA917672 35991_at AA917945 38319_at AA919102 34941_at AA921399 41368_at AA922934 40166_at AA923149 40982_at AA926957 37347_at AA926959 32125_at AA928996 32911_s_at AA931204 41623_s_at AA932443 41624_r_at AA932443 39506_at AA933984 35607_at AA934573 39440_f_at AA962207 40270_at AA969267 31736_at AA975427 41764_at AA976838 34905_at AA977136 34906_g_at AA977136 33116_f_at AA977163 33117_r_at AA977163 31739_at AA977513 33881_at AA977580 41760_at AA978033 41126_at AA978353 34167_s_at AA984230 35858_at AA996066 33448_at AB000095 32949_at AB000099 41031_at AB000114 36927_at AB000115 376_at AB000220 377_g_at AB000220 31713_s_at AB000275 40388_at AB000277 36696_at AB000359 36697_g_at AB000359 378_s_at AB000381 35299_at AB000409 39980_at AB000449 33124_at AB000450 32180_s_at AB000461 1303_at AB000462 41392_at AB000464 41391_at AB000466 35777_at AB000468 35238_at AB000509 37136_at AB000520 1890_at AB000584 35276_at AB000712 33904_at AB000714 40180_at AB000732 41592_at AB000734 35529_at AB000824 36067_at AB000887 1689_at AB000895 1690_at AB000896 1691_at AB000897 762_f_at AB000905 763_at AB001106 39249_at AB001325 31628_at AB001328 35622_at AB001451 33883_at AB001466 38303_at AB001523 39915_at AB001535 35306_at AB001636 33906_at AB001740 34521_at AB001872 35504_at AB001895 36220_at AB001915 40717_at AB001928 35093_at AB002058 31345_at AB002134 36035_at AB002135 34180_at AB002292 32071_at AB002293 39863_at AB002294 41613_at AB002295 38962_at AB002296 36844_at AB002297 40834_at AB002298 37036_at AB002299 40015_at AB002301 40016_g_at AB002301 37914_at AB002303 38314_at AB002304 35352_at AB002305 41381_at AB002306 38766_at AB002307 35313_at AB002308 40747_at AB002309 34372_at AB002310 32026_s_at AB002311 40092_at AB002312 34780_at AB002313 35030_i_at AB002314 35031_r_at AB002314 32801_at AB002315 36750_at AB002316 39589_at AB002317 39765_at AB002318 37943_at AB002319 35011_at AB002320 32592_at AB002321 32761_at AB002322 37300_at AB002323 36828_at AB002324 35609_at AB002325 38343_at AB002326 37652_at AB002328 34681_at AB002329 38030_at AB002330 32045_at AB002331 36080_at AB002332 35241_at AB002333 36025_at AB002335 33917_at AB002336 41464_at AB002337 31606_at AB002338 35057_at AB002339 32660_at AB002340 37286_at AB002341 39313_at AB002342 37092_at AB002343 41386_i_at AB002344 41387_r_at AB002344 35008_at AB002345 39797_at AB002347 34661_at AB002348 32685_at AB002349 38532_at AB002350 39544_at AB002351 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36964_at D42053 39785_at D42054 32078_at D42055 32788_at D42063 739_at D42072 40556_at D42073 37619_at D42084 40271_at D42085 33326_at D42087 1182_at D42108 35828_at D42123 314_at D42138 37718_at D43636 35638_at D43638 33873_at D43642 1183_at D43767 1680_at D43772 34470_at D43945 39783_at D43947 37293_at D43948 40054_at D43949 40417_at D43950 40048_at D43951 943_at D43968 39421_at D43969 1314_at D44466 38976_at D44497 35040_at D44708 31339_at D45027 315_at D45132 316_g_at D45132 1184_at D45248 41171_at D45248 35310_at D45288 39435_at D45333 38800_at D45352 40658_r_at D45371 41794_at D45399 41125_r_at D45421 38617_at D45906 944_s_at D49354 32003_at D49357 740_at D49394 741_g_at D49394 36631_at D49396 37395_at D49400 1185_at D49410 34617_at D49488 41750_at D49489 37044_at D49490 1186_at D49493 41245_at D49493 38523_f_at D49677 34338_at D49738 742_at D49742 39522_at D49817 31979_at D49818 35088_at D49919 1165_at D49950 36939_at D49958 35063_at D50030 40276_at D50063 945_at D50063 1836_at D50310 34428_at D50312 743_at D50370 38596_i_at D50402 38597_f_at D50402 38771_at D50405 35234_at D50406 37500_at D50419 744_at D50487 745_at D50495 33683_at D50525 33569_at D50532 33200_at D50550 35872_at D50640 746_at D50640 41627_at D50645 946_at D50663 1814_at D50683 1815_g_at D50683 1904_at D50692 35421_at D50810 40215_at D50840 37638_at D50857 37553_at D50863 40279_at D50911 40070_at D50912 35615_at D50914 33528_at D50915 36579_at D50916 37312_at D50917 38826_at D50918 33253_at D50919 34289_f_at D50920 35322_at D50922 40032_at D50923 31857_r_at D50924 40652_at D50925 36845_at D50926 32219_at D50927 32099_at D50928 32785_at D50929 40143_at D50930 35744_at D50931 40482_s_at D54318 38492_at D55639 41766_at D55649 36608_at D55654 36505_at D55655 317_at D55696 947_at D55716 33498_at D56495 32790_at D59253 37338_at D61391 747_at D63134 34602_at D63160 32445_at D63390 35800_at D63391 39795_at D63475 40828_at D63476 38472_at D63477 38089_at D63478 32561_at D63480 34743_at D63481 36741_at D63482 41078_at D63484 33281_at D63485 41728_at D63486 37648_at D63487 37962_r_at D63506 36436_at D63521 35895_at D63710 40104_at D63780 31495_at D63789 31496_g_at D63789 33473_at D63813 948_s_at D63861 32220_at D63874 40844_at D63875 37959_at D63876 37642_at D63877 40281_at D63878 35314_at D63880 40957_at D63881 748_s_at D63940 34861_at D63997 39663_at D63998 41762_at D64015 41763_g_at D64015 1657_at D64053 1658_g_at D64053 34579_r_at D64108 39286_at D64109 37218_at D64110 38673_s_at D64137 318_at D64142 319_g_at D64142 38808_at D64154 39155_at D67025 36207_at D67029 33102_at D67031 34461_at D67035 32422_at D70830 39044_s_at D73409 36308_at D76435 40140_at D76444 41422_at D78011 40272_at D78012 36149_at D78014 35839_at D78130 1659_s_at D78132 39864_at D78134 1166_at D78151 1816_at D78156 37978_at D78177 37626_at D78261 37627_g_at D78261 949_s_at D78275 40361_at D78333 36866_at D78334 37193_at D78335 1315_at D78361 34615_at D78367 1423_at D78514 1424_s_at D78577 40661_at D78579 40662_g_at D78579 32031_at D78586 749_at D78586 37749_at D78611 35844_at D79206 37695_at D79983 33889_s_at D79985 38050_at D79986 38158_at D79987 37469_at D79988 38852_at D79989 37598_at D79990 32644_at D79991 32661_s_at D79992 40128_at D79993 37225_at D79994 32671_at D79995 36942_at D79996 38847_at D79997 34858_at D79998 32849_at D80000 31863_at D80001 41150_r_at D80002 40411_at D80003 36970_at D80004 37031_at D80005 37734_at D80006 34731_at D80007 39677_at D80008 38709_at D80009 38098_at D80010 34034_at D80011 37683_at D80012 41440_at D82061 32299_at D82070 39284_at D82326 38855_s_at D82343 35020_at D82344 36491_at D82345 36768_at D82347 38811_at D82348 31671_at D82351 31672_g_at D82351 1660_at D83004 36604_at D83004 35946_at D83017 32598_at D83018 32674_at D83032 39065_s_at D83077 39166_s_at D83174 39167_r_at D83174 36763_at D83175 36170_at D83198 35308_at D83200 40732_at D83243 36533_at D83402 32076_at D83407 39930_at D83492 1296_at D83542 40715_at D83597 1509_at D83646 1510_g_at D83646 40759_at D83646 38879_at D83664 34011_at D83699 38148_at D83702 320_at D83703 32986_s_at D83760 31880_at D83767 41669_at D83776 36192_at D83777 34221_at D83778 38056_at D83779 38419_at D83780 34253_at D83781 37656_at D83782 40061_at D83784 37292_at D83785 33887_at D84064 38047_at D84109 1276_g_at D84110 1297_at D84110 38048_at D84110 38049_g_at D84110 34162_at D84111 34163_g_at D84111 31315_at D84143 34781_at D84145 39014_at D84239 41241_at D84273 40323_at D84276 34261_at D84307 1511_at D84361 38861_at D84371 32424_at D84424 34229_s_at D84454 34230_r_at D84454 37466_at D84488 40117_at D84557 1764_s_at D85131 32265_at D85245 750_at D85376 751_at D85418 1621_at D85423 752_s_at D85429 40656_at D85730 39079_at D85758 38665_at D85939 31927_s_at D86062 32686_at D86096 32688_at D86096 32689_s_at D86096 32690_s_at D86096 32691_s_at D86096 32692_at D86096 33936_at D86181 40710_at D86322 39317_at D86324 37356_r_at D86326 1167_s_at D86331 34483_at D86358 40012_at D86407 753_at D86425 33973_at D86519 1512_at D86550 36946_at D86550 40024_at D86640 40034_r_at D86864 34398_at D86956 38067_at D86957 34875_r_at D86958 38669_at D86959 34387_at D86960 37542_at D86961 37615_at D86962 40873_at D86963 32704_at D86964 37531_at D86965 37551_at D86966 31898_at D86967 37636_at D86969 36940_at D86970 32586_at D86971 36954_at D86972 36603_at D86973 34844_at D86975 33748_at D86976 37390_at D86977 38728_at D86978 31802_at D86979 37533_r_at D86980 38470_i_at D86981 38471_r_at D86981 40971_at D86982 39327_at D86983 33771_at D86984 37748_at D86985 34369_at D86987 39404_s_at D86988 35896_at D87002 715_s_at D87002 716_at D87002 736_f_at D87002 737_at D87002 754_s_at D87002 33542_at D87009 33654_at D87011 32361_s_at D87012 32362_r_at D87012 37281_at D87071 37586_at D87073 37265_at D87074 38122_at D87075 38342_at D87076 38892_at D87077 35359_at D87078 1622_at D87116 40113_at D87119 717_at D87119 34321_i_at D87120 34322_r_at D87120 38100_at D87127 950_at D87127 718_at D87258 719_g_at D87258 36123_at D87292 37764_at D87328 35166_at D87343 39533_at D87432 38487_at D87433 38393_at D87434 40123_at D87435 40447_at D87436 39770_at D87437 40765_at D87438 38436_at D87440 34835_at D87442 37045_at D87443 37751_at D87444 41634_at D87445 36971_at D87446 36034_at D87447 38834_at D87448 37888_at D87449 40086_at D87450 34883_at D87451 36154_at D87452 39377_at D87453 32237_at D87454 39405_at D87455 35633_at D87457 36903_at D87458 37190_at D87459 36211_at D87461 37191_at D87463 41101_at D87464 36155_at D87465 35039_at D87466 38062_at D87467 36307_at D87468 36499_at D87469 36612_at D87470 720_at D87673 721_g_at D87673 39761_at D87682 37336_at D87684 37694_at D87685 38536_at D87717 31907_at D87735 39563_at D87742 35874_at D87845 40438_at D87930 33547_i_at D87942 33548_f_at D87942 36933_at D87953 722_at D87957 37895_at D87969 40056_at D87989 34668_at D88152 40196_at D88153 37123_at D88154 33746_at D88208 37485_at D88308 33324_s_at D88357 36974_at D88378 951_at D88378 40225_at D88435 321_at D88460 39875_at D88460 322_at D88532 34479_at D88532 34708_at D88587 38565_at D88667 1959_at D88674 33367_s_at D88674 1425_at D88795 1168_at D88797 1169_at D88799 33288_i_at D88827 33289_f_at D88827 1277_at D89016 36167_at D89052 33880_at D89053 1426_at D89077 1427_g_at D89077 39624_at D89078 34953_i_at D89094 34954_r_at D89094 40733_f_at D89377 40734_r_at D89377 31744_at D89479 31446_s_at D89501 35725_at D89618 1817_at D89667 40576_f_at D89678 35480_at D89858 32075_at D89859 37106_at D89928 40131_at D89937 40132_g_at D89937 34498_at D89974 38187_at D90041 38912_at D90042 41048_at D90070 38638_at D90084 39160_at D90086 36103_at D90144 38279_at D90150 35192_at D90239 32468_f_at D90278 34884_at D90282 37491_at D90359 41684_at D90391 31989_s_at F08025 32934_i_at F08219 38660_at F27891 37493_at H04668 40319_at H05552 35283_at H05692 2089_s_at H06628 41840_r_at H08175 38328_at H10201 39560_at H10776 41247_at H12054 2090_i_at H12458 40657_r_at H15814 40618_at H15872 39879_s_at H16917 40932_at H18080 34453_at H19081 2091_at H23429 33168_at H24861 39848_at H49759 34809_at H53921 34559_at H55746 41446_f_at H68340 37521_s_at H82458 37522_r_at H82458 34983_at H87920 35783_at H93123 33248_at H94842 40954_at H94881 33538_at H96671 39518_at H97470 39103_s_at H98552 323_at X71875 1876_at M29893 1877_g_at M29893 1837_at M31468 1838_g_at M31468 1839_at M31469 1840_g_at M31469 952_at X55741 953_g_at X55741 1170_at X05825 723_s_at M29063 1892_s_at M12128 1171_s_at S66902 324_f_at X53280 724_at X69117 954_s_at L07395 1278_at X66036 1172_at M77693 1173_g_at M77693 1174_at J00119 1812_s_at X54559 725_i_at J03071 726_f_at J03071 1623_s_at J03358 325_s_at X51502 326_i_at L06498 327_f_at L06498 727_at L08237 1175_s_at Y00498 955_at X52606 1818_at M31470 956_at X02344 1819_at A08695 1820_g_at A08695 1743_s_at X15219 728_at X58531 1624_at X63465 957_at Z11501 729_i_at M55405 730_r_at M55405 731_f_at M55405 732_f_at M55406 733_at M57417 328_at M61872 734_at M64594 735_s_at M90360 329_s_at Z14227 330_s_at X06956 1661_i_at M21896 1662_r_at M21896 1513_at M24543 1514_g_at M24543 958_s_at AD001527 1625_at X03563 1176_at M25108 1663_at M32074 711_at X58840 712_s_at L23928 1905_s_at L41870 959_at M35543 960_g_at M35543 1177_at M36711 1921_at S62035 1922_g_at S62035 713_at X66867 693_g_at U02390 714_at U02390 331_at X14474 332_at X16576 1821_at X52987 333_s_at X64652 1279_s_at X66357 694_at X74955 1280_i_at Z25424 1281_f_at Z25424 1282_s_at Z25427 1283_at Z25428 1284_at Z25429 1285_at Z25431 1626_at Z25436 1627_at Z25437 1841_s_at S49953 1842_at S62138 1843_at J03407 1178_at K01614 1179_at Y00371 1180_g_at Y00371 334_s_at M36612 335_r_at L21990 311_s_at M10905 312_s_at L05186 1893_s_at X73067 313_at D14886 1628_at Z21818 1629_s_at D21211 1162_g_at L25665 1181_at L25665 1894_f_at L27065 1163_at S67334 1428_at X74497 695_at M96686 1164_at X78140 1142_at M8771 1143_s_at M87771 1144_at Z71929 1145_g_at Z71929 1146_at M12807 292_s_at L29219 696_at X16173 1147_at X12795 1903_at X08004 1936_s_at M13930 697_f_at X00264 1664_at M29645 936_s_at M98528 698_f_at M67508 1813_at M99624 699_s_at M21868 700_s_at X52229 701_s_at X73637 702_f_at X74862 1630_s_at Z29630 703_at L38429 293_at X73637 1790_s_at L33264 937_at S70622 938_at S71404 1631_at L25664 1632_at X77664 1937_at M26460 1881_at D43969 1882_g_at D43969 939_at A00127 1515_at X76771 1516_g_at X76771 294_s_at U04824 704_at U07809 705_at U09806 1608_at U11813 1609_g_at U11813 1286_s_at M15530 295_s_at U14755 296_at X79535 297_g_at X79535 298_at Z34280 1744_at Z29078 299_i_at M90355 300_f_at M90355 706_at U80947 1822_at Y07642 1823_g_at Y07642 1745_at M31213 1746_s_at U12597 1148_s_at L12260 918_at U18236 1149_at M33782 1883_s_at Z69745 1906_at M37191 1665_s_at M63193 1150_at X54134 1151_at X59357 919_at L01694 920_at L04288 707_s_at L07517 301_at L07518 1725_s_at X98025 302_at L07803 1726_at L09561 921_s_at L31848 303_at L13857 304_at L13858 305_g_at L13858 31737_at J00068 39063_at J00073 40114_at J00077 1152_i_at J00117 1153_f_at J00117 38291_at J00123 39052_at J00124 37019_at J00129 1610_s_at J00139 37913_at J00140 31479_f_at J00146 31525_s_at J00153 37039_at J00194 1770_at J00207 1791_s_at J00207 1666_at J00210 1021_at J00219 1611_s_at J00219 160038_s_at J00268 1590_s_at J00277 36642_at J00287 708_at J00301 1430_at J00306 37202_at J00307 709_at J00314 36681_at J02611 306_s_at J02621 40379_at J02625 1154_at J02645 37740_r_at J02683 37004_at J02761 691_g_at J02783 710_at J02783 1431_at J02843 39145_at J02854 1667_s_at J02871 33871_s_at J02876 40867_at J02902 922_at J02902 1517_at J02906 37023_at J02923 36543_at J02931 38029_at J02939 33063_at J02940 37833_at J02943 692_s_at J02947 35684_at J02958 32822_at J02966 35928_at J02969 33803_at J02973 39916_r_at J02984 1408_at J02986 31550_at J03019 40095_at J03037 671_at J03040 32631_at J03060 32632_g_at J03060 40889_at J03060 37400_at J03068 37401_g_at J03068 1155_at J03069 31493_s_at J03071 36784_at J03071 39711_at J03075 36795_at J03077 1156_at J03133 1409_at J03161 40109_at J03161 1157_s_at J03171 36675_r_at J03191 1591_s_at J03242 36782_s_at J03242 1388_g_at J03258 1410_at J03258 1771_s_at J03278 35133_at J03358 40176_at J03407 38081_at J03459 32305_at J03464 32306_g_at J03464 1287_at J03473 41146_at J03473 37394_at J03507 38691_s_at J03553 923_at J03589 40435_at J03592 40436_g_at J03592 307_at J03600 33815_at J03626 40357_at J03634 308_f_at J03756 309_f_at J03756 672_at J03764 310_s_at J03778 1389_at J03779 32343_at J03796 37949_at J03798 37989_at J03802 924_s_at J03805 38238_at J03810 36652_at J03824 36653_g_at J03824 40336_at J03826 36140_at J03827 34512_at J03853 35506_s_at J03870 39728_at J03909 925_at J03909 926_at J03910 38533_s_at J03925 33523_at J03930 37661_at J04027 673_at J04031 674_g_at J04031 39726_at J04040 1158_s_at J04046 40509_at J04058 37863_at J04076 40496_at J04080 1592_at J04088 1518_at J04101 1519_at J04102 1895_at J04111 32583_at J04111 37633_s_at J04129 36674_at J04130 41868_at J04131 37078_at J04132 35293_at J04137 291_s_at J04152 1159_at J04156 37200_at J04162 675_at J04164 676_g_at J04164 36797_at J04168 36798_g_at J04168 41221_at J04173 37892_at J04177 35418_at J04178 35419_g_at J04178 39758_f_at J04182 AFFX-BioB-3_at J04423 AFFX-BioB-3_st J04423 AFFX-BioB-5_at J04423 AFFX-BioB-5_st J04423 AFFX-BioB-M_at J04423 AFFX-BioB-M_st J04423 AFFX-BioC-3_at J04423 AFFX-BioC-3_st J04423 AFFX-BioC-5_at J04423 AFFX-BioC-5_st J04423 AFFX-BioDn-3_at J04423 AFFX-BioDn-3_st J04423 AFFX-BioDn-5_at J04423 AFFX-BioDn-5_st J04423 677_s_at J04430 1160_at J04444 270_at J04449 31887_at J04469 37299_at J04501 1593_at J04513 41806_at J04513 37670_at J04543 38126_at J04599 36109_at J04605 1288_s_at J04617 39757_at J04621 37054_at J04739 31697_s_at J04755 38486_at J04760 2092_s_at J04765 38780_at J04794 36997_at J04809 37124_i_at J04813 37125_f_at J04813 678_at J04948 36708_at J04970 40854_at J04973 2093_s_at J04977 1161_at J04988 679_at J04990 32615_at J05032 271_s_at J05036 40390_at J05037 35919_at J05068 31859_at J05070 37865_at J05081 34377_at J05096 41369_at J05125 40368_r_at J05158 35131_at J05213 33833_at J05243 1119_at J05249 680_s_at J05253 37413_at J05257 40695_at J05272 37592_at J05401 41376_i_at J05428 41377_f_at J05428 1594_at J05448 1120_at J05459 1121_g_at J05459 36036_at J05500 36037_g_at J05500 36038_r_at J05500 681_at J05556 38783_at J05581 38784_g_at J05581 927_s_at J05582 1824_s_at J05614 37948_at J05682 40316_at K00470 32272_at K00558 31619_at K00627 2094_s_at K00650 31623_f_at K01383 AFFX-TrpnX-3_at K01391 AFFX-TrpnX-5_at K01391 AFFX-TrpnX-M_at K01391 682_at K01900 272_at K02054 273_g_at K02054 683_at K02100 35111_at K02100 AFFX-YEL021w/URA3_at K02207 684_at K02215 35556_at K02402 37234_at K02566 37235_g_at K02566 41400_at K02581 35526_at K02766 37467_at K02882 37015_at K03000 1122_f_at K03183 36767_at K03191 40507_at K03195 40373_at K03203 36774_f_at K03204 32457_f_at K03207 32885_f_at K03208 1938_at K03218 685_f_at K03460 686_s_at K03498 687_at K03498 39122_at K03515 35601_at L00022 32159_at L00049 1390_s_at L00137 37175_at L00190 32855_at L00352 36746_s_at L00587 1772_s_at L00634 1773_at L00635 37488_at L00635 32469_at L00693 38474_at L00972 36901_at L01042 38949_at L01087 33619_at L01124 1123_at L01406 36809_at L01664 34106_at L01694 34886_at L02320 1289_at L02321 1290_g_at L02321 31596_f_at L02326 688_at L02426 32723_at L02547 37922_at L02648 33939_at L02750 928_at L02785 40693_at L02840 689_at L02867 34541_at L02867 32123_at L02870 929_at L02932 41407_at L03411 34215_at L03426 40313_at L03427 37717_at L03532 40773_at L03785 1291_s_at L03840 1497_at L04270 274_at L04282 41466_s_at L04282 34232_at L04288 35478_at L04489 36205_at L04490 37537_at L04510 38001_at L04569 40549_at L04658 1124_at L04731 39057_at L04733 1391_s_at L04751 2080_s_at L04791 35043_at L04791 690_s_at L04947 669_s_at L05072 31708_at L05095 35549_at L05096 33702_f_at L05144 275_at L05147 41226_at L05147 1498_at L05148 1125_s_at L05424 1126_s_at L05424 40493_at L05424 36930_at L05425 35580_at L05500 670_s_at L05515 34604_at L05568 1844_s_at L05624 1896_s_at L05628 41473_at L05779 40198_at L06132 36523_at L06133 1595_at L06139 1596_g_at L06139 35436_at L06147 33320_at L06175 39531_at L06237 37696_at L06328 36184_at L06419 32438_at L06498 31962_at L06499 649_s_at L06797 40408_at L06845 1774_at L06895 34543_at L06895 2081_s_at L07032 650_s_at L07044 31871_r_at L07077 32146_s_at L07261 33108_i_at L07335 33109_f_at L07335 651_at L07493 652_g_at L07493 40731_at L07515 653_at L07540 38863_at L07540 39269_at L07541 37713_at L07548 35211_at L07590 930_at L07590 37152_at L07592 1897_at L07594 1127_at L07597 36600_at L07633 654_at L07648 39072_at L07648 33064_at L07738 40816_at L07758 37203_at L07765 32138_at L07807 1727_at L07868 34585_at L07919 655_at L07949 32643_at L07956 31477_at L08044 276_at L08069 39118_at L08069 34054_at L08096 931_at L08177 277_at L08246 33146_at L08246 40543_at L08424 40544_g_at L08424 39321_at L08485 656_at L08488 41524_at L08488 2082_s_at L08599 37697_s_at L08666 37996_s_at L08835 37997_r_at L08835 37291_r_at L08850 37710_at L08895 37309_at L09159 37635_at L09190 1128_s_at L09230 31316_at L09234 34890_at L09235 40450_at L09561 33374_at L09708 32884_at L09749 33012_at L09753 32864_at L10102 31331_at L10123 34055_at L10126 34056_g_at L10126 40125_at L10284 39178_at L10333 38516_at L10338 41469_at L10343 37605_at L10347 38408_at L10373 37067_at L10374 39334_s_at L10377 33123_at L10379 32868_at L10386 31349_at L10403 1499_at L10413 38840_s_at L10678 1478_at L10717 1479_g_at L10717 2083_at L10822 40192_at L10844 39725_at L10910 41509_at L11066 34633_s_at L11238 1129_at L11239 38367_s_at L11245 1130_at L11284 1131_at L11285 1292_at L11329 38007_at L11353 31716_at L11369 37562_at L11370 39458_s_at L11372 657_at L11373 31546_at L11566 31811_r_at L11667 32080_at L11669 932_i_at L11672 933_f_at L11672 32903_at L11695 1293_s_at L11701 934_at L11702 38320_s_at L11706 38321_r_at L11706 34738_at L11931 2061_at L12002 1132_s_at L12060 935_at L12168 658_at L12350 659_g_at L12350 37767_at L12392 35042_at L12398 35220_at L12468 32544_s_at L12535 32545_r_at L12535 31822_at L12579 31506_s_at L12691 1133_at L12701 38789_at L12711 1480_at L12723 33703_f_at L12760 31544_at L13203 37754_at L13210 34612_at L13220 31328_at L13258 37134_f_at L13266 37135_f_at L13268 37902_at L13278 31706_at L13283 660_at L13286 31548_at L13291 40592_at L13329 32569_at L13385 38476_at L13434 33126_at L13435 278_at L13436 37701_at L13463 36117_at L13616 31893_at L13687 1728_at L13689 41562_at L13689 661_at L13698 41839_at L13698 1597_at L13720 1598_g_at L13720 37658_at L13720 1134_at L13738 40235_at L13738 279_at L13740 280_g_at L13740 35975_at L13744 36163_at L13761 39037_at L13773 662_at L13848 36153_at L13848 1294_at L13852 33260_at L13857 32857_at L13858 40745_at L13939 38129_at L13943 40290_f_at L13972 40291_r_at L13972 36672_at L13977 36991_at L14076 35854_at L14269 36298_at L14565 41127_at L14595 31861_at L14754 281_s_at L14778 1907_at L14812 31482_at L14813 31483_g_at L14813 32532_at L14837 41510_s_at L15189 34058_at L15309 1135_at L15388 40994_at L15388 1668_s_at L15409 39946_at L15533 35822_at L15702 1908_at L16464 32303_at L16464 37497_at L16499 282_at L16782 35434_at L16794 283_at L16842 1392_at L16862 38637_at L16895 39261_at L16896 1136_at L16991 32714_s_at L17075 40394_at L17128 39704_s_at L17131 31307_at L17325 31487_at L17328 31308_at L17330 35893_s_at L17418 31480_f_at L18877 33518_f_at L18920 663_at L18960 34278_at L18960 916_at L18983 917_g_at L18983 35855_s_at L19058 35856_r_at L19058 1271_g_at L19067 1295_at L19067 36645_at L19067 1272_at L19161 35934_at L19161 2062_at L19182 32791_at L19183 39729_at L19185 33768_at L19267 32296_at L19297 37393_at L19314 32998_at L19315 664_at L19593 36637_at L19605 895_at L19686 36989_at L19711 284_at L19778 285_g_at L19778 286_at L19779 40629_at L19783 287_at L19871 40516_at L19872 2063_at L20046 2064_g_at L20046 41175_at L20298 32886_at L20316 33317_at L20320 665_at L20321 1393_at L20348 35939_s_at L20433 40746_at L20814 39991_at L20815 36643_at L20817 39951_at L20826 1137_at L20852 36956_at L20852 1138_at L20859 40632_at L20860 1669_at L20861 31862_at L20861 33943_at L20941 666_at L20965 33705_at L20971 37053_at L20977 38457_at L21715 34035_at L21893 34826_at L21936 37462_i_at L21990 37463_r_at L21990 896_at L21998 1273_r_at L22005 1274_s_at L22005 41292_at L22009 1139_at L22075 33635_at L22075 667_at L22206 40400_at L22214 35718_at L22342 2065_s_at L22473 2066_at L22474 2067_f_at L22475 668_s_at L22524 32372_at L22569 38209_at L22647 31388_at L22650 2068_s_at L22846 1960_at L22967 32264_at L23134 1961_f_at L23210 40449_at L23320 2069_s_at L23805 1481_at L23808 1482_g_at L23808 39414_at L23849 31539_r_at L23852 1670_at L23959 37757_at L23959 38439_at L24123 1898_at L24203 36446_s_at L24521 1775_at L24559 1776_at L24564 39528_at L24564 32548_at L24804 1394_at L25080 1395_at L25081 37317_at L25107 34534_at L25119 33772_at L25124 33268_at L25270 38427_at L25286 1275_at L25441 37271_at L25444 38955_at L25615 37903_at L25665 1140_at L25851 1599_at L25876 38790_at L25879 32432_f_at L25899 288_s_at L25931 33461_at L26081 40081_at L26232 36019_at L26260 2070_i_at L26318 2071_s_at L26318 34006_s_at L26318 645_at L26336 36925_at L26336 36670_at L26339 33675_at L26494 31925_s_at L26584 37108_at L26953 32966_at L27050 1600_at L27071 33490_at L27071 1141_at L27080 37490_at L27213 36655_at L27476 32971_at L27479 1601_s_at L27559 1396_at L27560 38650_at L27560 36714_at L27586 38416_at L27706 33626_at L27745 36682_at L27841 1117_at L27943 38071_at L28010 32106_at L28101 32496_at L28168 1118_at L28175 38188_s_at L28821 36885_at L28824 39285_at L28957 37296_at L28997 36115_at L29217 646_s_at L29218 38763_at L29254 289_at L29277 39708_at L29277 35906_at L29339 34934_at L29376 33624_at L29385 33625_g_at L29385 39979_at L29433 37074_at L31529 32122_at L31573 1097_s_at L31584 36206_at L31801 38714_at L31860 41537_r_at L31881 40161_at L32137 33564_at L32140 35102_at L32164 36512_at L32179 290_s_at L32831 37114_at L32832 36364_at L32961 1397_at L32976 1398_g_at L32976 34401_at L32977 1825_at L33075 897_at L33243 1899_s_at L33262 38143_at L33404 37480_at L33410 32266_at L33477 34913_at L33798 31609_s_at L33799 1253_at L33801 40645_at L33801 36624_at L33842 1602_at L33881 1603_g_at L33881 266_s_at L33930 33644_at L34035 33902_at L34041 2072_at L34057 2073_s_at L34058 1483_at L34059 1484_at L34060 37289_at L34060 267_at L34075 36384_at L34081 37909_at L34155 35887_at L34219 38609_at L34355 34241_at L34357 39148_s_at L34363 34475_at L34408 35034_at L34409 1399_at L34587 31836_at L34600 268_at L34657 37397_at L34657 34328_s_at L34673 34219_at L34838 2074_at L34954 33909_at L35013 38036_at L35035 39530_at L35240 40568_at L35249 36371_at L35251 1671_s_at L35253 37733_at L35263 39944_at L35269 32498_at L35318 647_at L35545 33163_r_at L35546 41704_at L35592 41123_s_at L35594 41124_r_at L35594 32451_at L35848 33834_at L36033 1098_at L36051 31597_r_at L36055 34537_at L36069 34684_at L36140 40783_s_at L36151 1777_at L36463 1778_g_at L36463 39532_at L36463 40242_at L36529 41005_at L36531 1485_at L36642 1604_at L36644 1605_g_at L36644 1606_at L36645 2075_s_at L36719 41415_at L36720 36598_s_at L36818 1607_at L36844 1254_at L36861 1255_g_at L36861 1845_at L36870 36910_at L36870 32622_at L36983 40850_at L37033 40184_at L37042 38019_at L37043 648_at L37112 627_g_at L37112 1486_at L37127 39475_at L37199 898_s_at L37360 2076_s_at L37361 35024_at L37362 36186_at L37368 39874_at L37378 37985_at L37747 37184_at L37792 36799_at L37882 628_at L37882 39659_at L37936 AFFX-DapX-3_at L38424 AFFX-DapX-5_at L38424 AFFX-DapX-M_at L38424 39066_at L38486 1487_at L38487 1099_s_at L38503 34618_at L38517 899_at L38517 31724_at L38518 36125_s_at L38696 32449_at L38707 38567_at L38820 39064_at L38928 1256_at L38929 32577_s_at L38933 38423_at L38935 33657_at L38941 41196_at L38951 37991_at L38961 32670_at L38969 40221_at L39059 35006_at L39060 34497_at L39061 629_at L39064 35229_at L39211 32709_at L39833 630_at L39874 631_g_at L39874 38458_at L39945 38459_g_at L39945 632_at L40027 39627_at L40157 41611_at L40371 36312_at L40377 2077_at L40385 633_s_at L40386 269_at L40387 248_at L40388 35754_at L40391 41208_at L40392 37693_at L40393 33927_i_at L40396 33928_r_at L40396 36128_at L40397 31884_at L40399 36385_at L40400 36625_at L40401 35843_at L40402 33926_at L40403 41065_at L40407 41251_at L40410 38216_at L40411 40814_at L40586 40815_g_at L40586 34331_at L40636 38178_at L40802 37104_at L40904 33694_at L40933 34501_at L40992 34502_g_at L40992 249_at L41066 37369_s_at L41066 37370_i_at L41066 250_at L41067 40822_at L41067 33441_at L41143 32907_at L41147 36455_at L41162 36886_f_at L41268 900_at L41349 901_g_at L41349 634_at L41351 40886_at L41498 40887_g_at L41498 35033_at L41607 31598_s_at L41668 33649_at L41680 1729_at L41690 251_at L41816 32719_at L41827 1900_at L41870 32165_at L41887 1672_f_at L41913 902_at L41939 40579_at L42025 1568_s_at L42243 1569_r_at L42243 1588_at L42243 1589_s_at L42243 252_at L42324 253_g_at L42324 903_at L42373 635_s_at L42374 1257_s_at L42379 36386_at L42450 38844_at L42451 36718_s_at L42452 36719_r_at L42452 36628_at L42542 32482_at L42563 37659_at L42572 39015_f_at L42611 39016_r_at L42611 36334_at L42621 636_at L43338 637_at L43366 37574_at L43821 41349_at L43964 638_at L46353 38376_at L46590 32356_at L47208 904_s_at L47276 639_s_at L47345 37579_at L47738 640_at L48211 32052_at L48215 41424_at L48516 33720_at L48692 32416_at L48728 33139_s_at L49054 36669_at L49169 1570_f_at L49219 1571_f_at L49229 41203_at L49380 34584_at L75847 38923_at L76159 1100_at L76191 905_at L76200 35697_at L76259 34995_at L76380 32570_at L76465 641_at L76517 642_s_at L76528 1258_s_at L76568 1259_at L76568 40010_s_at L76569 643_at L76571 37505_at L76571 33509_at L76627 40683_at L76687 39068_at L76702 32734_at L76703 33183_at L76927 38136_at L76937 35621_at L77213 36803_at L77561 39534_at L77564 32032_at L77566 39825_at L77567 34440_at L77571 36255_at L77730 1101_at L77864 1488_at L77886 1846_at L78132 41792_at L78207 35490_at L78267 906_at L78440 644_at L78833 604_at L78833 605_at L78833 606_at L78833 625_at L78833 626_s_at L78833 38586_at M10050 1572_s_at M10051 37519_at M10058 AFFX-HUMRGE/M10098_3_at M10098 AFFX-HUMRGE/M10098_5_at M10098 AFFX-HUMRGE/M10098_M_at M10098 607_s_at M10321 1102_s_at M10901 36690_at M10901 31720_s_at M10905 31622_f_at M10943 39328_at M11058 38850_at M11119 34020_at M11166 32472_at M11186 254_at M11353 38634_at M11433 37236_at M11437 AFFX-HUMTFRR/M11507_3_at M11507 AFFX-HUMTFRR/M11507_5_at M11507 AFFX-HUMTFRR/M11507_M_at M11507 1103_at M11567 34072_s_at M11591 1104_s_at M11717 34168_at M11722 33218_at M11730 38388_at M11810 1901_s_at M12036 32313_at M12125 32314_g_at M12125 1826_at M12174 36636_at M12267 36247_f_at M12272 33992_at M12523 608_at M12529 35118_at M12625 1573_at M12783 38541_at M12792 35517_at M12807 40699_at M12824 1105_s_at M12886 1106_s_at M12959 34637_f_at M12963 34638_r_at M12963 31634_at M13057 31635_g_at M13057 35591_at M13142 32353_at M13143 31835_at M13149 31549_at M13150 1878_g_at M13194 1902_at M13194 36519_at M13194 1400_at M13207 1401_g_at M13207 2078_s_at M13228 33520_at M13232 32453_at M13299 37377_i_at M13452 37378_r_at M13452 609_f_at M13485 38428_at M13509 35016_at M13560 35817_at M13577 34523_at M13654 41854_at M13666 39008_at M13699 1107_s_at M13755 907_at M13792 36355_at M13903 34506_at M13928 1827_s_at M13929 34592_at M13932 34593_g_at M13932 32412_at M13934 32413_at M13934 2079_s_at M13970 255_s_at M13981 38544_at M13981 1574_s_at M13982 1847_s_at M13994 2038_g_at M13995 2060_at M13995 39409_at M14058 38125_at M14083 31574_i_at M14087 31575_f_at M14087 37550_at M14113 256_s_at M14199 36528_at M14218 34649_at M14219 36325_at M14306 2039_s_at M14333 40480_s_at M14333 40481_r_at M14333 1962_at M14502 38052_at M14539 31789_at M14564 37195_at M14565 38589_i_at M14630 38590_r_at M14630 257_at M14648 39071_at M14648 908_at M14660 909_g_at M14660 1909_at M14745 1910_s_at M14745 2040_s_at M14752 2041_i_at M14752 1575_at M14758 1576_g_at M14758 1673_at M14764 1879_at M14949 2042_s_at M15024 2043_s_at M15025 35752_s_at M15036 34959_at M15059 34960_g_at M15059 610_at M15169 33308_at M15182 910_at M15205 39402_at M15330 37752_at M15353 37918_at M15395 2044_s_at M15400 33452_at M15518 1884_s_at M15796 41209_at M15856 37452_at M15881 1674_at M15990 1402_at M16038 32616_at M16038 37105_at M16117 36108_at M16276 41138_at M16279 40738_at M16336 33666_at M16342 39340_at M16424 258_at M16441 259_s_at M16441 260_at M16447 38034_at M16505 37841_at M16541 40742_at M16591 2045_s_at M16592 1260_s_at M16594 1261_i_at M16594 38781_at M16594 38936_at M16652 31478_at M16653 33984_at M16660 1779_s_at M16750 AFFX-MurIL2_at M16762 33249_at M16801 37618_at M16937 33115_at M16938 33261_at M16941 32035_at M16942 36621_at M16961 40977_f_at M16965 35245_at M16967 36304_at M16973 41023_at M16974 37137_at M17016 35372_r_at M17017 36383_at M17254 1730_s_at M17446 32300_s_at M17589 31557_at M17733 41694_at M17754 31538_at M17885 31956_f_at M17886 31957_r_at M17886 39680_at M18078 38587_at M18079 611_at M18185 1108_s_at M18391 40488_at M18533 33274_f_at M18645 33699_at M18667 41238_s_at M18700 36105_at M18728 40757_at M18737 1262_s_at M19154 36790_at M19267 36791_g_at M19267 37862_at M19301 36114_r_at M19309 911_s_at M19311 38356_at M19481 33284_at M19507 612_s_at M19650 31963_at M19684 1489_s_at M19720 1490_at M19720 1780_at M19722 261_s_at M19828 37160_at M19888 39443_s_at M19961 1109_s_at M19989 1263_at M20137 32522_f_at M20469 32523_at M20470 38657_s_at M20471 31792_at M20560 40158_r_at M20642 36979_at M20681 31319_at M20707 41350_at M20776 32098_at M20777 32103_at M20786 31386_at M20812 37341_at M20867 31576_at M20919 912_s_at M21056 1403_s_at M21121 1404_r_at M21121 1405_i_at M21121 262_at M21154 263_g_at M21154 36684_at M21154 35807_at M21186 31840_at M21188 38680_at M21259 36734_at M21302 31317_r_at M21388 613_at M21389 913_at M21535 914_g_at M21535 2046_at M21536 36242_at M21539 1731_at M21574 1110_at M21624 34881_at M21812 34485_r_at M21868 36094_at M21984 1406_at M21985 1407_g_at M21985 1387_at M22005 1111_at M22092 1112_g_at M22092 38039_at M22246 34793_s_at M22299 34794_r_at M22299 39385_at M22324 37720_at M22382 37017_at M22430 614_at M22430 39407_at M22488 1113_at M22489 40367_at M22489 1114_at M22490 31314_at M22491 40764_at M22632 39971_at M22637 36157_at M22734 41223_at M22760 36666_at M22806 1939_at M22898 33993_at M22919 33994_g_at M22919 38460_at M22976 1848_at M22995 38756_at M22995 39791_at M23114 39790_at M23115 38727_at M23161 36802_at M23197 33978_at M23234 37001_at M23254 1577_at M23263 1578_g_at M23263 34888_at M23294 AFFX-YEL024w/RIP1_at M23316 36277_at M23323 1675_at M23379 36935_at M23379 2047_s_at M23410 264_at M23533 40857_f_at M23575 36893_at M23668 34636_at M23892 39839_at M24069 41730_at M24122 41731_g_at M24122 34608_at M24194 34609_g_at M24194 32640_at M24283 615_s_at M24351 36877_at M24364 40580_r_at M24398 36141_at M24400 31812_at M24470 37037_at M24486 AFFX-PheX-3_at M24537 AFFX-PheX-5_at M24537 AFFX-PheX-M_at M24537 32814_at M24594 915_at M24594 265_s_at M24736 616_s_at M24748 36680_at M24895 35846_at M24899 32520_at M24900 32200_at M24902 617_at M24902 35294_at M25077 35295_g_at M25077 31687_f_at M25079 1781_at M25269 245_at M25280 40366_at M25322 1264_at M25393 1265_g_at M25393 246_at M25629 37714_at M25667 1945_at M25753 34736_at M25753 36924_r_at M25756 32959_at M25809 AFFX-MurIL4_at M25892 1115_at M25897 36780_at M25915 36874_at M26004 40897_at M26061 1365_at M26062 618_at M26167 32378_at M26252 35766_at M26326 39333_at M26576 41148_at M26665 873_at M26679 35103_i_at M26682 35104_r_at M26682 874_at M26683 875_g_at M26683 1266_s_at M26692 2048_s_at M26747 247_s_at M26856 1366_i_at M26880 1367_f_at M26880 39655_at M26901 38927_i_at M27160 38928_r_at M27160 1579_at M27288 1580_f_at M27318 619_s_at M27394 36671_at M27396 1368_at M27492 1581_s_at M27504 35015_at M27533 876_at M27543 37535_at M27691 877_at M27691 38514_at M27749 33336_at M27819 34702_f_at M27826 AFFX-M27830_3_at M27830 AFFX-M27830_5_at M27830 AFFX-M27830_M_at M27830 41033_at M27878 39067_at M27937 1828_s_at M27968 1369_s_at M28130 1096_g_at M28170 1116_at M28170 1074_at M28209 620_at M28210 39244_at M28211 621_at M28211 622_at M28212 623_s_at M28213 624_at M28214 36110_at M28215 600_at M28215 31552_at M28219 34375_at M28225 32904_at M28393 601_s_at M28439 1075_f_at M28585 36816_s_at M28668 34663_at M28696 36668_at M28713 34926_at M28825 34927_at M28826 37835_at M28827 1076_at M28983 602_s_at M29037 2049_s_at M29039 33966_at M29053 36654_s_at M29065 33315_at M29204 38558_at M29273 31728_at M29335 878_s_at M29386 37624_at M29458 1077_at M29474 1582_at M29540 38277_at M29550 39780_at M29551 38932_at M29580 35931_at M29581 1370_at M29696 2050_s_at M29870 1371_s_at M29874 41814_at M29877 39253_s_at M29893 582_g_at M29960 603_at M29960 32905_s_at M30038 34037_at M30134 40741_at M30185 583_s_at M30257 35366_at M30269 32843_s_at M30448 32893_s_at M30474 31534_at M30607 34898_at M30704 40513_at M30773 879_at M30818 41468_at M30894 38733_at M30938 584_s_at M30938 585_at M30938 586_s_at M31153 37221_at M31158 1372_at M31165 1491_at M31166 587_at M31210 1782_s_at M31303 37838_at M31315 225_at M31328 40351_at M31328 41109_at M31452 39695_at M31516 32315_at M31520 1373_at M31523 1374_g_at M31523 33967_at M31525 33745_at M31606 37640_at M31642 36328_at M31651 33262_at M31659 1078_at M31661 1079_g_at M31661 1080_s_at M31667 38545_at M31682 40137_at M31724 588_at M31724 2051_at M31767 2052_g_at M31767 34513_at M31774 1885_at M31899 37687_i_at M31932 37688_f_at M31932 41038_at M32011 1375_s_at M32304 589_at M32313 1583_at M32315 590_at M32334 37795_at M32373 37093_at M32402 41723_s_at M32578 39055_at M32886 38700_at M33146 36889_at M33195 AFFX-HUMGAPDH/M33197_3_at M33197 AFFX-HUMGAPDH/M33197_3_st M33197 AFFX-HUMGAPDH/M33197_5_at M33197 AFFX-HUMGAPDH/M33197_5_st M33197 AFFX-HUMGAPDH/M33197_M_at M33197 AFFX-HUMGAPDH/M33197_M_st M33197 36993_at M33210 36601_at M33308 1492_f_at M33317 1493_r_at M33318 1494_f_at M33318 33530_at M33326 226_at M33336 227_g_at M33336 41768_at M33336 35482_at M33375 34603_at M33478 33321_r_at M33494 33913_at M33509 33838_at M33519 36493_at M33552 38952_s_at M33653 35282_r_at M33680 591_s_at M33684 1081_at M33764 40703_at M33875 37014_at M33882 39241_at M33987 1495_at M34057 2053_at M34064 2054_g_at M34064 1584_at M34065 592_at M34079 36161_at M34175 36215_at M34181 36359_at M34182 2055_s_at M34189 36646_at M34276 1585_at M34309 32787_at M34309 593_s_at M34353 37096_at M34379 37742_at M34423 34061_at M34428 36804_at M34455 40643_at M34480 40644_g_at M34480 880_at M34539 2056_at M34641 2057_g_at M34641 1082_at M34667 1496_at M34668 37907_at M34677 40858_at M34715 2058_s_at M35011 1083_s_at M35093 881_at M35198 38469_at M35252 1084_at M35296 228_at M35416 32776_at M35416 40337_at M35531 39736_at M35543 1586_at M35878 37319_at M35878 37952_at M35999 32806_at M36035 1376_at M36067 33780_at M36200 33987_at M36340 36585_at M36341 37417_at M36542 33567_at M36634 37418_at M36653 37419_g_at M36653 39300_at M36707 32154_at M36711 34471_at M36769 39763_at M36803 37187_at M36820 34022_at M36821 31621_s_at M36860 2059_s_at M36881 38378_at M37033 1783_at M37190 229_at M37197 32194_at M37197 1085_s_at M37238 35343_at M37400 882_at M37435 35670_at M37457 39337_at M37583 33299_at M37712 38465_at M37721 38006_at M37766 32861_s_at M37815 1732_at M37825 AFFX-MurIL10_at M37897 34019_at M37981 39085_at M37984 31467_at M38056 35721_at M38180 1587_at M38258 1830_s_at M38449 39389_at M38690 230_s_at M54914 883_s_at M54915 41158_at M54927 1940_at M54968 37479_at M54992 39176_f_at M54994 39177_r_at M54994 39208_i_at M54995 39209_r_at M54995 40249_at M55040 40075_at M55047 40159_r_at M55067 36817_at M55131 36876_at M55150 231_at M55153 38404_at M55153 38965_at M55172 232_at M55210 40258_at M55265 594_s_at M55265 36313_at M55267 37629_at M55268 1267_at M55284 1676_s_at M55409 36783_f_at M55422 34981_at M55513 32344_r_at M55514 34362_at M55531 35494_at M55536 35735_at M55542 32700_at M55543 39007_at M55593 39778_at M55621 31680_at M55630 41441_at M55654 37109_at M55671 36026_at M55674 233_s_at M55682 35610_at M55683 36599_at M55905 2035_s_at M55914 34463_at M55983 37621_at M57230 234_s_at M57399 34820_at M57399 31485_at M57423 33965_at M57506 37346_at M57567 40358_at M57609 32005_at M57703 37816_at M57729 40425_at M57730 34639_at M57732 37984_s_at M57763 32370_at M57888 35051_at M57892 32392_s_at M57951 39095_at M58018 1268_at M58028 37845_at M58285 1563_s_at M58286 40569_at M58297 32923_r_at M58378 34643_at M58458 41214_at M58459 38838_at M58460 34651_at M58525 32667_at M58526 40326_at M58583 39210_at M58597 31825_at M58600 1377_at M58603 1378_g_at M58603 38438_at M58603 2036_s_at M59040 38951_at M59217 32833_at M59287 34519_at M59305 1379_at M59371 595_at M59465 235_at M59488 40767_at M59499 34223_at M59818 596_s_at M59820 31692_at M59830 884_at M59911 885_g_at M59911 1086_at M59941 37494_at M59941 597_at M59964 37969_at M59979 36878_f_at M60028 38489_at M60047 34976_at M60052 36664_at M60091 40743_at M60092 31730_at M60094 236_at M60165 34138_at M60165 34698_at M60165 38037_at M60278 35404_at M60284 36871_at M60298 598_at M60299 1831_at M60314 1733_at M60315 39279_at M60315 1087_at M60459 37986_at M60459 237_s_at M60483 33181_at M60483 31542_at M60502 886_at M60527 1734_at M60556 1735_g_at M60556 1946_at M60614 1947_g_at M60614 37352_at M60618 37353_g_at M60618 36919_r_at M60626 599_at M60721 238_at M60724 37946_at M60724 2037_s_at M60725 33030_at M60747 580_at M60748 40842_at M60784 1380_at M60828 32126_at M60828 40019_at M60830 32590_at M60858 32181_at M60922 1911_s_at M60974 32155_at M61156 1088_at M61176 38409_at M61199 34581_s_at M61733 33346_r_at M61764 40821_at M61832 1477_s_at M61853 34078_s_at M61854 1455_f_at M61855 38906_at M61877 37634_at M61886 1269_at M61906 35373_at M61906 581_at M61916 887_at M62302 888_s_at M62302 1381_at M62303 38278_at M62324 1832_at M62397 35561_at M62397 33051_at M62400 1736_at M62402 1737_s_at M62403 41700_at M62424 36994_at M62762 37126_at M62800 36191_at M62810 36097_at M62831 39393_r_at M62839 37647_at M62840 40380_at M62843 31444_s_at M62895 31684_at M62896 35124_at M62982 32293_at M63108 32294_g_at M63108 239_at M63138 32470_at M63154 1564_at M63167 38068_at M63175 38473_at M63180 36879_at M63193 34155_s_at M63241 36190_at M63256 40776_at M63391 38851_at M63394 38194_s_at M63438 1382_at M63488 38481_at M63488 35823_at M63573 32323_at M63582 560_s_at M63589 38734_at M63603 35903_at M63623 37220_at M63835 1456_s_at M63838 35380_at M63896 40365_at M63904 38578_at M63928 36194_at M63959 33521_at M63962 38503_at M63967 36101_s_at M63978 31806_at M64082 31504_at M64098 38237_at M64099 34389_at M64108 41738_at M64110 1457_at M64174 41594_at M64174 240_at M64231 241_g_at M64231 2016_s_at M64241 39672_at M64322 31805_at M64347 2017_s_at M64349 39397_at M64497 34616_at M64554 242_at M64571 243_g_at M64571 32226_at M64571 1458_at M64572 31885_at M64572 32737_at M64595 244_at M64673 40200_at M64673 39189_at M64676 31573_at M64716 36853_at M64752 1251_g_at M64788 1270_at M64788 32207_at M64925 1383_at M64929 41167_at M64929 1384_at M64930 38197_at M64934 1089_i_at M64936 1090_f_at M64936 36727_at M64936 38825_at M64982 38371_at M64992 38094_at M65028 1677_at M65062 1678_g_at M65062 1091_at M65066 561_at M65085 562_g_at M65085 40105_at M65131 2018_at M65188 1092_at M65199 32874_at M65214 202_at M65217 32087_at M65217 1093_at M65254 1094_g_at M65254 41429_at M65254 563_at M65290 33955_at M65291 32249_at M65292 33050_at M67439 37995_s_at M67468 37008_r_at M68516 1792_g_at M68520 1833_at M68520 41772_at M68840 37376_at M68864 203_at M68891 37194_at M68891 2019_s_at M68892 33519_at M68895 1459_at M68941 1460_g_at M68941 40562_at M69013 564_at M69013 38612_at M69023 37668_at M69039 36099_at M69040 1461_at M69043 33024_at M69136 37628_at M69177 38326_at M69199 40304_at M69225 35967_at M69238 33757_f_at M69245 33669_at M69296 35938_at M72393 36098_at M72709 41459_at M73047 34725_at M73077 32366_at M73238 1095_s_at M73239 41433_at M73255 32430_at M73481 33996_at M73482 34450_at M73489 1252_at M73547 36182_at M73548 2020_at M73554 34596_at M73628 36749_at M73720 889_at M73780 2021_s_at M73812 33665_s_at M73832 32183_at M74002 565_at M74047 1912_s_at M74088 37178_at M74089 1923_at M74091 39251_at M74091 41060_at M74093 37523_at M74096 31823_at M74099 33290_at M74161 35077_at M74290 204_at M74297 205_g_at M74297 40393_at M74297 39988_at M74447 39336_at M74491 890_at M74524 1231_at M74525 40031_at M74542 32767_at M74558 1232_s_at M74587 36605_at M74719 32279_at M74826 37768_at M74905 37172_at M75106 32439_at M75110 36755_s_at M75914 1233_s_at M76125 38433_at M76125 40201_at M76180 32108_at M76231 34572_at M76424 36728_at M76446 36729_g_at M76446 33693_at M76482 39275_at M76558 39276_g_at M76558 35527_at M76559 35702_at M76665 32483_at M76676 39737_at M76729 1070_at M76766 40578_s_at M77016 35879_at M77140 33852_at M77142 34002_at M77144 2022_at M77198 2023_g_at M77198 40972_at M77198 31490_at M77235 38327_at M77348 1385_at M77349 32426_f_at M77481 33209_at M77698 891_at M77698 1071_at M77810 1072_g_at M77810 37741_at M77836 2024_s_at M79321 566_at M79462 567_s_at M79463 32186_at M80244 40840_at M80254 2025_s_at M80261 568_at M80335 569_g_at M80335 40826_at M80359 1462_s_at M80397 35017_f_at M80469 32001_s_at M80482 38088_r_at M80563 33348_at M80627 1793_at M80629 34354_at M80634 36988_at M80783 37027_at M80899 41210_at M81057 37707_i_at M81118 37708_r_at M81118 36773_f_at M81141 32369_at M81349 32494_at M81589 35503_at M81590 38066_at M81600 1073_at M81601 37556_at M81637 32760_at M81650 33259_at M81652 35012_at M81750 31330_at M81757 33545_at M81758 33551_s_at M81778 37371_at M81780 37372_at M81780 40919_at M81830 32280_at M81882 37183_at M81883 36854_s_at M81886 36855_r_at M81886 1738_at M81933 35407_at M81933 38747_at M81945 37374_at M82809 38788_at M82827 40067_at M82882 31817_at M82919 35489_at M82962 32210_at M83088 2026_at M83215 41739_s_at M83216 570_at M83221 41089_at M83363 34929_at M83554 AFFX-MurFAS_at M83649 38212_at M83651 38095_i_at M83664 38096_f_at M83664 1052_s_at M83667 40739_at M83670 1386_at M83738 36615_at M83751 40665_at M83772 35371_at M83822 1234_at M83941 39351_at M84349 206_at M84424 37825_at M84443 33141_at M84472 40282_s_at M84526 37095_r_at M84562 31329_at M84605 1653_at M84711 32543_at M84739 1362_s_at M84820 40334_at M85085 38496_at M85164 38497_at M85165 38666_at M85169 32277_at M85217 32340_s_at M85234 37145_at M85276 32845_at M85289 1235_at M86400 38448_at M86406 34499_at M86407 32063_at M86546 40634_at M86667 571_at M86667 572_at M86699 38999_s_at M86707 37739_at M86737 207_at M86752 33013_at M86808 573_at M86826 33265_at M86852 31551_at M86868 41313_at M86917 32991_f_at M86933 37709_at M86934 2027_at M87068 39264_at M87284 1053_at M87338 1054_at M87339 1055_g_at M87339 39263_at M87434 38517_at M87503 574_s_at M87507 1363_at M87770 39346_at M88108 40213_at M88163 36995_at M88249 38729_at M88279 34961_at M88282 38132_at M88338 39080_at M88458 35437_at M88461 36907_at M88468 39309_at M88714 38184_at M89470 32446_at M89473 34561_at M89796 1236_s_at M89914 38289_r_at M89914 37988_at M89957 37807_at M90299 31516_f_at M90354 31517_f_at M90355 31518_i_at M90356 31519_f_at M90356 31932_f_at M90357 31933_r_at M90357 32421_at M90359 32431_at M90366 1056_s_at M90391 34102_at M90424 32626_at M90516 31850_at M90656 892_at M90657 40370_f_at M90683 41239_r_at M90696 38417_at M91029 38585_at M91036 40359_at M91083 32941_at M91196 35868_at M91211 34915_at M91368 37532_at M91432 37076_at M91463 33607_at M91467 32450_at M91556 41103_at M91585 35225_at M91592 41618_at M91669 40619_at M91670 893_at M91670 894_g_at M91670 1794_at M92287 1795_g_at M92287 34251_at M92299 36558_at M92302 36559_g_at M92302 36557_at M92303 38631_at M92357 31481_s_at M92383 1880_at M92424 31977_at M92432 41754_at M92439 33382_at M92449 35168_f_at M92642 40448_at M92843 575_s_at M93036 33305_at M93056 37211_at M93107 33157_at M93119 31926_at M93133 36908_at M93221 40372_at M93283 35594_at M93284 870_f_at M93311 32676_at M93405 1463_at M93425 1364_at M93426 40740_at M93650 40189_at M93651 576_at M93718 32553_at M94046 36725_at M94055 33195_at M94065 208_at M94151 31841_at M94151 209_at M94167 33960_s_at M94172 577_at M94250 33677_at M94314 38391_at M94345 36987_at M94362 36662_at M94547 38016_at M94630 578_at M94633 39799_at M94856 35930_at M94893 36305_at M95167 39330_s_at M95178 41305_at M95549 38627_at M95585 871_s_at M95585 39925_at M95610 37649_at M95623 38434_at M95627 210_at M95678 1654_at M95712 40306_at M95712 31894_at M95724 579_at M95724 33155_at M95740 37855_at M95767 36931_at M95787 38782_at M95809 33159_at M95925 40127_at M95929 41020_at M95971 556_s_at M96233 33963_at M96326 2028_s_at M96577 41344_s_at M96684 557_s_at M96738 36281_at M96739 36326_at M96740 40948_at M96759 40687_at M96789 39556_at M96803 40817_at M96824 35679_s_at M96859 35680_r_at M96860 31578_at M96936 34620_at M96944 41761_at M96954 40386_r_at M96956 32188_at M96980 32189_g_at M96980 36517_at M96982 1565_s_at M96995 33855_at M96995 35044_i_at M97016 33158_at M97252 36899_at M97287 38218_at M97347 211_at M97388 32621_at M97388 33995_at M97496 212_at M97639 213_at M97675 214_at M97676 215_g_at M97676 40199_at M97676 1057_at M97815 41783_at M97815 33255_at M97856 34623_at M97925 32859_at M97935 32860_g_at M97935 AFFX-HUMISGF3A/M97935_3_at M97935 AFFX-HUMISGF3A/M97935_5_at M97935 AFFX-HUMISGF3A/M97935_MA_at M97935 AFFX-HUMISGF3A/M97935_MB_at M97935 33338_at M97936 33339_g_at M97936 36923_at M98045 39861_at M98343 36656_at M98399 35947_at M98447 38008_at M98528 216_at M98539 558_at 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41355_at N95229 33122_at N95393 38744_at N95406 33716_at N95443 39718_r_at N98607 39551_at N98667 39009_at N98670 36095_at N99340 160044_g_at NM_001098 160039_at NM_002747 160033_s_at NM_006297 41689_at R16035 40208_at R37702 41670_at R38263 38344_at R40666 34164_at R42599 33841_at R48209 39833_at R54564 35596_at R55188 32929_at R56605 38947_at R59327 41302_at R59606 35140_at R59697 34443_at R61362 32839_at R85997 39798_at R87876 38845_at R89044 34779_at R90942 36130_f_at R92331 39594_f_at R93527 41331_at R93981 38758_at R98910 1741_s_at S37730 559_s_at S38742 217_at S39329 34904_at S40369 40185_at S40719 39576_at S41458 37840_at S42457 37587_at S43855 32541_at S46622 32114_s_at S46950 31966_at S48220 34514_at S49816 34515_g_at S49816 35062_at S49953 32962_at S52028 538_at S53911 33658_at S54641 33975_at S55606 32322_at S56770 1849_s_at S57153 37711_at S57212 37712_g_at S57212 33391_r_at S57235 32157_at S57501 36744_at S58544 36575_at S59049 37756_at S59184 539_at S59184 33944_at 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38000_at S72370 37162_at S72869 32042_at S72904 34590_at S72921 1464_at S73149 31508_at S73591 39101_at S73840 39638_at S73885 853_at S74017 218_at S74221 542_at S74445 543_g_at S74445 31537_at S74683 39970_at S74720 36132_at S74728 36264_at S75168 1703_g_at S75174 1724_at S75174 38707_r_at S75174 40474_r_at S75295 36820_r_at S75313 39867_at S75463 1465_s_at S75881 32990_at S75989 31443_at S76346 1059_at S76475 1060_g_at S76475 854_at S76617 544_at S76638 545_g_at S76638 219_i_at S76756 220_r_at S76756 34916_s_at S76792 36202_at S76965 546_at S76965 1655_s_at S76978 1704_at S76992 547_s_at S77154 37983_at S77410 37179_at S77763 1545_g_at S77812 1567_at S77812 855_at S78085 1347_at S78187 35862_at S78203 35863_g_at S78203 40591_at S78234 37210_at S78296 221_s_at S78467 37671_at S78569 36209_at S78771 36210_g_at S78771 37412_at S78798 36619_r_at S78825 36024_at S79048 1348_s_at S79219 856_at S79267 31352_at S79281 34069_s_at S79325 34570_at S79522 222_at S79639 32164_at S79639 34591_at 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40252_g_at U00943 38490_r_at U00944 32185_at U00946 33147_at U00951 38063_at U00952 35558_at U00954 39461_s_at U00955 31566_at U00956 36632_at U00957 32135_at U00968 37228_at U01038 182_at U01062 37343_at U01062 36241_r_at U01120 1963_at U01134 1964_g_at U01134 39058_at U01147 36405_s_at U01156 36404_at U01157 36083_at U01160 38026_at U01244 1706_at U01337 1707_g_at U01337 34582_at U01824 183_at U01828 35422_at U01828 37609_at U01833 33896_at U01877 551_at U01877 39191_at U01922 41131_f_at U01923 41132_r_at U01923 38015_at U02019 33849_at U02020 35673_at U02082 38900_at U02309 1350_at U02388 33404_at U02390 41105_s_at U02478 38527_at U02493 33563_s_at U02519 36921_at U02556 1063_s_at U02566 552_at U02570 553_g_at U02570 41603_at U02609 35671_at U02619 36441_at U02632 36442_g_at U02632 1064_at U02680 38569_at U02683 1065_at U02687 34583_at U02687 38526_at U02882 1546_at U03056 39070_at U03057 39629_at U03090 41155_at U03100 41156_g_at U03100 36980_at U03105 2031_s_at U03106 37528_at U03109 31563_at U03115 1066_at U03187 35496_at U03270 37012_at U03271 38012_at U03272 31540_at U03397 35000_at U03398 33515_at U03399 33041_at U03493 40084_at U03494 40085_s_at U03495 554_at U03634 184_at U03642 37980_at U03644 40071_at U03688 859_at U03688 33517_f_at U03735 40808_at U03749 36641_at U03851 1067_at U03858 1068_g_at U03858 32983_at U03865 32551_at U03877 36327_at U03884 35173_at U03886 39937_at U03905 39938_g_at U03905 860_at U03911 861_g_at U03911 38719_at U03985 36535_at U04209 38858_at U04270 862_at U04313 863_g_at U04313 36270_at U04343 1069_at U04636 38677_at U04735 36314_at U04806 32702_at U04810 185_at U04840 40416_at U04847 32899_s_at U04897 40827_at U04953 39596_at U05012 39860_at U05040 555_at U05227 41091_at U05237 41026_f_at U05255 38017_at U05259 38018_g_at U05259 33431_at U05291 36590_at U05321 38414_at U05340 33311_at U05569 32414_at U05589 37489_s_at U05596 39978_at U05659 1796_s_at U05681 37747_at U05770 32805_at U05861 41140_at U05875 32100_r_at U06088 34551_at U06233 1050_at U06452 1051_g_at U06452 31889_at U06452 186_at U06454 39823_at U06631 39152_f_at U06632 39153_r_at U06632 33069_f_at U06641 35880_at U06698 31773_at U06715 40130_at U06863 517_at U07000 537_f_at U07000 518_at U07132 519_g_at U07132 34726_at U07139 37911_at U07158 33244_at U07223 36292_at U07225 32595_at U07231 187_at U07349 520_at U07358 36285_at U07364 2032_s_at U07375 1850_at U07418 34291_at U07424 39990_at U07559 1635_at U07563 1636_g_at U07563 1656_s_at U07563 32974_at U07563 32975_g_at U07563 1708_at U07620 1709_g_at U07620 864_at U07664 36195_at U07681 1351_at U07695 36880_at U07736 1029_s_at U07794 32587_at U07802 1710_s_at U07804 1030_s_at U07806 521_at U07807 34580_at U07882 36686_at U07919 39143_at U08015 37032_at U08021 1786_at U08023 40648_at U08023 33196_at U08191 35524_at U08198 33229_at U08316 865_at U08316 41567_at U08336 38478_at U08377 38447_at U08438 522_s_at U08471 33068_f_at U08854 38268_at U08989 31690_at U08997 31691_g_at U08997 35657_at U08998 38236_at U09002 32682_at U09087 37596_at U09117 38397_at U09196 31636_s_at U09210 39945_at U09278 39232_at U09284 188_at U09303 39721_at U09303 37254_at U09366 38603_at U09367 40245_at U09368 37264_at U09410 33597_at U09411 36295_at U09412 36392_at U09413 34989_at U09414 1711_at U09477 36581_at U09510 36582_g_at U09510 41607_at U09550 1031_at U09564 37042_at U09577 1637_at U09578 38274_at U09584 36613_at U09585 1547_at U09607 40363_r_at U09609 1238_at U09759 38431_at U09759 34811_at U09813 39412_at U09825 41713_at U09848 40241_at U09850 31407_at U09860 37998_at U09877 189_s_at U09937 36358_at U09953 39734_at U10117 35048_at U10301 35049_g_at U10301 36189_at U10323 40845_at U10324 40846_g_at U10324 36955_at U10362 32772_s_at U10473 35974_at U10485 36010_at U10492 37279_at U10550 2033_s_at U10564 35491_at U10685 34574_at U10686 36302_f_at U10688 34575_f_at U10689 31599_f_at U10691 34576_at U10693 34577_at U10694 36457_at U10860 40685_at U10868 40583_at U10886 2034_s_at U10906 39644_at U10991 40689_at U11037 35447_s_at U11098 35449_at U11276 39796_at U11292 36688_at U11313 38200_at U11690 37930_at U11700 40528_at U11701 1638_at U11732 38491_at U11732 1924_at U11791 36086_at U11791 1851_s_at U11821 39029_at U11861 37186_s_at U11863 1352_at U11870 1353_g_at U11870 1032_at U11872 1033_g_at U11872 41143_at U12022 41144_g_at U12022 34198_at U12128 40744_at U12134 1354_at U12140 1355_g_at U12140 31431_at U12255 31432_g_at U12255 36410_f_at U12431 866_at U12471 867_s_at U12471 33396_at U12472 1467_at U12535 34535_at U12569 34536_g_at U12569 1468_at U12595 33784_at U12597 38963_i_at U12707 38964_r_at U12707 190_at U12767 40659_at U12767 33522_at U12775 40673_at U12778 1469_at U12779 36179_at U12779 36074_at U12897 37660_at U12978 1239_s_at U13021 34448_s_at U13021 1240_at U13022 34449_at U13022 37245_at U13044 37275_at U13045 523_s_at U13061 38183_at U13219 36319_at U13220 39995_s_at U13395 36965_at U13616 33682_at U13666 41092_at U13680 41461_at U13695 524_at U13695 525_g_at U13695 526_s_at U13696 39320_at U13697 36143_at U13737 40065_s_at U13896 40246_at U13897 40737_at U13913 33773_at U13948 868_at U13991 34573_at U14187 869_at U14193 191_at U14383 37631_at U14391 1034_at U14394 1035_g_at U14394 1036_at U14407 34254_at U14417 527_at U14518 39637_at U14528 34693_at U14550 AFFX-hum_alu_at U14573 37705_at U14575 38644_at U14588 1241_at U14603 38415_at U14603 2015_s_at U14658 38556_at U14658 1993_s_at U14680 35388_at U14755 36346_at U14910 33660_at U14966 32436_at U14968 31385_at U14969 32437_at U14970 31511_at U14971 31568_at U14972 41609_at U15085 40806_at U15128 37746_r_at U15131 37226_at U15172 32060_at U15173 34092_at U15177 34667_at U15306 34658_at U15422 37938_at U15552 36518_at U15555 528_at U15590 1639_s_at U15642 1242_at U15655 38996_at U15655 37745_s_at U15780 41183_at U15782 529_at U15932 32648_at U15979 1994_at U16028 845_at U16031 35857_at U16125 39573_at U16126 34540_at U16127 530_at U16258 41848_f_at U16261 41849_r_at U16261 40044_at U16282 37460_at U16296 531_at U16307 1548_s_at U16720 37669_s_at U16799 846_s_at U16811 1995_at U16815 36349_at U16861 36941_at U16954 35559_at U16997 39927_at U17032 35462_at U17033 35461_at U17034 33331_at U17077 1996_s_at U17105 37055_at U17163 34343_at U17280 1965_s_at U17326 532_at U17418 533_g_at U17418 33135_at U17566 32383_at U17579 32384_g_at U17579 1640_at U17714 1712_s_at U17743 36929_at U17760 33922_at U17838 35751_at U17886 847_at U17969 33642_s_at U17986 40901_at U17989 39378_at U17999 40147_at U18009 192_at U18062 40750_at U18088 31725_s_at U18235 35458_r_at U18237 35096_at U18244 41511_at U18259 32683_at U18271 35616_at U18288 40404_s_at U18291 1243_at U18300 1356_at U18321 40413_at U18321 1966_i_at U18334 1967_f_at U18334 34836_at U18420 34741_at U18422 35956_s_at U18467 AFFX-YEL018w/_at U18530 38537_at U18543 31320_at U18548 32420_at U18549 33947_at U18550 1244_at U18671 36770_at U18671 35690_s_at U18760 35691_r_at U18760 33840_at U18914 36126_at U18919 36127_g_at U18919 34182_at U18932 35246_at U18934 37240_at U18937 37072_at U18945 34113_at U18991 33968_at U19107 31497_at U19142 31960_f_at U19143 31953_f_at U19144 33671_f_at U19145 37065_f_at U19146 31498_f_at U19147 1037_at U19180 1038_s_at U19247 848_at U19261 849_g_at U19261 33793_at U19345 33794_g_at U19345 828_at U19487 32666_at U19495 35122_at U19517 37944_at U19523 1549_s_at U19557 1997_s_at U19599 1998_i_at U19599 38442_at U19718 32841_at U19765 1999_s_at U19775 1550_at U19796 1551_g_at U19796 38528_at U19822 37258_at U19878 33440_at U19969 40748_at U19977 39319_at U20158 40345_at U20180 39219_at U20240 35457_at U20325 40646_at U20350 34284_at U20362 534_s_at U20391 35309_at U20428 32199_at U20489 34504_at U20530 35662_at U20536 32898_at U20582 31390_at U20648 1357_at U20657 37339_at U20657 38959_s_at U20759 38958_at U20760 535_s_at U20816 33496_at U20860 38220_at U20938 32589_at U20979 36912_at U20980 39781_at U20982 31610_at U21049 35460_at U21051 1470_at U21090 37057_s_at U21092 38038_at U21128 38201_at U21551 829_s_at U21689 193_at U21858 39494_at U21915 36495_at U21931 32906_at U21936 33552_at U21943 1552_i_at U22028 1553_r_at U22028 1554_f_at U22028 1555_f_at U22029 37730_at U22055 32309_at U22172 38150_at U22233 511_s_at U22322 1471_at U22376 1472_g_at U22376 1473_s_at U22376 1474_s_at U22376 1475_s_at U22376 1476_s_at U22376 41852_at U22377 1787_at U22398 39545_at U22398 1039_s_at U22431 39108_at U22526 33106_at U22662 512_at U22662 34275_s_at U22680 41781_at U22815 41782_g_at U22815 41780_at U22816 40063_at U22897 33990_at U22961 33991_g_at U22961 34426_at U22963 34427_g_at U22963 1358_s_at U22970 34758_at U23028 37678_at U23070 36178_at U23143 1040_s_at U23435 33923_s_at U23736 34569_at U23752 37334_at U23803 32779_s_at U23850 33238_at U23852 33389_at U23942 1556_at U23946 36962_at U24105 1557_at U24152 1558_g_at U24152 1559_at U24153 1560_g_at U24153 33456_at U24166 41250_at U24169 36196_at U24183 37330_at U24266 37331_g_at U24266 37332_r_at U24267 36811_at U24389 1452_at U24576 37068_at U24577 40766_at U24578 36388_at U25128 38298_at U25138 38405_at U25165 38435_at U25182 513_at U25265 31405_at U25341 194_at U25433 35319_at U25435 32491_at U25441 32492_g_at U25441 41774_at U25771 32337_at U25789 830_at U25801 36611_at U25849 37541_at U25956 1245_i_at U25975 33758_f_at U25988 41354_at U25997 39784_at U26032 41187_at U26162 36280_at U26174 31559_at U26209 37722_s_at U26266 33508_at U26398 1041_at U26403 32142_at U26424 2000_at U26455 2001_g_at U26455 32633_at U26591 40068_at U26648 35632_at U26710 514_at U26710 515_s_at U26712 39697_at U26726 1713_s_at U26727 36466_at U26742 36467_g_at U26742 1714_at U26914 35664_at U27109 1042_at U27185 1561_at U27193 1562_g_at U27193 41017_at U27266 38495_s_at U27328 33099_at U27330 36290_s_at U27331 36289_f_at U27333 39943_at U27459 37373_at U27460 2002_s_at U27467 1043_s_at U27516 37637_at U27655 40679_at U27699 34272_at U27768 195_s_at U28014 196_s_at U28015 831_at U28042 32981_at U28043 40560_at U28049 40406_at U28055 31677_at U28131 39087_at U28249 33566_at U28251 32902_at U28281 40407_at U28386 37192_at U28389 39664_at U28413 33208_at U28424 41741_at U28686 32443_at U28687 33098_at U28694 32549_at U28727 37706_at U28811 36020_at U28831 2003_s_at U28946 35653_at U28963 34642_at U28964 37405_at U29091 36949_at U29171 493_at U29171 32579_at U29175 36159_s_at U29185 35663_at U29195 38422_s_at U29332 38429_at U29344 36759_at U29589 37699_at U29607 37061_at U29615 197_at U29656 198_g_at U29656 2004_at U29671 35502_at U29700 35617_at U29725 38463_s_at U29926 36411_s_at U29943 40856_at U29953 34558_at U30185 37423_at U30246 36963_at U30255 39710_at U30521 40453_s_at U30826 37302_at U30872 36982_at U30888 35626_at U30894 36363_at U30930 31782_at U31099 37223_at U31116 494_at U31120 41482_at U31176 35281_at U31201 33510_s_at U31216 38179_at U31248 2005_s_at U31317 33384_at U31346 33385_g_at U31346 39666_at U31382 37735_at U31383 37908_at U31384 36887_f_at U31416 41629_at U31449 33688_at U31468 35265_at U31501 1948_f_at U31511 40876_at U31525 1044_s_at U31556 41275_at U31556 2006_at U31601 2007_g_at U31601 495_at U31628 39051_at U31767 34368_at U31814 35004_at U31875 39278_at U31905 38368_at U31930 35032_at U31973 33532_at U31986 38381_at U32315 496_s_at U32324 34856_at U32331 35945_at U32376 40653_at U32439 41133_at U32519 34454_r_at U32576 31845_at U32645 1359_at U32659 497_at U32680 36472_at U32849 32057_at U32907 1641_s_at U32986 38606_at U32989 33513_at U33017 199_s_at U33052 36835_at U33052 175_s_at U33053 39662_s_at U33055 36329_at U33147 2008_s_at U33199 38509_at U33202 1859_s_at U33203 39665_at U33267 2009_at U33284 34622_at U33317 31900_at U33429 31466_at U33547 37552_at U33632 38819_at U33635 2010_at U33760 1941_at U33761 35279_at U33821 498_at U33821 499_at U33822 35009_at U33837 1045_s_at U33838 34361_at U33849 35667_at U33920 36344_at U34038 36345_g_at U34038 39387_at U34044 36361_at U34051 36742_at U34249 33899_at U34252 41543_at U34360 2011_s_at U34584 33948_at U34587 1046_at U34605 40668_s_at U34624 38386_r_at U34683 31778_at U34802 32317_s_at U34804 31426_at U34806 40793_s_at U34846 33570_at U34962 34578_at U34976 2012_s_at U34994 35905_s_at U34995 33084_at U35100 1642_at U35113 1643_g_at U35113 38633_at U35113 2013_at U35117 36073_at U35139 33584_at U35146 1246_at U35234 1247_g_at U35234 31662_at U35246 39683_at U35340 36303_f_at U35376 37304_at U35451 31409_at U35459 36006_at U35612 38520_r_at U35735 40003_at U36221 41021_s_at U36310 41022_r_at U36310 38402_at U36336 40926_at U36341 31848_at U36448 40700_at U36500 37354_at U36501 37255_at U36601 31601_s_at U36610 36440_at U36759 1644_at U36764 38943_at U36787 34650_at U36798 33132_at U37012 1942_s_at U37022 1047_s_at U37055 37482_at U37100 33103_s_at U37122 38501_s_at U37139 40676_at U37139 500_at U37143 501_g_at U37143 39358_at U37146 35448_at U37219 39111_s_at U37220 33188_at U37221 32341_f_at U37230 35475_at U37251 36513_at U37283 176_at U37352 40786_at U37352 39233_at U37359 41308_at U37408 41309_g_at U37408 40726_at U37426 502_s_at U37431 1715_at U37518 37956_at U37519 36254_at U37529 36578_at U37547 1248_at U37689 35631_at U37689 503_at U37690 39684_at U37707 39384_at U38175 34462_at U38254 32634_s_at U38260 35666_at U38276 33725_at U38291 40055_s_at U38320 1048_at U38480 1049_g_at U38480 177_at U38545 32298_at U38805 39297_at U38810 39779_at U38847 41426_at U38864 35825_s_at U38896 38142_at U38904 178_f_at U38964 35859_f_at U38979 179_at U38980 2014_s_at U39064 32230_at U39067 33527_at U39196 33197_at U39226 35589_at U39231 832_at U39317 39083_at U39318 504_at U39318 36951_at U39400 36977_at U39412 33756_at U39447 33463_at U39487 34161_at U39573 36335_at U39576 1543_at U39657 1544_at U39817 37141_at U39840 31403_at U39905 38581_at U40038 38564_at U40152 36748_at U40215 833_at U40279 35365_at U40282 32289_at U40317 1797_at U40343 36311_at U40370 32418_at U40371 32419_at U40372 35658_at U40380 36332_at U40391 32072_at U40434 40007_at U40462 834_at U40462 41722_at U40490 35627_at U40571 40589_at U40572 1360_at U40622 1342_g_at U40705 1361_at U40705 32255_i_at U40705 32256_r_at U40705 37385_at U40763 158_at U40992 33533_at U40992 38107_at U40998 1798_at U41060 1026_s_at U41068 1027_at U41068 34842_at U41303 37650_at U41315 37022_at U41344 36973_at U41371 40490_at U41387 38041_at U41514 36156_at U41518 36996_at U41635 35316_at U41654 37335_at U41668 31321_at U41737 38757_at U41745 835_at U41745 33330_at U41763 34761_r_at U41766 38282_at U41767 36461_at U41804 37809_at U41813 38911_at U41815 41003_at U41816 39077_at U41843 36256_at U41901 34721_at U42031 36852_at U42349 36850_at U42360 36851_g_at U42360 34597_at U42387 40581_at U42390 40539_at U42391 33282_at U42408 34346_at U42412 33525_at U42766 36252_at U43030 505_at U43077 38580_at U43083 159_at U43142 836_at U43148 40458_at U43185 506_s_at U43185 507_s_at U43189 34735_at U43195 33754_at U43203 31679_at U43279 39078_at U43286 31532_at U43292 34997_r_at U43318 39618_at U43328 37268_at U43368 41044_at U43374 1522_at U43408 1523_g_at U43408 1028_at U43431 41004_at U43431 31915_at U43519 33804_at U43522 1645_at U43527 41596_s_at U43572 1716_at U43586 31427_at U43604 36377_at U43672 1989_at U43746 1990_g_at U43746 33202_f_at U43747 38330_at U43753 38868_at U43774 1991_s_at U43784 39237_at U43784 40333_at U43842 36393_at U43843 1249_at U43885 32979_at U43885 160_at U43899 1321_s_at U43916 508_at U43923 837_s_at U43944 36052_at U43959 36966_at U43965 36967_g_at U43965 32493_at U44059 31918_at U44060 161_at U44105 37604_at U44111 36953_at U44378 509_at U44378 510_g_at U44378 34722_at U44385 32136_r_at U44429 35488_at U44754 37252_at U44755 34774_at U44772 41029_at U44798 162_at U44839 38185_at U45255 38186_g_at U45255 36028_at U45285 838_s_at U45328 33535_at U45448 1717_s_at U45878 1646_at U45880 41151_at U45973 39323_at U45974 38960_at U45975 37685_at U45976 33553_r_at U45984 38916_at U46023 36920_at U46024 491_at U46116 492_g_at U46116 31968_at U46120 41389_s_at U46193 1524_at U46194 163_at U46461 839_at U46499 32909_at U46569 37321_at U46570 41800_s_at U46571 40008_at U46573 40409_at U46689 41659_at U46691 35816_at U46692 36469_at U46744 36471_f_at U46746 40898_at U46751 31389_at U46752 40890_at U46920 1971_g_at U46922 1992_at U46922 1525_s_at U47011 1526_i_at U47011 36667_at U47025 34984_at U47050 35134_at U47054 1250_at U47077 40129_at U47077 39165_at U47101 33489_at U47292 1913_at U47414 37723_at U47414 471_f_at U47634 1322_at U47677 33831_at U47741 38377_at U47742 840_at U47742 34003_at U47924 37942_at U47924 39973_at U47926 34405_at U47927 164_at U47931 165_g_at U47931 40274_at U48213 33095_i_at U48224 33096_r_at U48224 33549_at U48231 40624_at U48250 841_at U48250 842_at U48251 40730_at U48263 843_at U48296 166_at U48405 32423_at U48408 40009_at U48436 36148_at U48437 37990_at U48508 1007_s_at U48705 844_at U48707 472_at U48730 473_g_at U48730 41753_at U48734 825_at U48736 1926_at U48801 1788_s_at U48807 33568_at U48861 32847_at U48959 41747_s_at U49020 31560_at U49065 40421_at U49070 40389_at U49082 41453_at U49089 38524_at U49184 32977_at U49187 32978_g_at U49187 37007_at U49188 33721_at U49248 38939_r_at U49250 34410_at U49260 36959_at U49278 40110_at U49283 40111_g_at U49283 474_at U49379 37011_at U49392 40396_at U49395 167_at U49436 33550_at U49516 38425_at U49719 39524_at U49742 41180_i_at U49785 41181_r_at U49785 38444_at U49837 37229_at U49844 40483_at U49857 40484_g_at U49857 32153_s_at U49869 33701_at U49897 35634_at U49928 41195_at U49957 40696_at U50062 475_at U50062 476_s_at U50079 39968_at U50136 33526_at U50146 168_at U50196 38301_at U50196 31309_r_at U50277 39406_at U50330 36462_at U50383 39350_at U50410 1718_at U50523 34049_at U50525 1527_s_at U50527 34459_at U50529 1528_at U50531 1529_at U50534 1530_g_at U50534 1531_at U50535 1532_g_at U50535 39197_s_at U50536 826_at U50553 1008_f_at U50648 41682_s_at U50708 41683_i_at U50708 38475_at U50733 34267_r_at U50748 38120_at 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41778_at U53347 1010_at U53442 31897_at U53445 479_at U53446 1886_at U53476 1887_g_at U53476 38412_at U53588 36412_s_at U53831 35298_at U54558 35327_at U54559 36739_at U54617 34600_s_at U54644 40789_at U54645 1011_s_at U54778 35396_at U54804 37854_at U54996 39102_at U54999 39521_at U55054 40243_at U55184 37263_at U55206 41041_s_at U55209 41042_r_at U55209 37287_at U55258 37288_g_at U55258 34028_at U55312 40250_at U55766 40554_at U55853 38991_at U55980 33575_at U56102 41032_at U56387 32836_at U56417 32837_at U56418 31428_at U56420 31921_at U56421 40910_at U56637 34170_s_at U56813 480_at U56816 171_at U56833 806_at U56998 31702_at U57029 40327_at U57052 36317_at U57057 33599_at U57092 807_at U57092 808_at U57093 40669_at U57094 809_at U57094 34218_at U57099 1012_at U57317 40317_at U57352 481_at U57452 34169_s_at U57627 38164_at U57629 41401_at U57646 172_at U57650 37620_at U57693 40672_at U57721 34611_at U57796 33627_at U57843 33628_g_at U57843 34385_at U57877 36029_at U57911 32456_s_at 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32970_f_at U77327 38614_s_at U77413 32575_at U77456 35123_at U77494 34407_at U77594 820_at U77604 31355_at U77629 41045_at U77643 41040_at U77664 39702_at U77665 1927_s_at U77713 33543_s_at U77718 1633_g_at U77735 1652_at U77735 41539_at U77782 31711_at U77783 38953_at U77845 35414_s_at U77914 38774_at U77942 466_at U77948 1536_at U77949 36839_at U77949 34652_at U77968 39548_at U77970 36833_at U78027 38213_at U78027 35430_at U78082 35431_g_at U78082 34348_at U78095 40289_at U78107 32401_at U78110 31450_s_at U78166 37953_s_at U78181 40684_at U78190 37430_at U78294 38104_at U78302 37107_at U78305 41869_at U78310 38156_at U78313 41011_i_at U78516 41012_r_at U78516 36586_at U78521 36573_at U78524 35323_at U78525 1229_at U78556 1230_g_at U78556 31833_at U78575 32852_at U78678 33572_at U78722 1928_s_at U78733 35183_at U78735 821_s_at U78793 1209_at U78798 1330_at U78876 822_s_at U79115 39074_at U79241 37568_at U79242 34208_at U79245 40633_at U79246 36367_at U79247 41676_at U79248 36793_at 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32560_s_at W30959 32004_s_at W32483 41495_at W37606 36423_at W47047 36165_at W51774 39541_at W52003 34316_at W52024 34317_g_at W52024 40027_at W52999 37878_at W55917 38363_at W60864 39750_at W61005 36685_at W63793 35154_at W68046 33128_s_at W68521 32736_at W68830 38087_s_at W72186 41528_at W72239 41529_g_at W72239 41487_at W72400 41471_at W72424 32752_at W72440 38721_at W72733 35466_at W73046 35467_g_at W73046 34530_at W73822 32617_at W74442 41804_at W80358 41805_g_at W80358 38726_at W80399 37559_at W84438 40491_at W84531 38643_at W87466 39885_at W87858 39818_at W94101 152_f_at X00038 153_f_at X00088 32552_at X00129 AFFX-HSAC07/X00351_3_at X00351 AFFX-HSAC07/X00351_3_st X00351 AFFX-HSAC07/X00351_5_at X00351 AFFX-HSAC07/X00351_5_st X00351 AFFX-HSAC07/X00351_M_at X00351 AFFX-HSAC07/X00351_M_st X00351 32485_at X00371 32793_at X00437 32794_g_at X00437 36983_f_at X00442 38833_at X00457 1537_at X00588 37327_at X00588 1538_s_at X00695 38699_at X00734 429_f_at X00734 430_at X00737 31732_at X00948 1702_at X01057 36801_at X01059 37324_at X01060 36106_at X01388 40541_at X01630 36781_at X01683 40567_at X01703 35921_at X02133 41485_at X02152 1023_at X02158 33162_at X02160 39106_at X02162 37899_at X02308 36620_at X02317 36299_at X02330 33678_i_at X02344 33679_f_at X02344 34566_at X02404 37310_at X02419 1974_s_at X02469 431_at X02530 35315_at X02544 1333_f_at X02596 34679_at X02596 1024_at X02612 1025_g_at X02612 33455_at X02747 39255_at X02750 1539_at X02751 31719_at X02761 41445_at X02812 432_s_at X02883 433_at X02883 1852_at X02910 1540_f_at X02956 1541_f_at X02958 41654_at X02994 38570_at X03066 1853_at X03072 38796_at X03084 33377_at X03168 32771_at X03178 32276_at X03342 35730_at X03350 1802_s_at X03363 AFFX-CreX-3_at X03453 AFFX-CreX-3_st X03453 AFFX-CreX-5_at X03453 AFFX-CreX-5_st X03453 434_at X03473 435_g_at X03473 1917_at X03484 38742_s_at X03484 36805_s_at X03541 1975_s_at X03563 1681_at X03635 1334_s_at X03656 160022_at X03663 38042_at X03674 37975_at X04011 34160_at X04098 36138_at X04106 32754_at X04201 32225_at X04297 39598_at X04325 33759_at X04327 33908_at X04366 38389_at X04371 32953_at X04391 37449_i_at X04409 37450_r_at X04409 32612_at X04412 38299_at X04430 1335_at X04434 34718_at X04434 32275_at X04470 1520_s_at X04500 33341_at X04526 1542_at X04571 AFFX-ThrX-3_at X04603 AFFX-ThrX-5_at X04603 AFFX-ThrX-M_at X04603 436_at X04688 35332_at X04714 36990_at X04741 1323_at X04803 37307_at X04828 34625_at X05153 437_at X05232 32336_at X05236 33866_at X05276 37931_at X05299 37716_at X05323 40794_at X05332 1803_at X05360 32747_at X05409 40157_s_at X05451 40995_at X05608 36659_at X05610 39042_at X05615 1634_s_at X05839 37403_at X05908 35395_at X05997 39226_at X06026 1888_s_at X06182 39753_at X06256 36679_at X06272 31721_at X06290 1976_s_at X06292 1336_s_at X06318 37726_at X06323 35703_at X06374 38743_f_at X06409 160030_at X06562 1337_s_at X06614 32330_at X06617 786_at X06745 40875_s_at X06815 32312_at X06825 36661_s_at X06882 34023_at X06948 36591_at X06956 35819_at X06994 112_g_at X07024 154_at X07024 1217_g_at X07109 160029_at X07109 36584_at X07173 40749_at X07203 38611_at X07228 40118_at X07290 31858_at X07315 33474_at X07384 32480_at X07495 32250_at X07523 39657_at X07695 37582_at X07696 32458_f_at X07704 1804_at X07730 1805_g_at X07730 37639_at X07732 37328_at X07743 438_at X07767 1006_at X07820 34666_at X07834 160023_at X07876 39639_s_at X07948 32808_at X07979 32917_at X07994 39054_at X08020 41088_at X12433 37391_at X12451 35660_at X12453 35661_g_at X12453 40360_at X12458 440_at X12492 38119_at X12496 41317_at X12534 41318_g_at X12534 1806_at X12556 1807_g_at X12556 37927_at X12654 40211_at X12671 35231_at X12791 1218_at X12794 41310_f_at X12794 160032_at X12830 35415_at X12901 160028_s_at X12949 34464_at X13227 32943_at X13255 40702_at X13274 1854_at X13293 40896_at X13403 39239_at X13444 37585_at X13482 41231_f_at X13546 986_at X13589 987_g_at X13589 37033_s_at X13710 33819_at X13794 33820_g_at X13794 32755_at X13839 38775_at X13916 1338_s_at X13930 35135_at X13956 441_s_at X13967 36187_at X13973 32729_at X13988 37180_at X14034 31870_at X14046 35953_at X14329 34587_at X14346 35894_at X14362 32488_at X14420 1855_at X14445 113_i_at X14474 114_r_at X14474 38610_s_at X14487 37593_at X14608 36883_at X14640 1339_s_at X14675 36323_at X14766 35028_at X14767 115_at X14787 33312_at X14789 33313_g_at X14789 1977_s_at X14798 40415_at X14813 35027_at X14830 40195_at X14850 1767_s_at X14885 33653_at X14894 116_at X14968 38905_at X14968 37861_at X14975 32316_s_at X15183 442_at X15187 1865_at X15217 1866_g_at X15217 1918_at X15218 41499_at X15218 33767_at X15306 36490_s_at X15331 40862_i_at X15334 40863_r_at X15334 32625_at X15357 36762_at X15376 33480_at X15393 36589_at X15414 32945_i_at X15422 32946_r_at X15422 36651_at X15525 40116_at X15573 38453_at X15606 38454_g_at X15606 31997_at X15674 35585_at X15675 35130_at X15722 39329_at X15804 38902_r_at X15875 38722_at X15880 34802_at X15882 33676_at X15940 36300_at X15943 1219_at X15949 1220_g_at X15949 38111_at X15998 38112_g_at X15998 31584_at X16064 35201_at X16135 39294_at X16155 36203_at X16277 35408_i_at X16281 35409_r_at X16281 36794_at X16282 37013_at X16295 40422_at X16302 1919_at X16316 1340_s_at X16323 988_at X16354 40074_at X16396 39730_at X16416 33616_at X16576 32152_at X16609 37954_at X16662 31820_at X16663 39610_at X16665 31555_at X16666 33620_at X16667 40268_at X16706 32271_at X16707 37021_at X16832 38243_at X16841 31499_s_at X16863 1436_at X16866 38507_at X16867 36510_at X16901 35731_at X16983 AFFX-LysX-3_at X17013 AFFX-LysX-5_at X17013 AFFX-LysX-M_at X17013 36985_at X17025 1978_at X17033 41481_at X17033 32227_at X17042 35338_at X17094 31527_at X17206 36787_at X17254 38294_at X17360 443_at X17360 444_g_at X17360 39206_s_at X17406 39207_r_at X17406 41795_at X17576 989_at X17576 38180_f_at X17610 1521_at X17620 32473_at X17622 33932_at X17644 32410_at X17651 32786_at X51345 40371_at X51362 36606_at X51405 40512_at X51408 160036_at X51417 36911_at X51420 35251_at X51435 40103_at X51521 990_at X51602 991_g_at X51602 1500_at X51630 1943_at X51688 40697_at X51688 160021_r_at X51730 117_at X51757 35965_at X51757 36399_at X51779 38515_at X51801 31860_at X51804 40193_at X51956 36776_at X51985 160040_at X52001 31421_at X52005 34554_at X52008 31310_at X52009 39676_at X52011 37603_at X52015 38077_at X52022 1341_at X52056 36796_at X52075 34647_at X52104 32441_at X52142 37963_at X52151 32888_at X52213 41095_at X52221 992_at X52221 38785_at X52228 31707_at X52332 404_at X52425 1437_at X52479 39641_at X52486 35405_at X52520 789_at X52541 38354_at X52560 790_at X52599 791_g_at X52599 792_s_at X52611 33980_at X52638 32352_at X52730 405_at X52773 38522_s_at X52785 33667_at X52851 34791_at X52882 39098_at X52896 34605_at X52943 32531_at X52947 31696_at X52987 35101_at X52997 39754_at X53002 41024_f_at X53004 41025_r_at X53004 35055_at X53281 38794_at X53390 37880_at X53414 32750_r_at X53416 35194_at X53463 41266_at X53586 406_at X53587 35041_at X53655 38027_at X53742 32440_at X53777 39056_at X53793 32247_at X53795 37777_at X54131 407_at X54131 32916_at X54134 37765_at X54162 38384_at X54199 33929_at X54232 33447_at X54304 35300_at X54326 34641_at X54380 35379_at X54412 39775_at X54486 408_at X54489 37165_f_at X54534 993_at X54637 39599_at X54673 32342_at X54741 1221_at X54871 37362_at X54871 793_at X54936 118_at X54938 40690_at X54942 1316_at X55005 31554_at X55019 31816_at X55079 38124_at X55110 37799_at X55284 34181_at X55330 38043_at X55448 31975_at X55503 1979_s_at X55504 36297_at X55544 37066_at X55668 34645_at X55715 39110_at X55733 31886_at X55740 34548_at X55764 34549_g_at X55764 37386_i_at X55885 37387_r_at X55885 32394_s_at X55954 32395_r_at X55954 36766_at X55988 31441_at X55989 33979_at X55990 37448_s_at X56009 38446_at X56199 32547_at X56253 32530_at X56468 409_at X56468 39173_at X56597 37157_at X56667 1612_s_at X56681 41483_s_at X56681 41484_r_at X56681 38795_s_at X56687 37020_at X56692 39719_at X56777 39720_g_at X56777 39853_at X56789 39302_at X56807 39084_at X56832 32321_at X56841 35119_at X56932 39850_at X56958 1501_at X57025 38737_at X57025 34416_at X57110 33067_at X57130 410_s_at X57152 34606_s_at X57197 37272_at X57206 31681_at X57282 36274_at X57303 32324_at X57346 33322_i_at X57348 33323_r_at X57348 411_i_at X57351 41745_at X57352 33414_at X57398 40153_at X57522 37459_at X57527 41071_at X57655 38181_at X57766 33273_f_at X57809 35469_at X57830 36333_at X57958 33352_at X57985 41608_at X58022 40511_at X58072 34674_at X58079 32145_at X58141 36051_s_at X58199 31892_at X58288 994_at X58288 995_g_at X58288 35464_at X58377 33999_f_at X58398 34000_r_at X58398 35014_at X58401 160042_s_at X58431 39274_at X58521 41166_at X58529 37383_f_at X58536 1682_s_at X58723 33969_at X58822 38506_at X58840 40062_s_at X58851 32989_at X58964 1980_s_at X58965 33415_at X58965 34550_at X58987 996_at X59065 31847_at X59131 33982_f_at X59244 37380_at X59268 37381_g_at X59268 40414_at X59303 38521_at X59350 36882_at X59372 413_at X59372 414_at X59373 38441_s_at X59408 36122_at X59417 36124_at X59434 34314_at X59543 36922_at X59618 33524_at X59656 415_at X59656 38931_at X59739 35834_at X59766 998_s_at X59770 38418_at X59798 999_at X59812 40522_at X59834 32696_at X59841 38295_at X59842 32649_at X59871 38121_at X59892 1768_s_at X59932 32574_at X59960 37675_at X60036 32936_at X60155 1000_at X60188 40023_at X60201 41228_r_at X60221 1981_s_at X60287 37285_at X60364 38566_at X60382 36754_at X60435 31521_f_at X60484 35748_at X60489 35150_at X60592 35045_r_at X60655 32331_at X60673 34823_at X60708 1001_at X60957 40667_at X60992 31311_at X61070 31556_at X61072 31322_at X61079 33645_at X61094 33646_g_at X61094 38395_at X61100 32184_at X61118 37294_at X61123 36756_at X61177 AFFX-YEL002c/WBP1_at X61388 40362_at X61498 36902_at X61587 33681_at X61598 39617_at X61615 416_s_at X61755 32204_at X62025 36909_at X62048 794_at X62055 35820_at X62078 36272_r_at X62167 35599_at X62250 38065_at X62534 32716_at X62535 34664_at X62573 34665_g_at X62573 37003_at X62654 37344_at X62744 41352_at X62822 31439_f_at X63095 31930_f_at X63096 37164_at X63097 38787_at X63131 33933_at X63187 37206_at X63359 37365_at X63368 37691_at X63380 32961_at X63417 37993_at X63422 32318_s_at X63432 31928_at X63454 32602_at X63465 37882_at X63468 37295_at X63469 32435_at X63527 1613_s_at X63546 1614_s_at X63546 31526_f_at X63547 32535_at X63556 39746_at X63563 40791_at X63564 41090_s_at X63575 37613_at X63578 37614_g_at X63578 33491_at X63597 160031_at X63629 36120_at X63657 34796_at X63679 37333_at X63692 37643_at X63717 40375_at X63741 36085_at X63749 39097_at X63753 34555_at X63755 33478_at X63759 33479_g_at X63759 31351_at X63966 36826_at X64037 32556_at X64044 32698_at X64116 32699_s_at X64116 40768_s_at X64228 38992_at X64229 37544_at X64318 40881_at X64330 36162_at X64364 36569_at X64559 32663_at X64594 35940_at X64624 31509_at X64707 32278_at X64728 40649_at X64810 34350_at 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AnnotationDbi/inst/extdata/manyToOneBlackList.Rda0000644000175200017520000000035314710217313023066 0ustar00biocbuildbiocbuildMPR0 t([4ڞ:pkR]i%UJU^XT%,T6ޜ/w y. M߁g\2\1$At,$i(]в!RF= {;5DARBsLߙSO(͆$ a[$-ׁrpfݗx=o˖N͈s9QjAnnotationDbi/inst/extdata/org.testing.db/0000755000175200017520000000000014710217313021562 5ustar00biocbuildbiocbuildAnnotationDbi/inst/extdata/org.testing.db/DESCRIPTION0000644000175200017520000000106614710217313023273 0ustar00biocbuildbiocbuildPackage: org.testing.db Title: Genome wide annotation for Taeniopygia guttataTestingSubset Description: Genome wide annotation for Taeniopygia guttataTestingSubset, primarily based on mapping using Entrez Gene identifiers. Version: 0.1 Author: Some One Maintainer: Some One Depends: R (>= 2.7.0), methods, AnnotationDbi (>= 1.23.23) Suggests: annotate, RUnit Imports: methods, AnnotationDbi License: Artistic-2.0 organism: Taeniopygia guttataTestingSubset species: Taeniopygia guttataTestingSubset biocViews: OrgDb, annotation AnnotationDbi/inst/extdata/org.testing.db/NAMESPACE0000644000175200017520000000054014710217313023000 0ustar00biocbuildbiocbuildimport(methods) import(AnnotationDbi) ### Only put what is statically exported here. All the AnnObj instances ### created at load time are dynamically exported (refer to R/zzz.R for ### the details). export( org.testing, org.testing_dbconn, org.testing_dbfile, org.testing_dbschema, org.testing_dbInfo, org.testingORGANISM ) AnnotationDbi/inst/extdata/org.testing.db/R/0000755000175200017520000000000014710217313021763 5ustar00biocbuildbiocbuildAnnotationDbi/inst/extdata/org.testing.db/R/zzz.R0000644000175200017520000000250214710217313022742 0ustar00biocbuildbiocbuilddatacache <- new.env(hash=TRUE, parent=emptyenv()) org.testing <- function() showQCData("org.testing", datacache) org.testing_dbconn <- function() dbconn(datacache) org.testing_dbfile <- function() dbfile(datacache) org.testing_dbschema <- function(file="", show.indices=FALSE) dbschema(datacache, file=file, show.indices=show.indices) org.testing_dbInfo <- function() dbInfo(datacache) org.testingORGANISM <- "Taeniopygia guttataTestingSubset" .onLoad <- function(libname, pkgname) { require("methods", quietly=TRUE) ## Connect to the SQLite DB dbfile <- system.file("extdata", "org.testing.sqlite", package=pkgname, lib.loc=libname) assign("dbfile", dbfile, envir=datacache) dbconn <- dbFileConnect(dbfile) assign("dbconn", dbconn, envir=datacache) ## Create the OrgDb object sPkgname <- sub(".db$","",pkgname) db <- loadDb(system.file("extdata", paste(sPkgname, ".sqlite",sep=""), package=pkgname, lib.loc=libname), packageName=pkgname) dbNewname <- AnnotationDbi:::dbObjectName(pkgname,"OrgDb") ns <- asNamespace(pkgname) assign(dbNewname, db, envir=ns) namespaceExport(ns, dbNewname) packageStartupMessage(AnnotationDbi:::annoStartupMessages("org.testing.db")) } .onUnload <- function(libpath) { dbFileDisconnect(org.testing_dbconn()) } AnnotationDbi/inst/extdata/org.testing.db/inst/0000755000175200017520000000000014710217313022537 5ustar00biocbuildbiocbuildAnnotationDbi/inst/extdata/org.testing.db/inst/extdata/0000755000175200017520000000000014710217313024171 5ustar00biocbuildbiocbuildAnnotationDbi/inst/extdata/org.testing.db/inst/extdata/org.testing.sqlite0000644000175200017520001334600014710217313027666 0ustar00biocbuildbiocbuildSQLite format 3@ - sb&--)9G '_indexgenes_GID_indgenes!CREATE INDEX genes_GID_ind ON genes (GID)G'_indexgenes__id_indgenesCREATE INDEX genes__id_ind ON genes (_id) utablegenesgenesCREATE TABLE genes ( _id INTEGER PRIMARY KEY, GID VARCHAR(10) NOT NULL UNIQUE -- Gene ID ))=indexsqlite_autoindex_genes_1genest!!3tablemap_countsmap_countsCREATE TABLE map_counts (map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL)3G!indexsqlite_autoindex_map_counts_1map_countsE%%Mtablemap_metadatamap_metadataCREATE TABLE map_metadata (map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL)dtablemetadatametadataCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY,value VARCHAR(255))/Cindexsqlite_autoindex_metadataK1+ #xgXG#"1'Supporting packageAnnotationDbiDb typeOrgDb TAXID59729CENTRALIDGID*MSPECIESTaeniopygia guttataTestingSubset+MORGANISMTaeniopygia guttataTestingSubset#DBSCHEMANOSCHEMA_DB+DBSCHEMAVERSION2.1 1Supporting package Db type TAXID CENTRALID SPECIES ORGANISM DBSCHEMA+ DBSCHEMAVERSION   |qf[PE:/$ti^SH=2'wlaVK@5* N752013 M752011 L752009 K752008 J752007 I752006 H752004 G752003 F752002 E752001 D752000 C751999 B751998 A751997 @751996 ?751995 >751993 =751992 <751990 ;751989 :751988 9751987 8751986 7751985 6751984 5751983 4751982 3751981 2751980 1751979 0751978 /751977 .751976 -751975 ,751974 +751973 *751972 )751971 (751970 '751969 &751968 %751967 $751966 #751965 "751964 !751963 751962 751961 751960 751959 751958 751957 751956 751955 751954 751953 751952 751780 751779 751778 751777 751776 751775 751774 751773 751771 751770 751769 751607 751606 751605 751589 751588 751q6{@ J  N~\\o}rg\QF;0%uj_TI>3(xmbWLA6+  752013N 752011M 752009L 752008K 752007J 752006I 752004H 752003G 752002F 752001E 752000D 751999C 751998B 751997A 751996@ 751995? 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    LL  $*06<BHNTZ`flrx~ &,28>DJPV\bhntz "(.4:@FLRX^djpv|       !!""##$$%%&&''(())**++,,--..//00112233445566778899::;;<<==>>??@@AABBCCDDEEFFGGHHIIJJKKLLMMNNOOPPQQRRSSTTUUVVWWXXYYZZ[[\\]]^^__``aabbccddeeffgghhiijjkkllmmnnooppqqrrssttuuvvwwxxyyzz{{||}}~~ e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpx e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpx            !!""##$$%%&&''(())**++,,--..//00112233445566778899::;;<<==>>??@@AABBCCDDEEFFGGHHIIJJKK d (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxMMMMNNOOPPQQRRSSTTUUVVWWXXYYZZ[[\\]]^^__``aabbccddeeffgghhiijjkkllmmnnooppqqrrssttuuvvwwxxyyzz{{||}}~~ Cxph`XPH@80( xph`XPH@80( )tfXJ<. whYJ;,xiZK<-100189970100189969100189968100189967100189966100189965100189964100189963100189962100189961100189960100189959100189958100189957100189956100189955100189954100189952100189951100189950100189949100189948100189947100189946100189945100189944100189943100189942100189941100189940100189939100189938100189937100189936 100189935 100189934~ 100189933} 100189932| 100187707{ 100187706z 100187705y 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3950799` 3950800a 3950801b 3950802c 4357609d  751582 751583 751584 751585 751586 751588 751589 751605 751606 751607 751769 751770 I|qf[PE:/$ti^SH=2'wlaVK@5* 778447V 778446U 778445T 778444S 778443R 778442Q 778441P 778440O 752013N 752011M 752009L 752008K 752007J 752006I 752004H 752003G 752002F 752001E 752000D 751999C 751998B 751997A 751996@ 751995? 751993> 751992= 751990< 751989; 751988: 7519879 7519868 7519857 7519846 7519835 7519824 7519813 7519802 7519791 7519780 751977/ 751976. 751975- 751974, 751973+ 751972* 751971) 751970( 751969' 751968& 751967% 751966$ 751965# 751964" 751963! 751962 751961 751960 751959 751958 751957 751956 751955 751954 751953 751952 751780 751779 751778 751777 751776 751775 751774 751773Rysmga[UOIC=71+% }wqke_YSMGA;5/)#0031115IEABP& !GO:0031092IEACC% !GO:0030544IEAMF$ !GO:0030426IEACC# !GO:0030424IEACC" !GO:0019894IEAMF! !GO:0016491IEAMF  !GO:0016234IEACC !GO:0016044IEABP !GO:0015629IEACC !GO:0014059IEABP !GO:0014048IEABP !GO:0010642IEABP !GO:0010517IEABP !GO:0010040IEABP !GO:0008344IEABP !GO:0008270/ e@]^v_Q`,abbc=desfNg)hi_j:klpmKn&op\q7rsmtHu#v~wYx4yzj{E| }{~V\1" #g$B%&x'Q(*)*\+5,-g.@/0r1K2$3}4V5/67a8:9:l;E<=w>P?)@A[B4C DfE?FGqHJI#J|MT,* B CnOG '_indedtablemetadatametadataCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY,valuedtablemetadatametadataCREATE TABLE metadata (name VARCHAR(80) PRIMARY KEY,value VARCHAR(255))/Cindexsqlite_autoindex_metadata_1metadataE%%Mtablemap_metadatamap_metadataCREATE TABLE map_metadata (map_name VARCHAR(80) NOT NULL, source_name VARCHAR(80) NOT NULL, source_url VARCHAR(255) NOT NULL, source_date VARCHAR(20) NOT NULL)t!!3tablemap_countsmap_countsCREATE TABLE map_counts (map_name VARCHAR(80) PRIMARY KEY, count INTEGER NOT NULL)3G!indexsqlite_autoindex_map_counts_1map_counts utablegenesgenesCREATE TABLE genes ( _id INTEGER PRIMARY KEY, GID VARCHAR(10) NOT NULL UNIQUE -- Gene ID ))=indexsqlite_autoindex_genes_1genesG'_indexgenes__id_indgenesCREATE INDEX genes__id_ind ON genes (_id)G 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(08@HPX`hpx (08@HPX`hpx (08@HPX`hpx   !"#$%&')*,-./01235 6 7 8 9 ;<=?ABCDEFGHIJKLMNP Q!S"T#U$V%W&X'Y(Z)[*\+],^-_.`/a0b1d2e3f4g5h6i7j8k9l:m;n<o=p>q?s@tAuBvCwDxEyFzG{H|I d (08@HPX`hpx (08@HPX`hpx (08@HPX`hpx~K~KLMNOPQRSTUVWXYZ[\]^_`abcdefghijklmnopqrstuvwxyz{|}~ t`L8$p\H4  lXD0~k!GO:0043205>!GO:0042802 k!GO:0042273 M!GO:0034341/!GO:0032154!GO:0030970 !GO:0030424#!GO:0030027 !GO:0021517:!GO:0019001!GO:0016757 !GO:0016446!GO:0016021!GO:0016020!GO:0015643!GO:0010033!GO:0008542!GO:0008237 !GO:0008021!GO:0007369!GO:0007165!GO:0006869!GO:0006777!GO:0006412 r!GO:0006355!GO:0005938 >!GO:0005840 x!GO:0005802!GO:0005741!GO:0005739!GO:0005737!GO:0005634 !GO:0005634!GO:0005622!GO:0005515 u!GO:0005515!GO:0005515R!GO:0005261TI!GO:0005102H!GO:0004872G!GO:0004416 .F!GO:0003735 E!GO:00037050C!GO:0003676 B!GO:0001701@!GO:0044154  8 0@P`p 0@P`p 0@P`p!GO:0000045!GO:0000056!GO:0000060 !GO:0000079!GO:0000082r!GO:0000082W!GO:0000084!GO:0000118!GO:0000122!GO:0000122!GO:00001227!GO:0000122s!GO:0000122!GO:0000122 !GO:0000122 !GO:0000122 !GO:0000124 !GO:0000139!GO:0000149!GO:0000166 !GO:0000166!GO:0000166!GO:0000166J!GO:0000166!GO:0000166!GO:0000166!GO:0000166 !GO:0000166!GO:0000166!GO:0000166!GO:0000166*!GO:0000166s!GO:0000166!GO:0000166!GO:0000166!GO:0000166 !GO:0000166 7!GO:0000166 j!GO:0000166 !GO:0000166 !GO:0000166 X!GO:0000166 !GO:0000166 !GO:0000166 !GO:0000166 !GO:0000166 !GO:0000166 8!GO:0000166 !GO:0000166 !GO:0000178O!GO:0000184 !GO:0000184 !GO:0000186 {!GO:0000226 !GO:0000276!GO:0000276 8ztnhb\VPJD>82,& ~xrlf`ZTNHB<60*$ |vpjd^XRLF@:4.(" }^?"hJ* jM0uV6vV6ߘzޘ]ݘ@ܘ#ۘڗgٗJؗ-ח֖pՖSԖ6ӖҕwѕYЕ9yY;_?"hK.tW8x Y <   eH+qT7N}`C& lO2vY<eH+qS4wX:}^@ cE'߆ ޅj݅L܅,ۅ ڄnلO؄0ׄ!qSS[5ZYxXXW8VUxӁBi\qxR-V >}sjaWND:0' |rh^TJ@7.$18013/14.Un-12,19+15*20)19(19'4&24%11$3#1"23!14 11201222315Z724318122232727208 18 13 2 1 13102352851145515~1}25|8{11z4Ay22x2w5v1u1t9 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GO:0000287!GO:0000338 !GO:0000346!GO:0000413!GO:0000502!GO:0000502!GO:0000502!GO:0000502 !GO:0000502 !GO:0000720 !GO:0000724!GO:0000724 !GO:0000724 !GO:0000729 )!GO:0000774!GO:0000785!GO:0000785 !GO:0000785 !GO:0000790{!GO:0000790K!GO:0000902t!GO:0000910!GO:0000932s!GO:0000932!GO:0000932!GO:00009768!GO:0000976l!GO:0000979!GO:0000980|!GO:00009829!GO:0000987u!GO:0001046!GO:0001085L!GO:0001102}!GO:0001104I!GO:0001104 !GO:0001106!GO:0001190~!GO:0001523 !GO:0001542!GO:0001547!GO:0001553!GO:0001558 !GO:0001568!GO:0001569X!GO:0001570K!GO:0001641_!GO:0001642!GO:0001657]!GO:0001661!GO:0001662^!GO:0001662j!GO:0001662!GO:0001667Y!GO:0001671 /!GO:0001671 # 8$4DScs 0@P`p 0@P`p!GO:0001701M!GO:0001701k!GO:0001701)!GO:0001701!GO:0001701 k!GO:0001726!GO:0001750!GO:0001750?!GO:0001758!GO:0001764L!GO:0001764!GO:0001764 !GO:0001774!GO:0001824O!GO:0001917!GO:0001921!GO:0001936!GO:0001937!GO:0001944A!GO:0001956!GO:0001963!GO:0001964!GO:0001964l!GO:0001964L!GO:0001967!GO:0001967m!GO:0001975!GO:0001975M!GO:0002014 !GO:0002031!GO:0002039 l!GO:0002039 )!GO:0002053!GO:0002053*!GO:0002064!GO:0002070!GO:0002176v!GO:0002329+!GO:0002639,!GO:0002761 9!GO:0002829 :!GO:0002865 D!GO:0003006w!GO:0003007!GO:0003016B!GO:0003016 !GO:0003073N!GO:0003676!GO:0003676!GO:0003676:!GO:0003676!GO:0003676!GO:0003676!GO:0003676 8!GO:0003676 !GO:0003676 Z{rjaXPF<2( {rh_VMC90& zqh_VLB90& D1AC10B11A1@6?15>Z=Z<5;4A:19917817Z61751243332919010/4A.Un-22,1A+5*12)Z(6'6&2%2$4A#1A"27!5 1102151A2421Z23924Z1A1A12381A 1 4 1A 6 1322725171B1227241A2~4A}Un|5{1Bz20y27x3wUnv1u12t15s1rZq1p3o2nUnm15l~9k}1A 8 0@P`p 0@P`p 0@P`p!GO:0003676 !GO:0003676 !GO:0003677!GO:0003677!GO:0003677C!GO:0003677O!GO:0003677!GO:0003677!GO:0003677-!GO:0003677x!GO:0003677!GO:0003677!GO:0003677!GO:0003677!GO:0003677!GO:0003677!GO:0003677;!GO:0003677X!GO:0003677!GO:0003677!GO:0003677m!GO:0003677!GO:0003677!GO:0003677!GO:0003677 !GO:0003677 !GO:0003677 !GO:0003677 !GO:0003677 !GO:0003677 !GO:0003677 !GO:0003677 !GO:0003677 !GO:0003682P!GO:0003682!GO:0003682.!GO:0003682!GO:0003682 !GO:0003697!GO:0003697 !GO:0003700!GO:0003700!GO:0003700Q!GO:0003700!GO:0003700/!GO:0003700y!GO:0003700!GO:0003700!GO:0003700!GO:0003700<!GO:0003700Y!GO:0003700!GO:0003700n!GO:0003700!GO:0003705!GO:0003705 8 0@P`p 0@P`p 0@P`p!GO:0003707R!GO:0003707!GO:0003707z!GO:0003707!GO:0003707!GO:0003707!GO:0003707Z!GO:0003707!GO:0003708!GO:00037132!GO:0003713 !GO:0003713 !GO:0003723!GO:0003723P!GO:0003723t!GO:0003723!GO:0003723!GO:0003723:!GO:0003723!GO:0003723!GO:0003723d!GO:0003723!GO:0003723 !GO:0003723 !GO:0003723 !GO:0003723 !GO:0003725!GO:0003729 9!GO:0003729 *!GO:0003735!GO:0003735!GO:0003735 !GO:00037352!GO:0003735!GO:0003735!GO:0003735!GO:0003735!GO:0003735!GO:0003735!GO:0003735!GO:0003735e!GO:0003735!GO:0003735!GO:0003735!GO:0003735 !GO:0003735 +!GO:0003735 :!GO:0003735 \!GO:0003735 !GO:0003735 !GO:0003735 !GO:0003735 !GO:0003735 f!GO:0003735 n!GO:0003735 t!GO:0003735 + 8 0@P`p 0@P`p 0@P`p!GO:0003735 !GO:0003735 !GO:0003735 $!GO:0003735 E!GO:0003743u!GO:0003755!GO:0003779!GO:0003824 !GO:0003824!GO:0003824!GO:0003824!GO:0003824!GO:0003824!GO:0003824!GO:0003824 !GO:0003824 !GO:0003854!GO:0003899 !GO:0003899 !GO:0003899 !GO:0003899 !GO:0003924!GO:0003924!GO:0003924!GO:0003924!GO:0003924+!GO:0003924!GO:0003924!GO:0003924!GO:0003924 !GO:0004004 !GO:0004017 !GO:0004022 !GO:0004028!GO:0004129!GO:0004129!GO:0004129!GO:0004140 k!GO:0004169 !GO:0004170!GO:0004175!GO:0004175!GO:0004180 '!GO:0004197!GO:0004221!GO:0004221!GO:0004252 !GO:0004298!GO:0004298 !GO:0004339!GO:0004351!GO:0004351!GO:0004364 P!GO:0004386!GO:0004386!GO:0004386  8 0@P`p 0@P`p 0@P`p!GO:0004497!GO:0004540!GO:0004553!GO:0004553!GO:0004558!GO:0004582 !GO:0004672M!GO:0004672!GO:0004672 !GO:0004672 *!GO:0004674 +!GO:0004693X!GO:0004713N!GO:0004713 ,!GO:0004714O!GO:0004721 !GO:0004722 !GO:0004735 !GO:0004842!GO:0004842J!GO:0004846!GO:0004849 l!GO:0004861Y!GO:0004871!GO:0004871!GO:0004871!GO:0004871`!GO:0004871!GO:0004871!GO:0004871!GO:0004871!GO:0004871!GO:0004871&!GO:0004871,!GO:0004871@!GO:0004871,!GO:0004871t!GO:0004871 ;!GO:0004872!GO:0004872!GO:0004872!GO:0004872S!GO:0004872!GO:0004872!GO:0004872!GO:0004872!GO:00048726!GO:0004872E!GO:0004872a!GO:0004872n!GO:0004872!GO:0004872!GO:0004872!GO:0004872P!GO:0004872{!GO:0004872 8!1AQaq!1AQaq!1AQaq!GO:0004872!GO:0004872!GO:0004872'!GO:0004872-!GO:00048729!GO:0004872A!GO:0004872N!GO:0004872!GO:0004872[!GO:0004872!GO:0004872!GO:0004872 !GO:0004879T!GO:0004879!GO:0004879!GO:0004882U!GO:0004883\!GO:0004887|!GO:0004890!GO:0004930!GO:0004930!GO:0004930!GO:0004930b!GO:0004930!GO:0004930!GO:0004930!GO:0004930!GO:0004930!GO:0004930(!GO:0004930.!GO:0004930B!GO:0004949!GO:0004970!GO:0004970!GO:0004970!GO:00049707!GO:0004970F!GO:0004970o!GO:0004970!GO:0004970O!GO:0004971!GO:0004971G!GO:0004972!GO:0004972p!GO:0004972P!GO:0004990:!GO:0004993!GO:0005000;!GO:0005030Q!GO:0005057!GO:0005070 !GO:0005080 5!GO:0005085 |!GO:0005102_!GO:0005102V!GO:0005102^h|vpjd^e receptor, ionotropic, N-methyl D-aspartate 19kNR5A1nuclear receptor subfamily 5, group A, member 1ByCYP19A1cytochrome P450, family 19, subfamily A, polypeptide 19kNR3C2nuclear receptor subfamily 3, group C, member 20YGRIA2glutamate receptor, ionotropic, AMPA 2/ARandrogen receptor)IZFAND5zinc finger, AN1-type domain 56 a ALDH1A2aldehyde dehydrogenase 1 family, member A2X % HSD3B1hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1 + FOXP2forkhead box P2' I CNR1cannabinoid receptor 1 (brain) - SYT4synaptotagmin IV+SYT1synaptotagmin ILUCHL1ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase) 7MTNR1Bmelatonin receptor 1B 7MTNR1Amelatonin receptor 1A3_CREB1cAMP responsive elgrfaePd?c.ba `|_m^]]K\9[)ZYXtWbVSUAT.SRQwPfORN?M&L "",f+gindexgo_EVIDENCE_indgoCREATE INDEX go_EVIDENCE_ind ON go (EVIDENCE)8Oindexgo_GO_indgoCREATE TABLE temp ( GID TEXT, GOALL TEXT, EVIDENCEALL TEXT, ONTOLOGYALL TEXT )<!Sindexgo__id_indgoCREATE INDEX go__id_indq?!indexchromosome_CHROMOSOME_indchromosome0CREATE INDEX chromosome_CHROMOSOME_ind ON chromosome (CHROMOSOME)[1!sindexchromosome__id_indchromosome6CREATE INDEX chromosome__id_ind ON chromosome (_id)7Ytablegogo*CREATE TABLE go ( _id INTEGER NOT NULL, -- REFERENCES genes GO VARCHAR( 25 ) NOT NULL, -- data EVIDENCE VARCHAR( 25 ) NOT NULL, -- data ONTOLOGY VARCHAR( 25 ) NOT NULL, -- data FOREIGN KEY (_id) REFERENCES genes (_id) )8Oindexgo_GO_indgoA>STXBP1syntaxin binding protein 1==q=GABRA2gamma-aminobutyric acid (GABA) A receptor, alpha 2&<=b1Q*~0m>-w%EwLOC100187703uncharacterized LOC100187703.vUvRAP1ARAP1A, member of RAS oncogene familyBuyuCYP11A1cytochrome P450, family 11, subfamily A, polypeptide 1Mt tCYP17A1steroidogenic enzyme cytochrome P450 17a-hydroxylase/17,20 lyaseLssKCNC1potassium voltage-gated channel, Shaw-related subfamily, member 1/r%IrLOC100144431GABA-A receptor gamma4 subunitq7qPGRprogesterone receptor$p=pC13orf1SPRY domain containing 74oaoCKS1BCDC28 protein kinase regulatory subunit 1B%nAnTUBB2Ctubulin, beta 4B class IVb-mQmUBE2R2ubiquitin-conjugating enzyme E2R 2"l?lNPVFneuropeptide VF precursorMkkTRPV1transient receptor potential cation channel, subfamily V, member 1yoySLC7A6OSsolute carrier family 7, member 6 opposite strand&xExREEP5receptor accessory protein 5 Pb3V4t"xP%%3LOC100189963scotin protein-like.%ELOC100189962uncharacterized LOC1001899620%ILOC10018996140S ribosomal protein S25-likeC%oLOC100189960nudix (nucleoside diphosphate linked moiety)-likeO%LOC100189959retinoic acid receptor responder (tazarotene induced) 2-like1%KLOC100189958death-associated protein 1-like:%]LOC100189957RNA polymerase I 16 kDa polypeptide-like&%5LOC100189956CGI-105 protein-like#%/LOC100189955cornichon homolog7HBE1hemoglobin, epsilon 1B%mLOC100189952uncharacterized hypothalamus protein HSMNP1-like.%ELOC100189951uncharacterized LOC100189951'EWASF1WAS protein family, member 1: %]LOC100189949mitochondrial ribosomal protein S36-like, %ALOC100189948ribosomal protein L31-like$ %1LOC100189947cdna MGC75753-like. %ELOC100189946uncharacterized LOC100189946C %oLOC100189945DNA directed RNA polymerase II polypeptide E-like C{P#i2 h0 CE.%sLOC100189983transmembrane BAX inhibitor motif containing 4-like6-%ULOC100189982peptidylprolyl isomerase-like 1-like,SEPT3septin 3,+%ALOC100189980ribonuclease P 14 kDa-like$*%1LOC100189979microcephalin-like5)%SLOC100189978Phosphohistidine phosphatase 1-like!(9LYRM5LYR motif containing 5.'%ELOC100189976uncharacterized LOC100189976J&%}LOC100189975eukaryotic translation initiation factor 4E (eIF4E)-like%%CDBX2developing brain homeobox 24$%QLOC100189973stromal cell derived factor 1-like*#%=LOC100189972exosome component 5-like$"AMED7mediator complex subunit 7/!%GLOC100189970COMM domain containing 3-like1 %KLOC100189969fatty acid-binding protein-like*ERNF113A2zinc finger protein 183-like(%9LOC100189967fracture callus 1-like0%ILOC100189966S-100 protein alpha chain-like %)LOC100189965frequenin-like,%ALOC100189964ribosomal protein S11-like GZ s<$r>qG'A%7LOC100190003C35 protein cDNA-like5@%SLOC100190002ubiquitin specific protease 12-like*?%=LOC100190001aldo-keto reductase-like,>%ALOC100190000ribosomal protein L23-like6=%ULOC100189999proteasome subunit alpha type 6-like1<SC11orf75chromosome 11 open reading frame 752;%MLOC100189997recombination protein REC14-like.:%ELOC100189996uncharacterized LOC100189996$9=COMMD9COMM domain containing 9"8%-LOC100189994CD9 antigen-like7!TAGLNtransgelin46]SAMD12sterile alpha motif domain containing 1205%ILOC100189991transcription factor Dp 1-like34%OLOC100189990basic transcription factor 3-like.3%ELOC100189989uncharacterized LOC100189989J2B3GNT7UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7C1%oLOC100189987Rho/Cdc42/Rac GTPase-activating protein RICS-like,0%ALOC100189986ribosomal protein S18-like./%ELOC100189985uncharacterized LOC100189985 7h*o>r97OS%LOC100190021coiled-coil-helix-coiled-coil-helix domain containing 6-likeR%MYCT1myc target 1QAKIRIN2akirin 2YP%LOC100190018evectin-2 pleckstrin homology domain containing family B member 2-likeO%'LOC100190017oxytocin-like6N%ULOC100190016RNA polymerase II polypeptide H-like0MUTM6SF1transmembrane 6 superfamily member 1+L%?LOC100190014ribosomal protein S4-likeDK%qLOC100190013protein phosphatase 1 catalytic subunit alpha-like!J%+LOC100190012annexin A4-like.I%ELOC100190011uncharacterized LOC100190011FHPACSIN3protein kinase C and casein kinase substrate in neurons 3JG%}LOC100190009sm like protein U6 snRNA-associated Sm-like protein-like"F%-LOC100190008complexin 1-like;E%_LOC100190007BRCA2 and CDKN1A-interacting protein-like#D%/LOC100190006DPCD protein-like,C%ALOC100190005ribosomal protein L14-like@B%iLOC100190004Ras family small GTP binding protein RALA-like CU\|<sC-bQMRPL9mitochondrial ribosomal protein L9)a%;LOC100190036thioredoxin-like 2-like)`%;LOC100190035thioredoxin-like 2-like._%ELOC100190033uncharacterized LOC100190033=^%cLOC100190032amyloid beta precursor protein-binding-like=]%cLOC100190031putative dimethyladenosine transferase-likeW\%LOC100190030ATP synthase H+ transporting mitochondrial F0 complex subunit c-like;[%_LOC100190029TGF beta-inducible nuclear protein 1-likeEZ%sLOC100190028translocase of inner mitochondrial membrane 10-like3Y%OLOC100190027malignant T cell amplified 1-like9X%[LOC100190026p32 subunit of splicing factor SF2-like4W_STRBPspermatid perinuclear RNA binding proteinMV%LOC100190024phosphate cytidylyltransferase 1 choline beta isoform-likeOU%LOC100190023guanine nucleotide binding protein (G protein) gamma 10-likeVT%LOC100190022cofactor required for Sp1 transcriptional activation subunit 8-like 7Z)[Nj70t%ILOC1001900556-phosphogluconolactonase-like:skNR2F2nuclear receptor subfamily 2, group F, member 2$r=ALYREFdisulfide-isomerase-like5q%SLOC100190052phosphohistidine phosphatase 1-likeEp%sLOC100190051BCL2/adenovirus E1B 19kD interacting protein 1-likeAo%kLOC100190050postmeiotic segregation increased 2-like 6-likeEn%sLOC100190049hexamethylene bisacetamide-inducible protein 1-like m%)LOC100190048metaxin 2-likel3HBADhemoglobin, alpha 2;k%_LOC100190046cyclin-dependent kinase inhibitor 1B-like&j%5LOC100190045stathmin-like 3-like.i%ELOC100190044uncharacterized LOC1001900444h%QLOC100190043defender against cell death 1-like:g%]LOC100190042mitochondrial ribosomal protein L42-like.f%ELOC100190041uncharacterized LOC1001900416eeCMC2COX assembly mitochondrial protein 2 homolog9dcTRAPPC2Ltrafficking protein particle complex 2-like.c%ELOC100190038uncharacterized LOC100190038 1j*e4Y:`1,%ALOC100190073ribosomal protein L36-likeA%kLOC100190071S100 calcium binding protein beta (neural)-likeB%mLOC100190070molybdopterin synthase large subunit MOCS2B-like"%-LOC100190069prefoldin 2-like)%;LOC100190068preproenkephalin 1-like1LAMRlaminin receptor 1K%LOC100190066ATPase H+ transporting lysosomal 31 kDa V1 subunit E-like9~%[LOC100190065GrpE-like 1 mitochondrial precusor-likeN}NDUFC2NADH dehydrogenase (ubiquinone) 1, subcomplex unknown, 2, 14.5kDa.|%ELOC100190063uncharacterized LOC1001900631{%KLOC100190062nucleolar protein family A-like0zWNTHL1nth endonuclease III-like 1 (E. coli).y%ELOC100190060uncharacterized LOC100190060*x%=LOC100190059U3 snoRNP protein 4-like=w%cLOC100190058aldo-keto reductase family 7 member A2-likedv%/LOC100190057cytoplasmic dynein light chain (T-complex testis-specific protein 1 homolog)-like,u%ALOC100190056ribosomal protein S16-like .u?\!~FT.#%/LOC100190092RBX1 protein-likeB%mLOC100190090chaperonin containing TCP1 subunit 2 (beta)-like:%]LOC100190089phosphopantothenate cysteine ligase-like.UMZT1mitotic spindle organizing protein 1<%aLOC100190087NADH dehydrogenase 1 alpha subcomplex-like5aDECR12,4-dienoyl CoA reductase 1, mitochondrial&%5LOC100190085sorting nexin 3-like7%WLOC100190084ADP-ribosylation factor-like 10C-like=mIER3IP1immediate early response 3 interacting protein 18%YLOC100190082thioesterase superfamily member 2-like3 %O LOC100190081peripheral myelin protein 22-like, %A LOC100190080ribosomal protein S15-like6 %U LOC100190079Proteasome subunit alpha type 4-likeB %m LOC100190078CDC26 subunit of anaphase promoting complex-like3 %O LOC100190077somatostatin precursor pro-2-like,MCCDC25coiled-coil domain containing 25&CJMJD8jumonji domain containing 80%ILOC100190074mitotic phosphoprotein 44-like [Kt<j$[.)%E)LOC100190110ring finger protein 126-like,(%A(LOC100190109ribosomal protein L37-like7'%W'LOC100190108macrophage erythroblast attacher-like,&%A&LOC100190107N-acetyltransferase 5-likeC%%o%LOC100190106LSM6 homolog U6 small nuclear RNA associated-like1$%K$LOC100190105alpha-aspartyl dipeptidase-likeE#%s#LOC100190104cyclin-dependent kinase 2-associated protein 1-like,"%A"LOC100190103ribosomal protein L34-like$!=!SFT2D1SFT2 domain containing 15 _ ARFRP1ADP-ribosylation factor related protein 18%YLOC100190100solute carrier family 40 member 1-like(%9LOC100190099U11/U12 snRNP 48K-like4%QLOC100190098HESB like domain containing 1-like7%WLOC100190097putative hypothetical protein MGC2198:%]LOC100190096mitochondrial ribosomal protein L21-like!%+LOC100190095dynactin 6-like(%9LOC100190094metallothionein-I-like&?TMEM189transmembrane protein 189 ;y&}\qr;49%Q9LOC100190126Ras homolog enriched in brain-like+8%?8LOC100190125dUTP pyrophosphatase-like/7Q7C9orf16chromosome 9 open reading frame 16B6%m6LOC100190123myosin regulatory light chain isoform L20-B-likeW5%5LOC100190122ATP synthase H+ transporting mitochondrial F0 complex subunit f-like#4%/4LOC100190121maternal G10-like@3%i3LOC100190120RAB member of RAS oncogene family-like 2B-like72%W2LOC100190119Brix domain containing protein 1-likeE1%s1LOC100190118translocase of outer mitochondrial membrane 20-like0%%0LOC100190117Di-Ras2-like1/%K/LOC100190116PAK1 interacting protein 1-like4.%Q.LOC100190115signal sequence receptor beta-like;-%_-LOC100190114vacuolar proton-ATPase subunit ATP6H-likeP,%,LOC100190113translocase of inner mitochondrial membrane 9/10 homolog-like;+%_+LOC100190112MAD2 mitotic arrest deficient-like 2-likeF*%u*LOC100190111high-mobility group nucleosome binding domain 1-like ?k? tG^n?,K%AKLOC100190144ribosomal protein S26-likeCJ%oJLOC100190143macrophage migration inhibitory factor (MIF)-like?IuIRRP7Aribosomal RNA processing 7 homolog A (S. cerevisiae)!H9HLYRM1LYR motif containing 1AG%kGLOC100190140inhibitor-1 of protein phosphatase type 2A-likePFFAHSA2AHA1, activator of heat shock 90kDa protein ATPase homolog 2 (yeast),E%AELOC100190138ribosomal protein L24-like:D%]DLOC100190137alcohol dehydrogenase 5 (class III)-like'C%7CLOC100190136MGC89063 protein-like*B%=BLOC100190135stem cell antigen 2-like>A%eALOC100190134NADH dehydrogenase 1 alpha subcomplex 8-like$@%1@LOC100190133cdna MGC42090-like+?%??LOC100190132ribosomal protein S6-like2>%M>LOC100190131glycine N-methyltransferase-like)=%;=LOC100190130suppressor of Ty 4-like.<%Eg9m%[mLOC100190180ATP synthase e chain mitochondrial-like:l%]lLOC100190179mitochondrial ribosomal protein L17-like,k%AkLOC100190178ribosomal protein L7a-like,j%AjLOC100190177ribosomal protein S21-like9i%[iLOC100190175mitochondrial ribosomal protein L2-like2hYhAPITD1apoptosis-inducing, TAF9-like domain 1/g%GgLOC100190173cytokine induced protein-like/f%GfLOC100190172transmembrane protein 80-likeEe%seLOC100190171adaptor-related protein complex 2 mu 1 subunit-likeNd%dLOC100190170zinc binding alcohol dehydrogenase domain containing 1-likeQc% cLOC100190169regulatory factor X-associated ankyrin-containing protein-like,b%AbLOC100190168ribosomal protein S27-like1a%KaLOC100190167myelin protein zero-like 1-like0`%I`LOC100190166transmembrane protein 50B-like(_%9_LOC100190165LIM domain only 1-like<^%a^LOC100190164clathrin light polypeptide variant 1a-like ][#}E);]8|%Y|LOC100190196hydroxyacyl glutathione hydrolase-likeM{%{LOC100190195ubiquitin-conjugating enzyme E2 transcript variant 2A-likePz%zLOC100190194AHA1 activator of heat shock 90 protein ATPase homolog 1-like]y/yFSCN2fascin homolog 2, actin-bundling protein, retinal (Strongylocentrotus purpuratus))x%;xLOC100190192dickkopf homolog 3-like;w%_wLOC100190191p53 and DNA damage-regulated protein-like!v%+vLOC100190190calretinin-likeu+uSNCBsynuclein, beta5t%StLOC100190188JUN activation binding protein-likeKs%sLOC100190187activated RNA polymerase II transcription cofactor 4-like'r%7rLOC100190186ubiquitin-like 5-like+q%?qLOC100190185ribosomal protein L9-like5p%SpLOC100190184signal sequence receptor gamma-likeCo%ooLOC100190183DNA directed RNA polymerase II polypeptide K-like\n-nTAF13TAF13 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 18kDa Iu<Nl1I6 %ULOC10019021260S acidic ribosomal protein P1-like, %ALOC100190211ribosomal protein L30-likeA %kLOC100190210phosphatidylinositol transfer protein beta-like9 %[LOC100190209mitochondrial ribosomal protein S6-like8%YLOC100190208IscU iron-sulfur cluster scaffold-like4_NTPCRnucleoside-triphosphatase, cancer-related$%1LOC100190206MIZIP protein-likeB%mLOC100190205actin related protein 2/3 complex subunit 4-like<%aLOC100190204glutathione S-transferase class-alpha-like<%aLOC100190203vesicle-associated membrane protein 4-like2%MLOC100190202WW domain binding protein 2-like;oSYF2SYF2 homolog, RNA splicing factor (S. cerevisiae)9%[LOC100190200Nedd4 family interacting protein 1-like6%ULOC100190199biphenyl hydrolase-like protein-like>~%e~LOC100190198NADH dehydrogenase 1 alpha subcomplex 5-likeG}}COX19COX19 cytochrome c oxidase assembly homolog (S. cerevisiae) ,H#zKg8_,0%ILOC100190230kelch domain containing 3-like.%ELOC100190229uncharacterized LOC100190229=qPYCR2pyrroline-5-carboxylate reductase family, member 24%QLOC100190227TruB pseudouridine synthase 2-like.%ELOC100190226uncharacterized LOC100190226,MCCDC23coiled-coil domain containing 23C%oLOC100190224DNA directed RNA polymerase II polypeptide D-like.%ELOC100190223uncharacterized LOC100190223:%]LOC100190222mitochondrial ribosomal protein L12-like-%CLOC100190221ATP synthase subunit b-like,%ALOC100190220preprocholecystokinin-like.%ELOC100190219uncharacterized LOC100190219A%kLOC100190218DNA polymerase delta interacting protein 2-like1%KLOC100190217aspartate beta-hydroxylase-like";CLYBLcitrate lyase beta like>%eLOC100190215embryogenesis protein H beta 58 homolog-likeILAMTOR2late endosomal/lysosomal adaptor, MAPK and MTOR activator 2( %9LOC100190213churchill protein-like d^.<T#dJ.%}LOC100190247solution structure of the Bola-Like protein chain A-like>-%eLOC100190246U2 snRNP auxiliary factor small subunit-like.,%ELOC100190245uncharacterized LOC100190245.+%ELOC100190243uncharacterized LOC100190243F*%uLOC100190242high-mobility group nucleosome binding domain 1-like)1HPCAL1hippocalcin-like 1C(%oLOC100190240protein transport protein SEC61 beta subunit-like5'%SLOC100190239engulfment and cell motility 1-likeB&%mLOC100190238actin related protein 2/3 complex subunit 3-like.%%ELOC100190237uncharacterized LOC100190237C$%oLOC100190236DNA directed RNA polymerase II polypeptide C-like3#_ENY2enhancer of yellow 2 homolog (Drosophila)-"SCOQ9coenzyme Q9 homolog (S. cerevisiae)5!%SLOC100190233palmitoyl-protein thioesterase-like' %7LOC100190232ubiquitin-like 1-like=%cLOC100190231splicing factor arginine/serine-rich 7-like Yq@fV#Y.?%ELOC100190264uncharacterized LOC100190264.>%ELOC100190263optic atrophy 3 protein-like=DERL3derlin 3O<%LOC100190261growth-related translationally controlled tumor protein-like0;%ILOC10019026040S ribosomal protein S29-like-:%CLOC100190259RNA-binding protein 8A-like-9%CLOC100190258ubiquitously-expressed-like[8%LOC100190257ATP synthase H+ transporting mitochondrial F1 complex delta subunit-likeO7%LOC100190256ATP synthase mitochondrial F1 complex assembly factor 1-like76%WLOC100190255thymidine kinase 2 mitochondrial-like25%MLOC100190254Yip1 domain family member 6-likeD4%qLOC100190253small nuclear ribonucleoprotein polypeptide G-like!39LYRM4LYR motif containing 4.2%ELOC100190251uncharacterized LOC100190251"1%-LOC100190250C10 protein-like#0%/LOC100190249parathymosin-likeA/%kLOC100190248protein phosphatase 1 regulatory subunit 7-like 2xP YN2JP%}LOC100190281proteasome 26S subunit ATPase 3 interacting protein-likeCO%oLOC100190280proteaseome (prosome macropain) 28 subunit 3-like8N%YLOC100190279dynein light chain 2A cytoplasmic-likeKM ITPAinosine triphosphatase (nucleoside triphosphate pyrophosphatase)JL%}LOC100190277hematological and neurological expressed sequence 1-like>K%eLOC100190276NADH dehydrogenase 1 alpha subcomplex 2-like=J%cLOC100190275NADH dehydrogenase 1 beta subcomplex 9-like:I%]LOC100190274mitochondrial ribosomal protein L30-like*HILMAN2Llectin, mannose-binding 2-likeG+SELSselenoprotein S0F%ILOC100190271DnaJ subfamily C member 8-like3E%OLOC10019027026S ATPase complex subunit 4-likeBD%mLOC100190269growth arrest and DNA-damage-inducible beta-like%C%3LOC100190268glutaredoxin 5-like3B%OLOC100190267fetal globin-inducing factor-like A%)LOC100190266syndesmos-like,@%ALOC100190265ribosomal protein S13-like 9e%e,h#n92a%MLOC100190300axonemal dynein light chain-likeA`%kLOC100190299ubiquitin-conjugating enzyme E2I cluster 2-like._%ELOC100190297programmed cell death 5-like=^%cLOC100190296dolichol-phosphate mannosyltransferase-likeB]%mLOC100190295arginine-rich mutated in early stage tumors-like?\%gLOC100190294U6 snRNA-associated Sm-like protein LSm1-like;[%_LOC100190293mitochondrial ribosomal protein S18A-likeAZ{MMABmethylmalonic aciduria (cobalamin deficiency) cblB type6Y%ULOC10019029121 kDa signal peptidase subunit-like5X%SLOC10019029026S proteasome-associated pad1-like8W%YLOC100190289NADH dehydrogenase Fe-S protein 6-like V7RPS3Aribosomal protein S3A'U%7LOC100190286brain protein 44-like=T%cLOC100190285growth factor receptor-bound protein 2-like+S%?LOC100190284ribosomal protein S3-like?R%gLOC100190283iron-sulfur cluster scaffold protein Nfu-like(QGMEAF6MYST/Esa1-associated factor 6 Ig n1@$xI,r%ALOC100190317ribosomal protein L26-like,q%ALOC100190316ribosomal protein L26-like"p%-LOC100190315complexin 2-like.o%ELOC100190314uncharacterized LOC100190314$n=NUDCD2NudC domain containing 2m+SELKselenoprotein Knl%CLOC100190311tyrosine 3-monooxgenase/tryptophan 5-monooxgenase activation protein gamma polypeptide-likeIk%{LOC100190310ectonucleotide pyrophosphatase/phosphodiesterase 2-like1j%KLOC100190309p53-related protein kinase-like:i%]LOC100190308mitochondrial ribosomal protein S17-like.h%ELOC100190307uncharacterized LOC100190307?g%gLOC100190306ovarian carcinoma immunoreactive antigen-likeJSamz  ,8DPYckv )3=GR]hs~ ACT5C0 AHSA2F AKIRIN2 ALDH1A2 ALDH3A2U ALYREF APITD1hARARCE ARFRP1 ATP5A1-ATP6\ATP8[ B3GNT7BDNF C11orf75 C13orf1p C9orf167 CCDC23 CCDC25 CCDC58 CHD1WR CHD1ZS CKS1Bo CLYBL CMC2CNR1 COMMD9 COQ9COX1Y COX19}COX2ZCOX3] CREB1 CYBASC3z CYP11A1u CYP17A1t CYP19A1CYTBb DBX2DCXF DECR1 DERL3EGR1e ENY2ESR1B FNTM1g FNTM2f FOXP16 FOXP2 FSCN2y GABRA2=GAD1QGAD1V GRIA1 GRIA2 GRIA3 GRIA4 GRIK1 GRIK3 GRIK5 GRIK5 GRIN1 GRIN2AO GRIN2B GRIN2CP GRIN2DD GRIN3AGRM1CGRM2GRM3 GRM4IGRM8! HBAD HBE1 HINT1. HPCAL1 HSD3B1 HTR7G IER3IP1 ITPA 5vv~ 0BTfx,>Pbt(:L^pKA1J KANK1i KCNC1s LAMR LAMTOR2 LMAN2L%LOC100144431r%LOC100187703w%LOC100189935%LOC100189936%LOC100189937%LOC100189938%LOC100189939%LOC100189940%LOC100189941%LOC100189942%LOC100189944%LOC100189945%LOC100189946%LOC100189947%LOC100189948%LOC100189949%LOC100189951%LOC100189952%LOC100189955%LOC100189956%LOC100189957%LOC100189958%LOC100189959%LOC100189960%LOC100189961%LOC100189962%LOC100189963%LOC100189964%LOC100189965%LOC100189966%LOC100189967%LOC100189969%LOC100189970%LOC100189972%LOC100189973%LOC100189975%LOC100189976%LOC100189978%LOC100189979%LOC100189980%LOC100189982%LOC100189983%LOC100189985%LOC100189986%LOC100189987%LOC100189989%LOC100189990 2|| 0BTfx,>Pbt(:L^p%LOC100189994%LOC100189996%LOC100189997%LOC100189999%LOC100190000%LOC100190001%LOC100190002%LOC100190003%LOC100190004%LOC100190005%LOC100190006%LOC100190007%LOC100190008%LOC100190009%LOC100190011%LOC100190012%LOC100190013%LOC100190014%LOC100190016%LOC100190017%LOC100190018%LOC100190021%LOC100190022%LOC100190023%LOC100190024%LOC100190026%LOC100190027%LOC100190028%LOC100190029%LOC100190030%LOC100190031%LOC100190032%LOC100190033%LOC100190035%LOC100190036%LOC100190038%LOC100190041%LOC100190042%LOC100190043%LOC100190044%LOC100190045%LOC100190046%LOC100190048%LOC100190049%LOC100190050%LOC100190051%LOC100190052%LOC100190055%LOC100190056%LOC100190057 2|| 0BTfx,>Pbt(:L^p%LOC100190059%LOC100190060%LOC100190062%LOC100190063%LOC100190065%LOC100190066%LOC100190068%LOC100190069%LOC100190070%LOC100190071%LOC100190073%LOC100190074%LOC100190077 %LOC100190078 %LOC100190079 %LOC100190080 %LOC100190081 %LOC100190082%LOC100190084%LOC100190085%LOC100190087%LOC100190089%LOC100190090%LOC100190092%LOC100190094%LOC100190095%LOC100190096%LOC100190097%LOC100190098%LOC100190099%LOC100190100%LOC100190103"%LOC100190104#%LOC100190105$%LOC100190106%%LOC100190107&%LOC100190108'%LOC100190109(%LOC100190110)%LOC100190111*%LOC100190112+%LOC100190113,%LOC100190114-%LOC100190115.%LOC100190116/%LOC1001901170%LOC1001901181%LOC1001901192%LOC1001901203%LOC1001901214 2|| 0BTfx,>Pbt(:L^p%LOC1001901236%LOC1001901258%LOC1001901269%LOC100190127:%LOC100190128;%LOC100190129<%LOC100190130=%LOC100190131>%LOC100190132?%LOC100190133@%LOC100190134A%LOC100190135B%LOC100190136C%LOC100190137D%LOC100190138E%LOC100190140G%LOC100190143J%LOC100190144K%LOC100190145L%LOC100190146M%LOC100190147N%LOC100190148O%LOC100190149P%LOC100190150Q%LOC100190151R%LOC100190153T%LOC100190155V%LOC100190156W%LOC100190158X%LOC100190159Y%LOC100190160Z%LOC100190161[%LOC100190162\%LOC100190163]%LOC100190164^%LOC100190165_%LOC100190166`%LOC100190167a%LOC100190168b%LOC100190169c%LOC100190170d%LOC100190171e%LOC100190172f%LOC100190173g%LOC100190175i%LOC100190177j%LOC100190178k%LOC100190179l%LOC100190180m%LOC100190183o 2|| 0BTfx,>Pbt(:L^p%LOC100190185q%LOC100190186r%LOC100190187s%LOC100190188t%LOC100190190v%LOC100190191w%LOC100190192x%LOC100190194z%LOC100190195{%LOC100190196|%LOC100190198~%LOC100190199%LOC100190200%LOC100190202%LOC100190203%LOC100190204%LOC100190205%LOC100190206%LOC100190208%LOC100190209%LOC100190210%LOC100190211%LOC100190212%LOC100190213%LOC100190215%LOC100190217%LOC100190218%LOC100190219%LOC100190220%LOC100190221%LOC100190222%LOC100190223%LOC100190224%LOC100190226%LOC100190227%LOC100190229%LOC100190230%LOC100190231%LOC100190232%LOC100190233%LOC100190236%LOC100190237%LOC100190238%LOC100190239%LOC100190240%LOC100190242%LOC100190243%LOC100190245%LOC100190246%LOC100190247 2|| 0BTfx,>Pbt(:L^p%LOC100190249%LOC100190250%LOC100190251%LOC100190253%LOC100190254%LOC100190255%LOC100190256%LOC100190257%LOC100190258%LOC100190259%LOC100190260%LOC100190261%LOC100190263%LOC100190264%LOC100190265%LOC100190266%LOC100190267%LOC100190268%LOC100190269%LOC100190270%LOC100190271%LOC100190274%LOC100190275%LOC100190276%LOC100190277%LOC100190279%LOC100190280%LOC100190281%LOC100190283%LOC100190284%LOC100190285%LOC100190286%LOC100190289%LOC100190290%LOC100190291%LOC100190293%LOC100190294%LOC100190295%LOC100190296%LOC100190297%LOC100190299%LOC100190300%LOC100190301%LOC100190302%LOC100190303%LOC100190306%LOC100190307%LOC100190308%LOC100190309%LOC100190310 I .<JXft$/:DMXbmx$.9DNZcn{ SAMD12%LOC100190314%LOC100190315%LOC100190316%LOC100190317%LOC100190319 LOC751964" LOC751965# LOC751966$ LOC751967% LOC751968& LOC751969' LOC751970( LOC751972* LOC751973+ LOC751974, LOC7519791 LOC7519813 LOC7519824 LOC7519879 LOC751990< LOC751996@ LOC752004H LOC752009L LOC778445T LYRM1H LYRM4 LYRM5 MEAF6 MED7MGAM~ MGLUR5K MMAB MRPL9 MTNR1A MTNR1B MYCT1 MZT1 NCALDND1WND2XND3^ND4`ND4L_ND5aND6c NDUFC2 NEWENTRYdNGFANPVFl NR2F2 NR3C1h NR3C2 NR5A1 NTHL1 NTPCR NTRK27 NUDCD2NUS1{ OPN1SWN PACSIN3PGRq PYCR2 RAP1AvRARBURARG8 REEP5xRHO) RNF113A2 RPL17; RPL37: RPS3A RPUSD4 RRP7AI #{pf]SJA6+ ZFAND5 WASF1VT3MVIT2/UOX| UCK2S UCHL1 UBE2R2m TUBB2Cn TRPV1k TRAPPC2L TMEM189 TMEM188 TM6SF1 TAGLN TAF13nSYT4 SYT1 SYNPR5SYN22 SYF2 STXBP1> STRBPSOX3? SNCBu SNCA SLC7A6OSySI} SHFM1j SFT2D1! SEPT3 SEP15 SELS SELK SCAMP1rKhF mKX;} synuclein, alpha (non A4 component of amyloid precursor) Esodium/glucose cotransporterAribosomal protein L36-like7qprotein phosphatase 1 catalytic subunit alpha-like)Upeptidylprolyl isomerase-like 1-like=neuronal protein 22-like9metallothionein-I-like~9uhigh-mobility group nucleosome binding domain 1-like};{glutamate receptor, ionotropic, N-methyl-D-aspartate 3A|6qgamma-aminobutyric acid (GABA) A receptor, alpha 2={=disulfide-isomerase-likezIcofactor required for Sp1 transcriptional activation subunit 8-likey0camyloid beta precursor protein-binding-likex._TGF beta-inducible nuclear protein 1-likew(SRAN member RAS oncogene family-like\v"GMYST/Esa1-associated factor 6u6oDNA directed RNA polymerase II polypeptide C-liketNFubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase) }}AeEt.Lj515 kDa selenoprotein/a2,4-dienoyl CoA reductase 1, mitochondrial)U21 kDa signal peptidase subunit-like&O26S ATPase complex subunit 4-like(S26S proteasome-associated pad1-like#I40S ribosomal protein S25-like#I40S ribosomal protein S29-like"G40S ribosomal protein S9-likeJ5-hydroxytryptamine (serotonin) receptor 7, adenylate cyclase-coupledG#I6-phosphogluconolactonase-like)U60S acidic ribosomal protein P1-like._ADP-ribosylation factor related protein 1 *WADP-ribosylation factor-like 10C-likeCAHA1 activator of heat shock 90 protein ATPase homolog 1-likezJAHA1, activator of heat shock 90kDa protein ATPase homolog 2 (yeast)F?ATP synthase F0 subunit 6\?ATP synthase F0 subunit 8[JATP synthase H+ transporting mitochondrial F0 complex subunit c-likeJATP synthase H+ transporting mitochondrial F0 complex subunit f-like5 ;;h*i&<Wm-_,[ATP synthase e chain mitochondrial-likemBATP synthase mitochondrial F1 complex assembly factor 1-like CATP synthase subunit b-like]=ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1, cardiac muscle->ATPase H+ transporting lysosomal 31 kDa V1 subunit E-like)UAdenylate kinase 3 alpha like 1-likeY8sBCL2/adenovirus E1B 19kD interacting protein 1-like._BRCA2 and CDKN1A-interacting protein-like*WBrix domain containing protein 1-like2-C10 protein-like7C35 protein cDNA-like-CD9 antigen-like5mCDC26 subunit of anaphase promoting complex-like .aCDC28 protein kinase regulatory subunit 1Bo5CGI-105 protein-like"GCOMM domain containing 3-like=COMM domain containing 91eCOX assembly mitochondrial protein 2 homologACOX19 cytochrome c oxidase assembly homolog (S. cerevisiae)}<{CTD nuclear envelope phosphatase 1 regulatory subunit 1!EDEAD box polypeptide 48-like ??v0Bf>j:Vr6oDNA directed RNA polymerase II polypeptide D-like6oDNA directed RNA polymerase II polypeptide E-like6oDNA directed RNA polymerase II polypeptide K-likeo4kDNA polymerase delta interacting protein 2-like/DPCD protein-like%Di-Ras2-like0#IDnaJ subfamily C member 8-likeBDolichyl-phosphate beta-D-mannosyltransferase subunit 3-like"IGABA-A receptor gamma4 subunitr=GPP34/GMX33-like protein<,[GrpE-like 1 mitochondrial precusor-like'QHESB like domain containing 1-like+YIscU iron-sulfur cluster scaffold-like(SJUN activation binding protein-liket)WKN motif and ankyrin repeat domains 1i9LIM domain only 1-like_6oLSM6 homolog U6 small nuclear RNA associated-like% LWS opsinH9LYR motif containing 1H9LYR motif containing 49LYR motif containing 5._MAD2 mitotic arrest deficient-like 2-like+7MGC89063 protein-likeC+YMID1 interacting G12-like protein-like1MIZIP protein-like LLj6h7Xy1Vy?Mel-1c melatonin receptor9AN-acetyltransferase 5-like&GNADH dehydrogenase (ubiquinone) 1, subcomplex unknown, 2, 14.5kDa1eNADH dehydrogenase 1 alpha subcomplex 2-like1eNADH dehydrogenase 1 alpha subcomplex 5-like~1eNADH dehydrogenase 1 alpha subcomplex 8-likeA/aNADH dehydrogenase 1 alpha subcomplex-like0cNADH dehydrogenase 1 beta subcomplex 9-like+YNADH dehydrogenase Fe-S protein 6-like ENADH dehydrogenase subunit 1W ENADH dehydrogenase subunit 2X ENADH dehydrogenase subunit 3^ ENADH dehydrogenase subunit 4`!GNADH dehydrogenase subunit 4L_ ENADH dehydrogenase subunit 5a ENADH dehydrogenase subunit 6cNF-M3,[Nedd4 family interacting protein 1-like=NudC domain containing 2$KPAK1 interacting protein 1-like/"GPDZ domain containing 11-likeT(SPhosphohistidine phosphatase 1-like)UProteasome subunit alpha type 4-like 3iRAB member of RAS oncogene family-like 2B-like3 LLu(I}VwAP(URAP1A, member of RAS oncogene familyv/RBX1 protein-like RH2 opsin*-]RNA polymerase I 16 kDa polypeptide-like)URNA polymerase II polypeptide H-like5mRNA pseudouridylate synthase domain containing 4 CRNA-binding protein 8A-like3iRas family small GTP binding protein RALA-like'QRas homolog enriched in brain-like9yuRecord to support submission of GeneRIFs for a gene not in Gene (Poephila guttata; Taenopygia guttata; zebra finch).d6oRho/Cdc42/Rac GTPase-activating protein RICS-like CRibosomal protein L35a-like:#IS-100 protein alpha chain-like4kS100 calcium binding protein beta (neural)-like=SFT2 domain containing 1! SNAP-25b4=SPRY domain containing 7p(USRY (sex determining region Y)-box 3?!SWS2 opsin+6oSYF2 homolog, RNA splicing factor (S. cerevisiae)!ETAF10 RNA polymerase II-likeV-TAF13 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 18kDan 77_{Bh B-\'QTruB pseudouridine synthase 2-like9U11/U12 snRNP 48K-like1eU2 snRNP auxiliary factor small subunit-like=U3 snoRNP protein 4-like2gU6 snRNA-associated Sm-like protein LSm1-likeCUDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7%MUPF0687 protein C20orf27 homolog!EWAS protein family, member 1%MWW domain binding protein 2-like%MYip1 domain family member 6-like5mactin related protein 2/3 complex subunit 3-like5mactin related protein 2/3 complex subunit 4-like>activated RNA polymerase II transcription cofactor 4-likes6qactivity-regulated cytoskeleton-associated proteinE8sadaptor-related protein complex 2 mu 1 subunit-likee akirin 2-]alcohol dehydrogenase 5 (class III)-likeD.aaldehyde dehydrogenase 1 family, member A2 /aaldehyde dehydrogenase 3 family, member A2U0caldo-keto reductase family 7 member A2-like=aldo-keto reductase-like$Kalpha-aspartyl dipeptidase-like$ ``v :`/DgFn/aclat/androgen receptor ankyrin B,+annexin A4-like+Yapoptosis-inducing, TAF9-like domain 1h5marginine-rich mutated in early stage tumors-like$Kaspartate beta-hydroxylase-like5autophagy-related 12%Maxonemal dynein light chain-like&Obasic transcription factor 3-like!beta-actin0)Ubiphenyl hydrolase-like protein-like7brain protein 44-like%Obrain-derived neurotrophic factor-_cAMP responsive element binding protein 1+calretinin-likev"Icannabinoid receptor 1 (brain) 1cdna MGC42090-like@1cdna MGC75753-like5mchaperonin containing TCP1 subunit 2 (beta)-like'Schromo-helicase DNA-binding proteinR'Schromo-helicase DNA-binding proteinS(Schromosome 11 open reading frame 75'Qchromosome 9 open reading frame 1679churchill protein-like;citrate lyase beta like/aclathrin light polypeptide variant 1a-like^(Scoenzyme Q9 homolog (S. cerevisiae) RRx3J(9aHg derlin 3%Mcoiled-coil domain containing 23%Mcoiled-coil domain containing 25%Mcoiled-coil domain containing 58Bcoiled-coil-helix-coiled-coil-helix domain containing 6-like-complexin 1-like-complexin 2-like/cornichon homolog8scyclin-dependent kinase 2-associated protein 1-like#._cyclin-dependent kinase inhibitor 1B-like:ycytochrome P450, family 11, subfamily A, polypeptide 1u:ycytochrome P450, family 19, subfamily A, polypeptide 1%cytochrome bb'Scytochrome b, ascorbate dependent 3z"Icytochrome c oxidase subunit IY#Kcytochrome c oxidase subunit IIZ$Mcytochrome c oxidase subunit III]"Gcytokine induced protein-likegW/cytoplasmic dynein light chain (T-complex testis-specific protein 1 homolog)-like?dUTP pyrophosphatase-like8$Kdeath-associated protein 1-like'Qdefender against cell death 1-like derlin 3 Cdeveloping brain homeobox 2;dickkopf homolog 3-likex [[7id&g=)frequenin-like9fractu0cdolichol-phosphate mannosyltransferase-like%doublecortinF+dynactin 6-like+Ydynein light chain 2A cytoplasmic-like;early growth response 1e<{ectonucleotide pyrophosphatase/phosphodiesterase 2-like1eembryogenesis protein H beta 58 homolog-like(Sengulfment and cell motility 1-like._enhancer of yellow 2 homolog (Drosophila)3estrogen receptor 1B=}eukaryotic translation initiation factor 4E (eIF4E)-likeLevectin-2 pleckstrin homology domain containing family B member 2-like=exosome component 5-likeW/fascin homolog 2, actin-bundling protein, retinal (Strongylocentrotus purpuratus)y$Kfatty acid-binding protein-like&Ofetal globin-inducing factor-like@fibronectin type III and transmembrane containing protein 1g@fibronectin type III and transmembrane containing protein 2f+forkhead box P16+forkhead box P2 9fracture callus 1-like)frequenin-like IIv'S)TL,]glutamate decarboxylase 1 (brain, 67kDa)Q,]glutamate decarboxylase 1 (brain, 67kDa)V+[glutamate receptor AMPA tyep GluR3 flop&+[glutamate receptor AMPA type GluR1 flip"+[glutamate receptor AMPA type GluR1 flop#+[glutamate receptor AMPA type GluR2 flip$+[glutamate receptor AMPA type GluR2 flop%+[glutamate receptor AMPA type GluR3 flipL+[glutamate receptor AMPA type GluR4 flip'+[glutamate receptor AMPA type GluR4 flop(%Oglutamate receptor kainate type 1J*Yglutamate receptor, ionotropic, AMPA 1*Yglutamate receptor, ionotropic, AMPA 2*Yglutamate receptor, ionotropic, AMPA 3*Yglutamate receptor, ionotropic, AMPA 4:yglutamate receptor, ionotropic, N-methyl D-aspartate 1;{glutamate receptor, ionotropic, N-methyl D-aspartate 2AO;{glutamate receptor, ionotropic, N-methyl D-aspartate 2B;{glutamate receptor, ionotropic, N-methyl D-aspartate 2CP;{glutamate receptor, ionotropic, N-methyl D-aspartate 2DD DDr#Jq.dYr8-_glutamate receptor, ionotropic, kainate 1-_glutamate receptor, ionotropic, kainate 3-_glutamate receptor, ionotropic, kainate 5-_glutamate receptor, ionotropic, kainate 5&Qglutamate receptor, metabotropic 1C&Qglutamate receptor, metabotropic 2&Qglutamate receptor, metabotropic 3 &Qglutamate receptor, metabotropic 4I&Qglutamate receptor, metabotropic 8!3glutaredoxin 5-like/aglutathione S-transferase class-alpha-like%Mglycine N-methyltransferase-like>5mgrowth arrest and DNA-damage-inducible beta-like0cgrowth factor receptor-bound protein 2-likeBgrowth-related translationally controlled tumor protein-likeBguanine nucleotide binding protein (G protein) gamma 10-like=}hematological and neurological expressed sequence 1-like3hemoglobin, alpha 27hemoglobin, epsilon 18shexamethylene bisacetamide-inducible protein 1-like9uhigh-mobility group nucleosome binding domain 1-like* EE] Bw6N=j7melatonin r1hippocalcin-like 10ehistidine triad nucleotide binding protein 1.Q%hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1 +Yhydroxyacyl glutathione hydrolase-like|5mimmediate early response 3 interacting protein 14kinhibitor-1 of protein phosphatase type 2A-likeGF inosine triphosphatase (nucleoside triphosphate pyrophosphatase)2giron-sulfur cluster scaffold protein Nfu-like Cjumonji domain containing 8#Ikelch domain containing 3-like1laminin receptor 1Alate endosomal/lysosomal adaptor, MAPK and MTOR activator 2#Ilectin, mannose-binding 2-like*Wmacrophage erythroblast attacher-like'6omacrophage migration inhibitory factor (MIF)-likeJ&Omalignant T cell amplified 1-like,]maltase-glucoamylase (alpha-glucosidase)~/maternal G10-like4Amediator complex subunit 77melatonin receptor 1A7melatonin receptor 1B*Ymetabotropic type glutamate receptor 5K GG[ 9gHv'Rd*Yne)metaxin 2-like<{methylmalonic aciduria (cobalamin deficiency) cblB type1microcephalin-like-]mitochondrial ribosomal protein L12-like-]mitochondrial ribosomal protein L17-likel,[mitochondrial ribosomal protein L2-likei-]mitochondrial ribosomal protein L21-like-]mitochondrial ribosomal protein L30-like-]mitochondrial ribosomal protein L42-like'Qmitochondrial ribosomal protein L9-]mitochondrial ribosomal protein S17-like._mitochondrial ribosomal protein S18A-like-]mitochondrial ribosomal protein S36-like,[mitochondrial ribosomal protein S6-like#Imitotic phosphoprotein 44-like)Umitotic spindle organizing protein 15mmolybdopterin synthase large subunit MOCS2B-like*Wmotile sperm domain containing 1-likeQ%myc target 1$Kmyelin protein zero-like 1-likea5mmyosin regulatory light chain isoform L20-B-like6*Ynerve growth factor (beta polypeptide)A/neurocalcin delta RRpg?n,?l4/parathymosin-like(Spal?neuropeptide VF precursorl2ineurotrophic tyrosine kinase, receptor, type 27+ninjurin 1-likeW*Wnth endonuclease III-like 1 (E. coli)4knuclear receptor subfamily 2, group F, member 2Nnuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)h3knuclear receptor subfamily 3, group C, member 23knuclear receptor subfamily 5, group A, member 1Jnuclear undecaprenyl pyrophosphate synthase 1 homolog (S. cerevisiae){$Knucleolar protein family A-like._nucleoside-triphosphatase, cancer-related6onudix (nucleoside diphosphate linked moiety)-like1gopsin 1 (cone pigments), short-wave-sensitiveN!Eoptic atrophy 3 protein-like2govarian carcinoma immunoreactive antigen-like'oxytocin-like,[p32 subunit of splicing factor SF2-like._p53 and DNA damage-regulated protein-likew$Kp53-related protein kinase-like(Spalmitoyl-protein thioesterase-like/parathymosin-like cc)W*JgAm9)Uprotein kinase C inhibitor/ASWZ-like&Operipheral myelin protein 22-like @phosphate cytidylyltransferase 1 choline beta isoform-like4kphosphatidylinositol transfer protein beta-like(Sphosphohistidine phosphatase 1-like-]phosphopantothenate cysteine ligase-like4kpostmeiotic segregation increased 2-like 6-like@potassium channel tetramerisation domain containing 4-likeFpotassium voltage-gated channel, Shaw-related subfamily, member 1s-prefoldin 2-likeApreprocholecystokinin-like;preproenkephalin 1-like(Spresenilin associated rhomboid-likeX7progesterone receptorq!Eprogrammed cell death 5-like6oproteaseome (prosome macropain) 28 subunit 3-like=}proteasome 26S subunit ATPase 3 interacting protein-like+Yproteasome assembling chaperone 3-like[)Uproteasome subunit alpha type 6-like>protein kinase C and casein kinase substrate in neurons 3)Uprotein kinase C inhibitor/ASWZ-like KKKl;\~ @`4kprotein phosphatase 1 regulatory subunit 7-like6oprotein transport protein SEC61 beta subunit-like0cputative dimethyladenosine transferase-like*Wputative hypothetical protein MGC21987qpyrroline-5-carboxylate reductase family, member 2 Ereceptor accessory protein 5x%Mrecombination protein REC14-likeD regulatory factor X-associated ankyrin-containing protein-likec Eretinoic acid receptor alphaTBretinoic acid receptor responder (tazarotene induced) 2-like Eretinoic acid receptor, betaU!Gretinoic acid receptor, gamma8 rhodopsin)Aribonuclease P 14 kDa-like9uribosomal RNA processing 7 homolog A (S. cerevisiae)IAribosomal protein L14-like7ribosomal protein L17;Aribosomal protein L23-likeAribosomal protein L24-likeEAribosomal protein L26-likeAribosomal protein L26-likeAribosomal protein L30-likeAribosomal protein L31-likeAribosomal protein L34-like" SSm ,Ll%Df 9a7ribosomal protein L37:Aribosomal protein L37-like(Aribosomal protein L7a-likek?ribosomal protein L9-likeqAribosomal protein S11-likeAribosomal protein S13-likeAribosomal protein S15-like Aribosomal protein S16-likeAribosomal protein S18-likeAribosomal protein S21-likejAribosomal protein S26-likeKAribosomal protein S27-likeb?ribosomal protein S3-like7ribosomal protein S3A?ribosomal protein S4-like?ribosomal protein S6-like?!Ering finger protein 126-like)3scotin protein-like(Usecretory carrier membrane protein 1+selenoprotein K+selenoprotein S septin 37serotonin 1B receptor@'serum albumin1,[signal recognition particle 14 kDa-likeR'Qsignal sequence receptor beta-like.(Ssignal sequence receptor gamma-likep=}sm like protein U6 snRNA-associated Sm-like protein-like7qsmall nuclear ribonucleoprotein polypeptide G-like rr,j0g;fQAsyntaxin binding protein 1>+Ysolute carrier family 25 member 5-likeL+Ysolute carrier family 25 member 6-likeM+Ysolute carrier family 40 member 1-like5osolute carrier family 7, member 6 opposite strandy=}solution structure of the Bola-Like protein chain A-like&Osomatostatin precursor pro-2-like 5sorting nexin 3-like$Ksperm associated antigen 7-like;._spermatid perinuclear RNA binding protein0csplicing factor arginine/serine-rich 7-like6qsplit hand/foot malformation (ectrodactyly) type 1j5stathmin-like 3-like=stem cell antigen 2-likeB-]sterile alpha motif domain containing 12E steroidogenic enzyme cytochrome P450 17a-hydroxylase/17,20 lyaset'Qstromal cell derived factor 1-like*Ysucrase-isomaltase (alpha-glucosidase)};suppressor of Ty 4-like=#synapsin II2%synaptoporin5+synaptotagmin I-synaptotagmin IV )syndesmos-likeAsyntaxin binding protein 1> ff{/`Y8\+synuclein, betau+Ythioesterase superfamily member 2-like"Gthioredoxin family Trp26-likeN;thioredoxin-like 2-like;thioredoxin-like 2-like*Wthymidine kinase 2 mitochondrial-like0ctrafficking protein particle complex 2-like#Itranscription factor Dp 1-like!transgelinGtransient receptor potential cation channel, subfamily V, member 1k8stranslocase of inner mitochondrial membrane 10-likeCtranslocase of inner mitochondrial membrane 9/10 homolog-like,8stranslocase of outer mitochondrial membrane 20-like1)Utransmembrane 6 superfamily member 18stransmembrane BAX inhibitor motif containing 4-like#Itransmembrane protein 14C-like?transmembrane protein 189#Itransmembrane protein 50B-like`"Gtransmembrane protein 80-likefAtubulin, beta 4B class IVbnaCtyrosine 3-monooxgenase/tryptophan 5-monooxgenase activation protein gamma polypeptide-like Fa|$Fh4Vx^!E!Euncharacterized LOC100190155V(Subiquitin specific protease 12-like@ubiquitin-conjugating enzyme E2 transcript variant 2A-like{4kubiquitin-conjugating enzyme E2I cluster 2-like&Qubiquitin-conjugating enzyme E2R 2m7ubiquitin-like 1-like7ubiquitin-like 5-liker Cubiquitously-expressed-like Euncharacterized LOC100187703w!Euncharacterized LOC100189939!Euncharacterized LOC100189946!Euncharacterized LOC100189951!Euncharacterized LOC100189962!Euncharacterized LOC100189976!Euncharacterized LOC100189985!Euncharacterized LOC100189989!Euncharacterized LOC100189996!Euncharacterized LOC100190011!Euncharacterized LOC100190033!Euncharacterized LOC100190038!Euncharacterized LOC100190041!Euncharacterized LOC100190044!Euncharacterized LOC100190060!Euncharacterized LOC100190063!Euncharacterized LOC100190148O!Euncharacterized LOC100190149PXX :mM ;wtNATP synthase H+ transporting mitochondrial F1 complex delta subunit-likeu6oDNA directed RNA polymerase II polypeptide C-likev"GMYST/Esa1-associated factor 6w(SRAN member RAS oncogene family-like\x._TGF beta-inducible nuclear protein 1-likey0camyloid beta precursor protein-binding-likezIcofactor required for Sp1 transcriptional activation subunit 8-like{=disulfide-isomerase-like|6qgamma-aminobutyric acid (GABA) A receptor, alpha 2=};{glutamate receptor, ionotropic, N-methyl-D-aspartate 3A~9uhigh-mobility group nucleosome binding domain 1-like9metallothionein-I-like=neuronal protein 22-like)Upeptidylprolyl isomerase-like 1-like7qprotein phosphatase 1 catalytic subunit alpha-likeAribosomal protein L36-like Esodium/glucose cotransporter;} synuclein, alpha (non A4 component of amyloid precursor)!Euncharacterized LOC100190155VFubiquitin carboxyl-terminal !Euncharacterized LOC100190155V xV4hF[H"Izinc finger, AN1-type domain 5!Ezinc finger protein 346-like82,& ~~}}||{{zzyyxxwwvvuuttssrrqqppoonnmmllkkjjiihhggffeeddccbbaa``__^^]]\\[[ZZYYXXWWVVUUTTSSRRQQPPOONNMMLLKKJJIIHHGGFFEEDDCCBBAA@@??>>==<<;;::99887766554433221100//..--,,++**))((''&&%%$$##""!!     LL  $*06<BHNTZ`flrx~ &,28>DJPV\bhntz "(.4:@FLRX^djpv|       !!""##$$%%&&''(())**++,,--..//00112233445566778899::;;<<==>>??@@AABBCCDDEEFFGGHHIIJJKKLLMMNNOOPPQQRRSSTTUUVVWWXXYYZZ[[\\]]^^__``aabbccddeeffgghhiijjkkllmmnnooppqqrrssttuuvvwwxxyyzz{{||}}~~ e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpx e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpx            !!""##$$%%&&''(())**++,,--..//00112233445566778899::;;<<==>>??@@AABBCCDDEEFFGGHHIIJJKK d (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxMMMMNNOOPPQQRRSSTTUUVVWWXXYYZZ[[\\]]^^__``aabbccddeeffgghhiijjkkllmmnnooppqqrrssttuuvvwwxxyyzz{{||}}~~ Cxph`XPH@80( xph`XPH@80(  8 0@P`p 0@P`p 0@P`p!GO:0005102!GO:0005125Z!GO:0005154 !GO:0005159 6!GO:0005163!GO:0005168 !GO:0005179!GO:0005179 !GO:0005184 !GO:0005185$!GO:0005198 !GO:0005198!GO:0005198m!GO:0005198 a!GO:0005198 !GO:0005215!GO:0005215!GO:0005215!GO:0005215!GO:0005215!GO:00052158!GO:0005215H!GO:0005215q!GO:0005215$!GO:0005215Q!GO:0005215!GO:0005215;!GO:0005215!GO:0005215 B!GO:0005215 O!GO:0005216!GO:0005216!GO:0005216!GO:00052169!GO:0005216I!GO:0005216r!GO:0005216!GO:0005216R!GO:0005216!GO:0005216!GO:0005216!GO:0005230!GO:0005234!GO:0005234!GO:0005234!GO:0005234:!GO:0005234J!GO:0005234s!GO:0005234!GO:0005234S!GO:0005244!GO:0005246c!GO:0005249!GO:0005249!GO:0005261!GO:0005261t 8%5EUeu"2BRbr 0@P`p!GO:0005262!GO:0005262u!GO:0005262U!GO:0005267!GO:0005319!GO:0005344}!GO:0005488 C!GO:0005488 P!GO:0005496W!GO:0005496!GO:0005496]!GO:0005496!GO:0005504!GO:0005504 !GO:0005506!GO:0005506!GO:0005506~!GO:0005506 ^!GO:0005506 !GO:0005507!GO:0005507!GO:0005509!GO:0005509\!GO:0005509!GO:0005509!GO:0005509!GO:00055098!GO:0005509?!GO:0005509!GO:0005509!GO:0005509!GO:0005509 !GO:0005509 !GO:0005509 !GO:0005509 !GO:0005515!GO:0005515`!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515X!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515K!GO:0005515v!GO:0005515!GO:0005515!GO:0005515!GO:0005515 !GO:0005515!GO:00055151 8 0@P`p 0@P`p 0@P`p!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515V!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515=!GO:0005515U!GO:0005515V!GO:0005515^!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!!GO:00055159!GO:0005515@!GO:0005515H!GO:0005515J!GO:0005515Q!GO:0005515v!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515 !GO:0005515&!GO:0005515-!GO:0005515<!GO:0005515R!GO:0005515Z!GO:0005515!GO:0005515 8 0@P`p 0@P`p 0@P`p!GO:0005515!GO:0005515!GO:0005515!GO:0005515 !GO:0005515!GO:00055156!GO:0005515>!GO:0005515A!GO:0005515K!GO:0005515u!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515!GO:0005515 !GO:0005515 3!GO:0005515 ;!GO:0005515 D!GO:0005515 Q!GO:0005515 m!GO:0005515 w!GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 $!GO:0005515 *!GO:0005515 <!GO:0005515 Q!GO:0005515 T!GO:0005515 _!GO:0005515 u!GO:0005515 }!GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 #!GO:0005515 ,!GO:0005515 6!GO:0005515 E!GO:0005515 h!GO:0005515 m 8 0@P`p 0@P`p 0@P`p!GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 !GO:0005515 -!GO:0005515 7!GO:0005515 F!GO:0005515 N!GO:0005516!GO:0005520 !GO:0005524!GO:0005524!GO:0005524!GO:0005524S!GO:0005524!GO:0005524!GO:0005524!GO:0005524!GO:0005524 n!GO:0005524 !GO:0005524 Y!GO:0005524 9!GO:0005524 !GO:0005524 !GO:0005524 !GO:0005524 .!GO:0005525!GO:0005525!GO:0005525!GO:0005525!GO:0005525-!GO:0005525v!GO:0005525!GO:0005525!GO:0005525!GO:0005525 !GO:0005543!GO:0005543'!GO:0005544!GO:0005576!GO:0005576[!GO:0005576%!GO:0005576!GO:0005576 !GO:0005576 !GO:0005615!GO:0005615 !GO:0005622!GO:0005622!GO:00056222 8!1AQaq!1AQaq!1AQ`p!GO:0005622!GO:0005622!GO:0005622>!GO:0005622_!GO:0005622!GO:0005622 !GO:0005622!GO:00056223!GO:0005622!GO:0005622!GO:0005622!GO:0005622U!GO:0005622!GO:0005622!GO:0005622!GO:0005622.!GO:0005622f!GO:0005622w!GO:0005622!GO:0005622!GO:0005622!GO:0005622!GO:0005622!GO:0005622!GO:0005622!GO:0005622!GO:0005622 !GO:0005622 <!GO:0005622 ]!GO:0005622 {!GO:0005622 !GO:0005622 !GO:0005622 !GO:0005622 !GO:0005622 !GO:0005622 l!GO:0005622 o!GO:0005622 v!GO:0005622 -!GO:0005622 !GO:0005622 !GO:0005622 !GO:0005622 %!GO:0005622 D!GO:0005622 G!GO:0005634 !GO:0005634!GO:0005634!GO:0005634!GO:0005634Y!GO:0005634!GO:0005634!GO:00056343!GO:0005634}!GO:0005634!GO:0005634 8 0@P`p 0@P`p 0@P`p!GO:0005634!GO:0005634!GO:0005634?!GO:0005634`!GO:0005634x!GO:0005634!GO:0005634A!GO:0005634o!GO:0005634!GO:0005634!GO:0005634!GO:0005634!GO:0005634 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GO:0071300IEABP>! GO:0060324IEABP=! GO:0055114IEABP<! GO:0048738IEABP;! GO:0048566IEABP:! GO:0048384IEABP9! GO:0043065IEABP8! GO:0043010IEABP7! GO:0042904IEABP6! GO:0042574IEABP5! GO:0042573IEABP4! GO:0035799IEABP3! GO:0035115IEABP2! GO:0034097IEABP1! GO:0031076IEABP0! GO:0031016IEABP/! GO:0030902IEABP.! GO:0030900IEABP-! GO:0030326IEABP,! GO:0030324IEABP+! GO:0030182IEABP*! GO:0021915IEABP)! GO:0016620IEAMF(! GO:0016491IEAMF'! GO:0016331IEABP&! GO:0014032IEABP%! GO:0010628IEABP$! GO:0009954IEABP#! GO:0009952IEABP"! GO:0009855IEABP!! GO:0008285IEABP ! GO:0008284IEABP! GO:0008152IEABP! GO:0005737IEACC! GO:0005634IEACC! GO:0004028IEAMF! GO:0003007IEABP! GO:0001936IEABP! GO:0001758IEAMF 'XpX@(hP8 x`H0pX! GO:0001568IEABP! GO:0055114IEABP! GO:0050662IEAMF! GO:0045226IEABP! GO:0044237IEABP! GO:0016616IEAMF! GO:0016491IEAMF! GO:0009058IEABP! GO:0008831IEAMF! GO:0006694IEABP! GO:0003854IEAMF ! GO:0003824IEAMF ! GO:0000166IEAMF ! GO:0060501IEABP ! GO:0060013IEABP ! GO:0050679IEABP! GO:0048745IEABP! GO:0048286IEABP! GO:0046982IEAMF! GO:0045892IEABP! GO:0043565IEAMF! GO:0043010IEABP! GO:0042803IEAMF! GO:0042297IEABP! GO:0040007IEABP! GO:0030324IEABP~! GO:0021987IEABP}! GO:0021758ISSBP|! GO:0021758IEABP{! GO:0021757ISSBPz! GO:0021757IEABPy! GO:0021549IEABPx! GO:0009791IEABPw! GO:0009790IEABPv! GO:0008270IEAMFu! GO:0007519IEABPt! GO:0006355IEABPs! GO:0005622IEACCr! GO:0005515IEAMF 'XpX@(hP8 x`H0pXq! GO:0003700IEAMFp! GO:0003677IEAMFo! GO:0002053IEABPn! GO:0000122IEABPm! GO:0016021IEACCl! GO:0016020IEACCk! GO:0007188IEABPj! GO:0007186IEABPi! GO:0007165IEABPh! GO:0005886IEACCg! GO:0004949IEAMFf! GO:0004930IEAMFe! GO:0004872IEAMFd! GO:0004871IEAMFc! GO:0048471IEACCb! GO:0043005IEACCa! GO:0016020IEACC`! GO:0008021IEACC_! GO:0007269IEABP^! GO:0006810IEABP]! GO:0005515IEAMF\! GO:0005509IEAMF[! 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GO:0060088IEABP%! GO:0050910IEABP$! GO:0032426IEACC %cjQ8pW>% v]D+|c#! GO:0032421IEACC"! GO:0016324IEACC!! GO:0016020IEACC ! GO:0007605IEABP! GO:0005886IEACC! GO:0005515IEAMF! GO:0042274IEABP! GO:0030529IEACC! GO:0022627IEACC! GO:0015935IEACC! GO:0006412IEABP! GO:0006364IEABP! GO:0005840IEACC! GO:0003735IEAMF! GO:0003723IEAMF! GO:0000056IEABP! GO:0051603IEABP! GO:0019773IEACC! GO:0016787IEAMF! GO:0008233IEAMF! GO:0006511IEABP! GO:0006508IEABP ! GO:0005839IEACC ! GO:0005737IEACC ! GO:0005634IEACC ! GO:0005515IEAMF ! GO:0004298IEAMF! GO:0004175IEAMF! GO:0000932IEACC! GO:0000502IEACC! GO:0070979IEABP! GO:0031145IEABP! GO:0030071IEABP! GO:0005680IEACC! GO:0005515IEAMF! GO:0005576IEACC! 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!GO:0019226IEABPs !GO:0010646IEABPr !GO:0050877IEABPq !GO:0007267IEABPp !GO:0007154IEABPo !GO:0003008IEABPn !GO:2001056IEABPm !GO:2000116IEABPl !GO:0097202IEABPk !GO:0065009IEABPj !GO:0052548IEABPi !GO:0052547IEABPh !GO:0051345IEABPg !GO:0051336IEABPf !GO:0050790IEABPe !GO:0044093IEABPd !GO:0043281IEABPc !GO:0043280IEABPb !GO:0043085IEABPa !GO:0019222IEABP` !GO:0010952IEABP_ !GO:0010950IEABP^ !GO:0008152IEABP] !GO:1901215IEABP\ !GO:1901214IEABP[ !GO:0097285IEABPZ !GO:0070997IEABPY !GO:0065007IEABPX !GO:0060548IEABPW !GO:0051402IEABPV !GO:0050794IEABPU !GO:0050789IEABP (iw`I2zcL5}fO8! i& !GO:0051247IEABP% !GO:0051246IEABP$ !GO:0051174IEABP# !GO:0048522IEABP" !GO:0048518IEABP! !GO:0045937IEABP  !GO:0044267IEABP !GO:0044260IEABP !GO:0044238IEABP !GO:0044237IEABP !GO:0043412IEABP !GO:0043170IEABP !GO:0042327IEABP !GO:0042325IEABP !GO:0036211IEABP !GO:0033135IEABP !GO:0032270IEABP !GO:0032268IEABP !GO:0031401IEABP !GO:0031399IEABP !GO:0031325IEABP !GO:0031323IEABP !GO:0019538IEABP !GO:0019220IEABP !GO:0018209IEABP  !GO:0018193IEABP  !GO:0018105IEABP  !GO:0016310IEABP  !GO:0010604IEABP  !GO:0010562IEABP !GO:0009893IEABP !GO:0006796IEABP !GO:0006793IEABP !GO:0006468IEABP !GO:0006464IEABP !GO:0001934IEABP !GO:0001932IEABP !GO:0065008IEABP !GO:0051969IEABP !GO:0051239IEABP (hv_H1ybK4|eN7  hN !GO:0051046IEABPM !GO:0032940IEABPL !GO:0023061IEABPK !GO:0007269IEABPJ !GO:0006836IEABPI !GO:0046903IEABPH !GO:0003001IEABPG !GO:0001505IEABPF !GO:0023056IEABPE !GO:0001919IEABPD !GO:0001881IEABPC !GO:0045321IEABPB !GO:0042116IEABPA !GO:0002376IEABP@ !GO:0002274IEABP? !GO:0001775IEABP> !GO:0044765IEABP= !GO:0043112IEABP< !GO:0006898IEABP; !GO:0006897IEABP: !GO:0016192IEABP9 !GO:0051234IEABP8 !GO:0051179IEABP7 !GO:0051051IEABP6 !GO:0051049IEABP5 !GO:0044092IEABP4 !GO:0032879IEABP3 !GO:0032409IEABP2 !GO:0006810IEABP1 !GO:1901615IEABP0 !GO:1901564IEABP/ !GO:1901360IEABP. !GO:0018958IEABP- !GO:0009712IEABP, !GO:0006807IEABP+ !GO:0006725IEABP* !GO:0006584IEABP) !GO:0080090IEABP( !GO:0071704IEABP' !GO:0060255IEABP (hv_H1ybK4|eN7  hv !GO:0048008IEABPu !GO:0023057IEABPt !GO:0010648IEABPs !GO:0010640IEABPr !GO:0009968IEABPq !GO:0009966IEABPp !GO:0007167IEABPo !GO:0007166IEABPn !GO:0007169IEABPm !GO:0007165IEABPl !GO:0060191IEABPk !GO:0010039IEABPj !GO:0010035IEABPi !GO:0010038IEABPh !GO:0044708IEABPg !GO:0030534IEABPf !GO:0007626IEABPe !GO:0007610IEABPd !GO:0071840IEABPc !GO:0061024IEABPb !GO:0016043IEABPa !GO:0007005IEABP` !GO:0006996IEABP_ !GO:0019637IEABP^ !GO:0044710IEABP] !GO:0044281IEABP\ !GO:0044255IEABP[ !GO:0043436IEABPZ !GO:0032787IEABPY !GO:0019752IEABPX !GO:0006629IEABPW !GO:0006082IEABPV !GO:0007270IEABPU !GO:0060341IEABPT !GO:0051649IEABPS !GO:0051641IEABPR !GO:0051590IEABPQ !GO:0051588IEABPP !GO:0051050IEABPO !GO:0051047IEABP (hv_H1ybK4|eN7  h !GO:0032272IEABP !GO:0032271IEABP !GO:0031333IEABP !GO:0031113IEABP !GO:0031111IEABP !GO:0031110IEABP !GO:0031109IEABP !GO:0022607IEABP !GO:0010639IEABP !GO:0007017IEABP !GO:0006461IEABP !GO:0007010IEABP !GO:0000226IEABP !GO:0051937IEABP !GO:0050433IEABP !GO:0050432IEABP !GO:0015872IEABP  !GO:0015850IEABP  !GO:0015844IEABP  !GO:0014046IEABP  !GO:0006812IEABP  !GO:0071705IEABP !GO:0071702IEABP !GO:0051955IEABP !GO:0051952IEABP !GO:0046942IEABP !GO:0044070IEABP !GO:0043269IEABP !GO:0032890IEABP !GO:0015849IEABP !GO:0015837IEABP !GO:0015711IEABP~ !GO:0014047IEABP} !GO:0006865IEABP| !GO:0006835IEABP{ !GO:0006820IEABPz !GO:0006811IEABPy !GO:0051716IEABPx !GO:0048585IEABPw !GO:0048583IEABP (hv_H1ybK4|eN7  hF !GO:0016573IEABPE !GO:0016570IEABPD !GO:0016569IEABPC !GO:0016568IEABPB !GO:0010605IEABPA !GO:0009892IEABP@ !GO:0006475IEABP? !GO:0006473IEABP> !GO:0006325IEABP= !GO:0051276IEABP< !GO:0070887IEABP; !GO:0033554IEABP: !GO:0006979IEABP9 !GO:0045087IEABP8 !GO:0034097IEABP7 !GO:0006955IEABP6 !GO:0006950IEABP5 !GO:0006952IEABP4 !GO:0051354IEABP3 !GO:0051341IEABP2 !GO:0043086IEABP1 !GO:0032768IEABP0 !GO:0071822IEABP/ !GO:0070507IEABP. !GO:0070271IEABP- !GO:0065003IEABP, !GO:0051494IEABP+ !GO:0051493IEABP* !GO:0051258IEABP) !GO:0051129IEABP( !GO:0051128IEABP' !GO:0046785IEABP& !GO:0044087IEABP% !GO:0044085IEABP$ !GO:0043933IEABP# !GO:0043623IEABP" !GO:0043254IEABP! !GO:0034622IEABP  !GO:0033043IEABP !GO:0032886IEABP (hv_H1ybK4|eN7  hn !GO:0010466IEABPm !GO:0050865IEABPl !GO:0002694IEABPk !GO:0002682IEABPj !GO:0045333IEABPi !GO:0042773IEABPh !GO:0015980IEABPg !GO:0022900IEABPf !GO:0006119IEABPe !GO:0022904IEABPd !GO:0006091IEABPc !GO:1901617IEABPb !GO:1901576IEABPa !GO:1901566IEABP` !GO:1901362IEABP_ !GO:0046189IEABP^ !GO:0044249IEABP] !GO:0042423IEABP\ !GO:0019438IEABP[ !GO:0009713IEABPZ !GO:0009058IEABPY !GO:0040011IEABPX !GO:2001251IEABPW !GO:2000757IEABPV !GO:2000756IEABPU !GO:1902275IEABPT !GO:1901984IEABPS !GO:1901983IEABPR !GO:0051248IEABPQ !GO:0043543IEABPP !GO:0035065IEABPO !GO:0033044IEABPN !GO:0032269IEABPM !GO:0031400IEABPL !GO:0031324IEABPK !GO:0031057IEABPJ !GO:0031056IEABPI !GO:0018394IEABPH !GO:0018393IEABPG !GO:0018205IEABP (hv_H1ybK4|eN7  h !GO:0006875IEABP !GO:0006874IEABP !GO:0006873IEABP !GO:0030001IEABP !GO:0006816IEABP !GO:0071616IEABP !GO:0051193IEABP !GO:0051188IEABP !GO:0051186IEABP  !GO:0042180IEABP  !GO:0035384IEABP  !GO:0035383IEABP  !GO:0031326IEABP  !GO:0051196IEABP !GO:0019217IEABP !GO:0019216IEABP !GO:0010565IEABP !GO:0009889IEABP !GO:0009108IEABP !GO:0006732IEABP !GO:0006637IEABP !GO:0051971IEABP !GO:0051240IEABP !GO:0031646IEABP~ !GO:0010647IEABP} !GO:0097480IEABP| !GO:0097479IEABP{ !GO:0051656IEABPz !GO:0051650IEABPy !GO:0051648IEABPx !GO:0051640IEABPw !GO:0051048IEABPv !GO:0017157IEABPu !GO:0006887IEABPt !GO:0060627IEABPs !GO:0051130IEABPr !GO:0030100IEABPq !GO:2000117IEABPp !GO:0051346IEABPo !GO:0010951IEABP (hv_H1ybK4|eN7  h> !GO:0051583IEABP= !GO:0051581IEABP< !GO:0051580IEABP; !GO:0043271IEABP: !GO:0032225IEABP9 !GO:0001504IEABP8 !GO:2000021IEABP7 !GO:0072511IEABP6 !GO:0070838IEABP5 !GO:0060402IEABP4 !GO:0060401IEABP3 !GO:0055082IEABP2 !GO:0055080IEABP1 !GO:0055074IEABP0 !GO:0072507IEABP/ !GO:0055065IEABP. !GO:0051928IEABP- !GO:0051924IEABP, !GO:0051480IEABP+ !GO:0051283IEABP* !GO:0051282IEABP) !GO:0051279IEABP( !GO:0051209IEABP' !GO:0048878IEABP& !GO:0050801IEABP% !GO:0046907IEABP$ !GO:0043270IEABP# !GO:0042592IEABP" !GO:0032846IEABP! !GO:0032844IEABP  !GO:0032388IEABP !GO:0032386IEABP !GO:0072503IEABP !GO:0030003IEABP !GO:0019725IEABP !GO:0016482IEABP !GO:0010959IEABP !GO:0010524IEABP !GO:0010522IEABP !GO:0007204IEABP (hv_H1ybK4|eN7  hf !GO:0008277IEABPe !GO:0007186IEABPd !GO:0090407IEABPc !GO:0046173IEABPb !GO:0046165IEABPa !GO:0045913IEABP` !GO:0044723IEABP_ !GO:0044711IEABP^ !GO:0044283IEABP] !GO:0044262IEABP\ !GO:0043647IEABP[ !GO:0043255IEABPZ !GO:0032958IEABPY !GO:0031328IEABPX !GO:0019751IEABPW !GO:0016051IEABPV !GO:0010919IEABPU !GO:0010676IEABPT !GO:0010675IEABPS !GO:0009891IEABPR !GO:0006109IEABPQ !GO:0006066IEABPP !GO:0005975IEABPO !GO:0060078IEABPN !GO:0051899IEABPM !GO:0042391IEABPL !GO:0051621IEABPK !GO:0051620IEABPJ !GO:0015874IEABPI !GO:0051611IEABPH !GO:0051610IEABPG !GO:0006837IEABPF !GO:0090494IEABPE !GO:0090493IEABPD !GO:0051953IEABPC !GO:0051945IEABPB !GO:0051940IEABPA !GO:0051934IEABP@ !GO:0051589IEABP? !GO:0051584IEABP (hv_H1ybK4|eN7  h !GO:0044424IEACC  !GO:0043229IEACC  !GO:0043227IEACC  !GO:0043226IEACC  !GO:0043231IEACC  !GO:0005623IEACC !GO:0005575IEACC !GO:0005622IEACC !GO:0045202IEACC !GO:0048471IEACC !GO:0016234IEACC !GO:0043205IEACC !GO:0031092IEACC !GO:0030426IEACC !GO:0015629IEACC !GO:0005938IEACC~ !GO:0005856IEACC} !GO:0005829IEACC| !GO:0030424IEACC{ !GO:0005739IEACCz !GO:0005886IEACCy !GO:0005737IEACCx !GO:0005634IEACCw !GO:0071248IEABPv !GO:0071241IEABPu !GO:0046688IEABPt !GO:0031647IEABPs !GO:0010608IEABPr !GO:0010468IEABPq !GO:0010467IEABPp !GO:0071900IEABPo !GO:0051347IEABPn !GO:0051338IEABPm !GO:0045860IEABPl !GO:0045859IEABPk !GO:0043549IEABPj !GO:0033674IEABPi !GO:0070494IEABPh !GO:0070493IEABPg !GO:0045744IEABP (hv_H1ybK4|eN7  h6 !GO:0043014IEAMF5 !GO:0042393IEAMF4 !GO:0030544IEAMF3 !GO:0019894IEAMF2 !GO:0008198IEAMF1 !GO:0000287IEAMF0 !GO:0045502IEAMF/ !GO:0005509IEAMF. !GO:0042802IEAMF- !GO:0008270IEAMF, !GO:0044421IEACC+ !GO:0044420IEACC* !GO:0031012IEACC) !GO:0005578IEACC( !GO:0005576IEACC' !GO:0044446IEACC& !GO:0044433IEACC% !GO:0044422IEACC$ !GO:0031988IEACC# !GO:0031982IEACC" !GO:0031410IEACC! !GO:0031091IEACC  !GO:0031090IEACC !GO:0030659IEACC !GO:0016023IEACC !GO:0012506IEACC !GO:0012505IEACC !GO:0030667IEACC !GO:0030141IEACC !GO:0044463IEACC !GO:0030427IEACC !GO:0043232IEACC !GO:0043228IEACC !GO:0097458IEACC !GO:0042995IEACC !GO:0043005IEACC !GO:0044444IEACC !GO:0071944IEACC !GO:0016020IEACC !GO:0044464IEACC (cv_H1ybK4|eN7  {c^!GO:0043167IEAMF]!GO:0046872IEAMF\!GO:0005488IEAMF[!GO:0003674IEAMFZ!GO:0005509IEAMFY !GO:0003824IEAMFX !GO:1901567IEAMFW !GO:0050543IEAMFV !GO:0050542IEAMFU !GO:0043168IEAMFT !GO:0036041IEAMFS !GO:0033293IEAMFR !GO:0031406IEAMFQ !GO:0008289IEAMFP !GO:0005504IEAMFO !GO:0061134IEAMFN !GO:0043028IEAMFM !GO:0030234IEAMFL !GO:0030414IEAMFK !GO:0061135IEAMFJ !GO:0004869IEAMFI !GO:0004866IEAMFH !GO:0004857IEAMFG !GO:0015631IEAMFF !GO:0031072IEAMFE !GO:0008092IEAMFD !GO:0005506IEAMFC !GO:0046914IEAMFB !GO:0043169IEAMFA !GO:0043167IEAMF@ !GO:0046872IEAMF? !GO:0005488IEAMF> !GO:0003674IEAMF= !GO:0005515IEAMF< !GO:0016491IEAMF; !GO:0005507IEAMF: !GO:0051219IEAMF9 !GO:0050544IEAMF8 !GO:0048156IEAMF7 !GO:0043027IEAMF 'XpX@(hP8 x`H0pX!GO:0008283IEABP!GO:0007405IEABP!GO:0007399IEABP!GO:0072001IEABP!GO:0048856IEABP!GO:0048731IEABP!GO:0044707IEABP~!GO:0044699IEABP}!GO:0035295IEABP|!GO:0032502IEABP{!GO:0032501IEABPz!GO:0008150IEABPy!GO:0007275IEABPx!GO:0001655IEABPw!GO:0051965IEABPv!GO:0043066IEABPu!GO:0001662IEABPt!GO:0042490IEABPs!GO:0048839IEABPr!GO:0048167IEABPq!GO:0046668IEABPp!GO:0045666IEABPo!GO:0043524IEABPn!GO:0043523IEABPm!GO:0042596IEABPl!GO:0042493IEABPk!GO:0021675IEABPj!GO:0019222IEABPi!GO:0016358IEABPh!GO:0014047IEABPg!GO:0008038IEABPf!GO:0007631IEABPe!GO:0007611IEABPd!GO:0007610IEABPc!GO:0007412IEABPb!GO:0007411IEABPa!GO:0007406IEABP`!GO:0001657IEABP_!GO:0043169IEAMF 'XpX@(hP8 x`H0pX,!GO:0009605IEABP+!GO:0007409IEABP*!GO:0009653IEABP)!GO:0006935IEABP(!GO:0006928IEABP'!GO:0000904IEABP&!GO:0000902IEABP%!GO:2000647IEABP$!GO:2000178IEABP#!GO:2000177IEABP"!GO:2000026IEABP!!GO:0072091IEABP !GO:0072089IEABP!GO:0065007IEABP!GO:0061351IEABP!GO:0060284IEABP!GO:0051960IEABP!GO:0051239IEABP!GO:0051093IEABP!GO:0050794IEABP!GO:0050793IEABP!GO:0050789IEABP!GO:0050768IEABP!GO:0050767IEABP!GO:0048869IEABP!GO:0048699IEABP!GO:0048523IEABP!GO:0048519IEABP!GO:0048468IEABP!GO:0045596IEABP!GO:0045595IEABP !GO:0044767IEABP !GO:0044763IEABP !GO:0042127IEABP !GO:0030154IEABP !GO:0022008IEABP!GO:0010721IEABP!GO:0009987IEABP!GO:0008285IEABP 'XpX@(hP8 x`H0pXS!GO:0071702IEABPR!GO:0051649IEABPQ!GO:0051641IEABPP!GO:0051234IEABPO!GO:0051179IEABPN!GO:0046942IEABPM!GO:0044765IEABPL!GO:0032940IEABPK!GO:0015849IEABPJ!GO:0015711IEABPI!GO:0006865IEABPH!GO:0006835IEABPG!GO:0006820IEABPF!GO:0006811IEABPE!GO:0006810IEABPD!GO:0046903IEABPC!GO:0008037IEABPB!GO:0050890IEABPA!GO:0044708IEABP@!GO:0050877IEABP?!GO:0003008IEABP>!GO:0007154IEABP=!GO:0097485IEABP<!GO:0071840IEABP;!GO:0061564IEABP:!GO:0050896IEABP9!GO:0048858IEABP8!GO:0048812IEABP7!GO:0048667IEABP6!GO:0048666IEABP5!GO:0042330IEABP4!GO:0042221IEABP3!GO:0040011IEABP2!GO:0032990IEABP1!GO:0032989IEABP0!GO:0031175IEABP/!GO:0030182IEABP.!GO:0030030IEABP-!GO:0016043IEABP 'XpX@(hP8 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!GO:0005102IEAMF!GO:0044464IEACC!GO:0044444IEACC!GO:0044424IEACC!GO:0043229IEACC!GO:0043227IEACC!GO:0043226IEACC!GO:0031988IEACC!GO:0031982IEACC!GO:0031410IEACC!GO:0043231IEACC!GO:0005623IEACC!GO:0005575IEACC!GO:0005622IEACC!GO:0005737IEACC!GO:0048471IEACC!GO:0016023IEACC!GO:0051963IEABP!GO:0051962IEABP !GO:0051130IEABP !GO:0051128IEABP !GO:0050808IEABP !GO:0050807IEABP !GO:0050803IEABP!GO:0044089IEABP!GO:0044087IEABP!GO:0044085IEABP!GO:0022607IEABP!GO:0007416IEABP!GO:0006952IEABP!GO:0002209IEABP!GO:0043583IEABP!GO:0065008IEABP!GO:0051969IEABP~!GO:0050804IEABP}!GO:0044700IEABP|!GO:0044057IEABP{!GO:0035637IEABP 'XpX@(hP8 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x`H0pXo!GO:0010817IEABPn!GO:0010646IEABPm!GO:0009914IEABPl!GO:0007267IEABPk!GO:0007154IEABPj!GO:0006810IEABPi!GO:0046903IEABPh!GO:0003001IEABPg!GO:2001141IEABPf!GO:2000112IEABPe!GO:1901576IEABPd!GO:1901362IEABPc!GO:1901360IEABPb!GO:0090304IEABPa!GO:0080090IEABP`!GO:0071704IEABP_!GO:0065007IEABP^!GO:0060255IEABP]!GO:0051252IEABP\!GO:0051171IEABP[!GO:0050794IEABPZ!GO:0050789IEABPY!GO:0046483IEABPX!GO:0044271IEABPW!GO:0044260IEABPV!GO:0044249IEABPU!GO:0044238IEABPT!GO:0044237IEABPS!GO:0043170IEABPR!GO:0034654IEABPQ!GO:0034645IEABPP!GO:0034641IEABPO!GO:0032774IEABPN!GO:0031326IEABPM!GO:0031323IEABPL!GO:0019438IEABPK!GO:0019222IEABPJ!GO:0019219IEABPI!GO:0018130IEABP 'XpX@(hP8 x`H0pX!GO:0048856IEABP!GO:0048731IEABP!GO:0048513IEABP!GO:0048286IEABP!GO:0044767IEABP!GO:0044707IEABP!GO:0035295IEABP!GO:0032502IEABP!GO:0032501IEABP !GO:0030324IEABP !GO:0030323IEABP !GO:0007275IEABP !GO:0071840IEABP !GO:0016050IEABP!GO:0016043IEABP!GO:0006996IEABP!GO:0065008IEABP!GO:0060341IEABP!GO:0051649IEABP!GO:0051641IEABP!GO:0051234IEABP!GO:0051179IEABP!GO:0051050IEABP!GO:0051049IEABP~!GO:0051047IEABP}!GO:0051046IEABP|!GO:0048522IEABP{!GO:0048518IEABPz!GO:0046883IEABPy!GO:0046879IEABPx!GO:0044765IEABPw!GO:0044763IEABPv!GO:0044700IEABPu!GO:0044699IEABPt!GO:0032940IEABPs!GO:0032879IEABPr!GO:0023061IEABPq!GO:0023051IEABPp!GO:0023052IEABP 'XpX@(hP8 x`H0pX=!GO:0051240IEABP<!GO:0051239IEABP;!GO:0045927IEABP:!GO:0040014IEABP9!GO:0040008IEABP8!GO:0035264IEABP7!GO:0040007IEABP6!GO:0031647IEABP5!GO:0010608IEABP4!GO:0051094IEABP3!GO:0050793IEABP2!GO:0045598IEABP1!GO:0045597IEABP0!GO:0045595IEABP/!GO:0045444IEABP.!GO:0090066IEABP-!GO:0032535IEABP,!GO:0071310IEABP+!GO:0070848IEABP*!GO:0051716IEABP)!GO:0050896IEABP(!GO:0042221IEABP'!GO:0070887IEABP&!GO:0046890IEABP%!GO:0045834IEABP$!GO:0044710IEABP#!GO:0019216IEABP"!GO:0009893IEABP!!GO:0009891IEABP !GO:0008610IEABP!GO:0006629IEABP!GO:0060487IEABP!GO:0060479IEABP!GO:0048869IEABP!GO:0030855IEABP!GO:0030154IEABP!GO:0060429IEABP!GO:0009888IEABP!GO:0060541IEABP 'XpX@(hP8 x`H0pXd!GO:0006366IEABPc!GO:0061564IEABPb!GO:0048858IEABPa!GO:0048812IEABP`!GO:0048699IEABP_!GO:0048667IEABP^!GO:0048666IEABP]!GO:0048468IEABP\!GO:0032990IEABP[!GO:0032989IEABPZ!GO:0031175IEABPY!GO:0030182IEABPX!GO:0030030IEABPW!GO:0022008IEABPV!GO:0009653IEABPU!GO:0000904IEABPT!GO:0000902IEABPS!GO:0035270IEABPR!GO:0030900IEABPQ!GO:0021536IEABPP!GO:0007420IEABPO!GO:0007417IEABPN!GO:0007399IEABPM!GO:0051254IEABPL!GO:0051173IEABPK!GO:0031328IEABPJ!GO:0031325IEABPI!GO:0045935IEABPH!GO:0010628IEABPG!GO:0010604IEABPF!GO:0010557IEABPE!GO:0050878IEABPD!GO:0048609IEABPC!GO:0032941IEABPB!GO:0032504IEABPA!GO:0022414IEABP@!GO:0007589IEABP?!GO:0000003IEABP>!GO:0048732IEABP 'XpX@(hP8 x`H0pX !GO:0005694IEACC !GO:0000785IEACC !GO:0000228IEACC!GO:0044464IEACC!GO:0044424IEACC!GO:0043229IEACC!GO:0043227IEACC!GO:0043226IEACC!GO:0043231IEACC!GO:0005623IEACC!GO:0005575IEACC!GO:0005622IEACC!GO:0005719IEACC~!GO:0005667IEACC}!GO:0000790IEACC|!GO:0005634IEACC{!GO:0044267IEABPz!GO:0043412IEABPy!GO:0036211IEABPx!GO:0019538IEABPw!GO:0016310IEABPv!GO:0006796IEABPu!GO:0006793IEABPt!GO:0006464IEABPs!GO:2000113IEABPr!GO:0051253IEABPq!GO:0051172IEABPp!GO:0048523IEABPo!GO:0048519IEABPn!GO:0045934IEABPm!GO:0031327IEABPl!GO:0031324IEABPk!GO:0045892IEABPj!GO:0010629IEABPi!GO:0010605IEABPh!GO:0010558IEABPg!GO:0009892IEABPf!GO:0009890IEABPe!GO:0006357IEABP 'XpX@(hP8 x`H0pX2!GO:0000975IEAMF1!GO:0001076IEAMF0!GO:0000989IEAMF/!GO:0000988IEAMF.!GO:0033613IEAMF-!GO:0008134IEAMF,!GO:0001085IEAMF+!GO:0001071IEAMF*!GO:1901363IEAMF)!GO:0097159IEAMF(!GO:0005488IEAMF'!GO:0003676IEAMF&!GO:0003674IEAMF%!GO:0000980IEAMF$!GO:0003705IEAMF#!GO:0035497IEAMF"!GO:0001190IEAMF!!GO:0001102IEAMF !GO:0005515IEAMF!GO:0046983IEAMF!GO:0043565IEAMF!GO:0003700IEAMF!GO:0003677IEAMF!GO:0000791IEACC!GO:0044451IEACC!GO:0043234IEACC!GO:0032991IEACC!GO:0005654IEACC!GO:0070013IEACC!GO:0044454IEACC!GO:0044446IEACC!GO:0044428IEACC!GO:0044427IEACC!GO:0044422IEACC!GO:0043233IEACC!GO:0043232IEACC!GO:0043228IEACC !GO:0031981IEACC !GO:0031974IEACC 'XpX@(hP8 x`H0pXY!GO:0009152IEABPX!GO:0009150IEABPW!GO:0009117IEABPV!GO:0009058IEABPU!GO:0006807IEABPT!GO:0006796IEABPS!GO:0006793IEABPR!GO:0006753IEABPQ!GO:0006725IEABPP!GO:0006182IEABPO!GO:0006164IEABPN!GO:0006163IEABPM!GO:0006140IEABPL!GO:0006139IEABPK!GO:0008152IEABPJ!GO:0007166IEABPI!GO:0065007IEABPH!GO:0051716IEABPG!GO:0050896IEABPF!GO:0050794IEABPE!GO:0050789IEABPD!GO:0044763IEABPC!GO:0044700IEABPB!GO:0044699IEABPA!GO:0023052IEABP@!GO:0009987IEABP?!GO:0008150IEABP>!GO:0007154IEABP=!GO:0030828IEABP<!GO:0007186IEABP;!GO:0007165IEABP:!GO:0035326IEAMF9!GO:0001158IEAMF8!GO:0001012IEAMF7!GO:0000977IEAMF6!GO:0000976IEAMF5!GO:0000981IEAMF4!GO:0044212IEAMF3!GO:0001067IEAMF 'XpX@(hP8 x`H0pX!GO:0045937IEABP!GO:0044710IEABP~!GO:0044281IEABP}!GO:0044271IEABP|!GO:0044249IEABP{!GO:0044238IEABPz!GO:0044237IEABPy!GO:0034654IEABPx!GO:0034641IEABPw!GO:0031328IEABPv!GO:0031326IEABPu!GO:0031325IEABPt!GO:0031323IEABPs!GO:0030826IEABPr!GO:0030825IEABPq!GO:0030823IEABPp!GO:0030810IEABPo!GO:0030808IEABPn!GO:0030804IEABPm!GO:0030802IEABPl!GO:0030801IEABPk!GO:0030799IEABPj!GO:0019693IEABPi!GO:0019637IEABPh!GO:0019438IEABPg!GO:0019222IEABPf!GO:0019220IEABPe!GO:0019219IEABPd!GO:0018130IEABPc!GO:0045935IEABPb!GO:0010562IEABPa!GO:0009893IEABP`!GO:0009891IEABP_!GO:0009889IEABP^!GO:0009260IEABP]!GO:0009259IEABP\!GO:0009190IEABP[!GO:0009187IEABPZ!GO:0009165IEABP 'XpX@(hP8 x`H0pX'!GO:0005623IEACC&!GO:0005886IEACC%!GO:0043234IEACC$!GO:0032991IEACC#!GO:0044425IEACC"!GO:0031224IEACC!!GO:0016020IEACC !GO:0005575IEACC!GO:0005887IEACC!GO:0043235IEACC!GO:0016021IEACC!GO:1901576IEABP!GO:1901566IEABP!GO:1901564IEABP!GO:1901362IEABP!GO:1901360IEABP!GO:1901293IEABP!GO:1901137IEABP!GO:1901135IEABP!GO:1900544IEABP!GO:1900542IEABP!GO:1900373IEABP!GO:1900371IEABP!GO:0090407IEABP!GO:0080090IEABP!GO:0072522IEABP !GO:0072521IEABP !GO:0071704IEABP !GO:0055086IEABP !GO:0052652IEABP !GO:0051174IEABP!GO:0051173IEABP!GO:0051171IEABP!GO:0048522IEABP!GO:0048518IEABP!GO:0046483IEABP!GO:0046390IEABP!GO:0046068IEABP!GO:0045981IEABP 'XpX@(hP8 x`H0pXN!GO:0003001IEABPM!GO:0002791IEABPL!GO:0002790IEABPK!GO:0065008IEABPJ!GO:0048878IEABPI!GO:0042592IEABPH!GO:0033500IEABPG!GO:0007166IEABPF!GO:0065007IEABPE!GO:0051716IEABPD!GO:0050896IEABPC!GO:0050794IEABPB!GO:0050789IEABPA!GO:0044763IEABP@!GO:0044700IEABP?!GO:0044699IEABP>!GO:0023052IEABP=!GO:0009987IEABP<!GO:0008150IEABP;!GO:0007154IEABP:!GO:0050796IEABP9!GO:0042593IEABP8!GO:0007186IEABP7!GO:0007165IEABP6!GO:0005488IEAMF5!GO:0038023IEAMF4!GO:0004888IEAMF3!GO:0060089IEAMF2!GO:0003674IEAMF1!GO:0042562IEAMF0!GO:0097159IEAMF/!GO:0008502IEAMF.!GO:0004930IEAMF-!GO:0004871IEAMF,!GO:0004872IEAMF+!GO:0071944IEACC*!GO:0044464IEACC)!GO:0044459IEACC(!GO:0031226IEACC 'XpX@(hP8 x`H0pXu!GO:0060089IEAMFt!GO:0003674IEAMFs!GO:0008502IEAMFr!GO:0004930IEAMFq!GO:0004871IEAMFp!GO:0004872IEAMFo!GO:0044425IEACCn!GO:0031224IEACCm!GO:0016020IEACCl!GO:0005575IEACCk!GO:0016021IEACCj!GO:0090276IEABPi!GO:0090087IEABPh!GO:0071705IEABPg!GO:0071702IEABPf!GO:0060341IEABPe!GO:0051649IEABPd!GO:0051641IEABPc!GO:0051234IEABPb!GO:0051179IEABPa!GO:0051049IEABP`!GO:0051046IEABP_!GO:0046883IEABP^!GO:0046879IEABP]!GO:0044765IEABP\!GO:0042886IEABP[!GO:0032940IEABPZ!GO:0032879IEABPY!GO:0030073IEABPX!GO:0030072IEABPW!GO:0023061IEABPV!GO:0023051IEABPU!GO:0015833IEABPT!GO:0010817IEABPS!GO:0010646IEABPR!GO:0009914IEABPQ!GO:0007267IEABPP!GO:0006810IEABPO!GO:0046903IEABP 'XpX@(hP8 x`H0pX!GO:0007018IEABP!GO:0007017IEABP!GO:0006928IEABP!GO:0006810IEABP!GO:1901575IEABP!GO:0071704IEABP!GO:0044267IEABP!GO:0044265IEABP!GO:0044260IEABP!GO:0044257IEABP!GO:0044248IEABP!GO:0044238IEABP!GO:0044237IEABP!GO:0043632IEABP!GO:0043170IEABP !GO:0030163IEABP !GO:0019538IEABP !GO:0009987IEABP !GO:0009057IEABP !GO:0009056IEABP!GO:0008150IEABP!GO:0051603IEABP!GO:0006508IEABP!GO:0008152IEABP!GO:0019941IEABP!GO:0043407IEABP!GO:0016579IEABP!GO:0007409IEABP!GO:0007628IEABP!GO:0006950IEABP~!GO:0008283IEABP}!GO:0048747IEABP|!GO:0050905IEABP{!GO:0007412IEABPz!GO:0042755IEABPy!GO:0019896IEABPx!GO:0006511IEABPw!GO:0038023IEAMFv!GO:0004888IEAMF 'XpX@(hP8 x`H0pXC!GO:0048856IEABPB!GO:0048812IEABPA!GO:0048731IEABP@!GO:0048699IEABP?!GO:0048667IEABP>!GO:0048666IEABP=!GO:0048468IEABP<!GO:0044767IEABP;!GO:0044707IEABP:!GO:0032990IEABP9!GO:0032989IEABP8!GO:0032502IEABP7!GO:0032501IEABP6!GO:0031175IEABP5!GO:0030182IEABP4!GO:0030154IEABP3!GO:0030030IEABP2!GO:0022008IEABP1!GO:0016043IEABP0!GO:0007399IEABP/!GO:0009653IEABP.!GO:0007275IEABP-!GO:0007154IEABP,!GO:0000904IEABP+!GO:0000902IEABP*!GO:0050896IEABP)!GO:0007631IEABP(!GO:0007610IEABP'!GO:0051649IEABP&!GO:0051641IEABP%!GO:0051234IEABP$!GO:0051179IEABP#!GO:0046907IEABP"!GO:0044765IEABP!!GO:0044763IEABP !GO:0044699IEABP!GO:0030705IEABP!GO:0010970IEABP!GO:0008088IEABP 'XpX@(hP8 x`H0pXj!GO:0010741IEABPi!GO:0010648IEABPh!GO:0010646IEABPg!GO:0010627IEABPf!GO:0010605IEABPe!GO:0010563IEABPd!GO:0009968IEABPc!GO:0009966IEABPb!GO:0009892IEABPa!GO:0007243IEABP`!GO:0006796IEABP_!GO:0006793IEABP^!GO:0006469IEABP]!GO:0006468IEABP\!GO:0035556IEABP[!GO:0007165IEABPZ!GO:0001933IEABPY!GO:0001932IEABPX!GO:0000165IEABPW!GO:0070647IEABPV!GO:0070646IEABPU!GO:0043412IEABPT!GO:0036211IEABPS!GO:0006464IEABPR!GO:0044708IEABPQ!GO:0008344IEABPP!GO:0030534IEABPO!GO:0007626IEABPN!GO:0061061IEABPM!GO:0055002IEABPL!GO:0055001IEABPK!GO:0051146IEABPJ!GO:0042692IEABPI!GO:0050877IEABPH!GO:0003008IEABPG!GO:0071840IEABPF!GO:0061564IEABPE!GO:0048869IEABPD!GO:0048858IEABP 'XpX@(hP8 x`H0pX!GO:0065007IEABP!GO:0060255IEABP!GO:0051716IEABP!GO:0051348IEABP !GO:0051338IEABP !GO:0051248IEABP !GO:0051246IEABP !GO:0051174IEABP !GO:0050794IEABP!GO:0050790IEABP!GO:0050789IEABP!GO:0048585IEABP!GO:0048583IEABP!GO:0048523IEABP!GO:0048519IEABP!GO:0045936IEABP!GO:0045859IEABP!GO:0044700IEABP!GO:0044092IEABP~!GO:0043549IEABP}!GO:0043409IEABP|!GO:0043408IEABP{!GO:0043405IEABPz!GO:0043086IEABPy!GO:0042326IEABPx!GO:0042325IEABPw!GO:0033673IEABPv!GO:0032269IEABPu!GO:0032268IEABPt!GO:0031400IEABPs!GO:0031399IEABPr!GO:0031324IEABPq!GO:0031323IEABPp!GO:0023057IEABPo!GO:0023051IEABPn!GO:0023052IEABPm!GO:0019222IEABPl!GO:0019220IEABPk!GO:0016310IEABP 'XpX@(hP8 x`H0pX8!GO:0005102IEAMF7!GO:0001664IEAMF6!GO:0016790IEAMF5!GO:0016788IEAMF4!GO:0016787IEAMF3!GO:0003824IEAMF2!GO:0003674IEAMF1!GO:0005515IEAMF0!GO:0043130IEAMF/!GO:0004197IEAMF.!GO:0008242IEAMF-!GO:0031694IEAMF,!GO:0004221IEAMF+!GO:0043229IEACC*!GO:0043227IEACC)!GO:0043226IEACC(!GO:0043231IEACC'!GO:0071944IEACC&!GO:0016020IEACC%!GO:0044444IEACC$!GO:0044424IEACC#!GO:0044297IEACC"!GO:0097458IEACC!!GO:0042995IEACC !GO:0043005IEACC!GO:0044464IEACC!GO:0005623IEACC!GO:0005575IEACC!GO:0005634IEACC!GO:0005886IEACC!GO:0005737IEACC!GO:0005829IEACC!GO:0043025IEACC!GO:0030424IEACC!GO:0005622IEACC!GO:0080090IEABP!GO:0071901IEABP!GO:0071900IEABP!GO:0065009IEABP 'XpX@(hP8 x`H0pX_!GO:0065008IEABP^!GO:0065007IEABP]!GO:0051649IEABP\!GO:0051641IEABP[!GO:0044765IEABPZ!GO:0044763IEABPY!GO:0044707IEABPX!GO:0044700IEABPW!GO:0044699IEABPV!GO:0035637IEABPU!GO:0032940IEABPT!GO:0032501IEABPS!GO:0023061IEABPR!GO:0023052IEABPQ!GO:0019226IEABPP!GO:0009987IEABPO!GO:0050877IEABPN!GO:0007268IEABPM!GO:0007267IEABPL!GO:0007154IEABPK!GO:0006836IEABPJ!GO:0046903IEABPI!GO:0003008IEABPH!GO:0003001IEABPG!GO:0001505IEABPF!GO:0051234IEABPE!GO:0051179IEABPD!GO:0008150IEABPC!GO:0016079IEABPB!GO:0007269IEABPA!GO:0006810IEABP@!GO:0032182IEAMF?!GO:0008234IEAMF>!GO:0004175IEAMF=!GO:0070011IEAMF<!GO:0008238IEAMF;!GO:0008233IEAMF:!GO:0031690IEAMF9!GO:0005488IEAMF 'XpX@(hP8 x`H0pX!GO:0031090IEACC!GO:0030665IEACC!GO:0030662IEACC!GO:0030659IEACC!GO:0012506IEACC!GO:0045202IEACC!GO:0044464IEACC!GO:0044456IEACC~!GO:0044444IEACC}!GO:0044424IEACC|!GO:0043229IEACC{!GO:0043227IEACCz!GO:0043226IEACCy!GO:0031988IEACCx!GO:0031982IEACCw!GO:0031410IEACCv!GO:0030136IEACCu!GO:0030135IEACCt!GO:0016023IEACCs!GO:0043231IEACCr!GO:0005737IEACCq!GO:0005623IEACCp!GO:0005622IEACCo!GO:0005575IEACCn!GO:0042734IEACCm!GO:0043005IEACCl!GO:0030141IEACCk!GO:0030672IEACCj!GO:0008021IEACCi!GO:0016020IEACCh!GO:0097480IEABPg!GO:0097479IEABPf!GO:0051656IEABPe!GO:0051650IEABPd!GO:0051648IEABPc!GO:0051640IEABPb!GO:0048489IEABPa!GO:0006887IEABP`!GO:0016192IEABP 'XpX@(hP8 x`H0pX-! GO:0035637IEABP,! GO:0032940IEABP+! GO:0032501IEABP*! GO:0023061IEABP)! GO:0023052IEABP(! GO:0019226IEABP'! GO:0009987IEABP&! GO:0050877IEABP%! GO:0007268IEABP$! GO:0007267IEABP#! GO:0007154IEABP"! GO:0006836IEABP!! GO:0046903IEABP ! GO:0003008IEABP! GO:0003001IEABP! GO:0001505IEABP! GO:0051234IEABP! GO:0051179IEABP! GO:0008150IEABP! GO:0007269IEABP! GO:0006810IEABP!GO:0070325IEAMF!GO:0005102IEAMF!GO:0043169IEAMF!GO:0043167IEAMF!GO:0046872IEAMF!GO:0005488IEAMF!GO:0003674IEAMF!GO:0005515IEAMF!GO:0050750IEAMF!GO:0048306IEAMF!GO:0005509IEAMF !GO:0005215IEAMF !GO:0097060IEACC !GO:0097458IEACC !GO:0042995IEACC !GO:0044446IEACC!GO:0044433IEACC!GO:0044422IEACC 'XpX@(hP8 x`H0pXT! GO:0005488IEAMFS! GO:0003674IEAMFR! GO:0005509IEAMFQ! GO:0005515IEAMFP! GO:0005215IEAMFO! GO:0097458IEACCN! GO:0042995IEACCM! GO:0045202IEACCL! GO:0044464IEACCK! GO:0044456IEACCJ! GO:0044444IEACCI! GO:0044424IEACCH! GO:0043229IEACCG! GO:0043227IEACCF! GO:0043226IEACCE! GO:0031988IEACCD! GO:0031982IEACCC! GO:0031410IEACCB! GO:0030136IEACCA! GO:0030135IEACC@! GO:0016023IEACC?! GO:0043231IEACC>! GO:0005737IEACC=! GO:0005623IEACC<! GO:0005622IEACC;! GO:0005575IEACC:! GO:0048471IEACC9! GO:0043005IEACC8! GO:0008021IEACC7! GO:0016020IEACC6! GO:0065008IEABP5! GO:0065007IEABP4! GO:0051649IEABP3! GO:0051641IEABP2! GO:0044765IEABP1! GO:0044763IEABP0! GO:0044707IEABP/! GO:0044700IEABP.! GO:0044699IEABP 'XpX@(hP8 x`H0pX{! GO:0009790IEABPz! GO:0006355IEABPy! GO:0038023IEAMFx! GO:0004888IEAMFw! GO:0060089IEAMFv! GO:0003674IEAMFu! GO:0004949IEAMFt! GO:0004930IEAMFs! GO:0004871IEAMFr! GO:0004872IEAMFq! GO:0071944IEACCp! GO:0044464IEACCo! GO:0005623IEACCn! GO:0044425IEACCm! GO:0031224IEACCl! GO:0005575IEACCk! GO:0016020IEACCj! GO:0005886IEACCi! GO:0016021IEACCh! GO:0007187IEABPg! GO:0007166IEABPf! GO:0065007IEABPe! GO:0051716IEABPd! GO:0050896IEABPc! GO:0050794IEABPb! GO:0050789IEABPa! GO:0044763IEABP`! GO:0044700IEABP_! GO:0044699IEABP^! GO:0023052IEABP]! GO:0009987IEABP\! GO:0008150IEABP[! GO:0007154IEABPZ! GO:0007188IEABPY! GO:0007186IEABPX! GO:0007165IEABPW! GO:0043169IEAMFV! GO:0043167IEAMFU! GO:0046872IEAMF 'XpX@(hP8 x`H0pX"! GO:0031323IEABP!! GO:0019438IEABP ! GO:0019222IEABP! GO:0019219IEABP! GO:0018130IEABP! GO:0016070IEABP! GO:0010556IEABP! GO:0010468IEABP! GO:0010467IEABP! GO:0009987IEABP! GO:0009889IEABP! GO:0009059IEABP! GO:0009058IEABP! GO:0008150IEABP! GO:0006807IEABP! GO:0006725IEABP! GO:0006351IEABP! GO:0006139IEABP! GO:0008152IEABP! GO:0021987IEABP! GO:0021757IEABP ! GO:0021758IEABP ! GO:0000122IEABP ! GO:0021758ISSBP ! GO:0021757ISSBP ! GO:0060501IEABP! GO:0060013IEABP! GO:0048286IEABP! GO:0043010IEABP! GO:0042297IEABP! GO:0002053IEABP! GO:0040007IEABP! GO:0021549IEABP! GO:0048745IEABP! GO:0050679IEABP! GO:0009791IEABP~! GO:0007519IEABP}! GO:0030324IEABP|! GO:0045892IEABP 'XpX@(hP8 x`H0pXI! GO:0031324IEABPH! GO:0010629IEABPG! GO:0010605IEABPF! GO:0010558IEABPE! GO:0009892IEABPD! GO:0009890IEABPC! GO:0048856IEABPB! GO:0044767IEABPA! GO:0044707IEABP@! GO:0044699IEABP?! GO:0032502IEABP>! GO:0032501IEABP=! GO:0007275IEABP<! GO:2001141IEABP;! GO:2000112IEABP:! GO:1901576IEABP9! GO:1901362IEABP8! GO:1901360IEABP7! GO:0090304IEABP6! GO:0080090IEABP5! GO:0071704IEABP4! GO:0065007IEABP3! GO:0060255IEABP2! GO:0051252IEABP1! GO:0051171IEABP0! GO:0050794IEABP/! GO:0050789IEABP.! GO:0046483IEABP-! GO:0044271IEABP,! GO:0044260IEABP+! GO:0044249IEABP*! GO:0044238IEABP)! GO:0044237IEABP(! GO:0043170IEABP'! GO:0034654IEABP&! GO:0034645IEABP%! GO:0034641IEABP$! GO:0032774IEABP#! GO:0031326IEABP 'XpX@(hP8 x`H0pXp! GO:0007610IEABPo! GO:0050877IEABPn! GO:0009612IEABPm! GO:0003008IEABPl! GO:2000648IEABPk! GO:0072091IEABPj! GO:0072089IEABPi! GO:0010464IEABPh! GO:0010463IEABPg! GO:0030902IEABPf! GO:0022037IEABPe! GO:0007420IEABPd! GO:0007417IEABPc! GO:0007399IEABPb! GO:0050678IEABPa! GO:0050673IEABP`! GO:0048522IEABP_! GO:0048518IEABP^! GO:0042127IEABP]! GO:0008284IEABP\! GO:0008283IEABP[! GO:0061061IEABPZ! GO:0060538IEABPY! GO:0060537IEABPX! GO:0014706IEABPW! GO:0007517IEABPV! GO:0009888IEABPU! GO:0060541IEABPT! GO:0048731IEABPS! GO:0048513IEABPR! GO:0035295IEABPQ! GO:0030323IEABPP! GO:2000113IEABPO! GO:0051253IEABPN! GO:0051172IEABPM! GO:0048523IEABPL! GO:0048519IEABPK! GO:0045934IEABPJ! GO:0031327IEABP 'XpX@(hP8 x`H0pX! GO:0044767ISSBP! GO:0044707ISSBP! GO:0044699ISSBP! GO:0032502ISSBP! GO:0032501ISSBP! GO:0030900ISSBP! GO:0021756ISSBP! GO:0021544ISSBP! GO:0021537ISSBP! GO:0008150ISSBP ! GO:0007420ISSBP ! GO:0007417ISSBP ! GO:0007399ISSBP ! GO:0007275ISSBP ! GO:2000794IEABP! GO:2000027IEABP! GO:2000026IEABP! GO:0060502IEABP! GO:0060429IEABP! GO:0060428IEABP! GO:0060425IEABP! GO:0051239IEABP! GO:0050793IEABP! GO:0022603IEABP! GO:0009887IEABP~! GO:0009653IEABP}! GO:0060004IEABP|! GO:0007423IEABP{! GO:0001654IEABPz! GO:0050896IEABPy! GO:0050890IEABPx! GO:0044708IEABPw! GO:0031223IEABPv! GO:0010996IEABPu! GO:0009628IEABPt! GO:0009605IEABPs! GO:0007638IEABPr! GO:0007612IEABPq! GO:0007611IEABP 'XpX@(hP8 x`H0pX>! GO:0006694IEABP=! GO:0044237IEABP<! GO:0009058IEABP;! GO:0055114IEABP:! GO:0042802IEAMF9! GO:0046983IEAMF8! GO:0046914IEAMF7! GO:0043169IEAMF6! GO:0043167IEAMF5! GO:0046872IEAMF4! GO:0001071IEAMF3! GO:1901363IEAMF2! GO:0097159IEAMF1! GO:0005488IEAMF0! GO:0003676IEAMF/! GO:0003674IEAMF.! GO:0005515IEAMF-! GO:0046982IEAMF,! GO:0042803IEAMF+! GO:0043565IEAMF*! GO:0008270IEAMF)! GO:0003700IEAMF(! GO:0003677IEAMF'! GO:0044464IEACC&! GO:0005623IEACC%! GO:0005575IEACC$! GO:0005622IEACC#! GO:0021543IEABP"! GO:0048857IEABP!! GO:0030900IEABP ! GO:0021756IEABP! GO:0021544IEABP! GO:0021537IEABP! GO:0006357IEABP! GO:0006366IEABP! GO:0048857ISSBP! GO:0048856ISSBP! GO:0048731ISSBP! GO:0048513ISSBP 'XpX@(hP8 x`H0pXe! GO:0097159IEAMFd! GO:0036094IEAMFc! GO:0005488IEAMFb! GO:0003674IEAMFa! GO:0008831IEAMF`! GO:0003854IEAMF_! GO:0050662IEAMF^! GO:0016616IEAMF]! GO:0003824IEAMF\! GO:0016491IEAMF[! GO:0000166IEAMFZ! GO:0046379IEABPY! GO:0044723IEABPX! GO:0044264IEABPW! GO:0044262IEABPV! GO:0044260IEABPU! GO:0044249IEABPT! GO:0043170IEABPS! GO:0034645IEABPR! GO:0034637IEABPQ! GO:0033692IEABPP! GO:0016051IEABPO! GO:0009059IEABPN! GO:0005976IEABPM! GO:0005975IEABPL! GO:0000271IEABPK! GO:1901576IEABPJ! GO:1901362IEABPI! GO:1901360IEABPH! GO:0071704IEABPG! GO:0044238IEABPF! GO:0008610IEABPE! GO:0008202IEABPD! GO:0006629IEABPC! GO:0009987IEABPB! GO:0044710IEABPA! GO:0008150IEABP@! GO:0008152IEABP?! GO:0045226IEABP 'XpX@(hP8 x`H0pX ! GO:0034097IEABP ! GO:0021915IEABP ! GO:0043010IEABP ! GO:0001568IEABP! GO:0030902IEABP! GO:0009952IEABP! GO:0030900IEABP! GO:0008284IEABP! GO:0043065IEABP! GO:0030182IEABP! GO:0030324IEABP! GO:0003007IEABP! GO:0035115IEABP! GO:0030326IEABP~! GO:0042573IEABP}! GO:0060324IEABP|! GO:0048384IEABP{! GO:0031016IEABPz! GO:0010628IEABPy! GO:0009954IEABPx! GO:0048738IEABPw! GO:0048566IEABPv! GO:0014032IEABPu! GO:0016331IEABPt! GO:0031076IEABPs! GO:0071300IEABPr! GO:0042904IEABPq! GO:0042574IEABPp! GO:0035799IEABPo! GO:0001936IEABPn! GO:0009855IEABPm! GO:0008152IEABPl! GO:0055114IEABPk! GO:0033764IEAMFj! GO:0016229IEAMFi! GO:0048037IEAMFh! GO:0016614IEAMFg! GO:1901363IEAMFf! GO:1901265IEAMF 'XpX@(hP8 x`H0pX3! GO:0071704IEABP2! GO:0044255IEABP1! GO:0044238IEABP0! GO:0044237IEABP/! GO:0016101IEABP.! GO:0006721IEABP-! GO:0006720IEABP,! GO:0006629IEABP+! GO:0006081IEABP*! GO:0001523IEABP)! GO:0072189IEABP(! GO:0072001IEABP'! GO:0071695IEABP&! GO:0048856IEABP%! GO:0048799IEABP$! GO:0048731IEABP#! GO:0048513IEABP"! GO:0044767IEABP!! GO:0021700IEABP ! GO:0001655IEABP! GO:0065007IEABP! GO:0050794IEABP! GO:0050789IEABP! GO:0050678IEABP! GO:0050673IEABP! GO:0042127IEABP! GO:0009987IEABP! GO:0008283IEABP! GO:0001935IEABP! GO:0044707IEABP! GO:0044699IEABP! GO:0032502IEABP! GO:0032501IEABP! GO:0009799IEABP! GO:0007389IEABP! GO:0007275IEABP! GO:0044710IEABP! GO:0008150IEABP ! GO:0008285IEABP 'XpX@(hP8 x`H0pXZ! GO:0048568IEABPY! GO:0007423IEABPX! GO:0009790IEABPW! GO:0001654IEABPV! GO:1901701IEABPU! GO:1901700IEABPT! GO:0071396IEABPS! GO:0071310IEABPR! GO:0051716IEABPQ! GO:0050896IEABPP! GO:0044763IEABPO! GO:0042221IEABPN! GO:0033993IEABPM! GO:0032526IEABPL! GO:0070887IEABPK! GO:0010033IEABPJ! GO:1901576IEABPI! GO:0072330IEABPH! GO:0065008IEABPG! GO:0046394IEABPF! GO:0044711IEABPE! GO:0044283IEABPD! GO:0044281IEABPC! GO:0044249IEABPB! GO:0043436IEABPA! GO:0042905IEABP@! GO:0042445IEABP?! GO:0034754IEABP>! GO:0032787IEABP=! GO:0019752IEABP<! GO:0016114IEABP;! GO:0016102IEABP:! GO:0016053IEABP9! GO:0010817IEABP8! GO:0009058IEABP7! GO:0008610IEABP6! GO:0008299IEABP5! GO:0006082IEABP4! GO:0002138IEABP 'XpX@(hP8 x`H0pX! GO:0035108IEABP! GO:0035107IEABP! GO:0060322IEABP~! GO:0044700IEABP}! GO:0030522IEABP|! GO:0023052IEABP{! GO:0007154IEABPz! GO:0007165IEABPy! GO:0060255IEABPx! GO:0048518IEABPw! GO:0043170IEABPv! GO:0019222IEABPu! GO:0010604IEABPt! GO:0010468IEABPs! GO:0010467IEABPr! GO:0009893IEABPq! GO:0003002IEABPp! GO:0072359IEABPo! GO:0072358IEABPn! GO:0060537IEABPm! GO:0014706IEABPl! GO:0007507IEABPk! GO:0055123IEABPj! GO:0048565IEABPi! GO:0060485IEABPh! GO:0048869IEABPg! GO:0048864IEABPf! GO:0048863IEABPe! GO:0048762IEABPd! GO:0048468IEABPc! GO:0030154IEABPb! GO:0014033IEABPa! GO:0014031IEABP`! GO:0060429IEABP_! GO:0048729IEABP^! GO:0048598IEABP]! GO:0009888IEABP\! GO:0009653IEABP[! GO:0002009IEABP 'XpX@(hP8 x`H0pX(! GO:0043229IEACC'! GO:0043227IEACC&! GO:0043226IEACC%! GO:0043231IEACC$! GO:0044464IEACC#! GO:0044424IEACC"! GO:0005623IEACC!! GO:0005575IEACC ! GO:0005622IEACC! GO:0005634IEACC! GO:0005737IEACC! GO:0048523IEABP! GO:0048519IEABP! GO:0043009IEABP! GO:0009792IEABP! GO:0001944IEABP! GO:0007420IEABP! GO:0007417IEABP! GO:0048522IEABP! GO:0043068IEABP! GO:0043067IEABP! GO:0042981IEABP! GO:0016265IEABP! GO:0010942IEABP! GO:0010941IEABP! GO:0012501IEABP! GO:0008219IEABP ! GO:0006915IEABP ! GO:0048699IEABP ! GO:0022008IEABP ! GO:0007399IEABP ! GO:0060541IEABP! GO:0035295IEABP! GO:0030323IEABP! GO:0009887IEABP! GO:0035136IEABP! GO:0060173IEABP! GO:0048736IEABP! GO:0035113IEABP 'XpX@(hP8 x`H0pXO!GO:0007167IEABPN!GO:0007166IEABPM!GO:0007154IEABPL!GO:0007169IEABPK!GO:0007165IEABPJ!GO:0060537IEABPI!GO:0009888IEABPH!GO:0060322IEABPG!GO:0048731IEABPF!GO:0048513IEABPE!GO:0009887IEABPD!GO:0009653IEABPC!GO:0001501IEABPB!GO:0048856IEABPA!GO:0044767IEABP@!GO:0044707IEABP?!GO:0044699IEABP>!GO:0043009IEABP=!GO:0032502IEABP<!GO:0032501IEABP;!GO:0009792IEABP:!GO:0008150IEABP9!GO:0009790IEABP8!GO:0007275IEABP7!GO:0003016IEABP6!GO:0001944IEABP5!GO:0010761IEABP4!GO:0048008IEABP3!GO:0048745IEABP2!GO:0060324IEABP1!GO:0048705IEABP0!GO:0001701IEABP/! GO:0016903IEAMF.! GO:0003824IEAMF-! GO:0003674IEAMF,! GO:0004028IEAMF+! GO:0001758IEAMF*! GO:0016620IEAMF)! GO:0016491IEAMF 'XpX@(hP8 x`H0pXv!GO:0051092IEABPu!GO:0001701IEABPt!GO:0006357IEABPs!GO:0006351IEABPr!GO:0043066IEABPq!GO:0045944IEABPp!GO:0045893IEABPo!GO:0006355IEABPn!GO:0046914IEAMFm!GO:0043169IEAMFl!GO:0043167IEAMFk!GO:1901363IEAMFj!GO:0097159IEAMFi!GO:0005488IEAMFh!GO:0003676IEAMFg!GO:0003674IEAMFf!GO:0046872IEAMFe!GO:0008270IEAMFd!GO:0003677IEAMFc!GO:0007585IEABPb!GO:0003008IEABPa!GO:0072359IEABP`!GO:0072358IEABP_!GO:0051674IEABP^!GO:0051179IEABP]!GO:0048870IEABP\!GO:0040011IEABP[!GO:0016477IEABPZ!GO:0006928IEABPY!GO:0001667IEABPX!GO:0065007IEABPW!GO:0051716IEABPV!GO:0050896IEABPU!GO:0050794IEABPT!GO:0050789IEABPS!GO:0044763IEABPR!GO:0044700IEABPQ!GO:0023052IEABPP!GO:0009987IEABP 'XpX@(hP8 x`H0pX!GO:0008150IEABP!GO:0006807IEABP!GO:0006725IEABP!GO:0006139IEABP!GO:0008152IEABP!GO:0051259IEABP!GO:0030522IEABP!GO:0007283IEABP!GO:0003073IEABP!GO:0090003IEABP!GO:0060749IEABP!GO:0060742IEABP!GO:0060740IEABP!GO:0060736IEABP!GO:0060685IEABP!GO:0060599IEABP !GO:0060571IEABP !GO:0060520IEABP !GO:0048808IEABP !GO:0048645IEABP !GO:0048638IEABP!GO:0048608IEABP!GO:0045945IEABP!GO:0045726IEABP!GO:0045720IEABP!GO:0043568IEABP!GO:0042327IEABP!GO:0033148IEABP!GO:0019102IEABP!GO:0008584IEABP!GO:0060748IEABP~!GO:0009987IEABP}!GO:0010468IEABP|!GO:0043410IEABP{!GO:0050790IEABPz!GO:0030521IEABPy!GO:0043401IEABPx!GO:0050680IEABPw!GO:0008284IEABP 'XpX@(hP8 x`H0pXD!GO:0009893IEABPC!GO:0009891IEABPB!GO:2001141IEABPA!GO:2000112IEABP@!GO:1901576IEABP?!GO:1901362IEABP>!GO:1901360IEABP=!GO:0090304IEABP<!GO:0080090IEABP;!GO:0071704IEABP:!GO:0065007IEABP9!GO:0060255IEABP8!GO:0051252IEABP7!GO:0051171IEABP6!GO:0050794IEABP5!GO:0050789IEABP4!GO:0046483IEABP3!GO:0044271IEABP2!GO:0044260IEABP1!GO:0044249IEABP0!GO:0044238IEABP/!GO:0044237IEABP.!GO:0043170IEABP-!GO:0034654IEABP,!GO:0034645IEABP+!GO:0034641IEABP*!GO:0032774IEABP)!GO:0031326IEABP(!GO:0031323IEABP'!GO:0019438IEABP&!GO:0019222IEABP%!GO:0019219IEABP$!GO:0018130IEABP#!GO:0016070IEABP"!GO:0010556IEABP!!GO:0010467IEABP !GO:0009889IEABP!GO:0009059IEABP!GO:0009058IEABP 'XpX@(hP8 x`H0pXk!GO:0042127IEABPj!GO:0008283IEABPi!GO:0065009IEABPh!GO:0051091IEABPg!GO:0051090IEABPf!GO:0044093IEABPe!GO:0048856IEABPd!GO:0044767IEABPc!GO:0044707IEABPb!GO:0043009IEABPa!GO:0032502IEABP`!GO:0032501IEABP_!GO:0009792IEABP^!GO:0009790IEABP]!GO:0007275IEABP\!GO:0060548IEABP[!GO:0048523IEABPZ!GO:0048519IEABPY!GO:0044763IEABPX!GO:0044699IEABPW!GO:0043069IEABPV!GO:0043067IEABPU!GO:0042981IEABPT!GO:0016265IEABPS!GO:0010941IEABPR!GO:0012501IEABPQ!GO:0008219IEABPP!GO:0006915IEABPO!GO:0006366IEABPN!GO:0051254IEABPM!GO:0051173IEABPL!GO:0048522IEABPK!GO:0048518IEABPJ!GO:0031328IEABPI!GO:0031325IEABPH!GO:0045935IEABPG!GO:0010628IEABPF!GO:0010604IEABPE!GO:0010557IEABP 'XpX@(hP8 x`H0pX!GO:0048584IEABP!GO:0048583IEABP!GO:0043408IEABP!GO:0023056IEABP!GO:0023051IEABP !GO:0010740IEABP !GO:0010647IEABP !GO:0010646IEABP !GO:0010627IEABP !GO:0009967IEABP!GO:0009966IEABP!GO:0007243IEABP!GO:0035556IEABP!GO:0000165IEABP!GO:0030518IEABP!GO:0071495IEABP!GO:0071407IEABP!GO:0071396IEABP!GO:0071383IEABP!GO:0071310IEABP~!GO:0051716IEABP}!GO:0050896IEABP|!GO:0048545IEABP{!GO:0044700IEABPz!GO:0042221IEABPy!GO:0033993IEABPx!GO:0032870IEABPw!GO:0070887IEABPv!GO:0023052IEABPu!GO:0014070IEABPt!GO:0010033IEABPs!GO:0009755IEABPr!GO:0009725IEABPq!GO:0009719IEABPp!GO:0007154IEABPo!GO:0007165IEABPn!GO:0050678IEABPm!GO:0050673IEABPl!GO:0008285IEABP 'XpX@(hP8 x`H0pX9!GO:0007530IEABP8!GO:0061458IEABP7!GO:0046661IEABP6!GO:0046546IEABP5!GO:0045137IEABP4!GO:0008406IEABP3!GO:0007548IEABP2!GO:0061180IEABP1!GO:0061138IEABP0!GO:0060745IEABP/!GO:0060603IEABP.!GO:0060562IEABP-!GO:0060444IEABP,!GO:0060443IEABP+!GO:0060429IEABP*!GO:0060135IEABP)!GO:0051704IEABP(!GO:0048754IEABP'!GO:0048732IEABP&!GO:0048731IEABP%!GO:0048729IEABP$!GO:0048609IEABP#!GO:0048513IEABP"!GO:0044706IEABP!!GO:0044703IEABP !GO:0044702IEABP!GO:0035295IEABP!GO:0035239IEABP!GO:0032504IEABP!GO:0030879IEABP!GO:0022612IEABP!GO:0022414IEABP!GO:0007565IEABP!GO:0009888IEABP!GO:0009653IEABP!GO:0003006IEABP!GO:0002009IEABP!GO:0001763IEABP!GO:0000003IEABP 'XpX@(hP8 x`H0pX`!GO:0050793IEABP_!GO:0048589IEABP^!GO:0040008IEABP]!GO:0040007IEABP\!GO:0006359IEABP[!GO:0006383IEABPZ!GO:0051130IEABPY!GO:0071840IEABPX!GO:0061024IEABPW!GO:0051129IEABPV!GO:0051128IEABPU!GO:0045113IEABPT!GO:0045112IEABPS!GO:0016044IEABPR!GO:0016043IEABPQ!GO:0010605IEABPP!GO:0010558IEABPO!GO:0009892IEABPN!GO:0009890IEABPM!GO:0007009IEABPL!GO:0048009IEABPK!GO:0043567IEABPJ!GO:0007167IEABPI!GO:0007166IEABPH!GO:0007169IEABPG!GO:0051174IEABPF!GO:0045937IEABPE!GO:0042325IEABPD!GO:0019220IEABPC!GO:0016310IEABPB!GO:0010562IEABPA!GO:0006796IEABP@!GO:0006793IEABP?!GO:0033146IEABP>!GO:0033145IEABP=!GO:0033143IEABP<!GO:0030520IEABP;!GO:0030238IEABP:!GO:0018993IEABP 'XpX@(hP8 x`H0pX!GO:0061377IEABP!GO:0048610IEABP!GO:0030855IEABP!GO:0060572IEABP!GO:0060513IEABP!GO:0060512IEABP!GO:0048598IEABP!GO:0030850IEABP!GO:0016331IEABP~!GO:0001655IEABP}!GO:0060601IEABP|!GO:2000243IEABP{!GO:2000241IEABPz!GO:2000027IEABPy!GO:2000026IEABPx!GO:0060688IEABPw!GO:0060514IEABPv!GO:0051240IEABPu!GO:0051239IEABPt!GO:0051094IEABPs!GO:0048869IEABPr!GO:0045995IEABPq!GO:0045595IEABPp!GO:0045168IEABPo!GO:0045165IEABPn!GO:0042659IEABPm!GO:0031128IEABPl!GO:0030154IEABPk!GO:0022603IEABPj!GO:0010453IEABPi!GO:0007267IEABPh!GO:0003156IEABPg!GO:0001759IEABPf!GO:0001708IEABPe!GO:0048806IEABPd!GO:0035112IEABPc!GO:0030539IEABPb!GO:0048646IEABPa!GO:0009887IEABP 'XpX@(hP8 x`H0pX.!GO:0005623IEACC-!GO:0005575IEACC,!GO:0005622IEACC+!GO:0043234IEACC*!GO:0005886IEACC)!GO:0000790IEACC(!GO:0005737IEACC'!GO:0005634IEACC&!GO:0071822IEABP%!GO:0070271IEABP$!GO:0065003IEABP#!GO:0044085IEABP"!GO:0043933IEABP!!GO:0022607IEABP 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v]D+|c{!GO:0044249IEABPz!GO:0044238IEABPy!GO:0044237IEABPx!GO:0043170IEABPw!GO:0034645IEABPv!GO:0019538IEABPu!GO:0010467IEABPt!GO:0009987IEABPs!GO:0009059IEABPr!GO:0009058IEABPq!GO:0008150IEABPp!GO:0008152IEABPo!GO:0006364IEABPn!GO:0042274IEABPm!GO:0006412IEABPl!GO:1901265IEAMFk!GO:0036094IEAMFj!GO:1901363IEAMFi!GO:0097159IEAMFh!GO:0005488IEAMFg!GO:0003674IEAMFf!GO:0005515IEAMFe!GO:0000166IEAMFd!GO:0003676IEAMFc!GO:0005681IEACCb!GO:0030529IEACCa!GO:0044464IEACC`!GO:0044446IEACC_!GO:0044428IEACC^!GO:0044424IEACC]!GO:0044422IEACC\!GO:0043234IEACC[!GO:0043229IEACCZ!GO:0043227IEACCY!GO:0043226IEACCX!GO:0032991IEACCW!GO:0043231IEACC %cjQ8pW>% v]D+|c !GO:0044391IEACC!GO:0044444IEACC!GO:0044424IEACC!GO:0043232IEACC!GO:0043229IEACC!GO:0043228IEACC!GO:0043226IEACC!GO:0032991IEACC!GO:0005737IEACC!GO:0044464IEACC!GO:0005623IEACC!GO:0005575IEACC!GO:0022627IEACC!GO:0015935IEACC!GO:0030529IEACC!GO:0005840IEACC!GO:0005622IEACC!GO:1901360IEABP!GO:0090304IEABP !GO:0046483IEABP !GO:0034660IEABP !GO:0034641IEABP !GO:0034470IEABP !GO:0016072IEABP!GO:0016070IEABP!GO:0006807IEABP!GO:0006725IEABP!GO:0006396IEABP!GO:0006139IEABP!GO:0071840IEABP!GO:0044085IEABP!GO:0022613IEABP!GO:0042254IEABP!GO:1901576IEABP~!GO:0071704IEABP}!GO:0044267IEABP|!GO:0044260IEABP %cjQ8pW>% v]D+|cE!GO:0046719IEABPD!GO:0045184IEABPC!GO:0044766IEABPB!GO:0044764IEABPA!GO:0044763IEABP@!GO:0044699IEABP?!GO:0044419IEABP>!GO:0044003IEABP=!GO:0042592IEABP<!GO:0035821IEABP;!GO:0034613IEABP:!GO:0033036IEABP9!GO:0030581IEABP8!GO:0044403IEABP7!GO:0019048IEABP6!GO:0015031IEABP5!GO:0009987IEABP4!GO:0016032IEABP3!GO:0008150IEABP2!GO:0006886IEABP1!GO:0006858IEABP0!GO:0006810IEABP/!GO:0008104IEABP.!GO:0019060IEABP-!GO:1901363IEAMF,!GO:0097159IEAMF+!GO:0005488IEAMF*!GO:0003676IEAMF)!GO:0005198IEAMF(!GO:0003674IEAMF'!GO:0003723IEAMF&!GO:0003735IEAMF%!GO:0044445IEACC$!GO:0022626IEACC#!GO:0005829IEACC"!GO:0044446IEACC!!GO:0044422IEACC %cjQ8pW>% v]D+|cj!GO:0043226IEACCi!GO:0043231IEACCh!GO:0005623IEACCg!GO:0005575IEACCf!GO:0005622IEACCe!GO:0005829IEACCd!GO:0005634IEACCc!GO:0044464IEACCb!GO:0044444IEACCa!GO:0044424IEACC`!GO:0043229IEACC_!GO:0043227IEACC^!GO:0043226IEACC]!GO:0043231IEACC\!GO:0005737IEACC[!GO:0005623IEACCZ!GO:0005575IEACCY!GO:0005622IEACCX!GO:0005739IEACCW!GO:0005488IEAMFV!GO:0003674IEAMFU!GO:0005515IEAMFT!GO:0042802IEAMFS!GO:0071702IEABPR!GO:0070727IEABPQ!GO:0065008IEABPP!GO:0065007IEABPO!GO:0051817IEABPN!GO:0051708IEABPM!GO:0051704IEABPL!GO:0051701IEABPK!GO:0051649IEABPJ!GO:0051641IEABPI!GO:0051234IEABPH!GO:0051179IEABPG!GO:0048878IEABPF!GO:0046907IEABP %cjQ8pW>% v]D+|c!GO:0042803IEAMF!GO:0070013IEACC !GO:0044446IEACC !GO:0044429IEACC !GO:0044422IEACC !GO:0043233IEACC !GO:0031974IEACC!GO:0044464IEACC!GO:0044444IEACC!GO:0044424IEACC!GO:0043229IEACC!GO:0043227IEACC!GO:0043226IEACC!GO:0043231IEACC!GO:0005737IEACC!GO:0005623IEACC!GO:0005575IEACC~!GO:0005622IEACC}!GO:0005759IEACC|!GO:0005739IEACC{!GO:0071704IEABPz!GO:0044267IEABPy!GO:0044260IEABPx!GO:0044238IEABPw!GO:0044237IEABPv!GO:0043170IEABPu!GO:0019538IEABPt!GO:0009987IEABPs!GO:0008150IEABPr!GO:0008152IEABPq!GO:0006457IEABPp!GO:0044444IEACCo!GO:0005737IEACCn!GO:0044464IEACCm!GO:0044424IEACCl!GO:0043229IEACCk!GO:0043227IEACC %cjQ8pW>% v]D+|c4!GO:0016469IEACC3!GO:0033178IEACC2!GO:0055085IEABP1!GO:0051234IEABP0!GO:0051179IEABP/!GO:0044765IEABP.!GO:0044763IEABP-!GO:0044699IEABP,!GO:0034220IEABP+!GO:0015988IEABP*!GO:0015992IEABP)!GO:0015672IEABP(!GO:0009987IEABP'!GO:0008150IEABP&!GO:0006818IEABP%!GO:0006812IEABP$!GO:0006811IEABP#!GO:0006810IEABP"!GO:0015991IEABP!!GO:1901363IEAMF !GO:1901265IEAMF!GO:0097159IEAMF!GO:0060590IEAMF!GO:0060589IEAMF!GO:0036094IEAMF!GO:0030554IEAMF!GO:0030234IEAMF!GO:0017076IEAMF!GO:0000166IEAMF!GO:0042802IEAMF!GO:0046983IEAMF!GO:0005488IEAMF!GO:0003674IEAMF!GO:0005515IEAMF!GO:0000774IEAMF!GO:0051087IEAMF!GO:0051082IEAMF %cjQ8pW>% v]D+|cY!GO:0009058IEABPX!GO:0008150IEABPW!GO:0008152IEABPV!GO:0006412IEABPU!GO:0044769IEAMFT!GO:0043492IEAMFS!GO:0042625IEAMFR!GO:0022892IEAMFQ!GO:0022890IEAMFP!GO:0022891IEAMFO!GO:0022804IEAMFN!GO:0016820IEAMFM!GO:0016818IEAMFL!GO:0016817IEAMFK!GO:0016787IEAMFJ!GO:0016462IEAMFI!GO:0015405IEAMFH!GO:0015399IEAMFG!GO:0015078IEAMFF!GO:0015077IEAMFE!GO:0015075IEAMFD!GO:0016887IEAMFC!GO:0008324IEAMFB!GO:0022857IEAMFA!GO:0005215IEAMF@!GO:0017111IEAMF?!GO:0042626IEAMF>!GO:0019829IEAMF=!GO:0003824IEAMF<!GO:0042623IEAMF;!GO:0003674IEAMF:!GO:0046961IEAMF9!GO:0044425IEACC8!GO:0043234IEACC7!GO:0032991IEACC6!GO:0016020IEACC5!GO:0005575IEACC %cjQ8pW>% v]D+|c~!GO:0044446IEACC}!GO:0044422IEACC|!GO:0044391IEACC{!GO:0044444IEACCz!GO:0043232IEACCy!GO:0043228IEACCx!GO:0032991IEACCw!GO:0071944IEACCv!GO:0044424IEACCu!GO:0043229IEACCt!GO:0043227IEACCs!GO:0043226IEACCr!GO:0043231IEACCq!GO:0044464IEACCp!GO:0005623IEACCo!GO:0005575IEACCn!GO:0015935IEACCm!GO:0030529IEACCl!GO:0005840IEACCk!GO:0016020IEACCj!GO:0005886IEACCi!GO:0005737IEACCh!GO:0005634IEACCg!GO:0005622IEACCf!GO:1901576IEABPe!GO:0071704IEABPd!GO:0044267IEABPc!GO:0044260IEABPb!GO:0044249IEABPa!GO:0044238IEABP`!GO:0044237IEABP_!GO:0043170IEABP^!GO:0034645IEABP]!GO:0019538IEABP\!GO:0010467IEABP[!GO:0009987IEABPZ!GO:0009059IEABP %cjQ8pW>% v]D+|c#!GO:0006732IEABP"!GO:0008152IEABP!!GO:0006777IEABP !GO:0007600IEABP!GO:0050877IEABP!GO:0003008IEABP!GO:0044708IEABP!GO:0044707IEABP!GO:0042596IEABP!GO:0033555IEABP!GO:0032501IEABP!GO:0006950IEABP!GO:0006952IEABP!GO:0002209IEABP!GO:0065007IEABP!GO:0051716IEABP!GO:0050896IEABP!GO:0050794IEABP!GO:0050789IEABP!GO:0044763IEABP!GO:0044700IEABP!GO:0044699IEABP !GO:0023052IEABP !GO:0009987IEABP !GO:0008150IEABP !GO:0007186IEABP !GO:0007166IEABP!GO:0007154IEABP!GO:0007165IEABP!GO:0019233IEABP!GO:0001662IEABP!GO:0007610IEABP!GO:0007218IEABP!GO:0005198IEAMF!GO:0003674IEAMF!GO:0004872IEAMF!GO:0003735IEAMF %cjQ8pW>% v]D+|cH!GO:0005623IEACCG!GO:0005575IEACCF!GO:0005622IEACCE!GO:0019008IEACCD!GO:0005829IEACCC!GO:0005737IEACCB!GO:0005634IEACCA!GO:1901576IEABP@!GO:1901566IEABP?!GO:1901564IEABP>!GO:1901362IEABP=!GO:1901360IEABP<!GO:0090407IEABP;!GO:0071704IEABP:!GO:0051188IEABP9!GO:0051186IEABP8!GO:0046483IEABP7!GO:0044267IEABP6!GO:0044260IEABP5!GO:0044249IEABP4!GO:0044238IEABP3!GO:0044237IEABP2!GO:0043545IEABP1!GO:0043170IEABP0!GO:0032324IEABP/!GO:0019720IEABP.!GO:0019637IEABP-!GO:0019538IEABP,!GO:0018130IEABP+!GO:0009987IEABP*!GO:0009108IEABP)!GO:0009058IEABP(!GO:0008150IEABP'!GO:0006807IEABP&!GO:0006796IEABP%!GO:0006793IEABP$!GO:0051189IEABP %cjQ8pW>% v]D+|cm!GO:0009967IEABPl!GO:0009966IEABPk!GO:0007249IEABPj!GO:0007243IEABPi!GO:0007154IEABPh!GO:0035556IEABPg!GO:0007165IEABPf!GO:0050896IEABPe!GO:0050890IEABPd!GO:0044708IEABPc!GO:0044707IEABPb!GO:0044699IEABPa!GO:0032501IEABP`!GO:0008150IEABP_!GO:0007610IEABP^!GO:0050877IEABP]!GO:0003008IEABP\!GO:0048168IEABP[!GO:0043123IEABPZ!GO:0007613IEABPY!GO:0007611IEABPX!GO:0003824IEAMFW!GO:0005488IEAMFV!GO:0003674IEAMFU!GO:0005515IEAMFT!GO:0030366IEAMFS!GO:0016740IEAMFR!GO:0042802IEAMFQ!GO:0043234IEACCP!GO:0032991IEACCO!GO:0044444IEACCN!GO:0044464IEACCM!GO:0044424IEACCL!GO:0043229IEACCK!GO:0043227IEACCJ!GO:0043226IEACCI!GO:0043231IEACC %cjQ8pW>% v]D+|c!GO:0005575IEACC!GO:0005622IEACC!GO:0043025IEACC!GO:0001726IEACC!GO:0048471IEACC !GO:0005737IEACC !GO:0005634IEACC !GO:0065008IEABP !GO:0051969IEABP !GO:0051239IEABP!GO:0050804IEABP!GO:0048167IEABP!GO:0044057IEABP!GO:0035637IEABP!GO:0031644IEABP!GO:0019226IEABP!GO:0007268IEABP!GO:0007267IEABP!GO:0065007IEABP!GO:0051716IEABP~!GO:0050794IEABP}!GO:0050789IEABP|!GO:0048584IEABP{!GO:0048583IEABPz!GO:0048522IEABPy!GO:0048518IEABPx!GO:0044763IEABPw!GO:0044700IEABPv!GO:0043122IEABPu!GO:0023056IEABPt!GO:0023051IEABPs!GO:0023052IEABPr!GO:0010740IEABPq!GO:0010647IEABPp!GO:0010646IEABPo!GO:0010627IEABPn!GO:0009987IEABP %cjQ8pW>% v]D+|c7!GO:0044237IEABP6!GO:0043170IEABP5!GO:0034645IEABP4!GO:0019538IEABP3!GO:0010467IEABP2!GO:0009987IEABP1!GO:0009059IEABP0!GO:0009058IEABP/!GO:0008150IEABP.!GO:0008152IEABP-!GO:0006412IEABP,!GO:0005102IEAMF+!GO:0046983IEAMF*!GO:0043169IEAMF)!GO:0043167IEAMF(!GO:0046872IEAMF'!GO:0005488IEAMF&!GO:0003674IEAMF%!GO:0005515IEAMF$!GO:0044548IEAMF#!GO:0050786IEAMF"!GO:0048306IEAMF!!GO:0042803IEAMF !GO:0005509IEAMF!GO:0042802IEAMF!GO:0097458IEACC!GO:0044297IEACC!GO:0042995IEACC!GO:0031252IEACC!GO:0044444IEACC!GO:0044464IEACC!GO:0044424IEACC!GO:0043229IEACC!GO:0043227IEACC!GO:0043226IEACC!GO:0043231IEACC!GO:0005623IEACC %cjQ8pW>% v]D+|c\!GO:0044445IEACC[!GO:0044391IEACCZ!GO:0022626IEACCY!GO:0015934IEACCX!GO:0005829IEACCW!GO:0044444IEACCV!GO:0032991IEACCU!GO:0070013IEACCT!GO:0044446IEACCS!GO:0044428IEACCR!GO:0044424IEACCQ!GO:0044422IEACCP!GO:0043233IEACCO!GO:0043232IEACCN!GO:0043229IEACCM!GO:0043228IEACCL!GO:0043227IEACCK!GO:0043226IEACCJ!GO:0031981IEACCI!GO:0031974IEACCH!GO:0043231IEACCG!GO:0005634IEACCF!GO:0044464IEACCE!GO:0005623IEACCD!GO:0005575IEACCC!GO:0005737IEACCB!GO:0022625IEACCA!GO:0030529IEACC@!GO:0005840IEACC?!GO:0005730IEACC>!GO:0005622IEACC=!GO:1901576IEABP<!GO:0071704IEABP;!GO:0044267IEABP:!GO:0044260IEABP9!GO:0044249IEABP8!GO:0044238IEABP %cjQ8pW>% v]D+|c!GO:0043232IEACC!GO:0043228IEACC!GO:0005856IEACC~!GO:0044464IEACC}!GO:0044446IEACC|!GO:0044428IEACC{!GO:0044424IEACCz!GO:0044422IEACCy!GO:0043229IEACCx!GO:0043227IEACCw!GO:0043226IEACCv!GO:0031975IEACCu!GO:0031967IEACCt!GO:0031090IEACCs!GO:0012505IEACCr!GO:0005635IEACCq!GO:0005623IEACCp!GO:0016020IEACCo!GO:0005575IEACCn!GO:0005622IEACCm!GO:0005634IEACCl!GO:0005886IEACCk!GO:0043231IEACCj!GO:0045111IEACCi!GO:0031965IEACCh!GO:0051234IEABPg!GO:0051179IEABPf!GO:0044765IEABPe!GO:0044763IEABPd!GO:0044699IEABPc!GO:0009987IEABPb!GO:0008150IEABPa!GO:0006810IEABP`!GO:0055085IEABP_!GO:0005198IEAMF^!GO:0003674IEAMF]!GO:0003735IEAMF %cjQ8pW>% v]D+|c&! GO:0050794IEABP%! GO:0050789IEABP$! GO:0048285IEABP#! GO:0044784IEABP"! GO:0044772IEABP!! GO:0044770IEABP ! GO:0044763IEABP! GO:0044699IEABP! GO:0033043IEABP! GO:0022402IEABP! GO:0016043IEABP! GO:0010564IEABP! GO:0009987IEABP! GO:0008150IEABP! GO:0007346IEABP! GO:0007091IEABP! GO:0007088IEABP! GO:0007067IEABP! GO:0007049IEABP! GO:0006996IEABP! GO:0051726IEABP! GO:0000280IEABP! GO:0000278IEABP! GO:0070979IEABP! GO:0031145IEABP ! GO:0030071IEABP ! GO:0005488IEAMF ! GO:0005102IEAMF ! GO:0003674IEAMF ! GO:0005515IEAMF! GO:0005179IEAMF! GO:0005575IEACC! GO:0005576IEACC!GO:0005488IEAMF!GO:0003674IEAMF!GO:0005515IEAMF!GO:0071944IEACC %cjQ8pW>% v]D+|cK! GO:0005680IEACCJ! GO:0070647IEABPI! GO:0043412IEABPH! GO:0036211IEABPG! GO:0032446IEABPF! GO:0006464IEABPE! GO:0016567IEABPD! GO:0000209IEABPC! GO:1901575IEABPB! GO:0071704IEABPA! GO:0044267IEABP@! GO:0044265IEABP?! GO:0044260IEABP>! GO:0044257IEABP=! GO:0044248IEABP<! GO:0044238IEABP;! GO:0044237IEABP:! GO:0043632IEABP9! GO:0043170IEABP8! GO:0043161IEABP7! GO:0030163IEABP6! GO:0019538IEABP5! GO:0010498IEABP4! GO:0009057IEABP3! GO:0009056IEABP2! GO:0006511IEABP1! GO:0051603IEABP0! GO:0006508IEABP/! GO:0008152IEABP.! GO:0019941IEABP-! GO:1902099IEABP,! GO:1901990IEABP+! GO:1901987IEABP*! GO:0071840IEABP)! GO:0065007IEABP(! GO:0051783IEABP'! GO:0051128IEABP %cjQ8pW>% v]D+|cp! GO:0044237IEABPo! GO:0043632IEABPn! GO:0030163IEABPm! GO:0009987IEABPl! GO:0009057IEABPk! GO:0009056IEABPj! GO:0019941IEABPi! GO:0071704IEABPh! GO:0044238IEABPg! GO:0043170IEABPf! GO:0019538IEABPe! GO:0008150IEABPd! GO:0008152IEABPc! GO:0051603IEABPb! GO:0006511IEABPa! GO:0006508IEABP`! GO:0005488IEAMF_! GO:0003674IEAMF^! GO:0005515IEAMF]! GO:0044464IEACC\! GO:0044446IEACC[! GO:0044428IEACCZ! GO:0044424IEACCY! GO:0044422IEACCX! GO:0043234IEACCW! GO:0043229IEACCV! GO:0043227IEACCU! GO:0043226IEACCT! GO:0032991IEACCS! GO:0031461IEACCR! GO:0043231IEACCQ! GO:0005634IEACCP! GO:0005623IEACCO! GO:0005575IEACCN! GO:0005622IEACCM! GO:0000152IEACCL! GO:0000151IEACC %cjQ8pW>% v]D+|c! GO:0070003IEAMF! GO:0070011IEAMF! GO:0003824IEAMF! GO:0003674IEAMF! GO:0005515IEAMF! GO:0008233IEAMF! GO:0004298IEAMF! GO:0004175IEAMF ! GO:0016787IEAMF ! GO:0044444IEACC ! GO:0043232IEACC ! GO:0043228IEACC ! GO:0035770IEACC! GO:0030529IEACC! GO:0043234IEACC! GO:0032991IEACC! GO:0044464IEACC! GO:0044424IEACC! GO:0043229IEACC! GO:0043227IEACC! GO:0043226IEACC! GO:0043231IEACC! GO:0005623IEACC~! GO:0005575IEACC}! GO:0005622IEACC|! GO:0000932IEACC{! GO:0019773IEACCz! GO:0005839IEACCy! GO:0000502IEACCx! GO:0005737IEACCw! GO:0005634IEACCv! GO:1901575IEABPu! GO:0044267IEABPt! GO:0044265IEABPs! GO:0044260IEABPr! GO:0044257IEABPq! GO:0044248IEABP %cjQ8pW>% v]D+|c:! GO:0051234IEABP9! GO:0051179IEABP8! GO:0051169IEABP7! GO:0051168IEABP6! GO:0046907IEABP5! GO:0044763IEABP4! GO:0044699IEABP3! GO:0044085IEABP2! GO:0033753IEABP1! GO:0033750IEABP0! GO:0022613IEABP/! GO:0016482IEABP.! GO:0006913IEABP-! GO:0006810IEABP,! GO:0000054IEABP+! GO:0042254IEABP*! GO:1901576IEABP)! GO:0071704IEABP(! GO:0044267IEABP'! GO:0044260IEABP&! GO:0044249IEABP%! GO:0044238IEABP$! GO:0044237IEABP#! GO:0043170IEABP"! GO:0034645IEABP!! GO:0019538IEABP ! GO:0010467IEABP! GO:0009987IEABP! GO:0009059IEABP! GO:0009058IEABP! GO:0008150IEABP! GO:0008152IEABP! GO:0006364IEABP! GO:0042274IEABP! GO:0000056IEABP! GO:0006412IEABP! GO:0005488IEAMF %cjQ8pW>% v]D+|c_! GO:0044391IEACC^! GO:0044464IEACC]! GO:0044444IEACC\! GO:0044424IEACC[! GO:0043232IEACCZ! GO:0043229IEACCY! GO:0043228IEACCX! GO:0043226IEACCW! GO:0032991IEACCV! GO:0005737IEACCU! GO:0005623IEACCT! GO:0005575IEACCS! GO:0005622IEACCR! GO:0022627IEACCQ! GO:0015935IEACCP! GO:0030529IEACCO! GO:0005840IEACCN! GO:1901360IEABPM! GO:0090304IEABPL! GO:0046483IEABPK! GO:0034660IEABPJ! GO:0034641IEABPI! GO:0034470IEABPH! GO:0016072IEABPG! GO:0016070IEABPF! GO:0006807IEABPE! GO:0006725IEABPD! GO:0006396IEABPC! GO:0006139IEABPB! GO:0071840IEABPA! GO:0071428IEABP@! GO:0071426IEABP?! GO:0071166IEABP>! GO:0051656IEABP=! GO:0051649IEABP<! GO:0051641IEABP;! GO:0051640IEABP %cjQ8pW>% v]D+|c! GO:0009913IEABP! GO:0008544IEABP! GO:0007423IEABP! GO:0007399IEABP! GO:0009888IEABP! GO:0009887IEABP~! GO:0009790IEABP}! GO:0009653IEABP|! GO:0007275IEABP{! GO:0002093IEABPz! GO:0002064IEABPy! GO:0000904IEABPx! GO:0000902IEABPw! GO:0044707IEABPv! GO:0044699IEABPu! GO:0032501IEABPt! GO:0008150IEABPs! GO:0007600IEABPr! GO:0050877IEABPq! GO:0050954IEABPp! GO:0003008IEABPo! GO:0050910IEABPn! GO:0060088IEABPm! GO:0007605IEABPl! GO:1901363IEAMFk! GO:0097159IEAMFj! GO:0005488IEAMFi! GO:0003676IEAMFh! GO:0005198IEAMFg! GO:0003674IEAMFf! GO:0003723IEAMFe! GO:0003735IEAMFd! GO:0044445IEACCc! GO:0022626IEACCb! GO:0005829IEACCa! GO:0044446IEACC`! GO:0044422IEACC %cjQ8pW>% v]D+|c)! GO:0009612IEABP(! GO:0071840IEABP'! GO:0060429IEABP&! GO:0060122IEABP%! GO:0060119IEABP$! GO:0060117IEABP#! GO:0060113IEABP"! GO:0048869IEABP!! GO:0048856IEABP ! GO:0048839IEABP! GO:0048731IEABP! GO:0048699IEABP! GO:0048667IEABP! GO:0048666IEABP! GO:0048598IEABP! GO:0048568IEABP! GO:0048562IEABP! GO:0048513IEABP! GO:0048468IEABP! GO:0044767IEABP! GO:0044763IEABP! GO:0043588IEABP! GO:0043583IEABP! GO:0042491IEABP! GO:0042490IEABP! GO:0042472IEABP! GO:0042471IEABP! GO:0035315IEABP ! GO:0032989IEABP ! GO:0032502IEABP ! GO:0030855IEABP ! GO:0030182IEABP ! GO:0030154IEABP! GO:0030030IEABP! GO:0022008IEABP! GO:0016043IEABP! GO:0009987IEABP %cjQ8pW>% v]D+|cN!GO:0016043IEABPM!GO:0022607IEABPL!GO:0008150IEABPK!GO:0006461IEABPJ!GO:0051289IEABPI! GO:0005488IEAMFH! GO:0003674IEAMFG! GO:0005515IEAMFF! GO:0044446IEACCE! GO:0044422IEACCD! GO:0044424IEACCC! GO:0043232IEACCB! GO:0043229IEACCA! GO:0043228IEACC@! GO:0043226IEACC?! GO:0005622IEACC>! GO:0071944IEACC=! GO:0045177IEACC<! GO:0044464IEACC;! GO:0044459IEACC:! GO:0044425IEACC9! GO:0005623IEACC8! GO:0005575IEACC7! GO:0005886IEACC6! GO:0032426IEACC5! GO:0032421IEACC4! GO:0016324IEACC3! GO:0016020IEACC2! GO:0051606IEABP1! GO:0050982IEABP0! GO:0050974IEABP/! GO:0050906IEABP.! GO:0050896IEABP-! GO:0009628IEABP,! GO:0009605IEABP+! GO:0009582IEABP*! GO:0009581IEABP %cjQ8pW>% v]D+|cs!GO:0045184IEABPr!GO:0033036IEABPq!GO:0008150IEABPp!GO:0006810IEABPo!GO:0008104IEABPn!GO:0007186IEABPm!GO:0006886IEABPl!GO:0007264IEABPk!GO:0015031IEABPj!GO:0016790IEAMFi!GO:0016788IEAMFh!GO:0016787IEAMFg!GO:0016289IEAMFf!GO:0003824IEAMFe!GO:0003674IEAMFd!GO:0047617IEAMFc!GO:0044464IEACCb!GO:0044444IEACCa!GO:0044424IEACC`!GO:0043229IEACC_!GO:0043227IEACC^!GO:0043226IEACC]!GO:0043231IEACC\!GO:0005737IEACC[!GO:0005623IEACCZ!GO:0005575IEACCY!GO:0005622IEACCX!GO:0005739IEACCW!GO:0071840IEABPV!GO:0071822IEABPU!GO:0070271IEABPT!GO:0065003IEABPS!GO:0051259IEABPR!GO:0051262IEABPQ!GO:0044085IEABPP!GO:0043933IEABPO!GO:0051260IEABP %cjQ8pW>% v]D+|c!GO:0004871IEAMF!GO:0003924IEAMF!GO:0005525IEAMF!GO:0000166IEAMF!GO:0044424IEACC!GO:0043229IEACC!GO:0043227IEACC!GO:0043226IEACC!GO:0043231IEACC!GO:0044464IEACC!GO:0005623IEACC !GO:0005575IEACC !GO:0005737IEACC !GO:0005634IEACC !GO:0005622IEACC !GO:0007166IEABP!GO:0070727IEABP!GO:0051649IEABP!GO:0051641IEABP!GO:0046907IEABP!GO:0034613IEABP!GO:0065007IEABP!GO:0051716IEABP!GO:0050896IEABP!GO:0050794IEABP!GO:0050789IEABP~!GO:0044763IEABP}!GO:0044700IEABP|!GO:0044699IEABP{!GO:0023052IEABPz!GO:0009987IEABPy!GO:0007154IEABPx!GO:0035556IEABPw!GO:0007165IEABPv!GO:0071702IEABPu!GO:0051234IEABPt!GO:0051179IEABP %cjQ8pW>% v]D+|c=!GO:0005768IEACC<!GO:0005623IEACC;!GO:0005575IEACC:!GO:0005622IEACC9!GO:0005737IEACC8!GO:0010008IEACC7!GO:0005769IEACC6!GO:0044763IEABP5!GO:0044699IEABP4!GO:0009987IEABP3!GO:0008150IEABP2!GO:0007154IEABP1!GO:0060089IEAMF0!GO:0016818IEAMF/!GO:0016817IEAMF.!GO:0016787IEAMF-!GO:0016462IEAMF,!GO:0017111IEAMF+!GO:0003824IEAMF*!GO:0043168IEAMF)!GO:0043167IEAMF(!GO:0035639IEAMF'!GO:0032561IEAMF&!GO:0032555IEAMF%!GO:0032553IEAMF$!GO:0032550IEAMF#!GO:0032549IEAMF"!GO:0017076IEAMF!!GO:0001883IEAMF !GO:0001882IEAMF!GO:1901363IEAMF!GO:1901265IEAMF!GO:0097159IEAMF!GO:0036094IEAMF!GO:0005488IEAMF!GO:0003674IEAMF!GO:0019001IEAMF %cjQ8pW>% v]D+|cb!GO:0044464IEACCa!GO:0044444IEACC`!GO:0044424IEACC_!GO:0043229IEACC^!GO:0043227IEACC]!GO:0043226IEACC\!GO:0043231IEACC[!GO:0005623IEACCZ!GO:0005575IEACCY!GO:0005622IEACCX!GO:0005737IEACCW!GO:0005739IEACCV!GO:1901981IEAMFU!GO:0019902IEAMFT!GO:0019899IEAMFS!GO:0043168IEAMFR!GO:0043167IEAMFQ!GO:0008289IEAMFP!GO:0005543IEAMFO!GO:0005488IEAMFN!GO:0003674IEAMFM!GO:0032266IEAMFL!GO:0019903IEAMFK!GO:0005515IEAMFJ!GO:0035091IEAMFI!GO:0044446IEACCH!GO:0044440IEACCG!GO:0044422IEACCF!GO:0031090IEACCE!GO:0016020IEACCD!GO:0044464IEACCC!GO:0044444IEACCB!GO:0044424IEACCA!GO:0043229IEACC@!GO:0043227IEACC?!GO:0043226IEACC>!GO:0043231IEACC %cjQ8pW>% v]D+|c!GO:0043234IEACC!GO:0032991IEACC!GO:0044446IEACC!GO:0044430IEACC!GO:0044422IEACC!GO:0043232IEACC!GO:0043229IEACC!GO:0043228IEACC!GO:0043226IEACC~!GO:0015630IEACC}!GO:0044464IEACC|!GO:0044424IEACC{!GO:0005623IEACCz!GO:0005575IEACCy!GO:0005622IEACCx!GO:0008274IEACCw!GO:0005856IEACCv!GO:0005819IEACCu!GO:0005815IEACCt!GO:0005813IEACCs!GO:0005737IEACCr!GO:0070727IEABPq!GO:0051641IEABPp!GO:0051179IEABPo!GO:0044763IEABPn!GO:0044699IEABPm!GO:0034629IEABPl!GO:0034613IEABPk!GO:0033036IEABPj!GO:0031503IEABPi!GO:0009987IEABPh!GO:0008150IEABPg!GO:0008104IEABPf!GO:0033566IEABPe!GO:0005488IEAMFd!GO:0003674IEAMFc!GO:0005515IEAMF %cjQ8pW>% v]D+|c,!GO:0009057IEABP+!GO:0009056IEABP*!GO:0006511IEABP)!GO:0051603IEABP(!GO:0006508IEABP'!GO:0019941IEABP&!GO:0071704IEABP%!GO:0070647IEABP$!GO:0044267IEABP#!GO:0044260IEABP"!GO:0044238IEABP!!GO:0044237IEABP !GO:0043412IEABP!GO:0043170IEABP!GO:0036211IEABP!GO:0032446IEABP!GO:0019538IEABP!GO:0009987IEABP!GO:0008150IEABP!GO:0006464IEABP!GO:0008152IEABP!GO:0006513IEABP!GO:0030163IEABP!GO:0045116IEABP!GO:0043161IEABP!GO:0031146IEABP!GO:0016567IEABP!GO:0003824IEAMF!GO:0003674IEAMF!GO:0016874IEAMF!GO:0005488IEAMF !GO:0003674IEAMF !GO:0005515IEAMF !GO:0044450IEACC !GO:0044444IEACC !GO:0000931IEACC!GO:0000930IEACC %cjQ8pW>% v]D+|cQ!GO:0003824IEAMFP!GO:0046914IEAMFO!GO:0043169IEAMFN!GO:0043167IEAMFM!GO:0005488IEAMFL!GO:0003674IEAMFK!GO:0031625IEAMFJ!GO:0005515IEAMFI!GO:0019788IEAMFH!GO:0004842IEAMFG!GO:0046872IEAMFF!GO:0008270IEAMFE!GO:0044444IEACCD!GO:0005737IEACCC!GO:0080008IEACCB!GO:0044464IEACCA!GO:0044424IEACC@!GO:0043234IEACC?!GO:0032991IEACC>!GO:0005623IEACC=!GO:0005575IEACC<!GO:0005622IEACC;!GO:0000151IEACC:!GO:0031461IEACC9!GO:0031462IEACC8!GO:0031466IEACC7!GO:0005829IEACC6!GO:0031465IEACC5!GO:0031464IEACC4!GO:0031463IEACC3!GO:0019005IEACC2!GO:1901575IEABP1!GO:0044265IEABP0!GO:0044257IEABP/!GO:0044248IEABP.!GO:0043632IEABP-!GO:0010498IEABP %cjQ8pW>% v]D+|cv!GO:0032991IEACCu!GO:0015630IEACCt!GO:0015629IEACCs!GO:0005875IEACCr!GO:0005856IEACCq!GO:0005623IEACCp!GO:0005575IEACCo!GO:0005622IEACCn!GO:0005813IEACCm!GO:0005869IEACCl!GO:0043169IEAMFk!GO:0043167IEAMFj!GO:0005488IEAMFi!GO:0003674IEAMFh!GO:0046872IEAMFg!GO:0065008IEABPf!GO:0065007IEABPe!GO:0055082IEABPd!GO:0055080IEABPc!GO:0055065IEABPb!GO:0048878IEABPa!GO:0050801IEABP`!GO:0044763IEABP_!GO:0044699IEABP^!GO:0042592IEABP]!GO:0030003IEABP\!GO:0019725IEABP[!GO:0009987IEABPZ!GO:0008150IEABPY!GO:0006873IEABPX!GO:0006875IEABPW!GO:0044389IEAMFV!GO:0019899IEAMFU!GO:0019787IEAMFT!GO:0016881IEAMFS!GO:0016879IEAMFR!GO:0016874IEAMF %cjQ8pW>% v]D+|c!GO:0005575IEACC!GO:0005840IEACC!GO:0005622IEACC!GO:1901576IEABP!GO:0071704IEABP!GO:0044267IEABP!GO:0044260IEABP!GO:0044249IEABP!GO:0044238IEABP!GO:0044237IEABP!GO:0043170IEABP!GO:0034645IEABP!GO:0019538IEABP!GO:0010467IEABP !GO:0009987IEABP !GO:0009059IEABP !GO:0009058IEABP !GO:0008150IEABP !GO:0008152IEABP!GO:0006412IEABP!GO:0005488IEAMF!GO:0005515IEAMF!GO:0003824IEAMF!GO:0003674IEAMF!GO:0045502IEAMF!GO:0016740IEAMF!GO:0005815IEACC!GO:0044464IEACC!GO:0044446IEACC~!GO:0044430IEACC}!GO:0044424IEACC|!GO:0044422IEACC{!GO:0043234IEACCz!GO:0043232IEACCy!GO:0043229IEACCx!GO:0043228IEACCw!GO:0043226IEACC %cjQ8pW>% v]D+|c@!GO:0071840IEABP?!GO:0071822IEABP>!GO:0070271IEABP=!GO:0065003IEABP<!GO:0044763IEABP;!GO:0044699IEABP:!GO:0044085IEABP9!GO:0043933IEABP8!GO:0043623IEABP7!GO:0034622IEABP6!GO:0016043IEABP5!GO:0022607IEABP4!GO:0009987IEABP3!GO:0008150IEABP2!GO:0007005IEABP1!GO:0006996IEABP0!GO:0006461IEABP/!GO:0097250IEABP.!GO:1901363IEAMF-!GO:0097159IEAMF,!GO:0005488IEAMF+!GO:0003676IEAMF*!GO:0005198IEAMF)!GO:0003674IEAMF(!GO:0003723IEAMF'!GO:0003735IEAMF&!GO:0044444IEACC%!GO:0044424IEACC$!GO:0043232IEACC#!GO:0043229IEACC"!GO:0043228IEACC!!GO:0043226IEACC !GO:0032991IEACC!GO:0005737IEACC!GO:0030529IEACC!GO:0044464IEACC!GO:0005623IEACClhMhntz "(.4:@FLRX^djpv| $*06<BHNTZ`flrx~j4Y~#Hm7\&Kp:?d .SxBg 1V{ Ej4Y~#Hm7\&Kp:_)Ns=b , Q v  @e /TyCh 2W|!Fk5 Z!"$#I$n%&8']()'*L+q,-;.`/0*1O2t34>5c67-8R9w:;A/?S@wAB?CcDE+FOGsHI;J_KL' %cjQ8pW>% v]D+|ce!GO:0005623IEACCd!GO:0030529IEACCc!GO:0005575IEACCb!GO:0005622IEACCa!GO:0005634IEACC`!GO:0005737IEACC_!GO:0005689IEACC^!GO:0051540IEAMF]!GO:0005488IEAMF\!GO:0003674IEAMF[!GO:0005198IEAMFZ!GO:0051536IEAMFY!GO:0071840IEABPX!GO:0044085IEABPW!GO:0031163IEABPV!GO:0016043IEABPU!GO:0022607IEABPT!GO:0009058IEABPS!GO:0008150IEABPR!GO:0008152IEABPQ!GO:0016226IEABPP!GO:0044464IEACCO!GO:0044444IEACCN!GO:0044424IEACCM!GO:0043229IEACCL!GO:0043227IEACCK!GO:0043226IEACCJ!GO:0043231IEACCI!GO:0005737IEACCH!GO:0005623IEACCG!GO:0005622IEACCF!GO:0044425IEACCE!GO:0031224IEACCD!GO:0005575IEACCC!GO:0016020IEACCB!GO:0005739IEACCA!GO:0016021IEACC %cjQ8pW>% v]D+|c ! GO:0050794IEABP ! GO:0050789IEABP! GO:0044763IEABP! GO:0044700IEABP! GO:0044699IEABP! GO:0023052IEABP! GO:0009987IEABP! GO:0007154IEABP! GO:0035556IEABP! GO:0007165IEABP! GO:0071702IEABP! GO:0051234IEABP~! GO:0051179IEABP}! GO:0045184IEABP|! GO:0033036IEABP{! GO:0008150IEABPz! GO:0006810IEABPy! GO:0008104IEABPx! GO:0007186IEABPw! GO:0006886IEABPv! GO:0043001IEABPu! GO:0042147IEABPt! GO:0034067IEABPs! GO:0007369IEABPr! GO:0007264IEABPq! GO:0015031IEABPp!GO:0044464IEACCo!GO:0044446IEACCn!GO:0044428IEACCm!GO:0044424IEACCl!GO:0044422IEACCk!GO:0043229IEACCj!GO:0043227IEACCi!GO:0043226IEACCh!GO:0032991IEACCg!GO:0043231IEACCf!GO:0005681IEACC %cjQ8pW>% v]D+|c/! GO:0043226IEACC.! GO:0043231IEACC-! GO:0044464IEACC,! GO:0005623IEACC+! GO:0005575IEACC*! GO:0016020IEACC)! GO:0005802IEACC(! GO:0005794IEACC'! GO:0005737IEACC&! GO:0005634IEACC%! GO:0005622IEACC$! GO:0007166IEABP#! GO:0048193IEABP"! GO:0016482IEABP!! GO:0006893IEABP ! GO:0006892IEABP! GO:0051649IEABP! GO:0046907IEABP! GO:0044765IEABP! GO:0016197IEABP! GO:0016192IEABP! GO:0070727IEABP! GO:0051641IEABP! GO:0034613IEABP! GO:0033365IEABP! GO:0048856IEABP! GO:0048598IEABP! GO:0044767IEABP! GO:0044707IEABP! GO:0032502IEABP! GO:0032501IEABP! GO:0009790IEABP! GO:0009653IEABP! GO:0007275IEABP ! GO:0065007IEABP ! GO:0051716IEABP ! GO:0050896IEABP %cjQ8pW>% v]D+|cT!!GO:0044425IEACCS!!GO:0031224IEACCR!!GO:0016020IEACCQ!!GO:0005575IEACCP!!GO:0016021IEACCO!!GO:0051234IEABPN!!GO:0051179IEABPM!!GO:0008150IEABPL!!GO:0016192IEABPK!!GO:0006810IEABPJ! GO:0060089IEAMFI! GO:0043168IEAMFH! GO:0043167IEAMFG! GO:0035639IEAMFF! GO:0032561IEAMFE! GO:0032555IEAMFD! GO:0032553IEAMFC! GO:0032550IEAMFB! GO:0032549IEAMFA! GO:0017076IEAMF@! GO:0001883IEAMF?! GO:0001882IEAMF>! GO:1901363IEAMF=! GO:1901265IEAMF<! GO:0097159IEAMF;! GO:0036094IEAMF:! GO:0005488IEAMF9! GO:0003674IEAMF8! GO:0005515IEAMF7! GO:0019001IEAMF6! GO:0004871IEAMF5! GO:0005525IEAMF4! GO:0000166IEAMF3! GO:0044444IEACC2! GO:0044424IEACC1! GO:0043229IEACC0! GO:0043227IEACC %cjQ8pW>% v]D+|cy!"GO:0044422IEACCx!"GO:0044391IEACCw!"GO:0022626IEACCv!"GO:0015934IEACCu!"GO:0005829IEACCt!"GO:0044444IEACCs!"GO:0044424IEACCr!"GO:0043232IEACCq!"GO:0043229IEACCp!"GO:0043228IEACCo!"GO:0043226IEACCn!"GO:0032991IEACCm!"GO:0005737IEACCl!"GO:0030529IEACCk!"GO:0044464IEACCj!"GO:0005623IEACCi!"GO:0005575IEACCh!"GO:0022625IEACCg!"GO:0005840IEACCf!"GO:0005622IEACCe!"GO:1901576IEABPd!"GO:0071704IEABPc!"GO:0044267IEABPb!"GO:0044260IEABPa!"GO:0044249IEABP`!"GO:0044238IEABP_!"GO:0044237IEABP^!"GO:0043170IEABP]!"GO:0034645IEABP\!"GO:0019538IEABP[!"GO:0010467IEABPZ!"GO:0009987IEABPY!"GO:0009059IEABPX!"GO:0009058IEABPW!"GO:0008150IEABPV!"GO:0008152IEABPU!"GO:0006412IEABP %cjQ8pW>% 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(08@HPX`hpxBPSBBPSCBPSDBPSEBPSFBPSGBPSHBPSIBPSJBPSKBPSLBPSMBPSNBPSOBPSPBPSQBPSRBPSSBPSTBPSUBPSVBPSWBPSXBPSYBPSZBPS[BPS\BPS]BPS^BPS_BPS`BPSaBPSbBPScBPSdBPSeBPSfBPSgBPShBPSiBPSjBPSkBPSlBPSmBPSnBPSoBPSpBPSqBPSrBPSsBPStBPSuBPSvBPSwBPSxBPSyBPSBPSBPSBPSBPSBPSBPSBPSBPSBPSBPSBPTBPTBPTBPTBPTBPTBPTBPTBPT BPT!BPT"BPT#BPT$BPT%BPT&BPT'BPT(BPT)BPT*BPT+BPT,BPT-BPT.BPT/BPT0BPT1BPT2BPT3BPT4BPT5BPT6BPT7BPT8BPT9 e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxBPT;BPT<BPT=BPT>BPT?BPT@BPTABPTBBPTCBPTDBPTEBPTFBPTGBPTHBPTIBPTJBPTKBPTLBPThBPTiBPTjBPTkBPTlBPTmBPTnBPToBPTpBPTqBPTrBPTsBPTtBPTuBPTvBPTwBPTxBPTyBPTzBPT{BPT|BPT}BPT~BPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPTBPUBPUBPUBPU BPU BPU BPU BPU BPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPU e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxBPUBPUBPUBPUBPUBPUBPU BPU!BPU"BPU#BPU$BPU%BPU&BPU'BPU(BPU)BPU*BPU+BPU,BPU-BPU.BPU/BPU0BPU1BPU2BPU3BPU4BPU5BPU6BPU7BPU8BPU9BPU:BPU;BPU<BPU=BPU>BPU?BPU@BPUABPUBBPUCBPUDBPUEBPUFBPUGBPUHBPUIBPUJBPUKBPULBPUMBPUNBPUOBPUPBPUQBPURBPUSBPUTBPUUBPUVBPUWBPUXBPUYBPUZBPU[BPU\BPU]BPU^BPU_BPU`BPUaBPUbBPUcBPUdBPUeBPUfBPUgBPUhBPUiBPUjBPUkBPUlBPUmBPUnBPUoBPUpBPUqBPUrBPUsBPUtBPUuBPUvBPUwBPUxBPUyBPUzBPU{BPU|BPU}BPU~ e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPUBPVBPVBPVBPVBPVBPVBPVBPVBPVBPV BPV BPV BPV BPV BPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPV@BPVABPVBBPVCBPVDBPVEBPVFBPVGBPVH e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxBPVJBPVKBPVLBPVMBPVNBPVOBPVPBPVQBPVRBPVSBPVTBPVUBPVVBPVWBPVXBPVYBPVZBPV[BPV\BPV]BPV^BPV_BPV`BPVaBPVbBPVcBPVdBPVeBPVfBPVgBPVhBPViBPVjBPVkBPVlBPVmBPVnBPVoBPVpBPVqBPVrBPVsBPVtBPVuBPVvBPVwBPVxBPVyBPVzBPV{BPV|BPV}BPV~BPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPV e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxBPVBPVBPVBPVBPVBPVBPVBPVBPVBPVBPWBPWBPWBPWBPWBPWBPWBPWBPWBPW BPW BPW BPW-BPW.BPW/BPW0BPW1BPW2BPW3BPW4BPW5BPW6BPW7BPW8BPW9BPW:BPW;BPW<BPW=BPW>BPW?BPW@BPWABPWBBPWCBPWDBPWEBPWFBPWGBPWHBPWIBPWJBPWKBPWLBPW[BPW\BPW]BPW^BPW_BPW`BPWaBPWbBPWcBPWdBPWeBPWfBPWgBPWhBPWiBPWjBPWkBPWlBPWmBPWnBPWoBPWpBPWqBPWrBPWsBPWtBPWuBPWvBPWwBPWxBPWyBPWzBPW{BPW|BPW}BPW~BPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPW e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPWBPXBPXBPXBPXBPXBPXBPXBPXBPXBPX BPX BPX BPX BPX BPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXRBPXSBPXT e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxBPXVBPXWBPXXBPXYBPXZBPX[BPX\BPX]BPX^BPX_BPX`BPXaBPXbBPXcBPXdBPXeBPXfBPXgBPXhBPXiBPXjBPXkBPXlBPXmBPXnBPXoBPXpBPXqBPXrBPXsBPXtBPXuBPXvBPXwBPXxBPXyBPXzBPX{BPX|BPX}BPX~BPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPX e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPXBPYBPYBPYBPYBPYBPYBPYBPYLBPYMBPYNBPYOBPYPBPYQBPYRBPYSBPYTBPYUBPYVBPYWBPYXBPYYBPYZBPY[BPY\BPY]BPY^BPY_BPY`BPYaBPYbBPYcBPYdBPYeBPYfBPYgBPYhBPYiBPYjBPYkBPYlBPYmBPYnBPYoBPYpBPYqBPYr e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxBPYtBPYuBPYvBPYwBPYxBPYyBPYzBPY{BPY|BPY}BPY~BPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPYBPZBPZBPZBPZBPZBPZ e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxBPZBPZBPZBPZBPZBPZBPZBPZBPZ BPZ!BPZ"BPZ#BPZ$BPZ%BPZ&BPZ'BPZ(BPZ)BPZ*BPZ+BPZ,BPZ-BPZ.BPZ/BPZ0BPZ1BPZ2BPZ3BPZ4BPZ5BPZ6BPZ7BPZaBPZbBPZcBPZdBPZeBPZfBPZgBPZhBPZiBPZjBPZkBPZlBPZmBPZnBPZoBPZpBPZqBPZrBPZsBPZtBPZuBPZvBPZwBPZxBPZyBPZzBPZ{BPZ|BPZ}BPZ~BPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZ e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBPZBP[BP[BP[BP[BP[BP[BP[BP[BP[BP[BP[BP[BP[ BP[!BP["BP[#BP[$BP[%BP[&BP['BP[(BP[)BP[*BP[+BP[,BP[-BP[. e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxBP[0BP[1BP[2BP[3BP[4BP[5BP[6CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC CC CC CC CC CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC CC!CC"CC#CC$CC%CC&CC'CC(CC)CC*CC+CC,CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC CC CC CC CC CCCCCCCCCCCCCC e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC CC CC CC CC7CC8CC9CC:CC;CC<CC=CC>CC?CC@CCACCBCCCCCDCCECCFCCG e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCCICCJCCKCCLCCMCCNCCOCCiCCjCCkCClCCmCCnCCoCCpCCqCC$CC%CC&CC'CCCCCC CC!CC"CC#CC$CC%CC&CC'CC(CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC !CC "CC #CC $CC %CC &CC 'CC (CC )CC *CC +CC ,CC - e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCC /CC 0CC 1CC CC CC CC CC CC CC CC CC CC CC :CC ;CC <CC =CC >CC ?CC @CC ACC BCC CCC DCC ECC FCC GCC HCC ICC JCC KCC LCC MCC NCC OCC PCC QCC RCC SCC TCC UCC VCC WCC XCC YCC ZCC [CC \CC ]CC ^CC _CC `CC aCC bCC cCC dCC eCC fCC gCC hCC iCC jCC kCC lCC mCC nCC oCC pCC qCC rCC sCC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC H  $0<HT`lx ,8DP\ht(4@LXdp| >CC @CC ACC BCC} CCC DCC3 ECC FCC GCC HCC ICC H JCC# KCC%0 LCC& MCC's NCC( OCC* PCC, QCC.A RCC/[ SCC0 TCC2 UCC4 VCC5 WCC6 XCC8B YCC9D ZCC:f [CC; \CC=u ]CC?[ ^CC@ _CCB `CCD$ aCCE^ bCCF cCCGw dCCIK eCCKg fCCM gCCN hCCP iCCQ jCCS kCCTS lCCU mCCW( nCCY oCC[E pMF/ qMF^ rMF X sMF ^ tMF uMF vMF< wMF xMF yMFw zMF {MF |MF"c }MF$1 ~MF& MF( MF+1 MF. MF1 MF4f MF6 MF8 MF: e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC !CC "CC #CC $CC %CC &CC 'CC (CC )CC *CC +CC ,CC -CC .CC /CC 0CC 1CC 2CC 3CC 4CC 5CC 6CC 7CC 8CC 9CC :CC ;CC <CC =CC >CC ?CC @CC ACC BCC CCC DCC ECC FCC GCC HCC ICC JCC {CC |CC }CC ~CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CCCCCCCCCC.CC/CC0CC1CC2CC3CC4CC5CC6CC7CC8CC9CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC)CC*CC+CC,CC-CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCqCCrCCsCCtCCuCCvCCwCCxCCyCCzCC{CC| e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCC~CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC CC CC CC>CC?CC@CCACCBCCCCCDCCECCFCCGCCHCCICCJCCKCCLCCMCCNCCOCCPCCQCCRCCSCCTCCUCCVCCWCCXCCYCCZCC[CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCCCCCCCCCCCCCC CC CC CC CC CCCCCCCCCCCCCCCCCCCCCCCC!CC"CC#CC$CC%CC&CC'CC(CC)CC*CC+CC,CC-CC.CC/CC0CC1CC2CC3CC4CC5CC6CC7CC8CC%CC&CC'CC(CC)CC*CC+CC,CC-CC.CC]CC^CC_CC`CCaCCbCCcCCdCCeCCfCCgCChCCiCCjCCkCClCCmCCnCCoCCpCCqCCrCCsCCtCCuCCvCCwCCxCCyCCzCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCC4CC5CC6CC7CC8CC9CC:CC;CC<CC=CC>CC?CC@CCACCBCCCCCDCCECCFCCGCCHCCfCCgCChCCiCCjCCkCClCCmCCnCCoCCpCCqCCrCCsCCtCCuCCvCCwCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC"CC#CC$CC%CC&CC'CC(CC)CC*CC+CC,CC-CCCCCCCCCCCCCCCC e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCCCCCCCCCCCC2CC3CC4CC5CC6CC7CC8CC9CC:CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC;CC<CC=CC>CC?CC@CCACCBCCCCCDCCECCFCCGCCHCCICCJCCKCCLCCMCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC CC CC CC CC e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC CC!CChCCiCCjCCkCClCCmCCnCCoCCpCCqCCCCCCCCCCCCCCCCCCCCCC CCCCCCCCCCCCCCCCCCCClCCmCCnCCoCCpCCqCCrCCsCCtCCuCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC CC!CC"CC#CC$CC%CC&CC'CC(CC)CC*CC+CC,CC-CC.CC/CC0CC[CC\CC]CC^CC_CC`CCaCCbCCcCCdCCeCCfCCgCChCCiCCjCCkCClCCmCCnCCoCCpCCqCCrCCsCCtCCuCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCCCCCCCCyCCzCC{CC|CC}CC~CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC CC CC CC CC CC CC CC CC CC CC CC CC 9CC :CC ;CC <CC =CC >CC ?CC @CC ACC BCC CCC DCC ECC FCC G e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCC ICC JCC KCC LCC MCC NCC OCC PCC QCC mCC nCC oCC pCC qCC rCC sCC tCC uCC vCC wCC xCC yCC zCC {CC |CC }CC ~CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC!CC!CC!CC!CC!CC!CC!CC!CC!CC!CC!CC!CC!CC!CC!CC!CC"PCC"QCC"RCC"SCC"TCC"UCC"VCC"WCC"XCC"YCC"ZCC"[CC"\CC"]CC#CC# e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxCC#CC#CC#CC#CC#CC#CC#CC#ICC#JCC#KCC#LCC#MCC#NCC#OCC#PCC#QCC#RCC#SCC#TCC#UCC#VCC#WCC#XCC#YCC#ZCC#[CC#\CC#]CC#^CC#_CC#`CC#aCC#bCC#cCC#tCC#uCC#vCC#wCC#xCC$CC$CC$CC$CC$ CC$ CC$ CC$ CC$ CC$CC$CC$CC$CC$CC$CC$CC$CC$CC$CC$CC$CC$CC$CC$CC$CC$CC$CC$CC%CC%CC%CC%CC%CC%CC%CC%CC%CC%CC%CC%CC%CC%CC%CC%CC%CC%CC% CC%!CC%"CC%#CC%$CC%%CC%&CC%'CC%(CC%)CC%*CC%+CC%,CC%-CC%.CC%/ e (08@HPX`hpx (08@HPX`hpx 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Z!Z"Z#Z$Z%Z&Z'Z(Z)Z*Z+Z,Z-Z.Z/Z0Z1Z2Z3Z4Z5Z6Z7Z8Z9Z:Z;Z<Z=Z>Z?Z@ZAZBZCZDZEZFZGZHZIZJZKZLZMZNZOZPZQZRZSZTZUZVZWZXZYZZZ[Z\Z]Z^Z_Z`ZaZbZcZdZeZfZgZhZiZjZkZlZmZnZoZpZqZrZsZtZuZvZwZxZyZzZ{ e (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxZ}Z~ZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZ d (08@HPX`hpx (08@HPX`hpx (08@HPX`hpxZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZ[[[[[[[[[[ [ [ [ [ [[[[[[[[[[[[[[[[[[[ [!["[#[$[%[&['[([)[*[+[,[-[.[/[0[1[2[3[4[5[6[7[8[9[:[;[<[=[>[?[@[A[B[C[D[E[F !xph`XPH@80( [h[g[f[e[d[c[b[a[`[_[^[][\[[[Z[Y[X[W[V[U[T[S[R[Q[P[O[N[M[L[K[J[I[HAnnotationDbi/inst/extdata/org.testing.db/man/0000755000175200017520000000000014710217313022335 5ustar00biocbuildbiocbuildAnnotationDbi/inst/extdata/org.testing.db/man/org.TguttataTestingSubset.egBASE.Rd0000644000175200017520000000201414710217313030755 0ustar00biocbuildbiocbuild\name{org.TguttataTestingSubset.eg.db} \alias{org.TguttataTestingSubset.eg.db} \alias{org.TguttataTestingSubset.eg} \title{Bioconductor annotation data package} \description{ Welcome to the org.TguttataTestingSubset.eg.db annotation Package. This is an organism specific package. The purpose is to provide detailed information about the species abbreviated in the second part of the package name org.TguttataTestingSubset.eg.db. "Hs" is for Homo sapiens. This package is updated biannually. You can learn what objects this package supports with the following command: \code{ls("package:org.TguttataTestingSubset.eg.db")} Each of these objects has their own manual page detailing where relevant data was obtained along with examples of how to use it. Many of these objects also have a reverse map available. When this is true, expect to usually find relevant information on the same manual page as the forward map. } \examples{ ls("package:org.TguttataTestingSubset.eg.db") } \keyword{datasets} AnnotationDbi/inst/extdata/org.testing.db/man/org.TguttataTestingSubset.egORGANISM.Rd0000644000175200017520000000114514710217313031466 0ustar00biocbuildbiocbuild\name{org.TguttataTestingSubset.egORGANISM} \alias{org.TguttataTestingSubset.egORGANISM} \title{The Organism for org.TguttataTestingSubset.eg} \description{ org.TguttataTestingSubset.egORGANISM is an R object that contains a single item: a character string that names the organism for which org.TguttataTestingSubset.eg was built. } \details{ Although the package name is suggestive of the organism for which it was built, org.TguttataTestingSubset.egORGANISM provides a simple way to programmatically extract the organism name. } \examples{ org.TguttataTestingSubset.egORGANISM } \keyword{datasets} AnnotationDbi/inst/extdata/org.testing.db/man/org.TguttataTestingSubset.eg_dbconn.Rd0000644000175200017520000000553114710217313031654 0ustar00biocbuildbiocbuild \name{org.TguttataTestingSubset.eg_dbconn} \alias{org.TguttataTestingSubset.eg_dbconn} \alias{org.TguttataTestingSubset.eg_dbfile} \alias{org.TguttataTestingSubset.eg_dbschema} \alias{org.TguttataTestingSubset.eg_dbInfo} \title{Collect information about the package annotation DB} \description{ Some convenience functions for getting a connection object to (or collecting information about) the package annotation DB. } \usage{ org.TguttataTestingSubset.eg_dbconn() org.TguttataTestingSubset.eg_dbfile() org.TguttataTestingSubset.eg_dbschema(file="", show.indices=FALSE) org.TguttataTestingSubset.eg_dbInfo() } \arguments{ \item{file}{ A connection, or a character string naming the file to print to (see the \code{file} argument of the \code{\link[base]{cat}} function for the details). } \item{show.indices}{ The CREATE INDEX statements are not shown by default. Use \code{show.indices=TRUE} to get them. } } \details{ \code{org.TguttataTestingSubset.eg_dbconn} returns a connection object to the package annotation DB. IMPORTANT: Don't call \code{\link[DBI:dbConnect]{dbDisconnect}} on the connection object returned by \code{org.TguttataTestingSubset.eg_dbconn} or you will break all the \code{\link[AnnotationDbi:AnnDbObj-class]{AnnDbObj}} objects defined in this package! \code{org.TguttataTestingSubset.eg_dbfile} returns the path (character string) to the package annotation DB (this is an SQLite file). \code{org.TguttataTestingSubset.eg_dbschema} prints the schema definition of the package annotation DB. \code{org.TguttataTestingSubset.eg_dbInfo} prints other information about the package annotation DB. } \value{ \code{org.TguttataTestingSubset.eg_dbconn}: a DBIConnection object representing an open connection to the package annotation DB. \code{org.TguttataTestingSubset.eg_dbfile}: a character string with the path to the package annotation DB. \code{org.TguttataTestingSubset.eg_dbschema}: none (invisible \code{NULL}). \code{org.TguttataTestingSubset.eg_dbInfo}: none (invisible \code{NULL}). } \seealso{ \code{\link[DBI:dbSendQuery]{dbGetQuery}}, \code{\link[DBI:dbConnect]{dbConnect}}, \code{\link[AnnotationDbi:AnnDbObj-class]{dbconn}}, \code{\link[AnnotationDbi:AnnDbObj-class]{dbfile}}, \code{\link[AnnotationDbi:AnnDbObj-class]{dbschema}}, \code{\link[AnnotationDbi:AnnDbObj-class]{dbInfo}} } \examples{ ## Count the number of rows in the "genes" table: dbGetQuery(org.TguttataTestingSubset.eg_dbconn(), "SELECT COUNT(*) FROM genes") ## The connection object returned by org.TguttataTestingSubset.eg_dbconn() was ## created with: dbConnect(SQLite(), dbname=org.TguttataTestingSubset.eg_dbfile(), cache_size=64000, synchronous="off") org.TguttataTestingSubset.eg_dbschema() org.TguttataTestingSubset.eg_dbInfo() } \keyword{utilities} \keyword{datasets} AnnotationDbi/inst/extdata/resultTable.Rda0000644000175200017520000000123014710217313021645 0ustar00biocbuildbiocbuild r0b```b`@& `d`aEť9%!I9 @!V bL.:.v@wu 5=Gh 〆Bi*˟88ESd ,6Bυ<=q@_TΫ>p?*R:Љ|ŕx$?8 < 4ڛ;݁c_N9 9g9.$+}zþS;d޸uۤ3_.pH+s!?|iwfMZ␖^a)w!#/՛>{GQLUK7g0 ۴eY;|-yŖƚ_hk7*-=i>o-WwDݼ3W?T[ݛ/1Ţ,ǜc+]͕O\s.7%9q UZ+a_y@8R!9y05@3W\XY\ SS 1Y_lLEIYU #CK 3T3-  -,,  L ,9' WJbI^ZЇ@?vmVAnnotationDbi/inst/script/0000755000175200017520000000000014710217313016605 5ustar00biocbuildbiocbuildAnnotationDbi/inst/script/generateMultiCols.R0000644000175200017520000001653014710217313022363 0ustar00biocbuildbiocbuild## This script is used to pre-compute information about which cols() ## values have a many to one relationship with the _id cols in each ## table, and how bad that relationship is. The values are scanned ## across all the org packages and then collected into a vector so ## that they can be used by AnntoationDbi to make sensible ## recommendations about what cols() a user should ask for at once, or ## if multiple cols should be requested together. ## The final output is a named integer vector. The names of this ## vector are the values for cols(). And the values of this vector is ## a number that represents the max value ever seen for any given ## field, and the names are the names used by cols(). So this number ## is meant to be an indicator for how bad something can be when ## cols() is used. ## If cols() indicates potential danger, then the plan is to message() ## the user (or use warning("",immediately=TRUE)) and tell them that ## what they are doing is going to maybe take a long time. Hervé has ## suggested that I could just use count() at the front of the same ## query and just pre-call that to get a message that tells them how ## bad it is (so that they can escape if they wish). Paul asked me to ## add a parameter (in that case) so that users who know what they are ## doing can switch that safety off. Martin mentioned that being able ## to hit Ctrl-C is probably sufficient. I agree with Martin in this ## case. ############################################################################## ## ACK Combinatorics! ############################################################################## ## As for the actual problem. I am just going to put together a ## hand-made blacklist of cols that I know have many to one ## relationships based on this script here. This script will just ## learn which fields do that (not try to rate them). ## Then if the user uses more than a few of them, I will issue a ## warning as described above... The test can trap this warning maybe ## to make sure it goes out? ## So lets just do it for HUMAN ## library(org.Hs.eg.db) ## x <- org.Hs.eg.db getManyToOneStatus <- function(x){ cols <- cols(x) testManyToOne <- function(c, x){ k <- keys(x,"ENTREZID") res <- select(x, cols=c, keys=k, keytype="ENTREZID") if(length(unique(res[["ENTREZID"]])) < length(res[["ENTREZID"]])){ return(TRUE) }else{ return(FALSE) } } res <- unlist(lapply(cols, testManyToOne, x)) names(res) <- cols res } ## Tests ## This should be TRUE ## testManyToOne("PFAM", x) ## This should be FALSE: ## testManyToOne("SYMBOL", x) ## res <- getManyToOneStatus(x) ## so then do the above for all the org packages. require("org.Hs.eg.db") require("org.Mm.eg.db") require("org.At.tair.db") require("org.Bt.eg.db") require("org.Cf.eg.db") require("org.Gg.eg.db") require("org.Dm.eg.db") require("org.Rn.eg.db") require("org.Ce.eg.db") require("org.Xl.eg.db") require("org.Sc.sgd.db") require("org.Ss.eg.db") require("org.Dr.eg.db") require("org.EcK12.eg.db") require("org.EcSakai.eg.db") pkgs <- c(org.Hs.eg.db, org.Mm.eg.db, ## org.At.tair.db, ## exclude b/c tair is (atypical) org.Bt.eg.db, org.Cf.eg.db, org.Gg.eg.db, org.Dm.eg.db, org.Rn.eg.db, org.Ce.eg.db, org.Xl.eg.db, ## org.Sc.sgd.db, ## There is a problem with this one. org.Ss.eg.db, org.Dr.eg.db, org.EcK12.eg.db, org.EcSakai.eg.db) res <- lapply(pkgs, getManyToOneStatus) many2Ones = res save(many2Ones, file="many2Ones.Rda") ## then combine all these vectors into one vector. We want to have ## the vectors added together and then call unique, but we ALSO want ## to give preference to things being TRUE. So if you are true for ## one, you are always true from then on... ## So we just do this to sort so that the trues are in front (and will ## get grabbed by the final filtering) blackList <- sort(unlist(res), decreasing=TRUE) ## And then we call unique (which grabs the ones it sees 1st) blackList <- blackList[unique(names(blackList))] ## Then we just keep the ones that are marked as TRUE. blackList <- names(blackList[blackList]) ## and save it... save(blackList, file="manyToOneBlackList.Rda") ## TROUBLESHOOTING THE strange yeast issue: ### problem with yeast is just this one: ## x <- org.Sc.sgd.db ## k <- keys(x,"ENTREZID") ## debug(AnnotationDbi:::.select) ## debug(AnnotationDbi:::.extractData) ## res <- select(x, cols="ORF", keys=k, keytype="ENTREZID") ## gives us this: ## SELECT genes.gene_id,gene2systematic.systematic_name,sgd.sgd_id FROM genes LEFT JOIN gene2systematic USING ( systematic_name ) LEFT JOIN sgd USING ( systematic_name ); ## plus a huge where clause like WHERE genes.gene_id in ( '9164990','9 ## and this here ## res <- select(x, cols="COMMON", keys=k, keytype="ENTREZID") ## give us this: ## SELECT genes.gene_id,gene2systematic.gene_name,sgd.sgd_id FROM genes LEFT JOIN gene2systematic USING ( systematic_name ) LEFT JOIN sgd USING ( systematic_name ); ## which has the same problem (a bad join) ## OK, so I have a couple options: ## 1) add _id to gene2systematic and then simplify code ## BUT problem with adding _id is just that some of the rows will not ## have one? So: does that matter? would those rows EVER be joined ## in any meaningful way? It turns out that only in the context of ## keys() is that information worth anything. IOW you can't link it ## to anything, because the sgd table doesn't have rows where there ## isn't an _id. Is that true? - NO! Look at this (for example): ## select * from gene2systematic LEFT JOIN sgd USING (systematic_name) WHERE systematic_name IN ('AIP5','AGS1'); ## output shows that AIP5 has a _id and an sgd_id, so these exist for ## many of the systematic_name values even if they are not represented ## by a gene_name... ## AND actually: ALL of the systematic_name vals are in both sgd and ## gene2systematic. What are different are the gene_name vals. There ## are 10960 distinct gene names in gene2systematic but only 5872 of ## those are associated in sgd with an _id or a sgd id etc. ## So really it's just the gene_name field that can be a problem. But ## that data is only useful in the sense of "keys", since it can only ## connect if it is associated with one of the 8699 systematic_name ## fields (or one of the _id values) ## lets test this: ## add the _id col: It should be an integer and it should be NULL by default ## ALTER TABLE gene2systematic ADD COLUMN _id INTEGER NULL; ## then add the index on this col (it can't be a primary key for this table). ## CREATE INDEX g2s_id ON gene2systematic (_id); ## then an insert: ## And actually I am going to really want an insert that looks more like this: ## INSERT INTO gene2systematic SELECT sgd._id, g2s.gene_name, g2s.systematic_name FROM gene2systematic as g2s LEFT JOIN sgd USING (systematic_name) ; ## OR (ruled this out already) ## and for the sake of completeness, lets work out #2 1st... ## 2) figure out why sgd has fewer gene_name values than ## gene2systematic (and possibly fix that / adjust code to just use ## sgd table instead of gene2systematic) ## It's because table sgd has a not null constraint on sgd. So rows ## that have a gene_name and no sgd_id are excluded. So I can't do ## this approach (or shouldn't) AnnotationDbi/inst/unitTests/0000755000175200017520000000000014710217313017303 5ustar00biocbuildbiocbuildAnnotationDbi/inst/unitTests/test_bimap.R0000644000175200017520000001255414710217313021564 0ustar00biocbuildbiocbuildrequire(org.Hs.eg.db) require(RUnit) ## map is just to represent a classic Bimap map <- org.Hs.egSYMBOL ## map2 represents an AnnotationDbMap mapping made by some other process for BC ## map2 <- new("AnnotationDbMap", AnnotDb=org.Hs.eg.db, columns="SYMBOL") map3 <- AnnotationDbi:::makeFlatBimapUsingSelect(org.Hs.eg.db, col="SYMBOL") ## And another map object expected by most other tests. map2 <- AnnotationDbi:::makeFlatBimapUsingSelect(org.Hs.eg.db, col="ONTOLOGY") ##map3 <- AnnotationDbi:::flatten(map) # molecular function, cellular component, biological process bioconcepts <- c("MF", "CC", "BP") ## test ls test_ls <- function(){ res <- ls(map) checkTrue(is.character(res)) checkTrue(length(res) > 0) checkEquals(c("1","10","100"), head(res,n=3)) res2 <- ls(map3) checkTrue(is.character(res2)) checkTrue(length(res2) > 0) checkEquals(c("1","10","100"), head(res2,n=3)) } ## test Lkeys and Rkeys test_Lkeys <- function(){ lres <- Lkeys(map) checkTrue(length(lres) >0) checkTrue(!any(is.na(lres))) checkTrue(length(lres) == length(unique(lres))) lres2 <- Lkeys(map2) checkTrue(length(lres2) >0) checkTrue(!any(is.na(lres2))) checkTrue(length(lres2) == length(unique(lres2))) } test_Rkeys <- function(){ rres <- Rkeys(map) checkTrue(length(rres) >0) checkTrue(!any(is.na(rres))) checkTrue(length(rres) == length(unique(rres))) rres2 <- Rkeys(map2) checkTrue(length(rres2) >0) checkTrue(!any(is.na(rres2))) checkTrue(length(rres2) == length(unique(rres2))) } ## test revmap (add a test now that it seems to work... test_revmap <- function(){ rmap <- revmap(map) checkTrue(rmap@direction == -1) rmap2 <- revmap(map2) checkTrue(rmap2@direction == -1) } ## test mget test_mget <- function(){ k <- c("1","2") res <- mget(k, map) checkEquals(names(res), k) checkEquals(res[[1]], "A1BG") checkTrue(length(res)==length(k)) res2 <- mget(k, map2) checkEquals(names(res2), k) checkTrue(setequal(res2[[1]], bioconcepts)) checkTrue(length(res2)==length(k)) ## reverse test kr <- c("CC","MF") res3 <- mget(kr, revmap(map2)) checkEquals(names(res3), kr) checkEquals(res3[[1]][1], "1") checkTrue(length(res3)==length(kr)) } ## test as.list test_as.list <- function(){ res <- as.list(map) checkEquals(names(res)[1], "1") checkEquals(res[[1]][1], "A1BG") checkTrue(length(res)>1000) res2 <- as.list(map2) checkEquals(names(res2)[[1]], "1") checkTrue(setequal(res2[[1]], bioconcepts)) checkTrue(length(res2)>1000) ## reverse test res3 <- as.list(revmap(map2)) checkTrue(setequal(names(res3), bioconcepts)) checkEquals(res3[[1]][1], "1") checkIdentical(length(res3), 3L) } ## test as.character test_as.character <- function(){ res <- as.character(map) checkEquals(names(res)[1], "1") checkEquals(res[[1]][1], "A1BG") res2 <- as.character(map2) checkEquals(names(res2[1:3]), rep("1", 3)) checkTrue(setequal(res2[names(res2) == "1"], bioconcepts)) ## reverse test res3 <- as.character(revmap(map2)) checkTrue(setequal(names(res3[res3 == "1"]), bioconcepts)) checkIdentical(unname(res3[1:3]), rep("1", 3)) } ## test eapply test_eapply <- function(){ res <- eapply(map, length) checkEquals(names(res)[1], "1") checkTrue(res[[1]][1] == 1) res2 <- eapply(map2, length) checkEquals(names(res2)[1], "1") checkTrue(res2[[1]][1] == 3) } ## test get test_get <- function(){ k <- "1" res <- get(k, map) checkTrue(res == "A1BG") res2 <- get(k, map2) checkTrue(setequal(res2, bioconcepts)) ## reverse test kr <- "CC" res3 <- get(kr, revmap(map2)) checkTrue(res3[[1]][1] == "1") } ## test exists test_exists <- function(){ checkTrue(exists("2", map) == TRUE) checkTrue(exists("titi", map) == FALSE) checkTrue(exists("9", map2) == TRUE) checkTrue(exists("titi", map2) == FALSE) } ## test "[[" test_dblBrackets <- function(){ res <- map[["1"]] checkTrue(res == "A1BG") res2 <- map2[["1"]] checkTrue(setequal(res2, bioconcepts)) } test_head <- function(){ res <- head(map, n=3) checkTrue( class(res) == "AnnDbBimap" ) res2 <- head(map2, n=3) ## implement Lkeys and Rkeys checkTrue( class(res2) == "data.frame" ) checkTrue( dim(res2)[1] == 3 ) checkTrue( dim(res2)[2] == 2 ) } test_tail <- function(){ res <- tail(map, n=3) checkTrue( class(res) == "AnnDbBimap" ) res2 <- tail(map2, n=3) checkTrue( class(res2) == "data.frame" ) checkTrue( dim(res2)[1] == 3 ) checkTrue( dim(res2)[2] == 2 ) } ## test "$" test_Dollar <- function(){ res <- map$"1" checkTrue(res == "A1BG") res2 <- map2$"1" checkTrue(setequal(res2, bioconcepts)) } ## test toTable as.data.frame test_toTable <- function(){ res <- toTable(map) resdf <- as.data.frame(map) checkEquals(res, resdf) checkEquals(colnames(res), c("gene_id","symbol")) checkTrue(res[1,1]==1) checkTrue(res[1,2]=="A1BG") ## So one potential issue I have is that I get the "wrong" sort of headings? ## this is largely a cosmetic issue though... res2 <- toTable(map2) resdf2 <- as.data.frame(map2) checkEquals(res2, resdf2) checkEquals(colnames(res2), c("ENTREZID","ONTOLOGY")) checkTrue(res2[1,1]==1) checkTrue( setequal(res2[res2[["ENTREZID"]]==1, "ONTOLOGY"], bioconcepts) ) } test_sample <- function(){ res <- sample(map,size=2) checkTrue(length(res)==2) checkTrue(class(res)=="list") res2 <- sample(map2,size=2) checkTrue(length(res2)==2) checkTrue(class(res2)=="list") } AnnotationDbi/inst/unitTests/test_geneCentricDbs.R0000644000175200017520000000076614710217313023355 0ustar00biocbuildbiocbuildtest_getOrgPkg_load_only <- function() { ## check that map between chip and org package works with loaded ## but not attached org package if ("package:org.Hs.eg.db" %in% search()) { detach("package:org.Hs.eg.db") on.exit(attachNamespace("org.Hs.eg.db")) } pkg <- "hgu95av2.db" env <- loadNamespace(pkg) db <- get(pkg, env) keys <- head(AnnotationDbi::keys(db)) df <- AnnotationDbi::select(db, keys, "SYMBOL") checkIdentical(c(6L, 2L), dim(df)) } AnnotationDbi/inst/unitTests/test_mapIds.R0000644000175200017520000000445114710217313021706 0ustar00biocbuildbiocbuild## unit test to just check that mapIds is behaving itself require(org.Hs.eg.db) ## constants k <- head(keys(org.Hs.eg.db, 'ENTREZID')) # trace("mapIds", tracer=browser, signature ="AnnotationDb") ### The actual tests. ## Default is currently 'first' test_mapIds_default <- function(){ res <- mapIds(org.Hs.eg.db, keys=k, column='ALIAS', keytype='ENTREZID') checkTrue(length(res) == length(k)) checkTrue(res[[1]] == "A1B") checkTrue(class(res)=='character') } ## test other return types. ## "list" test_mapIds_CharacterList <- function(){ res <- mapIds(org.Hs.eg.db, keys=k, column='ALIAS', keytype='ENTREZID', multiVals="list") checkTrue(length(res) == length(k)) checkTrue(res[[1]][1] == "A1B") checkTrue(class(res)=='list') } ## "CharacterList" test_mapIds_CharacterList <- function(){ res <- mapIds(org.Hs.eg.db, keys=k, column='ALIAS', keytype='ENTREZID', multiVals="CharacterList") checkTrue(length(res) == length(k)) checkTrue(res[[1]][1] == "A1B") checkTrue(class(res)=='SimpleCharacterList') } ## "NAMultiples" test_mapIds_NAMultiples <- function(){ res <- mapIds(org.Hs.eg.db, keys=k, column='PFAM', keytype='ENTREZID', multiVals="asNA") checkTrue(length(res) == length(k)) checkTrue(res[['10']] == "PF00797") checkTrue(class(res)=='character') res <- mapIds(org.Hs.eg.db, "2", "PFAM", "ENTREZID", multiVals = "asNA") checkTrue(is.character(res)) checkIdentical(length(res), 1L) } ## "filterMultiples" test_mapIds_filterMultiples <- function(){ res <- mapIds(org.Hs.eg.db, keys=k, column='PFAM', keytype='ENTREZID', multiVals="filter") checkTrue(length(res) < length(k)) ## multi matchers means should be shorter checkTrue(res[['10']] == "PF00797") checkTrue(res[['1']] == "PF13895") checkTrue(class(res)=='character') res <- mapIds(org.Hs.eg.db, "2", "PFAM", "ENTREZID", multiVals = "filter") checkTrue(is.character(res)) checkIdentical(length(res), 0L) } ## CUSTOM function test_mapIds_FUN <- function(){ last <- function(x){ x[[length(x)]] } res <- mapIds(org.Hs.eg.db, keys=k, column='ALIAS', keytype='ENTREZID', multiVals=last) checkTrue(length(res) == length(k)) checkTrue(res[[1]] == "A1BG") checkTrue(class(res)=='character') } AnnotationDbi/inst/unitTests/test_select.R0000644000175200017520000003774514710217313021764 0ustar00biocbuildbiocbuild## One strategy is to put some of my examples (with expected output into here) ## - but this is fragile unless I also provide a localized example DB (which I ## probably should do anyways for other reasons, but is not necessarily useful ## here). ## Another strategy is that I should probably have tests for all my helper ## functions to make sure that they are returning what is expected. ## Generally, I want to make tests for each thing that can go wrong due to ## changes elsewhere. The strategy of writing tests for the helpers will ## catch some of this, but also I need to anticipate things that will change ## in the annotations etc. ## library(AnnotationDbi);AnnotationDbi:::.test() require(RSQLite) require(org.Hs.eg.db) require(org.At.tair.db) require(org.Sc.sgd.db) require(GO.db) require(hgu95av2.db) require("RUnit") x <- org.Hs.eg.db t <- org.At.tair.db s <- org.Sc.sgd.db cols <- c("CHR","PFAM","GO") keys <- c(1,10) jointype <- "genes.gene_id" ## changed from 'gene_id' quiet <- suppressWarnings # quieten warnings from 1:many mappings in select() ## resort and friends are really important as they are generic enough to ## be reused elsewhere. test_generateExtraRows <- function(){ ttab = data.frame(warpbreaks[1:10,]) ttab$breaks <- as.character(ttab$breaks) tkeys = ttab$breaks tkeys = c(26, tkeys[1:7], tkeys[7], 30, tkeys[8:10], tkeys[10]) res <- AnnotationDbi:::.generateExtraRows(ttab, tkeys, jointype='breaks') expLen <- sum(table(tkeys) * table(ttab$breaks)) checkTrue(expLen == dim(res)[1]) } test_dropUnwantedRows <- function() { fun <- AnnotationDbi:::.dropUnwantedRows ## no duplicates, no changes keys <- letters[1:5] tab <- data.frame(x=keys, y=LETTERS[1:5], z=LETTERS[5:1], row.names=NULL) checkIdentical(tab, fun(tab, keys, "x")) ## duplicate jointype element, duplicate dropped tab1 <- tab[c(1:5, 3L),] rownames(tab1) <- NULL checkIdentical(tab, fun(tab1, keys, "x")) ## unique all NA (other than jointype column) _retained_ tab1 <- tab tab1[3, 2:3] <- NA rownames(tab1) <- NULL checkIdentical(tab1, fun(tab1, keys, "x")) ## duplicate all NA, made unique tab1 <- tab tab1[3, 2:3] <- NA tab2 <- tab1[c(1:5, 3),] checkIdentical(tab1, fun(tab2, keys, "x")) ## duplicate key, dropped keys1 <- keys[c(1:5, 3)] checkIdentical(tab, fun(tab, keys1, "x")) } test_resort <- function() { fun <- resort_base ## from AnnotationDbi ## repeat keys returned keys <- letters[1:5] tab <- data.frame(x=keys, y=LETTERS[1:5], z=LETTERS[5:1], row.names=NULL, stringsAsFactors=FALSE) keys1 <- keys[c(1:5, 1)] tab1 <- tab[c(1:5, 1),] rownames(tab1) <- NULL checkIdentical(tab1, fun(tab, keys1, "x", names(tab))) ## keys with missing values returned tab1 <- tab tab1[3, 2:3] <- NA keys1 <- tab1[["x"]] checkIdentical(tab1, fun(tab1, keys, "x", names(tab))) ## multiple keys with missing values returned tab1 <- tab[c(3,4,3,4),] tab1[c(1,3), 2:3] <- NA keys1 <- keys[c(3,4,3,4)] rownames(tab1) <- NULL checkIdentical(tab1, fun(tab1[1:2,], keys1, "x", names(tab))) cols <- c("CHR","SYMBOL", "PFAM") keys <- c(1,10) res <- AnnotationDbi:::.extractData(x, cols, keytype="ENTREZID", keys) ## jumble res to simulate trouble resRO = res[order(sort(res$genes.gene_id,decreasing=TRUE)),] reqCols <- c("genes.gene_id","chromosomes.chromosome","gene_info.symbol", "pfam.pfam_id") Rres <- fun(resRO, keys, jointype, reqCols) checkIdentical(Rres$gene_id,Rres$gene_id) checkTrue(class(Rres) =="data.frame") ## now what if we have MORE keys? keys <- c(1, keys, keys) cols <- c("CHR","SYMBOL") res <- AnnotationDbi:::.extractData(x, cols, keytype="ENTREZID", keys) reqCols <- c("genes.gene_id","chromosomes.chromosome","gene_info.symbol") res2 <- fun(res, keys, jointype, reqCols) checkIdentical(as.numeric(as.character(res2$genes.gene_id)),keys) checkTrue(class(res) =="data.frame") } test_keytypes <- function(){ checkTrue("ENTREZID" %in% keytypes(x)) checkTrue("TAIR" %in% keytypes(t)) checkTrue("ENTREZID" %in% keytypes(t)) checkTrue("ORF" %in% keytypes(s)) checkTrue("ENTREZID" %in% keytypes(s)) } test_keys <- function(){ checkException(keys(org.Hs.eg.db, keytype="PROBEID")) egHskeys <- as.numeric(head(keys(x))) checkTrue(length(egHskeys[!is.na(egHskeys)])==6) rsHskeys <- head(keys(x, "REFSEQ")) checkTrue(any(grepl("N", rsHskeys))) egAtkeys <- as.numeric(head(keys(t,"ENTREZID"))) checkTrue(length(egAtkeys[!is.na(egAtkeys)])==6) rsAtkeys <- head(keys(t, "REFSEQ")) checkTrue(any(grepl("N", rsAtkeys))) tairAtkeys <- head(keys(t, "TAIR")) checkTrue(any(grepl("AT", tairAtkeys))) egSckeys <- as.numeric(head(keys(s, "ENTREZID"))) checkTrue(length(egSckeys[!is.na(egSckeys)])==6) rsSckeys <- head(keys(s, "REFSEQ")) checkTrue(any(grepl("N", rsSckeys))) orfSckeys <- head(keys(s, "ORF")) checkTrue(any(grepl("A", orfSckeys))) } test_keys_advancedArgs <- function(){ k1 <- keys(x, keytype="SYMBOL") checkTrue("A1BG" %in% k1) k2 <- keys(x, keytype="SYMBOL", pattern="BRCA") checkTrue("BRCA1" %in% k2) checkTrue(!("A1BG" %in% k2)) checkTrue(length(k2) < length(k1)) l1 <- length(keys(x, keytype="ENTREZID", column="PATH")) l2 <- length(keys(x, keytype="ENTREZID")) checkTrue(l1 < l2) k3 <- keys(x,keytype="ENTREZID",pattern="^MSX",column="SYMBOL") res <- select(x, k3, c("ENTREZID","SYMBOL"), "ENTREZID") checkTrue(any(grep("^MSX",res$SYMBOL))) } ######################################################################### ## These ones are to test out some real use cases... test_select1 <- function(){ keys <- head(keys(hgu95av2.db, "ALIAS"),n=2) cols <- c("SYMBOL","ENTREZID","PROBEID") res <- quiet(select(hgu95av2.db, keys, cols, keytype="ALIAS")) checkIdentical(c(3L, 4L), dim(res)) checkIdentical(c("ALIAS","SYMBOL","ENTREZID","PROBEID"), colnames(res)) } test_select2 <- function(){ keys <- head(keys(org.Hs.eg.db),n=2) cols <- c("PFAM","ENTREZID", "GO") res <- quiet(select(org.Hs.eg.db, keys, cols, keytype="ENTREZID")) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==5) checkIdentical(c("ENTREZID","PFAM","GO","EVIDENCE","ONTOLOGY"), colnames(res)) } test_select3 <- function(){ keys <- head(keys(org.Hs.eg.db,keytype="OMIM"),n=4) cols <- c("SYMBOL", "UNIPROT", "PATH") res <- quiet(select(hgu95av2.db, keys, cols, keytype="OMIM")) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==4) checkIdentical(c("OMIM","SYMBOL","UNIPROT","PATH"), colnames(res)) } test_select4 <- function(){ keys <- head(keys(org.Hs.eg.db),n=2) cols <- c("ACCNUM","REFSEQ") res <- quiet(select(org.Hs.eg.db, keys, cols)) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==3) checkIdentical(c("ENTREZID","ACCNUM","REFSEQ"), colnames(res)) } test_select5 <- function(){ keys <- head(keys(GO.db), n=4) cols <- c("TERM","ONTOLOGY","DEFINITION") res <- select(GO.db, keys, cols) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==4) checkIdentical(c("GOID","TERM","ONTOLOGY","DEFINITION"), colnames(res)) } test_select6 <- function(){ keys <- head(keys(hgu95av2.db)) cols <- c("SYMBOL","ENTREZID", "GO") ## tests for bad keys: checkException(select(hgu95av2.db, keys, cols, keytype="ENTREZID")) ## also catch bogus keytype arguments checkException(select(hgu95av2.db, keys, cols, keytype="FOO")) checkException(keys(hgu95av2.db, keytype="FOO")) } test_select7 <- function(){ cols <- c("SYMBOL","ENTREZID") ## 1st of all cols should be 1:1 cols keys <- head(keys(org.Hs.eg.db),n=3) keys <- c(1, keys, keys) res <- select(org.Hs.eg.db, keys, cols) checkTrue(class(res) =="data.frame") checkIdentical(keys, as.character(t(res$ENTREZID))) } test_select8 <- function(){ cols <- c("ENTREZID") keys <- head(keys(org.Hs.eg.db),n=3) res <- select(org.Hs.eg.db, keys, cols) checkTrue(class(res) =="data.frame") checkTrue(dim(res)[2] ==1) checkIdentical(as.character(keys), as.character(t(res$ENTREZID))) } test_select9 <- function(){ ## What about when we need to throw away extra cols? uniKeys <- head(keys(org.Hs.eg.db, keytype="UNIPROT")) cols <- c("SYMBOL", "PATH") res <- quiet(select(org.Hs.eg.db, keys=uniKeys, columns=cols, keytype="UNIPROT")) checkTrue(class(res) =="data.frame") checkTrue(dim(res)[2] ==3) checkIdentical(c("UNIPROT","SYMBOL","PATH"), colnames(res)) } test_select10 <- function(){ ## What about when we have to get data from Arabidopsis using various ## keytypes? cols <- c("SYMBOL","CHR") keys <- head(keys(t,"TAIR")) res <- quiet(select(t, keys, cols, keytype="TAIR")) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==3) checkIdentical(c("TAIR","SYMBOL","CHR"), colnames(res)) keys <- head(keys(t,"ENTREZID")) res <- quiet(select(t, keys, cols, keytype="ENTREZID")) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==3) checkIdentical(c("ENTREZID","SYMBOL","CHR"), colnames(res)) keys=head(keys(t,"REFSEQ")) res <- quiet(select(t, keys, cols , keytype="REFSEQ")) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==3) checkIdentical(c("REFSEQ","SYMBOL","CHR"), colnames(res)) } test_select11 <- function(){ ## how about different keytypes for yeast? keys <- head(keys(s, "REFSEQ")) cols <- c("CHR","PFAM") res <- quiet(select(s, keys, cols, keytype="REFSEQ")) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==3) checkIdentical(c("REFSEQ","CHR","PFAM"), colnames(res)) keys <- head(keys(s, "ENTREZID")) cols <- c("CHR","PATH") res <- quiet(select(s, keys, cols, keytype="ENTREZID")) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==3) checkIdentical(c("ENTREZID","CHR","PATH"), colnames(res)) keys <- head(keys(s, "ORF")) cols <- c("CHR","SGD") res <- select(s, keys, cols, keytype="ORF") checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==3) checkIdentical(c("ORF","CHR","SGD"), colnames(res)) ## And if you flip things the other way cols <- c("SGD","CHR") res <- select(s, keys, cols, keytype="ORF") checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==3) checkIdentical(c("ORF","SGD","CHR"), colnames(res)) ## Martins bug discoveries keys <- keys(s, keytype="GENENAME") checkTrue(length(keys) > 0) checkTrue(is.character(keys)) keys <- keys(s, keytype="CHRLOC") checkTrue(length(keys) > 0) checkTrue(is.character(keys)) res <- select(s, "YAL003W", "GENENAME") checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==3) checkIdentical(c("ORF","SGD","GENENAME"), colnames(res)) ## This works but is slow (therefore it's tested elsewhere) ## res <- select(s, keys="YAL003W", columns(s)) ## Another test to make sure we can join up to ORF properly keys <- keys(s,"ENTREZID") res <- select(s, columns="ORF", keys=keys, keytype="ENTREZID") checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==3) checkIdentical(c("ENTREZID","ORF","SGD"), colnames(res)) } test_select12 <- function(){ ## what happens when we use GO as an ID? keys <- "1" cols <- c("GO","ENTREZID") res <- quiet(select(x, keys, cols, keytype="ENTREZID")) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==4) checkIdentical(c("ENTREZID","GO","EVIDENCE","ONTOLOGY"), colnames(res)) keys <- "GO:0000018" cols <- c("GO","ENTREZID") res <- quiet(select(x, keys, cols, keytype="GO")) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==4) checkIdentical(c("GO","EVIDENCE","ONTOLOGY","ENTREZID"), colnames(res)) keys <- "GO:0000023" cols <- c("GO","ENTREZID") res <- quiet(select(t, keys, cols, keytype="GO")) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==4) checkIdentical(c("GO","EVIDENCE","ONTOLOGY","ENTREZID"), colnames(res)) keys <- "GO:0000023" cols <- c("ENTREZID","TAIR","GO") res <- quiet(select(t, keys, cols, keytype="GO")) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==5) checkIdentical(c("GO","EVIDENCE","ONTOLOGY","ENTREZID","TAIR"), colnames(res)) } test_select13 <- function(){ ## what happens with dropping unwanted rows? sym <- "ITGA7" res <- quiet(select(x, sym, "PFAM", keytype="ALIAS")) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==2) ## make sure no NAs are in res$PFAM checkTrue(length(res$PFAM)== length(res$PFAM[!is.na(res$PFAM)])) } test_select14 <- function(){ ## what happens when there are no results AT ALL? (should be all NAs) keys <- c("1001_at","1006_at","1007_s_at") res <- select(hgu95av2.db, keys, "PATH", keytype="PROBEID") checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==2) ## make sure all of res$PATH ARE NAs ## If this part fails it is a warning that the test is no longer valid, ## which would happen if some of these IDs were to be further annotated for ## PATH (unlikely since PATH is basically dead for this repos) checkTrue(length(res$PATH)== length(res$PATH[is.na(res$PATH)])) } test_select15 <- function(){ ## Another bug that seems to happen in post-processing... ## the code that resolves duplicated values is going a bit insane... ## (IOW .replaceValues()) if(!all(.Platform$OS.type == "windows", .Platform$r_arch == "i386")){ res <- select(x, keys="100008586", columns(x)) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==26) exp <- c("ENTREZID", "ACCNUM", "ALIAS", "ENSEMBL", "ENSEMBLPROT", "ENSEMBLTRANS", "ENZYME", "EVIDENCE", "EVIDENCEALL", "GENENAME", "GENETYPE", "GO", "GOALL", "IPI", "MAP", "OMIM", "ONTOLOGY", "ONTOLOGYALL", "PATH", "PFAM", "PMID", "PROSITE", "REFSEQ", "SYMBOL", "UCSCKG", "UNIPROT") checkIdentical(exp, colnames(res)) } } test_select16 <- function(){ ## What happens if we ask for probes back... ## (and pass in something else as a key) sk = c( 'MAPK3','TIE1' ) res <- select(hgu95av2.db, keys=sk, columns = c("PROBEID"), keytype="SYMBOL") checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==2) checkIdentical(c('SYMBOL','PROBEID'), colnames(res)) } ## NA values are now OK for legacySelect (in order to be consistent ## with other select methods which have greater respect for incoming NA values test_select_NAsInNAsOut <- function(){ ## NAs in should result in NAs out. ## Not that we like NAs but just because if possible: we want to ## preserve the geometry of the keys coming in. k=c('1', NA, NA, '10'); res <- select(x, k, 'SYMBOL', 'ENTREZID') checkTrue(dim(res)[1]==4) checkTrue(dim(res)[2]==2) checkIdentical(c('ENTREZID','SYMBOL'), colnames(res)) checkIdentical(k, res$ENTREZID) checkTrue(any(is.na(res$SYMBOL))) } ## Some new messages from AnnotationDbi:::.generateExtraRows() ## where I am calling it internally... ## these tests just make sure the right kinds of messages are being sent... test_select_XtoX <- function(){ k=c('1','1', NA, '10'); res <- tryCatch(select(org.Hs.eg.db, k, 'SYMBOL', 'ENTREZID'), message = function(x){return(x)}) checkTrue(grepl('many:1', res$message)) res <- tryCatch(select(org.Hs.eg.db, '1', 'ALIAS', 'ENTREZID'), message = function(x){return(x)}) checkTrue(grepl('1:many', res$message)) res <- tryCatch(select(org.Hs.eg.db, k, 'ALIAS', 'ENTREZID'), message = function(x){return(x)}) checkTrue(grepl('many:many', res$message)) res <- tryCatch(select(org.Hs.eg.db, c('1','10'), 'SYMBOL', 'ENTREZID'), message = function(x){return(x)}) checkTrue(grepl('1:1', res$message)) } ## TODO: deal with any fallout from having new messages in select() ## This will also cause me to have to silence select() in many places ## to avoid annoying repeats of the test_dbconn_and_dbfile <- function(){ resc <- dbconn(org.Hs.eg.db) m <- dbGetQuery(resc, "SELECT * FROM metadata") checkTrue(dim(m)[2] ==2) checkTrue(dim(m)[1] > 10) resf <- dbfile(org.Hs.eg.db) mf <- dbGetQuery(dbConnect(SQLite(), resf), "SELECT * FROM metadata") checkTrue(all(mf == m)) } ## Fast checking: ## BiocGenerics:::testPackage(pattern="^test_select.*\\.R$") AnnotationDbi/inst/unitTests/test_select_NOSCHEMA.R0000644000175200017520000001054214710217313023223 0ustar00biocbuildbiocbuild## this will install a testDb stashed in the ## ## this is the package name ## pkgName <- "org.testing.db" ## ## Get the package path ## pkgPath <- system.file("extdata", pkgName, package="AnnotationDbi") ## ## Then install it ## install.packages(pkgPath, repos=NULL) ## and load it #####install.packages(system.file('extdata','org.testing.db', package='AnnotationDbi'), repos=NULL) dir.create(testlib <- tempfile()) old_libPaths <- NULL .setUp <- function() { installed <- rownames(installed.packages(testlib)) if ("org.testing.db" %in% installed) return() pkg <- system.file("extdata", "org.testing.db", package="AnnotationDbi") suppressPackageStartupMessages(install.packages( pkg, lib = testlib, repos=NULL, type="source", INSTALL_opts="--no-test-load", verbose = FALSE, quiet = TRUE )) old_libPaths <<- .libPaths() .libPaths(c(testlib, old_libPaths)) finchCsomes <<- c(as.character(1:15),as.character(17:28), "MT","Un","W","Z","4A","1A","1B") finchCols <<- c("CHROMOSOME","SYMBOL","GENENAME","GID","GO","EVIDENCE", "ONTOLOGY","GOALL","EVIDENCEALL","ONTOLOGYALL") } .tearDown <- function() .libPaths(old_libPaths) ## lower level tests (more useful) test_keysLow <- function(){ x <- org.testing.db::org.testing.db res <- unique(AnnotationDbi:::.noSchemaKeys(x, "CHROMOSOME")) checkTrue(all(sort(res) == sort(finchCsomes))) } test_selectLow <- function(){ x <- org.testing.db::org.testing.db keys <- "100008579" cols <- "SYMBOL" keytype <- "GID" res <- AnnotationDbi:::.noSchemaSelect(x, keys, cols, keytype) checkTrue(all(res==c("100008579","EGR1"))) checkTrue(all(colnames(res)==c("GID","SYMBOL"))) keys <- "brain-derived neurotrophic factor" cols <- c("SYMBOL","GID") keytype <- "GENENAME" res <- AnnotationDbi:::.noSchemaSelect(x, keys, cols, keytype) checkTrue(all(res==c("brain-derived neurotrophic factor","BDNF","751584"))) checkTrue(all(colnames(res)==c("GENENAME","SYMBOL","GID"))) keys <- "brain-derived neurotrophic factor" cols <- c("GO","GID") keytype <- "GENENAME" res <- head(AnnotationDbi:::.noSchemaSelect(x, keys, cols, keytype),n=1) checkTrue(all(res==c("brain-derived neurotrophic factor","GO:0001657", "751584"))) checkTrue(all(colnames(res)==c("GENENAME","GO","GID"))) } ## high level tests (does this dispatch right etc.?) test_columns <- function(){ x <- org.testing.db::org.testing.db res <- columns(x) checkTrue(all(sort(res) == sort(finchCols))) } test_keytypes <- function(){ x <- org.testing.db::org.testing.db res <- keytypes(x) checkTrue(all(sort(res) == sort(finchCols))) } test_keys<- function(){ ## BOOM x <- org.testing.db::org.testing.db ## most basic case res <- keys(x, "CHROMOSOME") checkTrue(all(sort(res) == sort(finchCsomes))) res <- head(keys(x, "GID"), n=2) checkTrue(all(res==c("751582", "751583"))) res <- head(keys(x, "SYMBOL", pattern="BDNF")) checkTrue(res=="BDNF") res <- head(keys(x, "GID", pattern="BDNF", column="SYMBOL")) checkTrue(res=="751584") res <- head(keys(x, "SYMBOL", column="GID"),n=2) checkTrue(all(res==c("ACT5C","AHSA2"))) } test_select <- function(){ x <- org.testing.db::org.testing.db ## most basic case res <- select(x, keys="100008579", columns="SYMBOL", keytype="GID") checkTrue(all(res==c("100008579","EGR1"))) checkTrue(all(colnames(res)==c("GID","SYMBOL"))) ## return more than one column res <- select(x, keys="100008579", columns=c("SYMBOL","CHROMOSOME"), keytype="GID") checkTrue(all(res==c("100008579","EGR1","13"))) checkTrue(all(colnames(res)==c("GID","SYMBOL","CHROMOSOME"))) ## return GO and evidence codes suppressWarnings(res <- head(select(x, keys="100008579", columns=c("GO","EVIDENCE"), keytype="GID"),n=1)) checkTrue(all(res==c("100008579","GO:0000122","IEA"))) checkTrue(all(colnames(res)==c("GID","GO","EVIDENCE"))) ## test lookup from alt-key res <- select(x, keys="BDNF", columns="GENENAME", keytype="SYMBOL") checkTrue(all(res==c("BDNF","brain-derived neurotrophic factor"))) checkTrue(all(colnames(res)==c("SYMBOL","GENENAME"))) } AnnotationDbi/inst/unitTests/test_select_reactome.R0000644000175200017520000000735214710217313023632 0ustar00biocbuildbiocbuild## unit tests for methods associated with reactome.db require(reactome.db) r <- reactome.db test_cols <- function(){ res <- columns(r) checkTrue(length(res) >4) checkTrue("ENTREZID" %in% res) checkTrue("GO" %in% res) checkTrue("PATHNAME" %in% res) checkTrue("REACTOMEID" %in% res) } test_keytypes <- function(){ res <- keytypes(r) checkTrue(length(res) >4) checkTrue("ENTREZID" %in% res) checkTrue("GO" %in% res) checkTrue("PATHNAME" %in% res) checkTrue("REACTOMEID" %in% res) } test_keys <- function(){ res <- head(keys(r, keytype="ENTREZID")) checkTrue(length(res) > 0) checkTrue(length(res) == length(unique(res))) res2 <- head(keys(r, keytype="PATHNAME")) checkTrue(is.character(res2)) checkTrue(length(res2) == length(unique(res2))) } ## test function that gets table names test_getTables <- function(){ c <- c("ENTREZID", "PATHNAME") res <- AnnotationDbi:::.getTables(c, retVal="table") ##default for retVal checkTrue(length(res) ==2) checkIdentical(res, c("pathway2gene","pathway2name")) res2 <- AnnotationDbi:::.getTables(c, retVal="colname") checkTrue(length(res2) ==2) checkIdentical(res2, c("gene_id","path_name")) } ## Tests ability to get one table/query out. test_extractWithSimpleQuery <- function(){ table <- "pathway2gene" ## a table (in this case). (Could also be subquery) colType <- "gene_id" ## column we are interested in. k <- head(keys(r, keytype="ENTREZID"), n=2) res <- AnnotationDbi:::.extractWithSimpleQuery(r, table, colType, k) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==2) checkIdentical(c("DB_ID","gene_id"), colnames(res)) } ## Test ability to pull data out in vectorized fashion test_collateQueryResults <- function(){ tables <- c("pathway2gene", "reactome2go", "pathway2name") colType <- "gene_id" k <- head(keys(r, keytype="ENTREZID"), n=2) mergeID = "DB_ID" res <- AnnotationDbi:::.collateQueryResults(r, tables, colType, k, mergeID) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==4) checkIdentical(c("DB_ID","gene_id","go_id","path_name"), colnames(res)) } ## and tests for select: test_select_TYPICAL <- function(){ k <- head(keys(r, keytype="ENTREZID")) c <- c("ENTREZID","PATHNAME","GO","REACTOMEID") res <- select(r, keys=k, columns=c, keytype="ENTREZID") checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==4) checkIdentical(c("ENTREZID","PATHNAME","GO","REACTOMEID"), colnames(res)) } test_select_MISSING_EG <- function(){ k <- head(keys(r, keytype="ENTREZID")) c <- c("PATHNAME","GO") res <- select(r, keys=k, columns=c, keytype="ENTREZID") checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==3) checkIdentical(c("ENTREZID","PATHNAME","GO"), colnames(res)) } test_select_ONE_COL <- function(){ k <- head(keys(r, keytype="ENTREZID")) c <- c("ENTREZID") res <- select(r, keys=k, columns=c, keytype="ENTREZID") ## Boom no warning checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==1) checkIdentical(c("ENTREZID"), colnames(res)) } test_select_OTHERKEYTYPE <- function(){ ## This also checks if that we handle "BS keys" OK k <- head(keys(r, keytype="REACTOMEID")) k <- c(k[1:4], "109688") c <- c("ENTREZID","PATHNAME","GO") res <- select(r, keys=k, columns=c, keytype="REACTOMEID") checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==4) checkIdentical(c("REACTOMEID","ENTREZID","PATHNAME","GO"), colnames(res)) } test_select_PATHNAME <- function(){ k <- head(keys(r, "PATHNAME")) suppressWarnings(res <- select(r, k, "ENTREZID", "PATHNAME")) checkTrue(dim(res)[1]>0) checkTrue(dim(res)[2]==2) checkIdentical(c("PATHNAME","ENTREZID"), colnames(res)) } ## for convenience... ## debug(AnnotationDbi:::.selectReact) ## debug(AnnotationDbi:::.collateQueryResults) ## debug(AnnotationDbi:::.extractWithSimpleQuery) AnnotationDbi/man/0000755000175200017520000000000014710217313015077 5ustar00biocbuildbiocbuildAnnotationDbi/man/AnnDbObj-class.Rd0000644000175200017520000001222014710217313020103 0ustar00biocbuildbiocbuild\name{AnnDbObj-objects} \docType{class} \alias{AnnDbObj-objects} % Classes \alias{AnnDbObj} \alias{class:AnnDbObj} \alias{AnnDbObj-class} % Accessor-like methods \alias{dbconn} \alias{dbconn,SQLiteConnection-method} \alias{dbconn,environment-method} \alias{dbconn,AnnDbObj-method} \alias{dbfile} \alias{dbfile,SQLiteConnection-method} \alias{dbfile,environment-method} \alias{dbfile,AnnDbObj-method} \alias{dbmeta} \alias{dbmeta,DBIConnection-method} \alias{dbmeta,environment-method} \alias{dbmeta,AnnDbObj-method} \alias{dbschema} \alias{dbschema,DBIConnection-method} \alias{dbschema,environment-method} \alias{dbschema,AnnDbObj-method} \alias{dbInfo} \alias{dbInfo,DBIConnection-method} \alias{dbInfo,environment-method} \alias{dbInfo,AnnDbObj-method} \title{AnnDbObj objects} \description{ The AnnDbObj class is the most general container for storing any kind of SQLite-based annotation data. } \details{ Many classes in AnnotationDbi inherit directly or indirectly from the AnnDbObj class. One important particular case is the \link{AnnDbBimap} class which is the lowest class in the AnnDbObj hierarchy to also inherit the \link{Bimap} interface. } \section{Accessor-like methods}{ In the code snippets below, \code{x} is an AnnDbObj object. \describe{ \item{}{ \code{dbconn(x)}: Return a connection object to the SQLite DB containing \code{x}'s data. } } \describe{ \item{}{ \code{dbfile(x)}: Return the path (character string) to the SQLite DB (file) containing \code{x}'s data. } } \describe{ \item{}{ \code{dbmeta(x, name)}: Print the value of metadata whose name is 'name'. Also works if \code{x} is a DBIConnection object. } } \describe{ \item{}{ \code{dbschema(x, file="", show.indices=FALSE)}: Print the schema definition of the SQLite DB. Also works if \code{x} is a DBIConnection object. The \code{file} argument must be a connection, or a character string naming the file to print to (see the \code{file} argument of the \code{\link[base:cat]{cat}} function for the details). The CREATE INDEX statements are not shown by default. Use \code{show.indices=TRUE} to get them. } } \describe{ \item{}{ \code{dbInfo(x)}: Prints other information about the SQLite DB. Also works if \code{x} is a DBIConnection object. } } } \seealso{ \code{\link[DBI:dbConnect]{dbConnect}}, \code{\link[DBI:dbListTables]{dbListTables}}, \code{\link[DBI:dbListTables]{dbListFields}}, \code{\link[DBI:dbSendQuery]{dbGetQuery}}, \link{Bimap} } \examples{ library("hgu95av2.db") dbconn(hgu95av2ENTREZID) # same as hgu95av2_dbconn() dbfile(hgu95av2ENTREZID) # same as hgu95av2_dbfile() dbmeta(hgu95av2_dbconn(), "ORGANISM") dbmeta(hgu95av2_dbconn(), "DBSCHEMA") dbmeta(hgu95av2_dbconn(), "DBSCHEMAVERSION") library("DBI") dbListTables(hgu95av2_dbconn()) #lists all tables on connection ## If you use dbSendQuery instead of dbGetQuery ## (NOTE: for ease of use, this is defintitely NOT reccomended) ## Then you may need to know how to list results objects dbListResults(hgu95av2_dbconn()) #for listing results objects ## You can also list the fields by using this connection dbListFields(hgu95av2_dbconn(), "probes") dbListFields(hgu95av2_dbconn(), "genes") dbschema(hgu95av2ENTREZID) # same as hgu95av2_dbschema() ## According to the schema, the probes._id column references the genes._id ## column. Note that in all tables, the "_id" column is an internal id with ## no biological meaning (provided for allowing efficient joins between ## tables). ## The information about the probe to gene mapping is in probes: dbGetQuery(hgu95av2_dbconn(), "SELECT * FROM probes LIMIT 10") ## This mapping is in fact the ENTREZID map: toTable(hgu95av2ENTREZID)[1:10, ] # only relevant columns are retrieved dbInfo(hgu95av2GO) # same as hgu95av2_dbInfo() ##Advanced example: ##Sometimes you may wish to join data from across multiple databases at ##once: ## In the following example we will attach the GO database to the ## hgu95av2 database, and then grab information from separate tables ## in each database that meet a common criteria. library(hgu95av2.db) library("GO.db") attachSql <- paste('ATTACH "', GO_dbfile(), '" as go;', sep = "") dbGetQuery(hgu95av2_dbconn(), attachSql) sql <- 'SELECT DISTINCT a.go_id AS "hgu95av2.go_id", a._id AS "hgu95av2._id", g.go_id AS "GO.go_id", g._id AS "GO._id", g.term, g.ontology, g.definition FROM go_bp_all AS a, go.go_term AS g WHERE a.go_id = g.go_id LIMIT 10;' data <- dbGetQuery(hgu95av2_dbconn(), sql) data ## For illustration purposes, the internal id "_id" and the "go_id" ## from both tables is included in the output. This makes it clear ## that the "go_ids" can be used to join these tables but the internal ## ids can NOT. The internal IDs (which are always shown as _id) are ## suitable for joins within a single database, but cannot be used ## across databases. } \keyword{classes} \keyword{methods} AnnotationDbi/man/AnnDbPkg-checker.Rd0000644000175200017520000000103514710217313020413 0ustar00biocbuildbiocbuild\name{AnnDbPkg-checker} \alias{AnnDbPkg-checker} \alias{checkMAPCOUNTS} \title{Check the SQL data contained in an SQLite-based annotation package} \description{ Check the SQL data contained in an SQLite-based annotation package. } \usage{ checkMAPCOUNTS(pkgname) } \arguments{ \item{pkgname}{ The name of the SQLite-based annotation package to check. } } \author{H. Pagès} \seealso{ \code{\link[AnnotationForge:AnnDbPkg-maker]{AnnDbPkg-maker}} } \examples{ checkMAPCOUNTS("org.Sc.sgd.db") } \keyword{utilities} AnnotationDbi/man/AnnotationDb-class.Rd0000644000175200017520000002320614710217313021054 0ustar00biocbuildbiocbuild\name{AnnotationDb-objects} \docType{class} % Classes \alias{AnnotationDb} \alias{class:AnnotationDb} \alias{AnnotationDb-class} \alias{ChipDb-class} \alias{GODb-class} \alias{InparanoidDb-class} \alias{OrgDb-class} \alias{ReactomeDb-class} \alias{OrthologyDb-class} % Accessor-like methods \alias{loadDb} \alias{dbconn,AnnotationDb-method} \alias{saveDb} \alias{saveDb,AnnotationDb-method} \alias{show,AnnotationDb-method} \alias{metadata,AnnotationDb-method} \alias{names,AnnotationDb-method} \alias{species} \alias{species,AnnotationDb-method} \alias{dbfile,AnnotationDb-method} \alias{taxonomyId} \alias{taxonomyId,AnnotationDb-method} % select and select related methods \alias{cols} \alias{columns} \alias{columns,AnnotationDb-method} \alias{columns,OrgDb-method} \alias{columns,ChipDb-method} \alias{columns,GODb-method} \alias{columns,InparanoidDb-method} \alias{columns,Inparanoid8Db-method} \alias{columns,ReactomeDb-method} \alias{columns,OrthologyDb-method} \alias{keytypes} \alias{keytypes,OrgDb-method} \alias{keytypes,ChipDb-method} \alias{keytypes,GODb-method} \alias{keytypes,InparanoidDb-method} \alias{keytypes,Inparanoid8Db-method} \alias{keytypes,ReactomeDb-method} \alias{keytypes,OrthologyDb-method} % \alias{keys} %Not aliased here because it is already aliased in Bimap-keys.Rd % \alias{keys,AnnotationDb-method} \alias{keys} \alias{keys,OrgDb-method} \alias{keys,ChipDb-method} \alias{keys,GODb-method} \alias{keys,InparanoidDb-method} \alias{keys,Inparanoid8Db-method} \alias{keys,ReactomeDb-method} \alias{keys,OrthologyDb-method} \alias{select} % \alias{select,AnnotationDb-method} \alias{select,OrgDb-method} \alias{select,ChipDb-method} \alias{select,GODb-method} \alias{select,InparanoidDb-method} \alias{select,Inparanoid8Db-method} \alias{select,ReactomeDb-method} \alias{select,OrthologyDb-method} % mapIds should work for anything with select defined... \alias{mapIds} \alias{mapIds,AnnotationDb-method} \title{AnnotationDb objects and their progeny, methods etc.} \description{ \code{AnnotationDb} is the virtual base class for all annotation packages. It contain a database connection and is meant to be the parent for a set of classes in the Bioconductor annotation packages. These classes will provide a means of dispatch for a widely available set of \code{select} methods and thus allow the easy extraction of data from the annotation packages. \code{select}, \code{columns} and \code{keys} are used together to extract data from an \code{AnnotationDb} object (or any object derived from the parent class). Examples of classes derived from the \code{AnnotationDb} object include (but are not limited to): \code{ChipDb}, \code{OrgDb} \code{GODb}, \code{OrthologyDb} and \code{ReactomeDb}. \code{columns} shows which kinds of data can be returned for the \code{AnnotationDb} object. \code{keytypes} allows the user to discover which keytypes can be passed in to \code{select} or \code{keys} and the \code{keytype} argument. \code{keys} returns keys for the database contained in the \code{AnnotationDb} object . This method is already documented in the keys manual page but is mentioned again here because it's usage with \code{select} is so intimate. By default it will return the primary keys for the database, but if used with the \code{keytype} argument, it will return the keys from that keytype. \code{select} will retrieve the data as a data.frame based on parameters for selected \code{keys} \code{columns} and \code{keytype} arguments. Users should be warned that if you call \code{select} and request columns that have multiple matches for your keys, select will return a data.frame with one row for each possible match. This has the effect that if you request multiple columns and some of them have a many to one relationship to the keys, things will continue to multiply accordingly. So it's not a good idea to request a large number of columns unless you know that what you are asking for should have a one to one relationship with the initial set of keys. In general, if you need to retrieve a column (like GO) that has a many to one relationship to the original keys, it is most useful to extract that separately. \code{mapIds} gets the mapped ids (column) for a set of keys that are of a particular keytype. Usually returned as a named character vector. \code{saveDb} will take an AnnotationDb object and save the database to the file specified by the path passed in to the \code{file} argument. \code{loadDb} takes a .sqlite database file as an argument and uses data in the metadata table of that file to return an AnnotationDb style object of the appropriate type. \code{species} shows the genus and species label currently attached to the \code{AnnotationDb} objects database. \code{dbfile} gets the database file associated with an object. \code{dbconn} gets the datebase connection associated with an object. \code{taxonomyId} gets the taxonomy ID associated with an object (if available). } \usage{ columns(x) keytypes(x) keys(x, keytype, ...) select(x, keys, columns, keytype, ...) mapIds(x, keys, column, keytype, ..., multiVals) saveDb(x, file) loadDb(file, packageName=NA) } \arguments{ \item{x}{the \code{AnnotationDb} object. But in practice this will mean an object derived from an \code{AnnotationDb} object such as a \code{OrgDb} or \code{ChipDb} object.} \item{keys}{the keys to select records for from the database. All possible keys are returned by using the \code{keys} method.} \item{columns}{the columns or kinds of things that can be retrieved from the database. As with \code{keys}, all possible columns are returned by using the \code{columns} method.} \item{keytype}{the keytype that matches the keys used. For the \code{select} methods, this is used to indicate the kind of ID being used with the keys argument. For the \code{keys} method this is used to indicate which kind of keys are desired from \code{keys} } \item{column}{the column to search on (for \code{mapIds}). Different from \code{columns} in that it can only have a single element for the value} \item{...}{other arguments. These include: \describe{ \item{pattern:}{the pattern to match (used by keys)} \item{column:}{the column to search on. This is used by keys and is for when the thing you want to pattern match is different from the keytype, or when you want to simply want to get keys that have a value for the thing specified by the column argument.} \item{fuzzy:}{TRUE or FALSE value. Use fuzzy matching? (this is used with pattern by the keys method)} } } \item{multiVals}{What should \code{mapIds} do when there are multiple values that could be returned? Options include: \describe{ \item{first:}{This value means that when there are multiple matches only the 1st thing that comes back will be returned. This is the default behavior} \item{list:}{This will just returns a list object to the end user} \item{filter:}{This will remove all elements that contain multiple matches and will therefore return a shorter vector than what came in whenever some of the keys match more than one value} \item{asNA:}{This will return an NA value whenever there are multiple matches} \item{CharacterList:}{This just returns a SimpleCharacterList object} \item{FUN:}{You can also supply a function to the \code{multiVals} argument for custom behaviors. The function must take a single argument and return a single value. This function will be applied to all the elements and will serve a 'rule' that for which thing to keep when there is more than one element. So for example this example function will always grab the last element in each result: \code{ last <- function(x){x[[length(x)]]} } } } } \item{file}{an \code{sqlite} file path. A string the represents the full name you want for your sqlite database and also where to put it.} \item{packageName}{for internal use only} } \value{ \code{keys},\code{columns} and \code{keytypes} each return a character vector or possible values. \code{select} returns a data.frame. } \author{Marc Carlson} \seealso{ \code{keys}, \code{\link[DBI:dbConnect]{dbConnect}}, \code{\link[DBI:dbListTables]{dbListTables}}, \code{\link[DBI:dbListTables]{dbListFields}}, \code{\link[DBI:dbSendQuery]{dbGetQuery}}, \link{Bimap} } \examples{ require(hgu95av2.db) ## display the columns columns(hgu95av2.db) ## get the 1st 6 possible keys keys <- head( keys(hgu95av2.db) ) keys ## lookup gene symbol and gene type for the 1st 6 keys select(hgu95av2.db, keys=keys, columns = c("SYMBOL","GENETYPE")) ## get keys based on RefSeq keyref <- head( keys(hgu95av2.db, keytype="REFSEQ") ) keyref ## list supported key types keytypes(hgu95av2.db) ## lookup gene symbol and refseq ID based on refseq IDs by setting ## the keytype to "REFSEQ" and passing in refseq keys: select(hgu95av2.db, keys=keyref, columns = c("SYMBOL","REFSEQ"), keytype="REFSEQ") keys <- head(keys(hgu95av2.db, 'ENTREZID')) ## get a default result (captures only the 1st element) mapIds(hgu95av2.db, keys=keys, column='ALIAS', keytype='ENTREZID') ## or use a different option mapIds(hgu95av2.db, keys=keys, column='ALIAS', keytype='ENTREZID', multiVals="CharacterList") ## Or define your own function last <- function(x){x[[length(x)]]} mapIds(hgu95av2.db, keys=keys, column='ALIAS', keytype='ENTREZID', multiVals=last) ## For other ways to access the DB, you can use dbfile() or dbconn() to extract dbconn(hgu95av2.db) dbfile(hgu95av2.db) ## Try to retrieve an associated taxonomyId taxonomyId(hgu95av2.db) } \keyword{classes} \keyword{methods} AnnotationDbi/man/AnnotationDbi-internals.Rd0000644000175200017520000000157714710217313022126 0ustar00biocbuildbiocbuild\name{AnnotationDbi internals} \alias{debugSQL} \alias{class:FlatBimap} \alias{FlatBimap-class} \alias{FlatBimap} \alias{class:AnnObj} \alias{AnnObj-class} \alias{AnnObj} \alias{showQCData} \alias{class:L2Rlink} \alias{L2Rlink-class} \alias{L2Rlink} \alias{initialize,FlatBimap-method} \alias{initialize,L2Rlink-method} \alias{show,L2Rlink-method} \alias{dbGetTable} \alias{dbFileConnect} \alias{dbFileDisconnect} \alias{mergeToNamespaceAndExport} \alias{createAnnObjs.SchemaChoice} \alias{NCBICHIP_DB_SeedGenerator} \alias{getOrgPkgForSchema} \alias{filterSeeds} \alias{chooseCentralOrgPkgSymbol} \alias{mapIds_base} \alias{resort_base} \alias{testForValidKeytype} \alias{testSelectArgs} \title{AnnotationDbi internals} \description{ AnnotationDbi objects, classes and methods that are not intended to be used directly. } \keyword{internal} \keyword{methods} \keyword{classes} AnnotationDbi/man/Bimap-direction.Rd0000644000175200017520000001775614710217313020414 0ustar00biocbuildbiocbuild\name{Bimap-direction} \alias{Bimap-direction} \alias{direction} \alias{direction,FlatBimap-method} \alias{direction,AnnDbBimap-method} \alias{direction<-} \alias{direction<-,FlatBimap-method} \alias{direction<-,AnnDbBimap-method} \alias{direction<-,AnnDbMap-method} \alias{revmap} \alias{revmap,Bimap-method} \alias{revmap,AnnDbBimap-method} \alias{revmap,environment-method} \alias{revmap,list-method} \alias{Lkeys} \alias{Lkeys,FlatBimap-method} \alias{Lkeys,AnnDbBimap-method} \alias{Lkeys,ProbeAnnDbBimap-method} \alias{Lkeys,ProbeAnnDbMap-method} \alias{Lkeys,ProbeGo3AnnDbBimap-method} \alias{Lkeys,ProbeIpiAnnDbMap-method} \alias{Rkeys} \alias{Rkeys,FlatBimap-method} \alias{Rkeys,AnnDbBimap-method} \alias{Rkeys,Go3AnnDbBimap-method} \alias{Rkeys,AnnDbMap-method} \alias{Llength} \alias{Llength,Bimap-method} \alias{Llength,AnnDbBimap-method} \alias{Llength,ProbeAnnDbBimap-method} \alias{Llength,ProbeAnnDbMap-method} \alias{Llength,ProbeGo3AnnDbBimap-method} \alias{Llength,ProbeIpiAnnDbMap-method} \alias{Rlength} \alias{Rlength,Bimap-method} \alias{Rlength,AnnDbBimap-method} \alias{Rlength,Go3AnnDbBimap-method} \alias{Rlength,AnnDbMap-method} \alias{mappedLkeys} \alias{mappedLkeys,FlatBimap-method} \alias{mappedLkeys,AnnDbBimap-method} \alias{mappedLkeys,Go3AnnDbBimap-method} \alias{mappedLkeys,AgiAnnDbMap-method} \alias{mappedRkeys} \alias{mappedRkeys,FlatBimap-method} \alias{mappedRkeys,AnnDbBimap-method} \alias{mappedRkeys,Go3AnnDbBimap-method} \alias{mappedRkeys,AnnDbMap-method} \alias{count.mappedLkeys} \alias{count.mappedLkeys,Bimap-method} \alias{count.mappedLkeys,AnnDbBimap-method} \alias{count.mappedLkeys,Go3AnnDbBimap-method} \alias{count.mappedLkeys,AgiAnnDbMap-method} \alias{count.mappedRkeys} \alias{count.mappedRkeys,Bimap-method} \alias{count.mappedRkeys,AnnDbBimap-method} \alias{count.mappedRkeys,Go3AnnDbBimap-method} \alias{count.mappedRkeys,AnnDbMap-method} \alias{Lkeys<-} \alias{Lkeys<-,FlatBimap-method} \alias{Lkeys<-,AnnDbBimap-method} \alias{Rkeys<-} \alias{Rkeys<-,FlatBimap-method} \alias{Rkeys<-,AnnDbBimap-method} \alias{subset,Bimap-method} \alias{subset,AnnDbBimap-method} \title{Methods for getting/setting the direction of a Bimap object, and undirected methods for getting/counting/setting its keys} \description{ These methods are part of the \link{Bimap} interface (see \code{?\link{Bimap}} for a quick overview of the \link{Bimap} objects and their interface). They are divided in 2 groups: (1) methods for getting or setting the direction of a \link{Bimap} object and (2) methods for getting, counting or setting the left or right keys (or mapped keys only) of a \link{Bimap} object. Note that all the methods in group (2) are undirected methods i.e. what they return does NOT depend on the direction of the map (more on this below). } \usage{ ## Getting or setting the direction of a Bimap object direction(x) direction(x) <- value revmap(x, ...) ## Getting, counting or setting the left or right keys (or mapped ## keys only) of a Bimap object Lkeys(x) Rkeys(x) Llength(x) Rlength(x) mappedLkeys(x) mappedRkeys(x) count.mappedLkeys(x) count.mappedRkeys(x) Lkeys(x) <- value Rkeys(x) <- value \S4method{subset}{Bimap}(x, Lkeys = NULL, Rkeys = NULL, drop.invalid.keys = FALSE) \S4method{subset}{AnnDbBimap}(x, Lkeys = NULL, Rkeys = NULL, drop.invalid.keys = FALSE, objName = NULL) } \arguments{ \item{x}{ A \link{Bimap} object. } \item{value}{ A single integer or character string indicating the new direction in \code{direction(x) <- value}. A character vector containing the new keys (must be a subset of the current keys) in \code{Lkeys(x) <- value} and \code{Rkeys(x) <- value}. } \item{Lkeys, Rkeys, drop.invalid.keys, objName, ...}{Extra arguments for \code{revmap} and \code{subset}. Extra argument for \code{revmap} can be: \describe{ \item{\code{objName}}{ The name to give to the reversed map (only supported if \code{x} is an \link{AnnDbBimap} object). } } Extra arguments for \code{subset} can be: \describe{ \item{\code{Lkeys}}{ The new Lkeys. } \item{\code{Rkeys}}{ The new Rkeys. } \item{\code{drop.invalid.keys}}{ If \code{drop.invalid.keys=FALSE} (the default), an error will be raised if the new Lkeys or Rkeys contain invalid keys i.e. keys that don't belong to the current Lkeys or Rkeys. If \code{drop.invalid.keys=TRUE}, invalid keys are silently dropped. } \item{\code{objName}}{ The name to give to the submap (only supported if \code{x} is an \link{AnnDbBimap} object). } } } } \details{ All \link{Bimap} objects have a direction which can be left-to-right (i.e. the mapping goes from the left keys to the right keys) or right-to-left (i.e. the mapping goes from the right keys to the left keys). A \link{Bimap} object \code{x} that maps from left to right is considered to be a direct map. Otherwise it is considered to be an indirect map (when it maps from right to left). \code{direction} returns \code{1} on a direct map and \code{-1} otherwise. The direction of \code{x} can be changed with \code{direction(x) <- value} where value must be \code{1} or \code{-1}. An easy way to reverse a map (i.e. to change its direction) is to do \code{direction(x) <- - direction(x)}, or, even better, to use \code{revmap(x)} which is actually the recommended way for doing it. The \code{Lkeys} and \code{Rkeys} methods return respectively the left and right keys of a \link{Bimap} object. Unlike the \code{\link{keys}} method (see \code{?\link{keys}} for more information), these methods are direction-independent i.e. what they return does NOT depend on the direction of the map. Such methods are also said to be "undirected methods" and methods like the \code{\link{keys}} method are said to be "directed methods". All the methods described below are also "undirected methods". \code{Llength(x)} and \code{Rlength(x)} are equivalent to (but more efficient than) \code{length(Lkeys(x))} and \code{length(Rkeys(x))}, respectively. The \code{mappedLkeys} (or \code{mappedRkeys}) method returns the left keys (or right keys) that are mapped to at least one right key (or one left key). \code{count.mappedLkeys(x)} and \code{count.mappedRkeys(x)} are equivalent to (but more efficient than) \code{length(mappedLkeys(x))} and \code{length(mappedRkeys(x))}, respectively. These functions give overall summaries, if you want to know how many Rkeys correspond to a given Lkey you can use the \code{nhit} function. \code{Lkeys(x) <- value} and \code{Rkeys(x) <- value} are the undirected versions of \code{keys(x) <- value} (see \code{?\link{keys}} for more information) and \code{subset(x, Lkeys=new_Lkeys, Rkeys=new_Rkeys)} is provided as a convenient way to reduce the sets of left and right keys in one single function call. } \value{ \code{1L} or \code{-1L} for \code{direction}. A \link{Bimap} object of the same subtype as \code{x} for \code{revmap} and \code{subset}. A character vector for \code{Lkeys}, \code{Rkeys}, \code{mappedLkeys} and \code{mappedRkeys}. A single non-negative integer for \code{Llength}, \code{Rlength}, \code{count.mappedLkeys} and \code{count.mappedRkeys}. } \author{H. Pagès} \seealso{ \link{Bimap}, \link{Bimap-keys}, \link{BimapFormatting}, \link{Bimap-envirAPI}, \code{\link{nhit}} } \examples{ library(hgu95av2.db) ls(2) x <- hgu95av2GO x summary(x) direction(x) length(x) Llength(x) Rlength(x) keys(x)[1:4] Lkeys(x)[1:4] Rkeys(x)[1:4] count.mappedkeys(x) count.mappedLkeys(x) count.mappedRkeys(x) mappedkeys(x)[1:4] mappedLkeys(x)[1:4] mappedRkeys(x)[1:4] y <- revmap(x) y summary(y) direction(y) length(y) Llength(y) Rlength(y) keys(y)[1:4] Lkeys(y)[1:4] Rkeys(y)[1:4] ## etc... ## Get rid of all unmapped keys (left and right) z <- subset(y, Lkeys=mappedLkeys(y), Rkeys=mappedRkeys(y)) } \keyword{methods} AnnotationDbi/man/Bimap-envirAPI.Rd0000644000175200017520000000624314710217313020076 0ustar00biocbuildbiocbuild\name{Bimap-envirAPI} \alias{Bimap-envirAPI} \alias{ls} \alias{ls,Bimap-method} \alias{exists} \alias{exists,ANY,ANY,Bimap-method} \alias{exists,ANY,Bimap,missing-method} \alias{get} \alias{get,ANY,ANY,Bimap-method} \alias{get,ANY,Bimap,missing-method} \alias{[[,Bimap-method} \alias{$,Bimap-method} \alias{mget} \alias{mget,Bimap-method} \alias{mget,ANY,Bimap-method} \alias{eapply} \alias{eapply,Bimap-method} \alias{contents,Bimap-method} \alias{sample} \alias{sample,Bimap-method} \alias{sample,environment-method} \title{Environment-like API for Bimap objects} \description{ These methods allow the user to manipulate any \link{Bimap} object as if it was an environment. This environment-like API is provided for backward compatibility with the traditional environment-based maps. } \usage{ ls(name, pos = -1L, envir = as.environment(pos), all.names = FALSE, pattern, sorted = TRUE) exists(x, where, envir, frame, mode, inherits) get(x, pos, envir, mode, inherits) #x[[i]] #x$name ## Converting to a list mget(x, envir, mode, ifnotfound, inherits) eapply(env, FUN, ..., all.names, USE.NAMES) ## Additional convenience method sample(x, size, replace=FALSE, prob=NULL, ...) } \arguments{ \item{name}{ A \link{Bimap} object for \code{ls}. A key as a literal character string or a name (possibly backtick quoted) for \code{x$name}. } \item{pos, all.names, USE.NAMES, where, frame, mode, inherits}{ Ignored. } \item{envir}{ Ignored for \code{ls}. A \link{Bimap} object for \code{mget}, \code{get} and \code{exists}. } \item{pattern}{ An optional regular expression. Only keys matching 'pattern' are returned. } \item{x}{ The key(s) to search for for \code{exists}, \code{get} and \code{mget}. A \link{Bimap} object for \code{[[} and \code{x$name}. A \link{Bimap} object or an environment for \code{sample}. } \item{i}{ Single key specifying the map element to extract. } \item{ifnotfound}{ A value to be used if the key is not found. Only \code{NA} is currently supported. } \item{env}{ A \link{Bimap} object. } \item{FUN}{ The function to be applied (see original \code{\link[base:eapply]{eapply}} for environments for the details). } \item{...}{ Optional arguments to \code{FUN}. } \item{size}{ Non-negative integer giving the number of map elements to choose. } \item{replace}{ Should sampling be with replacement? } \item{prob}{ A vector of probability weights for obtaining the elements of the map being sampled. } \item{sorted}{ \code{logical(1)}. When TRUE (default), return primary keys in sorted order. } } \seealso{ \code{\link[base:ls]{ls}}, \code{\link[base:exists]{exists}}, \code{\link[base:get]{get}}, \code{\link[base:get]{mget}}, \code{\link[base:eapply]{eapply}}, \code{\link[base:sample]{sample}}, \link{BimapFormatting}, \link{Bimap} } \examples{ library(hgu95av2.db) x <- hgu95av2CHRLOC ls(x)[1:3] exists(ls(x)[1], x) exists("titi", x) get(ls(x)[1], x) x[[ls(x)[1]]] x$titi # NULL mget(ls(x)[1:3], x) eapply(x, length) sample(x, 3) } \keyword{methods} \keyword{interface} AnnotationDbi/man/Bimap-keys.Rd0000644000175200017520000001042514710217313017371 0ustar00biocbuildbiocbuild\name{Bimap-keys} \alias{Bimap-keys} \alias{keys,Bimap-method} \alias{length,Bimap-method} \alias{mappedkeys} \alias{mappedkeys,Bimap-method} \alias{mappedkeys,environment-method} \alias{mappedkeys,vector-method} \alias{count.mappedkeys} \alias{count.mappedkeys,Bimap-method} \alias{count.mappedkeys,ANY-method} \alias{isNA} \alias{isNA,Bimap-method} \alias{isNA,environment-method} \alias{isNA,ANY-method} \alias{keys<-} \alias{keys<-,Bimap-method} \alias{[,Bimap-method} \alias{show,AnnDbTable-method} \title{Methods for manipulating the keys of a Bimap object} \description{ These methods are part of the \link{Bimap} interface (see \code{?\link{Bimap}} for a quick overview of the \link{Bimap} objects and their interface). } \usage{ #length(x) isNA(x) mappedkeys(x) count.mappedkeys(x) keys(x) <- value #x[i] } \arguments{ \item{x}{ A \link{Bimap} object. If the method being caled is \code{keys(x)}, then x can also be a AnnotationDb object or one of that objects progeny. } \item{value}{ A character vector containing the new keys (must be a subset of the current keys). } \item{i}{ A character vector containing the keys of the map elements to extract. } } \details{ \code{keys(x)} returns the set of all valid keys for map \code{x}. For example, \code{keys(hgu95av2GO)} is the set of all probe set IDs for chip hgu95av2 from Affymetrix. Please Note that in addition to \code{Bimap} objest, \code{keys(x)} will also work for \code{AnnotationDb} objects and related objects such as \code{OrgDb} and \code{ChipDb} objects. Note also that the double bracket operator \code{[[} for \link{Bimap} objects is guaranteed to work only with a valid key and will raise an error if the key is invalid. (See \code{?`\link{Bimap-envirAPI}`} for more information about this operator.) \code{length(x)} is equivalent to (but more efficient than) \code{length(keys(x))}. A valid key is not necessarily mapped (\code{[[} will return an \code{NA} on an unmapped key). \code{isNA(x)} returns a logical vector of the same length as \code{x} where the \code{TRUE} value is used to mark keys that are NOT mapped and the \code{FALSE} value to mark keys that ARE mapped. \code{mappedkeys(x)} returns the subset of \code{keys(x)} where only mapped keys were kept. \code{count.mappedkeys(x)} is equivalent to (but more efficient than) \code{length(mappedkeys(x))}. Two (almost) equivalent forms of subsetting a \link{Bimap} object are provided: (1) by setting the keys explicitely and (2) by using the single bracket operator \code{[} for \link{Bimap} objects. Let's say the user wants to restrict the mapping to the subset of valid keys stored in character vector \code{mykeys}. This can be done either with \code{keys(x) <- mykeys} (form (1)) or with \code{y <- x[mykeys]} (form (2)). Please note that form (1) alters object \code{x} in an irreversible way (the original keys are lost) so form (2) should be preferred. All the methods described on this pages are "directed methods" i.e. what they return DOES depend on the direction of the \link{Bimap} object that they are applied to (see \code{?\link{direction}} for more information about this). } \value{ A character vector for \code{keys} and \code{mappedkeys}. A single non-negative integer for \code{length} and \code{count.mappedkeys}. A logical vector for \code{isNA}. A \link{Bimap} object of the same subtype as \code{x} for \code{x[i]}. } \author{H. Pagès} \seealso{ \link{Bimap}, \link{Bimap-envirAPI}, \link{Bimap-toTable}, \link{BimapFormatting}, \link{AnnotationDb}, \link{select}, \link{columns} } \examples{ library(hgu95av2.db) x <- hgu95av2GO x length(x) count.mappedkeys(x) x[1:3] links(x[1:3]) ## Keep only the mapped keys keys(x) <- mappedkeys(x) length(x) count.mappedkeys(x) x # now it is a submap ## The above subsetting can also be achieved with x <- hgu95av2GO[mappedkeys(hgu95av2GO)] ## mappedkeys() and count.mappedkeys() also work with an environment ## or a list z <- list(k1=NA, k2=letters[1:4], k3="x") mappedkeys(z) count.mappedkeys(z) ## retrieve the set of primary keys for the ChipDb object named 'hgu95av2.db' keys <- keys(hgu95av2.db) head(keys) } \keyword{methods} AnnotationDbi/man/Bimap-toTable.Rd0000644000175200017520000001530714710217313020014 0ustar00biocbuildbiocbuild\name{Bimap-toTable} \alias{Bimap-toTable} \alias{toTable} \alias{toTable,FlatBimap-method} \alias{toTable,Bimap-method} \alias{as.data.frame,Bimap-method} \alias{as.data.frame.Bimap} \alias{nrow} \alias{nrow,Bimap-method} \alias{nrow,FlatBimap-method} \alias{nrow,AnnDbTable-method} \alias{nrow,AnnDbBimap-method} \alias{nrow,Go3AnnDbBimap-method} \alias{ncol} \alias{ncol,Bimap-method} \alias{dim,Bimap-method} \alias{head,FlatBimap-method} \alias{tail,FlatBimap-method} \alias{links} \alias{links,Bimap-method} \alias{links,FlatBimap-method} \alias{links,AnnDbBimap-method} \alias{links,Go3AnnDbBimap-method} \alias{count.links} \alias{count.links,Bimap-method} \alias{count.links,Go3AnnDbBimap-method} \alias{nhit} \alias{nhit,Bimap-method} \alias{nhit,environment-method} \alias{nhit,list-method} \alias{colnames} \alias{colnames,FlatBimap-method} \alias{colnames,AnnDbBimap-method} \alias{colmetanames} \alias{colmetanames,FlatBimap-method} \alias{colmetanames,AnnDbBimap-method} \alias{Lkeyname} \alias{Lkeyname,Bimap-method} \alias{Lkeyname,AnnDbBimap-method} \alias{Rkeyname} \alias{Rkeyname,Bimap-method} \alias{Rkeyname,AnnDbBimap-method} \alias{keyname} \alias{keyname,Bimap-method} \alias{tagname} \alias{tagname,Bimap-method} \alias{tagname,AnnDbBimap-method} \alias{Rattribnames} \alias{Rattribnames,Bimap-method} \alias{Rattribnames,AnnDbBimap-method} \alias{Rattribnames<-} \alias{Rattribnames<-,FlatBimap-method} \alias{Rattribnames<-,AnnDbBimap-method} \alias{Rattribnames<-,Go3AnnDbBimap-method} \title{Methods for manipulating a Bimap object in a data-frame style} \description{ These methods are part of the \link{Bimap} interface (see \code{?\link{Bimap}} for a quick overview of the \link{Bimap} objects and their interface). } \usage{ ## Extract all the columns of the map (links + right attributes) toTable(x, ...) nrow(x) ncol(x) #dim(x) \S4method{head}{FlatBimap}(x, ...) \S4method{tail}{FlatBimap}(x, ...) ## Extract only the links of the map links(x) count.links(x) nhit(x) ## Col names and col metanames colnames(x, do.NULL=TRUE, prefix="col") colmetanames(x) Lkeyname(x) Rkeyname(x) keyname(x) tagname(x) Rattribnames(x) Rattribnames(x) <- value } \arguments{ \item{x}{ A \link{Bimap} object (or a list or an environment for \code{nhit}). } \item{...}{ Further arguments to be passed to or from other methods (see \code{\link[utils:head]{head}} or \code{\link[utils:head]{tail}} for the details). } \item{do.NULL}{ Ignored. } \item{prefix}{ Ignored. } \item{value}{ A character vector containing the names of the new right attributes (must be a subset of the current right attribute names) or NULL. } } \details{ \code{toTable(x)} turns \link{Bimap} object \code{x} into a data frame (see section "Flat representation of a bimap" in \code{?\link{Bimap}} for a short introduction to this concept). For simple maps (i.e. no tags and no right attributes), the resulting data frame has only 2 columns, one for the left keys and one for the right keys, and each row in the data frame represents a link (or edge) between a left and a right key. For maps with tagged links (i.e. a tag is associated to each link), \code{toTable(x)} has one additional colmun for the tags and there is still one row per link. For maps with right attributes (i.e. a set of attributes is associated to each right key), \code{toTable(x)} has one additional colmun per attribute. So for example if \code{x} has tagged links and 2 right attributes, \code{toTable(x)} will have 5 columns: one for the left keys, one for the right keys, one for the tags, and one for each right attribute (always the rightmost columns). Note that if at least one of the right attributes is multivalued then more than 1 row can be needed to represent the same link so the number of rows in \code{toTable(x)} can be strictly greater than the number of links in the map. \code{nrow(x)} is equivalent to (but more efficient than) \code{nrow(toTable(x))}. \code{ncol(x)} is equivalent to (but more efficient than) \code{ncol(toTable(x))}. \code{colnames(x)} is equivalent to (but more efficient than) \code{colnames(toTable(x))}. Columns are named accordingly to the names of the SQL columns where the data are coming from. An important consequence of this that they are not necessarily unique. \code{colmetanames(x)} returns the metanames for the column of \code{x} that are not right attributes. Valid column metanames are \code{"Lkeyname"}, \code{"Rkeyname"} and \code{"tagname"}. \code{Lkeyname}, \code{Rkeyname}, \code{tagname} and \code{Rattribnames} return the name of the column (or columns) containing the left keys, the right keys, the tags and the right attributes, respectively. Like \code{toTable(x)}, \code{links(x)} turns \code{x} into a data frame but the right attributes (if any) are dropped. Note that dropping the right attributes produces a data frame that has eventually less columns than \code{toTable(x)} and also eventually less rows because now exactly 1 row is needed to represent 1 link. \code{count.links(x)} is equivalent to (but more efficient than) \code{nrow(links(x))}. \code{nhit(x)} returns a named integer vector indicating the number of "hits" for each key in \code{x} i.e. the number of links that start from each key. } \value{ A data frame for \code{toTable} and \code{links}. A single integer for \code{nrow}, \code{ncol} and \code{count.links}. A character vector for \code{colnames}, \code{colmetanames} and \code{Rattribnames}. A character string for \code{Lkeyname}, \code{Rkeyname} and \code{tagname}. A named integer vector for \code{nhit}. } \author{H. Pagès} \seealso{ \link{Bimap}, \link{BimapFormatting}, \link{Bimap-envirAPI} } \examples{ library(GO.db) x <- GOSYNONYM x toTable(x)[1:4, ] toTable(x["GO:0007322"]) links(x)[1:4, ] links(x["GO:0007322"]) nrow(x) ncol(x) dim(x) colnames(x) colmetanames(x) Lkeyname(x) Rkeyname(x) tagname(x) Rattribnames(x) links(x)[1:4, ] count.links(x) y <- GOBPCHILDREN nhy <- nhit(y) # 'nhy' is a named integer vector identical(names(nhy), keys(y)) # TRUE table(nhy) sum(nhy == 0) # number of GO IDs with no children names(nhy)[nhy == max(nhy)] # the GO ID(s) with the most direct children ## Some sanity check sum(nhy) == count.links(y) # TRUE ## Changing the right attributes of the GOSYNONYM map (advanced ## users only) class(x) # GOTermsAnnDbBimap as.list(x)[1:3] colnames(x) colmetanames(x) tagname(x) # untagged map Rattribnames(x) Rattribnames(x) <- Rattribnames(x)[3:1] colnames(x) class(x) # AnnDbBimap as.list(x)[1:3] } \keyword{methods} AnnotationDbi/man/Bimap.Rd0000644000175200017520000001544514710217313016427 0ustar00biocbuildbiocbuild\name{Bimap} \docType{class} \alias{Bimap} % Classes \alias{Bimap} \alias{class:Bimap} \alias{Bimap-class} \alias{AnnDbBimap} \alias{class:AnnDbBimap} \alias{AnnDbBimap-class} \alias{GoAnnDbBimap} \alias{class:GoAnnDbBimap} \alias{GoAnnDbBimap-class} \alias{Go3AnnDbBimap} \alias{class:Go3AnnDbBimap} \alias{Go3AnnDbBimap-class} \alias{GOTermsAnnDbBimap} \alias{class:GOTermsAnnDbBimap} \alias{GOTermsAnnDbBimap-class} \alias{AnnDbMap} \alias{class:AnnDbMap} \alias{AnnDbMap-class} \alias{IpiAnnDbMap} \alias{class:IpiAnnDbMap} \alias{IpiAnnDbMap-class} \alias{AgiAnnDbMap} \alias{class:AgiAnnDbMap} \alias{AgiAnnDbMap-class} \alias{ProbeAnnDbBimap} \alias{class:ProbeAnnDbBimap} \alias{ProbeAnnDbBimap-class} \alias{ProbeGo3AnnDbBimap} \alias{class:ProbeGo3AnnDbBimap} \alias{ProbeGo3AnnDbBimap-class} \alias{ProbeAnnDbMap} \alias{class:ProbeAnnDbMap} \alias{ProbeAnnDbMap-class} \alias{ProbeIpiAnnDbMap} \alias{class:ProbeIpiAnnDbMap} \alias{ProbeIpiAnnDbMap-class} % Standard generic methods \alias{show,FlatBimap-method} \alias{show,AnnDbBimap-method} \alias{summary,Bimap-method} \alias{summary,AnnDbBimap-method} \title{Bimap objects and the Bimap interface} \description{ What we usually call "annotation maps" are in fact Bimap objects. In the following sections we present the bimap concept and the Bimap interface as it is defined in AnnotationDbi. } \section{Display methods}{ In the code snippets below, \code{x} is a Bimap object. \describe{ \item{}{ \code{show(x)}: Display minimal information about Bimap object \code{x}. } \item{}{ \code{summary(x)}: Display a little bit more information about Bimap object \code{x}. } } } \section{The bimap concept}{ A bimap is made of: \preformatted{ - 2 sets of objects: the left objects and the right objects. All the objects have a name and this name is unique in each set (i.e. in the left set and in the right set). The names of the left (resp. right) objects are called the left (resp. right) keys or the Lkeys (resp. the Rkeys). } \preformatted{ - Any number of links (edges) between the left and right objects. Note that the links can be tagged. In our model, for a given bimap, either none or all the links are tagged. } In other words, a bimap is a bipartite graph. Here are some examples: \preformatted{ 1. bimap B1: 4 left objects (Lkeys): "a", "b", "c", "d" 3 objects on the right (Rkeys): "A", "B", "C" Links (edges): "a" <--> "A" "a" <--> "B" "b" <--> "A" "d" <--> "C" Note that: - There can be any number of links starting from or ending at a given object. - The links in this example are untagged. } \preformatted{ 2. bimap B2: 4 left objects (Lkeys): "a", "b", "c", "d" 3 objects on the right (Rkeys): "A", "B", "C" Tagged links (edges): "a" <-"x"-> "A" "a" <-"y"-> "B" "b" <-"x"-> "A" "d" <-"x"-> "C" "d" <-"y"-> "C" Note that there are 2 links between objects "d" and "C": 1 with tag "x" and 1 with tag "y". } } \section{Flat representation of a bimap}{ The flat representation of a bimap is a data frame. For example, for B1, it is: \preformatted{ left right a A a B b A d C } If in addition the right objects have 1 multivalued attribute, for example, a numeric vector: \preformatted{ A <-- c(1.2, 0.9) B <-- character(0) C <-- -1:1 } then the flat representation of B1 becomes: \preformatted{ left right Rattrib1 a A 1.2 a A 0.9 a B NA b A 1.2 b A 0.9 d C -1 d C 0 d C 1 } Note that now the number of rows is greater than the number of links! } \section{AnnDbBimap and FlatBimap objects}{ An AnnDbBimap object is a bimap whose data are stored in a data base. A FlatBimap object is a bimap whose data (left keys, right keys and links) are stored in memory (in a data frame for the links). Conceptually, AnnDbBimap and FlatBimap objects are the same (only their internal representation differ) so it's natural to try to define a set of methods that make sense for both (so they can be manipulated in a similar way). This common interface is the Bimap interface. Note that both AnnDbBimap and FlatBimap objects have a read-only semantic: the user can subset them but cannot change their data. } \section{The "flatten" generic}{ \preformatted{ flatten(x) converts AnnDbBimap object x into FlatBimap object y with no loss of information } Note that a FlatBimap object can't be converted into an AnnDbBimap object (well, in theory maybe it could be, but for now the data bases we use to store the data of the AnnDbBimap objects are treated as read-only). This conversion from AnnDbBimap to FlatBimap is performed by the "flatten" generic function (with methods for AnnDbBimap objects only). } \section{Property0}{ The "flatten" generic plays a very useful role when we need to understand or explain exactly what a given Bimap method f will do when applied to an AnnDbBimap object. It's generally easier to explain what it does on a FlatBimap object and then to just say "and it does the same thing on an AnnDbBimap object". This is exactly what Property0 says: \preformatted{ for any AnnDbBimap object x, f(x) is expected to be indentical to f(flatten(x)) } Of course, this implies that the f method for AnnDbBimap objects return the same type of object than the f method for FlatBimap objects. In this sense, the "revmap" and "subset" Bimap methods are particular because they are expected to return an object of the same class as their argument x, so f(x) can't be identical to f(flatten(x)). For these methods, Property0 says: \preformatted{ for any AnnDbBimap object x, flatten(f(x)) is expected to be identical to f(flatten(x)) } Note to the AnnotationDbi maintainers/developpers: the \code{checkProperty0} function (AnnDbPkg-checker.R file) checks that Property0 is satisfied on all the AnnDbBimap objects defined in a given package (FIXME: checkProperty0 is currently broken). } \section{The Bimap interface in AnnotationDbi}{ The full documentation for the methods of the Bimap interface is splitted into 4 man pages: \link{Bimap-direction}, \link{Bimap-keys} and \link{Bimap-toTable}. } \seealso{ \link{Bimap-direction}, \link{Bimap-keys}, \link{Bimap-toTable}, \link{BimapFormatting}, \link{Bimap-envirAPI} } \examples{ library(hgu95av2.db) ls(2) hgu95av2GO # calls the "show" method summary(hgu95av2GO) hgu95av2GO2PROBE # calls the "show" method summary(hgu95av2GO2PROBE) } \keyword{classes} \keyword{interface} AnnotationDbi/man/BimapFiltering.Rd0000644000175200017520000000722614710217313020271 0ustar00biocbuildbiocbuild\name{toggleProbes} % \alias{exposeAllProbes} % \alias{exposeAllProbes,AnnDbBimap-method} % \alias{maskMultiProbes} % \alias{maskMultiProbes,AnnDbBimap-method} % \alias{maskSingleProbes} % \alias{maskSingleProbes,AnnDbBimap-method} \alias{toggleProbes} \alias{toggleProbes,ProbeAnnDbBimap-method} \alias{toggleProbes,ProbeAnnDbMap-method} \alias{toggleProbes,ProbeIpiAnnDbMap-method} \alias{toggleProbes,ProbeGo3AnnDbBimap-method} \alias{hasMultiProbes} \alias{hasMultiProbes,ProbeAnnDbBimap-method} \alias{hasMultiProbes,ProbeAnnDbMap-method} \alias{hasMultiProbes,ProbeIpiAnnDbMap-method} \alias{hasMultiProbes,ProbeGo3AnnDbBimap-method} \alias{hasSingleProbes} \alias{hasSingleProbes,ProbeAnnDbBimap-method} \alias{hasSingleProbes,ProbeAnnDbMap-method} \alias{hasSingleProbes,ProbeIpiAnnDbMap-method} \alias{hasSingleProbes,ProbeGo3AnnDbBimap-method} \alias{getBimapFilters} \alias{getBimapFilters,AnnDbBimap-method} \title{Methods for getting/setting the filters on a Bimap object} \description{ These methods are part of the \link{Bimap} interface (see \code{?\link{Bimap}} for a quick overview of the \link{Bimap} objects and their interface). Some of these methods are for getting or setting the filtering status on a \link{Bimap} object so that the mapping object can toggle between displaying all probes, only single probes (the defualt) or only multiply matching probes. Other methods are for viewing or setting the filter threshold value on a InpAnnDbBimap object. } \usage{ ## Making a Bimap object that does not prefilter to remove probes that ## match multiple genes: toggleProbes(x, value) hasMultiProbes(x) ##T/F test for exposure of single probes hasSingleProbes(x) ##T/F test for exposure of mulitply matched probes ## Looking at the SQL filter values for a Bimap getBimapFilters(x) } \arguments{ \item{x}{ A \link{Bimap} object. } \item{value}{ A character vector containing the new value that the Bimap should use as the filter. Or the value to toggle a probe mapping to: "all", "single", or "multiple". } } \details{ \code{toggleProbes(x)} is a methods for creating Bimaps that have an alternate filter for which probes get exposed based upon whether these probes map to multiple genes or not. \code{hasMultiProbes(x)} and \code{hasSingleProbes(x)} are provided to give a quick test about whether or not such probes are exposed in a given mapping. \code{getBimapFilters(x)} will list all the SQL filters applied to a Bimap object. } \value{ A \link{Bimap} object of the same subtype as \code{x} for \code{exposeAllProbes(x)}, \code{maskMultiProbes(x)} and \code{maskSingleProbes(x)}. A TRUE or FALSE value in the case of \code{hasMultiProbes(x)} and \code{hasSingleProbes(x)}. } \author{M. Carlson} \seealso{ \link{Bimap}, \link{Bimap-keys}, \link{Bimap-direction}, \link{BimapFormatting}, \link{Bimap-envirAPI}, \code{\link{nhit}} } \examples{ ## Make a Bimap that contains all the probes require("hgu95av2.db") mapWithMultiProbes <- toggleProbes(hgu95av2ENTREZID, "all") count.mappedLkeys(hgu95av2ENTREZID) count.mappedLkeys(mapWithMultiProbes) ## Check that it has both multiply and singly matching probes: hasMultiProbes(mapWithMultiProbes) hasSingleProbes(mapWithMultiProbes) ## Make it have Multi probes ONLY: OnlyMultiProbes = toggleProbes(mapWithMultiProbes, "multiple") hasMultiProbes(OnlyMultiProbes) hasSingleProbes(OnlyMultiProbes) ## Convert back to a default map with only single probes exposed OnlySingleProbes = toggleProbes(OnlyMultiProbes, "single") hasMultiProbes(OnlySingleProbes) hasSingleProbes(OnlySingleProbes) } \keyword{methods} AnnotationDbi/man/BimapFormatting.Rd0000644000175200017520000000172214710217313020453 0ustar00biocbuildbiocbuild\name{BimapFormatting} \alias{BimapFormatting} \alias{as.list} \alias{as.list,FlatBimap-method} \alias{as.list,Bimap-method} \alias{as.list.Bimap} \alias{as.list,IpiAnnDbMap-method} \alias{as.list,AgiAnnDbMap-method} \alias{as.list,GoAnnDbBimap-method} \alias{as.list,GOTermsAnnDbBimap-method} \alias{as.character,AnnDbBimap-method} \alias{as.character,FlatBimap-method} \title{Formatting a Bimap as a list or character vector} \description{ These functions format a Bimap as a list or character vector. } \usage{ ## Formatting as a list as.list(x, ...) ## Formatting as a character vector #as.character(x, ...) } \arguments{ \item{x}{ A \link{Bimap} object. } \item{...}{ Further arguments are ignored. } } \author{H. Pagès} \seealso{ \link{Bimap}, \link{Bimap-envirAPI} } \examples{ library(hgu95av2.db) as.list(hgu95av2CHRLOC)[1:9] as.list(hgu95av2ENTREZID)[1:9] as.character(hgu95av2ENTREZID)[1:9] } \keyword{methods} AnnotationDbi/man/GOColsAndKeytypes.Rd0000644000175200017520000000240114710217313020672 0ustar00biocbuildbiocbuild\name{GOID} \alias{GOID} \alias{TERM} \alias{ONTOLOGY} \alias{DEFINITION} \title{Descriptions of available values for \code{columns} and \code{keytypes} for GO.db.} \description{ This manual page enumerates the kinds of data represented by the values returned when the user calls \code{columns} or \code{keytypes} } \details{ All the possible values for \code{columns} and \code{keytypes} are listed below. \describe{ \item{GOID:}{GO Identifiers} \item{DEFINITION:}{The definition of a GO Term} \item{ONTOLOGY:}{Which of the three Gene Ontologies (BP, CC, or MF)} \item{TERM:}{The actual GO term} } To get the latest information about the date stamps and source URLS for the data used to make an annotation package, please use the metadata method as shown in the example below. } \author{Marc Carlson} \examples{ library(GO.db) ## List the possible values for columns columns(GO.db) ## List the possible values for keytypes keytypes(GO.db) ## get some values back keys <- head(keys(GO.db)) keys select(GO.db, keys=keys, columns=c("TERM","ONTOLOGY"), keytype="GOID") ## More infomation about the dates and original sources for these data: metadata(GO.db) } \keyword{utilities} \keyword{manip} AnnotationDbi/man/GOFrame.Rd0000644000175200017520000000276214710217313016655 0ustar00biocbuildbiocbuild\name{GOFrame} \docType{class} % Classes \alias{GOFrame} \alias{class:GOFrame} \alias{GOFrame-class} \alias{GOAllFrame} \alias{class:GOAllFrame} \alias{GOAllFrame-class} % methods \alias{GOFrame} \alias{GOFrame,data.frame,character-method} \alias{GOFrame,data.frame,missing-method} \alias{GOAllFrame} \alias{GOAllFrame,GOFrame-method} \alias{getGOFrameData} \alias{getGOFrameData,GOFrame-method} \alias{getGOFrameData,GOAllFrame-method} \title{GOFrame and GOAllFrame objects} \description{ These objects each contain a data frame which is required to be composed of 3 columns. The 1st column are GO IDs. The second are evidence codes and the 3rd are the gene IDs that match to the GO IDs using those evidence codes. There is also a slot for the organism that these anotations pertain to. } \details{ The GOAllFrame object can only be generated from a GOFrame object and its contructor method does this automatically from a GOFrame argument. The purpose of these objects is to create a safe way for annotation data about GO from non-traditional sources to be used for analysis packages like GSEABase and eventually GOstats. } \examples{ ## Make up an example genes = c(1,10,100) evi = c("ND","IEA","IDA") GOIds = c("GO:0008150","GO:0008152","GO:0001666") frameData = data.frame(cbind(GOIds,evi,genes)) library(AnnotationDbi) frame=GOFrame(frameData,organism="Homo sapiens") allFrame=GOAllFrame(frame) getGOFrameData(allFrame) } \keyword{classes} \keyword{interface} AnnotationDbi/man/GOTerms-class.Rd0000644000175200017520000000775614710217313020030 0ustar00biocbuildbiocbuild\name{GOTerms-class} \docType{class} \alias{class:GOTerms} \alias{GOTerms-class} \alias{GOTerms} \alias{initialize,GOTerms-method} % \alias{GOID} \alias{GOID,GOTerms-method} \alias{GOID,GOTermsAnnDbBimap-method} \alias{GOID,character-method} \alias{Term} \alias{Term,GOTerms-method} \alias{Term,GOTermsAnnDbBimap-method} \alias{Term,character-method} \alias{Ontology} \alias{Ontology,GOTerms-method} \alias{Ontology,GOTermsAnnDbBimap-method} \alias{Ontology,character-method} \alias{Definition} \alias{Definition,GOTerms-method} \alias{Definition,GOTermsAnnDbBimap-method} \alias{Definition,character-method} \alias{Synonym} \alias{Synonym,GOTerms-method} \alias{Synonym,GOTermsAnnDbBimap-method} \alias{Synonym,character-method} \alias{Secondary} \alias{Secondary,GOTerms-method} \alias{Secondary,GOTermsAnnDbBimap-method} \alias{Secondary,character-method} \alias{show,GOTerms-method} \title{Class "GOTerms"} \description{A class to represent Gene Ontology nodes} \section{Objects from the Class}{ Objects can be created by calls of the form \code{GOTerms(GOId, term, ontology, definition, synonym, secondary)}. GOId, term, and ontology are required. } \section{Slots}{ \describe{ \item{\code{GOID}:}{Object of class \code{"character"} A character string for the GO id of a primary node.} \item{\code{Term}:}{Object of class \code{"character"} A character string that defines the role of gene product corresponding to the primary GO id.} \item{\code{Ontology}:}{Object of class \code{"character"} Gene Ontology category. Can be MF - molecular function, CC - cellular component, or BP - biological process.} \item{\code{Definition}:}{Object of class \code{"character"} Further definition of the ontology of the primary GO id.} \item{\code{Synonym}:}{Object of class \code{"character"} other ontology terms that are considered to be synonymous to the primary term attached to the GO id (e.g. "type I programmed cell death" is a synonym of "apoptosis"). Synonymous here can mean that the synonym is an exact synonym of the primary term, is related to the primary term, is broader than the primary term, is more precise than the primary term, or name is related to the term, but is not exact, broader or narrower.} \item{\code{Secondary}:}{Object of class \code{"character"} GO ids that are secondary to the primary GO id as results of merging GO terms so that One GO id becomes the primary GO id and the rest become the secondary.} } } \section{Methods}{ \describe{ \item{GOID}{\code{signature(object = "GOTerms")}: The get method for slot GOID.} \item{Term}{\code{signature(object = "GOTerms")}: The get method for slot Term.} \item{Ontology}{\code{signature(object = "GOTerms")}: The get method for slot Ontology.} \item{Definition}{\code{signature(object = "GOTerms")}: The get method for slot Definition.} \item{Synonym}{\code{signature(object = "GOTerms")}: The get method for slot Synonym.} \item{Secondary}{\code{signature(object = "GOTerms")}: The get method for slot Secondary.} \item{show}{\code{signature(x = "GOTerms")}: The method for pretty print.} } } \references{\url{http://www.geneontology.org/}} \seealso{ \code{\link{makeGOGraph}} shows how to make GO mappings into graphNEL objects. } \note{GOTerms objects are used to represent primary GO nodes in the SQLite-based annotation data package GO.db} \examples{ gonode <- new("GOTerms", GOID="GO:1234567", Term="Test", Ontology="MF", Definition="just for testing") GOID(gonode) Term(gonode) Ontology(gonode) ##Or you can just use these methods on a GOTermsAnnDbBimap \dontrun{##I want to show an ex., but don't want to require GO.db require(GO.db) FirstTenGOBimap <- GOTERM[1:10] ##grab the 1st ten Term(FirstTenGOBimap) ##Or you can just use GO IDs directly ids = keys(FirstTenGOBimap) Term(ids) } } \keyword{methods} \keyword{classes} AnnotationDbi/man/KEGGFrame.Rd0000644000175200017520000000243514710217313017062 0ustar00biocbuildbiocbuild\name{KEGGFrame} \docType{class} % Classes \alias{KEGGFrame} \alias{class:KEGGFrame} \alias{KEGGFrame-class} % methods \alias{KEGGFrame} \alias{KEGGFrame,data.frame,character-method} \alias{KEGGFrame,data.frame,missing-method} \alias{getKEGGFrameData} \alias{getKEGGFrameData,KEGGFrame-method} \alias{getKEGGFrameData,KEGGAllFrame-method} \title{KEGGFrame objects} \description{ These objects each contain a data frame which is required to be composed of 2 columns. The 1st column are KEGG IDs. The second are the gene IDs that match to the KEGG IDs. There is also a slot for the organism that these anotations pertain to. \code{getKEGGFrameData} is just an accessor method and returns the data.frame contained in the KEGGFrame object and is mostly used by other code internally. } \details{ The purpose of these objects is to create a safe way for annotation data about KEGG from non-traditional sources to be used for analysis packages like GSEABase and eventually Category. } \examples{ ## Make up an example genes = c(2,9,9,10) KEGGIds = c("04610","00232","00983","00232") frameData = data.frame(cbind(KEGGIds,genes)) library(AnnotationDbi) frame=KEGGFrame(frameData,organism="Homo sapiens") getKEGGFrameData(frame) } \keyword{classes} \keyword{interface} AnnotationDbi/man/colsAndKeytypes.Rd0000644000175200017520000001234614710217313020515 0ustar00biocbuildbiocbuild\name{ACCNUM} \alias{ACCNUM} \alias{ALIAS} \alias{ARACYC} \alias{ARACYCENZYME} \alias{CHR} \alias{CHRLOC} \alias{CHRLOCEND} \alias{COMMON} \alias{DESCRIPTION} \alias{ENSEMBL} \alias{ENSEMBLPROT} \alias{ENSEMBLTRANS} \alias{ENTREZID} \alias{ENZYME} \alias{EVIDENCE} \alias{EVIDENCEALL} \alias{GENENAME} \alias{GO} \alias{GOALL} \alias{INTERPRO} \alias{IPI} \alias{MAP} \alias{OMIM} % \alias{ONTOLOGY} \alias{ONTOLOGYALL} \alias{ORF} \alias{PATH} \alias{PFAM} \alias{PMID} \alias{PROBEID} \alias{PROSITE} \alias{REFSEQ} \alias{SGD} \alias{SMART} \alias{SYMBOL} \alias{TAIR} \alias{UNIGENE} \alias{UNIPROT} \title{Descriptions of available values for \code{columns} and \code{keytypes}.} \description{ This manual page enumerates the kinds of data represented by the values returned when the user calls \code{columns} or \code{keytypes} } \details{ All the possible values for \code{columns} and \code{keytypes} are listed below. Users will have to actually use these methods to learn which of the following possible values actually apply in their case. \describe{ \item{ACCNUM:}{GenBank accession numbers} \item{ALIAS:}{Commonly used gene symbols} \item{ARACYC:}{KEGG Identifiers for arabidopsis as indicated by aracyc} \item{ARACYCENZYME:}{Aracyc enzyme names as indicated by aracyc} \item{CHR:}{Chromosome (deprecated for Bioc > 3.1) For this information you should look at a TxDb or OrganismDb object and search for an appropriate field like TXCHROM, EXONCHROM or CDSCHROM. This information can also be retrieved from these objects using an appropriate range based accesor like transcripts, transcriptsBy etc.} \item{CHRLOC:}{Chromosome and starting base of associated gene (deprecated for Bioc > 3.1) For this information you should look at a TxDb or OrganismDb object and search for an appropriate field like TXSTART etc. or even better use the associated range based accessors like transcripts or transcriptsBy to get back GRanges objects.} \item{CHRLOCEND:}{Chromosome and ending base of associated gene (deprecated for Bioc > 3.1) For this information you should look at a TxDb or OrganismDb object and search for an appropriate field like TXEND etc. or even better use the associated range based accessors like transcripts or transcriptsBy to get back GRanges objects.} \item{COMMON:}{Common name} \item{DESCRIPTION:}{The description of the associated gene} \item{ENSEMBL:}{The ensembl ID as indicated by ensembl} \item{ENSEMBLPROT:}{The ensembl protein ID as indicated by ensembl} \item{ENSEMBLTRANS:}{The ensembl transcript ID as indicated by ensembl} \item{ENTREZID:}{Entrez gene Identifiers} \item{ENZYME:}{Enzyme Commission numbers} \item{EVIDENCE:}{Evidence codes for GO associations with a gene of interest} \item{EVIDENCEALL:}{Evidence codes for GO (includes less specific terms)} \item{GENENAME:}{The full gene name} \item{GO:}{GO Identifiers associated with a gene of interest} \item{GOALL:}{GO Identifiers (includes less specific terms)} \item{INTERPRO:}{InterPro identifiers} \item{IPI:}{IPI accession numbers} \item{MAP:}{cytoband locations} \item{OMIM:}{Online Mendelian Inheritance in Man identifiers} \item{ONTOLOGY:}{For GO Identifiers, which Gene Ontology (BP, CC, or MF)} \item{ONTOLOGYALL:}{Which Gene Ontology (BP, CC, or MF), (includes less specific terms)} \item{ORF:}{Yeast ORF Identifiers} \item{PATH:}{KEGG Pathway Identifiers} \item{PFAM:}{PFAM Identifiers} \item{PMID:}{Pubmed Identifiers} \item{PROBEID:}{Probe or manufacturer Identifiers for a chip package} \item{PROSITE:}{Prosite Identifiers} \item{REFSEQ:}{Refseq Identifiers} \item{SGD:}{Saccharomyces Genome Database Identifiers} \item{SMART:}{Smart Identifiers} \item{SYMBOL:}{The official gene symbol} \item{TAIR:}{TAIR Identifiers} \item{UNIGENE:}{Unigene Identifiers} \item{UNIPROT:}{Uniprot Identifiers} } To get the latest information about the date stamps and source URLS for the data used to make an annotation package, please use the metadata method as shown in the example below. Unless otherwise indicated above, the majority of the data for any one package is taken from the source indicated by either it's name (if it's an org package) OR from the name of it's associated org package. So for example, org.Hs.eg.db is using "eg" in the name to indicate that most of the data in that package comes from NCBI entrez gene based data. And org.At.tair.db uses data that primarily comes from tair. For chip packages, the relevant information is the organism package that they depend on. So for example, hgu95av2.db depends on org.Hs.eg.db, and is thus primarily based on NCBI entrez gene ID information. } \author{Marc Carlson} \examples{ library(hgu95av2.db) ## List the possible values for columns columns(hgu95av2.db) ## List the possible values for keytypes keytypes(hgu95av2.db) ## get some values back keys <- head(keys(hgu95av2.db)) keys select(hgu95av2.db, keys=keys, columns=c("SYMBOL","PFAM"), keytype="PROBEID") ## More infomation about the dates and original sources for these data: metadata(hgu95av2.db) } \keyword{utilities} \keyword{manip} AnnotationDbi/man/createSimpleBimap.Rd0000644000175200017520000000447214710217313020763 0ustar00biocbuildbiocbuild\name{createSimpleBimap} \alias{createSimpleBimap} \title{Creates a simple Bimap from a SQLite database in an situation that is external to AnnotationDbi} \description{ This function allows users to easily make a simple Bimap object for extra tables etc that they may wish to add to their annotation packages. For most Bimaps, their definition is stored inside of AnnotationDbi. The addition of this function is to help ensure that this does not become a limitation, by allowing simple extra Bimaps to easily be defined external to AnnotationDbi. Usually, this will be done in the zzz.R source file of a package so that these extra mappings can be seemlessly integrated with the rest of the package. For now, this function assumes that users will want to use data from just one table. } \usage{ createSimpleBimap(tablename, Lcolname, Rcolname, datacache, objName, objTarget) } \arguments{ \item{tablename}{ The name of the database table to grab the mapping information from. } \item{Lcolname}{ The field name from the database table. These will become the Lkeys in the final mapping. } \item{Rcolname}{ The field name from the database table. These will become the Rkeys in the final mapping. } \item{datacache}{ The datacache object should already exist for every standard Annotation package. It is not exported though, so you will have to access it with ::: . It is needed to provide the connection information to the function. } \item{objName}{ This is the name of the mapping. } \item{objTarget}{ This is the name of the thing the mapping goes with. For most uses, this will mean the package name that the mapping belongs with. } } \examples{ ##You simply have to call this function to create a new mapping. For ##example, you could have created a mapping between the gene_name and ##the symbols fields from the gene_info table contained in the hgu95av2 ##package by doing this: library(hgu95av2.db) hgu95av2NAMESYMBOL <- createSimpleBimap("gene_info", "gene_name", "symbol", hgu95av2.db:::datacache, "NAMESYMBOL", "hgu95av2.db") } \keyword{utilities} AnnotationDbi/man/inpIDMapper.Rd0000644000175200017520000001557014710217313017546 0ustar00biocbuildbiocbuild\name{inpIDMapper} \alias{inpIDMapper} \alias{intraIDMapper} \alias{idConverter} \title{Convenience functions for mapping IDs through an appropriate set of annotation packages} \description{ These are a set of convenience functions that attempt to take a list of IDs along with some addional information about what those IDs are, what type of ID you would like them to be, as well as some information about what species they are from and what species you would like them to be from and then attempts to the simplest possible conversion using the organism and possible inparanoid annotation packages. By default, this function will drop ambiguous matches from the results. Please see the details section for more information about the parameters that can affect this. If a more complex treatment of how to handle multiple matches is required, then it is likely that a less convenient approach will be necessary. } \usage{ inpIDMapper(ids, srcSpecies, destSpecies, srcIDType="UNIPROT", destIDType="EG", keepMultGeneMatches=FALSE, keepMultProtMatches=FALSE, keepMultDestIDMatches = TRUE) intraIDMapper(ids, species, srcIDType="UNIPROT", destIDType="EG", keepMultGeneMatches=FALSE) idConverter(ids, srcSpecies, destSpecies, srcIDType="UNIPROT", destIDType="EG", keepMultGeneMatches=FALSE, keepMultProtMatches=FALSE, keepMultDestIDMatches = TRUE) } \arguments{ \item{ids}{a list or vector of original IDs to match} \item{srcSpecies}{The original source species in in paranoid format. In other words, the 3 letters of the genus followed by 2 letters of the species in all caps. Ie. 'HOMSA' is for Homo sapiens etc.} \item{destSpecies}{the destination species in inparanoid format} \item{species}{the species involved} \item{srcIDType}{The source ID type written exactly as it would be used in a mapping name for an eg package. So for example, 'UNIPROT' is how the uniprot mappings are always written, so we keep that convention here.} \item{destIDType}{the destination ID, written the same way as you would write the srcIDType. By default this is set to "EG" for entrez gene IDs} \item{keepMultGeneMatches}{Do you want to try and keep the 1st ID in those ambiguous cases where more than one protein is suggested? (You probably want to filter them out - hence the default is FALSE)} \item{keepMultProtMatches}{Do you want to try and keep the 1st ID in those ambiguous cases where more than one protein is suggested? (default = FALSE)} \item{keepMultDestIDMatches}{If you have mapped to a destination ID OTHER than an entrez gene ID, then it is possible that there may be multiple answers. Do you want to keep all of these or only return the 1st one? (default = TRUE)} } \value{ a list where the names of each element are the elements of the original list you passed in, and the values are the matching results. Elements that do not have a match are not returned. If you want things to align you can do some bookeeping. } \details{ inpIDMapper - This is a convenience function for getting an ID from one species mapped to an ID type of your choice from another organism of your choice. The only mappings used to do this are the mappings that are scored as 100 according to the inparanoid algorithm. This function automatically tries to join IDs by using FIVE different mappings in the sequence that follows: 1) initial IDs -> src organism Entrez Gene IDs 2) src organism Entrez Gene IDs -> sre organism Inparanoid ID 3) src organism Inparanoid ID -> dest organism Inparanoid ID 4) dest organism Inparanoid ID -> dest organism Entrez Gene ID 5) dest organism Entrez Gene ID -> final destination organism ID You can simplify this mapping as a series of steps like this: srcIDs ---> srcEGs ---> srcInp ---> destInp ---> destEGs ---> destIDs (1) (2) (3) (4) (5) There are two steps in this process where multiple mappings can really interfere with getting a clear answer. It's no coincidence that these are also adjacent to the two places where we have to tie the identity to a single gene for each organism. When this happens, any ambiguity is confounding. Preceding step \#2, it is critical that we only have ONE entrez gene ID per initial ID, and the parameter keepMultGeneMatches can be used to toggle whether to drop any ambiguous matches (the default) or to keep the 1st one in the hope of getting an additional hit. A similar thing is done preceding step \#4, where we have to be sure that the protein IDs we are getting back have all mapped to only one gene. We allow you to use the keepMultProtMatches parameter to make the same kind of decision as in step \#2, again, the default is to drop anything that is ambiguous. intraIDMapper - This is a convenience function to map within an organism and so it has a much simpler job to do. It will either map through one mapping or two depending whether the source ID or destination ID is a central ID for the relevant organism package. If the answer is neither, then two mappings will be needed. idConverter - This is mostly for convenient usage of these functions by developers. It is just a wrapper function that can pass along all the parameters to the appropriate function (intraIDMapper or inpIDMapper). It decides which function to call based on the source and destination organism. The disadvantage to using this function all the time is just that more of the parameters have to be filled out each time. } \author{Marc Carlson} \examples{ \dontrun{ ## This has to be in a dontrun block because otherwise I would have to ## expand the DEPENDS field for AnnotationDbi ## library("org.Hs.eg.db") ## library("org.Mm.eg.db") ## library("org.Sc.eg.db") ## library("hom.Hs.inp.db") ## library("hom.Mm.inp.db") ## library("hom.Sc.inp.db") ##Some IDs just for the example library("org.Hs.eg.db") ids = as.list(org.Hs.egUNIPROT)[10000:10500] ##get some ragged IDs ## Get entrez gene IDs (default) for uniprot IDs mapping from human to mouse. MouseEGs = inpIDMapper(ids, "HOMSA", "MUSMU") ##Get yeast uniprot IDs in exchange for uniprot IDs from human YeastUPs = inpIDMapper(ids, "HOMSA", "SACCE", destIDType="UNIPROT") ##Get yeast uniprot IDs but only return one ID per initial ID YeastUPSingles = inpIDMapper(ids, "HOMSA", "SACCE", destIDType="UNIPROT", keepMultDestIDMatches = FALSE) ##Test out the intraIDMapper function: HumanEGs = intraIDMapper(ids, species="HOMSA", srcIDType="UNIPROT", destIDType="EG") HumanPATHs = intraIDMapper(ids, species="HOMSA", srcIDType="UNIPROT", destIDType="PATH") ##Test out the wrapper function MousePATHs = idConverter(MouseEGs, srcSpecies="MUSMU", destSpecies="MUSMU", srcIDType="EG", destIDType="PATH") ##Convert from Yeast uniprot IDs to Human entrez gene IDs. HumanEGs = idConverter(YeastUPSingles, "SACCE", "HOMSA") } } \keyword{manip} AnnotationDbi/man/makeGOGraph.Rd0000644000175200017520000000113314710217313017511 0ustar00biocbuildbiocbuild\name{makeGOGraph} \alias{makeGOGraph} \title{A convenience function to generate graphs based on the GO.db package} \description{ \code{makeGOGraph} is a function to quickly convert any of the three Gene Ontologies in GO.db into a graphNEL object where each edge is given a weight of 1. } \usage{ makeGOGraph(ont = c("bp","mf","cc")) } \arguments{ \item{ont}{Specifies the ontology: "cc", "bp" or "mf".} } \author{Marc Carlson} \seealso{ \code{\link{GOTerms}} } \examples{ ## makes a GO graph from the CC ontology f <- makeGOGraph("cc") } \keyword{utilities} \keyword{manip} AnnotationDbi/man/make_eg_to_go_map.Rd0000644000175200017520000000132214710217313021000 0ustar00biocbuildbiocbuild\name{make_eg_to_go_map} \alias{make_eg_to_go_map} \alias{make_go_to_eg_map} \title{Create GO to Entrez Gene maps for chip-based packages} \description{ Create a new map object mapping Entrez ID to GO (or vice versa) given a chip annotation data package. This is a temporary solution until a more general pluggable map solution comes online. } \usage{ make_eg_to_go_map(chip) } \arguments{ \item{chip}{The name of the annotation data package.} } \value{ Either a \code{Go3AnnDbMap} or a \code{RevGo3AnnDbMap}. } \author{Seth Falcon and Hervé Pagès} \examples{ library("hgu95av2.db") eg2go = make_eg_to_go_map("hgu95av2.db") sample(eg2go, 2) go2eg = make_go_to_eg_map("hgu95av2.db") sample(go2eg, 2) } AnnotationDbi/man/orgPackageName.Rd0000644000175200017520000000140614710217313020233 0ustar00biocbuildbiocbuild\name{orgPackageName} \alias{orgPackageName} \title{Org package contained in annotation object} \description{ Get the name of the org package used by an annotation resource object. NOTE: This man page is for the \code{orgPackageName} \emph{S4 generic function} defined in the \pkg{AnnotationDbi} package. Bioconductor packages can define specific methods for annotation objects not supported by the default method. } \usage{ orgPackageName(x, ...) } \arguments{ \item{x}{ An annotation resource object. } \item{...}{ Additional arguments. } } \value{ A \code{character(1)} vector indicating the org package name. Specific methods defined in Bioconductor packages should behave as consistently as possible with the default method. } AnnotationDbi/man/organismKEGGFrame.Rd0000644000175200017520000000067314710217313020624 0ustar00biocbuildbiocbuild\name{organismKEGGFrame} \alias{organismKEGGFrame} \alias{organismKEGGFrame} \title{A data frame that maps species names to KEGG organisms} \description{ Create a data.frame that maps a species name (e.g. Homo sapeins) to the KEGG organsim notation (e.g. hsa). } \usage{ organismKEGGFrame() } \value{ A data.frame with 2 columns, species and organsim. } \author{Kayla Interdonato} \examples{ query <- organismKEGGFrame() head(query) } AnnotationDbi/man/print.probetable.Rd0000644000175200017520000000163114710217313020641 0ustar00biocbuildbiocbuild\name{print.probetable} \alias{print.probetable} \title{Print method for probetable objects} \usage{ \method{print}{probetable}(x, maxrows, \dots) } \description{ Prints class(x), nrow(x) and ncol(x), but not the elements of x. The motivation for having this method is that methods from the package \code{base} such as \code{\link[base:print.dataframe]{print.data.frame}} will try to print the values of all elements of \code{x}, which can take inconveniently much time and screen space if \code{x} is large. } \arguments{ \item{x}{an object of S3-class \code{probetable}.} \item{maxrows}{maximum number of rows to print.} \item{\dots}{further arguments that get ignored.} } \seealso{ \code{\link[base:print.dataframe]{print.data.frame}} } \examples{ a = as.data.frame(matrix(runif(1e6), ncol=1e3)) class(a) = c("probetable", class(a)) print(a) print(as.matrix(a[2:3, 4:6])) } \keyword{print} AnnotationDbi/man/toSQLStringSet.Rd0000644000175200017520000000200614710217313020231 0ustar00biocbuildbiocbuild\name{toSQLStringSet} \alias{toSQLStringSet} \title{Convert a vector to a quoted string for use as a SQL value list} \description{ Given a vector, this function returns a string with each element of the input coerced to character, quoted, and separated by ",". } \usage{ toSQLStringSet(names) } \arguments{ \item{names}{A vector of values to quote} } \details{ If \code{names} is a character vector with elements containing single quotes, these quotes will be doubled so as to escape the quote in SQL. } \value{ A character vector of length one that represents the input vector as a SQL value list. Each element is single quoted and elements are comma separated. } \author{Hervé Pagès} \note{ Do not use \code{sQuote} for generating SQL as that function is intended for display purposes only. In some locales, \code{sQuote} will generate fancy quotes which will break your SQL. } \examples{ toSQLStringSet(letters[1:4]) toSQLStringSet(c("'foo'", "ab'cd", "bar")) } \keyword{utilities} \keyword{manip} AnnotationDbi/man/unlist2.Rd0000644000175200017520000000246514710217313016775 0ustar00biocbuildbiocbuild\name{unlist2} \alias{unlist2} \title{A replacement for unlist() that does not mangle the names} \description{ \code{unlist2} is a replacement for \code{base::unlist()} that does not mangle the names. } \usage{ unlist2(x, recursive=TRUE, use.names=TRUE, what.names="inherited") } \arguments{ \item{x, recursive, use.names}{See \code{?unlist}.} \item{what.names}{\code{"inherited"} or \code{"full"}.} } \details{ Use this function if you don't like the mangled names returned by the standard \code{unlist} function from the base package. Using \code{unlist} with annotation data is dangerous and it is highly recommended to use \code{unlist2} instead. } \author{Hervé Pagès} \seealso{ \code{\link{unlist}} } \examples{ x <- list(A=c(b=-4, 2, b=7), B=3:-1, c(a=1, a=-2), C=list(c(2:-1, d=55), e=99)) unlist(x) unlist2(x) library(hgu95av2.db) egids <- c("10", "100", "1000") egids2pbids <- mget(egids, revmap(hgu95av2ENTREZID)) egids2pbids unlist(egids2pbids) # 1001, 1002, 10001 and 10002 are not real # Entrez ids but are the result of unlist() # mangling the names! unlist2(egids2pbids) # much cleaner! yes the names are not unique # but at least they are correct... } \keyword{utilities} \keyword{manip} AnnotationDbi/tests/0000755000175200017520000000000014710217313015466 5ustar00biocbuildbiocbuildAnnotationDbi/tests/AnnotationDbi_unit_tests.R0000644000175200017520000000014214710217313022620 0ustar00biocbuildbiocbuildrequire("AnnotationDbi") || stop("unable to load AnnotationDbi package") AnnotationDbi:::.test() AnnotationDbi/vignettes/0000755000175200017520000000000014710267466016352 5ustar00biocbuildbiocbuildAnnotationDbi/vignettes/AnnotationDbi.Rnw0000644000175200017520000006654114710217313021571 0ustar00biocbuildbiocbuild%\VignetteIndexEntry{2. (Deprecated) How to use bimaps from the ".db" annotation packages} %\VignetteDepends{hgu95av2.db} %\VignetteKeywords{annotation, database} %\VignettePackage{AnnotationDbi} %\VignetteEngine{knitr::knitr} \documentclass[11pt]{article} <>= BiocStyle::latex() @ %% Excercises and Questions \usepackage{theorem} \theoremstyle{break} \newtheorem{Ex}{Exercise} \theoremstyle{break} \newtheorem{Q}{Question} %% And solution or answer \newenvironment{solution}{\color{blue}}{\bigskip} \title{How to use bimaps from the ".db" annotation packages} \author{Marc Carlson, Hervé Pagès, Seth Falcon, Nianhua Li} <>= library(knitr) opts_chunk$set(tidy=FALSE) @ \begin{document} \maketitle \textbf{NOTE} The `bimap' interface to annotation resources is not recommend; instead, use the approach in the vignette \href{http://bioconductor.org/packages/release/bioc/vignettes/AnnotationDbi/inst/doc/IntroToAnnotationPackages.pdf}{Introduction To Bioconductor Annotation Packages}. \section{Introduction} \subsubsection{Purpose} AnnotationDbi is used primarily to create mapping objects that allow easy access from R to underlying annotation databases. As such, it acts as the R interface for all the standard annotation packages. Underlying each AnnotationDbi supported annotation package is at least one (and often two) annotation databases. AnnotationDbi also provides schemas for theses databases. For each supported model organism, a standard gene centric database is maintained from public sources and is packaged up as an appropriate organism or "org" package. \subsubsection{Database Schemas} For developers, a lot of the benefits of having the information loaded into a real database will require some knowledge about the database schema. For this reason the schemas that were used in the creation of each database type are included in AnnotationDbi. The currently supported schemas are listed in the DBschemas directory of AnnotationDbi. But it is also possible to simply print out the schema that a package is currently using by using its "\_dbschema" method. There is one schema/database in each kind of package. These schemas specify which tables and indices will be present for each package of that type. The schema that a particular package is using is also listed when you type the name of the package as a function to obtain quality control information. The code to make most kinds of the new database packages is also included in AnnotationDbi. Please see the vignette on SQLForge for more details on how to make additional database packages. \subsubsection{Internal schema Design of org packages} The current design of the organism packages is deliberately simple and gene centric. Each table in the database contains a unique kind of information and also an internal identifier called \_id. The internal \_id has no meaning outside of the context of a single database. But \_id does connect all the data within a single database. As an example if we wanted to connect the values in the genes table with the values in the kegg table, we could simply join the two tables using the internal \_id column. It is very important to note however that \_id does not have any absolute significance. That is, it has no meaning outside of the context of the database where it is used. It is tempting to think that an \_id could have such significance because within a single database, it looks and behaves similarly to an entrez gene ID. But \_id is definitely NOT an entrez gene ID. The entrez gene IDs are in another table entirely, and can be connected to using the internal \_id just like all the other meaningful information inside these databases. Each organism package is centered around one type of gene identifier. This identifier is found as the gene\_id field in the genes table and is both the central ID for the database as well as the foreign key that chip packages should join to. The chip packages are 'lightweight', and only contain information about the basic probe to gene mapping. You might wonder how such packages can provide access to all the other information that they do. This is possible because all the other data provided by chip packages comes from joins that are performed by AnnotationDbi behind the scenes at run time. All chip packages have a dependency on at least one organism package. The name of the organism package being depended on can be found by looking at its "ORGPKG" value. To learn about the schema from the appropriate organism package, you will need to look at the "\_dbschema" method for that package. In the case of the chip packages, the gene\_id that in these packages is mapped to the probe\_ids, is used as a foreign key to the appropriate organism package. Specialized packages like the packages for GO and KEGG, will have their own schemas but will also adhere to the use of an internal \_id for joins between their tables. As with the organism packages, this \_id is not suitable for use as a foreign key. For a complete listing of the different schemas used by various packages, users can use the \Rfunction{available.dbschemas} function. This list will also tell you which model organisms are supported. <<>= library(DBI) library(org.Hs.eg.db) library(AnnotationForge) available.dbschemas() @ \section{Examples} \subsubsection{Basic information} The \Rpackage{AnnotationDbi} package provides an interface to SQLite-based annotation packages. Each SQLite-based annotation package (identified by a ``.db'' suffix in the package name) contains a number of \Rclass{AnnDbBimap} objects in place of the \Rclass{environment} objects found in the old-style environment-based annotation packages. The API provided by \Rpackage{AnnotationDbi} allows you to treat the \Rclass{AnnDbBimap} objects like \Rclass{environment} instances. For example, the functions \verb+[[+, \Rfunction{get}, \Rfunction{mget}, and \Rfunction{ls} all behave the same as they did with the older environment based annotation packages. In addition, new methods like \Rfunction{[}, \Rfunction{toTable}, \Rfunction{subset} and others provide some additional flexibility in accessing the annotation data. <>= options(continue=" ", prompt="R> ", width=72L) @ <>= library(hgu95av2.db) @ The same basic set of objects is provided with the db packages: <>= ls("package:hgu95av2.db") @ \begin{Ex} Start an R session and use the \Rfunction{library} function to load the \Rpackage{hgu95av2.db} software package. Use search() to see that an organism package was also loaded and then use the approriate "\_dbschema" methods to the schema for the \Rpackage{hgu95av2.db} and \Rpackage{org.Hs.eg.db} packages. <>= library(hgu95av2.db) search() hgu95av2_dbschema() org.Hs.eg_dbschema() @ \end{Ex} It is possible to call the package name as a function to get some QC information about it. <>= qcdata = capture.output(hgu95av2()) head(qcdata, 20) @ Alternatively, you can get similar information on how many items are in each of the provided maps by looking at the MAPCOUNTs: <>= hgu95av2MAPCOUNTS @ To demonstrate the \Rclass{environment} API, we'll start with a random sample of probe set IDs. <>= all_probes <- ls(hgu95av2ENTREZID) length(all_probes) set.seed(0xa1beef) probes <- sample(all_probes, 5) probes @ The usual ways of accessing annotation data are also available. <>= hgu95av2ENTREZID[[probes[1]]] hgu95av2ENTREZID$"31882_at" syms <- unlist(mget(probes, hgu95av2SYMBOL)) syms @ The annotation packages provide a huge variety of information in each package. Some common types of information include gene symbols (SYMBOL), GO terms (GO), KEGG pathway IDs (KEGG), ENSEMBL IDs (ENSEMBL) and chromosome start and stop locations (CHRLOC and CHRLOCEND). Each mapping will have a manual page that you can read to describe the data in the mapping and where it came from. <>= ?hgu95av2CHRLOC @ \begin{Ex} For the probes in 'probes' above, use the annotation mappings to find the chromosome start locations. <>= mget(probes, hgu95av2CHRLOC, ifnotfound=NA)[1:2] @ \end{Ex} \subsubsection{Manipulating Bimap Objects} Many filtering operations on the annotation \Rclass{Bimap} objects require conversion of the \Rclass{AnnDbBimap} into a \Rclass{list}. In general, converting to lists will not be the most efficient way to filter the annotation data when using a SQLite-based package. Compare the following two examples for how you could get the 1st ten elements of the hgu95av2SYMBOL mapping. In the 1st case we have to get the entire mapping into list form, but in the second case we first subset the mapping object itself and this allows us to only convert the ten elements that we care about. <>= system.time(as.list(hgu95av2SYMBOL)[1:10]) ## vs: system.time(as.list(hgu95av2SYMBOL[1:10])) @ There are many different kinds of \Rclass{Bimap} objects in AnnotationDbi, but most of them are of class \Rclass{AnnDbBimap}. All /Rclass{Bimap} objects represent data as a set of left and right keys. The typical usage of these mappings is to search for right keys that match a set of left keys that have been supplied by the user. But sometimes it is also convenient to go in the opposite direction. The annotation packages provide many reverse maps as objects in the package name space for backwards compatibility, but the reverse mappings of almost any map is also available using \Rfunction{revmap}. Since the data are stored as tables, no extra disk space is needed to provide reverse mappings. <>= unlist(mget(syms, revmap(hgu95av2SYMBOL))) @ So now that you know about the \Rfunction{revmap} function you might try something like this: <>= as.list(revmap(hgu95av2PATH)["00300"]) @ Note that in the case of the PATH map, we don't need to use revmap(x) because hgu95av2.db already provides the PATH2PROBE map: <>= x <- hgu95av2PATH ## except for the name, this is exactly revmap(x) revx <- hgu95av2PATH2PROBE revx2 <- revmap(x, objName="PATH2PROBE") revx2 identical(revx, revx2) as.list(revx["00300"]) @ Note that most maps are reversible with \Rfunction{revmap}, but some (such as the more complex GO mappings), are not. Why is this? Because to reverse a mapping means that there has to be a "value" that will always become the "key" on the newly reversed map. And GO mappings have several distinct possibilities to choose from (GO ID, Evidence code or Ontology). In non-reversible cases like this, AnnotationDbi will usually provide a pre-defined reverse map. That way, you will always know what you are getting when you call \Rfunction{revmap} While we are on the subject of GO and GO mappings, there are a series of special methods for GO mappings that can be called to find out details about these IDs. \Rfunction{Term},\Rfunction{GOID}, \Rfunction{Ontology}, \Rfunction{Definition},\Rfunction{Synonym}, and \Rfunction{Secondary} are all useful ways of getting additional information about a particular GO ID. For example: <>= Term("GO:0000018") Definition("GO:0000018") @ \begin{Ex} Given the following set of RefSeq IDs: c("NG\_005114","NG\_007432","NG\_008063"), Find the Entrez Gene IDs that would correspond to those. Then find the GO terms that are associated with those entrez gene IDs. \Rpackage{org.Hs.eg.db} packages. <>= rs = ls(revmap(org.Hs.egREFSEQ))[4:6] EGs = mget(rs, revmap(org.Hs.egREFSEQ), ifnotfound=NA) ##Then get the GO terms. GOs = mget(unlist(EGs), org.Hs.egGO, ifnotfound=NA) GOs ##Extract the GOIDs from this list: GOIDs = as.character(unique(sapply(GOs, names))) ##Then look up what these terms are: Term(GOIDs) @ \end{Ex} \subsubsection{The Contents and Structure of Bimap Objects} Sometimes you may want to display or subset elements from an individual map. A \Rclass{Bimap} interface is available to access the data in table (\Rclass{data.frame}) format using \Rfunction{[} and \Rfunction{toTable}. <>= head(toTable(hgu95av2GO[probes])) @ The \Rfunction{toTable} function will display all of the information in a \Rclass{Bimap}. This includes both the left and right values along with any other attributes that might be attached to those values. The left and right keys of the \Rclass{Bimap} can be extracted using \Rfunction{Lkeys} and \Rfunction{Rkeys}. If is is necessary to only display information that is directly associated with the left to right links in a \Rclass{Bimap}, then the \Rfunction{links} function can be used. The \Rfunction{links} returns a data frame with one row for each link in the bimap that it is applied to. It only reports the left and right keys along with any attributes that are attached to the edge between these two values. Note that the order of the cols returned by \Rfunction{toTable} does not depend on the direction of the map. We refer to it as an 'undirected method': <>= toTable(x)[1:6, ] toTable(revx)[1:6, ] @ Notice however that the Lkeys are always on the left (1st col), the Rkeys always in the 2nd col For length() and keys(), the result does depend on the direction, hence we refer to these as 'directed methods': <>= length(x) length(revx) allProbeSetIds <- keys(x) allKEGGIds <- keys(revx) @ There are more 'undirected' methods listed below: <>= junk <- Lkeys(x) # same for all maps in hgu95av2.db (except pseudo-map # MAPCOUNTS) Llength(x) # nb of Lkeys junk <- Rkeys(x) # KEGG ids for PATH/PATH2PROBE maps, GO ids for # GO/GO2PROBE/GO2ALLPROBES maps, etc... Rlength(x) # nb of Rkeys @ Notice how they give the same result for x and revmap(x) You might be tempted to think that \Rfunction{Lkeys} and \Rfunction{Llength} will tell you all that you want to know about the left keys. But things are more complex than this, because not all keys are mapped. Often, you will only want to know about the keys that are mapped (ie. the ones that have a corresponding Rkey). To learn this you want to use the \Rfunction{mappedkeys} or the undirected variants \Rfunction{mappedLkeys} and \Rfunction{mappedRkeys}. Similarily, the \Rfunction{count.mappedkeys}, \Rfunction{count.mappedLkeys} and \Rfunction{count.mappedRkeys} methods are very fast ways to determine how many keys are mapped. Accessing keys like this is usually very fast and so it can be a decent strategy to subset the mapping by 1st using the mapped keys that you want to find. <>= x = hgu95av2ENTREZID[1:10] ## Directed methods mappedkeys(x) # mapped keys count.mappedkeys(x) # nb of mapped keys ## Undirected methods mappedLkeys(x) # mapped left keys count.mappedLkeys(x) # nb of mapped Lkeys @ If you want to find keys that are not mapped to anything, you might want to use \Rfunction{isNA}. <>= y = hgu95av2ENTREZID[isNA(hgu95av2ENTREZID)] # usage like is.na() Lkeys(y)[1:4] @ \begin{Ex} How many probesets do not have a GO mapping for the \Rpackage{hgu95av2.db} package? How many have no mapping? Find a probeset that has a GO mapping. Now look at the GO mappings for this probeset in table form. <>= count.mappedLkeys(hgu95av2GO) Llength(hgu95av2GO) - count.mappedLkeys(hgu95av2GO) mappedLkeys(hgu95av2GO)[1] toTable(hgu95av2GO["1000_at"]) @ \end{Ex} \subsubsection{Some specific examples} Lets use what we have learned to get information about the probes that are are not assigned to a chromosome: <>= x <- hgu95av2CHR Rkeys(x) chroms <- Rkeys(x)[23:24] chroms Rkeys(x) <- chroms toTable(x) @ To get this in the classic named-list format: <>= z <- as.list(revmap(x)[chroms]) names(z) z[["Y"]] @ Many of the common methods for accessing \Rclass{Bimap} objects return things in list format. This can be convenient. But you have to be careful about this if you want to use unlist(). For example the following will return multiple probes for each chromosome: <>= chrs = c("12","6") mget(chrs, revmap(hgu95av2CHR[1:30]), ifnotfound=NA) @ But look what happens here if we try to unlist that: <>= unlist(mget(chrs, revmap(hgu95av2CHR[1:30]), ifnotfound=NA)) @ Yuck! One trick that will sometimes help is to use Rfunction{unlist2}. But be careful here too. Depending on what step comes next, Rfunction{unlist2} may not really help you... <>= unlist2(mget(chrs, revmap(hgu95av2CHR[1:30]), ifnotfound=NA)) @ Lets ask if the probes in 'pbids' mapped to cytogenetic location "18q11.2"? <>= x <- hgu95av2MAP pbids <- c("38912_at", "41654_at", "907_at", "2053_at", "2054_g_at", "40781_at") x <- subset(x, Lkeys=pbids, Rkeys="18q11.2") toTable(x) @ To coerce this map to a named vector: <>= pb2cyto <- as.character(x) pb2cyto[pbids] @ The coercion of the reverse map works too but issues a warning because of the duplicated names for the reasons stated above: <>= cyto2pb <- as.character(revmap(x)) @ \subsubsection{Accessing probes that map to multiple targets} In many probe packages, some probes are known to map to multiple genes. The reasons for this can be biological as happens in the arabidopsis packages, but usually it is due to the fact that the genome builds that chip platforms were based on were less stable than desired. Thus what may have originally been a probe designed to measure one thing can end up measuring many things. Usually you don't want to use probes like this, because if they manufacturer doesn't know what they map to then their usefullness is definitely suspect. For this reason, by default all chip packages will normally hide such probes in the standard mappings. But sometimes you may want access to the answers that the manufacturer says such a probe will map to. In such cases, you will want to use the \Rfunction{toggleProbes} method. To use this method, just call it on a standard mapping and copy the result into a new mapping (you cannot alter the original mapping). Then treat the new mapping as you would any other mapping. <>= ## How many probes? dim(hgu95av2ENTREZID) ## Make a mapping with multiple probes exposed multi <- toggleProbes(hgu95av2ENTREZID, "all") ## How many probes? dim(multi) @ If you then decide that you want to make a mapping that has only multiple mappings or you wish to revert one of your maps back to the default state of only showing the single mappings then you can use \Rfunction{toggleProbes} to switch back and forth. <>= ## Make a mapping with ONLY multiple probes exposed multiOnly <- toggleProbes(multi, "multiple") ## How many probes? dim(multiOnly) ## Then make a mapping with ONLY single mapping probes singleOnly <- toggleProbes(multiOnly, "single") ## How many probes? dim(singleOnly) @ Finally, there are also a pair of test methods \Rfunction{hasMultiProbes} and \Rfunction{hasSingleProbes} that can be used to see what methods a mapping presently has exposed. <>= ## Test the multiOnly mapping hasMultiProbes(multiOnly) hasSingleProbes(multiOnly) ## Test the singleOnly mapping hasMultiProbes(singleOnly) hasSingleProbes(singleOnly) @ \subsubsection{Using SQL to access things directly} While the mapping objects provide a lot of convenience, sometimes there are definite benefits to writing a simple SQL query. But in order to do this, it is necessary to know a few things. The 1st thing you will need to know is some SQL. Fortunately, it is quite easy to learn enough basic SQL to get stuff out of a database. Here are 4 basic SQL things that you may find handy: First, you need to know about SELECT statements. A simple example would look something like this: SELECT * FROM genes; Which would select everything from the genes table. SELECT gene\_id FROM genes; Will select only the gene\_id field from the genes table. Second you need to know about WHERE clauses: SELECT gene\_id,\_id FROM genes WHERE gene\_id=1; Will only get records from the genes table where the gene\_id is = 1. Thirdly, you will want to know about an inner join: SELECT * FROM genes,chromosomes WHERE genes.\_id=chromosomes.\_id; This is only slightly more complicated to understand. Here we want to get all the records that are in both the 'genes' and 'chromosomes' tables, but we only want ones where the '\_id' field is identical. This is known as an inner join because we only want the elements that are in both of these tables with respect to '\_id'. There are other kinds of joins that are worth learning about, but most of the time, this is all you will need to do. Finally, it is worthwhile to learn about the AS keyword which is useful for making long queries easier to read. For the previous example, we could have written it this way to save space: SELECT * FROM genes AS g,chromosomes AS c WHERE g.\_id=c.\_id; In a simple example like this you might not see a lot of savings from using AS, so lets consider what happens when we want to also specify which fields we want: SELECT g.gene\_id,c.chromosome FROM genes AS g,chromosomes AS c WHERE g.\_id=c.\_id; Now you are most of the way there to being able to query the databases directly. The only other thing you need to know is a little bit about how to access these databases from R. With each package, you will also get a method that will print the schema for its database, you can view this to see what sorts of tables are present etc. <>= org.Hs.eg_dbschema() @ To access the data in a database, you will need to connect to it. Fortunately, each package will automatically give you a connection object to that database when it loads. <>= org.Hs.eg_dbconn() @ You can use this connection object like this: <>= query <- "SELECT gene_id FROM genes LIMIT 10;" result = dbGetQuery(org.Hs.eg_dbconn(), query) result @ \begin{Ex} Retrieve the entrez gene ID and chromosome by using a database query. Show how you could do the same thing by using \Rfunction{toTable} <>= sql <- "SELECT gene_id, chromosome FROM genes AS g, chromosomes AS c WHERE g._id=c._id;" dbGetQuery(org.Hs.eg_dbconn(),sql)[1:10,] ##OR toTable(org.Hs.egCHR)[1:10,] @ \end{Ex} \subsubsection{Combining data from multiple annotation packages at the SQL level} For a more complex example, consider the task of obtaining all gene symbols which are probed on a chip that have at least one GO BP ID annotation with evidence code IMP, IGI, IPI, or IDA. Here is one way to extract this using the environment-based packages: <>= ## Obtain SYMBOLS with at least one GO BP ## annotation with evidence IMP, IGI, IPI, or IDA. system.time({ bpids <- eapply(hgu95av2GO, function(x) { if (length(x) == 1 && is.na(x)) NA else { sapply(x, function(z) { if (z$Ontology == "BP") z$GOID else NA }) } }) bpids <- unlist(bpids) bpids <- unique(bpids[!is.na(bpids)]) g2p <- mget(bpids, hgu95av2GO2PROBE) wantedp <- lapply(g2p, function(x) { x[names(x) %in% c("IMP", "IGI", "IPI", "IDA")] }) wantedp <- wantedp[sapply(wantedp, length) > 0] wantedp <- unique(unlist(wantedp)) ans <- unlist(mget(wantedp, hgu95av2SYMBOL)) }) length(ans) ans[1:10] @ All of the above code could have been reduced to a single SQL query with the SQLite-based packages. But to put together this query, you would need to look 1st at the schema to know what tables are present: <>= hgu95av2_dbschema() @ This function will give you an output of all the create table statements that were used to generate the hgu95av2 database. In this case, this is a chip package, so you will also need to see the schema for the organism package that it depends on. To learn what package it depends on, look at the ORGPKG value: <>= hgu95av2ORGPKG @ Then you can see that schema by looking at its schema method: <>= org.Hs.eg_dbschema() @ So now we can see that we want to connect the data in the go\_bp, and symbol tables from the org.Hs.eg.sqlite database along with the probes data in the hgu95av2.sqlite database. How can we do that? It turns out that one of the great conveniences of SQLite is that it allows other databases to be `ATTACHed'. Thus, we can keep our data in many differnt databases, and then 'ATTACH' them to each other in a modular fashion. The databases for a given build have been built together and frozen into a single version specifically to allow this sort of behavoir. To use this feature, the SQLite ATTACH command requires the filename for the database file on your filesystem. Fortunately, R provides a nice system independent way of getting that information. Note that the name of the database is always the same as the name of the package, with the suffix '.sqlite'.: <>= orgDBLoc = system.file("extdata", "org.Hs.eg.sqlite", package="org.Hs.eg.db") attachSQL = paste("ATTACH '", orgDBLoc, "' AS orgDB;", sep = "") dbGetQuery(hgu95av2_dbconn(), attachSQL) @ Finally, you can assemble a cross-db sql query and use the helper function as follows. Note that when we want to refer to tables in the attached database, we have to use the 'orgDB' prefix that we specified in the 'ATTACH' query above.: <>= system.time({ SQL <- "SELECT DISTINCT probe_id,symbol FROM probes, orgDB.gene_info AS gi, orgDB.genes AS g, orgDB.go_bp AS bp WHERE bp._id=g._id AND gi._id=g._id AND probes.gene_id=g.gene_id AND bp.evidence IN ('IPI', 'IDA', 'IMP', 'IGI')" zz <- dbGetQuery(hgu95av2_dbconn(), SQL) }) #its a good idea to always DETACH your database when you are finished... dbGetQuery(hgu95av2_dbconn(), "DETACH orgDB" ) @ \begin{Ex} Retrieve the entrez gene ID, chromosome location information and cytoband infomration by using a single database query. <>= sql <- "SELECT gene_id, start_location, end_location, cytogenetic_location FROM genes AS g, chromosome_locations AS c, cytogenetic_locations AS cy WHERE g._id=c._id AND g._id=cy._id" dbGetQuery(org.Hs.eg_dbconn(),sql)[1:10,] @ \end{Ex} \begin{Ex} Expand on the example in the text above to combine data from the \Rpackage{hgu95av2.db} and \Rpackage{org.Hs.eg.db} with the \Rpackage{GO.db} package so as to include the GO ID, and term definition in the output. <>= orgDBLoc = system.file("extdata", "org.Hs.eg.sqlite", package="org.Hs.eg.db") attachSQL = paste("ATTACH '", orgDBLoc, "' AS orgDB;", sep = "") dbGetQuery(hgu95av2_dbconn(), attachSQL) goDBLoc = system.file("extdata", "GO.sqlite", package="GO.db") attachSQL = paste("ATTACH '", goDBLoc, "' AS goDB;", sep = "") dbGetQuery(hgu95av2_dbconn(), attachSQL) SQL <- "SELECT DISTINCT p.probe_id, gi.symbol, gt.go_id, gt.definition FROM probes AS p, orgDB.gene_info AS gi, orgDB.genes AS g, orgDB.go_bp AS bp, goDB.go_term AS gt WHERE bp._id=g._id AND gi._id=g._id AND p.gene_id=g.gene_id AND bp.evidence IN ('IPI', 'IDA', 'IMP', 'IGI') AND gt.go_id=bp.go_id" zz <- dbGetQuery(hgu95av2_dbconn(), SQL) dbGetQuery(hgu95av2_dbconn(), "DETACH orgDB") dbGetQuery(hgu95av2_dbconn(), "DETACH goDB") @ \end{Ex} The version number of R and packages loaded for generating the vignette were: <>= sessionInfo() @ \end{document} AnnotationDbi/vignettes/IntroToAnnotationPackages.Rnw0000644000175200017520000003452614710217313024126 0ustar00biocbuildbiocbuild%\VignetteIndexEntry{1. Introduction To Bioconductor Annotation Packages} %\VignetteDepends{org.Hs.eg.db, TxDb.Hsapiens.UCSC.hg19.knownGene, EnsDb.Hsapiens.v75} %\VignetteKeywords{annotation, database} %\VignettePackage{AnnotationDbi} %\VignetteEngine{knitr::knitr} \documentclass[11pt]{article} <>= BiocStyle::latex() @ %% Question, Exercise, Solution \usepackage{theorem} \theoremstyle{break} \newtheorem{Ext}{Exercise} \newtheorem{Question}{Question} \newenvironment{Exercise}{ \renewcommand{\labelenumi}{\alph{enumi}.}\begin{Ext}% }{\end{Ext}} \newenvironment{Solution}{% \noindent\textbf{Solution:}\renewcommand{\labelenumi}{\alph{enumi}.}% }{\bigskip} \title{AnnotationDbi: Introduction To Bioconductor Annotation Packages} \author{Marc Carlson} <>= library(knitr) opts_chunk$set(tidy=FALSE) @ \begin{document} \maketitle \begin{figure}[ht] \centering \includegraphics[width=.6\textwidth]{databaseTypes.pdf} \caption{Annotation Packages: the big picture} \label{fig:dbtypes} \end{figure} \Bioconductor{} provides extensive annotation resources. These can be \emph{gene centric}, or \emph{genome centric}. Annotations can be provided in packages curated by \Bioconductor, or obtained from web-based resources. This vignette is primarily concerned with describing the annotation resources that are available as packages. More advanced users who wish to learn about how to make new annotation packages should see the vignette titled "Creating select Interfaces for custom Annotation resources" from the \Rpackage{AnnotationForge} package. Gene centric \Rpackage{AnnotationDbi} packages include: \begin{itemize} \item Organism level: e.g. \Rpackage{org.Mm.eg.db}. \item Platform level: e.g. \Rpackage{hgu133plus2.db}, \Rpackage{hgu133plus2.probes}, \Rpackage{hgu133plus2.cdf}. \item System-biology level: \Rpackage{GO.db} \end{itemize} Genome centric \Rpackage{GenomicFeatures} packages include \begin{itemize} \item Transcriptome level: e.g. \Rpackage{TxDb.Hsapiens.UCSC.hg19.knownGene}, \Rpackage{EnsDb.Hsapiens.v75}. \item Generic genome features: Can generate via \Rpackage{GenomicFeatures} \end{itemize} One web-based resource accesses \href{http://www.biomart.org/}{biomart}, via the \Rpackage{biomaRt} package: \begin{itemize} \item Query web-based `biomart' resource for genes, sequence, SNPs, and etc. \end{itemize} The most popular annotation packages have been modified so that they can make use of a new set of methods to more easily access their contents. These four methods are named: \Rfunction{columns}, \Rfunction{keytypes}, \Rfunction{keys} and \Rfunction{select}. And they are described in this vignette. They can currently be used with all chip, organism, and \Rclass{TxDb} packages along with the popular GO.db package. For the older less popular packages, there are still conventient ways to retrieve the data. The \emph{How to use bimaps from the ".db" annotation packages} vignette in the \Rpackage{AnnotationDbi} package is a key reference for learnign about how to use bimap objects. Finally, all of the `.db' (and most other \Bioconductor{} annotation packages) are updated every 6 months corresponding to each release of \Bioconductor{}. Exceptions are made for packages where the actual resources that the packages are based on have not themselves been updated. \section{AnnotationDb objects and the select method} As previously mentioned, a new set of methods have been added that allow a simpler way of extracting identifier based annotations. All the annotation packages that support these new methods expose an object named exactly the same as the package itself. These objects are collectively called \Rclass{AnntoationDb} objects for the class that they all inherit from. The more specific classes (the ones that you will actually see in the wild) have names like \Rclass{OrgDb}, \Rclass{ChipDb} or \Rclass{TxDb} objects. These names correspond to the kind of package (and underlying schema) being represented. The methods that can be applied to all of these objects are \Rfunction{columns}, \Rfunction{keys}, \Rfunction{keytypes} and \Rfunction{select}. In addition, another accessor has recently been added which allows extraction of one column at at time. the \Rfunction{mapIds} method allows users to extract data into either a named character vector, a list or even a SimpleCharacterList. This method should work with all the different kinds of \Rclass{AnntoationDb} objects described below. \section{ChipDb objects and the select method} An extremely common kind of Annotation package is the so called platform based or chip based package type. This package is intended to make the manufacturer labels for a series of probes or probesets to a wide range of gene-based features. A package of this kind will load an \Rclass{ChipDb} object. Below is a set of examples to show how you might use the standard 4 methods to interact with an object of this type. First we need to load the package: <>= suppressPackageStartupMessages({ library(hgu95av2.db) }) @ If we list the contents of this package, we can see that one of the many things loaded is an object named after the package "hgu95av2.db": <>= ls("package:hgu95av2.db") @ We can look at this object to learn more about it: <>= hgu95av2.db @ If we want to know what kinds of data are retriveable via \Rfunction{select}, then we should use the \Rfunction{columns} method like this: <>= columns(hgu95av2.db) @ If we are further curious to know more about those values for columns, we can consult the help pages. Asking about any of these values will pull up a manual page describing the different fields and what they mean. <>= help("SYMBOL") @ If we are curious about what kinds of fields we could potentiall use as keys to query the database, we can use the \Rfunction{keytypes} method. In a perfect world, this method will return values very similar to what was returned by \Rfunction{columns}, but in reality, some kinds of values make poor keys and so this list is often shorter. <>= keytypes(hgu95av2.db) @ If we want to extract some sample keys of a particular type, we can use the \Rfunction{keys} method. <>= head(keys(hgu95av2.db, keytype="SYMBOL")) @ And finally, if we have some keys, we can use \Rfunction{select} to extract them. By simply using appropriate argument values with select we can specify what keys we want to look up values for (keys), what we want returned back (columns) and the type of keys that we are passing in (keytype) <>= #1st get some example keys k <- head(keys(hgu95av2.db,keytype="PROBEID")) # then call select select(hgu95av2.db, keys=k, columns=c("SYMBOL","GENENAME"), keytype="PROBEID") @ And as you can see, when you call the code above, select will try to return a data.frame with all the things you asked for matched up to each other. Finally if you wanted to extract only one column of data you could instead use the mapIds method like this: <>= #1st get some example keys k <- head(keys(hgu95av2.db,keytype="PROBEID")) # then call mapIds mapIds(hgu95av2.db, keys=k, column=c("GENENAME"), keytype="PROBEID") @ \section{OrgDb objects and the select method} An organism level package (an `org' package) uses a central gene identifier (e.g. Entrez Gene id) and contains mappings between this identifier and other kinds of identifiers (e.g. GenBank or Uniprot accession number, RefSeq id, etc.). The name of an org package is always of the form \emph{org...db} (e.g. \Rpackage{org.Sc.sgd.db}) where \emph{} is a 2-letter abbreviation of the organism (e.g. \Rpackage{Sc} for \emph{Saccharomyces cerevisiae}) and \emph{} is an abbreviation (in lower-case) describing the type of central identifier (e.g. \Rpackage{sgd} for gene identifiers assigned by the Saccharomyces Genome Database, or \Rpackage{eg} for Entrez Gene ids). Just as the chip packages load a \Rclass{ChipDb} object, the org packages will load a \Rclass{OrgDb} object. The following exercise should acquaint you with the use of these methods in the context of an organism package. %% select exercise \begin{Exercise} Display the \Rclass{OrgDb} object for the \Biocpkg{org.Hs.eg.db} package. Use the \Rfunction{columns} method to discover which sorts of annotations can be extracted from it. Is this the same as the result from the \Rfunction{keytypes} method? Use the \Rfunction{keytypes} method to find out. Finally, use the \Rfunction{keys} method to extract UNIPROT identifiers and then pass those keys in to the \Rfunction{select} method in such a way that you extract the gene symbol and KEGG pathway information for each. Use the help system as needed to learn which values to pass in to columns in order to achieve this. \end{Exercise} \begin{Solution} <>= library(org.Hs.eg.db) columns(org.Hs.eg.db) @ <>= help("SYMBOL") ## for explanation of these columns and keytypes values @ <>= keytypes(org.Hs.eg.db) uniKeys <- head(keys(org.Hs.eg.db, keytype="UNIPROT")) cols <- c("SYMBOL", "PATH") select(org.Hs.eg.db, keys=uniKeys, columns=cols, keytype="UNIPROT") @ \end{Solution} So how could you use select to annotate your results? This next exercise should hlep you to understand how that should generally work. \begin{Exercise} Please run the following code snippet (which will load a fake data result that I have provided for the purposes of illustration): <>= load(system.file("extdata", "resultTable.Rda", package="AnnotationDbi")) head(resultTable) @ The rownames of this table happen to provide entrez gene identifiers for each row (for human). Find the gene symbol and gene name for each of the rows in resultTable and then use the merge method to attach those annotations to it. \end{Exercise} \begin{Solution} <>= annots <- select(org.Hs.eg.db, keys=rownames(resultTable), columns=c("SYMBOL","GENENAME"), keytype="ENTREZID") resultTable <- merge(resultTable, annots, by.x=0, by.y="ENTREZID") head(resultTable) @ \end{Solution} \section{Using select with GO.db} When you load the GO.db package, a \Rclass{GODb} object is also loaded. This allows you to use the \Rfunction{columns}, \Rfunction{keys}, \Rfunction{keytypes} and \Rfunction{select} methods on the contents of the GO ontology. So if for example, you had a few GO IDs and wanted to know more about it, you could do it like this: <>= library(GO.db) GOIDs <- c("GO:0042254","GO:0044183") select(GO.db, keys=GOIDs, columns="DEFINITION", keytype="GOID") @ \section{Using select with TxDb packages} A \Rclass{TxDb} package (a 'TxDb' package) connects a set of genomic coordinates to various transcript oriented features. The package can also contain Identifiers to features such as genes and transcripts, and the internal schema describes the relationships between these different elements. All TxDb containing packages follow a specific naming scheme that tells where the data came from as well as which build of the genome it comes from. %% select exercise TxDb \begin{Exercise} Display the \Rclass{TxDb} object for the \Biocpkg{TxDb.Hsapiens.UCSC.hg19.knownGene} package. As before, use the \Rfunction{columns} and \Rfunction{keytypes} methods to discover which sorts of annotations can be extracted from it. Use the \Rfunction{keys} method to extract just a few gene identifiers and then pass those keys in to the \Rfunction{select} method in such a way that you extract the transcript ids and transcript starts for each. \end{Exercise} \begin{Solution} <>= library(TxDb.Hsapiens.UCSC.hg19.knownGene) txdb <- TxDb.Hsapiens.UCSC.hg19.knownGene txdb columns(txdb) keytypes(txdb) keys <- head(keys(txdb, keytype="GENEID")) cols <- c("TXID", "TXSTART") select(txdb, keys=keys, columns=cols, keytype="GENEID") @ \end{Solution} As is widely known, in addition to providing access via the \Rfunction{select} method, \Rclass{TxDb} objects also provide access via the more familiar \Rfunction{transcripts}, \Rfunction{exons}, \Rfunction{cds}, \Rfunction{transcriptsBy}, \Rfunction{exonsBy} and \Rfunction{cdsBy} methods. For those who do not yet know about these other methods, more can be learned by seeing the vignette called: \emph{Making and Utilizing TxDb Objects} in the \Rpackage{GenomicFeatures} package. \section{Using select with EnsDb packages} Similar to the \Rclass{TxDb} objects/packages discussed in the previous section, \Rclass{EnsDb} objects/packages provide genomic coordinates of gene models along with additional annotations (e.g. gene names, biotypes etc) but are tailored to annotations provided by Ensembl. The central methods \Rfunction{columns}, \Rfunction{keys}, \Rfunction{keytypes} and \Rfunction{select} are all implemented for \Rclass{EnsDb} objects. In addition, these methods allow also the use of the \Rclass{EnsDb} specific filtering framework to retrieve only selected information from the database (see vignette of the \Rpackage{ensembldb} package for more information). In the example below we first evaluate which columns, keys and keytypes are available for \Rclass{EnsDb} objects and fetch then the transcript ids, genomic start coordinate and transcript biotype for some genes. <>= library(EnsDb.Hsapiens.v75) edb <- EnsDb.Hsapiens.v75 edb ## List all columns columns(edb) ## List all keytypes keytypes(edb) ## Get the first keys <- head(keys(edb, keytype="GENEID")) ## Get the data select(edb, keys=keys, columns=c("TXID", "TXSEQSTART", "TXBIOTYPE"), keytype="GENEID") @ We can modify the queries above to retrieve only genes encoded on chromosome Y. To this end we use filter objects available for \Rclass{EnsDb} objects and its methods. <>= ## Retrieve all gene IDs of all lincRNAs encoded on chromosome Y linkY <- keys(edb, filter=list(GeneBiotypeFilter("lincRNA"), SeqNameFilter("Y"))) length(linkY) ## We get now all transcripts for these genes. txs <- select(edb, keys=linkY, columns=c("TXID", "TXSEQSTART", "TXBIOTYPE"), keytype="GENEID") nrow(txs) ## Alternatively, we could specify/pass the filters with the keys argument. txs <- select(edb, keys=list(GeneBiotypeFilter("lincRNA"), SeqNameFilter("Y")), columns=c("TXID", "TXSEQSTART", "TXBIOTYPE")) nrow(txs) @ The version number of R and packages loaded for generating the vignette were: <>= sessionInfo() @ \end{document} AnnotationDbi/vignettes/databaseTypes.pdf0000644000175200017520000000454514710217313021630 0ustar00biocbuildbiocbuild%PDF-1.3 % 1 0 obj <> endobj 2 0 obj <> endobj 3 0 obj <> endobj 4 0 obj <> endobj 5 0 obj <> stream xڵn7 st֥(6^)qf%z]MYsVߐ%QMfxcϏ\۾M,\#O^ďv+(VknG`j:p#`lv?%iv)el ڣeCghX@) gFhi0arhLAj=#YEO`fiode&"u*Z0-MȊ, wtD!Ά.)өlۮ?S_u1cU>Gu}γ{ %ʽrkvz,r&L~{wp~9Tt/{gĦ#mu`+7ucb.pD::ޓNk78*K'?^= sivOpApV߾E##hx=W>s +]9ݑ.`LȧKq»VqEB V'uP~ޛ}8k\8'8 *[}%}t'\pnvq,*7 #ݑ"4ZGKr7q_'ҕ@t&H~VSlp<5v]ZpX`^@j58!5g$*) w,y=AnI1J'{K`tf+{wFb@d9K >) F]]RsT鉈xyυ苍I+w,pϭdSŘwI'nnTC1%x h>*N xSVk-Fntb*7p]6ک; =8ZSj֛$w]hc3O/'$b> 'mZY<.Nٛ|X:?,.@}w* +7= PV7I)2Ca&kdEJI$)NVTbi%GO%q;Ck m[l@݉\OJ 9DCҜ5K9/h*xqrUpތUn W~]`zo%oL6BVӧN?2"anT idaJRR$JNH&_"s1(iwRw&I aMlbcHC;c endstream endobj 7 0 obj <> endobj 8 0 obj <>>> endobj xref 0 9 0000000000 65535 f 0000000015 00000 n 0000000066 00000 n 0000000111 00000 n 0000000283 00000 n 0000000380 00000 n 0000000000 65535 f 0000002008 00000 n 0000002096 00000 n trailer <> startxref 2153 %%EOF

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