BSgenome/DESCRIPTION0000644000175400017540000000331613175725526015025 0ustar00biocbuildbiocbuildPackage: BSgenome Title: Software infrastructure for efficient representation of full genomes and their SNPs Description: Infrastructure shared by all the Biostrings-based genome data packages. Version: 1.46.0 Encoding: UTF-8 Author: Hervé Pagès Maintainer: H. Pagès biocViews: Genetics, Infrastructure, DataRepresentation, SequenceMatching, Annotation, SNP Depends: R (>= 2.8.0), methods, BiocGenerics (>= 0.13.8), S4Vectors (>= 0.9.36), IRanges (>= 2.11.16), GenomeInfoDb (>= 1.13.1), GenomicRanges (>= 1.29.14), Biostrings (>= 2.35.3), rtracklayer (>= 1.25.8) Imports: methods, utils, stats, BiocGenerics, S4Vectors, IRanges, XVector, GenomeInfoDb, GenomicRanges, Biostrings, Rsamtools, rtracklayer Suggests: BiocInstaller, Biobase, BSgenome.Celegans.UCSC.ce2, BSgenome.Hsapiens.UCSC.hg38, BSgenome.Hsapiens.UCSC.hg38.masked, BSgenome.Mmusculus.UCSC.mm10, BSgenome.Rnorvegicus.UCSC.rn5, BSgenome.Scerevisiae.UCSC.sacCer1, TxDb.Hsapiens.UCSC.hg38.knownGene, TxDb.Mmusculus.UCSC.mm10.knownGene, SNPlocs.Hsapiens.dbSNP144.GRCh38, XtraSNPlocs.Hsapiens.dbSNP144.GRCh38, hgu95av2probe, RUnit License: Artistic-2.0 LazyLoad: yes Collate: utils.R OnDiskLongTable_old-class.R OnDiskLongTable-class.R OnDiskNamedSequences-class.R SNPlocs-class.R ODLT_SNPlocs-class.R OldFashionSNPlocs-class.R InjectSNPsHandler-class.R XtraSNPlocs-class.R BSgenome-class.R available.genomes.R injectSNPs.R getSeq-methods.R bsapply.R BSgenomeViews-class.R BSgenome-utils.R export-methods.R BSgenomeForge.R NeedsCompilation: no Packaged: 2017-10-30 22:44:38 UTC; biocbuild BSgenome/NAMESPACE0000644000175400017540000001133213175713516014527 0ustar00biocbuildbiocbuildimport(methods) importFrom(utils, read.table, available.packages, contrib.url, installed.packages, str) importFrom(stats, setNames) import(BiocGenerics) import(S4Vectors) import(IRanges) import(GenomeInfoDb) import(GenomicRanges) import(XVector) import(Biostrings) import(Rsamtools) import(rtracklayer) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Export S4 classes ### exportClasses( OnDiskLongTable_old, GRanges_OR_NULL, OnDiskLongTable, SNPlocs, ODLT_SNPlocs, OldFashionSNPlocs, InjectSNPsHandler, XtraSNPlocs, BSgenome, MaskedBSgenome, BSgenomeViews, ## BSgenomeForge classes: BSgenomeDataPkgSeed ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Export S3 methods ### S3method(as.data.frame, BSgenomeViews) ### We also export them thru the export() directive so that (a) they can be ### called directly, (b) tab-completion on the name of the generic shows them, ### and (c) methods() doesn't asterisk them. export( as.data.frame.BSgenomeViews ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Export S4 methods for generics not defined in BSgenome ### exportMethods( ## Methods for generics defined in the base package: length, names, dim, dimnames, as.character, as.list, as.data.frame, "[[", "$", unlist, nchar, ## Methods for generics defined in the methods package: coerce, show, ## Methods for generics defined in the BiocGenerics package: start, end, width, strand, organism, ## Methods for generics defined in the S4Vectors package: elementNROWS, ## Methods for generics defined in the IRanges package: ranges, Views, subject, score, ## Methods for generics defined in the GenomeInfoDb package: seqinfo, "seqinfo<-", seqnames, "seqnames<-", commonName, provider, providerVersion, releaseDate, releaseName, ## Methods for generics defined in the GenomicRanges package: granges, ## Methods for generics defined in the Biostrings package: getSeq, seqtype, alphabetFrequency, hasOnlyBaseLetters, uniqueLetters, letterFrequency, oligonucleotideFrequency, nucleotideFrequencyAt, consensusMatrix, consensusString, matchPWM, countPWM, vmatchPattern, vcountPattern, ## Methods for generics defined in the rtracklayer package: export ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Export non-generic functions ### export( ## OnDiskLongTable_old-class.R: saveAsOnDiskLongTable_old, saveRowidsForOnDiskLongTable_old, OnDiskLongTable_old, getBatchesFromOnDiskLongTable_old, getRowsByIndexFromOnDiskLongTable_old, getRowsByIdFromOnDiskLongTable_old, ## OnDiskLongTable-class.R: OnDiskLongTable, writeOnDiskLongTable, writeOnDiskLongTableRowids, getBatchesFromOnDiskLongTable, getBatchesBySeqnameFromOnDiskLongTable, getBatchesByOverlapsFromOnDiskLongTable, getRowsFromOnDiskLongTable, getRowsByIdFromOnDiskLongTable, ## OldFashionSNPlocs-class.R: newSNPlocs, ## XtraSNPlocs-class.R: newXtraSNPlocs, ## BSgenome-class.R: BSgenome, MaskedBSgenome, ## available.genomes.R: installed.genomes, available.genomes, getBSgenome, ## injectSNPs.R: installed.SNPs, available.SNPs, ## bsapply.R: bsapply, ## BSgenomeViews-class.R: BSgenomeViews, ## export-methods.R: writeBSgenomeToFasta, writeBSgenomeToTwobit, ## BSgenomeForge.R: forgeSeqlengthsFile, forgeSeqFiles, forgeMasksFiles ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Export S4 generics defined in BSgenome + export corresponding methods ### export( ## OnDiskLongTable_old-class.R: breakpoints, blocksizes, rowids, ## OnDiskLongTable-class.R: batchsizes, spatialIndex, ## SNPlocs-class.R: referenceGenome, compatibleGenomes, snpcount, snplocs, snpsBySeqname, snpsByOverlaps, snpsById, ## OldFashionSNPlocs-class.R: snpid2loc, snpid2alleles, snpid2grange, ## InjectSNPsHandler-class.R: SNPlocs_pkgname, ## BSgenome-class.R: sourceUrl, mseqnames, masknames, ## injectSNPs.R: injectSNPs, ## BSgenomeForge.R: forgeBSgenomeDataPkg, forgeMaskedBSgenomeDataPkg ) ### Exactly the same list as above. exportMethods( breakpoints, blocksizes, rowids, batchsizes, spatialIndex, referenceGenome, compatibleGenomes, snpcount, snplocs, snpsBySeqname, snpsByOverlaps, snpsById, snpid2loc, snpid2alleles, snpid2grange, SNPlocs_pkgname, sourceUrl, mseqnames, masknames, injectSNPs, forgeBSgenomeDataPkg, forgeMaskedBSgenomeDataPkg ) BSgenome/NEWS0000644000175400017540000000076313175713516014015 0ustar00biocbuildbiocbuildCHANGES IN VERSION 1.28.0 ------------------------- NEW FEATURES o Add seqnames() setter for BSgenome objects so users can rename the single sequences in those objects. This has been a popular user request for a while. SIGNIFICANT USER-VISIBLE CHANGES o Add sanity check to "getSeq" method for BSgenome objects, raising an error if the supplied BSgenome and GRanges objects are based on incompatible reference genomes. MISCELLANEOUS o Started the NEWS file (this file). BSgenome/R/0000755000175400017540000000000013175713516013511 5ustar00biocbuildbiocbuildBSgenome/R/BSgenome-class.R0000644000175400017540000005232513175713516016445 0ustar00biocbuildbiocbuild### ========================================================================= ### BSgenome objects ### ------------------------------------------------------------------------- setClass("BSgenome", contains="GenomeDescription", representation( ## Name of the BSgenome data package where the BSgenome object is ## defined. pkgname="character", ## On-disk "single" and "multiple" sequences. single_sequences="OnDiskNamedSequences", multiple_sequences="RdaCollection", ## Permanent URL to the place where the FASTA files that were used ## to produce the "single" and "multiple" sequences above can be ## found (and downloaded). source_url="character", ## Named vector representing the translation table from the original ## seqnames (as stored in self@seqinfo@seqnames, the 'seqinfo' slot ## being inherited from the GenomeDescription class) to the user ## seqnames. user_seqnames="character", ## For SNPs injection. injectSNPs_handler="InjectSNPsHandler", ## Used for caching the single and multiple on-disk sequences. .seqs_cache="environment", .link_counts="environment", ## TODO: Remove the 2 slots below once all the BSgenome data packages ## with masks have been split in 2 packages (naked BSgenome + ## MaskedBSgenome). nmask_per_seq="integer", masks="RdaCollection" ) ) setClass("MaskedBSgenome", contains="BSgenome", representation( ## Name of the BSgenome data package where the MaskedBSgenome object ## is defined. masks_pkgname="character", ## Only the single sequences can be masked. They should all have the ## same set of masks. nmask_per_seq="integer", masks="RdaCollection" ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Low-level helper functions used for delayed-loading/caching/unloading the ### sequences. ### ### Return a new link to a cached object. ### 'objname' is the name of the cached object. ### 'cache' is the caching environment. ### 'link_counts' is the environment where we keep track of the number of links ### for each cached object. When the number of links for a given cached object ### reaches 0, then it is removed from the cache. .newLinkToCachedObject <- function(objname, cache, link_counts) { ans <- new.env(parent=emptyenv()) if (exists(objname, envir=link_counts, inherits=FALSE)) link_count0 <- get(objname, envir=link_counts, inherits=FALSE) + 1L else link_count0 <- 1L reg.finalizer(ans, function(e) { link_count <- get(objname, envir=link_counts, inherits=FALSE) - 1L assign(objname, link_count, envir=link_counts) if (link_count == 0) { if (getOption("verbose")) cat("uncaching ", objname, "\n", sep="") remove(list=objname, envir=cache) } } ) assign(objname, link_count0, envir=link_counts) ans } setGeneric(".linkToCachedObject<-", signature="x", function(x, value) standardGeneric(".linkToCachedObject<-") ) setReplaceMethod(".linkToCachedObject", "SharedVector", function(x, value) { x@.link_to_cached_object <- value x } ) setReplaceMethod(".linkToCachedObject", "XString", function(x, value) { .linkToCachedObject(x@shared) <- value x } ) setReplaceMethod(".linkToCachedObject", "MaskedXString", function(x, value) { .linkToCachedObject(x@unmasked) <- value x } ) setReplaceMethod(".linkToCachedObject", "XStringSet", function(x, value) { ### This means that an XStringSet object with a "pool" slot of ### length != 1 will be permanently cached. if (length(x@pool) == 1L) x@pool@.link_to_cached_object_list[[1L]] <- value x } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The names of the built-in masks. ### BUILTIN_MASKNAMES <- c("AGAPS", "AMB", "RM", "TRF") ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Accessors. ### setMethod("length", "BSgenome", function(x) length(names(x))) setGeneric("sourceUrl", function(x) standardGeneric("sourceUrl")) setMethod("sourceUrl", "BSgenome", function(x) x@source_url) setGeneric("mseqnames", function(x) standardGeneric("mseqnames")) setMethod("mseqnames", "BSgenome", function(x) { ans <- names(x@multiple_sequences) if (length(ans) == 0L) ans <- NULL ans } ) setMethod("names", "BSgenome", function(x) c(seqnames(x), mseqnames(x))) setGeneric("masknames", function(x) standardGeneric("masknames")) setMethod("masknames", "BSgenome", function(x) { if (x@nmask_per_seq == 0L) return(NULL) ## TODO: Put this kind of checking in a validity method for BSgenome ## objects (that's what validity methods are for). if (x@nmask_per_seq > length(BUILTIN_MASKNAMES)) stop("internal anomaly: x@nmask_per_seq > ", length(BUILTIN_MASKNAMES)) BUILTIN_MASKNAMES[seq_len(x@nmask_per_seq)] } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### seqinfo() accessor and related. ### setMethod("seqinfo", "BSgenome", function(x) { ans <- x@seqinfo seqlevels(ans) <- x@user_seqnames ans } ) ### This is a restricted "seqinfo<-" method for BSgenome objects that ### only supports replacement of the sequence names, i.e., except for their ### sequence names, Seqinfo objects 'value' and 'seqinfo(x)' must be identical. setReplaceMethod("seqinfo", "BSgenome", function(x, new2old=NULL, pruning.mode=c("error", "coarse", "fine", "tidy"), value) { if (!is(value, "Seqinfo")) stop("the supplied 'seqinfo' must be a Seqinfo object") IN_THIS_CONTEXT <- paste0("when replacing the 'seqinfo' ", "of a BSgenome object") pruning.mode <- match.arg(pruning.mode) if (pruning.mode != "error") stop("'pruning.mode' not supported ", IN_THIS_CONTEXT) x_seqinfo <- seqinfo(x) if (is.null(new2old)) { ## Support no-op seqinfo(x) <- seqinfo(x). if (!identical(value, x_seqinfo)) stop("'new2old' must be specified ", IN_THIS_CONTEXT) return(x) } if (length(value) != length(x_seqinfo)) stop("the supplied 'seqinfo' must have the same length ", "as the current 'seqinfo' ", IN_THIS_CONTEXT) if (!identical(new2old, seq_along(value))) stop("'new2old' must be NULL or equal to 'seq_along(value)' ", IN_THIS_CONTEXT) new_seqnames <- seqnames(value) seqnames(x_seqinfo) <- new_seqnames if (!identical(value, x_seqinfo)) stop("the supplied and current 'seqinfo' can differ only ", "in their sequence names ", IN_THIS_CONTEXT) if (any(new_seqnames %in% mseqnames(x))) stop("the supplied 'seqnames' cannot match any of the ", "multiple sequence names (as returned by 'mseqnames(x)')") x@user_seqnames[] <- new_seqnames # using [] to preserve the names x } ) setReplaceMethod("seqnames", "BSgenome", function(x, value) { x_seqinfo <- seqinfo(x) seqnames(x_seqinfo) <- value seqinfo(x, new2old=seq_along(x_seqinfo)) <- x_seqinfo x } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### SNP related accessors ### setMethod("SNPlocs_pkgname", "BSgenome", function(x) SNPlocs_pkgname(x@injectSNPs_handler) ) setMethod("snpcount", "BSgenome", function(x) snpcount(x@injectSNPs_handler) ) setMethod("snplocs", "BSgenome", function(x, seqname, ...) snplocs(x@injectSNPs_handler, seqname, ...) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### BSgenome constructor ### ### 'seqnames' only used for sanity check. .makeBSgenomeSeqinfo <- function(single_sequences, circ_seqs, provider_version, seqnames) { seqlengths <- seqlengths(single_sequences) if (length(seqnames) == 0L) { seqnames <- names(seqlengths) } else if (!identical(names(seqlengths), seqnames)) { stop("sequence names found in file '", seqlengthsFilepath(single_sequences), "' are not identical to 'seqnames'. ", "May be the data on disk is corrupted?") } if (identical(circ_seqs, NA)) { is_circ <- NA } else { is_circ <- seqnames %in% circ_seqs } Seqinfo(seqnames=seqnames, seqlengths=seqlengths, isCircular=is_circ, genome=provider_version) } ### NOTES: ### - In BioC 2.14, the 'seqs_pkgname' and 'masks_pkgname' BSgenome slots ### were replaced with the 'pkgname' slot but the 2 corresponding ### arguments were kept for backward compatibility with existing ### BSgenome packages. ### - In BioC 3.1, the 'species' argument was replaced with the 'common_name' ### argument but the former was kept for backward compatibility with ### existing BSgenome packages. BSgenome <- function(organism, common_name, provider, provider_version, release_date, release_name, source_url, seqnames, circ_seqs=NA, mseqnames, seqs_pkgname, seqs_dirpath, nmask_per_seq=0, masks_pkgname=NA, masks_dirpath=NA, species=NA_character_) { twobit_filename <- "single_sequences.2bit" twobit_filepath <- file.path(seqs_dirpath, twobit_filename) if (file.exists(twobit_filepath)) { single_sequences <- TwobitNamedSequences(twobit_filepath) } else { fa_filename <- "single_sequences.fa" fa_filepath <- file.path(seqs_dirpath, fa_filename) farz_filename <- paste0(fa_filename, ".rz") farz_filepath <- file.path(seqs_dirpath, farz_filename) if (file.exists(farz_filepath)) { single_sequences <- FastaNamedSequences(farz_filepath) } else if (file.exists(fa_filepath)) { single_sequences <- FastaNamedSequences(fa_filepath) } else { single_sequences <- RdaNamedSequences(seqs_dirpath, seqnames) } } seqinfo <- .makeBSgenomeSeqinfo(single_sequences, circ_seqs, provider_version, seqnames) seqnames <- seqnames(seqinfo) if (missing(common_name)) common_name <- species genome_description <- GenomeDescription(organism, common_name, provider, provider_version, release_date, release_name, seqinfo) if (is.null(mseqnames)) mseqnames <- character(0) multiple_sequences <- RdaCollection(seqs_dirpath, mseqnames) names(user_seqnames) <- user_seqnames <- seqnames nmask_per_seq <- as.integer(nmask_per_seq) masks_dirpath <- as.character(masks_dirpath) if (nmask_per_seq == 0L || length(seqnames) == 0L) { masks <- RdaCollection(masks_dirpath, character(0)) } else { masks <- RdaCollection(masks_dirpath, paste0(seqnames, ".masks")) } new("BSgenome", genome_description, pkgname=seqs_pkgname, single_sequences=single_sequences, multiple_sequences=multiple_sequences, source_url=source_url, user_seqnames=user_seqnames, .seqs_cache=new.env(parent=emptyenv()), .link_counts=new.env(parent=emptyenv()), nmask_per_seq=nmask_per_seq, masks=masks ) } MaskedBSgenome <- function(ref_bsgenome, masks_pkgname, nmask_per_seq, masks_dirpath) { masks <- RdaCollection(masks_dirpath, paste0(seqnames(ref_bsgenome), ".masks")) new("MaskedBSgenome", ref_bsgenome, .seqs_cache=new.env(parent=emptyenv()), .link_counts=new.env(parent=emptyenv()), masks_pkgname=masks_pkgname, nmask_per_seq=as.integer(nmask_per_seq), masks=masks) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Coercion ### setMethod("as.list", "BSgenome", function(x) lapply(setNames(seqnames(x), seqnames(x)), function(seqname) x[[seqname]]) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "show" method ### .SHOW_BSGENOME_PREFIX <- "# " .SHOW_SEQSECTION_PREFIX <- "# " setMethod("show", "BSgenome", function(object) { mystrwrap <- function(line) writeLines(strwrap(line, width=getOption("width")+1, exdent=0L, prefix=.SHOW_BSGENOME_PREFIX)) if (!is.na(object@common_name)) cat(object@common_name, "genome:\n") GenomeInfoDb:::showGenomeDescription(object, margin=.SHOW_BSGENOME_PREFIX) if (!is.null(SNPlocs_pkgname(object))) cat(.SHOW_BSGENOME_PREFIX, "with SNPs injected from package: ", SNPlocs_pkgname(object), "\n", sep="") if (length(mseqnames(object)) == 0L) { what <- "sequence" } else { cat(.SHOW_BSGENOME_PREFIX, "\n", sep="") what <- "single sequence" } mystrwrap(paste0(length(seqnames(object)), " ", what, "s:")) if (length(seqnames(object)) != 0L) { printAtomicVectorInAGrid(seqnames(object), prefix=.SHOW_SEQSECTION_PREFIX) mystrwrap(paste0("(use 'seqnames()' to see all the ", what, " names, ", "use the '$' or '[[' operator to access a given ", what, ")")) } else { cat(.SHOW_SEQSECTION_PREFIX, "NONE\n", sep="") } if (length(mseqnames(object)) != 0L) { cat(.SHOW_BSGENOME_PREFIX, "\n", sep="") mystrwrap("multiple sequences:") printAtomicVectorInAGrid(mseqnames(object), prefix=.SHOW_SEQSECTION_PREFIX) mystrwrap(paste0("(use 'mseqnames()' to see all the ", "multiple sequence names, ", "use the '$' or '[[' operator to access a given ", "multiple sequence)")) } } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### List-element extraction (with [[). ### .loadBSgenomeSequence <- function(x, seqname, user_seqname) { idx <- match(user_seqname, x@user_seqnames) if (is.na(idx)) { # multiple sequence if (substr(seqname, 1L, 8L) == "upstream") { msg <- c( " Starting with BioC 3.0, the upstream sequences ", "are defunct.\n", " However they can easily be extracted ", "from the full genome\n sequences with something like ", "(for example for hg19):\n\n", " library(TxDb.Hsapiens.UCSC.hg19.knownGene)\n", " txdb <- TxDb.Hsapiens.UCSC.hg19.knownGene\n", " gn <- sort(genes(txdb))\n", " up1000 <- flank(gn, width=1000)\n", " library(BSgenome.Hsapiens.UCSC.hg19)\n", " genome <- BSgenome.Hsapiens.UCSC.hg19\n", " up1000seqs <- getSeq(genome, up1000)\n\n", " IMPORTANT: Make sure you use a TxDb package (or ", "TranscriptDb object)\n that contains a gene model ", "based on the exact same reference genome\n", " as the BSgenome object you pass to getSeq(). Note that ", "you can make\n your own custom TranscriptDb object from ", "various annotation resources.\n", " See the makeTxDbFromUCSC(), ", "makeTxDbFromBiomart(), and\n", " makeTxDbFromGFF() functions in the ", "GenomicFeatures package." ) .Defunct(msg=paste0(msg, collapse="")) } ans <- x@multiple_sequences[[seqname]] return(ans) } # single sequence ans <- x@single_sequences[[seqname]] ## Check the length of the sequence if (length(ans) != seqlengths(x)[[user_seqname]]) { stop(user_seqname, " sequence does not have the expected length. ", "May be the data on disk is corrupted?") } ## Inject the SNPs, if any snps <- snplocs(x, seqname) if (!is.null(snps)) .inplaceReplaceLetterAt(ans, snps$loc, snps$alleles_as_ambig) ## Load and set the built-in masks, if any nmask_per_seq <- length(masknames(x)) if (nmask_per_seq > 0L) { masks_objname <- paste0(seqname, ".masks") builtinmasks <- x@masks[[masks_objname]] if (length(builtinmasks) < nmask_per_seq) { masks_filepath <- rdaPath(x@masks, masks_objname) stop("expecting ", nmask_per_seq, " built-in masks per ", "single sequence, found only ", length(builtinmasks), " in file '", masks_filepath, "'. ", "May be the data on disk is corrupted?") } if (length(builtinmasks) > nmask_per_seq) builtinmasks <- builtinmasks[seq_len(nmask_per_seq)] if (!identical(names(builtinmasks), masknames(x))) { masks_filepath <- rdaPath(x@masks, masks_objname) stop("mask names found in file '", masks_filepath, "' are not ", "identical to the names returned by masknames(). ", "May be the data on disk is corrupted?") } masks(ans) <- builtinmasks } ans } .getBSgenomeSequence <- function(x, seqname, user_seqname) { seqs_cache <- x@.seqs_cache ## Using the 'if (!exists()) assign(); get()' approach is NOT 100% ## reliable: ## ## if (!exists(seqname, envir=seqs_cache, inherits=FALSE)) { ## ... ## assign(seqname, ans, envir=seqs_cache) ## } ## get(seqname, envir=seqs_cache, inherits=FALSE) ## ## because the symbol (seqname) can disappear from the cache between ## the moment we test for its presence and the moment we try to get it. ## It's not me being paranoid, we've seen this happen! One possible ## explanation for this is that the symbol was candidate for removal ## from the cache but that removal didn't happen yet because gc() had ## not yet been called (removal from the cache is implemented thru the ## finalizers registered on the objects that are copied from the cache ## and made available to the user). Then the call to get() would trigger ## garbbage collection and that in turn would trigger the removal of ## the symbol *before* get() had a chance to get to it. So now we use ## the 'try(get(...))' approach, which hopefully is 100% reliable! ans <- try(get(seqname, envir=seqs_cache, inherits=FALSE), silent=TRUE) if (is(ans, "try-error")) { ans <- .loadBSgenomeSequence(x, seqname, user_seqname) if (getOption("verbose")) cat("caching ", seqname, "\n", sep="") assign(seqname, ans, envir=seqs_cache) } .linkToCachedObject(ans) <- .newLinkToCachedObject( seqname, seqs_cache, x@.link_counts) ans } setMethod("[[", "BSgenome", function(x, i, j, ...) { ## 'x' is guaranteed to be a "BSgenome" object (if it's not, then the ## method dispatch algo will not even call this method), so nargs() is ## guaranteed to be >= 1 if (nargs() >= 3L) stop("too many subscripts") subscripts <- list(...) if (!missing(i)) subscripts$i <- i if (!missing(j)) subscripts$j <- j ## At this point, 'subscripts' should be guaranteed ## to be of length <= 1 if (length(subscripts) == 0L) stop("no index specified") i <- subscripts[[1]] if (length(i) < 1) stop("attempt to select less than one element") if (length(i) > 1) stop("attempt to select more than one element") if (is.character(i)) { user_seqname <- try(match.arg(i, names(x)), silent=TRUE) if (is(user_seqname, "try-error")) stop("no such sequence") } else { if (!is.numeric(i) || is.na(i)) stop("no such sequence") i <- as.integer(i) if (i < 1L || length(x) < i) stop("no such sequence") user_seqname <- names(x)[i] } ## Translate user-supplied sequence named back to original name. idx <- match(user_seqname, x@user_seqnames) if (is.na(idx)) { seqname <- user_seqname # multiple sequence } else { seqname <- names(x@user_seqnames)[[idx]] # single sequence } .getBSgenomeSequence(x, seqname, user_seqname) } ) setMethod("$", "BSgenome", function(x, name) x[[name]] ) BSgenome/R/BSgenome-utils.R0000644000175400017540000004166013175713516016500 0ustar00biocbuildbiocbuild## vmatchPattern/vcountPattern for BSgenome setMethod("vmatchPattern", "BSgenome", function(pattern, subject, max.mismatch=0, min.mismatch=0, with.indels=FALSE, fixed=TRUE, algorithm="auto", exclude="", maskList=logical(0), userMask=RangesList(), invertUserMask=FALSE) { matchFUN <- function(posPattern, negPattern, chr, seqlengths, max.mismatch = max.mismatch, min.mismatch = min.mismatch, with.indels = with.indels, fixed = fixed, algorithm = algorithm) { posMatches <- matchPattern(pattern = posPattern, subject = chr, max.mismatch = max.mismatch, min.mismatch = min.mismatch, with.indels = with.indels, fixed = fixed, algorithm = algorithm) negMatches <- matchPattern(pattern = negPattern, subject = chr, max.mismatch = max.mismatch, min.mismatch = min.mismatch, with.indels = with.indels, fixed = fixed, algorithm = algorithm) COUNTER <<- COUNTER + 1L seqnames <- names(seqlengths) GRanges(seqnames = Rle(factor(seqnames[COUNTER], levels = seqnames), length(posMatches) + length(negMatches)), ranges = c(as(posMatches, "IRanges"), as(negMatches, "IRanges")), strand = Rle(strand(c("+", "-")), c(length(posMatches), length(negMatches))), seqlengths = seqlengths) } if (!is(pattern, "DNAString")) pattern <- DNAString(pattern) algorithm <- Biostrings:::normargAlgorithm(algorithm) if (Biostrings:::isCharacterAlgo(algorithm)) stop("'subject' must be a single (non-empty) string ", "for this algorithm") pattern <- Biostrings:::normargPattern(pattern, DNAStringSet()) max.mismatch <- Biostrings:::normargMaxMismatch(max.mismatch) min.mismatch <- Biostrings:::normargMinMismatch(min.mismatch, max.mismatch) with.indels <- Biostrings:::normargWithIndels(with.indels) fixed <- Biostrings:::normargFixed(fixed, DNAStringSet()) posPattern <- pattern negPattern <- reverseComplement(posPattern) bsParams <- new("BSParams", X = subject, FUN = matchFUN, exclude = exclude, simplify = FALSE, maskList = logical(0), userMask = userMask, invertUserMask = invertUserMask) COUNTER <- 0L seqlengths <- seqlengths(subject) matches <- bsapply(bsParams, posPattern = posPattern, negPattern = negPattern, seqlengths = seqlengths, max.mismatch = max.mismatch, min.mismatch = min.mismatch, with.indels = with.indels, fixed = fixed, algorithm = algorithm) nms <- factor(names(matches), levels = names(seqlengths)) nms <- nms[unlist(lapply(matches, length), use.names=FALSE) > 0] matches <- do.call(c, unname(matches)) runValue(seqnames(matches)) <- nms matches } ) setMethod("vcountPattern", "BSgenome", function(pattern, subject, max.mismatch=0, min.mismatch=0, with.indels=FALSE, fixed=TRUE, algorithm="auto", exclude="", maskList=logical(0), userMask=RangesList(), invertUserMask=FALSE) { countFUN <- function(posPattern, negPattern, chr, max.mismatch = max.mismatch, min.mismatch = min.mismatch, with.indels = with.indels, fixed = fixed, algorithm = algorithm) { data.frame(strand = strand(c("+", "-")), count = c(countPattern(pattern = posPattern, subject = chr, max.mismatch = max.mismatch, min.mismatch = min.mismatch, with.indels = with.indels, fixed = fixed, algorithm = algorithm), countPattern(pattern = negPattern, subject = chr, max.mismatch = max.mismatch, min.mismatch = min.mismatch, with.indels = with.indels, fixed = fixed, algorithm = algorithm))) } if (!is(pattern, "DNAString")) pattern <- DNAString(pattern) algorithm <- Biostrings:::normargAlgorithm(algorithm) if (Biostrings:::isCharacterAlgo(algorithm)) stop("'subject' must be a single (non-empty) string ", "for this algorithm") pattern <- Biostrings:::normargPattern(pattern, DNAStringSet()) max.mismatch <- Biostrings:::normargMaxMismatch(max.mismatch) min.mismatch <- Biostrings:::normargMinMismatch(min.mismatch, max.mismatch) with.indels <- Biostrings:::normargWithIndels(with.indels) fixed <- Biostrings:::normargFixed(fixed, DNAStringSet()) posPattern <- pattern negPattern <- reverseComplement(posPattern) bsParams <- new("BSParams", X = subject, FUN = countFUN, exclude = exclude, simplify = FALSE, maskList = logical(0), userMask = userMask, invertUserMask = invertUserMask) counts <- bsapply(bsParams, posPattern = posPattern, negPattern = negPattern, max.mismatch = max.mismatch, min.mismatch = min.mismatch, with.indels = with.indels, fixed = fixed, algorithm = algorithm) cbind(data.frame(seqname = rep(factor(names(counts), levels = names(counts)), each = 2)), do.call(rbind, unname(counts))) } ) ## vmatchPDict/vcountPDict for BSgenome setMethod("vmatchPDict", "BSgenome", function(pdict, subject, max.mismatch=0, min.mismatch=0, fixed=TRUE, algorithm="auto", verbose=FALSE, exclude="", maskList=logical(0)) { matchFUN <- function(posPDict, negPDict, chr, seqlengths, max.mismatch = max.mismatch, min.mismatch = min.mismatch, fixed = fixed, algorithm = algorithm, verbose = verbose) { posMatches <- matchPDict(pdict = posPDict, subject = chr, max.mismatch = max.mismatch, min.mismatch = min.mismatch, fixed = fixed, algorithm = algorithm, verbose = verbose) posCounts <- elementNROWS(posMatches) negMatches <- matchPDict(pdict = negPDict, subject = chr, max.mismatch = max.mismatch, min.mismatch = min.mismatch, fixed = fixed, algorithm = algorithm, verbose = verbose) negCounts <- elementNROWS(negMatches) COUNTER <<- COUNTER + 1L seqnames <- names(seqlengths) GRanges(seqnames = Rle(factor(seqnames[COUNTER], levels = seqnames), sum(posCounts) + sum(negCounts)), ranges = c(unlist(posMatches), unlist(negMatches)), strand = Rle(strand(rep(c("+", "-"))), c(sum(posCounts), sum(negCounts))), index = c(Rle(seq_len(length(posMatches)), posCounts), Rle(seq_len(length(negMatches)), negCounts)), seqlengths = seqlengths) } if (is(pdict, "PDict")) stop("'pdict' must be a DNAStringSet object ") if (!is(pdict, "DNAStringSet")) pdict <- DNAStringSet(pdict) max.mismatch <- Biostrings:::normargMaxMismatch(max.mismatch) min.mismatch <- Biostrings:::normargMinMismatch(min.mismatch, max.mismatch) fixed <- Biostrings:::normargFixed(fixed, DNAStringSet()) algorithm <- Biostrings:::normargAlgorithm(algorithm) if (Biostrings:::isCharacterAlgo(algorithm)) stop("'subject' must be a single (non-empty) string ", "for this algorithm") if (!isTRUEorFALSE(verbose)) stop("'verbose' must be TRUE or FALSE") posPDict <- pdict negPDict <- reverseComplement(posPDict) bsParams <- new("BSParams", X = subject, FUN = matchFUN, exclude = exclude, simplify = FALSE, maskList = logical(0)) COUNTER <- 0L seqlengths <- seqlengths(subject) matches <- bsapply(bsParams, posPDict = PDict(posPDict, max.mismatch = max.mismatch), negPDict = PDict(negPDict, max.mismatch = max.mismatch), seqlengths = seqlengths, max.mismatch = max.mismatch, min.mismatch = min.mismatch, fixed = fixed, algorithm = algorithm, verbose = verbose) nms <- factor(names(matches), levels = names(seqlengths)) nms <- nms[unlist(lapply(matches, length), use.names=FALSE) > 0] matches <- do.call(c, unname(matches)) runValue(seqnames(matches)) <- nms matches } ) setMethod("vcountPDict", "BSgenome", function(pdict, subject, max.mismatch=0, min.mismatch=0, fixed=TRUE, algorithm="auto", collapse=FALSE, weight=1L, verbose=FALSE, exclude="", maskList=logical(0)) { countFUN <- function(posPDict, negPDict, chr, max.mismatch = max.mismatch, min.mismatch = min.mismatch, fixed = fixed, algorithm = algorithm, verbose = verbose) { posCounts <- countPDict(pdict = posPDict, subject = chr, max.mismatch = max.mismatch, min.mismatch = min.mismatch, fixed = fixed, algorithm = algorithm, verbose = verbose) negCounts <- countPDict(pdict = negPDict, subject = chr, max.mismatch = max.mismatch, min.mismatch = min.mismatch, fixed = fixed, algorithm = algorithm, verbose = verbose) DataFrame(strand = Rle(strand(c("+", "-")), c(length(posCounts), length(negCounts))), index = c(seq_len(length(posCounts)), seq_len(length(negCounts))), count = c(Rle(posCounts), Rle(negCounts))) } if (is(pdict, "PDict")) stop("'pdict' must be a DNAStringSet object ") if (!is(pdict, "DNAStringSet")) pdict <- DNAStringSet(pdict) max.mismatch <- Biostrings:::normargMaxMismatch(max.mismatch) min.mismatch <- Biostrings:::normargMinMismatch(min.mismatch, max.mismatch) fixed <- Biostrings:::normargFixed(fixed, DNAStringSet()) algorithm <- Biostrings:::normargAlgorithm(algorithm) if (Biostrings:::isCharacterAlgo(algorithm)) stop("'subject' must be a single (non-empty) string ", "for this algorithm") if (!identical(collapse, FALSE)) stop("'collapse' is not supported in BSgenome method") if (!identical(weight, 1L)) stop("'weight' is not supported in BSgenome method") if (!isTRUEorFALSE(verbose)) stop("'verbose' must be TRUE or FALSE") posPDict <- pdict negPDict <- reverseComplement(posPDict) bsParams <- new("BSParams", X = subject, FUN = countFUN, exclude = exclude, simplify = FALSE, maskList = logical(0)) counts <- bsapply(bsParams, posPDict = PDict(posPDict, max.mismatch = max.mismatch), negPDict = PDict(negPDict, max.mismatch = max.mismatch), max.mismatch = max.mismatch, min.mismatch = min.mismatch, fixed = fixed, algorithm = algorithm, verbose = verbose) DataFrame(DataFrame(seqname = Rle(factor(names(counts), levels = names(counts)), unlist(lapply(counts, nrow), use.names = FALSE))), do.call(rbind, unname(counts))) } ) ## matchPWM/countPWM for BSgenome setMethod("matchPWM", "BSgenome", function(pwm, subject, min.score="80%", exclude="", maskList=logical(0)) { matchFUN <- function(posPWM, negPWM, chr, seqlengths, min.score) { posMatches <- matchPWM(pwm = posPWM, subject = chr, min.score = min.score) posScores <- PWMscoreStartingAt(pwm = posPWM, subject = chr, starting.at = start(posMatches)) negMatches <- matchPWM(pwm = negPWM, subject = chr, min.score = min.score) negScores <- PWMscoreStartingAt(pwm = negPWM, subject = chr, starting.at = start(negMatches)) COUNTER <<- COUNTER + 1L seqnames <- names(seqlengths) GRanges(seqnames = Rle(factor(seqnames[COUNTER], levels = seqnames), length(posMatches) + length(negMatches)), ranges = c(as(posMatches, "IRanges"), as(negMatches, "IRanges")), strand = Rle(strand(c("+", "-")), c(length(posMatches), length(negMatches))), score = c(posScores, negScores), string = c(as.character(posMatches), as.character(reverseComplement(DNAStringSet(negMatches)))), seqlengths = seqlengths) } ## checking 'pwm' pwm <- Biostrings:::.normargPwm(pwm) ## checking 'min.score' min.score <- Biostrings:::.normargMinScore(min.score, pwm) posPWM <- pwm[DNA_BASES, , drop = FALSE] negPWM <- reverseComplement(posPWM) bsParams <- new("BSParams", X = subject, FUN = matchFUN, exclude = exclude, simplify = FALSE, maskList = logical(0)) COUNTER <- 0L seqlengths <- seqlengths(subject) matches <- bsapply(bsParams, posPWM = posPWM, negPWM = negPWM, seqlengths = seqlengths, min.score = min.score) nms <- factor(names(matches), levels = names(seqlengths)) nms <- nms[unlist(lapply(matches, length), use.names=FALSE) > 0] matches <- do.call(c, unname(matches)) runValue(seqnames(matches)) <- nms ## create compact DNAStringSet string <- factor(mcols(matches)[["string"]]) mcols(matches)[["string"]] <- DNAStringSet(levels(string))[as.integer(string)] matches } ) setMethod("countPWM", "BSgenome", function(pwm, subject, min.score="80%", exclude="", maskList=logical(0)) { countFUN <- function(posPWM, negPWM, chr, min.score) { data.frame(strand = strand(c("+", "-")), count = c(countPWM(pwm = posPWM, subject = chr, min.score = min.score), countPWM(pwm = negPWM, subject = chr, min.score = min.score))) } ## checking 'pwm' pwm <- Biostrings:::.normargPwm(pwm) ## checking 'min.score' min.score <- Biostrings:::.normargMinScore(min.score, pwm) posPWM <- pwm[DNA_BASES, , drop = FALSE] negPWM <- reverseComplement(posPWM) bsParams <- new("BSParams", X = subject, FUN = countFUN, exclude = exclude, simplify = FALSE, maskList = logical(0)) counts <- bsapply(bsParams, posPWM = posPWM, negPWM = negPWM, min.score = min.score) cbind(data.frame(seqname = rep(factor(names(counts), levels = names(counts)), each = 2)), do.call(rbind, unname(counts))) } ) BSgenome/R/BSgenomeForge.R0000644000175400017540000011030313175713516016314 0ustar00biocbuildbiocbuild### ========================================================================= ### The BSgenomeForge functions ### ------------------------------------------------------------------------- .getMasksObjname <- function(seqnames) { if (length(seqnames) == 0) return(character(0)) paste(seqnames, ".masks", sep="") } .saveObject <- function(object, objname, destdir=".", verbose=TRUE) { assign(objname, object) destfile <- file.path(destdir, paste(objname, ".rda", sep="")) if (verbose) cat("Saving '", objname, "' object to compressed data file '", destfile, "' ... ", sep="") ## Using compress="xz" (instead of compress="gzip") would produce a .rda ## file that is about 20% smaller on disk but it would also take almost 3x ## longer to load it later on with load(). Tested on hg19 chr1 with R-2.14 ## (2011-09-20 r57033). This is why we stick to compress="gzip". save(list=objname, file=destfile, compress="gzip") if (verbose) cat("DONE\n") remove(list=objname) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "getSeqSrcpaths" function. ### getSeqSrcpaths <- function(seqnames, prefix="", suffix=".fa", seqs_srcdir=".") { if (!is.null(seqnames) && !is.character(seqnames)) stop("'seqnames' must be a character vector (or NULL)") if (length(seqnames) == 0) { warning("'seqnames' is empty") return(character(0)) } if (!isSingleString(prefix)) stop("'prefix' must be a single string") if (!isSingleString(suffix)) stop("'suffix' must be a single string") if (!isSingleString(seqs_srcdir)) stop("'seqs_srcdir' must be a single string") srcfiles <- paste(prefix, seqnames, suffix, sep="") ans <- file.path(seqs_srcdir, srcfiles) is_OK <- file.exists(ans) if (!all(is_OK)) { files_not_found <- paste(ans[!is_OK], collapse=", ") stop("file(s) not found: ", files_not_found) } names(ans) <- seqnames ans } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The getSeqlengths() and forgeSeqlengthsFile() functions. ### getSeqlengths <- function(seqnames, prefix="", suffix=".fa", seqs_srcdir=".") { if (length(seqnames) == 0) { warning("'seqnames' is empty") return(integer(0)) } srcpaths <- getSeqSrcpaths(seqnames, prefix=prefix, suffix=suffix, seqs_srcdir=seqs_srcdir) sapply(seqnames, function(seqname) { srcpath <- srcpaths[[seqname]] ans <- fasta.seqlengths(srcpath) if (length(ans) == 0) stop("In file '", srcpath, "': no sequence found") if (length(ans) > 1) warning("In file '", srcpath, "': ", length(ans), " sequences found, using first sequence only") if (names(ans)[1] != seqname) warning("In file '", srcpath, "': sequence description \"", names(ans), "\" doesn't match user-specified ", "sequence name \"", seqname, "\"") ans[[1]] }, USE.NAMES=TRUE ) } forgeSeqlengthsFile <- function(seqnames, prefix="", suffix=".fa", seqs_srcdir=".", seqs_destdir=".", verbose=TRUE) { seqlengths <- getSeqlengths(seqnames, prefix=prefix, suffix=suffix, seqs_srcdir=seqs_srcdir) if (!isSingleString(seqs_destdir)) stop("'seqs_destdir' must be a single string") .saveObject(seqlengths, "seqlengths", destdir=seqs_destdir, verbose=verbose) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "forgeSeqFiles" function. ### .forgeRdaSeqFile <- function(name, prefix, suffix, seqs_srcdir, seqs_destdir, is.single.seq=TRUE, verbose=TRUE) { if (!isSingleString(name)) stop("'name' must be a single string") srcpath <- getSeqSrcpaths(name, prefix=prefix, suffix=suffix, seqs_srcdir=seqs_srcdir) if (verbose) cat("Loading FASTA file '", srcpath, "' in '", name, "' object ... ", sep="") seq <- readDNAStringSet(srcpath, "fasta") if (verbose) cat("DONE\n") if (is.single.seq) { if (length(seq) == 0) stop("file contains no DNA sequence") if (length(seq) > 1) warning("file contains ", length(seq), " sequences, ", "using the first sequence only") seq <- seq[[1]] # now 'seq' is a DNAString object } .saveObject(seq, name, destdir=seqs_destdir, verbose=verbose) } .forgeFastaRzFileFromFastaFiles <- function(seqnames, prefix, suffix, seqs_srcdir, seqs_destdir, ondisk_seq_format, verbose=TRUE) { if (!is.character(seqnames)) stop("'seqnames' must be a character vector") dest_filename <- "single_sequences.fa" dest_filepath <- file.path(seqs_destdir, dest_filename) for (seqname in seqnames) { srcpath <- getSeqSrcpaths(seqname, prefix=prefix, suffix=suffix, seqs_srcdir=seqs_srcdir) if (verbose) cat("Loading '", seqname, "' sequence from FASTA file '", srcpath, "' ... ", sep="") seq <- readDNAStringSet(srcpath, "fasta") if (verbose) cat("DONE\n") if (length(seq) == 0L) stop("file contains no DNA sequence") if (length(seq) > 1L) { warning("file contains ", length(seq), " sequences, ", "using the first sequence only") seq <- seq[1L] } if (verbose) cat("Appending '", seqname, "' sequence to FASTA file '", dest_filepath, "' ... ", sep="") names(seq) <- seqname writeXStringSet(seq, dest_filepath, append=TRUE, format="fasta", width=50L) if (verbose) cat("DONE\n") } ## Create the index. if (ondisk_seq_format == "fa") { ## "fa" format if (verbose) cat("Indexing FASTA file '", dest_filepath, "' ... ", sep="") indexFa(dest_filepath) if (verbose) cat("DONE\n") } else { ## "fa.rz" format if (verbose) cat("Compressing FASTA file '", dest_filepath, "' ... ", sep="") farz_filepath <- sprintf("%s.rz", dest_filepath) razip(dest_filepath, dest=farz_filepath) unlink(dest_filepath) if (verbose) cat("DONE\n") if (verbose) cat("Indexing compressed FASTA file '", farz_filepath, "' ... ", sep="") indexFa(farz_filepath) if (verbose) cat("DONE\n") } } .replace_non_ACGTN_with_N <- function(x) { af <- alphabetFrequency(x) non_ACGTN <- setdiff(names(af), c(DNA_BASES, "N")) if (sum(af[non_ACGTN]) == 0L) return(x) warning("DNA sequence contains letters not supported by UCSC twoBit ", "format (the format\n only supports A, C, G, T, and N). ", "Replacing them with Ns.") old <- paste(non_ACGTN, collapse="") new <- paste(rep.int("N", length(non_ACGTN)), collapse="") chartr(old, new, x) } .forgeTwobitFileFromFastaFiles <- function(seqnames, prefix, suffix, seqs_srcdir, seqs_destdir, verbose=TRUE) { if (!is.character(seqnames)) stop("'seqnames' must be a character vector") dest_filename <- "single_sequences.2bit" dest_filepath <- file.path(seqs_destdir, dest_filename) seqs <- setNames(vector(mode="list", length=length(seqnames)), seqnames) for (seqname in seqnames) { srcpath <- getSeqSrcpaths(seqname, prefix=prefix, suffix=suffix, seqs_srcdir=seqs_srcdir) if (verbose) cat("Loading '", seqname, "' sequence from FASTA file '", srcpath, "' ... ", sep="") seq <- readDNAStringSet(srcpath, "fasta") if (verbose) cat("DONE\n") if (length(seq) == 0L) stop("file contains no DNA sequence") if (length(seq) > 1L) { warning("file contains ", length(seq), " sequences, ", "using the first sequence only") seq <- seq[1L] } seq <- .replace_non_ACGTN_with_N(seq[[1L]]) seqs[[seqname]] <- seq } seqs <- DNAStringSet(seqs) if (verbose) cat("Writing all sequences to '", dest_filepath, "' ... ", sep="") export(seqs, dest_filepath, format="2bit") if (verbose) cat("DONE\n") } .copySeqFile <- function(seqfile_name, seqs_srcdir, seqs_destdir, verbose=TRUE) { src_filepath <- file.path(seqs_srcdir, seqfile_name) if (!file.exists(src_filepath)) stop("File not found: ", src_filepath) dest_filename <- "single_sequences.2bit" dest_filepath <- file.path(seqs_destdir, dest_filename) if (verbose) cat("Copying '", src_filepath, "' to '", dest_filepath, "' ... ", sep="") if (!file.copy(src_filepath, dest_filepath, copy.mode=FALSE, copy.date=FALSE)) { if (verbose) stop("FAILED") stop("Failed to copy '", src_filepath, "' to '", dest_filepath, "'") } if (verbose) cat("DONE\n") } .subsetTwobitFile <- function(seqfile_name, seqnames, seqs_srcdir, seqs_destdir, verbose=verbose) { src_filepath <- file.path(seqs_srcdir, seqfile_name) dest_filename <- "single_sequences.2bit" dest_filepath <- file.path(seqs_destdir, dest_filename) if (verbose) cat("Loading '", src_filepath, "' ... ", sep="") seqs <- import(src_filepath) if (verbose) cat("DONE\n") idx <- match(seqnames, names(seqs)) notfound_idx <- which(is.na(idx)) if (length(notfound_idx) != 0L) stop("sequence(s) not found: ", paste(seqnames[notfound_idx], collapse=", ")) seqs <- seqs[idx] if (verbose) cat("Writing sequences to '", dest_filepath, "' ... ", sep="") export(seqs, dest_filepath, format="2bit") if (verbose) cat("DONE\n") } forgeSeqFiles <- function(seqnames, mseqnames=NULL, seqfile_name=NA, prefix="", suffix=".fa", seqs_srcdir=".", seqs_destdir=".", ondisk_seq_format=c("2bit", "rda", "fa.rz", "fa"), verbose=TRUE) { if (length(seqnames) == 0L && is.na(seqfile_name)) warning("'seqnames' is empty") if (!(length(mseqnames) == 0L || is.character(mseqnames))) stop("'mseqnames' must be a character vector (or NULL)") if (!isSingleString(seqs_destdir)) stop("'seqs_destdir' must be a single string") ondisk_seq_format <- match.arg(ondisk_seq_format) if (ondisk_seq_format == "rda") { # "rda" format for (name in seqnames) { .forgeRdaSeqFile(name, prefix, suffix, seqs_srcdir, seqs_destdir, is.single.seq=TRUE, verbose=verbose) } } else if (ondisk_seq_format == "2bit") { # "2bit" format if (is.na(seqfile_name)) { .forgeTwobitFileFromFastaFiles(seqnames, prefix, suffix, seqs_srcdir, seqs_destdir, verbose=verbose) } else if (length(seqnames) == 0L) { .copySeqFile(seqfile_name, seqs_srcdir, seqs_destdir, verbose=verbose) } else { .subsetTwobitFile(seqfile_name, seqnames, seqs_srcdir, seqs_destdir, verbose=verbose) } } else { # "fa" and "fa.rz" formats .forgeFastaRzFileFromFastaFiles(seqnames, prefix, suffix, seqs_srcdir, seqs_destdir, ondisk_seq_format, verbose=verbose) } for (name in mseqnames) { .forgeRdaSeqFile(name, prefix, suffix, seqs_srcdir, seqs_destdir, is.single.seq=FALSE, verbose=verbose) } } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "forgeMasksFiles" function. ### ## AGAPS is the mask of "assembly gaps" (inter-contig Ns). ## If 'filetype' is: ## NA: then AGAPS is an empty mask; ## "gap": then AGAPS is extracted from a UCSC "gap" file; ## "agp": then AGAPS is extracted from an NCBI "agp" file. ## AGAPS is active by default. .forge.AGAPSmask <- function(seqname, mask_width, masks_srcdir, filetype, filename, fileprefix, filesuffix) { if (!isSingleStringOrNA(filetype)) stop("'filetype' must be a single string or NA") if (!isSingleStringOrNA(filename)) stop("'filename' must be a single string or NA") if (!isSingleStringOrNA(fileprefix)) stop("'fileprefix' must be a single string or NA") if (!isSingleStringOrNA(filesuffix)) stop("'filesuffix' must be a single string or NA") if (is.na(filetype)) { ans <- Mask(mask_width) desc(ans) <- "assembly gaps (empty)" } else { if (is.na(filename)) filename <- paste(fileprefix, seqname, filesuffix, sep="") filepath <- file.path(masks_srcdir, filename) if (filetype == "gap") ans <- read.gapMask(filepath, seqname=seqname, mask.width=mask_width) else ans <- read.agpMask(filepath, seqname=seqname, mask.width=mask_width) } active(ans) <- TRUE names(ans) <- "AGAPS" ans } ## AMB is the mask of "intra-contig ambiguities". ## AMB is active by default. .forge.AMBmask <- function(seq, AGAPSmask) { active(AGAPSmask) <- TRUE masks(seq) <- AGAPSmask amb_letters <- names(IUPAC_CODE_MAP)[nchar(IUPAC_CODE_MAP) > 1] for (amb_letter in amb_letters) seq <- maskMotif(seq, amb_letter) ans <- collapse(masks(seq)[-1]) desc(ans) <- "intra-contig ambiguities" if (isEmpty(ans)) desc(ans) <- paste(desc(ans), "(empty)") active(ans) <- TRUE names(ans) <- "AMB" ans } ## RM is the "RepeatMasker" mask (from the RepeatMasker .out file). ## RM is NOT active by default. .forge.RMmask <- function(seqname, mask_width, masks_srcdir, filename, fileprefix, filesuffix) { if (!isSingleStringOrNA(filename)) stop("'filename' must be a single string or NA") if (!isSingleStringOrNA(fileprefix)) stop("'fileprefix' must be a single string or NA") if (!isSingleStringOrNA(filesuffix)) stop("'filesuffix' must be a single string or NA") if (is.na(filename)) filename <- paste(fileprefix, seqname, filesuffix, sep="") filepath <- file.path(masks_srcdir, filename) if (file.exists(filepath)) { ans <- read.rmMask(filepath, seqname=seqname, mask.width=mask_width) desc(ans) <- "RepeatMasker" } else { ans <- Mask(mask_width) desc(ans) <- "RepeatMasker (empty)" } active(ans) <- FALSE names(ans) <- "RM" ans } ## TRF is the "Tandem Repeats Finder" mask (from the Tandem Repeats Finder ## .bed file). ## TRF is NOT active by default. .forge.TRFmask <- function(seqname, mask_width, masks_srcdir, filename, fileprefix, filesuffix) { if (!isSingleStringOrNA(filename)) stop("'filename' must be a single string or NA") if (!isSingleStringOrNA(fileprefix)) stop("'fileprefix' must be a single string or NA") if (!isSingleStringOrNA(filesuffix)) stop("'filesuffix' must be a single string or NA") if (is.na(filename)) filename <- paste(fileprefix, seqname, filesuffix, sep="") filepath <- file.path(masks_srcdir, filename) if (file.exists(filepath)) { ans <- read.trfMask(filepath, seqname=seqname, mask.width=mask_width) desc(ans) <- "Tandem Repeats Finder [period<=12]" } else { ans <- Mask(mask_width) desc(ans) <- "Tandem Repeats Finder [period<=12] (empty)" } active(ans) <- FALSE names(ans) <- "TRF" ans } .forgeMasksFile <- function(seqname, nmask_per_seq, seqs_destdir=".", ondisk_seq_format=c("2bit", "rda", "fa.rz", "fa"), masks_srcdir=".", masks_destdir=".", AGAPSfiles_type="gap", AGAPSfiles_name=NA, AGAPSfiles_prefix="", AGAPSfiles_suffix="_gap.txt", RMfiles_name=NA, RMfiles_prefix="", RMfiles_suffix=".fa.out", TRFfiles_name=NA, TRFfiles_prefix="", TRFfiles_suffix=".bed", verbose=TRUE) { if (!isSingleString(seqname)) stop("'seqname' must be a single string") if (!is.numeric(nmask_per_seq) || length(nmask_per_seq) != 1 || !(nmask_per_seq %in% 0:4)) stop("'nmask_per_seq' must be 0, 1, 2, 3 or 4") if (nmask_per_seq == 0) warning("forging an empty mask collection ('nmask_per_seq' is set to 0)") if (!isSingleString(seqs_destdir)) stop("'seqs_destdir' must be a single string") if (!isSingleString(masks_srcdir)) stop("'masks_srcdir' must be a single string") if (!isSingleString(masks_destdir)) stop("'masks_destdir' must be a single string") ## Load the sequence. ondisk_seq_format <- match.arg(ondisk_seq_format) if (ondisk_seq_format == "rda") { # "rda" format seqfile <- file.path(seqs_destdir, paste(seqname, ".rda", sep="")) load(seqfile) seq <- get(seqname) remove(list=seqname) } else if (ondisk_seq_format == "2bit") { # "2bit" format twobit_filename <- "single_sequences.2bit" twobit_filepath <- file.path(seqs_destdir, twobit_filename) twobitfile <- TwoBitFile(twobit_filepath) which <- GRanges(seqname, IRanges(1L, seqlengths(twobitfile)[[seqname]])) seq <- import(twobitfile, which=which)[[1L]] } else { # "fa" and "fa.rz" formats fa_filename <- "single_sequences.fa" if (ondisk_seq_format == "fa.rz") fa_filename <- paste0(fa_filename, ".rz") fa_filepath <- file.path(seqs_destdir, fa_filename) fafile <- FaFile(fa_filepath) ## TODO: Implement "[[" method for FaFile objects (in Rsamtools) and ## use it here (i.e. do 'seq <- fafile[[seqname]]' instead of the 2 ## lines below). param <- GRanges(seqname, IRanges(1L, seqlengths(fafile)[[seqname]])) seq <- scanFa(fafile, param=param)[[1L]] } mask_width <- length(seq) ## Start with an empty mask collection (i.e. a MaskCollection of ## length 0). masks <- new("MaskCollection", width=mask_width) if (nmask_per_seq >= 1) { AGAPSmask <- .forge.AGAPSmask(seqname, mask_width, masks_srcdir, AGAPSfiles_type, AGAPSfiles_name, AGAPSfiles_prefix, AGAPSfiles_suffix) masks <- append(masks, AGAPSmask) } if (nmask_per_seq >= 2) { AMBmask <- .forge.AMBmask(seq, AGAPSmask) masks <- append(masks, AMBmask) } if (nmask_per_seq >= 3) { RMmask <- .forge.RMmask(seqname, mask_width, masks_srcdir, RMfiles_name, RMfiles_prefix, RMfiles_suffix) masks <- append(masks, RMmask) } if (nmask_per_seq >= 4) { TRFmask <- .forge.TRFmask(seqname, mask_width, masks_srcdir, TRFfiles_name, TRFfiles_prefix, TRFfiles_suffix) masks <- append(masks, TRFmask) } objname <- .getMasksObjname(seqname) .saveObject(masks, objname, destdir=masks_destdir, verbose=verbose) } forgeMasksFiles <- function(seqnames, nmask_per_seq, seqs_destdir=".", ondisk_seq_format=c("2bit", "rda", "fa.rz", "fa"), masks_srcdir=".", masks_destdir=".", AGAPSfiles_type="gap", AGAPSfiles_name=NA, AGAPSfiles_prefix="", AGAPSfiles_suffix="_gap.txt", RMfiles_name=NA, RMfiles_prefix="", RMfiles_suffix=".fa.out", TRFfiles_name=NA, TRFfiles_prefix="", TRFfiles_suffix=".bed", verbose=TRUE) { if (length(seqnames) == 0) warning("'seqnames' is empty") for (seqname in seqnames) { .forgeMasksFile(seqname, nmask_per_seq, seqs_destdir=seqs_destdir, ondisk_seq_format=ondisk_seq_format, masks_srcdir=masks_srcdir, masks_destdir=masks_destdir, AGAPSfiles_type=AGAPSfiles_type, AGAPSfiles_name=AGAPSfiles_name, AGAPSfiles_prefix=AGAPSfiles_prefix, AGAPSfiles_suffix=AGAPSfiles_suffix, RMfiles_name=RMfiles_name, RMfiles_prefix=RMfiles_prefix, RMfiles_suffix=RMfiles_suffix, TRFfiles_name=TRFfiles_name, TRFfiles_prefix=TRFfiles_prefix, TRFfiles_suffix=TRFfiles_suffix, verbose=verbose) } } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The BSgenomeDataPkgSeed and MaskedBSgenomeDataPkgSeed classes and their ### low-level constructors. ### setClass("BSgenomeDataPkgSeed", representation( Package="character", Title="character", Description="character", Version="character", Author="character", Maintainer="character", Suggests="character", License="character", organism="character", common_name="character", provider="character", provider_version="character", release_date="character", release_name="character", source_url="character", organism_biocview="character", BSgenomeObjname="character", seqnames="character", # a single string containing R source code circ_seqs="character", # a single string containing R source code mseqnames="character", # a single string containing R source code PkgDetails="character", SrcDataFiles="character", PkgExamples="character", seqfile_name="character", seqfiles_prefix="character", seqfiles_suffix="character", ondisk_seq_format="character" ), prototype( Author="The Bioconductor Dev Team", Maintainer="Bioconductor Package Maintainer ", Suggests="", License="Artistic-2.0", source_url="-- information not available --", seqnames="NULL", # equivalent to "character(0)" circ_seqs="NULL", # equivalent to "character(0)" mseqnames="NULL", # equivalent to "character(0)" PkgDetails="", SrcDataFiles="-- information not available --", PkgExamples="", seqfile_name=NA_character_, seqfiles_prefix="", seqfiles_suffix=".fa", ondisk_seq_format="2bit" ) ) setClass("MaskedBSgenomeDataPkgSeed", representation( Package="character", Title="character", Description="character", Version="character", Author="character", Maintainer="character", RefPkgname="character", Suggests="character", License="character", source_url="character", organism_biocview="character", nmask_per_seq="integer", # a single integer PkgDetails="character", SrcDataFiles="character", PkgExamples="character", AGAPSfiles_type="character", AGAPSfiles_name="character", AGAPSfiles_prefix="character", AGAPSfiles_suffix="character", RMfiles_name="character", RMfiles_prefix="character", RMfiles_suffix="character", TRFfiles_name="character", TRFfiles_prefix="character", TRFfiles_suffix="character" ), prototype( Author="The Bioconductor Dev Team", Maintainer="Bioconductor Package Maintainer ", Suggests="", License="Artistic-2.0", source_url="-- information not available --", nmask_per_seq=0L, PkgDetails="", SrcDataFiles="-- information not available --", PkgExamples="", AGAPSfiles_type="gap", AGAPSfiles_name=as.character(NA), AGAPSfiles_prefix="", AGAPSfiles_suffix="_gap.txt", RMfiles_name=as.character(NA), RMfiles_prefix="", RMfiles_suffix=".fa.out", TRFfiles_name=as.character(NA), TRFfiles_prefix="", TRFfiles_suffix=".bed" ) ) ### Generic transformation of a named list into an S4 object with automatic ### coercion of the list elements to the required types. makeS4FromList <- function(Class, x) { if (!is.list(x) || is.null(names(x))) stop("'x' must be a named list") explicit_slots <- getSlots(Class)[names(x)] if (any(is.na(explicit_slots))) { invalid_names <- setdiff(names(x), names(getSlots(Class))) stop("some names in 'x' are not valid ", Class, " slots (", paste(invalid_names, collapse=", "), ")") } y <- lapply(seq_len(length(x)), function(i) { x_elt <- x[[i]] if (is(x_elt, explicit_slots[i])) return(x_elt) as(x_elt, explicit_slots[i]) }) names(y) <- names(x) y$Class <- Class do.call(new, y) } BSgenomeDataPkgSeed <- function(x) makeS4FromList("BSgenomeDataPkgSeed", x) MaskedBSgenomeDataPkgSeed <- function(x) makeS4FromList("MaskedBSgenomeDataPkgSeed", x) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "forgeBSgenomeDataPkg" generic and methods. ### setGeneric("forgeBSgenomeDataPkg", signature="x", function(x, seqs_srcdir=".", destdir=".", verbose=TRUE) standardGeneric("forgeBSgenomeDataPkg") ) setMethod("forgeBSgenomeDataPkg", "BSgenomeDataPkgSeed", function(x, seqs_srcdir=".", destdir=".", verbose=TRUE) { ## The Biobase package is needed for createPackage(). if (!requireNamespace("Biobase", quietly=TRUE)) stop("Couldn't load the Biobase package. Please install ", "the Biobase\n package and try again.") template_path <- system.file("pkgtemplates", "BSgenome_datapkg", package="BSgenome") BSgenome_version <- installed.packages()['BSgenome','Version'] symvals <- list( PKGTITLE=x@Title, PKGDESCRIPTION=x@Description, PKGVERSION=x@Version, AUTHOR=x@Author, MAINTAINER=x@Maintainer, BSGENOMEVERSION=BSgenome_version, SUGGESTS=x@Suggests, LICENSE=x@License, ORGANISM=x@organism, COMMONNAME=x@common_name, PROVIDER=x@provider, PROVIDERVERSION=x@provider_version, RELEASEDATE=x@release_date, RELEASENAME=x@release_name, SOURCEURL=x@source_url, ORGANISMBIOCVIEW=x@organism_biocview, BSGENOMEOBJNAME=x@BSgenomeObjname, SEQNAMES=ifelse(is.na(x@seqfile_name), x@seqnames, "NULL"), CIRCSEQS=x@circ_seqs, MSEQNAMES=x@mseqnames, PKGDETAILS=x@PkgDetails, SRCDATAFILES=x@SrcDataFiles, PKGEXAMPLES=x@PkgExamples ) ## Should never happen if (any(duplicated(names(symvals)))) { str(symvals) stop("'symvals' contains duplicated symbols") } ## All symvals should by single strings (non-NA) is_OK <- sapply(symvals, isSingleString) if (!all(is_OK)) { bad_syms <- paste(names(is_OK)[!is_OK], collapse=", ") stop("values for symbols ", bad_syms, " are not single strings") } Biobase::createPackage(x@Package, destdir, template_path, symvals) pkgdir <- file.path(destdir, x@Package) .seqnames <- eval(parse(text=x@seqnames)) .mseqnames <- eval(parse(text=x@mseqnames)) seqs_destdir <- file.path(pkgdir, "inst", "extdata") if (x@ondisk_seq_format == "rda") { ## Forge the "seqlengths.rda" file forgeSeqlengthsFile(.seqnames, prefix=x@seqfiles_prefix, suffix=x@seqfiles_suffix, seqs_srcdir=seqs_srcdir, seqs_destdir=seqs_destdir, verbose=verbose) } ## Forge the sequence files (either "2bit", "rda", "fa.rz", or "fa") forgeSeqFiles(.seqnames, mseqnames=.mseqnames, seqfile_name=x@seqfile_name, prefix=x@seqfiles_prefix, suffix=x@seqfiles_suffix, seqs_srcdir=seqs_srcdir, seqs_destdir=seqs_destdir, ondisk_seq_format=x@ondisk_seq_format, verbose=verbose) } ) setMethod("forgeBSgenomeDataPkg", "list", function(x, seqs_srcdir=".", destdir=".", verbose=TRUE) { y <- BSgenomeDataPkgSeed(x) forgeBSgenomeDataPkg(y, seqs_srcdir=seqs_srcdir, destdir=destdir, verbose=verbose) } ) .removeCommentLines <- function(infile=stdin(), outfile=stdout()) { if (is.character(infile)) { infile <- file(infile, "r") on.exit(close(infile)) } if (is.character(outfile)) { outfile <- file(outfile, "w") on.exit({close(infile); close(outfile)}) } while (TRUE) { lines <- readLines(infile, n=25000L) if (length(lines) == 0L) return() keep_it <- substr(lines, 1L, 1L) != "#" writeLines(lines[keep_it], outfile) } } ### A "comment aware" version of read.dcf(). read.dcf2 <- function(file, ...) { clean_file <- tempfile() .removeCommentLines(file, clean_file) on.exit(file.remove(clean_file)) read.dcf(clean_file, ...) } ### Return a named character vector. .readSeedFile <- function(file, verbose=TRUE) { if (!isSingleString(file)) stop("'file' must be a single string") if (file.exists(file)) { ## Using 'x["isdir"][[1]]' is safer than using 'x$isdir' or ## 'x[["isdir"]]' because it will fail if "isdir" is not a defined ## column isdir <- file.info(file)["isdir"][[1]] if (isdir) stop("'", file, "' is a directory, not a seed file") } else { file0 <- file seed_dir <- system.file("extdata", "GentlemanLab", package="BSgenome") file <- file.path(seed_dir, file) if (!file.exists(file)) { file <- paste(file, "-seed", sep="") if (!file.exists(file)) stop("seed file '", file0, "' not found") } if (verbose) cat("Seed file '", file0, "' not found, using file '", file, "'\n", sep="") } ans <- read.dcf2(file) # a character matrix if (nrow(ans) != 1) stop("seed file '", file, "' must have exactly 1 record") ans[1, , drop=TRUE] } setMethod("forgeBSgenomeDataPkg", "character", function(x, seqs_srcdir=".", destdir=".", verbose=TRUE) { y <- .readSeedFile(x, verbose=verbose) y <- as.list(y) if (missing(seqs_srcdir)) { seqs_srcdir <- y[["seqs_srcdir"]] if (is.null(seqs_srcdir)) stop("'seqs_srcdir' argument is missing, and the ", "'seqs_srcdir' field is missing in seed file") } y <- y[!(names(y) %in% "seqs_srcdir")] forgeBSgenomeDataPkg(y, seqs_srcdir=seqs_srcdir, destdir=destdir, verbose=verbose) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "forgeMaskedBSgenomeDataPkg" generic and methods. ### setGeneric("forgeMaskedBSgenomeDataPkg", signature="x", function(x, masks_srcdir=".", destdir=".", verbose=TRUE) standardGeneric("forgeMaskedBSgenomeDataPkg") ) setMethod("forgeMaskedBSgenomeDataPkg", "MaskedBSgenomeDataPkgSeed", function(x, masks_srcdir=".", destdir=".", verbose=TRUE) { ## The Biobase package is needed for createPackage(). if (!requireNamespace("Biobase", quietly=TRUE)) stop("Couldn't load the Biobase package. Please install ", "the Biobase\n package and try again.") require(x@RefPkgname, character.only=TRUE) || stop("the ", x@RefPkgname, " package is required") ref_envir <- as.environment(paste0("package:", x@RefPkgname)) ref_bsgenome <- get(x@RefPkgname, envir=ref_envir) template_path <- system.file("pkgtemplates", "MaskedBSgenome_datapkg", package="BSgenome") BSgenome_version <- installed.packages()['BSgenome','Version'] symvals <- list( PKGTITLE=x@Title, PKGDESCRIPTION=x@Description, PKGVERSION=x@Version, AUTHOR=x@Author, MAINTAINER=x@Maintainer, BSGENOMEVERSION=BSgenome_version, REFPKGNAME=x@RefPkgname, SUGGESTS=x@Suggests, LICENSE=x@License, ORGANISM=organism(ref_bsgenome), COMMONNAME=commonName(ref_bsgenome), PROVIDER=provider(ref_bsgenome), PROVIDERVERSION=providerVersion(ref_bsgenome), RELEASEDATE=releaseDate(ref_bsgenome), RELEASENAME=releaseName(ref_bsgenome), SOURCEURL=x@source_url, ORGANISMBIOCVIEW=x@organism_biocview, NMASKPERSEQ=as.character(x@nmask_per_seq), PKGDETAILS=x@PkgDetails, SRCDATAFILES=x@SrcDataFiles, PKGEXAMPLES=x@PkgExamples ) ## Should never happen if (any(duplicated(names(symvals)))) { str(symvals) stop("'symvals' contains duplicated symbols") } ## All symvals should by single strings (non-NA) is_OK <- sapply(symvals, isSingleString) if (!all(is_OK)) { bad_syms <- paste(names(is_OK)[!is_OK], collapse=", ") stop("values for symbols ", bad_syms, " are not single strings") } Biobase::createPackage(x@Package, destdir, template_path, symvals) ## Forge the "*.masks.rda" files seqs_destdir <- dirname(seqlengthsFilepath(ref_bsgenome@single_sequences)) pkgdir <- file.path(destdir, x@Package) masks_destdir <- file.path(pkgdir, "inst", "extdata") forgeMasksFiles(seqnames(ref_bsgenome), x@nmask_per_seq, seqs_destdir=seqs_destdir, ondisk_seq_format="2bit", masks_srcdir=masks_srcdir, masks_destdir=masks_destdir, AGAPSfiles_type=x@AGAPSfiles_type, AGAPSfiles_name=x@AGAPSfiles_name, AGAPSfiles_prefix=x@AGAPSfiles_prefix, AGAPSfiles_suffix=x@AGAPSfiles_suffix, RMfiles_name=x@RMfiles_name, RMfiles_prefix=x@RMfiles_prefix, RMfiles_suffix=x@RMfiles_suffix, TRFfiles_name=x@TRFfiles_name, TRFfiles_prefix=x@TRFfiles_prefix, TRFfiles_suffix=x@TRFfiles_suffix, verbose=verbose) } ) setMethod("forgeMaskedBSgenomeDataPkg", "list", function(x, masks_srcdir=".", destdir=".", verbose=TRUE) { y <- MaskedBSgenomeDataPkgSeed(x) forgeMaskedBSgenomeDataPkg(y, masks_srcdir=masks_srcdir, destdir=destdir, verbose=verbose) } ) setMethod("forgeMaskedBSgenomeDataPkg", "character", function(x, masks_srcdir=".", destdir=".", verbose=TRUE) { y <- .readSeedFile(x, verbose=verbose) y <- as.list(y) if (missing(masks_srcdir)) { masks_srcdir <- y[["masks_srcdir"]] if (is.null(masks_srcdir)) stop("'masks_srcdir' argument is missing, and the ", "'masks_srcdir' field is missing in seed file") } y <- y[!(names(y) %in% "masks_srcdir")] forgeMaskedBSgenomeDataPkg(y, masks_srcdir=masks_srcdir, destdir=destdir, verbose=verbose) } ) BSgenome/R/BSgenomeViews-class.R0000644000175400017540000003242513175713516017462 0ustar00biocbuildbiocbuild### ========================================================================= ### BSgenomeViews objects ### ------------------------------------------------------------------------- ### ### The BSgenomeViews class is a container for storing a set of genomic ### positions on a BSgenome object, called the "subject". ### ### We cannot (and should not try to) extend Views here, for the same ### reasons that we didn't make GRanges a subclass of IRanges. ### ### TODO: A cleaner class design would be to have 2 abstractions: IViews and ### GViews. For IViews: the subject is a Vector and the ranges slot is an ### IRanges object. Note that this is how the current Views class is defined. ### For GViews: the subject is a named List and the granges slot is a ### GRanges object. Both IViews and GViews would be direct subclasses of a ### more general Views class that contains List and has a subject slot. ### BSgenomeViews below then should become a subclass of GViews. setClass("BSgenomeViews", contains="List", representation( subject="BSgenome", granges="GRanges", elementMetadata="DataFrame" ), prototype( elementType="DNAString" ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Accessors ### setMethod("subject", "BSgenomeViews", function(x) x@subject) setMethod("granges", "BSgenomeViews", function(x, use.mcols=FALSE) { if (!isTRUEorFALSE(use.mcols)) stop("'use.mcols' must be TRUE or FALSE") ans <- x@granges if (use.mcols) mcols(ans) <- mcols(x) ans } ) setMethod("length", "BSgenomeViews", function(x) length(granges(x))) setMethod("names", "BSgenomeViews", function(x) names(granges(x))) setMethod("seqnames", "BSgenomeViews", function(x) seqnames(granges(x))) setMethod("start", "BSgenomeViews", function(x) start(granges(x))) setMethod("end", "BSgenomeViews", function(x) end(granges(x))) setMethod("width", "BSgenomeViews", function(x) width(granges(x))) setMethod("strand", "BSgenomeViews", function(x) strand(granges(x))) setMethod("ranges", "BSgenomeViews", function(x, use.mcols=FALSE) { if (!isTRUEorFALSE(use.mcols)) stop("'use.mcols' must be TRUE or FALSE") ans <- ranges(granges(x)) if (use.mcols) mcols(ans) <- mcols(x) ans } ) setMethod("elementNROWS", "BSgenomeViews", function(x) width(x)) setMethod("seqinfo", "BSgenomeViews", function(x) seqinfo(granges(x))) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Constructors ### BSgenomeViews <- function(subject, granges) { subject <- getBSgenome(subject) if (!is(granges, "GenomicRanges")) stop("'granges' must be a GRanges object") ans_seqinfo <- seqinfo(subject) ## Calling merge() is the standard way to check that 'subject' and ## 'granges' are based on the same reference genome. merge(ans_seqinfo, seqinfo(granges)) ans_granges <- granges(granges) seqlevels(ans_granges) <- seqlevels(ans_seqinfo) seqinfo(ans_granges) <- ans_seqinfo ans_mcols <- mcols(granges) if (is.null(ans_mcols)) ans_mcols <- S4Vectors:::make_zero_col_DataFrame(length(granges)) new("BSgenomeViews", subject=subject, granges=ans_granges, elementMetadata=ans_mcols) } ### Provided for convenience. Need to do some ugly tweaks with the supplied ### args because of the weird signature of the Views() generic. setMethod("Views", "BSgenome", function(subject, start=NULL, end=NULL, width=NULL, names=NULL) { if (!(is.null(end) && is.null(width) && is.null(names))) stop(wmsg("use call of the form 'Views(genome, gr)', ", "where 'genome' is a BSgenome object ", "and 'gr' a GRanges object, to create a ", "BSgenomeViews object")) if (!is(start, "GenomicRanges")) stop("the location of the views on the genome must be ", "specified as a GRanges object") BSgenomeViews(subject, start) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Displaying ### .makeNakedMatFromBSgenomeViews <- function(x) { lx <- length(x) nc <- ncol(mcols(x)) ans_seqnames <- as.character(seqnames(x)) ans_ranges <- showAsCell(ranges(x)) ans_strand <- as.character(strand(x)) ans_dna <- sapply(getSeq(subject(x), granges(x)), Biostrings:::toSeqSnippet, 23L) if (lx != 0L) ans_dna <- paste0("[", ans_dna, "]") ans <- cbind(seqnames=as.character(seqnames(x)), ranges=showAsCell(ranges(x)), strand=as.character(strand(x)), dna=ans_dna) if (nc > 0L) { tmp <- do.call(data.frame, lapply(mcols(x), showAsCell)) ans <- cbind(ans, `|`=rep.int("|", lx), as.matrix(tmp)) } ans } showBSgenomeViews <- function(x, margin="", print.classinfo=FALSE, print.seqinfo=FALSE) { lx <- length(x) nc <- ncol(mcols(x)) cat(class(x), " object with ", lx, " view", ifelse(lx == 1L, "", "s"), " and ", nc, " metadata column", ifelse(nc == 1L, "", "s"), ":\n", sep="") out <- S4Vectors:::makePrettyMatrixForCompactPrinting(x, .makeNakedMatFromBSgenomeViews) if (print.classinfo) { .COL2CLASS <- c( seqnames="Rle", ranges="IRanges", strand="Rle", dna="DNAStringSet" ) classinfo <- S4Vectors:::makeClassinfoRowForCompactPrinting(x, .COL2CLASS) ## A sanity check, but this should never happen! stopifnot(identical(colnames(classinfo), colnames(out))) out <- rbind(classinfo, out) } if (nrow(out) != 0L) rownames(out) <- paste0(margin, rownames(out)) ## We set 'max' to 'length(out)' to avoid the getOption("max.print") ## limit that would typically be reached when 'showHeadLines' global ## option is set to Inf. print(out, quote=FALSE, right=TRUE, max=length(out)) if (print.seqinfo) { cat(margin, "-------\n", sep="") cat(margin, "seqinfo: ", summary(seqinfo(x)), "\n", sep="") } } setMethod("show", "BSgenomeViews", function(object) showBSgenomeViews(object, margin=" ", print.classinfo=TRUE, print.seqinfo=TRUE) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Coercion ### .extract_dna_from_BSgenomeViews <- function(x, use.mcols=FALSE) { ## Doesn't work because getSeq() doesn't propagate the metadata cols of ## the GRanges object. Maybe it should? #getSeq(subject(x), granges(x, use.mcols=use.mcols)) if (!isTRUEorFALSE(use.mcols)) stop("'use.mcols' must be TRUE or FALSE") ans <- getSeq(subject(x), granges(x)) if (use.mcols) mcols(ans) <- mcols(x) ans } .from_BSgenomeViews_to_DNAStringSet <- function(from) .extract_dna_from_BSgenomeViews(from, use.mcols=TRUE) setAs("BSgenomeViews", "DNAStringSet", .from_BSgenomeViews_to_DNAStringSet) setAs("BSgenomeViews", "XStringSet", .from_BSgenomeViews_to_DNAStringSet) setMethod("as.character", "BSgenomeViews", function(x, ...) { x <- .extract_dna_from_BSgenomeViews(x) callGeneric(x, ...) } ) ### S3/S4 combo for as.data.frame.BSgenomeViews .as.data.frame.BSgenomeViews <- function(x, row.names=NULL, optional=FALSE) { if (!identical(row.names, NULL)) stop("\"as.data.frame\" method for BSgenomeViews objects ", "does not support the 'row.names' argument") df1 <- as.data.frame(granges(x, use.mcols=TRUE), row.names=NULL, optional=optional) df2 <- as.data.frame(.extract_dna_from_BSgenomeViews(x), row.names=NULL, optional=optional) colnames(df2) <- "dna" cbind(df1, df2) } as.data.frame.BSgenomeViews <- function(x, row.names=NULL, optional=FALSE, ...) .as.data.frame.BSgenomeViews(x, row.names=row.names, optional=optional, ...) setMethod("as.data.frame", "BSgenomeViews", as.data.frame.BSgenomeViews) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Subsetting ### setMethod("extractROWS", "BSgenomeViews", function(x, i) { x@granges <- extractROWS(x@granges, i) x@elementMetadata <- extractROWS(x@elementMetadata, i) x } ) ### Extracting a view. setMethod("getListElement", "BSgenomeViews", function(x, i, exact=TRUE) { i <- normalizeDoubleBracketSubscript(i, x, exact=exact, error.if.nomatch=TRUE) getSeq(subject(x), granges(x)[i])[[1L]] } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### DNAStringSet methods ### setMethod("seqtype", "BSgenomeViews", function(x) seqtype(new(x@elementType)) ) setMethod("nchar", "BSgenomeViews", function(x, type="chars", allowNA=FALSE) width(x) ) ### For some methods below we use ### do.call(callGeneric, as.list(match.call()[-1L])) ### instead of just calling callGeneric() with no args, and we also use the ### exact same formal args than in the method for DNAStringSet objects. This ### is to work around a bug (bug 16141) in callGeneric(). ### See https://bugs.r-project.org/bugzilla3/show_bug.cgi?id=16141 for the ### details. setMethod("unlist", "BSgenomeViews", function(x, recursive=TRUE, use.names=TRUE) { x <- .extract_dna_from_BSgenomeViews(x) callGeneric() } ) # Ideally, we'd like to just be able to do this: #setMethod("alphabetFrequency", "BSgenomeViews", # function(x, as.prob=FALSE, ...) # { # x <- .extract_dna_from_BSgenomeViews(x) # callGeneric() # } #) # Unfortunately, because of bug 16141 (see above), we have to do this: setMethod("alphabetFrequency", "BSgenomeViews", function(x, as.prob=FALSE, collapse=FALSE, baseOnly=FALSE) { x <- .extract_dna_from_BSgenomeViews(x) do.call(callGeneric, as.list(match.call()[-1L])) } ) setMethod("hasOnlyBaseLetters", "BSgenomeViews", function(x) { x <- .extract_dna_from_BSgenomeViews(x) callGeneric() } ) setMethod("uniqueLetters", "BSgenomeViews", function(x) { x <- .extract_dna_from_BSgenomeViews(x) callGeneric() } ) # Ideally, we'd like to just be able to do this: #setMethod("letterFrequency", "BSgenomeViews", # function(x, letters, OR="|", as.prob=FALSE, ...) # { # x <- .extract_dna_from_BSgenomeViews(x) # callGeneric() # } #) # Unfortunately, because of bug 16141 (see above), we have to do this: setMethod("letterFrequency", "BSgenomeViews", function(x, letters, OR="|", as.prob=FALSE, collapse=FALSE) { x <- .extract_dna_from_BSgenomeViews(x) do.call(callGeneric, as.list(match.call()[-1L])) } ) # Ideally, we'd like to just be able to do this: #setMethod("oligonucleotideFrequency", "BSgenomeViews", # function(x, width, step=1, as.prob=FALSE, as.array=FALSE, # fast.moving.side="right", with.labels=TRUE, ...) # { # x <- .extract_dna_from_BSgenomeViews(x) # callGeneric() # } #) # Unfortunately, because of bug 16141 (see above), we have to do this: setMethod("oligonucleotideFrequency", "BSgenomeViews", function(x, width, step=1, as.prob=FALSE, as.array=FALSE, fast.moving.side="right", with.labels=TRUE, simplify.as="matrix") { x <- .extract_dna_from_BSgenomeViews(x) do.call(callGeneric, as.list(match.call()[-1L])) } ) # Ideally, we'd like to just be able to do this: #setMethod("nucleotideFrequencyAt", "BSgenomeViews", # function(x, at, as.prob=FALSE, as.array=TRUE, # fast.moving.side="right", with.labels=TRUE, ...) # { # x <- .extract_dna_from_BSgenomeViews(x) # callGeneric() # } #) # Unfortunately, because of bug 16141 (see above), we have to do this: setMethod("nucleotideFrequencyAt", "BSgenomeViews", function(x, at, as.prob=FALSE, as.array=TRUE, fast.moving.side="right", with.labels=TRUE) { x <- .extract_dna_from_BSgenomeViews(x) do.call(callGeneric, as.list(match.call()[-1L])) } ) # Ideally, we'd like to just be able to do this: #setMethod("consensusMatrix", "BSgenomeViews", # function(x, as.prob=FALSE, shift=0L, width=NULL, ...) # { # x <- .extract_dna_from_BSgenomeViews(x) # callGeneric() # } #) # Unfortunately, because of bug 16141 (see above), we have to do this: setMethod("consensusMatrix", "BSgenomeViews", function(x, as.prob=FALSE, shift=0L, width=NULL, baseOnly=FALSE) { x <- .extract_dna_from_BSgenomeViews(x) do.call(callGeneric, as.list(match.call()[-1L])) } ) # Ideally, we'd like to just be able to do this: #setMethod("consensusString", "BSgenomeViews", # function(x, ...) # { # x <- .extract_dna_from_BSgenomeViews(x) # callGeneric() # } #) # Unfortunately, because of bug 16141 (see above), we have to do this: setMethod("consensusString", "BSgenomeViews", function(x, ambiguityMap=IUPAC_CODE_MAP, threshold=0.25, shift=0L, width=NULL) { x <- .extract_dna_from_BSgenomeViews(x) do.call(callGeneric, as.list(match.call()[-1L])) } ) ### TODO: Add more DNAStringSet methods... BSgenome/R/InjectSNPsHandler-class.R0000644000175400017540000001523313175713516020221 0ustar00biocbuildbiocbuild### ========================================================================= ### The "InjectSNPsHandler" class ### ------------------------------------------------------------------------- setClass("InjectSNPsHandler", representation( SNPlocs_pkgname="character", # single string getSNPcount="function", getSNPlocs="function", seqname_translation_table="character" # named character vector ) ) .check.seqname_translation_table <- function(x, SNPlocs_seqnames, bsgenome_seqnames) { if (!is.character(x) || any(is.na(x))) return("must be a character vector with no NAs") if (!all(x %in% SNPlocs_seqnames)) return("must have all its elements in 'names(getSNPcount())'") if (is.null(names(x)) || any(is.na(names(x))) || any(duplicated(names(x)))) return("must have unique non-NA names") if (!all(names(x) %in% bsgenome_seqnames)) return("has names incompatible with BSgenome seqnames") NULL } .get.seqname_translation_table <- function(SNPlocs_pkgname, bsgenome_pkgname, SNPlocs_seqnames, bsgenome_seqnames) { library(SNPlocs_pkgname, character.only=TRUE) pkgenvir <- as.environment(paste("package", SNPlocs_pkgname, sep=":")) COMPATIBLE_BSGENOMES <- try(get("COMPATIBLE_BSGENOMES", envir=pkgenvir, inherits=FALSE), silent=TRUE) if (is(COMPATIBLE_BSGENOMES, "try-error")) return(character(0)) if (!is.list(COMPATIBLE_BSGENOMES)) stop("cannot use package ", SNPlocs_pkgname, " for SNP injection:\n", " '", SNPlocs_pkgname, "::COMPATIBLE_BSGENOMES' is not a list") seqname_translation_table <- COMPATIBLE_BSGENOMES[[bsgenome_pkgname]] if (is.null(seqname_translation_table)) { warning(bsgenome_pkgname, " not in ", "'", SNPlocs_pkgname, "::COMPATIBLE_BSGENOMES'") return(character(0)) } pb <- .check.seqname_translation_table(seqname_translation_table, SNPlocs_seqnames, bsgenome_seqnames) if (!is.null(pb)) stop("cannot inject ", SNPlocs_pkgname, " in ", bsgenome_pkgname, ":\n", " bad seqname translation table (it ", pb, ")") seqname_translation_table } ### 'snps' can be a SNPlocs object or the name of a SNPlocs data package. ### Calling this constructor has the side effect to try to load the ### SNPlocs data package specified thru the 'snps' argument. InjectSNPsHandler <- function(snps, bsgenome_pkgname, bsgenome_seqnames) { if (is(snps, "SNPlocs")) { SNPlocs_pkgname <- snps@data_pkgname .getSNPcount <- function() snpcount(snps) .getSNPlocs <- function(...) snplocs(snps, ...) } else if (isSingleString(snps)) { SNPlocs_pkgname <- snps library(SNPlocs_pkgname, character.only=TRUE) pkgenvir <- as.environment(paste("package", SNPlocs_pkgname, sep=":")) snps <- try(get(SNPlocs_pkgname, envir=pkgenvir, inherits=FALSE), silent=TRUE) if (is(snps, "SNPlocs")) { .getSNPcount <- function() snpcount(snps) .getSNPlocs <- function(...) snplocs(snps, ...) } else { .getSNPcount <- try(get("getSNPcount", envir=pkgenvir, inherits=FALSE), silent=TRUE) if (!is.function(.getSNPcount)) stop("cannot use ", SNPlocs_pkgname, " for SNP injection:\n", " it doesn't seem to define (and export) a function ", "called 'getSNPcount'") .getSNPlocs <- try(get("getSNPlocs", envir=pkgenvir, inherits=FALSE), silent=TRUE) if (!is.function(.getSNPlocs)) stop("cannot use ", SNPlocs_pkgname, " for SNP injection:\n", " it doesn't seem to define (and export) a function ", "called 'getSNPlocs'") } } else { stop("'snps' must be a SNPlocs object or the name of ", "a SNPlocs data package") } seqname_translation_table <- .get.seqname_translation_table( SNPlocs_pkgname, bsgenome_pkgname, names(.getSNPcount()), bsgenome_seqnames) #if (length(seqname_translation_table) == 0L # && !all(bsgenome_seqnames %in% names(.getSNPcount()))) # stop("cannot inject ", SNPlocs_pkgname, " in ", # bsgenome_pkgname, ":\n", # " seqnames are incompatible and no seqname translation\n", # " table is provided") new("InjectSNPsHandler", SNPlocs_pkgname=SNPlocs_pkgname, getSNPcount=.getSNPcount, getSNPlocs=.getSNPlocs, seqname_translation_table=seqname_translation_table) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### SNP related accessors ### setGeneric("SNPlocs_pkgname", function(x) standardGeneric("SNPlocs_pkgname")) setMethod("SNPlocs_pkgname", "InjectSNPsHandler", function(x) { if (length(x@SNPlocs_pkgname) == 0L) return(NULL) x@SNPlocs_pkgname } ) setMethod("snpcount", "InjectSNPsHandler", function(x) { if (length(x@SNPlocs_pkgname) == 0L) return(NULL) ans <- x@getSNPcount() if (length(x@seqname_translation_table) == 0L) return(ans) ans <- ans[x@seqname_translation_table] names(ans) <- names(x@seqname_translation_table) ans } ) setMethod("snplocs", "InjectSNPsHandler", function(x, seqname, ...) { if (length(x@SNPlocs_pkgname) == 0L) return(NULL) if (!isSingleString(seqname)) stop("'seqname' must be a single string") if (!(seqname %in% names(snpcount(x)))) return(NULL) if (length(x@seqname_translation_table) != 0L) seqname <- x@seqname_translation_table[seqname] ans <- x@getSNPlocs(seqname, ...) if (NROW(ans) != x@getSNPcount()[seqname]) stop("reported SNP count for sequence ", seqname, " in package ", SNPlocs_pkgname(x), " does not match the ", "number of SNPs returned by ", SNPlocs_pkgname(x), ":::getSNPlocs()") ans } ) BSgenome/R/ODLT_SNPlocs-class.R0000644000175400017540000001306213175713516017104 0ustar00biocbuildbiocbuild### ========================================================================= ### ODLT_SNPlocs objects ### ------------------------------------------------------------------------- setClass("ODLT_SNPlocs", contains="SNPlocs", representation( snp_table="OnDiskLongTable" ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Low-level constructor ### new_ODLT_SNPlocs <- function(provider, provider_version, release_date, release_name, source_data_url, download_date, reference_genome, compatible_genomes, data_pkgname, data_dirpath) { snp_table <- OnDiskLongTable(data_dirpath) new("ODLT_SNPlocs", provider=provider, provider_version=provider_version, release_date=release_date, release_name=release_name, source_data_url=source_data_url, download_date=download_date, reference_genome=reference_genome, compatible_genomes=compatible_genomes, data_pkgname=data_pkgname, snp_table=snp_table) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### snpcount() ### setMethod("snpcount", "ODLT_SNPlocs", function(x) { spatial_index <- spatialIndex(x@snp_table) batch_seqnames <- seqnames(spatial_index) batches_per_seq <- runLength(batch_seqnames) batch_breakpoints <- breakpoints(x@snp_table) seq_breakpoints <- batch_breakpoints[cumsum(batches_per_seq)] setNames(S4Vectors:::diffWithInitialZero(seq_breakpoints), runValue(batch_seqnames)) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### snplocs() ### ### Used internally for SNP injection. Not intended for the end user. ### Must return a 2-col data-frame-like object with columns "loc" (integer) ### and "alleles_as_ambig" (character). ### setMethod("snplocs", "ODLT_SNPlocs", function(x, seqname) { df <- getBatchesBySeqnameFromOnDiskLongTable(x@snp_table, seqname) data.frame(loc=df[ , "pos"], alleles_as_ambig=decode_bytes_as_letters(df[ , "alleles"]), stringsAsFactors=FALSE) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### .as_naked_GRanges() and .as_GPos() ### .as_naked_GRanges <- function(df, seqinfo) { ans_seqnames <- df[ , "seqnames"] ans_ranges <- IRanges(df[ , "pos"], width=1L) ans_strand <- Rle(strand("*"), nrow(df)) GRanges(ans_seqnames, ans_ranges, ans_strand, seqinfo=seqinfo) } .as_GPos <- function(df, seqinfo, drop.rs.prefix=FALSE) { gr <- .as_naked_GRanges(df, seqinfo) alleles_as_ambig <- decode_bytes_as_letters(df[ , "alleles"]) rowids <- df$rowids if (is.null(rowids)) { ans_mcols <- DataFrame(alleles_as_ambig=alleles_as_ambig) } else { if (!drop.rs.prefix && length(gr) != 0L) rowids <- paste0("rs", rowids) ans_mcols <- DataFrame(RefSNP_id=rowids, alleles_as_ambig=alleles_as_ambig) } mcols(gr) <- ans_mcols as(gr, "GPos") } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### SNP extractors: snpsBySeqname(), snpsByOverlaps(), snpsById() ### .snpsBySeqname_ODLT_SNPlocs <- function(x, seqnames, drop.rs.prefix=FALSE) { if (!isTRUEorFALSE(drop.rs.prefix)) stop(wmsg("'drop.rs.prefix' must be TRUE or FALSE")) df <- getBatchesBySeqnameFromOnDiskLongTable(x@snp_table, seqnames, with.rowids=TRUE) x_spatial_index <- spatialIndex(x@snp_table) x_seqinfo <- seqinfo(x_spatial_index) .as_GPos(df, x_seqinfo, drop.rs.prefix=drop.rs.prefix) } setMethod("snpsBySeqname", "ODLT_SNPlocs", .snpsBySeqname_ODLT_SNPlocs) .snpsByOverlaps_ODLT_SNPlocs <- function(x, ranges, drop.rs.prefix=FALSE, ...) { ranges <- normarg_ranges(ranges) if (!isTRUEorFALSE(drop.rs.prefix)) stop(wmsg("'drop.rs.prefix' must be TRUE or FALSE")) dots <- list(...) if (isTRUE(dots$invert)) stop(wmsg("snpsByOverlaps() does not support 'invert=TRUE'")) if (is.null(maxgap <- dots$maxgap)) maxgap <- -1L if (is.null(minoverlap <- dots$minoverlap)) minoverlap <- 0L df <- getBatchesByOverlapsFromOnDiskLongTable(x@snp_table, ranges, maxgap=maxgap, minoverlap=minoverlap, with.rowids=TRUE) x_spatial_index <- spatialIndex(x@snp_table) x_seqinfo <- seqinfo(x_spatial_index) gr0 <- .as_naked_GRanges(df, x_seqinfo) idx <- which(overlapsAny(gr0, ranges, ...)) df <- df[idx, ] .as_GPos(df, x_seqinfo, drop.rs.prefix=drop.rs.prefix) } setMethod("snpsByOverlaps", "ODLT_SNPlocs", .snpsByOverlaps_ODLT_SNPlocs) .snpsById_ODLT_SNPlocs <- function(x, ids, ifnotfound=c("error", "warning", "drop")) { user_rowids <- ids2rowids(ids) ifnotfound <- match.arg(ifnotfound) x_rowids <- rowids(x@snp_table) rowidx <- rowids2rowidx(user_rowids, ids, x_rowids, ifnotfound) df <- getRowsFromOnDiskLongTable(x@snp_table, rowidx[[1L]], with.rowids=FALSE) df$rowids <- rowidx[[2L]] x_spatial_index <- spatialIndex(x@snp_table) x_seqinfo <- seqinfo(x_spatial_index) .as_GPos(df, x_seqinfo, drop.rs.prefix=TRUE) } setMethod("snpsById", "ODLT_SNPlocs", .snpsById_ODLT_SNPlocs) BSgenome/R/OldFashionSNPlocs-class.R0000644000175400017540000004221413175713516020232 0ustar00biocbuildbiocbuild### ========================================================================= ### OldFashionSNPlocs objects ### ------------------------------------------------------------------------- ### ### Implement old fashion on-disk storage used by SNPlocs packages < 0.99.20. ### TODO: Remove once all SNPlocs packages < 0.99.20 are gone. ### setClass("OldFashionSNPlocs", contains="SNPlocs", representation( ## Absolute path to local directory where to find the serialized ## objects containing the SNPs. data_dirpath="character", data_serialized_objnames="character", .data_cache="environment" ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Constructor ### ### Not intended to be used directly. ### 'download_url' argument is for backward compatibility with SNPlocs ### packages < 0.99.20. newSNPlocs <- function(provider, provider_version, release_date, release_name, source_data_url, download_date, reference_genome, compatible_genomes, data_pkgname, data_dirpath, download_url="") { if (missing(source_data_url)) source_data_url <- download_url if (file.exists(file.path(data_dirpath, "header.rds"))) return(new_ODLT_SNPlocs(provider, provider_version, release_date, release_name, source_data_url, download_date, reference_genome, compatible_genomes, data_pkgname, data_dirpath)) data_serialized_objnames <- c( "SNPcount", "all_rsids", paste(seqlevels(reference_genome), "_snplocs", sep="") ) new("OldFashionSNPlocs", provider=provider, provider_version=provider_version, release_date=release_date, release_name=release_name, source_data_url=source_data_url, download_date=download_date, reference_genome=reference_genome, compatible_genomes=compatible_genomes, data_pkgname=data_pkgname, data_dirpath=data_dirpath, data_serialized_objnames=data_serialized_objnames, .data_cache=new.env(hash=TRUE, parent=emptyenv())) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### snpcount() ### ### Creates objects "on-the-fly" (not serialized). ### WARNING: Improper calls to .get_SNPlocs_data() by the .create_object() ### function can lead to infinite recursive loops! .create_object <- function(objname) { if (objname == "empty_snplocs") { obj <- data.frame(loc=integer(0), alleles=raw(0)) return(obj) } if (objname == "empty_ufsnplocs") { obj <- data.frame(RefSNP_id=character(0), alleles_as_ambig=character(0), loc=integer(0), stringsAsFactors=FALSE) return(obj) } # add more here... stop("don't know how to create object '", objname, "'") } .get_SNPlocs_data <- function(x, objname, caching=TRUE) { datacache <- x@.data_cache not_cached <- !exists(objname, envir=datacache) if (not_cached) { if (objname %in% x@data_serialized_objnames) { filename <- paste(objname, ".rda", sep="") filepath <- file.path(x@data_dirpath, filename) load(filepath, envir=datacache) } else { assign(objname, .create_object(objname), envir=datacache) } } ans <- get(objname, envir=datacache) if (not_cached && !caching) rm(list=objname, envir=datacache) ans } setMethod("snpcount", "OldFashionSNPlocs", function(x) { objname <- "SNPcount" ans <- .get_SNPlocs_data(x, objname) if (!is.integer(ans) || !identical(names(ans), seqlevels(x))) stop("internal error: '", objname, "' data set is broken.\n", " Please contact the maintainer of the ", x@data_pkgname, "\n package.") ans } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### snplocs() ### ### Used internally for SNP injection. Not intended for the end user. ### Must return a 2-col data-frame-like object with columns "loc" (integer) ### and "alleles_as_ambig" (character). ### ### Load rs ids for a given sequence. Return them in an integer vector. .load_rsids <- function(x, seqname) { all_rsids <- .get_SNPlocs_data(x, "all_rsids") seq_pos <- match(seqname, names(snpcount(x))) offset <- .get_rsid_offsets(x)[seq_pos] idx <- seq_len(snpcount(x)[seq_pos]) + offset all_rsids[idx] } ### Load raw snplocs. .load_raw_snplocs <- function(x, seqname, caching) { objname <- paste(seqname, "_snplocs", sep="") ans <- .get_SNPlocs_data(x, objname, caching=caching) empty_snplocs <- .get_SNPlocs_data(x, "empty_snplocs") if (!identical(sapply(ans, class), sapply(empty_snplocs, class))) stop("internal error: unexpected col names and/or col types\n", " for the '", objname, "' data set.\n", " Please contact the maintainer of the ", x@data_pkgname, "\n package.") if (nrow(ans) != snpcount(x)[seqname]) stop("internal error: nb of rows in object '", objname, " ", "doesn't match the\n nb of SNPs reported by snpcount().\n", " Please contact the maintainer of the ", x@data_pkgname, "\n package.") ans } ### Get user-friendly snplocs. .get_ufsnplocs <- function(x, seqname, caching) { rsids <- as.character(.load_rsids(x, seqname)) snplocs <- .load_raw_snplocs(x, seqname, caching) alleles <- decode_bytes_as_letters(snplocs$alleles) data.frame(RefSNP_id=rsids, alleles_as_ambig=alleles, loc=snplocs$loc, stringsAsFactors=FALSE) } .SNPlocsAsGRanges <- function(x, ufsnplocs, seqname) { if (is(seqname, "Rle")) { if (length(seqname) != nrow(ufsnplocs) || !identical(levels(seqname), seqlevels(x))) stop("when an Rle, 'seqname' must be a factor Rle ", "of length 'nrow(ufsnplocs)' and levels 'SEQNAMES'") ans_seqnames <- seqname } else { if (!is.factor(seqname)) seqname <- factor(seqname, levels=seqlevels(x)) if (length(seqname) == 1L) ans_seqnames <- Rle(seqname, nrow(ufsnplocs)) else if (length(seqname) == nrow(ufsnplocs)) ans_seqnames <- Rle(seqname) else stop("'length(seqname)' must be 1 or 'nrow(ufsnplocs)'") } if (nrow(ufsnplocs) == 0L) ans_ranges <- IRanges() else ans_ranges <- IRanges(start=ufsnplocs$loc, width=1L) ans_strand <- Rle(strand("*"), nrow(ufsnplocs)) ans <- GRanges(seqnames=ans_seqnames, ranges=ans_ranges, strand=ans_strand, RefSNP_id=ufsnplocs$RefSNP_id, alleles_as_ambig=ufsnplocs$alleles_as_ambig) seqinfo(ans) <- seqinfo(x) ans } ### Returns a data frame (when 'as.GRanges=FALSE') or a GRanges object ### (when 'as.GRanges=TRUE'). setMethod("snplocs", "OldFashionSNPlocs", function(x, seqname, as.GRanges=FALSE, caching=TRUE) { if (!is.character(seqname) || any(is.na(seqname))) stop("'seqname' must be a character vector with no NAs") if (!all(seqname %in% seqlevels(x))) stop("all 'seqname' elements must be in: ", paste(seqlevels(x), collapse=", ")) if (!isTRUEorFALSE(as.GRanges)) stop("'as.GRanges' must be TRUE or FALSE") if (!isTRUEorFALSE(caching)) stop("'caching' must be TRUE or FALSE") if (!as.GRanges) { if (length(seqname) != 1L) stop("'seqname' must be of length 1 when 'as.GRanges' is FALSE") return(.get_ufsnplocs(x, seqname, caching)) } if (length(seqname) == 0L) { empty_ufsnplocs <- .get_SNPlocs_data(x, "empty_ufsnplocs") ans <- .SNPlocsAsGRanges(x, empty_ufsnplocs, character(0)) return(ans) } list_of_ufsnplocs <- lapply(seqname, .get_ufsnplocs, x=x, caching=caching) ufsnplocs <- do.call(rbind, list_of_ufsnplocs) seqnames <- Rle(factor(seqname, levels=seqlevels(x)), unlist(lapply(list_of_ufsnplocs, nrow), use.names=FALSE)) .SNPlocsAsGRanges(x, ufsnplocs, seqnames) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Old SNPlocs extractors (deprecated in BioC 3.5): ### snpid2loc() ### snpid2alleles() ### snpid2grange() ### ### Returns a named integer vector where each (name, value) pair corresponds ### to a supplied SNP id (typically an rs id). The name is the chromosome of ### the SNP id and the value is its position on the chromosome. setGeneric("snpid2loc", signature="x", function(x, snpid, ...) standardGeneric("snpid2loc") ) ### Returns a named character vector where each (name, value) pair corresponds ### to a supplied SNP id (typically an rs id). The name is the chromosome of ### the SNP id and the value is a single IUPAC code representing the associated ### alleles. setGeneric("snpid2alleles", signature="x", function(x, snpid, ...) standardGeneric("snpid2alleles") ) setGeneric("snpid2grange", signature="x", function(x, snpid, ...) standardGeneric("snpid2grange") ) .get_rsid_offsets <- function(x) { offsets <- c(0L, cumsum(snpcount(x))) offsets <- offsets[-length(offsets)] names(offsets) <- names(snpcount(x)) offsets } .normarg_snpid <- function(snpid) { if (!is.vector(snpid)) stop("'snpid' must be an integer or character vector") if (S4Vectors:::anyMissing(snpid)) stop("'snpid' cannot contain NAs") if (is.numeric(snpid)) { if (!is.integer(snpid)) snpid <- as.integer(snpid) return(snpid) } if (!is.character(snpid)) stop("'snpid' must be an integer or character vector") prefixes <- unique(substr(snpid, 1L, 2L)) if ("rs" %in% prefixes) { if (!setequal(prefixes, "rs")) stop("'snpid' cannot mix ids that are prefixed with \"rs\" ", "with ids that are not") ## Drop the "rs" prefix. snpid <- substr(snpid, 3, nchar(snpid)) } snpid <- suppressWarnings(as.integer(snpid)) if (S4Vectors:::anyMissing(snpid)) stop("cannot extract the digital part of some ids in 'snpid'") snpid } ### Returns a named integer vector where each (name, value) pair corresponds ### to a supplied SNP id (typically an rs id). The name is the chromosome of ### the SNP id and the value is the row index in the serialized snplocs data ### frame corresponding to the SNP id. .snpid2rowidx <- function(x, snpid) { if (length(snpid) == 0L) { idx <- integer(0) } else { all_rsids <- .get_SNPlocs_data(x, "all_rsids") idx <- match(snpid, all_rsids) bad_snpid_idx <- which(is.na(idx)) if (length(bad_snpid_idx) != 0L) { bad_snpid <- snpid[bad_snpid_idx] bad_snpid_in1string <- paste(bad_snpid, collapse=", ") stop(wmsg("SNP id(s) not found: ", bad_snpid_in1string, "\n\nPlease note that rsid2loc(), snpid2loc(), ", "rsid2alleles(), snpid2alleles(), rsidsToGRanges(), ", "and snpid2grange() are superseded by snpsById(). ", "The latter can be called with 'ifnotfound=\"drop\"' ", "to drop unknown SNP ids. See '?snpsById' for more ", "information.\n\n ")) } } seqidx <- findInterval(idx - 1L, cumsum(snpcount(x))) + 1L rowidx <- idx - .get_rsid_offsets(x)[seqidx] names(rowidx) <- names(snpcount(x))[seqidx] rowidx } .snpid2loc_OldFashionSNPlocs <- function(x, snpid, caching=TRUE) { rowidx <- .snpid2rowidx(x, snpid) if (length(rowidx) == 0L) { ans <- integer(0) } else { rowidx_list <- split(unname(rowidx), names(rowidx)) loc_list <- lapply(names(rowidx_list), function(seqname) { idx <- rowidx_list[[seqname]] .load_raw_snplocs(x, seqname, caching)$loc[idx] }) ans <- unsplit(loc_list, names(rowidx)) } names(ans) <- names(rowidx) ans } setMethod("snpid2loc", "OldFashionSNPlocs", function(x, snpid, caching=TRUE) { .Deprecated(msg=wmsg("snpid2loc() is deprecated. ", "Please use snpsById() instead.")) snpid <- .normarg_snpid(snpid) if (!isTRUEorFALSE(caching)) stop("'caching' must be TRUE or FALSE") .snpid2loc_OldFashionSNPlocs(x, snpid, caching=caching) } ) .snpid2alleles_OldFashionSNPlocs <- function(x, snpid, caching=TRUE) { rowidx <- .snpid2rowidx(x, snpid) if (length(rowidx) == 0L) { ans <- raw(0) } else { rowidx_list <- split(unname(rowidx), names(rowidx)) alleles_list <- lapply(names(rowidx_list), function(seqname) { idx <- rowidx_list[[seqname]] .load_raw_snplocs(x, seqname, caching)$alleles[idx] }) ans <- unsplit(alleles_list, names(rowidx)) } ans <- decode_bytes_as_letters(ans) names(ans) <- names(rowidx) ans } setMethod("snpid2alleles", "OldFashionSNPlocs", function(x, snpid, caching=TRUE) { .Deprecated(msg=wmsg("snpid2alleles() is deprecated. ", "Please use snpsById() instead.")) snpid <- .normarg_snpid(snpid) if (!isTRUEorFALSE(caching)) stop("'caching' must be TRUE or FALSE") .snpid2alleles_OldFashionSNPlocs(x, snpid, caching=caching) } ) .snpid2grange_OldFashionSNPlocs <- function(x, snpid, caching=TRUE) { snpid <- .normarg_snpid(snpid) if (!isTRUEorFALSE(caching)) stop("'caching' must be TRUE or FALSE") loc <- .snpid2loc_OldFashionSNPlocs(x, snpid, caching=caching) alleles <- .snpid2alleles_OldFashionSNPlocs(x, snpid, caching=caching) ufsnplocs <- data.frame(RefSNP_id=as.character(snpid), alleles_as_ambig=unname(alleles), loc=unname(loc), stringsAsFactors=FALSE) .SNPlocsAsGRanges(x, ufsnplocs, names(loc)) } setMethod("snpid2grange", "OldFashionSNPlocs", function(x, snpid, caching=TRUE) { .Deprecated(msg=wmsg("snpid2grange() is deprecated. ", "Please use snpsById() instead.")) .snpid2grange_OldFashionSNPlocs(x, snpid, caching=caching) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### NEW API: snpsBySeqname(), snpsByOverlaps(), snpsById() (similar to API ### for querying an XtraSNPlocs object) ### .get_GPos_by_seqname_from_SNPlocs <- function(x, seqnames, drop.rs.prefix) { gr <- snplocs(x, seqnames, as.GRanges=TRUE) if (!drop.rs.prefix && length(gr) != 0L) mcols(gr)$RefSNP_id <- paste0("rs", mcols(gr)$RefSNP_id) as(gr, "GPos") } .snpsBySeqname_OldFashionSNPlocs <- function(x, seqnames, drop.rs.prefix=FALSE) { if (!is.character(seqnames) || any(is.na(seqnames)) || any(duplicated(seqnames))) stop(wmsg("'seqnames' must be a character vector ", "with no NAs and no duplicates")) if (!all(seqnames %in% seqlevels(x))) stop(wmsg("'seqnames' must be a subset of: ", paste(seqlevels(x), collapse=", "))) if (!isTRUEorFALSE(drop.rs.prefix)) stop(wmsg("'drop.rs.prefix' must be TRUE or FALSE")) .get_GPos_by_seqname_from_SNPlocs(x, seqnames, drop.rs.prefix) } setMethod("snpsBySeqname", "OldFashionSNPlocs", .snpsBySeqname_OldFashionSNPlocs ) .snpsByOverlaps_OldFashionSNPlocs <- function(x, ranges, drop.rs.prefix=FALSE, ...) { ranges <- normarg_ranges(ranges) dots <- list(...) if (isTRUE(dots$invert)) stop(wmsg("snpsByOverlaps() does not support 'invert=TRUE'")) ## The only purpose of the line below is to check that 'x' and 'ranges' ## are based on the same reference genome (merge() will raise an error ## if they are not). merge(seqinfo(x), seqinfo(ranges)) seqlevels(ranges, pruning.mode="coarse") <- intersect(seqlevels(x), seqlevelsInUse(ranges)) snps_by_seqname <- .snpsBySeqname_OldFashionSNPlocs(x, seqlevels(ranges), drop.rs.prefix=drop.rs.prefix) subsetByOverlaps(snps_by_seqname, ranges, ...) } setMethod("snpsByOverlaps", "OldFashionSNPlocs", .snpsByOverlaps_OldFashionSNPlocs ) .snpsById_OldFashionSNPlocs <- function(x, ids, ifnotfound=c("error", "warning", "drop")) { user_rowids <- ids2rowids(ids) ifnotfound <- match.arg(ifnotfound) x_rowids <- .get_SNPlocs_data(x, "all_rsids") rowidx <- rowids2rowidx(user_rowids, ids, x_rowids, ifnotfound) gr <- .snpid2grange_OldFashionSNPlocs(x, rowidx[[2L]]) mcols(gr)[ , "RefSNP_id"] <- rowidx[[2L]] as(gr, "GPos") } setMethod("snpsById", "OldFashionSNPlocs", .snpsById_OldFashionSNPlocs) BSgenome/R/OnDiskLongTable-class.R0000644000175400017540000007504613175713516017732 0ustar00biocbuildbiocbuild### ========================================================================= ### OnDiskLongTable objects ### ------------------------------------------------------------------------- setClassUnion("GRanges_OR_NULL", c("GRanges", "NULL")) setClass("OnDiskLongTable", representation( ## A single string. dirpath="character", ## Whether on-disk storage is column- (the default) or batch-oriented. #bybatch="logical", ## A named ordinary list of length the nb of cols where all list ## elements are vector-like objects of length 0. The names on the list ## are interpreted as the column names and thus cannot be NAs or empty ## strings. header="list", ## An integer vector of length the nb of batches. Contains the ## cumulated nb of rows in the batches. A batch cannot be empty so ## 'breakpoints' must contain *strictly* sorted positive integers. ## If the table has zero rows, then 'breakpoints' is empty. Otherwise, ## its last element is the nb of rows in the table. breakpoints="integer", ## [OPTIONAL] A *sorted* *unstranded* GRanges object with 1 range per ## batch. The object must be naked i.e. no names and no metadata ## columns. spatial_index="GRanges_OR_NULL", ## Where to load and cache the row ids. The row ids are stored in a ## vector of *unique* integer values of length the nb of rows. This ## vector is typically big (OnDiskLongTable objects can have tens or ## hundreds of millions of rows), so can take a long time to load from ## disk to memory. Caching it allows fast translation from ## user-supplied row ids to row indices. .rowids_cache="environment" ), prototype( dirpath=NA_character_, #bybatch=FALSE, header=setNames(list(), character(0)) ) ) .get_OnDiskLongTable_nrow_from_breakpoints <- function(breakpoints) { breakpoints_len <- length(breakpoints) if (breakpoints_len == 0L) 0L else breakpoints[[breakpoints_len]] } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Validity ### .valid_OnDiskLongTable_dirpath <- function(dirpath) { if (!is.character(dirpath) || length(dirpath) != 1L) return(wmsg("'dirpath' must be a single string")) if (is.na(dirpath)) return(NULL) if (dirpath == "") return(wmsg("'dirpath' must be a non-empty string")) if (!dir.exists(dirpath)) return(wmsg("directory not found: ", dirpath)) NULL } .valid_OnDiskLongTable_header <- function(header) { if (!is.list(header)) return(wmsg("'header' must be a list")) colnames <- names(header) if (is.null(colnames)) return(wmsg("'header' must be a named list")) if (any(colnames %in% c(NA_character_, ""))) return(wmsg("'names(header)' cannot contain NAs or empty strings")) if (!all(lengths(header) == 0L)) return(wmsg("all list elements in 'header' must be ", "vector-like objects of length 0")) NULL } .valid_OnDiskLongTable_breakpoints <- function(breakpoints) { if (!is.integer(breakpoints) || S4Vectors:::anyMissing(breakpoints) || is.unsorted(breakpoints, strictly=TRUE) || length(breakpoints) != 0L && breakpoints[[1L]] <= 0L) return(wmsg("invalid breakpoints found for OnDiskLongTable object")) NULL } .valid_OnDiskLongTable_spatial_index <- function(spatial_index, breakpoints) { if (is.null(spatial_index)) return(NULL) if (!is(spatial_index, "GRanges")) return(wmsg("'spatial_index' must be a GRanges object or NULL")) if (length(spatial_index) != length(breakpoints)) return(wmsg("'spatial_index' must have the length of 'breakpoints'")) if (is.unsorted(spatial_index)) return(wmsg("'spatial_index' must be a sorted GRanges object")) if (!all(strand(spatial_index) == "*")) return(wmsg("'spatial_index' must be unstranded")) if (!is.null(names(spatial_index))) return(wmsg("'spatial_index' cannot have names")) if (ncol(mcols(spatial_index)) != 0L) return(wmsg("'spatial_index' cannot have metadata columns")) NULL } .valid_OnDiskLongTable <- function(x) { c(.valid_OnDiskLongTable_dirpath(x@dirpath), .valid_OnDiskLongTable_header(x@header), .valid_OnDiskLongTable_breakpoints(x@breakpoints), .valid_OnDiskLongTable_spatial_index(x@spatial_index, x@breakpoints)) } setValidity2("OnDiskLongTable", .valid_OnDiskLongTable) .check_OnDiskLongTable_dirpath <- function(dirpath) { errmsg <- .valid_OnDiskLongTable_dirpath(dirpath) if (!is.null(errmsg)) stop(errmsg) if (is.na(dirpath)) stop("'dirpath' must be a single string") } .check_OnDiskLongTable_rowids <- function(rowids) { if (!is.integer(rowids)) stop(wmsg("'rowids' must be an integer vector")) if (S4Vectors:::anyMissing(rowids) || anyDuplicated(rowids)) stop(wmsg("'rowids' cannot contain NAs or duplicated values")) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Read/write data to/from disk ### ### 'opath' is the relative path (with respect to 'dirpath') to the file that ### is to be read/written. It must NOT have the ".rds" extension. .make_filepath <- function(dirpath, opath) file.path(dirpath, paste0(opath, ".rds")) .read_object <- function(dirpath, opath) { filepath <- .make_filepath(dirpath, opath) suppressWarnings(readRDS(filepath)) } .write_object <- function(object, dirpath, opath, compress=TRUE, overwrite=FALSE) { filepath <- .make_filepath(dirpath, opath) if (!overwrite && file.exists(filepath)) stop(wmsg("file already exists: ", filepath)) saveRDS(object, file=filepath, compress=compress) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Read/write block to/from disk ### ### In all the functions below: ### b: batch number ### c: column number ### ### Make batch/col physical name from batch/col number. .BATCH_FMT <- "b%05d" # nb of batches must be <= 99999 .COL_FMT <- "c%03d" # nb of cols must be <= 999 .batch_physname <- function(b) sprintf(.BATCH_FMT, b) .col_physname <- function(c) sprintf(.COL_FMT, c) ### Make block physical name from batch/col numbers. .block_physname <- function(b, c, bybatch=FALSE) { batch_physname <- .batch_physname(b) col_physname <- .col_physname(c) #if (bybatch) { # block_physname <- file.path(batch_physname, col_physname) #} else { block_physname <- file.path(col_physname, batch_physname) #} block_physname } .read_OnDiskLongTable_block <- function(dirpath, b, c, bybatch=FALSE) { block_physname <- .block_physname(b, c, bybatch=bybatch) .read_object(dirpath, block_physname) } .write_OnDiskLongTable_block <- function(block_data, dirpath, b, c, bybatch=FALSE, compress=TRUE) { block_physname <- .block_physname(b, c, bybatch=bybatch) .write_object(block_data, dirpath, block_physname, compress=compress) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### .write_zero_row_OnDiskLongTable() ### .remove_file <- function(dirpath, filename) { filepath <- file.path(dirpath, filename) if (file.exists(filepath)) { if (!file.remove(filepath)) stop(wmsg("failed to remove file: ", filepath)) } } .remove_dirs <- function(dirpaths) { fail_idx <- which(as.logical(unlink(dirpaths, recursive=TRUE))) if (length(fail_idx) != 0L) stop(wmsg("failed to remove directories: ", paste0(dirpaths[fail_idx], collapse=", "))) } .write_zero_row_OnDiskLongTable <- function(df, dirpath, spatial_index) { ## Remove stuff. .remove_file(dirpath, "rowids.rds") colpaths <- file.path(dirpath, .col_physname(seq_len(ncol(df)))) .remove_dirs(colpaths) ## Create stuff. header <- df[0, , drop=FALSE] .write_object(header, dirpath, "header", overwrite=TRUE) for (c in seq_len(ncol(df))) { colpath <- colpaths[[c]] if (!dir.create(colpath, showWarnings=TRUE, mode="0775")) stop(wmsg("failed to create directory: ", colpath)) } .write_object(integer(0), dirpath, "breakpoints", overwrite=TRUE) if (!is.null(spatial_index)) { .write_object(spatial_index[0], dirpath, "spatial_index", overwrite=TRUE) } } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### .append_df_to_OnDiskLongTable() ### ### b_offset: batch index offset (integer) ### c: column number .write_OnDiskLongTable_column <- function(df_col, dirpath, breakpoints, b_offset, c, compress=TRUE) { batch_ranges <- as(PartitioningByEnd(breakpoints), "IRanges") for (b2 in seq_along(batch_ranges)) { b <- b_offset + b2 block_data <- extractROWS(df_col, batch_ranges[b2]) .write_OnDiskLongTable_block(block_data, dirpath, b, c, compress=compress) } } .append_df_to_OnDiskLongTable <- function(df, dirpath, batchsize, spatial_index, compress=TRUE) { ## Check existence of rowids.rds file. filepath <- file.path(dirpath, "rowids.rds") if (file.exists(filepath)) stop(wmsg("cannot append data to an ", "OnDiskLongTable object with row ids")) ## Check 'df' colnames. old_colnames <- names(.read_object(dirpath, "header")) if (!identical(colnames(df), old_colnames)) stop(wmsg("'colnames(df)' do not match the colnames found in ", file.path(dirpath, "header.rds"))) ## Load 'breakpoints' vector. breakpoints0 <- .read_object(dirpath, "breakpoints") ## Append 'df' columns. colpaths <- file.path(dirpath, .col_physname(seq_len(ncol(df)))) if (is.null(spatial_index)) { breakpoints <- end(breakInChunks(nrow(df), batchsize)) } else { breakpoints <- cumsum(batchsize) spatial_index0 <- .read_object(dirpath, "spatial_index") } b_offset <- length(breakpoints0) for (c in seq_len(ncol(df))) { colpath <- colpaths[[c]] if (!dir.exists(colpath)) stop(wmsg("directory not found: ", colpath)) .write_OnDiskLongTable_column(df[[c]], dirpath, breakpoints, b_offset, c, compress=compress) } ## Update 'breakpoints' vector. nrow0 <- .get_OnDiskLongTable_nrow_from_breakpoints(breakpoints0) breakpoints <- c(breakpoints0, nrow0 + breakpoints) .write_object(breakpoints, dirpath, "breakpoints", overwrite=TRUE) if (!is.null(spatial_index)) { ## Update 'spatial_index'. ## We use suppressWarnings() to avoid the "The 2 combined objects have ## no sequence levels in common" warning that would typically happen ## when writeOnDiskLongTable() is used in a loop to append data from ## different chromosomes (unless at each iteration the user is ## cautiously building and passing a 'spatial_index' with seqlevels ## set to all the chromosomes). spatial_index <- suppressWarnings(c(spatial_index0, spatial_index)) .write_object(spatial_index, dirpath, "spatial_index", overwrite=TRUE) } } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### writeOnDiskLongTable() and writeOnDiskLongTableRowids() ### .normarg_batchsize <- function(batchsize, totalsize) { if (!isSingleNumberOrNA(batchsize)) stop(wmsg("'batchsize' must be a single integer or NA")) if (!is.integer(batchsize)) batchsize <- as.integer(batchsize) if (is.na(batchsize)) return(totalsize) if (batchsize < 0L) stop(wmsg("'batchsize' cannot be negative")) if (batchsize == 0L && totalsize != 0L) stop(wmsg("'batchsize' can be 0 only if 'nrow(df)' is 0")) batchsize } ### Ignore the row names on 'df'. If 'df' is a DataFrame, 'metadata(df)' and ### 'mcols(df)' are also ignored. writeOnDiskLongTable <- function(df, dirpath=".", batchsize=NA, spatial_index=NULL, append=FALSE, compress=TRUE) { if (!is.data.frame(df) && !is(df, "DataFrame")) stop(wmsg("'df' must be a data.frame or DataFrame object")) .check_OnDiskLongTable_dirpath(dirpath) if (!isTRUEorFALSE(append)) stop(wmsg("'append' must be TRUE or FALSE")) if (is.null(spatial_index)) { batchsize <- .normarg_batchsize(batchsize, nrow(df)) } else { if (!identical(batchsize, NA)) stop(wmsg("'batchsize' must be NA when 'spatial_index' ", "is supplied")) if (!is(spatial_index, "GenomicRanges")) stop(wmsg("'spatial_index' must be a GenomicRanges object")) batchsize <- mcols(spatial_index)$batchsize if (is.null(batchsize)) stop(wmsg("'spatial_index' must have a \"batchsize\" ", "metadata column")) if (!is.numeric(batchsize)) stop(wmsg("'spatial_index' metadata column \"batchsize\" ", "must be numeric")) if (!is.integer(batchsize)) batchsize <- as.integer(batchsize) if (!isTRUE(all(batchsize >= 1L))) stop(wmsg("'spatial_index' metadata column \"batchsize\" ", "must contain positive numbers")) if (sum(batchsize) != nrow(df)) stop(wmsg("sum of values in 'spatial_index' metadata ", "column \"batchsize\" must equal 'nrow(df)'")) spatial_index <- unstrand(granges(spatial_index, use.names=FALSE)) } if (!append) .write_zero_row_OnDiskLongTable(df, dirpath, spatial_index) .append_df_to_OnDiskLongTable(df, dirpath, batchsize, spatial_index, compress=TRUE) } ### After row ids are saved, data cannot be appended to the OnDiskLongTable ### object. writeOnDiskLongTableRowids <- function(rowids, dirpath=".", compress=TRUE) { .check_OnDiskLongTable_rowids(rowids) .check_OnDiskLongTable_dirpath(dirpath) breakpoints <- .read_object(dirpath, "breakpoints") nrow <- .get_OnDiskLongTable_nrow_from_breakpoints(breakpoints) if (length(rowids) != nrow) stop(wmsg("length of 'rowids' is incompatible ", "with the OnDiskLongTable object in ", dirpath)) .write_object(rowids, dirpath, "rowids", compress=compress) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Constructor ### .friendly_read_object <- function(dirpath, opath) { object <- try(.read_object(dirpath, opath), silent=TRUE) if (inherits(object, "try-error")) stop(wmsg("Cannot open ", .make_filepath(dirpath, opath), ". ", "Please make sure that '", dirpath, "' is the path to a ", "valid OnDiskLongTable directory structure, that is, one ", "as written by writeOnDiskLongTable().")) object } OnDiskLongTable <- function(dirpath=".") { .check_OnDiskLongTable_dirpath(dirpath) header <- .friendly_read_object(dirpath, "header") breakpoints <- .friendly_read_object(dirpath, "breakpoints") spatial_index <- try(.read_object(dirpath, "spatial_index"), silent=TRUE) if (inherits(spatial_index, "try-error")) { spatial_index <- NULL } else if (!is(spatial_index, "GRanges")) { stop(wmsg("invalid 'spatial_index'")) } .rowids_cache <- new.env(parent=emptyenv()) new2("OnDiskLongTable", dirpath=dirpath, header=header, breakpoints=breakpoints, spatial_index=spatial_index, .rowids_cache=.rowids_cache) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Basic getters (from the matrix/data.frame API) ### setMethod("dim", "OnDiskLongTable", function(x) { x_nrow <- .get_OnDiskLongTable_nrow_from_breakpoints(x@breakpoints) x_ncol <- length(x@header) c(x_nrow, x_ncol) } ) setMethod("dimnames", "OnDiskLongTable", function(x) list(NULL, names(x@header)) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### OnDiskLongTable specific getters ### ### Generic defined in OnDiskLongTable_old-class.R #setGeneric("breakpoints", function(x) standardGeneric("breakpoints")) setMethod("breakpoints", "OnDiskLongTable", function(x) x@breakpoints) setGeneric("batchsizes", function(x) standardGeneric("batchsizes")) setMethod("batchsizes", "OnDiskLongTable", function(x) { x_breakpoints <- breakpoints(x) ans <- S4Vectors:::diffWithInitialZero(x_breakpoints) names(ans) <- names(x_breakpoints) ans } ) setGeneric("spatialIndex", function(x) standardGeneric("spatialIndex")) setMethod("spatialIndex", "OnDiskLongTable", function(x) x@spatial_index) ### Generic defined in OnDiskLongTable_old-class.R #setGeneric("rowids", function(x) standardGeneric("rowids")) ### Return NA if 'x' has no row ids. .get_rowids_path <- function(x) { if (is.na(x@dirpath)) return(NA_character_) rowids_path <- .make_filepath(x@dirpath, "rowids") if (!file.exists(rowids_path)) return(NA_character_) rowids_path } ### Return NULL or an integer vector with no NAs or duplicated values. setMethod("rowids", "OnDiskLongTable", function(x) { objname <- "rowids" ## 1. Try to get the row ids from the cache. rowids <- try(get(objname, envir=x@.rowids_cache, inherits=FALSE), silent=TRUE) if (!inherits(rowids, "try-error")) return(rowids) ## 2. Try to get the row ids from disk. rowids_path <- .get_rowids_path(x) if (is.na(rowids_path)) { rowids <- NULL } else { rowids <- readRDS(rowids_path) .check_OnDiskLongTable_rowids(rowids) if (length(rowids) != nrow(x)) stop(wmsg("length(rowids) != nrow(x)")) } ## 3. Cache the row ids. assign(objname, rowids, envir=x@.rowids_cache) rowids } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### "show" method ### setMethod("show", "OnDiskLongTable", function(object) { cat(class(object), " object with ", nrow(object), " row", if (nrow(object) >= 2L) "s" else "", " x ", ncol(object), " col", if (ncol(object) >= 2L) "s" else "", sep="") rowids_path <- .get_rowids_path(object) spatial_index <- spatialIndex(object) if (!is.na(rowids_path)) { if (is.null(spatial_index)) cat(" and ") else cat(", ") cat("row ids") } if (!is.null(spatial_index)) cat(" and spatial index") cat("\n") } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### getBatchesFromOnDiskLongTable() ### ### Return an integer vector of valid batch indices. .normarg_batchidx <- function(batchidx, x) { if (!is.integer(batchidx)) stop(wmsg("'batchidx' must be an integer vector")) if (S4Vectors:::anyMissingOrOutside(batchidx, 1L, length(breakpoints(x)))) stop(wmsg("'batchidx' contains NAs or invalid batch indices")) batchidx } ### Return an integer vector of valid column indices. .normarg_colidx <- function(colidx, x) { if (is.null(colidx)) return(seq_len(ncol(x))) if (is.character(colidx)) { colidx <- match(colidx, colnames(x)) if (S4Vectors:::anyMissing(colidx)) stop(wmsg("'colidx' contains invalid column names")) return(colidx) } if (!is.numeric(colidx)) stop(wmsg("'colidx' must be an integer or character vector")) if (!is.integer(colidx)) colidx <- as.integer(colidx) if (S4Vectors:::anyMissingOrOutside(colidx, 1L, ncol(x))) stop(wmsg("'colidx' contains NAs or invalid column indices")) colidx } ### batchidx: integer vector of batch indices. ### c: column number .read_OnDiskLongTable_batch_column <- function(x, batchidx, c) { if (length(batchidx) == 0L) return(x@header[[c]]) tmp <- lapply(batchidx, function(b) .read_OnDiskLongTable_block(x@dirpath, b, c)) S4Vectors:::quick_unlist(tmp) } ### seqnames: factor-Rle or NULL. ### rowids: integer vector of row ids, or NULL. .as_data.frame <- function(listData, seqnames=NULL, rowids=NULL) { if (!is.null(seqnames)) { seqnames <- S4Vectors:::decodeRle(seqnames) listData <- c(list(seqnames=seqnames), listData) } if (!is.null(rowids)) listData <- c(list(rowids=rowids), listData) data.frame(listData, stringsAsFactors=FALSE) } .as_DataFrame <- function(listData, seqnames=NULL, rowids=NULL, nrows) { if (!is.null(seqnames)) listData <- c(list(seqnames=seqnames), listData) if (!is.null(rowids)) listData <- c(list(rowids=rowids), listData) new("DataFrame", listData=listData, nrows=nrows) } ### batchidx: integer vector of batch indices. ### colidx: integer or character vector of column indices, or NULL. getBatchesFromOnDiskLongTable <- function(x, batchidx, colidx=NULL, with.rowids=FALSE, as.data.frame=FALSE) { if (!is(x, "OnDiskLongTable")) stop(wmsg("'x' must be an OnDiskLongTable object")) batchidx <- .normarg_batchidx(batchidx, x) colidx <- .normarg_colidx(colidx, x) names(colidx) <- colnames(x)[colidx] if (!isTRUEorFALSE(with.rowids)) stop(wmsg("'with.rowids' must be TRUE or FALSE")) if (!isTRUEorFALSE(as.data.frame)) stop(wmsg("'as.data.frame' must be TRUE or FALSE")) ans_listData <- lapply(colidx, function(c) .read_OnDiskLongTable_batch_column(x, batchidx, c)) x_batchsizes <- batchsizes(x) ans_batchsizes <- x_batchsizes[batchidx] x_spatial_index <- spatialIndex(x) if (is.null(x_spatial_index)) { ans_seqnames <- NULL } else { ans_seqnames <- rep.int(seqnames(x_spatial_index)[batchidx], ans_batchsizes) } ans_rowids <- NULL if (with.rowids) { x_rowids <- rowids(x) if (!is.null(x_rowids)) { rowidx <- successiveIRanges(x_batchsizes)[batchidx] ans_rowids <- extractROWS(x_rowids, rowidx) } } if (as.data.frame) .as_data.frame(ans_listData, ans_seqnames, ans_rowids) else .as_DataFrame(ans_listData, ans_seqnames, ans_rowids, nrows=sum(ans_batchsizes)) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### getBatchesBySeqnameFromOnDiskLongTable() ### .seqnames2batchidx <- function(seqnames, spatial_index) { if (!is.character(seqnames) || anyNA(seqnames) || any(duplicated(seqnames))) stop(wmsg("'seqnames' must be a character vector ", "with no NAs and no duplicates")) seqinfo <- seqinfo(spatial_index) seqlevels <- seqlevels(seqinfo) seqrank <- match(seqnames, seqlevels) if (anyNA(seqrank)) stop(wmsg("'seqnames' must be a subset of: ", paste(seqlevels, collapse=", "))) as.integer(successiveIRanges(runLength(seqnames(spatial_index)))[seqrank]) } ### seqnames: character vector of unique sequence names. ### colidx: integer or character vector of column indices, or NULL. getBatchesBySeqnameFromOnDiskLongTable <- function(x, seqnames, colidx=NULL, with.rowids=FALSE, as.data.frame=FALSE) { if (!is(x, "OnDiskLongTable")) stop(wmsg("'x' must be an OnDiskLongTable object")) x_spatial_index <- spatialIndex(x) if (is.null(x_spatial_index)) stop(wmsg("'x' has no spatial index: cannot use ", "getBatchesBySeqnameFromOnDiskLongTable() on it")) batchidx <- .seqnames2batchidx(seqnames, x_spatial_index) getBatchesFromOnDiskLongTable(x, batchidx, colidx=colidx, with.rowids=with.rowids, as.data.frame=as.data.frame) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### getBatchesByOverlapsFromOnDiskLongTable() ### ### ranges: GenomicRanges object. ### colidx: integer or character vector of column indices, or NULL. getBatchesByOverlapsFromOnDiskLongTable <- function(x, ranges, maxgap=-1L, minoverlap=0L, colidx=NULL, with.rowids=FALSE, as.data.frame=FALSE) { if (!is(x, "OnDiskLongTable")) stop(wmsg("'x' must be an OnDiskLongTable object")) x_spatial_index <- spatialIndex(x) if (is.null(x_spatial_index)) stop(wmsg("'x' has no spatial index: cannot use ", "getBatchesByOverlapsFromOnDiskLongTable() on it")) hits <- findOverlaps(ranges, x_spatial_index, maxgap=maxgap, minoverlap=minoverlap) batchidx <- sort(unique(subjectHits(hits))) getBatchesFromOnDiskLongTable(x, batchidx, colidx=colidx, with.rowids=with.rowids, as.data.frame=as.data.frame) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### getRowsFromOnDiskLongTable() ### ### Return an integer vector of valid row indices. .normarg_rowidx <- function(rowidx, x) { if (!is.integer(rowidx)) stop(wmsg("'rowidx' must be an integer vector")) if (S4Vectors:::anyMissingOrOutside(rowidx, 1L, nrow(x))) stop(wmsg("'rowidx' contains NAs or invalid row indices")) rowidx } .breakpoints2offsets <- function(breakpoints) { breakpoints_len <- length(breakpoints) if (breakpoints_len == 0L) return(integer(0)) c(0L, breakpoints[-breakpoints_len]) } ### Translation from row index to "row key". ### breakpoints: integer vector of break points. ### rowidx: integer vector containing valid row indices. ### Return a list of 2 integer vectors parallel to 'rowidx'. The 1st vector ### contains batch indices. The 2nd vector contains row indices relative to ### the batch indicated by the corresponding element in the 1st vector. ### In addition, if 'breakpoints' has names (i.e. batch names) then the 1st ### vector also has names indicating the batch associated with each row index ### in 'rowidx'. .rowidx2rowkeys <- function(breakpoints, rowidx) { batchidx <- findInterval(rowidx - 1L, breakpoints) + 1L names(batchidx) <- names(breakpoints)[batchidx] rowrelidx <- rowidx - .breakpoints2offsets(unname(breakpoints))[batchidx] list(batchidx, rowrelidx) } ### c: column number ### rowkeys: list of 2 integer vectors as returned by .rowidx2rowkeys() .read_OnDiskLongTable_column <- function(x, c, rowkeys) { if (length(rowkeys[[1L]]) == 0L) return(x@header[[c]]) list_of_keys <- split(unname(rowkeys[[2L]]), rowkeys[[1L]]) tmp <- lapply(seq_along(list_of_keys), function(i) { b <- as.integer(names(list_of_keys)[[i]]) block_data <- .read_OnDiskLongTable_block(x@dirpath, b, c) block_data[list_of_keys[[i]]] }) S4Vectors:::quick_unsplit(tmp, rowkeys[[1L]]) } ### rowidx: integer vector of row indices. ### colidx: integer or character vector of column indices, or NULL. ### Return a DataFrame (or data.frame) with 1 row per row id in 'rowidx'. ### Note that we do NOT set the row names to 'rowidx' on the returned DataFrame ### because we want to support duplicates in 'rowidx'. getRowsFromOnDiskLongTable <- function(x, rowidx, colidx=NULL, with.rowids=FALSE, as.data.frame=FALSE) { if (!is(x, "OnDiskLongTable")) stop(wmsg("'x' must be an OnDiskLongTable object")) rowidx <- .normarg_rowidx(rowidx, x) x_breakpoints <- breakpoints(x) rowkeys <- .rowidx2rowkeys(x_breakpoints, rowidx) colidx <- .normarg_colidx(colidx, x) names(colidx) <- colnames(x)[colidx] if (!isTRUEorFALSE(with.rowids)) stop(wmsg("'with.rowids' must be TRUE or FALSE")) if (!isTRUEorFALSE(as.data.frame)) stop(wmsg("'as.data.frame' must be TRUE or FALSE")) ans_listData <- lapply(colidx, function(c) .read_OnDiskLongTable_column(x, c, rowkeys)) x_spatial_index <- spatialIndex(x) if (is.null(x_spatial_index)) { ans_seqnames <- NULL } else { x_seqnames <- rep.int(seqnames(x_spatial_index), batchsizes(x)) ans_seqnames <- x_seqnames[rowidx] } ans_rowids <- NULL if (with.rowids) { x_rowids <- rowids(x) if (!is.null(x_rowids)) ans_rowids <- x_rowids[rowidx] } if (as.data.frame) .as_data.frame(ans_listData, ans_seqnames, ans_rowids) else .as_DataFrame(ans_listData, ans_seqnames, ans_rowids, nrows=length(rowidx)) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### getRowsByIdFromOnDiskLongTable() ### .rowids2rowidx <- function(x, rowids) { x_rowids <- rowids(x) if (is.null(x_rowids)) stop(wmsg("'x' has no row ids: cannot use ", "getRowsByIdFromOnDiskLongTable() on it")) if (!is.integer(rowids) || S4Vectors:::anyMissing(rowids)) stop(wmsg("'rowids' must be an integer vector with no NAs")) rowidx <- match(rowids, x_rowids) if (S4Vectors:::anyMissing(rowidx)) stop(wmsg("'rowids' contains invalid row ids")) rowidx } ### rowids: integer vector of row ids. ### colidx: integer or character vector of column indices, or NULL. ### Return a DataFrame (or data.frame) with 1 row per row id in 'rowids'. ### Note that we do NOT set the row names to 'rowids' on the returned DataFrame ### because we want to support duplicates in 'rowids'. getRowsByIdFromOnDiskLongTable <- function(x, rowids, colidx=NULL, with.rowids=FALSE, as.data.frame=FALSE) { if (!is(x, "OnDiskLongTable")) stop(wmsg("'x' must be an OnDiskLongTable object")) rowidx <- .rowids2rowidx(x, rowids) getRowsFromOnDiskLongTable(x, rowidx, colidx=colidx, with.rowids=with.rowids, as.data.frame=as.data.frame) } BSgenome/R/OnDiskLongTable_old-class.R0000644000175400017540000005327013175713516020563 0ustar00biocbuildbiocbuild### ========================================================================= ### OnDiskLongTable_old objects ### ------------------------------------------------------------------------- ### setClass("OnDiskLongTable_old", representation( dirpath="character", # Single string. colnames="character", # Vector of column names (no NAs, no # empty strings). breakpoints="integer", # Values must be positive and strictly # sorted. Last value matches nb of rows # in the table. .rowids_cache="environment" # Where to load and cache the row ids. # Row ids are unique integer values. # Used for fast translation from # user-supplied row ids to row indices. ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Low-level helpers ### .OnDiskLongTable_old_check_dirpath <- function(dirpath) { if (!isSingleString(dirpath) || dirpath == "") stop(wmsg("'dirpath' must be a single (non-empty) string")) if (!dir.exists(dirpath)) stop(wmsg("directory not found: ", dirpath)) } .OnDiskLongTable_old_check_breakpoints <- function(breakpoints) { if (!is.integer(breakpoints) || S4Vectors:::anyMissing(breakpoints) || is.unsorted(breakpoints, strictly=TRUE) || length(breakpoints) != 0L && breakpoints[[1L]] < 1L) stop(wmsg("invalid breakpoints found for OnDiskLongTable_old object")) } .OnDiskLongTable_old_check_rowids <- function(rowids) { if (!is.integer(rowids)) stop(wmsg("'rowids' must be an integer vector")) if (S4Vectors:::anyMissing(rowids) || anyDuplicated(rowids)) stop(wmsg("'rowids' cannot contain NAs or duplicated values")) } .OnDiskLongTable_old_get_nrow_from_breakpoints <- function(breakpoints) { if (length(breakpoints) == 0L) return(0L) breakpoints[[length(breakpoints)]] } .OnDiskLongTable_old_colidx2dirname <- function(colidx) sprintf("col%03d", colidx) .OnDiskLongTable_old_colidx2dirpath <- function(dirpath, colidx) file.path(dirpath, .OnDiskLongTable_old_colidx2dirname(colidx)) .OnDiskLongTable_old_blockidx2blockname <- function(blockidx) { not_na_idx <- which(!is.na(blockidx)) blockname <- character(length(blockidx)) blockname[not_na_idx] <- sprintf("b%05d", blockidx[not_na_idx]) blockname } .save_object <- function(dirpath, objname, value, compress=TRUE, compression_level, overwrite=FALSE) { filename <- paste0(objname, ".rda") filepath <- file.path(dirpath, filename) if (!overwrite && file.exists(filepath)) stop(wmsg("file already exists: ", filepath)) assign(objname, value) save(list=objname, file=filepath, compress=compress, compression_level=compression_level) } .load_object <- function(dirpath, objname) { filename <- paste0(objname, ".rda") filepath <- file.path(dirpath, filename) if (!file.exists(filepath)) stop(wmsg("file not found: ", filepath)) tmpenv <- new.env(parent=emptyenv()) if (!identical(load(filepath, envir=tmpenv), objname)) stop(wmsg(filepath, " does not seem to belong ", "to an OnDiskLongTable_old object")) get(objname, envir=tmpenv, inherits=FALSE) } ### colidx: column index of length 1. ### blockname: a valid block name. Can also be a valid block index as a ### single integer. .load_block <- function(x, colidx, blockname) { if (!is.character(blockname)) blockname <- .OnDiskLongTable_old_blockidx2blockname(blockname) col_dirpath <- .OnDiskLongTable_old_colidx2dirpath(x@dirpath, colidx) .load_object(col_dirpath, blockname) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### .write_zero_row_OnDiskLongTable_old() ### .remove_file <- function(dirpath, filename) { filepath <- file.path(dirpath, filename) if (file.exists(filepath)) { if (!file.remove(filepath)) stop(wmsg("failed to remove file: ", filepath)) } } .remove_dirs <- function(dirpaths) { fail_idx <- which(as.logical(unlink(dirpaths, recursive=TRUE))) if (length(fail_idx) != 0L) stop(wmsg("failed to remove directories: ", paste0(dirpaths[fail_idx], collapse=", "))) } .create_and_initialize_column_dir <- function(df_col, col_dirpath) { if (!dir.create(col_dirpath, showWarnings=TRUE, mode="0775")) stop(wmsg("failed to create directory: ", col_dirpath)) ## A "special block" is written in newly created column dir. It contains ## serialized zero-length column. blockname <- .OnDiskLongTable_old_blockidx2blockname(0L) block <- df_col[integer(0)] .save_object(col_dirpath, blockname, block) } .write_zero_row_OnDiskLongTable_old <- function(df, dirpath) { ## Remove stuff. .remove_file(dirpath, "rowids.rda") col_dirpaths <- .OnDiskLongTable_old_colidx2dirpath(dirpath, seq_len(ncol(df))) .remove_dirs(col_dirpaths) ## Create stuff. .save_object(dirpath, "colnames", colnames(df), overwrite=TRUE) for (j in seq_len(ncol(df))) .create_and_initialize_column_dir(df[[j]], col_dirpaths[[j]]) .save_object(dirpath, "breakpoints", integer(0), overwrite=TRUE) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### .append_batch_to_OnDiskLongTable_old() ### .write_column <- function(df_col, col_dirpath, breakpoints, blockidx_offset, compress, compression_level) { if (!dir.exists(col_dirpath)) stop(wmsg("directory not found: ", col_dirpath)) block_ranges <- PartitioningByEnd(breakpoints) for (b in seq_along(block_ranges)) { blockidx <- blockidx_offset + b blockname <- .OnDiskLongTable_old_blockidx2blockname(blockidx) block <- df_col[block_ranges[[b]]] .save_object(col_dirpath, blockname, block, compress, compression_level) } } .append_batch_to_OnDiskLongTable_old <- function(df, dirpath, batch_label, blocksize, compress, compression_level) { ## Check existence of rowids.rda file. filepath <- file.path(dirpath, "rowids.rda") if (file.exists(filepath)) stop(wmsg("cannot append data to an ", "OnDiskLongTable_old object with row ids")) ## Check 'df' colnames. old_colnames <- .load_object(dirpath, "colnames") if (!identical(colnames(df), old_colnames)) stop(wmsg("'colnames(df)' must be identical to colnames in ", file.path(dirpath, "colnames.rda"))) ## Load 'breakpoints' vector. breakpoints1 <- .load_object(dirpath, "breakpoints") ## Append 'df' columns. col_dirpaths <- .OnDiskLongTable_old_colidx2dirpath(dirpath, seq_len(ncol(df))) breakpoints2 <- end(breakInChunks(nrow(df), blocksize)) blockidx_offset <- length(breakpoints1) for (j in seq_len(ncol(df))) .write_column(df[[j]], col_dirpaths[[j]], breakpoints2, blockidx_offset, compress, compression_level) ## Update 'breakpoints' vector. if (!is.null(batch_label)) names(breakpoints2) <- rep.int(batch_label, length(breakpoints2)) nrow1 <- .OnDiskLongTable_old_get_nrow_from_breakpoints(breakpoints1) breakpoints <- c(breakpoints1, nrow1 + breakpoints2) .save_object(dirpath, "breakpoints", breakpoints, overwrite=TRUE) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### saveAsOnDiskLongTable_old() and saveRowidsForOnDiskLongTable_old() ### .normarg_blocksize <- function(blocksize, totalsize) { if (!isSingleNumberOrNA(blocksize)) stop(wmsg("'blocksize' must be a single integer or NA")) if (!is.integer(blocksize)) blocksize <- as.integer(blocksize) if (is.na(blocksize)) return(totalsize) if (blocksize < 0L) stop(wmsg("'blocksize' cannot be negative")) if (blocksize == 0L && totalsize != 0L) stop(wmsg("'blocksize' can be 0 only if 'nrow(df)' is 0")) blocksize } ### Ignore the row names on 'df'. If 'df' is a DataFrame, 'metadata(df)' and ### 'mcols(df)' are also ignored. saveAsOnDiskLongTable_old <- function(df, dirpath=".", append=FALSE, batch_label=NULL, blocksize=NA, compress=TRUE, compression_level) { if (!is.data.frame(df) && !is(df, "DataFrame")) stop(wmsg("'df' must be a data.frame or DataFrame object")) .OnDiskLongTable_old_check_dirpath(dirpath) if (!isTRUEorFALSE(append)) stop(wmsg("'append' must be TRUE or FALSE")) if (!(is.null(batch_label) || isSingleString(batch_label) && batch_label != "")) stop(wmsg("'batch_label' must be NULL or a single (non-empty) string")) blocksize <- .normarg_blocksize(blocksize, nrow(df)) if (!append) .write_zero_row_OnDiskLongTable_old(df, dirpath) .append_batch_to_OnDiskLongTable_old(df, dirpath, batch_label, blocksize, compress, compression_level) } ### After row ids are saved, data cannot be appended to the OnDiskLongTable_old ### object. saveRowidsForOnDiskLongTable_old <- function(rowids, dirpath=".", compress=TRUE, compression_level) { .OnDiskLongTable_old_check_rowids(rowids) .OnDiskLongTable_old_check_dirpath(dirpath) breakpoints <- .load_object(dirpath, "breakpoints") nrow <- .OnDiskLongTable_old_get_nrow_from_breakpoints(breakpoints) if (length(rowids) != nrow) stop(wmsg("length of 'rowids' is incompatible ", "with the OnDiskLongTable_old object in ", dirpath)) .save_object(dirpath, "rowids", rowids, compress, compression_level) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Constructor ### OnDiskLongTable_old <- function(dirpath=".") { .OnDiskLongTable_old_check_dirpath(dirpath) ans_colnames <- .load_object(dirpath, "colnames") ans_breakpoints <- .load_object(dirpath, "breakpoints") ans_rowids_cache <- new.env(parent=emptyenv()) ans <- new("OnDiskLongTable_old", dirpath=dirpath, colnames=ans_colnames, breakpoints=ans_breakpoints, .rowids_cache=ans_rowids_cache) .OnDiskLongTable_old_check_breakpoints(ans_breakpoints) ans } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Getters ### setGeneric("breakpoints", function(x) standardGeneric("breakpoints")) setMethod("breakpoints", "OnDiskLongTable_old", function(x) x@breakpoints) setGeneric("blocksizes", function(x) standardGeneric("blocksizes")) setMethod("blocksizes", "OnDiskLongTable_old", function(x) { x_breakpoints <- breakpoints(x) ans <- S4Vectors:::diffWithInitialZero(x_breakpoints) names(ans) <- names(x_breakpoints) ans } ) setGeneric("rowids", function(x) standardGeneric("rowids")) ### Return NULL or an integer vector with no NAs or duplicated values. setMethod("rowids", "OnDiskLongTable_old", function(x) { objname <- "rowids" ## 1. Try to get the row ids from the cache. ans <- try(get(objname, envir=x@.rowids_cache, inherits=FALSE), silent=TRUE) if (!is(ans, "try-error")) return(ans) ## 2. Try to find them on disk. filename <- paste0(objname, ".rda") filepath <- file.path(x@dirpath, filename) if (!file.exists(filepath)) return((assign(objname, NULL, envir=x@.rowids_cache))) ## 3. Load the row ids from disk. if (!identical(load(filepath, envir=x@.rowids_cache), objname)) stop(wmsg(filepath, " does not seem to belong ", "to an OnDiskLongTable_old object")) ans <- get(objname, envir=x@.rowids_cache, inherits=FALSE) .OnDiskLongTable_old_check_rowids(ans) if (length(ans) != nrow(x)) stop(wmsg("length(rowids) != nrow(x)")) ans } ) setMethod("dim", "OnDiskLongTable_old", function(x) { x_nrow <- .OnDiskLongTable_old_get_nrow_from_breakpoints(breakpoints(x)) x_ncol <- length(colnames(x)) c(x_nrow, x_ncol) } ) setMethod("dimnames", "OnDiskLongTable_old", function(x) list(NULL, x@colnames) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### "show" method ### setMethod("show", "OnDiskLongTable_old", function(object) { cat(class(object), " object with ", nrow(object), " row", if (nrow(object) >= 2L) "s" else "", " and ", ncol(object), " column", if (ncol(object) >= 2L) "s" else "", "\n", sep="") } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Get batches from OnDiskLongTable_old ### .normarg_batch_labels <- function(batch_labels, x_batch_labels) { if (is.null(x_batch_labels)) stop(wmsg("'x' has no batch labels (i.e. 'breakpoints(x)' has ", "no names): cannot use getBatchesFromOnDiskLongTable_old() ", "on it")) if (!is.character(batch_labels) || S4Vectors:::anyMissing(batch_labels) || anyDuplicated(batch_labels)) stop(wmsg("'batch_labels' must be a character vector ", "with no NAs and no duplicates")) batch_labels } .normarg_colidx <- function(colidx, x) { if (is.character(colidx)) { colidx <- match(colidx, colnames(x)) if (S4Vectors:::anyMissing(colidx)) stop(wmsg("'colidx' contains invalid column names")) return(colidx) } if (!is.numeric(colidx)) stop(wmsg("'colidx' must be an integer or character vector")) if (!is.integer(colidx)) colidx <- as.integer(colidx) if (S4Vectors:::anyMissingOrOutside(colidx, 1L, ncol(x))) stop(wmsg("'colidx' contains invalid column indices")) colidx } ### colidx: column index of length 1 .get_blocks_from_column <- function(x, colidx, blockidx) { if (length(blockidx) == 0L) blockidx <- 0L tmp <- lapply(blockidx, function(i) .load_block(x, colidx, i)) S4Vectors:::quick_unlist(tmp) } ### batch_labels: character vector of batch labels. ### colidx: integer or character vector. ### Return a DataFrame (or data.frame). getBatchesFromOnDiskLongTable_old <- function(x, batch_labels, colidx, with.batch_label=FALSE, with.rowids=FALSE, as.data.frame=FALSE) { if (!is(x, "OnDiskLongTable_old")) stop(wmsg("'x' must be an OnDiskLongTable_old object")) x_blocksizes <- blocksizes(x) x_batch_labels <- names(x_blocksizes) batch_labels <- .normarg_batch_labels(batch_labels, x_batch_labels) colidx <- .normarg_colidx(colidx, x) if (!isTRUEorFALSE(with.batch_label)) stop(wmsg("'with.batch_label' must be TRUE or FALSE")) if (!isTRUEorFALSE(with.rowids)) stop(wmsg("'with.rowids' must be TRUE or FALSE")) if (!isTRUEorFALSE(as.data.frame)) stop(wmsg("'as.data.frame' must be TRUE or FALSE")) hits <- findMatches(batch_labels, x_batch_labels) blockidx <- subjectHits(hits) ans_blocksizes <- x_blocksizes[blockidx] names(colidx) <- colnames(x)[colidx] ans_listData <- lapply(colidx, function(j) .get_blocks_from_column(x, j, blockidx)) if (with.batch_label) { batch_label_levels <- unique(x_batch_labels) ans_batch_label <- factor(batch_labels[queryHits(hits)], levels=batch_label_levels) ans_batch_label <- rep.int(ans_batch_label, ans_blocksizes) ans_listData[["batch_label"]] <- ans_batch_label } if (with.rowids) { rowidx <- as.integer(successiveIRanges(x_blocksizes)[blockidx]) ans_rowids <- rowids(x)[rowidx] } else { ans_rowids <- NULL } if (as.data.frame) { ans <- data.frame(ans_listData, row.names=ans_rowids, stringsAsFactors=FALSE) } else { ## Unfortunately, DataFrame cannot store its row names as an integer ## vector. if (!is.null(ans_rowids)) ans_rowids <- as.character(ans_rowids) ans <- new("DataFrame", listData=ans_listData, nrows=sum(ans_blocksizes), rownames=ans_rowids) } ans } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### getRowsByIndexFromOnDiskLongTable_old() ### .normarg_rowidx <- function(rowidx, x) { if (!is.integer(rowidx)) stop(wmsg("'rowidx' must be an integer vector")) if (S4Vectors:::anyMissingOrOutside(rowidx, 1L, nrow(x))) stop(wmsg("'rowidx' contains NAs or invalid row indices")) rowidx } .breakpoints2offsets <- function(breakpoints) { breakpoints_len <- length(breakpoints) if (breakpoints_len == 0L) return(integer(0)) c(0L, breakpoints[-breakpoints_len]) } ### Translation from row index to "row key". ### breakpoints: integer vector of break points. ### rowidx: integer vector containing valid row indices. ### Return a list of 2 integer vectors parallel to 'rowidx'. The 1st vector ### contains block indices. The 2nd vector contains row indices relative to ### the block indicated by the corresponding element in the 1st vector. ### In addition, if 'breakpoints' has names (i.e. "batch labels") then the ### 1st vector also has names indicating the label of the batch associated ### with each row index in 'rowidx'. .rowidx2rowkeys <- function(breakpoints, rowidx) { blockidx <- findInterval(rowidx - 1L, breakpoints) + 1L names(blockidx) <- names(breakpoints)[blockidx] rowrelidx <- rowidx - .breakpoints2offsets(unname(breakpoints))[blockidx] list(blockidx, rowrelidx) } ### colidx: column index of length 1 .get_values_from_column <- function(x, colidx, rowkeys) { if (length(rowkeys[[1L]]) == 0L) return(.load_block(x, colidx, 0L)) list_of_keys <- split(unname(rowkeys[[2L]]), rowkeys[[1L]]) tmp <- lapply(seq_along(list_of_keys), function(i) { blockidx <- as.integer(names(list_of_keys)[i]) keys <- list_of_keys[[i]] block <- .load_block(x, colidx, blockidx) block[keys] }) S4Vectors:::quick_unsplit(tmp, rowkeys[[1L]]) } ### rowidx: integer vector. ### colidx: integer or character vector. ### Return a DataFrame (or data.frame) with 1 row per row id in 'rowidx'. ### Note that we do NOT set the row names to 'rowidx' on the returned DataFrame ### because we want to support duplicates in 'rowidx'. getRowsByIndexFromOnDiskLongTable_old <- function(x, rowidx, colidx, with.batch_label=FALSE, as.data.frame=FALSE) { if (!is(x, "OnDiskLongTable_old")) stop(wmsg("'x' must be an OnDiskLongTable_old object")) rowidx <- .normarg_rowidx(rowidx, x) x_breakpoints <- breakpoints(x) rowkeys <- .rowidx2rowkeys(x_breakpoints, rowidx) colidx <- .normarg_colidx(colidx, x) if (!isTRUEorFALSE(with.batch_label)) stop(wmsg("'with.batch_label' must be TRUE or FALSE")) if (!isTRUEorFALSE(as.data.frame)) stop(wmsg("'as.data.frame' must be TRUE or FALSE")) names(colidx) <- colnames(x)[colidx] ans_listData <- lapply(colidx, function(j) .get_values_from_column(x, j, rowkeys)) if (with.batch_label) { batch_label_levels <- unique(names(x_breakpoints)) ans_listData[["batch_label"]] <- factor(names(rowkeys[[1L]]), levels=batch_label_levels) } if (as.data.frame) { ans <- data.frame(ans_listData, stringsAsFactors=FALSE) } else { ans <- new("DataFrame", listData=ans_listData, nrows=length(rowidx)) } ans } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### getRowsByIdFromOnDiskLongTable_old() ### .rowids2rowidx <- function(x, rowids) { x_rowids <- rowids(x) if (is.null(x_rowids)) stop(wmsg("'x' has no row ids: cannot use ", "getRowsByIdFromOnDiskLongTable_old() on it")) if (!is.integer(rowids) || S4Vectors:::anyMissing(rowids)) stop(wmsg("'rowids' must be an integer vector with no NAs")) rowidx <- match(rowids, x_rowids) if (S4Vectors:::anyMissing(rowidx)) stop(wmsg("'rowids' contains invalid row ids")) rowidx } ### rowids: integer vector. ### colidx: integer or character vector. ### Return a DataFrame (or data.frame) with 1 row per row id in 'rowids'. ### Note that we do NOT set the row names to 'rowids' on the returned DataFrame ### because we want to support duplicates in 'rowids'. getRowsByIdFromOnDiskLongTable_old <- function(x, rowids, colidx, with.batch_label=FALSE, as.data.frame=FALSE) { if (!is(x, "OnDiskLongTable_old")) stop(wmsg("'x' must be an OnDiskLongTable_old object")) rowidx <- .rowids2rowidx(x, rowids) getRowsByIndexFromOnDiskLongTable_old(x, rowidx, colidx, with.batch_label=with.batch_label, as.data.frame=as.data.frame) } BSgenome/R/OnDiskNamedSequences-class.R0000644000175400017540000002376013175713516020757 0ustar00biocbuildbiocbuild### ========================================================================= ### OnDiskNamedSequences objects ### ------------------------------------------------------------------------- setClass("OnDiskNamedSequences") # VIRTUAL class with no slots ### OnDiskNamedSequences API ### ------------------------ ### Concrete subclasses need to implement the following: ### - names() ### - seqlengthsFilepath() ### - seqinfo API (implementing seqinfo() is enough to make seqlengths(), ### seqlevels(), etc... work) ### - [[ -- load full sequence as XString object ### Default methods are provided for the following: ### - length() ### - seqnames() ### - show() ### - loadSubseqsFromLinearSequence() setGeneric("seqlengthsFilepath", function(x) standardGeneric("seqlengthsFilepath") ) setGeneric("loadSubseqsFromLinearSequence", function(x, seqname, ranges) standardGeneric("loadSubseqsFromLinearSequence") ) ### Low-level utilities ### Works on an XString object or any object 'x' for which seqlengths() is ### defined. .get_seqlength <- function(x, seqname) { if (!isSingleString(seqname)) stop("'seqname' must be a single string") if (is(x, "XString")) return(length(x)) x_seqlengths <- seqlengths(x) idx <- match(seqname, names(x_seqlengths)) if (is.na(idx)) stop("invalid sequence name: ", seqname) x_seqlengths[[idx]] } ### Default methods setMethod("length", "OnDiskNamedSequences", function(x) length(names(x))) setMethod("seqnames", "OnDiskNamedSequences", function(x) seqlevels(x)) setMethod("show", "OnDiskNamedSequences", function(object) { cat(class(object), " instance of length ", length(object), ":\n", sep="") GenomeInfoDb:::compactPrintNamedAtomicVector(seqlengths(object)) } ) ### Load regions from a single sequence as an XStringSet object. ### 'seqname' is ignored. setMethod("loadSubseqsFromLinearSequence", "XString", function(x, seqname, ranges) xvcopy(extractAt(x, ranges)) # ignores 'seqname' ) setMethod("loadSubseqsFromLinearSequence", "OnDiskNamedSequences", function(x, seqname, ranges) loadSubseqsFromLinearSequence(x[[seqname]], seqname, ranges) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### RdaNamedSequences objects ### ### The "dirpath" slot should contain 1 serialized XString object per ### sequence + a serialized named integer vector ('seqlengths.rda') ### containing the sequence names and lengths. ### setClass("RdaNamedSequences", contains=c("RdaCollection", "OnDiskNamedSequences"), representation( seqlengths="RdaCollection" ) ) setMethod("seqlengthsFilepath", "RdaNamedSequences", function(x) rdaPath(x@seqlengths, "seqlengths") ) setMethod("seqlevels", "RdaNamedSequences", function(x) names(x)) setMethod("seqlengths", "RdaNamedSequences", function(x) { ans <- x@seqlengths[["seqlengths"]] if (!is.integer(ans) || is.null(names(ans))) stop("serialized object in file '", seqlengthsFilepath(x), "' ", "must be a named integer vector") ans } ) setMethod("seqinfo", "RdaNamedSequences", function(x) { x_seqlengths <- seqlengths(x) x_seqlevels <- seqlevels(x) Seqinfo(x_seqlevels, x_seqlengths) } ) ### Constructor. RdaNamedSequences <- function(dirpath, seqnames) { sequences <- RdaCollection(dirpath, seqnames) seqlengths <- RdaCollection(dirpath, "seqlengths") new("RdaNamedSequences", sequences, seqlengths=seqlengths) } ### Load a full sequence as an XString object. setMethod("[[", "RdaNamedSequences", function(x, i, j, ...) { ans <- callNextMethod() if (!is(ans, "XString")) stop("serialized object in file '", rdaPath(x, i), "' ", "must be an XString object") updateObject(ans) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### FastaNamedSequences objects ### setClass("FastaNamedSequences", contains="OnDiskNamedSequences", representation( ## FaFile object pointing to the .fa/.fa.fai (or .fa.rz/.fa.rz.fai ## if RAZip compressed) files containing the sequences/index. fafile="FaFile" ) ) setMethod("names", "FastaNamedSequences", function(x) seqlevels(x@fafile)) setMethod("seqlengthsFilepath", "FastaNamedSequences", function(x) path(x@fafile) ) setMethod("seqinfo", "FastaNamedSequences", function(x) seqinfo(x@fafile)) ### Constructor. FastaNamedSequences <- function(filepath) { fafile <- FaFile(filepath) open(fafile) new("FastaNamedSequences", fafile=fafile) } ### We only support subetting by name. ### Load a full sequence as a DNAString object. setMethod("[[", "FastaNamedSequences", function(x, i, j, ...) { if (!missing(j) || length(list(...)) > 0L) stop("invalid subsetting") if (!is.character(i)) stop("a FastaNamedSequences object can only be subsetted by name") if (length(i) < 1L) stop("attempt to select less than one element") if (length(i) > 1L) stop("attempt to select more than one element") fafile <- x@fafile seqlength <- .get_seqlength(fafile, i) param <- GRanges(i, IRanges(1L, seqlength)) scanFa(fafile, param=param)[[1L]] } ) ### Load regions from a single sequence as a DNAStringSet object. ### TODO: Try the following optimization: reduce 'ranges' before calling ### scanFa(), then extract the regions from the DNAStringSet returned by ### scanFa(). This way, a given nucleotide is loaded only once. setMethod("loadSubseqsFromLinearSequence", "FastaNamedSequences", function(x, seqname, ranges) { if (!is(ranges, "Ranges")) stop("'ranges' must be a Ranges object") fafile <- x@fafile seqlength <- .get_seqlength(fafile, seqname) if (length(ranges) != 0L && (min(start(ranges)) < 1L || max(end(ranges)) > seqlength)) stop("trying to load regions beyond the boundaries ", "of non-circular sequence \"", seqname, "\"") param <- GRanges(seqname, ranges) scanFa(fafile, param=param) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### TwobitNamedSequences objects ### setClass("TwobitNamedSequences", contains="OnDiskNamedSequences", representation( ## TwoBitFile object pointing to the .2bit file containing the ## sequences. twobitfile="TwoBitFile" ) ) setMethod("names", "TwobitNamedSequences", function(x) seqlevels(x@twobitfile)) setMethod("seqlengthsFilepath", "TwobitNamedSequences", function(x) path(x@twobitfile) ) setMethod("seqinfo", "TwobitNamedSequences", function(x) seqinfo(x@twobitfile)) ### Constructor. TwobitNamedSequences <- function(filepath) { twobitfile <- TwoBitFile(filepath) new("TwobitNamedSequences", twobitfile=twobitfile) } ### We only support subetting by name. ### Load a full sequence as a DNAString object. setMethod("[[", "TwobitNamedSequences", function(x, i, j, ...) { if (!missing(j) || length(list(...)) > 0L) stop("invalid subsetting") if (!is.character(i)) stop("a FastaNamedSequences object can only be subsetted by name") if (length(i) < 1L) stop("attempt to select less than one element") if (length(i) > 1L) stop("attempt to select more than one element") twobitfile <- x@twobitfile seqlength <- .get_seqlength(twobitfile, i) which <- GRanges(i, IRanges(1L, seqlength)) import(twobitfile, which=which)[[1L]] } ) ### Load regions from a single sequence as a DNAStringSet object. setMethod("loadSubseqsFromLinearSequence", "TwobitNamedSequences", function(x, seqname, ranges) { if (!is(ranges, "Ranges")) stop("'ranges' must be a Ranges object") twobitfile <- x@twobitfile seqlength <- .get_seqlength(twobitfile, seqname) if (length(ranges) != 0L && (min(start(ranges)) < 1L || max(end(ranges)) > seqlength)) stop("trying to load regions beyond the boundaries ", "of non-circular sequence \"", seqname, "\"") which <- GRanges(seqname, ranges) import(twobitfile, which=which) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### loadSubseqsFromStrandedSequence() ### .loadSubseqsFromCircularSequence <- function(x, seqname, ranges) { if (!is(ranges, "Ranges")) stop("'ranges' must be a Ranges object") seqlength <- .get_seqlength(x, seqname) ranges_start <- start(ranges) ranges_end <- end(ranges) if (max(ranges_end - ranges_start) >= seqlength) stop("loading regions that are longer than the whole circular ", "sequence \"", seqname, "\" is not supported") start0 <- ranges_start - 1L # 0-based start shift <- start0 %% seqlength - start0 L_start <- ranges_start + shift end1 <- ranges_end + shift L_end <- pmin(end1, seqlength) R_start <- 1L R_end <- pmax(end1, seqlength) - seqlength L_ans <- loadSubseqsFromLinearSequence(x, seqname, IRanges(L_start, L_end)) R_ans <- loadSubseqsFromLinearSequence(x, seqname, IRanges(R_start, R_end)) xscat(L_ans, R_ans) } loadSubseqsFromStrandedSequence <- function(x, seqname, ranges, strand, is_circular=NA) { if (length(ranges) != length(strand)) stop("'ranges' and 'strand' must have the same length") if (!is.logical(is_circular) || length(is_circular) != 1L) stop("'is_circular' must be a single logical") if (is_circular %in% c(NA, FALSE)) { loadFUN <- loadSubseqsFromLinearSequence } else { loadFUN <- .loadSubseqsFromCircularSequence } ans <- loadFUN(x, seqname, ranges) idx <- which(strand == "-") ans[idx] <- reverseComplement(ans[idx]) ans } BSgenome/R/SNPlocs-class.R0000644000175400017540000001641613175713516016270 0ustar00biocbuildbiocbuild### ========================================================================= ### SNPlocs objects ### ------------------------------------------------------------------------- setClass("SNPlocs", representation( "VIRTUAL", ## Provider of the SNPs (e.g. "dbSNP"). provider="character", ## e.g. "dbSNP Human BUILD 149" provider_version="character", ## Official release date of the SNPs (e.g. "Nov 9, 2010"). release_date="character", ## Official release name of the SNPs (e.g. "Build 132"). release_name="character", ## URL to the place where the original SNP data was downloaded from. source_data_url="character", ## Date the original SNP data was downloaded. download_date="character", ## Reference genome of the SNPs. reference_genome="GenomeDescription", ## Named list of "sequence name translation tables" (one table per ## compatible genome and each table is represented by a named ## character vector). compatible_genomes="list", ## Name of the SNPlocs data package where the SNPlocs object is ## defined. data_pkgname="character" ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Accessors ### setMethod("provider", "SNPlocs", function(x) x@provider) setMethod("providerVersion", "SNPlocs", function(x) x@provider_version) setMethod("releaseDate", "SNPlocs", function(x) x@release_date) setMethod("releaseName", "SNPlocs", function(x) x@release_name) setGeneric("referenceGenome", function(x) standardGeneric("referenceGenome")) setMethod("referenceGenome", "SNPlocs", function(x) x@reference_genome) setGeneric("compatibleGenomes", function(x) standardGeneric("compatibleGenomes") ) setMethod("compatibleGenomes", "SNPlocs", function(x) x@compatible_genomes) setMethod("organism", "SNPlocs", function(object) organism(referenceGenome(object)) ) setMethod("commonName", "SNPlocs", function(object) commonName(referenceGenome(object)) ) setMethod("seqinfo", "SNPlocs", function(x) seqinfo(referenceGenome(x))) setMethod("seqnames", "SNPlocs", function(x) seqnames(referenceGenome(x))) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The 'show' method ### setMethod("show", "SNPlocs", function(object) { cat("# SNPlocs object for ", organism(object), " (", releaseName(object), ")\n", sep="") cat("# reference genome: ", providerVersion(referenceGenome(object)), "\n", sep="") cat("# nb of SNPs: ", sum(snpcount(object)), "\n", sep="") } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### snpcount() ### setGeneric("snpcount", function(x) standardGeneric("snpcount")) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### snplocs() ### ### Used internally for SNP injection. Not intended for the end user. ### Must return a 2-col data-frame-like object with columns "loc" (integer) ### and "alleles_as_ambig" (character). ### setGeneric("snplocs", signature="x", function(x, seqname, ...) standardGeneric("snplocs") ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### SNP extractors: snpsBySeqname(), snpsByOverlaps(), snpsById() ### setGeneric("snpsBySeqname", signature="x", function(x, seqnames, ...) standardGeneric("snpsBySeqname") ) ### Same args and signature as GenomicFeatures::transcriptsByOverlaps() ### EXCEPT for 'minoverlap' default value that we set to zero so we also ### get SNPs that are insertions (relevant for XtraSNPlocs objects). setGeneric("snpsByOverlaps", signature="x", function(x, ranges, ...) standardGeneric("snpsByOverlaps") ) setGeneric("snpsById", signature="x", function(x, ids, ...) standardGeneric("snpsById") ) ### TODO: Avoid code duplication between normarg_ranges() and ### GenomicAlignments:::.normarg_param(). normarg_ranges <- function(ranges) { if (isSingleString(ranges)) { tmp1 <- strsplit(ranges, ":", fixed=TRUE)[[1L]] if (length(tmp1) != 2L) stop(wmsg("when a character string, 'ranges' must be ", "of the form \"ch14:5201-5300\"")) tmp2 <- as.integer(strsplit(tmp1[2L], "-", fixed=TRUE)[[1L]]) if (length(tmp2) != 2L || any(is.na(tmp2))) stop(wmsg("when a character string, 'ranges' must be ", "of the form \"ch14:5201-5300\"")) ranges <- GRanges(tmp1[1L], IRanges(tmp2[1L], tmp2[2L])) return(ranges) } if (!is(ranges, "GenomicRanges")) stop(wmsg("'ranges' ranges must be a GenomicRanges object ", "or a character string of the form \"ch14:5201-5300\"")) ranges } ### Return an integer vector with no NAs parallel to 'ids'. ids2rowids <- function(ids) { if (!(is.character(ids) || is.numeric(ids))) stop(wmsg("'ids' must be a character or integer vector with no NAs")) if (S4Vectors:::anyMissing(ids)) stop(wmsg("'ids' cannot contain NAs")) if (is.character(ids)) { prefixes <- unique(substr(ids, 1L, 2L)) if ("rs" %in% prefixes) { if (!setequal(prefixes, "rs")) stop(wmsg("'ids' cannot mix SNP ids that are prefixed ", "with \"rs\" with SNP ids that are not")) ## Drop the "rs" prefix. ids <- substr(ids, 3L, nchar(ids)) } ids <- suppressWarnings(as.numeric(ids)) if (S4Vectors:::anyMissing(ids)) stop(wmsg("cannot extract the digital part of ", "some SNP ids in 'ids'")) } if (length(ids) != 0L && min(ids) < 0) stop(wmsg("'ids' contains unrealistic SNP ids")) if (!is.integer(ids)) { ids <- suppressWarnings(as.integer(ids)) if (S4Vectors:::anyMissing(ids)) stop(wmsg("'ids' contains SNP ids that are too big")) } ids } ### Return a list of 2 vectors parallel to each other. The 1st and 2nd vectors ### are respectively the row indices (integer vector) and the 'user_ids' vector ### (which can be character, numeric, or integer), with the not found entries ### removed from both of them. ### Note that, if 'ifnotfound="error"' then the 2 returned vectors are parallel ### to input vectors 'user_rowids' and 'user_ids'. rowids2rowidx <- function(user_rowids, user_ids, x_rowids, ifnotfound) { if (is.null(x_rowids)) stop(wmsg("BSgenome internal error: data contains no SNP ids")) rowidx <- match(user_rowids, x_rowids) notfound_idx <- which(is.na(rowidx)) if (length(notfound_idx) != 0L) { if (length(notfound_idx) <= 10L) { ids_to_show <- user_ids[notfound_idx] } else { ids_to_show <- c(user_ids[notfound_idx[1:9]], "...") } ids_to_show <- paste0(ids_to_show, collapse=", ") if (ifnotfound == "error") stop(wmsg("SNP ids not found: ", ids_to_show, "\n\nUse 'ifnotfound=\"drop\"' to drop them.")) if (ifnotfound == "warning") warning(wmsg("SNP ids not found: ", ids_to_show, "\n\nThey were dropped.")) rowidx <- rowidx[-notfound_idx] user_ids <- user_ids[-notfound_idx] } list(rowidx, user_ids) } BSgenome/R/XtraSNPlocs-class.R0000644000175400017540000003413213175713516017122 0ustar00biocbuildbiocbuild### ========================================================================= ### XtraSNPlocs objects ### ------------------------------------------------------------------------- ### setClassUnion("OnDiskLongTable_OR_old", c("OnDiskLongTable", "OnDiskLongTable_old") ) setClass("XtraSNPlocs", representation( ## Name of the XtraSNPlocs data package where the XtraSNPlocs ## object is defined. pkgname="character", ## OnDiskLongTable_old object containing the SNP data. snp_table="OnDiskLongTable_OR_old", ## Provider of the SNPs (e.g. "dbSNP"). provider="character", ## E.g. "dbSNP Human BUILD 141". provider_version="character", ## Official release date of the SNPs (e.g. "May 2014"). release_date="character", ## Official release name of the SNPs (e.g. "dbSNP Human BUILD 141"). release_name="character", ## URL to the place where the original SNP data was downloaded from. source_data_url="character", ## Date the original SNP data was downloaded. download_date="character", ## Reference genome of the SNPs. reference_genome="GenomeDescription" ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Low-level helpers ### .XTRASNPLOCS_COLUMNS <- c( "seqnames", "start", "end", "width", "strand", "RefSNP_id", "alleles", "snpClass", "loctype" ) ### Only some of the columns above are actually columns of the ### OnDiskLongTable_old component of an XtraSNPlocs object. We call them ### "physical" columns. The other columns are "computed" columns i.e. columns ### that we compute on demand. .XTRASNPLOCS_PHYSICAL_COLUMNS <- c( "snpClass", "alleles", "start", "width", "strand", "loctype" ) .XtraSNPlocs_check_user_supplied_columns <- function(columns) { if (!is.character(columns) || any(is.na(columns))) stop(wmsg("'columns' must be a character vector with no NAs")) if (!all(columns %in% .XTRASNPLOCS_COLUMNS)) stop(wmsg("valid columns: ", paste(.XTRASNPLOCS_COLUMNS, collapse=", "))) } .XtraSNPlocs_get_physical_from_user_supplied_columns <- function(columns) { physical_columns <- intersect(columns, .XTRASNPLOCS_PHYSICAL_COLUMNS) if ("end" %in% columns) physical_columns <- union(physical_columns, c("start", "width")) physical_columns } .XtraSNPlocs_get_DF_for_seqnames <- function(x, seqnames, columns, drop.rs.prefix) { physical_columns <- .XtraSNPlocs_get_physical_from_user_supplied_columns(columns) with_RefSNP_id <- "RefSNP_id" %in% columns DF0 <- getBatchesFromOnDiskLongTable_old(x@snp_table, seqnames, physical_columns, with.batch_label=TRUE, with.rowids=with_RefSNP_id, as.data.frame=with_RefSNP_id) if (with_RefSNP_id) { ans_RefSNP_id <- rownames(DF0) rownames(DF0) <- NULL DF0 <- DataFrame(DF0) if (!drop.rs.prefix && length(ans_RefSNP_id) != 0L) ans_RefSNP_id <- paste0("rs", ans_RefSNP_id) DF0[["RefSNP_id"]] <- ans_RefSNP_id } if ("seqnames" %in% columns) DF0[["seqnames"]] <- factor(DF0[["batch_label"]], levels=seqlevels(x)) if ("strand" %in% columns) { strand0 <- DF0[["strand"]] ans_strand <- rep.int("+", length(strand0)) minus_idx <- which(strand0 != as.raw(0L)) ans_strand[minus_idx] <- "-" DF0[["strand"]] <- ans_strand } if ("end" %in% columns) DF0[["end"]] <- DF0[["start"]] + DF0[["width"]] - 1L if ("loctype" %in% columns) DF0[["loctype"]] <- as.integer(DF0[["loctype"]]) DF0[columns] } ### 'rowidx' must be a list of 2 vectors parallel to each other, as returned ### by rowids2rowidx(). .XtraSNPlocs_get_DF_for_ids <- function(x, rowidx, columns) { physical_columns <- .XtraSNPlocs_get_physical_from_user_supplied_columns(columns) DF0 <- getRowsByIndexFromOnDiskLongTable_old(x@snp_table, rowidx[[1L]], physical_columns, with.batch_label=TRUE) if ("RefSNP_id" %in% columns) DF0[["RefSNP_id"]] <- rowidx[[2L]] if ("seqnames" %in% columns) DF0[["seqnames"]] <- factor(DF0[["batch_label"]], levels=seqlevels(x)) if ("strand" %in% columns) { strand0 <- DF0[["strand"]] ans_strand <- rep.int("+", length(strand0)) minus_idx <- which(strand0 != as.raw(0L)) ans_strand[minus_idx] <- "-" DF0[["strand"]] <- ans_strand } if ("end" %in% columns) DF0[["end"]] <- DF0[["start"]] + DF0[["width"]] - 1L if ("loctype" %in% columns) DF0[["loctype"]] <- as.integer(DF0[["loctype"]]) DF0[columns] } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Getters ### setMethod("dimnames", "XtraSNPlocs", function(x) list(NULL, .XTRASNPLOCS_COLUMNS) ) setMethod("dim", "XtraSNPlocs", function(x) { x_nrow <- nrow(x@snp_table) x_ncol <- length(.XTRASNPLOCS_COLUMNS) c(x_nrow, x_ncol) } ) setMethod("provider", "XtraSNPlocs", function(x) x@provider) setMethod("providerVersion", "XtraSNPlocs", function(x) x@provider_version) setMethod("releaseDate", "XtraSNPlocs", function(x) x@release_date) setMethod("releaseName", "XtraSNPlocs", function(x) x@release_name) setMethod("referenceGenome", "XtraSNPlocs", function(x) x@reference_genome) setMethod("organism", "XtraSNPlocs", function(object) organism(referenceGenome(object)) ) setMethod("commonName", "XtraSNPlocs", function(object) commonName(referenceGenome(object)) ) setMethod("seqinfo", "XtraSNPlocs", function(x) seqinfo(referenceGenome(x))) setMethod("seqnames", "XtraSNPlocs", function(x) seqnames(referenceGenome(x))) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Constructor ### ### Not intended to be used directly. ### 'download_url' argument is for backward compatibility with XtraSNPlocs ### packages <= 0.99.12. newXtraSNPlocs <- function(pkgname, snp_table_dirpath, provider, provider_version, release_date, release_name, source_data_url, download_date, reference_genome, download_url="") { if (missing(source_data_url)) source_data_url <- download_url snp_table <- OnDiskLongTable_old(snp_table_dirpath) stopifnot(identical(colnames(snp_table), .XTRASNPLOCS_PHYSICAL_COLUMNS)) new("XtraSNPlocs", pkgname=pkgname, snp_table=snp_table, provider=provider, provider_version=provider_version, release_date=release_date, release_name=release_name, source_data_url=source_data_url, download_date=download_date, reference_genome=reference_genome) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The 'show' method ### setMethod("show", "XtraSNPlocs", function(object) { cat("# ", class(object), " object for ", organism(object), " (", releaseName(object), ")\n", sep="") cat("# reference genome: ", providerVersion(referenceGenome(object)), "\n", sep="") cat("# nb of SNPs: ", nrow(object), "\n", sep="") } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### snpcount() ### .get_snpcount_from_blocksizes <- function(blocksizes, seqnames, class, pkgname) { ans <- integer(length(seqnames)) names(ans) <- seqnames ## Most of the times, 'names(blocksizes)' will be identical to ## 'seqnames'. However, in the unlikely situation where some ## chromosomes have no SNPs, these chromosomes will be missing ## from 'names(blocksizes)'. The sanity check below accomodates ## for that. m <- match(names(blocksizes), seqnames) if (any(is.na(m)) || !isStrictlySorted(m)) stop(wmsg("BSgenome internal error: ", "the data in this ", class, " object is not in the ", "expected format. Please contact the maintainer of the ", pkgname, " package.")) ans[m] <- blocksizes ans } setMethod("snpcount", "XtraSNPlocs", function(x) .get_snpcount_from_blocksizes(blocksizes(x@snp_table), seqlevels(x), class(x), x@pkgname) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### snpsBySeqname() ### .normarg_columns <- function(columns) { #IGNORED_COLUMNS <- c("seqnames", "start", "end", "width", "strand") #ignored_idx <- which(columns %in% IGNORED_COLUMNS) #if (length(ignored_idx) != 0L) # warning(wmsg("ignored columns (because they're implicit): ", # paste(IGNORED_COLUMNS[ignored_idx], collapse=", "))) columns <- setdiff(columns, "width") union(columns, c("seqnames", "start", "end", "strand")) } .get_GRanges_by_seqname_from_XtraSNPlocs <- function(x, seqnames, columns, drop.rs.prefix) { columns <- .normarg_columns(columns) DF <- .XtraSNPlocs_get_DF_for_seqnames(x, seqnames, columns, drop.rs.prefix) makeGRangesFromDataFrame(DF, keep.extra.columns=TRUE, seqinfo=seqinfo(x)) } ### Returns a GRanges object unless 'as.DataFrame=TRUE'. setMethod("snpsBySeqname", "XtraSNPlocs", function(x, seqnames, columns=c("seqnames", "start", "end", "strand", "RefSNP_id"), drop.rs.prefix=FALSE, as.DataFrame=FALSE) { if (!is.character(seqnames) || any(is.na(seqnames)) || any(duplicated(seqnames))) stop(wmsg("'seqnames' must be a character vector ", "with no NAs and no duplicates")) if (!all(seqnames %in% seqlevels(x))) stop(wmsg("'seqnames' must be a subset of: ", paste(seqlevels(x), collapse=", "))) .XtraSNPlocs_check_user_supplied_columns(columns) if (!isTRUEorFALSE(drop.rs.prefix)) stop(wmsg("'drop.rs.prefix' must be TRUE or FALSE")) if (!isTRUEorFALSE(as.DataFrame)) stop(wmsg("'as.DataFrame' must be TRUE or FALSE")) if (as.DataFrame) return(.XtraSNPlocs_get_DF_for_seqnames(x, seqnames, columns, drop.rs.prefix)) .get_GRanges_by_seqname_from_XtraSNPlocs(x, seqnames, columns, drop.rs.prefix) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### snpsByOverlaps() ### .to_DataFrame <- function(x, columns) { spatial_colnames <- c("seqnames", "start", "end", "width", "strand") spatial_colnames <- intersect(spatial_colnames, columns) spatial_cols <- vector(mode="list", length=length(spatial_colnames)) names(spatial_cols) <- spatial_colnames if ("seqnames" %in% spatial_colnames) spatial_cols[["seqnames"]] <- seqnames(x) if ("start" %in% spatial_colnames) spatial_cols[["start"]] <- start(x) if ("end" %in% spatial_colnames) spatial_cols[["end"]] <- end(x) if ("width" %in% spatial_colnames) spatial_cols[["width"]] <- width(x) if ("strand" %in% spatial_colnames) spatial_cols[["strand"]] <- strand(x) cbind(DataFrame(spatial_cols), mcols(x))[ , columns, drop=FALSE] } ### Returns a GRanges object unless 'as.DataFrame=TRUE'. ### Arguments passed thru ... are further arguments to be passed to ### subsetByOverlaps(). setMethod("snpsByOverlaps", "XtraSNPlocs", function(x, ranges, columns=c("seqnames", "start", "end", "strand", "RefSNP_id"), drop.rs.prefix=FALSE, as.DataFrame=FALSE, ...) { ranges <- normarg_ranges(ranges) dots <- list(...) if (isTRUE(dots$invert)) stop(wmsg("snpsByOverlaps() does not support 'invert=TRUE'")) ## The only purpose of the line below is to check that 'x' and 'ranges' ## are based on the same reference genome (merge() will raise an error ## if they are not). merge(seqinfo(x), seqinfo(ranges)) seqlevels(ranges, pruning.mode="coarse") <- intersect(seqlevels(x), seqlevelsInUse(ranges)) if (!isTRUEorFALSE(as.DataFrame)) stop(wmsg("'as.DataFrame' must be TRUE or FALSE")) snps_by_seqname <- snpsBySeqname(x, seqlevels(ranges), columns=columns, drop.rs.prefix=drop.rs.prefix) ans <- subsetByOverlaps(snps_by_seqname, ranges, ...) if (as.DataFrame) ans <- .to_DataFrame(ans, columns) ans } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### snpsById() ### .get_GRanges_by_id_from_XtraSNPlocs <- function(x, rowidx, columns) { columns <- .normarg_columns(columns) DF <- .XtraSNPlocs_get_DF_for_ids(x, rowidx, columns) makeGRangesFromDataFrame(DF, keep.extra.columns=TRUE, seqinfo=seqinfo(x)) } ### Returns a GRanges object unless 'as.DataFrame=TRUE'. ### If 'ifnotfound="error"' and if the function returns then the returned ### object is guaranteed to be parallel to 'ids'. setMethod("snpsById", "XtraSNPlocs", function(x, ids, columns=c("seqnames", "start", "end", "strand", "RefSNP_id"), ifnotfound=c("error", "warning", "drop"), as.DataFrame=FALSE) { user_rowids <- ids2rowids(ids) ifnotfound <- match.arg(ifnotfound) x_rowids <- rowids(x@snp_table) rowidx <- rowids2rowidx(user_rowids, ids, x_rowids, ifnotfound) .XtraSNPlocs_check_user_supplied_columns(columns) if (!isTRUEorFALSE(as.DataFrame)) stop(wmsg("'as.DataFrame' must be TRUE or FALSE")) if (as.DataFrame) return(.XtraSNPlocs_get_DF_for_ids(x, rowidx, columns)) .get_GRanges_by_id_from_XtraSNPlocs(x, rowidx, columns) } ) BSgenome/R/available.genomes.R0000644000175400017540000002040613175713516017212 0ustar00biocbuildbiocbuild### ========================================================================= ### available.genomes() and related utilities ### ------------------------------------------------------------------------- ### .BSGENOME_PREFIX <- "BSgenome." .has_BSgenome_prefix <- function(x) substr(x, 1L, nchar(.BSGENOME_PREFIX)) == .BSGENOME_PREFIX ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### installed.genomes() and available.genomes() ### .splitNameParts <- function(pkgs) { if (length(pkgs) == 0L) { ans <- data.frame(pkgname=character(0), organism=factor(), provider=factor(), provider_version=character(0), masked=logical(0), stringsAsFactors=FALSE) return(ans) } ## Remove ".masked" suffix. pkgs2 <- pkgs is_masked <- substr(pkgs2, nchar(pkgs2) - 6L, nchar(pkgs2)) == ".masked" idx <- which(is_masked) pkgs2[idx] <- substr(pkgs2[idx], 1L, nchar(pkgs2)[idx] - 7L) parts <- strsplit(pkgs2, ".", fixed=TRUE) nparts <- elementNROWS(parts) ## Some packages like BSgenome.Tgondii.ToxoDB.7.0 don't follow the rules ## and are made of more than 4 parts. has_more_than_4_parts <- which(nparts > 4L) for (i in has_more_than_4_parts) { tmp <- parts[[i]] parts[[i]] <- c(tmp[1:3], paste(tmp[4:length(tmp)], collapse=".")) } ## And just in case one day we start to see some packages with less than ## 4 parts. has_less_than_4_parts <- which(nparts < 4L) for (i in has_less_than_4_parts) { tmp <- parts[[i]] parts[[i]] <- c(tmp, rep.int(NA_character_, 4L - length(tmp))) } ## From now, any top-level element in 'parts' is guaranteed to be a ## character vector of length 4. uparts <- unlist(parts) idx4 <- (1:length(parts)) * 4L data.frame(pkgname=pkgs, organism=factor(uparts[idx4 - 2L]), provider=factor(uparts[idx4 - 1L]), provider_version=uparts[idx4], masked=is_masked, stringsAsFactors=FALSE) } installed.genomes <- function(splitNameParts=FALSE) { if (!isTRUEorFALSE(splitNameParts)) stop("'splitNameParts' must be TRUE or FALSE") pkgs <- installed.packages()[ , "Package"] pkgs <- pkgs[.has_BSgenome_prefix(pkgs)] names(pkgs) <- NULL if (splitNameParts) pkgs <- .splitNameParts(pkgs) pkgs } available.genomes <- function(splitNameParts=FALSE, type=getOption("pkgType")) { if (!isTRUEorFALSE(splitNameParts)) stop("'splitNameParts' must be TRUE or FALSE") contrib_url <- get_data_annotation_contrib_url(type) pkgs <- available.packages(contrib_url)[, "Package"] pkgs <- pkgs[.has_BSgenome_prefix(pkgs)] names(pkgs) <- NULL if (splitNameParts) pkgs <- .splitNameParts(pkgs) pkgs } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### getBSgenome() ### .stopOnAvailablePkg <- function(genome, is.source=FALSE) stop(genome, " package is not currently installed.\n", " You first need to install it, which you can do with:\n", " library(BiocInstaller)\n", " biocLite(\"", genome, "\"", ifelse(is.source, ", type=\"source\"", ""), ")") .stopOnMoreThanOneAvailablePkg <- function(genome, masked, is.source=FALSE) stop("Looks like there is more than one available ", ifelse(masked, "masked ", ""), "BSgenome data package\n", " that matches genome assembly (a.k.a. provider version): ", genome, "\n", " You first need to choose one (use 'available.genomes(", ifelse(is.source, "type=\"source\"", ""), ")' to get\n the list). ", "Then install it, which you can do with:\n", " library(BiocInstaller)\n", " biocLite(\"\"", ifelse(is.source, ", type=\"source\"", ""), ")") .getInstalledPkgnameFromProviderVersion <- function(genome, masked=FALSE) { ## 1) Search installed packages. inst_pkgs <- installed.genomes(splitNameParts=TRUE) inst_pkgs <- inst_pkgs[inst_pkgs[ , "masked"] == masked, , drop=FALSE] idx <- which(genome == inst_pkgs[ , "provider_version"]) if (length(idx) == 1L) return(inst_pkgs[idx , "pkgname"]) if (length(idx) >= 2L) stop("Looks like you have more than one installed ", ifelse(masked, "masked ", ""), "BSgenome data package\n", " that matches genome assembly (a.k.a. provider version): ", genome, "\n", " Please disambiguate by specifying the full name of the ", "package you want\n to use (use 'installed.genomes()' to ", "get the list).") ## 2) Search available packages. av_pkgs <- available.genomes(splitNameParts=TRUE) av_pkgs <- av_pkgs[av_pkgs[ , "masked"] == masked, ] idx <- which(genome == av_pkgs[ , "provider_version"]) if (length(idx) == 1L) { genome <- av_pkgs[idx , "pkgname"] .stopOnAvailablePkg(genome) } if (length(idx) >= 2L) .stopOnMoreThanOneAvailablePkg(genome, masked) ## 3) Search available source packages. if (getOption("pkgType") != "source") { av_srcpkgs <- available.genomes(splitNameParts=TRUE, type="source") av_srcpkgs <- av_srcpkgs[av_srcpkgs[ , "masked"] == masked, ] idx <- which(genome == av_srcpkgs[ , "provider_version"]) if (length(idx) == 1L) { genome <- av_srcpkgs[idx , "pkgname"] .stopOnAvailablePkg(genome, is.source=TRUE) } if (length(idx) >= 2L) .stopOnMoreThanOneAvailablePkg(genome, masked, is.source=TRUE) } ## All searches have failed. stop("Couldn't find a ", ifelse(masked, "masked ", ""), "BSgenome data package ", "that matches genome assembly\n (a.k.a. provider version): ", genome, "\n\n", " Please use 'available.genomes()' ", "(or 'available.genomes(type=\"source\")')\n", " to check the list of BSgenome data packages that are available ", "in the\n Bioconductor repositories for your version of ", "R/Bioconductor.\n If you don't find what you are looking for, ", "please see the BSgenomeForge\n vignette in the BSgenome software ", "package for how to forge a ", ifelse(masked, "masked ", ""), "BSgenome\n data package ", "for your organism of interest.") } .getBSgenomeObjectFromInstalledPkgname <- function(genome) { if (suppressWarnings(require(genome, quietly=TRUE, character.only=TRUE))) { ## 'genome' package is on the search list. pkgenvir <- as.environment(paste("package", genome, sep=":")) ans <- try(get(genome, envir=pkgenvir, inherits=FALSE), silent=TRUE) if (!is(ans, "BSgenome")) stop(genome, " doesn't look like a valid BSgenome data package") return(ans) } av_pkgs <- available.genomes() if (genome %in% av_pkgs) .stopOnAvailablePkg(genome) if (getOption("pkgType") != "source") { av_srcpkgs <- available.genomes(type="source") if (genome %in% av_srcpkgs) .stopOnAvailablePkg(genome, is.source=TRUE) } stop("Package ", genome, " is not available.\n", " Please see the BSgenomeForge vignette in the BSgenome software ", "package\n for how to forge a BSgenome data package for ", "your organism of interest.") } getBSgenome <- function(genome, masked=FALSE) { if (!isTRUEorFALSE(masked)) stop("'masked' must be TRUE or FALSE") if (is(genome, "BSgenome")) return(genome) if (!isSingleString(genome)) stop("'genome' must be a BSgenome object, or the full name of an ", "installed\n BSgenome data package, or a short string ", "specifying a genome assembly (a.k.a.\n provider version) ", "that refers unambiguously to an installed BSgenome data\n", " package") if (!.has_BSgenome_prefix(genome)) { genome <- .getInstalledPkgnameFromProviderVersion(genome, masked=masked) } else if (masked) { warning("'masked' is ignored when 'genome' is supplied as ", "a full package name") } .getBSgenomeObjectFromInstalledPkgname(genome) } BSgenome/R/bsapply.R0000644000175400017540000000526213175713516015313 0ustar00biocbuildbiocbuildsetClass("BSParams", representation=representation( X="BSgenome", FUN="function", exclude = "character", simplify="logical", maskList="logical", motifList="character", userMask="RangesList", invertUserMask="logical"), prototype=prototype( exclude=character(0), simplify=FALSE, maskList=logical(0), motifList=character(0), invertUserMask=FALSE, userMask=RangesList() ), validity=function(object) { msg <- TRUE if (length(object@maskList) > 0) { for(i in seq_len(length(object@maskList))) { if(!(names(object@maskList)[i] %in% masknames(object@X))) { msg <- "the names of 'maskList' must be vector of names corresponding to the default BSgenome masks." break } } } msg }) bsapply <- function(BSParams, ...) { if (!is(BSParams, "BSParams") || !isTRUE(validObject(BSParams, test=TRUE))) stop("'X' must be a valid BSgenome object") processSeqname <- function(seqname, ...) { seq <- BSParams@X[[seqname]] if (length(BSParams@maskList) > 0) { for(i in seq_len(length(BSParams@maskList))){ if(names(BSParams@maskList)[i] %in% masknames(BSParams@X)) { active(masks(seq))[names(BSParams@maskList)[i]] <- BSParams@maskList[[i]] } } } if (length(BSParams@motifList) > 0){ for(i in seq_len(length(BSParams@motifList))) { seq <- maskMotif(seq, BSParams@motifList[i]) } } seqMask <- userMask[[seqname]] if (length(seqMask) > 0) { seqMask <- Mask(length(seq), start(seqMask), end(seqMask)) if (BSParams@invertUserMask) seqMask <- gaps(seqMask) if (!is.null(masks(seq))) seqMask <- append(masks(seq), seqMask) masks(seq) <- seqMask } BSParams@FUN(seq, ...) } if (length(seqnames(BSParams@X)) > 0) seqnames <- seqnames(BSParams@X) else seqnames <- mseqnames(BSParams@X) exclude <- unname(BSParams@exclude[nzchar(BSParams@exclude)]) pariahIndex <- unique(unlist(lapply(exclude, grep, seqnames))) if (length(pariahIndex) > 0) seqnames <- seqnames[- pariahIndex] userMask <- reduce(BSParams@userMask) sapply(seqnames, processSeqname, ..., simplify=BSParams@simplify) } BSgenome/R/export-methods.R0000644000175400017540000000463613175713516016627 0ustar00biocbuildbiocbuild### ========================================================================= ### Some "export" methods for BSgenome objects ### ------------------------------------------------------------------------- ### ### Note: the export() generic is defined in the rtracklayer package. ### ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Export as FASTA file ### ### This is exported but not yet documented. ### TODO: Document this in export-methods.Rd (add \usage entry). writeBSgenomeToFasta <- function(x, filepath, compress=FALSE, compression_level=NA, verbose=TRUE) { if (!is(x, "BSgenome")) stop("'x' must be a BSgenome object") if (!isTRUEorFALSE(verbose)) stop("'verbose' must be TRUE or FALSE") append <- FALSE for (seqname in seqnames(x)) { dna <- x[[seqname]] masks(dna) <- NULL dna <- DNAStringSet(dna) names(dna) <- seqname if (verbose) cat("writing", seqname, "sequence to file ... ") writeXStringSet(dna, filepath=filepath, append=append, compress=compress, compression_level=compression_level) if (verbose) cat("OK\n") append <- TRUE } } setMethod("export", c("BSgenome", "FastaFile"), function(object, con, format, compress=FALSE, compression_level=NA, verbose=TRUE) { writeBSgenomeToFasta(object, path(con), compress=compress, compression_level=compression_level, verbose=verbose) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Export as twoBit file ### ### This is exported but not yet documented. ### TODO: Document this in export-methods.Rd (add \usage entry). writeBSgenomeToTwobit <- function(x, filepath, ...) { i <- 0L object <- bsapply( new("BSParams", X=x, FUN=function(chr) { i <<- i + 1 rtracklayer:::.DNAString_to_twoBit(chr, seqnames(x)[i]) })) invisible(rtracklayer:::.TwoBits_export(object, filepath)) } setMethod("export", c("BSgenome", "TwoBitFile"), function(object, con, format, ...) { if (!missing(format)) rtracklayer:::checkArgFormat(con, format) writeBSgenomeToTwobit(object, rtracklayer:::twoBitPath(path(con)), ...) } ) BSgenome/R/getSeq-methods.R0000644000175400017540000003676413175713516016545 0ustar00biocbuildbiocbuild### ========================================================================= ### The "getSeq" method for BSgenome objects. ### ------------------------------------------------------------------------- ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Low-level helpers called by "getSeq" method for BSgenome objects. ### .normargStrand <- function(strand, length) { if (is(strand, "Rle")) strand <- as.vector(strand) if (is.factor(strand)) strand <- as.vector(strand) if (!is.character(strand)) stop("invalid 'strand'") lvls <- levels(strand()) if (!all(strand %in% lvls)) stop("strand values must be in '", paste(lvls, collapse="' '"), "'") if (length(strand) > length) stop("too many elements in 'strand'") if (length(strand) < length) { if (length(strand) == 0L) stop("cannot recycle zero-length 'strand'") strand <- S4Vectors:::recycleVector(strand, length) } strand } ### Make 'strand' star-free. ### If applied on the output of .normargStrand(), then returns a character ### vector guaranteed to have only "+" or "-" elements (no "*"). ### If applied on the output of strand(GRanges), then returns a 'factor' Rle ### guaranteed to have only "+" or "-" elements (no "*"). .starfreeStrand <- function(strand) { ustrand <- unique(strand) if (length(ustrand) == 1L && ustrand == "*") { ## Strand is "*" for all the elements. Replace it by "+". strand[] <- "+" return(strand) } if ("*" %in% ustrand) stop("cannot mix \"*\" with other strand values") strand } ### Assumes 'names' is a character vector. .normGetSeqArgs <- function(names, start, end, width, strand) { start <- IRanges:::.normargSEW(start, "start") end <- IRanges:::.normargSEW(end, "end") width <- IRanges:::.normargSEW(width, "width") l0 <- length(names) l1 <- length(start) l2 <- length(end) l3 <- length(width) max0123 <- max(l0, l1, l2, l3) ## Recycling will fail for vectors of length 0. names <- S4Vectors:::recycleVector(names, max0123) start <- S4Vectors:::recycleVector(start, max0123) end <- S4Vectors:::recycleVector(end, max0123) width <- S4Vectors:::recycleVector(width, max0123) strand <- .starfreeStrand(.normargStrand(strand, max0123)) list(names=names, start=start, end=end, width=width, strand=strand) } ### Assumes 'x' is a RangesList object with names. .newGRangesFromNamedRangesList <- function(x, strand) { seqnames <- rep.int(names(x), elementNROWS(x)) ranges <- unlist(x, use.names=FALSE) strand <- .normargStrand(strand, length(ranges)) GRanges(seqnames=seqnames, ranges=ranges, strand=strand) } ### Assumes 'x' is a Ranges object with names. .newGRangesFromNamedRanges <- function(x, strand) { strand <- .normargStrand(strand, length(x)) GRanges(seqnames=names(x), ranges=unname(x), strand=strand) } ### Error messages refer to 'x' as "names" because of the context in which ### .toGRanges() is called. .toGRanges <- function(x, strand) { if (is(x, "RangesList") || is(x, "Ranges")) { if (is.null(names(x))) stop("when 'names' is a RangesList or Ranges object, ", "it must be named with the sequence names") if (is(x, "RangesList")) ans <- .newGRangesFromNamedRangesList(x, strand) else ans <- .newGRangesFromNamedRanges(x, strand) return(ans) } stop("invalid 'names'") } .drop_unused_seqlevels <- function(x) { seqlevels(x) <- seqlevelsInUse(x) x } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### .extractFromBSgenomeSingleSequences() ### ### 'names' must be a character vector or a GRanges object. ### If 'names' is character vector, then 'start', 'end', 'width', and 'strand' ### are assumed to be already normalized (and star-free for 'strand'). ### Otherwise, they are ignored and 'strand(names)' is assumed to be star-free. .extractFromBSgenomeSingleSequences <- function(x, names, start, end, width, strand) { if (is.character(names)) { #idx <- which(is.na(start) & is.na(width)) #if (length(idx) != 0L) # start[idx] <- 1L #idx <- which(is.na(end) & is.na(width)) #if (length(idx) != 0L) # end[idx] <- unname(seqlengths(x)[names]) #ranges <- IRanges(start=start, end=end, width=width) refwidths <- seqlengths(x)[names] ranges <- solveUserSEW(refwidths, start=start, end=end, width=width) names <- GRanges(seqnames=names, ranges=ranges, strand=strand) } ## Check that 'seqlengths(names)' is compatible with 'x'. #if (!all(names(seqlengths(names)) %in% names(seqlengths(x)))) # stop("sequence names in GRanges are incompatible with BSgenome object") #if (!all(is.na(seqlengths(names))) # && !identical(seqlengths(names), # seqlengths(x)[names(seqlengths(names))])) # stop("sequence lengths in GRanges are incompatible ", # "with BSgenome object") ## Split 'names' by sequence names. grl <- split(names, seqnames(names)) grl_seqlevels <- names(grl) ## Loop over the sequence names and extract the ranges. dnaset_list <- lapply(seq_len(length(grl)), function(i) { gr <- grl[[i]] if (length(gr) == 0L) return(DNAStringSet()) seqlevel <- grl_seqlevels[i] is_circular <- isCircular(x)[[seqlevel]] idx <- match(seqlevel, x@user_seqnames) if (is.na(idx)) stop("invalid sequence name: ", seqlevel) seqname <- names(x@user_seqnames)[[idx]] if (is.null(snplocs(x, seqname))) { ## Try to grab the subject sequence from the cache. subject <- try(get(seqname, envir=x@.seqs_cache, inherits=FALSE), silent=TRUE) if (is(subject, "try-error")) { ## The subject sequence was not in the cache. ans <- loadSubseqsFromStrandedSequence( x@single_sequences, seqname, ranges(gr), strand(gr), is_circular) return(ans) } ## The subject sequence was in the cache. .linkToCachedObject(subject) <- .newLinkToCachedObject( seqname, x@.seqs_cache, x@.link_counts) } else { subject <- x[[seqlevel]] } masks(subject) <- NULL loadSubseqsFromStrandedSequence( subject, seqlevel, ranges(gr), strand(gr), is_circular) } ) ## "unsplit" 'dnaset_list'. unsplit_list_of_XVectorList("DNAStringSet", dnaset_list, as.factor(seqnames(names))) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### .extractFromBSgenomeMultipleSequences() ### ### Assumes that 'strand' is star-free. .getOneSeqFromBSgenomeMultipleSequences <- function(x, name, start, end, width, strand, exact.match) { nhits <- 0L for (mseqname in mseqnames(x)) { mseq <- x[[mseqname]] if (exact.match) { ii <- which(names(mseq) == name) } else { ii <- grep(name, names(mseq)) } if (nhits == 0L && length(ii) == 1L) subject <- mseq[[ii]] nhits <- nhits + length(ii) } if (nhits == 0L) stop("sequence ", name, " not found") if (nhits > 1L) stop("sequence ", name, " found more than once, ", "please use a non-ambiguous name") ans <- subseq(subject, start=start, end=end, width=width) if (strand == "+") return(xvcopy(ans)) else return(reverseComplement(ans)) } ### Assumes 'x' is a list of DNAString objects and turns it into a ### DNAStringSet object. ### TODO: Find a better way to do this (current implementation is not very ### efficient). Also maybe make this a "DNAStringSet" method for list objects. .listOfDNAStringToDNAStringSet <- function(x) { if (length(x) == 0L) return(DNAStringSet()) subject <- do.call(xscat, x) DNAStringSet(successiveViews(subject, elementNROWS(x))) } ### 'names' must be a character vector or a GRanges object. ### If 'names' is character vector, then 'start', 'end', 'width', and 'strand' ### are assumed to be already normalized (and star-free for 'strand'). ### Otherwise, they are ignored and 'strand(names)' is assumed to be star-free. .extractFromBSgenomeMultipleSequences <- function(x, names, start, end, width, strand) { if (is.character(names)) { ans <- lapply(seq_len(length(names)), function(i) .getOneSeqFromBSgenomeMultipleSequences(x, names[i], start[i], end[i], width[i], strand[i], exact.match=FALSE) ) } else { ans <- lapply(seq_len(length(names)), function(i) { name <- as.character(seqnames(names))[i] start <- start(names)[i] width <- width(names)[i] strand <- as.character(strand(names))[i] .getOneSeqFromBSgenomeMultipleSequences(x, name, start, NA, width, strand, exact.match=TRUE) } ) } .listOfDNAStringToDNAStringSet(ans) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "getSeq" generic and methods for BSgenome and XStringSet objects. ### setMethod("getSeq", "BSgenome", function(x, names, start=NA, end=NA, width=NA, strand="+", as.character=FALSE) { if (!isTRUEorFALSE(as.character)) stop("'as.character' must be TRUE or FALSE") if (missing(names)) { names <- seqnames(x) } else { if (is(names, "Rle")) names <- as.vector(names) if (is.factor(names)) names <- as.vector(names) } if (is.character(names)) { args <- .normGetSeqArgs(names, start, end, width, strand) sseq_idx <- args$names %in% seqnames(x) sseq_args <- list(names=args$names[sseq_idx], start=args$start[sseq_idx], end=args$end[sseq_idx], width=args$width[sseq_idx], strand=args$strand[sseq_idx]) mseq_idx <- !sseq_idx mseq_args <- list(names=args$names[mseq_idx], start=args$start[mseq_idx], end=args$end[mseq_idx], width=args$width[mseq_idx], strand=args$strand[mseq_idx]) } else { if (!identical(c(start, end, width), c(NA, NA, NA))) stop("'start', 'end' and 'width' can only be specified when ", "'names' is either missing, a character vector/factor, ", "a character-Rle, or a factor-Rle") if (is(names, "GRanges") || is(names, "GRangesList")) { if (!identical(strand, "+")) stop("'strand' cannot be specified ", "when 'names' is a GRanges or GRangesList object") if (is(names, "GRangesList")) { unlisted_names <- unlist(names, use.names=FALSE) unlisted_ans <- getSeq(x, unlisted_names, as.character=as.character) return(relist(unlisted_ans, names)) } } else { names <- .toGRanges(names, strand) } ## We don't need the result of merge(). By calling merge() here ## we're just making sure that 'x' and 'names' are based on ## compatible reference genomes (merge() will raise an error if ## they are not). merge(seqinfo(x), seqinfo(names)) strand(names) <- .starfreeStrand(strand(names)) seqnames <- as.character(seqnames(names)) sseq_idx <- seqnames %in% seqnames(x) sseq_args <- list(names=.drop_unused_seqlevels(names[sseq_idx])) mseq_idx <- !sseq_idx mseq_args <- list(names=names[mseq_idx]) } ans <- rep.int(DNAStringSet(""), length(sseq_idx)) ans[sseq_idx] <- .extractFromBSgenomeSingleSequences(x, sseq_args$names, sseq_args$start, sseq_args$end, sseq_args$width, sseq_args$strand) ans[mseq_idx] <- .extractFromBSgenomeMultipleSequences(x, mseq_args$names, mseq_args$start, mseq_args$end, mseq_args$width, mseq_args$strand) if (is(names, "GRanges")) names(ans) <- names(names) else if (is.character(names)) names(ans) <- names if (as.character) return(as.character(ans)) if (length(ans) == 1L && is.character(names)) return(ans[[1L]]) # turn 1st and unique element into DNAString ans } ) setMethod("getSeq", "XStringSet", function(x, names) { stopifnot(is.character(names) || is(names, "GRanges") || is(names, "GRangesList"), !is.null(names(x))) if (is.character(names)) { found <- names %in% names(x) regexNames <- unlist(lapply(names[!found], grep, names(x), value=TRUE)) names <- c(names[found], regexNames) return(x[names]) } else if (is(names, "GRangesList")) { gr <- unlist(names, use.names=FALSE) } else { gr <- names } ignoringStrand <- any(strand(gr) != "*") && !hasMethod(reverseComplement, class(x)) if (ignoringStrand) { warning("some strand(x) != '*' but ", "strand has no meaning for ", class(x)) } rl <- as(gr, "RangesList") ans <- relist(unsplit(x[rl], rep(seqnames(gr), width(gr))), PartitioningByWidth(width(gr))) if (!ignoringStrand) { minus <- strand(gr) == "-" ans[minus] <- reverseComplement(ans[minus]) } if (is(names, "GRangesList")) { ans <- relist(ans, names) } ans } ) setMethod("[", c("XStringSet", "GenomicRanges"), function (x, i, j, ..., drop = TRUE) { if (!missing(j)) stop("invalid subsetting") getSeq(x, i, ...) }) setMethod("[", c("XStringSet", "GRangesList"), function (x, i, j, ..., drop = TRUE) { if (!missing(j)) stop("invalid subsetting") unstrsplit(getSeq(x, i, ...)) }) BSgenome/R/injectSNPs.R0000644000175400017540000000320713175713516015656 0ustar00biocbuildbiocbuild### ========================================================================= ### SNP injection ### ------------------------------------------------------------------------- .keep_snps_packages <- function(pkgs) { idx1 <- which(substr(pkgs, 1, 8) == "SNPlocs.") idx2 <- which(substr(pkgs, 1, 12) == "XtraSNPlocs.") idx <- c(idx1, idx2) pkgs[idx] } installed.SNPs <- function() { pkgs <- installed.packages()[ , "Package"] pkgs <- .keep_snps_packages(pkgs) names(pkgs) <- NULL return(pkgs) } available.SNPs <- function(type=getOption("pkgType")) { contrib_url <- get_data_annotation_contrib_url(type) pkgs <- available.packages(contrib_url)[, "Package"] pkgs <- .keep_snps_packages(pkgs) names(pkgs) <- NULL return(pkgs) } setGeneric("injectSNPs", signature="x", function(x, snps) standardGeneric("injectSNPs") ) ### 'snps' can be a SNPlocs object or the name of a SNPlocs package. setMethod("injectSNPs", "BSgenome", function(x, snps) { if (!is.null(SNPlocs_pkgname(x))) stop("SNPs were already injected in genome 'x'. ", "Injecting from more than 1 package is not supported.") ans <- x ## We want the original sequence names, not the user sequence names, ## so we use 'seqnames(x@seqinfo)' instead of 'seqnames(x)'. ans@injectSNPs_handler <- InjectSNPsHandler(snps, x@pkgname, seqnames(x@seqinfo)) ans@.seqs_cache <- new.env(parent=emptyenv()) ans@.link_counts <- new.env(parent=emptyenv()) ans } ) BSgenome/R/utils.R0000644000175400017540000000254513175713516015002 0ustar00biocbuildbiocbuild### ========================================================================= ### Some low-level internal (i.e. non-exported) utilities ### ------------------------------------------------------------------------- get_data_annotation_contrib_url <- function(type=getOption("pkgType")) { ## The BiocInstaller package is needed for biocinstallRepos(). if (!requireNamespace("BiocInstaller", quietly=TRUE)) { ## Sourcing this file will install and load the BiocInstaller package. suppressWarnings(source("http://bioconductor.org/biocLite.R", local=TRUE)) } contrib.url(BiocInstaller::biocinstallRepos()["BioCann"], type=type) } ### TODO: Move this to GenomeInfoDb. read_seqinfo_table <- function(filepath, genome=NA) { df <- read.table(filepath, stringsAsFactors=FALSE) seqnames <- df[[1L]] Seqinfo( seqnames=seqnames, seqlengths=df[[2L]], isCircular=df[[3L]], genome=genome ) } ### Encode/decode character vector of single letters as/from raw object. ### Used in SNPlocs packages to store IUPAC ambiguity letters on disk as ### a raw vector with 1 byte per letter. Alternatively a DNAString object ### could be used for that! encode_letters_as_bytes <- function(x) charToRaw(paste(x, collapse="")) decode_bytes_as_letters <- function(x) rawToChar(x, multiple=TRUE) BSgenome/TODO0000644000175400017540000000436713175713516014012 0ustar00biocbuildbiocbuild- Try harder to reproduce the following issue with parallel retrieval of sequences. Reported by email directly to me by Juri Reimand on 2014/11/19. Systems I tried this so far: OS R BioC could reproduce? petty Snow Leopard 3.2.2 3.1 no morelia Mavericks 3.2.2 3.1 no perceval Snow Leopard 3.2.2 3.2 no rhino04 Ubuntu 14.04.2 LTS 3.2.0 3.2 no rhino04 Ubuntu 14.04.2 LTS 3.2.0 3.1 no latitude Ubuntu 14.04.3 LTS 3.2.1 3.2 no latitude Ubuntu 14.04.3 LTS 3.2.1 3.1 no latitude Ubuntu 14.04.3 LTS 3.1.2 3.0 no latitude Ubuntu 14.04.3 LTS 3.1.1 2.14 no #+begin_src R ## test_mclapply_on_BSgenome.R file send by Juri Reimand on 2014/11/19 library(parallel) library(Biostrings) library(BSgenome) library(BSgenome.Hsapiens.UCSC.hg19) # simulate some DNA coordinates dfr = data.frame(chr=paste0("chr", rep(1:10, each=100)), pos=round(1e6*runif(1000))+1e6, stringsAsFactors=F) # fetch nucleotides with one command test_ref_all = getSeq(Hsapiens, dfr$chr, dfr$pos, dfr$pos, as.character=TRUE) # function to fetch nucleotides one by one get_seq = function(i, dfr) { cat('.') getSeq(Hsapiens, dfr[i,"chr"], dfr[i,"pos"], dfr[i,"pos"], as.character=T) } # use above function to retrieve nucleotides using single processor core test_ref_single_core = sapply(1:nrow(dfr), get_seq, dfr) # use above function to retrieve nucleotides using multiple processor cores test_ref_multicore = unlist(mclapply(1:nrow(dfr), get_seq, dfr, mc.cores=8)) table(test_ref_all==test_ref_single_core) #TRUE #1000 table(test_ref_multicore==test_ref_single_core) #FALSE TRUE # 23 977 R.Version() #$platform #[1] "x86_64-apple-darwin10.8.0" # #$arch #[1] "x86_64" # #$os #[1] "darwin10.8.0" # #$system #[1] "x86_64, darwin10.8.0" # #$status #[1] "" # #$major #[1] "3" # #$minor #[1] "1.0" # #$year #[1] "2014" # #$month #[1] "04" # #$day #[1] "10" # #$`svn rev` #[1] "65387" # #$language #[1] "R" # #$version.string #[1] "R version 3.1.0 (2014-04-10)" # #$nickname #[1] "Spring Dance" #+end_src BSgenome/build/0000755000175400017540000000000013175725526014413 5ustar00biocbuildbiocbuildBSgenome/build/vignette.rds0000644000175400017540000000052113175725526016750 0ustar00biocbuildbiocbuild}Q]O0CFbX|7Dɲ M|m@#57@p~s雃"ÜLc.K.nzABȩ/ʄ[^ axҥ{oEqۊ (IpAwP]t,dK*@5)^2QR&<2(xl6u{1X u}}?:xz}[A*2_WJ7lk؎:5T```Q?`OtlIY&|mN@3G@o?ӯZѐh^Vou5MNf 2qBSgenome/inst/0000755000175400017540000000000013175725526014271 5ustar00biocbuildbiocbuildBSgenome/inst/doc/0000755000175400017540000000000013175725526015036 5ustar00biocbuildbiocbuildBSgenome/inst/doc/BSgenomeForge.R0000644000175400017540000000374713175725450017652 0ustar00biocbuildbiocbuild### R code from vignette source 'BSgenomeForge.Rnw' ### Encoding: UTF-8 ################################################### ### code chunk number 1: BSgenomeForge.Rnw:193-196 ################################################### library(Biostrings) file <- system.file("extdata", "ce2chrM.fa.gz", package="BSgenome") fasta.seqlengths(file) ################################################### ### code chunk number 2: BSgenomeForge.Rnw:429-440 ################################################### library(BSgenome) seed_files <- system.file("extdata", "GentlemanLab", package="BSgenome") tail(list.files(seed_files, pattern="-seed$")) ## Display seed file for musFur1: musFur1_seed <- list.files(seed_files, pattern="\\.musFur1-seed$", full.names=TRUE) cat(readLines(musFur1_seed), sep="\n") ## Display seed file for rn4: rn4_seed <- list.files(seed_files, pattern="\\.rn4-seed$", full.names=TRUE) cat(readLines(rn4_seed), sep="\n") ################################################### ### code chunk number 3: BSgenomeForge.Rnw:453-455 (eval = FALSE) ################################################### ## library(BSgenome) ## forgeBSgenomeDataPkg("path/to/my/seed") ################################################### ### code chunk number 4: BSgenomeForge.Rnw:678-683 ################################################### library(BSgenome) seed_files <- system.file("extdata", "GentlemanLab", package="BSgenome") tail(list.files(seed_files, pattern="\\.masked-seed$")) rn4_masked_seed <- list.files(seed_files, pattern="\\.rn4\\.masked-seed$", full.names=TRUE) cat(readLines(rn4_masked_seed), sep="\n") ################################################### ### code chunk number 5: BSgenomeForge.Rnw:698-700 (eval = FALSE) ################################################### ## library(BSgenome) ## forgeMaskedBSgenomeDataPkg("path/to/my/seed") ################################################### ### code chunk number 6: BSgenomeForge.Rnw:742-743 ################################################### sessionInfo() BSgenome/inst/doc/BSgenomeForge.Rnw0000644000175400017540000007745013175713516020221 0ustar00biocbuildbiocbuild%\VignetteIndexEntry{How to forge a BSgenome data package} %\VignetteKeywords{Genome, BSgenome, DNA, Sequence, UCSC, BSgenome data package} %\VignettePackage{BSgenome} % % NOTE -- ONLY EDIT THE .Rnw FILE!!! The .tex file is % likely to be overwritten. % \SweaveOpts{keep.source=TRUE} \documentclass[10pt]{article} %\usepackage{amsmath} %\usepackage[authoryear,round]{natbib} % % NOTE -- There is an obscure issue with the use of \url from the hyperref % package that will trigger a MiKTeX/pdflatex error: % ! pdfTeX error (ext4): \pdfendlink ended up in different nesting level than \pd % fstartlink. % \AtBegShi@Output ...ipout \box \AtBeginShipoutBox % \fi \fi % l.96 \end{document} % % ! ==> Fatal error occurred, no output PDF file produced! % Transcript written on BSgenomeForge1.log. % The error is hard to reproduce. I've observed it on the r34270 version of this % vignette and with the following version of the MiKTeX/pdflatex command: % MiKTeX-pdfTeX 2.7.3147 (1.40.9) (MiKTeX 2.7) \usepackage{hyperref} \usepackage{underscore} \textwidth=6.5in \textheight=8.5in \parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \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}} \bibliographystyle{plainnat} \begin{document} \title{How to forge a BSgenome data package} \author{Herv\'e Pag\`es \\ Gentleman Lab \\ Fred Hutchinson Cancer Research Center \\ Seattle, WA} \date{\today} \maketitle \tableofcontents %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \section{Introduction} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% IMPORTANT NOTE: Starting with Bioconductor 2.14, the \Rfunction{forgeBSgenomeDataPkg} function doesn't handle masks anymore i.e. now it produces a \term{BSgenome data package} that contains only the bare sequences. A new function \Rfunction{forgeMaskedBSgenomeDataPkg} has been added to forge a \term{BSgenome data package} with masked sequences. This vignette has been updated to reflect these changes. This vignette describes the process of forging a \term{BSgenome data package}. It is intended for Bioconductor users who want to make a new \term{BSgenome data package}, not for regular users of these packages. Start {\R} (make sure you are using the latest release version), load the \Rpackage{BSgenome} package, and use the \Rfunction{available.genomes} function to get the list of \term{BSgenome data packages} available in the current release version of Bioconductor. So you confirm that none of those genomes suits your needs? And you want to make your own package? If you answer yes to these 2 questions, then you've come to the right place. Requirements: \begin{itemize} \item Some basic knowledge of the Unix/Linux command line is required. The commands that you will most likely need are: \code{cd}, \code{mkdir}, \code{mv}, \code{rmdir}, \code{tar}, \code{gunzip}, \code{unzip}, \code{ftp} and \code{wget}. Also you will need to create and edit some text files. \item You need access to a good Unix/Linux build machine with a decent amount of RAM (>= 4GB), especially if your genome is big. For smaller genomes, 2GB or even 1GB of RAM might be enough. \item You need the latest release versions of {\R} plus the \Rpackage{Biostrings} and \Rpackage{BSgenome} packages installed on the build machine. To check your installation, start {\R} and try to load the \Rpackage{BSgenome} package. \item Finally, you need to obtain the \term{source data files} of the genome that you want to build a package for. There are 2 groups of \term{source data files}: (1) the files containing the sequence data (those files are required), and (2) the files containing the mask data (those files are optional). For most organisms, these files have been made publicly available on the internet by genome providers like UCSC, NCBI, FlyBase, TAIR, etc. The next sections of this vignette explain how to obtain and prepare these files. \end{itemize} Refer to the \textit{R Installation and Administration} manual \footnote{\url{http://cran.r-project.org/doc/manuals/R-admin.html}} if you need to install {\R} or upgrade your {\R} version, and to the \textit{Bioconductor - Install} page \footnote{\url{http://bioconductor.org/install/}} on the Bioconductor website if you need to install or update the \Rpackage{Biostrings} or \Rpackage{BSgenome} packages. Questions, comments or bug reports about this vignette or about the BSgenomeForge functions are welcome. Please address them to the author (\code{hpages@fredhutch.org}) or post them on the Bioconductor support site \footnote{\url{https://support.bioconductor.org/}}. In the next section (``How to forge a BSgenome data package with bare sequences''), we describe how to forge a \term{BSgenome data package} with sequences that have no masks on them. If this is what you're after, then you'll be done at the end of the section. Only if you need to forge a package with masked sequences, you'll have to keep reading but you'll have to forge a \term{BSgenome data package} with bare sequences first. In this vignette, we call \term{target packages} the \term{BSgenome data packages} that we're going to forge (one target package with bare sequences and possibly a 2nd target package with masked sequences). %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \section{How to forge a BSgenome data package with bare sequences} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \subsection{Obtain and prepare the sequence data} \subsubsection{What do I need?} The sequence data must be in a single twoBit file (e.g. \textit{musFur1.2bit}) or in a collection of FASTA files (possibly gzip-compressed). If the latter, then you need 1 FASTA file per sequence that you want to put in the \term{target package}. In that case the name of each FASTA file must be of the form \textit{}\textit{}\textit{} where \textit{} is the name of the sequence in it and \textit{} and \textit{} are a prefix and a suffix (possibly empty) that are the same for all the FASTA files. \subsubsection{Examples} UCSC provides the genome sequences for Stickleback (gasAcu1) in various forms: (a) as a twoBit file (\textit{gasAcu1.2bit} located in \url{http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/bigZips/}, (b) as a big compressed tarball containing one file per chromosome (\textit{chromFa.tar.gz} located in the same folder), and (c) as a collection of compressed FASTA files (\texttt{chrI.fa.gz}, \texttt{chrII.fa.gz}, \texttt{chrIII.fa.gz}, ..., \texttt{chrXXI.fa.gz}, \texttt{chrM.fa.gz} and \texttt{chrUn.fa.gz} located in \url{http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/chromosomes/}). To forge a \term{BSgenome data package} for gasAcu1, the easiest would be to use (a) (the twoBit file). However it would also be possible to use (c) (the collection of compressed FASTA files). In that case the suffix would need to be set to \texttt{.fa.gz}. Note that the prefix here is empty and not \texttt{chr}, because \texttt{chr} is considered to be part of the sequence names (a commonly used chromosome naming convention at UCSC). Alternatively, the big compressed tarball (\texttt{chromFa.tar.gz}) could be used. After downloading and extracting it, we should end up with the same files as with (c). You can use the \Rfunction{fasta.seqlengths} function from the \Rpackage{Biostrings} package to get the lengths of the sequences in a FASTA file: <<>>= library(Biostrings) file <- system.file("extdata", "ce2chrM.fa.gz", package="BSgenome") fasta.seqlengths(file) @ For the \Rpackage{BSgenome.Mfuro.UCSC.musFur1} package, the twoBit file was used and downloaded with: \begin{verbatim} wget http://hgdownload.soe.ucsc.edu/goldenPath/musFur1/bigZips/musFur1.2bit \end{verbatim} For the \Rpackage{BSgenome.Rnorvegicus.UCSC.rn4} package, the big compressed tarball was used. It was downloaded and extracted with: \begin{verbatim} wget http://hgdownload.cse.ucsc.edu/goldenPath/rn4/bigZips/chromFa.tar.gz tar zxf chromFa.tar.gz \end{verbatim} \subsubsection{The \textit{} folder} So we assume that you've downloaded the \term{sequence data files} and that they are now located in a folder on your machine\footnote{Note that checking the md5sums after download is always a good idea.}. From now on, we'll refer to this folder as the \textit{} folder. Depending on what data files you downloaded (see previous sub-subsection), you might also need to extract and possibly rename the files. Note that all the \term{sequence data files} should be located directly in the \textit{} folder, not in subfolders of this folder. For example, depending on the genome, UCSC provides either a big \texttt{chromFa.tar.gz} or \texttt{chromFa.zip} file that contains the sequence data for all the chromosomes. But it could be that, after extraction of this big file, the individual FASTA files for each chromosome end up being located one level down the \textit{} folder (granted that you were in this folder when you extracted the file). If this is the case, then you will need to move them one level up (use \code{mv -i */*.fa .} for this, then remove all the empty subfolders with \code{rmdir *}). \subsection{Prepare the BSgenome data package seed file} \subsubsection{Overview} The \term{BSgenome data package seed file} will contain all the information needed by the \Rfunction{forgeBSgenomeDataPkg} function to forge the \term{target package}. The format of this file is DCF (Debian Control File), which is also the format used for the \texttt{DESCRIPTION} file of any {\R} package. The valid fields of a \term{seed file} are divided in 3 categories: \begin{enumerate} \item Standard \texttt{DESCRIPTION} fields. These fields are actually the mandatory fields found in any \texttt{DESCRIPTION} file. They will be copied to the \texttt{DESCRIPTION} file of the \term{target package}. \item Non-standard \texttt{DESCRIPTION} fields. These fields are specific to \term{seed files} and they will also be copied to the \texttt{DESCRIPTION} file of the \term{target package}. In addition, the values of these fields will be stored in the \Rclass{BSgenome} object that will be contained in the \term{target package}. This means that the users of the \term{target package} will be able to retrieve these values via the accessor methods defined for \Rclass{BSgenome} objects. See the man page for the \Rclass{BSgenome} class (\code{{?}`BSgenome-class`}) for a description of these methods. \item Additional fields that don't fall in the first 2 categories. \end{enumerate} The 3 following sub-subsections give an extensive description of all the valid fields of a \term{seed file}. Alternatively, the reader in a hurry can go directly to the last sub-subsection of this subsection for an example of a \term{seed file}. \subsubsection{Standard \texttt{DESCRIPTION} fields} \begin{itemize} \item \code{Package}: Name to give to the \term{target package}. The convention used for the packages built by the Bioconductor project is to use a name made of 4 parts separated by a dot. Part 1 is always \code{BSgenome}. Part 2 is the abbreviated name of the organism (when the name of the organism is made of 2 words, we put together the first letter of the first word in upper case followed by the entire second word in lower case e.g. \code{Rnorvegicus}). Part 3 is the name of the organisation who provided the genome (e.g. \code{UCSC}). Part 4 is the release string or number used by this organisation to identify this version of the genome (e.g. \code{rn4}). \item \code{Title}: The title of the \term{target package}. E.g. \code{Full genome sequences for Rattus norvegicus (UCSC version rn4)}. \item \code{Description}, \code{Version}, \code{Author}, \code{Maintainer}, \code{License}: Like the 2 previous fields, these are mandatory fields found in any \texttt{DESCRIPTION} file. Please refer to the \textit{The DESCRIPTION file} subsection of the \textit{Writing R Extensions} manual \footnote{\url{http://cran.r-project.org/doc/manuals/R-exts.html\#The-DESCRIPTION-file}} for more information about these fields. If you plan to distribute the \term{target package} that you are about to forge, please pickup the license carefully and make sure that it is compatible with the license of the \term{sequence data files} if any. \item \code{Suggests}: [OPTIONAL] If you're going to add examples to the \code{Examples} section of the \term{target package} (see \code{PkgExamples} field below for how to do this), use this field to list the packages used in these examples. \end{itemize} \subsubsection{Non-standard \texttt{DESCRIPTION} fields} \begin{itemize} \item \code{organism}: The scientific name of the organism in the format \code{Genus species} (e.g. \code{Rattus norvegicus}, \code{Homo sapiens}) or \code{Genus species subspecies} (e.g. \code{Homo sapiens neanderthalensis}). \item \code{common\_name}: The common name of the organism (e.g. \code{Rat} or \code{Human}). For organisms that have more than one commmon name (e.g. \code{Bovine} or \code{Cow} for Bos taurus), choose one. Note that for the packages built by the Bioconductor project from a UCSC genome, this field corresponds to the \code{SPECIES} column of the \textit{List of UCSC genome releases} table \footnote{\url{http://genome.ucsc.edu/FAQ/FAQreleases\#release1}}. \item \code{provider}: The provider of the \term{sequence data files} e.g. \code{UCSC}, \code{NCBI}, \code{BDGP}, \code{FlyBase}, etc... Should preferably match part 3 of the package name (field \code{Package}). \item \code{provider\_version}: The provider-side version of the genome. Should preferably match part 4 of the package name (field \code{Package}). For the packages built by the Bioconductor project from a UCSC genome, this field corresponds to the \code{UCSC VERSION} field of the \textit{List of UCSC genome releases} table. \item \code{release\_date}: When this assembly of the genome was released. For the packages built by the Bioconductor project from a UCSC genome, this field corresponds to the \code{RELEASE DATE} field of the \textit{List of UCSC genome releases} table. \item \code{release\_name}: The release name or build number of this assembly of the genome. For the packages built by the Bioconductor project from a UCSC genome, this field corresponds to the \code{RELEASE NAME} field of the \textit{List of UCSC genome releases} table. \item \code{source\_url}: The permanent URL where the \term{sequence data files} used to forge the \term{target package} can be found. \item \code{organism\_biocview}: The official biocViews term for this organism. This is generally the same as the \code{organism} field except that spaces should be replaced by underscores. The value of this field matters only if the \term{target package} is going to be added to a Bioconductor repository since it will determine under which subview of the \textit{Bioconductor Task View} for \textit{Organism} \footnote{\url{http://bioconductor.org/packages/release/Organism.html}} the package will appear. Note that this is the only field in this category that won't be stored in the \Rclass{BSgenome} object that will be contained in the \term{target package}. \end{itemize} \subsubsection{Other fields} \begin{itemize} \item \code{BSgenomeObjname}: Should match part 2 of the package name (see \code{Package} field above). \item \code{seqnames}: [OPTIONAL] Needed only if you are using a collection of \term{sequence data files}. In that case \code{seqnames} must be an {\R} expression returning the names of the single sequences to forge (in a character vector). E.g. \code{paste("chr", c(1:20, "X", "M", "Un", paste(c(1:20, "X", "Un"), "\_random", sep="")), sep="")}. \item \code{circ\_seqs}: [OPTIONAL] An {\R} expression returning the names of the circular sequences (in a character vector). If the \code{seqnames} field is specified, then \code{circ\_seqs} must be a subset of it. E.g. \code{"chrM"} for rn4 or \code{c("chrM", "2micron")} for the sacCer2 genome (Yeast) from UCSC. The default value for \code{circ\_seqs} is \code{NULL} (no circular sequence). \item \code{mseqnames}: [OPTIONAL] An {\R} expression returning the names of the multiple sequences to forge (in a character vector). E.g. \code{c("random", "chrUn")} for \code{rn5}. The default value for \code{mseqnames} is \code{NULL} (no multiple sequence). \item \code{PkgDetails}: [OPTIONAL] Some arbitrary text that will be copied to the \code{Details} section of the man page of the \term{target package}. \item \code{SrcDataFiles}: [OPTIONAL] Some arbitrary text that will be copied to the \code{Note} section of the man pages of the \term{target package}. \code{SrcDataFiles} should describe briefly where the \term{sequence data files} are coming from. Will typically contain URLs (permanent URLs are a must). \item \code{PkgExamples}: [OPTIONAL] Some {\R} code (possibly with comments) that will be added to the \code{Examples} section of the man page of the \term{target package}. Don't forget to list the packages used in these examples in the \code{Suggests} field. \item \code{seqs\_srcdir}: The absolute path to the folder containing the \term{sequence data files}. \item \code{seqfile\_name}: Required if the \term{sequence data files} is a single twoBit file (e.g. \code{musFur1.2bit}). Ignored otherwise. \item \code{seqfiles\_prefix}, \code{seqfiles\_suffix}: [OPTIONAL] Needed only if you are using a collection of \term{sequence data files}. The common prefix and suffix that need to be added to all the sequence names (fields \code{seqnames} and \code{mseqnames}) to get the name of the corresponding FASTA file. Default values are the empty prefix for \code{seqfiles\_prefix} and \code{.fa} for \code{seqfiles\_suffix}. \item \code{ondisk\_seq\_format}: [OPTIONAL] Specifies how the single sequences should be stored in the \term{target package}. Can be \code{2bit}, \code{rda}, \code{fa.rz}, or \code{fa}. If \code{2bit} (the default), then all the single sequences are stored in a single twoBit file. If \code{rda}, then each single sequence is stored in a separated serialized \Rclass{XString} object (one per single sequence). If \code{fa.rz} or \code{fa}, then all the single sequences are stored in a single FASTA file (compressed in the RAZip format if \code{fa.rz}). \end{itemize} \subsubsection{An example} The \term{seed files} used for the packages forged by the Bioconductor project are included in the \Rpackage{BSgenome} package: <<>>= library(BSgenome) seed_files <- system.file("extdata", "GentlemanLab", package="BSgenome") tail(list.files(seed_files, pattern="-seed$")) ## Display seed file for musFur1: musFur1_seed <- list.files(seed_files, pattern="\\.musFur1-seed$", full.names=TRUE) cat(readLines(musFur1_seed), sep="\n") ## Display seed file for rn4: rn4_seed <- list.files(seed_files, pattern="\\.rn4-seed$", full.names=TRUE) cat(readLines(rn4_seed), sep="\n") @ From now we assume that you have managed to prepare the \term{seed file} for your \term{target package}. \subsection{Forge the \term{target package}} To forge the \term{target package}, start \R, load the \Rpackage{BSgenome} package, and call the \Rfunction{forgeBSgenomeDataPkg} function on your \term{seed file}. For example, if the path to your \term{seed file} is \texttt{"path/to/my/seed"}, do: <>= library(BSgenome) forgeBSgenomeDataPkg("path/to/my/seed") @ Depending on the size of the genome and your hardware, this can take between 2 minutes and 1 or 2 hours. By default \Rfunction{forgeBSgenomeDataPkg} will create the source tree of the \term{target package} in the current directory. Once \Rfunction{forgeBSgenomeDataPkg} is done, ignore the warnings (if any), quit \R, and build the source package (tarball) with \begin{verbatim} R CMD build \end{verbatim} where \code{} is the path to the source tree of the package. Then check the package with \begin{verbatim} R CMD check \end{verbatim} where \code{} is the path to the tarball produced by \code{R CMD build}. Finally install the package with \begin{verbatim} R CMD INSTALL \end{verbatim} and use it! %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \section{How to forge a BSgenome data package with masked sequences} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \subsection{Obtain and prepare the mask data} \subsubsection{What do I need?} The mask data are not available for all organisms. What you download exactly depends of course on what's available and also on what built-in masks you want to have in the \term{2nd target package}. 4 kinds of built-in masks are currently supported by BSgenomeForge: \begin{itemize} \item the masks of assembly gaps, aka ``the AGAPS masks''; \item the masks of intra-contig ambiguities, aka ``the AMB masks''; \item the masks of repeat regions that were determined by the RepeatMasker software, aka ``the RM masks''; \item the masks of repeat regions that were determined by the Tandem Repeats Finder software (where only repeats with period less than or equal to 12 were kept), aka ``the TRF masks''. \end{itemize} For the AGAPS masks, you need UCSC ``gap'' or NCBI ``agp'' files. It can be one file per chromosome or a single big file containing the assembly gap information for all the chromosomes together. In the former case, the name of each file must be of the form \textit{}\textit{}\textit{}. Like for the FASTA files in group 1, \textit{} must be the name of the sequence (sequence names for FASTA files and AGAPS masks must match) and \textit{} and \textit{} must be a prefix and a suffix (possibly empty) that are the same for all the files (this prefix/suffix doesn't need to be, and typically is not, the same as for the FASTA files in group 1). You don't need any file for the AMB masks. For the RM masks, you need RepeatMasker \texttt{.out} files. Like for the AGAPS masks, it can be one file per chromosome or a single big file containing the RepeatMasker information for all the chromosomes together. In the former case, the name of each file must also be of the form \textit{}\textit{}\textit{}. Same comments apply as for the AGAPS masks above. For the TRF masks, you need Tandem Repeats Finder \texttt{.bed} files. Again, it can be one file per chromosome or a single big file. In the former case, the name of each file must also be of the form \textit{}\textit{}\textit{}). Same comments apply as for the AGAPS masks above. Again, for some organisms none of the masks above are available or only some of them are. \subsubsection{An example} Here is how the \term{mask data files} for the \Rpackage{BSgenome.Rnorvegicus.UCSC.rn4} package were obtained and prepared: \begin{itemize} \item AGAPS masks: all the \texttt{chr*\_gap.txt.gz} files (UCSC ``gap'' files) were downloaded from the UCSC \textit{database} folder \footnote{\url{http://hgdownload.cse.ucsc.edu/goldenPath/rn4/database/}} for \code{rn4}. This was done with the standard Unix/Linux \code{ftp} command: \begin{verbatim} ftp hgdownload.cse.ucsc.edu # login as "anonymous" cd goldenPath/rn4/database prompt mget chr*_gap.txt.gz \end{verbatim} Then all the downloaded files were uncompressed with: \begin{verbatim} for file in chr*_gap.txt.gz; do gunzip $file ; done \end{verbatim} \item RM masks: file \texttt{chromOut.tar.gz} was downloaded from the UCSC \textit{bigZips} folder and extracted with: \begin{verbatim} tar zxf chromOut.tar.gz \end{verbatim} \item TRF masks: file \texttt{chromTrf.tar.gz} was downloaded from the UCSC \textit{bigZips} folder and extracted with: \begin{verbatim} tar zxf chromTrf.tar.gz \end{verbatim} \end{itemize} \subsubsection{The \textit{} folder} From now we assume that you've downloaded (checking the md5sums is always a good idea) and possibly extracted all the \term{mask data files}, and that they are located in the \textit{} folder. Note that all the \term{mask data files} should be located directly in the \textit{} folder, not in subfolders of this folder. \subsection{Prepare the seed file for the masked BSgenome data package} \subsubsection{Overview} The \term{seed file} for the \term{BSgenome data package} with masked sequences (i.e. \term{2nd target package}) is similar to the \term{seed file} for the \term{BSgenome data package} containing the corresponding bare sequences (a.k.a. the \term{reference target package} i.e. the package you forged in the previous section). It will contain all the information needed by the \Rfunction{forgeMaskedBSgenomeDataPkg} function to forge the \term{2nd target package}. The fields of this \term{seed file} are described in the 3 following sub-subsections. Alternatively, the reader in a hurry can go directly to the last sub-subsection of this subsection for an example of \term{seed file}. \subsubsection{Standard \texttt{DESCRIPTION} fields} \begin{itemize} \item \code{Package}: Name to give to the \term{2nd target package}. The convention used for the packages built by the Bioconductor project is to use the same name as the \term{reference target package} with the \code{.masked} suffix added to it. \item \code{Title}: The title of the package. E.g. \code{Full masked genome sequences for Rattus norvegicus (UCSC version rn4)}. \item \code{Description}, \code{Version}, \code{Author}, \code{Maintainer}, \code{License}: See previous section. \end{itemize} \subsubsection{Non-standard \texttt{DESCRIPTION} fields} \begin{itemize} \item \code{organism\_biocview}: Same as for the \term{reference target package}. \item \code{source\_url}: The permanent URL where the \term{mask data files} used to forge this package can be found. \end{itemize} \subsubsection{Other fields} \begin{itemize} \item \code{RefPkgname}: The name of the \term{reference target package}. \item \code{nmask\_per\_seq}: The number of masks per sequence (1 to 4). \item \code{PkgDetails}, \code{PkgExamples}: See previous section. \item \code{SrcDataFiles}: [OPTIONAL] Some arbitrary text that will be copied to the \code{Note} section of the man pages of the \term{target package}. \code{SrcDataFiles} should describe briefly where the \term{mask data files} are coming from. Will typically contain URLs (permanent URLs are a must). \item \code{masks\_srcdir}: The path to the \textit{} folder. \item \code{AGAPSfiles\_type}: [OPTIONAL] Must be \code{gap} (the default) if the \term{source data files} containing the AGAPS masks information are UCSC ``gap'' files, or \code{agp} if they are NCBI ``agp'' files. \item \code{AGAPSfiles\_name}: [OPTIONAL] Omit this field if you have one \term{source data file} per single sequence for the AGAPS masks and use the \code{AGAPSfiles\_prefix} and \code{AGAPSfiles\_suffix} fields below instead. Otherwise, use this field to specify the name of the single big file. \item \code{AGAPSfiles\_prefix}, \code{AGAPSfiles\_suffix}: [OPTIONAL] Omit these fields if you have one single big \term{source data file} for all the AGAPS masks and use the \code{AGAPSfiles\_name} field above instead. Otherwise, use these fields to specify the common prefix and suffix that need to be added to all the single sequence names (field \code{seqnames}) to get the name of the file that contains the corresponding AGAPS mask information. Default values are the empty prefix for \code{AGAPSfiles\_prefix} and \code{\_gap.txt} for \code{AGAPSfiles\_suffix}. \item \code{RMfiles\_name}, \code{RMfiles\_prefix}, \code{RMfiles\_suffix}: [OPTIONAL] Those fields work like the \code{AGAPSfiles*} fields above but for the RM masks. Default values are the empty prefix for \code{RMfiles\_prefix} and \texttt{.fa.out} for \code{RMfiles\_suffix}. \item \code{TRFfiles\_name}, \code{TRFfiles\_prefix}, \code{TRFfiles\_suffix}: [OPTIONAL] Those fields work like the \code{AGAPSfiles*} fields above but for the TRF masks. Default values are the empty prefix for \code{TRFfiles\_prefix} and \texttt{.bed} for \code{TRFfiles\_suffix}. \end{itemize} \subsubsection{An example} The \term{seed files} used for the packages forged by the Bioconductor project are included in the \Rpackage{BSgenome} package: <<>>= library(BSgenome) seed_files <- system.file("extdata", "GentlemanLab", package="BSgenome") tail(list.files(seed_files, pattern="\\.masked-seed$")) rn4_masked_seed <- list.files(seed_files, pattern="\\.rn4\\.masked-seed$", full.names=TRUE) cat(readLines(rn4_masked_seed), sep="\n") @ From now we assume that you have managed to prepare the \term{seed file} for the \term{2nd target package}. \subsection{Forge the \term{2nd target package}} To forge the package, start \R, make sure the \term{reference target package} is installed (try to load it), load the \Rpackage{BSgenome} package, and call the \Rfunction{forgeMaskedBSgenomeDataPkg} function on the \term{seed file} you made for the \term{2nd target package}. For example, if the path to your \term{seed file} is \texttt{"path/to/my/seed"}, do: <>= library(BSgenome) forgeMaskedBSgenomeDataPkg("path/to/my/seed") @ Depending on the size of the genome and your hardware, this can take between 2 minutes and 1 or 2 hours. By default \Rfunction{forgeMaskedBSgenomeDataPkg} will create the source tree of the \term{2nd target package} in the current directory. Once \Rfunction{forgeMaskedBSgenomeDataPkg} is done, ignore the warnings (if any), quit \R, and build the source package (tarball) with \begin{verbatim} R CMD build \end{verbatim} where \code{} is the path to the source tree of the package. Then check the package with \begin{verbatim} R CMD check \end{verbatim} where \code{} is the path to the tarball produced by \code{R CMD build}. Finally install the package with \begin{verbatim} R CMD INSTALL \end{verbatim} and use it! 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BSgenome/inst/doc/GenomeSearching.R0000644000175400017540000002745413175725526020233 0ustar00biocbuildbiocbuild### R code from vignette source 'GenomeSearching.Rnw' ### Encoding: UTF-8 ################################################### ### code chunk number 1: b1 ################################################### library(BSgenome.Celegans.UCSC.ce2) ls("package:BSgenome.Celegans.UCSC.ce2") genome <- BSgenome.Celegans.UCSC.ce2 genome ################################################### ### code chunk number 2: b2 ################################################### class(genome) ################################################### ### code chunk number 3: b3 ################################################### organism(genome) provider(genome) providerVersion(genome) seqnames(genome) mseqnames(genome) ################################################### ### code chunk number 4: b4 ################################################### genome$chrI ################################################### ### code chunk number 5: b5 ################################################### chrI <- genome$chrI length(chrI) ################################################### ### code chunk number 6: b6 ################################################### afI <- alphabetFrequency(chrI) afI sum(afI) == length(chrI) ################################################### ### code chunk number 7: b7 ################################################### p1 <- "ACCCAGGGC" countPattern(p1, chrI) ################################################### ### code chunk number 8: b8 ################################################### countPattern(p1, chrI, max.mismatch=1) ################################################### ### code chunk number 9: b9 ################################################### m1 <- matchPattern(p1, chrI, max.mismatch=1) m1[4:6] class(m1) ################################################### ### code chunk number 10: b10 ################################################### mismatch(p1, m1[4:6]) ################################################### ### code chunk number 11: b11 ################################################### p2 <- DNAString("AAGCCTAAGCCTAAGCCTAA") m2 <- matchPattern(p2, chrI, max.mismatch=2) m2[1:4] p2 == m2[1:4] mismatch(p2, m2[1:4]) ################################################### ### code chunk number 12: b12 ################################################### m2[p2 == m2] m2[p2 != m2] ################################################### ### code chunk number 13: c1 ################################################### ce2dict0_file <- system.file("extdata", "ce2dict0.fa", package="BSgenome") ce2dict0 <- readDNAStringSet(ce2dict0_file, "fasta") ce2dict0 ################################################### ### code chunk number 14: c2 ################################################### writeHits <- function(seqname, matches, strand, file="", append=FALSE) { if (file.exists(file) && !append) warning("existing file ", file, " will be overwritten with 'append=FALSE'") if (!file.exists(file) && append) warning("new file ", file, " will have no header with 'append=TRUE'") hits <- data.frame(seqname=rep.int(seqname, length(matches)), start=start(matches), end=end(matches), strand=rep.int(strand, length(matches)), patternID=names(matches), check.names=FALSE) write.table(hits, file=file, append=append, quote=FALSE, sep="\t", row.names=FALSE, col.names=!append) } runAnalysis1 <- function(dict0, outfile="") { library(BSgenome.Celegans.UCSC.ce2) genome <- BSgenome.Celegans.UCSC.ce2 seqnames <- seqnames(genome) seqnames_in1string <- paste(seqnames, collapse=", ") cat("Target:", providerVersion(genome), "chromosomes", seqnames_in1string, "\n") append <- FALSE for (seqname in seqnames) { subject <- genome[[seqname]] cat(">>> Finding all hits in chromosome", seqname, "...\n") for (i in seq_len(length(dict0))) { patternID <- names(dict0)[i] pattern <- dict0[[i]] plus_matches <- matchPattern(pattern, subject) names(plus_matches) <- rep.int(patternID, length(plus_matches)) writeHits(seqname, plus_matches, "+", file=outfile, append=append) append <- TRUE rcpattern <- reverseComplement(pattern) minus_matches <- matchPattern(rcpattern, subject) names(minus_matches) <- rep.int(patternID, length(minus_matches)) writeHits(seqname, minus_matches, "-", file=outfile, append=append) } cat(">>> DONE\n") } } ################################################### ### code chunk number 15: c3 ################################################### runAnalysis1(ce2dict0, outfile="ce2dict0_ana1.txt") ################################################### ### code chunk number 16: c4 ################################################### hits1 <- read.table("ce2dict0_ana1.txt", header=TRUE) nrow(hits1) ################################################### ### code chunk number 17: c5 ################################################### table(hits1$seqname) ################################################### ### code chunk number 18: c6 ################################################### hits1_table <- table(hits1$patternID) hits1_table ################################################### ### code chunk number 19: c7 ################################################### hits1_table[hits1_table == max(hits1_table)] # pattern(s) with more hits ################################################### ### code chunk number 20: c8 ################################################### setdiff(names(ce2dict0), hits1$patternID) # pattern(s) with no hits ################################################### ### code chunk number 21: c9 ################################################### plotGenomeHits <- function(bsgenome, seqnames, hits) { chrlengths <- seqlengths(bsgenome)[seqnames] XMAX <- max(chrlengths) YMAX <- length(seqnames) plot.new() plot.window(c(1, XMAX), c(0, YMAX)) axis(1) axis(2, at=seq_len(length(seqnames)), labels=rev(seqnames), tick=FALSE, las=1) ## Plot the chromosomes for (i in seq_len(length(seqnames))) lines(c(1, chrlengths[i]), c(YMAX + 1 - i, YMAX + 1 - i), type="l") ## Plot the hits for (i in seq_len(nrow(hits))) { seqname <- hits$seqname[i] y0 <- YMAX + 1 - match(seqname, seqnames) if (hits$strand[i] == "+") { y <- y0 + 0.05 col <- "red" } else { y <- y0 - 0.05 col <- "blue" } lines(c(hits$start[i], hits$end[i]), c(y, y), type="l", col=col, lwd=3) } } ################################################### ### code chunk number 22: c10 (eval = FALSE) ################################################### ## plotGenomeHits(genome, seqnames(genome), hits1) ################################################### ### code chunk number 23: d1 ################################################### library(hgu95av2probe) tmpseq <- DNAStringSet(hgu95av2probe$sequence) someStats <- function(v) { GC <- DNAString("GC") CG <- DNAString("CG") sapply(seq_len(length(v)), function(i) { y <- v[[i]] c(alphabetFrequency(y)[1:4], GC=countPattern(GC, y), CG=countPattern(CG, y)) } ) } someStats(tmpseq[1:10]) ################################################### ### code chunk number 24: f1 ################################################### library(BSgenome.Hsapiens.UCSC.hg38.masked) genome <- BSgenome.Hsapiens.UCSC.hg38.masked chrY <- genome$chrY chrY chrM <- genome$chrM chrM ################################################### ### code chunk number 25: f2 ################################################### active(masks(chrY))["RM"] <- TRUE chrY ################################################### ### code chunk number 26: f3 ################################################### active(masks(chrY)) <- FALSE active(masks(chrY))["AGAPS"] <- TRUE alphabetFrequency(unmasked(chrY)) alphabetFrequency(chrY) ################################################### ### code chunk number 27: f4 ################################################### as(chrY, "XStringViews") ################################################### ### code chunk number 28: f5 ################################################### gaps(as(chrY, "XStringViews")) ################################################### ### code chunk number 29: f6 ################################################### width(gaps(as(chrY, "XStringViews"))) ################################################### ### code chunk number 30: f7 ################################################### gaps(chrY) alphabetFrequency(gaps(chrY)) ################################################### ### code chunk number 31: f8 ################################################### af0 <- alphabetFrequency(unmasked(chrY)) af1 <- alphabetFrequency(chrY) af2 <- alphabetFrequency(gaps(chrY)) all(af0 == af1 + af2) ################################################### ### code chunk number 32: f9 ################################################### active(masks(chrY)) <- TRUE af1 <- alphabetFrequency(chrY) af1 gaps(chrY) af2 <- alphabetFrequency(gaps(chrY)) af2 all(af0 == af1 + af2) ################################################### ### code chunk number 33: f10 ################################################### Ebox <- "CANNTG" active(masks(chrY)) <- FALSE countPattern(Ebox, chrY, fixed=FALSE) ################################################### ### code chunk number 34: f11 ################################################### countPattern(Ebox, chrY, fixed=c(pattern=FALSE,subject=TRUE)) ################################################### ### code chunk number 35: f12 ################################################### active(masks(chrY))[c("AGAPS", "AMB")] <- TRUE alphabetFrequency(chrY, baseOnly=TRUE) # no ambiguities countPattern(Ebox, chrY, fixed=FALSE) ################################################### ### code chunk number 36: f13 ################################################### chr2 <- genome$chr2 active(masks(chr2))[-2] <- FALSE alphabetFrequency(gaps(chr2)) ################################################### ### code chunk number 37: e1 ################################################### runOneStrandAnalysis <- function(dict0, bsgenome, seqnames, strand, outfile="", append=FALSE) { cat("\nTarget: strand", strand, "of", providerVersion(bsgenome), "chromosomes", paste(seqnames, collapse=", "), "\n") if (strand == "-") dict0 <- reverseComplement(dict0) pdict <- PDict(dict0) for (seqname in seqnames) { subject <- bsgenome[[seqname]] cat(">>> Finding all hits in strand", strand, "of chromosome", seqname, "...\n") mindex <- matchPDict(pdict, subject) matches <- extractAllMatches(subject, mindex) writeHits(seqname, matches, strand, file=outfile, append=append) append <- TRUE cat(">>> DONE\n") } } runAnalysis2 <- function(dict0, outfile="") { library(BSgenome.Celegans.UCSC.ce2) genome <- BSgenome.Celegans.UCSC.ce2 seqnames <- seqnames(genome) runOneStrandAnalysis(dict0, genome, seqnames, "+", outfile=outfile, append=FALSE) runOneStrandAnalysis(dict0, genome, seqnames, "-", outfile=outfile, append=TRUE) } ################################################### ### code chunk number 38: e2 ################################################### ce2dict0cw15 <- DNAStringSet(ce2dict0, end=15) ################################################### ### code chunk number 39: e3 ################################################### runAnalysis2(ce2dict0cw15, outfile="ce2dict0cw15_ana2.txt") ################################################### ### code chunk number 40: g1 ################################################### sessionInfo() BSgenome/inst/doc/GenomeSearching.Rnw0000644000175400017540000006612413175713516020571 0ustar00biocbuildbiocbuild%\VignetteIndexEntry{Efficient genome searching with Biostrings and the BSgenome data packages} %\VignetteKeywords{BSgenome, genome, DNA, RNA, Sequence, Biostrings, Sequence alignment, SNPs} %\VignettePackage{BSgenome} % % NOTE -- ONLY EDIT THE .Rnw FILE!!! The .tex file is % likely to be overwritten. % \SweaveOpts{keep.source=TRUE} \documentclass[10pt]{article} %\usepackage{amsmath} %\usepackage[authoryear,round]{natbib} \usepackage{hyperref} \usepackage{underscore} \textwidth=6.5in \textheight=8.5in %\parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \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}} \bibliographystyle{plainnat} \begin{document} %\setkeys{Gin}{width=0.55\textwidth} \title{Efficient genome searching with Biostrings and the BSgenome data packages} \author{Herv\'e Pag\`es} \maketitle \tableofcontents % --------------------------------------------------------------------------- \section{The Biostrings-based genome data packages} The Bioconductor project provides data packages that contain the full genome sequences of a given organism. These packages are called {\it Biostrings-based genome data packages} because the sequences they contain are stored in some of the basic containers defined in the \Rpackage{Biostrings} package, like the \Rclass{DNAString}, the \Rclass{DNAStringSet} or the \Rclass{MaskedDNAString} containers. Regardless of the particular sequence data that they contain, all the Biostrings-based genome data packages are very similar and can be manipulated in a consistent and easy way. They all require the \Rpackage{BSgenome} package in order to work properly. This package, unlike the Biostrings-based genome data packages, is a software package that provides the infrastructure needed to support them (this is why the Biostrings-based genome data packages are also called {\it BSgenome data packages}). The \Rpackage{BSgenome} package itself requires the \Rpackage{Biostrings} package. See the man page for the \Rfunction{available.genomes} function (\Rfunction{?available.genomes}) for more information about how to get the list of all the BSgenome data packages currently available in your version of Bioconductor (you need an internet connection so that \Rfunction{available.genomes} can query the Bioconductor package repositories). More genomes can be added if necessary. Note that the process of making a BSgenome data package is not yet documented but you are welcome to ask for help on the bioc-devel mailing list (\url{http://bioconductor.org/docs/mailList.html}) if you need a genome that is not yet available. % --------------------------------------------------------------------------- \section{Finding an arbitrary nucleotide pattern in a chromosome} In this section we show how to find (or just count) the occurences of some arbitrary nucleotide pattern in a chromosome. The basic tool for this is the \Rfunction{matchPattern} (or \Rfunction{countPattern}) function from the \Rpackage{Biostrings} package. First we need to install and load the BSgenome data package for the organism that we want to look at. In our case, we want to search chromosome I of {\it Caenorhabditis elegans}. UCSC provides several versions of the C. elegans genome: ce1, ce2 and ce4. These versions correspond to different {\it releases} from WormBase, which are the WS100, WS120 and WS170 releases, respectively. See \url{http://genome.ucsc.edu/FAQ/FAQreleases#release1} for the list of all UCSC genome releases and for the correspondance between UCSC versions and release names. The BSgenome data package for the ce2 genome is \Rpackage{BSgenome.Celegans.UCSC.ce2}. Note that ce1 and ce4 are not available in Bioconductor but they could be added if there is demand for them. See \Rfunction{?available.genomes} for how to install \Rpackage{BSgenome.Celegans.UCSC.ce2}. Then load the package and display the single object defined in it: <>= library(BSgenome.Celegans.UCSC.ce2) ls("package:BSgenome.Celegans.UCSC.ce2") genome <- BSgenome.Celegans.UCSC.ce2 genome @ \Robject{genome} is a \Rclass{BSgenome} object: <>= class(genome) @ When displayed, some basic information about the origin of the genome is shown (organism, provider, provider version, etc...) followed by the index of {\it single} sequences and eventually an additional index of {\it multiple} sequences. Methods (adequately called {\it accessor methods}) are defined for individual access to this information: <>= organism(genome) provider(genome) providerVersion(genome) seqnames(genome) mseqnames(genome) @ See the man page for the \Rclass{BSgenome} class (\Rfunction{?BSgenome}) for a complete list of accessor methods and their descriptions. Now we are ready to display chromosome I: <>= genome$chrI @ Note that this chrI sequence corresponds to the {\it forward} strand (aka {\it direct} or {\it sense} or {\it positive} or {\it plus} strand) of chromosome I. UCSC, and genome providers in general, don't provide files containing the nucleotide sequence of the {\it reverse} strand (aka {\it indirect} or {\it antisense} or {\it negative} or {\it minus} or {\it opposite} strand) of the chromosomes because these sequences can be deduced from the {\it forward} sequences by taking their reverse complements. The BSgenome data packages are no exceptions: they only provide the {\it forward} strand sequence of every chromosome. See \Rfunction{?reverseComplement} for more details about the reverse complement of a \Rclass{DNAString} object. It is important to remember that, in practice, the {\it reverse} strand sequence is almost never needed. The reason is that, in fact, a {\it reverse} strand analysis can (and should) always be transposed into a {\it forward} strand analysis. Therefore trying to compute the {\it reverse} strand sequence of an entire chromosome by applying \Rfunction{reverseComplement} to its {\it forward} strand sequence is almost always a bad idea. See the {\it Finding an arbitrary nucleotide pattern in an entire genome} section of this document for how to find arbitrary patterns in the {\it reverse} strand of a chromosome. % It seems like this page http://www.medterms.com/script/main/art.asp?articlekey=20468 % is lying about the noncoding (or coding, they are in fact contradicting themselves) % nature of the sense and antisense strands. The number of bases in this sequence can be retrieved with: <>= chrI <- genome$chrI length(chrI) @ Some basic stats: <>= afI <- alphabetFrequency(chrI) afI sum(afI) == length(chrI) @ Count all {\it exact} matches of pattern \Robject{"ACCCAGGGC"}: <>= p1 <- "ACCCAGGGC" countPattern(p1, chrI) @ Like most pattern matching functions in \Rpackage{Biostrings}, the \Rfunction{countPattern} and \Rfunction{matchPattern} functions support {\it inexact} matching. One form of inexact matching is to allow a few mismatching letters per match. Here we allow at most one: <>= countPattern(p1, chrI, max.mismatch=1) @ With the \Rfunction{matchPattern} function, the locations of the matches are stored in an \Rclass{XStringViews} object: <>= m1 <- matchPattern(p1, chrI, max.mismatch=1) m1[4:6] class(m1) @ The \Rfunction{mismatch} function (new in \Rpackage{Biostrings}~2) returns the positions of the mismatching letters for each match: <>= mismatch(p1, m1[4:6]) @ Note: The \Rfunction{mismatch} method is in fact a particular case of a (vectorized) {\it alignment} function where only ``replacements'' are allowed. Current implementation is slow but this will be addressed. It may happen that a match is {\it out of limits} like in this example: <>= p2 <- DNAString("AAGCCTAAGCCTAAGCCTAA") m2 <- matchPattern(p2, chrI, max.mismatch=2) m2[1:4] p2 == m2[1:4] mismatch(p2, m2[1:4]) @ The list of exact matches and the list of inexact matches can both be obtained with: <>= m2[p2 == m2] m2[p2 != m2] @ Note that the length of \Robject{m2[p2 == m2]} should be equal to \Robject{countPattern(p2, chrI, max.mismatch=0)}. % --------------------------------------------------------------------------- \section{Finding an arbitrary nucleotide pattern in an entire genome} Now we want to extend our analysis to the {\it forward} and {\it reverse} strands of all the C. elegans chromosomes. More precisely, here is the analysis we want to perform: \begin{itemize} \item{The input dictionary: } Our input is a dictionary of 50 patterns. Each pattern is a short nucleotide sequence of 15 to 25 bases (As, Cs, Gs and Ts only, no Ns). It is stored in a FASTA file called \Robject{"ce2dict0.fa"}. % ce2dict0.fa was generated with % > set.seed(23) % > ce2dict0 <- sapply(1:50, function(i) { x <- genome[[sample(seqnames(genome), 1)]]; start <- as.integer(runif(1, min=1, length(x)-20)); end <- start + as.integer(runif(1, min=14, max=25)); x <- subXString(x, start, end); if (sample(1:2, 1) == 2) x <- reverseComplement(x); as.character(x) }) % > names(ce2dict0) <- paste("pattern", 1:50, sep="") % > write.XStringViews(XStringViews(ce2dict0, "DNAString"), file="ce2dict0.fa", format="fasta") See the {\it Finding all the patterns of a constant width dictionary in an entire genome} section of this document for a very efficient way to deal with the special case where all the patterns in the input dictionary have the same length. \item{The target: } Our target (or subject) is the {\it forward} and {\it reverse} strands of the seven C. elegans chromosomes (14 sequences in total). We want to find and report all occurences (or hits) of every pattern in the target. Note that a given pattern can have 0, 1 or several hits in 0, 1 or 2 strands of 0, 1 or several chromosomes. \item{Exact or inexact matching? } We are interested in exact matches only (for now). \item{The output: } We want to put the results of this analysis in a file so we can send it to our collaborators for some post analysis work. Our collaborators are not necessarily familiar with R or Bioconductor so dumping a high-level R object (like a list or a data frame) into an .rda file is not an option. For maximum portability (one of our collaborators wants to use Microsoft Excel for the post analysis) we choose to put our results in a tabulated file where one line describes one hit. The columns (or fields) of this file will be (in this order): \begin{itemize} \item{seqname: } the name of the chromosome where the hit occurs. \item{start: } an integer giving the starting position of the hit. \item{end: } an integer giving the ending position of the hit. \item{strand: } a plus (\Robject{+}) for a hit in the positive strand or a minus (\Robject{-}) for a hit in the negative strand. \item{patternID: } we use the unique ID provided for every pattern in the \Robject{"ce2dict0.fa"} file. \end{itemize} \end{itemize} Let's start by loading the input dictionary with: <>= ce2dict0_file <- system.file("extdata", "ce2dict0.fa", package="BSgenome") ce2dict0 <- readDNAStringSet(ce2dict0_file, "fasta") ce2dict0 @ Here is how we can write the functions that will perform our analysis: <>= writeHits <- function(seqname, matches, strand, file="", append=FALSE) { if (file.exists(file) && !append) warning("existing file ", file, " will be overwritten with 'append=FALSE'") if (!file.exists(file) && append) warning("new file ", file, " will have no header with 'append=TRUE'") hits <- data.frame(seqname=rep.int(seqname, length(matches)), start=start(matches), end=end(matches), strand=rep.int(strand, length(matches)), patternID=names(matches), check.names=FALSE) write.table(hits, file=file, append=append, quote=FALSE, sep="\t", row.names=FALSE, col.names=!append) } runAnalysis1 <- function(dict0, outfile="") { library(BSgenome.Celegans.UCSC.ce2) genome <- BSgenome.Celegans.UCSC.ce2 seqnames <- seqnames(genome) seqnames_in1string <- paste(seqnames, collapse=", ") cat("Target:", providerVersion(genome), "chromosomes", seqnames_in1string, "\n") append <- FALSE for (seqname in seqnames) { subject <- genome[[seqname]] cat(">>> Finding all hits in chromosome", seqname, "...\n") for (i in seq_len(length(dict0))) { patternID <- names(dict0)[i] pattern <- dict0[[i]] plus_matches <- matchPattern(pattern, subject) names(plus_matches) <- rep.int(patternID, length(plus_matches)) writeHits(seqname, plus_matches, "+", file=outfile, append=append) append <- TRUE rcpattern <- reverseComplement(pattern) minus_matches <- matchPattern(rcpattern, subject) names(minus_matches) <- rep.int(patternID, length(minus_matches)) writeHits(seqname, minus_matches, "-", file=outfile, append=append) } cat(">>> DONE\n") } } @ Some important notes about the implementation of the \Rfunction{runAnalysis1} function: \begin{itemize} \item{} \Robject{subject <- genome[[seqname]]} is the code that actually loads a chromosome sequence into memory. Using only one sequence at a time is a good practice to avoid memory allocation problems on a machine with a limited amount of memory. For example, loading all the human chromosome sequences in memory would require more than 3GB of memory! \item{} We have 2 nested \Robject{for} loops: the outer loop walks thru the target (7 chromosomes) and the inner loop walks thru the set of patterns. Doing the other way around would be very inefficient, especially with a bigger number of patterns because this would require to load each chromosome sequence into memory as many times as the number of patterns. \Rfunction{runAnalysis1} loads each sequence only once. \item{} We find the matches in the minus strand (\Robject{minus_matches}) by first taking the reverse complement of the current pattern (with \Robject{rcpattern <- reverseComplement(pattern)}) and NOT by taking the reverse complement of the current subject. \end{itemize} Now we are ready to run the analysis and put the results in the \Robject{"ce2dict0_ana1.txt"} file: <>= runAnalysis1(ce2dict0, outfile="ce2dict0_ana1.txt") @ Here is some very simple example of post analysis: \begin{itemize} \item{} Get the total number of hits: <>= hits1 <- read.table("ce2dict0_ana1.txt", header=TRUE) nrow(hits1) @ \item{} Get the number of hits per chromosome: <>= table(hits1$seqname) @ \item{} Get the number of hits per pattern: <>= hits1_table <- table(hits1$patternID) hits1_table @ \item{} Get the pattern(s) with the higher number of hits: <>= hits1_table[hits1_table == max(hits1_table)] # pattern(s) with more hits @ \item{} Get the pattern(s) with no hits: <>= setdiff(names(ce2dict0), hits1$patternID) # pattern(s) with no hits @ \item{} And finally a function that can be used to plot the hits: <>= plotGenomeHits <- function(bsgenome, seqnames, hits) { chrlengths <- seqlengths(bsgenome)[seqnames] XMAX <- max(chrlengths) YMAX <- length(seqnames) plot.new() plot.window(c(1, XMAX), c(0, YMAX)) axis(1) axis(2, at=seq_len(length(seqnames)), labels=rev(seqnames), tick=FALSE, las=1) ## Plot the chromosomes for (i in seq_len(length(seqnames))) lines(c(1, chrlengths[i]), c(YMAX + 1 - i, YMAX + 1 - i), type="l") ## Plot the hits for (i in seq_len(nrow(hits))) { seqname <- hits$seqname[i] y0 <- YMAX + 1 - match(seqname, seqnames) if (hits$strand[i] == "+") { y <- y0 + 0.05 col <- "red" } else { y <- y0 - 0.05 col <- "blue" } lines(c(hits$start[i], hits$end[i]), c(y, y), type="l", col=col, lwd=3) } } @ Plot the hits found by \Rfunction{runAnalysis1} with: <>= plotGenomeHits(genome, seqnames(genome), hits1) @ \end{itemize} % --------------------------------------------------------------------------- \section{Some precautions when using \Rmethod{matchPattern}} Improper use of \Rmethod{matchPattern} (or \Rmethod{countPattern}) can affect performance. If needed, the \Rmethod{matchPattern} and \Rmethod{countPattern} methods convert their first argument (the pattern) to an object of the same class than their second argument (the subject) before they pass it to the subroutine that actually implements the fast search algorithm. So if you need to reuse the same pattern a high number of times, it's a good idea to convert it {\it before} to pass it to the \Rmethod{matchPattern} or \Rmethod{countPattern} method. This way the conversion is done only once: <>= library(hgu95av2probe) tmpseq <- DNAStringSet(hgu95av2probe$sequence) someStats <- function(v) { GC <- DNAString("GC") CG <- DNAString("CG") sapply(seq_len(length(v)), function(i) { y <- v[[i]] c(alphabetFrequency(y)[1:4], GC=countPattern(GC, y), CG=countPattern(CG, y)) } ) } someStats(tmpseq[1:10]) @ % The above example is Raphael's use case discussed on BioC on Feb 2006. % In Biostrings 1, the equivalent would be: % src <- sapply(1:100, % function(i) { % paste(sample(c("A","C","G","T"), 25, replace=TRUE), % collapse="") % } % ) % tmpseq <- DNAString(src) % someStats <- function(v) % { % GC <- DNAString("GC") % CG <- DNAString("CG") % sapply(1:length(v), % function(i) { % y <- v[i] % c(alphabetFrequency(y)[2:5], % GC=length(matchDNAPattern(GC, y)), % CG=length(matchDNAPattern(CG, y))) % } % ) % } % someStats(tmpseq[1:10]) % --------------------------------------------------------------------------- \section{Masking the chromosome sequences} Starting with Bioconductor 2.2, the chromosome sequences in a {\it BSgenome data package} can have built-in masks. Starting with Bioconductor 2.3, there can be up to 4 built-in masks per sequence. These will always be (in this order): (1) the mask of assembly gaps, (2) the mask of intra-contig ambiguities, (3) the mask of repeat regions that were determined by the RepeatMasker software, and (4) the mask of repeat regions that were determined by the Tandem Repeats Finder software (where only repeats with period less than or equal to 12 were kept). For a given package, all the sequences will always have the same number of masks. <>= library(BSgenome.Hsapiens.UCSC.hg38.masked) genome <- BSgenome.Hsapiens.UCSC.hg38.masked chrY <- genome$chrY chrY chrM <- genome$chrM chrM @ The built-in masks are named consistenly across all the BSgenome data packages available in Bioconductor: \begin{table}[ht] \begin{center} \begin{tabular}{l|l|l|l} \hline Name & Active by default & Short description & Long description \\ \hline AGAPS & yes & assembly gaps & Masks the big N-blocks that have been placed between the contigs during the assembly. This mask is consistent with the Gap track from UCSC Genome Browser.\\ AMB & yes & intra-contig ambiguities & Masks any IUPAC ambiguity letter that was found in the contig regions of the original sequence. Note that only As, Cs, Gs and Ts remain unmasked when the AGAPS and AMB masks are both active (before SNPs are eventually injected, see below). \\ RM & no & RepeatMasker & Masks the repeat regions determined by the RepeatMasker software. This mask is consistent with the RepeatMasker track from UCSC Genome Browser. \\ TRF & no & Tandem Repeats Finder & Masks the tandem repeat regions that were determined by the Tandem Repeats Finder software (with period of 12 or less). \\ \hline \end{tabular} \end{center} \caption{The built-in masks provided by the BSgenome data packages.} \end{table} When displaying a masked sequence (here a \Rclass{MaskedDNAString} object), the {\it masked width} and {\it masked ratio} are reported for each individual mask, as well as for all the masks together, and for all the active masks together. The {\it masked width} is the total number of nucleotide positions that are masked and the {\it masked ratio} is the {\it masked width} divided by the length of the sequence. To activate a mask, use the \Rmethod{active} replacement method in conjonction with the \Rmethod{masks} method. For example, to activate the RepeatMasker mask, do: <>= active(masks(chrY))["RM"] <- TRUE chrY @ As you can see, the {\it masked width} for all the active masks together (i.e. the total number of nucleotide positions that are masked by at least one active mask) is now the same as for the first mask. This represents a {\it masked ratio} of about 83\%. Now when we use a function that is {\it mask aware}, like \Rfunction{alphabetFrequency}, the masked regions of the input sequence are ignored: <>= active(masks(chrY)) <- FALSE active(masks(chrY))["AGAPS"] <- TRUE alphabetFrequency(unmasked(chrY)) alphabetFrequency(chrY) @ This output indicates that, for this chromosome, the assembly gaps correspond exactly to the regions in the sequence that were filled with the letter N. Note that this is not always the case: sometimes Ns, and other IUPAC ambiguity letters, can be found inside the contigs. When coercing a \Rclass{MaskedXString} object to an \Rclass{XStringViews} object, each non-masked region in the original sequence is converted into a view on the sequence: <>= as(chrY, "XStringViews") @ This can be used in conjonction with the \Rmethod{gaps} method to see the gaps between the views i.e. the masked regions themselves: <>= gaps(as(chrY, "XStringViews")) @ To extract the sizes of the assembly gaps: <>= width(gaps(as(chrY, "XStringViews"))) @ Note that, if applied directly to \Robject{chrY}, \Rmethod{gaps} returns a \Rclass{MaskedDNAString} object with a single mask masking the regions that are not masked in the original object: <>= gaps(chrY) alphabetFrequency(gaps(chrY)) @ In fact, for any \Rclass{MaskedDNAString} object, the following should always be \Robject{TRUE}, whatever the masks are: <>= af0 <- alphabetFrequency(unmasked(chrY)) af1 <- alphabetFrequency(chrY) af2 <- alphabetFrequency(gaps(chrY)) all(af0 == af1 + af2) @ With all chrY masks active: <>= active(masks(chrY)) <- TRUE af1 <- alphabetFrequency(chrY) af1 gaps(chrY) af2 <- alphabetFrequency(gaps(chrY)) af2 all(af0 == af1 + af2) @ Now let's compare three different ways of finding all the occurences of the \Robject{"CANNTG"} consensus sequence in chrY. The Ns in this pattern need to be treated as wildcards i.e. they must match any letter in the subject. Without the mask feature, the first way to do it would be to use the \Robject{fixed=FALSE} option in the call to \Rfunction{matchPattern} (or \Rfunction{countPattern}): <>= Ebox <- "CANNTG" active(masks(chrY)) <- FALSE countPattern(Ebox, chrY, fixed=FALSE) @ The problem with this method is that the Ns in the subject are also treated as wildcards hence the abnormally high number of matches. A better method is to specify the {\it side} of the matching problem (i.e. {\it pattern} or {\it subject}) where the Ns should be treated as wildcards: <>= countPattern(Ebox, chrY, fixed=c(pattern=FALSE,subject=TRUE)) @ Finally, \Rfunction{countPattern} being {\it mask aware}, this can be achieved more efficiently by just masking the assembly gaps and ambiguities: <>= active(masks(chrY))[c("AGAPS", "AMB")] <- TRUE alphabetFrequency(chrY, baseOnly=TRUE) # no ambiguities countPattern(Ebox, chrY, fixed=FALSE) @ Note that some chromosomes can have Ns outside the assembly gaps: <>= chr2 <- genome$chr2 active(masks(chr2))[-2] <- FALSE alphabetFrequency(gaps(chr2)) @ so it is recommended to always keep the AMB mask active (in addition to the AGAPS mask) whatever the sequence is. Note that not all functions that work with an \Rclass{XString} input are {\it mask aware} but more will be added in the near future. However, most of the times there is a alternate way to exclude some arbitrary regions from an analysis without having to use {\it mask aware} functions. This is described below in the {\it Hard masking} section. % --------------------------------------------------------------------------- \section{Hard masking} coming soon... % --------------------------------------------------------------------------- \section{Injecting known SNPs in the chromosome sequences} coming soon... % --------------------------------------------------------------------------- \section{Finding all the patterns of a constant width dictionary in an entire genome} The \Rfunction{matchPDict} function can be used instead of \Rfunction{matchPattern} for the kind of analysis described in the {\it Finding an arbitrary nucleotide pattern in an entire genome} section but it will be much faster (between 100x and 10000x faster depending on the size of the input dictionary). Note that a current limitation of \Rfunction{matchPDict} is that it only works with a dictionary of DNA patterns where all the patterns have the same number of nucleotides (constant width dictionary). See \Rfunction{?matchPDict} for more information. Here is how our \Rfunction{runAnalysis1} function can be modified in order to use \Rfunction{matchPDict} instead of \Rfunction{matchPattern}: <>= runOneStrandAnalysis <- function(dict0, bsgenome, seqnames, strand, outfile="", append=FALSE) { cat("\nTarget: strand", strand, "of", providerVersion(bsgenome), "chromosomes", paste(seqnames, collapse=", "), "\n") if (strand == "-") dict0 <- reverseComplement(dict0) pdict <- PDict(dict0) for (seqname in seqnames) { subject <- bsgenome[[seqname]] cat(">>> Finding all hits in strand", strand, "of chromosome", seqname, "...\n") mindex <- matchPDict(pdict, subject) matches <- extractAllMatches(subject, mindex) writeHits(seqname, matches, strand, file=outfile, append=append) append <- TRUE cat(">>> DONE\n") } } runAnalysis2 <- function(dict0, outfile="") { library(BSgenome.Celegans.UCSC.ce2) genome <- BSgenome.Celegans.UCSC.ce2 seqnames <- seqnames(genome) runOneStrandAnalysis(dict0, genome, seqnames, "+", outfile=outfile, append=FALSE) runOneStrandAnalysis(dict0, genome, seqnames, "-", outfile=outfile, append=TRUE) } @ Remember that \Rfunction{matchPDict} only works if all the patterns in the input dictionary have the same length so for this 2nd analysis, we will truncate the patterns in \Robject{ce2dict0} to 15 nucleotides: <>= ce2dict0cw15 <- DNAStringSet(ce2dict0, end=15) @ Now we can run this 2nd analysis and put the results in the \Robject{"ce2dict0cw15_ana2.txt"} file: <>= runAnalysis2(ce2dict0cw15, outfile="ce2dict0cw15_ana2.txt") @ % --------------------------------------------------------------------------- \section{Session info} <>= sessionInfo() @ \end{document} BSgenome/inst/doc/GenomeSearching.pdf0000644000175400017540000056605213175725526020605 0ustar00biocbuildbiocbuild%PDF-1.5 % 51 0 obj << /Length 2463 /Filter /FlateDecode >> stream xY[s۸~ϯ#5!ą ٗfmfj5}`$V-HM3ӝ}pp.@ ]* XTZե[xWU_Os:[϶_ٰ\<i_GiBOV쑧_?zA( ZckL]*tސZ>ឰO1d–?Шrւi C[nlÏ.YAg) u3jǎLg ml<F/W5yk+ >)#t&-բ*]{ K#E󯌩t@s](fXͨ/**mI`;< UҀhOG-B2DW+ރ%oXoK ӸYEs>p| ٴ9^2ԗLŹ 6^Օ=2^S3H0ͦ. 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Version: 1.3.17 organism: Homo sapiens species: Human provider: 1000 Genomes provider_version: human_b36_female release_date: Aug. 2009 release_name: human_b36_female source_url: ftp://ftp-trace.ncbi.nih.gov/1000genomes/ftp/pilot_data/technical/reference/ organism_biocview: Homo_sapiens BSgenomeObjname: Hsapiens seqnames: paste("chr", c(1:22, "X", "M"), sep="") circ_seqs: "chrM" mseqnames: "supercontigs" nmask_per_seq: 0 SrcDataFiles1: human_b36_female.fa.gz from ftp://ftp-trace.ncbi.nih.gov/1000genomes/ftp/pilot_data/technical/reference/ PkgExamples: Hsapiens seqlengths(Hsapiens) Hsapiens$chr1 # same as Hsapiens[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/1000genomes/human_b36_female BSgenome/inst/extdata/GentlemanLab/1000genomes/BSgenome.Hsapiens.1000g.b36female-tools/0000755000175400017540000000000013175713516031105 5ustar00biocbuildbiocbuildsplit_human_b36_female.sh0000755000175400017540000000332113175713516035672 0ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/1000genomes/BSgenome.Hsapiens.1000g.b36female-tools#!/bin/bash # # Run with: # ./split_human_b36_female.sh human_b36_female.fa # Then test the result with: # cat chr[1-9].fa chr??.fa chrX.fa chrM.fa supercontigs.fa > merged.fa # cmp merged.fa human_b36_female.fa set -e # Exit immediately if a simple command exits with a non-zero status # Note that in 'head -n NH $1 | tail -n NT' the NH and NT values # were obtained from R with: # library(Biostrings) # fi <- fasta.seqlengths("human_b36_female.fa") # fi24 <- fi[1:24] # NT <- fi24 %/% 60L + 2L # NT[13] <- NT[13] - 1L # NH <- cumsum(NT) head -n 4120830 $1 > chr1.fa head -n 8170017 $1 | tail -n 4049187 > chr2.fa head -n 11495049 $1 | tail -n 3325032 > chr3.fa head -n 14682935 $1 | tail -n 3187886 > chr4.fa head -n 17697234 $1 | tail -n 3014299 > chr5.fa head -n 20545569 $1 | tail -n 2848335 > chr6.fa head -n 23192594 $1 | tail -n 2647025 > chr7.fa head -n 25630509 $1 | tail -n 2437915 > chr8.fa head -n 27968398 $1 | tail -n 2337889 > chr9.fa head -n 30224645 $1 | tail -n 2256247 > chr10.fa head -n 32465520 $1 | tail -n 2240875 > chr11.fa head -n 34671347 $1 | tail -n 2205827 > chr12.fa head -n 36573731 $1 | tail -n 1902384 > chr13.fa head -n 38346542 $1 | tail -n 1772811 > chr14.fa head -n 40018859 $1 | tail -n 1672317 > chr15.fa head -n 41499315 $1 | tail -n 1480456 > chr16.fa head -n 42812229 $1 | tail -n 1312914 > chr17.fa head -n 44080850 $1 | tail -n 1268621 > chr18.fa head -n 45144379 $1 | tail -n 1063529 > chr19.fa head -n 46184980 $1 | tail -n 1040601 > chr20.fa head -n 46967387 $1 | tail -n 782407 > chr21.fa head -n 47795579 $1 | tail -n 828192 > chr22.fa head -n 50377476 $1 | tail -n 2581897 > chrX.fa head -n 50377754 $1 | tail -n 278 > chrM.fa tail -n 213994 $1 > supercontigs.fa BSgenome/inst/extdata/GentlemanLab/BSgenome.Amellifera.BeeBase.assembly4-seed0000644000175400017540000000131213175713516030034 0ustar00biocbuildbiocbuildPackage: BSgenome.Amellifera.BeeBase.assembly4 Title: Full genome sequences for Apis mellifera (BeeBase assembly4) Description: iFull genome sequences for Apis mellifera (Honey Bee) as provided by BeeBase (assembly4, Feb. 2008) and stored in Biostrings objects. Version: 1.4.2 organism: Apis mellifera common_name: Honey Bee provider: BeeBase provider_version: assembly4 release_date: Feb. 2008 release_name: assembly4 source_url: NA organism_biocview: Apis_mellifera BSgenomeObjname: Amellifera seqnames: paste("Group", 1:16, sep="") mseqnames: "GroupUn" PkgExamples: genome$Group1 # same as genome[["Group1"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Amellifera.BeeBase.assembly4/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Amellifera.BeeBase.assembly4-tools/0000755000175400017540000000000013175713516030334 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Amellifera.BeeBase.assembly4-tools/NOTES.TXT0000644000175400017540000000204613175713516031627 0ustar00biocbuildbiocbuildGot the assembly4_chromosomes.fa file from: sftp honeybee@genomes.tamu.edu (password: beehive) cd assembly4_chromosomes (information provided by Brian Herb and Rafael Irizarry) Downloaded the file on March 5, 2008 9260 FASTA records: o 16 big records (> 7M and < 30M base pairs each) from line - to line Group1: 1 - 427631 Group2: 427632 - 657235 Group3: 657236 - 851830 Group4: 851831 - 1026927 Group5: 1026928 - 1234081 Group6: 1234082 - 1487498 Group7: 1487499 - 1671056 Group8: 1671057 - 1859475 Group9: 1859476 - 2017804 Group10: 2017805 - 2198414 Group11: 2198415 - 2405872 Group12: 2405873 - 2567431 Group13: 2567432 - 2714100 Group14: 2714101 - 2856625 Group15: 2856626 - 3001765 Group16: 3001766 - 3102808 o 9244 small records (>= 564 and <= 167350 base pairs each) GroupUn.1 to GroupUn.9244: 3102809 - bottom (line 3809863) Use the splitbigfasta.sh script to split assembly4_chromosomes.fa BSgenome/inst/extdata/GentlemanLab/BSgenome.Amellifera.BeeBase.assembly4-tools/splitbigfasta.sh0000755000175400017540000000210213175713516033522 0ustar00biocbuildbiocbuild#!/bin/bash # # Run with: # ./splitbigfasta.sh assembly4_chromosomes.fa # Then test the result with: # cat Group?.fa Group??.fa > merged.fa # cmp merged.fa assembly4_chromosomes.fa set -e # Exit immediately if a simple command exits with a non-zero status tail -n +1 $1 | head -n 427631 > Group1.fa tail -n +427632 $1 | head -n 229604 > Group2.fa tail -n +657236 $1 | head -n 194595 > Group3.fa tail -n +851831 $1 | head -n 175097 > Group4.fa tail -n +1026928 $1 | head -n 207154 > Group5.fa tail -n +1234082 $1 | head -n 253417 > Group6.fa tail -n +1487499 $1 | head -n 183558 > Group7.fa tail -n +1671057 $1 | head -n 188419 > Group8.fa tail -n +1859476 $1 | head -n 158329 > Group9.fa tail -n +2017805 $1 | head -n 180610 > Group10.fa tail -n +2198415 $1 | head -n 207458 > Group11.fa tail -n +2405873 $1 | head -n 161559 > Group12.fa tail -n +2567432 $1 | head -n 146669 > Group13.fa tail -n +2714101 $1 | head -n 142525 > Group14.fa tail -n +2856626 $1 | head -n 145140 > Group15.fa tail -n +3001766 $1 | head -n 101043 > Group16.fa tail -n +3102809 $1 > GroupUn.fa BSgenome/inst/extdata/GentlemanLab/BSgenome.Amellifera.UCSC.apiMel2-seed0000644000175400017540000000151313175713516026674 0ustar00biocbuildbiocbuildPackage: BSgenome.Amellifera.UCSC.apiMel2 Title: Full genome sequences for Apis mellifera (UCSC version apiMel2) Description: Full genome sequences for Apis mellifera (Honey Bee) as provided by UCSC (apiMel2, Jan. 2005) and stored in Biostrings objects. Version: 1.4.2 organism: Apis mellifera common_name: Honey Bee provider: UCSC provider_version: apiMel2 release_date: Jan. 2005 release_name: Baylor College of Medicine HGSC v.Amel_2.0 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/apiMel2/bigZips/ organism_biocview: Apis_mellifera BSgenomeObjname: Amellifera SrcDataFiles: apiMel2.2bit from http://hgdownload.cse.ucsc.edu/goldenPath/apiMel2/bigZips/ PkgExamples: genome$Group1 # same as genome[["Group1"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Amellifera.UCSC.apiMel2/seqs seqfile_name: apiMel2.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Amellifera.UCSC.apiMel2.masked-seed0000644000175400017540000000241413175713516030140 0ustar00biocbuildbiocbuildPackage: BSgenome.Amellifera.UCSC.apiMel2.masked Title: Full masked genome sequences for Apis mellifera (UCSC version apiMel2) Description: Full genome sequences for Apis mellifera (Honey Bee) as provided by UCSC (apiMel2, Jan. 2005) and stored in Biostrings objects. The sequences are the same as in BSgenome.Amellifera.UCSC.apiMel2, except that each of them has the 3 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), and (3) the mask of repeats from RepeatMasker (RM mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Amellifera.UCSC.apiMel2 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/apiMel2/bigZips/ organism_biocview: Apis_mellifera nmask_per_seq: 3 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/apiMel2/database/ RM masks: GroupOut.zip from http://hgdownload.cse.ucsc.edu/goldenPath/apiMel2/bigZips/ PkgExamples: genome$Group1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$Group1) # same as BSgenome.Amellifera.UCSC.apiMel2$Group1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Amellifera.UCSC.apiMel2/masks AGAPSfiles_name: gap.txt RMfiles_suffix: .out BSgenome/inst/extdata/GentlemanLab/BSgenome.Athaliana.TAIR.04232008-seed0000644000175400017540000000234513175713516026134 0ustar00biocbuildbiocbuildPackage: BSgenome.Athaliana.TAIR.04232008 Title: Full genome sequences for Arabidopsis thaliana (TAIR version from April 23, 2008) Description: Full genome sequences for Arabidopsis thaliana as provided by TAIR (snapshot from April 23, 2008) and stored in Biostrings objects. Version: 1.4.2 organism: Arabidopsis thaliana common_name: Arabidopsis provider: TAIR provider_version: 04232008 release_date: NA release_name: dumped from ADB: Mar/14/08 source_url: ftp://ftp.arabidopsis.org/home/tair/Sequences/whole_chromosomes/ organism_biocview: Arabidopsis_thaliana BSgenomeObjname: Athaliana seqnames: paste("chr", c(1:5, "C", "M"), sep="") circ_seqs: c("chrC", "chrM") SrcDataFiles: all the chr*.fas file from ftp://ftp.arabidopsis.org/home/tair/Sequences/whole_chromosomes/ WARNING: This is where things are today (Oct 1st, 2008) but is probably NOT aimed to be the permanent URL for the 04232008 snapshot of the genome. TAIR might update the content of this folder in the future with a new snapshot and move the 04232008 snapshot to the OLD/ subfolder. PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Athaliana.TAIR.04232008/seqs seqfiles_suffix: .fas ondisk_seq_format: rda BSgenome/inst/extdata/GentlemanLab/BSgenome.Athaliana.TAIR.TAIR9-seed0000644000175400017540000000172713175713516026065 0ustar00biocbuildbiocbuildPackage: BSgenome.Athaliana.TAIR.TAIR9 Title: Full genome sequences for Arabidopsis thaliana (TAIR9) Description: Full genome sequences for Arabidopsis thaliana as provided by TAIR (TAIR9 Genome Release) and stored in Biostrings objects. Note that TAIR10 is an "annotation release" based on the same genome assembly as TAIR9. Version: 1.4.2 organism: Arabidopsis thaliana common_name: Arabidopsis provider: TAIR provider_version: TAIR9 release_date: June 9, 2009 release_name: TAIR9 Genome Release source_url: ftp://ftp.arabidopsis.org/home/tair/Genes/TAIR9_genome_release/ organism_biocview: Arabidopsis_thaliana BSgenomeObjname: Athaliana seqnames: paste("Chr", c(1:5, "M", "C"), sep="") circ_seqs: c("ChrM", "ChrC") SrcDataFiles: ftp://ftp.arabidopsis.org/home/tair/Genes/TAIR9_genome_release/TAIR9_chr_all.fas PkgExamples: genome$Chr1 # same as genome[["Chr1"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Athaliana.TAIR.TAIR9/seqs ondisk_seq_format: rda BSgenome/inst/extdata/GentlemanLab/BSgenome.Athaliana.TAIR.TAIR9-tools/0000755000175400017540000000000013175713516026353 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Athaliana.TAIR.TAIR9-tools/NOTES.TXT0000644000175400017540000001013413175713516027643 0ustar00biocbuildbiocbuildSequences ========= ftp://ftp.arabidopsis.org/home/tair/Genes/TAIR9_genome_release/ file: TAIR9_chr_all.fas R code used to split TAIR9_chr_all.fas into 1 FASTA file per sequence: splitTair9ChrAllFasta <- function(filepath) { NAMESMAP <- paste("Chr", c(1:5, "M", "C"), sep="") names(NAMESMAP) <- c(1:5, "mitochondria", "chloroplast") chr_all <- readDNAStringSet(filepath) shortnames <- sapply(strsplit(names(chr_all), " ", fixed=TRUE), function(xx) xx[1L]) if (!identical(shortnames, names(NAMESMAP))) stop(filepath, " doesn't contain the expected sequence names") names(chr_all) <- NAMESMAP for (i in seq_len(length(chr_all))) { out <- paste(NAMESMAP[i], ".fa", sep="") cat("Writing ", out, " file ... ", sep="") write.XStringSet(chr_all[i], filepath=out) cat("OK\n") } } splitTair9ChrAllFasta("TAIR9_chr_all.fas") Masks ===== This was an attempt at putting built-in masks in BSgenome.Athaliana.TAIR.TAIR9 but it didn't work! (see below why) The first published version of BSgenome.Athaliana.TAIR.TAIR9 (version 1.3.18) has NO built-in masks. Assembly gaps extracted from ftp://ftp.arabidopsis.org/home/tair/Genes/TAIR9_genome_release/TAIR9_gff3/Assembly_GFF/ file: tair9_Assembly_gaps.gff R code used to convert tair9_Assembly_gaps.gff into a UCSC-like "gap" file: tair9GapsGFF.to.UCSCGapFile <- function(infile, outfile) { gff <- read.table(infile, sep="\t", quote="") if (!identical(levels(gff[[3L]]), "gap")) stop("some rows have a feature type != \"gap\"") if (!identical(levels(gff[[7L]]), "+")) stop("some gaps are not on the + strand") if (!identical(levels(gff[[6L]]), ".") || !identical(levels(gff[[8L]]), ".")) stop("field 6 and 8 are not empty") gap <- gff[c(1L, 4L, 5L)] gap[[2L]] <- gap[[2L]] - 1L gap <- cbind(gap, 0L, "N", gap[[3L]] - gap[[2L]], ".", ".") write.table(gap, file=outfile, quote=FALSE, sep="\t", col.names=FALSE) } tair9GapsGFF.to.UCSCGapFile("tair9_Assembly_gaps.gff", "gap.txt") Problems with those assembly gaps: some of them have a size that doesn't match the size of the corresponding N-block in the sequence (as reported in TAIR9_chr_all.fas). Email sent to the TAIR curators on Dec 14, 2010: ----------------------------------------------------------------------- Hi TAIR curators, For my project, I need to use the whole chromosome TAIR9 sequences provided here ftp://ftp.arabidopsis.org/home/tair/Genes/TAIR9_genome_release/TAIR9_chr_all.fas and also I need to know the exact locations (and sizes) of the assembly gaps for those sequences. After looking at the tair9_Assembly_gaps.gff file (from ftp://ftp.arabidopsis.org/home/tair/Genes/TAIR9_genome_release/TAIR9_gff3/Assembly_GFF/), I found that some of the assembly gaps listed in this file are not compatible with the N-blocks found in the sequences. See at the end of this email for the exact list of problems I found. My question is: what could explain that the size of an assembly gap is not the same as the size of its corresponding N-block? Is this really intended? If not, is there another file somewhere on your site that contains the actual size of the assembly gaps? Thanks in advance, H. List of problems found in the tair9_Assembly_gaps.gff file: Line # | seqname | type | start end | NOTE 5 | Chr1 | gap | 14545722 14581721 | NOTE=Size_36000_centromeric BAC Pb: the size of the N-block found in the sequence is 35998! 15 | Chr1 | gap | 15345855 15346528 | NOTE=Size_674_exact sizes of the gaps are unknown Pb: the size of the N-block found in the sequence is 60! 35 | Chr3 | gap | 13589757 13589816 | NOTE=Size_60_centromeric BAC Pb: the size of the N-block found in the sequence is 56! 76 | Chr3 | gap | 15132295 15132547 | NOTE=Size_253_N's as sequence needs to be verified Pb: the size of the N-block found in the sequence is 251! 93 | Chr5 | gap | 11725025 11726024 | NOTE=Size_1000 Pb: the size of the N-block found in the sequence is 998! ----------------------------------------------------------------------- BSgenome/inst/extdata/GentlemanLab/BSgenome.Btaurus.UCSC.bosTau3-seed0000644000175400017540000000272613175713516026316 0ustar00biocbuildbiocbuildPackage: BSgenome.Btaurus.UCSC.bosTau3 Title: Full genome sequences for Bos taurus (UCSC version bosTau3) Description: Full genome sequences for Bos taurus (Cow) as provided by UCSC (bosTau3, Aug. 2006) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Bos taurus common_name: Cow provider: UCSC provider_version: bosTau3 release_date: Aug. 2006 release_name: Baylor College of Medicine HGSC Btau_3.1 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/bosTau3/bigZips/ organism_biocview: Bos_taurus BSgenomeObjname: Btaurus SrcDataFiles: bosTau3.2bit from http://hgdownload.soe.ucsc.edu/goldenPath/bosTau3/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## UCSC makes the upstream sequences for bosTau3 available for download ## here http://hgdownload.soe.ucsc.edu/goldenPath/bosTau3/bigZips/ ## Alternatively, the upstream sequences can be extracted from the full ## genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("bosTau3", "refGene") up1000seqs <- extractUpstreamSeqs(genome, txdb, width=1000) . ## See ?extractUpstreamSeqs in the GenomicFeatures package for more ## information about this. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Btaurus.UCSC.bosTau3/seqs seqfile_name: bosTau3.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Btaurus.UCSC.bosTau3.masked-seed0000644000175400017540000000265713175713516027564 0ustar00biocbuildbiocbuildPackage: BSgenome.Btaurus.UCSC.bosTau3.masked Title: Full masked genome sequences for Bos taurus (UCSC version bosTau3) Description: Full genome sequences for Bos taurus (Cow) as provided by UCSC (bosTau3, Aug. 2006) and stored in Biostrings objects. The sequences are the same as in BSgenome.Btaurus.UCSC.bosTau3, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Btaurus.UCSC.bosTau3 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/bosTau3/bigZips/ organism_biocview: Bos_taurus nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau3/database/ RM masks: bosTau3.fa.out.gz from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau3/bigZips/ TRF masks: bosTau3.trf.bed.gz from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau3/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Btaurus.UCSC.bosTau3$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Btaurus.UCSC.bosTau3/masks AGAPSfiles_name: gap.txt RMfiles_name: bosTau3.fa.out TRFfiles_name: bosTau3.trf.bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Btaurus.UCSC.bosTau4-seed0000644000175400017540000000275413175713516026320 0ustar00biocbuildbiocbuildPackage: BSgenome.Btaurus.UCSC.bosTau4 Title: Full genome sequences for Bos taurus (UCSC version bosTau4) Description: Full genome sequences for Bos taurus (Cow) as provided by UCSC (bosTau4, Oct. 2007) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Bos taurus common_name: Cow provider: UCSC provider_version: bosTau4 release_date: Oct. 2007 release_name: Baylor College of Medicine HGSC Btau_4.0 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/bosTau4/bigZips/ organism_biocview: Bos_taurus BSgenomeObjname: Btaurus circ_seqs: "chrM" SrcDataFiles: bosTau4.2bit from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau4/chromosomes/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## UCSC makes the upstream sequences for bosTau4 available for download ## here http://hgdownload.soe.ucsc.edu/goldenPath/bosTau4/bigZips/ ## Alternatively, the upstream sequences can be extracted from the full ## genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("bosTau4", "refGene") up1000seqs <- extractUpstreamSeqs(genome, txdb, width=1000) . ## See ?extractUpstreamSeqs in the GenomicFeatures package for more ## information about this. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Btaurus.UCSC.bosTau4/seqs seqfile_name: bosTau4.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Btaurus.UCSC.bosTau4.masked-seed0000644000175400017540000000265713175713516027565 0ustar00biocbuildbiocbuildPackage: BSgenome.Btaurus.UCSC.bosTau4.masked Title: Full masked genome sequences for Bos taurus (UCSC version bosTau4) Description: Full genome sequences for Bos taurus (Cow) as provided by UCSC (bosTau4, Oct. 2007) and stored in Biostrings objects. The sequences are the same as in BSgenome.Btaurus.UCSC.bosTau4, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Btaurus.UCSC.bosTau4 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/bosTau4/bigZips/ organism_biocview: Bos_taurus nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau4/database/ RM masks: bosTau4.fa.out.gz from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau4/bigZips/ TRF masks: bosTau4.trf.bed.gz from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau4/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Btaurus.UCSC.bosTau4$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Btaurus.UCSC.bosTau4/masks AGAPSfiles_name: gap.txt RMfiles_name: bosTau4.fa.out TRFfiles_name: bosTau4.trf.bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Btaurus.UCSC.bosTau6-seed0000644000175400017540000000353213175713516026315 0ustar00biocbuildbiocbuildPackage: BSgenome.Btaurus.UCSC.bosTau6 Title: Full genome sequences for Bos taurus (UCSC version bosTau6) Description: Full genome sequences for Bos taurus (Cow) as provided by UCSC (bosTau6, Nov. 2009) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Bos taurus common_name: Cow provider: UCSC provider_version: bosTau6 release_date: Nov. 2009 release_name: University of Maryland v3.1 source_url: http://hgdownload.soe.ucsc.edu/goldenPath/bosTau6/bigZips/ organism_biocview: Bos_taurus BSgenomeObjname: Btaurus seqnames: paste("chr", c(1:29, "X", "M"), sep="") circ_seqs: "chrM" mseqnames: "chrUn" SrcDataFiles: bosTau6.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau6/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for bosTau6 are not included in the BSgenome ## data package anymore. However they can easily be extracted from the ## full genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("bosTau6", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Btaurus.UCSC.bosTau6/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Btaurus.UCSC.bosTau6-tools/0000755000175400017540000000000013175713516026607 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Btaurus.UCSC.bosTau6-tools/splitbigfasta.R0000755000175400017540000000123313175713516031570 0ustar00biocbuildbiocbuild### library(Biostrings) bosTau6 <- readDNAStringSet("bosTau6.fa") ### Partitioning: is_chrUn <- grepl("^chrUn", names(bosTau6)) is_chrom <- !is_chrUn ### Send each chromosome to a FASTA file. seqnames <- paste("chr", c(1:29, "X", "M"), sep="") stopifnot(setequal(seqnames, names(bosTau6)[is_chrom])) for (seqname in seqnames) { seq <- bosTau6[match(seqname, names(bosTau6))] filename <- paste(seqname, ".fa", sep="") cat("writing ", filename, "\n", sep="") writeXStringSet(seq, file=filename, width=50L) } ### Send the 3286 chrUn_* sequences to 1 FASTA file. chrUn_mseq <- bosTau6[is_chrUn] writeXStringSet(chrUn_mseq, file="chrUn.fa", width=50L) BSgenome/inst/extdata/GentlemanLab/BSgenome.Btaurus.UCSC.bosTau6.masked-seed0000644000175400017540000000265713175713516027567 0ustar00biocbuildbiocbuildPackage: BSgenome.Btaurus.UCSC.bosTau6.masked Title: Full masked genome sequences for Bos taurus (UCSC version bosTau6) Description: Full genome sequences for Bos taurus (Cow) as provided by UCSC (bosTau6, Nov. 2009) and stored in Biostrings objects. The sequences are the same as in BSgenome.Btaurus.UCSC.bosTau6, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Btaurus.UCSC.bosTau6 source_url: http://hgdownload.soe.ucsc.edu/goldenPath/bosTau6/bigZips/ organism_biocview: Bos_taurus nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau6/database/ RM masks: bosTau6.fa.out.gz from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau6/bigZips/ TRF masks: bosTau6.trf.bed.gz from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau6/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Btaurus.UCSC.bosTau6$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Btaurus.UCSC.bosTau6/masks AGAPSfiles_name: gap.txt RMfiles_name: bosTau6.fa.out TRFfiles_name: bosTau6.trf.bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Btaurus.UCSC.bosTau8-seed0000644000175400017540000000366013175713516026321 0ustar00biocbuildbiocbuildPackage: BSgenome.Btaurus.UCSC.bosTau8 Title: Full genome sequences for Bos taurus (UCSC version bosTau8) Description: Full genome sequences for Bos taurus (Cow) as provided by UCSC (bosTau8, Jun. 2014) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Bos taurus common_name: Cow provider: UCSC provider_version: bosTau8 release_date: Jun. 2014 release_name: University of Maryland v3.1.1 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/bosTau8/bigZips/ organism_biocview: Bos_taurus BSgenomeObjname: Btaurus circ_seqs: "chrM" SrcDataFiles: bosTau8.2bit from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau8/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Extract the upstream sequences ## --------------------------------------------------------------------- ## The upstream sequences located in ## http://hgdownload.cse.ucsc.edu/goldenPath/bosTau8/bigZips/ ## are based on RefSeq genes (RefSeq Genes track in the Genome Browser). ## These can easily be extracted from the full genome sequences with: . library(GenomicFeatures) refGene_txdb <- suppressWarnings(makeTxDbFromUCSC("bosTau8", "refGene")) refGene_up1000seqs <- extractUpstreamSeqs(genome, refGene_txdb) . ## Note that you can make a TxDb object from various annotation ## resources. See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), and ## makeTxDbFromGFF() functions in the GenomicFeatures package for more ## information. ## IMPORTANT: Make sure you use a TxDb package (or TxDb object) that ## contains a gene model based on bosTau8 or on a compatible genome ## (i.e. a genome with sequences identical to the sequences in bosTau8). ## See ?extractUpstreamSeqs in the GenomicFeatures package for more ## information. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Btaurus.UCSC.bosTau8/seqs seqfile_name: bosTau8.sorted.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Celegans.UCSC.ce10-seed0000644000175400017540000000355613175713516025624 0ustar00biocbuildbiocbuildPackage: BSgenome.Celegans.UCSC.ce10 Title: Full genome sequences for Caenorhabditis elegans (UCSC version ce10) Description: Full genome sequences for Caenorhabditis elegans (Worm) as provided by UCSC (ce10, Oct. 2010) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Caenorhabditis elegans common_name: Worm provider: UCSC provider_version: ce10 release_date: Oct. 2010 release_name: WormBase v. WS220 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/ce10/bigZips/ organism_biocview: Caenorhabditis_elegans BSgenomeObjname: Celegans seqnames: paste("chr", c("I", "II", "III", "IV", "V", "X", "M"), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.tar.gz from ftp://hgdownload.cse.ucsc.edu/goldenPath/ce10/bigZips/ PkgExamples: genome$chrI # same as genome[["chrI"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for ce10 are not included in the BSgenome data ## package anymore. However they can easily be extracted from the full ## genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("ce10", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Celegans.UCSC.ce10/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Celegans.UCSC.ce11-seed0000644000175400017540000000166013175713516025617 0ustar00biocbuildbiocbuildPackage: BSgenome.Celegans.UCSC.ce11 Title: Full genome sequences for Caenorhabditis elegans (UCSC version ce11) Description: Full genome sequences for Caenorhabditis elegans (Worm) as provided by UCSC (ce11, Feb. 2013) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Caenorhabditis elegans common_name: Worm provider: UCSC provider_version: ce11 release_date: Feb. 2013 release_name: C. elegans Sequencing Consortium WBcel235 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/ce11/bigZips/ organism_biocview: Caenorhabditis_elegans BSgenomeObjname: Celegans seqnames: paste("chr", c("I", "II", "III", "IV", "V", "X", "M"), sep="") circ_seqs: "chrM" SrcDataFiles: ce11.2bit from http://hgdownload.soe.ucsc.edu/goldenPath/ce11/bigZips/ PkgExamples: genome$chrI # same as genome[["chrI"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Celegans.UCSC.ce11/seqs seqfile_name: ce11.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Celegans.UCSC.ce2-seed0000644000175400017540000000354313175713516025541 0ustar00biocbuildbiocbuildPackage: BSgenome.Celegans.UCSC.ce2 Title: Full genome sequences for Caenorhabditis elegans (UCSC version ce2) Description: Full genome sequences for Caenorhabditis elegans (Worm) as provided by UCSC (ce2, Mar. 2004) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Caenorhabditis elegans common_name: Worm provider: UCSC provider_version: ce2 release_date: Mar. 2004 release_name: WormBase v. WS120 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/ce2/bigZips/ organism_biocview: Caenorhabditis_elegans BSgenomeObjname: Celegans seqnames: paste("chr", c("I", "II", "III", "IV", "V", "X", "M"), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.zip from http://hgdownload.cse.ucsc.edu/goldenPath/ce2/bigZips/ PkgExamples: genome$chrI # same as genome[["chrI"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for ce2 are not included in the BSgenome data ## package anymore. However they can easily be extracted from the full ## genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("ce2", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Celegans.UCSC.ce2/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Celegans.UCSC.ce6-seed0000644000175400017540000000357613175713516025553 0ustar00biocbuildbiocbuildPackage: BSgenome.Celegans.UCSC.ce6 Title: Full genome sequences for Caenorhabditis elegans (UCSC version ce6) Description: Full genome sequences for Caenorhabditis elegans (Worm) as provided by UCSC (ce6, May 2008) and stored in Biostrings objects. Version: 1.4.2 Suggests: TxDb.Celegans.UCSC.ce6.ensGene organism: Caenorhabditis elegans common_name: Worm provider: UCSC provider_version: ce6 release_date: May 2008 release_name: WormBase v. WS190 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/ce6/bigZips/ organism_biocview: Caenorhabditis_elegans BSgenomeObjname: Celegans seqnames: paste("chr", c("I", "II", "III", "IV", "V", "X", "M"), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.tar.gz from ftp://hgdownload.cse.ucsc.edu/goldenPath/ce6/bigZips/ PkgExamples: genome$chrI # same as genome[["chrI"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for ce6 are not included in the BSgenome data ## package anymore. However they can easily be extracted from the full ## genome sequences with something like: . library(TxDb.Celegans.UCSC.ce6.ensGene) txdb <- TxDb.Celegans.UCSC.ce6.ensGene gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Celegans.UCSC.ce6/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Cfamiliaris.UCSC.canFam2-seed0000644000175400017540000000350313175713516027035 0ustar00biocbuildbiocbuildPackage: BSgenome.Cfamiliaris.UCSC.canFam2 Title: Full genome sequences for Canis lupus familiaris (UCSC version canFam2) Description: Full genome sequences for Canis lupus familiaris (Dog) as provided by UCSC (canFam2, May 2005) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Canis lupus familiaris common_name: Dog provider: UCSC provider_version: canFam2 release_date: May 2005 release_name: Broad Institute v2.0 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/canFam2/bigZips/ organism_biocview: Canis_familiaris BSgenomeObjname: Cfamiliaris seqnames: paste("chr", c(1:38, "X", "M", "Un"), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/canFam2/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## The upstream sequences for canFam2 (i.e. the sequences 1000 bases ## upstream of annotated transcription starts) can easily be extracted ## from the full genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("canFam2", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Cfamiliaris.UCSC.canFam2/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Cfamiliaris.UCSC.canFam2.masked-seed0000644000175400017540000000263013175713516030300 0ustar00biocbuildbiocbuildPackage: BSgenome.Cfamiliaris.UCSC.canFam2.masked Title: Full masked genome sequences for Canis lupus familiaris (UCSC version canFam2) Description: Full genome sequences for Canis lupus familiaris (Dog) as provided by UCSC (canFam2, May 2005) and stored in Biostrings objects. The sequences are the same as in BSgenome.Cfamiliaris.UCSC.canFam2, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Cfamiliaris.UCSC.canFam2 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/canFam2/bigZips/ organism_biocview: Canis_familiaris nmask_per_seq: 4 SrcDataFiles: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/canFam2/database/ RM masks: chromOut.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/canFam2/bigZips/ TRF masks: chromTrf.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/canFam2/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Cfamiliaris.UCSC.canFam2$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Cfamiliaris.UCSC.canFam2/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Cfamiliaris.UCSC.canFam3-seed0000644000175400017540000000361213175713516027037 0ustar00biocbuildbiocbuildPackage: BSgenome.Cfamiliaris.UCSC.canFam3 Title: Full genome sequences for Canis lupus familiaris (UCSC version canFam3) Description: Full genome sequences for Canis lupus familiaris (Dog) as provided by UCSC (canFam3, Sep. 2011) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Canis lupus familiaris common_name: Dog provider: UCSC provider_version: canFam3 release_date: Sep. 2011 release_name: Broad Institute v3.1 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/canFam3/bigZips/ organism_biocview: Canis_familiaris BSgenomeObjname: Cfamiliaris seqnames: paste("chr", c(1:38, "X", "M"), sep="") circ_seqs: "chrM" mseqnames: "chrUn" SrcDataFiles: canFam3.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/canFam3/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for canFam3 are not included in the BSgenome ## data package anymore. However they can easily be extracted from the ## full genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("canFam3", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Cfamiliaris.UCSC.canFam3/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Cfamiliaris.UCSC.canFam3-tools/0000755000175400017540000000000013175713516027332 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Cfamiliaris.UCSC.canFam3-tools/splitbigfasta.R0000755000175400017540000000123313175713516032313 0ustar00biocbuildbiocbuild### library(Biostrings) canFam3 <- readDNAStringSet("canFam3.fa") ### Partitioning: is_chrUn <- grepl("^chrUn", names(canFam3)) is_chrom <- !is_chrUn ### Send each chromosome to a FASTA file. seqnames <- paste("chr", c(1:38, "X", "M"), sep="") stopifnot(setequal(seqnames, names(canFam3)[is_chrom])) for (seqname in seqnames) { seq <- canFam3[match(seqname, names(canFam3))] filename <- paste(seqname, ".fa", sep="") cat("writing ", filename, "\n", sep="") writeXStringSet(seq, file=filename, width=50L) } ### Send the 1439 chrUn_* sequences to 1 FASTA file. chrUn_mseq <- canFam3[is_chrUn] writeXStringSet(chrUn_mseq, file="chrUn.fa", width=50L) BSgenome/inst/extdata/GentlemanLab/BSgenome.Cfamiliaris.UCSC.canFam3.masked-seed0000644000175400017540000000274113175713516030304 0ustar00biocbuildbiocbuildPackage: BSgenome.Cfamiliaris.UCSC.canFam3.masked Title: Full masked genome sequences for Canis lupus familiaris (UCSC version canFam3) Description: Full genome sequences for Canis lupus familiaris (Dog) as provided by UCSC (canFam3, Sep. 2011) and stored in Biostrings objects. The sequences are the same as in BSgenome.Cfamiliaris.UCSC.canFam3, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Cfamiliaris.UCSC.canFam3 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/canFam3/bigZips/ organism_biocview: Canis_familiaris nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/canFam3/database/ RM masks: canFam3.fa.out.gz from http://hgdownload.cse.ucsc.edu/goldenPath/canFam3/bigZips/ TRF masks: canFam3.trf.bed.gz from http://hgdownload.cse.ucsc.edu/goldenPath/canFam3/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Cfamiliaris.UCSC.canFam3$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Cfamiliaris.UCSC.canFam3/masks AGAPSfiles_name: gap.txt RMfiles_name: canFam3.fa.out TRFfiles_name: canFam3.trf.bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Dmelanogaster.UCSC.dm2-seed0000644000175400017540000000362713175713516026621 0ustar00biocbuildbiocbuildPackage: BSgenome.Dmelanogaster.UCSC.dm2 Title: Full genome sequences for Drosophila melanogaster (UCSC version dm2) Description: Full genome sequences for Drosophila melanogaster (Fly) as provided by UCSC (dm2, Apr. 2004) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Drosophila melanogaster common_name: Fly provider: UCSC provider_version: dm2 release_date: Apr. 2004 release_name: BDGP Release 4 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/dm2/bigZips/ organism_biocview: Drosophila_melanogaster BSgenomeObjname: Dmelanogaster seqnames: paste("chr", c("2L", "2R", "3L", "3R", "4", "X", "U", "M", "2h", "3h", "4h", "Xh", "Yh"), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.zip from http://hgdownload.cse.ucsc.edu/goldenPath/dm2/bigZips/ PkgExamples: genome$chr2L # same as genome[["chr2L"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for dm2 are not included in the BSgenome data ## package anymore. However they can easily be extracted from the full ## genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("dm2", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Dmelanogaster.UCSC.dm2/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Dmelanogaster.UCSC.dm2.masked-seed0000644000175400017540000000257613175713516030066 0ustar00biocbuildbiocbuildPackage: BSgenome.Dmelanogaster.UCSC.dm2.masked Title: Full masked genome sequences for Drosophila melanogaster (UCSC version dm2) Description: Full genome sequences for Drosophila melanogaster (Fly) as provided by UCSC (dm2, Apr. 2004) and stored in Biostrings objects. The sequences are the same as in BSgenome.Dmelanogaster.UCSC.dm2, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Dmelanogaster.UCSC.dm2 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/dm2/bigZips/ organism_biocview: Drosophila_melanogaster nmask_per_seq: 4 SrcDataFiles: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/dm2/database/ RM masks: chromOut.zip from http://hgdownload.cse.ucsc.edu/goldenPath/dm2/bigZips/ TRF masks: chromTrf.zip from http://hgdownload.cse.ucsc.edu/goldenPath/dm2/bigZips/ PkgExamples: genome$chr2L # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr2L) # same as BSgenome.Dmelanogaster.UCSC.dm2$$chr2L masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Dmelanogaster.UCSC.dm2/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Dmelanogaster.UCSC.dm3-seed0000644000175400017540000000447013175713516026617 0ustar00biocbuildbiocbuildPackage: BSgenome.Dmelanogaster.UCSC.dm3 Title: Full genome sequences for Drosophila melanogaster (UCSC version dm3) Description: Full genome sequences for Drosophila melanogaster (Fly) as provided by UCSC (dm3, Apr. 2006) and stored in Biostrings objects. Version: 1.4.2 Suggests: TxDb.Dmelanogaster.UCSC.dm3.ensGene organism: Drosophila melanogaster common_name: Fly provider: UCSC provider_version: dm3 release_date: Apr. 2006 release_name: BDGP Release 5 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/dm3/bigZips/ organism_biocview: Drosophila_melanogaster BSgenomeObjname: Dmelanogaster seqnames: paste("chr", c("2L", "2R", "3L", "3R", "4", "X", "U", "M", "2LHet", "2RHet", "3LHet", "3RHet", "XHet", "YHet", "Uextra"), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/dm3/bigZips/ PkgExamples: genome$chr2L # same as genome[["chr2L"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for dm3 are not included in the BSgenome data ## package anymore. However they can easily be extracted from the full ## genome sequences with something like: . library(TxDb.Dmelanogaster.UCSC.dm3.ensGene) txdb <- TxDb.Dmelanogaster.UCSC.dm3.ensGene . ## Because the chrU and chrUextra sequences are made of concatenated ## scaffolds (see http://genome.ucsc.edu/cgi-bin/hgGateway?db=dm3), ## extracting the upstream sequences for genes located on these ## scaffolds is not reliable. So we exclude them: exclude <- c("chrU", "chrUextra") up1000seqs <- extractUpstreamSeqs(genome, txdb, width=1000, exclude.seqlevels=exclude) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package for more information. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Dmelanogaster.UCSC.dm3/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Dmelanogaster.UCSC.dm3.masked-seed0000644000175400017540000000260313175713516030056 0ustar00biocbuildbiocbuildPackage: BSgenome.Dmelanogaster.UCSC.dm3.masked Title: Full masked genome sequences for Drosophila melanogaster (UCSC version dm3) Description: Full genome sequences for Drosophila melanogaster (Fly) as provided by UCSC (dm3, Apr. 2006) and stored in Biostrings objects. The sequences are the same as in BSgenome.Dmelanogaster.UCSC.dm3, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Dmelanogaster.UCSC.dm3 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/dm3/bigZips/ organism_biocview: Drosophila_melanogaster nmask_per_seq: 4 SrcDataFiles: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/dm3/database/ RM masks: chromOut.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/dm3/bigZips/ TRF masks: chromTrf.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/dm3/bigZips/ PkgExamples: genome$chr2L # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr2L) # same as BSgenome.Dmelanogaster.UCSC.dm3$chr2L masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Dmelanogaster.UCSC.dm3/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Dmelanogaster.UCSC.dm6-seed0000644000175400017540000000335713175713516026625 0ustar00biocbuildbiocbuildPackage: BSgenome.Dmelanogaster.UCSC.dm6 Title: Full genome sequences for Drosophila melanogaster (UCSC version dm6) Description: Full genome sequences for Drosophila melanogaster (Fly) as provided by UCSC (dm6, Aug. 2014) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Drosophila melanogaster common_name: Fly provider: UCSC provider_version: dm6 release_date: Aug. 2014 release_name: BDGP Release 6 + ISO1 MT source_url: http://hgdownload.cse.ucsc.edu/goldenPath/dm6/bigZips/ organism_biocview: Drosophila_melanogaster BSgenomeObjname: Dmelanogaster seqnames: seqnames(Seqinfo(genome="dm6")) circ_seqs: "chrM" SrcDataFiles: dm6.2bit from http://hgdownload.cse.ucsc.edu/goldenPath/dm6/bigZips/ PkgExamples: genome$chr2L # same as genome[["chr2L"]] . ## --------------------------------------------------------------------- ## Extract the upstream sequences ## --------------------------------------------------------------------- ## The upstream sequences can easily be extracted from the full genome ## sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("dm6", tablename="refGene") up1000seqs <- extractUpstreamSeqs(genome, txdb, width=1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object) that ## contains a gene model based on dm6 or on a compatible genome (i.e. ## a genome with sequences identical to the sequences in dm6). Note ## that you can make a TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), and ## makeTxDbFromGFF() functions in the GenomicFeatures package for more ## information. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Dmelanogaster.UCSC.dm6/seqs seqfile_name: dm6.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer10-seed0000644000175400017540000000371713175713516026152 0ustar00biocbuildbiocbuildPackage: BSgenome.Drerio.UCSC.danRer10 Title: Full genome sequences for Danio rerio (UCSC version danRer10) Description: Full genome sequences for Danio rerio (Zebrafish) as provided by UCSC (danRer10, Sep. 2014) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Danio rerio common_name: Zebrafish provider: UCSC provider_version: danRer10 release_date: Sep. 2014 release_name: Genome Reference Consortium GRCz10 source_url: http://hgdownload.soe.ucsc.edu/goldenPath/danRer10/bigZips/ organism_biocview: Danio_rerio BSgenomeObjname: Drerio circ_seqs: "chrM" SrcDataFiles: danRer10.2bit from http://hgdownload.soe.ucsc.edu/goldenPath/danRer10/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Extract the upstream sequences ## --------------------------------------------------------------------- ## The upstream sequences located in ## http://hgdownload.cse.ucsc.edu/goldenPath/danRer10/bigZips/ ## are based on RefSeq genes (RefSeq Genes track in the Genome Browser). ## These can easily be extracted from the full genome sequences with: . library(GenomicFeatures) refGene_txdb <- suppressWarnings(makeTxDbFromUCSC("danRer10", "refGene")) refGene_up1000seqs <- extractUpstreamSeqs(genome, refGene_txdb) . ## Note that you can make a TxDb object from various annotation ## resources. See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), and ## makeTxDbFromGFF() functions in the GenomicFeatures package for more ## information. ## IMPORTANT: Make sure you use a TxDb package (or TxDb object) that ## contains a gene model based on danRer10 or on a compatible genome ## (i.e. a genome with sequences identical to the sequences in ## danRer10). See ?extractUpstreamSeqs in the GenomicFeatures package ## for more information. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Drerio.UCSC.danRer10/seqs seqfile_name: danRer10.sorted.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer10-tools/0000755000175400017540000000000013175713516026437 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer10-tools/sort_danRer10.2bit.R0000644000175400017540000000113713175713516032046 0ustar00biocbuildbiocbuildlibrary(Biostrings) library(rtracklayer) danRer10 <- import("danRer10.2bit") seqlevels1 <- paste0("chr", c(1:25, "M")) tmp <- CharacterList(strsplit(names(danRer10), "_")) npart <- elementNROWS(tmp) stopifnot(all(npart <= 2L)) idx1 <- which(npart == 1L) stopifnot(setequal(names(danRer10)[idx1], seqlevels1)) idx2 <- which(npart == 2L) m2 <- matrix(unlist(tmp[idx2]), ncol=2L, byrow=TRUE) stopifnot(all(m2[ , 1L] == "chrUn")) oo2 <- order(m2[ , 2L]) seqlevels2 <- names(danRer10)[idx2[oo2]] danRer10_seqlevels <- c(seqlevels1, seqlevels2) export(danRer10[danRer10_seqlevels], "danRer10.sorted.2bit") BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer5-seed0000644000175400017540000000356013175713516026072 0ustar00biocbuildbiocbuildPackage: BSgenome.Drerio.UCSC.danRer5 Title: Full genome sequences for Danio rerio (UCSC version danRer5) Description: Full genome sequences for Danio rerio (Zebrafish) as provided by UCSC (danRer5, Jul. 2007) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Danio rerio common_name: Zebrafish provider: UCSC provider_version: danRer5 release_date: Jul. 2007 release_name: Sanger Institute Zv7 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/danRer5/bigZips/ organism_biocview: Danio_rerio BSgenomeObjname: Drerio seqnames: paste("chr", c(1:25, "M"), sep="") circ_seqs: "chrM" mseqnames: c("Zv7_NA", "Zv7_scaffold") SrcDataFiles: danRer5.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/danRer5/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for danRer5 are not included in the BSgenome ## data package anymore. However they can easily be extracted from the ## full genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("danRer5", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Drerio.UCSC.danRer5/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer5-tools/0000755000175400017540000000000013175713516026363 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer5-tools/NOTES.TXT0000644000175400017540000000034513175713516027656 0ustar00biocbuildbiocbuildDownloaded the danRer5.fa.gz file on July 27, 2009 5036 FASTA records: o 26 chromosome sequences (1, 2, ..., 25, M) o 4844 Zv7_NA* sequences o 166 Zv7_scaffold* sequences Use the splitbigfasta.sh script to split danRer5.fa BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer5-tools/splitbigfasta.sh0000755000175400017540000000353313175713516031562 0ustar00biocbuildbiocbuild#!/bin/bash # # Run with: # ./splitbigfasta.sh danRer5.fa # Then test the result with: # cat chr[1-9].fa chr??.fa Zv7_NA.fa Zv7_scaffold.fa chrM.fa > merged.fa # cmp merged.fa danRer5.fa set -e # Exit immediately if a simple command exits with a non-zero status # Note that in 'head -n NH $1 | tail -n NT' the NH and NT values # were obtained from R with: # library(Biostrings) # fi <- fasta.seqlengths("danRer5.fa") # fi25 <- fi[1:25] # NT <- fi25 %/% 50 + 2 # NH <- cumsum(NT) head -n 1124095 $1 > chr1.fa head -n 2211431 $1 | tail -n 1087336 > chr2.fa head -n 3470057 $1 | tail -n 1258626 > chr3.fa head -n 4322107 $1 | tail -n 852050 > chr4.fa head -n 5729536 $1 | tail -n 1407429 > chr5.fa head -n 6913551 $1 | tail -n 1184015 > chr6.fa head -n 8318793 $1 | tail -n 1405242 > chr7.fa head -n 9447929 $1 | tail -n 1129136 > chr8.fa head -n 10477749 $1 | tail -n 1029820 > chr9.fa head -n 11325342 $1 | tail -n 847593 > chr10.fa head -n 12217671 $1 | tail -n 892329 > chr11.fa head -n 13168147 $1 | tail -n 950476 > chr12.fa head -n 14239096 $1 | tail -n 1070949 > chr13.fa head -n 15369555 $1 | tail -n 1130459 > chr14.fa head -n 16302145 $1 | tail -n 932590 > chr15.fa head -n 17363560 $1 | tail -n 1061415 > chr16.fa head -n 18409770 $1 | tail -n 1046210 > chr17.fa head -n 19395399 $1 | tail -n 985629 > chr18.fa head -n 20319025 $1 | tail -n 923626 > chr19.fa head -n 21449600 $1 | tail -n 1130575 > chr20.fa head -n 22370748 $1 | tail -n 921148 > chr21.fa head -n 23150386 $1 | tail -n 779638 > chr22.fa head -n 24078148 $1 | tail -n 927762 > chr23.fa head -n 24884016 $1 | tail -n 805868 > chr24.fa head -n 25541542 $1 | tail -n 657526 > chr25.fa tail -n 333 $1 > chrM.fa # NH and NT found after several try-and-fail attempts head -n 27902547 $1 | tail -n 2361005 > Zv7_NA.fa head -n 28818810 $1 | tail -n 916263 > Zv7_scaffold.fa BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer5.masked-seed0000644000175400017540000000266313175713516027340 0ustar00biocbuildbiocbuildPackage: BSgenome.Drerio.UCSC.danRer5.masked Title: Full masked genome sequences for Danio rerio (UCSC version danRer5) Description: Full genome sequences for Danio rerio (Zebrafish) as provided by UCSC (danRer5, Jul. 2007) and stored in Biostrings objects. The sequences are the same as in BSgenome.Drerio.UCSC.danRer5, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Drerio.UCSC.danRer5 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/danRer5/bigZips/ organism_biocview: Danio_rerio nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/danRer5/database/ RM masks: danRer5.fa.out.gz from http://hgdownload.cse.ucsc.edu/goldenPath/danRer5/bigZips/ TRF masks: danRer5.trf.bed.gz from http://hgdownload.cse.ucsc.edu/goldenPath/danRer5/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Drerio.UCSC.danRer5$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Drerio.UCSC.danRer5/masks AGAPSfiles_name: gap.txt RMfiles_name: danRer5.fa.out TRFfiles_name: danRer5.trf.bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer6-seed0000644000175400017540000000356013175713516026073 0ustar00biocbuildbiocbuildPackage: BSgenome.Drerio.UCSC.danRer6 Title: Full genome sequences for Danio rerio (UCSC version danRer6) Description: Full genome sequences for Danio rerio (Zebrafish) as provided by UCSC (danRer6, Dec. 2008) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Danio rerio common_name: Zebrafish provider: UCSC provider_version: danRer6 release_date: Dec. 2008 release_name: Sanger Institute Zv8 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/danRer6/bigZips/ organism_biocview: Danio_rerio BSgenomeObjname: Drerio seqnames: paste("chr", c(1:25, "M"), sep="") circ_seqs: "chrM" mseqnames: c("Zv8_NA", "Zv8_scaffold") SrcDataFiles: danRer6.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/danRer6/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for danRer6 are not included in the BSgenome ## data package anymore. However they can easily be extracted from the ## full genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("danRer6", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Drerio.UCSC.danRer6/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer6-tools/0000755000175400017540000000000013175713516026364 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer6-tools/NOTES.TXT0000644000175400017540000000034613175713516027660 0ustar00biocbuildbiocbuildDownloaded the danRer6.fa.gz file on June 17, 2010 11724 FASTA records: o 26 chromosome sequences (1, 2, ..., 25, M) o 11418 Zv8_NA* sequences o 280 Zv8_scaffold* sequences Use the splitbigfasta.R script to split danRer6.fa BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer6-tools/splitbigfasta.R0000755000175400017540000000213113175713516031343 0ustar00biocbuildbiocbuild### library(Biostrings) danRer6 <- readDNAStringSet("danRer6.fa") idx1 <- grep("chr", names(danRer6), fixed=TRUE) idx2 <- grep("Zv8_NA", names(danRer6), fixed=TRUE) idx3 <- grep("Zv8_scaffold", names(danRer6), fixed=TRUE) ### Check that (idx1, idx2, idx3) forms a partition of seq_len(length(danRer6)). stopifnot(identical(sort(c(idx1, idx2, idx3)), seq_len(length(danRer6)))) ### Send each chromosome to a FASTA file. seqnames <- paste("chr", c(1:25, "M"), sep="") for (seqname in seqnames) { seq <- danRer6[match(seqname, names(danRer6))] filename <- paste(seqname, ".fa", sep="") cat("writing ", filename, "\n", sep="") write.XStringSet(seq, file=filename) } ### Send all the Zv8_NA* sequences to a single FASTA file. mseq2 <- danRer6[idx2] mseq2 <- mseq2[order(as.integer(substr(names(mseq2), nchar("Zv8_NA")+1L, 999L)))] write.XStringSet(mseq2, file="Zv8_NA.fa") ### Send all the Zv8_scaffold* sequences to a single FASTA file. mseq3 <- danRer6[idx3] mseq3 <- mseq3[order(as.integer(substr(names(mseq3), nchar("Zv8_scaffold")+1L, 999L)))] write.XStringSet(mseq3, file="Zv8_scaffold.fa") BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer6.masked-seed0000644000175400017540000000266313175713516027341 0ustar00biocbuildbiocbuildPackage: BSgenome.Drerio.UCSC.danRer6.masked Title: Full masked genome sequences for Danio rerio (UCSC version danRer6) Description: Full genome sequences for Danio rerio (Zebrafish) as provided by UCSC (danRer6, Dec. 2008) and stored in Biostrings objects. The sequences are the same as in BSgenome.Drerio.UCSC.danRer6, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Drerio.UCSC.danRer6 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/danRer6/bigZips/ organism_biocview: Danio_rerio nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/danRer6/database/ RM masks: danRer6.fa.out.gz from http://hgdownload.cse.ucsc.edu/goldenPath/danRer6/bigZips/ TRF masks: danRer6.trf.bed.gz from http://hgdownload.cse.ucsc.edu/goldenPath/danRer6/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Drerio.UCSC.danRer6$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Drerio.UCSC.danRer6/masks AGAPSfiles_name: gap.txt RMfiles_name: danRer6.fa.out TRFfiles_name: danRer6.trf.bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer7-seed0000644000175400017540000000355013175713516026073 0ustar00biocbuildbiocbuildPackage: BSgenome.Drerio.UCSC.danRer7 Title: Full genome sequences for Danio rerio (UCSC version danRer7) Description: Full genome sequences for Danio rerio (Zebrafish) as provided by UCSC (danRer7, Jul. 2010) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Danio rerio common_name: Zebrafish provider: UCSC provider_version: danRer7 release_date: Jul. 2010 release_name: Sanger Institute Zv9 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/danRer7/ organism_biocview: Danio_rerio BSgenomeObjname: Drerio seqnames: paste("chr", c(1:25, "M"), sep="") circ_seqs: "chrM" mseqnames: c("Zv9_NA", "Zv9_scaffold") SrcDataFiles: danRer7.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/danRer7/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for danRer7 are not included in the BSgenome ## data package anymore. However they can easily be extracted from the ## full genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("danRer7", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Drerio.UCSC.danRer7/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer7-tools/0000755000175400017540000000000013175713516026365 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer7-tools/NOTES.TXT0000644000175400017540000000034313175713516027656 0ustar00biocbuildbiocbuildDownloaded the danRer7.fa.gz file on March 8, 2011 1133 FASTA records: o 26 chromosome sequences (1, 2, ..., 25, M) o 995 Zv9_NA* sequences o 112 Zv9_scaffold* sequences Use the splitbigfasta.R script to split danRer7.fa BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer7-tools/splitbigfasta.R0000755000175400017540000000213113175713516031344 0ustar00biocbuildbiocbuild### library(Biostrings) danRer7 <- readDNAStringSet("danRer7.fa") idx1 <- grep("chr", names(danRer7), fixed=TRUE) idx2 <- grep("Zv9_NA", names(danRer7), fixed=TRUE) idx3 <- grep("Zv9_scaffold", names(danRer7), fixed=TRUE) ### Check that (idx1, idx2, idx3) forms a partition of seq_len(length(danRer7)). stopifnot(identical(sort(c(idx1, idx2, idx3)), seq_len(length(danRer7)))) ### Send each chromosome to a FASTA file. seqnames <- paste("chr", c(1:25, "M"), sep="") for (seqname in seqnames) { seq <- danRer7[match(seqname, names(danRer7))] filename <- paste(seqname, ".fa", sep="") cat("writing ", filename, "\n", sep="") write.XStringSet(seq, file=filename) } ### Send all the Zv9_NA* sequences to a single FASTA file. mseq2 <- danRer7[idx2] mseq2 <- mseq2[order(as.integer(substr(names(mseq2), nchar("Zv9_NA")+1L, 999L)))] write.XStringSet(mseq2, file="Zv9_NA.fa") ### Send all the Zv9_scaffold* sequences to a single FASTA file. mseq3 <- danRer7[idx3] mseq3 <- mseq3[order(as.integer(substr(names(mseq3), nchar("Zv9_scaffold")+1L, 999L)))] write.XStringSet(mseq3, file="Zv9_scaffold.fa") BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer7.masked-seed0000644000175400017540000000265313175713516027341 0ustar00biocbuildbiocbuildPackage: BSgenome.Drerio.UCSC.danRer7.masked Title: Full masked genome sequences for Danio rerio (UCSC version danRer7) Description: Full genome sequences for Danio rerio (Zebrafish) as provided by UCSC (danRer7, Jul. 2010) and stored in Biostrings objects. The sequences are the same as in BSgenome.Drerio.UCSC.danRer7, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Drerio.UCSC.danRer7 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/danRer7/ organism_biocview: Danio_rerio nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/danRer7/database/ RM masks: danRer7.fa.out.gz from http://hgdownload.cse.ucsc.edu/goldenPath/danRer7/bigZips/ TRF masks: danRer7.trf.bed.gz from http://hgdownload.cse.ucsc.edu/goldenPath/danRer7/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Drerio.UCSC.danRer7$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Drerio.UCSC.danRer7/masks AGAPSfiles_name: gap.txt RMfiles_name: danRer7.fa.out TRFfiles_name: danRer7.trf.bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Ecoli.NCBI.20080805-seed0000644000175400017540000001532513175713516025267 0ustar00biocbuildbiocbuildPackage: BSgenome.Ecoli.NCBI.20080805 Title: Escherichia coli full genomes Description: Escherichia coli full genomes for several strains as provided by NCBI on 2008/08/05 and stored in Biostrings objects. Version: 1.4.2 organism: Escherichia coli common_name: E. coli provider: NCBI provider_version: 2008/08/05 release_date: NA release_name: NA source_url: ftp://ftp.ncbi.nih.gov/genomes/Bacteria/ organism_biocview: Escherichia_coli BSgenomeObjname: Ecoli seqnames: c(paste("NC_", c("008253", "008563", "010468", "004431", "009801", "009800", "002655", "002695", "010498", "007946", "010473", "000913"), sep=""), "AC_000091") circ_seqs: c(paste("NC_", c("008253", "008563", "010468", "004431", "009801", "009800", "002655", "002695", "010498", "007946", "010473", "000913"), sep=""), "AC_000091") PkgDetails: The genome of Escherichia coli is made of a single circular DNA sequence. The full genomes for the following strains are present in this package (one sequence per strain): \describe{ \item{}{ Escherichia coli 536 \preformatted{ Taxonomy ID: 362663 Other names: "Escherichia coli strain 536", "Escherichia coli str. 536" Refseq: NC_008253 Length: 4,938,920 nt Seq.Status: Completed Sequencing center: University of Goettingen Completed: 2006/07/24 File: ftp://ftp.ncbi.nih.gov/genomes/Bacteria/Escherichia_coli_536/NC_008253.fna }} \item{}{ Escherichia coli APEC O1 \preformatted{ Taxonomy ID: 405955 Other names: "Escherichia coli strain APEC O1", "Escherichia coli str. APEC O1" Refseq: NC_008563 Length: 5,082,025 nt Seq.Status: Completed Sequencing center: Iowa State University Completed: 2006/11/08 File: ftp://ftp.ncbi.nih.gov/genomes/Bacteria/Escherichia_coli_APEC_O1/NC_008563.fna }} \item{}{ Escherichia coli ATCC 8739 \preformatted{ Taxonomy ID: 481805 Other names: "Escherichia coli C (ATCC 8739)", "Escherichia coli C str. ATCC 8739", "Escherichia coli strain ATCC 8739", "Escherichia coli str. ATCC 8739" Refseq: NC_010468 Length: 4,746,218 nt Seq.Status: Completed Sequencing center: US DOE Joint Genome Institute (JGI-PGF) Completed: 2008/03/17 File: ftp://ftp.ncbi.nih.gov/genomes/Bacteria/Escherichia_coli_C_ATCC_8739/NC_010468.fna }} \item{}{ Escherichia coli CFT073 \preformatted{ Taxonomy ID: 199310 Other names: "Escherichia coli strain CFT073", "Escherichia coli str. CFT073" Refseq: NC_004431 Length: 5,231,428 nt Seq.Status: Completed Sequencing center: Univ. Wisconsin Completed: 2002/12/09 File: ftp://ftp.ncbi.nih.gov/genomes/Bacteria/Escherichia_coli_CFT073/NC_004431.fna }} \item{}{ Escherichia coli E24377A \preformatted{ Taxonomy ID: 331111 Refseq: NC_009801 Length: 4,979,619 nt Seq.Status: Completed Sequencing center: TIGR Completed: 2007/09/13 File: ftp://ftp.ncbi.nih.gov/genomes/Bacteria/Escherichia_coli_E24377A/NC_009801.fna }} \item{}{ Escherichia coli HS \preformatted{ Taxonomy ID: 331112 Refseq: NC_009800 Length: 4,643,538 nt Seq.Status: Completed Sequencing center: TIGR Completed: 2007/09/13 File: ftp://ftp.ncbi.nih.gov/genomes/Bacteria/Escherichia_coli_HS/NC_009800.fna }} \item{}{ Escherichia coli O157:H7 EDL933 \preformatted{ Taxonomy ID: 155864 Refseq: NC_002655 Length: 5,528,445 nt Seq.Status: Completed Sequencing center: Univ. Wisconsin Completed: 2001/09/27 File: ftp://ftp.ncbi.nih.gov/genomes/Bacteria/Escherichia_coli_O157H7_EDL933/NC_002655.fna }} \item{}{ Escherichia coli O157:H7 str. Sakai \preformatted{ Taxonomy ID: 386585 Other names: "Escherichia coli O157:H7 strain Sakai" Refseq: NC_002695 Length: 5,498,450 nt Seq.Status: Completed Sequencing center: GIRC Completed: 2001/10/02 File: ftp://ftp.ncbi.nih.gov/genomes/Bacteria/Escherichia_coli_O157H7/NC_002695.fna }} \item{}{ Escherichia coli SMS-3-5 \preformatted{ Taxonomy ID: 439855 Other names: "Escherichia coli strain SMS-3-5", "Escherichia coli str. SMS-3-5" Refseq: NC_010498 Length: 5,068,389 nt Seq.Status: Completed Sequencing center: TIGR Completed: 2008/03/24 File: ftp://ftp.ncbi.nih.gov/genomes/Bacteria/Escherichia_coli_SMS_3_5/NC_010498.fna }} \item{}{ Escherichia coli UTI89 \preformatted{ Taxonomy ID: 364106 Other names: "Escherichia coli strain UTI89", "Escherichia coli str. UTI89" Refseq: NC_007946 Length: 5,065,741 nt Seq.Status: Completed Sequencing center: Washington University (WashU) Completed: 2006/04/07 File: ftp://ftp.ncbi.nih.gov/genomes/Bacteria/Escherichia_coli_UTI89/NC_007946.fna }} \item{}{ Escherichia coli str. K12 substr. DH10B \preformatted{ Taxonomy ID: 316385 Other names: "Escherichia coli DH10B", "Escherichia coli strain K12 substrain DH10B" Refseq: NC_010473 Length: 4,686,137 nt Seq.Status: Completed Sequencing center: University of Wisconsin-Madison Completed: 2008/03/17 File: ftp://ftp.ncbi.nih.gov/genomes/Bacteria/Escherichia_coli_K_12_substr__DH10B/NC_010473.fna }} \item{}{ Escherichia coli str. K12 substr. MG1655 \preformatted{ Taxonomy ID: 511145 Other names: "Escherichia coli MG1655", "Escherichia coli strain MG1655", "Escherichia coli str. MG1655" Refseq: NC_000913 Length: 4,639,675 nt Seq.Status: Completed Sequencing center: Univ. Wisconsin Completed: 2001/10/15 File: ftp://ftp.ncbi.nih.gov/genomes/Bacteria/Escherichia_coli_K12_substr__MG1655/NC_000913.fna }} \item{}{ Escherichia coli str. K12 substr. W3110 \preformatted{ Taxonomy ID: 316407 Other names: "Escherichia coli W3110", "Escherichia coli strain W3110", "Escherichia coli str. W3110" Refseq: AC_000091 Length: 4,646,332 nt Seq.Status: Completed Sequencing center: Nara Institute of Science and Technology Completed: 2006/03/01 File: ftp://ftp.ncbi.nih.gov/genomes/Bacteria/Escherichia_coli_W3110/AC_000091.fna }} } SrcDataFiles: Escherichia_coli_536/NC_008253.fna Escherichia_coli_APEC_O1/NC_008563.fna Escherichia_coli_C_ATCC_8739/NC_010468.fna Escherichia_coli_CFT073/NC_004431.fna Escherichia_coli_E24377A/NC_009801.fna Escherichia_coli_HS/NC_009800.fna Escherichia_coli_O157H7_EDL933/NC_002655.fna Escherichia_coli_O157H7/NC_002695.fna Escherichia_coli_SMS_3_5/NC_010498.fna Escherichia_coli_UTI89/NC_007946.fna Escherichia_coli_K_12_substr__DH10B/NC_010473.fna Escherichia_coli_K12_substr__MG1655/NC_000913.fna Escherichia_coli_W3110/AC_000091.fna from ftp://ftp.ncbi.nih.gov/genomes/Bacteria/ (downloaded on 2008/08/05) PkgExamples: ## The names of the sequences are the Refseq numbers! genome$NC_008253 # same as genome[["NC_008253"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Ecoli.NCBI.20080805/seqs seqfiles_suffix: .fna ondisk_seq_format: rda BSgenome/inst/extdata/GentlemanLab/BSgenome.Gaculeatus.UCSC.gasAcu1-seed0000644000175400017540000000401213175713516026720 0ustar00biocbuildbiocbuildPackage: BSgenome.Gaculeatus.UCSC.gasAcu1 Title: Full genome sequences for Gasterosteus aculeatus (UCSC version gasAcu1) Description: Full genome sequences for Gasterosteus aculeatus (Stickleback) as provided by UCSC (gasAcu1, Feb. 2006) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Gasterosteus aculeatus common_name: Stickleback provider: UCSC provider_version: gasAcu1 release_date: Feb. 2006 release_name: Broad Release 1.0 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/ organism_biocview: Gasterosteus_aculeatus BSgenomeObjname: Gaculeatus seqnames: paste("chr", c("I", "II", "III", "IV", "V", "VI", "VII", "VIII", "IX", "X", "XI", "XII", "XIII", "XIV", "XV", "XVI", "XVII", "XVIII", "XIX", "XX", "XXI", "M", "Un"), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/bigZips/ PkgExamples: genome$chrI # same as genome[["chrI"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for gasAcu1 are not included in the BSgenome ## data package anymore. However they can easily be extracted from the ## full genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("gasAcu1", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Gaculeatus.UCSC.gasAcu1/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Gaculeatus.UCSC.gasAcu1.masked-seed0000644000175400017540000000272113175713516030170 0ustar00biocbuildbiocbuildPackage: BSgenome.Gaculeatus.UCSC.gasAcu1.masked Title: Full masked genome sequences for Gasterosteus aculeatus (UCSC version gasAcu1) Description: Full genome sequences for Gasterosteus aculeatus (Stickleback) as provided by UCSC (gasAcu1, Feb. 2006) and stored in Biostrings objects. The sequences are the same as in BSgenome.Gaculeatus.UCSC.gasAcu1, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Gaculeatus.UCSC.gasAcu1 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/ organism_biocview: Gasterosteus_aculeatus nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/database/ RM masks: chromOut.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/bigZips/ TRF masks: chromTrf.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/bigZips/ PkgExamples: genome$chrI # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chrI) # same as BSgenome.Gaculeatus.UCSC.gasAcu1$chrI masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Gaculeatus.UCSC.gasAcu1/masks AGAPSfiles_name: gap.txt RMfiles_suffix: .fa.out TRFfiles_suffix: .bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Ggallus.UCSC.galGal3-seed0000644000175400017540000000375313175713516026222 0ustar00biocbuildbiocbuildPackage: BSgenome.Ggallus.UCSC.galGal3 Title: Full genome sequences for Gallus gallus (UCSC version galGal3) Description: Full genome sequences for Gallus gallus (Chicken) as provided by UCSC (galGal3, May 2006) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Gallus gallus common_name: Chicken provider: UCSC provider_version: galGal3 release_date: May 2006 release_name: WUSTL Gallus-gallus-2.1 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/galGal3/bigZips/ organism_biocview: Gallus_gallus BSgenomeObjname: Ggallus seqnames: paste("chr", c(1:28, 32, "M", "W", "Z", "E64", "E22C19W28_E50C23", paste(c(1:2, 4:8, 10:13, 16:18, 20, 22, 25, 28, "W", "Z", "E64", "E22C19W28_E50C23", "Un"), "_random", sep="")), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/galGal3/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for galGal3 are not included in the BSgenome ## data package anymore. However they can easily be extracted from the ## full genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("galGal3", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Ggallus.UCSC.galGal3/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Ggallus.UCSC.galGal3.masked-seed0000644000175400017540000000256313175713516027463 0ustar00biocbuildbiocbuildPackage: BSgenome.Ggallus.UCSC.galGal3.masked Title: Full masked genome sequences for Gallus gallus (UCSC version galGal3) Description: Full genome sequences for Gallus gallus (Chicken) as provided by UCSC (galGal3, May 2006) and stored in Biostrings objects. The sequences are the same as in BSgenome.Ggallus.UCSC.galGal3, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Ggallus.UCSC.galGal3 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/galGal3/bigZips/ organism_biocview: Gallus_gallus nmask_per_seq: 4 SrcDataFiles: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/galGal3/database/ RM masks: chromOut.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/galGal3/bigZips/ TRF masks: chromTrf.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/galGal3/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Ggallus.UCSC.galGal3$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Ggallus.UCSC.galGal3/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Ggallus.UCSC.galGal4-seed0000644000175400017540000000364013175713516026216 0ustar00biocbuildbiocbuildPackage: BSgenome.Ggallus.UCSC.galGal4 Title: Full genome sequences for Gallus gallus (UCSC version galGal4) Description: Full genome sequences for Gallus gallus (Chicken) as provided by UCSC (galGal4, Nov. 2011) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Gallus gallus common_name: Chicken provider: UCSC provider_version: galGal4 release_date: Nov. 2011 release_name: ICGSC Gallus_gallus-4.0 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/galGal4/bigZips/ organism_biocview: Gallus_gallus BSgenomeObjname: Ggallus seqnames: paste("chr", c(1:28, 32, "M", "W", "Z", "LGE64", "LGE22C19W28_E50C23"), sep="") circ_seqs: "chrM" mseqnames: c("random", "chrUn") SrcDataFiles: galGal4.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/galGal4/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for galGal4 are not included in the BSgenome ## data package anymore. However they can easily be extracted from the ## full genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("galGal4", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Ggallus.UCSC.galGal4/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Ggallus.UCSC.galGal4-tools/0000755000175400017540000000000013175713516026510 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Ggallus.UCSC.galGal4-tools/splitbigfasta.R0000755000175400017540000000213513175713516031473 0ustar00biocbuildbiocbuild### library(Biostrings) galGal4 <- readDNAStringSet("galGal4.fa") ### Partitioning: is_random <- grepl("^chr[^_]*_[^_]*_random$", names(galGal4)) is_chrUn <- grepl("^chrUn", names(galGal4)) is_chrom <- !(is_random | is_chrUn) ### Sanity check: stopifnot(all(is_random | is_chrUn | is_chrom)) stopifnot(!any(is_random & is_chrUn)) stopifnot(!any(is_random & is_chrom)) stopifnot(!any(is_chrUn & is_chrom)) ### Send each chromosome to a FASTA file. seqnames <- paste("chr", c(1:28, 32, "M", "W", "Z", "LGE64", "LGE22C19W28_E50C23"), sep="") stopifnot(setequal(seqnames, names(galGal4)[is_chrom])) for (seqname in seqnames) { seq <- galGal4[match(seqname, names(galGal4))] filename <- paste(seqname, ".fa", sep="") cat("writing ", filename, "\n", sep="") writeXStringSet(seq, file=filename, width=50L) } ### Send the 1805 chrNN_*_random sequences to 1 FASTA file. random_mseq <- galGal4[is_random] writeXStringSet(random_mseq, file="random.fa", width=50L) ### Send the 14093 chrUn_* sequences to 1 FASTA file. chrUn_mseq <- galGal4[is_chrUn] writeXStringSet(chrUn_mseq, file="chrUn.fa", width=50L) BSgenome/inst/extdata/GentlemanLab/BSgenome.Ggallus.UCSC.galGal4.masked-seed0000644000175400017540000000267413175713516027467 0ustar00biocbuildbiocbuildPackage: BSgenome.Ggallus.UCSC.galGal4.masked Title: Full masked genome sequences for Gallus gallus (UCSC version galGal4) Description: Full genome sequences for Gallus gallus (Chicken) as provided by UCSC (galGal4, Nov. 2011) and stored in Biostrings objects. The sequences are the same as in BSgenome.Ggallus.UCSC.galGal4, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Ggallus.UCSC.galGal4 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/galGal4/bigZips/ organism_biocview: Gallus_gallus nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/galGal4/database/ RM masks: galGal4.fa.out.gz from http://hgdownload.cse.ucsc.edu/goldenPath/galGal4/bigZips/ TRF masks: galGal4.trf.bed.gz from http://hgdownload.cse.ucsc.edu/goldenPath/galGal4/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Ggallus.UCSC.galGal4$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Ggallus.UCSC.galGal4/masks AGAPSfiles_name: gap.txt RMfiles_name: galGal4.fa.out TRFfiles_name: galGal4.trf.bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Ggallus.UCSC.galGal5-seed0000644000175400017540000000147313175713516026221 0ustar00biocbuildbiocbuildPackage: BSgenome.Ggallus.UCSC.galGal5 Title: Full genome sequences for Gallus gallus (UCSC version galGal5) Description: Full genome sequences for Gallus gallus (Chicken) as provided by UCSC (galGal5, Dec. 2015) and stored in Biostrings objects. Version: 1.4.2 organism: Gallus gallus common_name: Chicken provider: UCSC provider_version: galGal5 release_date: Dec. 2015 release_name: ICGC Gallus-gallus-5.0 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/galGal5/bigZips/ organism_biocview: Gallus_gallus BSgenomeObjname: Ggallus circ_seqs: "chrM" SrcDataFiles: galGal5.2bit from http://hgdownload.cse.ucsc.edu/goldenPath/galGal5/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Ggallus.UCSC.galGal5/seqs seqfile_name: galGal5.sorted.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Ggallus.UCSC.galGal5-tools/0000755000175400017540000000000013175713516026511 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Ggallus.UCSC.galGal5-tools/sort_galGal5.2bit.R0000644000175400017540000000176713175713516032031 0ustar00biocbuildbiocbuildlibrary(Biostrings) library(rtracklayer) galGal5 <- import("galGal5.2bit") seqlevels1 <- paste0("chr", c(1:28, 30:33, "M", "W", "Z", "LGE64")) tmp <- CharacterList(strsplit(names(galGal5), "_")) npart <- elementNROWS(tmp) stopifnot(all(npart <= 4L)) idx1 <- which(npart == 1L) stopifnot(setequal(names(galGal5)[idx1], seqlevels1)) idx2 <- which(npart == 2L) stopifnot(length(idx2) == 0L) idx4 <- which(npart == 4L) m4 <- matrix(unlist(tmp[idx4]), ncol=4L, byrow=TRUE) stopifnot(all(m4[ , 2L] == "NT")) stopifnot(all(m4[ , 4L] == "random")) chrom <- match(m4[ , 1L], seqlevels1) stopifnot(!anyNA(chrom)) oo4 <- order(chrom, m4[ , 3L]) seqlevels4 <- names(galGal5)[idx4[oo4]] idx3 <- which(npart == 3L) m3 <- matrix(unlist(tmp[idx3]), ncol=3L, byrow=TRUE) stopifnot(all(m3[ , 1L] == "chrUn")) stopifnot(all(m3[ , 2L] == "NT")) oo3 <- order(m3[ , 3L]) seqlevels3 <- names(galGal5)[idx3[oo3]] galGal5_seqlevels <- c(seqlevels1, seqlevels4, seqlevels3) export(galGal5[galGal5_seqlevels], "galGal5.sorted.2bit") BSgenome/inst/extdata/GentlemanLab/BSgenome.Hsapiens.NCBI.GRCh38-seed0000644000175400017540000002463013175713516026035 0ustar00biocbuildbiocbuildPackage: BSgenome.Hsapiens.NCBI.GRCh38 Title: Full genome sequences for Homo sapiens (GRCh38) Description: Full genome sequences for Homo sapiens (Human) as provided by NCBI (GRCh38, 2013-12-17) and stored in Biostrings objects. Version: 1.4.2 organism: Homo sapiens common_name: Human provider: NCBI provider_version: GRCh38 release_date: 2013-12-17 release_name: Genome Reference Consortium Human Build 38 source_url: ftp://ftp.ncbi.nlm.nih.gov/genbank/genomes/Eukaryotes/vertebrates_mammals/Homo_sapiens/GRCh38/ organism_biocview: Homo_sapiens BSgenomeObjname: Hsapiens seqnames: c("1", "2", "3", "4", "5", "6", "7", "8", "9", "10", "11", "12", "13", "14", "15", "16", "17", "18", "19", "20", "21", "22", "X", "Y", "MT", "HSCHR1_CTG1_UNLOCALIZED", "HSCHR1_CTG2_UNLOCALIZED", "HSCHR1_CTG3_UNLOCALIZED", "HSCHR1_CTG4_UNLOCALIZED", "HSCHR1_CTG5_UNLOCALIZED", "HSCHR1_CTG6_UNLOCALIZED", "HSCHR1_CTG7_UNLOCALIZED", "HSCHR1_CTG8_UNLOCALIZED", "HSCHR1_CTG9_UNLOCALIZED", "HSCHR2_RANDOM_CTG1", "HSCHR2_RANDOM_CTG2", "HSCHR3UN_CTG2", "HSCHR4_RANDOM_CTG4", "HSCHR5_RANDOM_CTG1", "HSCHR9_UNLOCALIZED_CTG1", "HSCHR9_UNLOCALIZED_CTG2", "HSCHR9_UNLOCALIZED_CTG3", "HSCHR9_UNLOCALIZED_CTG4", "HSCHR11_CTG1_UNLOCALIZED", "HSCHR14_CTG1_UNLOCALIZED", "HSCHR14_CTG2_UNLOCALIZED", "HSCHR14_CTG3_UNLOCALIZED", "HSCHR14_CTG4_UNLOCALIZED", "HSCHR14_CTG5_UNLOCALIZED", "HSCHR14_CTG6_UNLOCALIZED", "HSCHR14_CTG7_UNLOCALIZED", "HSCHR14_CTG8_UNLOCALIZED", "HSCHR15_RANDOM_CTG1", "HSCHR16_RANDOM_CTG1", "HSCHR17_RANDOM_CTG3", "HSCHR17_RANDOM_CTG4", "HSCHR17_RANDOM_CTG5", "HSCHR22_UNLOCALIZED_CTG1", "HSCHR22_UNLOCALIZED_CTG2", "HSCHR22_UNLOCALIZED_CTG3", "HSCHR22_UNLOCALIZED_CTG4", "HSCHR22_UNLOCALIZED_CTG5", "HSCHR22_UNLOCALIZED_CTG6", "HSCHR22_UNLOCALIZED_CTG7", "HSCHR22_UNLOCALIZED_CTG8", "HSCHR22_UNLOCALIZED_CTG9", "HSCHRY_RANDOM_CTG1", "HSCHRUN_RANDOM_100", "HSCHRUN_RANDOM_101", "HSCHRUN_RANDOM_102", "HSCHRUN_RANDOM_103", "HSCHRUN_RANDOM_104", "HSCHRUN_RANDOM_105", "HSCHRUN_RANDOM_106", "HSCHRUN_RANDOM_107", "HSCHRUN_RANDOM_108", "HSCHRUN_RANDOM_109", "HSCHRUN_RANDOM_110", "HSCHRUN_RANDOM_111", "HSCHRUN_RANDOM_112", "HSCHRUN_RANDOM_113", "HSCHRUN_RANDOM_114", "HSCHRUN_RANDOM_115", "HSCHRUN_RANDOM_116", "HSCHRUN_RANDOM_117", "HSCHRUN_RANDOM_118", "HSCHRUN_RANDOM_119", "HSCHRUN_RANDOM_120", "HSCHRUN_RANDOM_121", "HSCHRUN_RANDOM_122", "HSCHRUN_RANDOM_123", "HSCHRUN_RANDOM_124", "HSCHRUN_RANDOM_125", "HSCHRUN_RANDOM_126", "HSCHRUN_RANDOM_127", "HSCHRUN_RANDOM_128", "HSCHRUN_RANDOM_129", "HSCHRUN_RANDOM_130", "HSCHRUN_RANDOM_131", "HSCHRUN_RANDOM_132", "HSCHRUN_RANDOM_133", "HSCHRUN_RANDOM_134", "HSCHRUN_RANDOM_135", "HSCHRUN_RANDOM_136", "HSCHRUN_RANDOM_137", "HSCHRUN_RANDOM_138", "HSCHRUN_RANDOM_139", "HSCHRUN_RANDOM_140", "HSCHRUN_RANDOM_141", "HSCHRUN_RANDOM_142", "HSCHRUN_RANDOM_143", "HSCHRUN_RANDOM_144", "HSCHRUN_RANDOM_145", "HSCHRUN_RANDOM_146", "HSCHRUN_RANDOM_147", "HSCHRUN_RANDOM_148", "HSCHRUN_RANDOM_149", "HSCHRUN_RANDOM_154", "HSCHRUN_RANDOM_155", "HSCHRUN_RANDOM_156", "HSCHRUN_RANDOM_157", "HSCHRUN_RANDOM_158", "HSCHRUN_RANDOM_159", "HSCHRUN_RANDOM_160", "HSCHRUN_RANDOM_161", "HSCHRUN_RANDOM_162", "HSCHRUN_RANDOM_163", "HSCHRUN_RANDOM_164", "HSCHRUN_RANDOM_165", "HSCHRUN_RANDOM_166", "HSCHRUN_RANDOM_167", "HSCHRUN_RANDOM_168", "HSCHRUN_RANDOM_169", "HSCHRUN_RANDOM_170", "HSCHRUN_RANDOM_171", "HSCHRUN_RANDOM_172", "HSCHRUN_RANDOM_173", "HSCHRUN_RANDOM_174", "HSCHRUN_RANDOM_175", "HSCHRUN_RANDOM_176", "HSCHRUN_RANDOM_177", "HSCHRUN_RANDOM_178", "HSCHRUN_RANDOM_179", "HSCHRUN_RANDOM_180", "HSCHRUN_RANDOM_181", "HSCHRUN_RANDOM_182", "HSCHRUN_RANDOM_183", "HSCHRUN_RANDOM_184", "HSCHRUN_RANDOM_185", "HSCHRUN_RANDOM_186", "HSCHRUN_RANDOM_187", "HSCHRUN_RANDOM_188", "HSCHRUN_RANDOM_189", "HSCHRUN_RANDOM_190", "HSCHRUN_RANDOM_191", "HSCHRUN_RANDOM_192", "HSCHRUN_RANDOM_193", "HSCHRUN_RANDOM_194", "HSCHRUN_RANDOM_195", "HSCHRUN_RANDOM_196", "HSCHRUN_RANDOM_197", "HSCHRUN_RANDOM_198", "HSCHRUN_RANDOM_199", "HSCHRUN_RANDOM_200", "HSCHRUN_RANDOM_201", "HSCHRUN_RANDOM_202", "HSCHRUN_RANDOM_203", "HSCHRUN_RANDOM_204", "HSCHRUN_RANDOM_CTG1", "HSCHRUN_RANDOM_CTG10", "HSCHRUN_RANDOM_CTG11", "HSCHRUN_RANDOM_CTG16", "HSCHRUN_RANDOM_CTG17", "HSCHRUN_RANDOM_CTG19", "HSCHRUN_RANDOM_CTG2", "HSCHRUN_RANDOM_CTG20", "HSCHRUN_RANDOM_CTG21", "HSCHRUN_RANDOM_CTG22", "HSCHRUN_RANDOM_CTG23", "HSCHRUN_RANDOM_CTG24", "HSCHRUN_RANDOM_CTG25", "HSCHRUN_RANDOM_CTG26", "HSCHRUN_RANDOM_CTG27", "HSCHRUN_RANDOM_CTG28", "HSCHRUN_RANDOM_CTG29", "HSCHRUN_RANDOM_CTG30", "HSCHRUN_RANDOM_CTG33", "HSCHRUN_RANDOM_CTG34", "HSCHRUN_RANDOM_CTG35", "HSCHRUN_RANDOM_CTG36", "HSCHRUN_RANDOM_CTG4", "HSCHRUN_RANDOM_CTG42", "HSCHRUN_RANDOM_CTG6", "HSCHRUN_RANDOM_CTG9", "HSCHR1_1_CTG3", "HSCHR1_2_CTG3", "HSCHR1_1_CTG11", "HSCHR1_4_CTG31", "HSCHR1_1_CTG31", "HSCHR1_2_CTG31", "HSCHR1_3_CTG31", "HSCHR1_4_CTG32_1", "HSCHR1_3_CTG32_1", "HSCHR1_1_CTG32_1", "HSCHR1_2_CTG32_1", "HSCHR2_2_CTG1", "HSCHR2_3_CTG1", "HSCHR2_4_CTG1", "HSCHR2_1_CTG1", "HSCHR2_1_CTG5", "HSCHR2_1_CTG7", "HSCHR2_5_CTG7_2", "HSCHR2_4_CTG7_2", "HSCHR2_3_CTG7_2", "HSCHR2_2_CTG7_2", "HSCHR2_1_CTG7_2", "HSCHR2_3_CTG15", "HSCHR2_1_CTG15", "HSCHR3_1_CTG1", "HSCHR3_3_CTG1", "HSCHR3_4_CTG2_1", "HSCHR3_1_CTG2_1", "HSCHR3_2_CTG2_1", "HSCHR3_3_CTG2_1", "HSCHR3_5_CTG2_1", "HSCHR3_1_CTG3", "HSCHR3_2_CTG3", "HSCHR3_9_CTG3", "HSCHR4_1_CTG4", "HSCHR4_1_CTG6", "HSCHR4_1_CTG8_1", "HSCHR4_1_CTG9", "HSCHR4_4_CTG12", "HSCHR4_1_CTG12", "HSCHR4_2_CTG12", "HSCHR4_5_CTG12", "HSCHR4_3_CTG12", "HSCHR5_5_CTG1", "HSCHR5_4_CTG1", "HSCHR5_3_CTG1", "HSCHR5_1_CTG1", "HSCHR5_2_CTG1", "HSCHR5_6_CTG1", "HSCHR5_2_CTG1_1", "HSCHR5_3_CTG1_1", "HSCHR5_4_CTG1_1", "HSCHR5_1_CTG5", "HSCHR5_2_CTG5", "HSCHR6_MHC_APD_CTG1", "HSCHR6_1_CTG7", "HSCHR6_1_CTG6", "HSCHR6_1_CTG2", "HSCHR6_1_CTG8", "HSCHR6_1_CTG9", "HSCHR6_1_CTG3", "HSCHR6_1_CTG4", "HSCHR6_1_CTG5", "HSCHR7_1_CTG1", "HSCHR7_2_CTG4_4", "HSCHR7_1_CTG4_4", "HSCHR7_1_CTG6", "HSCHR7_2_CTG6", "HSCHR7_3_CTG6", "HSCHR7_2_CTG7", "HSCHR7_1_CTG7", "HSCHR8_4_CTG1", "HSCHR8_2_CTG1", "HSCHR8_1_CTG1", "HSCHR8_8_CTG1", "HSCHR8_3_CTG1", "HSCHR8_9_CTG1", "HSCHR8_1_CTG6", "HSCHR8_1_CTG7", "HSCHR8_5_CTG7", "HSCHR8_6_CTG7", "HSCHR8_4_CTG7", "HSCHR8_3_CTG7", "HSCHR8_2_CTG7", "HSCHR9_1_CTG1", "HSCHR9_1_CTG2", "HSCHR9_1_CTG3", "HSCHR9_1_CTG4", "HSCHR9_1_CTG5", "HSCHR10_1_CTG1", "HSCHR10_1_CTG3", "HSCHR10_1_CTG2", "HSCHR10_1_CTG4", "HSCHR11_1_CTG8", "HSCHR11_1_CTG6", "HSCHR11_1_CTG7", "HSCHR11_1_CTG5", "HSCHR11_1_CTG1_1", "HG142_HG150_NOVEL_TEST", "HG151_NOVEL_TEST", "HSCHR11_1_CTG3", "HSCHR11_1_CTG2", "HSCHR12_1_CTG1", "HSCHR12_2_CTG2", "HSCHR12_5_CTG2", "HSCHR12_1_CTG2", "HSCHR12_4_CTG2", "HSCHR12_1_CTG2_1", "HSCHR12_2_CTG2_1", "HSCHR12_3_CTG2_1", "HSCHR12_6_CTG2_1", "HSCHR12_4_CTG2_1", "HSCHR12_5_CTG2_1", "HSCHR12_7_CTG2_1", "HSCHR13_1_CTG3", "HSCHR13_1_CTG2", "HSCHR13_1_CTG6", "HSCHR13_1_CTG4", "HSCHR13_1_CTG1", "HSCHR13_1_CTG5", "HSCHR14_1_CTG1", "HSCHR14_7_CTG1", "HSCHR14_2_CTG1", "HSCHR14_3_CTG1", "HSCHR15_1_CTG1", "HSCHR15_3_CTG3", "HSCHR15_1_CTG3", "HSCHR15_1_CTG8", "HSCHR15_3_CTG8", "HSCHR15_2_CTG8", "HSCHR15_5_CTG8", "HSCHR16_CTG2", "HSCHR16_4_CTG1", "HSCHR16_3_CTG1", "HSCHR16_1_CTG1", "HSCHR16_1_CTG3_1", "HSCHR16_2_CTG3_1", "HSCHR17_1_CTG1", "HSCHR17_2_CTG2", "HSCHR17_1_CTG2", "HSCHR17_7_CTG4", "HSCHR17_4_CTG4", "HSCHR17_5_CTG4", "HSCHR17_1_CTG4", "HSCHR17_1_CTG5", "HSCHR17_2_CTG4", "HSCHR17_8_CTG4", "HSCHR17_9_CTG4", "HSCHR17_3_CTG4", "HSCHR17_1_CTG9", "HSCHR18_4_CTG1_1", "HSCHR18_1_CTG1_1", "HSCHR18_2_CTG1_1", "HSCHR18_2_CTG2", "HSCHR18_1_CTG2", "HSCHR18_1_CTG2_1", "HSCHR18_2_CTG2_1", "HSCHR18_3_CTG2_1", "HSCHR19_5_CTG2", "HSCHR19_4_CTG2", "HSCHR19_1_CTG2", "HSCHR19_2_CTG2", "HSCHR19_3_CTG2", "HSCHR19_1_CTG3_1", "HSCHR19_2_CTG3_1", "HSCHR19_3_CTG3_1", "HSCHR19LRC_COX1_CTG3_1", "HSCHR20_1_CTG1", "HSCHR20_1_CTG2", "HSCHR20_1_CTG4", "HSCHR20_1_CTG3", "HSCHR21_1_CTG1_1", "HSCHR21_8_CTG1_1", "HSCHR21_6_CTG1_1", "HSCHR21_2_CTG1_1", "HSCHR21_3_CTG1_1", "HSCHR21_4_CTG1_1", "HSCHR21_5_CTG2", "HSCHR22_1_CTG3", "HSCHR22_1_CTG6", "HSCHR22_1_CTG7", "HSCHR22_1_CTG4", "HSCHR22_1_CTG5", "HSCHR22_1_CTG2", "HSCHR22_1_CTG1", "HSCHRX_1_CTG3", "HSCHRX_2_CTG12", "HSCHR1_ALT2_1_CTG32_1", "HSCHR2_2_CTG7", "HSCHR2_2_CTG15", "HSCHR3_3_CTG3", "HSCHR4_6_CTG12", "HSCHR5_1_CTG1_1", "HSCHR5_3_CTG5", "HSCHR6_MHC_COX_CTG1", "HSCHR7_2_CTG1", "HSCHR8_6_CTG1", "HSCHR8_5_CTG1", "HSCHR11_2_CTG1", "HSCHR11_2_CTG1_1", "HSCHR12_3_CTG2", "HSCHR15_2_CTG3", "HSCHR15_4_CTG8", "HSCHR17_2_CTG1", "HSCHR17_3_CTG2", "HSCHR17_10_CTG4", "HSCHR17_6_CTG4", "HSCHR17_2_CTG5", "HSCHR18_ALT21_CTG2_1", "HSCHR18_ALT2_CTG2_1", "HSCHR19LRC_COX2_CTG3_1", "HSCHR22_2_CTG1", "HSCHRX_2_CTG3", "HSCHR3_4_CTG3", "HSCHR4_7_CTG12", "HSCHR6_MHC_DBB_CTG1", "HSCHR8_7_CTG1", "HSCHR11_3_CTG1", "HSCHR19LRC_LRC_I_CTG3_1", "HSCHR22_3_CTG1", "HSCHR3_5_CTG3", "HSCHR6_MHC_MANN_CTG1", "HSCHR19LRC_LRC_J_CTG3_1", "HSCHR3_6_CTG3", "HSCHR6_MHC_MCF_CTG1", "HSCHR19LRC_LRC_S_CTG3_1", "HSCHR3_7_CTG3", "HSCHR6_MHC_QBL_CTG1", "HSCHR19LRC_LRC_T_CTG3_1", "HSCHR3_8_CTG3", "HSCHR6_MHC_SSTO_CTG1", "HSCHR19LRC_PGF1_CTG3_1", "HSCHR6_8_CTG1", "HSCHR19LRC_PGF2_CTG3_1", "HSCHR19_4_CTG3_1", "HSCHR19KIR_FH15_B_HAP_CTG3_1", "HSCHR19KIR_G085_A_HAP_CTG3_1", "HSCHR19KIR_G085_BA1_HAP_CTG3_1", "HSCHR19KIR_G248_A_HAP_CTG3_1", "HSCHR19KIR_G248_BA2_HAP_CTG3_1", "HSCHR19KIR_GRC212_AB_HAP_CTG3_1", "HSCHR19KIR_GRC212_BA1_HAP_CTG3_1", "HSCHR19KIR_LUCE_A_HAP_CTG3_1", "HSCHR19KIR_LUCE_BDEL_HAP_CTG3_1", "HSCHR19KIR_RSH_A_HAP_CTG3_1", "HSCHR19KIR_RSH_BA2_HAP_CTG3_1", "HSCHR19KIR_T7526_A_HAP_CTG3_1", "HSCHR19KIR_T7526_BDEL_HAP_CTG3_1", "HSCHR19KIR_ABC08_A1_HAP_CTG3_1", "HSCHR19KIR_ABC08_AB_HAP_C_P_CTG3_1", "HSCHR19KIR_ABC08_AB_HAP_T_P_CTG3_1", "HSCHR19KIR_FH05_A_HAP_CTG3_1", "HSCHR19KIR_FH05_B_HAP_CTG3_1", "HSCHR19KIR_FH06_A_HAP_CTG3_1", "HSCHR19KIR_FH06_BA1_HAP_CTG3_1", "HSCHR19KIR_FH08_A_HAP_CTG3_1", "HSCHR19KIR_FH08_BAX_HAP_CTG3_1", "HSCHR19KIR_FH13_A_HAP_CTG3_1", "HSCHR19KIR_FH13_BA2_HAP_CTG3_1", "HSCHR19KIR_FH15_A_HAP_CTG3_1", "HSCHR19KIR_RP5_B_HAP_CTG3_1") circ_seqs: "MT" SrcDataFiles: GCA_000001405.15_GRCh38_top-level.fna.gz from ftp://ftp.ncbi.nlm.nih.gov/genbank/genomes/Eukaryotes/vertebrates_mammals/Homo_sapiens/GRCh38 PkgExamples: genome[["1"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.NCBI.GRCh38/seqs ondisk_seq_format: rda BSgenome/inst/extdata/GentlemanLab/BSgenome.Hsapiens.NCBI.GRCh38-tools/0000755000175400017540000000000013175713516026325 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Hsapiens.NCBI.GRCh38-tools/splitbigfasta.R0000755000175400017540000000170113175713516031306 0ustar00biocbuildbiocbuild### library(Biostrings) library(GenomeInfoDb) ### Download GCA_000001405.15_GRCh38_top-level.fna.gz from ### ftp://ftp.ncbi.nlm.nih.gov/genbank/genomes/Eukaryotes/vertebrates_mammals/Homo_sapiens/GRCh38 ### then uncompress with gunzip GCA_000001405.15_GRCh38_top-level.fna.gz GRCh38 <- readDNAStringSet("GCA_000001405.15_GRCh38_top-level.fna") m_data <- strsplit(names(GRCh38), "|", fixed=TRUE) fasta_headers <- matrix(unlist(m_data, use.names=FALSE), ncol=length(m_data)) GRCh38_accns <- fasta_headers[4L, ] stopifnot(!any(duplicated(GRCh38_accns))) GRCh38_accn2seqlevel <- GenomeInfoDb:::fetch_GenBankAccn2seqlevel_from_NCBI("GCF_000001405.26") stopifnot(setequal(GRCh38_accns, names(GRCh38_accn2seqlevel))) GRCh38_seqlevels <- GRCh38_accn2seqlevel[GRCh38_accns] for (i in seq_along(GRCh38)) { filename <- paste0(GRCh38_seqlevels[[i]], ".fa") cat("writing ", filename, "\n", sep="") writeXStringSet(GRCh38[i], file=filename, width=50L) } BSgenome/inst/extdata/GentlemanLab/BSgenome.Hsapiens.UCSC.hg17-seed0000644000175400017540000000364113175713516025666 0ustar00biocbuildbiocbuildPackage: BSgenome.Hsapiens.UCSC.hg17 Title: Full genome sequences for Homo sapiens (UCSC version hg17) Description: Full genome sequences for Homo sapiens (Human) as provided by UCSC (hg17, May 2004) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Homo sapiens common_name: Human provider: UCSC provider_version: hg17 release_date: May 2004 release_name: NCBI Build 35 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/hg17/bigZips/ organism_biocview: Homo_sapiens BSgenomeObjname: Hsapiens seqnames: paste("chr", c(1:22, "X", "Y", "M", "6_hla_hap1", "6_hla_hap2", paste(c((1:22)[-c(11, 14, 20, 21)], "X"), "_random", sep="")), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.zip from http://hgdownload.cse.ucsc.edu/goldenPath/hg17/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for hg17 are not included in the BSgenome data ## package anymore. However they can easily be extracted from the full ## genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("hg17", "knownGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.UCSC.hg17/seqs ondisk_seq_format: rda BSgenome/inst/extdata/GentlemanLab/BSgenome.Hsapiens.UCSC.hg17.masked-seed0000644000175400017540000000251413175713516027127 0ustar00biocbuildbiocbuildPackage: BSgenome.Hsapiens.UCSC.hg17.masked Title: Full masked genome sequences for Homo sapiens (UCSC version hg17) Description: Full genome sequences for Homo sapiens (Human) as provided by UCSC (hg17, May 2004) and stored in Biostrings objects. The sequences are the same as in BSgenome.Hsapiens.UCSC.hg17, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Hsapiens.UCSC.hg17 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/hg17/bigZips/ organism_biocview: Homo_sapiens nmask_per_seq: 4 SrcDataFiles: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/hg17/database/ RM masks: chromOut.zip from http://hgdownload.cse.ucsc.edu/goldenPath/hg17/bigZips/ TRF masks: chromTrf.zip from http://hgdownload.cse.ucsc.edu/goldenPath/hg17/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Hsapiens.UCSC.hg17$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.UCSC.hg17/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Hsapiens.UCSC.hg18-seed0000644000175400017540000000373513175713516025673 0ustar00biocbuildbiocbuildPackage: BSgenome.Hsapiens.UCSC.hg18 Title: Full genome sequences for Homo sapiens (UCSC version hg18) Description: Full genome sequences for Homo sapiens (Human) as provided by UCSC (hg18, Mar. 2006) and stored in Biostrings objects. Version: 1.4.2 Suggests: TxDb.Hsapiens.UCSC.hg18.knownGene organism: Homo sapiens common_name: Human provider: UCSC provider_version: hg18 release_date: Mar. 2006 release_name: NCBI Build 36.1 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/hg18/bigZips/ organism_biocview: Homo_sapiens BSgenomeObjname: Hsapiens seqnames: paste("chr", c(1:22, "X", "Y", "M", "5_h2_hap1", "6_cox_hap1", "6_qbl_hap2", "22_h2_hap1", paste(c((1:22)[-c(12, 14, 20)], "X"), "_random", sep="")), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.zip from http://hgdownload.cse.ucsc.edu/goldenPath/hg18/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for hg18 are not included in the BSgenome data ## package anymore. However they can easily be extracted from the full ## genome sequences with something like: . library(TxDb.Hsapiens.UCSC.hg18.knownGene) txdb <- TxDb.Hsapiens.UCSC.hg18.knownGene gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.UCSC.hg18/seqs ondisk_seq_format: rda BSgenome/inst/extdata/GentlemanLab/BSgenome.Hsapiens.UCSC.hg18.masked-seed0000644000175400017540000000251513175713516027131 0ustar00biocbuildbiocbuildPackage: BSgenome.Hsapiens.UCSC.hg18.masked Title: Full masked genome sequences for Homo sapiens (UCSC version hg18) Description: Full genome sequences for Homo sapiens (Human) as provided by UCSC (hg18, Mar. 2006) and stored in Biostrings objects. The sequences are the same as in BSgenome.Hsapiens.UCSC.hg18, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Hsapiens.UCSC.hg18 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/hg18/bigZips/ organism_biocview: Homo_sapiens nmask_per_seq: 4 SrcDataFiles: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/hg18/database/ RM masks: chromOut.zip from http://hgdownload.cse.ucsc.edu/goldenPath/hg18/bigZips/ TRF masks: chromTrf.zip from http://hgdownload.cse.ucsc.edu/goldenPath/hg18/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Hsapiens.UCSC.hg18$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.UCSC.hg18/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Hsapiens.UCSC.hg19-seed0000644000175400017540000000467513175713516025700 0ustar00biocbuildbiocbuildPackage: BSgenome.Hsapiens.UCSC.hg19 Title: Full genome sequences for Homo sapiens (UCSC version hg19) Description: Full genome sequences for Homo sapiens (Human) as provided by UCSC (hg19, Feb. 2009) and stored in Biostrings objects. Version: 1.4.2 Suggests: TxDb.Hsapiens.UCSC.hg19.knownGene organism: Homo sapiens common_name: Human provider: UCSC provider_version: hg19 release_date: Feb. 2009 release_name: Genome Reference Consortium GRCh37 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/hg19/bigZips/ organism_biocview: Homo_sapiens BSgenomeObjname: Hsapiens seqnames: paste("chr", c(1:22, "X", "Y", "M", "1_gl000191_random", "1_gl000192_random", "4_ctg9_hap1", "4_gl000193_random", "4_gl000194_random", "6_apd_hap1", "6_cox_hap2", "6_dbb_hap3", "6_mann_hap4", "6_mcf_hap5", "6_qbl_hap6", "6_ssto_hap7", "7_gl000195_random" , "8_gl000196_random", "8_gl000197_random", "9_gl000198_random", "9_gl000199_random", "9_gl000200_random", "9_gl000201_random", "11_gl000202_random", "17_ctg5_hap1", "17_gl000203_random", "17_gl000204_random", "17_gl000205_random", "17_gl000206_random", "18_gl000207_random", "19_gl000208_random", "19_gl000209_random", "21_gl000210_random", paste("Un_gl000", 211:249, sep="")), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.zip from http://hgdownload.cse.ucsc.edu/goldenPath/hg19/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for hg19 are not included in the BSgenome data ## package anymore. However they can easily be extracted from the full ## genome sequences with something like: . library(TxDb.Hsapiens.UCSC.hg19.knownGene) txdb <- TxDb.Hsapiens.UCSC.hg19.knownGene gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.UCSC.hg19/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Hsapiens.UCSC.hg19.masked-seed0000644000175400017540000000253213175713516027131 0ustar00biocbuildbiocbuildPackage: BSgenome.Hsapiens.UCSC.hg19.masked Title: Full masked genome sequences for Homo sapiens (UCSC version hg19) Description: Full genome sequences for Homo sapiens (Human) as provided by UCSC (hg19, Feb. 2009) and stored in Biostrings objects. The sequences are the same as in BSgenome.Hsapiens.UCSC.hg19, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Hsapiens.UCSC.hg19 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/hg19/bigZips/ organism_biocview: Homo_sapiens nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/hg19/database/ RM masks: chromOut.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/hg19/bigZips/ TRF masks: chromTrf.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/hg19/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Hsapiens.UCSC.hg19$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.UCSC.hg19/masks AGAPSfiles_name: gap.txt BSgenome/inst/extdata/GentlemanLab/BSgenome.Hsapiens.UCSC.hg38-seed0000644000175400017540000000427213175713516025672 0ustar00biocbuildbiocbuildPackage: BSgenome.Hsapiens.UCSC.hg38 Title: Full genome sequences for Homo sapiens (UCSC version hg38) Description: Full genome sequences for Homo sapiens (Human) as provided by UCSC (hg38, Dec. 2013) and stored in Biostrings objects. Version: 1.4.2 Suggests: TxDb.Hsapiens.UCSC.hg38.knownGene organism: Homo sapiens common_name: Human provider: UCSC provider_version: hg38 release_date: Dec. 2013 release_name: Genome Reference Consortium GRCh38 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/hg38/bigZips/ organism_biocview: Homo_sapiens BSgenomeObjname: Hsapiens circ_seqs: "chrM" SrcDataFiles: hg38.2bit from http://hgdownload.cse.ucsc.edu/goldenPath/hg38/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Extract the upstream sequences ## --------------------------------------------------------------------- ## The upstream sequences located in ## http://hgdownload.cse.ucsc.edu/goldenPath/hg38/bigZips/ ## are based on RefSeq genes (RefSeq Genes track in the Genome Browser). ## Upstream sequences based on UCSC genes (UCSC Genes track in the ## Genome Browser) can easily be extracted from the full genome ## sequences with: . library(TxDb.Hsapiens.UCSC.hg38.knownGene) knownGene_txdb <- TxDb.Hsapiens.UCSC.hg38.knownGene knownGene_up1000seqs <- extractUpstreamSeqs(genome, knownGene_txdb) . ## Or, to get upstream sequences based on RefSeq genes: . refGene_txdb <- makeTxDbFromUCSC("hg38", "refGene") refGene_up1000seqs <- extractUpstreamSeqs(genome, refGene_txdb) . ## Note that you can make a TxDb object from various annotation ## resources. See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), and ## makeTxDbFromGFF() functions in the GenomicFeatures package for more ## information. ## IMPORTANT: Make sure you use a TxDb package (or TxDb object) that ## contains a gene model based on hg38 or on a compatible genome (i.e. ## a genome with sequences identical to the sequences in hg38). See ## ?extractUpstreamSeqs in the GenomicFeatures package for more ## information. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.UCSC.hg38/seqs seqfile_name: hg38.sorted.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Hsapiens.UCSC.hg38.masked-seed0000644000175400017540000000263013175713516027131 0ustar00biocbuildbiocbuildPackage: BSgenome.Hsapiens.UCSC.hg38.masked Title: Full masked genome sequences for Homo sapiens (UCSC version hg38) Description: Full genome sequences for Homo sapiens (Human) as provided by UCSC (hg38, Dec. 2013) and stored in Biostrings objects. The sequences are the same as in BSgenome.Hsapiens.UCSC.hg38, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Hsapiens.UCSC.hg38 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/hg38/bigZips/ organism_biocview: Homo_sapiens nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/hg38/database/ RM masks: hg38.fa.out.gz from http://hgdownload.cse.ucsc.edu/goldenPath/hg38/bigZips/ TRF masks: hg38.trf.bed.gz from http://hgdownload.cse.ucsc.edu/goldenPath/hg38/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Hsapiens.UCSC.hg38$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.UCSC.hg38/masks AGAPSfiles_name: gap.txt.gz RMfiles_name: hg38.fa.out.gz TRFfiles_name: hg38.trf.bed.gz BSgenome/inst/extdata/GentlemanLab/BSgenome.Mfascicularis.NCBI.5.0-seed0000644000175400017540000000337413175713516026416 0ustar00biocbuildbiocbuildPackage: BSgenome.Mfascicularis.NCBI.5.0 Title: Full genome sequences for Macaca fascicularis (Macaca_fascicularis_5.0) Description: Full genome sequences for Macaca fascicularis (long-tailed macaque) as provided by NCBI (Macaca_fascicularis_5.0, 2013-06-12) and stored in Biostrings objects. Version: 1.4.2 organism: Macaca fascicularis common_name: long-tailed macaque provider: NCBI provider_version: Macaca_fascicularis_5.0 release_date: 2013-06-12 release_name: Macaca_fascicularis_5.0 source_url: ftp://ftp.ncbi.nlm.nih.gov/genomes/all/GCF_000364345.1_Macaca_fascicularis_5.0/ organism_biocview: Macaca_fascicularis BSgenomeObjname: Mfascicularis seqnames: circ_seqs: "MT" SrcDataFiles: GCF_000364345.1_Macaca_fascicularis_5.0_genomic.fna.gz from ftp://ftp.ncbi.nlm.nih.gov/genomes/all/GCF_000364345.1_Macaca_fascicularis_5.0/ PkgExamples: genome$MFA1 # same as genome[["MFA1"]] . ## --------------------------------------------------------------------- ## About the ordering of the sequences ## --------------------------------------------------------------------- ## The sequences in BSgenome object 'genome' are ordered like in the ## assembly report at the following URL url <- "ftp://ftp.ncbi.nlm.nih.gov/genomes/ASSEMBLY_REPORTS/All/GCF_000364345.1.assembly.txt" ## except that the MT sequence was moved from the last position to the ## position between the chromosomes (MFA* sequences) and the scaffolds ## (Scaffold* sequences): SequenceName <- read.table(url, sep="\t", stringsAsFactors=FALSE)[[1]] target_seqlevels <- SequenceName[c(1:21, 7601, 22:7600)] stopifnot(identical(seqlevels(genome), target_seqlevels)) seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Mfascicularis.NCBI.5.0/seqs seqfile_name: Macaca_fascicularis_5.0.sorted.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Mfascicularis.NCBI.5.0-tools/0000755000175400017540000000000013175713516026704 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Mfascicularis.NCBI.5.0-tools/fasta_to_sorted2bit.R0000644000175400017540000000245713175713516033000 0ustar00biocbuildbiocbuildlibrary(BSgenome) INFILE <- "GCF_000364345.1_Macaca_fascicularis_5.0_genomic.fna.gz" OUTFILE <- "Macaca_fascicularis_5.0.sorted.2bit" ## Fetch assembly report from: ## ftp://ftp.ncbi.nlm.nih.gov/genomes/ASSEMBLY_REPORTS/All/GCF_000364345.1.assembly.txt assembly_report <- GenomeInfoDb:::fetch_assembly_report("GCF_000364345.1") Mfascicularis <- readDNAStringSet(INFILE) ## Clean names on Mfascicularis to keep only the RefSeq accession. names(Mfascicularis) <- as.character(phead( CharacterList( strsplit(names(Mfascicularis), " ", fixed=TRUE) ), n=1 )) ## Order sequences in Mfascicularis like in assembly report. Mfascicularis <- Mfascicularis[assembly_report[ , "RefSeqAccn"]] ## Replace RefSeq accessions with official SequenceName from assembly report. SequenceName <- assembly_report[ , "SequenceName"] names(Mfascicularis) <- SequenceName ## Move MT sequence from last position to position after chromosomes (MFA* ## sequences) and before scaffolds (Scaffold* sequences). oo <- c(grep("^MFA", SequenceName), grep("^MT$", SequenceName), grep("^Scaffold", SequenceName)) Mfascicularis <- Mfascicularis[oo] ## Export as 2bit file. export.2bit(Mfascicularis, OUTFILE) BSgenome/inst/extdata/GentlemanLab/BSgenome.Mfuro.UCSC.musFur1-seed0000644000175400017540000000152313175713516025775 0ustar00biocbuildbiocbuildPackage: BSgenome.Mfuro.UCSC.musFur1 Title: Full genome sequences for Mustela putorius furo (UCSC version musFur1) Description: Full genome sequences for Mustela putorius furo (Ferret) as provided by UCSC (musFur1, Apr. 2011) and stored in Biostrings objects. Version: 1.4.2 organism: Mustela putorius furo common_name: Ferret provider: UCSC provider_version: musFur1 release_date: Apr. 2011 release_name: Ferret Genome Sequencing Consortium MusPutFur1.0 source_url: http://hgdownload.soe.ucsc.edu/goldenPath/musFur1/bigZips/ organism_biocview: Mustela_furo BSgenomeObjname: Mfuro SrcDataFiles: musFur1.2bit from http://hgdownload.soe.ucsc.edu/goldenPath/musFur1/bigZips/ PkgExamples: genome$GL896898 # same as genome[["GL896898"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Mfuro.UCSC.musFur1/seqs seqfile_name: musFur1.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmulatta.UCSC.rheMac2-seed0000644000175400017540000000356613175713516026421 0ustar00biocbuildbiocbuildPackage: BSgenome.Mmulatta.UCSC.rheMac2 Title: Full genome sequences for Macaca mulatta (UCSC version rheMac2) Description: Full genome sequences for Macaca mulatta (Rhesus) as provided by UCSC (rheMac2, Jan. 2006) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Macaca mulatta common_name: Rhesus provider: UCSC provider_version: rheMac2 release_date: Jan. 2006 release_name: Baylor College of Medicine HGSC v1.0 Mmul_051212 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/rheMac2/ organism_biocview: Macaca_mulatta BSgenomeObjname: Mmulatta seqnames: paste("chr", c(1:20, "X", "Ur"), sep="") circ_seqs: character(0) SrcDataFiles: chromFa.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rheMac2/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for rheMac2 are not included in the BSgenome ## data package anymore. However they can easily be extracted from the ## full genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("rheMac2", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Mmulatta.UCSC.rheMac2/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmulatta.UCSC.rheMac2.masked-seed0000644000175400017540000000372213175713516027656 0ustar00biocbuildbiocbuildPackage: BSgenome.Mmulatta.UCSC.rheMac2.masked Title: Full masked genome sequences for Macaca mulatta (UCSC version rheMac2) Description: Full genome sequences for Macaca mulatta (Rhesus) as provided by UCSC (rheMac2, Jan. 2006) and stored in Biostrings objects. The sequences are the same as in BSgenome.Mmulatta.UCSC.rheMac2, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. NOTE: In most assemblies available at UCSC, Tandem Repeats Finder repeats were filtered to retain only the repeats with period <= 12. However, the filtering was omitted for this assembly, so the TRF masks contain all Tandem Repeats Finder results. Version: 1.3.99 RefPkgname: BSgenome.Mmulatta.UCSC.rheMac2 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/rheMac2/ organism_biocview: Macaca_mulatta nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rheMac2/database/ RM masks: chromOut.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rheMac2/bigZips/ TRF masks: chromTrf.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rheMac2/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## NOTE: In most assemblies available at UCSC, Tandem Repeats ## Finder repeats were filtered to retain only the repeats ## with period <= 12. However, the filtering was omitted for ## this assembly, so, despite the description being displayed ## for this mask, it contains all the Tandem Repeats Finder ## results. masks(genome$chr1)$TRF ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Mmulatta.UCSC.rheMac2$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Mmulatta.UCSC.rheMac2/masks AGAPSfiles_name: gap.txt.gz BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmulatta.UCSC.rheMac3-seed0000644000175400017540000000356213175713516026416 0ustar00biocbuildbiocbuildPackage: BSgenome.Mmulatta.UCSC.rheMac3 Title: Full genome sequences for Macaca mulatta (UCSC version rheMac3) Description: Full genome sequences for Macaca mulatta (Rhesus) as provided by UCSC (rheMac3, Oct. 2010) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Macaca mulatta common_name: Rhesus provider: UCSC provider_version: rheMac3 release_date: Oct. 2010 release_name: Beijing Genomics Institute CR_1.0 source_url: http://hgdownload.soe.ucsc.edu/goldenPath/rheMac3/ organism_biocview: Macaca_mulatta BSgenomeObjname: Mmulatta seqnames: paste("chr", c(1:20, "X", "M"), sep="") circ_seqs: "chrM" mseqnames: "chrUn" SrcDataFiles: rheMac3.fa.gz from http://hgdownload.soe.ucsc.edu/goldenPath/rheMac3/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for rheMac3 are not included in the BSgenome ## data package anymore. However they can easily be extracted from the ## full genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("rheMac3", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Mmulatta.UCSC.rheMac3/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmulatta.UCSC.rheMac3-tools/0000755000175400017540000000000013175713516026705 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Mmulatta.UCSC.rheMac3-tools/splitbigfasta.R0000755000175400017540000000123413175713516031667 0ustar00biocbuildbiocbuild### library(Biostrings) rheMac3 <- readDNAStringSet("rheMac3.fa") ### Partitioning: is_chrUn <- grepl("^chrUn", names(rheMac3)) is_chrom <- !is_chrUn ### Send each chromosome to a FASTA file. seqnames <- paste("chr", c(1:20, "X", "M"), sep="") stopifnot(setequal(seqnames, names(rheMac3)[is_chrom])) for (seqname in seqnames) { seq <- rheMac3[match(seqname, names(rheMac3))] filename <- paste(seqname, ".fa", sep="") cat("writing ", filename, "\n", sep="") writeXStringSet(seq, file=filename, width=50L) } ### Send the 34081 chrUn_* sequences to 1 FASTA file. chrUn_mseq <- rheMac3[is_chrUn] writeXStringSet(chrUn_mseq, file="chrUn.fa", width=50L) BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmulatta.UCSC.rheMac3.masked-seed0000644000175400017540000000270413175713516027656 0ustar00biocbuildbiocbuildPackage: BSgenome.Mmulatta.UCSC.rheMac3.masked Title: Full masked genome sequences for Macaca mulatta (UCSC version rheMac3) Description: Full genome sequences for Macaca mulatta (Rhesus) as provided by UCSC (rheMac3, Oct. 2010) and stored in Biostrings objects. The sequences are the same as in BSgenome.Mmulatta.UCSC.rheMac3, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Mmulatta.UCSC.rheMac3 source_url: http://hgdownload.soe.ucsc.edu/goldenPath/rheMac3/ organism_biocview: Macaca_mulatta nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.soe.ucsc.edu/goldenPath/rheMac3/database/ RM masks: rheMac3.fa.out.gz from http://hgdownload.soe.ucsc.edu/goldenPath/rheMac3/bigZips/ TRF masks: rheMac3.trf.bed.gz from http://hgdownload.soe.ucsc.edu/goldenPath/rheMac3/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Mmulatta.UCSC.rheMac3$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Mmulatta.UCSC.rheMac3/masks AGAPSfiles_name: gap.txt.gz RMfiles_name: rheMac3.fa.out.gz TRFfiles_name: rheMac3.trf.bed.gz BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmulatta.UCSC.rheMac8-seed0000644000175400017540000000152413175713516026417 0ustar00biocbuildbiocbuildPackage: BSgenome.Mmulatta.UCSC.rheMac8 Title: Full genome sequences for Macaca mulatta (UCSC version rheMac8) Description: Full genome sequences for Macaca mulatta (Rhesus) as provided by UCSC (rheMac8, Nov. 2015) and stored in Biostrings objects. Version: 1.4.2 organism: Macaca mulatta common_name: Rhesus provider: UCSC provider_version: rheMac8 release_date: Nov. 2015 release_name: Baylor College of Medicine HGSC Mmul_8.0.1 source_url: http://hgdownload.soe.ucsc.edu/goldenPath/rheMac8/bigZips/ organism_biocview: Macaca_mulatta BSgenomeObjname: Mmulatta circ_seqs: "chrM" SrcDataFiles: rheMac8.2bit from http://hgdownload.soe.ucsc.edu/goldenPath/rheMac8/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Mmulatta.UCSC.rheMac8/seqs seqfile_name: rheMac8.sorted.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmulatta.UCSC.rheMac8-tools/0000755000175400017540000000000013175713516026712 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Mmulatta.UCSC.rheMac8-tools/sort_rheMac8.2bit.R0000644000175400017540000000127413175713516032236 0ustar00biocbuildbiocbuildlibrary(Biostrings) library(rtracklayer) rheMac8 <- import("rheMac8.2bit") seqlevels1 <- paste0("chr", c(1:20, "X", "Y", "M")) tmp <- CharacterList(strsplit(names(rheMac8), "_")) npart <- elementNROWS(tmp) stopifnot(all(npart <= 3L)) idx1 <- which(npart == 1L) stopifnot(setequal(names(rheMac8)[idx1], seqlevels1)) idx2 <- which(npart == 2L) stopifnot(length(idx2) == 0L) idx3 <- which(npart == 3L) m3 <- matrix(unlist(tmp[idx3]), ncol=3L, byrow=TRUE) stopifnot(all(m3[ , 1L] == "chrUn")) stopifnot(all(m3[ , 2L] == "NW")) oo3 <- order(m3[ , 3L]) seqlevels3 <- names(rheMac8)[idx3[oo3]] rheMac8_seqlevels <- c(seqlevels1, seqlevels3) export(rheMac8[rheMac8_seqlevels], "rheMac8.sorted.2bit") BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmusculus.UCSC.mm10-seed0000644000175400017540000000730013175713516026111 0ustar00biocbuildbiocbuildPackage: BSgenome.Mmusculus.UCSC.mm10 Title: Full genome sequences for Mus musculus (UCSC version mm10) Description: Full genome sequences for Mus musculus (Mouse) as provided by UCSC (mm10, Dec. 2011) and stored in Biostrings objects. Version: 1.4.2 Suggests: TxDb.Mmusculus.UCSC.mm10.knownGene organism: Mus musculus common_name: Mouse provider: UCSC provider_version: mm10 release_date: Dec. 2011 release_name: Genome Reference Consortium GRCm38 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/mm10/chromosomes/ organism_biocview: Mus_musculus BSgenomeObjname: Mmusculus seqnames: paste("chr", c(1:19, "X", "Y", "M", paste(c("1_GL456210", "1_GL456211", "1_GL456212", "1_GL456213", "1_GL456221", "4_GL456216", "4_GL456350", "4_JH584292", "4_JH584293", "4_JH584294", "4_JH584295", "5_GL456354", "5_JH584296", "5_JH584297", "5_JH584298", "5_JH584299", "7_GL456219", "X_GL456233", "Y_JH584300", "Y_JH584301", "Y_JH584302", "Y_JH584303"), "_random", sep=""), paste("Un_", c("GL456239", "GL456359", "GL456360", "GL456366", "GL456367", "GL456368", "GL456370", "GL456372", "GL456378", "GL456379", "GL456381", "GL456382", "GL456383", "GL456385", "GL456387", "GL456389", "GL456390", "GL456392", "GL456393", "GL456394", "GL456396", "JH584304"), sep="")), sep="") circ_seqs: "chrM" SrcDataFiles: chr1.fa.gz chr2.fa.gz chr3.fa.gz chr4.fa.gz chr5.fa.gz chr6.fa.gz chr7.fa.gz chr8.fa.gz chr9.fa.gz chr10.fa.gz chr11.fa.gz chr12.fa.gz chr13.fa.gz chr14.fa.gz chr15.fa.gz chr16.fa.gz chr17.fa.gz chr18.fa.gz chr19.fa.gz chrX.fa.gz chrY.fa.gz chrM.fa.gz chr1_GL456210_random.fa.gz chr1_GL456211_random.fa.gz chr1_GL456212_random.fa.gz chr1_GL456213_random.fa.gz chr1_GL456221_random.fa.gz chr4_GL456216_random.fa.gz chr4_GL456350_random.fa.gz chr4_JH584292_random.fa.gz chr4_JH584293_random.fa.gz chr4_JH584294_random.fa.gz chr4_JH584295_random.fa.gz chr5_GL456354_random.fa.gz chr5_JH584296_random.fa.gz chr5_JH584297_random.fa.gz chr5_JH584298_random.fa.gz chr5_JH584299_random.fa.gz chr7_GL456219_random.fa.gz chrX_GL456233_random.fa.gz chrY_JH584300_random.fa.gz chrY_JH584301_random.fa.gz chrY_JH584302_random.fa.gz chrY_JH584303_random.fa.gz chrUn_GL456239.fa.gz chrUn_GL456359.fa.gz chrUn_GL456360.fa.gz chrUn_GL456366.fa.gz chrUn_GL456367.fa.gz chrUn_GL456368.fa.gz chrUn_GL456370.fa.gz chrUn_GL456372.fa.gz chrUn_GL456378.fa.gz chrUn_GL456379.fa.gz chrUn_GL456381.fa.gz chrUn_GL456382.fa.gz chrUn_GL456383.fa.gz chrUn_GL456385.fa.gz chrUn_GL456387.fa.gz chrUn_GL456389.fa.gz chrUn_GL456390.fa.gz chrUn_GL456392.fa.gz chrUn_GL456393.fa.gz chrUn_GL456394.fa.gz chrUn_GL456396.fa.gz chrUn_JH584304.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/mm10/chromosomes/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## The upstream sequences for mm10 (i.e. the sequences 1000 bases ## upstream of annotated transcription starts) can easily be extracted ## from the full genome sequences with something like: . library(TxDb.Mmusculus.UCSC.mm10.knownGene) txdb <- TxDb.Mmusculus.UCSC.mm10.knownGene gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Mmusculus.UCSC.mm10/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmusculus.UCSC.mm10.masked-seed0000644000175400017540000000201013175713516027345 0ustar00biocbuildbiocbuildPackage: BSgenome.Mmusculus.UCSC.mm10.masked Title: Full masked genome sequences for Mus musculus (UCSC version mm10) Description: Full genome sequences for Mus musculus (Mouse) as provided by UCSC (mm10, Dec. 2011) and stored in Biostrings objects. The sequences are the same as in BSgenome.Mmusculus.UCSC.mm10, except that each of them has the 2 following masks on top: (1) the mask of assembly gaps (AGAPS mask), and (2) the mask of intra-contig ambiguities (AMB mask). Version: 1.3.99 RefPkgname: BSgenome.Mmusculus.UCSC.mm10 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/mm10/chromosomes/ organism_biocview: Mus_musculus nmask_per_seq: 2 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/mm10/database/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Mmusculus.UCSC.mm10$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Mmusculus.UCSC.mm10/masks AGAPSfiles_name: gap.txt BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmusculus.UCSC.mm8-seed0000644000175400017540000000357313175713516026050 0ustar00biocbuildbiocbuildPackage: BSgenome.Mmusculus.UCSC.mm8 Title: Full genome sequences for Mus musculus (UCSC version mm8) Description: Full genome sequences for Mus musculus (Mouse) as provided by UCSC (mm8, Feb. 2006) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Mus musculus common_name: Mouse provider: UCSC provider_version: mm8 release_date: Feb. 2006 release_name: NCBI Build 36 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/mm8/bigZips/ organism_biocview: Mus_musculus BSgenomeObjname: Mmusculus seqnames: paste("chr", c(1:19, "X", "Y", "M", paste(c(1, 5, 7, 8, 9, 10, 13, 15, 17, "X", "Y", "Un"), "_random", sep="")), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/mm8/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for mm8 are not included in the BSgenome data ## package anymore. However they can easily be extracted from the full ## genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("mm8", "knownGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Mmusculus.UCSC.mm8/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmusculus.UCSC.mm8.masked-seed0000644000175400017540000000251513175713516027306 0ustar00biocbuildbiocbuildPackage: BSgenome.Mmusculus.UCSC.mm8.masked Title: Full masked genome sequences for Mus musculus (UCSC version mm8) Description: Full genome sequences for Mus musculus (Mouse) as provided by UCSC (mm8, Feb. 2006) and stored in Biostrings objects. The sequences are the same as in BSgenome.Mmusculus.UCSC.mm8, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Mmusculus.UCSC.mm8 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/mm8/bigZips/ organism_biocview: Mus_musculus nmask_per_seq: 4 SrcDataFiles: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/mm8/database/ RM masks: chromOut.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/mm8/bigZips/ TRF masks: chromTrf.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/mm8/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Mmusculus.UCSC.mm8$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Mmusculus.UCSC.mm8/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmusculus.UCSC.mm9-seed0000644000175400017540000000363713175713516026052 0ustar00biocbuildbiocbuildPackage: BSgenome.Mmusculus.UCSC.mm9 Title: Full genome sequences for Mus musculus (UCSC version mm9) Description: Full genome sequences for Mus musculus (Mouse) as provided by UCSC (mm9, Jul. 2007) and stored in Biostrings objects. Version: 1.4.2 Suggests: TxDb.Mmusculus.UCSC.mm9.knownGene organism: Mus musculus common_name: Mouse provider: UCSC provider_version: mm9 release_date: Jul. 2007 release_name: NCBI Build 37 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/mm9/bigZips/ organism_biocview: Mus_musculus BSgenomeObjname: Mmusculus seqnames: paste("chr", c(1:19, "X", "Y", "M", paste(c(1, 3, 4, 5, 7, 8, 9, 13, 16, 17, "X", "Y", "Un"), "_random", sep="")), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/mm9/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for mm9 are not included in the BSgenome data ## package anymore. However they can easily be extracted from the full ## genome sequences with something like: . library(TxDb.Mmusculus.UCSC.mm9.knownGene) txdb <- TxDb.Mmusculus.UCSC.mm9.knownGene gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Mmusculus.UCSC.mm9/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmusculus.UCSC.mm9.masked-seed0000644000175400017540000000251513175713516027307 0ustar00biocbuildbiocbuildPackage: BSgenome.Mmusculus.UCSC.mm9.masked Title: Full masked genome sequences for Mus musculus (UCSC version mm9) Description: Full genome sequences for Mus musculus (Mouse) as provided by UCSC (mm9, Jul. 2007) and stored in Biostrings objects. The sequences are the same as in BSgenome.Mmusculus.UCSC.mm9, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Mmusculus.UCSC.mm9 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/mm9/bigZips/ organism_biocview: Mus_musculus nmask_per_seq: 4 SrcDataFiles: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/mm9/database/ RM masks: chromOut.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/mm9/bigZips/ TRF masks: chromTrf.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/mm9/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Mmusculus.UCSC.mm9$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Mmusculus.UCSC.mm9/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Ptroglodytes.UCSC.panTro2-seed0000644000175400017540000000372313175713516027373 0ustar00biocbuildbiocbuildPackage: BSgenome.Ptroglodytes.UCSC.panTro2 Title: Full genome sequences for Pan troglodytes (UCSC version panTro2) Description: Full genome sequences for Pan troglodytes (Chimp) as provided by UCSC (panTro2, Mar. 2006) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Pan troglodytes common_name: Chimp provider: UCSC provider_version: panTro2 release_date: Mar. 2006 release_name: CGSC Build 2 Version 1 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/panTro2/bigZips/ organism_biocview: Pan_troglodytes BSgenomeObjname: Ptroglodytes seqnames: paste("chr", c(1, "2a", "2b", 3:22, "X", "Y", "M", "Un", "6_hla_hap1", paste(c(1, "2a", "2b", 3:20, 22, "X", "Y"), "_random", sep="")), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/panTro2/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for panTro2 are not included in the BSgenome ## data package anymore. However they can easily be extracted from the ## full genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("panTro2", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Ptroglodytes.UCSC.panTro2/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Ptroglodytes.UCSC.panTro2.masked-seed0000644000175400017540000000262713175713516030640 0ustar00biocbuildbiocbuildPackage: BSgenome.Ptroglodytes.UCSC.panTro2.masked Title: Full masked genome sequences for Pan troglodytes (UCSC version panTro2) Description: Full genome sequences for Pan troglodytes (Chimp) as provided by UCSC (panTro2, Mar. 2006) and stored in Biostrings objects. The sequences are the same as in BSgenome.Ptroglodytes.UCSC.panTro2, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Ptroglodytes.UCSC.panTro2 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/panTro2/bigZips/ organism_biocview: Pan_troglodytes nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from ftp://hgdownload.cse.ucsc.edu/goldenPath/panTro2/database/ RM masks: chromOut.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/panTro2/bigZips/ TRF masks: chromTrf.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/panTro2/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Ptroglodytes.UCSC.panTro2$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Ptroglodytes.UCSC.panTro2/masks AGAPSfiles_name: gap.txt BSgenome/inst/extdata/GentlemanLab/BSgenome.Ptroglodytes.UCSC.panTro3-seed0000644000175400017540000000372613175713516027377 0ustar00biocbuildbiocbuildPackage: BSgenome.Ptroglodytes.UCSC.panTro3 Title: Full genome sequences for Pan troglodytes (UCSC version panTro3) Description: Full genome sequences for Pan troglodytes (Chimp) as provided by UCSC (panTro3, Oct. 2010) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Pan troglodytes common_name: Chimp provider: UCSC provider_version: panTro3 release_date: Oct. 2010 release_name: CGSC Build 2.1.3 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/panTro3/bigZips/ organism_biocview: Pan_troglodytes BSgenomeObjname: Ptroglodytes seqnames: paste("chr", c(1, "2A", "2B", 3:22, "X", "Y", "M"), sep="") circ_seqs: "chrM" mseqnames: c(paste("chr", c(1, "2A", "2B", 3:22, "X", "Y", "M"), "_random", sep=""), "chrUn") SrcDataFiles: panTro3.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/panTro3/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for panTro3 are not included in the BSgenome ## data package anymore. However they can easily be extracted from the ## full genome sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("panTro3", "refGene") gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Ptroglodytes.UCSC.panTro3/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Ptroglodytes.UCSC.panTro3-tools/0000755000175400017540000000000013175713516027664 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Ptroglodytes.UCSC.panTro3-tools/splitbigfasta.R0000755000175400017540000000160713175713516032652 0ustar00biocbuildbiocbuild### library(Biostrings) panTro3 <- readDNAStringSet("panTro3.fa") ### Send each chromosome to a FASTA file. seqnames <- paste("chr", c(1, "2A", "2B", 3:22, "X", "Y", "M"), sep="") for (seqname in seqnames) { seq <- panTro3[match(seqname, names(panTro3))] filename <- paste(seqname, ".fa", sep="") cat("writing ", filename, "\n", sep="") write.XStringSet(seq, file=filename, width=50L) } ### Send the chr*_random sequences to 1 FASTA file per sequence. for (seqname in seqnames) { mseq <- panTro3[grep(paste0(seqname, "_"), names(panTro3), fixed=TRUE)] filename <- paste(seqname, "_random.fa", sep="") cat("writing ", filename, "\n", sep="") write.XStringSet(mseq, file=filename, width=50L) } ### Send all the chrUn_* sequences to 1 FASTA file. chrUn_mseq <- panTro3[grep("chrUn_", names(panTro3), fixed=TRUE)] write.XStringSet(chrUn_mseq, file="chrUn.fa", width=50L) BSgenome/inst/extdata/GentlemanLab/BSgenome.Ptroglodytes.UCSC.panTro3.masked-seed0000644000175400017540000000273113175713516030635 0ustar00biocbuildbiocbuildPackage: BSgenome.Ptroglodytes.UCSC.panTro3.masked Title: Full masked genome sequences for Pan troglodytes (UCSC version panTro3) Description: Full genome sequences for Pan troglodytes (Chimp) as provided by UCSC (panTro3, Oct. 2010) and stored in Biostrings objects. The sequences are the same as in BSgenome.Ptroglodytes.UCSC.panTro3, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Ptroglodytes.UCSC.panTro3 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/panTro3/bigZips/ organism_biocview: Pan_troglodytes nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/panTro3/database/ RM masks: panTro3.fa.out.gz from http://hgdownload.cse.ucsc.edu/goldenPath/panTro3/bigZips/ TRF masks: panTro3.trf.bed.gz from http://hgdownload.cse.ucsc.edu/goldenPath/panTro3/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Ptroglodytes.UCSC.panTro3$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Ptroglodytes.UCSC.panTro3/masks AGAPSfiles_name: gap.txt RMfiles_name: panTro3.fa.out TRFfiles_name: panTro3.trf.bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Ptroglodytes.UCSC.panTro5-seed0000644000175400017540000000150413175713516027371 0ustar00biocbuildbiocbuildPackage: BSgenome.Ptroglodytes.UCSC.panTro5 Title: Full genome sequences for Pan troglodytes (UCSC version panTro5) Description: Full genome sequences for Pan troglodytes (Chimp) as provided by UCSC (panTro5, May 2016) and stored in Biostrings objects. Version: 1.4.2 organism: Pan troglodytes common_name: Chimp provider: UCSC provider_version: panTro5 release_date: May 2016 release_name: CGSC Build 3.0 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/panTro5/bigZips/ organism_biocview: Pan_troglodytes BSgenomeObjname: Ptroglodytes circ_seqs: "chrM" SrcDataFiles: panTro5.2bit from http://hgdownload.cse.ucsc.edu/goldenPath/panTro5/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Ptroglodytes.UCSC.panTro5/seqs seqfile_name: panTro5.sorted.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Ptroglodytes.UCSC.panTro5-tools/0000755000175400017540000000000013175713516027666 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Ptroglodytes.UCSC.panTro5-tools/sort_panTro5.2bit.R0000644000175400017540000000176613175713516033261 0ustar00biocbuildbiocbuildlibrary(Biostrings) library(rtracklayer) panTro5 <- import("panTro5.2bit") seqlevels1 <- paste0("chr", c(1, "2A", "2B", 3:22, "X", "Y", "M")) tmp <- CharacterList(strsplit(names(panTro5), "_")) npart <- elementNROWS(tmp) stopifnot(all(npart <= 4L)) idx1 <- which(npart == 1L) stopifnot(setequal(names(panTro5)[idx1], seqlevels1)) idx2 <- which(npart == 2L) stopifnot(length(idx2) == 0L) idx4 <- which(npart == 4L) m4 <- matrix(unlist(tmp[idx4]), ncol=4L, byrow=TRUE) stopifnot(all(m4[ , 2L] == "NW")) stopifnot(all(m4[ , 4L] == "random")) chrom <- match(m4[ , 1L], seqlevels1) stopifnot(!anyNA(chrom)) oo4 <- order(chrom, m4[ , 3L]) seqlevels4 <- names(panTro5)[idx4[oo4]] idx3 <- which(npart == 3L) m3 <- matrix(unlist(tmp[idx3]), ncol=3L, byrow=TRUE) stopifnot(all(m3[ , 1L] == "chrUn")) stopifnot(all(m3[ , 2L] == "NW")) oo3 <- order(m3[ , 3L]) seqlevels3 <- names(panTro5)[idx3[oo3]] panTro5_seqlevels <- c(seqlevels1, seqlevels4, seqlevels3) export(panTro5[panTro5_seqlevels], "panTro5.sorted.2bit") BSgenome/inst/extdata/GentlemanLab/BSgenome.Rnorvegicus.UCSC.rn4-seed0000644000175400017540000000365513175713516026364 0ustar00biocbuildbiocbuildPackage: BSgenome.Rnorvegicus.UCSC.rn4 Title: Full genome sequences for Rattus norvegicus (UCSC version rn4) Description: Full genome sequences for Rattus norvegicus (Rat) as provided by UCSC (rn4, Nov. 2004) and stored in Biostrings objects. Version: 1.4.2 Suggests: TxDb.Rnorvegicus.UCSC.rn4.ensGene organism: Rattus norvegicus common_name: Rat provider: UCSC provider_version: rn4 release_date: Nov. 2004 release_name: Baylor College of Medicine HGSC v3.4 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/rn4/bigZips/ organism_biocview: Rattus_norvegicus BSgenomeObjname: Rnorvegicus seqnames: paste("chr", c(1:20, "X", "M", "Un", paste(c(1:20, "X", "Un"), "_random", sep="")), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rn4/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for rn4 are not included in the BSgenome data ## package anymore. However they can easily be extracted from the full ## genome sequences with something like: . library(TxDb.Rnorvegicus.UCSC.rn4.ensGene) txdb <- TxDb.Rnorvegicus.UCSC.rn4.ensGene gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Rnorvegicus.UCSC.rn4/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Rnorvegicus.UCSC.rn4.masked-seed0000644000175400017540000000254413175713516027623 0ustar00biocbuildbiocbuildPackage: BSgenome.Rnorvegicus.UCSC.rn4.masked Title: Full masked genome sequences for Rattus norvegicus (UCSC version rn4) Description: Full genome sequences for Rattus norvegicus (Rat) as provided by UCSC (rn4, Nov. 2004) and stored in Biostrings objects. The sequences are the same as in BSgenome.Rnorvegicus.UCSC.rn4, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Rnorvegicus.UCSC.rn4 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/rn4/bigZips/ organism_biocview: Rattus_norvegicus nmask_per_seq: 4 SrcDataFiles: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/rn4/database/ RM masks: chromOut.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rn4/bigZips/ TRF masks: chromTrf.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rn4/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Rnorvegicus.UCSC.rn4$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Rnorvegicus.UCSC.rn4/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Rnorvegicus.UCSC.rn5-seed0000644000175400017540000000356713175713516026367 0ustar00biocbuildbiocbuildPackage: BSgenome.Rnorvegicus.UCSC.rn5 Title: Full genome sequences for Rattus norvegicus (UCSC version rn5) Description: Full genome sequences for Rattus norvegicus (Rat) as provided by UCSC (rn5, Mar. 2012) and stored in Biostrings objects. Version: 1.4.2 Suggests: TxDb.Rnorvegicus.UCSC.rn5.refGene organism: Rattus norvegicus common_name: Rat provider: UCSC provider_version: rn5 release_date: Mar. 2012 release_name: RGSC 5.0 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/rn5/bigZips/ organism_biocview: Rattus_norvegicus BSgenomeObjname: Rnorvegicus seqnames: paste("chr", c(1:20, "X", "M"), sep="") circ_seqs: "chrM" mseqnames: c("random", "chrUn") SrcDataFiles: rn5.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rn5/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Upstream sequences ## --------------------------------------------------------------------- ## Starting with BioC 3.0, the upstream1000, upstream2000, and ## upstream5000 sequences for rn5 are not included in the BSgenome data ## package anymore. However they can easily be extracted from the full ## genome sequences with something like: . library(TxDb.Rnorvegicus.UCSC.rn5.refGene) txdb <- TxDb.Rnorvegicus.UCSC.rn5.refGene gn <- sort(genes(txdb)) up1000 <- flank(gn, width=1000) up1000seqs <- getSeq(genome, up1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object), ## that contains a gene model based on the exact same reference genome ## as the BSgenome object you pass to getSeq(). Note that you can make ## your own custom TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), ## and makeTxDbFromGFF() functions in the GenomicFeatures ## package. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Rnorvegicus.UCSC.rn5/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Rnorvegicus.UCSC.rn5-tools/0000755000175400017540000000000013175713516026651 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Rnorvegicus.UCSC.rn5-tools/splitbigfasta.R0000755000175400017540000000202013175713516031625 0ustar00biocbuildbiocbuild### library(Biostrings) rn5 <- readDNAStringSet("rn5.fa") ### Partitioning: is_random <- grepl("^chr[^_]*_[^_]*_random$", names(rn5)) is_chrUn <- grepl("^chrUn", names(rn5)) is_chrom <- !(is_random | is_chrUn) ### Sanity check: stopifnot(all(is_random | is_chrUn | is_chrom)) stopifnot(!any(is_random & is_chrUn)) stopifnot(!any(is_random & is_chrom)) stopifnot(!any(is_chrUn & is_chrom)) ### Send each chromosome to a FASTA file. seqnames <- paste("chr", c(1:20, "X", "M"), sep="") stopifnot(setequal(seqnames, names(rn5)[is_chrom])) for (seqname in seqnames) { seq <- rn5[match(seqname, names(rn5))] filename <- paste(seqname, ".fa", sep="") cat("writing ", filename, "\n", sep="") writeXStringSet(seq, file=filename, width=50L) } ### Send the 1278 chrNN_*_random sequences to 1 FASTA file. random_mseq <- rn5[is_random] writeXStringSet(random_mseq, file="random.fa", width=50L) ### Send the 1439 chrUn_* sequences to 1 FASTA file. chrUn_mseq <- rn5[is_chrUn] writeXStringSet(chrUn_mseq, file="chrUn.fa", width=50L) BSgenome/inst/extdata/GentlemanLab/BSgenome.Rnorvegicus.UCSC.rn5.masked-seed0000644000175400017540000000263413175713516027624 0ustar00biocbuildbiocbuildPackage: BSgenome.Rnorvegicus.UCSC.rn5.masked Title: Full masked genome sequences for Rattus norvegicus (UCSC version rn5) Description: Full genome sequences for Rattus norvegicus (Rat) as provided by UCSC (rn5, Mar. 2012) and stored in Biostrings objects. The sequences are the same as in BSgenome.Rnorvegicus.UCSC.rn5, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Rnorvegicus.UCSC.rn5 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/rn5/bigZips/ organism_biocview: Rattus_norvegicus nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rn5/database/ RM masks: rn5.fa.out.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rn5/bigZips/ TRF masks: rn5.trf.bed.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rn5/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Rnorvegicus.UCSC.rn5$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Rnorvegicus.UCSC.rn5/masks AGAPSfiles_name: gap.txt RMfiles_name: rn5.fa.out TRFfiles_name: rn5.trf.bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Rnorvegicus.UCSC.rn6-seed0000644000175400017540000000330413175713516026355 0ustar00biocbuildbiocbuildPackage: BSgenome.Rnorvegicus.UCSC.rn6 Title: Full genome sequences for Rattus norvegicus (UCSC version rn6) Description: Full genome sequences for Rattus norvegicus (Rat) as provided by UCSC (rn6, Jul. 2014) and stored in Biostrings objects. Version: 1.4.2 Suggests: GenomicFeatures organism: Rattus norvegicus common_name: Rat provider: UCSC provider_version: rn6 release_date: Jul. 2014 release_name: RGSC Rnor_6.0 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/rn6/bigZips/ organism_biocview: Rattus_norvegicus BSgenomeObjname: Rnorvegicus seqnames: seqnames(Seqinfo(genome="rn6")) circ_seqs: "chrM" SrcDataFiles: rn6.2bit from http://hgdownload.cse.ucsc.edu/goldenPath/rn6/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] . ## --------------------------------------------------------------------- ## Extract the upstream sequences ## --------------------------------------------------------------------- ## The upstream sequences can easily be extracted from the full genome ## sequences with something like: . library(GenomicFeatures) txdb <- makeTxDbFromUCSC("rn6", tablename="refGene") up1000seqs <- extractUpstreamSeqs(genome, txdb, width=1000) . ## IMPORTANT: Make sure you use a TxDb package (or TxDb object) that ## contains a gene model based on rn6 or on a compatible genome (i.e. ## a genome with sequences identical to the sequences in rn6). Note ## that you can make a TxDb object from various annotation resources. ## See the makeTxDbFromUCSC(), makeTxDbFromBiomart(), and ## makeTxDbFromGFF() functions in the GenomicFeatures package for more ## information. seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Rnorvegicus.UCSC.rn6/seqs seqfile_name: rn6.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Scerevisiae.UCSC.sacCer1-seed0000644000175400017540000000154613175713516027073 0ustar00biocbuildbiocbuildPackage: BSgenome.Scerevisiae.UCSC.sacCer1 Title: Saccharomyces cerevisiae (Yeast) full genome (UCSC version sacCer1) Description: Saccharomyces cerevisiae (Yeast) full genome as provided by UCSC (sacCer1, Oct. 2003) and stored in Biostrings objects. Version: 1.4.2 organism: Saccharomyces cerevisiae common_name: Yeast provider: UCSC provider_version: sacCer1 release_date: Oct. 2003 release_name: SGD 1 Oct 2003 sequence source_url: http://hgdownload.cse.ucsc.edu/goldenPath/sacCer1/bigZips/ organism_biocview: Saccharomyces_cerevisiae BSgenomeObjname: Scerevisiae seqnames: paste("chr", c(1:16, "M"), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.zip from http://hgdownload.cse.ucsc.edu/goldenPath/sacCer1/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Scerevisiae.UCSC.sacCer1/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Scerevisiae.UCSC.sacCer2-seed0000644000175400017540000000174413175713516027074 0ustar00biocbuildbiocbuildPackage: BSgenome.Scerevisiae.UCSC.sacCer2 Title: Saccharomyces cerevisiae (Yeast) full genome (UCSC version sacCer2) Description: Saccharomyces cerevisiae (Yeast) full genome as provided by UCSC (sacCer2, June 2008) and stored in Biostrings objects. Version: 1.4.2 organism: Saccharomyces cerevisiae common_name: Yeast provider: UCSC provider_version: sacCer2 release_date: June 2008 release_name: SGD June 2008 sequence source_url: http://hgdownload.cse.ucsc.edu/goldenPath/sacCer2/bigZips/ organism_biocview: Saccharomyces_cerevisiae BSgenomeObjname: Scerevisiae seqnames: c(paste("chr", c("I", "II", "III", "IV", "V", "VI", "VII", "VIII", "IX", "X", "XI", "XII", "XIII", "XIV", "XV", "XVI", "M"), sep=""), "2micron") circ_seqs: c("chrM", "2micron") SrcDataFiles: chromFa.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/sacCer2/bigZips/ PkgExamples: genome$chrI # same as genome[["chrI"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Scerevisiae.UCSC.sacCer2/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Scerevisiae.UCSC.sacCer3-seed0000644000175400017540000000171313175713516027071 0ustar00biocbuildbiocbuildPackage: BSgenome.Scerevisiae.UCSC.sacCer3 Title: Saccharomyces cerevisiae (Yeast) full genome (UCSC version sacCer3) Description: Saccharomyces cerevisiae (Yeast) full genome as provided by UCSC (sacCer3, April 2011) and stored in Biostrings objects. Version: 1.4.2 organism: Saccharomyces cerevisiae common_name: Yeast provider: UCSC provider_version: sacCer3 release_date: April 2011 release_name: SGD April 2011 sequence source_url: http://hgdownload.cse.ucsc.edu/goldenPath/sacCer3/bigZips/ organism_biocview: Saccharomyces_cerevisiae BSgenomeObjname: Scerevisiae seqnames: paste("chr", c("I", "II", "III", "IV", "V", "VI", "VII", "VIII", "IX", "X", "XI", "XII", "XIII", "XIV", "XV", "XVI", "M"), sep="") circ_seqs: "chrM" SrcDataFiles: chromFa.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/sacCer3/bigZips/ PkgExamples: genome$chrI # same as genome[["chrI"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Scerevisiae.UCSC.sacCer3/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Sscrofa.UCSC.susScr3-seed0000644000175400017540000000155613175713516026316 0ustar00biocbuildbiocbuildPackage: BSgenome.Sscrofa.UCSC.susScr3 Title: Full genome sequences for Sus scrofa (UCSC version susScr3) Description: Full genome sequences for Sus scrofa (Pig) as provided by UCSC (susScr3, Aug. 2011) and stored in Biostrings objects. Version: 1.4.2 organism: Sus scrofa common_name: Pig provider: UCSC provider_version: susScr3 release_date: Aug. 2011 release_name: Swine Genome Sequencing Consortium Sscrofa10.2 source_url: http://hgdownload.soe.ucsc.edu/goldenPath/susScr3/bigZips/ organism_biocview: Sus_scrofa BSgenomeObjname: Sscrofa seqnames: paste0("chr", c(1:18, "X", "Y", "M")) circ_seqs: "chrM" mseqnames: "unplaced_scaffolds" SrcDataFiles: susScr3.fa.gz from http://hgdownload.soe.ucsc.edu/goldenPath/susScr3/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Sscrofa.UCSC.susScr3/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Sscrofa.UCSC.susScr3-tools/0000755000175400017540000000000013175713516026604 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Sscrofa.UCSC.susScr3-tools/splitbigfasta.R0000755000175400017540000000154013175713516031566 0ustar00biocbuildbiocbuild### library(Biostrings) susScr3 <- readDNAStringSet("susScr3.fa") ### Partitioning: is_chrom <- grepl("^chr", names(susScr3)) is_unplaced_scaffold <- grepl("^(GL|JH)", names(susScr3)) ### Sanity check: stopifnot(all(is_chrom | is_unplaced_scaffold)) stopifnot(!any(is_chrom & is_unplaced_scaffold)) ### Send each chromosome to a FASTA file. seqnames <- paste("chr", c(1:18, "X", "Y", "M"), sep="") stopifnot(setequal(seqnames, names(susScr3)[is_chrom])) for (seqname in seqnames) { seq <- susScr3[match(seqname, names(susScr3))] filename <- paste(seqname, ".fa", sep="") cat("writing ", filename, "\n", sep="") writeXStringSet(seq, file=filename, width=50L) } ### Send the 4562 unplaced scaffolds to 1 FASTA file. unplaced_scaffolds <- susScr3[is_unplaced_scaffold] writeXStringSet(unplaced_scaffolds, file="unplaced_scaffolds.fa", width=50L) BSgenome/inst/extdata/GentlemanLab/BSgenome.Sscrofa.UCSC.susScr3.masked-seed0000644000175400017540000000265713175713516027564 0ustar00biocbuildbiocbuildPackage: BSgenome.Sscrofa.UCSC.susScr3.masked Title: Full masked genome sequences for Sus scrofa (UCSC version susScr3) Description: Full genome sequences for Sus scrofa (Pig) as provided by UCSC (susScr3, Aug. 2011) and stored in Biostrings objects. The sequences are the same as in BSgenome.Sscrofa.UCSC.susScr3, except that each of them has the 4 following masks on top: (1) the mask of assembly gaps (AGAPS mask), (2) the mask of intra-contig ambiguities (AMB mask), (3) the mask of repeats from RepeatMasker (RM mask), and (4) the mask of repeats from Tandem Repeats Finder (TRF mask). Only the AGAPS and AMB masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Sscrofa.UCSC.susScr3 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/susScr3/bigZips/ organism_biocview: Sus_scrofa nmask_per_seq: 4 SrcDataFiles: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/susScr3/database/ RM masks: susScr3.fa.out.gz from http://hgdownload.cse.ucsc.edu/goldenPath/susScr3/bigZips/ TRF masks: susScr3.trf.bed.gz from http://hgdownload.cse.ucsc.edu/goldenPath/susScr3/bigZips/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Sscrofa.UCSC.susScr3$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Sscrofa.UCSC.susScr3/masks AGAPSfiles_name: gap.txt RMfiles_name: susScr3.fa.out TRFfiles_name: susScr3.trf.bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Tguttata.UCSC.taeGut1-seed0000644000175400017540000000173213175713516026454 0ustar00biocbuildbiocbuildPackage: BSgenome.Tguttata.UCSC.taeGut1 Title: Full genome sequences for Taeniopygia guttata (UCSC version taeGut1) Description: Full genome sequences for Taeniopygia guttata (Zebra finch) as provided by UCSC (taeGut1, Jul. 2008) and stored in Biostrings objects. Version: 1.4.2 organism: Taeniopygia guttata common_name: Zebra finch provider: UCSC provider_version: taeGut1 release_date: Jul. 2008 release_name: WUSTL v3.2.4 source_url: http://hgdownload.soe.ucsc.edu/goldenPath/taeGut1/bigZips/ organism_biocview: Taeniopygia_guttata BSgenomeObjname: Tguttata seqnames: paste0("chr", c(1, "1A", "1B", 2:4, "4A", 5:28, "LGE22", "LG2", "LG5", "Z", "M", "Un", paste0(c(1, "1A", "1B", 2:4, "4A", 5:28, "LGE22", "Z"), "_random"))) circ_seqs: "chrM" SrcDataFiles: chromFa.tar.gz from http://hgdownload.soe.ucsc.edu/goldenPath/taeGut1/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Tguttata.UCSC.taeGut1/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Tguttata.UCSC.taeGut1.masked-seed0000644000175400017540000000216313175713516027716 0ustar00biocbuildbiocbuildPackage: BSgenome.Tguttata.UCSC.taeGut1.masked Title: Full masked genome sequences for Taeniopygia guttata (UCSC version taeGut1) Description: Full genome sequences for Taeniopygia guttata (Zebra finch) as provided by UCSC (taeGut1, Jul. 2008) and stored in Biostrings objects. The sequences are the same as in BSgenome.Tguttata.UCSC.taeGut1, except that each of them has the 2 following masks on top: (1) the mask of assembly gaps (AGAPS mask), and (2) the mask of intra-contig ambiguities (AMB mask). Both masks are "active" by default. Version: 1.3.99 RefPkgname: BSgenome.Tguttata.UCSC.taeGut1 source_url: http://hgdownload.soe.ucsc.edu/goldenPath/taeGut1/database/ organism_biocview: Taeniopygia_guttata nmask_per_seq: 2 SrcDataFiles: AGAPS masks: all the chr*_gap.txt.gz files from http://hgdownload.cse.ucsc.edu/goldenPath/taeGut1/database/ PkgExamples: genome$chr1 # a MaskedDNAString object! ## To get rid of the masks altogether: unmasked(genome$chr1) # same as BSgenome.Tguttata.UCSC.taeGut1$chr1 masks_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Tguttata.UCSC.taeGut1/masks AGAPSfiles_suffix: _gap.txt.gz BSgenome/inst/extdata/GentlemanLab/BSgenome.Tguttata.UCSC.taeGut2-seed0000644000175400017540000000152713175713516026457 0ustar00biocbuildbiocbuildPackage: BSgenome.Tguttata.UCSC.taeGut2 Title: Full genome sequences for Taeniopygia guttata (UCSC version taeGut2) Description: Full genome sequences for Taeniopygia guttata (Zebra finch) as provided by UCSC (taeGut2, Feb. 2013) and stored in Biostrings objects. Version: 1.4.2 organism: Taeniopygia guttata common_name: Zebra finch provider: UCSC provider_version: taeGut2 release_date: Feb. 2013 release_name: WashU taeGut324 source_url: http://hgdownload.soe.ucsc.edu/goldenPath/taeGut2/bigZips/ organism_biocview: Taeniopygia_guttata BSgenomeObjname: Tguttata circ_seqs: "chrM" SrcDataFiles: taeGut2.2bit from http://hgdownload.soe.ucsc.edu/goldenPath/taeGut2/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.Tguttata.UCSC.taeGut2/seqs seqfile_name: taeGut2.sorted.2bit BSgenome/inst/extdata/GentlemanLab/BSgenome.Tguttata.UCSC.taeGut2-tools/0000755000175400017540000000000013175713516026747 5ustar00biocbuildbiocbuildBSgenome/inst/extdata/GentlemanLab/BSgenome.Tguttata.UCSC.taeGut2-tools/sort_taeGut2.2bit.R0000644000175400017540000000163513175713516032320 0ustar00biocbuildbiocbuildlibrary(Biostrings) library(rtracklayer) taeGut2 <- import("taeGut2.2bit") seqlevels1 <- paste0("chr", c(1, "1A", "1B", 2:4, "4A", 5:28, "LGE22", "LG2", "LG5", "Z", "M")) tmp <- CharacterList(strsplit(names(taeGut2), "_")) npart <- elementNROWS(tmp) stopifnot(all(npart <= 3L)) idx1 <- which(npart == 1L) stopifnot(setequal(names(taeGut2)[idx1], seqlevels1)) idx2 <- which(npart == 2L) m2 <- matrix(unlist(tmp[idx2]), ncol=2L, byrow=TRUE) stopifnot(all(m2[ , 1L] == "chrUn")) oo2 <- order(m2[ , 2L]) seqlevels2 <- names(taeGut2)[idx2[oo2]] idx3 <- which(npart == 3L) m3 <- matrix(unlist(tmp[idx3]), ncol=3L, byrow=TRUE) stopifnot(all(m3[ , 3L] == "random")) chrom <- factor(m3[ , 1L], levels=seqlevels1) stopifnot(!anyNA(chrom)) oo3 <- order(chrom, m3[ , 2L]) seqlevels3 <- names(taeGut2)[idx3[oo3]] taeGut2_seqlevels <- c(seqlevels1, seqlevels3, seqlevels2) export(taeGut2[taeGut2_seqlevels], "taeGut2.sorted.2bit") BSgenome/inst/extdata/GentlemanLab/BSgenome.influenza.NCBI.20100628-seed0000644000175400017540000000135213175713516026216 0ustar00biocbuildbiocbuildPackage: BSgenome.influenza.NCBI.20100628 Title: Nucleotide sequences of all influenza viruses in GenBank Description: Nucleotide sequences of all influenza viruses in GenBank as provided by NCBI on 2010/06/28 and stored in Biostrings objects. Version: 1.3.16 organism: NA common_name: NA provider: NCBI provider_version: 2010/06/28 release_date: NA release_name: NA source_url: ftp://ftp.ncbi.nih.gov/genomes/INFLUENZA/ organism_biocview: influenza BSgenomeObjname: influenza seqnames: character(0) mseqnames: "influenza" SrcDataFiles: influenza.fna.gz from ftp://ftp.ncbi.nih.gov/genomes/INFLUENZA/ (downloaded on 2010/06/28) seqs_srcdir: /fh/fast/morgan_m/BioC/BSgenomeForge/srcdata/BSgenome.influenza.NCBI.20100628/seqs seqfiles_suffix: .fna BSgenome/inst/extdata/GentlemanLab/ForgeAll.R0000644000175400017540000000750213175713516022072 0ustar00biocbuildbiocbuild####################################################################### ### Use this R script to forge all the BSgenome data packages ### ### To run this script in batch mode: ### R-3.1 CMD BATCH --vanilla path/to/ForgeAll.R >ForgeAll.log 2>&1 & ### library(BSgenome) BSgenome_datapkgs <- c( "BSgenome.Amellifera.BeeBase.assembly4", "BSgenome.Amellifera.UCSC.apiMel2", "BSgenome.Athaliana.TAIR.04232008", "BSgenome.Athaliana.TAIR.TAIR9", "BSgenome.Btaurus.UCSC.bosTau3", "BSgenome.Btaurus.UCSC.bosTau4", "BSgenome.Btaurus.UCSC.bosTau6", "BSgenome.Btaurus.UCSC.bosTau8", "BSgenome.Celegans.UCSC.ce2", "BSgenome.Celegans.UCSC.ce6", "BSgenome.Celegans.UCSC.ce10", "BSgenome.Celegans.UCSC.ce11", "BSgenome.Cfamiliaris.UCSC.canFam2", "BSgenome.Cfamiliaris.UCSC.canFam3", "BSgenome.Dmelanogaster.UCSC.dm2", "BSgenome.Dmelanogaster.UCSC.dm3", "BSgenome.Dmelanogaster.UCSC.dm6", "BSgenome.Drerio.UCSC.danRer5", "BSgenome.Drerio.UCSC.danRer6", "BSgenome.Drerio.UCSC.danRer7", "BSgenome.Drerio.UCSC.danRer10", "BSgenome.Ecoli.NCBI.20080805", "BSgenome.Gaculeatus.UCSC.gasAcu1", "BSgenome.Ggallus.UCSC.galGal3", "BSgenome.Ggallus.UCSC.galGal4", "BSgenome.Ggallus.UCSC.galGal5", "BSgenome.Hsapiens.UCSC.hg17", "BSgenome.Hsapiens.UCSC.hg18", "BSgenome.Hsapiens.UCSC.hg19", "BSgenome.Hsapiens.NCBI.GRCh38", "BSgenome.Hsapiens.UCSC.hg38", "BSgenome.Mfascicularis.NCBI.5.0", "BSgenome.Mfuro.UCSC.musFur1", "BSgenome.Mmulatta.UCSC.rheMac2", "BSgenome.Mmulatta.UCSC.rheMac3", "BSgenome.Mmulatta.UCSC.rheMac8", "BSgenome.Mmusculus.UCSC.mm8", "BSgenome.Mmusculus.UCSC.mm9", "BSgenome.Mmusculus.UCSC.mm10", "BSgenome.Ptroglodytes.UCSC.panTro2", "BSgenome.Ptroglodytes.UCSC.panTro3", "BSgenome.Ptroglodytes.UCSC.panTro5", "BSgenome.Rnorvegicus.UCSC.rn4", "BSgenome.Rnorvegicus.UCSC.rn5", "BSgenome.Rnorvegicus.UCSC.rn6", "BSgenome.Scerevisiae.UCSC.sacCer1", "BSgenome.Scerevisiae.UCSC.sacCer2", "BSgenome.Scerevisiae.UCSC.sacCer3", "BSgenome.Sscrofa.UCSC.susScr3", "BSgenome.Tguttata.UCSC.taeGut1", "BSgenome.Tguttata.UCSC.taeGut2" ) for (pkg in BSgenome_datapkgs) { cat("\n") cat("============================================================\n") cat("START FORGING ", pkg, "\n", sep="") cat("\n") forgeBSgenomeDataPkg(pkg) cat("\n") cat("END FORGING ", pkg, "\n", sep="") } MaskedBSgenome_datapkgs <- c( "BSgenome.Amellifera.UCSC.apiMel2.masked", "BSgenome.Btaurus.UCSC.bosTau3.masked", "BSgenome.Btaurus.UCSC.bosTau4.masked", "BSgenome.Btaurus.UCSC.bosTau6.masked", "BSgenome.Cfamiliaris.UCSC.canFam2.masked", "BSgenome.Cfamiliaris.UCSC.canFam3.masked", "BSgenome.Dmelanogaster.UCSC.dm2.masked", "BSgenome.Dmelanogaster.UCSC.dm3.masked", "BSgenome.Drerio.UCSC.danRer5.masked", "BSgenome.Drerio.UCSC.danRer6.masked", "BSgenome.Drerio.UCSC.danRer7.masked", "BSgenome.Gaculeatus.UCSC.gasAcu1.masked", "BSgenome.Ggallus.UCSC.galGal3.masked", "BSgenome.Ggallus.UCSC.galGal4.masked", "BSgenome.Hsapiens.UCSC.hg17.masked", "BSgenome.Hsapiens.UCSC.hg18.masked", "BSgenome.Hsapiens.UCSC.hg19.masked", "BSgenome.Hsapiens.UCSC.hg38.masked", "BSgenome.Mmulatta.UCSC.rheMac2.masked", "BSgenome.Mmulatta.UCSC.rheMac3.masked", "BSgenome.Mmusculus.UCSC.mm8.masked", "BSgenome.Mmusculus.UCSC.mm9.masked", "BSgenome.Mmusculus.UCSC.mm10.masked", "BSgenome.Ptroglodytes.UCSC.panTro2.masked", "BSgenome.Ptroglodytes.UCSC.panTro3.masked", "BSgenome.Rnorvegicus.UCSC.rn4.masked", "BSgenome.Rnorvegicus.UCSC.rn5.masked", "BSgenome.Sscrofa.UCSC.susScr3.masked", "BSgenome.Tguttata.UCSC.taeGut1.masked" ) for (pkg in MaskedBSgenome_datapkgs) { cat("\n") cat("============================================================\n") cat("START FORGING ", pkg, "\n", sep="") cat("\n") forgeMaskedBSgenomeDataPkg(pkg) cat("\n") cat("END FORGING ", pkg, "\n", sep="") } BSgenome/inst/extdata/GentlemanLab/bump_seed_version.sh0000755000175400017540000000045713175713516024325 0ustar00biocbuildbiocbuild#!/bin/bash set -e # Exit immediately if a simple command exits with a non-zero status #for seed in BSgenome.*-seed; 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Kc !1IrbU&Tcm\#X'i#yJLA'I_8W %"8HzmZY%U]&4/HFjўϵ-m](pk 6aiAPK(6q. ,X ?F[_Tkf8^<,x/GIԼЇLDHkې>TDD^"}l*IIJ XeWoz4QPJ'ƶYZ)&l6JѤ}q#@0%}kmuX,8??b\wO‡gMK)w\¢+J+!؉:v݄(n Qk% KpsCCїYSD29S&IhR2>^, Ƌ}A' !wa]ܔwnhΤX2kJvX^myS`TeeT0JhO]\_Cgt?PKyAQgnbPZ-G<7L C>>83G\6L+?ZqzQxI9>h^)B>?Lq:z7ԔTƁt./ءѭ1 qٽ 8e$>6v]qǟ.nެ/$Hz}ucSU`RaΓt[L=xr2eRĜMv }0SPVt 5eI|X`W޴3~-0K`2`V,zKA :T7J=z\$s~-vT D-+ Q@wǼ ~ywV>@^й%#9o)-І"/cB1K>QY.W2D xBHWDٰJ媃Ye?mH^ Mϼi[jOɰJ(=؋nl*dZfڒD9k۵Lx'eȘ}+ʉ:f_O9Uհu 1lϱU^eSʦosїlY-i?UDo7RY3⃊[cnpj63єtܬ#x#\V[$*B.ZꮅCLL`L„匄+oiWhdZ%eѕ`^Ex M\ŵbՇgF4v+h$5  ؔjV_w,.ٰwG_sV5~bB#D82&?.cB:m&S=:eq$]湶Ӯ^giq w!ͯ`RͅGL'G7S39vfLXcPzw+ 9jaذ b#*_;a !`ӀvPWeOo·¬[!n/7>avP㰄+.ɇx2w~.z{I=c#E[&(r RceG=>FM6&PXo0tGZAW:בucGiH,O&4-ךon)G02pXNbF]2MWX9DlZO=c yg WZpҫ{o?yfPG_3acX 0 G̾B,*Pã|Z!+Hd6>`Gՙw>ix t;mzn/e1gb@3̻#id'uG)"n-r8Q~;{Ʌ #bď.q)dy@;Gdrlxl^_\ys`l8>WXf@1;f,vJcWj]j]*=%(ve|[-YC=PlHEzJj.ziX;7m;(*P }K۲udOCw@%`0 9JXz[yJD&ab̟0m.r>ب4@6xzE褖J: CƑL84mKW,ac!%v^.`''(8oٲtR]\.FA}XfF.T" tjWޔFa 2 8adKVHR;QX)E/[dLw'̕(PIO2'!,1p]q-Uj|Y+P!\7p^(A ^ꡅI۪ ,Kz~r A{'a-|`)=SÞĦza0 3&|gS&Z '{7ͬB2J4~"УVfr 7vVVYs&R?ѹscYspn[4_ֲފBSgenome/inst/extdata/ce2dict0.fa0000644000175400017540000000307613175713516017632 0ustar00biocbuildbiocbuild>pattern01 GCGAAACTAGGAGAGGCT >pattern02 CTGTTAGCTAATTTTAAAAATAAAT >pattern03 ACTACCACCCAAATTTAGATATTC >pattern04 AAATTTTTTTTGTTGCAAATTTGA >pattern05 TCTTCTTGGCTTTGGTGGTACTTTT >pattern06 AACAATTATCTATAAT >pattern07 GGTTTTGGAGAGTGATGCACGT >pattern08 TTTAATGAACCCCAGCAACTC >pattern09 TACTGAAACTCCCGCGAG >pattern10 GAGGGGAAAAATAGGACGGAAATA >pattern11 AAAAAATCGTTTTATAGT >pattern12 CAGTTTTGATCAATGC >pattern13 ATCAAACAAATGTATTGCAA >pattern14 GTAGGGCTACTGTATGATTAATGT >pattern15 GACGGAGAAATATTTGCACAG >pattern16 AAAAACGAGAAAATGACATT >pattern17 TATGGTGAAAACTTTC >pattern18 GAAATATCGTCGGAAAATCGA >pattern19 TTATAATAAAATTTC >pattern20 ATAGCTTCTGGAGACATCCAT >pattern21 TTCTGAAACTTCCATTTTCACTCA >pattern22 AATAGAAGAATGCTGT >pattern23 AGTCGTATTGCGAAT >pattern24 GTTTTCTATCAATTTAAGAT >pattern25 GTTAAAATATCCGTTTAAA >pattern26 TTTTTTTTATTCCTAGTAA >pattern27 ACGATTTTGTGATGGCGATTTTG >pattern28 ATTTTAATTATAAACTA >pattern29 TCACCTTTCCGGTAGAAAACT >pattern30 TAATGGGTATTTGTTTATTTAAAC >pattern31 CTATGAAATGCCTAGCCGTT >pattern32 CGCCGGATGTCAGCAGCTTC >pattern33 ATGGTTTAAGATGATT >pattern34 GGAAATATTCTGAAAA >pattern35 GAAACGAGCGGGACAC >pattern36 ACCCTAAAAGACTCACCC >pattern37 GCGGGCGATTGCCAATGGAGCGCG >pattern38 GTGTGGCTGTTCAATATTGTAC >pattern39 GATATACGAACTTAA >pattern40 CCGGCATGTAAATGAGAA >pattern41 ATGAGATAAACACATCAAACTAC >pattern42 AAAATAAGATTCTATTAAAATA >pattern43 GTTTTAATTCTAATT >pattern44 CATCGTTTCAACCGTTCG >pattern45 TAAAAAATCAAAACTTTTG >pattern46 TTTTGAACAAAGCATGTCTAACTA >pattern47 TAAACGAATTTAGGATATAT >pattern48 AAGGACCAGGATTGGCACG >pattern49 AAATAACTGCGTAAAAACACAATA >pattern50 AAAATGCCGGAGCATTTTAAAG BSgenome/inst/pkgtemplates/0000755000175400017540000000000013175713516016765 5ustar00biocbuildbiocbuildBSgenome/inst/pkgtemplates/BSgenome_datapkg/0000755000175400017540000000000013175713516022157 5ustar00biocbuildbiocbuildBSgenome/inst/pkgtemplates/BSgenome_datapkg/DESCRIPTION0000644000175400017540000000074013175713516023666 0ustar00biocbuildbiocbuildPackage: @PKGNAME@ Title: @PKGTITLE@ Description: @PKGDESCRIPTION@ Version: @PKGVERSION@ Author: @AUTHOR@ Maintainer: @MAINTAINER@ Depends: BSgenome (>= @BSGENOMEVERSION@) Imports: BSgenome Suggests: @SUGGESTS@ License: @LICENSE@ organism: @ORGANISM@ common_name: @COMMONNAME@ provider: @PROVIDER@ provider_version: @PROVIDERVERSION@ release_date: @RELEASEDATE@ release_name: @RELEASENAME@ source_url: @SOURCEURL@ biocViews: AnnotationData, Genetics, BSgenome, @ORGANISMBIOCVIEW@ BSgenome/inst/pkgtemplates/BSgenome_datapkg/NAMESPACE0000644000175400017540000000046513175713516023403 0ustar00biocbuildbiocbuildimport(BSgenome) ### Don't export @PKGNAME@ or @BSGENOMEOBJNAME@ (the new and old names of the ### BSgenome object defined in this package): the object is created and its 2 ### names are dynamically exported at load time (refer to R/zzz.R for the ### details). #export(@PKGNAME@) #export(@BSGENOMEOBJNAME@) BSgenome/inst/pkgtemplates/BSgenome_datapkg/R/0000755000175400017540000000000013175713516022360 5ustar00biocbuildbiocbuildBSgenome/inst/pkgtemplates/BSgenome_datapkg/R/zzz.R0000644000175400017540000000217613175713516023346 0ustar00biocbuildbiocbuild### ### .pkgname <- "@PKGNAME@" .seqnames <- @SEQNAMES@ .circ_seqs <- @CIRCSEQS@ .mseqnames <- @MSEQNAMES@ .onLoad <- function(libname, pkgname) { if (pkgname != .pkgname) stop("package name (", pkgname, ") is not ", "the expected name (", .pkgname, ")") extdata_dirpath <- system.file("extdata", package=pkgname, lib.loc=libname, mustWork=TRUE) ## Make and export BSgenome object. bsgenome <- BSgenome( organism="@ORGANISM@", common_name="@COMMONNAME@", provider="@PROVIDER@", provider_version="@PROVIDERVERSION@", release_date="@RELEASEDATE@", release_name="@RELEASENAME@", source_url="@SOURCEURL@", seqnames=.seqnames, circ_seqs=.circ_seqs, mseqnames=.mseqnames, seqs_pkgname=pkgname, seqs_dirpath=extdata_dirpath ) ns <- asNamespace(pkgname) objname <- pkgname assign(objname, bsgenome, envir=ns) namespaceExport(ns, objname) old_objname <- "@BSGENOMEOBJNAME@" assign(old_objname, bsgenome, envir=ns) namespaceExport(ns, old_objname) } BSgenome/inst/pkgtemplates/BSgenome_datapkg/inst/0000755000175400017540000000000013175713516023134 5ustar00biocbuildbiocbuildBSgenome/inst/pkgtemplates/BSgenome_datapkg/inst/extdata/0000755000175400017540000000000013175725526024572 5ustar00biocbuildbiocbuildBSgenome/inst/pkgtemplates/BSgenome_datapkg/man/0000755000175400017540000000000013175713516022732 5ustar00biocbuildbiocbuildBSgenome/inst/pkgtemplates/BSgenome_datapkg/man/package.Rd0000644000175400017540000000276013175713516024621 0ustar00biocbuildbiocbuild\name{@PKGNAME@} \docType{package} \alias{@PKGNAME@-package} \alias{@PKGNAME@} \alias{@BSGENOMEOBJNAME@} \title{@PKGTITLE@} \description{ @PKGDESCRIPTION@ } \details{ @PKGDETAILS@ } \note{ This BSgenome data package was made from the following source data files: \preformatted{ @SRCDATAFILES@ } See \code{?\link[BSgenome]{BSgenomeForge}} and the BSgenomeForge vignette (\code{vignette("BSgenomeForge")}) in the \pkg{BSgenome} software package for how to make a BSgenome data package. } \author{@AUTHOR@} \seealso{ \itemize{ \item \link[BSgenome]{BSgenome} objects and the \code{\link[BSgenome]{available.genomes}} function in the \pkg{BSgenome} software package. \item \link[Biostrings]{DNAString} objects in the \pkg{Biostrings} package. \item The BSgenomeForge vignette (\code{vignette("BSgenomeForge")}) in the \pkg{BSgenome} software package for how to make a BSgenome data package. } } \examples{ @PKGNAME@ genome <- @PKGNAME@ head(seqlengths(genome)) @PKGEXAMPLES@ ## --------------------------------------------------------------------- ## Genome-wide motif searching ## --------------------------------------------------------------------- ## See the GenomeSearching vignette in the BSgenome software ## package for some examples of genome-wide motif searching using ## Biostrings and the BSgenome data packages: if (interactive()) vignette("GenomeSearching", package="BSgenome") } \keyword{package} \keyword{data} BSgenome/inst/pkgtemplates/MaskedBSgenome_datapkg/0000755000175400017540000000000013175713516023304 5ustar00biocbuildbiocbuildBSgenome/inst/pkgtemplates/MaskedBSgenome_datapkg/DESCRIPTION0000644000175400017540000000077413175713516025022 0ustar00biocbuildbiocbuildPackage: @PKGNAME@ Title: @PKGTITLE@ Description: @PKGDESCRIPTION@ Version: @PKGVERSION@ Author: @AUTHOR@ Maintainer: @MAINTAINER@ Depends: BSgenome (>= @BSGENOMEVERSION@), @REFPKGNAME@ Imports: BSgenome, @REFPKGNAME@ Suggests: @SUGGESTS@ License: @LICENSE@ organism: @ORGANISM@ common_name: @COMMONNAME@ provider: @PROVIDER@ provider_version: @PROVIDERVERSION@ release_date: @RELEASEDATE@ release_name: @RELEASENAME@ source_url: @SOURCEURL@ biocViews: AnnotationData, Genetics, BSgenome, @ORGANISMBIOCVIEW@ BSgenome/inst/pkgtemplates/MaskedBSgenome_datapkg/NAMESPACE0000644000175400017540000000041313175713516024521 0ustar00biocbuildbiocbuildimport(BSgenome) import(@REFPKGNAME@) ### Don't export @PKGNAME@ (the name of the MaskedBSgenome object defined in ### this package): the object is created and its name is dynamically exported ### at load time (refer to R/zzz.R for the details). #export(@PKGNAME@) BSgenome/inst/pkgtemplates/MaskedBSgenome_datapkg/R/0000755000175400017540000000000013175713516023505 5ustar00biocbuildbiocbuildBSgenome/inst/pkgtemplates/MaskedBSgenome_datapkg/R/zzz.R0000644000175400017540000000133113175713516024463 0ustar00biocbuildbiocbuild### ### .pkgname <- "@PKGNAME@" .nmask_per_seq <- @NMASKPERSEQ@ .onLoad <- function(libname, pkgname) { if (pkgname != .pkgname) stop("package name (", pkgname, ") is not ", "the expected name (", .pkgname, ")") extdata_dirpath <- system.file("extdata", package=pkgname, lib.loc=libname, mustWork=TRUE) ## Make and export MaskedBSgenome object. bsgenome <- MaskedBSgenome( ref_bsgenome=@REFPKGNAME@, masks_pkgname=pkgname, nmask_per_seq=.nmask_per_seq, masks_dirpath=extdata_dirpath ) ns <- asNamespace(pkgname) objname <- pkgname assign(objname, bsgenome, envir=ns) namespaceExport(ns, objname) } BSgenome/inst/pkgtemplates/MaskedBSgenome_datapkg/inst/0000755000175400017540000000000013175713516024261 5ustar00biocbuildbiocbuildBSgenome/inst/pkgtemplates/MaskedBSgenome_datapkg/inst/extdata/0000755000175400017540000000000013175725526025717 5ustar00biocbuildbiocbuildBSgenome/inst/pkgtemplates/MaskedBSgenome_datapkg/man/0000755000175400017540000000000013175713516024057 5ustar00biocbuildbiocbuildBSgenome/inst/pkgtemplates/MaskedBSgenome_datapkg/man/package.Rd0000644000175400017540000000432713175713516025747 0ustar00biocbuildbiocbuild\name{@PKGNAME@} \docType{package} \alias{@PKGNAME@-package} \alias{@PKGNAME@} \title{@PKGTITLE@} \description{ @PKGDESCRIPTION@ } \details{ @PKGDETAILS@ } \note{ The masks in this BSgenome data package were made from the following source data files: \preformatted{ @SRCDATAFILES@ } See \code{?\link[@REFPKGNAME@]{@REFPKGNAME@}} in the \pkg{@REFPKGNAME@} package for information about how the sequences were obtained. See \code{?\link[BSgenome]{BSgenomeForge}} and the BSgenomeForge vignette (\code{vignette("BSgenomeForge")}) in the \pkg{BSgenome} software package for how to make a BSgenome data package. } \author{@AUTHOR@} \seealso{ \itemize{ \item \link[@REFPKGNAME@]{@REFPKGNAME@} in the \pkg{@REFPKGNAME@} package for information about how the sequences were obtained. \item \link[BSgenome]{BSgenome} objects and the \code{\link[BSgenome]{available.genomes}} function in the \pkg{BSgenome} software package. \item \link[Biostrings]{MaskedDNAString} objects in the \pkg{Biostrings} package. \item The BSgenomeForge vignette (\code{vignette("BSgenomeForge")}) in the \pkg{BSgenome} software package for how to make a BSgenome data package. } } \examples{ @PKGNAME@ genome <- @PKGNAME@ head(seqlengths(genome)) @PKGEXAMPLES@ if ("AGAPS" \%in\% masknames(genome)) { ## Check that the assembly gaps contain only Ns: checkOnlyNsInGaps <- function(seq) { ## Replace all masks by the inverted AGAPS mask masks(seq) <- gaps(masks(seq)["AGAPS"]) unique_letters <- uniqueLetters(seq) if (any(unique_letters != "N")) stop("assembly gaps contain more than just Ns") } ## A message will be printed each time a sequence is removed ## from the cache: options(verbose=TRUE) for (seqname in seqnames(genome)) { cat("Checking sequence", seqname, "... ") seq <- genome[[seqname]] checkOnlyNsInGaps(seq) cat("OK\n") } } ## See the GenomeSearching vignette in the BSgenome software ## package for some examples of genome-wide motif searching using ## Biostrings and the BSgenome data packages: if (interactive()) vignette("GenomeSearching", package="BSgenome") } \keyword{package} \keyword{data} BSgenome/man/0000755000175400017540000000000013175713516014063 5ustar00biocbuildbiocbuildBSgenome/man/BSParams-class.Rd0000644000175400017540000000353513175713516017133 0ustar00biocbuildbiocbuild\name{BSParams-class} \docType{class} \alias{class:BSParams} \alias{BSParams-class} \alias{BSParams} \title{Class "BSParams"} \description{ A parameter class for representing all parameters needed for running the \code{bsapply} method. } \section{Objects from the Class}{ Objects can be created by calls of the form \code{new("BSParams", ...)}. } \section{Slots}{ \describe{ \item{\code{X}:}{ a BSgenome object that contains chromosomes that you wish to apply FUN on } \item{\code{FUN}:}{ the function to apply to each chromosome in the BSgenome object 'X' } \item{\code{exclude}:}{ this is a character vector with strings that will be used to filter out chromosomes whose names match these strings. } \item{\code{simplify}:}{ TRUE/FALSE value to indicate whether or not the function should try to simplify the output for you. } \item{\code{maskList}:}{ A named logical vector of maskStates preferred when used with a BSGenome object. When using the bsapply function, the masks will be set to the states in this vector. } \item{\code{motifList}:}{ A character vector which should contain motifs that the user wishes to mask from the sequence. } \item{\code{userMask}:}{ A \linkS4class{RangesList} object, where each element masks the corresponding chromosome in \code{X}. This allows the user to conveniently apply masks besides those included in \code{X}. } \item{\code{invertUserMask}:}{ A \code{logical} indicating whether to invert each mask in \code{userMask}. } } } \section{Methods}{ \describe{ \item{\code{bsapply(p)}}{Performs the function FUN using the parameters contained within \code{BSParams}.} } } \author{Marc Carlson} \seealso{ \code{\link{bsapply}} } \keyword{classes} BSgenome/man/BSgenome-class.Rd0000644000175400017540000002217613175713516017164 0ustar00biocbuildbiocbuild\name{BSgenome-class} \docType{class} % Classes: \alias{class:BSgenome} \alias{BSgenome-class} \alias{BSgenome} % Accessors: \alias{length,BSgenome-method} \alias{sourceUrl} \alias{sourceUrl,BSgenome-method} \alias{mseqnames} \alias{mseqnames,BSgenome-method} \alias{names,BSgenome-method} \alias{masknames} \alias{masknames,BSgenome-method} \alias{seqinfo,BSgenome-method} \alias{seqinfo<-,BSgenome-method} \alias{seqnames<-,BSgenome-method} % Constructor-like functions and generics: \alias{BSgenome} % Other methods: \alias{as.list,BSgenome-method} \alias{show,BSgenome-method} \alias{[[,BSgenome-method} \alias{$,BSgenome-method} \title{BSgenome objects} \description{ The BSgenome class is a container for storing the full genome sequences of a given organism. BSgenome objects are usually made in advance by a volunteer and made available to the Bioconductor community as "BSgenome data packages". See \code{?\link{available.genomes}} for how to get the list of "BSgenome data packages" curently available. } \section{Accessor methods}{ In the code snippets below, \code{x} is a BSgenome object. Note that, because the BSgenome class contains the \link[GenomeInfoDb]{GenomeDescription} class, then all the accessor methods for \link[GenomeInfoDb]{GenomeDescription} objects can also be used on \code{x}. \describe{ \item{\code{sourceUrl(x)}}{ Returns the source URL i.e. the permanent URL to the place where the FASTA files used to produce the sequences contained in \code{x} can be found (and downloaded). } \item{\code{seqnames(x)}, \code{seqnames(x) <- value}}{ Gets or sets the names of the single sequences contained in \code{x}. Each single sequence is stored in a \link[Biostrings]{DNAString} or \link[Biostrings]{MaskedDNAString} object and typically comes from a source file (FASTA) with a single record. The names returned by \code{seqnames(x)} usually reflect the names of those source files but a common prefix or suffix was eventually removed in order to keep them as short as possible. } \item{\code{seqlengths(x)}}{ Returns the lengths of the single sequences contained in \code{x}. See \code{?`\link[XVector]{length,XVector-method}`} and \code{?`\link[Biostrings]{length,MaskedXString-method}`} for the definition of the length of a \link[Biostrings]{DNAString} or \link[Biostrings]{MaskedDNAString} object. Note that the length of a masked sequence (\link[Biostrings]{MaskedXString} object) is not affected by the current set of active masks but the \code{nchar} method for \link[Biostrings]{MaskedXString} objects is. \code{names(seqlengths(x))} is guaranteed to be identical to \code{seqnames(x)}. } \item{\code{mseqnames(x)}}{ Returns the index of the multiple sequences contained in \code{x}. Each multiple sequence is stored in a \link[Biostrings]{DNAStringSet} object and typically comes from a source file (FASTA) with multiple records. The names returned by \code{mseqnames(x)} usually reflect the names of those source files but a common prefix or suffix was eventually removed in order to keep them as short as possible. } \item{\code{names(x)}}{ Returns the index of all sequences contained in \code{x}. This is the same as \code{c(seqnames(x), mseqnames(x))}. } \item{\code{length(x)}}{ Returns the length of \code{x}, i.e., the total number of sequences in it (single and multiple sequences). This is the same as \code{length(names(x))}. } \item{\code{x[[name]]}}{ Returns the sequence (single or multiple) in \code{x} named \code{name} (\code{name} must be a single string). No sequence is actually loaded into memory until this is explicitely requested with a call to \code{x[[name]]} or \code{x$name}. When loaded, a sequence is kept in a cache. It will be automatically removed from the cache at garbage collection if it's not in use anymore i.e. if there are no reference to it (other than the reference stored in the cache). With \code{options(verbose=TRUE)}, a message is printed each time a sequence is removed from the cache. } \item{\code{x$name}}{ Same as \code{x[[name]]} but \code{name} is not evaluated and therefore must be a literal character string or a name (possibly backtick quoted). } \item{\code{masknames(x)}}{ The names of the built-in masks that are defined for all the single sequences. There can be up to 4 built-in masks per sequence. These will always be (in this order): (1) the mask of assembly gaps, aka "the AGAPS mask"; (2) the mask of intra-contig ambiguities, aka "the AMB mask"; (3) the mask of repeat regions that were determined by the RepeatMasker software, aka "the RM mask"; (4) the mask of repeat regions that were determined by the Tandem Repeats Finder software (where only repeats with period less than or equal to 12 were kept), aka "the TRF mask". All the single sequences in a given package are guaranteed to have the same collection of built-in masks (same number of masks and in the same order). \code{masknames(x)} gives the names of the masks in this collection. Therefore the value returned by \code{masknames(x)} is a character vector made of the first N elements of \code{c("AGAPS", "AMB", "RM", "TRF")}, where N depends only on the BSgenome data package being looked at (0 <= N <= 4). The man page for most BSgenome data packages should provide the exact list and permanent URLs of the source data files that were used to extract the built-in masks. For example, if you've installed the BSgenome.Hsapiens.UCSC.hg38 package, load it and see the Note section in \code{?`\link[BSgenome.Hsapiens.UCSC.hg38]{BSgenome.Hsapiens.UCSC.hg38}`}. } } } \author{H. Pagès} \seealso{ \code{\link{available.genomes}}, \link[GenomeInfoDb]{GenomeDescription-class}, \link{BSgenome-utils}, \link[Biostrings]{DNAString-class}, \link[Biostrings]{DNAStringSet-class}, \link[Biostrings]{MaskedDNAString-class}, \code{\link{getSeq,BSgenome-method}}, \code{\link{injectSNPs}}, \link[XVector]{subseq,XVector-method}, \code{\link[base]{rm}}, \code{\link[base]{gc}} } \examples{ ## Loading a BSgenome data package doesn't load its sequences ## into memory: library(BSgenome.Celegans.UCSC.ce2) ## Number of sequences in this genome: length(Celegans) ## Display a summary of the sequences: Celegans ## Index of single sequences: seqnames(Celegans) ## Lengths (i.e. number of nucleotides) of the single sequences: seqlengths(Celegans) ## Load chromosome I from disk to memory (hence takes some time) ## and keep a reference to it: chrI <- Celegans[["chrI"]] # equivalent to Celegans$chrI chrI class(chrI) # a DNAString instance length(chrI) # with 15080483 nucleotides ## Single sequence can be renamed: seqnames(Celegans) <- sub("^chr", "", seqnames(Celegans)) seqlengths(Celegans) Celegans$I seqnames(Celegans) <- paste0("chr", seqnames(Celegans)) ## Multiple sequences: library(BSgenome.Rnorvegicus.UCSC.rn5) rn5 <- BSgenome.Rnorvegicus.UCSC.rn5 rn5 seqnames(rn5) rn5_chr1 <- rn5$chr1 mseqnames(rn5) rn5_random <- Rnorvegicus$random rn5_random class(rn5_random) # a DNAStringSet instance ## Character vector containing the description lines of the first ## 4 sequences in the original FASTA file: names(rn5_random)[1:4] ## --------------------------------------------------------------------- ## PASS-BY-ADDRESS SEMANTIC, CACHING AND MEMORY USAGE ## --------------------------------------------------------------------- ## We want a message to be printed each time a sequence is removed ## from the cache: options(verbose=TRUE) gc() # nothing seems to be removed from the cache rm(rn5_chr1, rn5_random) gc() # rn5_chr1 and rn5_random are removed from the cache (they are # not in use anymore) options(verbose=FALSE) ## Get the current amount of data in memory (in Mb): mem0 <- gc()["Vcells", "(Mb)"] system.time(rn5_chr2 <- rn5$chr2) # read from disk gc()["Vcells", "(Mb)"] - mem0 # 'rn5_chr2' occupies 20Mb in memory system.time(tmp <- rn5$chr2) # much faster! (sequence # is in the cache) gc()["Vcells", "(Mb)"] - mem0 # we're still using 20Mb (sequences # have a pass-by-address semantic # i.e. the sequence data are not # duplicated) ## subseq() doesn't copy the sequence data either, hence it is very ## fast and memory efficient (but the returned object will hold a ## reference to 'rn5_chr2'): y <- subseq(rn5_chr2, 10, 8000000) gc()["Vcells", "(Mb)"] - mem0 ## We must remove all references to 'rn5_chr2' before it can be ## removed from the cache (so the 20Mb of memory used by this ## sequence are freed): options(verbose=TRUE) rm(rn5_chr2, tmp) gc() ## Remember that 'y' holds a reference to 'rn5_chr2' too: rm(y) gc() options(verbose=FALSE) gc()["Vcells", "(Mb)"] - mem0 } \keyword{methods} \keyword{classes} BSgenome/man/BSgenome-utils.Rd0000644000175400017540000001245613175713516017217 0ustar00biocbuildbiocbuild\name{BSgenome-utils} \alias{BSgenome-utils} \alias{matchPWM,BSgenome-method} \alias{countPWM,BSgenome-method} \alias{vmatchPattern,BSgenome-method} \alias{vcountPattern,BSgenome-method} \alias{vmatchPDict,BSgenome-method} \alias{vcountPDict,BSgenome-method} \title{BSgenome utilities} \description{ Utilities for BSgenome objects. } \usage{ \S4method{matchPWM}{BSgenome}(pwm, subject, min.score = "80\%", exclude = "", maskList = logical(0)) \S4method{countPWM}{BSgenome}(pwm, subject, min.score = "80\%", exclude = "", maskList = logical(0)) \S4method{vmatchPattern}{BSgenome}(pattern, subject, max.mismatch = 0, min.mismatch = 0, with.indels = FALSE, fixed = TRUE, algorithm = "auto", exclude = "", maskList = logical(0), userMask = RangesList(), invertUserMask = FALSE) \S4method{vcountPattern}{BSgenome}(pattern, subject, max.mismatch = 0, min.mismatch = 0, with.indels = FALSE, fixed = TRUE, algorithm = "auto", exclude = "", maskList = logical(0), userMask = RangesList(), invertUserMask = FALSE) \S4method{vmatchPDict}{BSgenome}(pdict, subject, max.mismatch = 0, min.mismatch = 0, fixed = TRUE, algorithm = "auto", verbose = FALSE, exclude = "", maskList = logical(0)) \S4method{vcountPDict}{BSgenome}(pdict, subject, max.mismatch = 0, min.mismatch = 0, fixed = TRUE, algorithm = "auto", collapse = FALSE, weight = 1L, verbose = FALSE, exclude = "", maskList = logical(0)) } \arguments{ \item{pwm}{ A numeric matrix with row names A, C, G and T representing a Position Weight Matrix. } \item{pattern}{ A \link[Biostrings]{DNAString} object containing the pattern sequence. } \item{pdict}{ A \link[Biostrings]{DNAStringSet} object containing the pattern sequences. } \item{subject}{ A \link{BSgenome} object containing the subject sequences. } \item{min.score}{ The minimum score for counting a match. Can be given as a character string containing a percentage (e.g. \code{"85\%"}) of the highest possible score or as a single number. } \item{max.mismatch, min.mismatch}{ The maximum and minimum number of mismatching letters allowed (see \code{?`\link[Biostrings]{lowlevel-matching}`} for the details). If non-zero, an inexact matching algorithm is used. } \item{with.indels}{ If \code{TRUE} then indels are allowed. In that case, \code{min.mismatch} must be \code{0} and \code{max.mismatch} is interpreted as the maximum "edit distance" allowed between any pattern and any of its matches (see \code{?`\link[Biostrings]{matchPattern}`} for the details). } \item{fixed}{ If \code{FALSE} then IUPAC extended letters are interpreted as ambiguities (see \code{?`\link[Biostrings]{lowlevel-matching}`} for the details). } \item{algorithm}{ For \code{vmatchPattern} and \code{vcountPattern} one of the following: \code{"auto"}, \code{"naive-exact"}, \code{"naive-inexact"}, \code{"boyer-moore"}, \code{"shift-or"}, or \code{"indels"}. For \code{vmatchPDict} and \code{vcountPDict} one of the following: \code{"auto"}, \code{"naive-exact"}, \code{"naive-inexact"}, \code{"boyer-moore"}, or \code{"shift-or"}. } \item{collapse, weight}{ ignored arguments. } \item{verbose}{ \code{TRUE} or \code{FALSE}. } \item{exclude}{ A character vector with strings that will be used to filter out chromosomes whose names match these strings. } \item{maskList}{ A named logical vector of maskStates preferred when used with a BSGenome object. When using the bsapply function, the masks will be set to the states in this vector. } \item{userMask}{ A \linkS4class{RangesList}, containing a mask to be applied to each chromosome. See \code{\link{bsapply}}. } \item{invertUserMask}{ Whether the \code{userMask} should be inverted. } } \value{ A \link[GenomicRanges]{GRanges} object for \code{matchPWM} with two elementMetadata columns: "score" (numeric), and "string" (DNAStringSet). A \link[GenomicRanges]{GRanges} object for \code{vmatchPattern}. A \link[GenomicRanges]{GRanges} object for \code{vmatchPDict} with one elementMetadata column: "index", which represents a mapping to a position in the original pattern dictionary. A data.frame object for \code{countPWM} and \code{vcountPattern} with three columns: "seqname" (factor), "strand" (factor), and "count" (integer). A \link[S4Vectors]{DataFrame} object for \code{vcountPDict} with four columns: "seqname" ('factor' Rle), "strand" ('factor' Rle), "index" (integer) and "count" ('integer' Rle). As with \code{vmatchPDict} the index column represents a mapping to a position in the original pattern dictionary. } \author{P. Aboyoun} \seealso{ \code{\link[Biostrings]{matchPWM}}, \code{\link[Biostrings]{matchPattern}}, \code{\link[Biostrings]{matchPDict}}, \code{\link{bsapply}} } \examples{ library(BSgenome.Celegans.UCSC.ce2) data(HNF4alpha) pwm <- PWM(HNF4alpha) matchPWM(pwm, Celegans) countPWM(pwm, Celegans) pattern <- consensusString(HNF4alpha) vmatchPattern(pattern, Celegans, fixed = "subject") vcountPattern(pattern, Celegans, fixed = "subject") vmatchPDict(HNF4alpha[1:10], Celegans) vcountPDict(HNF4alpha[1:10], Celegans) } \keyword{methods} \keyword{utilities} BSgenome/man/BSgenomeForge.Rd0000644000175400017540000001327613175713516017045 0ustar00biocbuildbiocbuild\name{BSgenomeForge} \alias{BSgenomeForge} \alias{BSgenomeDataPkgSeed} \alias{class:BSgenomeDataPkgSeed} \alias{BSgenomeDataPkgSeed-class} \alias{forgeBSgenomeDataPkg} \alias{forgeBSgenomeDataPkg,BSgenomeDataPkgSeed-method} \alias{forgeBSgenomeDataPkg,list-method} \alias{forgeBSgenomeDataPkg,character-method} \alias{forgeSeqlengthsFile} \alias{forgeSeqFiles} \alias{forgeMasksFiles} \title{The BSgenomeForge functions} \description{ A set of functions for making a BSgenome data package. } \usage{ ## Top-level BSgenomeForge function: forgeBSgenomeDataPkg(x, seqs_srcdir=".", destdir=".", verbose=TRUE) ## Low-level BSgenomeForge functions: forgeSeqlengthsFile(seqnames, prefix="", suffix=".fa", seqs_srcdir=".", seqs_destdir=".", verbose=TRUE) forgeSeqFiles(seqnames, mseqnames=NULL, seqfile_name=NA, prefix="", suffix=".fa", seqs_srcdir=".", seqs_destdir=".", ondisk_seq_format=c("2bit", "rda", "fa.rz", "fa"), verbose=TRUE) forgeMasksFiles(seqnames, nmask_per_seq, seqs_destdir=".", ondisk_seq_format=c("2bit", "rda", "fa.rz", "fa"), masks_srcdir=".", masks_destdir=".", AGAPSfiles_type="gap", AGAPSfiles_name=NA, AGAPSfiles_prefix="", AGAPSfiles_suffix="_gap.txt", RMfiles_name=NA, RMfiles_prefix="", RMfiles_suffix=".fa.out", TRFfiles_name=NA, TRFfiles_prefix="", TRFfiles_suffix=".bed", verbose=TRUE) } \arguments{ \item{x}{ A BSgenomeDataPkgSeed object or the name of a BSgenome data package seed file. See the BSgenomeForge vignette in this package for more information. } \item{seqs_srcdir, masks_srcdir}{ Single strings indicating the path to the source directories i.e. to the directories containing the source data files. Only read access to these directories is needed. See the BSgenomeForge vignette in this package for more information. } \item{destdir}{ A single string indicating the path to the directory where the source tree of the target package should be created. This directory must already exist. See the BSgenomeForge vignette in this package for more information. } \item{ondisk_seq_format}{ Specifies how the single sequences should be stored in the forged package. Can be \code{"2bit"}, \code{"rda"}, \code{"fa.rz"}, or \code{"fa"}. If \code{"2bit"} (the default), then all the single sequences are stored in a single twoBit file. If \code{"rda"}, then each single sequence is stored in a separated serialized \link[Biostrings]{XString} object (one per single sequence). If \code{"fa.rz"} or \code{"fa"}, then all the single sequences are stored in a single FASTA file (compressed in the RAZip format if \code{"fa.rz"}). } \item{verbose}{ \code{TRUE} or \code{FALSE}. } \item{seqnames, mseqnames}{ A character vector containing the names of the single (for \code{seqnames}) and multiple (for \code{mseqnames}) sequences to forge. See the BSgenomeForge vignette in this package for more information. } \item{seqfile_name, prefix, suffix}{ See the BSgenomeForge vignette in this package for more information, in particular the description of the \code{seqfile_name}, \code{seqfiles_prefix} and \code{seqfiles_suffix} fields of a BSgenome data package seed file. } \item{seqs_destdir, masks_destdir}{ During the forging process the source data files are converted into serialized Biostrings objects. \code{seqs_destdir} and \code{masks_destdir} must be single strings indicating the path to the directories where these serialized objects should be saved. These directories must already exist. \code{forgeSeqlengthsFile} will produce a single .rda file. Both \code{forgeSeqFiles} and \code{forgeMasksFiles} will produce one .rda file per sequence. } \item{nmask_per_seq}{ A single integer indicating the desired number of masks per sequence. See the BSgenomeForge vignette in this package for more information. } \item{AGAPSfiles_type, AGAPSfiles_name, AGAPSfiles_prefix, AGAPSfiles_suffix, RMfiles_name, RMfiles_prefix, RMfiles_suffix, TRFfiles_name, TRFfiles_prefix, TRFfiles_suffix}{ These arguments are named accordingly to the corresponding fields of a BSgenome data package seed file. See the BSgenomeForge vignette in this package for more information. } } \details{ These functions are intended for Bioconductor users who want to make a new BSgenome data package, not for regular users of these packages. See the BSgenomeForge vignette in this package (\code{vignette("BSgenomeForge")}) for an extensive coverage of this topic. } \author{H. Pagès} \examples{ seqs_srcdir <- system.file("extdata", package="BSgenome") seqnames <- c("chrX", "chrM") ## Forge .rda sequence files: forgeSeqFiles(seqnames, prefix="ce2", suffix=".fa.gz", seqs_srcdir=seqs_srcdir, seqs_destdir=tempdir(), ondisk_seq_format="rda") ## Forge .2bit sequence files: forgeSeqFiles(seqnames, prefix="ce2", suffix=".fa.gz", seqs_srcdir=seqs_srcdir, seqs_destdir=tempdir(), ondisk_seq_format="2bit") ## Sanity checks: library(BSgenome.Celegans.UCSC.ce2) genome <- BSgenome.Celegans.UCSC.ce2 load(file.path(tempdir(), "chrX.rda")) stopifnot(genome$chrX == chrX) load(file.path(tempdir(), "chrM.rda")) stopifnot(genome$chrM == chrM) ce2_sequences <- import(file.path(tempdir(), "single_sequences.2bit")) ce2_sequences0 <- DNAStringSet(list(chrX=genome$chrX, chrM=genome$chrM)) stopifnot(identical(names(ce2_sequences0), names(ce2_sequences)) && all(ce2_sequences0 == ce2_sequences)) } \keyword{manip} BSgenome/man/BSgenomeViews-class.Rd0000644000175400017540000002402613175713516020176 0ustar00biocbuildbiocbuild\name{BSgenomeViews-class} \docType{class} \alias{class:BSgenomeViews} \alias{BSgenomeViews-class} % constructors \alias{BSgenomeViews} \alias{Views,BSgenome-method} % accessors \alias{subject,BSgenomeViews-method} \alias{granges,BSgenomeViews-method} \alias{length,BSgenomeViews-method} \alias{names,BSgenomeViews-method} \alias{seqnames,BSgenomeViews-method} \alias{start,BSgenomeViews-method} \alias{end,BSgenomeViews-method} \alias{width,BSgenomeViews-method} \alias{strand,BSgenomeViews-method} \alias{ranges,BSgenomeViews-method} \alias{elementNROWS,BSgenomeViews-method} \alias{seqinfo,BSgenomeViews-method} % coercion \alias{coerce,BSgenomeViews,DNAStringSet-method} \alias{coerce,BSgenomeViews,XStringSet-method} \alias{as.character,BSgenomeViews-method} \alias{as.data.frame,BSgenomeViews-method} % subsetting \alias{extractROWS,BSgenomeViews-method} \alias{getListElement,BSgenomeViews-method} % DNAStringSet methods \alias{seqtype,BSgenomeViews-method} \alias{nchar,BSgenomeViews-method} \alias{unlist,BSgenomeViews-method} \alias{alphabetFrequency,BSgenomeViews-method} \alias{hasOnlyBaseLetters,BSgenomeViews-method} \alias{uniqueLetters,BSgenomeViews-method} \alias{letterFrequency,BSgenomeViews-method} \alias{oligonucleotideFrequency,BSgenomeViews-method} \alias{nucleotideFrequencyAt,BSgenomeViews-method} \alias{consensusMatrix,BSgenomeViews-method} \alias{consensusString,BSgenomeViews-method} % displaying \alias{show,BSgenomeViews-method} \title{BSgenomeViews objects} \description{ The BSgenomeViews class is a container for storing a set of genomic positions on a \link{BSgenome} object, called the "subject" in this context. } \usage{ ## Constructor ## ------------ BSgenomeViews(subject, granges) ## Accessors ## --------- \S4method{subject}{BSgenomeViews}(x) \S4method{granges}{BSgenomeViews}(x, use.mcols=FALSE) \S4method{length}{BSgenomeViews}(x) \S4method{names}{BSgenomeViews}(x) \S4method{seqnames}{BSgenomeViews}(x) \S4method{start}{BSgenomeViews}(x) \S4method{end}{BSgenomeViews}(x) \S4method{width}{BSgenomeViews}(x) \S4method{strand}{BSgenomeViews}(x) \S4method{ranges}{BSgenomeViews}(x, use.mcols=FALSE) \S4method{elementNROWS}{BSgenomeViews}(x) \S4method{seqinfo}{BSgenomeViews}(x) ## DNAStringSet methods ## -------------------- \S4method{seqtype}{BSgenomeViews}(x) \S4method{nchar}{BSgenomeViews}(x, type="chars", allowNA=FALSE) \S4method{unlist}{BSgenomeViews}(x, recursive=TRUE, use.names=TRUE) \S4method{alphabetFrequency}{BSgenomeViews}(x, as.prob=FALSE, collapse=FALSE, baseOnly=FALSE) \S4method{hasOnlyBaseLetters}{BSgenomeViews}(x) \S4method{uniqueLetters}{BSgenomeViews}(x) \S4method{letterFrequency}{BSgenomeViews}(x, letters, OR="|", as.prob=FALSE, collapse=FALSE) \S4method{oligonucleotideFrequency}{BSgenomeViews}(x, width, step=1, as.prob=FALSE, as.array=FALSE, fast.moving.side="right", with.labels=TRUE, simplify.as="matrix") \S4method{nucleotideFrequencyAt}{BSgenomeViews}(x, at, as.prob=FALSE, as.array=TRUE, fast.moving.side="right", with.labels=TRUE) \S4method{consensusMatrix}{BSgenomeViews}(x, as.prob=FALSE, shift=0L, width=NULL, baseOnly=FALSE) \S4method{consensusString}{BSgenomeViews}(x, ambiguityMap=IUPAC_CODE_MAP, threshold=0.25, shift=0L, width=NULL) } \arguments{ \item{subject}{ A \link{BSgenome} object or the name of a reference genome specified in a way that is accepted by the \code{\link{getBSgenome}} function. In that case the corresponding BSgenome data package needs to be already installed (see \code{?\link{getBSgenome}} for the details). } \item{granges}{ A \link[GenomicRanges]{GRanges} object containing ranges relative to the genomic sequences stored in \code{subject}. } \item{x}{ A BSgenomeViews object. } \item{use.mcols}{ \code{TRUE} or \code{FALSE} (the default). Whether the metadata columns on \code{x} (accessible with \code{mcols(x)}) should be propagated to the returned object or not. } \item{type, allowNA, recursive, use.names}{ Ignored. } \item{as.prob, letters, OR, width}{ See \code{?\link[Biostrings]{alphabetFrequency}} and \code{?\link[Biostrings]{oligonucleotideFrequency}} in the \pkg{Biostrings} package. } \item{collapse, baseOnly}{ See \code{?\link[Biostrings]{alphabetFrequency}} in the \pkg{Biostrings} package. } \item{step, as.array, fast.moving.side, with.labels, simplify.as, at}{ See \code{?\link[Biostrings]{oligonucleotideFrequency}} in the \pkg{Biostrings} package. } \item{shift, ambiguityMap, threshold}{ See \code{?\link[Biostrings]{consensusMatrix}} in the \pkg{Biostrings} package. } } \section{Constructors}{ \describe{ \item{}{ \code{BSgenomeViews(subject, granges)}: Make a BSgenomeViews object by putting the views specified by \code{granges} on top of the genomic sequences stored in \code{subject}. See above for how argument \code{subject} and \code{granges} should be specified. } \item{}{ \code{Views(subject, granges)}: Equivalent to \code{BSgenomeViews(subject, granges)}. Provided for convenience. } } } \section{Accessors}{ In the code snippets below, \code{x} is a BSgenomeViews object. \describe{ \item{}{ \code{subject(x)}: Return the \link{BSgenome} object containing the full genomic sequences on top of which the views in \code{x} are defined. } \item{}{ \code{granges(x, use.mcols=FALSE)}: Return the genomic ranges of the views as a \link[GenomicRanges]{GRanges} object. These ranges are relative to the genomic sequences stored in \code{subject(x)}. } \item{}{ \code{length(x)}: The number of views in \code{x}. } \item{}{ \code{names(x)}: The names of the views in \code{x}. } \item{}{ \code{seqnames(x)}, \code{start(x)}, \code{end(x)}, \code{width(x)}, \code{strand(x)}: Equivalent to \code{seqnames(granges(x))}, \code{start(granges(x))}, \code{end(granges(x))}, \code{width(granges(x))}, \code{strand(granges(x))}, respectively. } \item{}{ \code{ranges(x, use.mcols=FALSE)}: Equivalent to \code{ranges(granges(x, use.mcols), use.mcols)}. } \item{}{ \code{elementNROWS(x)}: Equivalent to \code{width(x)}. } \item{}{ \code{seqinfo(x)}: Equivalent to \code{seqinfo(subject(x))} and to \code{seqinfo(granges(x))} (both are guaranteed to be the same). See \code{?\link[GenomeInfoDb]{seqinfo}} in the \pkg{GenomeInfoDb} package for more information. } } } \section{Coercion}{ In the code snippets below, \code{x} is a BSgenomeViews object. \describe{ \item{}{ \code{as(x, "DNAStringSet")}: Turn \code{x} into a \link[Biostrings]{DNAStringSet} object by extxracting the DNA sequence corresponding to each view. Alternatively \code{as(x, "XStringSet")} can be used for this, and is equivalent to \code{as(x, "DNAStringSet")}. } \item{}{ \code{as.character(x)}: Equivalent to \code{as.character(as(x, "DNAStringSet"))}. } \item{}{ \code{as.data.frame(x)}: Turn \code{x} into a data.frame. } } } \section{Subsetting}{ \describe{ \item{}{ \code{x[i]}: Select the views specified by \code{i}. } \item{}{ \code{x[[i]]}: Extract the one view specified by \code{i}. } } } \section{DNAStringSet methods}{ For convenience, some methods defined for \link[Biostrings]{DNAStringSet} objects in the \pkg{Biostrings} package can be used directly on a BSgenomeViews object. In that case, everything happens like if the BSgenomeViews object \code{x} was turned into a \link[Biostrings]{DNAStringSet} object (with \code{as(x, "DNAStringSet")}) before it's passed to the method for \link[Biostrings]{DNAStringSet} objects. At the moment, the list of such methods is: \code{\link[Biostrings]{seqtype}}, \code{\link[Biostrings]{nchar,XStringSet-method}}, \code{\link[Biostrings]{unlist,XStringSet-method}}, \code{\link[Biostrings]{alphabetFrequency}}, \code{\link[Biostrings]{hasOnlyBaseLetters}}, \code{\link[Biostrings]{uniqueLetters}}, \code{\link[Biostrings]{letterFrequency}}, \code{\link[Biostrings]{oligonucleotideFrequency}}, \code{\link[Biostrings]{nucleotideFrequencyAt}}, \code{\link[Biostrings]{consensusMatrix}}, and \code{\link[Biostrings]{consensusString}}. See the corresponding man page in the \pkg{Biostrings} package for a description of these methods. } \author{H. Pagès} \seealso{ \itemize{ \item The \link{BSgenome} class. \item The \link[GenomicRanges]{GRanges} class in the \pkg{GenomicRanges} package. \item The \link[Biostrings]{DNAStringSet} class in the \pkg{Biostrings} package. \item The \link[GenomeInfoDb]{seqinfo} and related getters in the \pkg{GenomeInfoDb} package for getting the sequence information stored in an object. \item \link[GenomicFeatures]{TxDb} objects in the \pkg{GenomicFeatures} package. } } \examples{ library(BSgenome.Mmusculus.UCSC.mm10) genome <- BSgenome.Mmusculus.UCSC.mm10 library(TxDb.Mmusculus.UCSC.mm10.knownGene) txdb <- TxDb.Mmusculus.UCSC.mm10.knownGene ex <- exons(txdb, columns=c("exon_id", "tx_name", "gene_id")) v <- Views(genome, ex) v subject(v) granges(v) seqinfo(v) as(v, "DNAStringSet") v10 <- v[1:10] # select the first 10 views subject(v10) # same as subject(v) granges(v10) seqinfo(v10) # same as seqinfo(v) as(v10, "DNAStringSet") alphabetFrequency(v10) alphabetFrequency(v10, collapse=TRUE) v12 <- v[width(v) <= 12] # select the views of 12 nucleotides or less head(as.data.frame(v12)) trinucleotideFrequency(v12, simplify.as="collapsed") ## BSgenomeViews objects are list-like objects. That is, the ## BSgenomeViews class derives from List and typical list/List ## operations (e.g. [[, elementNROWS(), unlist(), elementType(), ## etc...) work on these objects: is(v12, "List") # TRUE v12[[2]] head(elementNROWS(v12)) # elementNROWS(v) is the same as width(v) unlist(v12) elementType(v12) } \keyword{methods} \keyword{classes} BSgenome/man/SNPlocs-class.Rd0000644000175400017540000001773613175713516017014 0ustar00biocbuildbiocbuild\name{SNPlocs-class} \docType{class} \alias{class:SNPlocs} \alias{SNPlocs-class} \alias{SNPlocs} \alias{class:ODLT_SNPlocs} \alias{ODLT_SNPlocs-class} \alias{ODLT_SNPlocs} \alias{class:OldFashionSNPlocs} \alias{OldFashionSNPlocs-class} \alias{OldFashionSNPlocs} % accessors \alias{provider,SNPlocs-method} \alias{providerVersion,SNPlocs-method} \alias{releaseDate,SNPlocs-method} \alias{releaseName,SNPlocs-method} \alias{referenceGenome} \alias{referenceGenome,SNPlocs-method} \alias{compatibleGenomes} \alias{compatibleGenomes,SNPlocs-method} \alias{organism,SNPlocs-method} \alias{commonName,SNPlocs-method} \alias{seqinfo,SNPlocs-method} \alias{seqnames,SNPlocs-method} % constructors \alias{new_ODLT_SNPlocs} \alias{newSNPlocs} % displaying \alias{show,SNPlocs-method} % SNP extractors \alias{snpcount} \alias{snpcount,SNPlocs-method} \alias{snpcount,ODLT_SNPlocs-method} \alias{snpcount,OldFashionSNPlocs-method} \alias{snplocs} \alias{snplocs,SNPlocs-method} \alias{snplocs,ODLT_SNPlocs-method} \alias{snplocs,OldFashionSNPlocs-method} \alias{snpsBySeqname} \alias{snpsBySeqname,SNPlocs-method} \alias{snpsBySeqname,ODLT_SNPlocs-method} \alias{snpsBySeqname,OldFashionSNPlocs-method} \alias{snpsByOverlaps} \alias{snpsByOverlaps,SNPlocs-method} \alias{snpsByOverlaps,ODLT_SNPlocs-method} \alias{snpsByOverlaps,OldFashionSNPlocs-method} \alias{snpsById} \alias{snpsById,SNPlocs-method} \alias{snpsById,ODLT_SNPlocs-method} \alias{snpsById,OldFashionSNPlocs-method} % Old SNPlocs extractors (deprecated) \alias{snpid2loc} \alias{snpid2loc,SNPlocs-method} \alias{snpid2loc,OldFashionSNPlocs-method} \alias{snpid2alleles} \alias{snpid2alleles,SNPlocs-method} \alias{snpid2alleles,OldFashionSNPlocs-method} \alias{snpid2grange} \alias{snpid2grange,SNPlocs-method} \alias{snpid2grange,OldFashionSNPlocs-method} \title{SNPlocs objects} \description{ The SNPlocs class is a container for storing known SNP locations (of class \emph{snp}) for a given organism. SNPlocs objects are usually made in advance by a volunteer and made available to the Bioconductor community as \emph{SNPlocs data packages}. See \code{?\link{available.SNPs}} for how to get the list of \emph{SNPlocs and \link{XtraSNPlocs} data packages} curently available. The main focus of this man page is on how to extract SNPs from an SNPlocs object. } \usage{ snpcount(x) snpsBySeqname(x, seqnames, ...) \S4method{snpsBySeqname}{SNPlocs}(x, seqnames, drop.rs.prefix=FALSE) snpsByOverlaps(x, ranges, ...) \S4method{snpsByOverlaps}{SNPlocs}(x, ranges, drop.rs.prefix=FALSE, ...) snpsById(x, ids, ...) \S4method{snpsById}{SNPlocs}(x, ids, ifnotfound=c("error", "warning", "drop")) } \arguments{ \item{x}{ A SNPlocs object. } \item{seqnames}{ The names of the sequences for which to get SNPs. Must be a subset of \code{seqlevels(x)}. NAs and duplicates are not allowed. } \item{...}{ Additional arguments, for use in specific methods. Arguments passed to the \code{snpsByOverlaps} method for SNPlocs objects thru \code{...} are used internally in the call to \code{\link[IRanges]{subsetByOverlaps}()}. See \code{?IRanges::\link[IRanges]{subsetByOverlaps}} in the \pkg{IRanges} package and \code{?GenomicRanges::\link[GenomicRanges]{subsetByOverlaps}} in the \pkg{GenomicRanges} package for more information about the \code{subsetByOverlaps()} generic and its method for \link[GenomicRanges]{GenomicRanges} objects. } \item{drop.rs.prefix}{ Should the \code{rs} prefix be dropped from the returned RefSNP ids? (RefSNP ids are stored in the \code{RefSNP_id} metadata column of the returned object.) } \item{ranges}{ One or more genomic regions of interest specified as a \link[GenomicRanges]{GRanges} or \link[GenomicRanges]{GPos} object. A single region of interest can be specified as a character string of the form \code{"ch14:5201-5300"}. } \item{ids}{ The RefSNP ids to look up (a.k.a. rs ids). Can be integer or character vector, with or without the \code{"rs"} prefix. NAs are not allowed. } \item{ifnotfound}{ What to do if SNP ids are not found. } } \value{ \code{snpcount} returns a named integer vector containing the number of SNPs for each sequence in the reference genome. \code{snpsBySeqname}, \code{snpsByOverlaps}, and \code{snpsById} return an \emph{unstranded} \link[GenomicRanges]{GPos} object with 1 element (genomic position) per SNP and the following metadata columns: \itemize{ \item \code{RefSNP_id}: RefSNP ID (aka "rs id"). Character vector with no NAs and no duplicates. \item \code{alleles_as_ambig}: A character vector with no NAs containing the alleles for each SNP represented by an IUPAC nucleotide ambiguity code. See \code{?\link[Biostrings]{IUPAC_CODE_MAP}} in the \pkg{Biostrings} package for more information. The alleles are always reported with respect to the positive strand. } Note that this \link[GenomicRanges]{GPos} object is \emph{unstranded} i.e. all the SNPs in it have their strand set to \code{"*"}. If \code{ifnotfound="error"}, the object returned by \code{snpsById} is guaranteed to be \emph{parallel} to \code{ids}, that is, the i-th element in the \link[GenomicRanges]{GPos} object corresponds to the i-th element in \code{ids}. } \author{H. Pagès} \seealso{ \itemize{ \item \code{\link{available.SNPs}} \item \link[GenomicRanges]{GPos} and \link[GenomicRanges]{GRanges} objects in the \pkg{GenomicRanges} package. \item \link{XtraSNPlocs} packages and objects for molecular variations of class other than \emph{snp} e.g. of class \emph{in-del}, \emph{heterozygous}, \emph{microsatellite}, etc... \item \code{IRanges::\link[IRanges]{subsetByOverlaps}} in the \pkg{IRanges} package and \code{GenomicRanges::\link[GenomicRanges]{subsetByOverlaps}} in the \pkg{GenomicRanges} package for more information about the \code{subsetByOverlaps()} generic and its method for \link[GenomicRanges]{GenomicRanges} objects. \item \code{\link{injectSNPs}} \item \code{\link[Biostrings]{IUPAC_CODE_MAP}} in the \pkg{Biostrings} package. } } \examples{ library(SNPlocs.Hsapiens.dbSNP144.GRCh38) snps <- SNPlocs.Hsapiens.dbSNP144.GRCh38 snpcount(snps) ## --------------------------------------------------------------------- ## snpsBySeqname() ## --------------------------------------------------------------------- ## Get all SNPs located on chromosome 22 or MT: snpsBySeqname(snps, c("22", "MT")) ## --------------------------------------------------------------------- ## snpsByOverlaps() ## --------------------------------------------------------------------- ## Get all SNPs overlapping some genomic region of interest: snpsByOverlaps(snps, "22:33.63e6-33.64e6") ## With the regions of interest being all the known CDS for hg38 ## located on chromosome 22 or MT (except for the chromosome naming ## convention, hg38 is the same as GRCh38): library(TxDb.Hsapiens.UCSC.hg38.knownGene) txdb <- TxDb.Hsapiens.UCSC.hg38.knownGene my_cds <- cds(txdb) seqlevels(my_cds, pruning.mode="coarse") <- c("chr22", "chrM") seqlevelsStyle(my_cds) # UCSC seqlevelsStyle(snps) # NCBI seqlevelsStyle(my_cds) <- seqlevelsStyle(snps) genome(my_cds) <- genome(snps) my_snps <- snpsByOverlaps(snps, my_cds) my_snps table(my_snps \%within\% my_cds) ## --------------------------------------------------------------------- ## snpsById() ## --------------------------------------------------------------------- ## Lookup some RefSNP ids: my_rsids <- c("rs10458597", "rs12565286", "rs7553394") \dontrun{ snpsById(snps, my_rsids) # error, rs7553394 not found } ## The following example uses more than 2GB of memory, which is more ## than what 32-bit Windows can handle: is_32bit_windows <- .Platform$OS.type == "windows" && .Platform$r_arch == "i386" if (!is_32bit_windows) { snpsById(snps, my_rsids, ifnotfound="drop") } } \keyword{methods} \keyword{classes} BSgenome/man/XtraSNPlocs-class.Rd0000644000175400017540000002341213175713516017637 0ustar00biocbuildbiocbuild\name{XtraSNPlocs-class} \docType{class} \alias{class:XtraSNPlocs} \alias{XtraSNPlocs-class} \alias{XtraSNPlocs} % getters \alias{colnames,XtraSNPlocs-method} \alias{dim,XtraSNPlocs-method} \alias{provider,XtraSNPlocs-method} \alias{providerVersion,XtraSNPlocs-method} \alias{releaseDate,XtraSNPlocs-method} \alias{releaseName,XtraSNPlocs-method} \alias{referenceGenome,XtraSNPlocs-method} \alias{organism,XtraSNPlocs-method} \alias{commonName,XtraSNPlocs-method} \alias{species,XtraSNPlocs-method} \alias{seqinfo,XtraSNPlocs-method} \alias{seqnames,XtraSNPlocs-method} % constructor \alias{newXtraSNPlocs} % displaying \alias{show,XtraSNPlocs-method} % SNP extractors \alias{snpcount,XtraSNPlocs-method} \alias{snpsBySeqname,XtraSNPlocs-method} \alias{snpsByOverlaps,XtraSNPlocs-method} \alias{snpsById,XtraSNPlocs-method} \title{XtraSNPlocs objects} \description{ The XtraSNPlocs class is a container for storing extra SNP locations and alleles for a given organism. While a \link{SNPlocs} object can store only molecular variations of class \emph{snp}, an XtraSNPlocs object contains molecular variations of other classes (\emph{in-del}, \emph{heterozygous}, \emph{microsatellite}, \emph{named-locus}, \emph{no-variation}, \emph{mixed}, \emph{multinucleotide-polymorphism}). XtraSNPlocs objects are usually made in advance by a volunteer and made available to the Bioconductor community as \emph{XtraSNPlocs data packages}. See \code{?\link{available.SNPs}} for how to get the list of \emph{\link{SNPlocs} and XtraSNPlocs data packages} curently available. The main focus of this man page is on how to extract SNPs from an XtraSNPlocs object. } \usage{ \S4method{snpcount}{XtraSNPlocs}(x) \S4method{snpsBySeqname}{XtraSNPlocs}(x, seqnames, columns=c("seqnames", "start", "end", "strand", "RefSNP_id"), drop.rs.prefix=FALSE, as.DataFrame=FALSE) \S4method{snpsByOverlaps}{XtraSNPlocs}(x, ranges, columns=c("seqnames", "start", "end", "strand", "RefSNP_id"), drop.rs.prefix=FALSE, as.DataFrame=FALSE, ...) \S4method{snpsById}{XtraSNPlocs}(x, ids, columns=c("seqnames", "start", "end", "strand", "RefSNP_id"), ifnotfound=c("error", "warning", "drop"), as.DataFrame=FALSE) \S4method{colnames}{XtraSNPlocs}(x, do.NULL=TRUE, prefix="col") } \arguments{ \item{x}{ An XtraSNPlocs object. } \item{seqnames}{ The names of the sequences for which to get SNPs. NAs and duplicates are not allowed. The supplied \code{seqnames} must be a subset of \code{seqlevels(x)}. } \item{columns}{ The names of the columns to return. Valid column names are: \code{seqnames}, \code{start}, \code{end}, \code{width}, \code{strand}, \code{RefSNP_id}, \code{alleles}, \code{snpClass}, \code{loctype}. See Details section below for a description of these columns. } \item{drop.rs.prefix}{ Should the \code{rs} prefix be dropped from the returned RefSNP ids? (RefSNP ids are stored in the \code{RefSNP_id} metadata column of the returned object.) } \item{as.DataFrame}{ Should the result be returned in a \link[S4Vectors]{DataFrame} instead of a \link[GenomicRanges]{GRanges} object? } \item{ranges}{ One or more regions of interest specified as a \link[GenomicRanges]{GRanges} object. A single region of interest can be specified as a character string of the form \code{"ch14:5201-5300"}. } \item{...}{ Additional arguments, for use in specific methods. Arguments passed to the \code{snpsByOverlaps} method for XtraSNPlocs objects thru \code{...} are used internally in the call to \code{\link[IRanges]{subsetByOverlaps}()}. See \code{?IRanges::\link[IRanges]{subsetByOverlaps}} in the \pkg{IRanges} package and \code{?GenomicRanges::\link[GenomicRanges]{subsetByOverlaps}} in the \pkg{GenomicRanges} package for more information about the \code{subsetByOverlaps()} generic and its method for \link[GenomicRanges]{GenomicRanges} objects. } \item{ids}{ The RefSNP ids to look up (a.k.a. \emph{rs ids}). Can be integer or character vector, with or without the \code{"rs"} prefix. NAs are not allowed. } \item{ifnotfound}{ What to do if SNP ids are not found. } \item{do.NULL, prefix}{ These arguments are ignored. } } \value{ \code{snpcount} returns a named integer vector containing the number of SNPs for each chromosome in the reference genome. \code{snpsBySeqname} and \code{snpsById} both return a \link[GenomicRanges]{GRanges} object with 1 element per SNP, unless \code{as.DataFrame} is set to \code{TRUE} in which case they return a \link[S4Vectors]{DataFrame} with 1 row per SNP. When a \link[GenomicRanges]{GRanges} object is returned, the columns requested via the \code{columns} argument are stored as metada columns of the object, except for the following columns: \code{seqnames}, \code{start}, \code{end}, \code{width}, and \code{strand}. These "spatial columns" (in the sense that they describe the genomic locations of the SNPs) can be accessed by calling the corresponding getter on the \link[GenomicRanges]{GRanges} object. Summary of available columns (\code{my_snps} being the returned object): \itemize{ \item \code{seqnames}: The name of the chromosome where each SNP is located. Access with \code{seqnames(my_snps)} when \code{my_snps} is a \link[GenomicRanges]{GRanges} object. \item \code{start} and \code{end}: The starting and ending coordinates of each SNP with respect to the chromosome indicated in \code{seqnames}. Coordinated are 1-based and with respect to the 5' end of the plus strand of the chromosome in the reference genome. Access with \code{start(my_snps)}, \code{end(my_snps)}, or \code{ranges(my_snps)} when \code{my_snps} is a \link[GenomicRanges]{GRanges} object. \item \code{width}: The number of nucleotides spanned by each SNP \emph{on the reference genome} (e.g. a width of 0 means the SNP is an insertion). Access with \code{width( my_snps)} when \code{my_snps} is a \link[GenomicRanges]{GRanges} object. \item \code{strand}: The strand that the alleles of each SNP was reported to. Access with \code{strand(my_snps)} when \code{my_snps} is a \link[GenomicRanges]{GRanges} object. \item \code{RefSNP_id}: The RefSNP id (a.k.a. \emph{rs id}) of each SNP. Access with \code{mcols(my_snps)$RefSNP_id} when \code{my_snps} is a \link[GenomicRanges]{GRanges} object. \item \code{alleles}: The alleles of each SNP in the format used by dbSNP. Access with \code{mcols(my_snps)$alleles} when \code{my_snps} is a \link[GenomicRanges]{GRanges} object. \item \code{snpClass}: Class of each SNP. Possible values are \code{in-del}, \code{heterozygous}, \code{microsatellite}, \code{named-locus}, \code{no-variation}, \code{mixed}, and \code{multinucleotide-polymorphism}. Access with \code{mcols(my_snps)$snpClass} when \code{my_snps} is a \link[GenomicRanges]{GRanges} object. \item \code{loctype}: See \url{ftp://ftp.ncbi.nih.gov/snp/00readme.txt} for the 6 loctype codes used by dbSNP, and their meanings. WARNING: The code assigned to each SNP doesn't seem to be reliable. For example, loctype codes 1 and 3 officially stand for insertion and deletion, respectively. However, when looking at the SNP ranges it actually seems to be the other way around. Access with \code{mcols(my_snps)$loctype} when \code{my_snps} is a \link[GenomicRanges]{GRanges} object. } \code{colnames(x)} returns the names of the available columns. } \author{H. Pagès} \seealso{ \itemize{ \item \code{\link{available.SNPs}} \item \link[GenomicRanges]{GRanges} objects in the \pkg{GenomicRanges} package. \item \link{SNPlocs} packages and objects for molecular variations of class \emph{snp}. } } \examples{ library(XtraSNPlocs.Hsapiens.dbSNP144.GRCh38) snps <- XtraSNPlocs.Hsapiens.dbSNP144.GRCh38 snpcount(snps) colnames(snps) ## --------------------------------------------------------------------- ## snpsBySeqname() ## --------------------------------------------------------------------- ## Get the location, RefSNP id, and alleles for all "extra SNPs" ## located on chromosome 22 or MT: snpsBySeqname(snps, c("ch22", "chMT"), columns=c("RefSNP_id", "alleles")) ## --------------------------------------------------------------------- ## snpsByOverlaps() ## --------------------------------------------------------------------- ## Get the location, RefSNP id, and alleles for all "extra SNPs" ## overlapping some regions of interest: snpsByOverlaps(snps, "ch22:33.63e6-33.64e6", columns=c("RefSNP_id", "alleles")) ## With the regions of interest being all the known CDS for hg38 ## (except for the chromosome naming convention, hg38 is the same ## as GRCh38): library(TxDb.Hsapiens.UCSC.hg38.knownGene) txdb <- TxDb.Hsapiens.UCSC.hg38.knownGene hg38_cds <- cds(txdb) seqlevelsStyle(hg38_cds) # UCSC seqlevelsStyle(snps) # dbSNP seqlevelsStyle(hg38_cds) <- seqlevelsStyle(snps) genome(hg38_cds) <- genome(snps) snpsByOverlaps(snps, hg38_cds, columns=c("RefSNP_id", "alleles")) ## --------------------------------------------------------------------- ## snpsById() ## --------------------------------------------------------------------- ## Get the location and alleles for some RefSNP ids: my_rsids <- c("rs367617508", "rs398104919", "rs3831697", "rs372470289", "rs141568169", "rs34628976", "rs67551854") snpsById(snps, my_rsids, c("RefSNP_id", "alleles")) ## See ?XtraSNPlocs.Hsapiens.dbSNP144.GRCh38 for more examples of using ## snpsBySeqname() and snpsById(). } \keyword{methods} \keyword{classes} BSgenome/man/available.genomes.Rd0000644000175400017540000001216713175713516017735 0ustar00biocbuildbiocbuild\name{available.genomes} \alias{available.genomes} \alias{installed.genomes} \alias{getBSgenome} \title{Find available/installed genomes} \description{ \code{available.genomes} gets the list of BSgenome data packages that are available in the Bioconductor repositories for your version of R/Bioconductor. \code{installed.genomes} gets the list of BSgenome data packages that are currently installed on your system. \code{getBSgenome} searchs the installed BSgenome data packages for the specified genome and returns it as a \link{BSgenome} object. } \usage{ available.genomes(splitNameParts=FALSE, type=getOption("pkgType")) installed.genomes(splitNameParts=FALSE) getBSgenome(genome, masked=FALSE) } \arguments{ \item{splitNameParts}{ Whether to split or not the package names in parts. In that case the result is returned in a data frame with 5 columns. } \item{type}{ Character string indicating the type of package (\code{"source"}, \code{"mac.binary"} or \code{"win.binary"}) to look for. } \item{genome}{ A \link{BSgenome} object, or the full name of an installed BSgenome data package, or a short string specifying a genome assembly (a.k.a. provider version) that refers unambiguously to an installed BSgenome data package. } \item{masked}{ \code{TRUE} or \code{FALSE}. Whether to search for the \emph{masked} BSgenome object (i.e. the object that contains the masked sequences) or not (the default). } } \details{ A BSgenome data package contains the full genome sequences for a given organism. Its name typically has 4 parts (5 parts if it's a \emph{masked} BSgenome data package i.e. if it contains masked sequences) separated by a dot e.g. \code{BSgenome.Mmusculus.UCSC.mm10} or \code{BSgenome.Mmusculus.UCSC.mm10.masked}: \enumerate{ \item The 1st part is always \code{BSgenome}. \item The 2nd part is the name of the organism in abbreviated form e.g. \code{Mmusculus}, \code{Hsapiens}, \code{Celegans}, \code{Scerevisiae}, \code{Ecoli}, etc... \item The 3rd part is the name of the organisation who provided the genome sequences. We formally refer to it as the \emph{provider} of the genome. E.g. \code{UCSC}, \code{NCBI}, \code{TAIR}, etc... \item The 4th part is the release string or number used by this organisation for this particular genome assembly. We formally refer to it as the \emph{provider version} of the genome. E.g. \code{hg38}, \code{GRCh38}, \code{hg19}, \code{mm10}, \code{susScr3}, etc... \item If the package contains masked sequences, its name has the \code{.masked} suffix added to it, which is typically the 5th part. } A BSgenome data package contains a single top-level object (a \link{BSgenome} object) named like the package itself that can be used to access the genome sequences. } \value{ For \code{available.genomes} and \code{installed.genomes}: by default (i.e. if \code{splitNameParts=FALSE}), a character vector containing the names of the BSgenome data packages that are available (for \code{available.genomes}) or currently installed (for \code{installed.genomes}). If \code{splitNameParts=TRUE}, the list of packages is returned in a data frame with one row per package and the following columns: \code{pkgname} (character), \code{organism} (factor), \code{provider} (factor), \code{provider_version} (character), and \code{masked} (logical). For \code{getBSgenome}: the \link{BSgenome} object containing the sequences for the specified genome. Or an error if the object cannot be found in the BSgenome data packages currently installed. } \author{H. Pagès} \seealso{ \itemize{ \item \link{BSgenome} objects. \item \code{\link[utils]{available.packages}}. } } \examples{ ## --------------------------------------------------------------------- ## available.genomes() and installed.genomes() ## --------------------------------------------------------------------- # What genomes are currently installed: installed.genomes() # What genomes are available: available.genomes() # Split the package names in parts: av_gen <- available.genomes(splitNameParts=TRUE) table(av_gen$organism) table(av_gen$provider) # Make your choice and install with: if (interactive()) { library(BiocInstaller) biocLite("BSgenome.Scerevisiae.UCSC.sacCer1") } # Have a coffee 8-) # Load the package and display the index of sequences for this genome: library(BSgenome.Scerevisiae.UCSC.sacCer1) Scerevisiae # same as BSgenome.Scerevisiae.UCSC.sacCer1 ## --------------------------------------------------------------------- ## getBSgenome() ## --------------------------------------------------------------------- ## Specify the full name of an installed BSgenome data package: genome <- getBSgenome("BSgenome.Celegans.UCSC.ce2") genome ## Specify a genome assembly (a.k.a. provider version): genome <- getBSgenome("hg38") class(genome) # BSgenome object providerVersion(genome) genome$chrM genome <- getBSgenome("hg38", masked=TRUE) class(genome) # MaskedBSgenome object providerVersion(genome) genome$chr22 } \keyword{manip} BSgenome/man/bsapply.Rd0000644000175400017540000000532013175713516016024 0ustar00biocbuildbiocbuild\name{bsapply} \alias{bsapply} \title{bsapply} \description{ Apply a function to each chromosome in a genome. } \usage{ bsapply(BSParams, ...) } \arguments{ \item{BSParams}{ a BSParams object that holds the various parameters needed to configure the bsapply function } \item{...}{ optional arguments to 'FUN'. } } \details{ By default the exclude parameter is set to not exclude anything. A popular option will probably be to set this to "rand" so that random bits of unassigned contigs are filtered out. } \value{ If \code{BSParams} sets \code{simplify=FALSE}, an ordinary list is returned containing the results generated using the remaining BSParams specifications. If \code{BSParams} sets \code{simplify=TRUE}, an \code{sapply}-like simplification is performed on the results. } \author{Marc Carlson} \seealso{ \link{BSParams-class}, \link{BSgenome-class}, \link{BSgenome-utils} } \examples{ ## Load the Worm genome: library("BSgenome.Celegans.UCSC.ce2") ## Count the alphabet frequencies for every chromosome but exclude ## mitochrondrial and scaffold ones: params <- new("BSParams", X = Celegans, FUN = alphabetFrequency, exclude = c("M", "_")) bsapply(params) ## Or we can do this same function with simplify = TRUE: params <- new("BSParams", X = Celegans, FUN = alphabetFrequency, exclude = c("M", "_"), simplify = TRUE) bsapply(params) ## Examples to show how we might look for a string (in this case an ## ebox motif) across the whole genome. Ebox <- DNAStringSet("CACGTG") pdict0 <- PDict(Ebox) params <- new("BSParams", X = Celegans, FUN = countPDict, simplify = TRUE) bsapply(params, pdict = pdict0) params@FUN <- matchPDict bsapply(params, pdict = pdict0) ## And since its really overkill to use matchPDict to find a single pattern: params@FUN <- matchPattern bsapply(params, pattern = "CACGTG") ## Examples on how to use the masks library(BSgenome.Hsapiens.UCSC.hg38.masked) genome <- BSgenome.Hsapiens.UCSC.hg38.masked ## I can make things verbose if I want to see the chromosomes getting processed. options(verbose=TRUE) ## For the 1st example, lets use default masks params <- new("BSParams", X = genome, FUN = alphabetFrequency, exclude = c(1:8,"M","X","_"), simplify = TRUE) bsapply(params) if (interactive()) { ## Set up the motifList to filter out all double T's and all double C's params@motifList <-c("TT","CC") bsapply(params) ## Get rid of the motifList params@motifList=as.character() } ##Enable all standard masks params@maskList <- c(RM=TRUE,TRF=TRUE) bsapply(params) ##Disable all standard masks params@maskList <- c(AGAPS=FALSE,AMB=FALSE) bsapply(params) } \keyword{manip} BSgenome/man/export-methods.Rd0000644000175400017540000000644613175713516017346 0ustar00biocbuildbiocbuild\name{export-methods} \alias{export-methods} \alias{writeBSgenomeToFasta} \alias{export,BSgenome,FastaFile,ANY-method} \alias{writeBSgenomeToTwobit} \alias{export,BSgenome,TwoBitFile,ANY-method} \title{Export a BSgenome object as a FASTA or twoBit file} \description{ \code{\link[rtracklayer]{export}} methods for \link{BSgenome} objects. NOTE: The \code{\link[rtracklayer]{export}} generic function and most of its methods are defined and documented in the \pkg{rtracklayer} package. This man page only documents the 2 \code{\link[rtracklayer]{export}} methods define in the \pkg{BSgenome} package. } \usage{ \S4method{export}{BSgenome,FastaFile,ANY}(object, con, format, compress=FALSE, compression_level=NA, verbose=TRUE) \S4method{export}{BSgenome,TwoBitFile,ANY}(object, con, format, ...) } \arguments{ \item{object}{ The \link{BSgenome} object to export. } \item{con}{ A \link[rtracklayer]{FastaFile} or \link[rtracklayer]{TwoBitFile} object. Alternatively \code{con} can be a single string containing the path to a FASTA or twoBit file, in which case either the file extension or the \code{format} argument needs to be \code{"fasta"}, \code{"twoBit"}, or \code{"2bit"}. Also note that in this case, the \code{\link[rtracklayer]{export}} method that is called is either the method with signature \code{c("ANY", "character", "missing")} or the method with signature \code{c("ANY", "character", "character")}, both defined in the \pkg{rtracklayer} package. If \code{object} is a \link{BSgenome} object and the file extension or the \code{format} argument is \code{"fasta"}, \code{"twoBit"}, or \code{"2bit"}, then the flow eventually reaches one of 2 methods documented here. } \item{format}{ If not missing, should be \code{"fasta"}, \code{"twoBit"}, or \code{"2bit"} (case insensitive for \code{"twoBit"} and \code{"2bit"}). } \item{compress, compression_level}{ Forwarded to \code{\link{writeXStringSet}}. See \code{?\link{writeXStringSet}} for the details. } \item{verbose}{ Whether or not the function should display progress. \code{TRUE} by default. } \item{...}{ Extra arguments. The method for \link[rtracklayer]{TwoBitFile} objects forwards them to \code{\link{bsapply}}. } } \seealso{ \itemize{ \item \link{BSgenome} objects. \item The \code{\link[rtracklayer]{export}} generic, and \link[rtracklayer]{FastaFile} and \link[rtracklayer]{TwoBitFile} objects in the \pkg{rtracklayer} package. } } \author{Michael Lawrence} \examples{ library(BSgenome.Celegans.UCSC.ce2) genome <- BSgenome.Celegans.UCSC.ce2 ## Export as FASTA file. out1_file <- file.path(tempdir(), "Celegans.fasta") export(genome, out1_file) ## Export as twoBit file. out2_file <- file.path(tempdir(), "Celegans.2bit") export(genome, out2_file) ## Sanity checks: dna0 <- DNAStringSet(as.list(genome)) system.time(dna1 <- import(out1_file)) stopifnot(identical(names(dna0), names(dna1)) && all(dna0 == dna1)) system.time(dna2 <- import(out2_file)) # importing twoBit is 10-20x # faster than importing non # compressed FASTA stopifnot(identical(names(dna0), names(dna2)) && all(dna0 == dna2)) } \keyword{methods} \keyword{utilities} BSgenome/man/getSeq-methods.Rd0000644000175400017540000003174713175713516017257 0ustar00biocbuildbiocbuild\name{getSeq-methods} \alias{getSeq} \alias{getSeq,BSgenome-method} \alias{getSeq,XStringSet-method} \alias{[,XStringSet,GenomicRanges-method} \alias{[,XStringSet,GRangesList-method} \title{getSeq methods for BSgenome and XStringSet objects} \description{ \code{\link[Biostrings]{getSeq}} methods for extracting a set of sequences (or subsequences) from a \link{BSgenome} or \link[Biostrings]{XStringSet} object. For XStringSets, there are also convenience methods on \code{[} that delegate to \code{getSeq}. } \usage{ \S4method{getSeq}{BSgenome}(x, names, start=NA, end=NA, width=NA, strand="+", as.character=FALSE) \S4method{getSeq}{XStringSet}(x, names) } \arguments{ \item{x}{ A \link{BSgenome} or \link[Biostrings]{XStringSet} object. See the \code{\link{available.genomes}} function for how to install a genome. } \item{names}{ When \code{x} is a \link{BSgenome}, \code{names} must be a character vector containing the names of the sequences in \code{x} where to get the subsequences from, or a \link[GenomicRanges]{GRanges} object, or a \link[GenomicRanges]{GRangesList} object, or a named \link[IRanges]{RangesList} object, or a named \link[IRanges]{Ranges} object. The \link[IRanges]{RangesList} or \link[IRanges]{Ranges} object must be named according to the sequences in \code{x} where to get the subsequences from. If \code{names} is missing, then \code{seqnames(x)} is used. See \code{?`\link{BSgenome-class}`} for details on how to get the lists of single sequences and multiple sequences (respectively) contained in a \link{BSgenome} object. When \code{x} is a \link[Biostrings]{XStringSet} object, \code{names} must be a character vector, \link[GenomicRanges]{GRanges} or \link[GenomicRanges]{GRangesList} object. } \item{start, end, width}{ Vector of integers (eventually with NAs) specifying the locations of the subsequences to extract. These are not needed (and it's an error to supply them) when \code{names} is a \link[GenomicRanges]{GRanges}, \link[GenomicRanges]{GRangesList}, \link[IRanges]{RangesList}, or \link[IRanges]{Ranges} object. } \item{strand}{ A vector containing \code{"+"}s or/and \code{"-"}s. This is not needed (and it's an error to supply it) when \code{names} is a \link[GenomicRanges]{GRanges} or \link[GenomicRanges]{GRangesList} object. } \item{as.character}{ \code{TRUE} or \code{FALSE}. Should the extracted sequences be returned in a standard character vector? } \item{...}{Additional arguments. (Currently ignored.)} } \details{ L, the number of sequences to extract, is determined as follow: \itemize{ \item If \code{names} is a \link[GenomicRanges]{GRanges} or \link[IRanges]{Ranges} object then L = \code{length(names)}. \item If \code{names} is a \link[GenomicRanges]{GRangesList} or \link[IRanges]{RangesList} object then L = \code{length(unlist(names))}. \item Otherwise, L is the length of the longest of \code{names}, \code{start}, \code{end} and \code{width} and all these arguments are recycled to this length. \code{NA}s and negative values in these 3 arguments are solved according to the rules of the SEW (Start/End/Width) interface (see \code{?\link[IRanges]{solveUserSEW}} for the details). } If \code{names} is neither a \link[GenomicRanges]{GRanges} or \link[GenomicRanges]{GRangesList} object, then the \code{strand} argument is also recycled to length L. Here is how the names passed to the \code{names} argument are matched to the names of the sequences in \link{BSgenome} object \code{x}. For each \code{name} in \code{names}: \itemize{ \item (1): If \code{x} contains a single sequence with that name then this sequence is used for extraction; \item (2): Otherwise the names of all the elements in all the multiple sequences are searched. If the \code{names} argument is a character vector then \code{name} is treated as a regular expression and \code{\link[base]{grep}} is used for this search, otherwise (i.e. when the names are supplied via a higher level object like \link[GenomicRanges]{GRanges} or \link[GenomicRanges]{GRangesList}) then \code{name} must match exactly the name of the sequence. If exactly 1 sequence is found, then it is used for extraction, otherwise (i.e. if no sequence or more than 1 sequence is found) then an error is raised. } There are convenience methods for extracting sequences from \link[Biostrings]{XStringSet} objects using a \link[GenomicRanges:GenomicRanges-class]{GenomicRanges} or \link[GenomicRanges]{GRangesList} subscript (character subscripts are implicitly supported). Both methods are simple wrappers around \code{getSeq}, although the GRangesList method differs from the \code{getSeq} behavior in that the within-element results are concatenated and returned as an XStringSet, rather than an XStringSetList. See the examples. } \value{ Normally a \link[Biostrings]{DNAStringSet} object (or character vector if \code{as.character=TRUE}). With the 2 following exceptions: \enumerate{ \item A \link[Biostrings]{DNAStringSetList} object (or \link[IRanges]{CharacterList} object if \code{as.character=TRUE}) of the same shape as \code{names} if \code{names} is a \link[GenomicRanges]{GRangesList} object. \item A \link[Biostrings]{DNAString} object (or single character string if \code{as.character=TRUE}) if L = 1 and \code{names} is not a \link[GenomicRanges]{GRanges}, \link[GenomicRanges]{GRangesList}, \link[IRanges]{RangesList}, or \link[IRanges]{Ranges} object. } } \note{ Be aware that using \code{as.character=TRUE} can be very inefficient when extracting a "big" amount of DNA sequences (e.g. millions of short sequences or a small number of very long sequences). Note that the masks in \code{x}, if any, are always ignored. In other words, masked regions in the genome are extracted in the same way as unmasked regions (this is achieved by dropping the masks before extraction). See \code{?`\link[Biostrings]{MaskedDNAString-class}`} for more information about masked DNA sequences. } \author{H. Pagès; improvements suggested by Matt Settles and others} \seealso{ \code{\link[Biostrings]{getSeq}}, \code{\link{available.genomes}}, \link{BSgenome-class}, \link[Biostrings]{DNAString-class}, \link[Biostrings]{DNAStringSet-class}, \link[Biostrings]{MaskedDNAString-class}, \link[GenomicRanges]{GRanges-class}, \link[GenomicRanges]{GRangesList-class}, \link[IRanges]{RangesList-class}, \link[IRanges]{Ranges-class}, \code{\link[base]{grep}} } \examples{ ## --------------------------------------------------------------------- ## A. SIMPLE EXAMPLES ## --------------------------------------------------------------------- ## Load the Caenorhabditis elegans genome (UCSC Release ce2): library(BSgenome.Celegans.UCSC.ce2) ## Look at the index of sequences: Celegans ## Get chromosome V as a DNAString object: getSeq(Celegans, "chrV") ## which is in fact the same as doing: Celegans$chrV \dontrun{ ## Never try this: getSeq(Celegans, "chrV", as.character=TRUE) ## or this (even worse): getSeq(Celegans, as.character=TRUE) } ## Get the first 20 bases of each chromosome: getSeq(Celegans, end=20) ## Get the last 20 bases of each chromosome: getSeq(Celegans, start=-20) ## --------------------------------------------------------------------- ## B. EXTRACTING SMALL SEQUENCES FROM DIFFERENT CHROMOSOMES ## --------------------------------------------------------------------- myseqs <- data.frame( chr=c("chrI", "chrX", "chrM", "chrM", "chrX", "chrI", "chrM", "chrI"), start=c(NA, -40, 8510, 301, 30001, 9220500, -2804, -30), end=c(50, NA, 8522, 324, 30011, 9220555, -2801, -11), strand=c("+", "-", "+", "+", "-", "-", "+", "-") ) getSeq(Celegans, myseqs$chr, start=myseqs$start, end=myseqs$end) getSeq(Celegans, myseqs$chr, start=myseqs$start, end=myseqs$end, strand=myseqs$strand) ## --------------------------------------------------------------------- ## C. USING A GRanges OBJECT ## --------------------------------------------------------------------- gr1 <- GRanges(seqnames=c("chrI", "chrI", "chrM"), ranges=IRanges(start=101:103, width=9)) gr1 # all strand values are "*" getSeq(Celegans, gr1) # treats strand values as if they were "+" strand(gr1)[] <- "-" getSeq(Celegans, gr1) strand(gr1)[1] <- "+" getSeq(Celegans, gr1) strand(gr1)[2] <- "*" if (interactive()) getSeq(Celegans, gr1) # Error: cannot mix "*" with other strand values gr2 <- GRanges(seqnames=c("chrM", "NM_058280_up_1000"), ranges=IRanges(start=103:102, width=9)) gr2 if (interactive()) { ## Because the sequence names are supplied via a GRanges object, they ## are not treated as regular expressions: getSeq(Celegans, gr2) # Error: sequence NM_058280_up_1000 not found } ## --------------------------------------------------------------------- ## D. USING A GRangesList OBJECT ## --------------------------------------------------------------------- gr1 <- GRanges(seqnames=c("chrI", "chrII", "chrM", "chrII"), ranges=IRanges(start=101:104, width=12), strand="+") gr2 <- shift(gr1, 5) gr3 <- gr2 strand(gr3) <- "-" grl <- GRangesList(gr1, gr2, gr3) getSeq(Celegans, grl) ## --------------------------------------------------------------------- ## E. EXTRACTING A HIGH NUMBER OF RANDOM 40-MERS FROM A GENOME ## --------------------------------------------------------------------- extractRandomReads <- function(x, density, readlength) { if (!is.integer(readlength)) readlength <- as.integer(readlength) start <- lapply(seqnames(x), function(name) { seqlength <- seqlengths(x)[name] sample(seqlength - readlength + 1L, seqlength * density, replace=TRUE) }) names <- rep.int(seqnames(x), elementNROWS(start)) ranges <- IRanges(start=unlist(start), width=readlength) strand <- strand(sample(c("+", "-"), length(names), replace=TRUE)) gr <- GRanges(seqnames=names, ranges=ranges, strand=strand) getSeq(x, gr) } ## With a density of 1 read every 100 genome bases, the total number of ## extracted 40-mers is about 1 million: rndreads <- extractRandomReads(Celegans, 0.01, 40) ## Notes: ## - The short sequences in 'rndreads' can be seen as the result of a ## simulated high-throughput sequencing experiment. A non-realistic ## one though because: ## (a) It assumes that the underlying technology is perfect (the ## generated reads have no technology induced errors). ## (b) It assumes that the sequenced genome is exactly the same as ## the reference genome. ## (c) The simulated reads can contain IUPAC ambiguity letters only ## because the reference genome contains them. In a real ## high-throughput sequencing experiment, the sequenced genome ## of course doesn't contain those letters, but the sequencer ## can introduce them in the generated reads to indicate ## ambiguous base-calling. ## - Those reads are coming from the plus and minus strands of the ## chromosomes. ## - With a density of 0.01 and the reads being only 40-base long, the ## average coverage of the genome is only 0.4 which is low. The total ## number of reads is about 1 million and it takes less than 10 sec. ## to generate them. ## - A higher coverage can be achieved by using a higher density and/or ## longer reads. For example, with a density of 0.1 and 100-base reads ## the average coverage is 10. The total number of reads is about 10 ## millions and it takes less than 1 minute to generate them. ## - Those reads could easily be mapped back to the reference by using ## an efficient matching tool like matchPDict() for performing exact ## matching (see ?matchPDict for more information). Typically, a ## small percentage of the reads (4 to 5\% in our case) will hit the ## reference at multiple locations. This is especially true for such ## short reads, and, in a lower proportion, is still true for longer ## reads, even for reads as long as 300 bases. ## --------------------------------------------------------------------- ## F. SEE THE BSgenome CACHE IN ACTION ## --------------------------------------------------------------------- options(verbose=TRUE) first20 <- getSeq(Celegans, end=20) first20 gc() stopifnot(length(ls(Celegans@.seqs_cache)) == 0L) ## One more gc() call is needed in order to see the amount of memory in ## used after all the chromosomes have been removed from the cache: gc() ## --------------------------------------------------------------------- ## G. USING '[' FOR CONVENIENT EXTRACTION ## --------------------------------------------------------------------- seqs <- getSeq(Celegans) seqs[gr1] seqs[grl] } \keyword{manip} BSgenome/man/injectSNPs.Rd0000644000175400017540000001176713175713516016406 0ustar00biocbuildbiocbuild\name{injectSNPs} \alias{class:InjectSNPsHandler} \alias{InjectSNPsHandler-class} \alias{InjectSNPsHandler} \alias{injectSNPs} \alias{injectSNPs,BSgenome-method} \alias{SNPlocs_pkgname} \alias{SNPlocs_pkgname,InjectSNPsHandler-method} \alias{SNPlocs_pkgname,BSgenome-method} \alias{snpcount,InjectSNPsHandler-method} \alias{snpcount,BSgenome-method} \alias{snplocs,InjectSNPsHandler-method} \alias{snplocs,BSgenome-method} \alias{available.SNPs} \alias{installed.SNPs} \title{SNP injection} \description{ Inject SNPs from a SNPlocs data package into a genome. } \usage{ injectSNPs(x, snps) SNPlocs_pkgname(x) \S4method{snpcount}{BSgenome}(x) \S4method{snplocs}{BSgenome}(x, seqname, ...) ## Related utilities available.SNPs(type=getOption("pkgType")) installed.SNPs() } \arguments{ \item{x}{ A \link[BSgenome:BSgenome-class]{BSgenome} object. } \item{snps}{ A \link{SNPlocs} object or the name of a SNPlocs data package. This object or package must contain SNP information for the single sequences contained in \code{x}. If a package, it must be already installed (\code{injectSNPs} won't try to install it). } \item{seqname}{ The name of a single sequence in \code{x}. } \item{type}{ Character string indicating the type of package (\code{"source"}, \code{"mac.binary"} or \code{"win.binary"}) to look for. } \item{...}{ Further arguments to be passed to \code{\link{snplocs}} method for \link{SNPlocs} objects. } } \value{ \code{injectSNPs} returns a copy of the original genome \code{x} where some or all of the single sequences from \code{x} are altered by injecting the SNPs stored in \code{snps}. The SNPs in the altered genome are represented by an IUPAC ambiguity code at each SNP location. \code{SNPlocs_pkgname}, \code{snpcount} and \code{snplocs} return \code{NULL} if no SNPs were injected in \code{x} (i.e. if \code{x} is not a \link{BSgenome} object returned by a previous call to \code{injectSNPs}). Otherwise \code{SNPlocs_pkgname} returns the name of the package from which the SNPs were injected, \code{snpcount} the number of SNPs for each altered sequence in \code{x}, and \code{snplocs} their locations in the sequence whose name is specified by \code{seqname}. \code{available.SNPs} returns a character vector containing the names of the SNPlocs and XtraSNPlocs data packages that are currently available on the Bioconductor repositories for your version of R/Bioconductor. A SNPlocs data package contains basic information (location and alleles) about the known molecular variations of class \emph{snp} for a given organism. A XtraSNPlocs data package contains information about the known molecular variations of other classes (\emph{in-del}, \emph{heterozygous}, \emph{microsatellite}, \emph{named-locus}, \emph{no-variation}, \emph{mixed}, \emph{multinucleotide-polymorphism}) for a given organism. Only SNPlocs data packages can be used for SNP injection for now. \code{installed.SNPs} returns a character vector containing the names of the SNPlocs and XtraSNPlocs data packages that are already installed. } \note{ \code{injectSNPs}, \code{SNPlocs_pkgname}, \code{snpcount} and \code{snplocs} have the side effect to try to load the SNPlocs data package that was specified thru the \code{snps} argument if it's not already loaded. } \author{H. Pagès} \seealso{ \link{BSgenome-class}, \code{\link[Biostrings]{IUPAC_CODE_MAP}}, \code{\link[Biostrings]{injectHardMask}}, \code{\link[Biostrings]{letterFrequencyInSlidingView}}, \code{\link[Biostrings]{.inplaceReplaceLetterAt}} } \examples{ ## What SNPlocs data packages are already installed: installed.SNPs() ## What SNPlocs data packages are available: available.SNPs() if (interactive()) { ## Make your choice and install with: source("http://bioconductor.org/biocLite.R") biocLite("SNPlocs.Hsapiens.dbSNP144.GRCh38") } ## Inject SNPs from dbSNP into the Human genome: library(BSgenome.Hsapiens.UCSC.hg38.masked) genome <- BSgenome.Hsapiens.UCSC.hg38.masked SNPlocs_pkgname(genome) genome2 <- injectSNPs(genome, "SNPlocs.Hsapiens.dbSNP144.GRCh38") genome2 # note the extra "with SNPs injected from ..." line SNPlocs_pkgname(genome2) snpcount(genome2) head(snplocs(genome2, "chr1")) alphabetFrequency(genome$chr1) alphabetFrequency(genome2$chr1) ## Find runs of SNPs of length at least 25 in chr1. Might require ## more memory than some platforms can handle (e.g. 32-bit Windows ## and maybe some Mac OS X machines with little memory): is_32bit_windows <- .Platform$OS.type == "windows" && .Platform$r_arch == "i386" is_macosx <- substr(R.version$os, start=1, stop=6) == "darwin" if (!is_32bit_windows && !is_macosx) { chr1 <- injectHardMask(genome2$chr1) ambiguous_letters <- paste(DNA_ALPHABET[5:15], collapse="") lf <- letterFrequencyInSlidingView(chr1, 25, ambiguous_letters) sl <- slice(as.integer(lf), lower=25) v1 <- Views(chr1, start(sl), end(sl)+24) v1 max(width(v1)) # length of longest SNP run } } \keyword{manip} BSgenome/vignettes/0000755000175400017540000000000013175725526015324 5ustar00biocbuildbiocbuildBSgenome/vignettes/BSgenomeForge.Rnw0000644000175400017540000007745013175713516020507 0ustar00biocbuildbiocbuild%\VignetteIndexEntry{How to forge a BSgenome data package} %\VignetteKeywords{Genome, BSgenome, DNA, Sequence, UCSC, BSgenome data package} %\VignettePackage{BSgenome} % % NOTE -- ONLY EDIT THE .Rnw FILE!!! The .tex file is % likely to be overwritten. % \SweaveOpts{keep.source=TRUE} \documentclass[10pt]{article} %\usepackage{amsmath} %\usepackage[authoryear,round]{natbib} % % NOTE -- There is an obscure issue with the use of \url from the hyperref % package that will trigger a MiKTeX/pdflatex error: % ! pdfTeX error (ext4): \pdfendlink ended up in different nesting level than \pd % fstartlink. % \AtBegShi@Output ...ipout \box \AtBeginShipoutBox % \fi \fi % l.96 \end{document} % % ! ==> Fatal error occurred, no output PDF file produced! % Transcript written on BSgenomeForge1.log. % The error is hard to reproduce. I've observed it on the r34270 version of this % vignette and with the following version of the MiKTeX/pdflatex command: % MiKTeX-pdfTeX 2.7.3147 (1.40.9) (MiKTeX 2.7) \usepackage{hyperref} \usepackage{underscore} \textwidth=6.5in \textheight=8.5in \parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \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}} \bibliographystyle{plainnat} \begin{document} \title{How to forge a BSgenome data package} \author{Herv\'e Pag\`es \\ Gentleman Lab \\ Fred Hutchinson Cancer Research Center \\ Seattle, WA} \date{\today} \maketitle \tableofcontents %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \section{Introduction} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% IMPORTANT NOTE: Starting with Bioconductor 2.14, the \Rfunction{forgeBSgenomeDataPkg} function doesn't handle masks anymore i.e. now it produces a \term{BSgenome data package} that contains only the bare sequences. A new function \Rfunction{forgeMaskedBSgenomeDataPkg} has been added to forge a \term{BSgenome data package} with masked sequences. This vignette has been updated to reflect these changes. This vignette describes the process of forging a \term{BSgenome data package}. It is intended for Bioconductor users who want to make a new \term{BSgenome data package}, not for regular users of these packages. Start {\R} (make sure you are using the latest release version), load the \Rpackage{BSgenome} package, and use the \Rfunction{available.genomes} function to get the list of \term{BSgenome data packages} available in the current release version of Bioconductor. So you confirm that none of those genomes suits your needs? And you want to make your own package? If you answer yes to these 2 questions, then you've come to the right place. Requirements: \begin{itemize} \item Some basic knowledge of the Unix/Linux command line is required. The commands that you will most likely need are: \code{cd}, \code{mkdir}, \code{mv}, \code{rmdir}, \code{tar}, \code{gunzip}, \code{unzip}, \code{ftp} and \code{wget}. Also you will need to create and edit some text files. \item You need access to a good Unix/Linux build machine with a decent amount of RAM (>= 4GB), especially if your genome is big. For smaller genomes, 2GB or even 1GB of RAM might be enough. \item You need the latest release versions of {\R} plus the \Rpackage{Biostrings} and \Rpackage{BSgenome} packages installed on the build machine. To check your installation, start {\R} and try to load the \Rpackage{BSgenome} package. \item Finally, you need to obtain the \term{source data files} of the genome that you want to build a package for. There are 2 groups of \term{source data files}: (1) the files containing the sequence data (those files are required), and (2) the files containing the mask data (those files are optional). For most organisms, these files have been made publicly available on the internet by genome providers like UCSC, NCBI, FlyBase, TAIR, etc. The next sections of this vignette explain how to obtain and prepare these files. \end{itemize} Refer to the \textit{R Installation and Administration} manual \footnote{\url{http://cran.r-project.org/doc/manuals/R-admin.html}} if you need to install {\R} or upgrade your {\R} version, and to the \textit{Bioconductor - Install} page \footnote{\url{http://bioconductor.org/install/}} on the Bioconductor website if you need to install or update the \Rpackage{Biostrings} or \Rpackage{BSgenome} packages. Questions, comments or bug reports about this vignette or about the BSgenomeForge functions are welcome. Please address them to the author (\code{hpages@fredhutch.org}) or post them on the Bioconductor support site \footnote{\url{https://support.bioconductor.org/}}. In the next section (``How to forge a BSgenome data package with bare sequences''), we describe how to forge a \term{BSgenome data package} with sequences that have no masks on them. If this is what you're after, then you'll be done at the end of the section. Only if you need to forge a package with masked sequences, you'll have to keep reading but you'll have to forge a \term{BSgenome data package} with bare sequences first. In this vignette, we call \term{target packages} the \term{BSgenome data packages} that we're going to forge (one target package with bare sequences and possibly a 2nd target package with masked sequences). %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \section{How to forge a BSgenome data package with bare sequences} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \subsection{Obtain and prepare the sequence data} \subsubsection{What do I need?} The sequence data must be in a single twoBit file (e.g. \textit{musFur1.2bit}) or in a collection of FASTA files (possibly gzip-compressed). If the latter, then you need 1 FASTA file per sequence that you want to put in the \term{target package}. In that case the name of each FASTA file must be of the form \textit{}\textit{}\textit{} where \textit{} is the name of the sequence in it and \textit{} and \textit{} are a prefix and a suffix (possibly empty) that are the same for all the FASTA files. \subsubsection{Examples} UCSC provides the genome sequences for Stickleback (gasAcu1) in various forms: (a) as a twoBit file (\textit{gasAcu1.2bit} located in \url{http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/bigZips/}, (b) as a big compressed tarball containing one file per chromosome (\textit{chromFa.tar.gz} located in the same folder), and (c) as a collection of compressed FASTA files (\texttt{chrI.fa.gz}, \texttt{chrII.fa.gz}, \texttt{chrIII.fa.gz}, ..., \texttt{chrXXI.fa.gz}, \texttt{chrM.fa.gz} and \texttt{chrUn.fa.gz} located in \url{http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/chromosomes/}). To forge a \term{BSgenome data package} for gasAcu1, the easiest would be to use (a) (the twoBit file). However it would also be possible to use (c) (the collection of compressed FASTA files). In that case the suffix would need to be set to \texttt{.fa.gz}. Note that the prefix here is empty and not \texttt{chr}, because \texttt{chr} is considered to be part of the sequence names (a commonly used chromosome naming convention at UCSC). Alternatively, the big compressed tarball (\texttt{chromFa.tar.gz}) could be used. After downloading and extracting it, we should end up with the same files as with (c). You can use the \Rfunction{fasta.seqlengths} function from the \Rpackage{Biostrings} package to get the lengths of the sequences in a FASTA file: <<>>= library(Biostrings) file <- system.file("extdata", "ce2chrM.fa.gz", package="BSgenome") fasta.seqlengths(file) @ For the \Rpackage{BSgenome.Mfuro.UCSC.musFur1} package, the twoBit file was used and downloaded with: \begin{verbatim} wget http://hgdownload.soe.ucsc.edu/goldenPath/musFur1/bigZips/musFur1.2bit \end{verbatim} For the \Rpackage{BSgenome.Rnorvegicus.UCSC.rn4} package, the big compressed tarball was used. It was downloaded and extracted with: \begin{verbatim} wget http://hgdownload.cse.ucsc.edu/goldenPath/rn4/bigZips/chromFa.tar.gz tar zxf chromFa.tar.gz \end{verbatim} \subsubsection{The \textit{} folder} So we assume that you've downloaded the \term{sequence data files} and that they are now located in a folder on your machine\footnote{Note that checking the md5sums after download is always a good idea.}. From now on, we'll refer to this folder as the \textit{} folder. Depending on what data files you downloaded (see previous sub-subsection), you might also need to extract and possibly rename the files. Note that all the \term{sequence data files} should be located directly in the \textit{} folder, not in subfolders of this folder. For example, depending on the genome, UCSC provides either a big \texttt{chromFa.tar.gz} or \texttt{chromFa.zip} file that contains the sequence data for all the chromosomes. But it could be that, after extraction of this big file, the individual FASTA files for each chromosome end up being located one level down the \textit{} folder (granted that you were in this folder when you extracted the file). If this is the case, then you will need to move them one level up (use \code{mv -i */*.fa .} for this, then remove all the empty subfolders with \code{rmdir *}). \subsection{Prepare the BSgenome data package seed file} \subsubsection{Overview} The \term{BSgenome data package seed file} will contain all the information needed by the \Rfunction{forgeBSgenomeDataPkg} function to forge the \term{target package}. The format of this file is DCF (Debian Control File), which is also the format used for the \texttt{DESCRIPTION} file of any {\R} package. The valid fields of a \term{seed file} are divided in 3 categories: \begin{enumerate} \item Standard \texttt{DESCRIPTION} fields. These fields are actually the mandatory fields found in any \texttt{DESCRIPTION} file. They will be copied to the \texttt{DESCRIPTION} file of the \term{target package}. \item Non-standard \texttt{DESCRIPTION} fields. These fields are specific to \term{seed files} and they will also be copied to the \texttt{DESCRIPTION} file of the \term{target package}. In addition, the values of these fields will be stored in the \Rclass{BSgenome} object that will be contained in the \term{target package}. This means that the users of the \term{target package} will be able to retrieve these values via the accessor methods defined for \Rclass{BSgenome} objects. See the man page for the \Rclass{BSgenome} class (\code{{?}`BSgenome-class`}) for a description of these methods. \item Additional fields that don't fall in the first 2 categories. \end{enumerate} The 3 following sub-subsections give an extensive description of all the valid fields of a \term{seed file}. Alternatively, the reader in a hurry can go directly to the last sub-subsection of this subsection for an example of a \term{seed file}. \subsubsection{Standard \texttt{DESCRIPTION} fields} \begin{itemize} \item \code{Package}: Name to give to the \term{target package}. The convention used for the packages built by the Bioconductor project is to use a name made of 4 parts separated by a dot. Part 1 is always \code{BSgenome}. Part 2 is the abbreviated name of the organism (when the name of the organism is made of 2 words, we put together the first letter of the first word in upper case followed by the entire second word in lower case e.g. \code{Rnorvegicus}). Part 3 is the name of the organisation who provided the genome (e.g. \code{UCSC}). Part 4 is the release string or number used by this organisation to identify this version of the genome (e.g. \code{rn4}). \item \code{Title}: The title of the \term{target package}. E.g. \code{Full genome sequences for Rattus norvegicus (UCSC version rn4)}. \item \code{Description}, \code{Version}, \code{Author}, \code{Maintainer}, \code{License}: Like the 2 previous fields, these are mandatory fields found in any \texttt{DESCRIPTION} file. Please refer to the \textit{The DESCRIPTION file} subsection of the \textit{Writing R Extensions} manual \footnote{\url{http://cran.r-project.org/doc/manuals/R-exts.html\#The-DESCRIPTION-file}} for more information about these fields. If you plan to distribute the \term{target package} that you are about to forge, please pickup the license carefully and make sure that it is compatible with the license of the \term{sequence data files} if any. \item \code{Suggests}: [OPTIONAL] If you're going to add examples to the \code{Examples} section of the \term{target package} (see \code{PkgExamples} field below for how to do this), use this field to list the packages used in these examples. \end{itemize} \subsubsection{Non-standard \texttt{DESCRIPTION} fields} \begin{itemize} \item \code{organism}: The scientific name of the organism in the format \code{Genus species} (e.g. \code{Rattus norvegicus}, \code{Homo sapiens}) or \code{Genus species subspecies} (e.g. \code{Homo sapiens neanderthalensis}). \item \code{common\_name}: The common name of the organism (e.g. \code{Rat} or \code{Human}). For organisms that have more than one commmon name (e.g. \code{Bovine} or \code{Cow} for Bos taurus), choose one. Note that for the packages built by the Bioconductor project from a UCSC genome, this field corresponds to the \code{SPECIES} column of the \textit{List of UCSC genome releases} table \footnote{\url{http://genome.ucsc.edu/FAQ/FAQreleases\#release1}}. \item \code{provider}: The provider of the \term{sequence data files} e.g. \code{UCSC}, \code{NCBI}, \code{BDGP}, \code{FlyBase}, etc... Should preferably match part 3 of the package name (field \code{Package}). \item \code{provider\_version}: The provider-side version of the genome. Should preferably match part 4 of the package name (field \code{Package}). For the packages built by the Bioconductor project from a UCSC genome, this field corresponds to the \code{UCSC VERSION} field of the \textit{List of UCSC genome releases} table. \item \code{release\_date}: When this assembly of the genome was released. For the packages built by the Bioconductor project from a UCSC genome, this field corresponds to the \code{RELEASE DATE} field of the \textit{List of UCSC genome releases} table. \item \code{release\_name}: The release name or build number of this assembly of the genome. For the packages built by the Bioconductor project from a UCSC genome, this field corresponds to the \code{RELEASE NAME} field of the \textit{List of UCSC genome releases} table. \item \code{source\_url}: The permanent URL where the \term{sequence data files} used to forge the \term{target package} can be found. \item \code{organism\_biocview}: The official biocViews term for this organism. This is generally the same as the \code{organism} field except that spaces should be replaced by underscores. The value of this field matters only if the \term{target package} is going to be added to a Bioconductor repository since it will determine under which subview of the \textit{Bioconductor Task View} for \textit{Organism} \footnote{\url{http://bioconductor.org/packages/release/Organism.html}} the package will appear. Note that this is the only field in this category that won't be stored in the \Rclass{BSgenome} object that will be contained in the \term{target package}. \end{itemize} \subsubsection{Other fields} \begin{itemize} \item \code{BSgenomeObjname}: Should match part 2 of the package name (see \code{Package} field above). \item \code{seqnames}: [OPTIONAL] Needed only if you are using a collection of \term{sequence data files}. In that case \code{seqnames} must be an {\R} expression returning the names of the single sequences to forge (in a character vector). E.g. \code{paste("chr", c(1:20, "X", "M", "Un", paste(c(1:20, "X", "Un"), "\_random", sep="")), sep="")}. \item \code{circ\_seqs}: [OPTIONAL] An {\R} expression returning the names of the circular sequences (in a character vector). If the \code{seqnames} field is specified, then \code{circ\_seqs} must be a subset of it. E.g. \code{"chrM"} for rn4 or \code{c("chrM", "2micron")} for the sacCer2 genome (Yeast) from UCSC. The default value for \code{circ\_seqs} is \code{NULL} (no circular sequence). \item \code{mseqnames}: [OPTIONAL] An {\R} expression returning the names of the multiple sequences to forge (in a character vector). E.g. \code{c("random", "chrUn")} for \code{rn5}. The default value for \code{mseqnames} is \code{NULL} (no multiple sequence). \item \code{PkgDetails}: [OPTIONAL] Some arbitrary text that will be copied to the \code{Details} section of the man page of the \term{target package}. \item \code{SrcDataFiles}: [OPTIONAL] Some arbitrary text that will be copied to the \code{Note} section of the man pages of the \term{target package}. \code{SrcDataFiles} should describe briefly where the \term{sequence data files} are coming from. Will typically contain URLs (permanent URLs are a must). \item \code{PkgExamples}: [OPTIONAL] Some {\R} code (possibly with comments) that will be added to the \code{Examples} section of the man page of the \term{target package}. Don't forget to list the packages used in these examples in the \code{Suggests} field. \item \code{seqs\_srcdir}: The absolute path to the folder containing the \term{sequence data files}. \item \code{seqfile\_name}: Required if the \term{sequence data files} is a single twoBit file (e.g. \code{musFur1.2bit}). Ignored otherwise. \item \code{seqfiles\_prefix}, \code{seqfiles\_suffix}: [OPTIONAL] Needed only if you are using a collection of \term{sequence data files}. The common prefix and suffix that need to be added to all the sequence names (fields \code{seqnames} and \code{mseqnames}) to get the name of the corresponding FASTA file. Default values are the empty prefix for \code{seqfiles\_prefix} and \code{.fa} for \code{seqfiles\_suffix}. \item \code{ondisk\_seq\_format}: [OPTIONAL] Specifies how the single sequences should be stored in the \term{target package}. Can be \code{2bit}, \code{rda}, \code{fa.rz}, or \code{fa}. If \code{2bit} (the default), then all the single sequences are stored in a single twoBit file. If \code{rda}, then each single sequence is stored in a separated serialized \Rclass{XString} object (one per single sequence). If \code{fa.rz} or \code{fa}, then all the single sequences are stored in a single FASTA file (compressed in the RAZip format if \code{fa.rz}). \end{itemize} \subsubsection{An example} The \term{seed files} used for the packages forged by the Bioconductor project are included in the \Rpackage{BSgenome} package: <<>>= library(BSgenome) seed_files <- system.file("extdata", "GentlemanLab", package="BSgenome") tail(list.files(seed_files, pattern="-seed$")) ## Display seed file for musFur1: musFur1_seed <- list.files(seed_files, pattern="\\.musFur1-seed$", full.names=TRUE) cat(readLines(musFur1_seed), sep="\n") ## Display seed file for rn4: rn4_seed <- list.files(seed_files, pattern="\\.rn4-seed$", full.names=TRUE) cat(readLines(rn4_seed), sep="\n") @ From now we assume that you have managed to prepare the \term{seed file} for your \term{target package}. \subsection{Forge the \term{target package}} To forge the \term{target package}, start \R, load the \Rpackage{BSgenome} package, and call the \Rfunction{forgeBSgenomeDataPkg} function on your \term{seed file}. For example, if the path to your \term{seed file} is \texttt{"path/to/my/seed"}, do: <>= library(BSgenome) forgeBSgenomeDataPkg("path/to/my/seed") @ Depending on the size of the genome and your hardware, this can take between 2 minutes and 1 or 2 hours. By default \Rfunction{forgeBSgenomeDataPkg} will create the source tree of the \term{target package} in the current directory. Once \Rfunction{forgeBSgenomeDataPkg} is done, ignore the warnings (if any), quit \R, and build the source package (tarball) with \begin{verbatim} R CMD build \end{verbatim} where \code{} is the path to the source tree of the package. Then check the package with \begin{verbatim} R CMD check \end{verbatim} where \code{} is the path to the tarball produced by \code{R CMD build}. Finally install the package with \begin{verbatim} R CMD INSTALL \end{verbatim} and use it! %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \section{How to forge a BSgenome data package with masked sequences} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \subsection{Obtain and prepare the mask data} \subsubsection{What do I need?} The mask data are not available for all organisms. What you download exactly depends of course on what's available and also on what built-in masks you want to have in the \term{2nd target package}. 4 kinds of built-in masks are currently supported by BSgenomeForge: \begin{itemize} \item the masks of assembly gaps, aka ``the AGAPS masks''; \item the masks of intra-contig ambiguities, aka ``the AMB masks''; \item the masks of repeat regions that were determined by the RepeatMasker software, aka ``the RM masks''; \item the masks of repeat regions that were determined by the Tandem Repeats Finder software (where only repeats with period less than or equal to 12 were kept), aka ``the TRF masks''. \end{itemize} For the AGAPS masks, you need UCSC ``gap'' or NCBI ``agp'' files. It can be one file per chromosome or a single big file containing the assembly gap information for all the chromosomes together. In the former case, the name of each file must be of the form \textit{}\textit{}\textit{}. Like for the FASTA files in group 1, \textit{} must be the name of the sequence (sequence names for FASTA files and AGAPS masks must match) and \textit{} and \textit{} must be a prefix and a suffix (possibly empty) that are the same for all the files (this prefix/suffix doesn't need to be, and typically is not, the same as for the FASTA files in group 1). You don't need any file for the AMB masks. For the RM masks, you need RepeatMasker \texttt{.out} files. Like for the AGAPS masks, it can be one file per chromosome or a single big file containing the RepeatMasker information for all the chromosomes together. In the former case, the name of each file must also be of the form \textit{}\textit{}\textit{}. Same comments apply as for the AGAPS masks above. For the TRF masks, you need Tandem Repeats Finder \texttt{.bed} files. Again, it can be one file per chromosome or a single big file. In the former case, the name of each file must also be of the form \textit{}\textit{}\textit{}). Same comments apply as for the AGAPS masks above. Again, for some organisms none of the masks above are available or only some of them are. \subsubsection{An example} Here is how the \term{mask data files} for the \Rpackage{BSgenome.Rnorvegicus.UCSC.rn4} package were obtained and prepared: \begin{itemize} \item AGAPS masks: all the \texttt{chr*\_gap.txt.gz} files (UCSC ``gap'' files) were downloaded from the UCSC \textit{database} folder \footnote{\url{http://hgdownload.cse.ucsc.edu/goldenPath/rn4/database/}} for \code{rn4}. This was done with the standard Unix/Linux \code{ftp} command: \begin{verbatim} ftp hgdownload.cse.ucsc.edu # login as "anonymous" cd goldenPath/rn4/database prompt mget chr*_gap.txt.gz \end{verbatim} Then all the downloaded files were uncompressed with: \begin{verbatim} for file in chr*_gap.txt.gz; do gunzip $file ; done \end{verbatim} \item RM masks: file \texttt{chromOut.tar.gz} was downloaded from the UCSC \textit{bigZips} folder and extracted with: \begin{verbatim} tar zxf chromOut.tar.gz \end{verbatim} \item TRF masks: file \texttt{chromTrf.tar.gz} was downloaded from the UCSC \textit{bigZips} folder and extracted with: \begin{verbatim} tar zxf chromTrf.tar.gz \end{verbatim} \end{itemize} \subsubsection{The \textit{} folder} From now we assume that you've downloaded (checking the md5sums is always a good idea) and possibly extracted all the \term{mask data files}, and that they are located in the \textit{} folder. Note that all the \term{mask data files} should be located directly in the \textit{} folder, not in subfolders of this folder. \subsection{Prepare the seed file for the masked BSgenome data package} \subsubsection{Overview} The \term{seed file} for the \term{BSgenome data package} with masked sequences (i.e. \term{2nd target package}) is similar to the \term{seed file} for the \term{BSgenome data package} containing the corresponding bare sequences (a.k.a. the \term{reference target package} i.e. the package you forged in the previous section). It will contain all the information needed by the \Rfunction{forgeMaskedBSgenomeDataPkg} function to forge the \term{2nd target package}. The fields of this \term{seed file} are described in the 3 following sub-subsections. Alternatively, the reader in a hurry can go directly to the last sub-subsection of this subsection for an example of \term{seed file}. \subsubsection{Standard \texttt{DESCRIPTION} fields} \begin{itemize} \item \code{Package}: Name to give to the \term{2nd target package}. The convention used for the packages built by the Bioconductor project is to use the same name as the \term{reference target package} with the \code{.masked} suffix added to it. \item \code{Title}: The title of the package. E.g. \code{Full masked genome sequences for Rattus norvegicus (UCSC version rn4)}. \item \code{Description}, \code{Version}, \code{Author}, \code{Maintainer}, \code{License}: See previous section. \end{itemize} \subsubsection{Non-standard \texttt{DESCRIPTION} fields} \begin{itemize} \item \code{organism\_biocview}: Same as for the \term{reference target package}. \item \code{source\_url}: The permanent URL where the \term{mask data files} used to forge this package can be found. \end{itemize} \subsubsection{Other fields} \begin{itemize} \item \code{RefPkgname}: The name of the \term{reference target package}. \item \code{nmask\_per\_seq}: The number of masks per sequence (1 to 4). \item \code{PkgDetails}, \code{PkgExamples}: See previous section. \item \code{SrcDataFiles}: [OPTIONAL] Some arbitrary text that will be copied to the \code{Note} section of the man pages of the \term{target package}. \code{SrcDataFiles} should describe briefly where the \term{mask data files} are coming from. Will typically contain URLs (permanent URLs are a must). \item \code{masks\_srcdir}: The path to the \textit{} folder. \item \code{AGAPSfiles\_type}: [OPTIONAL] Must be \code{gap} (the default) if the \term{source data files} containing the AGAPS masks information are UCSC ``gap'' files, or \code{agp} if they are NCBI ``agp'' files. \item \code{AGAPSfiles\_name}: [OPTIONAL] Omit this field if you have one \term{source data file} per single sequence for the AGAPS masks and use the \code{AGAPSfiles\_prefix} and \code{AGAPSfiles\_suffix} fields below instead. Otherwise, use this field to specify the name of the single big file. \item \code{AGAPSfiles\_prefix}, \code{AGAPSfiles\_suffix}: [OPTIONAL] Omit these fields if you have one single big \term{source data file} for all the AGAPS masks and use the \code{AGAPSfiles\_name} field above instead. Otherwise, use these fields to specify the common prefix and suffix that need to be added to all the single sequence names (field \code{seqnames}) to get the name of the file that contains the corresponding AGAPS mask information. Default values are the empty prefix for \code{AGAPSfiles\_prefix} and \code{\_gap.txt} for \code{AGAPSfiles\_suffix}. \item \code{RMfiles\_name}, \code{RMfiles\_prefix}, \code{RMfiles\_suffix}: [OPTIONAL] Those fields work like the \code{AGAPSfiles*} fields above but for the RM masks. Default values are the empty prefix for \code{RMfiles\_prefix} and \texttt{.fa.out} for \code{RMfiles\_suffix}. \item \code{TRFfiles\_name}, \code{TRFfiles\_prefix}, \code{TRFfiles\_suffix}: [OPTIONAL] Those fields work like the \code{AGAPSfiles*} fields above but for the TRF masks. Default values are the empty prefix for \code{TRFfiles\_prefix} and \texttt{.bed} for \code{TRFfiles\_suffix}. \end{itemize} \subsubsection{An example} The \term{seed files} used for the packages forged by the Bioconductor project are included in the \Rpackage{BSgenome} package: <<>>= library(BSgenome) seed_files <- system.file("extdata", "GentlemanLab", package="BSgenome") tail(list.files(seed_files, pattern="\\.masked-seed$")) rn4_masked_seed <- list.files(seed_files, pattern="\\.rn4\\.masked-seed$", full.names=TRUE) cat(readLines(rn4_masked_seed), sep="\n") @ From now we assume that you have managed to prepare the \term{seed file} for the \term{2nd target package}. \subsection{Forge the \term{2nd target package}} To forge the package, start \R, make sure the \term{reference target package} is installed (try to load it), load the \Rpackage{BSgenome} package, and call the \Rfunction{forgeMaskedBSgenomeDataPkg} function on the \term{seed file} you made for the \term{2nd target package}. For example, if the path to your \term{seed file} is \texttt{"path/to/my/seed"}, do: <>= library(BSgenome) forgeMaskedBSgenomeDataPkg("path/to/my/seed") @ Depending on the size of the genome and your hardware, this can take between 2 minutes and 1 or 2 hours. By default \Rfunction{forgeMaskedBSgenomeDataPkg} will create the source tree of the \term{2nd target package} in the current directory. Once \Rfunction{forgeMaskedBSgenomeDataPkg} is done, ignore the warnings (if any), quit \R, and build the source package (tarball) with \begin{verbatim} R CMD build \end{verbatim} where \code{} is the path to the source tree of the package. Then check the package with \begin{verbatim} R CMD check \end{verbatim} where \code{} is the path to the tarball produced by \code{R CMD build}. Finally install the package with \begin{verbatim} R CMD INSTALL \end{verbatim} and use it! If you want to distribute this package, you need to distribute it with the \term{reference target package} since it depends on it. %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \section{Session information} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% The output in this vignette was produced under the following conditions: <<>>= sessionInfo() @ \end{document} BSgenome/vignettes/GenomeSearching.Rnw0000644000175400017540000006612413175713516021057 0ustar00biocbuildbiocbuild%\VignetteIndexEntry{Efficient genome searching with Biostrings and the BSgenome data packages} %\VignetteKeywords{BSgenome, genome, DNA, RNA, Sequence, Biostrings, Sequence alignment, SNPs} %\VignettePackage{BSgenome} % % NOTE -- ONLY EDIT THE .Rnw FILE!!! The .tex file is % likely to be overwritten. % \SweaveOpts{keep.source=TRUE} \documentclass[10pt]{article} %\usepackage{amsmath} %\usepackage[authoryear,round]{natbib} \usepackage{hyperref} \usepackage{underscore} \textwidth=6.5in \textheight=8.5in %\parskip=.3cm \oddsidemargin=.1in \evensidemargin=.1in \headheight=-.3in \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}} \bibliographystyle{plainnat} \begin{document} %\setkeys{Gin}{width=0.55\textwidth} \title{Efficient genome searching with Biostrings and the BSgenome data packages} \author{Herv\'e Pag\`es} \maketitle \tableofcontents % --------------------------------------------------------------------------- \section{The Biostrings-based genome data packages} The Bioconductor project provides data packages that contain the full genome sequences of a given organism. These packages are called {\it Biostrings-based genome data packages} because the sequences they contain are stored in some of the basic containers defined in the \Rpackage{Biostrings} package, like the \Rclass{DNAString}, the \Rclass{DNAStringSet} or the \Rclass{MaskedDNAString} containers. Regardless of the particular sequence data that they contain, all the Biostrings-based genome data packages are very similar and can be manipulated in a consistent and easy way. They all require the \Rpackage{BSgenome} package in order to work properly. This package, unlike the Biostrings-based genome data packages, is a software package that provides the infrastructure needed to support them (this is why the Biostrings-based genome data packages are also called {\it BSgenome data packages}). The \Rpackage{BSgenome} package itself requires the \Rpackage{Biostrings} package. See the man page for the \Rfunction{available.genomes} function (\Rfunction{?available.genomes}) for more information about how to get the list of all the BSgenome data packages currently available in your version of Bioconductor (you need an internet connection so that \Rfunction{available.genomes} can query the Bioconductor package repositories). More genomes can be added if necessary. Note that the process of making a BSgenome data package is not yet documented but you are welcome to ask for help on the bioc-devel mailing list (\url{http://bioconductor.org/docs/mailList.html}) if you need a genome that is not yet available. % --------------------------------------------------------------------------- \section{Finding an arbitrary nucleotide pattern in a chromosome} In this section we show how to find (or just count) the occurences of some arbitrary nucleotide pattern in a chromosome. The basic tool for this is the \Rfunction{matchPattern} (or \Rfunction{countPattern}) function from the \Rpackage{Biostrings} package. First we need to install and load the BSgenome data package for the organism that we want to look at. In our case, we want to search chromosome I of {\it Caenorhabditis elegans}. UCSC provides several versions of the C. elegans genome: ce1, ce2 and ce4. These versions correspond to different {\it releases} from WormBase, which are the WS100, WS120 and WS170 releases, respectively. See \url{http://genome.ucsc.edu/FAQ/FAQreleases#release1} for the list of all UCSC genome releases and for the correspondance between UCSC versions and release names. The BSgenome data package for the ce2 genome is \Rpackage{BSgenome.Celegans.UCSC.ce2}. Note that ce1 and ce4 are not available in Bioconductor but they could be added if there is demand for them. See \Rfunction{?available.genomes} for how to install \Rpackage{BSgenome.Celegans.UCSC.ce2}. Then load the package and display the single object defined in it: <>= library(BSgenome.Celegans.UCSC.ce2) ls("package:BSgenome.Celegans.UCSC.ce2") genome <- BSgenome.Celegans.UCSC.ce2 genome @ \Robject{genome} is a \Rclass{BSgenome} object: <>= class(genome) @ When displayed, some basic information about the origin of the genome is shown (organism, provider, provider version, etc...) followed by the index of {\it single} sequences and eventually an additional index of {\it multiple} sequences. Methods (adequately called {\it accessor methods}) are defined for individual access to this information: <>= organism(genome) provider(genome) providerVersion(genome) seqnames(genome) mseqnames(genome) @ See the man page for the \Rclass{BSgenome} class (\Rfunction{?BSgenome}) for a complete list of accessor methods and their descriptions. Now we are ready to display chromosome I: <>= genome$chrI @ Note that this chrI sequence corresponds to the {\it forward} strand (aka {\it direct} or {\it sense} or {\it positive} or {\it plus} strand) of chromosome I. UCSC, and genome providers in general, don't provide files containing the nucleotide sequence of the {\it reverse} strand (aka {\it indirect} or {\it antisense} or {\it negative} or {\it minus} or {\it opposite} strand) of the chromosomes because these sequences can be deduced from the {\it forward} sequences by taking their reverse complements. The BSgenome data packages are no exceptions: they only provide the {\it forward} strand sequence of every chromosome. See \Rfunction{?reverseComplement} for more details about the reverse complement of a \Rclass{DNAString} object. It is important to remember that, in practice, the {\it reverse} strand sequence is almost never needed. The reason is that, in fact, a {\it reverse} strand analysis can (and should) always be transposed into a {\it forward} strand analysis. Therefore trying to compute the {\it reverse} strand sequence of an entire chromosome by applying \Rfunction{reverseComplement} to its {\it forward} strand sequence is almost always a bad idea. See the {\it Finding an arbitrary nucleotide pattern in an entire genome} section of this document for how to find arbitrary patterns in the {\it reverse} strand of a chromosome. % It seems like this page http://www.medterms.com/script/main/art.asp?articlekey=20468 % is lying about the noncoding (or coding, they are in fact contradicting themselves) % nature of the sense and antisense strands. The number of bases in this sequence can be retrieved with: <>= chrI <- genome$chrI length(chrI) @ Some basic stats: <>= afI <- alphabetFrequency(chrI) afI sum(afI) == length(chrI) @ Count all {\it exact} matches of pattern \Robject{"ACCCAGGGC"}: <>= p1 <- "ACCCAGGGC" countPattern(p1, chrI) @ Like most pattern matching functions in \Rpackage{Biostrings}, the \Rfunction{countPattern} and \Rfunction{matchPattern} functions support {\it inexact} matching. One form of inexact matching is to allow a few mismatching letters per match. Here we allow at most one: <>= countPattern(p1, chrI, max.mismatch=1) @ With the \Rfunction{matchPattern} function, the locations of the matches are stored in an \Rclass{XStringViews} object: <>= m1 <- matchPattern(p1, chrI, max.mismatch=1) m1[4:6] class(m1) @ The \Rfunction{mismatch} function (new in \Rpackage{Biostrings}~2) returns the positions of the mismatching letters for each match: <>= mismatch(p1, m1[4:6]) @ Note: The \Rfunction{mismatch} method is in fact a particular case of a (vectorized) {\it alignment} function where only ``replacements'' are allowed. Current implementation is slow but this will be addressed. It may happen that a match is {\it out of limits} like in this example: <>= p2 <- DNAString("AAGCCTAAGCCTAAGCCTAA") m2 <- matchPattern(p2, chrI, max.mismatch=2) m2[1:4] p2 == m2[1:4] mismatch(p2, m2[1:4]) @ The list of exact matches and the list of inexact matches can both be obtained with: <>= m2[p2 == m2] m2[p2 != m2] @ Note that the length of \Robject{m2[p2 == m2]} should be equal to \Robject{countPattern(p2, chrI, max.mismatch=0)}. % --------------------------------------------------------------------------- \section{Finding an arbitrary nucleotide pattern in an entire genome} Now we want to extend our analysis to the {\it forward} and {\it reverse} strands of all the C. elegans chromosomes. More precisely, here is the analysis we want to perform: \begin{itemize} \item{The input dictionary: } Our input is a dictionary of 50 patterns. Each pattern is a short nucleotide sequence of 15 to 25 bases (As, Cs, Gs and Ts only, no Ns). It is stored in a FASTA file called \Robject{"ce2dict0.fa"}. % ce2dict0.fa was generated with % > set.seed(23) % > ce2dict0 <- sapply(1:50, function(i) { x <- genome[[sample(seqnames(genome), 1)]]; start <- as.integer(runif(1, min=1, length(x)-20)); end <- start + as.integer(runif(1, min=14, max=25)); x <- subXString(x, start, end); if (sample(1:2, 1) == 2) x <- reverseComplement(x); as.character(x) }) % > names(ce2dict0) <- paste("pattern", 1:50, sep="") % > write.XStringViews(XStringViews(ce2dict0, "DNAString"), file="ce2dict0.fa", format="fasta") See the {\it Finding all the patterns of a constant width dictionary in an entire genome} section of this document for a very efficient way to deal with the special case where all the patterns in the input dictionary have the same length. \item{The target: } Our target (or subject) is the {\it forward} and {\it reverse} strands of the seven C. elegans chromosomes (14 sequences in total). We want to find and report all occurences (or hits) of every pattern in the target. Note that a given pattern can have 0, 1 or several hits in 0, 1 or 2 strands of 0, 1 or several chromosomes. \item{Exact or inexact matching? } We are interested in exact matches only (for now). \item{The output: } We want to put the results of this analysis in a file so we can send it to our collaborators for some post analysis work. Our collaborators are not necessarily familiar with R or Bioconductor so dumping a high-level R object (like a list or a data frame) into an .rda file is not an option. For maximum portability (one of our collaborators wants to use Microsoft Excel for the post analysis) we choose to put our results in a tabulated file where one line describes one hit. The columns (or fields) of this file will be (in this order): \begin{itemize} \item{seqname: } the name of the chromosome where the hit occurs. \item{start: } an integer giving the starting position of the hit. \item{end: } an integer giving the ending position of the hit. \item{strand: } a plus (\Robject{+}) for a hit in the positive strand or a minus (\Robject{-}) for a hit in the negative strand. \item{patternID: } we use the unique ID provided for every pattern in the \Robject{"ce2dict0.fa"} file. \end{itemize} \end{itemize} Let's start by loading the input dictionary with: <>= ce2dict0_file <- system.file("extdata", "ce2dict0.fa", package="BSgenome") ce2dict0 <- readDNAStringSet(ce2dict0_file, "fasta") ce2dict0 @ Here is how we can write the functions that will perform our analysis: <>= writeHits <- function(seqname, matches, strand, file="", append=FALSE) { if (file.exists(file) && !append) warning("existing file ", file, " will be overwritten with 'append=FALSE'") if (!file.exists(file) && append) warning("new file ", file, " will have no header with 'append=TRUE'") hits <- data.frame(seqname=rep.int(seqname, length(matches)), start=start(matches), end=end(matches), strand=rep.int(strand, length(matches)), patternID=names(matches), check.names=FALSE) write.table(hits, file=file, append=append, quote=FALSE, sep="\t", row.names=FALSE, col.names=!append) } runAnalysis1 <- function(dict0, outfile="") { library(BSgenome.Celegans.UCSC.ce2) genome <- BSgenome.Celegans.UCSC.ce2 seqnames <- seqnames(genome) seqnames_in1string <- paste(seqnames, collapse=", ") cat("Target:", providerVersion(genome), "chromosomes", seqnames_in1string, "\n") append <- FALSE for (seqname in seqnames) { subject <- genome[[seqname]] cat(">>> Finding all hits in chromosome", seqname, "...\n") for (i in seq_len(length(dict0))) { patternID <- names(dict0)[i] pattern <- dict0[[i]] plus_matches <- matchPattern(pattern, subject) names(plus_matches) <- rep.int(patternID, length(plus_matches)) writeHits(seqname, plus_matches, "+", file=outfile, append=append) append <- TRUE rcpattern <- reverseComplement(pattern) minus_matches <- matchPattern(rcpattern, subject) names(minus_matches) <- rep.int(patternID, length(minus_matches)) writeHits(seqname, minus_matches, "-", file=outfile, append=append) } cat(">>> DONE\n") } } @ Some important notes about the implementation of the \Rfunction{runAnalysis1} function: \begin{itemize} \item{} \Robject{subject <- genome[[seqname]]} is the code that actually loads a chromosome sequence into memory. Using only one sequence at a time is a good practice to avoid memory allocation problems on a machine with a limited amount of memory. For example, loading all the human chromosome sequences in memory would require more than 3GB of memory! \item{} We have 2 nested \Robject{for} loops: the outer loop walks thru the target (7 chromosomes) and the inner loop walks thru the set of patterns. Doing the other way around would be very inefficient, especially with a bigger number of patterns because this would require to load each chromosome sequence into memory as many times as the number of patterns. \Rfunction{runAnalysis1} loads each sequence only once. \item{} We find the matches in the minus strand (\Robject{minus_matches}) by first taking the reverse complement of the current pattern (with \Robject{rcpattern <- reverseComplement(pattern)}) and NOT by taking the reverse complement of the current subject. \end{itemize} Now we are ready to run the analysis and put the results in the \Robject{"ce2dict0_ana1.txt"} file: <>= runAnalysis1(ce2dict0, outfile="ce2dict0_ana1.txt") @ Here is some very simple example of post analysis: \begin{itemize} \item{} Get the total number of hits: <>= hits1 <- read.table("ce2dict0_ana1.txt", header=TRUE) nrow(hits1) @ \item{} Get the number of hits per chromosome: <>= table(hits1$seqname) @ \item{} Get the number of hits per pattern: <>= hits1_table <- table(hits1$patternID) hits1_table @ \item{} Get the pattern(s) with the higher number of hits: <>= hits1_table[hits1_table == max(hits1_table)] # pattern(s) with more hits @ \item{} Get the pattern(s) with no hits: <>= setdiff(names(ce2dict0), hits1$patternID) # pattern(s) with no hits @ \item{} And finally a function that can be used to plot the hits: <>= plotGenomeHits <- function(bsgenome, seqnames, hits) { chrlengths <- seqlengths(bsgenome)[seqnames] XMAX <- max(chrlengths) YMAX <- length(seqnames) plot.new() plot.window(c(1, XMAX), c(0, YMAX)) axis(1) axis(2, at=seq_len(length(seqnames)), labels=rev(seqnames), tick=FALSE, las=1) ## Plot the chromosomes for (i in seq_len(length(seqnames))) lines(c(1, chrlengths[i]), c(YMAX + 1 - i, YMAX + 1 - i), type="l") ## Plot the hits for (i in seq_len(nrow(hits))) { seqname <- hits$seqname[i] y0 <- YMAX + 1 - match(seqname, seqnames) if (hits$strand[i] == "+") { y <- y0 + 0.05 col <- "red" } else { y <- y0 - 0.05 col <- "blue" } lines(c(hits$start[i], hits$end[i]), c(y, y), type="l", col=col, lwd=3) } } @ Plot the hits found by \Rfunction{runAnalysis1} with: <>= plotGenomeHits(genome, seqnames(genome), hits1) @ \end{itemize} % --------------------------------------------------------------------------- \section{Some precautions when using \Rmethod{matchPattern}} Improper use of \Rmethod{matchPattern} (or \Rmethod{countPattern}) can affect performance. If needed, the \Rmethod{matchPattern} and \Rmethod{countPattern} methods convert their first argument (the pattern) to an object of the same class than their second argument (the subject) before they pass it to the subroutine that actually implements the fast search algorithm. So if you need to reuse the same pattern a high number of times, it's a good idea to convert it {\it before} to pass it to the \Rmethod{matchPattern} or \Rmethod{countPattern} method. This way the conversion is done only once: <>= library(hgu95av2probe) tmpseq <- DNAStringSet(hgu95av2probe$sequence) someStats <- function(v) { GC <- DNAString("GC") CG <- DNAString("CG") sapply(seq_len(length(v)), function(i) { y <- v[[i]] c(alphabetFrequency(y)[1:4], GC=countPattern(GC, y), CG=countPattern(CG, y)) } ) } someStats(tmpseq[1:10]) @ % The above example is Raphael's use case discussed on BioC on Feb 2006. % In Biostrings 1, the equivalent would be: % src <- sapply(1:100, % function(i) { % paste(sample(c("A","C","G","T"), 25, replace=TRUE), % collapse="") % } % ) % tmpseq <- DNAString(src) % someStats <- function(v) % { % GC <- DNAString("GC") % CG <- DNAString("CG") % sapply(1:length(v), % function(i) { % y <- v[i] % c(alphabetFrequency(y)[2:5], % GC=length(matchDNAPattern(GC, y)), % CG=length(matchDNAPattern(CG, y))) % } % ) % } % someStats(tmpseq[1:10]) % --------------------------------------------------------------------------- \section{Masking the chromosome sequences} Starting with Bioconductor 2.2, the chromosome sequences in a {\it BSgenome data package} can have built-in masks. Starting with Bioconductor 2.3, there can be up to 4 built-in masks per sequence. These will always be (in this order): (1) the mask of assembly gaps, (2) the mask of intra-contig ambiguities, (3) the mask of repeat regions that were determined by the RepeatMasker software, and (4) the mask of repeat regions that were determined by the Tandem Repeats Finder software (where only repeats with period less than or equal to 12 were kept). For a given package, all the sequences will always have the same number of masks. <>= library(BSgenome.Hsapiens.UCSC.hg38.masked) genome <- BSgenome.Hsapiens.UCSC.hg38.masked chrY <- genome$chrY chrY chrM <- genome$chrM chrM @ The built-in masks are named consistenly across all the BSgenome data packages available in Bioconductor: \begin{table}[ht] \begin{center} \begin{tabular}{l|l|l|l} \hline Name & Active by default & Short description & Long description \\ \hline AGAPS & yes & assembly gaps & Masks the big N-blocks that have been placed between the contigs during the assembly. This mask is consistent with the Gap track from UCSC Genome Browser.\\ AMB & yes & intra-contig ambiguities & Masks any IUPAC ambiguity letter that was found in the contig regions of the original sequence. Note that only As, Cs, Gs and Ts remain unmasked when the AGAPS and AMB masks are both active (before SNPs are eventually injected, see below). \\ RM & no & RepeatMasker & Masks the repeat regions determined by the RepeatMasker software. This mask is consistent with the RepeatMasker track from UCSC Genome Browser. \\ TRF & no & Tandem Repeats Finder & Masks the tandem repeat regions that were determined by the Tandem Repeats Finder software (with period of 12 or less). \\ \hline \end{tabular} \end{center} \caption{The built-in masks provided by the BSgenome data packages.} \end{table} When displaying a masked sequence (here a \Rclass{MaskedDNAString} object), the {\it masked width} and {\it masked ratio} are reported for each individual mask, as well as for all the masks together, and for all the active masks together. The {\it masked width} is the total number of nucleotide positions that are masked and the {\it masked ratio} is the {\it masked width} divided by the length of the sequence. To activate a mask, use the \Rmethod{active} replacement method in conjonction with the \Rmethod{masks} method. For example, to activate the RepeatMasker mask, do: <>= active(masks(chrY))["RM"] <- TRUE chrY @ As you can see, the {\it masked width} for all the active masks together (i.e. the total number of nucleotide positions that are masked by at least one active mask) is now the same as for the first mask. This represents a {\it masked ratio} of about 83\%. Now when we use a function that is {\it mask aware}, like \Rfunction{alphabetFrequency}, the masked regions of the input sequence are ignored: <>= active(masks(chrY)) <- FALSE active(masks(chrY))["AGAPS"] <- TRUE alphabetFrequency(unmasked(chrY)) alphabetFrequency(chrY) @ This output indicates that, for this chromosome, the assembly gaps correspond exactly to the regions in the sequence that were filled with the letter N. Note that this is not always the case: sometimes Ns, and other IUPAC ambiguity letters, can be found inside the contigs. When coercing a \Rclass{MaskedXString} object to an \Rclass{XStringViews} object, each non-masked region in the original sequence is converted into a view on the sequence: <>= as(chrY, "XStringViews") @ This can be used in conjonction with the \Rmethod{gaps} method to see the gaps between the views i.e. the masked regions themselves: <>= gaps(as(chrY, "XStringViews")) @ To extract the sizes of the assembly gaps: <>= width(gaps(as(chrY, "XStringViews"))) @ Note that, if applied directly to \Robject{chrY}, \Rmethod{gaps} returns a \Rclass{MaskedDNAString} object with a single mask masking the regions that are not masked in the original object: <>= gaps(chrY) alphabetFrequency(gaps(chrY)) @ In fact, for any \Rclass{MaskedDNAString} object, the following should always be \Robject{TRUE}, whatever the masks are: <>= af0 <- alphabetFrequency(unmasked(chrY)) af1 <- alphabetFrequency(chrY) af2 <- alphabetFrequency(gaps(chrY)) all(af0 == af1 + af2) @ With all chrY masks active: <>= active(masks(chrY)) <- TRUE af1 <- alphabetFrequency(chrY) af1 gaps(chrY) af2 <- alphabetFrequency(gaps(chrY)) af2 all(af0 == af1 + af2) @ Now let's compare three different ways of finding all the occurences of the \Robject{"CANNTG"} consensus sequence in chrY. The Ns in this pattern need to be treated as wildcards i.e. they must match any letter in the subject. Without the mask feature, the first way to do it would be to use the \Robject{fixed=FALSE} option in the call to \Rfunction{matchPattern} (or \Rfunction{countPattern}): <>= Ebox <- "CANNTG" active(masks(chrY)) <- FALSE countPattern(Ebox, chrY, fixed=FALSE) @ The problem with this method is that the Ns in the subject are also treated as wildcards hence the abnormally high number of matches. A better method is to specify the {\it side} of the matching problem (i.e. {\it pattern} or {\it subject}) where the Ns should be treated as wildcards: <>= countPattern(Ebox, chrY, fixed=c(pattern=FALSE,subject=TRUE)) @ Finally, \Rfunction{countPattern} being {\it mask aware}, this can be achieved more efficiently by just masking the assembly gaps and ambiguities: <>= active(masks(chrY))[c("AGAPS", "AMB")] <- TRUE alphabetFrequency(chrY, baseOnly=TRUE) # no ambiguities countPattern(Ebox, chrY, fixed=FALSE) @ Note that some chromosomes can have Ns outside the assembly gaps: <>= chr2 <- genome$chr2 active(masks(chr2))[-2] <- FALSE alphabetFrequency(gaps(chr2)) @ so it is recommended to always keep the AMB mask active (in addition to the AGAPS mask) whatever the sequence is. Note that not all functions that work with an \Rclass{XString} input are {\it mask aware} but more will be added in the near future. However, most of the times there is a alternate way to exclude some arbitrary regions from an analysis without having to use {\it mask aware} functions. This is described below in the {\it Hard masking} section. % --------------------------------------------------------------------------- \section{Hard masking} coming soon... % --------------------------------------------------------------------------- \section{Injecting known SNPs in the chromosome sequences} coming soon... % --------------------------------------------------------------------------- \section{Finding all the patterns of a constant width dictionary in an entire genome} The \Rfunction{matchPDict} function can be used instead of \Rfunction{matchPattern} for the kind of analysis described in the {\it Finding an arbitrary nucleotide pattern in an entire genome} section but it will be much faster (between 100x and 10000x faster depending on the size of the input dictionary). Note that a current limitation of \Rfunction{matchPDict} is that it only works with a dictionary of DNA patterns where all the patterns have the same number of nucleotides (constant width dictionary). See \Rfunction{?matchPDict} for more information. Here is how our \Rfunction{runAnalysis1} function can be modified in order to use \Rfunction{matchPDict} instead of \Rfunction{matchPattern}: <>= runOneStrandAnalysis <- function(dict0, bsgenome, seqnames, strand, outfile="", append=FALSE) { cat("\nTarget: strand", strand, "of", providerVersion(bsgenome), "chromosomes", paste(seqnames, collapse=", "), "\n") if (strand == "-") dict0 <- reverseComplement(dict0) pdict <- PDict(dict0) for (seqname in seqnames) { subject <- bsgenome[[seqname]] cat(">>> Finding all hits in strand", strand, "of chromosome", seqname, "...\n") mindex <- matchPDict(pdict, subject) matches <- extractAllMatches(subject, mindex) writeHits(seqname, matches, strand, file=outfile, append=append) append <- TRUE cat(">>> DONE\n") } } runAnalysis2 <- function(dict0, outfile="") { library(BSgenome.Celegans.UCSC.ce2) genome <- BSgenome.Celegans.UCSC.ce2 seqnames <- seqnames(genome) runOneStrandAnalysis(dict0, genome, seqnames, "+", outfile=outfile, append=FALSE) runOneStrandAnalysis(dict0, genome, seqnames, "-", outfile=outfile, append=TRUE) } @ Remember that \Rfunction{matchPDict} only works if all the patterns in the input dictionary have the same length so for this 2nd analysis, we will truncate the patterns in \Robject{ce2dict0} to 15 nucleotides: <>= ce2dict0cw15 <- DNAStringSet(ce2dict0, end=15) @ Now we can run this 2nd analysis and put the results in the \Robject{"ce2dict0cw15_ana2.txt"} file: <>= runAnalysis2(ce2dict0cw15, outfile="ce2dict0cw15_ana2.txt") @ % --------------------------------------------------------------------------- \section{Session info} <>= sessionInfo() @ \end{document}

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