Biobase/DESCRIPTION0000644000175400017540000000210413175724631014660 0ustar00biocbuildbiocbuildPackage: Biobase Title: Biobase: Base functions for Bioconductor Version: 2.38.0 Author: R. Gentleman, V. Carey, M. Morgan, S. Falcon Description: Functions that are needed by many other packages or which replace R functions. Suggests: tools, tkWidgets, ALL, RUnit, golubEsets Depends: R (>= 2.10), BiocGenerics (>= 0.3.2), utils Imports: methods Maintainer: Bioconductor Package Maintainer License: Artistic-2.0 Collate: tools.R strings.R environment.R vignettes.R packages.R AllGenerics.R VersionsClass.R VersionedClasses.R methods-VersionsNull.R methods-VersionedClass.R DataClasses.R methods-aggregator.R methods-container.R methods-MIAxE.R methods-MIAME.R methods-AssayData.R methods-AnnotatedDataFrame.R methods-eSet.R methods-ExpressionSet.R methods-MultiSet.R methods-SnpSet.R methods-NChannelSet.R anyMissing.R rowOp-methods.R updateObjectTo.R methods-ScalarObject.R zzz.R LazyLoad: yes biocViews: Infrastructure NeedsCompilation: yes Packaged: 2017-10-30 22:37:13 UTC; biocbuild Biobase/NAMESPACE0000644000175400017540000000602513175713325014375 0ustar00biocbuildbiocbuilduseDynLib(Biobase, copyEnv_sym=copyEnv, sublist_extract) import(methods) importFrom(BiocGenerics, combine, updateObject, updateObjectFromSlots, getObjectSlots, annotation, "annotation<-" ) importFrom(utils, head, tail, menu, packageDescription, read.table, write.table, .DollarNames) exportClasses(aggregator, container, eSet, MIAxE, MIAME, characterORMIAME, annotatedDataset, AssayData, data.frameOrNULL, AnnotatedDataFrame, Versions, VersionsNull, Versioned, VersionedBiobase, ExpressionSet, MultiSet, SnpSet, NChannelSet, ScalarObject, ScalarInteger, ScalarLogical, ScalarNumeric, ScalarCharacter) exportMethods("[", "[[", "$", abstract, aggenv, aggfun, annotatedDataFrameFrom, annotation, channel, channelNames, coerce, combine, content, contents, description, dimnames, "dimnames<-", dims, experimentData, expinfo, exprs, featureNames, featureData, fData, fvarLabels, fvarMetadata, hybridizations, initfun, length, locked, makeDataPackage, normControls, notes, otherInfo, pData, phenoData, preproc, protocolData, sampleNames, samples, se.exprs, selectChannels, snpCall, snpCallProbability, storageMode, varLabels, varMetadata, "annotation<-", "channelNames<-", "description<-", "dimLabels<-", "experimentData<-", "exprs<-", "featureNames<-", "featureData<-", "fData<-", "fvarLabels<-", "fvarMetadata<-", "notes<-", "preproc<-", "pData<-", "phenoData<-", "protocolData<-", "sampleNames<-", "snpCall<-", "snpCallProbability<-", "varLabels<-", "varMetadata<-", "assayData<-", "se.exprs<-", "storageMode<-", "write.exprs", dim, dimLabels, assayData, pubMedIds, "pubMedIds<-", isVersioned, isCurrent, classVersion, "classVersion<-", updateObject, updateObjectTo, initialize, show, Compare, AnnotatedDataFrame, ExpressionSet) export(Aggregate, addVigs2WinMenu, anyMissing, as.data.frame.ExpressionSet, assayDataNew, assayDataValidMembers, assayDataElementNames, assayDataElement, assayDataElementReplace, "assayDataElement<-", cache, copyEnv, copySubstitute, createPackage, dumpPackTxt, esApply, getPkgVigs, isUnique, listLen, matchpt, mkScalar, multiassign, NChannelSet, note, openPDF,openVignette, package.version, reverseSplit, rowMax, rowMedians, rowMin, rowQ, readExpressionSet, read.AnnotatedDataFrame, read.MIAME, MIAME, selectSome, strbreak, subListExtract, testBioCConnection, lcSuffix, lcPrefix, lcPrefixC, updateOldESet, userQuery, validMsg, write.AnnotatedDataFrame) S3method(.DollarNames, "eSet") S3method(.DollarNames, "ExpressionSet") S3method(head, "AnnotatedDataFrame") S3method(tail, "AnnotatedDataFrame") Biobase/NEWS0000644000175400017540000001254113175713325013655 0ustar00biocbuildbiocbuildCHANGES IN VERSION 2.37 ----------------------- BUG FIXES o '$' completion on eSet and ExpressionSet works in RStudio. CHANGES IN VERSION 2.33 ----------------------- BUG FIXES o exprs<- enforces value with correct dim, dimnames. CHANGES IN VERSION 2.31 ----------------------- NEW FEATURES o tab completion implemented for eSet classes o head and tail.AnnotatedDataFrame methods introduced CHANGES IN VERSION 2.27 ----------------------- NEW FEATURES o Add write.AnnotatedDataFrame function; request of samuel.granjeaud CHANGES IN VERSION 2.21 ----------------------- USER VISIBLE CHANGES o channelNames<-,NChannelSet,*-methods allow re-naming channels o NChannelSet validity requires all assayDataElementNames() to be levels in varMetadata()$channel. BUG FIXES o Updating an AnnotatedDataFrame no longer duplicates metadata from partially matching column names. CHANGES IN VERSION 2.19 ----------------------- USER VISIBLE CHANGES o dimnames(), rownames(), colnames() and setters work on eSet-derived objects CHANGES IN VERSION 2.17 ----------------------- USER VISIBLE CHANGES o l2e(), previously deprecated, has been made defunct. o All objects made defunct in previous release cycles have been removed. This includes geneNames, getExpData, eList, reporterNames, getBiocRepos, read.exprSet, updateOldMiame, df2pD, read.pD, read.phenoData, exprData, exprList, and phenoData. CHANGES IN VERSION 2.11 ---------------------- USER VISIBLE CHANGES o 'l2e' deprecated, use 'list2env' in base instead o MIAME class moved to subclass of MIAxE virtual class NEW FEATURES o Added MIAxE virtual class to hold experiment meta-data classes CHANGES IN VERSION 2.7 ---------------------- USER VISIBLE CHANGES o 'show,eSet-method' summarizes protocolData, if available. o 'snpCall' 'snpCallProbability' accessors added for SnpSet. BUG FIXES o 'selectSome' returns short factors as character() CHANGES IN VERSION 2.5 ---------------------- USER VISIBLE CHANGES o 'protocolData' slot added to eSet class to store protocol metadata stored in microarray data files; can be accessed by protocolData and set by protocolData<-. o 'sampleNames,NChannelSet-method' returns a vector when the sample names of each channel are the same. CHANGES IN VERSION 2.1 ---------------------- NEW FEATURES o 'makeDataPacakge' method for ExpressionSet now accepts a 'description' argument for the generated manual page. BUG FIXES o combine,matrix,matrix-method would record 'NA' for entries in the second matrix with niether rows nor columns present in the first. o openPDF now checks for NULL or zero-length pdfviewer option CHANGES IN VERSION 2.0 ---------------------- SIGNIFICANT USER-VISIBLE CHANGES o 'combine' on data.frame columns with mismatched levels causes a warning, rather than error. o updateObject does not warn about duplicating locked environment, unlesss verbose=TRUE NEW FEATURES o 'combine' now works to combine rows of ExpressionSet BUG FIXES o AnnotatedDataFrame 'show' listed additional varMetadata column names incorrectly when labelDescription was not the first. NEWLY DEFUNCT CLASSES, METHODS, FUNCTIONS, DATA SETS o Defunct S4 Classes 1) annotatedDataset - class definition still exits to support phenoData conversion 2) exprMatrix - removed class definition 3) exprSet - class definition still exists to allow conversion to ExpressionSet 4) phenoData - class definition still exists to allow conversion to AnnotatedDataFrame o Defunct Generics/Methods 1) addVarMetadataEntry - S4 generic definition removed 2) as.data.frame.exprSet - S3 method removed 3) convertVarLabels - S4 generic definition removed 4) eList - S4 methods remain with .Defunct messages 5) "eList<-" - S4 methods remain with .Defunct messages 6) exprs2excel - S4 generic definition removed 7) getExpData - S4 methods remain with .Defunct messages 8) geneNames - S4 methods remain with .Defunct messages 9) "geneNames<-" - S4 methods remain with .Defunct messages 10) getUnits - S4 generic definition removed 11) getVarMetadata - S4 generic definition removed 12) iter - S4 generic definition removed 13) reporterInfo - S4 generic definition removed 14) "reporterInfo<-" - S4 generic definition removed 15) reporterNames - S4 methods remain with .Defunct messages 16) "reporterNames<-" - S4 methods remain with .Defunct messages 17) split (for use with exprSet objects) - S4 generic definition removed 18) update2MIAME - S4 generic definition removed o Defunct functions 1) df2pD - function stub with .Defunct message 2) read.exprSet - function stub with .Defunct message 3) read.pD - function stub with .Defunct message 4) read.phenoData - function stub with .Defunct message 5) updateOldMiame - function stub with .Defunct message o Defunct data sets 1) bbsym 2) eset - use sample.ExpressionSet instead 3) golubMergeSub 4) sample.eSet - use sample.MultiSet instead 4) sample.exprSet.1 - use sample.ExpressionSet instead 5) sample.exprSet - use sample.ExpressionSet instead 6) SWPD 7) swrep Biobase/R/0000755000175400017540000000000013175713325013354 5ustar00biocbuildbiocbuildBiobase/R/AllGenerics.R0000644000175400017540000001635513175713325015701 0ustar00biocbuildbiocbuildsetGeneric("abstract", function(object) standardGeneric("abstract")) setGeneric("aggenv", function(object) standardGeneric("aggenv")) setGeneric("aggfun", function(object) standardGeneric("aggfun")) setGeneric("annotatedDataFrameFrom", function(object, byrow, ...) standardGeneric("annotatedDataFrameFrom")) setGeneric("assayData", function(object)standardGeneric("assayData")) setGeneric("assayData<-", function(object, value) standardGeneric("assayData<-")) setGeneric("channelNames", function(object, ...) standardGeneric("channelNames")) setGeneric("channel", function(object, name, ...) standardGeneric("channel")) setGeneric("content", function(object) standardGeneric("content")) setGeneric("description", function(object, ...) standardGeneric("description")) setGeneric("description<-", function(object, value) standardGeneric("description<-")) setGeneric("dims", function(object) standardGeneric("dims")) setGeneric("dimnames") setGeneric("dimnames<-") setGeneric("dimLabels", function(object) standardGeneric("dimLabels")) setGeneric("dimLabels<-", function(object, value) standardGeneric("dimLabels<-")) setGeneric("esApply", function(X, MARGIN, FUN, ...) standardGeneric("esApply"), signature=c("X")) setGeneric("experimentData", function(object) standardGeneric("experimentData")) setGeneric("experimentData<-",function(object, value) standardGeneric("experimentData<-")) setGeneric("expinfo", function(object) standardGeneric("expinfo")) setGeneric("exprs", function(object) standardGeneric("exprs")) setGeneric("exprs<-", function(object, value) standardGeneric("exprs<-")) setGeneric("featureNames", function(object) standardGeneric("featureNames")) setGeneric("featureNames<-", function(object, value) standardGeneric("featureNames<-")) setGeneric("featureData", function(object) standardGeneric("featureData")) setGeneric("featureData<-", function(object, value) standardGeneric("featureData<-")) setGeneric("fData", function(object) standardGeneric("fData")) setGeneric("fData<-", function(object, value) standardGeneric("fData<-")) setGeneric("fvarLabels", function(object) standardGeneric("fvarLabels")) setGeneric("fvarLabels<-", function(object, value) standardGeneric("fvarLabels<-")) setGeneric("fvarMetadata", function(object) standardGeneric("fvarMetadata")) setGeneric("fvarMetadata<-", function(object, value) standardGeneric("fvarMetadata<-")) setGeneric("hybridizations", function(object) standardGeneric("hybridizations")) setGeneric("initfun", function(object) standardGeneric("initfun")) setGeneric("locked", function(object) standardGeneric("locked")) setGeneric("makeDataPackage", function(object, author, email, packageName=deparse(substitute(object)), packageVersion=package_version("1.0.0"), license="Artistic-2.0", biocViews="ExperimentData", filePath=tempdir(), ...) standardGeneric("makeDataPackage"), signature="object") setGeneric("normControls", function(object) standardGeneric("normControls")) setGeneric("notes", function(object) standardGeneric("notes")) setGeneric("notes<-", function(object, value) standardGeneric("notes<-")) setGeneric("otherInfo", function(object) standardGeneric("otherInfo")) setGeneric("pData", function(object) standardGeneric("pData")) setGeneric("pData<-", function(object, value) standardGeneric("pData<-")) setGeneric("phenoData", function(object) standardGeneric("phenoData")) setGeneric("phenoData<-", function(object, value) standardGeneric("phenoData<-")) setGeneric("preproc", function(object) standardGeneric("preproc")) setGeneric("preproc<-", function(object, value) standardGeneric("preproc<-")) setGeneric("protocolData", function(object) standardGeneric("protocolData")) setGeneric("protocolData<-", function(object, value) standardGeneric("protocolData<-")) setGeneric("pubMedIds", function(object) standardGeneric("pubMedIds")) setGeneric("pubMedIds<-", function(object, value) standardGeneric("pubMedIds<-")) setGeneric("sampleNames", function(object) standardGeneric("sampleNames")) setGeneric("sampleNames<-", function(object, value) standardGeneric("sampleNames<-")) setGeneric("samples", function(object) standardGeneric("samples")) setGeneric("se.exprs", function(object) standardGeneric("se.exprs")) setGeneric("se.exprs<-", function(object, value) standardGeneric("se.exprs<-")) setGeneric("selectChannels", function(object, names, ...) standardGeneric("selectChannels")) setGeneric("selectSomeIndex", function(object, ...) standardGeneric("selectSomeIndex")) setGeneric("snpCall", function(object, ...) standardGeneric("snpCall")) setGeneric("snpCall<-", function(object, ..., value) standardGeneric("snpCall<-")) setGeneric("snpCallProbability", function(object, ...) standardGeneric("snpCallProbability")) setGeneric("snpCallProbability<-", function(object, ..., value) standardGeneric("snpCallProbability<-")) setGeneric("storageMode", function(object) standardGeneric("storageMode")) setGeneric("storageMode<-", function(object, value) standardGeneric("storageMode<-")) setGeneric("varLabels", function(object) standardGeneric("varLabels")) setGeneric("varLabels<-", function(object, value) standardGeneric("varLabels<-")) setGeneric("varMetadata", function(object) standardGeneric("varMetadata")) setGeneric("varMetadata<-", function(object, value) standardGeneric("varMetadata<-")) setGeneric("write.exprs", function(x,...) standardGeneric("write.exprs")) ## Version-related generics setGeneric("classVersion", function(object) standardGeneric("classVersion")) setGeneric("classVersion<-", function(object, value) standardGeneric("classVersion<-")) setGeneric("isCurrent", function(object, value) standardGeneric("isCurrent")) setGeneric("isVersioned", function(object) standardGeneric("isVersioned")) ## updateObjectTo setGeneric("updateObjectTo", function(object, template, ..., verbose=FALSE) { result <- standardGeneric("updateObjectTo") if (!is(result, class(template))) # or strict equality? stop("updateObjectTo returned class '", class(result), "' ", "expected class '", class(template), "'") validObject(result) result }) ## Generics for Constructors: AnnotatedDataFrame and ExpresssionSet setGeneric("AnnotatedDataFrame", function(data, varMetadata, ...) standardGeneric("AnnotatedDataFrame")) setGeneric("ExpressionSet", function(assayData, phenoData=annotatedDataFrameFrom(assayData, byrow=FALSE), featureData=annotatedDataFrameFrom(assayData, byrow=TRUE), experimentData=MIAME(), annotation=character(), protocolData=annotatedDataFrameFrom(assayData, byrow=FALSE), ...) standardGeneric("ExpressionSet"), signature="assayData") Biobase/R/DataClasses.R0000644000175400017540000002236513175713325015676 0ustar00biocbuildbiocbuild# ========================================================================== # aggregator: a simple aggregator (R. Gentleman, 2001) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - # Data are aggregated in the environment env if they are not there then the # get assigned with initfun, if they are there they get aggregated with agfun # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - .aggregator <- setClass("aggregator", representation( aggenv = "environment", initfun = "function", aggfun = "function" ), prototype = list( initfun = function(name, val) 1, aggfun = function(name, current, val) current + 1 ) ) # ========================================================================== # container: lists containing objects of specified class (R. Gentleman, 2001) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - .container <- setClass("container", representation( x = "list", content = "character", locked = "logical" ), prototype = list( x = vector("list", 0), content = "object", locked = FALSE ) ) # ========================================================================== # phenoData (DEFUNCT) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setClass("phenoData", representation( pData = "data.frame", varLabels = "list", varMetadata = "data.frame" ), contains="Versioned", validity = function(object) { paste("class phenoData is defunct,", "convert using as(<>, \"AnnotatedDataFrame\")") } ) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setOldClass("data.frame") setClassUnion("data.frameOrNULL", c("data.frame", "NULL")) # ========================================================================== # MIAxE: a VIRTUAL class for experiment meta-data # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - .MIAxe <- setClass("MIAxE", representation("VIRTUAL"), contains="Versioned", prototype = prototype(.Versioned(versions=c(MIAxE="1.0.0"))) ) # MIAME: a class for microarray data - MIAME information (Rafael A. Irizarry) # More info: http://www.mged.org/Workgroups/MIAME/miame_1.1.html .MIAME <- setClass("MIAME", representation( name = "character", lab = "character", contact = "character", title = "character", abstract = "character", url = "character", pubMedIds = "character", samples = "list", hybridizations = "list", normControls = "list", preprocessing = "list", other = "list" ), contains=c("MIAxE"), prototype = prototype( .Versioned(versions=c(classVersion("MIAxE"), MIAME="1.1.0")), name = "", lab = "", contact = "", title = "", abstract = "", url = "", pubMedIds = "", samples = list(), hybridizations = list(), normControls = list(), preprocessing = list(), other = list() ) ) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - # trick so that Plobs works # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setClassUnion("characterORMIAME", c("MIAME", "character")) # ========================================================================== # annotatedDataset (DEFUNCT) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setClass("annotatedDataset", representation( reporterInfo = "data.frameOrNULL", phenoData = "phenoData", "VIRTUAL" ), contains=c("VersionedBiobase")) # ========================================================================== # AnnotatedDataFrame: A data.frame, with annotations about columns named # in the data slot contained in the metadata slot. The data slot has # columns identifying different entities (e.g., genes, samples) and # the columns contain attributes of those entities (e.g., control or # spike-in information for genes, age or sex for samples). The number # of columns in the data slot equals the number of rows in the # metadata slot. # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - .AnnotatedDataFrame <- setClass("AnnotatedDataFrame", representation(varMetadata = "data.frame", data = "data.frame", dimLabels = "character"), contains=c("Versioned"), prototype = prototype( .Versioned(versions=list(AnnotatedDataFrame="1.1.0")), varMetadata = new( "data.frame" ), data = new( "data.frame" ), dimLabels=c("rowNames", "columnNames"))) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setClassUnion("AssayData", c("list", "environment")) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - # eSet: A VIRTUAL class containing assay data (typically, one or many # different sets of results obtained from one or many samples in a # single experiment), phenotypic data (describing the samples involved # in the experiment), experimental data (describing the methods and # protocols used), and an annotation (linking to separately maintained # chip annotation information). # # When assayData contains several sets of results, each set must have # the same dimension (e.g., columns representing genes, rows # representing samples, all assayData members providing information # for the same number of genes and samples). # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - .eSet <- setClass("eSet", representation(assayData = "AssayData", phenoData = "AnnotatedDataFrame", featureData = "AnnotatedDataFrame", experimentData = "MIAxE", annotation = "character", protocolData="AnnotatedDataFrame", "VIRTUAL"), contains="VersionedBiobase", prototype = prototype( .VersionedBiobase(versions=c(eSet="1.3.0")), assayData = list(), # use initialize to set as env, so # different instances have # different envs phenoData = .AnnotatedDataFrame( dimLabels=c("sampleNames", "sampleColumns")), featureData = .AnnotatedDataFrame( dimLabels=c("featureNames", "featureColumns")), annotation = character(), protocolData = .AnnotatedDataFrame( dimLabels=c("sampleNames", "sampleColumns")))) .ExpressionSet <- setClass("ExpressionSet", representation(experimentData="MIAME"), contains = "eSet", prototype = prototype( .VersionedBiobase( versions=c(classVersion("eSet"), ExpressionSet="1.0.0")), experimentData=.MIAME())) .NChannelSet <- setClass("NChannelSet", contains = "eSet", prototype = prototype( .VersionedBiobase( versions=c(classVersion("eSet"), NChannelSet="1.0.0")), phenoData = .AnnotatedDataFrame( data=data.frame(), varMetadata=data.frame( labelDescription=character(0), channelDescription=factor())))) .MultiSet <- setClass("MultiSet", # any element in assayData slot contains = "eSet", prototype = prototype( .VersionedBiobase( versions=c(classVersion("eSet"), MultiSet="1.0.0")))) .SnpSet <- setClass("SnpSet", # call, callProbability contains = "eSet", prototype = prototype( .VersionedBiobase( versions=c(classVersion("eSet"), SnpSet="1.0.0")))) # ========================================================================== # exprSet (DEFUNCT) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setClass("exprSet", representation( exprs = "matrix", se.exprs = "matrix", description = "characterORMIAME", annotation = "character", notes = "character" ), contains = c("annotatedDataset"), # contains VersionedBiobase implicitly validity = function(object) paste("class exprSet is defunct,", "convert using as(<>, \"ExpressionSet\")") ) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - .ScalarObject <- setClass("ScalarObject", contains="VIRTUAL", validity=function(object) { if (length(object) != 1L) paste(class(object), "must have length one") else TRUE }) .ScalarLogical <- setClass("ScalarLogical", contains=c("ScalarObject", "logical"), prototype=NA) .ScalarCharacter <- setClass("ScalarCharacter", contains=c("ScalarObject", "character"), prototype="") .ScalarInteger <- setClass("ScalarInteger", contains=c("ScalarObject", "integer"), prototype=NA_integer_) .ScalarNumeric <- setClass("ScalarNumeric", contains=c("ScalarObject", "numeric"), prototype=NA_real_) Biobase/R/VersionedClasses.R0000644000175400017540000000066013175713325016755 0ustar00biocbuildbiocbuild## Versions previously defined .VersionsNull <- setClass("VersionsNull", contains="Versions") .Versioned <- setClass("Versioned", representation(.__classVersion__ = "Versions")) .VersionedBiobase <- setClass("VersionedBiobase", contains="Versioned", prototype=prototype( .__classVersion__ = .Versions( R = getRversion(), Biobase = package_version(packageDescription("Biobase", NULL, "Version"))))) Biobase/R/VersionsClass.R0000644000175400017540000001053313175713325016277 0ustar00biocbuildbiocbuild## ========================================================================== ## Versions: version string information ## - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ## methods and class defined together so available for prototypes elsewhere .Versions <- setClass("Versions", contains="list") setMethod("initialize", signature(.Object="Versions"), function(.Object, ...) callNextMethod(.Object, .asValidVersions(list(...)))) .isValidVersion <- function(versions) { tryCatch(all(as.integer(versions)==versions) && all(versions >= 0) && length(versions) > 1, error=function(err) FALSE, warning=function(warn) {}) } .asValidVersions <- function(versions) { res <- list() for (i in seq(along=versions)) res[i] <- if (!is.character(versions[[i]]) && .isValidVersion(versions[[i]])) versions[i] else unclass(numeric_version(versions[[i]])) names(res) <- names(versions) res } ## update setMethod("updateObject", signature(object="Versions"), function(object, ..., verbose=FALSE) { if (verbose) message("updateObject(object = 'Versions')") if (!isS4(object)) do.call(new, c("Versions", object)) else object }) ## access setMethod("[", signature=signature(x="Versions"), function(x, i, j, ..., drop = FALSE) { ## 'dispatch' on i to avoid S4 complaint about j 'missing' if (is(i, "character") && !all(i %in% names(x))) { bad <- unique(i[!i %in% names(x)]) cl <- deparse(match.call()[[2]]) stop(sprintf("'[' indices '%s' not found in '%s'", paste(bad, collapse="', '"), cl)) } as(callNextMethod(), "Versions") }) ## assign setReplaceMethod("[", signature(x="Versions"), function(x, i, j, value) { lst <- x@.Data names(lst) <- names(x) lst[i] <- .asValidVersions(value) x@.Data <- lst names(x) <- names(lst) x }) setReplaceMethod("[[", signature(x="Versions"), function(x, i, j, value) { lst <- x@.Data names(lst) <- names(x) lst[[i]] <- unlist(.asValidVersions(value)) x@.Data <- lst names(x) <- names(lst) x }) setReplaceMethod("$", signature(x="Versions"), function(x, name, value) { x[[name]] <- value; x }) ## Compare .as.numeric_version <- function(x) numeric_version(as(x, "character")) .canVersionCompare <- function(e1, e2) { if (length(e1) != length(e2)) stop(sprintf("cannot compare versions with length '%d', '%d'", length(e1), length(e2))) if (length(e1)>1 && (!all(names(e1) %in% names(e2)) || !all(names(e2) %in% names(e1)))) stop("cannot compare versions with different names") TRUE } setMethod("Compare", signature=signature( e1="Versions", e2="Versions"), function(e1, e2) { .canVersionCompare(e1, e2) e2 <- e2[names(e1)] e1 <- .as.numeric_version(e1) e2 <- .as.numeric_version(e2) callNextMethod(e1, e2) }) setMethod("Compare", signature=signature( e1="Versions", e2="character"), function(e1, e2) { .canVersionCompare(e1, e2) if (length(e2) > 1) e2 <- e2[names(e1)] e1 <- .as.numeric_version(e1) e2 <- numeric_version(e2) callNextMethod(e1, e2) }) setMethod("Compare", signature=signature( e1="character", e2="Versions"), function(e1, e2) callGeneric(e2,e1)) ## show setAs("Versions", "character", function(from) { if (length(from)) sapply(from, paste, collapse=".") else "Versioned; no version string" }) setMethod("show", signature(object="Versions"), function(object) print(as(object, "character"))) Biobase/R/anyMissing.R0000644000175400017540000000050213175713325015615 0ustar00biocbuildbiocbuildanyMissing <- function(x=NULL) { .Call("anyMissing", x); } ############################################################################ # HISTORY: # 2007-08-14 # o Created. See also R-devel thread "hasNA()/anyNA()?" on 2007-08-13. ############################################################################ Biobase/R/environment.R0000644000175400017540000000673213175713325016053 0ustar00biocbuildbiocbuild# ========================================================================== # Functions to operate with the environment: # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - # .initContents; .buildBiobaseOpts; # multiassign; copyEnv # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - .initContents <- function() { makeG = TRUE if( isGeneric("contents", where = .GlobalEnv ) ) if( identical(names(formals(contents)), c("object", "all.names")) ) makeG = FALSE if(makeG) setGeneric("contents", function(object, all.names) standardGeneric("contents")) setMethod("contents", "environment", function(object, all.names) { if (missing(all.names)) all.names <- FALSE as.list(object, all.names=all.names) } ) } # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - .buildBiobaseOpts <- function() { BioC <- getOption("BioC") if (is.null(BioC)) { BioC <- list() class(BioC) <- "BioCOptions" } Base <- BioC$Base if (is.null(Base)) { Base <- list() class(Base) <- "BioCPkg" } if (is.null(Base$urls)) Base$urls <- list( bioc = "http://bioconductor.org") ##RI: I added this to make my life easier. Should it be TRUE? ##AJR: NO. I've run across a few cases when it would completely ## break functionality, i.e. when tcltk isn't part of the R ## package (on weird, and development-based machines if (is.null(Base$use.widgets)) Base$use.widgets <- FALSE BioC$Base <- Base options("BioC"=BioC) } # ========================================================================== # RG: # multiput and multiget # ideally these will be internalized at some point # FIXME: I think Luke's Dynamic variables should be used rather than # the on.exit kludge # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - multiassign <- function (x, value, envir = parent.frame(), inherits = FALSE) { if( ! is.environment(envir) ) stop("envir argument is not an environment") if( missing(value) ) { nx <- names(x) if( any(nchar(nx) == 0) ) stop("value is missing and x does not have named components") value <- x x <- nx } lenx <- length(x) for(i in 1:lenx) { i2 <- (i-1)%%lenx+1 if( is.list(x) ) { if( is.list(value) ) assign(x[[i]], value[[i2]], envir=envir, inherits=inherits) else assign(x[[i]], value[i2], envir=envir, inherits=inherits) } else { if( is.list(value) ) assign(x[i], value[[i2]], envir=envir, inherits=inherits) else assign(x[i], value[i2], envir=envir, inherits=inherits) } } } #### Functions for lists and environments listLen <- function(x) .Call("listLen", x, PACKAGE="Biobase") .new_env_size <- function(n) { ## helper function returns suggested size for new environments that ## will be used as hashtables given expected number of elements 'n'. max(29L, as.integer(n * 1.20)) } copyEnv <- function(oldEnv, newEnv, all.names=FALSE) { if (missing(newEnv)) newEnv <- new.env(hash=TRUE, parent=parent.env(oldEnv), size=.new_env_size(length(oldEnv))) .Call(copyEnv_sym, oldEnv, newEnv, all.names) } ## Deprecated in v 2.11.2 l2e <- function(vals, envir) { .Defunct("list2env", package="base") } Biobase/R/methods-AnnotatedDataFrame.R0000644000175400017540000004733113175713325020632 0ustar00biocbuildbiocbuildsetMethod("initialize", signature(.Object="AnnotatedDataFrame"), function(.Object, data = data.frame(), varMetadata = data.frame(), ...) { tryCatch({ if (missing(varMetadata)) { if (!missing(data)) checkClass(data, "data.frame", class(.Object)) varMetadata <- data.frame(labelDescription = rep(NA, ncol(data))) row.names(varMetadata) <- as.character(colnames(data)) } else { checkClass(varMetadata, "data.frame", class(.Object)) if (!"labelDescription" %in% colnames(varMetadata)) varMetadata[["labelDescription"]] <- rep(NA, nrow(varMetadata)) row.names(varMetadata) <- names(data) } varMetadata[["labelDescription"]] <- as.character(varMetadata[["labelDescription"]]) }, error=function(err) { stop(conditionMessage(err), "\n AnnotatedDataFrame 'initialize' could not update varMetadata:", "\n perhaps pData and varMetadata are inconsistent?") }) callNextMethod(.Object, data=data, varMetadata=varMetadata, ...) }) validAnnotatedDataFrame <- function( object ) { msg <- NULL if (!is(object, "AnnotatedDataFrame")) msg <- c(msg, paste("cannot validate", class(object), "as AnnotatedDataFrame" )) if (length(row.names(varMetadata(object))) != length(colnames(pData(object)))) msg <- c(msg, paste("all AnnotatedDataFrame pData column names", "must be present as rows in varMetadata", "and vice versa")) else if (any(row.names(varMetadata(object)) != colnames(pData(object)))) msg <- c(msg, paste("AnnotatedDataFrame colnames of data differ", "from row.names of varMetadata")) if ( !("labelDescription" %in% colnames(varMetadata(object)))) msg <- c(msg, paste("AnnotatedDataFrame varMetadata", "missing labelDescription column")) if (length(dimLabels(object))!=2) msg <- c(msg, "dimLabels must be a character vector of length 2") if (is.null(msg)) TRUE else msg } setValidity("AnnotatedDataFrame", validAnnotatedDataFrame) setAs("AnnotatedDataFrame", "data.frame", function(from) { pData(from) }) setMethod("updateObject", signature(object="AnnotatedDataFrame"), function(object, ..., verbose=FALSE) { if (verbose) message("updateObject(object = 'AnnotatedDataFrame')") object <- asS4(object) if (isVersioned(object) && isCurrent(object)["AnnotatedDataFrame"]) callNextMethod() else { ## version 1.0.0. -> 1.1.0 needs a new slot "dimLabels" to <- new(class(object)) varMetadata(to) <- updateObject(varMetadata(object)) pData(to) <- updateObject(pData(object)) to } }) annotatedDataFrameFromMatrix <- function(object, byrow=FALSE, ...) { ## contract: 'object' is matrix-like, with dim, rownames, colnames ## methods. Returns AnnotatedDataFrame with appropriate dimensions. dims <- dim(object) if (is.null(dims) || all(dims==0)) annotatedDataFrameFrom(NULL, byrow=byrow, ...) else { n <- if (byrow) dims[1] else dims[2] nms <- if(byrow) rownames(object) else colnames(object) data <- data.frame(numeric(n), row.names=nms)[,FALSE] dimLabels <- if (byrow) c("featureNames", "featureColumns") else c("sampleNames", "sampleColumns") AnnotatedDataFrame(data=data, dimLabels=dimLabels) } } setMethod("annotatedDataFrameFrom", signature(object="matrix"), annotatedDataFrameFromMatrix) annotatedDataFrameFromNull <- function(object, byrow=FALSE, ...) { dimLabels <- if (byrow) c("featureNames", "featureColumns") else c("sampleNames", "sampleColumns") AnnotatedDataFrame(data=data.frame(), dimLabels=dimLabels) } setMethod("annotatedDataFrameFrom", signature(object="NULL"), annotatedDataFrameFromNull) annotatedDataFrameFromAssayData <- function(object, byrow=FALSE, ...) { eltNames <- if (is(object, "environment")) ls(object) else names(object) if (length(eltNames)==0) annotatedDataFrameFrom(NULL, byrow=byrow, ...) else annotatedDataFrameFrom(object[[eltNames[1]]], byrow=byrow, ...) } setMethod("annotatedDataFrameFrom", signature(object="AssayData"), annotatedDataFrameFromAssayData) head.AnnotatedDataFrame <- function(x, n=6L, ...) { ## essentially, utils:::head.data.frame stopifnot(length(x) == 1L) n <- if (n < 0L) { max(nrow(x) + n, 0L) } else min(n, nrow(x)) x[seq_len(n), ] } tail.AnnotatedDataFrame <- function(x, n=6L, ...) { ## essentially, utils:::tail.data.frame stopifnot(length(x) == 1L) nrx <- nrow(x) n <- if (n < 0L) max(nrx + n, 0L) else min(n, nrx) x[seq.int(to = nrx, length.out = n), , drop = FALSE] } setMethod("dimnames", "AnnotatedDataFrame", function(x) { dimnames(pData(x)) }) setReplaceMethod("dimnames", "AnnotatedDataFrame", function(x, value) { sampleNames(x) <- value[[1]] varLabels(x) <- value[[2]] x }) setMethod("dim", "AnnotatedDataFrame", function( x ) { d <- dim(pData(x)) names(d) <- dimLabels(x) d }) setMethod("dimLabels", "AnnotatedDataFrame", function(object) { object@dimLabels }) setReplaceMethod("dimLabels", signature=signature( object="AnnotatedDataFrame", value="character"), function(object, value) { object@dimLabels <- value object }) setMethod("pData", "AnnotatedDataFrame", function(object) object@data) setReplaceMethod("pData", signature=signature( object="AnnotatedDataFrame", value="data.frame"), function(object, value) { idx <- match(names(value), rownames(varMetadata(object))) varMetadata <- varMetadata(object)[idx,,drop=FALSE] row.names(varMetadata) <- names(value) initialize(object, data=value, varMetadata=varMetadata) }) setMethod("sampleNames", "AnnotatedDataFrame", function(object) row.names(object@data)) setReplaceMethod("sampleNames", signature(object="AnnotatedDataFrame", value="ANY"), function(object, value) { if (!is.null(value) && (length(value) != dim(object@data)[[1]])) stop("number of new names (", length(value), ") ", "should equal number of rows in AnnotatedDataFrame (", dim( object )[[1]], ")") row.names(object@data) <- value object }) setMethod("featureNames", signature(object="AnnotatedDataFrame"), function(object) sampleNames(object)) setReplaceMethod("featureNames", signature(object="AnnotatedDataFrame", value="ANY"), function(object, value) { sampleNames(object) <- value object }) setMethod("varLabels", "AnnotatedDataFrame", function(object) colnames(object@data)) setReplaceMethod("varLabels", signature("AnnotatedDataFrame", "ANY"), function(object, value) { if (!is.null(value) && (length(value) != dim(object@data)[[2]])) stop("number of new varLabels (", length(value), ") ", "should equal number of columns in AnnotatedDataFrame (", dim(object)[[2]], ")") if (!is.null(value)) { ## silently ignore attempts to set colnames to NULL colnames(object@data) <- value row.names(object@varMetadata) <- value } object }) setMethod("varMetadata", "AnnotatedDataFrame", function(object) object@varMetadata ) setReplaceMethod("varMetadata", c("AnnotatedDataFrame", "data.frame"), function(object, value) { if (!("labelDescription" %in% colnames(value))) warning("'varMetadata' must have column 'labelDescription'") rinfo <- .row_names_info(value) if (0L != length(varLabels(object))) { if (0L <= rinfo) { ## not 'automatic' bad <- setdiff(row.names(value), varLabels(object)) if (0L != length(bad)) { fmt <- "'%s' not in 'varLabels()'" nms <- paste(selectSome(bad), collapse="', '") stop(sprintf(fmt, nms)) } } if (ncol(object) != abs(rinfo)) { fmt <- "varMetadata has %d row(s), 'value' has %d" stop(sprintf(fmt, ncol(object), nrow(value))) } if (0 < ncol(pData(object))) row.names(value) <- names(pData(object)) } object@varMetadata <- value object }) setMethod("[", signature(x="AnnotatedDataFrame"), function(x, i, j, ..., drop) { if (missing(drop)) drop = FALSE else if (drop) stop("'AnnotatedDataFrame' does not support drop = TRUE") if(missing(j)) { mD <- x@varMetadata pD <- x@data[i,,drop = drop] } else { mD <- x@varMetadata[j,,drop = drop] if( missing( i )) pD <- x@data[,j,drop = drop] else pD <- x@data[i,j,drop = drop] } initialize(x, data=pD, varMetadata=mD) }) ##setMethod("$", "AnnotatedDataFrame", function(x, name) `$`(pData(x), name)) setMethod("$", "AnnotatedDataFrame", function(x, name) { eval(substitute(pData(x)$NAME_ARG, list(NAME_ARG=name))) }) setReplaceMethod("$", "AnnotatedDataFrame", function(x, name, value) { x[[name]] <- value x }) setMethod("[[", "AnnotatedDataFrame", function(x, i, j, ...) pData(x)[[i]] ) setReplaceMethod("[[", signature=signature(x="AnnotatedDataFrame"), function(x, i, j, ..., value) { pData(x)[[i]] <- value for (metadata in names(list(...))) varMetadata(x)[i, metadata] <- list(...)[[metadata]] x }) setAs("phenoData", "AnnotatedDataFrame", function(from) { from <- asS4(from) ## data data <- from@pData ## varMetadata cnames <- colnames(data) varMetadata <- from@varMetadata if (all(dim(varMetadata)==0)) { varMetadata <- data.frame(numeric(length(cnames)),row.names=cnames)[,FALSE] } ## varLabels -- as column in varMetadata,or warn varLabels <- from@varLabels if (length(varLabels)>0 && !("labelDescription" %in% colnames(varMetadata))) varMetadata[["labelDescription"]] <- as.character(varLabels[cnames]) else if (length(varLabels)>0) warning("contents of varLabels ignored\n", call.=FALSE) else varMetadata[["labelDescription"]] <- as.character(rep(NA, nrow(varLabels))) AnnotatedDataFrame( data=data, varMetadata=varMetadata, dimLabels=c("sampleNames", "sampleColumns")) }) setAs("data.frame", "AnnotatedDataFrame", function(from) AnnotatedDataFrame(data=from)) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - selectSome <- function(obj, maxToShow=5) { len <- length(obj) if (maxToShow<3) maxToShow <- 3 if (len > maxToShow) { maxToShow <- maxToShow-1 bot <- ceiling(maxToShow/2) top <- len-(maxToShow-bot-1) nms <- obj[c(1:bot, top:len)] c(as.character(nms[1:bot]), "...", as.character(nms[-c(1:bot)])) } else if (is.factor(obj)) as.character(obj) else obj } setMethod("selectSomeIndex", signature(object="data.frame"), function(object, maxToShow=5, byrow=TRUE, ...) { len <- if (byrow) dim(object)[[1]] else dim(object)[[2]] if (maxToShow < 3) maxToShow <- 3 if (len > maxToShow) { maxToShow <- maxToShow - 1 bot <- ceiling(maxToShow/2) top <- len-(maxToShow-bot-1) list(1:bot, "...", top:len) } else if (len >= 1) list(1:len, NULL, NULL) else list(NULL, NULL, NULL) }) .wrapcat <- function(lbl, nms, total, ..., indent=2, exdent=4) { lbl <- sprintf("%s:", lbl) txt <- paste(c(lbl, nms), collapse=" ") ext <- if (length(nms) < total) sprintf("(%d total)", total) else character() txt <- paste(c(lbl, nms, ext), collapse=" ") cat(strwrap(txt, ..., indent=indent, exdent=exdent), sep="\n") } .showAnnotatedDataFrame <- function(object, labels=list(0)) { lbls <- list(object=paste0("An object of class '", class(object), "'"), sampleNames=dimLabels(object)[[1]], varMetadata="varMetadata", varLabels="varLabels") lbls[names(labels)] <- labels if (ncol(object) == 0) { # early exit for empty objects cat(lbls[["object"]], ": none\n", sep="") return() } ## create a simplified object for extracting names idx <- selectSomeIndex(pData(object), maxToShow=4) idy <- selectSomeIndex(pData(object), byrow=FALSE, maxToShow=4) pData <- pData(object)[c(idx[[1]], idx[[3]]), c(idy[[1]], idy[[3]]), drop=FALSE] rnms <- rownames(pData) nms <- c(rnms[idx[[1]]], idx[[2]], if (!is.null(idx[[1]])) rnms[-idx[[1]]] else NULL) cat(lbls$object, "\n", sep="") .wrapcat(lbls$sampleNames, nms, nrow(object)) cnms <- colnames(pData) if (length(cnms) > 0) { vars <- c(cnms[idy[[1]]], idy[[2]], cnms[-idy[[1]]]) .wrapcat(lbls$varLabels, vars, ncol(object)) mnms <- selectSome(colnames(varMetadata(object)), maxToShow=4) .wrapcat(lbls$varMetadata, mnms, length(mnms)) } else cat("\n ", lbls$varLabels, ": none", sep="") } setMethod("show", signature=signature(object="AnnotatedDataFrame"), function(object) .showAnnotatedDataFrame(object)) setMethod("combine", signature(x="AnnotatedDataFrame", y="AnnotatedDataFrame"), function(x, y) { if (class(x) != class(y)) { fmt <- "'%s' objects have diffrenent classes '%s', '%s'" txt0 <- "combine,AnnotatedDataFrame,AnnotatedDataFrame-method" stop(sprintf(fmt, txt0, class(x), class(y))) } if (!identical(dimLabels(x),dimLabels(y))) { fmt <- paste("AnnotatedDataFrame dimLabels differ:\n", " %s\n", " %s\n try 'updateObject'?") stop(sprintf(fmt, paste(dimLabels(x), collapse=", "), paste(dimLabels(y), collapse=", "))) } pDataX <- pData(x) pDataY <- pData(y) pData <- combine(pDataX, pDataY) varMetadataX <- varMetadata(x) varMetadataY <- varMetadata(y) ## labelDescription is required, likely a factor with ## conflicting levels if (is.factor(varMetadataX$labelDescription) && is.factor(varMetadataY$labelDescription)) { f <- factor(c(as.character(varMetadataX$labelDescription), as.character(varMetadataY$labelDescription))) varMetadataX$labelDescription <- factor(as.character(varMetadataX$labelDescription), levels=levels(f)) varMetadataY$labelDescription <- factor(as.character(varMetadataY$labelDescription), levels=levels(f)) } vM <- combine(varMetadataX, varMetadataY) initialize(x, data=pData, varMetadata=vM) }) read.AnnotatedDataFrame <- function(filename, path, sep = "\t", header = TRUE, quote = "", stringsAsFactors = FALSE, row.names = 1L, varMetadata.char="#", widget = getOption("BioC")$Base$use.widgets, sampleNames = character(0), ...) { if(!(is.character(varMetadata.char) && (identical(nchar(varMetadata.char), 1L)))) stop("Invalid 'varMetadata.char'") ## For backward (or forward?) compatibility: if(widget) stop("Sorry: tkWidgets is not available for read.AnnotatedDataFrame") if(length(sampleNames)>0) stop("'sampleNames' argument is not supported, provide the sample", "names in the input file and use the option 'row.names'.") if(!missing(path)) filename = file.path(path, filename) pData = read.table(filename, sep=sep, header=header, quote=quote, stringsAsFactors=stringsAsFactors, row.names=row.names, comment.char=varMetadata.char, ...) ## read varMetadata section (the lines with leading "#") vmd = grep(paste0("^", varMetadata.char), readLines(filename), value=TRUE) svmd = strsplit(vmd, ": *") varNames = sub("^# *", "", sapply(svmd, "[", 1L)) varMetad = sapply(svmd, "[", 2L) ## link varMetadata names with pData colnames mt = match(colnames(pData), varNames) varMetad = ifelse(!is.na(mt), varMetad[mt], "") vmd = data.frame(labelDescription=varMetad, row.names=colnames(pData)) ## add provenance information. Alapping it on as an attribute is a ## bit tacky, if Martin likes the idea at all, maybe this can be ## made a proper slot... provenance = sprintf("Read from file %s on %s at %s.", filename, Sys.info()["nodename"], date()) attr(vmd, "provenance") = provenance AnnotatedDataFrame(data=pData, varMetadata=vmd) } write.AnnotatedDataFrame <- function(x, file="", varMetadata.char="#", ..., append=FALSE, fileEncoding="") { ## file handling from write.table if (file == "") file <- stdout() else if (is.character(file)) { file <- if (nzchar(fileEncoding)) file(file, ifelse(append, "a", "w"), encoding = fileEncoding) else file(file, ifelse(append, "a", "w")) on.exit(close(file)) } else if (!isOpen(file, "w")) { open(file, "w") on.exit(close(file)) } if (!inherits(file, "connection")) stop("'file' must be a character string or connection") writeLines(sprintf("%s %s: %s", varMetadata.char, varLabels(x), varMetadata(x)$labelDescription), file) write.table(pData(x), file, append=append, fileEncoding=fileEncoding, ...) } setMethod("AnnotatedDataFrame", signature(data="missing", varMetadata="missing"), function(data, varMetadata, dimLabels=c("rowNames", "columnNames"), ...) { .AnnotatedDataFrame(data=data.frame(), varMetadata=data.frame(), dimLabels=dimLabels, ...) }) setMethod("AnnotatedDataFrame", signature(data="data.frame", varMetadata="missing"), function(data, varMetadata, dimLabels=c("rowNames", "columnNames"), ...) { varMetadata <- data.frame(labelDescription = rep(NA, ncol(data))) row.names(varMetadata) <- names(data) .AnnotatedDataFrame(data=data, varMetadata=varMetadata, dimLabels=dimLabels,...) }) setMethod("AnnotatedDataFrame", signature(data="data.frame", varMetadata="data.frame"), function(data, varMetadata, dimLabels=c("rowNames", "columnNames"), ...) { if (!"labelDescription" %in% colnames(varMetadata)) varMetadata[["labelDescription"]] <- rep(NA, nrow(varMetadata)) row.names(varMetadata) <- names(data) varMetadata[["labelDescription"]] <- as.character(varMetadata[["labelDescription"]]) .AnnotatedDataFrame(data=data, varMetadata=varMetadata, dimLabels=dimLabels, ...) }) Biobase/R/methods-AssayData.R0000644000175400017540000002546613175713325017027 0ustar00biocbuildbiocbuildassayDataNew <- function(storage.mode = c("lockedEnvironment", "environment", "list"), ...) { storage.mode <- match.arg(storage.mode) ## defaults to "lockedEnvironment" assayData <- switch(storage.mode, lockedEnvironment =, environment = new.env(parent=emptyenv()), list = list()) arglist <- list(...) if((length(arglist)>0L) && ((is.null(names(arglist))) || any(names(arglist)==""))) stop("all arguments must be named") for (nm in names(arglist)) { elt <- arglist[[nm]] if (!is.null(dimnames(elt))) dimnames(elt) <- lapply(dimnames(elt), unname) assayData[[nm]] <- elt } if (storage.mode == "lockedEnvironment") assayDataEnvLock(assayData) msg <- assayDataValidMembers(assayData) if (!is.logical(msg)) stop(msg) assayData } assayDataValidMembers <- function(assayData, required) { msg <- NULL eltNames <- if ("list" == assayDataStorageMode(assayData)) names(assayData) else ls(assayData) if (!missing(required)) { absent <- required[!required %in% eltNames] if (length(absent) != 0) msg <- c(msg, paste0("'AssayData' missing '", absent ,"'" , collapse = "\n\t")) } dimsOk <- sapply(eltNames, function(elt) tryCatch(length(dim(assayData[[elt]]))>1, error=function(err) FALSE)) if (!all(dimsOk)) msg <- c(msg, paste0("'AssayData' elements with invalid dimensions: '", paste(eltNames[!dimsOk], collapse="' '"), "'")) if (length(assayData)>1) { eltRowNames <- rownames(assayData[[eltNames[[1]]]]) rowNamesOk <- all(sapply(eltNames[-1], function(elt) all(eltRowNames == rownames(assayData[[elt]])))) if (!rowNamesOk) msg <- c(msg, "'AssayData' elements with different rowNames") } if (is.null(msg)) TRUE else msg } assayDataStorageMode <- function(object) { if (is(object, "list")) "list" else if (environmentIsLocked(object)) "lockedEnvironment" else "environment" } setMethod("storageMode", "AssayData", assayDataStorageMode) assayDataStorageModeReplace <- function(object, value) { storageMode <- assayDataStorageMode(object) if (storageMode == value) return(object) names <- if (storageMode == "list") names(object) else ls(object) switch(value, lockedEnvironment = { assayData <- new.env(parent=emptyenv()) for (nm in names) assayData[[nm]] <- object[[nm]] assayDataEnvLock(assayData) assayData }, environment = { assayData <- new.env(parent=emptyenv()) for (nm in names) assayData[[nm]] <- object[[nm]] assayData }, list = as.list(object)) } setReplaceMethod("storageMode", signature=c(object="AssayData", value="character"), assayDataStorageModeReplace) assayDataEnvLock <- function(assayData) lockEnvironment(assayData, bindings=TRUE) assayDataSubsetElements <- function(object, elts, storageMode = assayDataStorageMode(object)) { if (any(duplicated(elts))) stop("'AssayData' element names must be unique") names <- if (storageMode(object)=="list") names(object) else ls(object) if (!all(elts %in% names)) stop("'AssayData' missing elements: '", paste0(elts[!elts %in% names], collapse="', '"), "'") switch(storageMode, lockedEnvironment = { assayData <- new.env(parent = emptyenv()) for (nm in elts) assayData[[nm]] <- object[[nm]] assayDataEnvLock(assayData) assayData }, environment = { assayData <- new.env(parent = emptyenv()) for (nm in elts) assayData[[nm]] <- object[[nm]] assayData }, list = { object[elts] }) } setMethod("assayData", signature=signature(object="AssayData"), function(object) object) .assayDataDimnames <- function(assayData) { switch(storageMode(assayData), lockedEnvironment=, environment = { result <- vector("list", length(assayData)) names(result) <- ls(assayData) for (nm in ls(assayData)) result[[nm]] <- dimnames(assayData[[nm]]) result }, list=lapply(assayData, dimnames)) } setMethod("sampleNames", signature(object="AssayData"), function(object) { if (!length(object)) return(character(0)) safe.colnames <- function(x) if (ncol(x) == 0) character(0) else colnames(x) switch(assayDataStorageMode(object), list=safe.colnames(object[[1]]), safe.colnames(object[[ls(object)[1]]])) }) setReplaceMethod("sampleNames", signature(object="AssayData", value="list"), function(object, value) { .names_found_unique <- function(names, table) { ok <- !is.null(names) && all(names %in% table) && !any(duplicated(names)) if (!ok) { txt <- "'sampleNames' replacement list must have unique named elements corresponding to assayData element names" stop(paste(strwrap(txt, exdent=2), colapse="\n")) } } mode <- assayDataStorageMode(object) switch(mode, lockedEnvironment = { .names_found_unique(names(value), ls(object)) object <- copyEnv(object) }, environment = { .names_found_unique(names(value), ls(object)) }, list= { .names_found_unique(names(value), names(object)) }) for (nm in names(value)) { dn <- dimnames(object[[nm]]) if (is.null(dn)) dn <- vector("list", length(dim(object[[nm]]))) dn[[2]] <- value[[nm]] dimnames(object[[nm]]) <- dn } if (mode == "lockedEnvironment") assayDataEnvLock(object) object }) setReplaceMethod("sampleNames", signature(object="AssayData", value="ANY"), function(object, value) { mode <- assayDataStorageMode(object) dims <- switch(mode, lockedEnvironment=, environment = { result <- vector("list", length(object)) names(result) <- ls(object) for (nm in ls(object)) result[[nm]] <- ncol(object[[nm]]) result }, list = { lapply(object, ncol) }) if (length(dims)==0 && length(value) !=0) return(object) # early exit; no samples to name if (!all(dims==length(value))) { txt <- sprintf("'value' length (%d) must equal sample number in AssayData (%d)", length(value), dims[[1]]) stop(paste(strwrap(txt, exdent=2), collapse="\n")) } nms <- switch(mode, lockedEnvironment = { object <- copyEnv(object) ls(object) }, environment = ls(object), list = names(object)) for (nm in nms) { dn <- dimnames(object[[nm]]) if (is.null(dn)) dn <- vector("list", length(dim(object[[nm]]))) dn[[2]] <- value dimnames(object[[nm]]) <- dn } if (mode == "lockedEnvironment") assayDataEnvLock(object) object }) setMethod("featureNames", signature(object="AssayData"), function(object) { if (!length(object)) return(character(0)) safe.rownames <- function(x) if (nrow(x) == 0) character(0) else rownames(x) switch(assayDataStorageMode(object), list=safe.rownames(object[[1]]), safe.rownames(object[[ls(object)[1]]])) }) setReplaceMethod("featureNames", signature(object="AssayData", value="ANY"), function(object, value) { mode <- assayDataStorageMode(object) dims <- switch(mode, lockedEnvironment=, environment = { result <- vector("list", length(object)) names(result) <- ls(object) for (nm in ls(object)) result[[nm]] <- nrow(object[[nm]]) result }, list = lapply(object, nrow)) if (length(dims)==0 && length(value) !=0) return(object) # early exit; no features to name if (!all(dims==length(value))) { txt <- sprintf("'value' length (%d) must equal feature number in AssayData (%d)", length(value), dims[[1]]) stop(paste(strwrap(txt, exdent=2), collapse="\n")) } nms <- switch(mode, lockedEnvironment = { object <- copyEnv(object) ls(object) }, environment = ls(object), list=names(object)) for (nm in nms) { dn <- dimnames(object[[nm]]) if (is.null(dn)) dn <- vector("list", length(dim(object[[nm]]))) dn[[1]] <- value dimnames(object[[nm]]) <- dn } if (mode == "lockedEnvironment") assayDataEnvLock(object) object }) setMethod("combine", c("AssayData", "AssayData"), function(x, y, ...) { storage.mode <- assayDataStorageMode(x) nmfunc <- if ("environment"==class(x)) ls else names if (assayDataStorageMode(y) != storage.mode) stop("assayData must have same storage, but are '", storage.mode, "', '", assayDataStorageMode(y)) if (length(nmfunc(x)) != length(nmfunc(y))) stop("assayData have different numbers of elements:\n\t", paste(nmfunc(x), collapse=" "), "\n\t", paste(nmfunc(y), collapse=" ")) if (!all(nmfunc(x) == nmfunc(y))) stop(paste("assayData have different element names:", paste(nmfunc(x), collapse=" "), paste(nmfunc(y), collapse=" "), sep="\n\t")) if ("list" == storage.mode) { aData <- lapply(names(x), function(nm) combine(x[[nm]],y[[nm]])) names(aData) <- names(x) } else { aData <- new.env(parent=emptyenv()) for (nm in ls(x)) aData[[nm]] <- combine(x[[nm]], y[[nm]]) if ("lockedEnvironment" == storage.mode) assayDataEnvLock(aData) } aData }) assayDataDim <- function(object) { nms <- if (assayDataStorageMode(object) == "list") names(object) else ls(object) if ( length( nms ) == 0 ) return( NA ) d <- dim( object[[ nms[[1]] ]]) names(d) <- c( "Features", "Samples", rep("...", max(length(d)-2, 0))) d } ##FIXME: RG says I don't know if you should ignore non-matrix objects or ## not - for now I have put in an informative error message assayDataDims <- function(object) { nms <- if (assayDataStorageMode(object) == "list") names(object) else ls(object) if (length(nms) == 0) return(matrix(integer(0), nrow = 2, ncol = 0, dimnames = list(c("Features", "Samples"), character(0)))) d <- sapply(nms, function(i) dim(object[[i]])) rownames(d) <- c("Features", "Samples", rep("...", nrow(d)-2)) colnames(d) <- nms d[,order(colnames(d)), drop=FALSE] } Biobase/R/methods-ExpressionSet.R0000644000175400017540000002445513175713325017765 0ustar00biocbuildbiocbuildsetMethod("initialize", "ExpressionSet", function(.Object, assayData, phenoData, featureData, exprs=new("matrix"), ... ) { if (missing(assayData)) { if (missing(phenoData)) phenoData <- annotatedDataFrameFrom(exprs, byrow=FALSE) if (missing(featureData)) featureData <- annotatedDataFrameFrom(exprs, byrow=TRUE) .Object <- callNextMethod(.Object, phenoData = phenoData, featureData = featureData, exprs = exprs, ...) } else if (missing(exprs)) { if (missing(phenoData)) phenoData <- annotatedDataFrameFrom(assayData, byrow=FALSE) if (missing(featureData)) featureData <- annotatedDataFrameFrom(assayData, byrow=TRUE) .Object <- callNextMethod(.Object, assayData = assayData, phenoData = phenoData, featureData = featureData, ...) } else stop("provide at most one of 'assayData' or 'exprs' to initialize ExpressionSet", call.=FALSE) .harmonizeDimnames(.Object) }) .harmonizeDimnames <- function(object) { err <- function(conflicts) stop("assayData element dimnames conflict: ", paste(names(conflicts), collapse=", ")) okNames <- list(featureNames(featureData(object)), sampleNames(phenoData(object))) dimNames <- .assayDataDimnames(assayData(object)) dimConflict <- function(dimNames, okNames, dim) { nm <- lapply(dimNames, "[[", dim) isConflict <- !sapply(nm, function(x, y) { is.null(x) || isTRUE(all.equal(x, y, check.attr=FALSE)) }, okNames[[dim]]) isNamed <- sapply(lapply(nm, names), length) > 0 isNull <- sapply(nm, is.null) if (all(!isConflict & !isNamed & !isNull)) return (FALSE) if (any(isConflict & !isNull)) err(isConflict[!isNull]) TRUE } if (dimConflict(dimNames, okNames, 1)) featureNames(assayData(object)) <- okNames[[1]] if (dimConflict(dimNames, okNames, 2)) sampleNames(assayData(object)) <- okNames[[2]] object } setAs("exprSet", "ExpressionSet", function(from) { from <- asS4(from) desc <- from@description desc <- if (class(desc)!="MIAME") { txt <- "missing or mis-formed MIAME 'description' in original object; creating new, empty description" warning(paste0(strwrap(txt, indent=2), collapse="\n ")) MIAME() } else updateObject(desc) exprs <- from@exprs phenoData <- as(from@phenoData, "AnnotatedDataFrame") annotation <- from@annotation dims <- dim(exprs) if (all(dim(from@se.exprs) == dims)) { se.exprs <- from@se.exprs colnames(se.exprs) <- colnames(exprs) .ExpressionSet(phenoData=phenoData, experimentData=desc, annotation=annotation, exprs=exprs, se.exprs=se.exprs) } else { txt <- "missing or mis-formed 'se.exprs' in original object; creating ExpressionSet without se.exprs" warning(paste0(strwrap(txt, indent=2), collapse="\n ")) .ExpressionSet(phenoData=phenoData, experimentData=desc, annotation=annotation, exprs=exprs) } }) setValidity("ExpressionSet", function(object) { msg <- validMsg(NULL, isValidVersion(object, "ExpressionSet")) msg <- validMsg(msg, assayDataValidMembers(assayData(object), c("exprs"))) if(class(experimentData(object)) != "MIAME") msg <- validMsg(msg, "experimentData slot in ExpressionSet must be 'MIAME' object") if (is.null(msg)) TRUE else msg }) setAs("ExpressionSet", "data.frame", function (from) data.frame(t(exprs(from)), pData(from))) as.data.frame.ExpressionSet <- function(x, row.names=NULL, optional=FALSE, ...) as(x, "data.frame") setMethod("exprs", signature(object="ExpressionSet"), function(object) assayDataElement(object,"exprs")) setReplaceMethod("exprs", signature(object="ExpressionSet",value="matrix"), function(object, value) assayDataElementReplace(object, "exprs", value)) .esApply <- function(X, MARGIN, FUN, ...) { parent <- environment(FUN) if (is.null(parent)) parent <- emptyenv() e1 <- new.env(parent=parent) multiassign(names(pData(X)), pData(X), envir=e1) environment(FUN) <- e1 apply(exprs(X), MARGIN, FUN, ...) } setMethod("esApply", signature=signature(X="ExpressionSet"), .esApply) setMethod("makeDataPackage", signature(object="ExpressionSet"), function(object, author, email, packageName, packageVersion, license, biocViews, filePath, description=paste(abstract(object), collapse="\n\n"), ...) { if( missing(email) || !(is.character(email) && (length(email) == 1) && grep("@", email) == 1 ) ) stop("invalid email address") sym = list( AUTHOR = author, VERSION=as.character(package_version(packageVersion)), LICENSE=license, TITLE = paste("Experimental Data Package:",packageName), MAINTAINER = paste0(author, ", <", email, ">"), BVIEWS = biocViews, DESCRIPTION = description, FORMAT = pD2Rd(phenoData(object))) res = createPackage(packageName, destinationDir=filePath, originDir = system.file("ExpressionSet", package="Biobase"), symbolValues = sym, unlink=TRUE) ##save the data file datadir = file.path(res$pkgdir, "data") dir.create(datadir, showWarnings=FALSE) outfile = file.path(datadir, paste0(packageName, ".rda")) assign(packageName, object) save(list=packageName, file = outfile) return(res) }) setMethod("write.exprs", signature(x="ExpressionSet"), function(x, file="tmp.txt", quote=FALSE, sep="\t", col.names=NA, ...){ write.table(exprs(x), file=file, quote=quote, sep=sep, col.names=col.names, ...) }) readExpressionSet <- function(exprsFile, phenoDataFile, experimentDataFile, notesFile, path, annotation, ## arguments to read.* methods exprsArgs=list(sep=sep, header=header, row.names=row.names, quote=quote, ...), phenoDataArgs=list(sep=sep, header=header, row.names=row.names, quote=quote, stringsAsFactors=stringsAsFactors, ...), experimentDataArgs=list(sep=sep, header=header, row.names=row.names, quote=quote, stringsAsFactors=stringsAsFactors, ...), sep = "\t", header = TRUE, quote = "", stringsAsFactors = FALSE, row.names = 1L, ## widget widget = getOption("BioC")$Base$use.widgets, ...) { if (!missing(widget) && widget != FALSE) stop("sorry, widgets not yet available") ## exprs if (missing(exprsFile)) stop("exprs can not be missing!") exprsArgs$file=exprsFile ex = as.matrix(do.call(read.table, exprsArgs)) ## phenoData if (!missing(phenoDataFile)) { phenoDataArgs$file=phenoDataFile pd = do.call(read.AnnotatedDataFrame, phenoDataArgs) if (!identical(sampleNames(pd), colnames(ex))) stop("Column names of expression matrix must be identical to\n", "the sample names of the phenodata table.\n", "You could use 'options(error=recover)' to compare the", "values of 'sampleNames(pd)' and 'colnames(ex)'.\n") } else { pd = annotatedDataFrameFrom(ex, byrow=FALSE) } obj = ExpressionSet(ex, phenoData=pd) ## FIXME: these should probably added to obj before, or simultaneously to, exprs; ## as is this can provoke a lot of copying ## experimentData if (!missing(experimentDataFile)) experimentDataArgs$file=experimentDataFile if (!is.null(experimentDataArgs$file)) experimentData(obj) <- do.call(read.MIAME, experimentDataArgs) ## annotation if (!missing(annotation)) annotation(obj) <- annotation ## notes if (!missing(notesFile)) notes(obj) <- readLines(notesFile) validObject(obj) obj } setMethod(ExpressionSet, "missing", function(assayData, phenoData=AnnotatedDataFrame(), featureData=AnnotatedDataFrame(), experimentData=MIAME(), annotation=character(), protocolData=AnnotatedDataFrame(), ...) { .ExpressionSet( assayData=assayDataNew(exprs=new("matrix")), phenoData=phenoData, featureData=featureData, experimentData=experimentData, annotation=annotation, protocolData=protocolData, ...) }) setMethod(ExpressionSet, "environment", function(assayData, phenoData=annotatedDataFrameFrom(assayData, byrow=FALSE), featureData=annotatedDataFrameFrom(assayData, byrow=TRUE), experimentData=MIAME(), annotation=character(), protocolData=annotatedDataFrameFrom(assayData, byrow=FALSE), ...) { .ExpressionSet(assayData=assayData, phenoData=phenoData, featureData=featureData, experimentData=experimentData, annotation=annotation, protocolData=protocolData, ...) }) setMethod(ExpressionSet, "matrix", function(assayData, phenoData=annotatedDataFrameFrom(assayData, byrow=FALSE), featureData=annotatedDataFrameFrom(assayData, byrow=TRUE), experimentData=MIAME(), annotation=character(), protocolData=annotatedDataFrameFrom(assayData, byrow=FALSE), ...) { assayData <- assayDataNew(exprs=assayData) .ExpressionSet(assayData=assayData, phenoData=phenoData, featureData=featureData, experimentData=experimentData, annotation=annotation, protocolData=protocolData, ...) }) .DollarNames.ExpressionSet <- .DollarNames.eSet Biobase/R/methods-MIAME.R0000644000175400017540000001617113175713325015776 0ustar00biocbuildbiocbuildsetMethod("isCurrent", signature(object="MIAME", value="missing"), function(object, value) { cver <- callNextMethod() MIAMEres <- all(c(cver, "pubMedIds" %in% names(getObjectSlots(object)))) if("MIAxE" %in% names(cver)) { res <- c(cver["MIAxE"], MIAMEres) names(res) <- c("MIAxE", "MIAME") } else {res <- MIAMEres; names(res) <- "MIAME"} res }) setMethod("updateObject", signature(object="MIAME"), function(object, ..., verbose=FALSE) { if (verbose) message("updateObject(object = 'MIAME')") object <- asS4(object) if (isVersioned(object) && isCurrent(object)["MIAME"]) callNextMethod() else object <- updateObjectFromSlots(object, ..., verbose=verbose) classVersion(object) <- classVersion(class(object)) object }) # ========================================================================== setMethod("show", "MIAME", function(object) { tmp <- c("samples","hybridizations","normalization controls","preprocessing") Index <-c(length(object@samples) > 0, length(object@hybridizations) > 0, length(object@normControls) > 0, length(object@preprocessing) > 0) cat("Experiment data\n") cat(" Experimenter name:",object@name,"\n") cat(" Laboratory:",object@lab,"\n") cat(" Contact information:",object@contact,"\n") cat(" Title:",object@title,"\n") cat(" URL:",object@url,"\n") # deal with legacy MIAME objects! pmids = try( pubMedIds(object), silent=TRUE ) if (!inherits(pmids, "try-error")) cat(" PMIDs:",pmids,"\n") # end of dealing! if(length(object@abstract) > 0 && all(object@abstract!="")) cat("\n Abstract: A",length(strsplit(object@abstract," ")[[1]]), "word abstract is available. Use 'abstract' method.\n") else cat(" No abstract available.\n") if(any(Index)) cat(" Information is available on:", paste(tmp[Index],collapse=", "),"\n") nO = notes(object) if (length(nO) > 0) { cat(" notes:\n" ) if( is.list(nO) ) { nms = names(nO) ##a print width for the values, so we stay inside the margins pw = options("width")[[1]] - 6 for(i in 1:length(nO) ) { cat(" ", nms[i], ":", sep="") cat(" ", strbreak(nO[[i]], width=pw, exdent=0), sep="\n ") } } } } ) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("abstract","MIAME",function(object) object@abstract) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("samples","MIAME",function(object) object@samples) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("hybridizations","MIAME",function(object) object@hybridizations) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("normControls","MIAME",function(object) object@normControls) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("preproc","MIAME",function(object) object@preprocessing) setReplaceMethod("preproc", "MIAME", function(object, value) { object@preprocessing <- value object }) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("pubMedIds","MIAME",function(object) object@pubMedIds) setReplaceMethod("pubMedIds","MIAME",function(object,value){ object@pubMedIds = value object }) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("otherInfo","MIAME",function(object) object@other) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("expinfo","MIAME", function(object) { tmp <- c(object@name, object@lab, object@contact, object@title, object@url) names(tmp) <- c("name","lab","contact","title","url") return(tmp) } ) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("notes", signature(object="MIAME"), function(object) object@other) setReplaceMethod("notes", signature(object="MIAME", value="list"), function(object, value) { object@other <- value object }) setReplaceMethod("notes", signature(object="MIAME", value="character"), function(object, value) { object@other <- append(object@other, value) object }) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - MIAME <- function(name = "", lab = "", contact = "", title = "", abstract = "", url = "", pubMedIds = "", samples = list(), hybridizations = list(), normControls = list(), preprocessing = list(), other = list()) { .MIAME(name=name, lab=lab, contact=contact, title=title, abstract=abstract, url=url, pubMedIds=pubMedIds, samples=samples, hybridizations=hybridizations, normControls=normControls, preprocessing=preprocessing, other=other) } # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - read.MIAME <- function(filename=NULL,widget=getOption("BioC")$Base$use.widgets,...) { if(!is.null(filename)) { miame <- scan(filename,what="c",quiet=TRUE,sep="\n",...) MIAME(name=miame[1], lab=miame[2], contact=miame[3], title=miame[4], abstract=miame[5], url=miame[6]) } else if(widget) { requireNamespace("tkWidgets", quietly=TRUE) || stop("Requires tkWidgets") tmp <- tkWidgets::tkMIAME() MIAME(name=tmp$ExperimentName, lab=tmp$LabName, contact=tmp$ContactInfo, title=tmp$ExperimentTitle, abstract=tmp$Description, url=tmp$URL) } else MIAME() } # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("combine", c("MIAME", "MIAME"), function(x, y, ...) { if (identical(x,y)) return (x) for (sl in names(getSlots(class(x)))) { if (identical(slot(x,sl),slot(y,sl))) next slot(x,sl) <- switch(sl, ## multiple elements possible name=, lab=, contact=, title=, url=, pubMedIds=, samples=, hybridizations=, normControls=, preprocessing=, other= { c(slot(x,sl),slot(y,sl)) }, ## just a single entry abstract= { paste(slot(x,sl), slot(y,sl), collapse="\n") }, .__classVersion__= { stop("'MIAME' objects have different class version strings") }, ## unknown { warning("\n unknown or conflicting information in MIAME field '", sl,"'; using information from object 'x'") slot(x,sl) }) } x }) Biobase/R/methods-MIAxE.R0000644000175400017540000000037613175713325016051 0ustar00biocbuildbiocbuild# ================================== # MIAxE Class Methods # ---------------------------------- setMethod("show", signature=signature(object="MIAxE"), function(object) { cat(class( object ), "\n", sep="") }) Biobase/R/methods-MultiSet.R0000644000175400017540000000016413175713325016707 0ustar00biocbuildbiocbuildsetMethod("initialize", signature(.Object="MultiSet"), function(.Object, ...) callNextMethod()) Biobase/R/methods-NChannelSet.R0000644000175400017540000002175213175713325017311 0ustar00biocbuildbiocbuildNChannelSet <- .NChannelSet .init_NChannelSet <- # copy constructor, validation selectMethod(initialize, "ANY") setMethod("initialize", "NChannelSet", function(.Object, assayData, phenoData, ...) { mySlots <- slotNames(.Object) dotArgs <- list(...) isSlot <- names(dotArgs) %in% mySlots if (missing(assayData)) { assayData <- do.call(assayDataNew, dotArgs[!isSlot], envir=parent.frame()) } if (missing(phenoData)) { phenoData <- annotatedDataFrameFrom(assayData, byrow=FALSE) } if (is.null(varMetadata(phenoData)[["channel"]])) { varMetadata(phenoData)[["channel"]] <- factor(rep("_ALL_", nrow(varMetadata(phenoData))), levels=c(assayDataElementNames(assayData), "_ALL_")) } ## ensure sample names OK -- all assayData with names; ## phenoData with correct names from assayData nms <- if (storageMode(assayData) == "list") names(assayData) else ls(assayData) assaySampleNames <- vector("list", length(nms)) names(assaySampleNames) <- nms for (nm in nms) { cnames <- colnames(assayData[[nm]]) assaySampleNames[[nm]] <- if (is.null(cnames)) { sampleNames(phenoData) } else cnames } sampleNames(assayData) <- assaySampleNames sampleNames(phenoData) <- sampleNames(assayData) do.call(callNextMethod, c(.Object, assayData = assayData, phenoData = phenoData, dotArgs[isSlot])) }) .invalid_NChannelAssayNames <- function(object) { phenoChannels <- levels(varMetadata(object)[["channel"]]) assayChannels <- c("_ALL_", assayDataElementNames(object)) setdiff(union(assayChannels, phenoChannels), intersect(assayChannels, phenoChannels)) } setValidity("NChannelSet", function(object) { msg <- validMsg(NULL, isValidVersion(object, "NChannelSet")) if (!"channel" %in% names(varMetadata(object))) { txt <- "\n 'NChannelSet' varMetadata must have a 'channel' column" msg <- validMsg(msg, txt) } else { channel <- varMetadata(object)[["channel"]] if (!is(channel, "factor")) { txt <- paste("\n 'NChannelSet' varMetadata column 'channel'", "must be class 'factor'") msg <- validMsg(msg, txt) } else if (0 < length(levels(channel))) { if (length(.invalid_NChannelAssayNames(object))) { txt <- 'NChannelSet levels(varMetadata(object)$channel) / assayDataElementNames() mismatch; see ?"channelNames<-,NChannelSet,character-method"' txt <- paste(strwrap(c("\n", txt), exdent=2), collapse="\n ") msg <- validMsg(msg, txt) } } if (!("_ALL_" %in% levels(channel))) { txt <- paste("\n 'NChannelSet' varMetadata 'channel'", "requires '_ALL_' as a level") msg <- validMsg(msg, txt) } } if (is.null(msg)) TRUE else msg }) .assayDataGets_NChannelSet <- function(object, value) { phenoData <- phenoData(object) ## update channel names, making some attempt to preserve order from <- channelNames(object) to <- assayDataElementNames(value) lvls <- c(from[from %in% to], to[!to %in% from], "_ALL_") varMetadata(phenoData)$channel <- factor(as.character(varMetadata(phenoData)$channel), levels=lvls) .init_NChannelSet(object, assayData=value, phenoData=phenoData) } setReplaceMethod("assayData", c("NChannelSet", "environment"), .assayDataGets_NChannelSet) setReplaceMethod("assayData", c("NChannelSet", "list"), .assayDataGets_NChannelSet) setMethod("channelNames", "NChannelSet", function(object, ...) { nms <- assayDataElementNames(object) lvls <- levels(varMetadata(object)$channel) if (all(nms %in% lvls)) ## FIXME: this accomodates invalid (previous) NChannelSet instances ## order to match channelNames nms <- lvls[lvls %in% nms] nms }) setGeneric("channelNames<-", function(object, ..., value) standardGeneric("channelNames<-")) setReplaceMethod("channelNames", c("NChannelSet", "character"), function(object, ..., value) { if (!is.null(names(value))) { ## re-name & re-order channelNames(object) <- as.list(value) } else { ## re-order if (!all(sort(value) == sort(channelNames(object)))) stop("'value' elements must include all channelNames()") varMetadata(object)$channel <- factor(varMetadata(object)$channel, levels=c(value, "_ALL_")) validObject(object) } object }) setReplaceMethod("channelNames", c("NChannelSet", "list"), function(object, ..., value) { from <- unlist(value, use.names=FALSE) if (!all(sort(from) == sort(channelNames(object)))) stop("'value' elements must include all channelNames()") to <- names(value) if (any(duplicated(to))) stop("duplicated channelNames are not allowed") assayData <- assayData(object) levels(varMetadata(object)$channel) <- c(value, list("_ALL_" = "_ALL")) if (is.list(assayData)) { idx <- match(from, names(assayData)) names(assayData)[idx] <- to } else { env <- new.env(parent=emptyenv()) for (i in seq_along(value)) env[[ to[i] ]] = assayData[[ from[i] ]] if (storageMode(object) == "lockedEnvironment") assayDataEnvLock(env) assayData <- env } assayData(object) <- assayData object }) setMethod("channel", signature = signature( object = "NChannelSet", name = "character"), function(object, name, ...) { if (length(name) != 1) stop("\n 'NChannelSet' channel 'name' must be one element", "\n was: '", paste0(name, collapse="', '"), "'") obj <- selectChannels(object, name) # subset phenoData appropriately sampleNames(phenoData(obj)) <- sampleNames(assayData(obj)) ExpressionSet(assayData(obj)[[name]], phenoData = phenoData(obj), featureData = featureData(obj), experimentData = experimentData(obj), annotation=annotation(obj), protocolData=protocolData(obj), ...) }) setMethod("selectChannels", signature = signature( object = "NChannelSet", names="character"), function(object, names, ...) { if (any(duplicated(names))) stop("NChannelSet' channels 'names' must be unique") channelNames <- channelNames(object) badNames <- !names %in% channelNames if (any(badNames)) stop("NChannelSet' channels 'names' must be channels") dropChannels <- channelNames[!channelNames %in% names] if (0 == length(dropChannels)) return(object) ## assayData assayData <- assayDataSubsetElements(assayData(object), names) ## phenoData -- drop unneeded info metadata <- varMetadata(object)[["channel"]] okMetadata <- !metadata %in% dropChannels phenoData <- phenoData(object)[,okMetadata] ## reduce factor levels varMetadata(phenoData)[["channel"]] <- factor(metadata[okMetadata], levels=unique(c(names, "_ALL_"))) initialize(object, assayData = assayData, phenoData = phenoData, featureData = featureData(object), experimentData=experimentData(object), annotation=annotation(object), protocolData=protocolData(object), ...) }) setMethod("sampleNames", signature=signature(object="NChannelSet"), function(object) { assayData <- assayData(object) nms <- if (storageMode(object) == "list") names(assayData) else ls(assayData) res <- vector("list", length(nms)) names(res) <- nms for (nm in nms) res[[nm]] <- colnames(assayData[[nm]]) ident <- sapply(res[-1], function(elt, ref) all(elt==ref), res[[1]]) if (all(ident)) res[[1]] else res }) setReplaceMethod("sampleNames", c("NChannelSet", "list"), function(object, value) { assayData <- assayData(object) sampleNames(assayData) <- value phenoData <- phenoData(object) sampleNames(phenoData) <- sampleNames(assayData) protocolData <- protocolData(object) sampleNames(protocolData) <- sampleNames(assayData) .init_NChannelSet(object, assayData=assayData, phenoData=phenoData, protocolData=protocolData) }) Biobase/R/methods-ScalarObject.R0000644000175400017540000000114313175713325017473 0ustar00biocbuildbiocbuildmkScalar <- function(obj) { switch(typeof(obj), character=.ScalarCharacter(obj), logical=.ScalarLogical(obj), integer=.ScalarInteger(obj), double=.ScalarNumeric(obj), stop("no scalar class implemented for type: ", typeof(obj))) } setMethod("show", "ScalarObject", function(object) { cat(object, "\n") }) setMethod("show", "ScalarCharacter", function(object) { if (is.na(object)) cat(NA, "\n") else cat(sprintf('"%s"\n', object)) }) Biobase/R/methods-SnpSet.R0000644000175400017540000000374613175713325016366 0ustar00biocbuildbiocbuildsetMethod("initialize", "SnpSet", function(.Object, assayData = assayDataNew(call = call, callProbability = callProbability, ...), phenoData = annotatedDataFrameFrom(assayData, byrow=FALSE), featureData = annotatedDataFrameFrom(assayData, byrow=TRUE), experimentData = MIAME(), annotation = character(), protocolData = phenoData[,integer(0)], call = new("matrix"), callProbability = matrix(numeric(), nrow=nrow(call), ncol=ncol(call), dimnames=dimnames(call)), ...) { callNextMethod(.Object, assayData = assayData, phenoData = phenoData, featureData = featureData, experimentData = experimentData, annotation = annotation, protocolData = protocolData) }) setValidity("SnpSet", function(object) { assayDataValidMembers(assayData(object), c("call", "callProbability")) }) setMethod("exprs", c("SnpSet"), function(object) assayDataElement(object, "call")) setReplaceMethod("exprs", c("SnpSet", "matrix"), function(object, value) { assayDataElementReplace(object, "call", value) }) setMethod(snpCall, "SnpSet", function(object, ...) { assayDataElement(object, "call") }) setMethod(snpCallProbability, "SnpSet", function(object, ...) { assayDataElement(object, "callProbability") }) setReplaceMethod("snpCall", c("SnpSet", "matrix"), function(object, ..., value) { assayDataElementReplace(object, "call", value) }) setReplaceMethod("snpCallProbability", c("SnpSet", "matrix"), function(object, ..., value) { assayDataElementReplace(object, "callProbability", value) }) Biobase/R/methods-VersionedClass.R0000644000175400017540000000771313175713325020074 0ustar00biocbuildbiocbuild## ========================================================================== ## Versioned: mix-in class to add version information ## - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ## initialize -- see VersionedClasses setMethod("initialize", signature(.Object="Versioned"), function(.Object, versions = list(), ...) { .Object <- callNextMethod(.Object, ...) classVersion(.Object)[names(versions)] <- versions .Object }) ## validity setValidity("Versioned", function(object) { msg <- NULL if (!isVersioned(object)) msg <- validMsg(msg, "missing version string") if (is.null(msg)) TRUE else msg }) isValidVersion <- function(object, nm) {# utility msg <- NULL if (!isS4(object)) msg <- validMsg(msg, "not an S4 object") if (isVersioned(object) && !all(isCurrent(object)[nm])) { vers <- isCurrent(object)[nm] vers[is.na(vers)] <- FALSE names(vers) <- nm bad <- names(vers[vers==FALSE]) msg <- validMsg(msg, paste0("out-of-date class version '", bad, "'")) } msg } ## isVersioned setMethod("isVersioned", signature(object="ANY"), function(object) FALSE) setMethod("isVersioned", signature(object="character"), function(object) { ## need to check getNamespace("Biobase") during Biobase installation length(object) > 0 && nchar(object)>0 && (isClass(object) || isClass(object, where=getNamespace("Biobase"))) && extends(getClass(object), "Versioned") }) setMethod("isVersioned", signature(object="Versioned"), function(object) ".__classVersion__" %in% names(attributes(object))) ## classVersion setMethod("classVersion", signature(object="ANY"), function(object) .VersionsNull()) setMethod("classVersion", signature(object="character"), function(object) { if (isVersioned(object)) attr(getClass(object)@prototype, ".__classVersion__") else callNextMethod() }) setMethod("classVersion", signature(object="Versioned"), function(object) { if (isVersioned(object)) { if (isS4(object@.__classVersion__)) object@.__classVersion__ else ## force update to S4 instance ## user needs to recognize need for update updateObject(object@.__classVersion__) } else callNextMethod() }) setReplaceMethod("classVersion", signature(object="Versioned", value="Versions"), function(object, value) { object@.__classVersion__ <- value object }) ## isCurrent setMethod("isCurrent", signature(object="ANY"), function(object, value) NA) setMethod("isCurrent", signature(object="Versioned", value="missing"), function(object, value) isCurrent(object, class(object))) setMethod("isCurrent", signature(object="Versioned", value="character"), function(object, value) { # vers <- classVersion(value) # if(!all(names(vers) %in% names(classVersion(object)))) { # res <- FALSE # names(res) <- value # return(res) # } vers <- classVersion(value) if (extends(class(object),value) && isVersioned(object) && all(names(vers) %in% names(classVersion(object)))) { res <- classVersion(object)[names(vers)] == vers names(res) <- names(vers) } else { res <- FALSE names(res) <- value } res <- c(S4=isS4(object), res) res }) ## show setMethod("show", signature(object="Versioned"), function(object) callNextMethod()) Biobase/R/methods-VersionsNull.R0000644000175400017540000000053613175713325017607 0ustar00biocbuildbiocbuild## Unversioned ## setMethod("initialize", signature(.Object="VersionsNull"), function(.Object, ...) { if (!missing(...)) warning("ignoring arguments to '.VersionsNull()')") .Object }) setMethod("show", signature(object="VersionsNull"), function(object) print("No version")) Biobase/R/methods-aggregator.R0000644000175400017540000000336513175713325017271 0ustar00biocbuildbiocbuildsetMethod("initialize", signature(.Object="aggregator"), function(.Object, aggenv=new.env(hash=TRUE), ...) { callNextMethod(.Object, aggenv=aggenv, ...) }) # ========================================================================== setMethod("aggenv", "aggregator", function(object) object@aggenv) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("initfun", "aggregator", function(object) object@initfun) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("aggfun", "aggregator", function(object) object@aggfun) # ========================================================================== Aggregate <- function(x, agg) { if( !is(agg, "aggregator") ) stop("second argument must be an aggregator") if( is.null(x) || length(x) == 0 ) return() if(is.character(x)) { for( i in 1:length(x) ) { nm <- x[i] if( !exists(nm, envir=aggenv(agg), inherits=FALSE) ) assign(nm, envir=aggenv(agg), initfun(agg)(nm, x)) else { v1 <- get(nm, envir=aggenv(agg)) assign(nm, aggfun(agg)(nm, v1), envir=aggenv(agg)) } } } else if(is.list(x)) { nms <- names(x) for( i in 1:length(x) ) { nm <- nms[i] if( !exists(nm, envir=aggenv(agg), inherits=FALSE) ) assign(nm, envir=aggenv(agg), initfun(agg)(nm, x[[i]])) else { v1 <- get(nm, envir=aggenv(agg)) assign(nm, envir=aggenv(agg), aggfun(agg)(nm, v1, x[[i]])) } } } else stop("bad type for Aggregate") } # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Biobase/R/methods-container.R0000644000175400017540000000301413175713325017120 0ustar00biocbuildbiocbuild# ========================================================================== setMethod("content", "container", function(object) object@content) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("locked", "container", function(object) object@locked) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("[", "container", def = function(x, i, j, ..., drop = F) { .container(content = content(x), x = x@x[i], locked = locked(x)) } ) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("[[", "container", function(x, i, j, ...) { x@x[[i]] } ) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setReplaceMethod("[[", "container", function(x, i, j,..., value) { if( locked(x) ) stop("cannot assign into a locked container") cv <- class(value) cont <- content(x) if( !extends(cv, cont) ) stop("the container is class '", cont, "' the object is class '", cv, "' cannot assign") x@x[[i]] <- value x } ) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("length", "container", function(x) length(x@x)) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("show", "container", function(object) { cat("Container of ", content(object), "\n", sep="") print(object@x) } ) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Biobase/R/methods-eSet.R0000644000175400017540000007123313175713325016046 0ustar00biocbuildbiocbuild# ========================================================================== # eSet Class Validator # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("initialize", signature(.Object="eSet"), function(.Object, assayData, phenoData=annotatedDataFrameFrom(assayData, byrow=FALSE), featureData=annotatedDataFrameFrom(assayData, byrow=TRUE), experimentData=MIAME(), annotation=character(0), protocolData=phenoData[,integer(0)], ...) { ## NB: Arguments provided in '...' are used to initialize ## slots if possible (when called from some subclass). ## Otherwise, extra args in '...' are added as elements ## to assayData. We do this to allow subclasses to ## rely on default contructor behavior for initializing ## slots. ## ## NB2: Extra args to the assayData constructor will ## be passed along as long as current class doesn't ## have a slot with a matching name. mySlots <- slotNames(.Object) dotArgs <- list(...) isSlot <- names(dotArgs) %in% mySlots if (missing(assayData)) assayData <- do.call(assayDataNew, dotArgs[!isSlot], envir=parent.frame()) else { checkClass(assayData, "AssayData", class(.Object)) nms <- if (storageMode(assayData)=="list") names(assayData) else ls(assayData) dupNames <- nms %in% names(dotArgs[!isSlot]) if (any(dupNames)) warning("initialize argument(s) '", paste(nms[dupNames], collapse="' '"), "' also present in 'assayData'; argument(s) ignored") } if (!missing(phenoData)) checkClass(phenoData, "AnnotatedDataFrame", class(.Object)) dimLabels(phenoData) <- c("sampleNames", "sampleColumns") if (!missing(featureData)) checkClass(featureData, "AnnotatedDataFrame", class(.Object)) dimLabels(featureData) <- c("featureNames", "featureColumns") ## create the protocolData, if necessary if (!missing(protocolData)) { checkClass(protocolData, "AnnotatedDataFrame", class(.Object)) dimLabels(protocolData) <- c("sampleNames", "sampleColumns") } ## coordinate sample names adSampleNames <- sampleNames(assayData) if (all(sapply(adSampleNames, is.null))) sampleNames(assayData) <- sampleNames(phenoData) pdSampleNames <- sampleNames(protocolData) if (all(sapply(pdSampleNames, is.null))) sampleNames(protocolData) <- sampleNames(phenoData) ## where do feature names come from? assayData or featureData adFeatureNames <- featureNames(assayData) if (all(sapply(adFeatureNames, is.null))) featureNames(assayData) <- featureNames(featureData) ## create new instance from 'extra' dotArgs, and from instance for (s in names(dotArgs)[isSlot]) slot(.Object, s) <- dotArgs[[s]] callNextMethod(.Object, assayData=assayData, phenoData=phenoData, featureData=featureData, experimentData=experimentData, annotation=annotation, protocolData=protocolData) }) updateOldESet <- function(from, toClass, ...) { # to MultiExpressionSet from <- asS4(from) ophenoData <- asS4(phenoData(from)) metadata <- ophenoData@varMetadata if (all(dim(metadata)==0)) { warning("replacing apparently empty varMetadata") metadata <- data.frame(numeric(ncol(ophenoData@pData)))[,FALSE] } if (!is.null(metadata[["varName"]])) { row.names(metadata) <- metadata[["varName"]] metadata[["varName"]] <- NULL } else if (!is.null(names(ophenoData@pData))) { row.names(metadata) <- names(ophenoData@pData) } if (!is.null(metadata[["varLabels"]])) { names(metadata)[names(metadata)=="varLabels"] <- "labelDescription" metadata[["labelDescription"]] <- as.character(metadata[["labelDescription"]]) } ## phenoData pData <- ophenoData@pData phenoData <- AnnotatedDataFrame(data=pData, varMetadata=metadata) ## sampleNames if (any(sampleNames(assayData(from))!=sampleNames(phenoData))) { warning("creating assayData colnames from phenoData sampleNames") sampleNames(assayData(from)) <- sampleNames(phenoData) } ## reporterNames if (length(from@reporterNames) == dim(from)[[1]]) { if (any(sapply(assayData(from),rownames)!=from@reporterNames)) warning("creating assayData featureNames from reporterNames") featureNames(assayData(from)) <- from@reporterNames } else { warning("creating numeric assayData featureNames") featureNames(assayData(from)) <- 1:dim(from)[[1]] } if (sum(dups <- duplicated(featureNames(assayData(from))))>0) { warning("removing ", sum(dups), " duplicated featureNames") from@assayData <- lapply(from@assayData, function(elt) elt[!dups,]) } ## description description <- from@description if (is(description,"MIAME")) { if (length(from@notes)!=0) { warning("addding 'notes' to 'description'") description@other <- c(description@other,from@notes) } if (length(from@history)!=0) { warning("adding 'history' to 'description'") description@other <- c(description@other,from@history) } } else { warning("'description' is not of class MIAME; ignored") description <- NULL } ## reporterInfo if (any(dim(from@reporterInfo)!=0)) warning("reporterInfo data not transfered to '",toClass, "' object") ## new object object <- new(toClass, assayData = from@assayData, phenoData = phenoData, featureData = annotatedDataFrameFrom(from@assayData, byrow=TRUE), experimentData = updateObject(description), annotation = from@annotation) validObject(object) object } setAs("eSet", "ExpressionSet", function(from, to) updateOldESet(from, "ExpressionSet")) setAs("eSet", "MultiSet", function(from, to) updateOldESet(from, "MultiSet")) updateESetTo <- function(object, template, ..., verbose=FALSE) { if (verbose) message("updateESetTo(object = 'eSet' template = '", class(template), "')") ## cannot instantiate a 'virtual' class, so use accessor functions ## to update class components. Better than direct slot access? funcs <- c("assayData", "phenoData", "experimentData", "annotation") eval(parse(text=paste(funcs,"(template)<-", "updateObject(", funcs, "(object), ..., verbose=verbose)"))) result <- try(featureData(template) <- featureData(object), silent=TRUE) if (class(result)=="try-error") featureData(template) <- annotatedDataFrameFrom(assayData(object), byrow=TRUE) vers <- classVersion("eSet") classVersion(template)[names(vers)] <- vers # current class version, eSet & 'below' only template } setMethod("updateObject", signature(object="eSet"), function(object, ..., verbose=FALSE) { if (verbose) message("updateObject(object = 'eSet')") object <- asS4(object) if (isVersioned(object) && isCurrent(object)["eSet"]) return(callNextMethod()) ## storage.mode likely to be useful to update versioned classes, too storage.mode.final <- storageMode(object) storage.mode <- if (storage.mode.final == "lockedEnvironment") "environment" else storage.mode.final additionalSlots <- setdiff(slotNames(class(object)), slotNames("eSet")) names(additionalSlots) <- additionalSlots if (!isVersioned(object)) { object <- updateESetTo(object, new(class(object), storage.mode=storage.mode), ..., verbose=verbose) storageMode(object) <- storage.mode.final } else if (classVersion(object)["eSet"]=="1.0.0") { ## added featureData slot; need to update phenoData object <- do.call(new, c(list(class(object), assayData = updateObject(assayData(object), ..., verbose=verbose), phenoData = AnnotatedDataFrame(data=pData(object), varMetadata=varMetadata(object)), featureData = annotatedDataFrameFrom(assayData(object), byrow=TRUE), experimentData = updateObject(experimentData(object), ..., verbose=verbose), annotation = annotation(object)), lapply(additionalSlots, function(x) slot(object, x)))) } else if (classVersion(object)["eSet"]=="1.1.0") { ## added scanDates slot object <- do.call(new, c(list(class(object), assayData = updateObject(assayData(object)), phenoData = updateObject(phenoData(object)), featureData = updateObject(featureData(object)), experimentData = updateObject(experimentData(object)), annotation = annotation(object)), lapply(additionalSlots, function(x) slot(object, x)))) } else if (classVersion(object)["eSet"]=="1.2.0") { ## added protocolData slot, removed scanDates slot scanDates <- object@scanDates protocolData <- phenoData(object)[,integer(0)] if (length(scanDates) > 0) { protocolData[["ScanDate"]] <- scanDates } object <- do.call(new, c(list(class(object), assayData = updateObject(assayData(object)), phenoData = updateObject(phenoData(object)), featureData = updateObject(featureData(object)), experimentData = updateObject(experimentData(object)), annotation = annotation(object), protocolData = protocolData), lapply(additionalSlots, function(x) updateObject(slot(object, x))))) } else { stop("cannot update object of class '", class(object), "', claiming to be eSet version '", as(classVersion(object)["eSet"], "character"), "'") } object }) setMethod("updateObjectTo", signature(object="eSet", template="eSet"), updateESetTo) setValidity("eSet", function(object) { msg <- validMsg(NULL, isValidVersion(object, "eSet")) dims <- dims(object) if (ncol(dims) > 0) { ## assayData msg <- validMsg(msg, assayDataValidMembers(assayData(object))) if (any(dims[1,] != dims[1,1])) msg <- validMsg(msg, "row numbers differ for assayData members") if (any(dims[2,] != dims[2,1])) msg <- validMsg(msg, "sample numbers differ for assayData members") ## featureData if (dims[1,1] != dim( featureData(object))[[1]]) msg <- validMsg(msg, "feature numbers differ between assayData and featureData") if (!identical(featureNames(assayData(object)), featureNames(featureData(object)))) msg <- validMsg(msg, "featureNames differ between assayData and featureData") ## phenoData if (dims[2,1] != dim(phenoData(object))[[1]]) msg <- validMsg(msg, "sample numbers differ between assayData and phenoData") if (!identical(sampleNames(assayData(object)), sampleNames(phenoData(object)))) msg <- validMsg(msg, "sampleNames differ between assayData and phenoData") ## protocolData if (dim(phenoData(object))[[1]] != dim(protocolData(object))[[1]]) msg <- validMsg(msg, "sample numbers differ between phenoData and protocolData") if (!identical(sampleNames(phenoData(object)), sampleNames(protocolData(object)))) msg <- validMsg(msg, "sampleNames differ between phenoData and protocolData") } if (is.null(msg)) TRUE else msg }) setMethod("preproc", "eSet", function(object) preproc(experimentData(object))) setReplaceMethod("preproc", signature=signature(object="eSet"), function(object, value) { ed <- experimentData(object) preproc(ed) <- value object@experimentData <- ed object }) setMethod("show", signature=signature(object="eSet"), function(object) { cat(class(object), " (storageMode: ", storageMode(object), ")\n", sep="") adim <- dim(object) if (length(adim)>1) cat("assayData:", if (length(adim)>1) paste(adim[[1]], "features,", adim[[2]], "samples") else NULL, "\n") cat(" element names:", paste(assayDataElementNames(object), collapse=", "), "\n") .showAnnotatedDataFrame(protocolData(object), labels=list(object="protocolData")) .showAnnotatedDataFrame(phenoData(object), labels=list(object="phenoData")) .showAnnotatedDataFrame(featureData(object), labels=list( object="featureData", sampleNames="featureNames", varLabels="fvarLabels", varMetadata="fvarMetadata")) cat("experimentData: use 'experimentData(object)'\n") pmids <- pubMedIds(object) if (length(pmids) > 0 && all(pmids != "")) cat(" pubMedIds:", paste(pmids, sep=", "), "\n") cat("Annotation:", annotation(object), "\n") }) setMethod("storageMode", "eSet", function(object) storageMode(assayData(object))) setReplaceMethod("storageMode", signature=signature( object="eSet", value="character"), function(object, value) { ad <- assayData(object) storageMode(ad) <- value object@assayData <- ad object }) setMethod("sampleNames", signature(object="eSet"), function(object) sampleNames(phenoData(object))) setReplaceMethod("sampleNames", signature=signature(object="eSet", value="ANY"), function(object, value) { pd <- phenoData(object) sampleNames(pd) <- value ad <- assayData(object) sampleNames(ad) <- value prd <- protocolData(object) if (nrow(prd) == 0) { prd <- pd[,integer(0)] } else { sampleNames(prd) <- value } object@phenoData <- pd object@protocolData <- prd unsafeSetSlot(object, "assayData", ad) }) setMethod("featureNames", signature=signature(object="eSet"), function(object) featureNames(assayData(object))) setReplaceMethod("featureNames", signature=signature(object="eSet", value="ANY"), function(object, value) { fd <- featureData(object) featureNames(fd) <- value ad <- assayData(object) featureNames(ad) <- value object@featureData <- fd unsafeSetSlot(object, "assayData", ad) }) setMethod("dimnames", "eSet", function(x) { list(featureNames(x), sampleNames(x)) }) setReplaceMethod("dimnames", "eSet", function(x, value) { featureNames(x) <- value[[1]] sampleNames(x) <- value[[2]] x }) setMethod("dim", "eSet", function(x) assayDataDim(assayData(x))) setMethod("dims", "eSet", function(object) assayDataDims(assayData(object))) setMethod("[", "eSet", function(x, i, j, ..., drop = FALSE) { if (missing(drop)) drop <- FALSE if (missing(i) && missing(j)) { if (!missing(...)) stop("specify genes or samples to subset; use '", substitute(x), "$", names(list(...))[[1]], "' to access phenoData variables") return(x) } if (!isVersioned(x) || !isCurrent(x)["eSet"]) x <- updateObject(x) if (!missing(j)) { phenoData(x) <- phenoData(x)[j,, ..., drop = drop] protocolData(x) <- protocolData(x)[j,, ..., drop = drop] } if (!missing(i)) featureData(x) <- featureData(x)[i,,..., drop=drop] ## assayData; implemented here to avoid function call orig <- assayData(x) storage.mode <- assayDataStorageMode(orig) assayData(x) <- switch(storage.mode, environment =, lockedEnvironment = { aData <- new.env(parent=emptyenv()) if (missing(i)) # j must be present for(nm in ls(orig)) aData[[nm]] <- orig[[nm]][, j, ..., drop = drop] else { # j may or may not be present if (missing(j)) for(nm in ls(orig)) aData[[nm]] <- orig[[nm]][i,, ..., drop = drop] else for(nm in ls(orig)) aData[[nm]] <- orig[[nm]][i, j, ..., drop = drop] } if ("lockedEnvironment" == storage.mode) assayDataEnvLock(aData) aData }, list = { if (missing(i)) # j must be present lapply(orig, function(obj) obj[, j, ..., drop = drop]) else { # j may or may not be present if (missing(j)) lapply(orig, function(obj) obj[i,, ..., drop = drop]) else lapply(orig, function(obj) obj[i, j, ..., drop = drop]) } }) x }) ## $ stops dispatching ?! ##setMethod("$", "eSet", function(x, name) `$`(phenoData(x), name)) setMethod("$", "eSet", function(x, name) { eval(substitute(phenoData(x)$NAME_ARG, list(NAME_ARG=name))) }) .DollarNames.eSet <- function(x, pattern = "") grep(pattern, names(pData(x)), value=TRUE) setReplaceMethod("$", "eSet", function(x, name, value) { phenoData(x)[[name]] = value x }) setMethod("[[", "eSet", function(x, i, j, ...) phenoData(x)[[i]]) setReplaceMethod("[[", "eSet", function(x, i, j, ..., value) { phenoData(x)[[i, ...]] <- value x }) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - setMethod("assayData", "eSet", function(object) object@assayData) setReplaceMethod("assayData", signature=signature( object="eSet", value="AssayData"), function(object, value) { object@assayData <- value object }) assayDataElementNames <- function(object) { if (storageMode(object) == "list") names(assayData(object)) else ls(assayData(object)) } assayDataElement <- function(object, elt) assayData(object)[[elt]] .validate_assayDataElementReplace <- function(obj, value) { if (!is.null(value)) { dimvalue <- dim(value) dimobj <- dim(obj)[seq_along(dimvalue)] if (!isTRUE(all.equal(unname(dimvalue), unname(dimobj)))) stop("object and replacement value have different dimensions") } if (!is.null(value)) { if (!is.null(dimnames(value))) { ## validate and harmonize dimnames vd <- Map(function(od, vd) { if (is.null(vd)) ## update vd to contain indexes into matrix od <- seq_along(od) else if (!setequal(od, vd)) stop("object and replacement value dimnames differ") od }, dimnames(obj), dimnames(value)) ## re-arrange value to have dimnames in same order as obj value <- do.call(`[`, c(list(value), vd, drop=FALSE)) } dimnames(value) <- dimnames(obj) } value } assayDataElementReplace <- function(obj, elt, value, validate=TRUE) { ## 'validate' added later, needs to be last for position matching if (validate) value <- .validate_assayDataElementReplace(obj, value) storage.mode <- storageMode(obj) switch(storageMode(obj), "lockedEnvironment" = { aData <- copyEnv(assayData(obj)) if (is.null(value)) rm(list=elt, envir=aData) else aData[[elt]] <- value assayDataEnvLock(aData) assayData(obj) <- aData }, "environment" = { if (is.null(value)) rm(list=elt, envir=assayData(obj)) else assayData(obj)[[elt]] <- value }, list = assayData(obj)[[elt]] <- value) obj } `assayDataElement<-` <- function(obj, elt, ..., value) ## 'value' is always the last argument, but needs to be 3rd for ## assayDataElementReplace assayDataElementReplace(obj, elt, value, ...) setMethod("phenoData", "eSet", function(object) object@phenoData) setReplaceMethod("phenoData", signature=signature( object="eSet", value="AnnotatedDataFrame"), function(object, value) { object@phenoData <- value if (nrow(protocolData(object)) == 0) { protocolData(object) <- value[,integer(0)] } object }) setMethod("pData", "eSet", function(object) pData(phenoData(object))) setReplaceMethod("pData", signature=signature( object="eSet", value="data.frame"), function(object, value) { pd <- phenoData(object) pData(pd) <- value phenoData(object) <- pd object }) setMethod("varMetadata", signature=signature(object="eSet"), function(object) varMetadata(phenoData(object))) setReplaceMethod("varMetadata", signature=signature( object="eSet", value="data.frame"), function(object, value) { pd <- phenoData(object) varMetadata(pd) <- value object@phenoData <- pd object }) setMethod("varLabels", signature=signature(object="eSet"), function(object) varLabels(phenoData(object))) setReplaceMethod("varLabels", signature=signature( object="eSet", value="ANY"), function(object, value) { pd <- phenoData(object) varLabels(pd) <- value object@phenoData <- pd object }) setMethod("featureData", signature(object="eSet"), function(object) object@featureData) setReplaceMethod("featureData", signature=signature( object="eSet", value="AnnotatedDataFrame"), function(object, value) { object@featureData <- value object }) setMethod("fData", signature=signature(object="eSet"), function(object) pData(featureData(object))) setReplaceMethod("fData", signature=signature( object="eSet", value="data.frame"), function(object, value) { fd <- featureData(object) pData(fd) <- value object@featureData <- fd object }) setMethod("fvarMetadata", signature=signature(object="eSet"), function(object) varMetadata(featureData(object))) setReplaceMethod("fvarMetadata", signature=signature( object="eSet", value="data.frame"), function(object, value) { fd <- featureData(object) varMetadata(fd) <- value object@featureData <- fd object }) setMethod("fvarLabels", signature=signature(object="eSet"), function(object) varLabels(featureData(object))) setReplaceMethod("fvarLabels", signature=signature( object="eSet", value="ANY"), function(object, value) { pd <- featureData(object) varLabels(pd) <- value object@featureData <- pd object }) setMethod("experimentData", signature(object="eSet"), function(object) object@experimentData) setReplaceMethod("experimentData", signature=signature( object="eSet", value="MIAME"), function(object, value) { object@experimentData <- value object }) setMethod("description", signature(object="eSet"), function(object, ...) { experimentData(object) }) setReplaceMethod("description", signature=signature( object="eSet", value="MIAME"), function(object, value) { object@experimentData <- value object }) setMethod("notes", signature(object="eSet"), function(object) otherInfo(experimentData(object))) setReplaceMethod("notes", signature=signature( object="eSet", value="ANY"), function(object, value) { ed <- experimentData(object) notes(ed) <- value object@experimentData <- ed object }) setMethod("pubMedIds", signature(object="eSet"), function(object) pubMedIds(experimentData(object))) setReplaceMethod("pubMedIds", signature=signature( object="eSet", value="character"), function(object, value) { ed <- experimentData(object) pubMedIds(ed) <- value object@experimentData <- ed object }) setMethod("abstract", "eSet", function(object) abstract(experimentData(object))) setMethod("annotation", "eSet", definition = function(object) object@annotation) setReplaceMethod("annotation", signature=signature( object="eSet", value="character"), function(object, value) { object@annotation <- value object }) setMethod("protocolData", "eSet", function(object) { tryCatch(object@protocolData, error = function(x) { phenoData(object)[,integer(0)] }) }) setReplaceMethod("protocolData", signature=signature( object="eSet", value="AnnotatedDataFrame"), function(object, value) { if (class(try(object@protocolData, silent = TRUE)) == "try-error") object <- updateObject(object) object@protocolData <- value object }) setMethod("combine", signature=signature( x="eSet", y="eSet"), function(x, y, ...) { if (class(x) != class(y)) stop("objects must be the same class, but are '", class(x), "', '", class(y), "'") if (any(annotation(x) != annotation(y))) stop("objects have different annotations: ", annotation(x), ", ", annotation(y)) if (!isCurrent(x)[["eSet"]]) x <- updateObject(x) assayData(x) <- combine(assayData(x), assayData(y)) phenoData(x) <- combine(phenoData(x), phenoData(y)) featureData(x) <- combine(featureData(x), featureData(y)) experimentData(x) <- combine(experimentData(x),experimentData(y)) protocolData(x) <- combine(protocolData(x), protocolData(y)) ## annotation -- constant x }) Biobase/R/packages.R0000644000175400017540000000707713175713325015270 0ustar00biocbuildbiocbuild# ========================================================================== # Functions to operate with packages: # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - # createPackage; package.version; dumpPackTxt # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - # uses strings.R # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - createPackage <- function(pkgname, destinationDir, originDir, symbolValues, unlink=FALSE, quiet=FALSE) { ## check arguments for (a in c("pkgname", "destinationDir", "originDir")) if (!is.character(get(a)) || length(get(a))!=1) stop("'", a, "' must be character(1)") ## check whether destinationDir, originDir exist and are directories for (a in c("destinationDir", "originDir")) if(!file.exists(get(a)) || !file.info(get(a))$isdir) stop("'", a, "' must be a directory (", get(a), ")") ## locate / remove / create destination directory pkgdir = file.path(destinationDir, pkgname) if (!quiet) cat("Creating package in", pkgdir, "\n") if (file.exists(pkgdir)) { if (unlink) { unlink(pkgdir, recursive=TRUE) if (file.exists(pkgdir)) { stop("directory '", pkgdir, "' exists and could not be removed; ", "remove it manually or choose another destination directory") } else { if(!quiet) cat("existing", pkgdir, "was removed.\n") } } else stop("directory '", pkgdir, "' exists; use unlink=TRUE ", "to remove it, or choose another destination directory") } ## if (file.exists) ## predefined symbols symbolValues = append(symbolValues, list(TODAY=date(), PKGNAME=pkgname)) ## copy (from strings.R) copySubstitute(dir(originDir, full.names=TRUE), pkgdir, symbolValues, recursive=TRUE) return(list(pkgdir=pkgdir)) } # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - package.version <- function(pkg, lib.loc = NULL) { curWarn <- getOption("warn") on.exit(options(warn=curWarn),add=TRUE) options(warn=-1) desc <- packageDescription(pkg, lib.loc, "Version") if (is.na(desc)) stop("package '", pkg, "' does not exist") desc } # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - dumpPackTxt <- function (package) { # stolen from "library" to get descriptive info out on stdout pkgpath <- find.package(package) # outFile <- tempfile("Rlibrary") # outConn <- file(outFile, open = "w") docFiles <- file.path(pkgpath, c("TITLE", "DESCRIPTION", "INDEX")) headers <- c("", "Description:\n\n", "Index:\n\n") footers <- c("\n", "\n", "") for (i in which(file.exists(docFiles))) { writeLines(headers[i], sep = "") writeLines(readLines(docFiles[i]) ) writeLines(footers[i], sep = "") } # close(outConn) # file.show(outFile, delete.file = TRUE) } # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ##strictly internal, not for export ##take an AnnotatedDataFrame object and create a valid format ## section for a man page pD2Rd <- function(pD) { if(!inherits(pD, "AnnotatedDataFrame") ) stop("only works for AnnotatedDataFrames") fmt = "\\format{\n The format is:\n An \\code{ExpressionSetObject} with covariates:\n" covs = "\\itemize{" vMD = varMetadata(pD) vL = varLabels(pD) for(i in 1:length(vL) ) { item = paste0("\\item \\code{", vL[i], "}: ", vMD[i,1]) covs = paste(covs, item, sep="\n") } paste0(fmt, covs, "\n}\n}\n") } Biobase/R/rowOp-methods.R0000644000175400017540000000277713175713325016263 0ustar00biocbuildbiocbuildsetGeneric("rowMedians", function(x, na.rm=FALSE, ...) { # Backward compatibility for rowMedians(imat=...) if (missing(x)) { args <- list(...); if (is.element("imat", names(args))) { x <- args$imat; .Deprecated(msg="The name of the matrix argument for Biobase::rowMedians() has been changed from 'imat' to 'x'."); } } standardGeneric("rowMedians") }) setMethod("rowMedians", signature(x="matrix"), function(x, na.rm=FALSE, ...) { na.rm <- as.logical(na.rm); hasNAs <- TRUE; # Add as an argument? /2007-08-24 .Call("rowMedians", x, na.rm, hasNAs, TRUE, PACKAGE="Biobase"); }) setMethod("rowMedians", signature(x="ExpressionSet"), function(x, na.rm=FALSE, ...) { rowMedians(exprs(x), na.rm=na.rm, ...); }) setGeneric("rowQ", function(imat, which) standardGeneric("rowQ")) setMethod("rowQ", signature(imat="matrix", which="numeric"), function(imat, which) { if (any(is.na(imat))) stop("cannot handle missing values.") if (length(which) != 1 || !is.finite(which)) stop("'which' must be length one and finite numeric") if(is.integer(imat)) imat <- structure(as.numeric(imat), dim=dim(imat)) .Call("rowQ", imat, which, PACKAGE="Biobase") }) setMethod("rowQ", signature(imat="ExpressionSet", which="numeric"), function(imat, which) rowQ(exprs(imat), which)) rowMin <- function(imat) rowQ(imat, 1) rowMax <- function(imat) rowQ(imat, ncol(imat)) Biobase/R/strings.R0000644000175400017540000000366113175713325015176 0ustar00biocbuildbiocbuild# ========================================================================== # Functions to deal with strings: # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - # strbreak # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - strbreak <- function(x, width=getOption("width"), exdent=2, collapse="\n") { width <- as.integer(width) if(is.na(width) || width<=1) stop("invalid argument 'width'") exdent <- as.integer(exdent) if(is.na(exdent) || exdent>width) stop("invalid argument 'exdent'") ww <- width-exdent lb <- paste0(collapse, paste(rep(" ", exdent), collapse="")) rv <- character(length(x)) for(i in seq(along=x)) { first <- 1 last <- width if(nchar(x[i])>width) { f <- seq(width+1, nchar(x[i]), ww) first <- c(first, f) last <- c(last, f+ww-1) } rv[i] <- paste(substring(x[i], first=first, last=last), collapse=lb) } return(rv) } # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - lcSuffix <- function(x, ignore.case = FALSE) { x <- as.character(x) if( ignore.case ) x <- toupper(x) nc <- nchar(x, type="char") for(i in 1:min(nc)) { ## The +1 and +2 are because substr is funny ss = substr(x, nc - i + 1, nc) if( any(ss != ss[1] )) { if (i == 1L) # trailing char mismatch return("") return(substr(x[1], nc - i + 2, nc)) } } return(substr(x[1], nc - i + 1, nc)) } lcPrefix <- function(x, ignore.case=FALSE) { x <- as.character(x) if (ignore.case) x <- toupper(x) nc <- nchar(x, type="char") for (i in 1:min(nc)) { ss <- substr(x, 1, i) if (any(ss != ss[1])) { return(substr(x[1], 1, i-1)) } } substr(x[1], 1, i) } lcPrefixC <- function(x, ignore.case=FALSE) { .Call("lc_prefix", x, ignore.case) } Biobase/R/tools.R0000644000175400017540000002710013175713325014637 0ustar00biocbuildbiocbuild# ========================================================================== # Uncategorized tools for Biobase # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - # testBioCConnection # openPDF # listLen; reverseSplit # rowQ; rowMedians; rowMin; rowMax # copySubstitute # isUnique # cache # userQuery # ========================================================================== testBioCConnection <- function() { ## Stifle the "connected to www.... garbage output curNetOpt <- getOption("internet.info") on.exit(options(internet.info=curNetOpt), add=TRUE) options(internet.info=3) ## First check to make sure they have HTTP capability. If they do ## not, there is no point to this exercise. http <- as.logical(capabilities(what="http/ftp")) if (http == FALSE) return(FALSE) ## find out where we think that bioC is bioCoption <- getOption("BIOC") if (is.null(bioCoption)) bioCoption <- "http://www.bioconductor.org" ## Now check to see if we can connect to the BioC website biocURL <- url(paste0(bioCoption,"/main.html")) options(show.error.messages=FALSE) test <- try(readLines(biocURL)[1]) options(show.error.messages=TRUE) if (inherits(test,"try-error")) return(FALSE) else close(biocURL) return(TRUE) } # ========================================================================== openPDF <- function(file, bg=TRUE) { OST <- .Platform$OS.type if (OST=="windows") shell.exec(file) else if (OST == "unix") { bioCOpt <- getOption("BioC") pdf <- getOption("pdfviewer") msg <- NULL if (is.null(pdf)) msg <- "getOption('pdfviewer') is NULL" else if (length(pdf)==1 && nchar(pdf[[1]])==0) msg <- "getOption('pdfviewer') is ''" if (!is.null(msg)) stop(msg, "; please use 'options(pdfviewer=...)'") cmd <- paste(pdf,file) if( bg ) cmd <- paste(cmd, "&") system(cmd) } return(TRUE) } # ========================================================================== reverseSplit = function(inList) { if (length(inList)==0) { return(inList) } lens = sapply(inList, length) nms = rep(names(inList), lens) vals = unlist(inList) split(nms, vals) } # ========================================================================== copySubstitute = function(src, dest, symbolValues, symbolDelimiter = "@", allowUnresolvedSymbols = FALSE, recursive = FALSE, removeExtension = "\\.in$") { ## Check integrity of arguments (...lots of bureaucracy) mess = NULL if (!is.list(symbolValues) && !is.vector(symbolValues)) mess = "'symbolValues' must be a list or vector." if (!all(sapply(symbolValues, is.character))) mess = "'symbolValues' must only contain characters." if (is.null(names(symbolValues)) || any(names(symbolValues)=="")) mess = "'symbolValues' must have non-empty names." if (!(is.character(symbolDelimiter) && length(symbolDelimiter)==1 && all(nchar(symbolDelimiter)==1))) mess = "'symbolDelimiter' must be a single character." if (!is.logical(allowUnresolvedSymbols)) mess = "'allowUnresolvedSymbols' must be of type logical." if(!is.null(mess)) stop(mess) ## Here the actual subsitution and copying work is done ## cin and cout are single files or connections cpSubsCon = function(cin, cout) { txt = readLines(cin) for (i in seq(along=symbolValues)) { txt = gsub(nm[i], symbolValues[[i]], txt, fixed=TRUE) if (any(is.na(txt))) stop("trying to replace ", nm[i], " by an NA") } ## check for unresolved symbols if(!allowUnresolvedSymbols) { re = regexpr(paste0(symbolDelimiter, ".+", symbolDelimiter), txt) wh = which(re>0) if(length(wh)>0) { ml = attr(re, "match.length") mess = "UNRESOLVED SYMBOLS:\n" mess <- paste0(mess, paste(sapply(wh, function(i) { paste("Line", i, ":", substr(txt[i], re[i], re[i] + ml[i])) }), collapse="\n")) stop(mess) } } ## finito writeLines(text=txt, con=cout) } ## Substitution on filenames subsFileName = function(x) { res = gsub(removeExtension, "", x) for (i in seq(along=symbolValues)) { res = gsub(nm[i], symbolValues[[i]], res) if (any(is.na(res))) stop("trying to replace ", nm[i], " by an NA") } return(res) } ## Iterate over character vectors of filenames and ## recursively descend into directories cpSubs = function(src, dest) { usage = paste("\n* Usage:", "\n* with recursive=FALSE:", "\n* 'src' a connection open for reading or a file name AND", "\n* 'dest' a connection open for writing or a file name", "\n* with recursive=TRUE:", "\n* 'src' a vector of file and directory names and 'dest' a directory name\n\n") if (!recursive) { ## {file,connection} to {file,connection} if ((("connection" %in% class(src) && isOpen(src, rw="r")) || (is.character(src) && length(src)==1)) && (("connection" %in% class(dest) && isOpen(dest, rw="w")) || (is.character(dest) && length(dest)==1))) { if(is.character(dest)) dest = subsFileName(dest) cpSubsCon(src, dest) return(invisible(NULL)) } } else { ## recursive: file(s) and/or directory(ies) to directory if (is.character(src) && is.character(dest) && length(dest==1)) { ## if 'dest' does not exist, create if (file.access(dest) != 0) { if (!dir.create(dest)) stop("'dest' does not exist, and cannot be created: ", dest) } ## process src isdir = file.info(src)$isdir for (k in seq(along=src)) { ## name of source file or directory (without path) tmp = unlist(strsplit(src[k], .Platform$file.sep)) tmp = subsFileName(tmp[length(tmp)]) ## name of destination file or directory (with path) destname = file.path(dest, tmp) if (isdir[k]) { if(!dir.create(destname)) stop("directory cannot be created: ", destname) cpSubs(dir(src[k], full.names=TRUE), destname) } else cpSubsCon(src[k], destname) } ## for k return(invisible(NULL)) } ## if(is.character...) } ## if(recursive)else stop(usage) } ## cpSubs ## DO IT! nm = paste0(symbolDelimiter, names(symbolValues), symbolDelimiter) cpSubs(src, dest) } # ========================================================================== note <- function(...) { ## A "less drastic" version of warning() if (nargs() > 0) { message <- paste("Note:",...,"\n") cat(message) } } ## ================================================== isUnique = function(x){ rv = rep(TRUE, length(x)) if(length(x)>=2) { ord = order(x) ox = x[ord] ## compare consecutive values neq = (ox[-length(ox)]!=ox[-1]) ## a value is unique if neither its predecessor nor successor ## in the ordered vector are the same rv[ord] = c(neq, TRUE) & c(TRUE, neq) } return(rv) } ## - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ## O.Sklyar, EBI, 2006 matchpt <- function(x, y) { storage.mode(x)="double" if (is.vector(x)) x <- matrix(x, ncol = 1L, nrow = length(x)) if (!(is.matrix(x) && is.numeric(x))) stop("'x' must be a numeric matrix.") if (!missing(y)) { storage.mode(y)="double" if (is.vector(y)) y <- matrix(y, ncol = 1L, nrow = length(y)) if (!(is.matrix(y) && is.numeric(y))) stop("y must be a numeric matrix.") if (ncol(x) != ncol(y)) stop("x and y must have the same number of columns.") } else { y <- NULL } res <- .Call("matchpt", x, y, PACKAGE = "Biobase") res <- as.data.frame(res) rownames(res) <- rownames(x) return(res) } ## - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - cache <- function(expr, dir=".", prefix="tmp_R_cache_") { pexpr <- parse(text=deparse(substitute(expr))) pexpr <- as.list(pexpr[[1]]) name <- as.character(pexpr[[2]]) RHS <- pexpr[[3]] cachefile <- file.path(dir, paste0(prefix, name, ".RData")) if(file.exists(cachefile)) { load(cachefile) assign(name, get(name), envir=parent.frame()) } else { dir.create(dir, recursive=TRUE, showWarnings=FALSE) assign(name, eval(RHS, envir=parent.frame()), envir=parent.frame()) save(list=name, file=cachefile, envir=parent.frame()) } invisible(get(name, envir=parent.frame())) } ## - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - validMsg <- function(msg, result) { if (is.character(result)) { append(msg, result) } else msg } checkClass <- function(object, expected, prefix="", call.=FALSE, ...) { if (!is(object, expected)) stop(prefix, " '", deparse(substitute(object)), "' is class '", paste(class(object), collapse="', '"), "' but should be or extend '", paste(expected, collapse="', '"), "'", call.=call., ...) } ## - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - userQuery <- function(msg, allowed=c("y","n"), default = "n", case.sensitive = FALSE) { ## Prompts the user with a string and for an answer ## repeats until it gets allowable input if(interactive()){ repeat { allowMsg <- paste0("[", paste(allowed,collapse="/"), "] ") outMsg <- paste(msg, allowMsg) cat(outMsg) if(case.sensitive) ans <- readLines(n=1) else ans <- tolower(readLines(n=1)) if (ans %in% allowed) break else cat(ans, "is not a valid response, try again.\n") } return(ans) }else{ return(default) } } unsafeSetSlot <- function(obj, slot, value) { ## This function _assumes_ that there is exactly on references to ## 'obj'; the number of references is not usually detectable from ## casual perusal of the code, because R only maintains the ## _illusion_ of pass by value. Use this with the greatest care, ## if at all. invisible(.Call("unsafe_set_slot", obj, slot, value)) } subListExtract <- function(L, name, simplify=FALSE, keep.names=TRUE) { ## Return a list or vector obtained by extracting the element named ## 'name' from each inner list of L. ## ## L - list ## name - character vector length 1, name of inner list element ## simplify - return an atomic vector or error if TRUE ## keep.names - if TRUE, keep names of L on result ## ## this is just a mockup, to play with the desired interface ## and behavior. will be replaced with a C version. .Call(sublist_extract, L, name, simplify, keep.names) ## f <- function(x) { ## wh <- match(name, names(x), 0) ## if (wh > 0) ## x[[wh]] ## else # would be nice to have index in msg ## stop("bad inner list, no element named ", name) ## } ## if (!simplify) ## ans <- lapply(L, f) ## else { ## ans <- sapply(L, f) ## if (is.list(ans)) ## stop("unable to simplify") ## } ## if (!keep.names) ## names(ans) <- NULL ## ans } Biobase/R/updateObjectTo.R0000644000175400017540000000144313175713325016415 0ustar00biocbuildbiocbuildsetMethod("updateObjectTo", signature(object="ANY", template="ANY"), function(object, template, ..., verbose=FALSE) { if (verbose) message("updateObject(object = 'ANY', template = 'ANY') default for object = '", class(object), "' template = ", class(template), "'") if (class(object)==class(template)) object else { tryCatch(as(object, class(template)), error=function(err) { stop("\nupdateObjectTo:\n ", "cannot convert object of class '", class(object), "' ", "to template class '", class(template), "'")}) } }) Biobase/R/vignettes.R0000644000175400017540000000672213175713325015516 0ustar00biocbuildbiocbuild## Functions to detect and open vignettes: ## uses tools.R getPkgVigs = function(package=NULL) { pkgs <- .packages() if( !is.null(package) ) { if( !is.character(package) ) stop("`package' must be a character vector of package names") rows <- match(package, pkgs) if( all(is.na(rows)) ) stop("packages '", paste(package, collapse="', '"), "' are not loaded") if( any(is.na(rows)) ) warning("packages '", paste(package[is.na(rows)], collapse="', '"), "' are not loaded") pkgs <- pkgs[rows[!is.na(rows)]] } vigrds = file.path(find.package(pkgs), "Meta", "vignette.rds") ## construct data frame with: package, path, title pkgVigs = vector(mode="list", length=length(vigrds)) for(j in seq(along=vigrds)) { if (file.exists(vigrds[j])) { v = readRDS(vigrds[j]) f = v[, "PDF"] f = ifelse(f=="", as.character(NA), file.path(dirname(dirname(vigrds[j])), "doc", f)) tit = v[, "Title"] tit[tit==""] = as.character(NA) rv= data.frame(package = pkgs[j], filename = f, title = tit, stringsAsFactors=FALSE) pkgVigs[[j]] = rv } } ## for j do.call(rbind, args=pkgVigs) } # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - openVignette = function(package=NULL) { vig = getPkgVigs(package) if (is.null(vig)) { txt <- "" if (!is.null(package)) { ss <- if (length(package)==1) "" else "s" pkgs <- paste(package, collapse=", ") txt <- sprintf(" for package%s %s", ss, pkgs) } warning("no vignettes found", txt) } else { hasnofile = is.na(vig$filename) vig$title[hasnofile] = paste(vig$title[hasnofile], "[-]") vig = vig[order(hasnofile, tolower(vig$package), tolower(vig$title)), ] index = menu(paste(vig$package, "-", vig$tit), title = paste("Please select a vignette:", if(any(hasnofile)) "(entries marked by '[-]' have no PDF file)" else "" )) if (index>0) { vif = vig$filename[index] if(!is.na(vif)) { openPDF(vif) cat("Opening", vif, "\n") ## browseURL(paste0("file://", vig[index])) } else { stop("Sorry, no PDF file could be found for this vignette.\n", "Please reinstall the package with built vignettes.") } } } } #----------------------------------------------------------- # add package vignettes to the menu bar of the Windows Rgui ##---------------------------------------------------------- addVigs2WinMenu = function(pkgName) { if ((.Platform$OS.type == "windows") && (.Platform$GUI == "Rgui") && interactive()) { vigFile = system.file("Meta", "vignette.rds", package=pkgName) if (!file.exists(vigFile)) { warning(sprintf("%s contains no vignette, nothing is added to the menu bar", pkgName)) } else { vigMtrx = readRDS(vigFile) vigs = file.path(find.package(pkgName), "doc", vigMtrx[, "PDF"]) names(vigs) = vigMtrx[,"Title"] if (!"Vignettes" %in% winMenuNames()) winMenuAdd("Vignettes") pkgMenu = paste("Vignettes", pkgName, sep="/") winMenuAdd(pkgMenu) for (i in seq(along=vigs)) winMenuAddItem(pkgMenu, names(vigs)[i], paste0("shell.exec(\"", vigs[i], "\")")) } ## else ans = TRUE } else { ans = FALSE } ## else ans } Biobase/R/zzz.R0000644000175400017540000000166213175713325014341 0ustar00biocbuildbiocbuild# ========================================================================== # Biobase package initialization # ========================================================================== .onLoad <- function(libname, pkgname) { ## need contents to load at library attach - not at build time .initContents() ## in environment.R .buildBiobaseOpts() ## in environment.R } .onAttach <- function(libname, pkgname) { msg0 <- "Vignettes contain introductory material; view with 'browseVignettes()'. To cite Bioconductor, see 'citation(\"Biobase\")', and for packages 'citation(\"pkgname\")'." msg <- strwrap(paste(msg0, collapse=""), exdent=4, indent=4) packageStartupMessage(paste(c("Welcome to Bioconductor\n", msg), collapse="\n"), "\n") addVigs2WinMenu("Biobase") } .onUnload <- function( libpath ) { library.dynam.unload( "Biobase", libpath ) } Biobase/build/0000755000175400017540000000000013175724631014254 5ustar00biocbuildbiocbuildBiobase/build/vignette.rds0000644000175400017540000000053013175724631016611 0ustar00biocbuildbiocbuild‹S]KÃ0ÍÚº/‚ˆ?`ÿÃdDQ|˺$$Ùfßüã:Óí¦k‡{h’{sî9÷\šç>!$"q‘(öÇ8õKÛ'e@Òóûé•P/Ì–+=é²¹ÂÛ‹ëwmÀZ¡ä#¸éŒâ‹©óa t v¤u^lRMö³;åÀÒ™2<å[0—#IE–:E±#Ê$§ ýP4DAZoè_šÏþ÷µU¾ÊT“}øÓÔðîü™!¤WMÌé†wËOpo!°ƒ:¿§ëÕá:Ýu@G’å…! 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>;׊ɲ-rÐО†ˆÄy±k &ÜiU«žCG”²t¼›—f,H«ê@Éï Ga½%ye9 $ òù+°¿T¿1| $]¿¿ØÏ$È'\a0Ç &û†œ)A©2gN“[nË7ì}>ÒТ£.™Î­ÛXX"Ù4ÐÛæ“V’”$Þ+¦Äè¦ÝàX^j ç­Ñ‡¦áÅë:QÝý² ¢n×gó!pZ§¬ò@â3ЄÒ8Nô‡À_S·;ÇZ©wËß”çIéZË3F%À´€ 4m“ª“LNi‚ž à’×ON©ÕPœéáPë±ûröß””Dj_Ì[mî¤@Ù*¥bÙËn>®ΰp,;•Ÿ‹¼œ-Æ>ÊSuò¥u1óך³R˜;´íãÙ í]Cw"ÿ {?幨µs¦]gv”Åb‡tÁëZíJTǬ8Æól ¨ B £ú•–ñ×3oÙŠ¾Yæô,ËvÉ)Ê”cDnYóÕ’·í;å)¿ñà—Ð]j3£Ùçj) Û„ÃîÓwLéNƒ¸\/`ºF-/IÐÜг"Y‹Ñ˜áGˆ-A®oëÙ¤J fÓA>±oKÓȤbW ·­b«4Lcñÿ†á+¡Ë¸Ö_@cõ‘)0‡k˜° J;x,}¯w¦ì)1¦T‰…[ÿÃôC´?[ÀÅa«kÀË™ÅÒîÓšìêèv¸‰KD…¥_– †©e…D¿;³ªa>XÜÑùs›ÕFâïŒ;2 zWÄòE?x˵½Æ9`Í3—)ÑžoC¥J~MÄ÷˜#Ъ‹œŸ™’#3ެDR)Ï®ç ßaÅž§"â.Ñ÷æuÐFÔ{æ‰eBäé«‘• 2óÄn'°Ïÿ‡ˆaŽÖÔ×x¸CŸÊ|ÒÉß ÛòejO|q¥(;o_%¦€dQ•ôºãhYâÁkÝúì›9“H7^…|A½— dvMH^ûŒ8nϬ–·ö=_EÉ £‚Ê¿7†©ç<Ê`Ð5 Gó"ØÚ éFjF¨­Ç†cqª¼Ó¤"j+·ü ß!?†æõ®k5•ԇ䤅¡ùU‚Tî•v·²«Û?.^/à}eeš×ò3Ï=}QwãÙù+ÿφŘ+”ÕÔ$hvmB|½™ÈgBìê”äÀûÆ'ò xwæEH_öTX±€¹¼¬ˆBÔ¨Ý>0 ‹YZBiobase/data/aaMap.R0000644000175400017540000000302413175713325015225 0ustar00biocbuildbiocbuildaaMap <- structure(list(name = structure(c(1, 5, 4, 6, 14, 8, 9, 10, 12, 11, 13, 3, 15, 7, 2, 16, 17, 20, 18, 19), .Label = c("alanine", "arginine", "asparagine", "aspartic.acid", "cysteine", "glutamic.acid", "glutamine", "glycine", "histidine", "isoleucine", "leucine", "lysine", "methionine", "phenylalanine", "proline", "serine", "threonine", "tryptophan", "tyrosine", "valine"), class = "factor"), let.1 = structure(c(1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20), .Label = c("A", "C", "D", "E", "F", "G", "H", "I", "K", "L", "M", "N", "P", "Q", "R", "S", "T", "V", "W", "Y"), class = "factor"), let.3 = structure(c(1, 5, 4, 7, 14, 8, 9, 10, 12, 11, 13, 3, 15, 6, 2, 16, 17, 20, 18, 19), .Label = c("ala", "arg", "asn", "asp", "cys", "gln", "glu", "gly", "his", "ile", "leu", "lys", "met", "phe", "pro", "ser", "thr", "trp", "tyr", "val"), class = "factor"), scProp = structure(c(1, 2, 2, 2, 1, 1, 2, 1, 2, 1, 1, 2, 1, 2, 2, 2, 2, 1, 1, 2), .Label = c("nonpolar", "polar"), class = "factor"), hyPhilic = c(FALSE, NA, TRUE, TRUE, FALSE, NA, TRUE, FALSE, TRUE, FALSE, FALSE, TRUE, NA, TRUE, TRUE, NA, NA, FALSE, NA, NA), acidic = c(NA, NA, TRUE, TRUE, NA, NA, FALSE, NA, FALSE, NA, NA, FALSE, NA, FALSE, FALSE, NA, NA, NA, NA, NA)), .Names = c("name", "let.1", "let.3", "scProp", "hyPhilic", "acidic"), class = "data.frame", row.names = c("1", "2", "3", "4", "5", "6", "7", "8", "9", "10", "11", "12", "13", "14", "15", "16", "17", "18", "19", "20")) Biobase/data/geneCov.R0000644000175400017540000000076513175713325015605 0ustar00biocbuildbiocbuildgeneCov <- structure(list(cov1 = c(1, 1, 1, 1, 1, 1, 1, 1, 1, 1, 1, 1, 1, 2, 2, 2, 2, 2, 2, 2, 2, 2, 2, 2, 2, 2), cov2 = c(1, 1, 1, 1, 2, 2, 2, 2, 2, 2, 2, 2, 2, 2, 2, 2, 2, 2, 2, 1, 1, 1, 1, 1, 1, 1), cov3 = c(1, 1, 1, 1, 1, 1, 1, 1, 2, 2, 2, 2, 2, 2, 2, 2, 2, 3, 3, 3, 3, 3, 3, 3, 3, 3)), .Names = c("cov1", "cov2", "cov3" ), row.names = c("A", "B", "C", "D", "E", "F", "G", "H", "I", "J", "K", "L", "M", "N", "O", "P", "Q", "R", "S", "T", "U", "V", "W", "X", "Y", "Z"), class = "data.frame") Biobase/data/geneCovariate.rda0000644000175400017540000000066313175713325017335 0ustar00biocbuildbiocbuild‹…’=LÂ@Ƕhh‚!‘‰ÁwrÑ"ø… ~¡a¹àaL %mƒ_³³³®:3ãêÇæ ‰‘ÈFbĈ+z-÷ TÐKÚ÷»÷þ÷î½»KFRSrJF H`FJû¹òy˜õîÑñ}?y-[æÇÏÝ<Î;Ì“…;ù)‰=äqÉ<*ÀṌ¦;G×B½I\횘P"³Q€ÀÀ<ÀÀ"À@``` XXØØØHlì yEò.1I(«³Cá/©ó ÞùÒ?Biobase/data/geneData.R0000644000175400017540000036527313175713325015737 0ustar00biocbuildbiocbuildgeneData <- structure(c(192.742, 97.137, 45.8192, 22.5445, 96.7875, 89.073, 265.964, 110.136, 43.0794, 10.9187, 751.227, 76.9437, 105.378, 40.4826, 58.1706, 257.619, 129.056, 61.7251, -40.9349, 284.407, 178.745, 79.7368, 9903.19, 61.2671, 120.544, 50.0962, 42.5285, 36.8936, 234.698, 26.9561, 58.124, 40.616, 125.063, 49.9943, 33.1246, 148.494, 66.6936, 19.1364, 165.75, 179.989, 151.72, 553.87, 72.2579, -30.1595, 65.1004, 1781.95, 3311.18, 4478.99, 3835.31, 4252.98, 5449.81, 79.7636, 3.75133, 44.3623, 197.782, 831.418, 541.391, 117.151, 144.719, 70.46, 55.4337, 224.167, 238.342, 130.794, 54.0728, 107.263, 382.255, 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„pãÙc‚—Lpœ³5r®“\,ÓU$¤ëê„ôšÉÏ®h7ÞÓ›íÕ?YP(ѯµÍvùÖ¥-¶ Æ§¡ö|Ö!šôžÇ1ªæi=ãsÏ€|býÕk€Å wyo$W0˜åÛr…Óèô¹yü]Têª"‹* ‡E¡Qü]ÉáB@ï' Biobase/inst/0000755000175400017540000000000013175724631014132 5ustar00biocbuildbiocbuildBiobase/inst/CITATION0000644000175400017540000000165613175713325015275 0ustar00biocbuildbiocbuildcitEntry(entry="Article", author = "Huber, W. and Carey, V. J. and Gentleman, R. and Anders, S. and Carlson, M. and Carvalho, B. S. and Bravo, H. C. and Davis, S. and Gatto, L. and Girke, T. and Gottardo, R. and Hahne, F. and Hansen, K. D. and Irizarry, R. A. and Lawrence, M. and Love, M. I. and MacDonald, J. and Obenchain, V. and {Ole\'s}, A. K. and {Pag\`es}, H. and Reyes, A. and Shannon, P. and Smyth, G. K. and Tenenbaum, D. and Waldron, L. and Morgan, M. ", title = "{O}rchestrating high-throughput genomic analysis with {B}ioconductor", journal = "Nature Methods", year = "2015", volume = "12", number = "2", pages = "115--121", url = "http://www.nature.com/nmeth/journal/v12/n2/full/nmeth.3252.html", textVersion = paste( "Orchestrating high-throughput genomic analysis with Bioconductor.", "W. Huber, V.J. Carey, R. Gentleman, ..., M. Morgan", "Nature Methods, 2015:12, 115.") ) Biobase/inst/Code/0000755000175400017540000000000013175713325015002 5ustar00biocbuildbiocbuildBiobase/inst/Code/DESCRIPTION0000644000175400017540000000031113175713325016503 0ustar00biocbuildbiocbuildPackage: @PKGNAME@ Title: Greek mythology package Version: @VERSION@ Author: @AUTHOR@ Description: Package automatically created on @TODAY@. Maintainer: Some One <@AUTHOR@@mtolympus.gr> License: LGPL Biobase/inst/Code/R/0000755000175400017540000000000013175713325015203 5ustar00biocbuildbiocbuildBiobase/inst/Code/R/get@PKGNAME@.R0000644000175400017540000000013313175713325017305 0ustar00biocbuildbiocbuild## for example, a very simple accessor function: get@PKGNAME@ = function(n) @PKGNAME@[n] Biobase/inst/Code/man/0000755000175400017540000000000013175713325015555 5ustar00biocbuildbiocbuildBiobase/inst/Code/man/@PKGNAME@.Rd0000644000175400017540000000074713175713325017336 0ustar00biocbuildbiocbuild\name{@PKGNAME@} \docType{data} \alias{@PKGNAME@} \title{Greek mythology package: @TITLE@} \description{Greek mythology package: @TITLE@} \usage{ data(@PKGNAME@) } \format{@FORMAT@} \details{According to @AUTHOR@'s Theogony, Zeus lay with Mnemosyne for nine days, and she gave birth to the Muses, who rejoice in their bright dancing places on Mount Helicon.} \seealso{\code{\link[@PKGNAME@:get@PKGNAME@]{get@PKGNAME@}}} \examples{ data(@PKGNAME@) @PKGNAME@ } \keyword{datasets} Biobase/inst/Code/man/get@PKGNAME@.Rd0000644000175400017540000000053613175713325020032 0ustar00biocbuildbiocbuild\name{get@PKGNAME@} \alias{get@PKGNAME@} \title{Accessor function - Greek mythology package: @TITLE@} \description{Accessor function - Greek mythology package: @TITLE@} \usage{ get@PKGNAME@(n) } \arguments{\item{n}{Integer.}} \value{A character vector of the same size as \code{n}.} \examples{ data(@PKGNAME@) get@PKGNAME@(1:3) } \keyword{datasets} Biobase/inst/ExpressionSet/0000755000175400017540000000000013175713325016743 5ustar00biocbuildbiocbuildBiobase/inst/ExpressionSet/DESCRIPTION0000644000175400017540000000032413175713325020450 0ustar00biocbuildbiocbuildPackage: @PKGNAME@ Title: @TITLE@ Version: @VERSION@ Author: @AUTHOR@ Description: Data Package automatically created on @TODAY@. Maintainer: @MAINTAINER@ Depends: Biobase License: @LICENSE@ biocViews: @BVIEWS@ Biobase/inst/ExpressionSet/man/0000755000175400017540000000000013175713325017516 5ustar00biocbuildbiocbuildBiobase/inst/ExpressionSet/man/@PKGNAME@.Rd0000644000175400017540000000026413175713325021271 0ustar00biocbuildbiocbuild\name{@PKGNAME@} \docType{data} \alias{@PKGNAME@} \title{@TITLE@} \description{@DESCRIPTION@} \usage{ data(@PKGNAME@) } @FORMAT@ \examples{ data(@PKGNAME@) } \keyword{datasets} Biobase/inst/doc/0000755000175400017540000000000013175724631014677 5ustar00biocbuildbiocbuildBiobase/inst/doc/BiobaseDevelopment.R0000644000175400017540000001750413175724626020604 0ustar00biocbuildbiocbuild### R code from vignette source 'BiobaseDevelopment.Rnw' ################################################### ### code chunk number 1: Biobase ################################################### options(width=69) library(Biobase) ################################################### ### code chunk number 2: eSet-class ################################################### getClass("eSet") ################################################### ### code chunk number 3: eSet-validity ################################################### getValidity(getClass("eSet")) ################################################### ### code chunk number 4: ExpressionSet-initialize (eval = FALSE) ################################################### ## obj <- new("ExpressionSet", phenoData = new("AnnotatedDataFrame"), experimentData = new("MIAME"), annotation = character(), exprs = new("matrix")) ################################################### ### code chunk number 5: newAssayData (eval = FALSE) ################################################### ## assayDataNew("environment", elt) ################################################### ### code chunk number 6: assayData-storageMode ################################################### data(sample.ExpressionSet) storageMode(sample.ExpressionSet) tryCatch(assayData(sample.ExpressionSet)$exprs <- log(exprs(sample.ExpressionSet)), error=function(err) cat(conditionMessage(err))) exprs(sample.ExpressionSet) <- log(exprs(sample.ExpressionSet)) ################################################### ### code chunk number 7: ExpressionSet-class ################################################### getClass("ExpressionSet") getValidity(getClass("ExpressionSet")) ################################################### ### code chunk number 8: SwirlSet-class ################################################### setClass("SwirlSet", contains="eSet") ################################################### ### code chunk number 9: SwirlSet-initialize ################################################### setMethod("initialize", "SwirlSet", function(.Object, R = new("matrix"), G = new("matrix"), Rb = new("matrix"), Gb = new("matrix"), ...) { callNextMethod(.Object, R=R, G=G, Rb=Rb, Gb=Gb, ...) }) ################################################### ### code chunk number 10: SwirlSet-initialize-2 ################################################### setMethod("initialize", "SwirlSet", function(.Object, assayData=assayDataNew( R=R, G=G, Rb=Rb, Gb=Gb), R = new("matrix"), G = new("matrix"), Rb = new("matrix"), Gb = new("matrix"), ...) { if (!missing(assayData) && any(!missing(R), !missing(G), !missing(Rb), !missing(Gb))) { warning("using 'assayData'; ignoring 'R', 'G', 'Rb', 'Gb'") } callNextMethod(.Object, assayData=assayData, ...) }) ################################################### ### code chunk number 11: SwirlSet-new ################################################### new("SwirlSet") ################################################### ### code chunk number 12: initialize-.Object (eval = FALSE) ################################################### ## setMethod("initialize", "MySet", ## function(.Object, ...) { ## .Object <- callNextMethod(.Object, ...) ## }) ## . ################################################### ### code chunk number 13: SwirlSet-validity ################################################### setValidity("SwirlSet", function(object) { assayDataValidMembers(assayData(object), c("R", "G", "Rb", "Gb")) }) ################################################### ### code chunk number 14: validity-sometimes (eval = FALSE) ################################################### ## myFancyFunction <- function(obj) { ## assayData(obj) <- fancyAssaydData # obj invalid... ## phenoData(obj) <- justAsFancyPhenoData # but now valid ## validObject(obj) ## obj ## } ################################################### ### code chunk number 15: updateObject-eg ################################################### data(sample.ExpressionSet) classVersion(sample.ExpressionSet) obj <- updateObject(sample.ExpressionSet) ################################################### ### code chunk number 16: isCurrent ################################################### isCurrent(sample.ExpressionSet)[c("eSet", "ExpressionSet")] ################################################### ### code chunk number 17: MultiSet-obj ################################################### setClass("MySet", contains = "eSet", prototype = prototype( new("VersionedBiobase", versions=c(classVersion("eSet"), MySet="1.0.0")))) obj <- new("MySet") classVersion(obj) ################################################### ### code chunk number 18: MultiSetRevised ################################################### setClass("MySet", contains = "eSet", prototype = prototype( new("VersionedBiobase", versions=c(classVersion("eSet"), MySet="1.0.1")))) isCurrent(obj) ################################################### ### code chunk number 19: updateObject-MultiSet ################################################### setMethod("updateObject", signature(object="MySet"), function(object, ..., verbose=FALSE) { if (verbose) message("updateObject(object = 'MySet')") object <- callNextMethod() if (isCurrent(object)["MySet"]) return(object) ## Create an updated instance. if (!isVersioned(object)) ## Radical surgery -- create a new, up-to-date instance new("MySet", assayData = updateObject(assayData(object), ...., verbose=verbose), phenoData = updateObject(phenoData(object), ..., verbose=verbose), experimentData = updateObject(experimentData(object), ..., verbose=verbose), annotation = updateObject(annotation(object), ..., verbose=verbose)) else { ## Make minor changes, and update version by consulting class definition classVersion(object)["MySet"] <- classVersion("MySet")["MySet"] object } }) ################################################### ### code chunk number 20: updateObject ################################################### classVersion(updateObject(obj)) ################################################### ### code chunk number 21: classVersion-AnnotatedDataFrame ################################################### classVersion(new("AnnotatedDataFrame")) ################################################### ### code chunk number 22: SwirlSet-version ################################################### setClass("SwirlSet", contains = "eSet", prototype = prototype( new("VersionedBiobase", versions=c(classVersion("eSet"), SwirlSet="1.0.0")))) classVersion(new("SwirlSet")) ################################################### ### code chunk number 23: arbitraryClassVersions ################################################### obj <- new("SwirlSet") classVersion(obj)["MyID"] <- "0.0.1" classVersion(obj) classVersion(updateObject(obj)) ################################################### ### code chunk number 24: BiobaseDevelopment.Rnw:680-681 ################################################### toLatex(sessionInfo()) Biobase/inst/doc/BiobaseDevelopment.Rnw0000644000175400017540000006745113175713325021151 0ustar00biocbuildbiocbuild% % NOTE -- ONLY EDIT THE .Rnw FILE!!! The .tex file is % likely to be overwritten. % %\VignetteIndexEntry{Notes for eSet developers} %\VignetteDepends{} %\VignetteKeywords{Expression Analysis} %\VignettePackage{Biobase} \documentclass[]{article} \usepackage{times} \usepackage{hyperref} \newcommand{\Rfunction}[1]{{\texttt{#1}}} \newcommand{\Robject}[1]{{\texttt{#1}}} \newcommand{\Rpackage}[1]{{\textit{#1}}} \newcommand{\Rmethod}[1]{{\texttt{#1}}} \newcommand{\Rfunarg}[1]{{\texttt{#1}}} \newcommand{\Rclass}[1]{{\textit{#1}}} \textwidth=6.2in \textheight=8.5in %\parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \newcommand{\R}{\textsf{R}} \newcommand{\eSet}{\Robject{eSet}} \newcommand{\ExpressionSet}{\Robject{ExpressionSet}} \newcommand{\Biobase}{\Rpackage{Biobase}} \newcommand{\term}[1]{\emph{#1}} \newcommand{\mref}[2]{\htmladdnormallinkfoot{#2}{#1}} \begin{document} \title{\Biobase{} development and the new \eSet} \author{\mref{mailto:mtmorgan@fhcrc.org}{Martin T. Morgan}} \date{7 August, 2006} \maketitle Revised 4 September, 2006 -- \Robject{featureData} slot. Revised 20 April 2007 -- minor wording changes; \Rfunarg{verbose} and other arguments passed through \Rmethod{updateObject} example; introduce a second variant of \Rmethod{initialize} illustrating its use as a copy constructor. Revised 4 November, 2010 -- \Robject{experimentData} slot as \Rclass{MIAxE} class. \Rclass{MIAME} class is now subclass of \Rclass{MIAxE}. \section{Introduction} These notes help \emph{developers} who are interested in using and extending the \eSet{} class hierarchy, and using features in \Biobase. The information here is not useful to regular users of \Biobase. This document illustrates the \Biobase{} structures and approaches that make it it easy for developers to creatively use and extend the \eSet{} class hierarchy. The document starts with a brief description of the motivation for change, and a comparison of the old (before August, 2006) and new \eSet{}s and related functionality (e.g.,the \Rclass{Versioned} class and \Rfunction{updateObject} methods). We then illustrate how \eSet{} can be extended to handle additional types of data, and how new methods can exploit the \eSet{} class hierarchy. We conclude with a brief summary of lessons learned, useful developer-related side-effects of efforts to revise \eSet{}, and possible directions for future development. \section{Comparing old and new} What is an \eSet{}? \begin{itemize} \item Coordinate high through-put (e.g., gene expression) and phenotype data. \item Provide common data container for diverse Bioconductor packages. \end{itemize} Motivation for change (August, 2006). \begin{itemize} \item What was broken? Complex data structure. Inconsistent object validity. No straight-forward way to extend \eSet{} to new data types. \item What forward-looking design goals did we have? Flexible storage model. Class hierarchy to promote code reuse and facilitate extension to new data objects. Methods for updating serialized instances. \end{itemize} Key features in the redesign. \begin{itemize} \item Simplified data content. \item Structured class hierarchy . \item Alternative storage modes. \item More validity checking. \item Conversion of example data in \Biobase{}, and many other data sets elsewhere in Bioconductor, to \Rclass{ExpressionSet}. \item \Rclass{Versioned} class information (in the development branch). \item \Rfunction{updateObject} methods (in the development branch). \end{itemize} \section{A quick tour} <>= options(width=69) library(Biobase) @ \subsection{The \eSet{} object: high-throughput experiments} Purpose. \begin{itemize} \item Coordinate and contain high-throughput genomic data. \end{itemize} Structure: virtual base class. <>= getClass("eSet") @ \begin{itemize} \item \Robject{assayData}: high-throughput data. \item \Robject{phenoData}: sample covariates. \item \Robject{featureData}: feature covariates. \item \Robject{experimentData}: experimental description. \item \Robject{annotation}: assay description. \item See below, and \verb|?"eSet-class"| \end{itemize} \subsubsection{\Robject{assayData}: high-throughput data} Purpose. \begin{itemize} \item Efficiently and flexibly contain high-volume data. \end{itemize} Structure: \Rclass{list}, \Rclass{environment}, or \Rclass{lockEnvironment} class union. \begin{itemize} \item Each element of \Rclass{list} / \Rclass{environment} / \Rclass{lockEnvironment} is a matrix \item Rows: \emph{features}, e.g., gene names. \item Columns: \emph{samples} represented on each chip. \item All matricies must have the same dimensions, row names, and column names. \item Subclasses determine which matricies \emph{must} be present. \item See \verb|?"AssayData-class"| \end{itemize} \subsubsection{\Robject{phenoData}: sample covariates} Purpose. \begin{itemize} \item Contain and document sample covariates. \end{itemize} Structure: \Rclass{AnnotatedDataFrame}. \begin{itemize} \item \Robject{data}: \Rclass{data.frame}. \begin{itemize} \item Rows: sample identifiers. \item Columns: measured covariates. \end{itemize} \item \Robject{varMetadata}: \Rclass{data.frame}. \begin{itemize} \item Rows: measured covariate labels. \item Columns: covariate descriptors. \end{itemize} \item See \verb|?"AnnotatedDataFrame-class"| \end{itemize} \subsubsection{\Robject{featureData}: feature covariates} Purpose. \begin{itemize} \item Contain and document feature covariates specific to the experiment; use the \Robject{annotation} slot for chip-level descriptions. \end{itemize} Structure: \Rclass{AnnotatedDataFrame}. \begin{itemize} \item \Robject{data}: \Rclass{data.frame}. \begin{itemize} \item Rows: feature identifiers. These match row names of \Robject{assayData}. \item Columns: measured covariates. \end{itemize} \item \Robject{varMetadata}: \Rclass{data.frame}. \begin{itemize} \item Rows: measured covariate labels. \item Columns: covariate descriptors. \end{itemize} \item See \verb|?"AnnotatedDataFrame-class"| \end{itemize} \subsubsection{\Robject{experimentData}: experiment description} Purpose. \begin{itemize} \item Summarize where and how the experiment was performed. \end{itemize} Structure: \Rclass{MIAxE} virtual class \begin{itemize} \item[] {In Biobase version 2.11 the \Rclass{MIAxE} virtual class was introduced as a general container for experiment meta-data. The \Rclass{MIAME} class is now a subclass of \Rclass{MIAxE}. See \verb|?"MIAxE-class"|. The \Rclass{MIAME} class structure is as follows} \end{itemize} \begin{itemize} \item \Robject{title}: experiment title. \item \Robject{name}: experimenter name(s). \item \Robject{preprocessing}: \Robject{list} of pre-processing steps. \item Additional slots. \item See \verb|?"MIAME-class"|. \end{itemize} \subsubsection{\Robject{annotation}: assay description} Purpose. \begin{itemize} \item Link experiment to annotation package. \end{itemize} Structure: \Rclass{character} \begin{itemize} \item Label identifying annotation package. \end{itemize} %% Methods \subsection{Important \eSet{} methods} Initialization. \begin{itemize} \item \eSet{} is \verb|VIRTUAL|, initialize via subclass \Rfunction{callNextMethod} \end{itemize} Accessors (get, set). \begin{itemize} \item \Rfunction{assayData(obj); assayData(obj) <- value}: access or assign \Robject{assayData} \item \Rfunction{phenoData(obj); phenoData(obj) <- value}: access or assign \Robject{phenoData} \item \Rfunction{experimentData(obj); experimentData(obj) <- value}: access or assign \Robject{experimentData} \item \Rfunction{annotation(obj); annotation(obj) <- value}: access or assign \Robject{annotation} \end{itemize} Subsetting. \begin{itemize} \item \Rfunction{obj[i, j]}: select genes $i$ and samples $j$. \item \Rfunction{obj\$name; obj\$name <- value}: retrieve or assign covariate \Robject{name} in \Robject{phenoData} \end{itemize} \subsubsection{Additional \eSet{} methods} \begin{itemize} \item \Rfunction{show}. \item \Rfunction{storageMode}: influence how \Robject{assayData} is stored. \item \Rfunction{updateObject}: update \eSet{} objects to their current version. \item \Rfunction{validObject}: ensure that \eSet{} is valid. \end{itemize} The \Rfunction{validObject} method is particularly important to \eSet{}, ensuring that \eSet{} contains consistent structure to data. <>= getValidity(getClass("eSet")) @ The validity methods for \eSet{} reflect our design goals. All \Robject{assayData} members must have identical row and column dimensions and \Robject{featureNames}. The names and numbers of samples must be the same in \Robject{assayData} and \Robject{phenoData} slots. Validity methods are defined for the classes underlying each slot as well. For instance, the validity methods for \Robject{AnnotatedDataFrame} check that variables used in \Robject{pData} are at least minimally described in \Robject{varMetadata}. %% Subclasses \subsection{Subclasses of \eSet} \Biobase{} defines three classes that extend \eSet{}. \ExpressionSet{} (discussed further below) is meant to contain microarray gene expression data. \Rclass{SnpSet} is a preliminary class to contain SNP data; other classes in development (e.g., in \Rpackage{oligo}) may provide alternative implementations for SNP data. \Rclass{MultiSet} is an \ExpressionSet-like class, but without restriction on the names (though not structure) of elements in the \Robject{assayData} slot. \subsubsection{\ExpressionSet} Purpose: \begin{itemize} \item Contain gene expression data. \end{itemize} Required \Robject{assayData} members. \begin{itemize} \item \Robject{exprs}, a matrix of expression values. \end{itemize} Important methods. \begin{itemize} \item Initialization (additional details below): <>= obj <- new("ExpressionSet", phenoData = new("AnnotatedDataFrame"), experimentData = new("MIAME"), annotation = character(), exprs = new("matrix")) @ \item \Rfunction{exprs(obj), exprs(obj) <- value}: get or set \Robject{exprs}; methods defined for \Rclass{ExpressionSet}, \Rclass{AssayData}. \end{itemize} \subsubsection{\Rclass{MultiSet} and \Rclass{SnpSet}} \Rclass{MultiSet}. \begin{itemize} \item Purpose: flexibly contain a collection of expression data matricies. \item Required \Robject{assayData} members: none. \end{itemize} \Rclass{SnpSet}. \begin{itemize} \item Purpose: contain genomic SNP calls. \item Required \Robject{assayData} members: \Robject{call}, \Robject{callProbability}. \end{itemize} \section{Comments on \Robject{assayData}: high-throughput data storage} The \Robject{assayData} slot is meant to store high-throughput data. The idea is that the slot contains identically sized matrices containing expression or other data. All matrices in the slot must have the same dimension, and are structured so that rows represent `features' and columns represent `samples'. Validity methods enforce that row and column names of slot elements are identical. For technical reasons, creating instance of \Rclass{AssayData} is slightly different from the way this is usually done in \R{}. Normally, one creates an instance of a class with an expression like \Rfunction{new("ExpressionSet", ...)}, with the \ldots representing additional arguments. \Rclass{AssayData} objects are created with <>= assayDataNew("environment", elt) @ where \Robject{elt} might be a matrix of expression values. For the curious, the reason for this setup stems from our desire to have a class that \Rfunction{is} a list or environment, rather than a class that has a slot that contains a list or environment. The \Rfunction{is} relationship is desirable to avoid unnecessary function calls to access slots, and requires that a class \Rfunction{contain} the base type (e.g., \Rclass{environment}). Until recently an \R{} object could not \Rfunction{contain} an \Rclass{environment}. The \Robject{assayData} slot of \ExpressionSet{} objects must contain a matrix named \Robject{exprs}. Nonetheless, the \ExpressionSet{} validity method tries to be liberal -- it guarantees that the object has an \Robject{exprs} element, but allows for other elements too. The prudent developer wanting consistent additional data elements should derive a class from \ExpressionSet{} that enforces the presence of their desired elements. The \Rclass{AssayData} class allows for data elements to be stored in three different ways (see \Rfunction{?storageMode} and \Rfunction{?"storageMode<-"} for details): as a \Robject{list}, \Robject{environment}, or \Robject{lockedEnvironment}. Developers are probably familiar with \Robject{list} objects; a drawback is that \Robject{exprs} elements may be large, and some operations on lists in \R{} may trigger creation of many copies of the the \Robject{exprs} element. This can be expensive in both space and time. Environments are nearly unique in \R{}, in that they are passed by reference rather than value. This eliminates some copying, but has the unfortunate consequence that side-effects occur -- modifications to an environment inside a function influence the value of elements outside the function. For these reasons, environments can be useful as `read only' arguments to functions, but can have unexpected consequences when functions modify their arguments. Locked environments implemented in \Biobase{} try to strike a happy medium, allowing pass by reference for most operations but triggering (whole-environment) copying when elements in the environment are modified. The locking mechanism is enforced by only allowing known `safe' operations to occur, usually by channeling user actions through the accessor methods: <>= data(sample.ExpressionSet) storageMode(sample.ExpressionSet) tryCatch(assayData(sample.ExpressionSet)$exprs <- log(exprs(sample.ExpressionSet)), error=function(err) cat(conditionMessage(err))) exprs(sample.ExpressionSet) <- log(exprs(sample.ExpressionSet)) @ The \Rfunction{setReplaceMethod} for \Robject{exprs} (and \Robject{assayData}) succeeds by performing a deep copy of the entire environment. Because this is very inefficient, the recommended paradigm to update an element in a \Robject{lockedEnvironment} is to extract it, make many changes, and then reassign it. Developers can study \Robject{assayData} methods to learn more about how to lock and unlock environment bindings. \Biobase{} allows the experienced user to employ (and run the risks of) environments, but the expectation is that most user objects are construced with the default \Robject{lockedEnvironment} or \Robject{list}. A longer term consideration in designing \Rclass{AssayData} was to allow more flexible methods of data storage, e.g., through database-hosted arrays. This is facilitated by using generic functions such as \Rfunction{exprs()} for data access, so that classes derived from \Rclass{AssayData} can provide implementations appropriate for their underlying storage mode. \section{Extending \eSet} A designer wanting to implement \eSet{} for a particular type of data creates a class that `contains' \eSet{}. The steps for doing this are described below. One example of such a class is \ExpressionSet, designed to hold a matrix of gene expression values in the \Robject{assayData} slot. <>= getClass("ExpressionSet") getValidity(getClass("ExpressionSet")) @ The data structure of an \ExpressionSet{} is identical to that of \eSet, and in fact is inherited (without additional slot creation) from \eSet{}. The main difference is that the validity methods of \eSet{} are augmented by a method to check that the \Robject{assayData} slot contains an entity named \Robject{"exprs"}. A valid \ExpressionSet{} object must also satisfy all the validity requirements of \eSet{}, but the developer does not explicitly invoke validity checking of the parts of the data structure inherited from \eSet{}. \subsection{Implementing a new class: a \Rclass{SwirlSet} example} We want the \emph{Swirl} data set (see the \Robject{SW} two color data set that motivates this class) to contain four elements in the \Robject{assayData} slot: \Robject{R}, \Robject{G}, \Robject{Rb}, \Robject{Gb}. To derive a class from \eSet{} for this data, we create a class, and provide initializaation and validation methods. We create a class as follows: <>= setClass("SwirlSet", contains="eSet") @ Notice that there are no new data elements in \Rclass{SwirlSet} compared with \eSet{}. The \Rfunction{initialize} method is written as <>= setMethod("initialize", "SwirlSet", function(.Object, R = new("matrix"), G = new("matrix"), Rb = new("matrix"), Gb = new("matrix"), ...) { callNextMethod(.Object, R=R, G=G, Rb=Rb, Gb=Gb, ...) }) @ % A slightly different \Rmethod{initialize} method allows the user to specify either the \Robject{assayData} or the \Robject{assayData} content. In advanced use, this has the advantage that \Rmethod{initialize} can be used as a `copy constructor' to update several slots simultaneously. <>= setMethod("initialize", "SwirlSet", function(.Object, assayData=assayDataNew( R=R, G=G, Rb=Rb, Gb=Gb), R = new("matrix"), G = new("matrix"), Rb = new("matrix"), Gb = new("matrix"), ...) { if (!missing(assayData) && any(!missing(R), !missing(G), !missing(Rb), !missing(Gb))) { warning("using 'assayData'; ignoring 'R', 'G', 'Rb', 'Gb'") } callNextMethod(.Object, assayData=assayData, ...) }) @ The structure of the \Rfunction{initialize} method is a bit different from those often seen in \R{}. Often, \Rfunction{initialize} has only \Robject{.Object} as a named argument, or, if there are other named arguments, they correspond to slot names. Here our initialize method accepts four arguments, named after the \Robject{assayData} elements. Inside the \Rfunction{initialize} method, the named arguments are passed to the next initialization method in the hierarch (i.e., \Rfunction{initialize} defined for \eSet). The \eSet{} \Rfunction{initialize} method then uses these arguments to populate the data slots in \Robject{.Object}. In particular, \eSet{} places all arguments other \Rfunction{phenoData}, \Rfunction{experimentData}, and \Rfunction{annotation} into the \Robject{assayData} slot. The \eSet{} \Rfunction{initialize} method then returns the result to the \Rfunction{initialize} method of \Rclass{SwirlSet}, which returns a \Rclass{SwirlSet} object to the user: <>= new("SwirlSet") @ General programing guidelines emerge from experience with the \Rfunction{initialize} method of \eSet{} and derived classes. First, an appropriate strategy is to name only those data elements that will be manipulated directly by the \Rfunction{initialize} method. For instance, the definition above did \emph{not} name \Robject{phenoData} and other \eSet{} slots by name. To do so is not incorrect, but would require that they be explicitly named (e.g., \Rfunction{phenoData=phenoData}) in the \Rfunction{callNextMethod} code. Second, the arguments \Robject{R, G, Rb, Rg} are present in the \Rfunction{initialize} method to provide defaults consistent with object construction; the `full' form of \Rfunction{callNextMethod}, replicating the named arguments, is required in the version of \R{} in which this class was developed. Third, named arguments can be manipulated before \Rfunction{callNextMethod} is invoked. Fourth, the return value of \Rfunction{callNextMethod} can be captured\ldots <>= setMethod("initialize", "MySet", function(.Object, ...) { .Object <- callNextMethod(.Object, ...) }) . @ and manipulated before being returned to the user. Finally, it is the responsbilitiy of the developer to ensure that a valid object is created; \Rfunction{callNextMethod} is a useful way to exploit correctly designed \Rfunction{initialize} methods for classes that the object extends, but the developer is free to use other techniques to create valid versions of their class. A validity method might complete our new class. A validity method is essential to ensure that the unique features of \Rclass{SwirlSet} -- our reason for designing the new class -- are indeed present. We define our validity method to ensure that the \Robject{assayData} slot contains our four types of expression elements: <>= setValidity("SwirlSet", function(object) { assayDataValidMembers(assayData(object), c("R", "G", "Rb", "Gb")) }) @ Notice that we do not have to explicitly request that the validity of other parts of the \Rclass{SwirlSet} object are valid; this is done for us automatically. Objects are checked for validity when they are created, but not when modified. This is partly for efficiency reasons, and partly because object updates might transiently make them invalid. So a good programing practice is to ensure validity after modification, e.g., <>= myFancyFunction <- function(obj) { assayData(obj) <- fancyAssaydData # obj invalid... phenoData(obj) <- justAsFancyPhenoData # but now valid validObject(obj) obj } @ Assigning \Robject{fancyAssaydData} might invalidate the object, but \Robject{justAsFancyPhenoData} restores validity. \section{\Rclass{Versioned}} One problem encountered in the Bioconductor project is that data objects stored to disk become invalid as the underlying class definition changes. For instance, earlier releases of \Biobase{} contain a sample \Rclass{eSet} object. But under the changes discussed here, \eSet{} is virtual and the stored object is no longer valid. The challenge is to easily identify invalid objects, and to provide a mechanism for updating old objects to their new representation. \Biobase{} introduces the \Rclass{Versioned} and \Rclass{VersionedBiobase} classes to facilitate this. These classes are incorporated into key \Biobase class definitions.\Biobase also defines \Rmethod{updateObject} methods (the \Rfunction{updateObject} generic function is defined in the \Rpackage{BiocGenerics} package) for conveniently updating old objects to their new representation. <>= data(sample.ExpressionSet) classVersion(sample.ExpressionSet) obj <- updateObject(sample.ExpressionSet) @ The version information for this object is a named list. The first two elements indicate the version of R and Biobase used to create the object. The latter two elements are contained in the class prototype, and the class prototype is consulted to see if the instance of an object is 'current'. These lists can be subsetted in the usual way, e.g., <>= isCurrent(sample.ExpressionSet)[c("eSet", "ExpressionSet")] @ Versioned classes, \Rfunction{updateObject} and related methods simplify the long-term maintenance of data objects. Take the fictious \Rclass{MySet} as an example. <>= setClass("MySet", contains = "eSet", prototype = prototype( new("VersionedBiobase", versions=c(classVersion("eSet"), MySet="1.0.0")))) obj <- new("MySet") classVersion(obj) @ This is a new class, and might undergo changes in its structure at some point in the future. When these changes are introduced, the developer will change the version number of the class in its prototype (the last line, below): <>= setClass("MySet", contains = "eSet", prototype = prototype( new("VersionedBiobase", versions=c(classVersion("eSet"), MySet="1.0.1")))) isCurrent(obj) @ and add code to update to the new version <>= setMethod("updateObject", signature(object="MySet"), function(object, ..., verbose=FALSE) { if (verbose) message("updateObject(object = 'MySet')") object <- callNextMethod() if (isCurrent(object)["MySet"]) return(object) ## Create an updated instance. if (!isVersioned(object)) ## Radical surgery -- create a new, up-to-date instance new("MySet", assayData = updateObject(assayData(object), ...., verbose=verbose), phenoData = updateObject(phenoData(object), ..., verbose=verbose), experimentData = updateObject(experimentData(object), ..., verbose=verbose), annotation = updateObject(annotation(object), ..., verbose=verbose)) else { ## Make minor changes, and update version by consulting class definition classVersion(object)["MySet"] <- classVersion("MySet")["MySet"] object } }) @ The code after \Rfunction{if(!isVersioned)} illustrates one way of performing `radical surgery, creating a new up-to-date instance by updating all slots. The \Rfunction{else} clause represents more modest changes, using methods to update stale information. \Rfunction{updateObject} then returns a new, enhanced object: <>= classVersion(updateObject(obj)) @ As in the example, versioning helps in choosing which modifications to perform -- minor changes for a slightly out-of-date object, radical surgery for something more ancient. Version information might also be used in methods, where changing class representation might facilitate more efficient routines. \subsection{\Rclass{Versioned} versus \Rclass{VersionedBiobase}} The information on \R{} and \Biobase{} versions is present in \eSet{} derived classes because \eSet{} contains \Rclass{VersionedBiobase}. On the other hand, \Rclass{AnnotatedDataFrame} contains \Rclass{Versioned}, and has only information about its own class version. <>= classVersion(new("AnnotatedDataFrame")) @ The rationale for this is that \Rclass{AnnotatedDataFrame} is and will likely remain relatively simple, and details about \R{} and \Biobase{} are probably irrelevant to its use. On the other hand, some aspects of \eSet{} and the algorithms that operate on them are more cutting edge and subject to changes in \R{} or \Biobase{}. Knowing the version of \R{} and \Biobase{} used to create an instance might provide valuable debugging information. \subsection{Adding \Rclass{Versioned} information to your own classes} The key to versioning your own classes is to define your class to \Rfunction{contain} \Rclass{Versioned} or \Rclass{VersionedBiobase}, and to add the version information in the prototype. For instance, to add a class-specific version stamp to \Rclass{SwirlSet} we would modify the class defintion to <>= setClass("SwirlSet", contains = "eSet", prototype = prototype( new("VersionedBiobase", versions=c(classVersion("eSet"), SwirlSet="1.0.0")))) classVersion(new("SwirlSet")) @ See additional examples in the \Rclass{Versioned} help page. It is also possible to add arbitrary information to particular instances. <>= obj <- new("SwirlSet") classVersion(obj)["MyID"] <- "0.0.1" classVersion(obj) classVersion(updateObject(obj)) @ There is additional documentation about these classes and methods in \Biobase{}. \section{Summary} This document summarizes \Biobase, outlining strategies that developers using \Biobase{} may find useful. The main points are to introduce the \eSet{} class hierarchy, to illustrate how developers can effectively extend this class, and to introduce class versions as a way of tracking and easily updating objects. 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endstream endobj startxref 208799 %%EOF Biobase/inst/doc/ExpressionSetIntroduction.R0000644000175400017540000001470313175724627022251 0ustar00biocbuildbiocbuild### R code from vignette source 'ExpressionSetIntroduction.Rnw' ################################################### ### code chunk number 1: init ################################################### options(width=65) ################################################### ### code chunk number 2: install-pkg (eval = FALSE) ################################################### ## source("http://bioconductor.org/biocLite.R") ## biocLite(c("Biobase")) ################################################### ### code chunk number 3: loadlib ################################################### library("Biobase") ################################################### ### code chunk number 4: convert (eval = FALSE) ################################################### ## library(convert) ## as(object, "ExpressionSet") ################################################### ### code chunk number 5: read-table-geneData ################################################### dataDirectory <- system.file("extdata", package="Biobase") exprsFile <- file.path(dataDirectory, "exprsData.txt") exprs <- as.matrix(read.table(exprsFile, header=TRUE, sep="\t", row.names=1, as.is=TRUE)) ################################################### ### code chunk number 6: exprsFile (eval = FALSE) ################################################### ## exprsFile <- "c:/path/to/exprsData.txt" ################################################### ### code chunk number 7: geneData-peak ################################################### class(exprs) dim(exprs) colnames(exprs) head(exprs[,1:5]) ################################################### ### code chunk number 8: ExpressionSet-basic ################################################### minimalSet <- ExpressionSet(assayData=exprs) ################################################### ### code chunk number 9: pData ################################################### pDataFile <- file.path(dataDirectory, "pData.txt") pData <- read.table(pDataFile, row.names=1, header=TRUE, sep="\t") dim(pData) rownames(pData) summary(pData) ################################################### ### code chunk number 10: geneCovariate-geneData-name-match ################################################### all(rownames(pData)==colnames(exprs)) ################################################### ### code chunk number 11: colnames ################################################### names(pData) ################################################### ### code chunk number 12: sapplyClasses ################################################### sapply(pData, class) ################################################### ### code chunk number 13: simpleSubsetting ################################################### pData[c(15, 20), c("gender", "type")] pData[pData$score>0.8,] ################################################### ### code chunk number 14: metadata-create ################################################### metadata <- data.frame(labelDescription= c("Patient gender", "Case/control status", "Tumor progress on XYZ scale"), row.names=c("gender", "type", "score")) ################################################### ### code chunk number 15: AnnotatedDataFrame ################################################### phenoData <- new("AnnotatedDataFrame", data=pData, varMetadata=metadata) phenoData ################################################### ### code chunk number 16: AnnotatedDataFrame-subset ################################################### head(pData(phenoData)) phenoData[c("A","Z"),"gender"] pData(phenoData[phenoData$score>0.8,]) ################################################### ### code chunk number 17: annotation ################################################### annotation <- "hgu95av2" ################################################### ### code chunk number 18: R.MIAME ################################################### experimentData <- new("MIAME", name="Pierre Fermat", lab="Francis Galton Lab", contact="pfermat@lab.not.exist", title="Smoking-Cancer Experiment", abstract="An example ExpressionSet", url="www.lab.not.exist", other=list( notes="Created from text files" )) ################################################### ### code chunk number 19: ExpressionSetFinally ################################################### exampleSet <- ExpressionSet(assayData=exprs, phenoData=phenoData, experimentData=experimentData, annotation="hgu95av2") ################################################### ### code chunk number 20: ExpressionSet-minimal ################################################### minimalSet <- ExpressionSet(assayData=exprs) ################################################### ### code chunk number 21: helpExpressionSet (eval = FALSE) ################################################### ## help("ExpressionSet-class") ################################################### ### code chunk number 22: showExpressionSet ################################################### exampleSet ################################################### ### code chunk number 23: usingDollar ################################################### exampleSet$gender[1:5] exampleSet$gender[1:5] == "Female" ################################################### ### code chunk number 24: featureNames ################################################### featureNames(exampleSet)[1:5] ################################################### ### code chunk number 25: sampleNames ################################################### sampleNames(exampleSet)[1:5] varLabels(exampleSet) ################################################### ### code chunk number 26: exprs ################################################### mat <- exprs(exampleSet) dim(mat) ################################################### ### code chunk number 27: first10 ################################################### vv <- exampleSet[1:5, 1:3] dim(vv) featureNames(vv) sampleNames(vv) ################################################### ### code chunk number 28: males ################################################### males <- exampleSet[ , exampleSet$gender == "Male"] males ################################################### ### code chunk number 29: ExpressionSetIntroduction.Rnw:489-490 ################################################### toLatex(sessionInfo()) Biobase/inst/doc/ExpressionSetIntroduction.Rnw0000644000175400017540000004304113175713325022604 0ustar00biocbuildbiocbuild% NOTE -- ONLY EDIT THE .Rnw FILE!!! The .tex file is % likely to be overwritten. % %\VignetteDepends{Biobase} %\VignetteIndexEntry{An introduction to Biobase and ExpressionSets} %\VignetteKeywords{tutorial, environment, graphics, ExpressionSet} % %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \documentclass[12pt]{article} \usepackage{amsmath,fullpage} \usepackage[authoryear,round]{natbib} \usepackage{hyperref} \usepackage{theorem} \usepackage{float} \usepackage{ifthen} \newcommand{\scscst}{\scriptscriptstyle} \newcommand{\scst}{\scriptstyle} \newcommand{\R}{{\textsf{R}}} \newcommand{\code}[1]{{\texttt{#1}}} \newcommand{\term}[1]{{\emph{#1}}} \newcommand{\Rpackage}[1]{\textsf{#1}} \newcommand{\Rfunction}[1]{\texttt{#1}} \newcommand{\Robject}[1]{\texttt{#1}} \newcommand{\Rclass}[1]{{\textit{#1}}} \newcommand{\Rmethod}[1]{{\textit{#1}}} \newcommand{\Rfunarg}[1]{{\textit{#1}}} %% Excercises and Questions \usepackage{theorem} \theoremstyle{break} \newtheorem{Ex}{Exercise} \theoremstyle{break} \newtheorem{Q}{Question} %% And solution or answer \newenvironment{solution}{% \begin{center} \begin{minipage}{0.75\textwidth} %% \color{blue} }{ \end{minipage} \end{center} \bigskip% } \bibliographystyle{plainnat} \title{An Introduction to Bioconductor's \Rclass{ExpressionSet} Class} \author{Seth Falcon, Martin Morgan, and Robert Gentleman} \date{6 October, 2006; revised 9 February, 2007} \begin{document} <>= options(width=65) @ \maketitle \section{Introduction} \Rpackage{Biobase} is part of the Bioconductor project, and is used by many other packages. \Rpackage{Biobase} contains standardized data structures to represent genomic data. The \Rclass{ExpressionSet} class is designed to combine several different sources of information into a single convenient structure. An \Rclass{ExpressionSet} can be manipulated (e.g., subsetted, copied) conveniently, and is the input or output from many Bioconductor functions. The data in an \Rclass{ExpressionSet} is complicated, consisting of expression data from microarray experiments (\code{assayData}; \code{assayData} is used to hint at the methods used to access different data components, as we will see below), `meta-data' describing samples in the experiment (\code{phenoData}), annotations and meta-data about the features on the chip or technology used for the experiment (\code{featureData}, \code{annotation}), information related to the protocol used for processing each sample (and usually extracted from manufacturer files, \code{protocolData}), and a flexible structure to describe the experiment (\code{experimentData}). The \Rclass{ExpressionSet} class coordinates all of this data, so that you do not usually have to worry about the details. However, an \Rclass{ExpressionSet} needs to be created in the first place, and creation can be complicated. In this introduction we learn how to create and manipulate \Rclass{ExpressionSet} objects, and practice some basic \R{} skills. \section{Preliminaries} \subsection{Installing Packages} If you are reading this document and have not yet installed any software on your computer, visit \url{http://bioconductor.org} and follow the instructions for installing \R{} and Bioconductor. Once you have installed \R{} and Bioconductor, you are ready to go with this document. In the future, you might find that you need to install one or more additional packages. The best way to do this is to start an \R{} session and evaluate commands like <>= source("http://bioconductor.org/biocLite.R") biocLite(c("Biobase")) @ %% \subsection{Loading Packages} The definition of the \Rclass{ExpressionSet} class along with many methods for manipulating \Rclass{ExpressionSet} objects are defined in the \Rpackage{Biobase} package. In general, you need to load class and method definitions before you use them. When using Bioconductor, this means loading \R{} packages using \Rfunction{library} or \Rfunction{require}. <>= library("Biobase") @ \begin{Ex} What happens when you try to load a package that is not installed? \end{Ex} \begin{solution} When using \Rfunction{library}, you get an error message. With \Rfunction{require}, the return value is \Robject{FALSE} and a warning is printed. \end{solution} \section{Building an ExpressionSet From .CEL and other files} Many users have access to .CEL or other files produced by microarray chip manufacturer hardware. Usually the strategy is to use a Bioconductor package such as \Rpackage{affyPLM}, \Rpackage{affy}, \Rpackage{oligo}, or \Rpackage{limma}, to read these files. These Bioconductor packages have functions (e.g., \Rfunction{ReadAffy}, \Rfunction{expresso}, or \Rfunction{justRMA} in \Rpackage{affy}) to read CEL files and perform preliminary preprocessing, and to represent the resulting data as an \Rclass{ExpressionSet} or other type of object. Suppose the result from reading and preprocessing CEL or other files is named \Robject{object}, and \Robject{object} is different from \Rclass{ExpressionSet}; a good bet is to try, e.g., <>= library(convert) as(object, "ExpressionSet") @ %% It might be the case that no converter is available. The path then is to extract relevant data from \Robject{object} and use this to create an \Rclass{ExpressionSet} using the instructions below. \section{Building an ExpressionSet From Scratch} As mentioned in the introduction, the data from many high-throughput genomic experiments, such as microarray experiments, usually consist of several conceptually distinct parts: assay data, phenotypic meta-data, feature annotations and meta-data, and a description of the experiment. We'll construct each of these components, and then assemble them into an \Rclass{ExpressionSet}. \subsection{Assay data} One important part of the experiment is a matrix of `expression' values. The values are usually derived from microarrays of one sort or another, perhaps after initial processing by manufacturer software or Bioconductor packages. The matrix has $F$ rows and $S$ columns, where $F$ is the number of features on the chip and $S$ is the number of samples. A likely scenario is that your assay data is in a 'tab-delimited' text file (as exported from a spreadsheet, for instance) with rows corresponding to features and columns to samples. The strategy is to read this file into \R{} using the \Rfunction{read.table} command, converting the result to a \Rclass{matrix}. A typical command to read a tab-delimited file that includes column `headers' is <>= dataDirectory <- system.file("extdata", package="Biobase") exprsFile <- file.path(dataDirectory, "exprsData.txt") exprs <- as.matrix(read.table(exprsFile, header=TRUE, sep="\t", row.names=1, as.is=TRUE)) @ %% The first two lines create a file path pointing to where the assay data is stored; replace these with a character string pointing to your own file, e.g, <>= exprsFile <- "c:/path/to/exprsData.txt" @ %% (Windows users: note the use of \verb+/+ rather than \verb+\+; this is because \R{} treats the \verb+\+ character as an `escape' sequence to change the meaning of the subsequent character). See the help pages for \Rfunction{read.table} for more detail. A common variant is that the character separating columns is a comma (``comma-separated values'', or ``csv'' files), in which case the \Robject{sep} argument might be \Robject{sep=","}. It is always important to verify that the data you have read matches your expectations. At a minimum, check the class and dimensions of \Robject{geneData} and take a peak at the first several rows <>= class(exprs) dim(exprs) colnames(exprs) head(exprs[,1:5]) @ %% At this point, we can create a minimal \Rclass{ExpressionSet} object using the \code{ExpressionSet} constructor: <>= minimalSet <- ExpressionSet(assayData=exprs) @ % We'll get more benefit from expression sets by creating a richer object that coordinates phenotypic and other data with our expression data, as outlined in the following sections. \subsection{Phenotypic data} Phenotypic data summarizes information about the samples (e.g., sex, age, and treatment status; referred to as `covariates'). The information describing the samples can be represented as a table with $S$ rows and $V$ columns, where $V$ is the number of covariates. An example of phenotypic data can be input with <>= pDataFile <- file.path(dataDirectory, "pData.txt") pData <- read.table(pDataFile, row.names=1, header=TRUE, sep="\t") dim(pData) rownames(pData) summary(pData) @ %% There are three columns of data, and 26 rows. Note that the number of rows of phenotypic data match the number of columns of expression data, and indeed that the row and column names are identically ordered: <>= all(rownames(pData)==colnames(exprs)) @ %% This is an essential feature of the relationship between the assay and phenotype data; \Rclass{ExpressionSet} will complain if these names do not match. Phenotypic data can take on a number of different forms. For instance, some covariates might reasonably be represented as numeric values. Other covariates (e.g., gender, tissue type, or cancer status) might better be represented as \Robject{factor} objects (see the help page for \Robject{factor} for more information). It is especially important that the phenotypic data are encoded correctly; the \Robject{colClasses} argument to \Rfunction{read.table} can be helpful in correctly inputing (and ignoring, if desired) columns from the file. \begin{Ex} What class does \Rfunction{read.table} return? \end{Ex} \begin{Ex} Determine the column names of \Robject{pData}. Hint: \Robject{apropos("name")}. \end{Ex} \begin{solution} <>= names(pData) @ \end{solution} \begin{Ex} Use \Rfunction{sapply} to determine the classes of each column of \Robject{pData}. Hint: read the help page for \Rfunction{sapply}. \end{Ex} \begin{solution} <>= sapply(pData, class) @ \end{solution} \begin{Ex} What is the sex and Case/Control status of the 15th and 20th samples? And for the sample(s) with \Robject{score} greater than $0.8$. \end{Ex} \begin{solution} <>= pData[c(15, 20), c("gender", "type")] pData[pData$score>0.8,] @ \end{solution} Investigators often find that the meaning of simple column names does not provide enough information about the covariate -- What is the cryptic name supposed to represent? What units are the covariates measured in? We can create a data frame containing such meta-data (or read the information from a file using \Rfunction{read.table}) with <>= metadata <- data.frame(labelDescription= c("Patient gender", "Case/control status", "Tumor progress on XYZ scale"), row.names=c("gender", "type", "score")) @ %% This creates a \Rclass{data.frame} object with a single column called \code{labelDescription}, and with row names identical to the column names of the \Rclass{data.frame} containing the phenotypic data. The column \Robject{labelDescription} \emph{must} be present; other columns are optional. Bioconductor's \Rpackage{Biobase} package provides a class called \Rclass{AnnotatedDataFrame} that conveniently stores and manipulates the phenotypic data and its metadata in a coordinated fashion. Create and view an \Rclass{AnnotatedDataFrame} instance with: <>= phenoData <- new("AnnotatedDataFrame", data=pData, varMetadata=metadata) phenoData @ %% Some useful operations on an \Rclass{AnnotatedDataFrame} include \Rmethod{sampleNames}, \Rmethod{pData} (to extract the original \Robject{pData} \Rclass{data.frame}), and \Rmethod{varMetadata}. In addition, \Rclass{AnnotatedDataFrame} objects can be subset much like a \Rclass{data.frame}: <>= head(pData(phenoData)) phenoData[c("A","Z"),"gender"] pData(phenoData[phenoData$score>0.8,]) @ %% \subsection{Annotations and feature data} Meta-data on features is as important as meta-data on samples, and can be very large and diverse. A single chip design (i.e., collection of features) is likely to be used in many different experiments, and it would be inefficient to repeatedly collect and coordinate the same meta-data for each \Rclass{ExpressionSet} instance. Instead, the ideas is to construct specialized meta-data packages for each type of chip or instrument. Many of these packages are available from the Bioconductor web site. These packages contain information such as the gene name, symbol and chromosomal location. There are other meta-data packages that contain the information that is provided by other initiatives such as GO and KEGG. The \Rpackage{annotate} and \Rpackage{AnnotationDbi} packages provides basic data manipulation tools for the meta-data packages. The appropriate way to create annotation data for features is very straight-forward: we provide a character string identifying the type of chip used in the experiment. For instance, the data we are using is from the Affymetrix hgu95av2 chip: <>= annotation <- "hgu95av2" @ %% It is also possible to record information about features that are unique to the experiment (e.g., flagging particularly relevant features). This is done by creating or modifying an \Robject{AnnotatedDataFrame} like that for \Robject{phenoData} but with row names of the \Rclass{AnnotatedDataFrame} matching rows of the assay data. \subsection{Experiment description} Basic description about the experiment (e.g., the investigator or lab where the experiment was done, an overall title, and other notes) can be recorded by creating a \Rclass{MIAME} object. One way to create a \Rclass{MIAME} object is to use the \Rfunction{new} function: <>= experimentData <- new("MIAME", name="Pierre Fermat", lab="Francis Galton Lab", contact="pfermat@lab.not.exist", title="Smoking-Cancer Experiment", abstract="An example ExpressionSet", url="www.lab.not.exist", other=list( notes="Created from text files" )) @ %% Usually, \Rfunction{new} takes as arguments the class name and pairs of names and values corresponding to different slots in the class; consult the help page for \Rclass{MIAME} for details of available slots. \subsection{Assembling an \Rclass{ExpressionSet}} An \Rclass{ExpressionSet} object is created by assembling its component parts and callng the \code{ExpressionSet} constructor: <>= exampleSet <- ExpressionSet(assayData=exprs, phenoData=phenoData, experimentData=experimentData, annotation="hgu95av2") @ %% Note that the names on the right of each equal sign can refer to any object of appropriate class for the argument. See the help page for \Rclass{ExpressionSet} for more information. We created a rich data object to coordinate diverse sources of information. Less rich objects can be created by providing less information. As mentioned earlier, a minimal expression set can be created with <>= minimalSet <- ExpressionSet(assayData=exprs) @ %% Of course this object has no information about phenotypic or feature data, or about the chip used for the assay. \section{\Rclass{ExpressionSet} Basics} Now that you have an \Rclass{ExpressionSet} instance, let's explore some of the basic operations. You can get an overview of the structure and available methods for \Rclass{ExpressionSet} objects by reading the help page: <>= help("ExpressionSet-class") @ When you print an \Rclass{ExpressionSet} object, a brief summary of the contents of the object is displayed (displaying the entire object would fill your screen with numbers): <>= exampleSet @ \subsection{Accessing Data Elements} A number of accessor functions are available to extract data from an \Rclass{ExpressionSet} instance. You can access the columns of the phenotype data (an \Rclass{AnnotatedDataFrame} instance) using \verb+$+: <>= exampleSet$gender[1:5] exampleSet$gender[1:5] == "Female" @ %% You can retrieve the names of the features using \Rfunction{featureNames}. For many microarray datasets, the feature names are the probe set identifiers. <>= featureNames(exampleSet)[1:5] @ %% The unique identifiers of the samples in the data set are available via the \Rfunction{sampleNames} method. The \Rfunction{varLabels} method lists the column names of the phenotype data: <>= sampleNames(exampleSet)[1:5] varLabels(exampleSet) @ %% Extract the expression matrix of sample information using \Rfunction{exprs}: <>= mat <- exprs(exampleSet) dim(mat) @ \subsubsection{Subsetting} Probably the most useful operation to perform on \Rclass{ExpressionSet} objects is subsetting. Subsetting an \Rclass{ExpressionSet} is very similar to subsetting the expression matrix that is contained within the \Rclass{ExpressionSet}, the first argument subsets the features and the second argument subsets the samples. Here are some examples: Create a new \Rclass{ExpressionSet} consisting of the 5 features and the first 3 samples: <>= vv <- exampleSet[1:5, 1:3] dim(vv) featureNames(vv) sampleNames(vv) @ %% Create a subset consisting of only the male samples: <>= males <- exampleSet[ , exampleSet$gender == "Male"] males @ \section{What was used to create this document} The version number of \R{} and the packages and their versions that were used to generate this document are listed below. <>= toLatex(sessionInfo()) @ \end{document} Biobase/inst/doc/ExpressionSetIntroduction.pdf0000644000175400017540000046436613175724627022637 0ustar00biocbuildbiocbuild%PDF-1.5 %ÐÔÅØ 66 0 obj << /Length 2640 /Filter /FlateDecode >> stream xÚY[oÛÈ~ϯú²M83^º@MwÓ¦h±‹¬ßºJ[´¬Æ– Š^Çýõ=×™¡D'vdÉ™ÃsýÎ…ï/Þ¼ûPV W˜ªraqq½¨iÊzQ…ÖÔ~q±YüsùÃ~µöE±ü¸²ËýÊÕËq8¬Ö.,7pç ~ãî@ÏhÛxàÿïwp7V´ç°‡?øÑ¡ ßÁŸãê_{÷!Øœ ×:Ó¶vQ0?}¹VÁ.ûãqwØÿÚ|fʹõ…)Z=òg }Û!}ys [_V7¯}pÆU¦lZ>ô+ìâvy"€€V["‘[ä™$xËOþËn@Ñá·áñ>ɵŧt3èX|Z"ÅØå%)§g2ð¤Zþ7DßÚß!­=ʰðÀÓ,Ö®6m¨™åŠIþ|5ž•W»Öø«¾çø¬ÿ]?ö‰±–¹ ±ûK”DìÕÉúiÕ$²Bµ¨Å‚ÕÂÖÆÙP’‚mQ™"„Å:¦t skWkk])®äAî–›’A\‰H‚}¬YÙ¬É+0šë½n¾ìXŒhæt¤tÆÖA}‚Ä…w5Åò> u_·ËÃ5ÿgûƒ†xgîÆ±irc|6ð¹{!{ƒ_þ§§‡¨«ÖEgØðÖŒ‘‡ÜðèÿÄk1}ºq‡#ö²×v‡™ŸW\ ݯ?š9‚ÿ›ë%:\—X¾ªÀ¤¥)!æè¤èB<µÛ‰€ •káßȬ³ªTÑq¹ÿöÞ¦iwvrÈõ‹‹¡WÚn9Š=ZÞ׫Þû£F=Ûr(qPÜÉ›¯˜Ää½fµ.]^°ÍŒrˆ·&|Œ¦J«ƒ±¡Ñ#W·ò£èg§À‡ÚõÆ–~ªÝ Ƀ»¶¢XRD¢«SH½Cy/#‘ÏâÃ#D7D“Wªmð(ÔÞ5/õ%×ìô¬URãNÔ¼ç÷ìr×~;áL‰lßDœ`¶÷ÂgŸèðáç}ƒœ"×âû9sÚð¨~5KÓx­Ù‰¨U©hËwì#ÿ÷¡Z”8ǽ¿Á³7¢ Ã`ájó`M éHÆ|÷ª¥ ™4X&œóD™“´ò„/Ô2pBN¸Ì PŸì3¹FöàÖZQ}`Qälrˆ»ó“”B®öbºHÚÀƒ{/_¤ô O¯4!ëvÆALM!2)þq¡²5çPÔĴ”“¦ÎT7’_ Er&ÕvcYÂ;ÑÒ­"–2Õ«ý›VJ‘£fð1C€-ÓÒ°…eÿEH2Hó`ÑHð(u‘l‚79D5Ïšínë´õI^`È´xbçBÏebY²1“G¢êšc‚“VÈ59«ñ1g ŽÂkžàωý]‡`|ÍóýñÊÔeùÑnLeÏìb±5¾Œfލ=É ½¸ìb6¥âÆ5E>º5Þ£2õ&&HÞ§É‚i÷qÊt+ÿ·O¼+‹0rdhV±id k¡ZÚ&縴íKLJÇž3"¶6¡ŽÕ+õðu[V‹ÚhË·³g‚› Þžt1N*®ý,q :hÏ¥,S4ˆn¤‚›: INBœ–-ªÉìRSûc¹H•”}Ë»³>‡±§,¡ì=Áµ™÷“v ¼A - gÜÓÇÆç†o»“Š^WZmåþ»‰§‡X#keĤ¿H( V½C{œ«ézR¸ ¹ëî¬>¡„ˈ<³†÷MeÊä[÷ú.˜PчL:WaxSûsàv£* G¯§zŸ´§¢¿ÆÕ†•ÔЧªSØÅÕxEßç§â(¸dXÖ*b—f²ó&ê³Rá¹ÈÄ}ÏE¦«) UÑ%ÐmVw¥ñ›p V(Ü© ¡S ÍW;ÅÖø×ukßÖ¦!¦ÍuÞ/ú–Šzâa“¥µXʾäÈpéµ Ä'­:z€[“Ša!Aø¤nïF¾~BåCƒH±-,SÖ¡ËQy8Áƒ. µ)I<xIE‚¢ÒÎÍd 6K(ÂL¿žËÁq0q+é;ý²^þU* d$õɘK½}¾Òo¡Pl_[èW.&{ª“z)á¼/¢ô¾ÈâÁs4ftt\gŒ~R à~Á”;Ú¬è×!­~"™€_ÁÁØwÙ“Ó5t,”-©ö)­Ÿ™Í·,ڲδ_’¡?âk*{æšU^#“ê÷aÒáÑùT`úÊ1>é¼Iès Äy*¾²ª„Q´YÙ4§­ìKúù9€uóÚC0maKƸiŠˆUµ¯‹Ì„Œå…ÍIÕ¼Ù]ip¥ÕW…á­€J×éÝ1Çf†¶p¦±Xù4Ç=,Ë–ÇÏBO!@'‘§bàÚ6!ÐTÐÓa'â_¸!È&gè4ôÇD-Íóq6Ü£•’Ç› › t·ä¦û-ç¸_V^ǧ°ø¼ª<]mûôeb*+¾È«ã÷¯Ö!>Ö‚RtÝeÙÐúeŒµÍ´'Á­cîûÖ)ºbÑ#þ–7Ë‘ºú)\ÞhÏÁnJ½¨Ü5Ø;ÑEÕJå¯vê79uÂÀ59ÍõÈä¸Çä-úÝG_"3Dº1 ÖÎÀuü ±ÓÑÒYvwO®ˆR4Tú#üy‡¿Kg§N±>¡äb$] ÛY?†š´i¦e·ÌÅÚŠ‹ÓÛØP ¡yÃØ¦1éù´r§\3Н'§böL®2šÚ 5ž Í"¥­‰¾:]“~0ðö<±Òj]/ÖÙ›TÛ“`€ëóäŸõ"sn8‡C¡>êo [匰ÈÄKF‰\”y¹E{7¤F‚óF ”2eqXnÓòq¿ÔÄ]y˜—EægU®‘œ Í\ëN´OiÓÙiîy:éÂi: q)Ö€kémé¼€ Ü—:"Î,#S§ÿ9%.itJ¬Î¸sV•:—¦Fr9ðÛîÔrŸ´¬xy:ÐènùÐW¾~­Kï–QI3ˆ#õÍQ¦Ñniúå©bÉ+ws[ÊYŽi#Ë>¤qw7ûY +ª×dXꦎ©f;™ì¬kCˆzˆÅ$óùnÒGy>s¸?õ´mÄmê&P2¬[Ë|ý jðÄ£Ø)~N×–&ü¢¿1û&<ÛE? 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print(sample.ExpressionSet) print(exprs(sample.ExpressionSet)[1,]) print(pData(sample.ExpressionSet)[1:2,1:3]) ################################################### ### code chunk number 3: R ################################################### print(rbind(exprs(sample.ExpressionSet[1,]), sex <- t(pData(sample.ExpressionSet))[1,])) ################################################### ### code chunk number 4: R ################################################### medContr <- function( y, x ) { ys <- split(y,x) median(ys[[1]]) - median(ys[[2]]) } ################################################### ### code chunk number 5: R ################################################### print(apply(exprs(sample.ExpressionSet[1,,drop=F]), 1, medContr, pData(sample.ExpressionSet)[["sex"]])) ################################################### ### code chunk number 6: R ################################################### medContr1 <- function(y) { ys <- split(y,sex) median(ys[[1]]) - median(ys[[2]]) } print(esApply( sample.ExpressionSet, 1, medContr1)[1]) ################################################### ### code chunk number 7: esApply.Rnw:126-127 ################################################### sessionInfo() Biobase/inst/doc/esApply.Rnw0000644000175400017540000000721713175713325017011 0ustar00biocbuildbiocbuild% % NOTE -- ONLY EDIT THE .Rnw FILE!!! The .tex file is % likely to be overwritten. % % \VignetteIndexEntry{esApply Introduction} %\VignetteDepends{Biobase} %\VignetteKeywords{Expression Analysis} %\VignettePackage{Biobase} \documentclass[12pt]{article} \usepackage{amsmath,fullpage} \usepackage[authoryear,round]{natbib} \usepackage{hyperref} \textwidth=6.2in \textheight=8.5in %\parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \newcommand{\scscst}{\scriptscriptstyle} \newcommand{\scst}{\scriptstyle} \newcommand{\Rfunction}[1]{{\texttt{#1}}} \newcommand{\Robject}[1]{{\texttt{#1}}} \newcommand{\Rpackage}[1]{{\textit{#1}}} \newcommand{\Rmethod}[1]{{\texttt{#1}}} \newcommand{\Rfunarg}[1]{{\texttt{#1}}} \newcommand{\Rclass}[1]{{\textit{#1}}} \bibliographystyle{plainnat} \begin{document} \section*{A note on {\tt esApply}} {\tt ExpressionSet}s are complex objects. \Robject{exprs(ExpressionSet)} produces $G \times N$, where $G$ is the number of genes on a chip and $N$ is the number of tissues analyzed, and \Robject{pData(ExpressionSet)} produces $N \times p$, where $p$ is the number of phenotypic or demographic, etc., variables collected. Abstractly, we are often interested in evaluating functions $f(y;x)$ where $y$ is an $N$-vector of expression results for a specific gene and $x$ is an $N$-dimensional structure, coordinated with $y$, that distinguishes elements of $y$ for processing in the function $f$. A basic problem is to guarantee that the $j$th element of $y$ is correctly associated with the $j$th component of $x$. <>= library(Biobase) data(sample.ExpressionSet) @ As an example, let's consider \Robject{sample.ExpressionSet}, which is an \Rclass{ExpressionSet} supplied with Biobase. We will print a little report, then the first $N$-vector of gene expressions and some covariate data: <>= print(sample.ExpressionSet) print(exprs(sample.ExpressionSet)[1,]) print(pData(sample.ExpressionSet)[1:2,1:3]) @ Now let's see how expressions and a covariate are related: <>= print(rbind(exprs(sample.ExpressionSet[1,]), sex <- t(pData(sample.ExpressionSet))[1,])) @ A function that evaluates the difference in median expression across strata defined using an abstract covariate \Robject{x} is <>= medContr <- function( y, x ) { ys <- split(y,x) median(ys[[1]]) - median(ys[[2]]) } @ We can apply this to a small \Rclass{ExpressionSet} that gives back the data listed above: <>= print(apply(exprs(sample.ExpressionSet[1,,drop=F]), 1, medContr, pData(sample.ExpressionSet)[["sex"]])) @ That's a bit clumsy. This is where \Rfunction{esApply} comes in. We pay for some simplicity by following a strict protocol for the definition of the statistical function to be applied. <>= medContr1 <- function(y) { ys <- split(y,sex) median(ys[[1]]) - median(ys[[2]]) } print(esApply( sample.ExpressionSet, 1, medContr1)[1]) @ The manual page on \Rfunction{esApply} has a number of additional examples that show how applicable functions can be constructed and used. The important thing to note is that the applicable functions {\em know} the names of the covariates in the \Robject{pData} dataframe. This is achieved by having an environment populated with all the variables in \Rclass{phenoData(ExpressionSet)} put in as the environment of the function that will be applied. If that function already has an environment we retain that but in the second position. 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<- TRUE else higherV <- FALSE } if(platform == "windows"){ if(isPkg && higherV && regexpr("Win32URL", i)[1] > 0){ sourceURL <- gsub("^Win32URL: *(.*)", "\\1", i) isPkg = FALSE } }else{ if(isPkg && higherV && regexpr("/Source/", i)[1] > 0){ sourceURL <- gsub("^SourceURL: *(.*)", "\\1", i) isPkg <- FALSE } } } return(sourceURL) } getPkgDisc <- function (isDevel){ on.exit(options(show.error.messages = TRUE)) if(isDevel) URL <- "http://www.bioconductor.org/packages/devel/distrib/PACKAGES" else URL <- "http://www.bioconductor.org/packages/release/distrib/PACKAGES" con <- url(URL) options(show.error.messages = FALSE) tryMe <- try(readLines(con)) options(show.error.messages = TRUE) if(inherits(tryMe, "try-error")) stop("The url for BioC PACKAGES is incorrect") close(con) return(tryMe) } getFileName <- function(url){ temp <- unlist(strsplit(url, "/")) return(temp[length(temp)]) } Biobase/inst/scripts/getBioCHelp0000644000175400017540000000227513175713325017675 0ustar00biocbuildbiocbuildGetBioC is a function that gets the required Bioconductor libraries from correct web sites and install them to the R library on a local machine. The function takes the following arguements: libName: a character string for the name of the Bioconductor library to be installed. Current valid names include "all" - all the released packages; "affy" - package "affy" plus packages included in "exprs"; "CDNA" - package "CDNA" plus packages included in "exprs"; and "exprs" - packages "Biobase", "annotate", "genefilter", "geneploter", "edd", "Roc", and "tkWidgets". destdir: a character string for the directory on a local machine where the downloaded packages will be stored. isDevel: a boolean indicating whether the released (FALSE) or developer (TRUE) version of the packages will be downloaded and installed. verbose: a boolean indicating whether any error related to the downloading process will be (TRUE) printed out on the screen. Error messages will still be returned but invisible if verbose is set to FALSE. Source getBioC.R on a local machine and run the function with proper arguements will allow for obtaining and installing all the required packages for a Bioconductor library. Biobase/inst/scripts/getBioCPkgNames.R0000644000175400017540000000214213175713325020703 0ustar00biocbuildbiocbuild# This function provides a widget for users to select packages to # download from Bioconductor. # getBioCWidget <- function(bundle = TRUE){ nameList <- list() popList <- function(toPut){ nameList[[toPut]] <<- "BioC Package" } if(bundle) pkgNames <- getBioCBundle() else pkgNames <- getBioCPkgNames() trash <- sapply(pkgNames, popList) selected <- listSelect(nameList, "Select packages from the list", NULL, NULL) toGet <- NULL for(i in names(selected)){ if(selected[[i]]){ toGet <- c(toGet, i) } } getBioC(libName = toGet, destdir = NULL, isDevel = FALSE, verbose = TRUE, bundle = bundle) } getBioCPkgNames <- function(){ pkgNames <- NULL biocURL <- getDefaultRep(bioCOnly = TRUE) repository <- getRep(biocURL[[1]]) for(i in repository){ if(isPak(i)){ pkgNames <- c(pkgNames, gsub("^Package: *(.*)", "\\1", i)) } } return(unique(pkgNames)) } getBioCBundle <- function(){ return(c("exprs", "affy", "cdna")) } Biobase/inst/scripts/makeExpressionSetPackage.R0000644000175400017540000000373013175713325022672 0ustar00biocbuildbiocbuild ##take a phenoData object and create a valid - sort of - format ## section for a man page pD2Rd <- function(pD) { if(!inherits(pD, "AnnotatedDataFrame") ) stop("only works for AnnotatedDataFrames") fmt = "\\format{\n The format is:\n An \\code{ExpressionSetObject} with covariates:\n" covs = "\\itemize{" vMD = varMetadata(pD) vL = varLabels(pD) for(i in 1:length(vL) ) { item = paste("\\item \\code{", vL[i], "}: ", vMD[i,1], sep="") covs = paste(covs, item, sep="\n") } paste(fmt, covs, "\n}\n}\n", sep="") } makeExpressionSetPackage = function(expS, author, filePath=tempdir(), version = "1.0.0", license, email, biocViews="ExperimentData", packageName ) { if( !inherits(expS, "ExpressionSet") ) stop("only works for ExpressionSets") if( missing(email) || !(is.character(email) && (length(email) == 1) && grep("@", email) == 1 ) ) stop("invalid email address") if( !is.package_version(version) ) version = package_version(version) if(missing(license) ) license= "The Artistic License, Version 2.0" if( missing(packageName) ) pkgname = deparse(substitute(expS)) sym = list(AUTHOR = author, VERSION=as.character(version), LICENSE=license, TITLE = paste("Experimental Data Package:",pkgname), MAINTAINER = paste(author, ", <", email, ">", sep = ""), BVIEWS = biocViews, DESCRIPTION = "place holder 1", FORMAT = "An instance of the ExpressionSet class") res = createPackage(pkgname, destinationDir=filePath, originDir = system.file("ExpressionSet", package="Biobase"), symbolValues = sym, unlink=TRUE) ##save the data file assign(pkgname, expS) save(list=pkgname, file = file.path( res$pkgdir, "data", paste(pkgname, ".rda", sep=""))) return(res) } library(ALL) data(ALL) makeExpressionSetPackage(ALL, author="Robert Gentleman", email="rgentlem@foo") x=pD2Rd(phenoData(ALL)) Biobase/inst/scripts/query.packages.R0000644000175400017540000001523013175713325020665 0ustar00biocbuildbiocbuild# This function queries the repository for packages and finds the urls # for all the packages a given package depends on. The urls will be # returned as list that contains the repository, url, and version # number of the package and a list of the urls for all the packages the # package depends on. # # pkgName: a character string for the name of the package whose # dependency will be queried. # pkgVersion: a integer for the version number of the packages on # which a given package depends. Default is to get the largest versin # number. # type: a character string for the type of the package. Should be # either "unix" or "windows". # repositories: a list of urls for the respositories to be # searched. The default is bioconductor and then CRAN. # query.packages <- function (pkgName, pkgVersion = NULL, type = "unix", repositories = getDefaultRep(bioCOnly = FALSE)){ on.exit(options(show.error.messages = TRUE)) pkgFound <- FALSE collectedItem <- NULL pkgPat <- getPkgPat(pkgName) returnList <- list(repository = NULL, packUrl = NULL, version = ifelse(is.null(pkgVersion), -1, pkgVersion), type = ifelse(is.null(type), .Platform$OS.type, type), depends = NULL) tempRep <- NULL tempSUrl <- NULL tempZUrl <- NULL tempDep <- NULL tempVer <- -1 listReady <- FALSE doList <- function(){ if(is.null(pkgVersion)){ if(tempRep == paste(getOption("repositories"), "/PACKAGES", sep = "")){ tempSUrl <<- paste(getOption("repositories"), "/", pkgName, "_", tempVer, ".tar.gz", sep = "") tempZUrl <<- avlCheck(pkgName) } if(tempVer >= returnList$version){ returnList$repository <<- tempRep if(!is.null(tempSUrl) && !is.null(tempZUrl)) returnList$packUrl <<- ifelse(type == "unix", tempSUrl, tempZUrl) returnList$version <<- tempVer if(!is.null(tempDep)) returnList$depends <<- formatLine(tempDep) listReady <<- TRUE pkgFound <<- FALSE } }else{ if(tempVer == returnList$version){ returnList$repository <<- tempRep if(!is.null(tempSUrl) && !is.null(tempZUrl)) returnList$packUrl <<- ifelse(type == "unix", tempSUrl, tempZUrl) returnList$version <<- tempVer if(!is.null(tempDep)) returnList$depends <<- formatLine(tempDep) listReady <<- TRUE pagFound <<- FALSE } } } for(i in repositories){ pakRep <- getRep(i) tempRep <- i for(j in pakRep){ if(isPak(j)){ # doList whenever we see a match if(pkgFound) doList() if(regexpr(pkgPat, j) == 1) pkgFound <- TRUE else pkgFound <- FALSE } if(pkgFound){ switch(sub("(^.*): .*", "\\1", j), "Version" = tempVer <- sub("^.*: *(.*)","\\1",j), "SourceURL" = tempSUrl <- sub("^.*(http://.*)","\\1",j), "Win32URL" = tempZUrl <- sub("^.*(http://.*)","\\1",j), "Depends" = tempDep <- getDepends(j)) } } # do list again in case the match is the last one if(pkgFound) doList() # Taken out to be in line with the new format of PACKAGES # if(listReady) # break } if(listReady) return(returnList) else{ toPut <- ifelse(is.null(pkgVersion), "", paste(" Version", pkgVersion)) print(paste("Can not find package ", pkgName, toPut, " in repositories", sep = "")) return(NULL) } } getDefaultRep <- function (bioCOnly = FALSE){ if(bioCOnly) return(list(BioC = "http://www.bioconductor.org/packages/release/distrib/PACKAGES")) else return(list(BioC = "http://www.bioconductor.org/packages/release/distrib/PACKAGES", CRAN = paste(getOption("repositories"), "/PACKAGES", sep = ""))) } getRep <- function(rep){ on.exit(options(show.error.messages = TRUE)) con <- url(rep) options(show.error.messages = FALSE) tryMe <- try(readLines(con)) #for testing using a local file only #tryMe <- try(readLines("PACKAGES")) options(show.error.messages = TRUE) if(inherits(tryMe, "try-error")) stop(paste("Invalid repository url", rep)) close(con) return(tryMe) } getPkgPat <- function(pkgName){ return(paste("Package: *", pkgName, sep = "")) } isPak <- function(aLine){ return(ifelse(regexpr("Package:.*", aLine) == 1, TRUE, FALSE)) } getDepends <- function(dep){ on.exit(options(show.error.messages = TRUE)) depList <- NULL options(show.error.messages = FALSE) tryMe <- try(sub("^.*: *(.*)","\\1",dep)) options(show.error.messages = TRUE) if(tryMe == "" || is.null(tryMe) || is.na(tryMe)){ depList <- NULL }else{ dep <- sub("^.*: *(.*)","\\1",dep) deps <- unlist(strsplit(dep, ",")) for(i in 1:length(deps)){ depList[[i]] <- deps[i] } } return(depList) } formatLine <- function(aLine){ return(gsub("^ *(.*)", "\\1", aLine)) } avlCheck <- function(pkgName){ on.exit(options(show.error.message = TRUE)) options(show.error.messages = FALSE) tryMe <- try(url(paste("http://cran.r-project.org/bin/", "windows/contrib/", pkgName, ".zip", sep = ""), "r")) if(!inherits(tryMe, "try-error")){ close(tryMe) return(paste("http://cran.r-project.org/bin/", "windows/contrib/", pkgName, ".zip", sep = "")) } tryMe <- try(url(paste("http://cran.r-project.org/bin/", "windows/base/", pkgName, ".zip", sep = ""), "r")) if(!inherits(tryMe, "try-error")){ close(tryMe) return(paste("http://cran.r-project.org/bin/", "windows/base/", pkgName, ".zip", sep = "")) }else{ return("Unavailable") } } Biobase/inst/testClass.R0000644000175400017540000000100413175713325016213 0ustar00biocbuildbiocbuild#some simple test classes to see if things are working at all library(methods) setClass("foo", representation(a="numeric", b="numeric")) setClass("bar", representation(c="numeric", b="character")) setClass("baz", "foo", representation(d="list", e="logical")) #load up Biobase so we can test library(Biobase) f1 <- new("foo", a=10,b=15) l1 <- list(a=f1) nc1 <- new("container", x=l1, content="foo", locked=FALSE) b1 <- new("bar", b="AAA", c=10) #this should fail... nc1[[1]] <- b1 nc1[[1]] v<-nc1[1] Biobase/inst/unitTests/0000755000175400017540000000000013175713325016132 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16248 17262 19092 21971 19426 21580 17467 "AFFX-HSAC07/X00351_5_at" 19541 9857 15363 6858 11636 17374 9902 13309 20371 10761 "AFFX-HSAC07/X00351_M_at" 27768 13271 20794 12511 14738 23936 17778 16775 25052 15420 "AFFX-HSAC07/X00351_3_at" 24477 17671 20166 18311 15303 21605 20434 14547 22296 17384 "AFFX-HUMTFRR/M11507_5_at" 149 218 497 254 217 366 159 677 118 140 "AFFX-HUMTFRR/M11507_M_at" 19 -8 399 100 -6 -236 -90 473 -68 -109 "AFFX-HUMTFRR/M11507_3_at" 229 -61 859 216 222 138 81 795 72 89 "AFFX-M27830_5_at" 6418 92 207 170 1491 12616 281 584 30139 15215 "AFFX-M27830_M_at" 27707 2029 2582 851 2967 13679 765 1365 9827 12263 "AFFX-M27830_3_at" 456 344 822 323 963 816 -6 685 211 190 "AFFX-HSAC07/X00351_3_st" 622 601 1041 968 1218 4062 1668 1122 1562 546 "AFFX-HUMGAPDH/M33197_5_st" 72 -68 129 -56 35 -252 133 252 -16 53 "AFFX-HUMGAPDH/M33197_M_st" 267 257 8 268 95 0 220 124 308 131 "AFFX-HUMGAPDH/M33197_3_st" -70 440 158 84 262 294 183 223 180 66 "AFFX-HSAC07/X00351_5_st" -299 -155 -232 -132 -105 -105 -90 -245 -211 -399 "AFFX-HSAC07/X00351_M_st" 193 660 435 -4 133 1062 216 516 166 -52 "A28102_at" 241 430 96 65 260 91 261 555 308 472 "AB000114_at" -38 4 31 -212 28 68 45 168 34 249 "AB000115_at" 251 131 138 1147 128 327 123 149 219 585 "AB000220_at" 98 68 40 35 46 96 51 31 167 202 "AB000409_at" -260 181 -120 -77 0 -354 125 134 121 161 "AB000449_at" 149 70 283 285 833 190 353 372 249 275 "AB000450_at" 275 406 113 172 390 199 259 122 209 360 "AB000460_at" 2573 1963 1082 1548 2222 2867 2548 884 1128 1604 "AB000462_at" 168 81 111 239 246 102 566 175 142 197 "AB000464_at" 1151 1021 530 582 592 750 181 454 336 383 "AB000466_at" -885 -1036 -1281 -451 -1046 -1940 -322 -990 -394 -355 "AB000467_at" -883 -800 -703 -369 -1123 -1394 -781 -1115 -538 -872 "AB000468_at" -106 16 272 769 1766 -170 767 247 515 258 "AB000584_at" -685 -260 -315 -277 -420 -331 62 105 102 -297 "AB000895_at" 147 -891 -124 -365 -637 -331 -518 -490 -10 -444 "AB000896_at" -328 114 -63 -39 -59 -633 7 -165 123 148 "AB000897_at" -77 -23 -114 -56 -57 -247 -112 -43 111 54 "AB000905_at" 301 79 163 -27 138 185 89 182 228 139 "AB001106_at" 111 228 261 180 863 266 258 182 305 191 "AB001325_at" 1016 521 695 853 872 1839 475 898 719 781 "AB002314_at" -60 -202 -6 8 -139 -2 145 74 103 86 "AB002315_at" 190 -8 311 195 285 44 50 185 246 210 "AB002318_at" 1233 510 1111 802 1652 2356 410 591 584 359 "AB002365_at" 207 551 13 -67 -8 141 3 64 -28 40 "AB002366_at" 0 -266 33 39 38 -58 18 -26 -163 -216 "AB002380_at" 43 -16 149 136 35 112 46 221 164 30 "AB002382_at" 767 604 176 346 583 705 403 141 60 185 "AB002409_at" 195 105 -171 102 -103 -236 82 -64 -143 -20 "AB002559_at" 1214 1080 1053 674 708 1260 1051 1747 1320 730 "AB003102_at" 461 537 868 432 1263 750 615 545 252 439 "AB003103_at" 48 187 41 92 445 91 150 93 80 63 "AB003177_at" 311 1037 887 342 1019 750 749 761 472 849 "AB003698_at" 115 175 189 159 705 279 298 199 231 148 "AB004884_at" 494 585 864 754 1655 1028 629 569 355 930 "AB006190_at" 473 859 525 542 852 948 422 771 348 489 "AC000061_cds2_at" 82 860 217 235 149 823 194 247 226 216 "AC000061_cds3_at" -70 -77 -105 -142 -149 -138 -54 -60 -38 -93 "AC000062_at" -14 30 -27 -27 -16 -49 14 19 -66 -81 "AC000064_cds1_at" 226 632 253 250 402 527 137 286 145 127 "AC000064_cds2_at" 111 286 84 86 218 205 167 245 40 161 "AC000066_at" -74 -86 -19 -54 -39 -79 -73 28 34 -57 Biobase/inst/unitTests/VersionedClass_data/raw/pData.tab0000644000175400017540000000130113175713325024354 0ustar00biocbuildbiocbuild"Samples" "ALL.AML" "BM.PB" "T.B.cell" "FAB" "Date" "Gender" "pctBlasts" "Treatment" "PS" "Source" "39" 39 "ALL" "BM" "B-cell" NA "" "F" NA NA 0.78 "DFCI" "40" 40 "ALL" "BM" "B-cell" NA "5/16/1980" "F" NA NA 0.68 "DFCI" "42" 42 "ALL" "BM" "B-cell" NA NA "F" NA NA 0.42 "DFCI" "47" 47 "ALL" "BM" "B-cell" NA "9/5/1986" "M" NA NA 0.81 "DFCI" "48" 48 "ALL" "BM" "B-cell" NA "2/28/1992" "F" NA NA 0.94 "DFCI" "49" 49 "ALL" "BM" "B-cell" NA NA "M" NA NA 0.84 "DFCI" "41" 41 "ALL" "BM" "B-cell" NA NA "F" NA NA 0.99 "DFCI" "43" 43 "ALL" "BM" "B-cell" NA NA "F" NA NA 0.66 "DFCI" "44" 44 "ALL" "BM" "B-cell" NA "11/19/1998" "F" NA NA 0.97 "DFCI" "45" 45 "ALL" "BM" "B-cell" NA "11/19/1998" "M" NA NA 0.88 "DFCI" Biobase/inst/unitTests/VersionedClass_data/raw/varMetadata.tab0000644000175400017540000000064713175713325025570 0ustar00biocbuildbiocbuild"labelDescription" "Samples" "Sample index" "ALL.AML" "Factor, indicating ALL or AML" "BM.PB" "Factor, sample from marrow or peripheral blood" "T.B.cell" "Factor, T cell or B cell leuk." "FAB" "Factor, FAB classification" "Date" "Date sample obtained" "Gender" "Factor, gender of patient" "pctBlasts" "pct of cells that are blasts" "Treatment" "response to treatment" "PS" "Prediction strength" "Source" "Source of sample" Biobase/inst/unitTests/test_AnnotatedDataFrame.R0000644000175400017540000002644313175713325023007 0ustar00biocbuildbiocbuilddat <- list(x=factor(1:10), y=I(1:10), z=I(letters[1:10])) obj1 <- new("AnnotatedDataFrame", data=data.frame(x=factor(1:10), y=I(1:10), z=I(letters[1:10]), row.names=LETTERS[1:10]), varMetadata=data.frame( labelDescription=names(dat), class=sapply(dat, class), typeof=sapply(dat, typeof), mode=sapply(dat, mode), row.names=c("x","y","z"))) obj2 <- local({ obj2 <- obj1 sampleNames(obj2) <- letters[1:dim(obj1)[[1]]] obj2 }) checkAsp <- function(obj1, obj) { cidx <- colnames(obj1) checkTrue(all(sapply(obj[,cidx, drop=FALSE], typeof)==sapply(obj1, typeof))) checkTrue(all(sapply(obj[,cidx, drop=FALSE], class)==sapply(obj1, class))) checkTrue(all(sapply(obj[,cidx, drop=FALSE], mode)==sapply(obj1, mode))) } checkData <- function(obj1, obj2, obj) { checkTrue(all(colnames(obj1) %in% colnames(obj))) checkTrue(all(colnames(obj2) %in% colnames(obj))) checkAsp(obj1, obj) checkAsp(obj2, obj) } checkVarMetadata <- function(obj1, obj2, obj) { checkTrue(all(colnames(obj1) %in% colnames(obj))) checkTrue(all(colnames(obj2) %in% colnames(obj))) checkTrue(all(rownames(obj1) %in% rownames(obj))) checkTrue(all(rownames(obj2) %in% rownames(obj))) checkAsp(obj1, obj) checkAsp(obj2, obj) } check <- function(obj1, obj2, obj) { checkData(pData(obj1), pData(obj2), pData(obj)) checkVarMetadata(varMetadata(obj1), varMetadata(obj2), varMetadata(obj)) } checkUnchangedPData <- function(p1, p2, p) { checkTrue(all(sapply(colnames(p1), function(nm) { identical(p[1:dim(p1)[[1]],nm], p1[,nm]) }))) checkTrue(all(sapply(colnames(p2), function(nm) { identical(p[dim(p1)[[1]] + 1:dim(p1)[[1]],nm], p2[,nm]) }))) } testEmptyCombine <- function() { obj <- new("AnnotatedDataFrame") checkTrue(identical(obj, combine(obj, obj))) } testAnnotatedDataFrameCombine <- function() { oldw <- options("warn") ## duplicate sampleNames checkTrue(identical(obj1, combine(obj1,obj1))) ## two distint pData obj <- combine(obj1, obj2) check(obj1, obj2, obj) checkTrue(identical(varMetadata(obj1), varMetadata(obj))) # varMetadata unchanged checkTrue(identical(varMetadata(obj2), varMetadata(obj))) ## warning about coercing pData factors obj2a <- obj2 pData(obj2a)[["x"]] <- factor(letters[1:10]) on.exit(options(oldw)) options(warn=2) checkException(combine(obj1,obj2a), silent=TRUE) options(oldw) ## varMetadata with different numbers of columns obj4 <- obj2 varMetadata(obj4)[,"int"] <- 1:dim(varMetadata(obj1))[[1]] varMetadata(obj4)[,"char"] <- I(letters[1:dim(varMetadata(obj1))[[1]]]) obj <- combine(obj1, obj4) checkUnchangedPData(pData(obj1), pData(obj4), pData(obj)) check(obj1, obj4, obj) ## varMetadata content mismatch obj3 <- obj2 varMetadata(obj3)[,1] <- varMetadata(obj3)[,4] colnames(varMetadata(obj3)) <- colnames(varMetadata(obj2)) checkException(combine(obj1, obj3), silent=TRUE) ## varMetadata multi-column mismatch obj3 <- obj2 varMetadata(obj3)[,1:2] <- varMetadata(obj3)[,4:3] colnames(varMetadata(obj3)) <- colnames(varMetadata(obj2)) checkException(suppressWarnings(combine(obj1, obj3)), silent=TRUE) ## varMetadata extra columns obj5 <- obj2 pData(obj5)[,"int"] <- 1:dim(pData(obj1))[[1]] pData(obj5)[,"char"] <- I(letters[1:dim(pData(obj1))[[1]]]) varMetadata(obj5)[c("int","char"),] <- NA obj <- combine(obj1, obj5) checkUnchangedPData(pData(obj1), pData(obj5), pData(obj)) check(obj1, obj5, obj) ## varMetadata with conflicting information (NAs) obj6 <- obj2 varMetadata(obj6)[2,"typeof"] <- NA checkException(suppressWarnings(combine(obj1, obj6)), silent=TRUE) } testVarMetadataAssign <- function() { ## previously coerced labelData to 'character' obj2 <- obj1 varMetadata(obj2) <- varMetadata(obj1) checkTrue(identical(obj1, obj2)) to <- AnnotatedDataFrame(data.frame(Sample=1:5)) df <- data.frame(labelDescription="foo", row.names="Sample") varMetadata(to) <- df checkTrue(validObject(to)) ## avoid varMetatadata duplication via partial match ## https://stat.ethz.ch/pipermail/bioconductor/2014-February/057883.html adf <- AnnotatedDataFrame(data.frame(xx=1:5)) varMetadata(adf)["xx", "labelDescription"] <- "lbl" adf$x <- 1:5 checkIdentical(c("lbl", NA), varMetadata(adf)$labelDescription) } testMetadataFactors <- function() { pd = data.frame(covar="Z") vmd = data.frame(labelDescription=I("Meta 'covar'")) rownames(vmd) = colnames(pd) rownames(pd) = "Z" a = new("AnnotatedDataFrame", data=pd, varMetadata=vmd) ## factor recode should throw a warning oldw=options("warn") on.exit(options(oldw)) options(warn=2) pd = data.frame(covar=LETTERS[1]) rownames(pd) = LETTERS[1] b = new("AnnotatedDataFrame", data=pd, varMetadata=vmd) checkException(combine(a,b), silent=TRUE) options(oldw) } testNoSharedCols <- function() { obj1 <- new("AnnotatedDataFrame", data=data.frame(x=factor(1:10)), varMetadata=data.frame(labelDescription="x", row.names=c("x"))) obj2 <- new("AnnotatedDataFrame", data=data.frame(y=factor(1:10), row.names=letters[1:10]), varMetadata=data.frame(labelDescription="y", row.names=c("y"))) obj <- combine(obj1,obj2) checkTrue(all(pData(obj)[1:10,colnames(pData(obj1)),drop=FALSE]==pData(obj1))) checkTrue(all(pData(obj)[11:20,colnames(pData(obj2)),drop=FALSE]==pData(obj2))) } testPhenoDataFactors <- function() { data(sample.ExpressionSet) suppressWarnings(obj1 <- updateObject(sample.ExpressionSet)) obj2 <- obj1 sampleNames(obj2) <- letters[1:dim(obj1)[[2]]] obj1 <- phenoData(obj1) obj2 <- phenoData(obj2) obj <- combine(obj1, obj2) checkTrue(all(pData(obj)[1:nrow(obj1),colnames(pData(obj1)),drop=FALSE]== pData(obj1))) checkTrue(all(pData(obj)[nrow(obj1)+1:nrow(obj2),colnames(pData(obj2)), drop=FALSE] == pData(obj2))) } testDimLabels <- function() { x <- new("AnnotatedDataFrame") y <- x y@dimLabels <- c("x","y") checkException(combine(x,y), silent=TRUE) } testNewCovariate <- function() { x <- new("AnnotatedDataFrame",data=data.frame(x=1:10)) x$y <- 1:10 checkTrue(validObject(x)) x[["z"]] <- 1:10 checkTrue(validObject(x)) x <- new("AnnotatedDataFrame",data=data.frame(x=1:10)) varMetadata(x)$meta1 <- TRUE x[["w"]] <- letters[1:10] checkTrue(identical(dim(varMetadata(x)), as.integer(c(2,2)))) checkTrue(identical(varMetadata(x)["x",,drop=TRUE], list(labelDescription=as.character(NA),meta1=TRUE))) x <- new("AnnotatedDataFrame",data=data.frame(x=1:10)) pData(x) <- pData(x)[1:5,,drop=FALSE] checkTrue(validObject(x)) checkTrue(identical(as.vector(dim(x),"integer"), as.integer(c(5,1)))) } testReplaceCovariates <- function() { ## previously tried to update rather than replace varMetadata adf <- new("AnnotatedDataFrame", data=data.frame(x=1:3)) pData(adf) <- data.frame(y=1:3) checkTrue(validObject(adf)) checkEquals("y", varLabels(adf)) pData(adf)[,"z"] <- 3:1 checkTrue(validObject(adf)) checkEquals(c("y","z"), varLabels(adf)) checkEquals(data.frame(y=1:3, z=3:1), pData(adf)) pData(adf)[,"y"] <- NULL checkTrue(validObject(adf)) checkEquals("z", varLabels(adf)) checkEquals(data.frame(z=3:1), pData(adf)) } testNewCovariateOnEmptyADF <- function() { adf <- new("AnnotatedDataFrame", data=data.frame(1:3)[,FALSE,drop=FALSE]) ## was failing to create varMetadata labelDescription pData(adf)$x <- 1:3 checkTrue(validObject(adf, complete=TRUE)) obj <- obj1 pData(obj)[["Z"]] <- NA checkTrue(validObject(obj, complete=TRUE)) } testBadInitializeArugments <- function() { checkException(new("AnnotatedDataFrame", data=NULL), silent=TRUE) checkException(new("AnnotatedDataFrame", varMetadata=NULL), silent=TRUE) checkException(new("AnnotatedDataFrame", data=data.frame(), varMetadata=NULL), silent=TRUE) } testNewWithVarMetadata <- function() { df <- data.frame(x=1:6, y=rep(c("Low", "High"),3), z=I(LETTERS[1:6]), row.names=paste("Sample", 1:6, sep="_")) metaData <- data.frame(labelDescription=c( "Numbers", "Factor levels", "Character")) ## standard obj <- new("AnnotatedDataFrame", data=df, varMetadata=metaData) checkTrue(validObject(obj)) ## varMetadata with inconsistent row names -- silent conversion row.names(metaData) <- 1:3 obj <- new("AnnotatedDataFrame", data=df, varMetadata=metaData) checkTrue(validObject(obj)) checkTrue(all(row.names(varMetadata(obj))==names(pData(obj)))) } testAnnotatedDataFrameFrom <- function() { ## empty matrix m <- matrix(0,0,0) a <- annotatedDataFrameFrom(m, byrow=TRUE) checkTrue(validObject(a)) checkTrue(all.equal(c(0,0), as.vector(dim(a)))) a <- annotatedDataFrameFrom(m, byrow=FALSE) checkTrue(validObject(a)) checkTrue(all.equal(c(0,0), as.vector(dim(a)))) ## matrix m <- matrix(0,5,10, dimnames=list(letters[1:5], LETTERS[1:10])) a <- annotatedDataFrameFrom(m, byrow=TRUE) checkIdentical(letters[1:5], sampleNames(a)) a <- annotatedDataFrameFrom(m, byrow=FALSE) checkIdentical(LETTERS[1:10], sampleNames(a)) ## assayData -- empty env ad <- assayDataNew() checkTrue(validObject(annotatedDataFrameFrom(ad, byrow=TRUE))) checkTrue(validObject(annotatedDataFrameFrom(ad, byrow=FALSE))) ## assayData -- empty list ad <- assayDataNew(storage.mode="list") checkIdentical("list", storageMode(ad)) checkTrue(validObject(annotatedDataFrameFrom(ad, byrow=TRUE))) checkTrue(validObject(annotatedDataFrameFrom(ad, byrow=FALSE))) ## assayData -- non-empty env ad <- assayDataNew(m=m) checkIdentical("lockedEnvironment", storageMode(ad)) a <- annotatedDataFrameFrom(ad, byrow=TRUE) checkIdentical(letters[1:5], sampleNames(a)) a <- annotatedDataFrameFrom(ad, byrow=FALSE) checkIdentical(LETTERS[1:10], sampleNames(a)) ## assayData -- non-empty list ad <- assayDataNew(m=m, storage.mode="list") checkIdentical("list", storageMode(ad)) a <- annotatedDataFrameFrom(ad, byrow=TRUE) checkIdentical(letters[1:5], sampleNames(a)) a <- annotatedDataFrameFrom(ad, byrow=FALSE) checkIdentical(LETTERS[1:10], sampleNames(a)) } testAnnotatedDataFrameDimnames <- function() { adf0 <- AnnotatedDataFrame(data.frame(x=1:5, y=5:1, row.names=letters[1:5]), data.frame(foo=1:2, row.names=c("x", "y"))) adf <- adf0 dimnames(adf) <- dimnames(adf) checkIdentical(adf0, adf) adf <- adf0 exp <- list(LETTERS[seq_len(nrow(adf0))], letters[seq_len(ncol(adf0))]) dimnames(adf) <- exp checkIdentical(exp, dimnames(adf)) df0 <- varMetadata(adf0) rownames(df0) <- exp[[2]] checkIdentical(df0, varMetadata(adf)) adf <- adf0 dimnames(adf) <- NULL checkTrue(validObject(adf)) checkIdentical(list(as.character(1:5), colnames(adf0)), dimnames(adf)) } Biobase/inst/unitTests/test_AssayData.R0000644000175400017540000000446613175713325021200 0ustar00biocbuildbiocbuildcheckAssayDataCombine <- function(nr, nc) { obj1 <- assayDataNew(exprs= matrix(runif(nr*nc), nrow=nr, ncol=nc, dimnames=list( if (nr > 0) letters[1:nr] else NULL, if (nc > 0) LETTERS[1:nc] else NULL))) obj <- combine(obj1,obj1) checkTrue(!identical(obj, obj1)) # different environments checkTrue(identical(obj1$exprs, obj$exprs)) storageMode(obj1) <- "list" obj <- combine(obj1,obj1) checkTrue(identical(obj1, obj)) # same list checkTrue(identical(obj1$exprs, obj$exprs)) if (nc > 2) { ## combine distinct cols obj1 <- assayDataNew(exprs= matrix(runif(nr*nc), nrow=nr, ncol=nc, dimnames=list( if (nr > 0) letters[1:nr] else nr, LETTERS[1:nc]))) obj2 <- obj1 sampleNames(obj2)[3] <- letters[3] obj <- combine(obj1, obj2) checkTrue(all(dim(obj$exprs)==c(nr,nc+1))) checkTrue(identical(obj$exprs[,1:nc],obj1$exprs)) checkTrue(identical(obj$exprs[,nc+1], obj2$exprs[,3])) } if (nc > 1) { ## inconsistent data -- list, otherwise both copies change! storageMode(obj1) <- "list" obj2 <- obj1 obj2$exprs[,1] <- runif(nr) checkException(combine(obj1, obj2), silent=TRUE) } } testAssayDataNew_named_dims <- function() { nms0 <- list(letters[1:5], LETTERS[1:2]) nms <- Map(setNames, nms0, nms0) exprs <- matrix(0, nrow=5, ncol=2, dimnames=nms) checkIdentical(nms0[[1]], featureNames(assayDataNew(exprs=exprs))) checkIdentical(nms0[[2]], sampleNames(assayDataNew(exprs=exprs))) } testAssayDataCombine <- function() { checkAssayDataCombine(5,3) checkAssayDataCombine(0,0) checkAssayDataCombine(1,0) checkAssayDataCombine(0,1) } testAssayDataCombineRows <- function() { m <- matrix(1:20, nrow=5, dimnames=list(LETTERS[1:5], letters[1:4])) obj <- assayDataNew(exprs=m) obj1 <- assayDataNew(exprs=m[1:3,]) obj2 <- assayDataNew(exprs=m[4:5,]) checkEquals(obj, combine(obj1, obj2)) obj3 <- assayDataNew(exprs=m[3:5,]) checkEquals(obj, combine(obj1, obj3)) # overlapping } Biobase/inst/unitTests/test_DataClasses.R0000644000175400017540000000106013175713325021500 0ustar00biocbuildbiocbuildtestNew <- function() { ## create instances of non-virtual objects with simple call to "new" nms <- ls(getNamespace("Biobase"),all=TRUE) classes <- gsub(".__C__", "", nms[grep(".__C__", nms)]) isVirtual <- sapply(classes, function(nm) getClass(nm)@virtual) res <- lapply(classes[!isVirtual], function(x) suppressWarnings(new(x))) } test_MIAME_construction <- function() { checkTrue(validObject(new("MIAME"))) checkTrue(validObject(MIAME())) checkIdentical(new("MIAME", name="mytest"), MIAME(name="mytest")) } Biobase/inst/unitTests/test_EsetSubclasses.R0000644000175400017540000004736313175713325022261 0ustar00biocbuildbiocbuildbaseClass <- list(eSet = NULL) ## featureSubclases <- ## list(PmOneChannelExpressionSet = c("pm"), ## PmMmOneChannelExpressionSet = c("pm", "mm"), ## PmMmOneChannelSNPSet = c("pm", "mm")) featureSubclases <- NULL targetSubclasses <- list(ExpressionSet = c("exprs"), MultiSet = c("myElt", "yourElt"), SnpSet = c("call", "callProbability")) allClasses <- c( baseClass, featureSubclases, targetSubclasses ) allSubclasses <- c( featureSubclases, targetSubclasses ) exprsEnabledSubclasses <- c("ExpressionSet","SnpSet") nonEmptySubclasses <- exprsEnabledSubclasses modes <- c("lockedEnvironment","environment","list") .features <- 20 .samples <- 10 helperNew <- function(obj, ...) { .pData <- data.frame(numeric(.samples), row.names=I(1:.samples))[,FALSE] .fData <- data.frame(numeric(.features), row.names=I(1:.features))[,FALSE] args <- function(names) { obj <- lapply(names, function(nm) new("matrix", nr = .features, nc = .samples)) names(obj) <- names c(obj, list(phenoData = new("AnnotatedDataFrame", data=.pData), featureData = new("AnnotatedDataFrame", data=.fData) )) } argsSnpN <- function(n) { list(call = new("array", dim=c(.features,.samples, n)), callProbability = new("array", dim=c(.features,.samples, n)), phenoData = new("AnnotatedDataFrame", data=.pData), featuerData = new("AnnotatedDataFrame", data=.fData)) } argsSnpDetail <- function(names) { obj <- lapply(names, function(nm) { if (nm != "copyNumber") new("array", dim=c(.features, .samples, 2)) else new("array",dim=c(.features, .samples, 3)) }) names(obj) <- names c(obj, list(phenoData = new("AnnotatedDataFrame", data=.pData), featureData = new("AnnotatedDataFrame", data=.fData))) } dots <- if (length(list(...))>0) list(...) else NULL switch(obj, SnpSetDetail = do.call(new, c(obj,argsSnpDetail(allClasses[[obj]]), dots)), SnpSet2 = do.call(new, c(obj,argsSnpN(2),dots)), SnpSet4 = do.call(new, c(obj,argsSnpN(8),dots)), eSet = new("eSet", ...), ## default do.call(new, c(obj, args(allClasses[[obj]]), dots))) } helperFillWithNoise <- function( obj ) { aData <- assayData(obj) storage.mode <- storageMode(obj) names <- if (is(aData,"environment")) ls(aData) else names(aData) if (is(aData,"environment")) aData <- new.env(parent=emptyenv()) adim <- as.numeric(dim(obj)) n <- prod(adim) for( nm in names ) { if (length(adim)==2) aData[[nm]] <- matrix(runif(n), nr=adim[[1]], nc=adim[[2]]) else aData[[nm]] <- array(runif(n),adim) } sampleNames(aData) <- sampleNames(obj) featureNames(aData) <- featureNames(obj) if (storage.mode=="lockedEnvironment") lockEnvironment(aData, bindings=TRUE) assayData(obj) <- aData obj } testNewSubclassCreation <- function() { for (mode in modes) lapply( names(allSubclasses), new, storage.mode=mode) } testStorageMode <- function() { lapply(names(allSubclasses), function(s) { obj <- new(s) checkTrue(class(assayData(obj))=="environment") obj <- new(s, storage.mode="list") checkTrue(class(assayData(obj))=="list") obj <- new(s, storage.mode="environment") checkTrue(class(assayData(obj))=="environment") ## is helperNew behaving? obj <- helperNew(s) checkTrue(class(assayData(obj))=="environment") obj <- helperNew(s, storage.mode="list") checkTrue(class(assayData(obj))=="list") obj <- helperNew(s, storage.mode="environment") checkTrue(class(assayData(obj))=="environment") }) ## update storage modes data(sample.ExpressionSet) storageMode(sample.ExpressionSet) <- "environment" checkTrue(storageMode(sample.ExpressionSet)=="environment") storageMode(sample.ExpressionSet) <- "lockedEnvironment" checkTrue(storageMode(sample.ExpressionSet)=="lockedEnvironment") storageMode(sample.ExpressionSet) <- "list" checkTrue(storageMode(sample.ExpressionSet)=="list") storageMode(sample.ExpressionSet) <- "environment" checkTrue(storageMode(sample.ExpressionSet)=="environment") } testNewValidSubclasses <- function() { for (mode in modes) lapply(names(allSubclasses), function( s ) { obj <- new(s, storage.mode=mode) checkTrue(validObject(obj)) }) for (mode in modes) lapply(names(allSubclasses), function(s) { obj <- helperNew(s, storage.mode=mode) checkTrue(class(obj)==s) checkTrue(validObject(obj)) }) } testPreallocSubclasses <- function() { for (mode in modes) lapply(names(allSubclasses), function(s) { obj <- helperNew(s, storage.mode=mode) checkTrue( all( dim(obj)[1:2] == c( .features, .samples ))) checkTrue( all( dim(phenoData(obj)) == c( .samples, 0 ))) }) } testInitializeWithNames <- function() { ## do names applied to one component get picked up? exprs <- matrix(1:10, ncol=2, dimnames=list(list(), c("A", "B"))) phenoData <- new("AnnotatedDataFrame", data=data.frame(x=1:2, row.names=c("A","B"))) obj <- new("ExpressionSet", phenoData=phenoData, exprs=exprs) checkTrue(identical(sampleNames(obj), c("A","B"))) exprs <- matrix(1:10, ncol=2) phenoData <- new("AnnotatedDataFrame", data=data.frame(x=1:2)) obj <- new("ExpressionSet", phenoData=phenoData, exprs=exprs) checkTrue(identical(sampleNames(obj), c("1", "2"))) exprs <- matrix(1:10, ncol=2) phenoData <- new("AnnotatedDataFrame", data=data.frame(x=1:2, row.names=c("A", "B"))) obj <- new("ExpressionSet", phenoData=phenoData, exprs=exprs) checkTrue(identical(sampleNames(obj), c("A", "B"))) } testValidation <- function() { errMsg <- c("sample numbers differ between assayData and phenoData", "sampleNames differ between assayData and phenoData", "sample numbers differ between phenoData and protocolData", "sampleNames differ between phenoData and protocolData" ) for (mode in modes) lapply(names(allSubclasses), function(s) { obj <- helperNew(s, storage.mode=mode) checkTrue(validObject( obj )) phenoData(obj) <- new("AnnotatedDataFrame") checkEquals( validObject( obj, test = TRUE ), errMsg) }) } testNColSubclasses <- function() { for (mode in modes) lapply(nonEmptySubclasses, function( s ) { obj <- new( s, storage.mode = mode ) checkTrue( ncol( obj ) == 0 ) }) for (mode in modes) lapply(names(allSubclasses), function( s ) { obj <- helperNew(s, storage.mode=mode) checkTrue( ncol( obj ) == .samples ) }) } testSubsetEsetSubclasses <- function() { subset <- function(s, ...) { obj <- helperNew(s, ...) obj1 <- obj[1:15, 1:5] checkTrue(validObject(obj1)) checkTrue(all(dims(obj1)[1:2,] == c( 15, 5 ))) ## original unmodified if (storageMode(obj)!="environment") { checkTrue(validObject(obj)) checkTrue(all(dims(obj)[1:2,] == c(.features,.samples))) obj <- obj[1:15, 1:5] checkTrue(validObject(obj)) checkTrue(all(dims(obj)[1:2,] == c( 15, 5 ))) } } for (mode in modes ) lapply(names(allSubclasses), subset, storage.mode=mode) } testAssayDataReplacement <- function() { lapply(names(allSubclasses), function( s ) { obj <- helperNew(s) assayData(obj) <- new.env() }) } testAssayDataElement <- function() { checkObj <- function(obj) { m <- new("matrix",0, nr=0, nc=0, dimnames=list(list(),list())) checkTrue(identical(assayDataElementNames(obj), "exprs")) checkTrue(identical(assayDataElement(obj, "exprs"), m)) obj <- assayDataElementReplace(obj, "exprs", m) checkTrue(identical(assayDataElement(obj, "exprs"), m)) } checkObj(new("ExpressionSet")) checkObj(new("ExpressionSet", storage.mode="list")) checkObj(new("ExpressionSet", storage.mode="environment")) } testOtherSlots <- function() { for (mode in modes) lapply(names(allSubclasses), function( s ) { obj <- helperNew(s, storage.mode=mode) experimentData( obj ) <- new( "MIAME" ) annotation( obj ) <- new( "character" ) }) } testShow <- function() { # just 'does it show' capture.output( for (mode in modes) lapply(names(allSubclasses), function( s ) { obj <- helperNew (s, storage.mode=mode) tryCatch(show(obj), error=function(e) checkTrue( 1==0 )) }) ) } testSampleNames <- function() { nameCheck <- function( obj ) { checkTrue( all( sampleNames( obj ) == sampleNames( phenoData( obj )))) checkException( sampleNames( obj ) <- 1:(.features+1), silent=TRUE ) sampleNames( obj ) <- letters[ 1:dim( obj )[[2]] %% 26 ] checkTrue(all(sampleNames(assayData(obj)) == sampleNames(obj))) checkTrue(validObject(obj), "original") orig <- sampleNames(obj) mod <- 1:length(orig) obj1 <- obj sampleNames(obj1) <- mod checkTrue(all(sampleNames(obj) == orig)) if (storageMode(obj)!="environment") checkTrue(validObject(obj), "after modification") else checkEquals(validObject(obj, test = TRUE ), "sampleNames differ between assayData and phenoData") checkTrue(all(sampleNames(obj1)==mod)) checkTrue(validObject(obj1)) sampleNames(assayData(obj)) <- mod validObject(obj,test=TRUE) checkEquals(validObject( obj, test = TRUE ), "sampleNames differ between assayData and phenoData") } for (mode in modes) lapply(names(allSubclasses), function(s) nameCheck(helperNew(s, storage.mode=mode))) } testExprs <- function() { exprsCheck <- function(obj) { newExprs <- switch(class(obj), SnpSet2 = { ex <- new("array", dim = c(.features, .samples, 2)) ex[,,] <- runif(length(ex)) ex }, SnpSet4 = { ex <- new("array", dim = c(.features, .samples, 8)) ex[,,] <- runif(length(ex)) ex }, SnpSetDetail = { ex <- new("array", dim = c(.features, .samples, 2)) ex[,,] <- runif(length(ex)) ex }, { ex <- new("matrix", nr = .features, nc = .samples) ex[,] <- runif(length(ex)) ex }) fNames <- featureNames(obj) sNames <- sampleNames(obj) oldExprs <- exprs(obj) exprs(obj) <- newExprs checkTrue( identical(unname(exprs(obj)), newExprs)) if (storageMode(obj)!="environment") checkTrue(!identical(exprs(obj), oldExprs)) sampleNames(assayData(obj)) <- sNames featureNames(assayData(obj)) <- fNames checkTrue(validObject(obj)) obj } lapply(exprsEnabledSubclasses, function(s) exprsCheck(helperNew(s))) for (mode in modes) lapply(exprsEnabledSubclasses, function(s) exprsCheck(helperNew(s, storage.mode=mode))) ## copy semantics lapply(exprsEnabledSubclasses, function(s) { obj <- helperNew(s, storage.mode="lockedEnvironment") oldExprs <- exprs(obj) obj1 <- exprsCheck(obj) checkTrue( identical(exprs(obj), oldExprs)) checkTrue(!identical(exprs(obj1),exprs(obj))) checkTrue(validObject(obj1)) }) lapply(exprsEnabledSubclasses, function(s) { # lockedEnvironment implicit obj <- helperNew(s) oldExprs <- exprs(obj) obj1 <- exprsCheck(obj) checkTrue( identical(exprs(obj), oldExprs)) checkTrue(!identical(exprs(obj1),exprs(obj))) checkTrue(validObject(obj1)) }) } testCombineEsetSubclasses <- function() { combineEmpty <- function(s, ...) { if (s=="MultiSet") return(TRUE) obj1 <- new(s) obj2 <- new(s) obj <- combine(obj1,obj2) checkTrue(validObject(obj)) } combineObj <- function(s, ...) { obj1 <- helperFillWithNoise(helperNew(s,...)) obj2 <- helperFillWithNoise(helperNew(s,...)) sampleNames(obj2) <- letters[1:length(sampleNames(obj2))%%26] obj <- combine(obj1,obj2) checkTrue(validObject(obj)) checkTrue(all.equal(obj[,1:.samples],obj1)) checkTrue(all.equal(obj[,(.samples+1):(2*.samples)],obj2)) } for (mode in modes) lapply(names(allSubclasses), combineEmpty, storage.mode=mode) for (mode in modes) lapply(names(allSubclasses), combineObj, storage.mode=mode) } testSetAs <- function() { setClass("SwirlSet", contains="eSet", where=.GlobalEnv) setMethod("initialize", "SwirlSet", function(.Object, assayData = assayDataNew( R=R, G=G, Rb=Rb, Gb=Gb, ...), phenoData = annotatedDataFrameFrom(assayData, byrow=FALSE), featureData = annotatedDataFrameFrom(assayData, byrow=TRUE), experimentData = new("MIAME"), annotation = character(), R = new("matrix"), G = new("matrix"), Rb = new("matrix"), Gb = new("matrix"), ... ) { callNextMethod(.Object, assayData = assayData, phenoData = phenoData, featureData = featureData, experimentData = experimentData, annotation = annotation) }, where=.GlobalEnv) setValidity("SwirlSet", function(object) { assayDataValidMembers(assayData(object), c("R", "G", "Rb", "Gb")) }, where=.GlobalEnv) checkNewAndOld <- function(new, old) { if (class(old)=="exprSet") { pDataOld <- slot(slot(old, "phenoData"), "pData") exprsOld <- slot(old, "exprs") sampleNamesOld <- as.character(pDataOld$Samples) geneNamesOld <- rownames(exprsOld) } else { pDataOld <- pData(old) exprsOld <- exprs(old) sampleNamesOld <- sampleNames(old) geneNamesOld <- geneNames(old) } checkTrue(identical(pData(new), pDataOld)) checkTrue(all.equal(exprs(new),exprsOld,check.attributes=FALSE)) checkTrue(identical(sampleNames(new),sampleNamesOld)) checkTrue(identical(featureNames(new),geneNamesOld)) } checkNewGolubMerge <- function(new,old) { checkTrue(identical(pData(new),pData(old))) checkTrue(all.equal(exprs(new),exprs(old),check.attributes=FALSE)) checkTrue(identical(sampleNames(new),sampleNames(old))) checkTrue(identical(featureNames(new),featureNames(old))) } checkNewSampleEset <- function(new, old) { if (class(old)=="eSet") { pDataOld <- slot(slot(old, "phenoData"), "pData") assayDataOld <- slot(old, "assayData") exprsOld <- assayDataOld[["exprs"]] } else { pDataOld <- pData(old) exprsOld <- exprs(old) sampleNamesOld <- sampleNames(old) geneNamesOld <- geneNames(old) } checkTrue(identical(pData(new),pDataOld)) checkTrue(all(names(assayDataOld) == names(assayData(new)))) dups <- duplicated(old@reporterNames) mapply(function(x,y) checkTrue(all.equal(x[!dups,],y,check.attributes=FALSE)), assayDataOld, assayData(new)) checkTrue(identical(sampleNames(new),old@sampleNames)) checkTrue(identical(featureNames(new),old@reporterNames[!dups])) } opts <- options() options(warn=-1) ## would like to be able to specify storage.mode, but how to specify?... fp <- system.file(package="Biobase", "unitTests", "VersionedClass_data", "devel", "exprSet.Rda") load(fp) suppressMessages(e <- as(exprSet,"ExpressionSet")) checkNewAndOld(e,exprSet) library(golubEsets) data(Golub_Merge) gm <- as(Golub_Merge,"ExpressionSet") checkNewGolubMerge(gm,Golub_Merge) pubMedIds(gm) = "10521349" checkNewGolubMerge(gm,Golub_Merge) fp <- system.file(package="Biobase", "unitTests", "VersionedClass_data", "devel", "sample.eSet.rda") load(fp) suppressMessages(es <- updateOldESet(sample.eSet, "SwirlSet")) checkNewSampleEset(es, sample.eSet) options(opts) removeClass("SwirlSet", where=.GlobalEnv) } testFeatureNamesReplace <- function() { e <- new("ExpressionSet", exprs=matrix(nrow=5,ncol=2)) featureNames(e) <- letters[5:1] checkIdentical(letters[5:1], featureNames(e)) checkTrue(validObject(e)) } testExtraSlotClassInitialize1 <- function() { setClass("ExtraSlotSet", contains="eSet", representation=representation( extraSlot="character"), where=.GlobalEnv) ## pass if no error e <- new("ExtraSlotSet") removeClass("ExtraSlotSet", where=.GlobalEnv) } testExtraSlotClassInitialize2 <- function() { setClass("ExtraSlotSet", contains="eSet", representation=representation( extraSlot="character"), where=.GlobalEnv) e <- new("ExtraSlotSet", R=matrix(0,5,3), G=matrix(0,5,3), extraSlot="hello", storage.mode="environment") checkEquals("hello", e@extraSlot) checkEquals(c("G", "R"), ls(assayData(e))) checkEquals("environment", storageMode(e)) removeClass("ExtraSlotSet", where=.GlobalEnv) } testExtraSlotClassInitialize3 <- function() { setClass("ExtraSlotSet", contains="eSet", representation=representation( extraSlot="character"), where=.GlobalEnv) e <- new("ExtraSlotSet", assayData=assayDataNew( R=new("matrix"), G=new("matrix"), storage.mode="environment"), extraSlot="hello") checkEquals("hello", e@extraSlot) checkEquals(c("G", "R"), ls(assayData(e))) checkEquals("environment", storageMode(e)) removeClass("ExtraSlotSet", where=.GlobalEnv) } testExtraSlotClassInitialize4 <- function() { setClass("ExtraSlotSet", contains="eSet", representation=representation( extraSlot="character"), where=.GlobalEnv) oldopts <- options() options(warn=2) on.exit(options(oldopts)) checkException(new("ExtraSlotSet", assayData=assayDataNew( R=matrix(0,3,5), storage.mode="environment"), R=new("matrix")), silent=TRUE) removeClass("ExtraSlotSet", where=.GlobalEnv) } testEsetUnsafeSetSlot <- function() { library(Biobase) data(sample.ExpressionSet) orig <- sampleNames(sample.ExpressionSet) obj <- sample.ExpressionSet obj <- `sampleNames<-`(obj, letters[1:26]) checkIdentical(sampleNames(obj), letters[1:26]) checkIdentical(sampleNames(sample.ExpressionSet), orig) } testEsetfeatureDataAccess <- function() { data(sample.ExpressionSet) checkTrue(all(dim(fData(sample.ExpressionSet))==c(500,0))) checkTrue(all(dim(fvarMetadata(sample.ExpressionSet))==c(0,1))) checkTrue(length(fvarLabels(sample.ExpressionSet))==0) adf <- new("AnnotatedDataFrame", data=data.frame(x=rep(0,500)), varMetadata=data.frame(labelDescription=c("X"))) obj <- sample.ExpressionSet featureData(obj) <- adf featureNames(obj) <- featureNames(obj) checkTrue(validObject(obj)) checkTrue(all(dim(fData(obj))==c(500,1))) checkTrue(all(dim(fvarMetadata(obj))==c(1,1))) checkTrue(fvarLabels(obj)=="x") obj <- sample.ExpressionSet fData(obj) <- pData(adf) checkTrue(all(dim(fData(obj))==c(500,1))) checkTrue(all(fData(obj)==pData(adf))) # Names differ fvarMetadata(obj) <- varMetadata(adf) checkTrue(all(dim(fvarMetadata(obj))==c(1,1))) checkTrue(all.equal(fvarMetadata(obj), varMetadata(adf), check.attributes=FALSE)) fvarLabels(obj) <- "y" checkTrue(fvarLabels(obj)=="y") } Biobase/inst/unitTests/test_ExpressionSet.R0000644000175400017540000001506013175713325022131 0ustar00biocbuildbiocbuildtestCombineFeatureData <- function() { data(sample.ExpressionSet) # use as source for exprs data suppressWarnings(obj <- updateObject(sample.ExpressionSet)[1:20,1:10]) obj1 <- new("ExpressionSet", phenoData=phenoData(obj), exprs=exprs(obj)) obj2 <- obj1 pData(featureData(obj1))[["x"]] <- FALSE pData(featureData(obj1))[["y"]] <- FALSE varMetadata(featureData(obj1)) <- data.frame(labelDescription=c("the x", "the y"), row.names=c("x", "y")) validObject(obj1) sampleNames(obj2) <- letters[1:dim(obj1)[[2]]] pData(featureData(obj2))[["y"]] <- FALSE pData(featureData(obj2))[["z"]] <- TRUE varMetadata(featureData(obj2)) <- data.frame(labelDescription=c("the y", "the z"), row.names=c("y", "z")) validObject(obj2) obj <- combine(obj1,obj2) checkTrue(all(varLabels(featureData(obj1)) %in% varLabels(featureData(obj)))) checkTrue(all(varLabels(featureData(obj2)) %in% varLabels(featureData(obj)))) ## conflicting feature pData pData(featureData(obj2))[["y"]] <- TRUE validObject(obj2) checkException(suppressWarnings(combine(obj1, obj2)), silent=TRUE) } testCombineRows <- function() { data(sample.ExpressionSet) obj <- sample.ExpressionSet checkEquals(obj, combine(obj[1:250,], obj[251:500,])) checkEquals(obj, combine(obj[,1:13], obj[,14:26])) ## overlapping checkEquals(obj, combine(obj[1:300,], obj[250:500,])) checkEquals(obj, combine(obj[,1:20], obj[,15:26])) } testAddTextNotes <- function() { eset <- new("ExpressionSet") notes(eset) <- "a note" checkTrue(identical(notes(eset), list("a note"))) notes(eset) <- "another" checkTrue(identical(notes(eset), list("a note", "another"))) } testExtraSlotExpressionClassInitialize1 <- function() { setClass("ExtraSlotExpressionSet", contains="ExpressionSet", representation=representation( extraSlot="character"), where=.GlobalEnv) ## pass if no error checkTrue(validObject(new("ExtraSlotExpressionSet"))) removeClass("ExtraSlotExpressionSet", where=.GlobalEnv) } testExtraSlotExpressionClassInitialize2 <- function() { setClass("ExtraSlotExpressionSet", contains="ExpressionSet", representation=representation( extraSlot="character"), where=.GlobalEnv) e <- new("ExtraSlotExpressionSet", exprs=new("matrix"), extraSlot="hello", storage.mode="environment") checkEquals("hello", e@extraSlot) checkEquals("exprs", ls(assayData(e))) checkEquals("environment", storageMode(e)) removeClass("ExtraSlotExpressionSet", where=.GlobalEnv) } testExtraSlotExpressionClassInitialize3 <- function() { setClass("ExtraSlotExpressionSet", contains="ExpressionSet", representation=representation( extraSlot="character"), where=.GlobalEnv) e <- new("ExtraSlotExpressionSet", assayData=assayDataNew( exprs=new("matrix"), storage.mode="environment"), extraSlot="hello") checkEquals("hello", e@extraSlot) checkEquals("exprs", ls(assayData(e))) checkEquals("environment", storageMode(e)) removeClass("ExtraSlotExpressionSet", where=.GlobalEnv) } testDollar <- function() { data(sample.ExpressionSet) s1 <- sample.ExpressionSet$sex s2 <- sample.ExpressionSet$se # we expect partial matching to work checkTrue(!is.null(s1), msg="$sex broken") checkTrue(!is.null(s2), msg="$se broken (pmatch)") checkEquals(s1, s2, msg="pmatch equality") } testSubset2 <- function() { data(sample.ExpressionSet) es <- sample.ExpressionSet x <- runif(ncol(es)) ldesc <- "Random variate" es[["RVar", labelDescription=ldesc]] <- x checkEquals(es[["RVar"]], x) checkEquals(varMetadata(es)["RVar", "labelDescription"], ldesc) } testHarmonizeAssayDataDimnames <- function() { checkHarmonizeOne <- function(exprs) { es <- new("ExpressionSet", exprs=exprs) checkTrue(validObject(es)) } checkHarmonizeTwo <- function (exprs, se.exprs) { es <- new("ExpressionSet", exprs=exprs, se.exprs=se.exprs) checkTrue(validObject(es)) okNames <- list(featureNames(featureData(es)), sampleNames(phenoData(es))) dimNames <- Biobase:::.assayDataDimnames(assayData(es)) checkTrue(all(sapply(dimNames, identical, okNames))) } checkCreation <- function(exprs, se.exprs) { checkHarmonizeOne(exprs) checkHarmonizeTwo(exprs, se.exprs) ## names on both dimnames nexprs <- exprs dimnames(nexprs) <- lapply(dimnames(nexprs), function(x) { names(x) <- as.vector(letters[seq(1, length(x))]) x }) checkHarmonizeOne(nexprs) checkHarmonizeTwo(nexprs, se.exprs) ## names on colnames nexprs <- exprs cnms <- colnames(nexprs) names(cnms) <- letters[seq(1, length(cnms))] colnames(nexprs) <- cnms checkHarmonizeOne(nexprs) checkHarmonizeTwo(nexprs, se.exprs) ## names on rownames nexprs <- exprs rnms <- rownames(nexprs) names(rnms) <- letters[seq(1, length(rnms))] rownames(nexprs) <- rnms checkHarmonizeOne(nexprs) checkHarmonizeTwo(nexprs, se.exprs) } se.exprs <- matrix(0, 5, 2) exprs <- matrix(0, 5, 2) dimnames(exprs) <- list(LETTERS[1:5], letters[1:2]) dimnames(se.exprs) <- NULL checkCreation(exprs, se.exprs) dimnames(se.exprs) <- list(LETTERS[1:5], NULL) checkCreation(exprs, se.exprs) dimnames(se.exprs) <- list(NULL, letters[1:2]) checkCreation(exprs, se.exprs) ## errors dimnames(se.exprs) <- list(letters[1:5], letters[1:2]) checkException(checkCreation(exprs, se.exprs), silent=TRUE) dimnames(se.exprs) <- list(LETTERS[1:5], LETTERS[1:2]) checkException(checkCreation(exprs, se.exprs), silent=TRUE) dimnames(se.exprs) <- list(letters[1:5], LETTERS[1:2]) checkException(checkCreation(exprs, se.exprs), silent=TRUE) } testExprsReplacement <- function() { exprs <- se.exprs <- matrix(1:50, 10, 5) eset <- ExpressionSet(list2env(list(exprs=exprs, se.exprs=se.exprs))) exprs(eset) <- exprs(eset) checkTrue(validObject(eset)) ## shuffled names ok exprs(eset) <- exprs(eset)[sample(rownames(eset)), sample(colnames(eset))] checkTrue(validObject(eset)) checkException({ exprs(eset) <- exprs(eset)[, 1:3] }, silent=TRUE) checkException({ exprs(eset) <- exprs(eset)[, c(1:4, 1)] }, silent=TRUE) } Biobase/inst/unitTests/test_NChannelSet.R0000644000175400017540000002277213175713325021470 0ustar00biocbuildbiocbuildtestNew <- function() { ## default constructor obj <- new("NChannelSet") checkTrue(length(channelNames(obj))==0) } testNew2 <- function() { ## assayData from arguments not matching slots obj <- new("NChannelSet", R=matrix(0,10,5), G=matrix(0,10,5)) checkTrue(all(c("R", "G") %in% channelNames(obj))) checkTrue(all(dim(obj)==c(10,5))) } testNew3 <- function() { ## explicit assayData, infered phenoData obj <- new("NChannelSet", assayData=assayDataNew( R=matrix(0,10,5), G=matrix(1,10,5))) checkTrue(all(c("R", "G") %in% channelNames(obj))) checkTrue(all(c(10,5)==dim(obj))) obj <- new("NChannelSet", R=matrix(0,10,5, dimnames=list(NULL, LETTERS[1:5])), G=matrix(0,10,5, dimnames=list(NULL, letters[1:5]))) checkTrue(all(c("R", "G") %in% channelNames(obj))) checkTrue(all(c(10,5)==dim(obj))) obj <- new("NChannelSet", R=matrix(0,10,5, dimnames=list(NULL, LETTERS[1:5])), G=matrix(0,10,5)) checkTrue(all(c("R", "G") %in% channelNames(obj))) checkTrue(all(c(10,5)==dim(obj))) obj <- new("NChannelSet", R=matrix(0,10,5), G=matrix(0,10,5, dimnames=list(NULL, LETTERS[1:5]))) checkTrue(all(c("R", "G") %in% channelNames(obj))) checkTrue(all(c(10,5)==dim(obj))) } testNew4 <- function() { ## no assayData, zero-row phenoData data <- data.frame(x=numeric(), y=numeric(), z=numeric()) varMetadata <- data.frame(labelDescription=character(ncol(data)), channel=factor(rep("_ALL_", ncol(data)))) phenoData <- new("AnnotatedDataFrame", data=data, varMetadata=varMetadata) checkTrue(validObject(new("NChannelSet", phenoData=phenoData))) } testNew5 <- function() { ## explicit assayData, phenoData R <- matrix(0, 10, 3, dimnames=list(NULL, LETTERS[1:3])) G <- matrix(1, 10, 3, dimnames=list(NULL, LETTERS[1:3])) assayData <- assayDataNew(R=R, G=G) data <- data.frame(x=numeric(ncol(R)), y=numeric(ncol(R)), z=numeric(ncol(R))) varMetadata <- data.frame(labelDescription=character(ncol(data)), channel=factor(rep("_ALL_", ncol(data)), levels=c("R", "G", "_ALL_"))) phenoData <- new("AnnotatedDataFrame", data=data, varMetadata=varMetadata) obj <- new("NChannelSet", assayData=assayData, phenoData=phenoData) checkTrue(nrow(varMetadata)==ncol(data)) checkTrue(all(varMetadata(obj)[["channel"]] == "_ALL_")) } testNew5a <- function() { ## explicit assayData, phenoData; no names R <- matrix(0, 10, 5) G <- matrix(1, 10, 5) assayData <- assayDataNew(R=R, G=G) data <- data.frame(x=numeric(ncol(R))) varMetadata <- data.frame(labelDescription=character(ncol(data)), channel=factor( rep("__ALL__", ncol(data)), levels=c("R", "G", "_ALL_"))) phenoData <- new("AnnotatedDataFrame", data=data, varMetadata=varMetadata) obj <- new("NChannelSet", assayData=assayData, phenoData=phenoData) } testNew6 <- function() { ## silently add 'channel' to varMetadata R <- matrix(0, 10, 5) G <- matrix(1, 10, 5) assayData <- assayDataNew(R=R, G=G) data <- data.frame(x=numeric(ncol(R))) phenoData <- new("AnnotatedDataFrame", data=data) obj <- new("NChannelSet", assayData=assayData, phenoData=phenoData) checkTrue(validObject(obj)) varMetadata <- data.frame(labelDescription=character(ncol(data))) phenoData <- new("AnnotatedDataFrame", data=data) obj <- new("NChannelSet", assayData=assayData, phenoData=phenoData) checkTrue(validObject(obj)) } testAssayDataGets <- function() { assayData <- assayDataNew(R = matrix(0, 10, 5), G = matrix(1,10,5)) obj <- NChannelSet(assayData = assayData) exp <- -1 * assayData(obj)[["G"]] assayDataElement(obj, "G") <- exp checkIdentical(exp, assayData(obj)[["G"]]) exp <- assayData(obj)[["R"]] assayDataElement(obj, "G") <- NULL checkIdentical("R", channelNames(obj)) checkIdentical("R", assayDataElementNames(obj)) checkIdentical(exp, assayData(obj)[["R"]]) } testDifferentSampleNames <- function() { ## channels have different identifiers assayData <- assayDataNew(R = matrix(0,10,5, dimnames=list(NULL, LETTERS[1:5])), G = matrix(1,10,5, dimnames=list(NULL, letters[1:5]))) obj <- new("NChannelSet", assayData = assayData) checkTrue(sampleNames(obj)[["R"]] == LETTERS[1:5] && sampleNames(obj)[["G"]] == letters[1:5]) } testSampleNamesUpdate <- function() { assayData <- assayDataNew(R = matrix(0,10,5), G = matrix(1,10,5)) obj <- new("NChannelSet", assayData = assayData) sampleNames(obj) <- list(R=LETTERS[1:5]) checkTrue(validObject(obj)) checkTrue(all(sampleNames(obj)[["R"]] == LETTERS[1:5])) sampleNames(obj) <- list(R=LETTERS[5:1], G=letters[5:1]) checkTrue(validObject(obj)) checkTrue(all(sampleNames(obj)[["R"]] == LETTERS[5:1]) && all(sampleNames(obj)[["G"]] == letters[5:1])) ## drop to character when smaple names identic sampleNames(obj) <- LETTERS[1:5] checkIdentical(LETTERS[1:5], sampleNames(obj)) checkIdentical(list(G=LETTERS[1:5], R=LETTERS[1:5]), eapply(assayData(obj), colnames)) checkException(sampleNames(obj) <- list(LETTERS[1:5]), silent=TRUE) # unnamed repleacement checkException(sampleNames(obj) <- list(X=LETTERS[1:5]) , silent=TRUE) # misnamed repleacement } testSelectChannels <- function() { obj <- new("NChannelSet", assayData=assayDataNew( R=matrix(0,10,5), G=matrix(1,10,5))) objR <- selectChannels(obj, "R") checkTrue(channelNames(objR) == "R") checkIdentical(dim(obj), dim(objR)) objRG <- selectChannels(obj, c("R", "G")) checkTrue(all(c("R", "G") %in% channelNames(objRG))) checkIdentical(dim(obj), dim(objRG)) checkException(selectChannels(obj, c("G", "G")), silent=TRUE) } testSelectChannelsCommonPhenoData <- function() { obj <- new("NChannelSet", assayData=assayDataNew( R=matrix(0,10,5), G=matrix(0,10,5)), phenoData=new("AnnotatedDataFrame", data=data.frame( r=letters[1:5], g=LETTERS[1:5], both=1:5), varMetadata=data.frame( labelDescription=c( "r data", "g data", "both data"), channel=factor( c("R", "G", "_ALL_"))))) objR <- selectChannels(obj, "R") checkIdentical("R", channelNames(objR)) checkTrue(all(c("r", "both") %in% names(pData(objR)) & !"g" %in% names(pData(objR)))) checkIdentical(c("R", "_ALL_"), levels(varMetadata(objR)[["channel"]])) objG <- selectChannels(obj, "G") checkIdentical("G", channelNames(objG)) checkTrue(all(c("g", "both") %in% names(pData(objG)) & !"r" %in% names(pData(objG)))) checkIdentical(c("G", "_ALL_"), levels(varMetadata(objG)[["channel"]])) objRG <- selectChannels(obj, c("R", "G")) checkTrue(all(c("R", "G") %in% channelNames(objRG))) checkTrue(all(c("r", "g", "both") %in% names(pData(objRG)))) checkTrue(all(c("R", "G") %in% levels(varMetadata(objRG)[["channel"]]))) } testChannel <- function() { obj <- new("NChannelSet", assayData=assayDataNew( R=matrix(1,10,5), G=matrix(2,10,5)), phenoData=new("AnnotatedDataFrame", data=data.frame( r=letters[1:5], g=LETTERS[1:5], both=1:5), varMetadata=data.frame( labelDescription=c( "r data", "g data", "both data"), channel=factor( c("R", "G", "_ALL_"))))) robj <- channel(obj, "R") checkTrue(validObject(robj)) checkTrue(all(varLabels(robj) %in% c("r", "both"))) checkIdentical(assayDataElementNames(robj), "exprs") gobj <- channel(obj, "G") checkTrue(validObject(gobj)) checkTrue(all(varLabels(gobj) %in% c("g", "both"))) checkIdentical(assayDataElementNames(gobj), "exprs") } testChannelNames_replace <- function() { obj <- NChannelSet(R=matrix(-1, 5, 5), G=matrix(1, 5, 5)) checkIdentical(c("G", "R"), channelNames(obj)) channelNames(obj) <- c(Gn="G", Rd="R") ## rename checkIdentical(c("Gn", "Rd"), channelNames(obj)) channelNames(obj) <- c("Rd", "Gn") ## reorder checkIdentical(c("Rd", "Gn"), channelNames(obj)) checkTrue(all(assayData(obj)[["Gn"]] == 1)) exp <- "'value' elements must include all channelNames()" obs <- tryCatch(channelNames(obj) <- "X", error=conditionMessage) checkIdentical(exp, obs) obs <- tryCatch(channelNames(obj) <- c(X="Gn"), error=conditionMessage) checkIdentical(exp, obs) exp <- "duplicated channelNames are not allowed" obs <- tryCatch(channelNames(obj) <- c(X="Gn", X="Rd"), error=conditionMessage) checkIdentical(exp, obs) } Biobase/inst/unitTests/test_SnpSet.R0000644000175400017540000000110413175713325020524 0ustar00biocbuildbiocbuildtestSnpSetAccessors <- function() { set.seed(1) nms <- list(paste("rs", 1:100, sep="_"), LETTERS[1:10]) m <- matrix(runif(1000), 100, dimnames=nms) n <- matrix(runif(1000), 100, dimnames=nms) sset <- new("SnpSet", call=m, callProbability=n) checkEquals(m, snpCall(sset)) checkEquals(n, snpCallProbability(sset)) m <- matrix(runif(1000), 100, dimnames=nms) n <- matrix(runif(1000), 100, dimnames=nms) snpCall(sset) <- m snpCallProbability(sset) <- n checkEquals(m, snpCall(sset)) checkEquals(n, snpCallProbability(sset)) } Biobase/inst/unitTests/test_UpdateObject.R0000644000175400017540000001361613175713325021674 0ustar00biocbuildbiocbuildtestUpdateObjectToDefaults <- function() { x <- 1:10 checkTrue(identical(1:10, updateObjectTo(x, 10:1))) x <- as.numeric(1:10) checkTrue(identical(as.integer(1:10), updateObjectTo(x, integer()))) checkTrue(!identical(as.numeric(1:10), updateObjectTo(x, integer()))) } testUpdateObjectToSetClass <- function() { setClass("A", representation(x="numeric"), prototype=prototype(x=1:10), where=.GlobalEnv) a <- new("A") a1 <- new("A",x=10:1) checkTrue(identical(a, updateObjectTo(a, a1))) setClass("B", representation(x="numeric"), where=.GlobalEnv) b <- new("B") checkException(updateObjectTo(a, b), silent=TRUE) setAs("A", "B", function(from) { b <- new("B") b@x <- from@x b }, where=.GlobalEnv) obj <- updateObjectTo(a,b) checkTrue(class(obj)=="B") checkIdentical(obj@x, a@x) removeMethod("coerce", c("A","B"), where=.GlobalEnv) removeClass("B", where=.GlobalEnv) removeClass("A", where=.GlobalEnv) } testUpdateExpressionSet <- function() { opts <- options() options(warn=-1) obj <- new("ExpressionSet") checkTrue(all.equal(obj, updateObject(obj))) checkTrue(!identical(new("ExpressionSet"), updateObject(obj))) # different environments obj <- new("ExpressionSet", storage.mode="list") checkTrue(identical(obj, updateObject(obj))) checkTrue(identical(new("ExpressionSet", storage.mode="list"), updateObject(obj))) # same class -- list data(sample.ExpressionSet) classVersion(sample.ExpressionSet)["eSet"] <- "1.0.0" checkException(validObject(sample.ExpressionSet), silent=TRUE) suppressMessages(obj <- updateObject(sample.ExpressionSet)) checkTrue(isVersioned(obj)) checkTrue(all(isCurrent(obj))) checkTrue(validObject(obj)) checkTrue(identical(lapply(ls(assayData(obj), all=TRUE), function(x) x), lapply(ls(assayData(sample.ExpressionSet),all=TRUE), function(x) x))) checkTrue(identical(annotation(obj), annotation(sample.ExpressionSet))) suppressMessages(obj1a <- updateObjectTo(sample.ExpressionSet, new("ExpressionSet"))) ## next better written as(sample.ExpressionSet, "MultiSet") suppressMessages(obj1b <- updateObjectTo(sample.ExpressionSet, new("MultiSet"))) obj2 <- updateObject(obj) # stop after eSet options(opts) } testUpdateESetMisc <- function() { opts <- options() options(warn=-1) idx <- c("phenoData", "experimentData", "featureData") fun <- function(nm) isS4(eval(parse(text=paste(nm,"(obj)", sep="")))) load(system.file("unitTests", "VersionedClass_data", "devel", "sample.exprSet.rda", package="Biobase")) suppressMessages(obj <- as(sample.exprSet, "ExpressionSet")) checkTrue(validObject(obj, complete=TRUE)) checkTrue(all(sapply(idx, fun))) load(system.file("unitTests", "VersionedClass_data", "devel", "sample.eSet.rda", package="Biobase")) obj <- as(sample.eSet, "MultiSet") checkTrue(validObject(obj, complete=TRUE)) checkTrue(all(sapply(idx, fun))) load(system.file("unitTests", "VersionedClass_data", "devel", "eset.rda", package="Biobase")) obj <- as(eset, "ExpressionSet") checkTrue(validObject(obj, complete=TRUE)) checkTrue(all(sapply(idx, fun))) options(opts) } testUpdateMiscPreviousInstances <- function() { opts <- options("warn") options(warn=-1) on.exit(options(opts)) rda <- dir(system.file("unitTests", "VersionedClass_data", package="Biobase"), full.names=TRUE, recursive=TRUE, pattern="^([^(ExpressionSet)]).*\\.Rda") ok <- sapply(rda, function(nm) { env <- new.env(parent=emptyenv()) load(nm, env) tryCatch({ eapply(env, function(elt) { suppressMessages(obj <- updateObject(elt)) checkTrue(isS4(obj)) checkTrue(validObject(obj, complete=TRUE)) }) TRUE }, error=function(...) FALSE) }) checkTrue(all(ok), msg=sprintf("failed: '%s'", paste(rda[!ok], collapse="' '"))) } testUpdatePreviousExpressionSet <- function() { opts <- options("warn") options(warn=-1) on.exit(options(opts)) rda <- dir(system.file("unitTests", "VersionedClass_data", package="Biobase"), full.names=TRUE, recursive=TRUE, pattern="^ExpressionSet.*\\.Rda") ok <- sapply(rda, function(nm) { env <- new.env(parent=emptyenv()) load(nm, env) tryCatch({ eapply(env, function(elt) { suppressMessages(obj <- updateObject(elt)) checkTrue(validObject(obj, complete=TRUE)) ## S4 idx <- c("phenoData", "experimentData", "featureData") ok <- sapply(idx, function(nm) { isS4(eval(parse(text=paste(nm,"(obj)", sep="")))) }) checkTrue(all(ok)) ## content checkIdentical(exprs(obj), slot(elt, "assayData")[["exprs"]]) checkIdentical(pData(phenoData(obj)), slot(slot(elt, "phenoData"), "data")) checkIdentical(varMetadata(phenoData(obj)), slot(slot(elt, "phenoData"), "varMetadata")) nms <- names(getSlots("MIAME")) nms <- nms[!nms %in% ".__classVersion__"] lapply(nms, function(nm) checkIdentical(slot(experimentData(obj), nm), slot(slot(elt, "experimentData"), nm))) }) TRUE }, error=function(...) FALSE) }) checkTrue(all(ok), msg=sprintf("failed: '%s'", paste(rda[!ok], collapse="' '"))) } Biobase/inst/unitTests/test_VersionedClass.R0000644000175400017540000001162713175713325022247 0ustar00biocbuildbiocbuildnonvirtualClasses <- NULL instanceDir <- system.file("unitTests", "VersionedClass_data", package="Biobase") .setUp <- function() { nms <- ls(getNamespace("Biobase"),all=TRUE) classes <- gsub(".__C__", "", nms[grep(".__C__", nms)]) classes <- classes[!classes %in% "phenoData"] isVirtual <- sapply(classes, function(nm) getClass(nm)@virtual) nonvirtualClasses <<- classes[!isVirtual] } testNewVersioned <- function() { new("Versioned") new("VersionedBiobase") ## Biobase:::.unversionedObj v <- new("Versioned", versions=list(x="1.0.0")) checkTrue(classVersion(v)["x"]=="1.0.0") ## use class definition defined in RUnit.R ## a <- new("A") ## checkTrue(all(classVersion(a) == classVersion(new("VersionedBiobase", versions=list(A="1.0.1"))))) ## checkTrue(all(a@x==10:1)) ## a <- new("A", x=1:10) ## checkTrue(all(classVersion(a) == classVersion(new("VersionedBiobase", versions=list(A="1.0.1"))))) ## checkTrue(all(a@x==1:10)) ## a <- new("A", x=1:10, versions=list(x="1.0.1")) ## checkTrue(all(a@x==1:10)) ## checkTrue(all(classVersion(a) == classVersion(new("VersionedBiobase", versions=list(A="1.0.1",x="1.0.1"))))) } testIsVersioned <- function() { checkTrue(isVersioned(new("VersionedBiobase"))) checkTrue(isVersioned("VersionedBiobase")) checkTrue(!isVersioned(1:10)) } testClassVersion <- function() { classVersion(new("Versioned")) classVersion(new("VersionedBiobase")) checkTrue(is(classVersion(new("VersionedBiobase")),"Versions")) checkTrue(all(classVersion("VersionedBiobase") == classVersion(new("VersionedBiobase")))) } testClassVersionReplace <- function() { ref <- obj <- new("VersionedBiobase") classVersion(obj)["x"] <- "1.0.0" checkTrue(all(classVersion(obj)[names(classVersion(ref))] == classVersion(ref))) checkTrue(classVersion(obj)["x"] == "1.0.0") y <- new("Versions", y="1.0.1") classVersion(obj)[names(y)] <- y checkTrue(all(classVersion(obj)[names(classVersion(ref))] == classVersion(ref))) checkTrue(classVersion(obj)["x"] == "1.0.0") checkTrue(classVersion(obj)["y"] == "1.0.1") checkTrue(classVersion(obj)["y"] != "1.0.0") obj <- ref classVersion(obj) <- y checkTrue(classVersion(obj)["y"] == "1.0.1") } testClassVersionSubset <- function() { obj <- new("Versions", x="1.0.0") checkTrue(obj[1]=="1.0.0") checkTrue(obj["x"]=="1.0.0") checkException(obj["y"], silent=TRUE) } testClassVersionCompare <- function() { obj <- new("Versions", x="1.0.0", y="2.0.1") checkTrue(all(obj == c(x="1.0.0", y="2.0.1"))) checkTrue(all(obj == c(y="2.0.1", x="1.0.0")), msg="versions in different order") checkTrue(!any(obj == c(y="1.0.0", x="2.0.1")), msg="incorrectly named elements") checkTrue(!all(obj == c(y="1.0.0", x="1.0.0")), msg="one element incorrect elements") checkException(all(obj == c(x="1.0.0", z="2.0.1")), msg="different version elements", silent=TRUE) checkException(obj == c(x="1.0.0"), msg="different version lengths", silent=TRUE) ## as above, but comparing version objects checkTrue(all(obj == new("Versions", x="1.0.0", y="2.0.1"))) checkTrue(all(obj == new("Versions", y="2.0.1", x="1.0.0"))) checkTrue(!any(obj == new("Versions", x="2.0.1", y="1.0.0"))) checkTrue(!all(obj == new("Versions", x="1.0.0", y="1.0.0"))) checkException(all(obj == new("Versions", x="1.0.0", z="2.0.1")), msg="different version elements", silent=TRUE) checkException(obj == new("Versions", x="1.0.0"), msg="different version lengths", silent=TRUE) } testIsCurrent <- function() { checkTrue(is.na(isCurrent(1:10))) checkTrue(all(isCurrent(new("VersionedBiobase")))) } testDevelInstanceArchived <- function() { ## archived devel instance? instances <- sub(".Rda", "", list.files(path=file.path(instanceDir, "devel"), pattern=".*.Rda")) checkTrue(all(nonvirtualClasses %in% instances), msg=paste(nonvirtualClasses[!nonvirtualClasses %in% instances], collapse=" ")) } testDevelInstanceIsCurrent <- function() { ## overall class is current instanceEnv <- new.env(parent=emptyenv()) lapply(nonvirtualClasses, function(cls) { cls <- paste(cls, ".Rda", sep="") load(file.path(instanceDir, "devel", cls), instanceEnv) }) instances <- sub(".Rda", "", list.files(path=file.path(instanceDir, "devel"), pattern=".*.Rda")) instances <- instances[!instances %in% "Versioned"] current <- sapply(instances, function(obj) { vers <- isCurrent(get(obj, env=instanceEnv))[c("S4", obj)] all(vers[!is.na(vers)]) }) currentv <- current[!is.na(current)] checkTrue(all(currentv), msg=paste(names(currentv)[!currentv], collapse=" ")) } Biobase/inst/unitTests/test_cache.R0000644000175400017540000000166713175713325020371 0ustar00biocbuildbiocbuildtest_cache_basic <- function() { pre <- "tmp_R_TEST_" cfile <- file.path(tempdir(), paste(pre, "theVar.RData", sep="")) on.exit(file.remove(cfile), add=TRUE) expensive <- function(n) n + 1 cache(theVar <- expensive(5), dir=tempdir(), prefix=pre) checkEquals(6, theVar) checkTrue(file.exists(cfile)) ## call again remove(theVar) cache(theVar <- expensive(5), dir=tempdir(), prefix=pre) checkEquals(6, theVar) } test_cache_infunc <- function() { pre <- "tmp_R_TEST_" cfile <- file.path(tempdir(), paste(pre, "theVar.RData", sep="")) on.exit(file.remove(cfile), add=TRUE) expensive <- function(n) n + 1 aFunc <- function() { m <- 1 cache(theVar <- expensive(m), dir=tempdir(), prefix=pre) theVar } val <- aFunc() checkEquals(2, val) checkTrue(file.exists(cfile)) ## call again remove(val) val <- aFunc() checkEquals(2, val) } Biobase/inst/unitTests/test_checkClass.R0000644000175400017540000000026413175713325021361 0ustar00biocbuildbiocbuildtestCheckData_S3ExtendedDataFrame<- function() { df <- data.frame(foo=1:2) class(df) = c("bar", class(df)) Biobase:::checkClass(df, "data.frame") checkTrue(TRUE) } Biobase/inst/unitTests/test_combine.R0000644000175400017540000000076713175713325020742 0ustar00biocbuildbiocbuildtestCombineOne <- function() { data(sample.ExpressionSet) checkIdentical(sample.ExpressionSet, combine(sample.ExpressionSet)) } testCombineTwo <- function() { data(sample.ExpressionSet) x <- sample.ExpressionSet checkTrue(all.equal(x, combine(x[,1:5],x[,seq(6, ncol(x))]))) } testCombineThree <- function() { data(sample.ExpressionSet) x <- sample.ExpressionSet y <- combine(x[,1:5],x[, 6:10], x[,seq(11, ncol(x))]) checkTrue(all.equal(x, y)) } Biobase/inst/unitTests/test_copyEnv.R0000644000175400017540000000062313175713325020740 0ustar00biocbuildbiocbuildbasic_test <- function() { env1 <- new.env(hash=TRUE, parent=emptyenv()) env1$a <- 1:3 env1$b <- "foo" env1[[".hidden"]] <- 3.1 z <- copyEnv(env1) checkEquals(env1$a, z$a) checkEquals(env1$b, z$b) checkTrue(!exists(".hidden", z)) z <- copyEnv(env1, all.names=TRUE) checkEquals(env1[[".hidden"]], z[[".hidden"]]) env1$a[1] <- 10L checkEquals(1L, z$a[1]) } Biobase/inst/unitTests/test_esApply.R0000644000175400017540000000406013175713325020731 0ustar00biocbuildbiocbuildtest_esApply_base <- function() { data(sample.ExpressionSet) target <- with(pData(sample.ExpressionSet), apply(exprs(sample.ExpressionSet), 1, sum)) current <- esApply(sample.ExpressionSet, 1, sum) checkIdentical(target, current) } test_esApply_lexical_scope <- function() { data(sample.ExpressionSet) f <- function() { x <- 0 function(y) x <<- x + 1 } target <- with(pData(sample.ExpressionSet), apply(exprs(sample.ExpressionSet), 1, f())) current <- esApply(sample.ExpressionSet, 1, f()) checkIdentical(target, current) } test_esApply_local_scope <- function() { data(sample.ExpressionSet) target <- with(pData(sample.ExpressionSet), apply(exprs(sample.ExpressionSet), 1, function(x) { xx <- split(x, sex) mean(xx[[1]]) - mean(xx[[2]]) })) current <- esApply(sample.ExpressionSet, 1, function(x) { xx <- split(x, sex) mean(xx[[1]]) - mean(xx[[2]]) }) checkIdentical(target, current) f <- function(x) { xx <- split(x, sex) mean(xx[[1]]) - mean(xx[[2]]) } current <- esApply(sample.ExpressionSet, 1, f) checkIdentical(target, current) f <- function(x, s) { xx <- split(x, s) mean(xx[[1]])-mean(xx[[2]]) } sex=sample.ExpressionSet[["sex"]] current <- esApply(sample.ExpressionSet, 1, f, s=sex) checkIdentical(target, current) } test_esApply_global_args <- function() { data(sample.ExpressionSet) f <- function(x, t) t*sum(x) target <- with(pData(sample.ExpressionSet), apply(exprs(sample.ExpressionSet), 1, f, 10)) current <- esApply(sample.ExpressionSet, 1, f, 10) checkIdentical(target, current, msg="unnamed global arg") current <- esApply(sample.ExpressionSet, 1, f, t=10) checkIdentical(target, current, msg="named global arg") } Biobase/inst/unitTests/test_subListExtract.R0000644000175400017540000000356313175713325022303 0ustar00biocbuildbiocbuildlibrary("Biobase") ## simple test list innerL <- list(i=4L, d=1.23, l=FALSE, n=NULL, na=NA, s="foo", c=3+4i, r=charToRaw("g")) len <- 20L L <- rep(list(innerL), len) names(L) <- paste("X", 1:len, sep="") ## unit tests for basic API test_extract_all_types <- function() { for (w in names(innerL)) { if (is.null(innerL[[w]])) want <- vector(mode="list", length=len) else want <- as.list(rep(innerL[[w]], len)) names(want) <- names(L) checkEquals(want, subListExtract(L, w)) } } test_simplify_extract_all_types <- function() { for (w in names(innerL)) { if (is.null(innerL[[w]])) next else want <- rep(innerL[[w]], len) names(want) <- names(L) checkEquals(want, subListExtract(L, w, simplify=TRUE), msg=paste("extracting", w)) } } test_basic_extract <- function() { want <- as.list(rep(4L, len)) names(want) <- names(L) checkEquals(want, subListExtract(L, "i")) checkEquals(names(L), names(subListExtract(L, "i"))) checkEquals(NULL, names(subListExtract(L, "i", keep.names=FALSE))) } test_simplify_extract <- function() { want <- rep(4L, len) names(want) <- names(L) checkEquals(want, subListExtract(L, "i", simplify=TRUE)) } test_simplify_fails_extract <- function() { L[[1]] <- list(d=matrix(1:10, ncol=2)) checkException(subListExtract(L, "i", simplify=TRUE), silent=TRUE) } test_extract_bad_inner <- function() { L[[3]] <- list(foo=1) checkException(subListExtract(L, "i"), silent=TRUE) } test_extract_from_empty <- function() { checkEquals(list(), subListExtract(list(), "foo")) ## but you can't simplify checkException(subListExtract(list(), "foo", simplify=TRUE)) } Biobase/inst/unitTests/test_unsaveSetSlot.R0000644000175400017540000000377013175713325022142 0ustar00biocbuildbiocbuild## Use of unsafeSetSlot is currently 'safe' inside a repelacement ## method, because under specific conditions the object is duplicated ## (referenced exactly once) on the way in. This test tries to catch ## any changes to R that eliminate this duplication, and hence ## invalidates the unsafe slot assignments used in Biobase testUnsafeSetSlotInSlotAssignment1 <- function() { ## calls like set(x) <- value setClass("A", representation=representation(x="numeric"), where=.GlobalEnv) on.exit(removeClass("A", .GlobalEnv)) setGeneric("set<-", function(object, value) standardGeneric("set<-"), where=.GlobalEnv) setReplaceMethod("set", signature=signature(object="A"), function(object, value) { Biobase:::unsafeSetSlot(object, "x", value) }, where=.GlobalEnv) on.exit(removeMethod("set<-", c(object="A"), .GlobalEnv)) on.exit(removeGeneric("set<-", .GlobalEnv)) b <- a <- new("A", x=1:10) set(a) <- 10:1 checkIdentical(a@x, 10:1) checkIdentical(b@x, 1:10) } testUnsafeSetSlotInSlotAssignment2 <- function() { ## calls like x <- "set<-"(x, value) setClass("A", representation=representation(x="numeric"), where=.GlobalEnv) on.exit(removeClass("A", .GlobalEnv)) setGeneric("set<-", function(object, value) standardGeneric("set<-"), where=.GlobalEnv) setReplaceMethod("set", signature=signature(object="A"), function(object, value) { object@x <- value Biobase:::unsafeSetSlot(object, "x", value) }, where=.GlobalEnv) on.exit(removeMethod("set<-", c(object="A"), .GlobalEnv)) on.exit(removeGeneric("set<-", .GlobalEnv)) b <- a <- new("A", x=1:10) a <- "set<-"(a, 10:1) checkIdentical(a@x, 10:1) checkIdentical(b@x, 1:10) } Biobase/inst/unitTests/utilities.R0000644000175400017540000000235113175713325020271 0ustar00biocbuildbiocbuild## these assume we're in Biobase/inst/unitTests createCurrentInstances <- function(instanceDir = "VersionedClass_data") { require("Biobase") classes <- getClasses("package:Biobase") isVirtual <- sapply(classes, function(nm) getClass(nm)@virtual) nonvirtualClasses <- classes[!isVirtual] instances <- sub(".Rda", "", list.files(path=file.path(instanceDir, "devel"), pattern=".*.Rda")) need <- nonvirtualClasses[!nonvirtualClasses %in% instances] if (length(need)!=0) { cat("need:", need, "\n") lapply(need, function(cls) { cat("creating", cls, "\n") assign(cls, new(cls)) save(list=cls, file=file.path(instanceDir, "devel", paste(cls, ".Rda", sep=""))) }) } else cat("no instances need creating\n") } createComponentClasses <- function(ExpressionSet, vers="devel", instanceDir = "VersionedClass_data") { MIAME <- experimentData(ExpressionSet) AnnotatedDataFrame <- phenoData(ExpressionSet) cat("creating MIAME\n") save(MIAME, file=file.path(instanceDir, vers, "MIAME.Rda")) cat("creating AnnotatedDataFrame\n") save(AnnotatedDataFrame, file=file.path(instanceDir, vers, "AnnotatedDataFrame.Rda")) } Biobase/man/0000755000175400017540000000000013175713325013726 5ustar00biocbuildbiocbuildBiobase/man/Aggregate.Rd0000644000175400017540000000230213175713325016100 0ustar00biocbuildbiocbuild\name{Aggregate} \alias{Aggregate} \title{A Simple Aggregation Mechanism. } \description{ Given an environment and an aggregator (an object of class \code{aggregate} simple aggregations are made. } \usage{ Aggregate(x, agg) } \arguments{ \item{x}{ The data to be aggregated. } \item{agg}{The aggregator to be used. } } \details{ Given some data, \code{x} the user can accumulate (or aggregate) information in \code{env} using the two supplied functions. See the accompanying documentation for a more complete example of this function and its use. } \value{ No value is returned. This function is evaluated purely for side effects. The symbols and values in \code{env} are altered. } \author{R. Gentleman } \seealso{ \code{\link{new.env}}, \code{\link{class:aggregator}} } \examples{ agg1 <- new("aggregator") Aggregate(letters[1:10], agg1) # the first 10 letters should be symbols in env1 with values of 1 Aggregate(letters[5:11], agg1) # now letters[5:10] should have value 2 bb <- mget(letters[1:11], env=aggenv(agg1), ifnotfound=NA) t1 <- as.numeric(bb); names(t1) <- names(bb) t1 # a b c d e f g h i j k # 1 1 1 1 2 2 2 2 2 2 1 } \keyword{programming} \keyword{methods} Biobase/man/Biobase-package.Rd0000644000175400017540000000236413175713325017157 0ustar00biocbuildbiocbuild\name{Biobase-package} \alias{Biobase-package} \alias{Biobase} \docType{package} \title{Biobase Package Overview} \description{ Biobase Package Overview } \details{ Important data classes: \code{\link{ExpressionSet}}, \code{\link{AnnotatedDataFrame}} \code{\link{MIAME}}. Full help on methods and associated functions is available from within class help pages. Additional data classes: \code{\link{eSet}}, \code{\link{MIAxE}}, \code{\link{MultiSet}}. Additional manipulation and data structuring classes: \code{\link{Versioned}}, \code{\link{VersionedBiobase}}, \code{\link{aggregator}}, \code{\link{container}}. Vignette routines: \code{\link{openVignette}}, \code{\link{getPkgVigs}}, \code{\link{openPDF}}. Package manipulation functions: \code{\link{createPackage}} and \code{\link{package.version}} Data sets: \code{\link{aaMap}}, \code{\link{sample.ExpressionSet}}, \code{\link{geneData}}. Introductory information is available from vignettes, type \code{openVignette()}. Full listing of documented articles is available in HTML view by typing \code{help.start()} and selecting \code{Biobase} package from the \code{Packages} menu or via \code{library(help="Biobase")}. } \author{ O. Sklyar } \keyword{package} Biobase/man/ScalarObject-class.Rd0000644000175400017540000000227113175713325017656 0ustar00biocbuildbiocbuild\name{ScalarObject-class} \docType{class} \alias{ScalarObject-class} \alias{ScalarCharacter-class} \alias{ScalarLogical-class} \alias{ScalarInteger-class} \alias{ScalarNumeric-class} \alias{mkScalar} \alias{show,ScalarObject-method} \alias{show,ScalarCharacter-method} \title{Utility classes for length one (scalar) objects} \usage{ mkScalar(obj) } \arguments{ \item{obj}{An object of type \code{character}, \code{logical}, \code{integer}, or \code{double}} } \description{ These classes represent scalar quantities, such as a string or a number and are useful because they provide their own validity checking. The classes \code{ScalarCharacter}, \code{ScalarLogical}, \code{ScalarInteger}, and \code{ScalarNumeric} all extend their respective base vector types and can be used interchangeably (except they should always have length one). The \code{mkScalar} factory function provides a convenient way of creating \code{Scalar} objects (see the examples section below). } \author{Seth Falcon} \examples{ v <- list(mkScalar("a single string"), mkScalar(1), mkScalar(1L), mkScalar(TRUE)) sapply(v, class) sapply(v, length) } \keyword{classes} Biobase/man/abstract.Rd0000644000175400017540000000231613175713325016022 0ustar00biocbuildbiocbuild\name{abstract} \alias{abstract} \alias{pubMedIds} \alias{pubMedIds<-} \alias{experimentData} \alias{experimentData<-} \title{Retrieve Meta-data from eSets and ExpressionSets.} \description{ These generic functions access generic data, abstracts, PubMed IDs and experiment data from instances of the \code{\link{eSet-class}} or \code{\link{ExpressionSet-class}}. } \usage{ abstract(object) pubMedIds(object) pubMedIds(object) <- value experimentData(object) experimentData(object) <- value } \arguments{ \item{object}{Object, possibly derived from \code{eSet-class} or \code{MIAME-class}} \item{value}{Value to be assigned; see class of \code{object} (e.g., \code{\link{eSet-class}}) for specifics.} } \value{ \code{abstract} returns a character vector containing the abstract (as in a published paper) associated with \code{object}. \code{pubMedIds} returns a character vector of PUBMED IDs associated with the experiment. \code{experimentData} returns an object representing the description of an experiment, e.g., an object of \code{\link{MIAME-class}} } \author{Biocore} \seealso{\code{\link{ExpressionSet-class}}, \code{\link{eSet-class}}, \code{\link{MIAME-class}}} \keyword{manip} Biobase/man/addVig2Menu.Rd0000644000175400017540000000165113175713325016325 0ustar00biocbuildbiocbuild\name{addVigs2WinMenu} \alias{addVigs2WinMenu} \concept{addVig2Menu} \concept{addVig4Win} \concept{addVig4Unix} \concept{addNonExisting} \concept{addPDF2Vig} \title{Add Menu Items to an Existing/New Menu of Window} \description{ This function adds a menu item for a package's vignettes. } \usage{ addVigs2WinMenu(pkgName) } \arguments{ \item{pkgName}{\code{pkgName} - a character string for the name of an R package} } \details{ The original functions \code{addVig2Menu}, \code{addVig4Win}, \code{addVig4Unix}, \code{addNonExisting}, \code{addPDF2Vig} have been replaced by \code{addVigs2WinMenu}, please use those instead. } \value{ The functions do not return any value. } \author{Jianhua Zhang and Jeff Gentry} \examples{ # Only works for windows now if(interactive() && .Platform$OS.type == "windows" && .Platform$GUI == "Rgui"){ addVigs2WinMenu("Biobase") } } \keyword{interface} Biobase/man/annotatedDataFrameFrom-methods.Rd0000644000175400017540000000245013175713325022225 0ustar00biocbuildbiocbuild\name{annotatedDataFrameFrom-methods} \docType{methods} \alias{annotatedDataFrameFrom} \alias{annotatedDataFrameFrom,AssayData-method} \alias{annotatedDataFrameFrom,matrix-method} \alias{annotatedDataFrameFrom,NULL-method} \title{Methods for Function annotatedDataFrameFrom in Package `Biobase'} \description{ \code{annotatedDataFrameFrom} is a convenience for creating \code{\link{AnnotatedDataFrame}} objects. } \section{Methods}{ Use the method with \code{annotatedDataFrameFrom(object, byrow=FALSE, ...)}; the argument \code{byrow} \emph{must} be specified. \describe{ \item{\code{signature(object="assayData")}}{This method creates an \code{AnnotatedDataFrame} using sample (when \code{byrow=FALSE}) or feature (\code{byrow=TRUE}) names and dimensions of an \code{\link{AssayData}} object as a template.} \item{\code{signature(object="matrix")}}{This method creates an \code{AnnotatedDataFrame} using column (when \code{byrow=FALSE}) or row (\code{byrow=TRUE}) names and dimensions of a \code{\link{matrix}} object as a template.} \item{\code{signature(object="NULL")}}{This method (called with 'NULL' as the object) creates an empty \code{AnnotatedDataFrame}; provides \code{dimLabels} based on value of \code{byrow}.} }} \author{Biocore team} \keyword{methods} Biobase/man/anyMissing.Rd0000644000175400017540000000133213175713325016335 0ustar00biocbuildbiocbuild\name{anyMissing} \alias{anyMissing} \title{Checks if there are any missing values in an object or not} \description{ Checks if there are any missing values in an object or not. } \usage{anyMissing(x=NULL)} \arguments{ \item{x}{A \code{\link[base]{vector}}.} } \value{ Returns \code{\link[base:logical]{TRUE}} if a missing value was detected, otherwise \code{\link[base:logical]{FALSE}}. } \details{ The implementation of this method is optimized for both speed and memory. } \author{Henrik Bengtsson (\url{http://www.braju.com/R/})} \examples{ x <- rnorm(n=1000) x[seq(300,length(x),by=100)] <- NA stopifnot(anyMissing(x) == any(is.na(x))) } \keyword{iteration} \keyword{logic} Biobase/man/assayData.Rd0000644000175400017540000000152213175713325016127 0ustar00biocbuildbiocbuild\name{assayData} \alias{assayData} \alias{assayData<-} \title{Retrieve assay data from eSets and ExpressionSets.} \description{ This generic function accesses assay data stored in an object derived from the \code{\link{eSet}} or \code{\link{ExpressionSet}} class. } \usage{ assayData(object) assayData(object) <- value } \arguments{ \item{object}{Object derived from class eSet} \item{value}{Named list or environment containing one or more matrices with identical dimensions} } \value{ \code{assayData} applied to \code{eSet}-derived classes returns a list or environment; applied to \code{ExpressionSet}, the method returns an environment. See the class documentation for specific details. } \author{Biocore} \seealso{\code{\link{eSet-class}}, \code{\link{ExpressionSet-class}}, \code{\link{SnpSet-class}}} \keyword{manip} Biobase/man/cache.Rd0000644000175400017540000000506613175713325015267 0ustar00biocbuildbiocbuild\name{cache} \alias{cache} \docType{methods} \title{Evaluate an expression if its value is not already cached.} \description{ Cache the evaluation of an expression in the file system. } \usage{ cache(expr, dir=".", prefix="tmp_R_cache_") } \arguments{ \item{expr}{An expression of the form \code{LHS <- RHS}, Where \code{LHS} is a variable name, \code{RHS} is any valid expression, and \code{<-} must be used (\code{=} will not work).} \item{dir}{A string specifying the directory into which cache files should be written (also where to go searching for an appropriate cache file).} \item{prefix}{A string giving the prefix to use when naming and searching for cache files. The default is \code{"tmp_R_cache_"}} } \details{ This function can be useful during the development of computationally intensive workflows, for example in vignettes or scripts. The function uses a cache file in \code{dir} which defaults to the current working directory whose name is obtained by \code{paste(prefix, name, ".RData", sep="")}. When \code{cache} is called and the cache file exists, it is loaded and the object whose name is given on the left of \code{<-} in \code{expr} is returned. In this case, \code{expr} is \emph{not} evaluted. When \code{cache} is called and the cache file does not exist, \code{expr} is evaluted, its value is saved into a cache file, and then its value is returned. The \code{expr} argument must be of the form of \code{someVar <- {expressions}}. That is, the left hand side must be a single symbol name and the next syntactic token must be \code{<-}. To flush the cache and force recomputation, simply remove the cache files. You can use \code{\link{file.remove}} to do this. } \value{ The (cached) value of \code{expr}. } \author{ Wolfgang Huber, \email{huber@ebi.ac.uk} Seth Falcon, \email{sfalcon@fhcrc.org} } \section{Note}{ The first version of this function had a slightly different interface which is no longer functional. The old version has arguments \code{name} and \code{expr} and the intended usage is: \code{foo <- cache("foo", expr)}. } \examples{ bigCalc <- function() runif(10) cache(myComplicatedObject <- bigCalc()) aCopy <- myComplicatedObject remove(myComplicatedObject) cache(myComplicatedObject <- bigCalc()) stopifnot(all.equal(myComplicatedObject, aCopy)) allCacheFiles <- list.files(".", pattern="^tmp_R_cache_.*\\\\.RData$", full.name=TRUE) file.remove(allCacheFiles) } \keyword{manip} \keyword{array} Biobase/man/channel.Rd0000644000175400017540000000135013175713325015624 0ustar00biocbuildbiocbuild\name{channel} \alias{channel} \title{Create a new ExpressionSet instance by selecting a specific channel} \description{ This generic function extracts a specific element from an object, returning a instance of the ExpressionSet class. } \usage{ channel(object, name, ...) } \arguments{ \item{object}{An S4 object, typically derived from class \code{\link{eSet}}} \item{name}{The name of the channel, a (length one) character vector.} \item{...}{Additional arguments.} } \value{ An instance of class \code{\link{ExpressionSet}}. } \author{Biocore} \examples{ obj <- NChannelSet( R=matrix(runif(100), 20, 5), G=matrix(runif(100), 20, 5)) ## G channel as ExpressionSet channel(obj, "G") } \keyword{manip} Biobase/man/channelNames.Rd0000644000175400017540000000274413175713325016620 0ustar00biocbuildbiocbuild\name{channelNames} \alias{channelNames} \alias{channelNames<-} \title{Retrieve and set channel names from object} \description{ This generic function reports or updates the channels in an object. } \usage{ channelNames(object, ...) channelNames(object, ...) <- value } \arguments{ \item{object}{An S4 object, typically derived from class \code{\link{eSet}}} \item{value}{Replacement value, either a character vector (to re-order existing channel names or a named character vector or list (to change channel names from the vector elements to the corresponding names).} \item{...}{Additional argument, not currently used.} } \details{ \code{channelNames} returns the names of the channels in a defined order. Change the order using the replacement method with a permuation of the channel names as \code{value}. Rename channels using the replacement method with a named list, where the vector elements are a permutation of the current channels, with corresponding names the new identifier for the channel. } \value{ \code{character}. } \author{Biocore} \examples{ ## channelNames default to alphabetical order of channels obj <- NChannelSet( R=matrix(runif(100), 20, 5), G=matrix(-runif(100), 20, 5)) channelNames(obj) channelNames(obj) <- c(Gn="G", Rd="R") ## rename channelNames(obj) channelNames(obj) <- c("Rd", "Gn") ## reorder channelNames(obj) all(assayData(obj)[["Gn"]] <= 0) all(assayData(obj)[["Rd"]] >= 0) } \keyword{manip} Biobase/man/class.AnnotatedDataFrame.Rd0000644000175400017540000002141313175713325021004 0ustar00biocbuildbiocbuild\name{AnnotatedDataFrame} \docType{class} \alias{class:AnnotatedDataFrame} \alias{AnnotatedDataFrame} \alias{AnnotatedDataFrame-class} \alias{AnnotatedDataFrame,missing,missing-method} \alias{AnnotatedDataFrame,data.frame,missing-method} \alias{AnnotatedDataFrame,data.frame,data.frame-method} \alias{dimLabels} \alias{dimLabels<-} \alias{[,AnnotatedDataFrame-method} \alias{[[<-,AnnotatedDataFrame-method} \alias{[[,AnnotatedDataFrame-method} \alias{$<-,AnnotatedDataFrame-method} \alias{$,AnnotatedDataFrame-method} \alias{coerce,AnnotatedDataFrame,data.frame-method} \alias{combine,AnnotatedDataFrame,AnnotatedDataFrame-method} \alias{initialize,AnnotatedDataFrame-method} \alias{coerce,data.frame,AnnotatedDataFrame-method} \alias{coerce,phenoData,AnnotatedDataFrame-method} \alias{head.AnnotatedDataFrame} \alias{tail.AnnotatedDataFrame} \alias{dim,AnnotatedDataFrame-method} \alias{dimnames,AnnotatedDataFrame-method} \alias{dimnames<-,AnnotatedDataFrame-method} \alias{dimLabels,AnnotatedDataFrame-method} \alias{dimLabels<-,AnnotatedDataFrame,character-method} \alias{ncol,AnnotatedDataFrame-method} \alias{pData<-,AnnotatedDataFrame,data.frame-method} \alias{pData,AnnotatedDataFrame-method} \alias{varMetadata<-,AnnotatedDataFrame,data.frame-method} \alias{varMetadata,AnnotatedDataFrame-method} \alias{sampleNames<-,AnnotatedDataFrame,ANY-method} \alias{sampleNames,AnnotatedDataFrame-method} \alias{featureNames,AnnotatedDataFrame-method} \alias{featureNames<-,AnnotatedDataFrame-method} \alias{show,AnnotatedDataFrame-method} \alias{updateObject,AnnotatedDataFrame-method} \alias{varLabels<-,AnnotatedDataFrame-method} \alias{varLabels,AnnotatedDataFrame-method} \title{ Class Containing Measured Variables and Their Meta-Data Description. } \description{ An \code{AnnotatedDataFrame} consists of two parts. There is a collection of samples and the values of variables measured on those samples. There is also a description of each variable measured. The components of an \code{AnnotatedDataFrame} can be accessed with \code{\link{pData}} and \code{\link{varMetadata}}. } \section{Extends}{ Versioned } \section{Creating Objects}{ \code{AnnotatedDataFrame(data, varMetadata, dimLabels=c("rowNames", "columnNames"), ...)} \code{AnnotatedDataFrame} instances are created using \code{AnnotatedDataFrame}. The function can take three arguments, \code{data} is a \code{data.frame} of the samples (rows) and measured variables (columns). \code{varMetadata} is a \code{data.frame} with the number of rows equal to the number of columns of the \code{data} argument. \code{varMetadata} describes aspects of each measured variable. \code{dimLabels} provides aesthetic control for labeling rows and columns in the \code{show} method. \code{varMetadata} and \code{dimLabels} can be missing. \code{as(data.frame, "AnnotatedDataFrame")} coerces a \code{data.frame} to an \code{AnnotatedDataFrame}. \code{\link{annotatedDataFrameFrom}} may be a convenient way to create an \code{AnnotatedDataFrame} from \code{\link{AssayData-class}}. } \section{Slots}{ Class-specific slots: \describe{ \item{\code{data}:}{A \code{data.frame} containing samples (rows) and measured variables (columns).} \item{\code{dimLabels}:}{A \code{character} vector of length 2 that provides labels for the rows and columns in the \code{show} method.} \item{\code{varMetadata}:}{A \code{data.frame} with number of rows equal number of columns in \code{data}, and at least one column, named \code{labelDescription}, containing a textual description of each variable.} \item{\code{.__classVersion__}:}{A \code{Versions} object describing the R and Biobase version numbers used to created the instance. Intended for developer use.} } } \section{Methods}{ Class-specific methods. \describe{ \item{\code{as(annotatedDataFrame, "data.frame")}}{Coerce objects of \code{AnnotatedDataFrame} to \code{data.frame}.} \item{\code{combine(, }:}{Bind data from one \code{AnnotatedDataFrame} to a second \code{AnnotatedDataFrame}, returning the result as an \code{AnnotatedDataFrame}. Row (sample) names in each argument must be unique. Variable names present in both arguments occupy a single column in the resulting \code{AnnotatedDataFrame}. Variable names unique to either argument create columns with values assigned for those samples where the variable is present. \code{varMetadata} in the returned \code{AnnotatedDataFrame} is updated to reflect the combination.} \item{\code{pData()}, \code{pData()<-}:}{Set and retrieve the data (samples and variables) in the \code{AnnotatedDataFrame}} \item{\code{varMetadata()}, \code{varMetadata()<-}:}{Set and retrieve the meta-data (variables and their descriptions) in the \code{AnnotatedDataFrame}} \item{\code{featureNames()}, \code{featureNames()<-}:}{Set and retrieve the feature names in \code{AnnotatedDataFrame}; a synonym for \code{sampleNames}.} \item{\code{sampleNames()}, \code{sampleNames()<-}:}{Set and retrieve the sample names in \code{AnnotatedDataFrame}} \item{\code{varLabels()}, \code{varLabels()<-}:}{Set and retrieve the variable labels in the \code{AnnotatedDataFrame}} \item{ \code{dimLabels()}, \code{dimLabels() <- }}{Retrieve labels used for display of \code{AnnotatedDataFrame}, e.g., \sQuote{rowNames}, \sQuote{columnNames}.} } Standard generic methods: \describe{ \item{\code{initialize()}:}{Object instantiation, used by \code{new}; not to be called directly by the user.} \item{\code{as(, "AnnotatedDataFrame")}:}{Convert a \code{data.frame} to an AnnotatedDataFrame.} \item{\code{as(,)}:}{Convert old-style \code{phenoData-class} objects to \code{AnnotatedDataFrame}, issuing warnings as appropriate.} \item{\code{validObject()}:}{Validity-checking method, ensuring coordination between \code{data} and \code{varMetadata} elements} \item{\code{updateObject(object, ..., verbose=FALSE)}}{Update instance to current version, if necessary. See \code{\link{updateObject}}} \item{\code{isCurrent(object)}}{Determine whether version of object is current. See \code{\link{isCurrent}}} \item{\code{isVersioned(object)}}{Determine whether object contains a 'version' string describing its structure . See \code{\link{isVersioned}}} \item{\code{show()}}{Abbreviated display of object} \item{\code{[,}:}{Subset operation, taking two arguments and indexing the sample and variable. Returns an \code{AnnotatedDataFrame}, i.e., including relevant metadata. Unlike a \code{data.frame}, setting \code{drop=TRUE} generates an error. } \item{\code{[[}, \code{$}:}{Selector returning a variable (column of \code{pData}).} \item{\code{[[, ...]]<-}, \code{$ <- }:}{Replace or add a variable to \code{pData}. ... can include named arguments (especially \code{labelDescription}) to be added to \code{varMetadata}.} \item{\code{head(, n = 6L, ...)}, \code{tail(, n=6L, ...)}}{Select the first (last for tail) \code{n} rows; negative \code{n} returns the first (last) \code{nrow() - n} rows.} \item{\code{dim()}, \code{ncol()}:}{Number of samples and variables (\code{dim}) and variables (\code{ncol}) in the argument.} \item{\code{dimnames()}, \code{rownames()}, \code{colnames()}:}{row and column names.} } } \author{V.J. Carey, after initial design by R. Gentleman } \seealso{ \code{\link{eSet}}, \code{\link{ExpressionSet}}, \code{\link{read.AnnotatedDataFrame}} } \examples{ df <- data.frame(x=1:6, y=rep(c("Low", "High"),3), z=I(LETTERS[1:6]), row.names=paste("Sample", 1:6, sep="_")) metaData <- data.frame(labelDescription=c( "Numbers", "Factor levels", "Characters")) AnnotatedDataFrame() AnnotatedDataFrame(data=df) AnnotatedDataFrame(data=df, varMetadata=metaData) as(df, "AnnotatedDataFrame") obj <- AnnotatedDataFrame() pData(obj) <- df varMetadata(obj) <- metaData validObject(obj) } \keyword{classes} Biobase/man/class.AssayData.Rd0000644000175400017540000000754313175713325017204 0ustar00biocbuildbiocbuild\name{AssayData-class} \docType{class} \alias{AssayData-class} \alias{AssayData} \alias{assayData,AssayData-method} \alias{combine,AssayData,AssayData-method} \alias{featureNames,AssayData-method} \alias{featureNames<-,AssayData-method} \alias{sampleNames,AssayData-method} \alias{sampleNames<-,AssayData,ANY-method} \alias{sampleNames<-,AssayData,list-method} \alias{storageMode,AssayData-method} \alias{storageMode<-,AssayData,character-method} \alias{assayDataNew} \alias{assayDataValidMembers} \title{Class "AssayData"} \description{ Container class defined as a class union of \code{list} and \code{environment}. Designed to contain one or more matrices of the same dimension. } \section{Methods}{ \describe{ \item{combine}{\code{signature(x = "AssayData", y = "AssayData")}: This method uses \code{cbind} to create new AssayData elements that contain the samples of both arguments \code{x} and \code{y}. Both AssayData arguments to combine must have the same collection of elements. The elements must have identical numbers of rows (features). The numerical contents of any columns (samples) present in the same element of different AssayData must be identical. The storageMode of the AssayData arguments must be identical, and the function returns an AssayData with storageMode matching the incoming mode. See also \code{\link{combine,eSet,eSet-method}}} \item{featureNames}{\code{signature(object = "AssayData")}} \item{featureNames<-}{\code{signature(object = "AssayData", value = "ANY")}: Return or set the feature names as a character vector. These are the row names of the AssayData elements. \code{value} can be a character or numeric vector; all entries must be unique.} \item{sampleNames}{\code{signature(object = "AssayData")}} \item{sampleNames<-}{\code{signature(object = "AssayData", value="ANY")}: Return or set the sample names. These are the column names of the the AssayData elements and the row names of \code{phenoData}. \code{value} can be a character or numeric vector.} \item{storageMode}{\code{signature(object = "AssayData")}} \item{storageMode<-}{\code{signature(object = "AssayData", value="character")}: Return or set the storage mode for the instance. \code{value} can be one of three choices: \code{"lockedEnvironment"}, \code{"environment"}, and \code{"list"}. Environments offer a mechanism for storing data that avoids some of the copying that occurs when using lists. Locked environment help to ensure data integrity. Note that environments are one of the few R objects that are pass-by-reference. This means that if you modify a copy of an environment, you also modify the original. For this reason, we recommend using lockedEnvironment whenever possible. } } Additional functions operating on \code{AssayData} include: \describe{ \item{assayData[[name]]}{Select element \code{name} from \code{assayData}.} \item{assayDataNew(storage.mode = c("lockedEnvironment", "environment", "list"), ...)}{Use \code{storage.mode} to create a new list or environment containing the named elements in \code{...}} \item{assayDataValidMembers(assayData, required)}{Validate \code{assayData}, ensuring that the named elements \code{required} are present, matrices are of the same dimension, and \code{featureNames} (rownames) are consistent (identical or \code{NULL}) across entries.} \item{assayDataElement(object, element)}{See \code{\link{eSet-class}}} \item{assayDataElementReplace(object, element, value, validate=TRUE)}{ See \code{\link{eSet-class}}} \item{assayDataElementNames(object)}{See \code{\link{eSet-class}}} } } \author{Biocore} \seealso{ \code{\link{eSet-class}} \code{\link{ExpressionSet-class}} } \keyword{classes} Biobase/man/class.ExpressionSet.Rd0000644000175400017540000002343413175713325020142 0ustar00biocbuildbiocbuild\name{ExpressionSet} \docType{class} \alias{class:ExpressionSet} \alias{ExpressionSet} \alias{ExpressionSet-class} \alias{ExpressionSet,missing-method} \alias{ExpressionSet,environment-method} \alias{ExpressionSet,matrix-method} \alias{exprs,ExpressionSet-method} \alias{exprs<-,ExpressionSet,matrix-method} \alias{initialize,ExpressionSet-method} \alias{coerce,exprSet,ExpressionSet-method} \alias{coerce,eSet,ExpressionSet-method} \alias{coerce,ExpressionSet,data.frame-method} \alias{esApply,ExpressionSet-method} \alias{updateObject,ExpressionSet-method} \alias{makeDataPackage,ExpressionSet-method} \alias{as.data.frame.ExpressionSet} \alias{write.exprs} \alias{write.exprs,ExpressionSet-method} \title{ Class to Contain and Describe High-Throughput Expression Level Assays. } \description{ Container for high-throughput assays and experimental metadata. \code{ExpressionSet} class is derived from \code{\link{eSet}}, and requires a matrix named \code{exprs} as assayData member. } \usage{ ## Instance creation ExpressionSet(assayData, phenoData=annotatedDataFrameFrom(assayData, byrow=FALSE), featureData=annotatedDataFrameFrom(assayData, byrow=TRUE), experimentData=MIAME(), annotation=character(), protocolData=annotatedDataFrameFrom(assayData, byrow=FALSE), ...) ## Additional methods documented below } \arguments{ \item{assayData}{A \code{matrix} of expression values, or an \code{environment}. When \code{assayData} is a \code{matrix}, the rows represent probe sets (\sQuote{features} in \code{ExpressionSet} parlance). Columns represent samples. When present, row names identify features and column names identify samples. Row and column names must be unique, and consistent with row names of \code{featureData} and \code{phenoData}, respectively. The assay data can be retrieved with \code{exprs()}. When \code{assayData} is an environment, it contains identically dimensioned matrices like that described in the previous paragraph. One of the elements of the environment must be named \sQuote{exprs}; this element is returned with \code{exprs()}. } \item{phenoData}{An optional \code{AnnotatedDataFrame} containing information about each sample. The number of rows in \code{phenoData} must match the number of columns in \code{assayData}. Row names of \code{phenoData} must match column names of the matrix / matricies in \code{assayData}.} \item{featureData}{An optional \code{AnnotatedDataFrame} containing information about each feature. The number of rows in \code{featureData} must match the number of rows in \code{assayData}. Row names of \code{featureData} must match row names of the matrix / matricies in \code{assayData}.} \item{experimentData}{An optional \code{MIAME} instance with meta-data (e.g., the lab and resulting publications from the analysis) about the experiment.} \item{annotation}{A \code{character} describing the platform on which the samples were assayed. This is often the name of a Bioconductor chip annotation package, which facilitated down-stream analysis.} \item{protocolData}{An optional \code{AnnotatedDataFrame} containing equipment-generated information about protocols. The number of rows and row names of \code{protocolData} must agree with the dimension and column names of \code{assayData}.} \item{\dots}{Additional arguments, passed to \code{new("ExpressionSet", ...)} and available for classes that extend \code{ExpressionSet}. } } \section{Extends}{ Directly extends class \code{\link{eSet}}. } \section{Creating Objects}{ \code{ExpressionSet} instances are usually created through \code{ExpressionSet()}. } \section{Slots}{ Inherited from \code{eSet}: \describe{ \item{\code{assayData}:}{Contains matrices with equal dimensions, and with column number equal to \code{nrow(phenoData)}. \code{assayData} must contain a matrix \code{exprs} with rows representing features (e.g., probe sets) and columns representing samples. Additional matrices of identical size (e.g., representing measurement errors) may also be included in \code{assayData}. Class:\code{\link{AssayData-class}}} \item{\code{phenoData}:}{See \code{\link{eSet}}} \item{\code{featureData}:}{See \code{\link{eSet}}} \item{\code{experimentData}:}{See \code{\link{eSet}}} \item{\code{annotation}:}{See \code{\link{eSet}}} \item{\code{protocolData}:}{See \code{\link{eSet}}} } } \section{Methods}{ Class-specific methods. \describe{ \item{\code{as(exprSet,"ExpressionSet")}}{Coerce objects of \code{\link{exprSet-class}} to \code{ExpressionSet}} \item{\code{as(object,"data.frame")}}{Coerce objects of \code{\link{ExpressionSet-class}} to \code{data.frame} by transposing the expression matrix and concatenating \code{phenoData}} \item{\code{exprs(ExpressionSet)}, \code{exprs(ExpressionSet,matrix)<-}}{Access and set elements named \code{exprs} in the \code{AssayData-class} slot.} \item{\code{esApply(ExpressionSet, MARGIN, FUN, ...)}}{'apply'-like function to conveniently operate on \code{ExpressionSet} objects. See \code{\link{esApply}}.} \item{\code{write.exprs(ExpressionSet)}}{Write expression values to a text file. It takes the same arguments as \code{write.table}} } Derived from \code{\link{eSet}}: \describe{ \item{\code{updateObject(object, ..., verbose=FALSE)}}{Update instance to current version, if necessary. See \code{\link{updateObject}} and \code{\link{eSet}}} \item{\code{isCurrent(object)}}{Determine whether version of object is current. See \code{\link{isCurrent}}} \item{\code{isVersioned(object)}}{Determine whether object contains a 'version' string describing its structure . See \code{\link{isVersioned}}} \item{\code{assayData(ExpressionSet)}:}{See \code{\link{eSet}}} \item{\code{sampleNames(ExpressionSet)} and \code{sampleNames(ExpressionSet)<-}:}{See \code{\link{eSet}}} \item{\code{featureNames(ExpressionSet)}, \code{featureNames(ExpressionSet, value)<-}:}{See \code{\link{eSet}}} \item{\code{dims(ExpressionSet)}:}{See \code{\link{eSet}}} \item{\code{phenoData(ExpressionSet)}, \code{phenoData(ExpressionSet,value)<-}:}{See \code{\link{eSet}}} \item{\code{varLabels(ExpressionSet)}, \code{varLabels(ExpressionSet, value)<-}:}{See \code{\link{eSet}}} \item{\code{varMetadata(ExpressionSet)}, \code{varMetadata(ExpressionSet,value)<-}:}{See \code{\link{eSet}}} \item{\code{pData(ExpressionSet)}, \code{pData(ExpressionSet,value)<-}:}{See \code{\link{eSet}}} \item{\code{varMetadata(ExpressionSet)}, \code{varMetadata(ExpressionSet,value)}}{See \code{\link{eSet}}} \item{\code{experimentData(ExpressionSet)},\code{experimentData(ExpressionSet,value)<-}:}{See \code{\link{eSet}}} \item{\code{pubMedIds(ExpressionSet)}, \code{pubMedIds(ExpressionSet,value)}}{See \code{\link{eSet}}} \item{\code{abstract(ExpressionSet)}:}{See \code{\link{eSet}}} \item{\code{annotation(ExpressionSet)}, \code{annotation(ExpressionSet,value)<-}}{See \code{\link{eSet}}} \item{\code{protocolData(ExpressionSet)}, \code{protocolData(ExpressionSet,value)<-}}{See \code{\link{eSet}}} \item{\code{combine(ExpressionSet,ExpressionSet)}:}{See \code{\link{eSet}}} \item{\code{storageMode(ExpressionSet)}, \code{storageMode(ExpressionSet,character)<-}:}{See \code{\link{eSet}}} } Standard generic methods: \describe{ \item{\code{initialize(ExpressionSet)}:}{Object instantiation, used by \code{new}; not to be called directly by the user.} \item{\code{updateObject(ExpressionSet)}:}{Update outdated versions of \code{ExpressionSet} to their current definition. See \code{\link{updateObject}}, \code{\link{Versions-class}}.} \item{\code{validObject(ExpressionSet)}:}{Validity-checking method, ensuring that \code{exprs} is a member of \code{assayData}. \code{checkValidity(ExpressionSet)} imposes this validity check, and the validity checks of \code{eSet}.} \item{\code{makeDataPackage(object, author, email, packageName, packageVersion, license, biocViews, filePath, description=paste(abstract(object), collapse="\n\n"), ...)}}{ Create a data package based on an ExpressionSet object. See \code{\link{makeDataPackage}}.} \item{\code{as(exprSet,ExpressionSet)}:}{Coerce \code{exprSet} to \code{ExpressionSet}.} \item{\code{as(eSet,ExpressionSet)}:}{Coerce the \code{eSet} portion of an object to \code{ExpressionSet}.} \item{\code{show(ExpressionSet)}}{See \code{\link{eSet}}} \item{\code{dim(ExpressionSet)}, \code{ncol}}{See \code{\link{eSet}}} \item{\code{ExpressionSet[(index)}:}{See \code{\link{eSet}}} \item{\code{ExpressionSet$}, \code{ExpressionSet$<-}}{See \code{\link{eSet}}} \item{\code{ExpressionSet[[i]]}, \code{ExpressionSet[[i]]<-}}{See \code{\link{eSet}}} } } \author{Biocore team} \seealso{ \code{\link{eSet-class}}, \code{\link{ExpressionSet-class}}. } \examples{ # create an instance of ExpressionSet ExpressionSet() ExpressionSet(assayData=matrix(runif(1000), nrow=100, ncol=10)) # update an existing ExpressionSet data(sample.ExpressionSet) updateObject(sample.ExpressionSet) # information about assay and sample data featureNames(sample.ExpressionSet)[1:10] sampleNames(sample.ExpressionSet)[1:5] experimentData(sample.ExpressionSet) # subset: first 10 genes, samples 2, 4, and 10 expressionSet <- sample.ExpressionSet[1:10,c(2,4,10)] # named features and their expression levels subset <- expressionSet[c("AFFX-BioC-3_at","AFFX-BioDn-5_at"),] exprs(subset) # samples with above-average 'score' in phenoData highScores <- expressionSet$score > mean(expressionSet$score) expressionSet[,highScores] # (automatically) coerce to data.frame lm(score~AFFX.BioDn.5_at + AFFX.BioC.3_at, data=subset) } \keyword{classes} Biobase/man/class.MIAME.Rd0000644000175400017540000001154113175713325016153 0ustar00biocbuildbiocbuild\name{MIAME} \docType{class} \alias{class:MIAME} \alias{MIAME} \alias{MIAME-class} \alias{abstract,MIAME-method} \alias{combine,MIAME,MIAME-method} \alias{expinfo,MIAME-method} \alias{hybridizations,MIAME-method} \alias{normControls,MIAME-method} \alias{otherInfo,MIAME-method} \alias{preproc} \alias{preproc,MIAME-method} \alias{preproc<-,MIAME-method} \alias{preproc<-} \alias{notes,MIAME-method} \alias{notes<-,MIAME,list-method} \alias{notes<-,MIAME,character-method} \alias{pubMedIds,MIAME-method} \alias{pubMedIds<-,MIAME,ANY-method} \alias{samples,MIAME-method} \alias{show,MIAME-method} \alias{updateObject,MIAME-method} \alias{isCurrent,MIAME,missing-method} \alias{samples} \concept{abstract} \concept{expinfo} \concept{hybridizations} \concept{normControls} \concept{preproc} \title{ Class for Storing Microarray Experiment Information } \description{ Class \code{MIAME} covers MIAME entries that are not covered by other classes in Bioconductor. Namely, experimental design, samples, hybridizations, normalization controls, and pre-processing information. The \code{MIAME} class is derived from \code{\link{MIAxE}}.} \section{Slots}{ \describe{ \item{\code{name}:}{Object of class \code{character} containing the experimenter name} \item{\code{lab}:}{Object of class \code{character} containing the laboratory where the experiment was conducted} \item{\code{contact}:}{Object of class \code{character} containing contact information for lab and/or experimenter} \item{\code{title}:}{Object of class \code{character} containing a single-sentence experiment title } \item{\code{abstract}:}{Object of class \code{character} containing an abstract describing the experiment} \item{\code{url}:}{Object of class \code{character} containing a URL for the experiment} \item{\code{samples}:}{Object of class \code{list} containing information about the samples} \item{\code{hybridizations}:}{Object of class \code{list} containing information about the hybridizations} \item{\code{normControls}:}{Object of class \code{list} containing information about the controls such as house keeping genes} \item{\code{preprocessing}:}{Object of class \code{list} containing information about the pre-processing steps used on the raw data from this experiment} \item{\code{pubMedIds}:}{Object of class \code{character} listing strings of PubMed identifiers of papers relevant to the dataset} \item{\code{other}:}{Object of class \code{list} containing other information for which none of the above slots does not applies} } } \section{Methods}{ Constructor methods: \describe{ \item{\code{MIAME()}:}{ \code{MIAME(name = "", lab = "", contact = "", title = "", abstract = "", url = "", pubMedIds = "" , samples = "", hybridizations = list(), normControls = list(), preprocessing = list(), other = list())}: Creates a new \code{MIAME} object with slots as defined above.} } Class-specific methods: \describe{ \item{\code{abstract(MIAME)}:}{An accessor function for \code{abstract}.} \item{\code{combine(MIAME,MIAME)}:}{Combine two objects of \code{MIAME-class}, issuing warnings when ambiguities encountered.} \item{\code{expinfo(MIAME)}:}{An accessor function for \code{name}, \code{lab}, \code{contact}, \code{title}, and \code{url}.} \item{\code{hybridizations(MIAME)}:}{An accessor function for \code{hybridizations}.} \item{\code{normControls(MIAME)}:}{An accessor function for \code{normControls}.} \item{\code{notes(MIAME), notes(MIAME) <- value}:}{Accessor functions for \code{other}. \code{notes(MIAME) <- character} \emph{appends} character to notes; use \code{notes(MIAME) <- list} to replace the notes entirely.} \item{\code{otherInfo(MIAME)}:}{An accessor function for \code{other}.} \item{\code{preproc(MIAME)}:}{An accessor function for \code{preprocessing}.} \item{\code{pubMedIds(MIAME), pubMedIds(MIAME) <- value}:}{Accessor function for \code{pubMedIds}.} \item{\code{samples(MIAME)}:}{An accessor function for \code{samples}.} } Standard generic methods: \describe{ \item{\code{updateObject(object, \dots, verbose=FALSE)}}{Update instance to current version, if necessary. See \code{\link{updateObject}}} \item{\code{isCurrent(object)}}{Determine whether version of object is current. See \code{\link{isCurrent}}} \item{\code{isVersioned(object)}}{Determine whether object contains a 'version' string describing its structure . See \code{\link{isVersioned}}} \item{\code{show(MIAME)}:}{Renders information about the MIAME information } } } \references{ \url{http://www.mged.org/Workgroups/MIAME/miame_1.1.html} } \seealso{ \code{\link{class:characterORMIAME}}, \code{\link{read.MIAME}} } \author{ Rafael A. Irizarry } \keyword{classes} Biobase/man/class.MIAxE.Rd0000644000175400017540000000234713175713325016232 0ustar00biocbuildbiocbuild\name{MIAxE} \docType{class} \alias{MIAxE} \alias{class:MIAxE} \alias{MIAxE-class} \alias{show,MIAxE-method} \title{MIAxE objects} \description{ The \code{MIAxE} virtual class is a general container for storing experiment metadata. Information such as experimental design, samples, normalization methods and pre-processing information can be stored in these objets. The \code{MIAxE} class is virtual and \code{MIAxE} objects cannot be instantiated directly. The following classes derive directly from the \code{MIAxE} class: MIAME. } \section{Slots}{ Introduced in \code{MIAxE}: \describe{ \item{\code{.__classVersion__}:}{A \code{Versions} object describing the \code{MIAxE} version number. Intended for developer use.} } } \section{Methods}{ Standard generic methods: \describe{ \item{\code{show(object)}}{Informatively display object contents.} } } \author{Biocore team} \seealso{ Related classes \code{\link{MIAME-class}}, \code{\link{ExpressionSet-class}}. Derived classes \code{\link{MIAME-class}}. } \examples{ # Create a new class MyData <- setClass("MyData", contains="MIAxE") MyData() # MIAxE objects cannot be instantiated directly try(new("MIAxE")) } \keyword{classes} Biobase/man/class.MultiSet.Rd0000644000175400017540000001225513175713325017074 0ustar00biocbuildbiocbuild\name{MultiSet} \docType{class} \alias{class:MultiSet} \alias{MultiSet} \alias{MultiSet-class} \alias{initialize,MultiSet-method} \alias{coerce,eSet,MultiSet-method} \title{ Class to Contain and Describe High-Throughput Expression Level Assays. } \description{ Container for high-throughput assays and experimental metadata. \code{MutliSet} is derived from \code{\link{eSet-class}}. \code{MultiSet} differs from \code{\link{ExpressionSet-class}} because \code{MultiSet} can contain any element(s) in \code{assayData} (\code{ExpressionSet} must have an element named \code{exprs}). } \section{Extends}{ Directly extends class \code{\link{eSet}}. } \section{Creating Objects}{ \code{new('MultiSet', phenoData = [AnnotatedDataFrame], experimentData = [MIAME], annotation = [character], protocolData = [AnnotatedDataFrame], ...) } \code{updateOldESet(oldESet,"MultiSet")} \code{MultiSet} instances are usually created through \code{new("MultiSet", ...)}. The \code{...} arguments to \code{new} are matrices of expression data (with features corresponding to rows and samples to columns), \code{phenoData}, \code{experimentData}, \code{annotation}, and \code{protocolData}. \code{phenoData}, \code{experimentData}, \code{annotation}, and \code{protocolData} can be missing, in which case they are assigned default values. \code{\link{updateOldESet}} will take a serialized instance (e.g., saved to a disk file with \code{save} object created with earlier definitions of the \code{eSet-class}, and update the object to \code{MultiSet}. Warnings are issued when direct translation is not possible; incorrectly created \code{oldESet} instances may not be updated. } \section{Slots}{ Inherited from \code{eSet}: \describe{ \item{\code{assayData}:}{Contains zero or more matrices with equal dimensions, and with column number equal to \code{nrow(phenoData)}. Each matrix in \code{assayData} has rows representing features (e.g., reporters) and columns representing samples. Class:\code{\link{AssayData-class}}} \item{\code{phenoData}:}{See \code{\link{eSet-class}}} \item{\code{experimentData}:}{See \code{\link{eSet-class}}} \item{\code{annotation}:}{See \code{\link{eSet-class}}} \item{\code{protocolData}:}{See \code{\link{eSet-class}}} } } \section{Methods}{ Class-specific methods: none Derived from \code{\link{eSet-class}}: \describe{ \item{\code{updateObject(object, ..., verbose=FALSE)}}{Update instance to current version, if necessary. See \code{\link{updateObject}} and \code{\link{eSet}}} \item{\code{isCurrent(object)}}{Determine whether version of object is current. See \code{\link{isCurrent}}} \item{\code{isVersioned(object)}}{Determine whether object contains a 'version' string describing its structure . See \code{\link{isVersioned}}} \item{\code{sampleNames(MultiSet)} and \code{sampleNames(MultiSet)<-}:}{See \code{\link{eSet-class}}} \item{\code{featureNames(MultiSet)}, \code{featureNames(MultiSet, value)<-}:}{See \code{\link{eSet-class}}} \item{\code{dims(MultiSet)}:}{See \code{\link{eSet-class}}} \item{\code{phenoData(MultiSet)}, \code{phenoData(MultiSet,value)<-}:}{See \code{\link{eSet-class}}} \item{\code{varLabels(MultiSet)}, \code{varLabels(MultiSet, value)<-}:}{See \code{\link{eSet-class}}} \item{\code{varMetadata(MultiSet)}, \code{varMetadata(MultiSet,value)<-}:}{See \code{\link{eSet-class}}} \item{\code{pData(MultiSet)}, \code{pData(MultiSet,value)<-}:}{See \code{\link{eSet-class}}} \item{\code{varMetadata(MultiSet)}, \code{varMetadata(MultiSet,value)}}{See \code{\link{eSet-class}}} \item{\code{experimentData(MultiSet)},\code{experimentData(MultiSet,value)<-}:}{See \code{\link{eSet-class}}} \item{\code{pubMedIds(MultiSet)}, \code{pubMedIds(MultiSet,value)}}{See \code{\link{eSet-class}}} \item{\code{abstract(MultiSet)}:}{See \code{\link{eSet-class}}} \item{\code{annotation(MultiSet)}, \code{annotation(MultiSet,value)<-}}{See \code{\link{eSet-class}}} \item{\code{protocolData(MultiSet)}, \code{protocolData(MultiSet,value)<-}}{See \code{\link{eSet-class}}} \item{\code{combine(MultiSet,MultiSet)}:}{See \code{\link{eSet-class}}} \item{\code{storageMode(eSet)}, \code{storageMode(eSet,character)<-}:}{See \code{\link{eSet-class}}} } Standard generic methods: \describe{ \item{\code{initialize(MultiSet)}:}{Object instantiation, used by \code{new}; not to be called directly by the user.} \item{\code{validObject(MultiSet)}:}{Validity-checking method, ensuring that all elements of \code{assayData} are matricies with equal dimensions.} \item{\code{as(eSet,MultiSet)}:}{Coerce the \code{eSet} portion of an object to \code{MultiSet}.} \item{\code{show(MultiSet)}}{See \code{\link{eSet-class}}} \item{\code{dim(MultiSet)}, \code{ncol}}{See \code{\link{eSet-class}}} \item{\code{MultiSet[(index)}:}{See \code{\link{eSet-class}}} \item{\code{MultiSet$}, \code{MultiSet$<-}}{See \code{\link{eSet-class}}} } } \author{Biocore team} \seealso{ \code{\link{eSet-class}}, \code{\link{ExpressionSet-class}} } \examples{ # create an instance of ExpressionSet new("MultiSet") } \keyword{classes} Biobase/man/class.NChannelSet.Rd0000644000175400017540000002053413175713325017467 0ustar00biocbuildbiocbuild\name{NChannelSet-class} \docType{class} \alias{NChannelSet-class} \alias{NChannelSet} \alias{class.NChannelSet} \alias{assayData<-,NChannelSet,environment-method} \alias{assayData<-,NChannelSet,list-method} \alias{channelNames,NChannelSet-method} \alias{channelNames<-,NChannelSet,character-method} \alias{channelNames<-,NChannelSet,list-method} \alias{channel,NChannelSet,character-method} \alias{sampleNames,NChannelSet-method} \alias{sampleNames<-,NChannelSet,list-method} \alias{selectChannels,NChannelSet,character-method} \alias{initialize,NChannelSet-method} \title{Class to contain data from multiple channel array technologies} \description{ Container for high-throughput assays and experimental meta-data. Data are from experiments where a single \sQuote{chip} contains several (more than 1) different \sQuote{channels}. All channels on a chip have the same set of\sQuote{features}. An experiment consists of a collection of several N-channel chips; each chip is a \sQuote{sample}. An \code{NChannelSet} provides a way to coordinate assay data (expression values) with phenotype information and references to chip annotation data; it extends the \code{\link{eSet}} class. An \code{NChannelSet} allows channels to be extracted (using the \code{channels} method, mentioned below), and subsets of features or samples to be selected (using \code{[, ]}). Selection and subsetting occur so that relevant phenotypic data is maintained by the selection or subset.} \section{Objects from the Class}{ Objects can be created by calls of the form \code{NChannelSet( assayData, phenoData, ...)}. See the examples below. } \section{Slots}{ \describe{ \item{\code{assayData}:}{ Object of class \code{\link{AssayData}}, usually an environment containing matrices of identical size. Each matrix represents a single channel. Columns in each matrix correspond to samples, rows to features. Once created, \code{NChannelSet} manages coordination of samples and channels. } \item{\code{phenoData}:}{ Object of class \code{\link{AnnotatedDataFrame}}. The \code{data} component of the \code{AnnotatedDataFrame} is \code{data.frame} with number of rows equal to the number of samples. Columns of the \code{data} component correspond to measured covariates. The \code{varMetadata} component consists of mandatory columns \code{labelDescription} (providing a textual description of each column label in the \code{data} component) and \code{channel}. The \code{channel} of \code{varMetadata} is a \code{factor}, with levels equal to the names of the \code{assayData} channels, plus the special symbol \code{_ALL_}. The \code{channel} column is used to indicate which channel(s) the corresponding column in the \code{data} component of \code{AnnotatedDataFrame} correspond; the \code{_ALL_} symbol indicates that the \code{data} column is applicable to all channels. \code{varMetadata} may contain additional columns with arbitrary information. Once created, \code{NChannelSet} coordinates selection and subsetting of channels in \code{phenoData}. } \item{\code{featureData}:}{ Object of class \code{\link{AnnotatedDataFrame}}, used to contain feature data that is unique to this experiment; feature-level descriptions common to a particular chip are usually referenced through the \code{annotation} slot. } \item{\code{experimentData}:}{ Object of class \code{\link{MIAME}} containing descriptions of the experiment. } \item{\code{annotation}:}{ Object of class \code{"character"}. Usually a length-1 character string identifying the chip technology used during the experiment. The annotation string is used to retrieve information about features, e.g., using the \code{annotation} package.} \item{\code{protocolData}:}{ Object of class \code{"character"}. A character vector identifying the dates the samples were scanned during the experiment.} \item{\code{.__classVersion__}:}{ Object of class \code{\link{Versions}}, containing automatically created information about the class definition Biobase package version, and other information about the user system at the time the instance was created. See \code{\link{classVersion}} and \code{\link{updateObject}} for examples of use. } } } \section{Extends}{ Class \code{"\linkS4class{eSet}"}, directly. Class \code{"\linkS4class{VersionedBiobase}"}, by class "eSet", distance 2. Class \code{"\linkS4class{Versioned}"}, by class "eSet", distance 3. } \section{Methods}{ Methods with class-specific functionality: \describe{ \item{\code{channel(object, name, ...)}}{ \code{signature(object="NChannelSet", name="character")}. Return an \code{ExperessionSet} created from the channel and corresponding phenotype of argument \code{name}. \code{name} must have length 1. Arguments \code{...} are rarely used, but are passed to the \code{ExpressionSet} constructor, for instance to influence \code{storage.mode}. } \item{\code{channelNames(object)}, \code{channelNames(object) <- value}}{ \code{signature(object = "NChannelSet")}. Obtain, reorder, or rename channels contained in \code{object}. See \code{\link{channelNames}}. } \item{\code{selectChannels(object, names, ...}}{ \code{signature(object = "NChannelSet", names = "character")}. Create a new \code{NChannelSet} from \code{object}, containing only channels in \code{names}. The \code{...} is not used by this method. } \item{\code{object[features, samples]}}{ \code{signature(object = "NChannelSet", features = "ANY", samples = "ANY")}. Create a new \code{NChannelSet} from \code{object}, containing only elements matching \code{features} and \code{samples}; either index may be missing, or a character, numeric, or logical vector. } \item{\code{sampleNames(object) <- value}}{ \code{signature(object = "NChannelSet", value = "list")} assign each (named) element of \code{value} to the \code{sampleNames} of the correspondingly named elements of \code{assayData} in \code{object}. } } Methods with functionality derived from \code{\link{eSet}}: \code{annotation}, \code{annotation<-}, \code{assayData}, \code{assayData<-}, \code{classVersion}, \code{classVersion<-}, \code{dim}, \code{dims}, \code{experimentData}, \code{experimentData<-}, \code{featureData}, \code{featureData<-}, \code{phenoData}, \code{phenoData<-}, \code{protocolData}, \code{protocolData<-}, \code{pubMedIds}, \code{pubMedIds<-}, \code{sampleNames}, \code{sampleNames<-}, \code{storageMode}, \code{storageMode<-}, \code{varMetadata}, \code{varMetadata<-}, \code{isCurrent}, \code{isVersioned}, \code{updateObject}. Additional methods: \code{coerce} (\sQuote{as}, to convert between objects, if possible), \code{initialize} (used internally for creating objects), \code{show} (invoked automatically when the object is displayed to the screen) } \author{Martin Morgan } \seealso{ \code{\linkS4class{eSet}}, \code{\linkS4class{ExpressionSet}}. } \examples{ ## An empty NChannelSet obj <- NChannelSet() ## An NChannelSet with two channels (R, G) and no phenotypic data obj <- NChannelSet(R=matrix(0,10,5), G=matrix(0,10,5)) ## An NChannelSet with two channels and channel-specific phenoData R <- matrix(0, 10, 3, dimnames=list(NULL, LETTERS[1:3])) G <- matrix(1, 10, 3, dimnames=list(NULL, LETTERS[1:3])) assayData <- assayDataNew(R=R, G=G) data <- data.frame(ChannelRData=numeric(ncol(R)), ChannelGData=numeric(ncol(R)), ChannelRAndG=numeric(ncol(R))) varMetadata <- data.frame(labelDescription=c( "R-specific phenoData", "G-specific phenoData", "Both channel phenoData"), channel=factor(c("R", "G", "_ALL_"))) phenoData <- AnnotatedDataFrame(data=data, varMetadata=varMetadata) obj <- NChannelSet(assayData=assayData, phenoData=phenoData) obj ## G channel as NChannelSet selectChannels(obj, "G") ## G channel as ExpressionSet channel(obj, "G") ## Samples "A" and "C" obj[,c("A", "C")] } \keyword{classes} Biobase/man/class.SnpSet.Rd0000644000175400017540000001254613175713325016545 0ustar00biocbuildbiocbuild\name{SnpSet} \docType{class} \alias{class:SnpSet} \alias{SnpSet} \alias{SnpSet-class} \alias{exprs<-,SnpSet,matrix-method} \alias{exprs,SnpSet-method} \alias{snpCall,SnpSet-method} \alias{snpCall<-,SnpSet,matrix-method} \alias{snpCallProbability,SnpSet-method} \alias{snpCallProbability<-,SnpSet,matrix-method} \alias{initialize,SnpSet-method} \title{ Class to Contain Objects Describing High-Throughput SNP Assays. } \description{ Container for high-throughput assays and experimental metadata. \code{SnpSet} class is derived from \code{\link{eSet}}, and requires matrices \code{call}, \code{callProbability} as assay data members.} \section{Extends}{ Directly extends class \code{\link{eSet}}. } \section{Creating Objects}{ \code{new('SnpSet', phenoData = [AnnotatedDataFrame], experimentData = [MIAME], annotation = [character], protocolData = [AnnotatedDataFrame], call = [matrix], callProbability = [matrix], ...) } \code{SnpSet} instances are usually created through \code{new("SnpSet", ...)}. Usually the arguments to \code{new} include \code{call} (a matrix of genotypic calls, with features (SNPs) corresponding to rows and samples to columns), \code{phenoData}, \code{experimentData}, \code{annotation}, and \code{protocolData}. \code{phenoData}, \code{experimentData}, \code{annotation} and \code{protocolData} can be missing, in which case they are assigned default values. } \section{Slots}{ Inherited from \code{eSet}: \describe{ \item{\code{assayData}:}{Contains matrices with equal dimensions, and with column number equal to \code{nrow(phenoData)}. \code{assayData} must contain a matrix \code{call} with rows representing features (e.g., SNPs) and columns representing samples, and a matrix \code{callProbability} describing the certainty of the call. The content of \code{call} and \code{callProbability} are not enforced by the class. Additional matrices of identical size may also be included in \code{assayData}. Class:\code{\link{AssayData-class}}} \item{\code{phenoData}:}{See \code{\link{eSet}}} \item{\code{experimentData}:}{See \code{\link{eSet}}} \item{\code{annotation}:}{See \code{\link{eSet}}} \item{\code{protocolData}:}{See \code{\link{eSet}}} } } \section{Methods}{ Class-specific methods: \describe{ \item{\code{snpCall(SnpSet)}, \code{snpCall(SnpSet,matrix)<-}}{Access and set elements named \code{call} in the \code{AssayData} slot.} \item{\code{exprs(SnpSet)}, \code{exprs(SnpSet,matrix)<-}}{Synonym for \code{snpCall}.} \item{\code{snpCallProbability(SnpSet)}, \code{snpCallProbability<-(SnpSet,matrix)<-}}{ Access and set elements named \code{callProbability} in the \code{AssayData} slot.} } Derived from \code{\link{eSet}}: \describe{ \item{\code{updateObject(object, ..., verbose=FALSE)}}{Update instance to current version, if necessary. See \code{\link{updateObject}} and \code{\link{eSet}}} \item{\code{isCurrent(object)}}{Determine whether version of object is current. See \code{\link{isCurrent}}} \item{\code{isVersioned(object)}}{Determine whether object contains a 'version' string describing its structure . See \code{\link{isVersioned}}} \item{\code{sampleNames(SnpSet)} and \code{sampleNames(SnpSet)<-}:}{See \code{\link{eSet}}} \item{\code{featureNames(SnpSet)}, \code{featureNames(SnpSet, value)<-}:}{See \code{\link{eSet}}} \item{\code{dims(SnpSet)}:}{See \code{\link{eSet}}} \item{\code{phenoData(SnpSet)}, \code{phenoData(SnpSet,value)<-}:}{See \code{\link{eSet}}} \item{\code{varLabels(SnpSet)}, \code{varLabels(SnpSet, value)<-}:}{See \code{\link{eSet}}} \item{\code{varMetadata(SnpSet)}, \code{varMetadata(SnpSet,value)<-}:}{See \code{\link{eSet}}} \item{\code{pData(SnpSet)}, \code{pData(SnpSet,value)<-}:}{See \code{\link{eSet}}} \item{\code{varMetadata(SnpSet)}, \code{varMetadata(SnpSet,value)}}{See \code{\link{eSet}}} \item{\code{experimentData(SnpSet)},\code{experimentData(SnpSet,value)<-}:}{See \code{\link{eSet}}} \item{\code{pubMedIds(SnpSet)}, \code{pubMedIds(SnpSet,value)}}{See \code{\link{eSet}}} \item{\code{abstract(SnpSet)}:}{See \code{\link{eSet}}} \item{\code{annotation(SnpSet)}, \code{annotation(SnpSet,value)<-}}{See \code{\link{eSet}}} \item{\code{protocolData(SnpSet)}, \code{protocolData(SnpSet,value)<-}}{See \code{\link{eSet}}} \item{\code{combine(SnpSet,SnpSet)}:}{See \code{\link{eSet}}} \item{\code{storageMode(eSet)}, \code{storageMode(eSet,character)<-}:}{See \code{\link{eSet}}} } Standard generic methods: \describe{ \item{\code{initialize(SnpSet)}:}{Object instantiation, used by \code{new}; not to be called directly by the user.} \item{\code{validObject(SnpSet)}:}{Validity-checking method, ensuring that \code{call} and \code{callProbability} is a member of \code{assayData}. \code{checkValidity(SnpSet)} imposes this validity check, and the validity checks of \code{eSet}.} \item{\code{show(SnpSet)}}{See \code{\link{eSet}}} \item{\code{dim(SnpSet)}, \code{ncol}}{See \code{\link{eSet}}} \item{\code{SnpSet[(index)}:}{See \code{\link{eSet}}} \item{\code{SnpSet$}, \code{SnpSet$<-}}{See \code{\link{eSet}}} } } \author{Martin Morgan, V.J. Carey, after initial design by R. Gentleman } \seealso{ \code{\link{eSet}}, \code{\link{ExpressionSet}} } \keyword{classes} Biobase/man/class.Versioned.Rd0000644000175400017540000000525113175713325017262 0ustar00biocbuildbiocbuild\name{Versioned} \docType{class} \alias{Versioned-class} \alias{Versioned} \alias{initialize,Versioned-method} \alias{isVersioned,Versioned-method} \alias{classVersion,Versioned-method} \alias{classVersion<-,Versioned,Versions-method} \alias{isCurrent,Versioned,missing-method} \alias{isCurrent,Versioned,character-method} \alias{show,Versioned-method} \title{Class "Versioned"} \description{ Use this class as a `superclass' for classes requiring information about versions. } \section{Methods}{ The following are defined; package developers may write additional methods. \describe{ \item{\code{new("Versioned", ..., versions=list())}}{Create a new \code{Versioned-class} instance, perhaps with additional named version elements (the contents of \code{versions}) added. Named elements of \code{versions} are character strings that can be coerced using \code{\link{package_version}}, or \code{package_version} instances.} \item{\code{classVersion(object)}}{Obtain version information about instance \code{object}. See \code{\link{classVersion}}.} \item{\code{classVersion(object) <- value}}{Set version information on instance \code{object} to \code{value}; useful when \code{object} is an instance of a class that contains \code{VersionClass}. See \code{\link{classVersion}}.} \item{\code{classVersion(object)["id"] <- value}}{Create or update version information \code{"id"} on instance \code{object} to \code{value}; useful when \code{object} is an instance of a class that contains \code{VersionClass}. See \code{\link{classVersion}}.} \item{\code{show(object)}}{Default method returns \code{invisible}, to avoid printing confusing information when your own class does not have a \code{show} method defined. Use \code{classVersion(object)} to get or set version information.} } } \author{Biocore} \seealso{ \code{\link{Versions-class}} } \examples{ obj <- new("Versioned", versions=list(A="1.0.0")) obj classVersion(obj) A <- setClass("A", contains="Versioned") classVersion("A") a <- A() a # 'show' nothing by default classVersion(a) B <- setClass("B", contains="Versioned", prototype=prototype(new("Versioned",versions=list(B="1.0.0")))) classVersion("B") b <- B() classVersion(b) classVersion(b)["B"] <- "1.0.1" classVersion(b) classVersion("B") classVersion("B") < classVersion(b) classVersion(b) == "1.0.1" C <- setClass("C", representation(x="numeric"), contains=("VersionedBiobase"), prototype=prototype(new("VersionedBiobase", versions=c(C="1.0.1")))) setMethod("show", signature(object="C"), function(object) print(object@x)) c <- C(x=1:10) c classVersion(c) } \keyword{classes} Biobase/man/class.VersionedBiobase.Rd0000644000175400017540000000201113175713325020536 0ustar00biocbuildbiocbuild\name{VersionedBiobase} \docType{class} \alias{VersionedBiobase-class} \alias{VersionedBiobase} \title{Class "VersionedBiobase"} \description{ Use this class as a `superclass' for classes requiring information about versions. By default, the class contains versions for R and Biobase. See \code{\link{Versioned-class}} for additional details. } \section{Methods}{ set \code{\link{Versioned-class}} for methods. } \author{Biocore} \seealso{ \code{\link{Versioned-class}} } \examples{ obj <- new("VersionedBiobase") classVersion(obj) obj <- new("VersionedBiobase", versions=list(A="1.0.0")) classVersion(obj) A <- setClass("A", contains="VersionedBiobase") classVersion("A") a <- A() classVersion(a) obj <- new("VersionedBiobase", versions=c(MyVersion="1.0.0")) classVersion(obj) B <- setClass("B", contains="VersionedBiobase", prototype=prototype(new("VersionedBiobase",versions=list(B="1.0.0")))) classVersion("B") b <- B() classVersion(b) removeClass("A") removeClass("B") } \keyword{classes} Biobase/man/class.Versions.Rd0000644000175400017540000000546213175713325017140 0ustar00biocbuildbiocbuild\name{Versions} \docType{class} \alias{Versions-class} \alias{Versions} \alias{initialize,Versions-method} \alias{[,Versions-method} \alias{[<-,Versions-method} \alias{[[<-,Versions-method} \alias{$<-,Versions-method} \alias{Compare,Versions,Versions-method} \alias{Compare,Versions,character-method} \alias{Compare,character,Versions-method} \alias{updateObject,Versions-method} \alias{show,Versions-method} \alias{coerce,Versions,character-method} \title{Class "Versions"} \description{ A class to record version number information. This class is used to report versions; to add version information to your own class, use \code{\link{Versioned-class}}. } \section{Methods}{ The following are defined; package developers may write additional methods. \describe{ \item{\code{new("Versions", ...)}}{Create a new \code{Versions-class} instance, perhaps with named version elements (the contents of \code{...}) added. Named elements of \code{versions} are character strings that can be coerced using \code{\link{package_version}}, or \code{package_version} instances, \code{Versions-class} objects.} \item{\code{object["id"]}}{Obtain version information \code{"id"} from \code{object}.} \item{\code{object["id"] <- value}}{Create or update version information \code{"id"} on instance \code{object}.} \item{\code{object[["id"]]}}{Obtain version information \code{"id"} from \code{object}. The result is a list of integers, corresponding to entries in the version string.} \item{\code{object[["id"]] <- value}}{Create or update version information \code{"id"} on instance \code{object}.} \item{\code{object$id}}{Obtain version information \code{"id"} from \code{object}.The result is a list of integers, corresponding to entries in the version string.} \item{\code{object$id <- value}}{Create or update version information \code{"id"} on instance \code{object}.} \item{\code{show(object)}}{Display version information.} \item{\code{updateObject(object)}}{Update \code{object} to the current \code{Versions-class} representation. Note that this does \emph{not} update another class that uses \code{Versions-class} to track the class version.} \item{\code{as(object, "character")}}{Convert \code{object} to character representation, e.g., \code{1.0.0}} \item{\code{object1 < object2}}{Compare \code{object1} and \code{object2} using version class information. Symbols in addition to \code{<} are admissible; see \code{?Ops}} } } \author{Biocore} \seealso{ \code{\link{classVersion}} \code{\link{isCurrent}} \code{\link{isVersioned}} } \examples{ obj <- new("Versions", A="1.0.0") obj obj["A"] <- "1.0.1" obj obj["B"] <- "2.0" obj obj1 <- obj obj1["B"] <- "2.0.1" obj1 == obj obj1["B"] > "2.0.0" obj["B"] == "2.0" # TRUE! } \keyword{classes} Biobase/man/class.VersionsNull.Rd0000644000175400017540000000143713175713325017771 0ustar00biocbuildbiocbuild\name{VersionsNull} \docType{class} \alias{VersionsNull-class} \alias{VersionsNull} \alias{initialize,VersionsNull-method} \alias{show,VersionsNull-method} \title{Class "VersionsNull"} \description{ A class used to represent the `version' of unversioned objects. Useful primarily for method dispatch. } \section{Methods}{ The following are defined; package developers may write additional methods. \describe{ \item{\code{new("VersionsNull", ...)}}{Create a new \code{VersionsNull-class} instance, ignoring any additional arguments.} \item{\code{show(object)}}{Display ``No version''.} } } \author{Biocore} \seealso{ \code{\link{classVersion}} } \examples{ obj <- new("VersionsNull") obj obj <- new("VersionsNull", A="1.0.0") # warning obj } \keyword{classes} Biobase/man/class.aggregator.Rd0000644000175400017540000000373013175713325017446 0ustar00biocbuildbiocbuild\name{aggregator} \docType{class} \alias{class:aggregator} \alias{aggregator} \alias{aggregator-class} \alias{initialize,aggregator-method} \alias{aggenv,aggregator-method} \alias{aggfun,aggregator-method} \alias{initfun,aggregator-method} \concept{aggenv} \concept{aggfun} \concept{initfun} \title{A Simple Class for Aggregators } \description{ A class of objects designed to help aggregate calculations over an iterative computation. The aggregator consists of three objects. An environment to hold the values. A function that sets up an initial value the first time an object is seen. An aggregate function that increments the value of an object seen previously. } \section{Creating Objects}{ \code{new('aggregator', aggenv = [environment], initfun = [function], aggfun = [function])} } \section{Slots}{ \describe{ \item{\code{aggenv}:}{Object of class 'environment', holds the values between iterations} \item{\code{initfun}:}{Object of class 'function' specifies how to initialize the value for a name the first time it is encountered} \item{\code{aggfun}:}{Object of class 'function' used to increment (or perform any other function) on a name} } } \section{Methods}{ \describe{ \item{\code{aggenv(aggregator)}:}{Used to access the environment of the aggregator} \item{\code{aggfun(aggregator)}:}{Used to access the function that aggregates} \item{\code{initfun(aggregator)}:}{Used to access the initializer function} } } \seealso{ \code{\link{Aggregate}} } \details{ This class is used to help aggregate different values over function calls. A very simple example is to use leave one out cross-validation for prediction. At each stage we first perform feature selection and then cross-validate. To keep track of how often each feature is selected we can use an aggregator. At the end of the cross-validation we can extract the names of the features chosen from \code{aggenv}. } \keyword{methods} \keyword{classes} Biobase/man/class.characterORmiame.Rd0000644000175400017540000000062413175713325020531 0ustar00biocbuildbiocbuild\name{class:characterORMIAME} \docType{class} \alias{class:characterORMIAME} \alias{characterORMIAME-class} \concept{characterORMIAME} \title{Class to Make Older Versions Compatible} \description{This class can be either \code{character} or \code{MIAME}.} \section{Methods}{ No methods defined with class "characterORMIAME" in the signature. } \seealso{See also \code{\link{MIAME}}} \keyword{classes} Biobase/man/class.container.Rd0000644000175400017540000000330513175713325017304 0ustar00biocbuildbiocbuild\name{container} \docType{class} \alias{class:container} \alias{container} \alias{container-class} \alias{[,container-method} \alias{[[<-,container-method} \alias{[[,container-method} \alias{content,container-method} \alias{length,container-method} \alias{locked,container-method} \alias{show,container-method} \concept{content} \concept{locked} \title{A Lockable List Structure with Constraints on Content} \description{Container class that specializes the list construct of R to provide content and access control } \section{Creating Objects}{ \code{new('container', x = [list], content = [character], locked = [logical])} } \section{Slots}{ \describe{ \item{x}{list of entities that are guaranteed to share a certain property} \item{content}{tag describing container contents} \item{locked}{boolean indicator of locked status. Value of TRUE implies assignments into the container are not permitted} } } \section{Methods}{ Class-specific methods: \describe{ \item{\code{content(container)}}{returns \code{content} slot of argument} \item{\code{locked(container)}}{returns \code{locked} slot of argument} } Standard methods defined for 'container': \describe{ \item{\code{show(container)}}{prints container} \item{\code{length(container)}}{returns number of elements in the container} \item{\code{[[(index)} and \code{[[(index, value)}}{access and replace elements in the container } \item{\code{[(index)}}{make a subset of a container (which will itself be a container)} } } \examples{ x1 <- new("container", x=vector("list", length=3), content="lm") lm1 <- lm(rnorm(10)~runif(10)) x1[[1]] <- lm1 } \keyword{methods} \keyword{classes} Biobase/man/class.eSet.Rd0000644000175400017540000003266013175713325016230 0ustar00biocbuildbiocbuild\name{eSet} \docType{class} \alias{class:eSet} \alias{eSet} \alias{eSet-class} \alias{[,eSet-method} \alias{$,eSet-method} \alias{$<-,eSet-method} \alias{[[,eSet-method} \alias{[[<-,eSet-method} \alias{abstract,eSet-method} \alias{annotation,eSet-method} \alias{annotation<-,eSet,character-method} \alias{assayData,eSet-method} \alias{assayData<-,eSet,AssayData-method} \alias{assayDataElement} \alias{assayDataElement<-} \alias{assayDataElementNames} \alias{assayDataElementReplace} \alias{combine,eSet,ANY-method} \alias{combine,eSet,eSet-method} \alias{description,eSet-method} \alias{description<-,eSet,MIAME-method} \alias{dimnames} \alias{dimnames<-} \alias{dimnames,eSet-method} \alias{dimnames<-,eSet-method} \alias{dim,eSet-method} \alias{dims,eSet-method} \alias{experimentData,eSet-method} \alias{experimentData<-,eSet,MIAME-method} \alias{exprs,eSet-method} \alias{exprs<-,eSet,AssayData-method} \alias{featureData,eSet-method} \alias{featureData<-,eSet,AnnotatedDataFrame-method} \alias{featureNames,eSet-method} \alias{featureNames<-,eSet-method} \alias{fData,eSet-method} \alias{fData<-,eSet,data.frame-method} \alias{fvarLabels,eSet-method} \alias{fvarLabels<-,eSet-method} \alias{fvarMetadata,eSet-method} \alias{fvarMetadata<-,eSet,data.frame-method} \alias{initialize,eSet-method} \alias{ncol,eSet-method} \alias{notes,eSet-method} \alias{notes<-,eSet,ANY-method} \alias{pData,eSet-method} \alias{pData<-,eSet,data.frame-method} \alias{phenoData,eSet-method} \alias{phenoData<-,eSet,AnnotatedDataFrame-method} \alias{pubMedIds,eSet-method} \alias{pubMedIds<-,eSet,character-method} \alias{preproc,eSet-method} \alias{preproc<-,eSet-method} \alias{protocolData,eSet-method} \alias{protocolData<-,eSet,character-method} \alias{sampleNames,eSet-method} \alias{sampleNames<-,eSet,ANY-method} \alias{show,eSet-method} \alias{storageMode,eSet-method} \alias{storageMode<-,eSet,character-method} \alias{varLabels,eSet-method} \alias{varLabels<-,eSet-method} \alias{varMetadata,eSet-method} \alias{varMetadata<-,eSet,data.frame-method} \alias{storageMode,eSet-method} \alias{storageMode<-,eSet,character-method} \alias{updateObject,eSet-method} \alias{updateObjectTo,eSet,eSet-method} \alias{listOrEnv} \alias{SW} \concept{exprs} \concept{annotation} \concept{combine} \concept{description} \concept{ncol} \concept{notes} \concept{featureNames} \concept{sampleNames} \title{ Class to Contain High-Throughput Assays and Experimental Metadata } \description{ Container for high-throughput assays and experimental metadata. Classes derived from \code{eSet} contain one or more identical-sized matrices as \code{assayData} elements. Derived classes (e.g., \code{\link{ExpressionSet-class}}, \code{\link{SnpSet-class}}) specify which elements must be present in the \code{assayData} slot. \code{eSet} object cannot be instantiated directly; see the examples for usage. } \section{Creating Objects}{ \code{eSet} is a virtual class, so instances cannot be created. Objects created under previous definitions of \code{eSet-class} can be coerced to the current classes derived from \code{eSet} using \code{updateOldESet}. } \section{Slots}{ Introduced in \code{eSet}: \describe{ \item{\code{assayData}:}{Contains matrices with equal dimensions, and with column number equal to \code{nrow(phenoData)}. Class:\code{\link{AssayData-class}}} \item{\code{phenoData}:}{Contains experimenter-supplied variables describing sample (i.e., columns in \code{assayData}) phenotypes. Class: \code{\link{AnnotatedDataFrame-class}}} \item{\code{featureData}:}{Contains variables describing features (i.e., rows in \code{assayData}) unique to this experiment. Use the \code{annotation} slot to efficiently reference feature data common to the annotation package used in the experiment. Class: \code{\link{AnnotatedDataFrame-class}}} \item{\code{experimentData}:}{Contains details of experimental methods. Class: \code{\link{MIAME-class}}} \item{\code{annotation}:}{Label associated with the annotation package used in the experiment. Class: \code{character}} \item{\code{protocolData}:}{Contains microarray equipment-generated variables describing sample (i.e., columns in \code{assayData}) phenotypes. Class: \code{\link{AnnotatedDataFrame-class}}} \item{\code{.__classVersion__}:}{A \code{Versions} object describing the R and Biobase version numbers used to created the instance. Intended for developer use.} } } \section{Methods}{ Methods defined in derived classes (e.g., \code{\link{ExpressionSet-class}}, \code{\link{SnpSet-class}}) may override the methods described here. Class-specific methods: \describe{ \item{\code{sampleNames(object)} and \code{sampleNames(object)<-value}:}{Coordinate accessing and setting sample names in \code{assayData} and \code{phenoData}} \item{\code{featureNames(object)}, \code{featureNames(object) <- value}:}{Coordinate accessing and setting of feature names (e.g, genes, probes) in \code{assayData}.} \item{\code{dimnames(object)}, \code{dimnames(object) <- value}:}{Also \code{rownames} and \code{colnames}; access and set feature and sample names.} \item{\code{dims(object)}:}{Access the common dimensions (\code{dim}) or column numbers (\code{ncol}), or dimensions of all members (\code{dims}) of \code{assayData}.} \item{\code{phenoData(object)}, \code{phenoData(object) <- value}:}{Access and set \code{phenoData}. Adding new columns to \code{phenoData} is often more easily done with \code{eSetObject[["columnName"]] <- value}.} \item{\code{pData(object)}, \code{pData(object) <- value}:}{Access and set sample data information. Adding new columns to \code{pData} is often more easily done with \code{eSetObject[["columnName"]] <- value}.} \item{\code{varMetadata(object)}, \code{varMetadata(eSet,value)}}{Access and set metadata describing variables reported in \code{pData}} \item{\code{varLabels(object)}, \code{varLabels(eSet, value)<-}:}{Access and set variable labels in \code{phenoData}.} \item{\code{featureData(object)}, \code{featureData(object) <- value}:}{Access and set \code{featureData}.} \item{\code{fData(object)}, \code{fData(object) <- value}:}{Access and set feature data information.} \item{\code{fvarMetadata(object)}, \code{fvarMetadata(eSet,value)}}{Access and set metadata describing features reported in \code{fData}} \item{\code{fvarLabels(object)}, \code{fvarLabels(eSet, value)<-}:}{Access and set variable labels in \code{featureData}.} \item{\code{assayData(object), assayData(object) <- value}:}{ \code{signature(object = "eSet", value = "AssayData")}: Access and replace the \code{AssayData} slot of an \code{eSet} instance. \code{assayData} returns a list or environment; elements in \code{assayData} not accessible in other ways (e.g., via \code{exprs} applied directly to the \code{eSet}) can most reliably be accessed with, e.g., \code{assayData(obj)[["se.exprs"]]}.} \item{\code{experimentData(object)},\code{experimentData(object) <- value}:}{Access and set details of experimental methods} \item{\code{description(object)},\code{description(object) <- value}:}{Synonymous with experimentData.} \item{\code{notes(object)},\code{notes(object) <- value}:}{ \code{signature(object="eSet", value="list")} Retrieve and set unstructured notes associated with \code{eSet}. \code{signature(object="eSet", value="character")} As with value="list", but \emph{append} value to current list of notes.} \item{\code{pubMedIds(object)}, \code{pubMedIds(eSet,value)}}{Access and set PMIDs in \code{experimentData}.} \item{\code{abstract(object)}:}{Access abstract in \code{experimentData}.} \item{\code{annotation(object)}, \code{annotation(object) <- value}}{Access and set annotation label indicating package used in the experiment.} \item{\code{protocolData(object)}, \code{protocolData(object) <- value}}{Access and set the protocol data.} \item{\code{preproc(object)}, \code{preproc(object) <- value}:}{\code{signature(object="eSet", value="list")} Access and set \code{preprocessing} information in the \code{\link{MIAME-class}} object associated with this \code{eSet}.} \item{\code{combine(eSet,eSet)}:}{Combine two \code{eSet} objects. To be combined, eSets must have identical numbers of \code{featureNames}, distinct \code{sampleNames}, and identical \code{annotation}.} \item{\code{storageMode(object)}, \code{storageMode(eSet,character)<-}:}{Change storage mode of \code{\link{assayData}}. Can be used to 'unlock' environments, or to change between \code{list} and \code{environment} modes of storing \code{assayData}.} } Standard generic methods: \describe{ \item{\code{initialize(object)}:}{Object instantiation, can be called by derived classes but not usually by the user.} \item{\code{validObject(object)}:}{Validity-checking method, ensuring (1) all assayData components have the same number of features and samples; (2) the number and names of \code{phenoData} rows match the number and names of \code{assayData} columns} \item{\code{as(eSet, "ExpressionSet")}}{Convert instance of class \code{"eSet"} to instance of \code{\link{ExpressionSet-class}}, if possible.} \item{\code{as(eSet, "MultiSet")}}{Convert instance of class \code{"eSet"} to instance of \code{\link{MultiSet-class}}, if possible.} \item{\code{updateObject(object, ..., verbose=FALSE)}}{Update instance to current version, if necessary. Usually called through class inheritance rather than directly by the user. See \code{\link{updateObject}}} \item{\code{updateObjectTo(object, template, ..., verbose=FALSE)}}{Update instance to current version by updating slots in \code{template}, if necessary. Usually call by class inheritance, rather than directly by the user. See \code{\link{updateObjectTo}}} \item{\code{isCurrent(object)}}{Determine whether version of object is current. See \code{\link{isCurrent}}} \item{\code{isVersioned(object)}}{Determine whether object contains a 'version' string describing its structure . See \code{\link{isVersioned}}} \item{\code{show(object)}}{Informatively display object contents.} \item{\code{dim(object)}, \code{ncol}}{Access the common dimensions (\code{dim}) or column numbers (\code{ncol}), of all memebers (\code{dims}) of \code{assayData}.} \item{\code{object[(index)}:}{Conducts subsetting of matrices and phenoData components } \item{\code{object$name}, \code{object$name<-value}}{Access and set \code{name} column in \code{phenoData}} \item{\code{object[[i, ...]]}, \code{object[[i, ...]]<-value}}{Access and set column \code{i} (character or numeric index) in \code{phenoData}. The ... argument can include named variables (especially \code{labelDescription}) to be added to varMetadata.} } Additional functions: \describe{ \item{assayDataElement(object, element)}{Return matrix \code{element} from \code{assayData} slot of \code{object}.} \item{assayDataElement(object, element, validate=TRUE) <- value)}{Set element \code{element} in \code{assayData} slot of \code{object} to matrix \code{value}. If \code{validate=TRUE}, check that value row and column names of conform to object.} \item{assayDataElementReplace(object, element, value, validate=TRUE)}{Set element \code{element} in \code{assayData} slot of \code{object} to matrix \code{value}. If \code{validate=TRUE}, check that row and column names of value conform to object.} \item{assayDataElementNames(object)}{Return element names in \code{assayData} slot of \code{object}} \item{\code{updateOldESet}}{Update versions of \code{eSet} constructued using \code{listOrEnv} as \code{assayData} slot (before May, 2006).} } } \author{Biocore team} \seealso{ Method use in \code{\link{ExpressionSet-class}}. Related classes \code{\link{AssayData-class}}, \code{\link{AnnotatedDataFrame-class}}, \code{\link{MIAME-class}}. Derived classes \code{\link{ExpressionSet-class}}, \code{\link{SnpSet-class}}. To update objects from previous class versions, see \code{\link{updateOldESet}}. } \examples{ # update previous eSet-like class oldESet to existing derived class \dontrun{updateOldESet(oldESet, "ExpressionSet")} # create a new, ad hoc, class, for personal use # all methods outlined above are available automatically .MySet <- setClass("MySet", contains="eSet") .MySet() # Create a more robust class, with constructor and validation methods # to ensure assayData contains specific matricies .TwoColorSet <- setClass("TwoColorSet", contains="eSet") TwoColorSet <- function(phenoData=AnnotatedDataFrame(), experimentData=MIAME(), annotation=character(), R=new("matrix"), G=new("matrix"), Rb=new("matrix"), Gb=new("matrix"), ...) { .TwoColorSet(phenoData=phenoData, experimentData=experimentData, annotation=annotation, R=R, G=G, Rb=Rb, Gb=Gb, ...) } setValidity("TwoColorSet", function(object) { assayDataValidMembers(assayData(object), c("R", "G", "Rb", "Gb")) }) TwoColorSet() # eSet objects cannot be instantiated directly, only derived objects try(new("eSet")) removeClass("MySet") removeClass("TwoColorSet") } \keyword{classes} Biobase/man/classVersion.Rd0000644000175400017540000000361513175713325016675 0ustar00biocbuildbiocbuild\name{classVersion} \alias{classVersion} \alias{classVersion<-} \alias{classVersion,ANY-method} \alias{classVersion,character-method} \title{Retrieve information about versioned classes} \description{ These generic functions return version information for classes derived from \code{\link{Versioned-class}}, or \code{\link{VersionsNull-class}} for unversioned objects. The version information is an object of \code{\link{Versions-class}}. By default, \code{classVersion} has the following behaviors: \describe{ \item{\code{classVersion(Versioned-instance)}}{Returns a \code{Versions-class} object obtained from the object.} \item{\code{classVersion{"class"}}}{Consults the definition of \code{class} and return the current version information, if available.} \item{\code{classVersion(ANY)}}{Return a \code{\link{VersionsNull-class}} object to indicate no version information available.} } By default, the \code{classVersion<-} method has the following behavior: \describe{ \item{\code{classVersion(Versioned-instance)["id"] <- value}}{Assign (update or add) \code{value} to \code{Versions-instance}. \code{value} is coerced to a valid version description. see \code{\link{Versions-class}} for additional access methods.} } } \usage{ classVersion(object) classVersion(object) <- value } \arguments{ \item{object}{Object whose version is to be determined, as described above.} \item{value}{\code{Version-class} object to assign to object of \code{Versioned-class} object.} } \value{ \code{classVersion} returns an instance of \code{\link{Versions-class}} } \author{Biocore team} \seealso{\code{\link{Versions-class}}} \examples{ obj <- new("VersionedBiobase") classVersion(obj) classVersion(obj)["Biobase"] classVersion(1:10) # no version classVersion("ExpressionSet") # consult ExpressionSet prototype classVersion(obj)["MyVersion"] <- "1.0.0" classVersion(obj) } \keyword{manip} Biobase/man/contents.Rd0000644000175400017540000000151413175713325016053 0ustar00biocbuildbiocbuild\name{contents} \alias{contents} \title{Function to retrieve contents of environments} \description{ The contents method is used to retrieve the values stored in an environment. } \usage{ contents(object, all.names) } \arguments{ \item{object}{The environment (data table) that you want to get all contents from} \item{all.names}{a logical indicating whether to copy all values in \code{as.list.environment}} } \value{ A named list is returned, where the elements are the objects stored in the environment. The names of the elements are the names of the objects. The \code{all.names} argument is identical to the one used in \code{as.list.environment}. } \author{R. Gentleman} \seealso{\code{\link{as.list.environment}}} \examples{ z <- new.env() multiassign(letters, 1:26, envir=z) contents(z) } \keyword{manip} Biobase/man/copyEnv.Rd0000644000175400017540000000164113175713325015642 0ustar00biocbuildbiocbuild\name{copyEnv} \alias{copyEnv} \title{List-Environment interactions} \description{ These functions can be used to make copies of environments, or to get/assign all of the objects inside of an environment. } \usage{ copyEnv(oldEnv, newEnv, all.names=FALSE) } \arguments{ \item{oldEnv}{An environment to copy from} \item{newEnv}{An environment to copy to. If missing, a new environment with the same parent environment as oldEnv.} \item{all.names}{Whether to retrieve objects with names that start with a dot.} } \details{ \code{copyEnv}: This function will make a copy of the contents from \code{oldEnv} and place them into \code{newEnv}. } \author{Jeff Gentry and R. Gentleman} \seealso{\code{\link{environment}}, \code{\link{as.list}}} \examples{ z <- new.env(hash=TRUE, parent=emptyenv(), size=29L) multiassign(c("a","b","c"), c(1,2,3), z) a <- copyEnv(z) ls(a) } \keyword{utilities} Biobase/man/copySubstitute.Rd0000644000175400017540000001107513175713325017267 0ustar00biocbuildbiocbuild\name{copySubstitute} \alias{copySubstitute} \title{Copy Between Connections or Files with Configure-Like Name-Value Substitution} \description{ Copy files, directory trees or between connections and replace all occurences of a symbol by the corresponding value. } \usage{ copySubstitute(src, dest, symbolValues, symbolDelimiter="@", allowUnresolvedSymbols=FALSE, recursive = FALSE, removeExtension = "\\\\.in$") } \arguments{ \item{src}{Source, either a character vector with filenames and/or directory names, or a connection object.} \item{dest}{Destination, either a character vector of length 1 with the name of an existing, writable directory, or a connection object. The class of the \code{dest} argument must match that of the \code{src} argument.} \item{symbolValues}{A named list of character strings.} \item{symbolDelimiter}{A character string of length one with a single character in it.} \item{allowUnresolvedSymbols}{Logical. If \code{FALSE}, then the function will execute \code{\link[base:stop]{stop}} if it comes across symbols that are not defined in \code{symbolValues}.} \item{recursive}{Logical. If \code{TRUE}, the function works recursively down a directory tree (see details).} \item{removeExtension}{Character. Matches to this regular expression are removed from filenames and directory names.} } \details{ Symbol substitution: this is best explained with an example. If the list \code{symbolValues} contains an element with name \code{FOO} and value \code{bar}, and symbolDelimiter is \code{@}, then any occurrence of \code{@FOO@} is replaced by \code{bar}. This applies both the text contents of the files in \code{src} as well as to the filenames. See examples. If \code{recursive} is \code{FALSE}, both \code{src} and \code{dest} must be connection or a filenames. The text in \code{src} is read through the function \code{\link[base:readLines]{readLines}}, symbols are replaced by their values, and the result is written to \code{dest} through the function \code{\link[base:readLines]{writeLines}}. If \code{recursive} is \code{TRUE}, \code{\link[Biobase:copySubstitute]{copySubstitute}} works recursively down a directory tree (see details and example). \code{src} must be a character vector with multiple filenames or directory names, \code{dest} a directory name. One use of this function is in \code{\link[Biobase:createPackage]{createPackage}} for the automatic generation of packages from a template package directory. } \value{ None. The function is called for its side effect. } \author{Wolfgang Huber \url{http://www.dkfz.de/mga/whuber}} \keyword{connection} \keyword{programming} \examples{ ## create an example file infile = tempfile() outfile = tempfile() writeLines(text=c("We will perform in @WHAT@:", "So, thanks to @WHOM@ at once and to each one,", "Whom we invite to see us crown'd at @WHERE@."), con = infile) ## create the symbol table z = list(WHAT="measure, time and place", WHOM="all", WHERE="Scone") ## run copySubstitute copySubstitute(infile, outfile, z) ## display the results readLines(outfile) ##-------------------------------------------------------------- ## This is a slightly more complicated example that demonstrates ## how copySubstitute works on nested directories ##-------------------------------------------------------------- d = tempdir() my.dir.create = function(x) {dir.create(x); return(x)} unlink(file.path(d, "src"), recursive=TRUE) unlink(file.path(d, "dest"), recursive=TRUE) ## create some directories and files: src = my.dir.create(file.path(d, "src")) dest = file.path(d, "dest") d1 = my.dir.create(file.path(src, "dir1.in")) d2 = my.dir.create(file.path(src, "dir2@FOO@.in")) d3 = my.dir.create(file.path(d2, "dir3")) d4 = my.dir.create(file.path(d3, "dir4")) d5 = my.dir.create(file.path(d4, "dir5@BAR@")) writeLines(c("File1:", "FOO: @FOO@"), file.path(d1, "file1.txt.in")) writeLines(c("File2:", "BAR: @BAR@"), file.path(d2, "file2.txt.in")) writeLines(c("File3:", "SUN: @SUN@"), file.path(d3, "file3.txt.in")) writeLines(c("File4:", "MOON: @MOON@"), file.path(d4, "@SUN@.txt")) ## call copySubstitute copySubstitute(src, dest, recursive=TRUE, symbolValues = list(FOO="thefoo", BAR="thebar", SUN="thesun", MOON="themoon")) ## view the result listsrc = dir(src, full.names=TRUE, recursive=TRUE) listdest = dir(dest, full.names=TRUE, recursive=TRUE) listsrc listdest cat(unlist(lapply(listsrc, readLines)), sep="\n") cat(unlist(lapply(listdest, readLines)), sep="\n") } Biobase/man/createPackage.Rd0000644000175400017540000000503113175713325016733 0ustar00biocbuildbiocbuild\name{createPackage} \alias{createPackage} \title{Create a Package Directory from a Template} \description{ Create a package directory from a template, with symbol-value substitution } \usage{ createPackage(pkgname, destinationDir, originDir, symbolValues, unlink=FALSE, quiet=FALSE) } \arguments{ \item{pkgname}{Character. The name of the package to be written.} \item{destinationDir}{Character. The path to a directory where the package is to be written.} \item{originDir}{Character. The path to a directory that contains the template package. Usually, this will contain a file named \code{DESCRIPTION}, and subdirectories \code{R}, \code{man}, \code{data}. In all files and filenames, symbols will be replaced by their respective values, see the parameter \code{symbolValues}.} \item{symbolValues}{Named list of character strings. The symbol-to-value mapping. See \code{\link[Biobase:copySubstitute]{copySubstitute}} for details.} \item{unlink}{Logical. If \code{TRUE}, and \code{destinationDir} already contains a file or directory with the name \code{pkgname}, try to unlink (remove) it.} \item{quiet}{Logical. If \code{TRUE}, do not print information messages.} } \details{The intended use of this function is for the automated mass production of data packages, such as the microarray annotation, CDF, and probe sequence packages. No syntactic or other checking of the package is performed. For this, use R CMD check. The symbols \code{@PKGNAME@} and \code{@DATE@} are automatically defined with the values of \code{pkgname} and \code{date()}, respectively. } \value{ The function returns a \code{list} with one element \code{pkgdir}: the path to the package. } \seealso{\code{\link[Biobase:copySubstitute]{copySubstitute}}, the reference manual \emph{Writing R extensions}.} \author{Wolfgang Huber \url{http://www.dkfz.de/mga/whuber}} \keyword{programming} \examples{ sym = list(AUTHOR = "Hesiod", VERSION = "1.0", TITLE = "the nine muses", FORMAT = "Character vector containg the names of the 9 muses.") res = createPackage("muses", destinationDir = tempdir(), originDir = system.file("Code", package="Biobase"), symbolValues = sym, unlink = TRUE, quiet = FALSE) muses = c("Calliope", "Clio", "Erato", "Euterpe", "Melpomene", "Polyhymnia", "Terpsichore", "Thalia", "Urania") dir.create(file.path(res$pkgdir, "data")) save(muses, file = file.path(res$pkgdir, "data", "muses.rda")) res$pkgdir } Biobase/man/data.aaMap.Rd0000644000175400017540000000140213175713325016141 0ustar00biocbuildbiocbuild\name{data:aaMap} \alias{data:aaMap} \alias{aaMap} \docType{data} \title{Dataset: Names and Characteristics of Amino Acids } \usage{data(aaMap)} \description{ The \code{aaMap} data frame has 20 rows and 6 columns. Includes elementary information about amino acids. } \format{ This data frame contains the following columns: \describe{ \item{name}{amino acid name} \item{let.1}{one-letter code} \item{let.3}{three-letter code} \item{scProp}{side chain property at pH 7 (polar/nonpolar)} \item{hyPhilic}{logical: side chain is hydrophilic at pH 7} \item{acidic}{logical: side chain is acidic at pH 7} } } \source{ Nei M and Kumar S: Molecular evolution and phylogenetics (Oxford 2000), Table 1.2 } \examples{ data(aaMap) } \keyword{datasets} Biobase/man/data.geneData.Rd0000644000175400017540000000134713175713325016642 0ustar00biocbuildbiocbuild\name{data:geneData} \alias{data:geneData} \alias{geneData} \alias{data:geneCov} \alias{geneCov} \alias{data:geneCovariate} \alias{geneCovariate} \alias{data:seD} \alias{seD} \docType{data} \title{Sample expression matrix and phenotype data.frames.} \usage{data(geneData)} \description{ The \code{geneData} data.frame has 500 rows and 26 columns. It consists of a subset of real expression data from an Affymetrix U95v2 chip. The data are anonymous. The covariate data \code{geneCov} and \code{geneCovariate} are made up. The standard error data \code{seD} is also made up. } \format{ A 500 by 26 data frame. } \source{ The J. Ritz Laboratory (S. Chiaretti). } \examples{ data(geneData) data(geneCovariate) data(seD) } \keyword{datasets} Biobase/man/data.reporter.Rd0000644000175400017540000000227313175713325016773 0ustar00biocbuildbiocbuild\name{reporter} \alias{data:reporter} \alias{reporter} \docType{data} \title{Example data.frame representing reporter information} \description{ The \code{reporter} object is a 500 by 1 data frame. The rows represent the 500 probe IDs in the \code{geneData} data. The values in \code{reporter} are the predefined probe types for the probes. \code{reporter} is used in conjunction with the \code{geneData} object and its associates. } \usage{data(reporter)} \format{ A 500 by 1 data frame } \details{ There are 10 predefined probe types: \itemize{ \item \code{AFFX-} Quality Control (QC) \item \code{_f_} SequenceFamily \item \code{_g_} CommonGroups \item \code{_s_} SimilarityConstraint \item \code{_r_} RulesDropped \item \code{_i_} Incomplete \item \code{_b_} AmbiguousProbeSet \item \code{_l_} LongProbeSet \item \code{_at} AntiSenseTarget \item \code{_st} SenseTarget } } \source{ Affymetrix GeneChip Expression Analysis Data Analysis Fundamentals (\url{http://www.affymetrix.com/Auth/support/downloads/manuals/data_analysis_fundamentals_manual.pdf}) } \examples{ data(reporter) ## maybe str(reporter) ; plot(reporter) ... } \keyword{datasets} Biobase/man/data.sample.ExpressionSet.Rd0000644000175400017540000000170513175713325021223 0ustar00biocbuildbiocbuild\name{data:sample.ExpressionSet} \alias{data:sample.ExpressionSet} \alias{sample.ExpressionSet} \docType{data} \title{Dataset of class 'ExpressionSet'} \usage{data(sample.ExpressionSet)} \format{ The data for 26 cases, labeled A to Z and 500 genes. Each case has three covariates: sex (male/female); type (case/control); and score (testing score). } \description{ The expression data are real but anonymized. The data are from an experiment that used Affymetrix U95v2 chips. The data were processed by dChip and then exported to R for analysis. The data illustrate \code{\link{ExpressionSet-class}}, with \code{assayData} containing the required matrix element \code{exprs} and an additional matrix \code{se.exprs}. \code{se.exprs} has the same dimensions as \code{exprs}. The phenoData and standard error estimates (se.exprs) are made up. The information in the "description" slot is fake. } \examples{ data(sample.ExpressionSet) } \keyword{datasets} Biobase/man/data.sample.MultiSet.Rd0000644000175400017540000000126313175713325020155 0ustar00biocbuildbiocbuild\name{data:sample.MultiSet} \alias{data:sample.MultiSet} \alias{sample.MultiSet} \docType{data} \title{Data set of class 'MultiSet'} \usage{data(sample.MultiSet)} \format{ The data for 4 cases, labeled a to d and 500 genes. Each case has five covariates: SlideNumber: number; FileName: name; Cy3: genotype labeled Cy3; Cy5: genotype labeled Cy5; Date: date. } \description{ The expression data are real but anonymized. The data are from an experiment that used Affymetrix U95v2 chips. The data were processed by dChip and then exported to R for analysis. The phenoData, standard error estimates, and description data are fake. } \examples{ data(sample.MultiSet) } \keyword{datasets} Biobase/man/defunct.Rd0000644000175400017540000000250413175713325015646 0ustar00biocbuildbiocbuild\name{Deprecated and Defunct} \title{Biobase Deprecated and Defunct} \alias{class:annotatedDataset} \alias{annotatedDataset} \alias{annotatedDataset-class} \alias{initialize,annotatedDataset-method} \alias{class:exprList} \alias{exprList} \alias{exprList-class} \alias{class:exprMatrix} \alias{exprMatrix} \alias{exprMatrix-class} \alias{class:exprSet} \alias{exprSet} \alias{exprSet-class} \alias{initialize,exprSet-method} \alias{class:phenoData} \alias{phenoData-class} \alias{initialize,phenoData-method} \alias{data:sample.eSet} \alias{sample.eSet} \alias{data:sample.exprSet.1} \alias{sample.exprSet.1} \alias{data:sample.exprSet} \alias{sample.exprSet} \alias{df2pD} \alias{read.pD} \alias{read.exprSet} \alias{read.phenoData} \alias{geneNames} \alias{geneNames,ExpressionSet-method} \alias{geneNames<-} \alias{geneNames<-,ExpressionSet,character-method} \alias{getExpData} \alias{getExpData,eSet,character-method} \alias{eList} \alias{eList,eSet-method} \alias{eList<-} \alias{eList<-,eSet,AssayData-method} \alias{reporterNames} \alias{reporterNames,eSet-method} \alias{reporterNames<-} \alias{reporterNames<-,eSet,character-method} \alias{updateOldMiame} \alias{l2e} \alias{biocReposList} \description{ The function, class, or data object you have asked for has been deprecated or made defunct. } \keyword{internal} Biobase/man/description.Rd0000644000175400017540000000137413175713325016545 0ustar00biocbuildbiocbuild\name{description} \alias{description} \alias{description<-} \title{Retrieve and set overall experimental information eSet-like classes.} \description{ These generic functions access experimental information associated with \code{\link{eSet-class}}. } \usage{ description(object, \dots) description(object) <- value } \arguments{ \item{object}{Object, possibly derived from class \code{\link{eSet-class}}.} \item{value}{Structured information describing the experiment, e.g., of \code{\link{MIAME-class}}.} \item{\dots}{Further arguments to be used by other methods. } } \value{ \code{description} returns an object of \code{\link{MIAME-class}}. } \author{Biocore} \seealso{\code{\link{eSet-class}}, \code{\link{MIAME-class}}} \keyword{manip} Biobase/man/dims.Rd0000644000175400017540000000101113175713325015142 0ustar00biocbuildbiocbuild\name{dims} \alias{dims} \title{Retrieve dimensions of all elements in a list or environment} \description{ This function returns the dimensions of element members in lists or environments such as \code{AssayData-class}. } \usage{ dims(object) } \arguments{ \item{object}{List or environment object containing one or several matrices} } \value{ matrix of row and column dimensions, (in rows) for each element in \code{object} (columns). } \author{Biocore} \seealso{\code{\link{eSet-class}}} \keyword{manip} Biobase/man/dumpPackTxt.Rd0000644000175400017540000000075613175713325016471 0ustar00biocbuildbiocbuild\name{dumpPackTxt} \alias{dumpPackTxt} \title{Dump Textual Description of a Package } \description{ Dump textual description of a package } \usage{ dumpPackTxt(package) } \arguments{ \item{package}{Character string naming an R package} } \details{ dumps DESCRIPTION and INDEX files from package sources } \value{ \code{stdout} output } \author{} \note{ Other approaches using formatDL are feasible } \examples{ dumpPackTxt("stats") } \keyword{ models } Biobase/man/esApply.Rd0000644000175400017540000000552313175713325015637 0ustar00biocbuildbiocbuild\name{esApply} \alias{esApply} \title{ An apply-like function for ExpressionSet and related structures. } \description{ \code{esApply} is a wrapper to \code{apply} for use with \code{ExpressionSet}s. The application of a function to rows of an expression array usually involves variables in \code{pData}. \code{esApply} uses a special evaluation paradigm to make this easy. The function \code{FUN} may reference any data in \code{pData} by name. } \usage{ esApply(X, MARGIN, FUN, \dots) } \arguments{ \item{X}{An instance of class \code{\link{ExpressionSet}}.} \item{MARGIN}{The margin to apply to, either 1 for rows (samples) or 2 for columns (features).} \item{FUN}{Any function } \item{\dots}{Additional parameters for \code{FUN}.} } \details{ The \code{pData} from \code{X} is installed in an environment. This environment is installed as the environment of \code{FUN}. This will then provide bindings for any symbols in \code{FUN} that are the same as the names of the \code{pData} of \code{X}. If \code{FUN} has an environment already it is retained but placed after the newly created environment. Some variable shadowing could occur under these circumstances. } \value{ The result of \code{with(pData(x), apply(exprs(X), MARGIN, FUN, ...))}. } \author{V.J. Carey , R. Gentleman } \seealso{ \code{\link{apply}}, \code{\link{ExpressionSet}} } \examples{ data(sample.ExpressionSet) ## sum columns of exprs res <- esApply(sample.ExpressionSet, 1, sum) ## t-test, spliting samples by 'sex' f <- function(x) { xx <- split(x, sex) t.test(xx[[1]], xx[[2]])$p.value } res <- esApply(sample.ExpressionSet, 1, f) ## same, but using a variable passed in the function call f <- function(x, s) { xx <- split(x, s) mean(xx[[1]]) - mean(xx[[2]]) } sex <- sample.ExpressionSet[["sex"]] res <- esApply(sample.ExpressionSet, 1, f, s = sex) # obtain the p-value of the t-test for sex difference mytt.demo <- function(y) { ys <- split(y, sex) t.test(ys[[1]], ys[[2]])$p.value } sexPValue <- esApply(sample.ExpressionSet, 1, mytt.demo) # obtain the p-value of the slope associated with score, adjusting for sex # (if we were concerned with sign we could save the z statistic instead at coef[3,3] myreg.demo <- function(y) { summary(lm(y ~ sex + score))$coef[3,4] } scorePValue <- esApply(sample.ExpressionSet, 1, myreg.demo) # a resampling method resamp <- function(ESET) { ntiss <- ncol(exprs(ESET)) newind <- sample(1:ntiss, size = ntiss, replace = TRUE) ESET[newind,] } # a filter q3g100filt <- function(eset) { apply(exprs(eset), 1, function(x) quantile(x,.75) > 100) } # filter after resampling and then apply set.seed(123) rest <- esApply({bool <- q3g100filt(resamp(sample.ExpressionSet)); sample.ExpressionSet[bool,]}, 1, mytt.demo) } \keyword{models} \keyword{methods} Biobase/man/exprs.Rd0000644000175400017540000000147613175713325015366 0ustar00biocbuildbiocbuild\name{exprs} \alias{exprs} \alias{exprs<-} \alias{se.exprs} \alias{se.exprs<-} \title{Retrieve expression data from eSets.} \description{ These generic functions access the expression and error measurements of assay data stored in an object derived from the \code{\link{eSet-class}}. } \usage{ exprs(object) exprs(object) <- value se.exprs(object) se.exprs(object) <- value } \arguments{ \item{object}{Object derived from class \code{eSet}.} \item{value}{Matrix with rows representing features and columns samples.} } \value{ \code{exprs} returns a (usually large!) matrix of expression values; \code{se.exprs} returns the corresponding matrix of standard errors, when available. } \author{Biocore} \seealso{\code{\link{eSet-class}}, \code{\link{ExpressionSet-class}}, \code{\link{SnpSet-class}}} \keyword{manip} Biobase/man/featureData.Rd0000644000175400017540000000250413175713325016443 0ustar00biocbuildbiocbuild\name{featureData} \alias{featureData} \alias{featureData<-} \alias{fData} \alias{fData<-} \alias{fvarLabels} \alias{fvarLabels<-} \alias{fvarMetadata} \alias{fvarMetadata<-} \title{Retrieve information on features recorded in eSet-derived classes.} \description{ These generic functions access feature data (experiment specific information about features) and feature meta-data (e.g., descriptions of feature covariates). } \usage{ featureData(object) featureData(object) <- value fData(object) fData(object) <- value fvarLabels(object) fvarLabels(object) <- value fvarMetadata(object) fvarMetadata(object) <- value } \arguments{ \item{object}{Object, possibly derived from \code{\link{eSet-class}} or \code{\link{AnnotatedDataFrame-class}}.} \item{value}{Value to be assigned to corresponding object.} } \value{ \code{featureData} returns an object containing information on both variable values and variable meta-data. \code{fvarLabels} returns a character vector of measured variable names. \code{fData} returns a data frame with features as rows, variables as columns. \code{fvarMetadata} returns a data frame with variable names as rows, description tags (e.g., unit of measurement) as columns. } \author{Biocore} \seealso{ \code{\linkS4class{eSet}}, \code{\linkS4class{ExpressionSet}} } \keyword{manip} Biobase/man/featureNames.Rd0000644000175400017540000000161513175713325016637 0ustar00biocbuildbiocbuild\name{featureNames} \alias{featureNames} \alias{featureNames<-} \alias{sampleNames} \alias{sampleNames<-} \title{Retrieve feature and sample names from eSets.} \description{ These generic functions access the feature names (typically, gene or SNP identifiers) and sample names stored in an object derived from the \code{\link{eSet-class}}. } \usage{ featureNames(object) featureNames(object) <- value sampleNames(object) sampleNames(object) <- value } \arguments{ \item{object}{Object, possibly derived from class \code{eSet}.} \item{value}{Character vector containing feature or sample names.} } \value{ \code{featureNames} returns a (usually long!) character vector uniquely identifying each feature.\code{sampleNames} returns a (usually shorter) character vector identifying samples. } \author{Biocore} \seealso{\code{\link{ExpressionSet-class}}, \code{\link{SnpSet-class}}} \keyword{manip} Biobase/man/getPkgVigs.Rd0000644000175400017540000000120213175713325016262 0ustar00biocbuildbiocbuild\name{getPkgVigs} \alias{getPkgVigs} \title{List Vignette Files for a Package} \description{ This function will return a listing of all vignettes stored in a package's \code{doc} directory. } \usage{ getPkgVigs(package = NULL) } \arguments{ \item{package}{A character vector of packages to search or \code{NULL}. The latter is for all attached packages (in \code{\link{search}()}).} } \value{ A data.frame with columns \code{package}, \code{filename}, \code{title}. } \author{Jeff Gentry, modifications by Wolfgang Huber.} \seealso{\code{\link{openVignette}}} \examples{ z <- getPkgVigs() z # and look at them } \keyword{utilities} Biobase/man/internals.Rd0000644000175400017540000000061113175713325016212 0ustar00biocbuildbiocbuild\name{Internals} \alias{aggenv} \alias{aggfun} \alias{content} \alias{expinfo} \alias{hybridizations} \alias{initfun} \alias{locked} \alias{normControls} \alias{otherInfo} %classes \alias{data.frameOrNULL-class} \alias{listOrEnv-class} %methods \alias{contents,environment-method} \title{Internals} \description{ Use help.search("your keyword", package="Biobase"). } \keyword{internal} Biobase/man/isCurrent.Rd0000644000175400017540000000371113175713325016175 0ustar00biocbuildbiocbuild\name{isCurrent} \alias{isCurrent} \alias{isCurrent,ANY,ANY-method} \title{Use version information to test whether class is current} \description{ This generic function uses \code{\link{Versioned-class}} information to ask whether an instance of a class (e.g., read from disk) has current version information. By default, \code{isCurrent} has the following behaviors: \describe{ \item{\code{isCurrent(Versioned-instance)}}{Returns a vector of logicals, indicating whether each version matches the current version from the class prototype.} \item{\code{isCurrent(ANY)}}{Return \code{NA}, indicating that the version cannot be determined} \item{\code{isCurrent(Versioned-instance, "class")}}{Returns a logical vector indicating whether version identifiers shared between \code{Versioned-instance} and \code{"class"} are current.} } Starting with R-2.6 / Bioconductor 2.1 / Biobase 1.15.1, \code{isCurrent(Versioned-instance, ...)} returns an element \code{S4} indicating whether the class has the `S4' bit set; a value of \code{FALSE} indicates that the object needs to be recreated. } \usage{ isCurrent(object, value) } \arguments{ \item{object}{Object whose version is to be determined, as described above.} \item{value}{(Optional) character string identifying a class with which to compare versions.} } \value{ \code{isCurrent} returns a logical vector. } \author{Biocore team} \seealso{\code{\link{Versions-class}}} \examples{ obj <- new("VersionedBiobase") isCurrent(obj) isCurrent(1:10) # NA A <- setClass("A", contains="VersionedBiobase", prototype=prototype(new("VersionedBiobase", versions=c(A="1.0.0")))) a <- A() classVersion(a) isCurrent(a, "VersionedBiobase") # is the 'VersionedBiobase' portion current? classVersion(a)["A"] <- "1.0.1" classVersion(a) isCurrent(a, "VersionedBiobase") isCurrent(a) # more recent, so does not match 'current' defined by prototype removeClass("A") } \keyword{manip} Biobase/man/isUnique.Rd0000644000175400017540000000076413175713325016026 0ustar00biocbuildbiocbuild\name{isUnique} \alias{isUnique} \title{Determine Unique Elements} \description{ Determines which elements of a vector occur exactly once. } \usage{ isUnique(x) } \arguments{ \item{x}{a vector} } \value{A logical vector of the same length as \code{x}, in which \code{TRUE} indicates uniqueness.} \seealso{\code{\link[base:unique]{unique}},\code{\link[base:duplicated]{duplicated}}.} \author{Wolfgang Huber} \examples{ x <- c(9:20, 1:5, 3:7, 0:8) isUnique(x) } \keyword{logic} \keyword{manip} Biobase/man/isVersioned.Rd0000644000175400017540000000255513175713325016516 0ustar00biocbuildbiocbuild\name{isVersioned} \alias{isVersioned} \alias{isVersioned,ANY-method} \alias{isVersioned,character-method} \title{Determine whether object or class contains versioning information} \description{ This generic function checks to see whether \code{\link{Versioned-class}} information is present. When the argument to \code{isVersioned} is a character string, the prototype of the class corresponding to the string is consulted. By default, \code{isVersioned} has the following behaviors: \describe{ \item{\code{isVersioned(Versioned-instance)}}{Returns \code{TRUE} when the instance have version information.} \item{\code{isCurrent("class-name")}}{Returns \code{TRUE} when the named class extends \code{\link{Versioned-class}}.} \item{\code{isVersioned(ANY)}}{Returns \code{FALSE}} } } \usage{ isVersioned(object) } \arguments{ \item{object}{Object or class name to check for version information, as described above.} } \value{ \code{isVersioned} returns a logical indicating whether version information is present. } \author{Biocore team} \seealso{\code{\link{Versions-class}}} \examples{ obj <- new("VersionedBiobase") isVersioned(obj) isVersioned(1:10) # FALSE A <- setClass("A", contains="VersionedBiobase", prototype=prototype(new("VersionedBiobase", versions=c(A="1.0.0")))) a <- A() isVersioned(a) removeClass("A") } \keyword{manip} Biobase/man/lcSuffix.Rd0000644000175400017540000000330213175713325015776 0ustar00biocbuildbiocbuild\name{lcSuffix} \alias{lcSuffix} \alias{lcPrefix} \alias{lcPrefixC} \title{Compute the longest common prefix or suffix of a string} \description{ These functions find the longest common prefix or suffix among the strings in a character vector. } \usage{ lcPrefix(x, ignore.case=FALSE) lcPrefixC(x, ignore.case=FALSE) lcSuffix(x, ignore.case=FALSE) } \arguments{ \item{x}{ a character vector. } \item{ignore.case}{ A logical value indicating whether or not to ignore the case in making comparisons. } } \details{ Computing the longest common suffix is helpful for truncating names of objects, like microarrays, that often have a common suffix, such as .CEL. There are some potential problems with the approach used if multibyte character encodings are being used. \code{lcPrefixC} is a faster implementation in C. It only handles ascii characters. } \value{ The common prefix or suffix. } \author{ R. Gentleman } \seealso{ \code{\link{nchar}}, \code{\link{nchar}}} \examples{ s1 <- c("ABC.CEL", "DEF.CEL") lcSuffix(s1) s2 <- c("ABC.123", "ABC.456") lcPrefix(s2) CHK <- stopifnot CHK(".CEL" == lcSuffix(s1)) CHK("bc" == lcSuffix(c("abc", "333abc", "bc"))) CHK("c" == lcSuffix(c("c", "abc", "xxxc"))) CHK("" == lcSuffix(c("c", "abc", "xxx"))) CHK("ABC." == lcPrefix(s2)) CHK("ab" == lcPrefix(c("abcd", "abcd123", "ab", "abc", "abc333333"))) CHK("a" == lcPrefix(c("abcd", "abcd123", "ax"))) CHK("a" == lcPrefix(c("a", "abcd123", "ax"))) CHK("" == lcPrefix(c("a", "abc", "xxx"))) CHK("ab" == lcPrefixC(c("abcd", "abcd123", "ab", "abc", "abc333333"))) CHK("a" == lcPrefixC(c("abcd", "abcd123", "ax"))) CHK("a" == lcPrefixC(c("a", "abcd123", "ax"))) CHK("" == lcPrefixC(c("a", "abc", "xxx"))) } \keyword{ manip } Biobase/man/listLen.Rd0000644000175400017540000000147013175713325015631 0ustar00biocbuildbiocbuild\name{listLen} \alias{listLen} \title{Lengths of list elements} \description{ This function returns an integer vector with the length of the elements of its argument, which is expected to be a list. } \usage{ listLen(x) } \arguments{ \item{x}{A list} } \details{ This function returns a vector of the same length as the list \code{x} containing the lengths of each element. The current implementation is intended for lists containing vectors and the C-level length function is used to determine length. This means no dispatch is done for the elements of the list. If your list contains S4 objects, you should use \code{sapply(x, length)} instead. } \author{Jeff Gentry and R. Gentleman} \seealso{\code{\link{sapply}}} \examples{ foo = lapply(1:8, rnorm) listLen(foo) } \keyword{utilities} Biobase/man/makeDataPackage.Rd0000644000175400017540000000375513175713325017212 0ustar00biocbuildbiocbuild\name{makeDataPackage} \alias{makeDataPackage} \alias{makeDataPackage,ANY-method} \title{Make an R package from a data object} \description{ This generic creates a valid R package from an R data object. } \usage{ makeDataPackage(object, author, email, packageName=deparse(substitute(object)), packageVersion=package_version("1.0.0"), license="Artistic-2.0", biocViews="ExperimentData", filePath=tempdir(), \dots) } \arguments{ \item{object}{An instance of an R data object.} \item{author}{The author, as a character string.} \item{email}{A valid email address for the maintainer, as a character string.} \item{packageName}{The name of the package, defaults to the name of the object instance.} \item{packageVersion}{The version number, as a character string.} \item{license}{The license, as a character string.} \item{biocViews}{A character vector of valid biocViews views.} \item{filePath}{The location to create the package.} \item{\dots}{Additional arguments to specific methods.} } \details{ The function makes use of various tools in R and Bioconductor to automatically generate the source files for a valid R package. } \value{ The return value is that from a call to \code{link{createPackage}} which is invoked once the default arguments are set up. The data instance is stored in the data directory with a name the same as that of the resulting package. } \note{Developers implementing derived methods might force correct package name evaluation by including 'packageName' in any \code{callNextMethod()}.} \author{R. Gentleman} \seealso{\code{\link{createPackage}}} \examples{ data(sample.ExpressionSet) ## package created in tempdir() s1 <- makeDataPackage(sample.ExpressionSet, author = "Foo Author", email = "foo@bar", packageName = "FooBarPkg", packageVersion = "1.0.0") } \keyword{manip} Biobase/man/matchpt.Rd0000644000175400017540000000330013175713325015651 0ustar00biocbuildbiocbuild\name{matchpt} \alias{matchpt} \docType{methods} \title{Nearest neighbor search.} \description{ Find the nearest neighbors of a set of query points in the same or another set of points in an n-dimensional real vector space, using the Euclidean distance. } \usage{ matchpt(x, y) } \arguments{ \item{x}{A matrix (or vector) of coordinates. Each row represents a point in an \code{ncol(x)}-dimensional real vector space.} \item{y}{Optional, matrix (or vector) with the same number of columns as \code{x}.} } \details{ If \code{y} is provided, the function searches for each point in \code{x} its nearest neighbor in \code{y}. If \code{y} is missing, it searches for each point in \code{x} its nearest neighbor in \code{x}, excluding that point itself. In the case of ties, only the neighbor with the smaller index is given. The implementation is simple and of complexity \code{nrow(x)} times \code{nrow(y)}. For larger problems, please consider one of the many more efficient nearest neighbor search algorithms. } \value{ A \code{data.frame} with two columns and \code{nrow(x)} rows. The first column is the index of the nearest neighbor, the second column the distance to the nearest neighbor. If \code{y} was given, the index is a row number in \code{y}, otherwise, in \code{x}. The row names of the result are those of \code{x}. } \author{ Oleg Sklyar \email{osklyar@ebi.ac.uk} } \examples{ a <- matrix(c(2,2,3,5,1,8,-1,4,5,6), ncol=2L, nrow=5L) rownames(a) = LETTERS[seq_len(nrow(a))] matchpt(a) b <- c(1,2,4,5,6) d <- c(5.3, 3.2, 8.9, 1.3, 5.6, -6, 4.45, 3.32) matchpt(b, d) matchpt(d, b) } \keyword{manip} \keyword{array} Biobase/man/multiassign.Rd0000644000175400017540000000406313175713325016557 0ustar00biocbuildbiocbuild\name{multiassign} \alias{multiassign} \title{Assign Values to a Names} \description{ Assign values to names in an environment. } \usage{ multiassign(x, value, envir = parent.frame(), inherits=FALSE) } \arguments{ \item{x}{A vector or list of names, represented by strings.} \item{value}{a vector or list of values to be assigned.} \item{envir}{the \code{\link{environment}} to use. See the details section.} \item{inherits}{should the enclosing frames of the environment be inspected?} } \details{ The \code{pos} argument can specify the environment in which to assign the object in any of several ways: as an integer (the position in the \code{\link{search}} list); as the character string name of an element in the search list; or as an \code{\link{environment}} (including using \code{\link{sys.frame}} to access the currently active function calls). The \code{envir} argument is an alternative way to specify an environment, but is primarily there for back compatibility. If \code{value} is missing and \code{x} has names then the values in each element of \code{x} are assigned to the names of \code{x}. } \value{ This function is invoked for its side effect, which is assigning the \code{values} to the variables in \code{x}. If no \code{envir} is specified, then the assignment takes place in the currently active environment. If \code{inherits} is \code{TRUE}, enclosing environments of the supplied environment are searched until the variable \code{x} is encountered. The value is then assigned in the environment in which the variable is encountered. If the symbol is not encountered then assignment takes place in the user's workspace (the global environment). If \code{inherits} is \code{FALSE}, assignment takes place in the initial frame of \code{envir}. } \examples{ #-- Create objects 'r1', 'r2', ... 'r6' -- nam <- paste("r",1:6, sep=".") multiassign(nam, 11:16) ls(pat="^r..$") #assign the values in y to variables with the names from y y<-list(a=4,d=mean,c="aaa") multiassign(y) } \keyword{data} Biobase/man/note.Rd0000644000175400017540000000124213175713325015161 0ustar00biocbuildbiocbuild\name{note} \alias{note} \title{Informational Messages} \description{ Generates an informational message that corresponds to its argument(s). Similar to warning() except prefaced by "Note:" instead of "Warning message:". } \usage{ note(...) } \arguments{ \item{\dots}{character vectors (which are pasted together) or NULL} } \details{ This function essentially cat()'s the created string to the screen. It is intended for messages to the user that are deemed to be 'informational', as opposed to warnings, etc. } \author{Jeff Gentry} \seealso{\code{\link{warning}},\code{\link{stop}}} \examples{ note("This is an example of a note") } \keyword{utilities} Biobase/man/notes.Rd0000644000175400017540000000142313175713325015345 0ustar00biocbuildbiocbuild\name{notes} \alias{notes} \alias{notes<-} \title{Retrieve and set eSet notes.} \description{ These generic functions access notes (unstructured descriptive data) associated \code{\link{eSet-class}}. \code{notes() <- } is unusual, in that the character vector is appended to the list of notes; use \code{notes() <- } to entirely replace the list. } \usage{ notes(object) notes(object) <- value } \arguments{ \item{object}{Object, possibly derived from class \code{eSet-class}.} \item{value}{Character vector containing unstructured information describing the experinement.} } \value{ \code{notes} returns a list. } \author{Biocore} \seealso{\code{\link{ExpressionSet-class}}, \code{\link{SnpSet-class}}} \keyword{manip} Biobase/man/openPDF.Rd0000644000175400017540000000177213175713325015517 0ustar00biocbuildbiocbuild\name{openPDF} \alias{openPDF} \title{Open PDF Files in a Standard Viewer} \description{ Displays the specified PDF file. } \usage{ openPDF(file, bg=TRUE) } \arguments{ \item{file}{A character string, indicating the file to view} \item{bg}{Should the pdf viewer be opened in the background.} } \details{ Currently this function works on Windows and Unix platforms. Under Windows, whatever program is associated with the file extension will be used. Under Unix, the function will use the program named in the % option "pdfViewer" (default is 'acroread'). -- the code checks pdfviewer! % and that's the option that options() documents. option "pdfviewer" (see \code{help(options)} for information on how this is set.) The \code{bg} argument is only interpreted on Unix. } \value{ This function is executed for its side effects. The specified PDF file is opened in the PDF viewer and \code{TRUE} is returned. } \author{ Jeff Gentry} \examples{ \dontrun{openPDF("annotate.pdf")} } \keyword{utilities} Biobase/man/openVignette.Rd0000644000175400017540000000166613175713325016675 0ustar00biocbuildbiocbuild\name{openVignette} \alias{openVignette} \title{ Open a Vignette or Show Vignette Selection Menu} \description{ Using the data returned by \code{vignette} this function provides a simple easy to use interface for opening vignettes. } \usage{ openVignette(package=NULL) } \arguments{ \item{package}{character string indicating the package to be used.} } \details{ If \code{package} is NULL then all packages are scanned for vignettes. The list of vignettes is presented to the user via the \code{menu} command. The user may select one of the vignettes to be opened in a PDF viewer. } \value{ No value is returned; this function is run entirely for the side effect of opening the pdf document in the PDF viewer. } \author{R. Gentleman } \seealso{\code{\link{vignette}}, \code{\link{openPDF}}, \code{\link{menu}}, \code{\link{getPkgVigs}}} \examples{ if( interactive() ) openVignette("Biobase") } \keyword{ utilities } Biobase/man/package.version.Rd0000644000175400017540000000163413175713325017300 0ustar00biocbuildbiocbuild\name{package.version} \alias{package.version} \title{Report Version of a Package} \description{ Will report the version number of a requested installed package } \usage{ package.version(pkg, lib.loc = NULL) } \arguments{ \item{pkg}{The name of the package} \item{lib.loc}{a character vector describing the location of R library trees to search through, or `NULL'. The default value of `NULL' corresponds to all libraries currently known.} } \details{ This function is a convenience wrapper around \code{package.description}, and will report simply the version number of the requested package. If the package does not exist or if the DESCRIPTION file can not be read, then an error will be thrown. } \value{ A character string reporting the version number. } \author{Jeff Gentry} \seealso{\code{\link{package.description}}} \examples{ package.version("Biobase") } \keyword{utilities} Biobase/man/phenoData.Rd0000644000175400017540000000252713175713325016126 0ustar00biocbuildbiocbuild\name{phenoData} \alias{phenoData} \alias{phenoData<-} \alias{varLabels} \alias{varLabels<-} \alias{varMetadata} \alias{varMetadata<-} \alias{pData} \alias{pData<-} \title{Retrieve information on experimental phenotypes recorded in eSet and ExpressionSet-derived classes.} \description{ These generic functions access the phenotypic data (e.g., covariates) and meta-data (e.g., descriptions of covariates) associated with an experiment. } \usage{ phenoData(object) phenoData(object) <- value varLabels(object) varLabels(object) <- value varMetadata(object) varMetadata(object) <- value pData(object) pData(object) <- value } \arguments{ \item{object}{Object, possibly derived from \code{\link{eSet-class}} or \code{\linkS4class{AnnotatedDataFrame}}.} \item{value}{Value to be assigned to corresponding object.} } \value{ \code{phenoData} returns an object containing information on both variable values and variable meta-data. \code{varLabels} returns a character vector of measured variables. \code{pData} returns a data frame with samples as rows, variables as columns. \code{varMetadata} returns a data frame with variable names as rows, description tags (e.g., unit of measurement) as columns. } \author{Biocore} \seealso{\code{\link{eSet-class}}, \code{\link{ExpressionSet-class}}, \code{\link{SnpSet-class}}} \keyword{manip} Biobase/man/protocolData.Rd0000644000175400017540000000137013175713325016651 0ustar00biocbuildbiocbuild\name{protocolData} \alias{protocolData} \alias{protocolData<-} \alias{protocolData<-,eSet,AnnotatedDataFrame-method} \title{Protocol Metadata} \description{ This generic function handles methods for adding and retrieving protocol metadata for the samples in eSets. } \usage{ protocolData(object) protocolData(object) <- value } \arguments{ \item{object}{Object derived from class eSet} \item{value}{Object of class AnnotatedDataFrame} } \value{ \code{protocolData(object)} returns an AnnotatedDataFrame containing the protocol metadata for the samples. } \author{Biocore} \seealso{\code{phenoData}, \code{\link{AnnotatedDataFrame-class}}, \code{\link{eSet-class}}, \code{\link{ExpressionSet-class}}, \code{\link{SnpSet-class}}} \keyword{manip} Biobase/man/read.AnnotatedDataFrame.Rd0000644000175400017540000000617313175713325020620 0ustar00biocbuildbiocbuild\name{read.AnnotatedDataFrame} \alias{read.AnnotatedDataFrame} \alias{write.AnnotatedDataFrame} \concept{AnnotatedDataFrame} \title{Read and write 'AnnotatedDataFrame'} \description{ Create an instance of class AnnotatedDataFrame by reading a file, or save an AnnotatedDataFrame to a file. } \usage{ read.AnnotatedDataFrame(filename, path, sep = "\t", header = TRUE, quote = "", stringsAsFactors = FALSE, row.names = 1L, varMetadata.char="#", widget = getOption("BioC")$Base$use.widgets, sampleNames = character(0), ...) write.AnnotatedDataFrame(x, file="", varMetadata.char="#", ..., append=FALSE, fileEncoding="") } \arguments{ \item{filename, file}{file or connection from which to read / write.} \item{x}{An instance of class \code{AnnotatedDataFrame}.} \item{path}{(optional) directory in which to find \code{filename}.} \item{row.names}{this argument gets passed on to \code{\link{read.table}} and will be used for the row names of the phenoData slot.} \item{varMetadata.char}{lines beginning with this character are used for the \code{varMetadata} slot. See examples.} \item{sep, header, quote, stringsAsFactors, ...}{further arguments that get passed on to \code{\link{read.table}} or \code{write.table}.} \item{widget}{logical. Currently this is \emph{not} implemented, and setting this option to \code{TRUE} will result in an error. In a precursor of this function, \code{read.phenoData}, this option could be used to open an interactive GUI widget for entering the data.} \item{sampleNames}{optional argument that could be used in conjunction with \code{widget}; do not use.} \item{append, fileEncoding}{Arguments as described in \code{\link{write.table}}}. } \details{ The function \code{\link{read.table}} is used to read \code{pData}. The argument \code{varMetadata.char} is passed on to that function as its argument \code{comment.char}. Lines beginning with \code{varMetadata.char} are expected to contain further information on the column headers of \code{pData}. The format is of the form: \code{# variable: textual explanation of the variable, units, measurement method, etc.} (assuming that \code{#} is the value of \code{varMetadata.char}). See also examples. \code{write.AnnotatedDataFrame} outputs \code{varLabels} and \code{varMetadata(x)$labelDescription} as commented header lines, and \code{pData(x)} as a with \code{write.table}. } \value{ \code{read.AnnotatedDataFrame}: An instance of class \code{AnnotatedDataFrame} \code{write.AnnotatedDataFrame}: \code{NULL}, invisibly. } \author{Martin Morgan and Wolfgang Huber, based on \code{read.phenoData} by Rafael A. Irizarry.} \seealso{\code{\link{AnnotatedDataFrame}} for additional methods, \code{\link{read.table}} for details of reading in phenotypic data} \examples{ exampleFile = system.file("extdata", "pData.txt", package="Biobase") adf <- read.AnnotatedDataFrame(exampleFile) adf head(pData(adf)) head(noquote(readLines(exampleFile)), 11) write.AnnotatedDataFrame(adf) # write to console by default } \keyword{file} \keyword{manip} Biobase/man/read.MIAME.Rd0000644000175400017540000000245113175713325015761 0ustar00biocbuildbiocbuild\name{read.MIAME} \alias{read.MIAME} \title{ Read MIAME Information into an Instance of Class 'MIAME' } \description{ Reads MIAME information from a file or using a widget. } \usage{ read.MIAME(filename = NULL, widget = getOption("BioC")$Base$use.widgets, ...) } \arguments{ \item{filename}{Filename from which to read MIAME information.} \item{widget}{Logical. If \code{TRUE} and a filename is not given, a widget is used to enter information.} \item{\dots}{Further arguments to \code{scan}.} } \details{ Notice that the \code{\link{MIAME}} class tries to cover the MIAME entries that are not covered by other classes in Bioconductor. Namely, experimental design, samples, hybridizations, normalization controls, and pre-processing information. The function \code{\link{scan}} is used to read. The file must be a flat file with the different entries for the instance of MIAME class separated by carriage returns. The order should be: name, lab, contact, title, abstract, and url. Alternatively a widget can be used. } \value{An object of class \code{\link{MIAME}}.} \author{Rafael Irizarry } \seealso{\code{\link{MIAME}},\code{\link[tkWidgets]{tkMIAME}} } \examples{ miame <- read.MIAME(widget=FALSE) ##creates an empty instance show(miame) } \keyword{file} Biobase/man/readExpressionSet.Rd0000644000175400017540000000732313175713325017671 0ustar00biocbuildbiocbuild\name{readExpressionSet} \alias{readExpressionSet} \concept{ExpressionSet} \title{Read 'ExpressionSet'} \description{ Create an instance of class ExpressionSet by reading data from files. \sQuote{widget} functionality is not implemented for readExpressionSet. } \usage{ readExpressionSet(exprsFile, phenoDataFile, experimentDataFile, notesFile, path, annotation, ## arguments to read.* methods exprsArgs=list(sep=sep, header=header, row.names=row.names, quote=quote, ...), phenoDataArgs=list(sep=sep, header=header, row.names=row.names, quote=quote, stringsAsFactors=stringsAsFactors, ...), experimentDataArgs=list(sep=sep, header=header, row.names=row.names, quote=quote, stringsAsFactors=stringsAsFactors, ...), sep = "\t", header = TRUE, quote = "", stringsAsFactors = FALSE, row.names = 1L, ## widget widget = getOption("BioC")$Base$use.widgets, ...) } \arguments{ \item{exprsFile}{(character) File or connection from which to read expression values. The file should contain a matrix with rows as features and columns as samples. \code{\link{read.table}} is called with this as its \code{file} argument and further arguments given by \code{exprsArgs}.} \item{phenoDataFile}{(character) File or connection from which to read phenotypic data. \code{\link{read.AnnotatedDataFrame}} is called with this as its \code{file} argument and further arguments given by \code{phenoDataArgs}.} \item{experimentDataFile}{(character) File or connection from which to read experiment data. \code{\link{read.MIAME}} is called with this as its \code{file} argument and further arguments given by \code{experimentDataArgs}.} \item{notesFile}{(character) File or connection from which to read notes; \code{\link{readLines}} is used to input the file.} \item{path}{(optional) directory in which to find all the above files.} \item{annotation}{(character) A single character string indicating the annotation associated with this ExpressionSet.} \item{exprsArgs}{A list of arguments to be used with \code{\link{read.table}} when reading in the expression matrix.} \item{phenoDataArgs}{A list of arguments to be used (with \code{\link{read.AnnotatedDataFrame}}) when reading the phenotypic data.} \item{experimentDataArgs}{A list of arguments to be used (with \code{\link{read.MIAME}}) when reading the experiment data.} \item{sep, header, quote, stringsAsFactors, row.names}{arguments used by the \code{\link{read.table}}-like functions.} \item{widget}{A boolean value indicating whether widgets can be used. Widgets are NOT yet implemented for \code{read.AnnotatedDataFrame}.} \item{\dots}{Further arguments that can be passed on to the \code{\link{read.table}}-like functions.} } \details{ Expression values are read using the \code{\link{read.table}} function. Phenotypic data are read using the \code{\link{read.AnnotatedDataFrame}} function. Experiment data are read using the \code{\link{read.MIAME}} function. Notes are read using the \code{\link{readLines}} function. The return value must be a valid \code{ExpressionSet}. Only the \code{exprsFile} argument is required. } \value{ An instance of the \code{\linkS4class{ExpressionSet}} class. } \author{Martin Morgan } \seealso{\code{\link{ExpressionSet}} for additional methods.} \examples{ exprsFile = system.file("extdata", "exprsData.txt", package="Biobase") phenoFile = system.file("extdata", "pData.txt", package="Biobase") ## Read ExpressionSet with appropriate parameters obj = readExpressionSet(exprsFile, phenoFile, sep = "\t", header=TRUE) obj } \keyword{file} \keyword{manip} Biobase/man/reverseSplit.Rd0000644000175400017540000000163113175713325016705 0ustar00biocbuildbiocbuild\name{reverseSplit} \alias{reverseSplit} \title{ A function to reverse the role of names and values in a list. } \description{ Given a list with names \code{x} and values in a set \code{y} this function returns a list with names in \code{y} and values in \code{x}. } \usage{ reverseSplit(inList) } \arguments{ \item{inList}{ A named list with values that are vectors. } } \details{ First the list is unrolled to provide a two long vectors, names are repeated, once for each of their values. Then the names are \code{split} by the values. This turns out to be useful for inverting mappings between one set of identifiers and an other. } \value{ A list with length equal to the number of distinct values in the input list and values from the names of the input list. } \author{ R. Gentleman } \seealso{ \code{\link{split}}} \examples{ l1 = list(a=1:4, b=c(2,3), d=c(4,5)) reverseSplit(l1) } \keyword{ manip } Biobase/man/rowMedians.Rd0000644000175400017540000000315413175713325016330 0ustar00biocbuildbiocbuild\name{rowMedians} \alias{rowMedians} \alias{rowMedians,matrix-method} \alias{rowMedians,ExpressionSet-method} \title{Calculates the median for each row in a matrix} \description{ Calculates the median for each row in a matrix. } \usage{rowMedians(x, na.rm=FALSE, ...)} \arguments{ \item{x}{A \code{\link[base]{numeric}} NxK \code{\link[base]{matrix}}.} \item{na.rm}{If \code{\link[base:logical]{TRUE}}, \code{\link[base]{NA}}s are excluded first, otherwise not.} \item{...}{Not use.} } \value{ Returns a \code{\link[base]{numeric}} \code{\link[base]{vector}} of length N. } \section{Missing values}{ Missing values are excluded before calculating the medians. } \details{ The implementation of \code{rowMedians()} is optimized for both speed and memory. To avoid coercing to \code{\link[base]{double}}s (and hence memory allocation), there is a special implementation for \code{\link[base]{integer}} matrices. That is, if \code{x} is an \code{\link[base]{integer}} \code{\link[base]{matrix}}, then \code{rowMedians(as.double(x))} would require three times the memory of \code{rowMedians(x)}, but all this is avoided. } \author{Henrik Bengtsson} \seealso{ See \code{rowMeans()} in \code{\link[base]{colSums}}(). } \examples{ set.seed(1) x <- rnorm(n=234*543) x[sample(1:length(x), size=0.1*length(x))] <- NA dim(x) <- c(234,543) y1 <- rowMedians(x, na.rm=TRUE) y2 <- apply(x, MARGIN=1, FUN=median, na.rm=TRUE) stopifnot(all.equal(y1, y2)) x <- cbind(x1=3, x2=c(4:1, 2:5)) stopifnot(all.equal(rowMeans(x), rowMedians(x))) } \keyword{manip} Biobase/man/rowQ.Rd0000644000175400017540000000207013175713325015144 0ustar00biocbuildbiocbuild\name{rowQ} \alias{rowQ} \alias{rowQ,matrix,numeric-method} \alias{rowQ,ExpressionSet,numeric-method} \alias{rowMin} \alias{rowMax} \title{A function to compute empirical row quantiles.} \description{ This function computes the requested quantile for each row of a matrix, or of an \code{ExpressionSet}. } \usage{ rowQ(imat, which) rowMax(imat) rowMin(imat) } \arguments{ \item{imat}{Either a matrix or an \code{ExpressionSet}.} \item{which}{An integer indicating which order statistic should be returned.} } \details{ \code{rowMax} and \code{rowMin} simply call \code{rowQ} with the appropriate argument set. The argument \code{which} takes values between 1, for the minimum per row, and \code{ncol(imat)}, for the maximum per row. } \value{ A vector of length equal to the number of rows of the input matrix containing the requested quantiles. } \author{R. Gentleman} \seealso{ \code{\link{rowMedians}}. \code{rowMeans()} in \code{\link[base]{colSums}}(). } \examples{ data(sample.ExpressionSet) rowMin(sample.ExpressionSet) rowQ(sample.ExpressionSet, 4) } Biobase/man/selectChannels.Rd0000644000175400017540000000127013175713325017150 0ustar00biocbuildbiocbuild\name{selectChannels} \alias{selectChannels} \title{Create a new NChannelSet instance by selecting specific channels} \description{ This generic function extracts specific elements from an object, returning a instance of that object. } \usage{ selectChannels(object, names, ...) } \arguments{ \item{object}{An S4 object, typically derived from class \code{\link{eSet}}} \item{names}{Character vector of named channels.} \item{...}{Additional arguments.} } \value{ Instance of class \code{object}. } \author{Biocore} \examples{ obj <- NChannelSet(R=matrix(runif(100), 20, 5), G=matrix(runif(100), 20, 5)) ## G channel as NChannelSet selectChannels(obj, "G") } \keyword{manip} Biobase/man/selectSome.Rd0000644000175400017540000000230613175713325016321 0ustar00biocbuildbiocbuild\name{selectSome} \alias{selectSome} \title{Extract elements of a vector for concise rendering} \description{ Extract the first and last several elements of a vector for concise rendering; insert ellipses to indicate elided elements. This function is primarily meant for developer rather than end-user use. } \usage{ selectSome(obj, maxToShow=5) } \arguments{ \item{obj}{A vector.} \item{maxToShow}{The number of elements (including "...") to render.} } \details{ This function can be used in 'show' methods to give users exemplars of the tokens used in a vector. For example, an \code{\link{ExpressionSet}} built from a yeast experiment might have features enumerated using systematic gene names (e.g., YPR181C) or standard gene names (e.g., SEC23). The \code{\link{show}} method for \code{\link{ExpressionSet}} uses \code{selectSome} to alert the user to the tokens used, and thereby to indicate what vocabulary must be understood to work with the feature names. } \value{ A string vector with at most \code{maxToShow} plus 1 elements, where an ellipsis ("...") is included to indicate incompleteness of the excerpt. } \author{Martin Morgan } \examples{ selectSome(1:20) } \keyword{utilities} Biobase/man/snpCall.Rd0000644000175400017540000000155013175713325015612 0ustar00biocbuildbiocbuild\name{snpCall} \alias{snpCall} \alias{snpCall<-} \alias{snpCallProbability} \alias{snpCallProbability<-} \title{Get and retrieve SNP call and call probability data.} \description{ These generic functions access the calls and call probabilities stored in objects. } \usage{ snpCall(object, ...) snpCall(object, ...) <- value snpCallProbability(object, ...) snpCallProbability(object, ...) <- value } \arguments{ \item{object}{Object, possibly derived from class \code{SnpSet}.} \item{value}{Matrix with rows representing SNP calls or call probabilities and columns samples.} \item{...}{Additional arguments available to methods.} } \value{ \code{snpCall} returns a matrix of SNP calls; \code{snpCallProbability} returns the corresponding matrix of standard errors, when available. } \author{Biocore} \seealso{\code{\link{SnpSet-class}}} \keyword{manip} Biobase/man/storageMode.Rd0000644000175400017540000000133313175713325016466 0ustar00biocbuildbiocbuild\name{storageMode} \alias{storageMode} \alias{storageMode<-} \title{Retrieve or set storage mode for eSets.} \description{ These generic functions report or change the storage mode used for \code{assayData}. } \usage{ storageMode(object) storageMode(object) <- value } \arguments{ \item{object}{Object, derived from class \code{eSet}} \item{value}{Character vector containing \code{"lockedEnvironment"},\code{"environment"}, or \code{"list"}. See \code{AssayData-class} for details.} } \value{ \code{storageMode} returns a length-1 character vector } \author{Biocore} \seealso{\code{\link{AssayData-class}}, \code{\link{eSet-class}} \code{\link{ExpressionSet-class}}, \code{\link{SnpSet-class}}} \keyword{manip} Biobase/man/strbreak.Rd0000644000175400017540000000157013175713325016035 0ustar00biocbuildbiocbuild\name{strbreak} \alias{strbreak} \title{Break Character Strings to Fit Width} \description{ Inserts line breaks (\code{collapse}) into input character strings. The main intention of this function is to prepare long strings for printing, so the output is not wider than \code{width}. } \usage{ strbreak(x, width=getOption("width"), exdent=2, collapse="\n") } \arguments{ \item{x}{a character vector} \item{width}{a positive integer giving the width of the output.} \item{exdent}{a positive integer specifying the indentation of subsequent lines after the first line.} \item{collapse}{a character. This is inserted to break lines.} } \author{Wolfgang Huber \url{http://www.ebi.ac.uk/huber}} \seealso{\code{\link{strwrap}}, \code{\link{substring}}} \examples{ longString = paste(rep(LETTERS, 10), collapse="", sep="") cat(strbreak(longString)) } \keyword{character} Biobase/man/subListExtract.Rd0000644000175400017540000000353413175713325017202 0ustar00biocbuildbiocbuild\name{subListExtract} \alias{subListExtract} \title{Extract the same element from the sublists of a list} \description{ Given a list of lists, this function can be used to extract a named element from each sublist. } \usage{ subListExtract(L, name, simplify = FALSE, keep.names = TRUE) } \arguments{ \item{L}{A list of named lists} \item{name}{The name of the element in the sublists that should be extracted. This should be a length one character vector.} \item{simplify}{When \code{TRUE}, the return value will be an atomic vector. If any extracted sublist value has length not equal to one and \code{simplify=TRUE}, an error will be raised. When \code{FALSE}, a list is returned containing the extracted elements.} \item{keep.names}{If \code{TRUE} (default), the names of \code{L} will be attached to the returned vector.} } \details{ This function is implemented in C and is intended to be faster than calling \code{lapply} or \code{sapply}. } \value{ If \code{simplify=FALSE}, a list will be returned having the same length as \code{L}, but with each element containing the element named \code{name} from the corresponding inner list of \code{L}. When \code{simplify=TRUE}, an atomic vector will be returned containing the extracted elements. If any of the inner list elements do not have length one or cannot be put inside an atomic vector, an error will be raised. } \author{Seth Falcon} \examples{ list_size = 500000 innerL = list(foo="foo", bar="bar") L = rep(list(innerL), list_size) system.time({j0 = sapply(L, function(x) x$foo)}) system.time({j1 = subListExtract(L, "foo", simplify=TRUE)}) stopifnot(all.equal(j0, j1)) LS = L[1:3] names(LS) = LETTERS[1:3] subListExtract(LS, "bar", simplify=TRUE) subListExtract(LS, "bar", simplify=FALSE) subListExtract(LS, "bar", simplify=TRUE, keep.names=FALSE) } \keyword{manip} Biobase/man/testBioCConnection.Rd0000644000175400017540000000102013175713325017742 0ustar00biocbuildbiocbuild\name{testBioCConnection} \alias{testBioCConnection} \title{A function to check internet connectivity to Bioconductor} \description{ This function will attempt to determine if the user has internet connectivity to the Bioconductor website. This is useful in many situations dealing with code that uses automated downloads and other such things. } \usage{ testBioCConnection() } \value{ TRUE if a connection is possible, FALSE if not. } \author{Jeff Gentry} \examples{ z <- testBioCConnection() } \keyword{utilities} Biobase/man/updateObjectTo.Rd0000644000175400017540000000276113175713325017137 0ustar00biocbuildbiocbuild\name{updateObjectTo} \alias{updateObjectTo} \alias{updateObjectTo,ANY,ANY-method} \title{Update an object to the class definition of a template} \description{ The \code{updateObjectTo} generic function returns an instance of \code{object} updated to the class definition of \code{template}. It requires that the class of the returned object be the same as the class of the \code{template} argument, and that the object is valid. Usually, updating proceeds by modifying slots in \code{template} with information from \code{object}, and returning \code{template}. Use \code{\link{as}} to coerce an object from one type to another; \code{updateObjectTo} might be useful to update a virtual superclass. By default, \code{updateObjectTo} has the following behavior: \describe{ \item{\code{updateObjectTo(ANY-object,ANY-template)}}{Attempt \code{as(ANY-object,class(ANY-template))}.} } } \usage{ updateObjectTo(object, template, \dots, verbose=FALSE) } \arguments{ \item{object}{Object to be updated.} \item{template}{Instance representing a template for updating object.} \item{\dots}{Additional arguments, for use in specific update methods.} \item{verbose}{A logical, indicating whether information about the update should be reported. Use \code{message} to report this.} } \value{ \code{updateObjectTo} returns a valid instance of \code{template}. } \author{Biocore team} \seealso{ \code{\link[BiocGenerics]{updateObject}}, \code{\link{Versions-class}} } \keyword{manip} Biobase/man/updateOldESet.Rd0000644000175400017540000000200613175713325016715 0ustar00biocbuildbiocbuild\name{updateOldESet} \alias{updateOldESet} \title{Update previously created eSet object to current eSet structure} \description{ This function updates \code{eSet} objects created in previous versions of Biobase to the current class structure. Warnings indicate when coercions change how data in the \code{from} object are altered. If the \code{from} object was not a valid object of the original eSet class, then \code{updateOldESet} may fail. } \usage{ updateOldESet(from, toClass, ...) } \arguments{ \item{from}{Object created using a previous version of the eSet class.} \item{toClass}{Character string identifying new class, e.g., \code{"ExpressionSet"}} \item{...}{Additional arguments passed to the initialization method for class \code{toClass}} } \value{ Valid object of class \code{toClass}. } \author{Biocore} \seealso{\code{\link{eSet-class}}, \code{\link{ExpressionSet-class}}, \code{\link{SnpSet-class}}} \examples{ \dontrun{ updateOldESet(oldESet, "ExpressionSet") }} \keyword{manip} Biobase/man/userQuery.Rd0000644000175400017540000000122713175713325016223 0ustar00biocbuildbiocbuild\name{userQuery} \alias{userQuery} \title{A function to query the user for input} \description{ This function will output a given message and seek a response from the user, repeating the message until the input is from a valid set provided by the code. } \usage{ userQuery(msg, allowed = c("y", "n"), default = "n", case.sensitive = FALSE) } \arguments{ \item{msg}{The output message} \item{allowed}{Allowed input from the user} \item{default}{Default response if called in batch mode} \item{case.sensitive}{Is the response case sensitive? Defaults to \code{FALSE}} } \value{ The input from the user } \author{Jeff Gentry} \keyword{utilities} Biobase/man/validMsg.Rd0000644000175400017540000000117413175713325015766 0ustar00biocbuildbiocbuild\name{validMsg} \alias{validMsg} \title{Conditionally append result to validity message} \description{ This function facilitates constructing messages during S4 class validation, and is meant for developer rather than end-user use. } \usage{ validMsg(msg, result) } \arguments{ \item{msg}{A character vector or NULL.} \item{result}{Any vector.} } \details{ This function appends \code{result} to \code{msg}, but only if \code{result} is a character vector. } \author{Martin Morgan } \examples{ msg <- NULL validMsg(msg, FALSE) # still NULL msg <- validMsg(msg, "one") validMsg(msg, "two") } \keyword{utilities} Biobase/src/0000755000175400017540000000000013175724631013744 5ustar00biocbuildbiocbuildBiobase/src/Rinit.c0000644000175400017540000000212713175724631015177 0ustar00biocbuildbiocbuild#include #include #include SEXP anyMissing(SEXP); SEXP copyEnv(SEXP e1, SEXP e2, SEXP all); SEXP listToEnv(SEXP, SEXP); SEXP listLen(SEXP); SEXP rowQ(SEXP, SEXP); SEXP rowMedians(SEXP, SEXP, SEXP, SEXP); SEXP rowQuantiles(SEXP, SEXP); SEXP unsafe_set_slot(SEXP obj, SEXP slot, SEXP value); SEXP lc_prefix(SEXP, SEXP); SEXP sublist_extract(SEXP, SEXP, SEXP, SEXP); /* Automate using sed or something. */ #if _MSC_VER >= 1000 __declspec(dllexport) #endif static const R_CallMethodDef R_CallDef[] = { {"anyMissing", (DL_FUNC)&anyMissing, 1}, {"copyEnv", (DL_FUNC)©Env, 3}, {"listToEnv", (DL_FUNC)&listToEnv, 2}, {"listLen", (DL_FUNC)&listLen, 1}, {"rowQ", (DL_FUNC)&rowQ, 2}, {"rowMedians", (DL_FUNC)&rowMedians, 4}, {"unsafe_set_slot", (DL_FUNC)&unsafe_set_slot, 3}, {"lc_prefix", (DL_FUNC)&lc_prefix, 2}, {"sublist_extract", (DL_FUNC)&sublist_extract, 4}, {NULL, NULL, 0}, }; void R_init_Biobase(DllInfo *info) { R_registerRoutines(info,NULL,R_CallDef,NULL,NULL); } Biobase/src/anyMissing.c0000644000175400017540000000403413175724631016232 0ustar00biocbuildbiocbuild/*************************************************************************** Public methods: anyMissing(SEXP x) TO DO: Support list():s too. Copyright Henrik Bengtsson, 2007 **************************************************************************/ /* Include R packages */ #include SEXP anyMissing(SEXP x) { SEXP ans; int n, ii; PROTECT(ans = allocVector(LGLSXP, 1)); LOGICAL(ans)[0] = 0; n = length(x); /* anyMissing() on zero-length objects should always return FALSE, just like any(double(0)). */ if (n == 0) { UNPROTECT(1); return(ans); } switch (TYPEOF(x)) { case REALSXP: for (ii=0; ii < n; ii++) { if ISNAN(REAL(x)[ii]) { LOGICAL(ans)[0] = 1; break; } } break; case INTSXP: for (ii=0; ii < n; ii++) { if (INTEGER(x)[ii] == NA_INTEGER) { LOGICAL(ans)[0] = 1; break; } } break; case LGLSXP: for (ii=0; ii < n; ii++) { if (LOGICAL(x)[ii] == NA_LOGICAL) { LOGICAL(ans)[0] = 1; break; } } break; case CPLXSXP: for (ii=0; ii < n; ii++) { if (ISNAN(COMPLEX(x)[ii].r) || ISNAN(COMPLEX(x)[ii].i)) { LOGICAL(ans)[0] = 1; break; } } break; case STRSXP: for (ii=0; ii < n; ii++) { if (STRING_ELT(x, ii) == NA_STRING) { LOGICAL(ans)[0] = 1; break; } } break; case RAWSXP: /* no such thing as a raw NA */ break; default: break; /* warningcall(call, _("%s() applied to non-vector of type '%s'"), "anyMissing", type2char(TYPEOF(x))); */ } /* switch() */ UNPROTECT(1); /* ans */ return(ans); } // anyMissing() /*************************************************************************** HISTORY: 2007-08-14 [HB] o Created using do_isna() in src/main/coerce.c as a template. **************************************************************************/ Biobase/src/envir.c0000644000175400017540000001513513175724631015240 0ustar00biocbuildbiocbuild/* Copyright R. Gentleman, 2003 */ #include #include #include #include /* speed up the conversion, this could become as.environment at some time we might want to check the names though */ SEXP listLen(SEXP x) { SEXP ans; int i; int *lens; if (!Rf_isNewList(x)) error("arg 'x' must be a 'list', not '%s'", type2char(TYPEOF(x))); PROTECT(ans = allocVector(INTSXP, length(x))); lens = INTEGER(ans); for(i = 0; i < length(x); i++) lens[i] = length(VECTOR_ELT(x, i)); UNPROTECT(1); return(ans); } SEXP copyEnv(SEXP e1, SEXP e2, SEXP all) { SEXP nms, sym, val; int i, all_nms; if (!(isEnvironment(e1) && isEnvironment(e2) && isLogical(all))) error("invalid arguments"); all_nms = INTEGER(all)[0]; if (all_nms == NA_LOGICAL) error("arg 'all' must be TRUE or FALSE, not NA"); PROTECT(nms = R_lsInternal(e1, all_nms)); for (i = 0; i < length(nms); i++) { /* no inheritance in lookup */ PROTECT(sym = install(CHAR(STRING_ELT(nms, i)))); val = findVarInFrame3(e1, sym, TRUE); INCREMENT_NAMED(val); defineVar(sym, val, e2); UNPROTECT(1); } UNPROTECT(1); return(e2); } SEXP listToEnv(SEXP x, SEXP env) { SEXP name, nm, nx, sym; int i; if( !Rf_isNewList(x) ) error("first argument must be a list, found %s", type2char(TYPEOF(x))); if( !isEnvironment(env) ) error("second argument must be an environment, found %s", type2char(TYPEOF(env))); PROTECT(nm = getAttrib(x, R_NamesSymbol)); if( length(nm) != length(x) ) error("all elements must have names"); for( i=0; i= ncol ) error("cannot calculate order statistic on object with %d columns", ncol); PROTECT(ans = allocVector(REALSXP, nrow)); rowData = (double *) R_alloc(ncol, sizeof(double)); for( i=0; i min_nc) break; } ans = mkString(prefix); Free(prefix); UNPROTECT(1); return ans; } #ifdef ALLDONENOW ##looks like we need to either expose some of the ls functionality ##or copy a lot of code - my preference is to expose the ls ## code looks a lot like do_ls; but we get the objects too... ## with a duplicate - I suppose -- otherwise it will be a problem.... SEXP envToList(SEXP env, SEXP allnames) { SEXP nms, ans; int i, k, n; if( !isEnvironment(env) ) error("argument must be an environment"); if( !isLogical(allnames) ) error("second argument must be a logical"); all = asLogical(allNames); if (all == NA_LOGICAL) all = 0; /* Step 1 : Compute the Vector Size */ k = 0; n = length(env); for (i = 0; i < n; i++) { if (VECTOR_ELT(env, i) == R_NilValue) k += BuiltinSize(all, 0); else if (isEnvironment(VECTOR_ELT(env, i))) { if (HASHTAB(VECTOR_ELT(env, i)) != R_NilValue) k += HashTableSize(HASHTAB(VECTOR_ELT(env, i)), all); else k += FrameSize(FRAME(VECTOR_ELT(env, i)), all); } else error("invalid envir= argument"); } /* Step 2 : Allocate and Fill the Result */ nms = allocVector(STRSXP, k); ans = allocVector(VECSXP, k); k = 0; for (i = 0; i < n; i++) { if (VECTOR_ELT(env, i) == R_NilValue) { BuiltinNames(all, 0, nms, &k); } else if (isEnvironment(VECTOR_ELT(env, i))) { if (HASHTAB(VECTOR_ELT(env, i)) != R_NilValue) { HashTableNames(HASHTAB(VECTOR_ELT(env, i)), all, nms, &k); } else { FrameNames(FRAME(VECTOR_ELT(env, i)), all, nms, &k); } } } UNPROTECT(1); sortVector(ans, FALSE); return ans; } #endif Biobase/src/matchpt.c0000644000175400017540000000351113175724631015550 0ustar00biocbuildbiocbuild/* finds nearest neighbour, either for every point in one array (if only one is given) or nearest neighbour in the second array for every point in the first */ /* O.Sklyar, EBI, 2006 */ #include #include #define INDEX(i, j, n) ((i) + (j)*(n)) /* - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - */ SEXP matchpt(SEXP x, SEXP y) { int * dimx; double dist, mdist, tmp, *dx, *dy, *pd; int i, j, k, index, nptx, npty, ncol, noY, *pidx; SEXP res, namesres, idx, d; dimx = INTEGER(GET_DIM(x)); nptx = dimx[0]; ncol = dimx[1]; dx = REAL(x); if (y != R_NilValue) { dy = REAL(y); npty = INTEGER(GET_DIM(y))[0]; noY = 0; } else { dy = dx; npty = nptx; noY = 1; } PROTECT(d = allocVector(REALSXP, nptx)); PROTECT(idx = allocVector(INTSXP, nptx)); pd = REAL(d); pidx = INTEGER(idx); for (i = 0; i SEXP rowMedians_Real(SEXP x, int nrow, int ncol, int narm, int hasna, int byrow); SEXP rowMedians_Integer(SEXP x, int nrow, int ncol, int narm, int hasna, int byrow); /* TEMPLATE rowMedians_(...): - SEXP rowMedians_Real(...); - SEXP rowMedians_Integer(...); */ #define METHOD rowMedians #define X_TYPE 'i' #include "rowMedians_TYPE-template.h" #define X_TYPE 'r' #include "rowMedians_TYPE-template.h" #undef METHOD SEXP rowMedians(SEXP x, SEXP naRm, SEXP hasNA, SEXP byRow) { int narm, hasna, byrow; SEXP ans; int nrow, ncol; /* Argument 'x': */ if (!isMatrix(x)) error("Argument 'x' must be a matrix."); /* Argument 'naRm': */ if (!isLogical(naRm)) error("Argument 'naRm' must be a single logical."); if (length(naRm) != 1) error("Argument 'naRm' must be a single logical."); narm = LOGICAL(naRm)[0]; if (narm != TRUE && narm != FALSE) error("Argument 'naRm' must be either TRUE or FALSE."); /* Argument 'hasNA': */ hasna = LOGICAL(hasNA)[0]; /* Argument 'byRow': */ byrow = INTEGER(byRow)[0]; /* Get dimensions of 'x'. */ PROTECT(ans = getAttrib(x, R_DimSymbol)); if (byrow) { nrow = INTEGER(ans)[0]; ncol = INTEGER(ans)[1]; } else { nrow = INTEGER(ans)[1]; ncol = INTEGER(ans)[0]; } /* Double matrices are more common to use. */ if (isReal(x)) { ans = rowMedians_Real(x, nrow, ncol, narm, hasna, byrow); } else if (isInteger(x)) { ans = rowMedians_Integer(x, nrow, ncol, narm, hasna, byrow); } else { UNPROTECT(1); error("Argument 'x' must be a numeric."); } UNPROTECT(1); return(ans); } /* rowMedians() */ /*************************************************************************** HISTORY: 2013-01-13 [HB] o Added argument 'byRow' to rowMedians() and dropped colMedians(). o Using internal arguments 'by_row' instead of 'by_column'. 2011-12-11 [HB] o BUG FIX: rowMediansReal(..., na.rm=TRUE) did not handle NaN:s, only NA:s. Note that NaN:s does not exist for integers. 2011-10-12 [HJ] o Added colMedians(). o Now rowMediansInteger/Real() can operate also by columns, cf. argument 'by_column'. 2007-08-14 [HB] o Added checks for user interrupts every 1000 line. o Added argument 'hasNA' to rowMedians(). 2005-12-07 [HB] o BUG FIX: When calculating the median of an even number (non-NA) values, the length of the second sort was one element too short, which made the method to freeze, i.e. rPsort(rowData, qq, qq) is now (...qq+1, qq). 2005-11-24 [HB] o By implementing a special version for integers, there is no need to coerce to double in R, which would take up twice the amount of memory. o rowMedians() now handles NAs too. o Adopted from rowQuantiles.c in Biobase of Bioconductor. **************************************************************************/ Biobase/src/rowMedians_TYPE-template.h0000644000175400017540000001355713175724631020712 0ustar00biocbuildbiocbuild/*********************************************************************** TEMPLATE: SEXP rowMedians_(...) GENERATES: SEXP rowMedians_Integer(SEXP x, int nrow, int ncol, int narm, int hasna, int byrow) SEXP rowMedians_Real(SEXP x, int nrow, int ncol, int narm, int hasna, int byrow) Arguments: The following macros ("arguments") should be defined for the template to work as intended. - METHOD: the name of the resulting function - X_TYPE: 'i' or 'r' Authors: Adopted from rowQuantiles.c by R. Gentleman. Template by Henrik Bengtsson. Copyright: Henrik Bengtsson, 2007-2013 ***********************************************************************/ #include #include #include /* Expand arguments: X_TYPE => (X_C_TYPE, X_IN_C, X_ISNAN, [METHOD_NAME]) */ #include "templates-types.h" #if X_TYPE == 'i' #define PSORT iPsort #elif X_TYPE == 'r' #define PSORT rPsort #endif SEXP METHOD_NAME(SEXP x, int nrow, int ncol, int narm, int hasna, int byrow) { SEXP ans; int isOdd; int ii, jj, kk, qq; int *colOffset; X_C_TYPE *rowData, *xx, value; xx = X_IN_C(x); /* R allocate memory for the 'rowData'. This will be taken care of by the R garbage collector later on. */ rowData = (X_C_TYPE *) R_alloc(ncol, sizeof(X_C_TYPE)); /* R allocate a double vector of length 'nrow' Note that 'nrow' means 'ncol' if byrow=FALSE. */ PROTECT(ans = allocVector(REALSXP, nrow)); /* If there are no missing values, don't try to remove them. */ if (hasna == FALSE) narm = FALSE; /* When narm == FALSE, isOdd and qq are the same for all rows */ if (narm == FALSE) { isOdd = (ncol % 2 == 1); qq = (int)(ncol/2) - 1; } else { isOdd = FALSE; qq = 0; } value = 0; /* Pre-calculate the column offsets */ colOffset = (int *) R_alloc(ncol, sizeof(int)); // HJ begin if (byrow) { for(jj=0; jj < ncol; jj++) colOffset[jj] = (int)jj*nrow; } else { for(jj=0; jj < ncol; jj++) colOffset[jj] = jj; } // HJ end if (hasna == TRUE) { for(ii=0; ii < nrow; ii++) { if(ii % 1000 == 0) R_CheckUserInterrupt(); int rowIdx = byrow ? ii : ncol*ii; //HJ kk = 0; /* The index of the last non-NA value detected */ for(jj=0; jj < ncol; jj++) { value = xx[rowIdx+colOffset[jj]]; //HJ if (X_ISNAN(value)) { if (narm == FALSE) { kk = -1; break; } } else { rowData[kk] = value; kk = kk + 1; } } if (kk == 0) { REAL(ans)[ii] = R_NaN; } else if (kk == -1) { REAL(ans)[ii] = R_NaReal; } else { /* When narm == TRUE, isOdd and qq may change with row */ if (narm == TRUE) { isOdd = (kk % 2 == 1); qq = (int)(kk/2) - 1; } /* Permute x[0:kk-1] so that x[qq] is in the correct place with smaller values to the left, ... */ PSORT(rowData, kk, qq+1); value = rowData[qq+1]; if (isOdd == TRUE) { REAL(ans)[ii] = (double)value; } else { if (narm == TRUE || !X_ISNAN(value)) { /* Permute x[0:qq-2] so that x[qq-1] is in the correct place with smaller values to the left, ... */ PSORT(rowData, qq+1, qq); if (X_ISNAN(rowData[qq])) REAL(ans)[ii] = R_NaReal; else REAL(ans)[ii] = ((double)(rowData[qq] + value))/2; } else { REAL(ans)[ii] = (double)value; } } } } } else { for(ii=0; ii < nrow; ii++) { if(ii % 1000 == 0) R_CheckUserInterrupt(); int rowIdx = byrow ? ii : ncol*ii; //HJ for(jj=0; jj < ncol; jj++) rowData[jj] = xx[rowIdx+colOffset[jj]]; //HJ /* Permute x[0:ncol-1] so that x[qq] is in the correct place with smaller values to the left, ... */ PSORT(rowData, ncol, qq+1); value = rowData[qq+1]; if (isOdd == TRUE) { REAL(ans)[ii] = (double)value; } else { /* Permute x[0:qq-2] so that x[qq-1] is in the correct place with smaller values to the left, ... */ PSORT(rowData, qq+1, qq); REAL(ans)[ii] = (double)((rowData[qq] + value))/2; } } } /* if (hasna ...) */ UNPROTECT(1); return(ans); } /* Undo template macros */ #undef PSORT #include "templates-types_undef.h" /*************************************************************************** HISTORY: 2013-04-23 [HB] o BUG FIX: The integer template of rowMedians_() would not handle ties properly. This was because ties were calculated as '(double)((rowData[qq] + value)/2)' instead of '((double)(rowData[qq] + value))/2'. 2013-01-13 [HB] o Merged rowMedians_Integer() and rowMedians_Read() into template rowMedians_(). 2013-01-13 [HB] o Using internal arguments 'by_row' instead of 'by_column'. 2011-12-11 [HB] o BUG FIX: rowMediansReal(..., na.rm=TRUE) did not handle NaN:s, only NA:s. Note that NaN:s does not exist for integers. 2011-10-12 [HJ] o Added colMedians(). o Now rowMediansInteger/Real() can operate also by columns, cf. argument 'by_column'. 2007-08-14 [HB] o Added checks for user interrupts every 1000 line. o Added argument 'hasNA' to rowMedians(). 2005-12-07 [HB] o BUG FIX: When calculating the median of an even number (non-NA) values, the length of the second sort was one element too short, which made the method to freeze, i.e. rPsort(rowData, qq, qq) is now (...qq+1, qq). 2005-11-24 [HB] o By implementing a special version for integers, there is no need to coerce to double in R, which would take up twice the amount of memory. o rowMedians() now handles NAs too. o Adopted from rowQuantiles.c in Biobase of Bioconductor. **************************************************************************/ Biobase/src/sublist_extract.c0000644000175400017540000001170713175724631017335 0ustar00biocbuildbiocbuild#include static SEXP list_el(SEXP list, SEXP name) { SEXP elmt = R_NilValue; SEXP names = getAttrib(list, R_NamesSymbol); SEXP cur_name; const char *cname = CHAR(name); int i, found = 0; for (i = 0; i < length(list); i++) { cur_name = STRING_ELT(names, i); if (cur_name == name || strcmp(CHAR(cur_name), cname) == 0) { elmt = VECTOR_ELT(list, i); found = 1; break; } } if (!found) error("no element named '%s'", cname); return elmt; } Rboolean checkScalarLogical(SEXP v, Rboolean na_ok) { if (!isLogical(v)) error("expecting a logical vector, found a %s", type2char(TYPEOF(v))); if (length(v) != 1) error("expecting a logical vector of length one, found length %d", length(v)); if (!na_ok && LOGICAL(v)[0] == NA_LOGICAL) error("found NA where TRUE/FALSE needed"); return TRUE; } static void fill_integer(SEXP L, SEXP name, SEXP dest) { SEXP el; int *ansi; int i; ansi = INTEGER(dest); for (i = 0; i < length(L); i++) { el = list_el(VECTOR_ELT(L, i), name); if (length(el) != 1) error("unable to simplify, element %d has length %d", i, length(el)); ansi[i] = INTEGER(el)[0]; } } static void fill_double(SEXP L, SEXP name, SEXP dest) { SEXP el; double *ansd; int i; ansd = REAL(dest); for (i = 0; i < length(L); i++) { el = list_el(VECTOR_ELT(L, i), name); if (length(el) != 1) error("unable to simplify, element %d has length %d", i, length(el)); ansd[i] = REAL(el)[0]; } } static void fill_logical(SEXP L, SEXP name, SEXP dest) { SEXP el; int *ansi; int i; ansi = LOGICAL(dest); for (i = 0; i < length(L); i++) { el = list_el(VECTOR_ELT(L, i), name); if (length(el) != 1) error("unable to simplify, element %d has length %d", i, length(el)); ansi[i] = LOGICAL(el)[0]; } } static void fill_complex(SEXP L, SEXP name, SEXP dest) { SEXP el; Rcomplex *anscplx; int i; anscplx = COMPLEX(dest); for (i = 0; i < length(L); i++) { el = list_el(VECTOR_ELT(L, i), name); if (length(el) != 1) error("unable to simplify, element %d has length %d", i, length(el)); anscplx[i] = COMPLEX(el)[0]; } } static void fill_string(SEXP L, SEXP name, SEXP dest) { SEXP el; int i; for (i = 0; i < length(L); i++) { el = list_el(VECTOR_ELT(L, i), name); if (length(el) != 1) error("unable to simplify, element %d has length %d", i, length(el)); SET_STRING_ELT(dest, i, STRING_ELT(el, 0)); } } static void fill_raw(SEXP L, SEXP name, SEXP dest) { SEXP el; unsigned char *ansr; int i; ansr = RAW(dest); for (i = 0; i < length(L); i++) { el = list_el(VECTOR_ELT(L, i), name); if (length(el) != 1) error("unable to simplify, element %d has length %d", i, length(el)); ansr[i] = RAW(el)[0]; } } SEXP sublist_extract(SEXP L, SEXP namev, SEXP simplify, SEXP keep_names) { SEXP name, el, ans, ansnms; int i; if (!isNewList(L)) error("'L' must be a list"); if (!isString(namev) || length(namev) != 1) error("'name' must be a character vector of length one"); name = STRING_ELT(namev, 0); if (name == NA_STRING) error("'name' cannot be NA"); checkScalarLogical(simplify, 0); checkScalarLogical(keep_names, 0); if (LOGICAL(simplify)[0]) { if (!length(L)) error("can't extract from an empty list when simplify=TRUE"); el = list_el(VECTOR_ELT(L, 0), name); if (length(el) != 1) error("unable to simplify, element 0 has length %d", length(el)); PROTECT(ans = allocVector(TYPEOF(el), length(L))); switch (TYPEOF(el)) { case REALSXP: fill_double(L, name, ans); break; case INTSXP: fill_integer(L, name, ans); break; case LGLSXP: fill_logical(L, name, ans); break; case CPLXSXP: fill_complex(L, name, ans); break; case STRSXP: fill_string(L, name, ans); break; case RAWSXP: fill_raw(L, name, ans); break; default: error("unample to simplify when type is '%s'", type2char(TYPEOF(el))); break; } } else { PROTECT(ans = allocVector(VECSXP, length(L))); for (i = 0; i < length(L); i++) { SET_VECTOR_ELT(ans, i, list_el(VECTOR_ELT(L, i), name)); } } if (LOGICAL(keep_names)[0]) { ansnms = duplicate(getAttrib(L, R_NamesSymbol)); setAttrib(ans, R_NamesSymbol, ansnms); } UNPROTECT(1); return ans; } Biobase/src/templates-types.h0000644000175400017540000000162113175724631017255 0ustar00biocbuildbiocbuild/* * Sets type-specific macros */ #define CONCAT(x,y) x ##_## y #define CONCAT_MACROS(x,y) CONCAT(x,y) /* Data type macros for argument 'x' */ #if X_TYPE == 'i' #ifndef METHOD_NAME #define METHOD_NAME CONCAT_MACROS(METHOD, Integer) #endif #define X_C_TYPE int #define X_IN_C INTEGER #define X_ISNAN(x) (x == NA_INTEGER) #elif X_TYPE == 'r' #ifndef METHOD_NAME #define METHOD_NAME CONCAT_MACROS(METHOD, Real) #endif #define X_C_TYPE double #define X_IN_C REAL #define X_ISNAN(x) ISNAN(x) #endif /* Data type macros for result ('ans') */ #ifndef ANS_TYPE /* Default to same as 'x' */ #define ANS_TYPE X_TYPE #endif #if ANS_TYPE == 'i' #define ANS_SXP INTSXP #define ANS_NA NA_INTEGER #define ANS_C_TYPE int #define ANS_IN_C INTEGER #elif ANS_TYPE == 'r' #define ANS_SXP REALSXP #define ANS_NA NA_REAL #define ANS_C_TYPE double #define ANS_IN_C REAL #endif Biobase/src/templates-types_undef.h0000644000175400017540000000032313175724631020434 0ustar00biocbuildbiocbuild#undef CONCAT #undef CONCAT_MACROS #undef METHOD_NAME #undef X_C_TYPE #undef X_IN_C #undef X_ISNAN #undef ANS_SXP #undef ANS_NA #undef ANS_C_TYPE #undef ANS_IN_C #undef X_TYPE #undef ANS_TYPE #undef MARGIN Biobase/tests/0000755000175400017540000000000013175713325014315 5ustar00biocbuildbiocbuildBiobase/tests/test-all.R0000644000175400017540000000004613175713325016165 0ustar00biocbuildbiocbuildBiocGenerics:::testPackage("Biobase") Biobase/tests/test-rowMedians.R0000644000175400017540000000570713175713325017536 0ustar00biocbuildbiocbuildlibrary(Biobase) set.seed(1) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - # Consistency checks # - - - - - - - - - - - - - - - - - - - - - - - - - - - - # rowMedians() by rowQ() rowMedians2 <- function(imat) { nr <- ncol(imat) half <- (nr + 1)/2 if (nr%%2 == 1) { return(rowQ(imat, half)) } else { return((rowQ(imat, half) + rowQ(imat, half+1))/2) } } cat("Consistency checks:\n") set.seed(1) for (kk in 1:20) { cat("Random test #", kk, "\n", sep="") # Simulate data in a matrix of any shape nrow <- sample(2000, size=1) ncol <- sample(2000, size=1) x <- rnorm(nrow*ncol) dim(x) <- c(nrow, ncol) # Add NAs? nas <- sample(c(TRUE,FALSE), size=1) if (nas) { nna <- sample(nrow*ncol, size=1) x[sample(length(x), size=nna)] <- NA } na.rm <- nas t1 <- system.time({ y1 <- rowMedians(x, na.rm=na.rm) }) t2 <- system.time({ y2 <- apply(x, MARGIN=1, FUN=median, na.rm=na.rm) }) # When all values of 'y2' are NA, 'y2' is logical if (is.logical(y2)) y2 <- as.double(y2) stopifnot(all.equal(y1,y2)) cat(sprintf("rowMedians()/apply(): %.3g\n", (t1/t2)[3])) if (!nas) { t3 <- system.time({ y3 <- rowMedians2(x) }) stopifnot(all.equal(y1,y3)) cat(sprintf("rowMedians()/rowMedians2(): %.3g\n", (t1/t3)[3])) } } # - - - - - - - - - - - - - - - - - - - - - - - - - - - - # Benchmarking # - - - - - - - - - - - - - - - - - - - - - - - - - - - - cat("Benchmarking:\n") # Simulate data in a matrix of any shape nrow <- 1000 ncol <- 1000 x <- rnorm(nrow*ncol) dim(x) <- c(nrow, ncol) gc() t0 <- system.time({ for (rr in 1:20) y0 <- apply(x, MARGIN=1, FUN=median, na.rm=FALSE) }) gc() t1 <- system.time({ for (rr in 1:20) y1 <- rowMedians(x, na.rm=FALSE) }) gc() stopifnot(all.equal(y0,y1)) cat(sprintf("rowMedians()/apply(): %.3g\n", (t1/t0)[3])) # - - - - - - - - - - - - - - - - - - - - - - - - - - - - # Consistency checks # - - - - - - - - - - - - - - - - - - - - - - - - - - - - cat("Consistency checks without NAs:\n") for (kk in 1:20) { cat("Random test #", kk, "\n", sep="") # Simulate data in a matrix of any shape nrow <- sample(1000, size=1) ncol <- sample(1000, size=1) x <- rnorm(nrow*ncol) dim(x) <- c(nrow, ncol) t0 <- system.time({ y0 <- apply(x, MARGIN=1, FUN=median, na.rm=FALSE) }) t1 <- system.time({ y1 <- rowMedians(x, na.rm=FALSE) }) stopifnot(all.equal(y0,y1)) } # for (kk in ...) cat("Consistency checks with NAs:\n") for (kk in 1:20) { cat("Random test #", kk, "\n", sep="") # Simulate data in a matrix of any shape nrow <- sample(1000, size=1) ncol <- sample(1000, size=1) x <- rnorm(nrow*ncol) dim(x) <- c(nrow, ncol) # Add NAs nna <- sample(nrow*ncol-1, size=1) x[sample(length(x), size=nna)] <- NA t0 <- system.time({ y0 <- apply(x, MARGIN=1, FUN=median, na.rm=TRUE) y0[is.na(y0)] <- NA }) t1 <- system.time({ y1 <- rowMedians(x, na.rm=TRUE) }) stopifnot(all.equal(y0,y1)) } # for (kk in ...) Biobase/vignettes/0000755000175400017540000000000013175724631015165 5ustar00biocbuildbiocbuildBiobase/vignettes/BiobaseDevelopment.Rnw0000644000175400017540000006745113175713325021437 0ustar00biocbuildbiocbuild% % NOTE -- ONLY EDIT THE .Rnw FILE!!! The .tex file is % likely to be overwritten. % %\VignetteIndexEntry{Notes for eSet developers} %\VignetteDepends{} %\VignetteKeywords{Expression Analysis} %\VignettePackage{Biobase} \documentclass[]{article} \usepackage{times} \usepackage{hyperref} \newcommand{\Rfunction}[1]{{\texttt{#1}}} \newcommand{\Robject}[1]{{\texttt{#1}}} \newcommand{\Rpackage}[1]{{\textit{#1}}} \newcommand{\Rmethod}[1]{{\texttt{#1}}} \newcommand{\Rfunarg}[1]{{\texttt{#1}}} \newcommand{\Rclass}[1]{{\textit{#1}}} \textwidth=6.2in \textheight=8.5in %\parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \newcommand{\R}{\textsf{R}} \newcommand{\eSet}{\Robject{eSet}} \newcommand{\ExpressionSet}{\Robject{ExpressionSet}} \newcommand{\Biobase}{\Rpackage{Biobase}} \newcommand{\term}[1]{\emph{#1}} \newcommand{\mref}[2]{\htmladdnormallinkfoot{#2}{#1}} \begin{document} \title{\Biobase{} development and the new \eSet} \author{\mref{mailto:mtmorgan@fhcrc.org}{Martin T. Morgan}} \date{7 August, 2006} \maketitle Revised 4 September, 2006 -- \Robject{featureData} slot. Revised 20 April 2007 -- minor wording changes; \Rfunarg{verbose} and other arguments passed through \Rmethod{updateObject} example; introduce a second variant of \Rmethod{initialize} illustrating its use as a copy constructor. Revised 4 November, 2010 -- \Robject{experimentData} slot as \Rclass{MIAxE} class. \Rclass{MIAME} class is now subclass of \Rclass{MIAxE}. \section{Introduction} These notes help \emph{developers} who are interested in using and extending the \eSet{} class hierarchy, and using features in \Biobase. The information here is not useful to regular users of \Biobase. This document illustrates the \Biobase{} structures and approaches that make it it easy for developers to creatively use and extend the \eSet{} class hierarchy. The document starts with a brief description of the motivation for change, and a comparison of the old (before August, 2006) and new \eSet{}s and related functionality (e.g.,the \Rclass{Versioned} class and \Rfunction{updateObject} methods). We then illustrate how \eSet{} can be extended to handle additional types of data, and how new methods can exploit the \eSet{} class hierarchy. We conclude with a brief summary of lessons learned, useful developer-related side-effects of efforts to revise \eSet{}, and possible directions for future development. \section{Comparing old and new} What is an \eSet{}? \begin{itemize} \item Coordinate high through-put (e.g., gene expression) and phenotype data. \item Provide common data container for diverse Bioconductor packages. \end{itemize} Motivation for change (August, 2006). \begin{itemize} \item What was broken? Complex data structure. Inconsistent object validity. No straight-forward way to extend \eSet{} to new data types. \item What forward-looking design goals did we have? Flexible storage model. Class hierarchy to promote code reuse and facilitate extension to new data objects. Methods for updating serialized instances. \end{itemize} Key features in the redesign. \begin{itemize} \item Simplified data content. \item Structured class hierarchy . \item Alternative storage modes. \item More validity checking. \item Conversion of example data in \Biobase{}, and many other data sets elsewhere in Bioconductor, to \Rclass{ExpressionSet}. \item \Rclass{Versioned} class information (in the development branch). \item \Rfunction{updateObject} methods (in the development branch). \end{itemize} \section{A quick tour} <>= options(width=69) library(Biobase) @ \subsection{The \eSet{} object: high-throughput experiments} Purpose. \begin{itemize} \item Coordinate and contain high-throughput genomic data. \end{itemize} Structure: virtual base class. <>= getClass("eSet") @ \begin{itemize} \item \Robject{assayData}: high-throughput data. \item \Robject{phenoData}: sample covariates. \item \Robject{featureData}: feature covariates. \item \Robject{experimentData}: experimental description. \item \Robject{annotation}: assay description. \item See below, and \verb|?"eSet-class"| \end{itemize} \subsubsection{\Robject{assayData}: high-throughput data} Purpose. \begin{itemize} \item Efficiently and flexibly contain high-volume data. \end{itemize} Structure: \Rclass{list}, \Rclass{environment}, or \Rclass{lockEnvironment} class union. \begin{itemize} \item Each element of \Rclass{list} / \Rclass{environment} / \Rclass{lockEnvironment} is a matrix \item Rows: \emph{features}, e.g., gene names. \item Columns: \emph{samples} represented on each chip. \item All matricies must have the same dimensions, row names, and column names. \item Subclasses determine which matricies \emph{must} be present. \item See \verb|?"AssayData-class"| \end{itemize} \subsubsection{\Robject{phenoData}: sample covariates} Purpose. \begin{itemize} \item Contain and document sample covariates. \end{itemize} Structure: \Rclass{AnnotatedDataFrame}. \begin{itemize} \item \Robject{data}: \Rclass{data.frame}. \begin{itemize} \item Rows: sample identifiers. \item Columns: measured covariates. \end{itemize} \item \Robject{varMetadata}: \Rclass{data.frame}. \begin{itemize} \item Rows: measured covariate labels. \item Columns: covariate descriptors. \end{itemize} \item See \verb|?"AnnotatedDataFrame-class"| \end{itemize} \subsubsection{\Robject{featureData}: feature covariates} Purpose. \begin{itemize} \item Contain and document feature covariates specific to the experiment; use the \Robject{annotation} slot for chip-level descriptions. \end{itemize} Structure: \Rclass{AnnotatedDataFrame}. \begin{itemize} \item \Robject{data}: \Rclass{data.frame}. \begin{itemize} \item Rows: feature identifiers. These match row names of \Robject{assayData}. \item Columns: measured covariates. \end{itemize} \item \Robject{varMetadata}: \Rclass{data.frame}. \begin{itemize} \item Rows: measured covariate labels. \item Columns: covariate descriptors. \end{itemize} \item See \verb|?"AnnotatedDataFrame-class"| \end{itemize} \subsubsection{\Robject{experimentData}: experiment description} Purpose. \begin{itemize} \item Summarize where and how the experiment was performed. \end{itemize} Structure: \Rclass{MIAxE} virtual class \begin{itemize} \item[] {In Biobase version 2.11 the \Rclass{MIAxE} virtual class was introduced as a general container for experiment meta-data. The \Rclass{MIAME} class is now a subclass of \Rclass{MIAxE}. See \verb|?"MIAxE-class"|. The \Rclass{MIAME} class structure is as follows} \end{itemize} \begin{itemize} \item \Robject{title}: experiment title. \item \Robject{name}: experimenter name(s). \item \Robject{preprocessing}: \Robject{list} of pre-processing steps. \item Additional slots. \item See \verb|?"MIAME-class"|. \end{itemize} \subsubsection{\Robject{annotation}: assay description} Purpose. \begin{itemize} \item Link experiment to annotation package. \end{itemize} Structure: \Rclass{character} \begin{itemize} \item Label identifying annotation package. \end{itemize} %% Methods \subsection{Important \eSet{} methods} Initialization. \begin{itemize} \item \eSet{} is \verb|VIRTUAL|, initialize via subclass \Rfunction{callNextMethod} \end{itemize} Accessors (get, set). \begin{itemize} \item \Rfunction{assayData(obj); assayData(obj) <- value}: access or assign \Robject{assayData} \item \Rfunction{phenoData(obj); phenoData(obj) <- value}: access or assign \Robject{phenoData} \item \Rfunction{experimentData(obj); experimentData(obj) <- value}: access or assign \Robject{experimentData} \item \Rfunction{annotation(obj); annotation(obj) <- value}: access or assign \Robject{annotation} \end{itemize} Subsetting. \begin{itemize} \item \Rfunction{obj[i, j]}: select genes $i$ and samples $j$. \item \Rfunction{obj\$name; obj\$name <- value}: retrieve or assign covariate \Robject{name} in \Robject{phenoData} \end{itemize} \subsubsection{Additional \eSet{} methods} \begin{itemize} \item \Rfunction{show}. \item \Rfunction{storageMode}: influence how \Robject{assayData} is stored. \item \Rfunction{updateObject}: update \eSet{} objects to their current version. \item \Rfunction{validObject}: ensure that \eSet{} is valid. \end{itemize} The \Rfunction{validObject} method is particularly important to \eSet{}, ensuring that \eSet{} contains consistent structure to data. <>= getValidity(getClass("eSet")) @ The validity methods for \eSet{} reflect our design goals. All \Robject{assayData} members must have identical row and column dimensions and \Robject{featureNames}. The names and numbers of samples must be the same in \Robject{assayData} and \Robject{phenoData} slots. Validity methods are defined for the classes underlying each slot as well. For instance, the validity methods for \Robject{AnnotatedDataFrame} check that variables used in \Robject{pData} are at least minimally described in \Robject{varMetadata}. %% Subclasses \subsection{Subclasses of \eSet} \Biobase{} defines three classes that extend \eSet{}. \ExpressionSet{} (discussed further below) is meant to contain microarray gene expression data. \Rclass{SnpSet} is a preliminary class to contain SNP data; other classes in development (e.g., in \Rpackage{oligo}) may provide alternative implementations for SNP data. \Rclass{MultiSet} is an \ExpressionSet-like class, but without restriction on the names (though not structure) of elements in the \Robject{assayData} slot. \subsubsection{\ExpressionSet} Purpose: \begin{itemize} \item Contain gene expression data. \end{itemize} Required \Robject{assayData} members. \begin{itemize} \item \Robject{exprs}, a matrix of expression values. \end{itemize} Important methods. \begin{itemize} \item Initialization (additional details below): <>= obj <- new("ExpressionSet", phenoData = new("AnnotatedDataFrame"), experimentData = new("MIAME"), annotation = character(), exprs = new("matrix")) @ \item \Rfunction{exprs(obj), exprs(obj) <- value}: get or set \Robject{exprs}; methods defined for \Rclass{ExpressionSet}, \Rclass{AssayData}. \end{itemize} \subsubsection{\Rclass{MultiSet} and \Rclass{SnpSet}} \Rclass{MultiSet}. \begin{itemize} \item Purpose: flexibly contain a collection of expression data matricies. \item Required \Robject{assayData} members: none. \end{itemize} \Rclass{SnpSet}. \begin{itemize} \item Purpose: contain genomic SNP calls. \item Required \Robject{assayData} members: \Robject{call}, \Robject{callProbability}. \end{itemize} \section{Comments on \Robject{assayData}: high-throughput data storage} The \Robject{assayData} slot is meant to store high-throughput data. The idea is that the slot contains identically sized matrices containing expression or other data. All matrices in the slot must have the same dimension, and are structured so that rows represent `features' and columns represent `samples'. Validity methods enforce that row and column names of slot elements are identical. For technical reasons, creating instance of \Rclass{AssayData} is slightly different from the way this is usually done in \R{}. Normally, one creates an instance of a class with an expression like \Rfunction{new("ExpressionSet", ...)}, with the \ldots representing additional arguments. \Rclass{AssayData} objects are created with <>= assayDataNew("environment", elt) @ where \Robject{elt} might be a matrix of expression values. For the curious, the reason for this setup stems from our desire to have a class that \Rfunction{is} a list or environment, rather than a class that has a slot that contains a list or environment. The \Rfunction{is} relationship is desirable to avoid unnecessary function calls to access slots, and requires that a class \Rfunction{contain} the base type (e.g., \Rclass{environment}). Until recently an \R{} object could not \Rfunction{contain} an \Rclass{environment}. The \Robject{assayData} slot of \ExpressionSet{} objects must contain a matrix named \Robject{exprs}. Nonetheless, the \ExpressionSet{} validity method tries to be liberal -- it guarantees that the object has an \Robject{exprs} element, but allows for other elements too. The prudent developer wanting consistent additional data elements should derive a class from \ExpressionSet{} that enforces the presence of their desired elements. The \Rclass{AssayData} class allows for data elements to be stored in three different ways (see \Rfunction{?storageMode} and \Rfunction{?"storageMode<-"} for details): as a \Robject{list}, \Robject{environment}, or \Robject{lockedEnvironment}. Developers are probably familiar with \Robject{list} objects; a drawback is that \Robject{exprs} elements may be large, and some operations on lists in \R{} may trigger creation of many copies of the the \Robject{exprs} element. This can be expensive in both space and time. Environments are nearly unique in \R{}, in that they are passed by reference rather than value. This eliminates some copying, but has the unfortunate consequence that side-effects occur -- modifications to an environment inside a function influence the value of elements outside the function. For these reasons, environments can be useful as `read only' arguments to functions, but can have unexpected consequences when functions modify their arguments. Locked environments implemented in \Biobase{} try to strike a happy medium, allowing pass by reference for most operations but triggering (whole-environment) copying when elements in the environment are modified. The locking mechanism is enforced by only allowing known `safe' operations to occur, usually by channeling user actions through the accessor methods: <>= data(sample.ExpressionSet) storageMode(sample.ExpressionSet) tryCatch(assayData(sample.ExpressionSet)$exprs <- log(exprs(sample.ExpressionSet)), error=function(err) cat(conditionMessage(err))) exprs(sample.ExpressionSet) <- log(exprs(sample.ExpressionSet)) @ The \Rfunction{setReplaceMethod} for \Robject{exprs} (and \Robject{assayData}) succeeds by performing a deep copy of the entire environment. Because this is very inefficient, the recommended paradigm to update an element in a \Robject{lockedEnvironment} is to extract it, make many changes, and then reassign it. Developers can study \Robject{assayData} methods to learn more about how to lock and unlock environment bindings. \Biobase{} allows the experienced user to employ (and run the risks of) environments, but the expectation is that most user objects are construced with the default \Robject{lockedEnvironment} or \Robject{list}. A longer term consideration in designing \Rclass{AssayData} was to allow more flexible methods of data storage, e.g., through database-hosted arrays. This is facilitated by using generic functions such as \Rfunction{exprs()} for data access, so that classes derived from \Rclass{AssayData} can provide implementations appropriate for their underlying storage mode. \section{Extending \eSet} A designer wanting to implement \eSet{} for a particular type of data creates a class that `contains' \eSet{}. The steps for doing this are described below. One example of such a class is \ExpressionSet, designed to hold a matrix of gene expression values in the \Robject{assayData} slot. <>= getClass("ExpressionSet") getValidity(getClass("ExpressionSet")) @ The data structure of an \ExpressionSet{} is identical to that of \eSet, and in fact is inherited (without additional slot creation) from \eSet{}. The main difference is that the validity methods of \eSet{} are augmented by a method to check that the \Robject{assayData} slot contains an entity named \Robject{"exprs"}. A valid \ExpressionSet{} object must also satisfy all the validity requirements of \eSet{}, but the developer does not explicitly invoke validity checking of the parts of the data structure inherited from \eSet{}. \subsection{Implementing a new class: a \Rclass{SwirlSet} example} We want the \emph{Swirl} data set (see the \Robject{SW} two color data set that motivates this class) to contain four elements in the \Robject{assayData} slot: \Robject{R}, \Robject{G}, \Robject{Rb}, \Robject{Gb}. To derive a class from \eSet{} for this data, we create a class, and provide initializaation and validation methods. We create a class as follows: <>= setClass("SwirlSet", contains="eSet") @ Notice that there are no new data elements in \Rclass{SwirlSet} compared with \eSet{}. The \Rfunction{initialize} method is written as <>= setMethod("initialize", "SwirlSet", function(.Object, R = new("matrix"), G = new("matrix"), Rb = new("matrix"), Gb = new("matrix"), ...) { callNextMethod(.Object, R=R, G=G, Rb=Rb, Gb=Gb, ...) }) @ % A slightly different \Rmethod{initialize} method allows the user to specify either the \Robject{assayData} or the \Robject{assayData} content. In advanced use, this has the advantage that \Rmethod{initialize} can be used as a `copy constructor' to update several slots simultaneously. <>= setMethod("initialize", "SwirlSet", function(.Object, assayData=assayDataNew( R=R, G=G, Rb=Rb, Gb=Gb), R = new("matrix"), G = new("matrix"), Rb = new("matrix"), Gb = new("matrix"), ...) { if (!missing(assayData) && any(!missing(R), !missing(G), !missing(Rb), !missing(Gb))) { warning("using 'assayData'; ignoring 'R', 'G', 'Rb', 'Gb'") } callNextMethod(.Object, assayData=assayData, ...) }) @ The structure of the \Rfunction{initialize} method is a bit different from those often seen in \R{}. Often, \Rfunction{initialize} has only \Robject{.Object} as a named argument, or, if there are other named arguments, they correspond to slot names. Here our initialize method accepts four arguments, named after the \Robject{assayData} elements. Inside the \Rfunction{initialize} method, the named arguments are passed to the next initialization method in the hierarch (i.e., \Rfunction{initialize} defined for \eSet). The \eSet{} \Rfunction{initialize} method then uses these arguments to populate the data slots in \Robject{.Object}. In particular, \eSet{} places all arguments other \Rfunction{phenoData}, \Rfunction{experimentData}, and \Rfunction{annotation} into the \Robject{assayData} slot. The \eSet{} \Rfunction{initialize} method then returns the result to the \Rfunction{initialize} method of \Rclass{SwirlSet}, which returns a \Rclass{SwirlSet} object to the user: <>= new("SwirlSet") @ General programing guidelines emerge from experience with the \Rfunction{initialize} method of \eSet{} and derived classes. First, an appropriate strategy is to name only those data elements that will be manipulated directly by the \Rfunction{initialize} method. For instance, the definition above did \emph{not} name \Robject{phenoData} and other \eSet{} slots by name. To do so is not incorrect, but would require that they be explicitly named (e.g., \Rfunction{phenoData=phenoData}) in the \Rfunction{callNextMethod} code. Second, the arguments \Robject{R, G, Rb, Rg} are present in the \Rfunction{initialize} method to provide defaults consistent with object construction; the `full' form of \Rfunction{callNextMethod}, replicating the named arguments, is required in the version of \R{} in which this class was developed. Third, named arguments can be manipulated before \Rfunction{callNextMethod} is invoked. Fourth, the return value of \Rfunction{callNextMethod} can be captured\ldots <>= setMethod("initialize", "MySet", function(.Object, ...) { .Object <- callNextMethod(.Object, ...) }) . @ and manipulated before being returned to the user. Finally, it is the responsbilitiy of the developer to ensure that a valid object is created; \Rfunction{callNextMethod} is a useful way to exploit correctly designed \Rfunction{initialize} methods for classes that the object extends, but the developer is free to use other techniques to create valid versions of their class. A validity method might complete our new class. A validity method is essential to ensure that the unique features of \Rclass{SwirlSet} -- our reason for designing the new class -- are indeed present. We define our validity method to ensure that the \Robject{assayData} slot contains our four types of expression elements: <>= setValidity("SwirlSet", function(object) { assayDataValidMembers(assayData(object), c("R", "G", "Rb", "Gb")) }) @ Notice that we do not have to explicitly request that the validity of other parts of the \Rclass{SwirlSet} object are valid; this is done for us automatically. Objects are checked for validity when they are created, but not when modified. This is partly for efficiency reasons, and partly because object updates might transiently make them invalid. So a good programing practice is to ensure validity after modification, e.g., <>= myFancyFunction <- function(obj) { assayData(obj) <- fancyAssaydData # obj invalid... phenoData(obj) <- justAsFancyPhenoData # but now valid validObject(obj) obj } @ Assigning \Robject{fancyAssaydData} might invalidate the object, but \Robject{justAsFancyPhenoData} restores validity. \section{\Rclass{Versioned}} One problem encountered in the Bioconductor project is that data objects stored to disk become invalid as the underlying class definition changes. For instance, earlier releases of \Biobase{} contain a sample \Rclass{eSet} object. But under the changes discussed here, \eSet{} is virtual and the stored object is no longer valid. The challenge is to easily identify invalid objects, and to provide a mechanism for updating old objects to their new representation. \Biobase{} introduces the \Rclass{Versioned} and \Rclass{VersionedBiobase} classes to facilitate this. These classes are incorporated into key \Biobase class definitions.\Biobase also defines \Rmethod{updateObject} methods (the \Rfunction{updateObject} generic function is defined in the \Rpackage{BiocGenerics} package) for conveniently updating old objects to their new representation. <>= data(sample.ExpressionSet) classVersion(sample.ExpressionSet) obj <- updateObject(sample.ExpressionSet) @ The version information for this object is a named list. The first two elements indicate the version of R and Biobase used to create the object. The latter two elements are contained in the class prototype, and the class prototype is consulted to see if the instance of an object is 'current'. These lists can be subsetted in the usual way, e.g., <>= isCurrent(sample.ExpressionSet)[c("eSet", "ExpressionSet")] @ Versioned classes, \Rfunction{updateObject} and related methods simplify the long-term maintenance of data objects. Take the fictious \Rclass{MySet} as an example. <>= setClass("MySet", contains = "eSet", prototype = prototype( new("VersionedBiobase", versions=c(classVersion("eSet"), MySet="1.0.0")))) obj <- new("MySet") classVersion(obj) @ This is a new class, and might undergo changes in its structure at some point in the future. When these changes are introduced, the developer will change the version number of the class in its prototype (the last line, below): <>= setClass("MySet", contains = "eSet", prototype = prototype( new("VersionedBiobase", versions=c(classVersion("eSet"), MySet="1.0.1")))) isCurrent(obj) @ and add code to update to the new version <>= setMethod("updateObject", signature(object="MySet"), function(object, ..., verbose=FALSE) { if (verbose) message("updateObject(object = 'MySet')") object <- callNextMethod() if (isCurrent(object)["MySet"]) return(object) ## Create an updated instance. if (!isVersioned(object)) ## Radical surgery -- create a new, up-to-date instance new("MySet", assayData = updateObject(assayData(object), ...., verbose=verbose), phenoData = updateObject(phenoData(object), ..., verbose=verbose), experimentData = updateObject(experimentData(object), ..., verbose=verbose), annotation = updateObject(annotation(object), ..., verbose=verbose)) else { ## Make minor changes, and update version by consulting class definition classVersion(object)["MySet"] <- classVersion("MySet")["MySet"] object } }) @ The code after \Rfunction{if(!isVersioned)} illustrates one way of performing `radical surgery, creating a new up-to-date instance by updating all slots. The \Rfunction{else} clause represents more modest changes, using methods to update stale information. \Rfunction{updateObject} then returns a new, enhanced object: <>= classVersion(updateObject(obj)) @ As in the example, versioning helps in choosing which modifications to perform -- minor changes for a slightly out-of-date object, radical surgery for something more ancient. Version information might also be used in methods, where changing class representation might facilitate more efficient routines. \subsection{\Rclass{Versioned} versus \Rclass{VersionedBiobase}} The information on \R{} and \Biobase{} versions is present in \eSet{} derived classes because \eSet{} contains \Rclass{VersionedBiobase}. On the other hand, \Rclass{AnnotatedDataFrame} contains \Rclass{Versioned}, and has only information about its own class version. <>= classVersion(new("AnnotatedDataFrame")) @ The rationale for this is that \Rclass{AnnotatedDataFrame} is and will likely remain relatively simple, and details about \R{} and \Biobase{} are probably irrelevant to its use. On the other hand, some aspects of \eSet{} and the algorithms that operate on them are more cutting edge and subject to changes in \R{} or \Biobase{}. Knowing the version of \R{} and \Biobase{} used to create an instance might provide valuable debugging information. \subsection{Adding \Rclass{Versioned} information to your own classes} The key to versioning your own classes is to define your class to \Rfunction{contain} \Rclass{Versioned} or \Rclass{VersionedBiobase}, and to add the version information in the prototype. For instance, to add a class-specific version stamp to \Rclass{SwirlSet} we would modify the class defintion to <>= setClass("SwirlSet", contains = "eSet", prototype = prototype( new("VersionedBiobase", versions=c(classVersion("eSet"), SwirlSet="1.0.0")))) classVersion(new("SwirlSet")) @ See additional examples in the \Rclass{Versioned} help page. It is also possible to add arbitrary information to particular instances. <>= obj <- new("SwirlSet") classVersion(obj)["MyID"] <- "0.0.1" classVersion(obj) classVersion(updateObject(obj)) @ There is additional documentation about these classes and methods in \Biobase{}. \section{Summary} This document summarizes \Biobase, outlining strategies that developers using \Biobase{} may find useful. The main points are to introduce the \eSet{} class hierarchy, to illustrate how developers can effectively extend this class, and to introduce class versions as a way of tracking and easily updating objects. It is anticipated that \eSet{}-derived classes will play an increasingly important role in \Biobase{} development. \section{Session Information} The version number of \R{} and packages loaded for generating the vignette were: <>= toLatex(sessionInfo()) @ \end{document} Biobase/vignettes/ExpressionSetIntroduction.Rnw0000644000175400017540000004304113175713325023072 0ustar00biocbuildbiocbuild% NOTE -- ONLY EDIT THE .Rnw FILE!!! The .tex file is % likely to be overwritten. % %\VignetteDepends{Biobase} %\VignetteIndexEntry{An introduction to Biobase and ExpressionSets} %\VignetteKeywords{tutorial, environment, graphics, ExpressionSet} % %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \documentclass[12pt]{article} \usepackage{amsmath,fullpage} \usepackage[authoryear,round]{natbib} \usepackage{hyperref} \usepackage{theorem} \usepackage{float} \usepackage{ifthen} \newcommand{\scscst}{\scriptscriptstyle} \newcommand{\scst}{\scriptstyle} \newcommand{\R}{{\textsf{R}}} \newcommand{\code}[1]{{\texttt{#1}}} \newcommand{\term}[1]{{\emph{#1}}} \newcommand{\Rpackage}[1]{\textsf{#1}} \newcommand{\Rfunction}[1]{\texttt{#1}} \newcommand{\Robject}[1]{\texttt{#1}} \newcommand{\Rclass}[1]{{\textit{#1}}} \newcommand{\Rmethod}[1]{{\textit{#1}}} \newcommand{\Rfunarg}[1]{{\textit{#1}}} %% Excercises and Questions \usepackage{theorem} \theoremstyle{break} \newtheorem{Ex}{Exercise} \theoremstyle{break} \newtheorem{Q}{Question} %% And solution or answer \newenvironment{solution}{% \begin{center} \begin{minipage}{0.75\textwidth} %% \color{blue} }{ \end{minipage} \end{center} \bigskip% } \bibliographystyle{plainnat} \title{An Introduction to Bioconductor's \Rclass{ExpressionSet} Class} \author{Seth Falcon, Martin Morgan, and Robert Gentleman} \date{6 October, 2006; revised 9 February, 2007} \begin{document} <>= options(width=65) @ \maketitle \section{Introduction} \Rpackage{Biobase} is part of the Bioconductor project, and is used by many other packages. \Rpackage{Biobase} contains standardized data structures to represent genomic data. The \Rclass{ExpressionSet} class is designed to combine several different sources of information into a single convenient structure. An \Rclass{ExpressionSet} can be manipulated (e.g., subsetted, copied) conveniently, and is the input or output from many Bioconductor functions. The data in an \Rclass{ExpressionSet} is complicated, consisting of expression data from microarray experiments (\code{assayData}; \code{assayData} is used to hint at the methods used to access different data components, as we will see below), `meta-data' describing samples in the experiment (\code{phenoData}), annotations and meta-data about the features on the chip or technology used for the experiment (\code{featureData}, \code{annotation}), information related to the protocol used for processing each sample (and usually extracted from manufacturer files, \code{protocolData}), and a flexible structure to describe the experiment (\code{experimentData}). The \Rclass{ExpressionSet} class coordinates all of this data, so that you do not usually have to worry about the details. However, an \Rclass{ExpressionSet} needs to be created in the first place, and creation can be complicated. In this introduction we learn how to create and manipulate \Rclass{ExpressionSet} objects, and practice some basic \R{} skills. \section{Preliminaries} \subsection{Installing Packages} If you are reading this document and have not yet installed any software on your computer, visit \url{http://bioconductor.org} and follow the instructions for installing \R{} and Bioconductor. Once you have installed \R{} and Bioconductor, you are ready to go with this document. In the future, you might find that you need to install one or more additional packages. The best way to do this is to start an \R{} session and evaluate commands like <>= source("http://bioconductor.org/biocLite.R") biocLite(c("Biobase")) @ %% \subsection{Loading Packages} The definition of the \Rclass{ExpressionSet} class along with many methods for manipulating \Rclass{ExpressionSet} objects are defined in the \Rpackage{Biobase} package. In general, you need to load class and method definitions before you use them. When using Bioconductor, this means loading \R{} packages using \Rfunction{library} or \Rfunction{require}. <>= library("Biobase") @ \begin{Ex} What happens when you try to load a package that is not installed? \end{Ex} \begin{solution} When using \Rfunction{library}, you get an error message. With \Rfunction{require}, the return value is \Robject{FALSE} and a warning is printed. \end{solution} \section{Building an ExpressionSet From .CEL and other files} Many users have access to .CEL or other files produced by microarray chip manufacturer hardware. Usually the strategy is to use a Bioconductor package such as \Rpackage{affyPLM}, \Rpackage{affy}, \Rpackage{oligo}, or \Rpackage{limma}, to read these files. These Bioconductor packages have functions (e.g., \Rfunction{ReadAffy}, \Rfunction{expresso}, or \Rfunction{justRMA} in \Rpackage{affy}) to read CEL files and perform preliminary preprocessing, and to represent the resulting data as an \Rclass{ExpressionSet} or other type of object. Suppose the result from reading and preprocessing CEL or other files is named \Robject{object}, and \Robject{object} is different from \Rclass{ExpressionSet}; a good bet is to try, e.g., <>= library(convert) as(object, "ExpressionSet") @ %% It might be the case that no converter is available. The path then is to extract relevant data from \Robject{object} and use this to create an \Rclass{ExpressionSet} using the instructions below. \section{Building an ExpressionSet From Scratch} As mentioned in the introduction, the data from many high-throughput genomic experiments, such as microarray experiments, usually consist of several conceptually distinct parts: assay data, phenotypic meta-data, feature annotations and meta-data, and a description of the experiment. We'll construct each of these components, and then assemble them into an \Rclass{ExpressionSet}. \subsection{Assay data} One important part of the experiment is a matrix of `expression' values. The values are usually derived from microarrays of one sort or another, perhaps after initial processing by manufacturer software or Bioconductor packages. The matrix has $F$ rows and $S$ columns, where $F$ is the number of features on the chip and $S$ is the number of samples. A likely scenario is that your assay data is in a 'tab-delimited' text file (as exported from a spreadsheet, for instance) with rows corresponding to features and columns to samples. The strategy is to read this file into \R{} using the \Rfunction{read.table} command, converting the result to a \Rclass{matrix}. A typical command to read a tab-delimited file that includes column `headers' is <>= dataDirectory <- system.file("extdata", package="Biobase") exprsFile <- file.path(dataDirectory, "exprsData.txt") exprs <- as.matrix(read.table(exprsFile, header=TRUE, sep="\t", row.names=1, as.is=TRUE)) @ %% The first two lines create a file path pointing to where the assay data is stored; replace these with a character string pointing to your own file, e.g, <>= exprsFile <- "c:/path/to/exprsData.txt" @ %% (Windows users: note the use of \verb+/+ rather than \verb+\+; this is because \R{} treats the \verb+\+ character as an `escape' sequence to change the meaning of the subsequent character). See the help pages for \Rfunction{read.table} for more detail. A common variant is that the character separating columns is a comma (``comma-separated values'', or ``csv'' files), in which case the \Robject{sep} argument might be \Robject{sep=","}. It is always important to verify that the data you have read matches your expectations. At a minimum, check the class and dimensions of \Robject{geneData} and take a peak at the first several rows <>= class(exprs) dim(exprs) colnames(exprs) head(exprs[,1:5]) @ %% At this point, we can create a minimal \Rclass{ExpressionSet} object using the \code{ExpressionSet} constructor: <>= minimalSet <- ExpressionSet(assayData=exprs) @ % We'll get more benefit from expression sets by creating a richer object that coordinates phenotypic and other data with our expression data, as outlined in the following sections. \subsection{Phenotypic data} Phenotypic data summarizes information about the samples (e.g., sex, age, and treatment status; referred to as `covariates'). The information describing the samples can be represented as a table with $S$ rows and $V$ columns, where $V$ is the number of covariates. An example of phenotypic data can be input with <>= pDataFile <- file.path(dataDirectory, "pData.txt") pData <- read.table(pDataFile, row.names=1, header=TRUE, sep="\t") dim(pData) rownames(pData) summary(pData) @ %% There are three columns of data, and 26 rows. Note that the number of rows of phenotypic data match the number of columns of expression data, and indeed that the row and column names are identically ordered: <>= all(rownames(pData)==colnames(exprs)) @ %% This is an essential feature of the relationship between the assay and phenotype data; \Rclass{ExpressionSet} will complain if these names do not match. Phenotypic data can take on a number of different forms. For instance, some covariates might reasonably be represented as numeric values. Other covariates (e.g., gender, tissue type, or cancer status) might better be represented as \Robject{factor} objects (see the help page for \Robject{factor} for more information). It is especially important that the phenotypic data are encoded correctly; the \Robject{colClasses} argument to \Rfunction{read.table} can be helpful in correctly inputing (and ignoring, if desired) columns from the file. \begin{Ex} What class does \Rfunction{read.table} return? \end{Ex} \begin{Ex} Determine the column names of \Robject{pData}. Hint: \Robject{apropos("name")}. \end{Ex} \begin{solution} <>= names(pData) @ \end{solution} \begin{Ex} Use \Rfunction{sapply} to determine the classes of each column of \Robject{pData}. Hint: read the help page for \Rfunction{sapply}. \end{Ex} \begin{solution} <>= sapply(pData, class) @ \end{solution} \begin{Ex} What is the sex and Case/Control status of the 15th and 20th samples? And for the sample(s) with \Robject{score} greater than $0.8$. \end{Ex} \begin{solution} <>= pData[c(15, 20), c("gender", "type")] pData[pData$score>0.8,] @ \end{solution} Investigators often find that the meaning of simple column names does not provide enough information about the covariate -- What is the cryptic name supposed to represent? What units are the covariates measured in? We can create a data frame containing such meta-data (or read the information from a file using \Rfunction{read.table}) with <>= metadata <- data.frame(labelDescription= c("Patient gender", "Case/control status", "Tumor progress on XYZ scale"), row.names=c("gender", "type", "score")) @ %% This creates a \Rclass{data.frame} object with a single column called \code{labelDescription}, and with row names identical to the column names of the \Rclass{data.frame} containing the phenotypic data. The column \Robject{labelDescription} \emph{must} be present; other columns are optional. Bioconductor's \Rpackage{Biobase} package provides a class called \Rclass{AnnotatedDataFrame} that conveniently stores and manipulates the phenotypic data and its metadata in a coordinated fashion. Create and view an \Rclass{AnnotatedDataFrame} instance with: <>= phenoData <- new("AnnotatedDataFrame", data=pData, varMetadata=metadata) phenoData @ %% Some useful operations on an \Rclass{AnnotatedDataFrame} include \Rmethod{sampleNames}, \Rmethod{pData} (to extract the original \Robject{pData} \Rclass{data.frame}), and \Rmethod{varMetadata}. In addition, \Rclass{AnnotatedDataFrame} objects can be subset much like a \Rclass{data.frame}: <>= head(pData(phenoData)) phenoData[c("A","Z"),"gender"] pData(phenoData[phenoData$score>0.8,]) @ %% \subsection{Annotations and feature data} Meta-data on features is as important as meta-data on samples, and can be very large and diverse. A single chip design (i.e., collection of features) is likely to be used in many different experiments, and it would be inefficient to repeatedly collect and coordinate the same meta-data for each \Rclass{ExpressionSet} instance. Instead, the ideas is to construct specialized meta-data packages for each type of chip or instrument. Many of these packages are available from the Bioconductor web site. These packages contain information such as the gene name, symbol and chromosomal location. There are other meta-data packages that contain the information that is provided by other initiatives such as GO and KEGG. The \Rpackage{annotate} and \Rpackage{AnnotationDbi} packages provides basic data manipulation tools for the meta-data packages. The appropriate way to create annotation data for features is very straight-forward: we provide a character string identifying the type of chip used in the experiment. For instance, the data we are using is from the Affymetrix hgu95av2 chip: <>= annotation <- "hgu95av2" @ %% It is also possible to record information about features that are unique to the experiment (e.g., flagging particularly relevant features). This is done by creating or modifying an \Robject{AnnotatedDataFrame} like that for \Robject{phenoData} but with row names of the \Rclass{AnnotatedDataFrame} matching rows of the assay data. \subsection{Experiment description} Basic description about the experiment (e.g., the investigator or lab where the experiment was done, an overall title, and other notes) can be recorded by creating a \Rclass{MIAME} object. One way to create a \Rclass{MIAME} object is to use the \Rfunction{new} function: <>= experimentData <- new("MIAME", name="Pierre Fermat", lab="Francis Galton Lab", contact="pfermat@lab.not.exist", title="Smoking-Cancer Experiment", abstract="An example ExpressionSet", url="www.lab.not.exist", other=list( notes="Created from text files" )) @ %% Usually, \Rfunction{new} takes as arguments the class name and pairs of names and values corresponding to different slots in the class; consult the help page for \Rclass{MIAME} for details of available slots. \subsection{Assembling an \Rclass{ExpressionSet}} An \Rclass{ExpressionSet} object is created by assembling its component parts and callng the \code{ExpressionSet} constructor: <>= exampleSet <- ExpressionSet(assayData=exprs, phenoData=phenoData, experimentData=experimentData, annotation="hgu95av2") @ %% Note that the names on the right of each equal sign can refer to any object of appropriate class for the argument. See the help page for \Rclass{ExpressionSet} for more information. We created a rich data object to coordinate diverse sources of information. Less rich objects can be created by providing less information. As mentioned earlier, a minimal expression set can be created with <>= minimalSet <- ExpressionSet(assayData=exprs) @ %% Of course this object has no information about phenotypic or feature data, or about the chip used for the assay. \section{\Rclass{ExpressionSet} Basics} Now that you have an \Rclass{ExpressionSet} instance, let's explore some of the basic operations. You can get an overview of the structure and available methods for \Rclass{ExpressionSet} objects by reading the help page: <>= help("ExpressionSet-class") @ When you print an \Rclass{ExpressionSet} object, a brief summary of the contents of the object is displayed (displaying the entire object would fill your screen with numbers): <>= exampleSet @ \subsection{Accessing Data Elements} A number of accessor functions are available to extract data from an \Rclass{ExpressionSet} instance. You can access the columns of the phenotype data (an \Rclass{AnnotatedDataFrame} instance) using \verb+$+: <>= exampleSet$gender[1:5] exampleSet$gender[1:5] == "Female" @ %% You can retrieve the names of the features using \Rfunction{featureNames}. For many microarray datasets, the feature names are the probe set identifiers. <>= featureNames(exampleSet)[1:5] @ %% The unique identifiers of the samples in the data set are available via the \Rfunction{sampleNames} method. The \Rfunction{varLabels} method lists the column names of the phenotype data: <>= sampleNames(exampleSet)[1:5] varLabels(exampleSet) @ %% Extract the expression matrix of sample information using \Rfunction{exprs}: <>= mat <- exprs(exampleSet) dim(mat) @ \subsubsection{Subsetting} Probably the most useful operation to perform on \Rclass{ExpressionSet} objects is subsetting. Subsetting an \Rclass{ExpressionSet} is very similar to subsetting the expression matrix that is contained within the \Rclass{ExpressionSet}, the first argument subsets the features and the second argument subsets the samples. Here are some examples: Create a new \Rclass{ExpressionSet} consisting of the 5 features and the first 3 samples: <>= vv <- exampleSet[1:5, 1:3] dim(vv) featureNames(vv) sampleNames(vv) @ %% Create a subset consisting of only the male samples: <>= males <- exampleSet[ , exampleSet$gender == "Male"] males @ \section{What was used to create this document} The version number of \R{} and the packages and their versions that were used to generate this document are listed below. <>= toLatex(sessionInfo()) @ \end{document} Biobase/vignettes/esApply.Rnw0000644000175400017540000000721713175713325017277 0ustar00biocbuildbiocbuild% % NOTE -- ONLY EDIT THE .Rnw FILE!!! The .tex file is % likely to be overwritten. % % \VignetteIndexEntry{esApply Introduction} %\VignetteDepends{Biobase} %\VignetteKeywords{Expression Analysis} %\VignettePackage{Biobase} \documentclass[12pt]{article} \usepackage{amsmath,fullpage} \usepackage[authoryear,round]{natbib} \usepackage{hyperref} \textwidth=6.2in \textheight=8.5in %\parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \newcommand{\scscst}{\scriptscriptstyle} \newcommand{\scst}{\scriptstyle} \newcommand{\Rfunction}[1]{{\texttt{#1}}} \newcommand{\Robject}[1]{{\texttt{#1}}} \newcommand{\Rpackage}[1]{{\textit{#1}}} \newcommand{\Rmethod}[1]{{\texttt{#1}}} \newcommand{\Rfunarg}[1]{{\texttt{#1}}} \newcommand{\Rclass}[1]{{\textit{#1}}} \bibliographystyle{plainnat} \begin{document} \section*{A note on {\tt esApply}} {\tt ExpressionSet}s are complex objects. \Robject{exprs(ExpressionSet)} produces $G \times N$, where $G$ is the number of genes on a chip and $N$ is the number of tissues analyzed, and \Robject{pData(ExpressionSet)} produces $N \times p$, where $p$ is the number of phenotypic or demographic, etc., variables collected. Abstractly, we are often interested in evaluating functions $f(y;x)$ where $y$ is an $N$-vector of expression results for a specific gene and $x$ is an $N$-dimensional structure, coordinated with $y$, that distinguishes elements of $y$ for processing in the function $f$. A basic problem is to guarantee that the $j$th element of $y$ is correctly associated with the $j$th component of $x$. <>= library(Biobase) data(sample.ExpressionSet) @ As an example, let's consider \Robject{sample.ExpressionSet}, which is an \Rclass{ExpressionSet} supplied with Biobase. We will print a little report, then the first $N$-vector of gene expressions and some covariate data: <>= print(sample.ExpressionSet) print(exprs(sample.ExpressionSet)[1,]) print(pData(sample.ExpressionSet)[1:2,1:3]) @ Now let's see how expressions and a covariate are related: <>= print(rbind(exprs(sample.ExpressionSet[1,]), sex <- t(pData(sample.ExpressionSet))[1,])) @ A function that evaluates the difference in median expression across strata defined using an abstract covariate \Robject{x} is <>= medContr <- function( y, x ) { ys <- split(y,x) median(ys[[1]]) - median(ys[[2]]) } @ We can apply this to a small \Rclass{ExpressionSet} that gives back the data listed above: <>= print(apply(exprs(sample.ExpressionSet[1,,drop=F]), 1, medContr, pData(sample.ExpressionSet)[["sex"]])) @ That's a bit clumsy. This is where \Rfunction{esApply} comes in. We pay for some simplicity by following a strict protocol for the definition of the statistical function to be applied. <>= medContr1 <- function(y) { ys <- split(y,sex) median(ys[[1]]) - median(ys[[2]]) } print(esApply( sample.ExpressionSet, 1, medContr1)[1]) @ The manual page on \Rfunction{esApply} has a number of additional examples that show how applicable functions can be constructed and used. The important thing to note is that the applicable functions {\em know} the names of the covariates in the \Robject{pData} dataframe. This is achieved by having an environment populated with all the variables in \Rclass{phenoData(ExpressionSet)} put in as the environment of the function that will be applied. If that function already has an environment we retain that but in the second position. Thus, there is some potential for variable shadowing. \section{Session Information} The version number of R and packages loaded for generating the vignette were: \begin{verbatim} <>= sessionInfo() @ \end{verbatim} \end{document} Biobase/vignettes/legacy/0000755000175400017540000000000013175713325016427 5ustar00biocbuildbiocbuildBiobase/vignettes/legacy/Biobase.Rnw0000644000175400017540000003247613175713325020477 0ustar00biocbuildbiocbuild% % NOTE -- ONLY EDIT Biobase.Rnw!!! % Biobase.tex file will get overwritten. % %\VignetteIndexEntry{Biobase Primer} %\VignetteDepends{} %\VignetteKeywords{Expression Analysis} %\VignettePackage{Biobase} \documentclass{article} \usepackage{hyperref} \textwidth=6.2in \textheight=8.5in %\parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \newcommand{\Rfunction}[1]{{\texttt{#1}}} \newcommand{\Robject}[1]{{\texttt{#1}}} \newcommand{\Rpackage}[1]{{\textsf{#1}}} \newcommand{\Rmethod}[1]{{\texttt{#1}}} \newcommand{\Rfunarg}[1]{{\texttt{#1}}} \newcommand{\Rclass}[1]{{\textit{#1}}} \newcommand{\classdef}[1]{% {\em #1} } %%FIXME: Jianhua, can you go through the current class definitions for %%exprSet and phenoData etc and update the documentation here accordingly. \begin{document} \title{Textual Description of Biobase} \maketitle \section*{Introduction} Biobase is part of the Bioconductor project. It is meant to be the location of any reusable (or non--specific) functionality. Biobase will be required by most of the other Bioconductor libraries. \section{Data Structures} Part of the Biobase functionality is the standardization of data structures for genomic data. Currently we have designed some data structures to handle microarray data. The \classdef{exprSet} class has the following slots: \begin{description} \item[exprs] A matrix of expression levels. Arrays are columns and genes are rows. \item[se.exprs] A matrix of standard errors for expressions if they are available. It will have length 0 if they are not. \item[phenoData] An object of class \verb+phenoData+ that contains phenotypic and/or experimental data. \item[description] A description of the experiment (object of class MIAME) \item[annotation] A character string indicating the base name for the associated annotation. \item[notes] A set of notes describing aspects or features of the data, the analysis, processing done, etc. \end{description} These data are extremely large and complex. To deal with them effectively we will need better tools for combining data and documentation. The \verb+exprSet+ class represents an initial attempt by the Bioconductor project to provide better tools for documenting and handling these large and complex data sets. The expression data represent experimentally derived data. In most cases these data will benefit from making use of biologically relevant meta-data. The meta-data are very large and diverse. In order to facilitate interactions and explorations we have taken the approach of constructing a specialized meta-data package for each chip or instrument. Many of these packages are available from the Bioconductor web site. These packages contain information such as the gene name, symbol and chromosomal location. There are other meta-data packages that contain the information that is provided by other initiatives such as GO and KEGG. These data can then be linked to the \verb+exprSet+ via the \verb+annotation+ slot. The \textit{annotate} package provides basic data manipulation tools for the meta-data packages. The \texttt{phenoData} class has the following slots: \begin{description} \item[pData] A dataframe where the rows are cases and the columns are variables. \item[varLabels] A list of labels and descriptions for the variables represented by the columns of \verb+pData+. \item[varMetaData] A \Rclass{data.frame} defining meta-data for the variables contained in the \Robject{pData} slot. \end{description} Instances of this class are essentially \verb+data.frame+'s with some additional documentation on the variables stored in the \verb+varLabels+ and \Robject{varMetaData} slots. %%FIXME: does this currently exist? It should be easy to require that %%the names of the pData data.frame are the same, and in the same %%order as the column names of the exprs A mechanism for ensuring that the elements of the \verb+phenoData+ slot of an instance of \verb+exprSet+ are in the same order as the columns of the \verb+exprs+ array is needed. It is important that these be properly aligned since analyses will require this and automatic tools for checking will probably be better than ad hoc ones. In addition to the class definitions a number of special methods (or functions) have been defined to operate on instances of these classes. Some particular attention has been paid to subsetting operations. Instances of both \verb+phenoData+ and \verb+exprSet+ are closed under subsetting operations. That is, any subset of one of these objects retains its class. There are also specialized print methods for objects of both classes. We consider an instance of an \verb+exprSet+ to be an expression array with some additional information. Thus there are two subscripts, one for the rows and one for the columns. For that reason subsetting works in the following ways: \begin{itemize} \item If the first subscript is given then the appropriate subset of rows from \verb+exprs+ and \verb+se.exprs+ is taken. All the data in \verb+phenoData+ is propagated since no subset of cases was made. \item If the second subscript is given then the appropriate set of columns from \verb+exprs+ and \verb+se.exprs+ is taken. At the same time the corresponding set of {\em rows} of \verb+phenoData+ are taken. \end{itemize} \subsection{An exprSet Vignette} In the data directory for Biobase there is a small anonymized data set. It consists of expression level data for 500 genes on 26 patients. The data can be accessed with the command \verb+data(geneData)+. There are three artificial covariates provided as well. These can be accessed using \verb+data(geneCovariate)+ once the Biobase library is attached. %%FIXME: is there a better way to do this? The following vignette shows how to read in these data and to create an instance of the \verb+exprSet+ class using those data. The first step is to create an object of \verb+phenoData+ calss. This object is used to store the phenotype data. We will use the example data frame \verb+geneCovariate+ to create such an object. <>= library(Biobase) @ %%<>= %%data(geneCov) %%data(geneData) %%covN <- list(cov1 = "Covariate 1; 2 levels", %% cov2 = "Covariate 2; 2 levels", %% cov3 = "Covariate 3; 3 levels") %% %%pD <- new("phenoData", pData=geneCov, varLabels=covN) %%eSet <- new("exprSet", exprs=geneData, phenoData=pD) %% %%@ <>= data(geneCovariate) head(geneCovariate) phenoD <- new("phenoData", pData=geneCovariate, varLabels=list("sex"="Female/Male","type"="Case/Control","score"="Testing Score") ) phenoD @ We also need a \verb+MIAME+ object to represent the background information, such as the names of the experimenter and laboratory, for this data set. <>= descr <- new("MIAME", name="Pierre Fermat", lab="Francis Galton Lab", contact="pfermat@lab.not.exist", title="Smoking-Cancer Experiment", abstract="An example object of expression set (exprSet) class", url="www.lab.not.exist", other=list( notes="An example object of expression set (exprSet) class") ) descr @ Moreover, we need a \verb+data.frame+ object to group the reporters (probes) at this data set (chip). The definition of probe types is applied from \textit{Affymetrix GeneChip Expression Analysis Data Analysis Fundamentals} (\url{http://www.affymetrix.com/Auth/support/downloads/manuals/data_analysis_fundamentals_manual.pdf}), and the result is stored in the \verb+data.frame+ object \Robject{reporter}. This is a one-column data frame. The rows represent the probe ids in the data set, and the values in the data frame are the predefined types associated with each probe. <>= data(reporter) head(reporter) @ The data frame \Robject{geneData}, containing 500 probes and 26 samples, is a subset of real expression data from an Affymetrix U95v2 chip. The \Robject{seD} is a \Rclass{matrix} object containing the standard errors of \Robject{geneData}. Finaly, we can put all objects together to create the \verb+exprSet+ object. <>= data(geneData) data(seD) exSet <- new("exprSet", exprs = geneData, se.exprs = seD, phenoData = phenoD, annotation = "hgu95av2", description = descr, notes = descr@other$notes, reporterInfo = reporter ) exSet @ If instead, you have the data stored in files, e.g. \texttt{.csv} files and want to read it in using \Rfunction{read.table} you will need to do some conversion. \Rfunction{read.table} reads data into a \Robject{data.frame}, and this is fine for the phenotypic data, but not for the expression data. You will need to convert the \Robject{data.frame} into a matrix. The code example gives a short example of the commands that you would need to execute if you have the expression data stored in a file named \texttt{myexprs.csv} and the phenotypic data in a file named \texttt{mycovs.csv}. \begin{verbatim} myExprs = read.csv("myexprs.csv") myExprsmat = as.matrix(myExprs) myCovs = read.csv("mycovs.csv") if( ncol(myExprsmat) != nrow(myCovs) ) print("ERROR: these should be the same") \end{verbatim} You should probably also check to ensure that you have the appropriate samples names used as row names for \Robject{myCovs} and as column names for \Robject{myExprsmat}, and they must be in the same order. So, again some pseudo-code that gives the essential ingredients is given next. If you are unclear on the difference between a \Robject{matrix} and a \Robject{data.frame} then you should consult one of the very many introductory texts on using R as well as the manual pages and documents that come with R. \begin{verbatim} if( !all.equal( row.names(myCovs), dimnames(myExprsmat)[[2]] ) ) print("ERROR: samples names are wrong") \end{verbatim} Now, we are almost ready to create an instance of an \Robject{exprSet} object. The missing piece is a list of descriptions for the covariates that constitute the phenotypic data. Suppose that we have two variables, one the age of the patient in years and the other the particular translocation they are known to have. And suppose that in the \Robject{data.frame} \Robject{myCovs} the column names are \texttt{age} and \texttt{translocation}. Then we could make up the covariate descriptions as follows. \begin{verbatim} covDesc = list(age="age of the patient in years", translocation="known translocation") \end{verbatim} The purpose of this level of documentation is to help others who might want to re-analyze your data, or you, if at some time in the future you need to go back and see what was done. By carefully annotating the data, in a self-describing way, you increase the chances that you will understand what was done. Below is the simplest form for creating an \Robject{exprSet}. We note that typically you would fill in more details, like the name of the chip used and some additional data describing the experiment itself. \begin{verbatim} myphenoData = new("phenoData", pData=myCovs, varLabels=covDesc) myEset = new("exprSet", exprs=myExprsmat, phenoData=myphenoData) \end{verbatim} \section{Aggregate} When performing an interative computation such as cross--validation or bootstrapping it is often useful to be able to aggregate certain intermediate results. The \verb+Aggregate+ functions (and soon the Aggregate class) provide some simple tools for doing this. The strategy employed is to maintain the summary statistics in an environment. This is passed to the iterative function. It does not need to be returned since environments have a {\em pass--by--reference} semantic. Once the function has finished the environment can be queried for the summary statistics. One simple task that people often want to carry out is to determine in a cross--validation calculation which genes are selected the most often. In some sense these genes may form a more stable basis for inference. Achieving that using an Aggregator is very straight forward. At each iteration we will pass the names of the selected genes to the Aggregator. It has two functions, one for initializing and one for updating (or aggregating). The aggregator also has an environment. This environment stores the data that is being aggregated. For our cross--validation example the process goes as follows: \begin{enumerate} \item At each iteration Aggregate is called with the list of genes selected. \item For each gene in that list we check to see if it was selected before. \begin{enumerate} \item If not then \verb+initfun+ is called with that gene name. The value returned by \verb+initfun+ is then associated with the gene name in the aggregation environment. \item If so, then the current value is obtained and \verb+agfun+ is called with the the gene name and the current value. This returns a new value that is then associated with the gene name in the aggregation environment. \end{enumerate} \end{enumerate} Basically we are using this as a form of updating hash table. At the same time we are slightly subverting R's usual pass--by--value semantics. %\section*{Resampling exprSet's} %need to fill this in again \section{Session Information} The version number of R and packages loaded for generating the vignette were: <>= toLatex(sessionInfo()) @ \end{document} Biobase/vignettes/legacy/Bioconductor.Rnw0000644000175400017540000000577313175713325021565 0ustar00biocbuildbiocbuild% % NOTE -- ONLY EDIT THE .Rnw FILE!!! The .tex file is % likely to be overwritten. % %\VignetteIndexEntry{Bioconductor Overview} %\VignetteDepends{} %\VignetteKeywords{Documentation} %\VignettePackage{Biobase} \documentclass[12pt]{article} \usepackage{times} \usepackage{hyperref} \textwidth=6.2in \textheight=8.5in %\parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \newcommand{\scscst}{\scriptscriptstyle} \newcommand{\scst}{\scriptstyle} \bibliographystyle{plainnat} \begin{document} \title{What is Bioconductor} \maketitle \section*{Prequisites} Bioconductor is a project to develop innovative software tools for use in computational biology. It is based on the R language ({\url www.r-project.org}). You should already be quite familiar with R before using Bioconductor. There are several on--line resources that can help you get started using R. They can be found from the R website. Some users find this a very steep learning curve; your experience may be similar. Bioconductor packages provide flexible interactive tools for carrying out a number of different computational tasks. They are generally not as fast as other analysis tools (since they are interactive) and often reflect current ideas. Most can be improved and interested users should file bug reports and feature requests on the Bioconductor mailing list. Bioconductor welcome collaboration in many different forms. These include new packages, fixes or additions to existing packages and help on different projects that are currently underway. Please see the {\em Current Projects} web page to see if there are any projects that are intersting to you. \subsection*{How to report a bug} Please provide enough information for us to help you. This typically includes the platform (windows, Unix, Macintosh) that you are using as well as version numbers for R and for the package that seems to be working incorrectly. Include a small complete example that can be run and demonstrates the problem. In some cases it is also important that you describe what you thought you should get. Please note: \begin{itemize} \item bugs in R should be reported to the R community \item missing features are not bugs -- they are feature requests. \end{itemize} \section{Bioconductor Design} Bioconductor relies on the R package system to distribute code and data. Most packages use S4 methods and classes (as described in {\em Programming with Data} by J. M. Chambers). This adherence to object oriented programming makes it easier to build component software and helps to deal with the complexity of the data. One of the important Bioconductor packages is {\em annotate}. This package provides access to various genomic annotation data. This package makes use of various web resources and precompiled data packages to provide tools for exploring biological data. \section{Session Information} The version number of R and packages loaded for generating the vignette were: \begin{verbatim} <>= sessionInfo() @ \end{verbatim} \end{document} Biobase/vignettes/legacy/HowTo.Rnw0000644000175400017540000000575013175713325020166 0ustar00biocbuildbiocbuild% % NOTE -- ONLY EDIT THE .Rnw FILE!!! The .tex file is % likely to be overwritten. % % \VignetteIndexEntry{Notes for writing introductory 'how to' documents} %\VignetteDepends{} %\VignetteKeywords{Expression Analysis} %\VignettePackage{Biobase} \documentclass[12pt]{article} \usepackage{times} \usepackage{hyperref} \newcommand{\Rfunction}[1]{{\texttt{#1}}} \newcommand{\Robject}[1]{{\texttt{#1}}} \newcommand{\Rpackage}[1]{{\textit{#1}}} \newcommand{\Rmethod}[1]{{\texttt{#1}}} \newcommand{\Rfunarg}[1]{{\texttt{#1}}} \newcommand{\Rclass}[1]{{\textit{#1}}} \textwidth=6.2in \textheight=8.5in %\parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \newcommand{\scscst}{\scriptscriptstyle} \newcommand{\scst}{\scriptstyle} \bibliographystyle{plainnat} \begin{document} \section*{How to write a HowTo} One of the goals of the Bioconductor project is to produce (and encourage others to produce) documentation on how to perform various tasks. Our main interest is in tasks associated with computational biology. However, we hope to produce HowTo documents for a wide variety of tasks. R has a very good mechanism for documenting individual functions, methods and classes. However, there are many situations where the task that we want to perform requires the use of many components. In other cases we would like to document the overall purpose of an R package rather than the individual functions. In this document we provide some advice on how to construct a document to describe how to perform a task. In most cases HowTo's will be written using \Rfunction{Sweave} in the \Rpackage{tools} package. In this document we give some general advice on how to write a HowTo. Of courese there is no \textit{right} way to do this but we feel that we can provide a few design principles that will help authors write better HowTo's. These design principles are listed below: \begin{itemize} \item It should be short (2 pages at most) and explicit. \item It should be about a single topic. \item It should contain runnable code and rely on data that are available in R or the libraries needed to carry out the task being documented. \item HowTo's should not be about single functions. The function documentation is the right place to document that. HowTo's should document a process or task and will typically involve several functions. \item To paraphrase Paul Halmos, you should imagine that you are writing a document for a friend who is as smart and has the same general level of knowledge as you but who does not know how to do the specific task at hand. \item Make use of the indexing system. The title of the document should be included in the \verb+% \VignetteIndexEntry+. It should contain the word \verb+HowTo+ to easily allow for programmatic manipulation and sorting of the HowTo's. \end{itemize} \section{Session Information} The version number of R and packages loaded for generating the vignette were: \begin{verbatim} <>= sessionInfo() @ \end{verbatim} \end{document} Biobase/vignettes/legacy/Qviews.Rnw0000644000175400017540000001164613175713325020405 0ustar00biocbuildbiocbuild%\VignetteIndexEntry{quick views of eSet instances} %\VignetteDepends{Biobase, ALL} %\VignetteKeywords{Data representation, Analysis} %\VignettePackage{Biobase} % % NOTE -- ONLY EDIT THE .Rnw FILE!!! The .tex file is % likely to be overwritten. % \documentclass[12pt]{article} \usepackage{amsmath,fullpage} \usepackage[authoryear,round]{natbib} \usepackage{hyperref} \textwidth=6.2in \textheight=8.5in %\parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \newcommand{\scscst}{\scriptscriptstyle} \newcommand{\scst}{\scriptstyle} \newcommand{\Rfunction}[1]{{\texttt{#1}}} \newcommand{\Robject}[1]{{\texttt{#1}}} \newcommand{\Rpackage}[1]{{\textit{#1}}} \newcommand{\Rmethod}[1]{{\texttt{#1}}} \newcommand{\Rfunarg}[1]{{\texttt{#1}}} \newcommand{\Rclass}[1]{{\textit{#1}}} \textwidth=6.2in \bibliographystyle{plainnat} \begin{document} %\setkeys{Gin}{width=0.55\textwidth} \title{quick view tools for eSets} \author{VJ Carey} \maketitle \tableofcontents \section{Introduction} In teaching a course where a large number of datasets are introduced over a short period of time, the relationship between data content and software infrastructure can be hard to master. This document introduces a number of experimental approaches to getting rapid access to key elements of eSet derivatives. We will work with the ALL data for demonstration. <>= if (!("Biobase" %in% search())) library(Biobase) if (!("ALL" %in% search())) library(ALL) if (!("ALL" %in% objects())) data(ALL) <>= library(Biobase) library(ALL) data(ALL) ALL @ \section{An alternative to the current show method} It could be nice to tell the package from which the dataset was loaded. <>= dataSource = function(dsn) { if (!is(dsn, "character")) dsn = try(deparse(substitute(dsn))) if (inherits(dsn, "try-error")) stop("can't parse dsn arg") dd = data()$results if (is.na(match(dsn, dd[,"Item"]))) return(NULL) paste("package:", dd[ dd[,"Item"] == dsn, "Package" ], sep="") } <>= setGeneric("peek", function(x,maxattr=10)standardGeneric("peek")) setMethod("peek", c("eSet", "numeric"), function(x,maxattr=10) { ds = dataSource(deparse(substitute(x))) if (!is.null(ds)) ds = paste(" [from ", ds, "]", sep="") else ds = "" cat(deparse(substitute(x)), ds, ":\n", sep="") cat("Platform annotation: ", annotation(x),"\n") cat("primary assay results are:\n") print(dim(x)) cat("sample attributes are:\n") vn = rownames(varMetadata(x)) ld = substr(varMetadata(x)$labelDescription,1,50) dd = data.frame("labelDescription[truncated]"=ld) rownames(dd) = vn if ((ndd <- nrow(dd)) <= maxattr) show(dd) else { cat("first", maxattr, "of", ndd, "attributes:\n") show(dd[1:maxattr,,drop=FALSE]) } cat("----------\n") cat("use varTable to see values/freqs of all sample attributes\n") cat("----------\n") }) setMethod("peek", c("eSet", "missing"), function(x,maxattr=10) { ds = dataSource(deparse(substitute(x))) if (!is.null(ds)) ds = paste(" [from ", ds, "]", sep="") else ds = "" cat(deparse(substitute(x)), ds, ":\n", sep="") cat("Platform annotation: ", annotation(x),"\n") cat("primary assay results are:\n") print(dim(x)) cat("sample attributes are:\n") vn = rownames(varMetadata(x)) ld = substr(varMetadata(x)$labelDescription,1,50) dd = data.frame("labelDescription[truncated]"=ld) rownames(dd) = vn if ((ndd <- nrow(dd)) <= maxattr) show(dd) else { cat("first", maxattr, "of", ndd, "attributes:\n") show(dd[1:maxattr,,drop=FALSE]) } cat("----------\n") cat("use varTable to see values/freqs of all sample attributes\n") cat("----------\n") }) setGeneric("varTable", function(x, full=FALSE, max=Inf) standardGeneric("varTable")) setMethod("varTable", c("eSet", "missing", "ANY"), function(x, full=FALSE, max=Inf) varTable(x, FALSE, max)) setMethod("varTable", c("eSet", "logical", "ANY"), function(x, full=FALSE, max=Inf) { ans = lapply( names(pData(x)), function(z)table(x[[z]]) ) tans = lapply(ans, names) kp = 1:min(max,length(tans)) if (!full) ans = sapply(tans, selectSome, 3)[kp] else ans = tans[kp] names(ans) = names(pData(x))[kp] ans }) setGeneric("varNames", function(x) standardGeneric("varNames")) setMethod("varNames", "eSet", function(x) names(pData(x))) @ We use \texttt{peek} to get a concise view: <>= peek(ALL) @ \section{Sample characterization} Getting a handle on sample characterization requires survey of variable names. <>= varNames(ALL) @ In addition, we need to know values taken. This can be very cumbersome. We have a few parameters on how much detail is provided. <>= varTable(ALL, max=4) @ In the above, we are only showing 4 attributes. By default all attributes would be shown. Note that the report on range of values is truncated and is character mode. We can show the full range of values using the \texttt{full} parameter. <>= varTable(ALL, full=TRUE, max=4) @ \end{document}