BSgenome/DESCRIPTION0000644000126300012640000000211312227133625015342 0ustar00biocbuildphs_compbioPackage: BSgenome Title: Infrastructure for Biostrings-based genome data packages Description: Infrastructure shared by all the Biostrings-based genome data packages Version: 1.30.0 Author: Herve Pages Maintainer: H. Pages biocViews: Genetics, Infrastructure, DataRepresentation, SequenceMatching, Annotation, SNP Depends: R (>= 2.8.0), methods, BiocGenerics (>= 0.1.2), IRanges (>= 1.13.6), GenomicRanges (>= 1.11.46), Biostrings (>= 2.23.3) Import: methods, BiocGenerics, IRanges, GenomicRanges, Biostrings Suggests: RUnit, BSgenome.Celegans.UCSC.ce2 (>= 1.3.11), BSgenome.Hsapiens.UCSC.hg19 (>= 1.3.11), SNPlocs.Hsapiens.dbSNP.20100427, hgu95av2probe, Biobase License: Artistic-2.0 LazyLoad: yes Collate: utils.R available.genomes.R GenomeDescription-class.R SNPlocs-class.R InjectSNPsHandler-class.R BSgenome-class.R injectSNPs.R getSeq-methods.R bsapply.R BSgenome-utils.R GenomeData-class.R GenomeDataList-class.R gdapply.R gdReduce.R BSgenomeForge.R Packaged: 2013-10-15 03:33:41 UTC; biocbuild BSgenome/NAMESPACE0000644000126300012640000000314612227064204015056 0ustar00biocbuildphs_compbioimport(methods) import(BiocGenerics) import(IRanges) import(GenomicRanges) import(Biostrings) exportClasses( GenomeDescription, SNPlocs, InjectSNPsHandler, BSgenome, GenomeData, GenomeDataList, ## BSgenomeForge classes: BSgenomeDataPkgSeed ) export( ## Non-generic functions: installed.genomes, available.genomes, GenomeDescription, newSNPlocs, BSgenome, installed.SNPs, available.SNPs, bsapply, GenomeData, GenomeDataList, ## Generic functions: organism, species, provider, providerVersion, releaseDate, releaseName, bsgenomeName, referenceGenome, compatibleGenomes, snpcount, snplocs, snpid2loc, snpid2alleles, snpid2grange, sourceUrl, SNPlocs, SNPlocs_pkgname, SNPcount, mseqnames, masknames, injectSNPs, gdapply, gdApply, gdReduce, gdreduce, ## BSgenomeForge functions: forgeSeqlengthsFile, forgeSeqFiles, forgeMasksFiles, forgeBSgenomeDataPkg ) exportMethods( ## Methods for generics defined elsewhere: names, show, length, "[[", "$", score, getSeq, matchPWM, countPWM, vmatchPattern, vcountPattern, ## Methods for generics defined in this package: organism, species, provider, providerVersion, releaseDate, releaseName, bsgenomeName, seqinfo, "seqinfo<-", seqnames, referenceGenome, compatibleGenomes, snpcount, snplocs, snpid2loc, snpid2alleles, snpid2grange, sourceUrl, SNPlocs, SNPlocs_pkgname, SNPcount, mseqnames, masknames, injectSNPs, gdapply, gdReduce, ## BSgenomeForge methods: forgeBSgenomeDataPkg ) BSgenome/NEWS0000644000126300012640000000076312227064204014340 0ustar00biocbuildphs_compbioCHANGES 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/0000755000126300012640000000000012227064177014045 5ustar00biocbuildphs_compbioBSgenome/R/BSgenome-class.R0000644000126300012640000004465412227064177017007 0ustar00biocbuildphs_compbio### ========================================================================= ### The "BSgenome" class ### ------------------------------------------------------------------------- setClass("BSgenome", contains="GenomeDescription", representation( ## source_url: permanent URL to the place where the FASTA files used ## to produce the sequences below 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", ## mseqnames: names of "multiple" sequences (e.g. upstream) mseqnames="character", ## where to find the serialized objects containing the sequences seqs_pkgname="character", seqs_dirpath="character", ## where to find the serialized objects containing the masks nmask_per_seq="integer", masks_pkgname="character", masks_dirpath="character", ## for SNPs injection injectSNPs_handler="InjectSNPsHandler", .seqs_cache="environment", .link_counts="environment" ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Low-level helper functions used for delayed-loading/caching/unloading the ### sequences. ### .getObjFilepath <- function(objname, objdir) { ## Should never happen. if (objdir == "") ## TODO: Put this kind of checking in a validity method for BSgenome ## objects (that's what validity methods are for). stop("internal anomaly: objdir is \"\"") filename <- paste(objname, ".rda", sep="") filepath <- file.path(objdir, filename) if (!file.exists(filepath)) stop("file '", filepath, "' doesn't exist") filepath } .loadSingleObject <- function(objname, objdir, objpkgname) { filepath <- .getObjFilepath(objname, objdir) tmp_env <- new.env(parent=emptyenv()) loaded_names <- load(filepath, envir=tmp_env) ## Check that we get only 1 object if (length(loaded_names) != 1L) stop("file '", filepath, "' contains 0 or more than 1 serialized object. ", "May be the ", objpkgname, " package is corrupted?") ## ... and that it has the expected name if (loaded_names != objname) stop("the serialized object in file '", filepath, "' ", "doesn't have the expected name. ", "May be the ", objpkgname, " package is corrupted?") ans <- get(objname, envir=tmp_env) ## TODO: This is temporary code to make temporarily broken BSgenome ## data packages work despite the big internal renaming I made in ## IRanges >= 1.3.76. Remove it after all the BSgenome data packages ## have been reforged. if (is(ans, "XString") || is(ans, "XStringSet")) ans <- updateObject(ans) return(ans) } ### 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") ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Accessor methods. ### setMethod("length", "BSgenome", function(x) length(names(x))) setGeneric("sourceUrl", function(x) standardGeneric("sourceUrl")) setMethod("sourceUrl", "BSgenome", function(x) x@source_url) 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) ) setGeneric("mseqnames", function(x) standardGeneric("mseqnames")) setMethod("mseqnames", "BSgenome", function(x) { if (length(x@mseqnames) == 0L) NULL else x@mseqnames } ) 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, force=FALSE, 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") if (!identical(force, FALSE)) stop("'force' 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 } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Constructor-like functions and generics ### .makeSeqinfo <- function(seqnames, circ_seqs, seqs_pkgname, seqs_dirpath, provider_version) { objname <- "seqlengths" seqlengths <- .loadSingleObject(objname, seqs_dirpath, seqs_pkgname) if (!identical(names(seqlengths), seqnames)) { filepath <- .getObjFilepath(objname, seqs_dirpath) stop("sequence names found in file '", filepath, "' are not ", "identical to 'seqnames'. ", "May be the ", seqs_pkgname, " package 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) } BSgenome <- function(organism, species, provider, provider_version, release_date, release_name, source_url, seqnames, circ_seqs=NA, mseqnames, seqs_pkgname, seqs_dirpath, nmask_per_seq, masks_pkgname, masks_dirpath) { seqinfo <- .makeSeqinfo(seqnames, circ_seqs, seqs_pkgname, seqs_dirpath, provider_version) user_seqnames <- seqnames(seqinfo) names(user_seqnames) <- user_seqnames if (is.null(mseqnames)) mseqnames <- character(0) new("BSgenome", GenomeDescription(organism, species, provider, provider_version, release_date, release_name, seqinfo), source_url=source_url, user_seqnames=user_seqnames, mseqnames=mseqnames, seqs_pkgname=seqs_pkgname, seqs_dirpath=seqs_dirpath, nmask_per_seq=as.integer(nmask_per_seq), masks_pkgname=masks_pkgname, masks_dirpath=masks_dirpath, .seqs_cache=new.env(parent=emptyenv()), .link_counts=new.env(parent=emptyenv()) ) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### 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)) showSequenceIndex <- function(names, prefix) { index_width <- getOption("width") + 2L - nchar(prefix) col_width <- max(nchar(names)) ncols <- index_width %/% (col_width + 2L) col <- 1L for (name in names) { if (col == 1L) cat(prefix) cat(format(name, width=col_width)) if (col == ncols) { cat("\n") col <- 1L } else { cat(" ") col <- col + 1L } } if (col != 1L) cat("\n") } if (!is.na(object@species)) { cat(object@species, "genome\n") cat(.SHOW_BSGENOME_PREFIX, "\n", sep="") } 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="") cat(.SHOW_BSGENOME_PREFIX, "\n", sep="") if (length(mseqnames(object)) != 0L) mystrwrap("single sequences (see '?seqnames'):") else mystrwrap("sequences (see '?seqnames'):") if (length(seqnames(object)) != 0L) showSequenceIndex(seqnames(object), .SHOW_SEQSECTION_PREFIX) else cat(.SHOW_SEQSECTION_PREFIX, "NONE\n", sep="") cat(.SHOW_BSGENOME_PREFIX, "\n", sep="") if (length(mseqnames(object)) != 0L) { mystrwrap("multiple sequences (see '?mseqnames'):") showSequenceIndex(mseqnames(object), .SHOW_SEQSECTION_PREFIX) cat(.SHOW_BSGENOME_PREFIX, "\n", sep="") } mystrwrap("(use the '$' or '[[' operator to access a given sequence)") } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Subsetting. ### .loadBSgenomeSequence <- function(objname, bsgenome, user_seqname) { seqs_pkgname <- bsgenome@seqs_pkgname seqs_dirpath <- bsgenome@seqs_dirpath nmask_per_seq <- length(masknames(bsgenome)) masks_pkgname <- bsgenome@masks_pkgname masks_dirpath <- bsgenome@masks_dirpath ans <- .loadSingleObject(objname, seqs_dirpath, seqs_pkgname) if (!is(ans, "XString")) return(ans) ## Check the length of the sequence if (length(ans) != seqlengths(bsgenome)[[user_seqname]]) { seq_filepath <- .getObjFilepath(objname, seqs_dirpath) stop("sequence found in file '", seq_filepath, "' does ", "not have the length reported by seqlengths(). ", "May be the ", seqs_pkgname, " package is corrupted?") } ## Inject the SNPs, if any snps <- SNPlocs(bsgenome, objname) if (!is.null(snps)) .inplaceReplaceLetterAt(ans, snps$loc, snps$alleles_as_ambig) ## Load and set the built-in masks, if any if (nmask_per_seq > 0L) { masks_objname <- paste(objname, ".masks", sep="") builtinmasks <- .loadSingleObject(masks_objname, masks_dirpath, masks_pkgname) if (length(builtinmasks) < nmask_per_seq) { masks_filepath <- .getObjFilepath(masks_objname, masks_dirpath) stop("expecting ", nmask_per_seq, " built-in masks per ", "single sequence, found only ", length(builtinmasks), " in file '", masks_filepath, "'. ", "May be the ", masks_pkgname, " package is corrupted?") } if (length(builtinmasks) > nmask_per_seq) builtinmasks <- builtinmasks[seq_len(nmask_per_seq)] if (!identical(names(builtinmasks), masknames(bsgenome))) { masks_filepath <- .getObjFilepath(masks_objname, masks_dirpath) stop("mask names found in file '", masks_filepath, "' are not ", "identical to the names returned by masknames(). ", "May be the ", masks_pkgname, " package is corrupted?") } masks(ans) <- builtinmasks } ans } .getBSgenomeSequence <- function(objname, bsgenome, user_seqname) { seqs_cache <- bsgenome@.seqs_cache ## Using the 'if (!exists()) assign(); get()' approach is NOT 100% ## reliable: ## ## if (!exists(objname, envir=seqs_cache, inherits=FALSE)) { ## ... ## assign(objname, ans, envir=seqs_cache) ## } ## get(objname, envir=seqs_cache, inherits=FALSE) ## ## because the symbol (objname) 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(objname, envir=seqs_cache, inherits=FALSE), silent=TRUE) if (is(ans, "try-error")) { ans <- .loadBSgenomeSequence(objname, bsgenome, user_seqname) if (getOption("verbose")) cat("caching ", objname, "\n", sep="") assign(objname, ans, envir=seqs_cache) } .linkToCachedObject(ans) <- .newLinkToCachedObject( objname, seqs_cache, bsgenome@.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)) { name <- try(match.arg(i, names(x)), silent=TRUE) if (is(name, "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") name <- names(x)[i] } ## Translate user-supplied sequence named back to original name. idx <- match(name, x@user_seqnames) if (is.na(idx)) { objname <- name } else { objname <- names(x@user_seqnames)[[idx]] } .getBSgenomeSequence(objname, x, name) } ) setReplaceMethod("[[", "BSgenome", function(x, i, j,..., value) { stop("attempt to modify the value of a \"BSgenome\" object") } ) setMethod("$", "BSgenome", function(x, name) x[[name]] ) BSgenome/R/BSgenome-utils.R0000644000126300012640000005431412227064177017034 0ustar00biocbuildphs_compbio## 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, asRangedData=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()) if (!missing(asRangedData)) { msg <- c("the 'asRangedData' argument is deprecated ", "and will be removed soon") .Deprecated(msg=msg) } if (asRangedData) { msg <- "using 'asRangedData=TRUE' is defunct" .Defunct(msg=msg) } 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(as.list(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(as.list(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), asRangedData=FALSE) { 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 <- elementLengths(posMatches) negMatches <- matchPDict(pdict = negPDict, subject = chr, max.mismatch = max.mismatch, min.mismatch = min.mismatch, fixed = fixed, algorithm = algorithm, verbose = verbose) negCounts <- elementLengths(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") if (!missing(asRangedData)) { msg <- c("the 'asRangedData' argument is deprecated ", "and will be removed soon") .Deprecated(msg=msg) } if (asRangedData) { msg <- "using 'asRangedData=TRUE' is defunct" .Defunct(msg=msg) } 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(as.list(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(as.list(counts)))) } ) ## matchPWM/countPWM for BSgenome setMethod("matchPWM", "BSgenome", function(pwm, subject, min.score="80%", exclude="", maskList=logical(0), asRangedData=FALSE) { 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) if (!missing(asRangedData)) { msg <- c("the 'asRangedData' argument is deprecated ", "and will be removed soon") .Deprecated(msg=msg) } if (asRangedData) { msg <- "using 'asRangedData=TRUE' is defunct" .Defunct(msg=msg) } 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(as.list(matches))) runValue(seqnames(matches)) <- nms ## create compact DNAStringSet string <- factor(elementMetadata(matches)[["string"]]) elementMetadata(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(as.list(counts)))) } ) setGeneric("vmatchLRPatterns", signature = "subject", function(Lpattern, Rpattern, max.gaplength, subject, max.Lmismatch=0, max.Rmismatch=0, with.Lindels=FALSE, with.Rindels=FALSE, Lfixed=TRUE, Rfixed=TRUE, ...) standardGeneric("vmatchLRPatterns")) setMethod("vmatchLRPatterns", "BSgenome", function(Lpattern, Rpattern, max.gaplength, subject, max.Lmismatch=0, max.Rmismatch=0, with.Lindels=FALSE, with.Rindels=FALSE, Lfixed=TRUE, Rfixed=TRUE, exclude = "", userMask = RangesList(), invertUserMask = FALSE) { matchFUN <- function(posLPattern, negLPattern, posRPattern, negRPattern, chr, max.gaplength, subject, max.Lmismatch, max.Rmismatch, with.Lindels, with.Rindels, Lfixed, Rfixed) { posMatches <- matchLRPatterns(posLPattern, posRPattern, max.gaplength, chr, max.Lmismatch, max.Rmismatch, with.Lindels, with.Rindels, Lfixed, Rfixed) negMatches <- IRanges() if (append(posLPattern, posRPattern) != append(negRPattern, negLPattern)) negMatches <- matchLRPatterns(negLPattern, negRPattern, max.gaplength, chr, max.Lmismatch, max.Rmismatch, with.Lindels, with.Rindels, Lfixed, Rfixed) strings <- c(as.character(posMatches), as.character(negMatches)) strand <- rep(c("+", "-"), c(length(posMatches), length(negMatches))) ord <- order(strand, strings) rngs <- c(as(posMatches, "IRanges"), as(negMatches, "IRanges")) RangedData(rngs[ord], string = Rle(strings[ord]), strand = Rle(strand[ord]), space = "1") } if (!is(Lpattern, "DNAString")) pattern <- DNAString(Lpattern) if (!is(Rpattern, "DNAString")) pattern <- DNAString(Rpattern) Lpattern <- Biostrings:::normargPattern(Lpattern, DNAStringSet()) Rpattern <- Biostrings:::normargPattern(Rpattern, DNAStringSet()) max.gaplength <- Biostrings:::normargMaxMismatch(max.gaplength) max.Lmismatch <- Biostrings:::normargMaxMismatch(max.Lmismatch) max.Rmismatch <- Biostrings:::normargMaxMismatch(max.Rmismatch) with.Lindels <- Biostrings:::normargWithIndels(with.Lindels) with.Rindels <- Biostrings:::normargWithIndels(with.Rindels) Lfixed <- Biostrings:::normargFixed(Lfixed, DNAStringSet()) Rfixed <- Biostrings:::normargFixed(Rfixed, DNAStringSet()) posLPattern <- Lpattern negLPattern <- reverseComplement(posLPattern) posRPattern <- Rpattern negRPattern <- reverseComplement(posRPattern) bsParams <- new("BSParams", X = subject, FUN = matchFUN, exclude = exclude, simplify = TRUE, userMask = userMask, invertUserMask = invertUserMask ) matches <- bsapply(bsParams, posLPattern = posLPattern, negLPattern = negLPattern, posRPattern = posRPattern, negRPattern = negRPattern, max.gaplength = max.gaplength, max.Lmismatch = max.Lmismatch, max.Rmismatch = max.Rmismatch, with.Lindels = with.Lindels, with.Rindels = with.Rindels, Lfixed = Lfixed, Rfixed = Rfixed) nms <- names(matches) matches <- do.call(c, unname(matches)) names(matches) <- nms matches } ) BSgenome/R/BSgenomeForge.R0000644000126300012640000005745412227064177016671 0ustar00biocbuildphs_compbio### ========================================================================= ### 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)) { missing_files <- paste(ans[!is_OK], collapse=", ") stop(missing_files, ": file(s) 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.info(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. ### .forgeSeqFile <- 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) } forgeSeqFiles <- function(seqnames, mseqnames=NULL, prefix="", suffix=".fa", seqs_srcdir=".", seqs_destdir=".", verbose=TRUE) { if (length(seqnames) == 0) { warning("'seqnames' is empty") } else { ## just for the side effect of checking the arguments getSeqSrcpaths(seqnames, prefix=prefix, suffix=suffix, seqs_srcdir=seqs_srcdir) } if (length(mseqnames) != 0) { if (!is.character(mseqnames)) stop("'mseqnames' must be a character vector (or NULL)") ## just for the side effect of checking the arguments getSeqSrcpaths(mseqnames, prefix=prefix, suffix=suffix, seqs_srcdir=seqs_srcdir) } if (!isSingleString(seqs_destdir)) stop("'seqs_destdir' must be a single string") for (name in seqnames) { .forgeSeqFile(name, prefix, suffix, seqs_srcdir, seqs_destdir, is.single.seq=TRUE, verbose=verbose) } for (name in mseqnames) { .forgeSeqFile(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=".", 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") ## Get the length of the sequence. seqfile <- file.path(seqs_destdir, paste(seqname, ".rda", sep="")) load(seqfile) seq <- get(seqname) 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) } remove(seq, list=seqname) 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=".", 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, 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" class and its low-level constructor. ### setClass( "BSgenomeDataPkgSeed", representation( Package="character", Title="character", Description="character", Version="character", Author="character", Maintainer="character", License="character", organism="character", species="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 nmask_per_seq="integer", # a single integer PkgDetails="character", SrcDataFiles1="character", SrcDataFiles2="character", PkgExamples="character", seqfiles_prefix="character", seqfiles_suffix="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 ", 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)" nmask_per_seq=0L, PkgDetails="", SrcDataFiles1="-- information not available --", SrcDataFiles2="", PkgExamples="", seqfiles_prefix="", seqfiles_suffix=".fa", 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) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The "forgeBSgenomeDataPkg" generic and methods. ### setGeneric("forgeBSgenomeDataPkg", signature="x", function(x, seqs_srcdir=".", masks_srcdir=".", destdir=".", verbose=TRUE) standardGeneric("forgeBSgenomeDataPkg") ) setMethod("forgeBSgenomeDataPkg", "BSgenomeDataPkgSeed", function(x, seqs_srcdir=".", masks_srcdir=".", destdir=".", verbose=TRUE) { require(Biobase) || stop("the Biobase package is required") template_path <- system.file("BSgenomeDataPkg-template", 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, LIC=x@License, ORGANISM=x@organism, SPECIES=x@species, 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=x@seqnames, CIRCSEQS=x@circ_seqs, MSEQNAMES=x@mseqnames, NMASKPERSEQ=as.character(x@nmask_per_seq), PKGDETAILS=x@PkgDetails, SRCDATAFILES1=x@SrcDataFiles1, SRCDATAFILES2=x@SrcDataFiles2, 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") } createPackage(x@Package, destdir, template_path, symvals) pkgdir <- file.path(destdir, x@Package) ## Just to avoid codetools "no visible binding" NOTEs .seqnames <- .mseqnames <- NULL .nmask_per_seq <- 0 ## Sourcing this file will set the values of the '.seqnames', ## '.mseqnames' and '.nmask_per_seq' variables source(file.path(pkgdir, "R", "zzz.R"), local=TRUE) ## Forge the "seqlengths.rda" file seqs_destdir <- file.path(pkgdir, "inst", "extdata") forgeSeqlengthsFile(.seqnames, prefix=x@seqfiles_prefix, suffix=x@seqfiles_suffix, seqs_srcdir=seqs_srcdir, seqs_destdir=seqs_destdir, verbose=verbose) ## Forge the sequence "*.rda" files forgeSeqFiles(.seqnames, mseqnames=.mseqnames, prefix=x@seqfiles_prefix, suffix=x@seqfiles_suffix, seqs_srcdir=seqs_srcdir, seqs_destdir=seqs_destdir, verbose=verbose) if (.nmask_per_seq > 0) { ## Forge the "*.masks.rda" files masks_destdir <- file.path(pkgdir, "inst", "extdata") forgeMasksFiles(.seqnames, .nmask_per_seq, seqs_destdir=seqs_destdir, 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("forgeBSgenomeDataPkg", "list", function(x, seqs_srcdir=".", masks_srcdir=".", destdir=".", verbose=TRUE) { y <- BSgenomeDataPkgSeed(x) forgeBSgenomeDataPkg(y, seqs_srcdir=seqs_srcdir, masks_srcdir=masks_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$isdir' or ## 'x[["isdir"]]' because it will fail if "isdir" is not a defined ## column isdir <- file.info(file)["isdir"][[1]] if (isdir) stop("'", file, "' is a directory, not a seed file") } else { file0 <- file seed_dir <- system.file("extdata", "GentlemanLab", package="BSgenome") file <- file.path(seed_dir, file) if (!file.exists(file)) { file <- paste(file, "-seed", sep="") if (!file.exists(file)) stop("seed file '", file0, "' not found") } if (verbose) cat("Seed file '", file0, "' not found, using file '", file, "'\n", sep="") } ans <- read.dcf2(file) # a character matrix if (nrow(ans) != 1) stop("seed file '", file, "' must have exactly 1 record") ans[1, , drop=TRUE] } setMethod("forgeBSgenomeDataPkg", "character", function(x, seqs_srcdir=".", masks_srcdir=".", destdir=".", verbose=TRUE) { y <- .readSeedFile(x, verbose=verbose) y <- as.list(y) if (missing(seqs_srcdir)) { seqs_srcdir <- y[["seqs_srcdir"]] if (is.null(seqs_srcdir)) stop("'seqs_srcdir' argument is missing, and the ", "'seqs_srcdir' field is missing in seed file") } if (missing(masks_srcdir) && !is.null(y[["masks_srcdir"]])) masks_srcdir <- y[["masks_srcdir"]] y <- y[!(names(y) %in% c("seqs_srcdir", "masks_srcdir"))] forgeBSgenomeDataPkg(y, seqs_srcdir=seqs_srcdir, masks_srcdir=masks_srcdir, destdir=destdir, verbose=verbose) } ) BSgenome/R/GenomeData-class.R0000644000126300012640000000656712227064177017315 0ustar00biocbuildphs_compbio## A container for data in the form of a list of chromosomes. Each ## sub-element can be anything setClass("GenomeData", contains = "SimpleList") ### FIXME: ideally there would be some sort of GenomeDescription ### object that encapsulates this information. For now, we store all ### the metadata fields in the SimpleList metadata list. ### At least that way, all the metadata is in one place. setMethod("providerVersion", "GenomeData", function(x) metadata(x)$providerVersion) setMethod("organism", "GenomeData", function(x) metadata(x)$organism) setMethod("provider", "GenomeData", function(x) metadata(x)$provider) GenomeData <- function(listData = list(), providerVersion = metadata[["providerVersion"]], organism = metadata[["organism"]], provider = metadata[["provider"]], metadata = list(), elementMetadata = NULL, ...) { if (!is.list(metadata)) stop("'metadata' must be a list") md <- list(organism = organism, provider = provider, providerVersion = providerVersion, ...) metadata[names(md)] <- md new("GenomeData", listData = listData, metadata = metadata, elementMetadata = elementMetadata) } setMethod("show", "GenomeData", function(object) { cat("A GenomeData instance") if (!is.null(organism(object))) cat(" for", organism(object)) if (!is.null(provider(object)) || !is.null(providerVersion(object))) { cat("\nbuild: ") if (!is.null(provider(object))) cat(provider(object), " ", sep = "") if (!is.null(providerVersion(object))) cat(providerVersion(object)) } cat("\n") nms <- names(object) if (is.null(nms)) nms <- seq_len(length(object)) cat(BiocGenerics:::labeledLine("chromosomes", nms)) }) setValidity("GenomeData", function(object) { org <- organism(object) prov <- provider(object) provVer <- providerVersion(object) if (!is.null(org) && !isSingleString(org)) "organism must be a single string or NULL" else if (!is.null(prov) && !isSingleString(prov)) "provider must be a single string or NULL" else if (!is.null(provVer) && !isSingleString(provVer)) "providerVersion must be a single string or NULL" else NULL }) ## coersion to data.frame methods setAs("GenomeData", "data.frame", function(from) { ind <- names(from) if (is.null(ind)) ind <- seq(length(from)) ans <- do.call(rbind, sapply(ind, function(chr) { cbind(as(from[[chr]], "data.frame"), chromosome = chr) }, simplify = FALSE)) row.names(ans) <- NULL ans }) ## seems common to store Ranges inside GenomeData, so tie into IRanges here setAs("GenomeData", "RangesList", function(from) { ans <- do.call("RangesList", lapply(from, as, "Ranges")) metadata(ans) <- metadata(from) universe(ans) <- providerVersion(from) ans }) setAs("GenomeData", "RangedData", function(from) { ans <- do.call("c", lapply(from, as, "RangedData")) names(ans) <- names(from) metadata(ans) <- metadata(from) universe(ans) <- providerVersion(from) ans }) BSgenome/R/GenomeDataList-class.R0000644000126300012640000000261312227064177020135 0ustar00biocbuildphs_compbio## Conceptually a list of GenomeData objects setClass("GenomeDataList", prototype = prototype(elementType = "GenomeData"), contains = "SimpleList") setValidity("GenomeDataList", function(object) { ## each element must be a "GenomeData" if (!identical(elementType(object), "GenomeData")) return("The elementType(object) is not 'GenomeData'") TRUE }) GenomeDataList <- function(listData = list(), metadata = list(), elementMetadata = NULL) { new("GenomeDataList", listData = listData, metadata = metadata, elementMetadata = elementMetadata) } setAs("GenomeDataList", "data.frame", function(from) { ind <- names(from) if (is.null(ind)) ind <- seq(length(from)) ans <- do.call(rbind, sapply(ind, function(sample) { cbind(as(from[[sample]], "data.frame"), sample = sample) }, simplify = FALSE)) row.names(ans) <- NULL ans }) setAs("GenomeDataList", "RangedDataList", function(from) { ans <- do.call(RangedDataList, lapply(from, as, "RangedData")) metadata(ans) <- metadata(from) elementMetadata(ans) <- elementMetadata(from) ans }) BSgenome/R/GenomeDescription-class.R0000644000126300012640000001137612227064177020721 0ustar00biocbuildphs_compbio### ========================================================================= ### The "GenomeDescription" class ### ------------------------------------------------------------------------- setClass("GenomeDescription", representation( ## organism: "Homo sapiens", "Mus musculus", etc... organism="character", ## species: "Human", "Mouse", etc... species="character", ## provider: "UCSC", "BDGP", etc... provider="character", ## provider_version: "hg18", "mm8", "sacCer1", etc... provider_version="character", ## release_date: "Mar. 2006", "Feb. 2006", "Oct. 2003", etc... release_date="character", ## release_name: "NCBI Build 36.1", "NCBI Build 36", ## "SGD 1 Oct 2003 sequence", etc... release_name="character", ## names, lengths, and circularity flags of the genome sequences seqinfo="Seqinfo" ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Accessor methods. ### setGeneric("organism", function(x) standardGeneric("organism")) setMethod("organism", "GenomeDescription", function(x) x@organism) setGeneric("species", function(x) standardGeneric("species")) setMethod("species", "GenomeDescription", function(x) x@species) setGeneric("provider", function(x) standardGeneric("provider")) setMethod("provider", "GenomeDescription", function(x) x@provider) setGeneric("providerVersion", function(x) standardGeneric("providerVersion")) setMethod("providerVersion", "GenomeDescription", function(x) x@provider_version) setGeneric("releaseDate", function(x) standardGeneric("releaseDate")) setMethod("releaseDate", "GenomeDescription", function(x) x@release_date) setGeneric("releaseName", function(x) standardGeneric("releaseName")) setMethod("releaseName", "GenomeDescription", function(x) x@release_name) setGeneric("bsgenomeName", function(x) standardGeneric("bsgenomeName")) setMethod("bsgenomeName", "GenomeDescription", function(x) { part1 <- "BSgenome" tmp <- strsplit(organism(x), " ", fixed=TRUE)[[1L]] part2 <- paste(substr(tmp[1L], start=1L, stop=1L), tmp[2L], sep="") part3 <- provider(x) part4 <- providerVersion(x) paste(part1, part2, part3, part4, sep=".") } ) setMethod("seqinfo", "GenomeDescription", function(x) x@seqinfo) setMethod("seqnames", "GenomeDescription", function(x) { ans <- seqnames(seqinfo(x)) if (length(ans) == 0L) ans <- NULL ans } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Validity. ### setValidity("GenomeDescription", function(object) { SINGLE_STRING_SLOTS <- setdiff(slotNames("GenomeDescription"), "seqinfo") .validSlot <- function(slotname) { slotval <- slot(object, slotname) if (isSingleStringOrNA(slotval)) return(NULL) problem <- paste("slot '", slotname, "' must be a ", "single string (or NA)", sep="") return(problem) } unlist(lapply(SINGLE_STRING_SLOTS, .validSlot)) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Constructor-like functions ### GenomeDescription <- function(organism, species, provider, provider_version, release_date, release_name, seqinfo) { if (identical(organism, "NA")) organism <- NA_character_ if (identical(species, "NA")) species <- NA_character_ if (identical(release_date, "NA")) release_date <- NA_character_ if (identical(release_name, "NA")) release_name <- NA_character_ new("GenomeDescription", organism=organism, species=species, provider=provider, provider_version=provider_version, release_date=release_date, release_name=release_name, seqinfo=seqinfo) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### The 'show' method ### showGenomeDescription <- function(x, margin="", print.seqlengths=FALSE) { cat(margin, "organism: ", organism(x), " (", species(x), ")\n", sep="") cat(margin, "provider: ", provider(x), "\n", sep="") cat(margin, "provider version: ", providerVersion(x), "\n", sep="") cat(margin, "release date: ", releaseDate(x), "\n", sep="") cat(margin, "release name: ", releaseName(x), "\n", sep="") if (print.seqlengths) { cat(margin, "---\n", sep="") GenomicRanges:::showSeqlengths(x, margin=margin) } } setMethod("show", "GenomeDescription", function(object) { showGenomeDescription(object, margin="| ", print.seqlengths=TRUE) } ) BSgenome/R/InjectSNPsHandler-class.R0000644000126300012640000001365412227064177020562 0ustar00biocbuildphs_compbio### ========================================================================= ### 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 } ### Calling this constructor has the side effect of loading the SNPlocs ### package! InjectSNPsHandler <- function(SNPlocs_pkgname, bsgenome_pkgname, bsgenome_seqnames) { if (!isSingleString(SNPlocs_pkgname)) stop("'SNPlocs_pkgname' must be a single string") library(SNPlocs_pkgname, character.only=TRUE) pkgenvir <- as.environment(paste("package", SNPlocs_pkgname, sep=":")) getSNPcount <- try(get("getSNPcount", envir=pkgenvir, inherits=FALSE), silent=TRUE) if (!is.function(getSNPcount)) stop("cannot use package ", 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 package ", SNPlocs_pkgname, " for SNP injection:\n", " it doesn't seem to define (and export) a function called ", "'getSNPlocs'") 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) } 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 } ) setGeneric("SNPcount", function(x) standardGeneric("SNPcount")) 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 } ) setGeneric("SNPlocs", signature="x", function(x, seqname) standardGeneric("SNPlocs")) 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/SNPlocs-class.R0000644000126300012640000003555512227064177016631 0ustar00biocbuildphs_compbio### ========================================================================= ### SNPlocs objects ### ------------------------------------------------------------------------- setClass("SNPlocs", representation( ## provider of the SNPs (e.g. "dbSNP") provider="character", ## creation date (in compact format) of the flat files found at ## download_url (look at 2nd line of each file e.g. ## CREATED ON: 2012-06-08 14:53, and use the most recent date in ## case of mixed dates, e.g. "20120608") 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 download_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", ## package name and absolute path to local directory where to find ## the serialized objects containing the SNPs data_pkgname="character", data_dirpath="character", data_serialized_objnames="character", .data_cache="environment" ) ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Constructor ### ### Not intended to be used directly. newSNPlocs <- function(provider, provider_version, release_date, release_name, download_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("SNPlocs", provider=provider, provider_version=provider_version, release_date=release_date, release_name=release_name, download_url=download_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())) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### 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(x) organism(referenceGenome(x))) setMethod("species", "SNPlocs", function(x) species(referenceGenome(x))) 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(class(object), " object for ", organism(object), " (", provider(object), " ", releaseName(object), ")\n", sep="") } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### snpcount() and snplocs() ### ### 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 } setGeneric("snpcount", function(x) standardGeneric("snpcount")) setMethod("snpcount", "SNPlocs", 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 } ) ### 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_rsid_offsets <- function(x) { offsets <- c(0L, cumsum(snpcount(x))) offsets <- offsets[-length(offsets)] names(offsets) <- names(snpcount(x)) offsets } ### 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] } ### 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 <- safeExplode(rawToChar(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 } setGeneric("snplocs", signature="x", function(x, seqname, ...) standardGeneric("snplocs") ) ### Returns a data frame (when 'as.GRanges=FALSE') or a GRanges object ### (when 'as.GRanges=TRUE'). setMethod("snplocs", "SNPlocs", 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) } ) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### snpid2loc(), snpid2alleles(), and snpid2grange() ### .normargSnpid <- function(snpid) { if (!is.vector(snpid)) stop("'snpid' must be an integer or character vector") if (IRanges:::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 (IRanges:::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("SNP id(s) not found: ", bad_snpid_in1string) } } seqidx <- findInterval(idx - 1L, cumsum(snpcount(x))) + 1L rowidx <- idx - .get_rsid_offsets(x)[seqidx] names(rowidx) <- names(snpcount(x))[seqidx] rowidx } ### 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") ) setMethod("snpid2loc", "SNPlocs", function(x, snpid, caching=TRUE) { snpid <- .normargSnpid(snpid) if (!isTRUEorFALSE(caching)) stop("'caching' must be TRUE or FALSE") 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 } ) ### 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") ) setMethod("snpid2alleles", "SNPlocs", function(x, snpid, caching=TRUE) { snpid <- .normargSnpid(snpid) if (!isTRUEorFALSE(caching)) stop("'caching' must be TRUE or FALSE") 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 <- safeExplode(rawToChar(ans)) names(ans) <- names(rowidx) ans } ) setGeneric("snpid2grange", signature="x", function(x, snpid, ...) standardGeneric("snpid2grange") ) setMethod("snpid2grange", "SNPlocs", function(x, snpid, caching=TRUE) { snpid <- .normargSnpid(snpid) if (!isTRUEorFALSE(caching)) stop("'caching' must be TRUE or FALSE") loc <- snpid2loc(x, snpid, caching=caching) alleles <- snpid2alleles(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)) } ) BSgenome/R/available.genomes.R0000644000126300012640000000353612227064177017553 0ustar00biocbuildphs_compbio.splitNameParts <- function(pkgs) { parts <- strsplit(pkgs, ".", fixed=TRUE) nparts <- elementLengths(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], stringsAsFactors=FALSE) } installed.genomes <- function(splitNameParts=FALSE) { if (!isTRUEorFALSE(splitNameParts)) stop("'splitNameParts' must be TRUE or FALSE") pkgs <- installed.packages()[ , "Package"] pkgs <- pkgs[substr(pkgs, 1, 9) == "BSgenome."] names(pkgs) <- NULL if (splitNameParts) pkgs <- .splitNameParts(pkgs) return(pkgs) } available.genomes <- function(splitNameParts=FALSE, type=getOption("pkgType")) { if (!isTRUEorFALSE(splitNameParts)) stop("'splitNameParts' must be TRUE or FALSE") url <- getDataAnnotationContribUrl(type) pkgs <- available.packages(url)[, "Package"] pkgs <- pkgs[substr(pkgs, 1, 9) == "BSgenome."] names(pkgs) <- NULL if (splitNameParts) pkgs <- .splitNameParts(pkgs) return(pkgs) } BSgenome/R/bsapply.R0000644000126300012640000000571312227064177015650 0ustar00biocbuildphs_compbiosetClass("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) if (BSParams@simplify) { sapply(seqnames, processSeqname, ...) } else { GenomeData(lapply(structure(seqnames, names = seqnames), processSeqname, ...), providerVersion = providerVersion(BSParams@X), organism = organism(BSParams@X), provider = provider(BSParams@X)) } } BSgenome/R/gdReduce.R0000644000126300012640000000320512227064177015712 0ustar00biocbuildphs_compbiogdreduce <- function(...) .Deprecated("gdReduce") setGeneric("gdReduce", function(f, ..., init, right=FALSE, accumulate=FALSE, gdArgs=list()) standardGeneric("gdReduce"), signature="...") setMethod(gdReduce, "GenomeDataList", function(f, ..., init, right=FALSE, accumulate=FALSE, gdArgs=list()) { args <- list(...) if (length(args) > 1L) stop("'...' must satisfy 'length(...) == 1' in\n ", "'gdReduce,GenomeDataList-method'") gdlist <- args[[1]] gdnames <- lapply(gdlist, names) nms <- unique(unlist(gdnames)) listData <- if (missing(init)) lapply(nms, function(nm) { ok <- sapply(gdnames, match, x=nm, nomatch=0L) > 0L Reduce(f, lapply(gdlist[ok], "[[", nm), right=right, accumulate=accumulate) }) else lapply(nms, function(nm) { ok <- sapply(gdnames, match, x=nm, nomatch=0L) > 0L Reduce(f, lapply(gdlist[ok], "[[", nm), init=init, right=right, accumulate=accumulate) }) names(listData) <- nms do.call(GenomeData, c(list(listData=listData), gdArgs)) }) setMethod(gdReduce, "GenomeData", function(f, ..., init, right=FALSE, accumulate=FALSE, gdArgs=list()) { if (missing(init)) gdReduce(f, GenomeDataList(list(...)), right=right, accumulate=accumulate, gdArgs=gdArgs) else gdReduce(f, GenomeDataList(list(...)), init=init, right=right, accumulate=accumulate, gdArgs=gdArgs) }) BSgenome/R/gdapply.R0000644000126300012640000000217012227064177015630 0ustar00biocbuildphs_compbio## An apply-type function for working with GenomeData and GenomeDataList objects: gdApply <- function(...) { msg <- "gdApply() is defunct. Use gdapply() instead [all lowercase]." .Defunct(msg=msg) } setGeneric("gdapply", function(X, FUN, ...) { standardGeneric("gdapply") }) setMethod("gdapply", signature(X = "GenomeDataList", FUN = "function"), function(X, FUN, ...) { new.elements <- lapply(X, gdapply, FUN, ...) cls <- lapply(new.elements, class) ucl <- unique(unlist(cls)) if (identical(ucl, "GenomeData")) GenomeDataList(new.elements, metadata(X)) else new.elements }) setMethod("gdapply", signature(X = "GenomeData", FUN = "function"), function(X, FUN, ...) { new.elements <- lapply(X, FUN, ...) cls <- lapply(new.elements, class) ucl <- unique(unlist(cls)) if (length(ucl) == 1) GenomeData(new.elements, metadata = metadata(X)) else new.elements }) BSgenome/R/getSeq-methods.R0000644000126300012640000003615712227064177017075 0ustar00biocbuildphs_compbio### ========================================================================= ### 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 <- IRanges:::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 <- IRanges:::recycleVector(names, max0123) start <- IRanges:::recycleVector(start, max0123) end <- IRanges:::recycleVector(end, max0123) width <- IRanges:::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), elementLengths(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, "RangedData")) { if ("strand" %in% colnames(x)) { if (!identical(strand, "+")) stop("'strand' cannot be specified when 'names' ", "is a RangedData object with a strand column") } else { strand <- Rle(strand(.normargStrand(strand, nrow(x)))) values(x) <- DataFrame(strand=strand) } return(as(x, "GRanges")) } 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'") } .dropUnusedGRangesSeqnamesLevels <- function(x) { ## There should be a better way to drop unused levels! seqnames <- as.character(seqnames(x)) GRanges(seqnames=seqnames, ranges=ranges(x), strand=strand(x), seqlengths=seqlengths(x)[unique(seqnames)]) } ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### .extractFromBSgenomeSingleSequences() ### .getSeqsFromDNAString <- function(subject, start, end, subject_is_circ, subject_name) { if (length(start) == 0L) return(DNAStringSet()) subject_len <- length(subject) if (is.na(subject_is_circ) || !subject_is_circ) { if (min(start) < 1L || max(end) > subject_len) stop("cannot extract DNA sequences beyond the ", "boundaries of non-circular chromosome \"", subject_name, "\"") return(DNAStringSet(subject, start=start, end=end)) } if (max(end - start) >= subject_len) stop("cannot extract DNA sequences that span more than ", "the total length of circular chromosome \"", subject_name, "\"") start0 <- start - 1L # 0-based start shift <- start0 %% subject_len - start0 L_start <- start + shift end1 <- end + shift L_end <- pmin(end1, subject_len) R_start <- 1L R_end <- pmax(end1, subject_len) - subject_len L_ans <- DNAStringSet(subject, start=L_start, end=L_end) R_ans <- DNAStringSet(subject, start=R_start, end=R_end) xscat(L_ans, R_ans) } ### Assumes 'ranges' and 'strand' have the same length and that this ### length is >= 1. Also assumes that 'strand' is star-free. .extractSeqsFromStrandedDNAString <- function(subject, ranges, strand, subject_is_circ, subject_name) { rglist <- split(unname(ranges), strand) plus_ranges <- rglist[["+"]] plus_dnaset <- .getSeqsFromDNAString(subject, start(plus_ranges), end(plus_ranges), subject_is_circ, subject_name) plus_dnaset <- xvcopy(plus_dnaset) minus_ranges <- rglist[["-"]] minus_dnaset <- .getSeqsFromDNAString(subject, start(minus_ranges), end(minus_ranges), subject_is_circ, subject_name) minus_dnaset <- reverseComplement(minus_dnaset) unsplit_list_of_XVectorList("DNAStringSet", list(plus_dnaset, minus_dnaset), as.factor(strand)) } ### '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)) { 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()) subject_name <- grl_seqlevels[i] subject <- x[[subject_name]] masks(subject) <- NULL subject_is_circ <- isCircular(x)[[subject_name]] .extractSeqsFromStrandedDNAString(subject, ranges(gr), strand(gr), subject_is_circ, subject_name) } ) ## "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, elementLengths(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 method for BSgenome 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=.dropUnusedGRangesSeqnamesLevels( 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 (as.character) ans <- as.character(ans) else if (length(ans) == 1L && is.character(names)) ans <- ans[[1L]] # turn 1st and unique element into DNAString ans } ) BSgenome/R/injectSNPs.R0000644000126300012640000000265712227064177016222 0ustar00biocbuildphs_compbio### ========================================================================= ### SNP injection ### ------------------------------------------------------------------------- installed.SNPs <- function() { pkgs <- installed.packages()[ , "Package"] pkgs <- pkgs[substr(pkgs, 1, 8) == "SNPlocs."] names(pkgs) <- NULL return(pkgs) } available.SNPs <- function(type=getOption("pkgType")) { url <- getDataAnnotationContribUrl(type) pkgs <- available.packages(url)[, "Package"] pkgs <- pkgs[substr(pkgs, 1, 8) == "SNPlocs."] names(pkgs) <- NULL return(pkgs) } setGeneric("injectSNPs", signature="x", function(x, SNPlocs_pkgname) standardGeneric("injectSNPs") ) setMethod("injectSNPs", "BSgenome", function(x, SNPlocs_pkgname) { 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(SNPlocs_pkgname, x@seqs_pkgname, seqnames(x@seqinfo)) ans@.seqs_cache <- new.env(parent=emptyenv()) ans@.link_counts <- new.env(parent=emptyenv()) ans } ) BSgenome/R/utils.R0000644000126300012640000000110412227064177015324 0ustar00biocbuildphs_compbio### ========================================================================= ### Some low-level internal (i.e. non-exported) utilities ### ------------------------------------------------------------------------- getDataAnnotationContribUrl <- function(type=getOption("pkgType")) { ## Just to avoid codetools "no visible binding" NOTE biocinstallRepos <- NULL ## Sourcing this file will define the 'biocinstallRepos' function suppressWarnings(source("http://bioconductor.org/biocLite.R", local=TRUE)) contrib.url(biocinstallRepos()["BioCann"], type=type) } BSgenome/TODO0000644000126300012640000000131512227064204014323 0ustar00biocbuildphs_compbio- RangesList - Make GenomicRanges() accept IRanges as 'start' parameter #+begin_src R library("GenomicFeatures") library("Rsamtools") library("BSgenome") st <- system.time bamFile <- "NA19239.SLX.maq.SRP000033.2009_09.subset.bam" tx <- loadFeatures("ucsc-human.sqlite") ## FIXME: need to align chromosome naming conventions. ## bam file uses "1" and tx db uses "chr1". ## ## one solution is: ## runValue(bigPat@unlistData@seqnames) <- ## paste("chr", runValue(bigPat@unlistData@seqnames), sep = "") ## st(bigTarget <- transcripts(tx)) ## or load serialized? st(bigPat <- readBAMasAlignments1(bamFile)) st(olaps <- findOverlaps(bigPat[1:500], bigTarget)) #+end_src BSgenome/build/0000755000126300012640000000000012227133625014736 5ustar00biocbuildphs_compbioBSgenome/build/vignette.rds0000644000126300012640000000052012227133625017272 0ustar00biocbuildphs_compbio‹}Q]Oƒ0íCFbüX|ïƒÏü7Dɲ M|m @#´5Ä7ù°@ïÜpøÐö~žsï雃š"C©¡Lc¡.KË.n¢¹z¯–AB¹È©/Ê„º[^ëÄâ¡ ””aÊxÒ¥Ž{oE¥ÀqÛŠ (IpAÂw’P]ûtÇ,d”K¬‹*@Æ5“)^2QÉR¹&<Â2¥§ñªÿ(¢xl6uÜ{1X ÿ¬ÞÂu}}?:xã–°zíÙÀ¢}Ã[ßA* Ÿ”‡2_WÁJÛ7§åì™ìlkŒÉØŽ’:¿ÒëÈ5T`’±„çê×`À`½Q?`¶OtlÆI¾ÿÀôY³&÷ޱñ|mN@ð3”G@o?Ó¯Z”Ñh^ŠÚ²óV÷ou5M³Nf¤‚‰ è´2ºq©ú•·û½­ÖYBSgenome/inst/0000755000126300012640000000000012227064200014604 5ustar00biocbuildphs_compbioBSgenome/inst/BSgenomeDataPkg-template/0000755000126300012640000000000012227064200021350 5ustar00biocbuildphs_compbioBSgenome/inst/BSgenomeDataPkg-template/DESCRIPTION0000644000126300012640000000070012227064200023053 0ustar00biocbuildphs_compbioPackage: @PKGNAME@ Title: @PKGTITLE@ Description: @PKGDESCRIPTION@ Version: @PKGVERSION@ Author: @AUTHOR@ Maintainer: @MAINTAINER@ Depends: BSgenome (>= @BSGENOMEVERSION@) Imports: BSgenome License: @LIC@ organism: @ORGANISM@ species: @SPECIES@ provider: @PROVIDER@ provider_version: @PROVIDERVERSION@ release_date: @RELEASEDATE@ release_name: @RELEASENAME@ source_url: @SOURCEURL@ biocViews: AnnotationData, Genetics, BSgenome, @ORGANISMBIOCVIEW@ BSgenome/inst/BSgenomeDataPkg-template/NAMESPACE0000644000126300012640000000046512227064200022574 0ustar00biocbuildphs_compbioimport(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/BSgenomeDataPkg-template/R/0000755000126300012640000000000012227064200021551 5ustar00biocbuildphs_compbioBSgenome/inst/BSgenomeDataPkg-template/R/zzz.R0000644000126300012640000000240412227064200022531 0ustar00biocbuildphs_compbio### ### .pkgname <- "@PKGNAME@" .seqnames <- @SEQNAMES@ .circ_seqs <- @CIRCSEQS@ .mseqnames <- @MSEQNAMES@ .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 BSgenome object. bsgenome <- BSgenome( organism="@ORGANISM@", species="@SPECIES@", 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, nmask_per_seq=.nmask_per_seq, masks_pkgname=pkgname, masks_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/BSgenomeDataPkg-template/inst/0000755000126300012640000000000012227064200022325 5ustar00biocbuildphs_compbioBSgenome/inst/BSgenomeDataPkg-template/inst/extdata/0000755000126300012640000000000012227064200023757 5ustar00biocbuildphs_compbioBSgenome/inst/BSgenomeDataPkg-template/man/0000755000126300012640000000000012227064200022123 5ustar00biocbuildphs_compbioBSgenome/inst/BSgenomeDataPkg-template/man/package.Rd0000644000126300012640000000324012227064200024004 0ustar00biocbuildphs_compbio\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{ @SRCDATAFILES1@ @SRCDATAFILES2@ } See \code{?\link[BSgenome]{BSgenomeForge}} and the BSgenomeForge vignette (\code{vignette("BSgenomeForge")}) in the BSgenome software package for how to make a BSgenome data package. } \author{@AUTHOR@} \seealso{ \link[BSgenome]{BSgenome-class}, \link[Biostrings]{DNAString-class}, \code{\link[BSgenome]{available.genomes}}, \link[BSgenome]{BSgenomeForge} } \examples{ @PKGNAME@ genome <- @PKGNAME@ 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/inst/doc/0000755000126300012640000000000012227133625015361 5ustar00biocbuildphs_compbioBSgenome/inst/doc/BSgenomeForge.R0000644000126300012640000000212612227133531020163 0ustar00biocbuildphs_compbio### R code from vignette source 'BSgenomeForge.Rnw' ################################################### ### code chunk number 1: BSgenomeForge.Rnw:162-165 ################################################### library(Biostrings) file <- system.file("extdata", "ce2chrM.fa", package="BSgenome") fasta.info(file) ################################################### ### code chunk number 2: BSgenomeForge.Rnw:494-499 ################################################### library(BSgenome) seed_files <- system.file("extdata", "GentlemanLab", package="BSgenome") list.files(seed_files, pattern="-seed$") rn4_seed <- list.files(seed_files, pattern="rn4", full.names=TRUE) cat(readLines(rn4_seed), sep="\n") ################################################### ### code chunk number 3: BSgenomeForge.Rnw:512-514 (eval = FALSE) ################################################### ## library(BSgenome) ## forgeBSgenomeDataPkg("path/to/my/seed") ################################################### ### code chunk number 4: BSgenomeForge.Rnw:545-546 ################################################### sessionInfo() BSgenome/inst/doc/BSgenomeForge.Rnw0000644000126300012640000005740412227064200020535 0ustar00biocbuildphs_compbio%\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} This document 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 your answer is 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 section of this document explains 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 document or about the BSgenomeForge functions are welcome. Please address them to the author (\code{hpages@fhcrc.org}) or post them on The Bioconductor Project Mailing List (\code{bioconductor@r-project.org}). Don't forget to visit the Bioconductor website \footnote{\url{http://bioconductor.org/}} and subscribe to this list if you've not already done so. In this document, we call \term{target package} the \term{BSgenome data package} that we want to forge. \section{Obtain and prepare the source data files} As mentioned earlier, there are 2 groups of \term{source data files}: (1) the files containing the sequence data (required), and (2) the files containing the mask data (optional). \subsection{Sequence data (group 1)} Group 1 must be FASTA files. You need 1 file per sequence that you want to put in the \term{target package}. The name of each 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 (eventually empty) that are the same for all the files. For example the FASTA files available at UCSC in the ``Data set by chromosome'' section for Stickleback (\url{http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/chromosomes/}) could already be considered to have names of this form (\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}). However, because the files will need to be uncompressed after download and before they can be used by the forging process, the suffix will need to be set to \texttt{.fa}, not \texttt{.fa.gz}. Also the prefix here is empty, not \texttt{chr}, because \texttt{chr} is considered to be part of the sequence names (a chromosome naming convention commonly used at UCSC). Note that, alternatively, you can download and extract the big \texttt{chromFa.tar.gz} tarball located in the ``Full data set'' section (aka the \textit{bigZips} folder) for Stickleback (\url{http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/bigZips/}): it should contain the same files as the ``Data set by chromosome'' folder. You can use the \Rfunction{fasta.info} function from the \Rpackage{Biostrings} package to see what's in a FASTA file: <<>>= library(Biostrings) file <- system.file("extdata", "ce2chrM.fa", package="BSgenome") fasta.info(file) @ \subsection{Mask data (group 2)} 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{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 (eventually 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. \subsection{An example} Here is how the \term{source data files} for the \Rpackage{BSgenome.Rnorvegicus.UCSC.rn4} package were obtained and prepared: \begin{itemize} \item Group 1: \begin{itemize} \item Single sequences: file \texttt{chromFa.tar.gz} was downloaded from the UCSC \textit{bigZips} folder \footnote{\url{http://hgdownload.cse.ucsc.edu/goldenPath/rn4/bigZips/}} for \code{rn4} and extracted with: \begin{verbatim} tar zxf chromFa.tar.gz \end{verbatim} \item Multiple sequences: files \texttt{upstream1000.fa.gz}, \texttt{upstream2000.fa.gz} and \texttt{upstream5000.fa.gz} were downloaded from the same \textit{bigZips} folder and uncompressed with: \begin{verbatim} for file in upstream*.fa.gz; do gunzip $file ; done \end{verbatim} \end{itemize} \item Group 2: \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} \end{itemize} \subsection{The \textit{} and \textit{} folders} From now we assume that you've downloaded (checking the md5sums is always a good idea), extracted, and eventually renamed all the \term{source data files}, and that they are located in the \textit{} folder for group 1 and in the \textit{} folder for group 2. Note that all the \term{source data files} should be located directly in the \textit{} and \textit{} folders, not in subfolders of these folders. 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 *}). \section{Prepare the BSgenome data package seed file} \subsection{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 those 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 2 first categories. \end{enumerate} The 3 following subsections give an extensive descriptions of all the valid fields of a \term{seed file}. Alternatively, the reader in a hurry can go directly to the last subsection of this section for an example of \term{seed file}. \subsection{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 names 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 package. E.g. \code{Rattus norvegicus full genome (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} section 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 package that you are going to forge, please pickup the license carefully and make sure that it is compatible with the license of the \term{source data files} if any. \end{itemize} \subsection{Non-standard \texttt{DESCRIPTION} fields} \begin{itemize} \item \code{organism}: The full name of the organism (e.g. \code{Rattus norvegicus}). \item \code{species}: The name of the species. 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{source 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{source data files} used to forge this 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} \subsection{Other fields} \begin{itemize} \item \code{BSgenomeObjname}: Should match part 2 of the package name (field \code{Package}). \item \code{seqnames}: 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). This must be a subset of the \code{seqnames} specified above. 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{paste("upstream", c("1000", "2000", "5000"), sep="")}. The default value for \code{mseqnames} is \code{NULL} (no multiple sequence). \item \code{nmask\_per\_seq}: [OPTIONAL] The number of masks per sequence (0 to 4). The default value for \code{nmask\_per\_seq} is \code{0} (no mask). \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{SrcDataFiles1}, \code{SrcDataFiles2}: [OPTIONAL] Some arbitrary text that will be copied to the \code{Note} section of the man pages of the \term{target package}. \code{SrcDataFiles1} should describe briefly where the \term{source data files} for the sequences are coming from. \code{SrcDataFiles2} should do the same for the masks. Permanent URLs are a must. \item \code{PkgExamples}: [OPTIONAL] Some {\R} code (eventually with comments) that will be added to the \code{Examples} section of the man page of the \term{target package}. \item \code{seqs\_srcdir}, \code{masks\_srcdir}: The path to the \textit{} and \textit{} folders, respectively. \item \code{seqfiles\_prefix}, \code{seqfiles\_suffix}: [OPTIONAL] 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{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} \subsection{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") list.files(seed_files, pattern="-seed$") rn4_seed <- list.files(seed_files, pattern="rn4", 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 package. \section{Forge the \term{target package}} To forge the 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}. 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################################################### ### code chunk number 2: b2 ################################################### class(Celegans) ################################################### ### code chunk number 3: b3 ################################################### organism(Celegans) provider(Celegans) providerVersion(Celegans) seqnames(Celegans) mseqnames(Celegans) ################################################### ### code chunk number 4: b4 ################################################### Celegans$chrI ################################################### ### code chunk number 5: b5 ################################################### chrI <- Celegans$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) seqnames <- seqnames(Celegans) seqnames_in1string <- paste(seqnames, collapse=", ") cat("Target:", providerVersion(Celegans), "chromosomes", seqnames_in1string, "\n") append <- FALSE for (seqname in seqnames) { subject <- Celegans[[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$end[i]), c(y, y), type="l", col=col, lwd=3) } } ################################################### ### code chunk number 22: c10 (eval = FALSE) ################################################### ## plotGenomeHits(Celegans, seqnames(Celegans), hits1) ################################################### ### code chunk number 23: d1 ################################################### library(hgu95av2probe) tmpseq <- DNAStringSet(hgu95av2probe$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.hg19) chrY <- Hsapiens$chrY chrY chrM <- Hsapiens$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 <- Hsapiens$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) seqnames <- seqnames(Celegans) runOneStrandAnalysis(dict0, Celegans, seqnames, "+", outfile=outfile, append=FALSE) runOneStrandAnalysis(dict0, Celegans, 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.Rnw0000644000126300012640000006573112227064200021113 0ustar00biocbuildphs_compbio%\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") Celegans @ \Robject{Celegans} is a \Rclass{BSgenome} object: <>= class(Celegans) @ 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(Celegans) provider(Celegans) providerVersion(Celegans) seqnames(Celegans) mseqnames(Celegans) @ 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: <>= Celegans$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 <- Celegans$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 <- Celegans[[sample(seqnames(Celegans), 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) seqnames <- seqnames(Celegans) seqnames_in1string <- paste(seqnames, collapse=", ") cat("Target:", providerVersion(Celegans), "chromosomes", seqnames_in1string, "\n") append <- FALSE for (seqname in seqnames) { subject <- Celegans[[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 <- Celegans[[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(Celegans, seqnames(Celegans), 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$sequence) someStats <- function(v) { GC <- DNAString("GC") CG <- DNAString("CG") sapply(seq_len(length(v)), function(i) { y <- v[[i]] c(alphabetFrequency(y)[1:4], GC=countPattern(GC, y), CG=countPattern(CG, y)) } ) } someStats(tmpseq[1:10]) @ % The above example is Raphael's use case discussed on BioC on Feb 2006. % In Biostrings 1, the equivalent would be: % src <- sapply(1:100, % function(i) { % paste(sample(c("A","C","G","T"), 25, replace=TRUE), % collapse="") % } % ) % tmpseq <- DNAString(src) % someStats <- function(v) % { % GC <- DNAString("GC") % CG <- DNAString("CG") % sapply(1:length(v), % function(i) { % y <- v[i] % c(alphabetFrequency(y)[2:5], % GC=length(matchDNAPattern(GC, y)), % CG=length(matchDNAPattern(CG, y))) % } % ) % } % someStats(tmpseq[1:10]) % --------------------------------------------------------------------------- \section{Masking the chromosome sequences} Starting with Bioconductor 2.2, the chromosome sequences in a {\it BSgenome data package} can have built-in masks. Starting with Bioconductor 2.3, there can be up to 4 built-in masks per sequence. These will always be (in this order): (1) the mask of assembly gaps, (2) the mask of intra-contig ambiguities, (3) the mask of repeat regions that were determined by the RepeatMasker software, and (4) the mask of repeat regions that were determined by the Tandem Repeats Finder software (where only repeats with period less than or equal to 12 were kept). For a given package, all the sequences will always have the same number of masks. <>= library(BSgenome.Hsapiens.UCSC.hg19) chrY <- Hsapiens$chrY chrY chrM <- Hsapiens$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 <- Hsapiens$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) seqnames <- seqnames(Celegans) runOneStrandAnalysis(dict0, Celegans, seqnames, "+", outfile=outfile, append=FALSE) runOneStrandAnalysis(dict0, Celegans, 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.pdf0000644000126300012640000063213112227133625021120 0ustar00biocbuildphs_compbio%PDF-1.4 %ÐÔÅØ 1 0 obj << /S /GoTo /D (section.1) >> endobj 4 0 obj (The Biostrings-based genome data packages) endobj 5 0 obj << /S /GoTo /D (section.2) >> endobj 8 0 obj (Finding an arbitrary nucleotide pattern in a chromosome) endobj 9 0 obj << /S /GoTo /D (section.3) 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5ustar00biocbuildphs_compbioBSgenome/inst/extdata/GentlemanLab/1000genomes/BSgenome.Hsapiens.1000g.b36female-seed0000644000126300012640000000166612227064202031142 0ustar00biocbuildphs_compbioPackage: BSgenome.Hsapiens.1000g.b36female Title: Full human_b36_female genome from the 1000 Genomes project Description: Full human_b36_female genome (from the 1000 Genomes project) stored in Biostrings objects. 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/0000755000126300012640000000000012227064202031426 5ustar00biocbuildphs_compbiosplit_human_b36_female.sh0000755000126300012640000000331312227064202036214 0ustar00biocbuildphs_compbioBSgenome/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.info("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 $1 > supercontigs.fa BSgenome/inst/extdata/GentlemanLab/BSgenome.Amellifera.BeeBase.assembly4-seed0000644000126300012640000000132612227064204030364 0ustar00biocbuildphs_compbioPackage: BSgenome.Amellifera.BeeBase.assembly4 Title: Apis mellifera (Honey Bee) full genome (BeeBase assembly4) Description: Apis mellifera (Honey Bee) full genome as provided by BeeBase (assembly4, Feb. 2008) and stored in Biostrings objects. Version: 1.3.19 organism: Apis mellifera species: Honey Bee provider: BeeBase provider_version: assembly4 release_date: Feb. 2008 release_name: assembly4 source_url: NA organism_biocview: Apis_mellifera BSgenomeObjname: Amellifera seqnames: paste("Group", 1:16, sep="") mseqnames: "GroupUn" nmask_per_seq: 0 PkgExamples: genome$Group1 # same as genome[["Group1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Amellifera.BeeBase.assembly4/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Amellifera.BeeBase.assembly4-tools/0000755000126300012640000000000012227064203030656 5ustar00biocbuildphs_compbioBSgenome/inst/extdata/GentlemanLab/BSgenome.Amellifera.BeeBase.assembly4-tools/NOTES.TXT0000644000126300012640000000204612227064203032151 0ustar00biocbuildphs_compbioGot 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.sh0000755000126300012640000000210212227064203034044 0ustar00biocbuildphs_compbio#!/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 $1 > GroupUn.fa BSgenome/inst/extdata/GentlemanLab/BSgenome.Amellifera.UCSC.apiMel2-seed0000644000126300012640000000230512227064204027217 0ustar00biocbuildphs_compbioPackage: BSgenome.Amellifera.UCSC.apiMel2 Title: Apis mellifera (Honey Bee) full genome (UCSC version apiMel2) Description: Apis mellifera (Honey Bee) full genome as provided by UCSC (apiMel2, Jan. 2005) and stored in Biostrings objects. Version: 1.3.19 organism: Apis mellifera species: Honey Bee provider: UCSC provider_version: apiMel2 release_date: Jan. 2005 release_name: Baylor College of Medicine HGSC v.Amel_2.0 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/apiMel2/bigZips/ organism_biocview: Apis_mellifera BSgenomeObjname: Amellifera seqnames: paste("Group", c(1:16, "Un"), sep="") nmask_per_seq: 3 SrcDataFiles1: sequences: http://hgdownload.cse.ucsc.edu/goldenPath/apiMel2/bigZips/GroupFa.zip SrcDataFiles2: AGAPS masks: http://hgdownload.cse.ucsc.edu/goldenPath/apiMel2/database/gap.txt.gz RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/apiMel2/bigZips/GroupOut.zip PkgExamples: genome$Group1 # same as genome[["Group1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Amellifera.UCSC.apiMel2/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Amellifera.UCSC.apiMel2/masks AGAPSfiles_name: gap.txt RMfiles_suffix: .out BSgenome/inst/extdata/GentlemanLab/BSgenome.Athaliana.TAIR.01222004-seed0000644000126300012640000000214612227064204026446 0ustar00biocbuildphs_compbioPackage: BSgenome.Athaliana.TAIR.01222004 Title: Arabidopsis thaliana full genome (TAIR version from January 22, 2004) Description: Arabidopsis thaliana full genome as provided by TAIR (snapshot from January 22, 2004) and stored in Biostrings objects. Version: 1.3.19 organism: Arabidopsis thaliana species: Arabidopsis provider: TAIR provider_version: 01222004 release_date: NA release_name: NA source_url: ftp://ftp.arabidopsis.org/home/tair/Sequences/whole_chromosomes/ organism_biocview: Arabidopsis_thaliana BSgenomeObjname: Athaliana seqnames: c("chr1", "chr2", "chr3", "chr4", "chr5", "mitochondria", "chloroplast") circ_seqs: c("mitochondria", "chloroplast") nmask_per_seq: 0 SrcDataFiles1: ATH1_chr1.1con.01222004 ATH1_chr2.1con.01222004 ATH1_chr3.1con.01222004 ATH1_chr4.1con.01222004 ATH1_chr5.1con.01222004 mitochondrial_genomic_sequence ATH1_chloroplast.1con.01072002 from ftp://ftp.arabidopsis.org/home/tair/Sequences/whole_chromosomes/OLD/ PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Athaliana.TAIR.01222004/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Athaliana.TAIR.04232008-seed0000644000126300012640000000232012227064204026450 0ustar00biocbuildphs_compbioPackage: BSgenome.Athaliana.TAIR.04232008 Title: Arabidopsis thaliana full genome (TAIR version from April 23, 2008) Description: Arabidopsis thaliana full genome as provided by TAIR (snapshot from April 23, 2008) and stored in Biostrings objects. Version: 1.3.19 organism: Arabidopsis thaliana species: Arabidopsis provider: TAIR provider_version: 04232008 release_date: NA release_name: dumped from ADB: Mar/14/08 source_url: ftp://ftp.arabidopsis.org/home/tair/Sequences/whole_chromosomes/ organism_biocview: Arabidopsis_thaliana BSgenomeObjname: Athaliana seqnames: paste("chr", c(1:5, "C", "M"), sep="") circ_seqs: c("chrC", "chrM") nmask_per_seq: 0 SrcDataFiles1: all the chr*.fas file from ftp://ftp.arabidopsis.org/home/tair/Sequences/whole_chromosomes/ WARNING: This is where things are today (Oct 1st, 2008) but is probably NOT aimed to be the permanent URL for the 04232008 snapshot of the genome. TAIR might update the content of this folder in the future with a new snapshot and move the 04232008 snapshot to the OLD/ subfolder. PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Athaliana.TAIR.04232008/seqs seqfiles_suffix: .fas BSgenome/inst/extdata/GentlemanLab/BSgenome.Athaliana.TAIR.TAIR9-seed0000644000126300012640000000170212227064204026401 0ustar00biocbuildphs_compbioPackage: BSgenome.Athaliana.TAIR.TAIR9 Title: Arabidopsis thaliana full genome (TAIR9) Description: Arabidopsis thaliana full genome 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: 1.3.19 organism: Arabidopsis thaliana species: 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") nmask_per_seq: 0 SrcDataFiles1: ftp://ftp.arabidopsis.org/home/tair/Genes/TAIR9_genome_release/TAIR9_chr_all.fas PkgExamples: genome$Chr1 # same as genome[["Chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Athaliana.TAIR.TAIR9/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Athaliana.TAIR.TAIR9-tools/0000755000126300012640000000000012227064204026676 5ustar00biocbuildphs_compbioBSgenome/inst/extdata/GentlemanLab/BSgenome.Athaliana.TAIR.TAIR9-tools/NOTES.TXT0000644000126300012640000001013412227064204030166 0ustar00biocbuildphs_compbioSequences ========= 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-seed0000644000126300012640000000250412227064204026633 0ustar00biocbuildphs_compbioPackage: BSgenome.Btaurus.UCSC.bosTau3 Title: Bos taurus (Cow) full genome (UCSC version bosTau3) Description: Bos taurus (Cow) full genome as provided by UCSC (bosTau3, Aug. 2006) and stored in Biostrings objects. Version: 1.3.19 organism: Bos taurus species: 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 seqnames: paste("chr", c(1:29, "X"), sep="") mseqnames: "chrUn.scaffolds" nmask_per_seq: 4 SrcDataFiles1: sequences: all the *.fa.gz files from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau3/chromosomes/ SrcDataFiles2: AGAPS masks: http://hgdownload.cse.ucsc.edu/goldenPath/bosTau3/database/gap.txt.gz RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/bosTau3/bigZips/bosTau3.fa.out.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/bosTau3/bigZips/bosTau3.trf.bed.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Btaurus.UCSC.bosTau3/seqs masks_srcdir: /shared/silo_researcher/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-seed0000644000126300012640000000275312227064204026642 0ustar00biocbuildphs_compbioPackage: BSgenome.Btaurus.UCSC.bosTau4 Title: Bos taurus (Cow) full genome (UCSC version bosTau4) Description: Bos taurus (Cow) full genome as provided by UCSC (bosTau4, Oct. 2007) and stored in Biostrings objects. Version: 1.3.19 organism: Bos taurus species: 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 seqnames: paste("chr", c(1:29, "X", "M"), sep="") circ_seqs: "chrM" mseqnames: c("chrUn.scaffolds", "upstream1000", "upstream2000", "upstream5000") nmask_per_seq: 4 SrcDataFiles1: sequences: all the *.fa.gz files from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau4/chromosomes/ + the upstream*.fa.gz files from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau4/bigZips/ SrcDataFiles2: AGAPS masks: http://hgdownload.cse.ucsc.edu/goldenPath/bosTau4/database/gap.txt.gz RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/bosTau4/bigZips/bosTau4.fa.out.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/bosTau4/bigZips/bosTau4.trf.bed.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Btaurus.UCSC.bosTau4/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Btaurus.UCSC.bosTau4/masks AGAPSfiles_name: gap.txt RMfiles_name: bosTau4.fa.out TRFfiles_name: bosTau4.trf.bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Btaurus.UCSC.bosTau6-seed0000644000126300012640000000270212227064204026636 0ustar00biocbuildphs_compbioPackage: BSgenome.Btaurus.UCSC.bosTau6 Title: Bos taurus (Cow) full genome (UCSC version bosTau6) Description: Bos taurus (Cow) full genome as provided by UCSC (bosTau6, Nov. 2009) and stored in Biostrings objects. Version: 1.3.19 organism: Bos taurus species: Cow provider: UCSC provider_version: bosTau6 release_date: Nov. 2009 release_name: University of Maryland v3.1 source_url: http://hgdownload.soe.ucsc.edu/goldenPath/bosTau6/bigZips/ organism_biocview: Bos_taurus BSgenomeObjname: Btaurus seqnames: paste("chr", c(1:29, "X", "M"), sep="") circ_seqs: "chrM" mseqnames: c("chrUn", "upstream1000", "upstream2000", "upstream5000") nmask_per_seq: 4 SrcDataFiles1: sequences: http://hgdownload.soe.ucsc.edu/goldenPath/bosTau6/bigZips/bosTau6.fa.gz + the upstream*.fa.gz files from http://hgdownload.cse.ucsc.edu/goldenPath/bosTau6/bigZips/ SrcDataFiles2: AGAPS masks: http://hgdownload.cse.ucsc.edu/goldenPath/bosTau6/database/gap.txt.gz RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/bosTau6/bigZips/bosTau6.fa.out.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/bosTau6/bigZips/bosTau6.trf.bed.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Btaurus.UCSC.bosTau6/seqs masks_srcdir: /shared/silo_researcher/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.bosTau6-tools/0000755000126300012640000000000012227064204027132 5ustar00biocbuildphs_compbioBSgenome/inst/extdata/GentlemanLab/BSgenome.Btaurus.UCSC.bosTau6-tools/splitbigfasta.R0000755000126300012640000000123312227064204032113 0ustar00biocbuildphs_compbio### 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.Celegans.UCSC.ce10-seed0000644000126300012640000000175512227064204026146 0ustar00biocbuildphs_compbioPackage: BSgenome.Celegans.UCSC.ce10 Title: Caenorhabditis elegans (Worm) full genome (UCSC version ce10) Description: Caenorhabditis elegans (Worm) full genome as provided by UCSC (ce10, Oct. 2010) and stored in Biostrings objects. Version: 1.3.19 organism: Caenorhabditis elegans species: 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" mseqnames: c("upstream1000", "upstream2000", "upstream5000") nmask_per_seq: 0 SrcDataFiles1: chromFa.tar.gz upstream1000.fa.gz upstream2000.fa.gz upstream5000.fa.gz from ftp://hgdownload.cse.ucsc.edu/goldenPath/ce10/bigZips/ PkgExamples: genome$chrI # same as genome[["chrI"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Celegans.UCSC.ce10/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Celegans.UCSC.ce2-seed0000644000126300012640000000173612227064204026066 0ustar00biocbuildphs_compbioPackage: BSgenome.Celegans.UCSC.ce2 Title: Caenorhabditis elegans (Worm) full genome (UCSC version ce2) Description: Caenorhabditis elegans (Worm) full genome as provided by UCSC (ce2, Mar. 2004) and stored in Biostrings objects. Version: 1.3.19 organism: Caenorhabditis elegans species: Worm provider: UCSC provider_version: ce2 release_date: Mar. 2004 release_name: WormBase v. WS120 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/ce2/bigZips/ organism_biocview: Caenorhabditis_elegans BSgenomeObjname: Celegans seqnames: paste("chr", c("I", "II", "III", "IV", "V", "X", "M"), sep="") circ_seqs: "chrM" mseqnames: c("upstream1000", "upstream2000", "upstream5000") nmask_per_seq: 0 SrcDataFiles1: chromFa.zip upstream1000.zip upstream2000.zip upstream5000.zip from http://hgdownload.cse.ucsc.edu/goldenPath/ce2/bigZips/ PkgExamples: genome$chrI # same as genome[["chrI"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Celegans.UCSC.ce2/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Celegans.UCSC.ce6-seed0000644000126300012640000000174412227064204026071 0ustar00biocbuildphs_compbioPackage: BSgenome.Celegans.UCSC.ce6 Title: Caenorhabditis elegans (Worm) full genome (UCSC version ce6) Description: Caenorhabditis elegans (Worm) full genome as provided by UCSC (ce6, May 2008) and stored in Biostrings objects. Version: 1.3.19 organism: Caenorhabditis elegans species: 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" mseqnames: c("upstream1000", "upstream2000", "upstream5000") nmask_per_seq: 0 SrcDataFiles1: chromFa.tar.gz upstream1000.fa.gz upstream2000.fa.gz upstream5000.fa.gz from ftp://hgdownload.cse.ucsc.edu/goldenPath/ce6/bigZips/ PkgExamples: genome$chrI # same as genome[["chrI"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Celegans.UCSC.ce6/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Cfamiliaris.UCSC.canFam2-seed0000644000126300012640000000242012227064204027355 0ustar00biocbuildphs_compbioPackage: BSgenome.Cfamiliaris.UCSC.canFam2 Title: Canis lupus familiaris full genome (UCSC version canFam2) Description: Canis lupus familiaris full genome as provided by UCSC (canFam2, May 2005) and stored in Biostrings objects. Version: 1.3.19 organism: Canis lupus familiaris species: Dog provider: UCSC provider_version: canFam2 release_date: May 2005 release_name: Broad Institute v2.0 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/canFam2/bigZips/ organism_biocview: Canis_familiaris BSgenomeObjname: Cfamiliaris seqnames: paste("chr", c(1:38, "X", "M", "Un"), sep="") circ_seqs: "chrM" nmask_per_seq: 4 SrcDataFiles1: sequences: chromFa.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/canFam2/bigZips/ SrcDataFiles2: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/canFam2/database/ RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/canFam2/bigZips/chromOut.tar.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/canFam2/bigZips/chromTrf.tar.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Cfamiliaris.UCSC.canFam2/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Cfamiliaris.UCSC.canFam2/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Cfamiliaris.UCSC.canFam3-seed0000644000126300012640000000270312227064204027362 0ustar00biocbuildphs_compbioPackage: BSgenome.Cfamiliaris.UCSC.canFam3 Title: Canis lupus familiaris (Dog) full genome (UCSC version canFam3) Description: Canis lupus familiaris (Dog) full genome as provided by UCSC (canFam3, Sep. 2011) and stored in Biostrings objects. Version: 1.3.19 organism: Canis lupus familiaris species: 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: c("chrUn", paste("upstream", c("1000", "2000", "5000"), sep="")) nmask_per_seq: 4 SrcDataFiles1: sequences: canFam3.fa.gz and the upstream*.fa.gz files from http://hgdownload.cse.ucsc.edu/goldenPath/canFam3/bigZips/ SrcDataFiles2: AGAPS masks: http://hgdownload.cse.ucsc.edu/goldenPath/canFam3/database/gap.txt.gz RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/canFam3/bigZips/canFam3.fa.out.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/canFam3/bigZips/canFam3.trf.bed.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Cfamiliaris.UCSC.canFam3/seqs masks_srcdir: /shared/silo_researcher/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.Cfamiliaris.UCSC.canFam3-tools/0000755000126300012640000000000012227064203027654 5ustar00biocbuildphs_compbioBSgenome/inst/extdata/GentlemanLab/BSgenome.Cfamiliaris.UCSC.canFam3-tools/splitbigfasta.R0000755000126300012640000000123312227064203032635 0ustar00biocbuildphs_compbio### 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.Dmelanogaster.UCSC.dm2-seed0000644000126300012640000000264712227064204027145 0ustar00biocbuildphs_compbioPackage: BSgenome.Dmelanogaster.UCSC.dm2 Title: Drosophila melanogaster (Fly) full genome (UCSC version dm2) Description: Drosophila melanogaster (Fly) full genome as provided by UCSC (dm2, Apr. 2004) and stored in Biostrings objects. Version: 1.3.19 organism: Drosophila melanogaster species: 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" mseqnames: paste("upstream", c("1000", "2000", "5000"), sep="") nmask_per_seq: 4 SrcDataFiles1: sequences: chromFa.zip, upstream1000.fa.gz, upstream2000.fa.gz, upstream5000.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/dm2/bigZips/ SrcDataFiles2: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/dm2/database/ RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/dm2/bigZips/chromOut.zip TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/dm2/bigZips/chromTrf.zip PkgExamples: genome$chr2L # same as genome[["chr2L"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Dmelanogaster.UCSC.dm2/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Dmelanogaster.UCSC.dm2/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Dmelanogaster.UCSC.dm3-seed0000644000126300012640000000271512227064204027142 0ustar00biocbuildphs_compbioPackage: BSgenome.Dmelanogaster.UCSC.dm3 Title: Drosophila melanogaster (Fly) full genome (UCSC version dm3) Description: Drosophila melanogaster (Fly) full genome as provided by UCSC (dm3, Apr. 2006) and stored in Biostrings objects. Version: 1.3.19 organism: Drosophila melanogaster species: 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" mseqnames: c("upstream1000", "upstream2000", "upstream5000") nmask_per_seq: 4 SrcDataFiles1: sequences: chromFa.tar.gz, upstream1000.fa.gz, upstream2000.fa.gz, upstream5000.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/dm3/bigZips/ SrcDataFiles2: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/dm3/database/ RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/dm3/bigZips/chromOut.tar.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/dm3/bigZips/chromTrf.tar.gz PkgExamples: genome$chr2L # same as genome[["chr2L"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Dmelanogaster.UCSC.dm3/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Dmelanogaster.UCSC.dm3/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer5-seed0000644000126300012640000000271612227064204026417 0ustar00biocbuildphs_compbioPackage: BSgenome.Drerio.UCSC.danRer5 Title: Danio rerio (Zebrafish) full genome (UCSC version danRer5) Description: Danio rerio (Zebrafish) full genome as provided by UCSC (danRer5, Jul. 2007) and stored in Biostrings objects. Version: 1.3.19 organism: Danio rerio species: Zebrafish provider: UCSC provider_version: danRer5 release_date: Jul. 2007 release_name: Sanger Institute Zv7 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/danRer5/bigZips/ organism_biocview: Danio_rerio BSgenomeObjname: Drerio seqnames: paste("chr", c(1:25, "M"), sep="") circ_seqs: "chrM" mseqnames: c("Zv7_NA", "Zv7_scaffold", paste("upstream", c("1000", "2000", "5000"), sep="")) nmask_per_seq: 4 SrcDataFiles1: sequences: danRer5.fa.gz, upstream1000.fa.gz, upstream2000.fa.gz and upstream5000.fa.gz files from http://hgdownload.cse.ucsc.edu/goldenPath/danRer5/bigZips/ SrcDataFiles2: AGAPS masks: http://hgdownload.cse.ucsc.edu/goldenPath/danRer5/database/gap.txt.gz RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/danRer5/bigZips/danRer5.fa.out.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/danRer5/bigZips/danRer5.trf.bed.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Drerio.UCSC.danRer5/seqs masks_srcdir: /shared/silo_researcher/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.danRer5-tools/0000755000126300012640000000000012227064202026704 5ustar00biocbuildphs_compbioBSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer5-tools/NOTES.TXT0000644000126300012640000000034512227064202030177 0ustar00biocbuildphs_compbioDownloaded 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.sh0000755000126300012640000000352512227064202032104 0ustar00biocbuildphs_compbio#!/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.info("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 $1 | tail -n 916263 > Zv7_scaffold.fa BSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer6-seed0000644000126300012640000000271612227064204026420 0ustar00biocbuildphs_compbioPackage: BSgenome.Drerio.UCSC.danRer6 Title: Danio rerio (Zebrafish) full genome (UCSC version danRer6) Description: Danio rerio (Zebrafish) full genome as provided by UCSC (danRer6, Dec. 2008) and stored in Biostrings objects. Version: 1.3.19 organism: Danio rerio species: Zebrafish provider: UCSC provider_version: danRer6 release_date: Dec. 2008 release_name: Sanger Institute Zv8 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/danRer6/bigZips/ organism_biocview: Danio_rerio BSgenomeObjname: Drerio seqnames: paste("chr", c(1:25, "M"), sep="") circ_seqs: "chrM" mseqnames: c("Zv8_NA", "Zv8_scaffold", paste("upstream", c("1000", "2000", "5000"), sep="")) nmask_per_seq: 4 SrcDataFiles1: sequences: danRer6.fa.gz, upstream1000.fa.gz, upstream2000.fa.gz and upstream5000.fa.gz files from http://hgdownload.cse.ucsc.edu/goldenPath/danRer6/bigZips/ SrcDataFiles2: AGAPS masks: http://hgdownload.cse.ucsc.edu/goldenPath/danRer6/database/gap.txt.gz RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/danRer6/bigZips/danRer6.fa.out.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/danRer6/bigZips/danRer6.trf.bed.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Drerio.UCSC.danRer6/seqs masks_srcdir: /shared/silo_researcher/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.danRer6-tools/0000755000126300012640000000000012227064202026705 5ustar00biocbuildphs_compbioBSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer6-tools/NOTES.TXT0000644000126300012640000000034612227064202030201 0ustar00biocbuildphs_compbioDownloaded 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.R0000755000126300012640000000213112227064202031664 0ustar00biocbuildphs_compbio### 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.danRer7-seed0000644000126300012640000000270712227064204026421 0ustar00biocbuildphs_compbioPackage: BSgenome.Drerio.UCSC.danRer7 Title: Danio rerio (Zebrafish) full genome (UCSC version danRer7) Description: Danio rerio (Zebrafish) full genome as provided by UCSC (danRer7, Jul. 2010) and stored in Biostrings objects. Version: 1.3.19 organism: Danio rerio species: 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", paste("upstream", c("1000", "2000", "5000"), sep="")) nmask_per_seq: 4 SrcDataFiles1: sequences: danRer7.fa.gz, upstream1000.fa.gz, upstream2000.fa.gz and upstream5000.fa.gz files from http://hgdownload.cse.ucsc.edu/goldenPath/danRer7/bigZips/ SrcDataFiles2: AGAPS masks: http://hgdownload.cse.ucsc.edu/goldenPath/danRer7/database/gap.txt.gz RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/danRer7/bigZips/danRer7.fa.out.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/danRer7/bigZips/danRer7.trf.bed.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Drerio.UCSC.danRer7/seqs masks_srcdir: /shared/silo_researcher/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.Drerio.UCSC.danRer7-tools/0000755000126300012640000000000012227064203026707 5ustar00biocbuildphs_compbioBSgenome/inst/extdata/GentlemanLab/BSgenome.Drerio.UCSC.danRer7-tools/NOTES.TXT0000644000126300012640000000034312227064203030200 0ustar00biocbuildphs_compbioDownloaded 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.R0000755000126300012640000000213112227064203031666 0ustar00biocbuildphs_compbio### 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.Ecoli.NCBI.20080805-seed0000644000126300012640000001533412227064204025612 0ustar00biocbuildphs_compbioPackage: 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: 1.3.19 organism: Escherichia coli species: 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") nmask_per_seq: 0 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 }} } SrcDataFiles1: 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: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Ecoli.NCBI.20080805/seqs seqfiles_suffix: .fna BSgenome/inst/extdata/GentlemanLab/BSgenome.Gaculeatus.UCSC.gasAcu1-seed0000644000126300012640000000307112227064204027247 0ustar00biocbuildphs_compbioPackage: BSgenome.Gaculeatus.UCSC.gasAcu1 Title: Gasterosteus aculeatus (Stickleback) full genome (UCSC version gasAcu1) Description: Gasterosteus aculeatus (Stickleback) full genome as provided by UCSC (gasAcu1, Feb. 2006) and stored in Biostrings objects. Version: 1.3.19 organism: Gasterosteus aculeatus species: 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" mseqnames: paste("upstream", c("1000", "2000", "5000"), sep="") nmask_per_seq: 4 SrcDataFiles1: sequences: chromFa.tar.gz + upstream*.fa.gz files from http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/bigZips/ SrcDataFiles2: AGAPS masks: http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/database/gap.txt.gz RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/bigZips/chromOut.tar.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/gasAcu1/bigZips/chromTrf.tar.gz PkgExamples: genome$chrI # same as genome[["chrI"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Gaculeatus.UCSC.gasAcu1/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Gaculeatus.UCSC.gasAcu1/masks AGAPSfiles_name: gap.txt RMfiles_suffix: .fa.out TRFfiles_suffix: .bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Ggallus.UCSC.galGal3-seed0000644000126300012640000000300712227064204026535 0ustar00biocbuildphs_compbioPackage: BSgenome.Ggallus.UCSC.galGal3 Title: Gallus gallus (Chicken) full genome (UCSC version galGal3) Description: Gallus gallus (Chicken) full genome as provided by UCSC (galGal3, May 2006) and stored in Biostrings objects. Version: 1.3.19 organism: Gallus gallus species: Chicken provider: UCSC provider_version: galGal3 release_date: May 2006 release_name: WUSTL Gallus-gallus-2.1 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/galGal3/bigZips/ organism_biocview: Gallus_gallus BSgenomeObjname: Ggallus seqnames: paste("chr", c(1:28, 32, "M", "W", "Z", "E64", "E22C19W28_E50C23", paste(c(1:2, 4:8, 10:13, 16:18, 20, 22, 25, 28, "W", "Z", "E64", "E22C19W28_E50C23", "Un"), "_random", sep="")), sep="") circ_seqs: "chrM" mseqnames: paste("upstream", c("1000", "2000", "5000"), sep="") nmask_per_seq: 4 SrcDataFiles1: sequences: chromFa.tar.gz, upstream1000.fa.gz, upstream2000.fa.gz, upstream5000.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/galGal3/bigZips/ SrcDataFiles2: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/galGal3/database/ RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/galGal3/bigZips/chromOut.tar.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/galGal3/bigZips/chromTrf.tar.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Ggallus.UCSC.galGal3/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Ggallus.UCSC.galGal3/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Ggallus.UCSC.galGal4-seed0000644000126300012640000000276412227064204026547 0ustar00biocbuildphs_compbioPackage: BSgenome.Ggallus.UCSC.galGal4 Title: Gallus gallus (Chicken) full genome (UCSC version galGal4) Description: Gallus gallus (Chicken) full genome as provided by UCSC (galGal4, Nov. 2011) and stored in Biostrings objects. Version: 1.3.19 organism: Gallus gallus species: 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", paste("upstream", c("1000", "2000", "5000"), sep="")) nmask_per_seq: 4 SrcDataFiles1: sequences: galGal4.fa.gz, upstream1000.fa.gz, upstream2000.fa.gz, upstream5000.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/galGal4/bigZips/ SrcDataFiles2: AGAPS masks: http://hgdownload.cse.ucsc.edu/goldenPath/galGal4/database/gap.txt.gz RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/galGal4/bigZips/galGal4.fa.out.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/galGal4/bigZips/galGal4.trf.bed.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Ggallus.UCSC.galGal4/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Ggallus.UCSC.galGal4/masks AGAPSfiles_name: gap.txt RMfiles_name: galGal4.fa.out TRFfiles_name: galGal4.trf.bed BSgenome/inst/extdata/GentlemanLab/BSgenome.Ggallus.UCSC.galGal4-tools/0000755000126300012640000000000012227064202027031 5ustar00biocbuildphs_compbioBSgenome/inst/extdata/GentlemanLab/BSgenome.Ggallus.UCSC.galGal4-tools/splitbigfasta.R0000755000126300012640000000213512227064202032014 0ustar00biocbuildphs_compbio### library(Biostrings) galGal4 <- readDNAStringSet("galGal4.fa") ### Partitioning: is_random <- grepl("^chr[^_]*_[^_]*_random$", 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.Hsapiens.UCSC.hg17-seed0000644000126300012640000000262212227064204026207 0ustar00biocbuildphs_compbioPackage: BSgenome.Hsapiens.UCSC.hg17 Title: Homo sapiens (Human) full genome (UCSC version hg17) Description: Homo sapiens (Human) full genome as provided by UCSC (hg17, May 2004) and stored in Biostrings objects. Version: 1.3.19 organism: Homo sapiens species: 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" mseqnames: paste("upstream", c("1000", "2000", "5000"), sep="") nmask_per_seq: 4 SrcDataFiles1: sequences: chromFa.zip, upstream1000.zip, upstream2000.zip, upstream5000.zip from http://hgdownload.cse.ucsc.edu/goldenPath/hg17/bigZips/ SrcDataFiles2: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/hg17/database/ RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/hg17/bigZips/chromOut.zip TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/hg17/bigZips/chromTrf.zip PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.UCSC.hg17/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.UCSC.hg17/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Hsapiens.UCSC.hg18-seed0000644000126300012640000000265512227064204026216 0ustar00biocbuildphs_compbioPackage: BSgenome.Hsapiens.UCSC.hg18 Title: Homo sapiens (Human) full genome (UCSC version hg18) Description: Homo sapiens (Human) full genome as provided by UCSC (hg18, Mar. 2006) and stored in Biostrings objects. Version: 1.3.19 organism: Homo sapiens species: Human provider: UCSC provider_version: hg18 release_date: Mar. 2006 release_name: NCBI Build 36.1 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/hg18/bigZips/ organism_biocview: Homo_sapiens BSgenomeObjname: Hsapiens seqnames: paste("chr", c(1:22, "X", "Y", "M", "5_h2_hap1", "6_cox_hap1", "6_qbl_hap2", "22_h2_hap1", paste(c((1:22)[-c(12, 14, 20)], "X"), "_random", sep="")), sep="") circ_seqs: "chrM" mseqnames: paste("upstream", c("1000", "2000", "5000"), sep="") nmask_per_seq: 4 SrcDataFiles1: sequences: chromFa.zip, upstream1000.zip, upstream2000.zip, upstream5000.zip from http://hgdownload.cse.ucsc.edu/goldenPath/hg18/bigZips/ SrcDataFiles2: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/hg18/database/ RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/hg18/bigZips/chromOut.zip TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/hg18/bigZips/chromTrf.zip PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.UCSC.hg18/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.UCSC.hg18/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Hsapiens.UCSC.hg19-seed0000644000126300012640000000365312227064204026216 0ustar00biocbuildphs_compbioPackage: BSgenome.Hsapiens.UCSC.hg19 Title: Homo sapiens (Human) full genome (UCSC version hg19) Description: Homo sapiens (Human) full genome as provided by UCSC (hg19, Feb. 2009) and stored in Biostrings objects. Version: 1.3.19 organism: Homo sapiens species: 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" mseqnames: paste("upstream", c("1000", "2000", "5000"), sep="") nmask_per_seq: 4 SrcDataFiles1: sequences: chromFa.zip, upstream1000.zip, upstream2000.zip, upstream5000.zip from http://hgdownload.cse.ucsc.edu/goldenPath/hg19/bigZips/ SrcDataFiles2: AGAPS masks: http://hgdownload.cse.ucsc.edu/goldenPath/hg19/database/gap.txt.gz RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/hg19/bigZips/chromOut.tar.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/hg19/bigZips/chromTrf.tar.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.UCSC.hg19/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Hsapiens.UCSC.hg19/masks AGAPSfiles_name: gap.txt BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmulatta.UCSC.rheMac2-seed0000644000126300012640000000376412227064204026744 0ustar00biocbuildphs_compbioPackage: BSgenome.Mmulatta.UCSC.rheMac2 Title: Macaca mulatta (Rhesus) full genome (UCSC version rheMac2) Description: Macaca mulatta (Rhesus) full genome as provided by UCSC (rheMac2, Jan. 2006) and stored in Biostrings objects. NOTE: In most assemblies available at UCSC, Tandem Repeats Finder repeats were filtered to retain only the repeats with period <= 12. However, the filtering was omitted for this assembly, so the TRF masks contain all Tandem Repeats Finder results. Version: 1.3.19 organism: Macaca mulatta species: Rhesus provider: UCSC provider_version: rheMac2 release_date: Jan. 2006 release_name: Baylor College of Medicine HGSC v1.0 Mmul_051212 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/rheMac2/ organism_biocview: Macaca_mulatta BSgenomeObjname: Mmulatta seqnames: paste("chr", c(1:20, "X", "Ur"), sep="") circ_seqs: character(0) mseqnames: paste("upstream", c(1:2, 5), "000", sep="") nmask_per_seq: 4 SrcDataFiles1: sequences: chromFa.tar.gz, upstream1000.fa.gz, upstream2000.fa.gz, upstream5000.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rheMac2/bigZips/ SrcDataFiles2: AGAPS masks: gap.txt.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rheMac2/database/ RM and TRF masks: chromOut.tar.gz and chromTrf.tar.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rheMac2/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] ## 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) seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Mmulatta.UCSC.rheMac2/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Mmulatta.UCSC.rheMac2/masks AGAPSfiles_name: gap.txt.gz BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmusculus.UCSC.mm10-seed0000644000126300012640000000571112227064204026440 0ustar00biocbuildphs_compbioPackage: BSgenome.Mmusculus.UCSC.mm10 Title: Mus musculus (Mouse) full genome (UCSC version mm10) Description: Mus musculus (Mouse) full genome as provided by UCSC (mm10, Dec. 2011) and stored in Biostrings objects. Version: 1.3.19 organism: Mus musculus species: 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" nmask_per_seq: 2 SrcDataFiles1: sequences: 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/ SrcDataFiles2: AGAPS masks: http://hgdownload.cse.ucsc.edu/goldenPath/mm10/database/gap.txt.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Mmusculus.UCSC.mm10/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Mmusculus.UCSC.mm10/masks AGAPSfiles_name: gap.txt BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmusculus.UCSC.mm8-seed0000644000126300012640000000261612227064204026370 0ustar00biocbuildphs_compbioPackage: BSgenome.Mmusculus.UCSC.mm8 Title: Mus musculus (Mouse) full genome (UCSC version mm8) Description: Mus musculus (Mouse) full genome as provided by UCSC (mm8, Feb. 2006) and stored in Biostrings objects. Version: 1.3.19 organism: Mus musculus species: 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" mseqnames: paste("upstream", c("1000", "2000", "5000"), sep="") nmask_per_seq: 4 SrcDataFiles1: sequences: chromFa.tar.gz, upstream1000.fa.gz, upstream2000.fa.gz, upstream5000.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/mm8/bigZips/ SrcDataFiles2: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/mm8/database/ RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/mm8/bigZips/chromOut.tar.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/mm8/bigZips/chromTrf.tar.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Mmusculus.UCSC.mm8/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Mmusculus.UCSC.mm8/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Mmusculus.UCSC.mm9-seed0000644000126300012640000000262012227064204026364 0ustar00biocbuildphs_compbioPackage: BSgenome.Mmusculus.UCSC.mm9 Title: Mus musculus (Mouse) full genome (UCSC version mm9) Description: Mus musculus (Mouse) full genome as provided by UCSC (mm9, Jul. 2007) and stored in Biostrings objects. Version: 1.3.19 organism: Mus musculus species: Mouse provider: UCSC provider_version: mm9 release_date: Jul. 2007 release_name: NCBI Build 37 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/mm9/bigZips/ organism_biocview: Mus_musculus BSgenomeObjname: Mmusculus seqnames: paste("chr", c(1:19, "X", "Y", "M", paste(c(1, 3, 4, 5, 7, 8, 9, 13, 16, 17, "X", "Y", "Un"), "_random", sep="")), sep="") circ_seqs: "chrM" mseqnames: paste("upstream", c("1000", "2000", "5000"), sep="") nmask_per_seq: 4 SrcDataFiles1: sequences: chromFa.tar.gz, upstream1000.fa.gz, upstream2000.fa.gz, upstream5000.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/mm9/bigZips/ SrcDataFiles2: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/mm9/database/ RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/mm9/bigZips/chromOut.tar.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/mm9/bigZips/chromTrf.tar.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Mmusculus.UCSC.mm9/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Mmusculus.UCSC.mm9/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Ptroglodytes.UCSC.panTro2-seed0000644000126300012640000000277012227064204027717 0ustar00biocbuildphs_compbioPackage: BSgenome.Ptroglodytes.UCSC.panTro2 Title: Pan troglodytes (Chimp) full genome (UCSC version panTro2) Description: Pan troglodytes (Chimp) full genome as provided by UCSC (panTro2, Mar. 2006) and stored in Biostrings objects. Version: 1.3.19 organism: Pan troglodytes species: 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" mseqnames: paste("upstream", c("1000", "2000", "5000"), sep="") nmask_per_seq: 4 SrcDataFiles1: sequences: chromFa.tar.gz, upstream1000.fa.gz, upstream2000.fa.gz, upstream5000.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/panTro2/bigZips/ SrcDataFiles2: AGAPS masks: gap.txt.gz from ftp://hgdownload.cse.ucsc.edu/goldenPath/panTro2/database/ RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/panTro2/bigZips/chromOut.tar.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/panTro2/bigZips/chromTrf.tar.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Ptroglodytes.UCSC.panTro2/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Ptroglodytes.UCSC.panTro2/masks AGAPSfiles_name: gap.txt BSgenome/inst/extdata/GentlemanLab/BSgenome.Ptroglodytes.UCSC.panTro3-seed0000644000126300012640000000305512227064204027715 0ustar00biocbuildphs_compbioPackage: BSgenome.Ptroglodytes.UCSC.panTro3 Title: Pan troglodytes (Chimp) full genome (UCSC version panTro3) Description: Pan troglodytes (Chimp) full genome as provided by UCSC (panTro3, Oct. 2010) and stored in Biostrings objects. Version: 1.3.19 organism: Pan troglodytes species: Chimp provider: UCSC provider_version: panTro3 release_date: Oct. 2010 release_name: CGSC Build 2.1.3 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/panTro3/bigZips/ organism_biocview: Pan_troglodytes BSgenomeObjname: Ptroglodytes seqnames: paste("chr", c(1, "2A", "2B", 3:22, "X", "Y", "M"), sep="") circ_seqs: "chrM" mseqnames: c(paste("chr", c(1, "2A", "2B", 3:22, "X", "Y", "M"), "_random", sep=""), "chrUn", paste("upstream", c("1000", "2000", "5000"), sep="")) nmask_per_seq: 4 SrcDataFiles1: sequences: panTro3.fa.gz, upstream1000.fa.gz, upstream2000.fa.gz, upstream5000.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/panTro3/bigZips/ SrcDataFiles2: AGAPS masks: http://hgdownload.cse.ucsc.edu/goldenPath/panTro3/database/gap.txt.gz RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/panTro3/bigZips/panTro3.fa.out.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/panTro3/bigZips/panTro3.trf.bed.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Ptroglodytes.UCSC.panTro3/seqs masks_srcdir: /shared/silo_researcher/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.panTro3-tools/0000755000126300012640000000000012227064203030206 5ustar00biocbuildphs_compbioBSgenome/inst/extdata/GentlemanLab/BSgenome.Ptroglodytes.UCSC.panTro3-tools/splitbigfasta.R0000755000126300012640000000160712227064203033174 0ustar00biocbuildphs_compbio### 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.Rnorvegicus.UCSC.rn4-seed0000644000126300012640000000263612227064204026705 0ustar00biocbuildphs_compbioPackage: BSgenome.Rnorvegicus.UCSC.rn4 Title: Rattus norvegicus (Rat) full genome (UCSC version rn4) Description: Rattus norvegicus (Rat) full genome as provided by UCSC (rn4, Nov. 2004) and stored in Biostrings objects. Version: 1.3.19 organism: Rattus norvegicus species: 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" mseqnames: paste("upstream", c("1000", "2000", "5000"), sep="") nmask_per_seq: 4 SrcDataFiles1: sequences: chromFa.tar.gz, upstream1000.fa.gz, upstream2000.fa.gz, upstream5000.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rn4/bigZips/ SrcDataFiles2: AGAPS masks: all the chr*_gap.txt.gz files from ftp://hgdownload.cse.ucsc.edu/goldenPath/rn4/database/ RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/rn4/bigZips/chromOut.tar.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/rn4/bigZips/chromTrf.tar.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Rnorvegicus.UCSC.rn4/seqs masks_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Rnorvegicus.UCSC.rn4/masks BSgenome/inst/extdata/GentlemanLab/BSgenome.Rnorvegicus.UCSC.rn5-seed0000644000126300012640000000262112227064204026700 0ustar00biocbuildphs_compbioPackage: BSgenome.Rnorvegicus.UCSC.rn5 Title: Rattus norvegicus (Rat) full genome (UCSC version rn5) Description: Rattus norvegicus (Rat) full genome as provided by UCSC (rn5, Mar. 2012) and stored in Biostrings objects. Version: 1.3.19 organism: Rattus norvegicus species: Rat provider: UCSC provider_version: rn5 release_date: Mar. 2012 release_name: RGSC 5.0 source_url: http://hgdownload.cse.ucsc.edu/goldenPath/rn5/bigZips/ organism_biocview: Rattus_norvegicus BSgenomeObjname: Rnorvegicus seqnames: paste("chr", c(1:20, "X", "M"), sep="") circ_seqs: "chrM" mseqnames: c("random", "chrUn", paste("upstream", c("1000", "2000", "5000"), sep="")) nmask_per_seq: 4 SrcDataFiles1: sequences: rn5.fa.gz, upstream1000.fa.gz, upstream2000.fa.gz, upstream5000.fa.gz from http://hgdownload.cse.ucsc.edu/goldenPath/rn5/bigZips/ SrcDataFiles2: AGAPS masks: http://hgdownload.cse.ucsc.edu/goldenPath/rn5/database/gap.txt.gz RM masks: http://hgdownload.cse.ucsc.edu/goldenPath/rn5/bigZips/rn5.fa.out.gz TRF masks: http://hgdownload.cse.ucsc.edu/goldenPath/rn5/bigZips/rn5.trf.bed.gz PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Rnorvegicus.UCSC.rn5/seqs masks_srcdir: /shared/silo_researcher/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.rn5-tools/0000755000126300012640000000000012227064202027172 5ustar00biocbuildphs_compbioBSgenome/inst/extdata/GentlemanLab/BSgenome.Rnorvegicus.UCSC.rn5-tools/splitbigfasta.R0000755000126300012640000000202012227064202032146 0ustar00biocbuildphs_compbio### library(Biostrings) rn5 <- readDNAStringSet("rn5.fa") ### Partitioning: is_random <- grepl("^chr[^_]*_[^_]*_random$", names(rn5)) is_chrUn <- grepl("^chrUn", names(rn5)) is_chrom <- !(is_random | is_chrUn) ### Sanity check: stopifnot(all(is_random | is_chrUn | is_chrom)) stopifnot(!any(is_random & is_chrUn)) stopifnot(!any(is_random & is_chrom)) stopifnot(!any(is_chrUn & is_chrom)) ### Send each chromosome to a FASTA file. seqnames <- paste("chr", c(1:20, "X", "M"), sep="") stopifnot(setequal(seqnames, names(rn5)[is_chrom])) for (seqname in seqnames) { seq <- rn5[match(seqname, names(rn5))] filename <- paste(seqname, ".fa", sep="") cat("writing ", filename, "\n", sep="") writeXStringSet(seq, file=filename, width=50L) } ### Send the 1278 chrNN_*_random sequences to 1 FASTA file. random_mseq <- rn5[is_random] writeXStringSet(random_mseq, file="random.fa", width=50L) ### Send the 1439 chrUn_* sequences to 1 FASTA file. chrUn_mseq <- rn5[is_chrUn] writeXStringSet(chrUn_mseq, file="chrUn.fa", width=50L) BSgenome/inst/extdata/GentlemanLab/BSgenome.Scerevisiae.UCSC.sacCer1-seed0000644000126300012640000000160412227064204027411 0ustar00biocbuildphs_compbioPackage: BSgenome.Scerevisiae.UCSC.sacCer1 Title: Saccharomyces cerevisiae (Yeast) full genome (UCSC version sacCer1) Description: Saccharomyces cerevisiae (Yeast) full genome as provided by UCSC (sacCer1, Oct. 2003) and stored in Biostrings objects. Version: 1.3.19 organism: Saccharomyces cerevisiae species: Yeast provider: UCSC provider_version: sacCer1 release_date: Oct. 2003 release_name: SGD 1 Oct 2003 sequence source_url: http://hgdownload.cse.ucsc.edu/goldenPath/sacCer1/bigZips/ organism_biocview: Saccharomyces_cerevisiae BSgenomeObjname: Scerevisiae seqnames: paste("chr", c(1:16, "M"), sep="") circ_seqs: "chrM" nmask_per_seq: 0 SrcDataFiles1: chromFa.zip from http://hgdownload.cse.ucsc.edu/goldenPath/sacCer1/bigZips/ PkgExamples: genome$chr1 # same as genome[["chr1"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Scerevisiae.UCSC.sacCer1/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Scerevisiae.UCSC.sacCer2-seed0000644000126300012640000000177412227064204027422 0ustar00biocbuildphs_compbioPackage: 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: 1.3.19 organism: Saccharomyces cerevisiae species: 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") nmask_per_seq: 0 SrcDataFiles1: http://hgdownload.cse.ucsc.edu/goldenPath/sacCer2/bigZips/chromFa.tar.gz PkgExamples: genome$chrI # same as genome[["chrI"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Scerevisiae.UCSC.sacCer2/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.Scerevisiae.UCSC.sacCer3-seed0000644000126300012640000000174312227064204027417 0ustar00biocbuildphs_compbioPackage: BSgenome.Scerevisiae.UCSC.sacCer3 Title: Saccharomyces cerevisiae (Yeast) full genome (UCSC version sacCer3) Description: Saccharomyces cerevisiae (Yeast) full genome as provided by UCSC (sacCer3, April 2011) and stored in Biostrings objects. Version: 1.3.19 organism: Saccharomyces cerevisiae species: Yeast provider: UCSC provider_version: sacCer3 release_date: April 2011 release_name: SGD April 2011 sequence source_url: http://hgdownload.cse.ucsc.edu/goldenPath/sacCer3/bigZips/ organism_biocview: Saccharomyces_cerevisiae BSgenomeObjname: Scerevisiae seqnames: paste("chr", c("I", "II", "III", "IV", "V", "VI", "VII", "VIII", "IX", "X", "XI", "XII", "XIII", "XIV", "XV", "XVI", "M"), sep="") circ_seqs: "chrM" nmask_per_seq: 0 SrcDataFiles1: http://hgdownload.cse.ucsc.edu/goldenPath/sacCer3/bigZips/chromFa.tar.gz PkgExamples: genome$chrI # same as genome[["chrI"]] seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.Scerevisiae.UCSC.sacCer3/seqs BSgenome/inst/extdata/GentlemanLab/BSgenome.influenza.NCBI.20100628-seed0000644000126300012640000000140112227064204026534 0ustar00biocbuildphs_compbioPackage: 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 species: 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" nmask_per_seq: 0 SrcDataFiles1: ftp://ftp.ncbi.nih.gov/genomes/INFLUENZA/influenza.fna.gz (downloaded on 2010/06/28) seqs_srcdir: /shared/silo_researcher/Morgan_M/BioC/BSgenomeForge/srcdata/BSgenome.influenza.NCBI.20100628/seqs seqfiles_suffix: .fna BSgenome/inst/extdata/GentlemanLab/ForgeAll.R0000644000126300012640000000320412227064204022410 0ustar00biocbuildphs_compbio####################################################################### ### Use this R script to forge all the BSgenome data packages ### library(BSgenome) pkgs <- 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.Celegans.UCSC.ce2", "BSgenome.Celegans.UCSC.ce6", "BSgenome.Celegans.UCSC.ce10", "BSgenome.Cfamiliaris.UCSC.canFam2", "BSgenome.Cfamiliaris.UCSC.canFam3", "BSgenome.Dmelanogaster.UCSC.dm2", "BSgenome.Dmelanogaster.UCSC.dm3", "BSgenome.Drerio.UCSC.danRer5", "BSgenome.Drerio.UCSC.danRer6", "BSgenome.Drerio.UCSC.danRer7", "BSgenome.Ecoli.NCBI.20080805", "BSgenome.Gaculeatus.UCSC.gasAcu1", "BSgenome.Ggallus.UCSC.galGal3", "BSgenome.Ggallus.UCSC.galGal4", "BSgenome.Hsapiens.UCSC.hg17", "BSgenome.Hsapiens.UCSC.hg18", "BSgenome.Hsapiens.UCSC.hg19", "BSgenome.Mmulatta.UCSC.rheMac2", "BSgenome.Mmusculus.UCSC.mm8", "BSgenome.Mmusculus.UCSC.mm9", "BSgenome.Mmusculus.UCSC.mm10", "BSgenome.Ptroglodytes.UCSC.panTro2", "BSgenome.Ptroglodytes.UCSC.panTro3", "BSgenome.Rnorvegicus.UCSC.rn4", "BSgenome.Rnorvegicus.UCSC.rn5", "BSgenome.Scerevisiae.UCSC.sacCer1", "BSgenome.Scerevisiae.UCSC.sacCer2", "BSgenome.Scerevisiae.UCSC.sacCer3" ) for (pkg in pkgs) { cat("\n") cat("============================================================\n") cat("START FORGING ", pkg, "\n", sep="") cat("\n") forgeBSgenomeDataPkg(pkg) cat("\n") cat("END FORGING ", pkg, "\n", sep="") } BSgenome/inst/extdata/GentlemanLab/bump_seed_version.sh0000755000126300012640000000036112227064204024642 0ustar00biocbuildphs_compbio#!/bin/bash set -e # Exit immediately if a simple command exits with a non-zero status for seed in BSgenome.*-seed; do mv $seed ${seed}.old cat ${seed}.old | sed -r "s/^Version: 1\.3\.16$/Version: 1.3.17/" > $seed rm ${seed}.old done BSgenome/inst/extdata/ce2chrM.fa0000644000126300012640000003337412227064204020047 0ustar00biocbuildphs_compbio>chrM CAGTAAATAGTTTAATAAAAATATAGCATTTGGGTTGCTAAGATATTATT ACTGATAGAATTTTTAGTTTAATTTAGAATGTATCACTTACAATGATGGG GTTTAAAATTCTATAGTAAAAGTGTTTTTTGTTTTAGCTGTTTTAAGTAG GATTATTAGATATATTAATATTGACCCTATAAAAAGAAGTTTTTTTCTTA TCTTTTCACTACTTTTTAGTATACCAGTTATTTCAATGAGAATACATATT TGGTTTTCTTACTTTATTTGTTTATTATTTTTAAGTGGTATTTTTGTTAT TTTGGTATATTTTTCTAGTTTATCTAAAATTAATGTAGTGAAAAGTTATA TAGCTGTGTTTTTACTTTTGTTAAGAATGTTATATTTTTCTCCCACAGTA TTAACTTATAGAAGATATTTAGGTTTAAGAGGTTTTTATTATAGTATTTA CTGGTTTATTTTTTGTTTTATTTTAGTATGTTTATTATTTTTTATAAATT TTAGTAGTTATTTTTTAAATTTTTCAGGTGCTTTACGTAAAGTTTAAAAT TATGTTTTTATTTGTTAGATTATTTATATTTATTTTTAAATGACAACGTT TAATTTTTATTCTAATTTCTTTAGAATTTATAATGTTGAGATTATTTTTA AAATTTTCTTATGTTTTAGGGGAAATAATGTTTTTTTATTTTATGTGTTT TTCTGTTATTTCAAGAATCCTGGGTATGGTAGTTATAGTAGGTAATATAA AATTTTTTGGTAGTGATAATTGTATTTTTTAGTAACAGATATAAGTTAAG TTTAAACTATTGATCTTCAAAATCAAAAATTTATTTCTGTAGAGATAATA GTATAAATAAGTATGTTTCTTTTTCGCAGAAATGGTTTTTTATCTTATAA AGTTTTCTTTCAGGGAATTAAAATTTGATCATGGTTTAAGATGATTTAAA ATGGTATTATCTAAATTTGATTTACAGAGTAGGCAATAAAAATTTACCTC GGCAATTTATCGCTTGTAAAATACTTGTTCCAGAATAATCGGCTAGACTT GTTAAAGCTTGTACTTTAATTGATGTTAATTATGAAATTATTATATTTTC TTTTAGATCTATGGTAGAATTTGGATTTATATTAGTGAATTTTCATAATT TTAAGATTTGTTGAACAAAGCAGATTAGTACCTGGTTAGACAAAAATTAA AAGAGCAGGAGTAAAGTTGTATTTAAACTGAAAAGATATTGGCAGACATT CTAAATTATCTTTGGAGGCTGAGTAGTAACTGAGAACCCTCATTAACTAC TTAATTTTTTGACTCGTGTATGATCGTTTATTTTATTCTTAAGGATTATA ATAAAAAATTTTTAATTTATTAAAATAGATATATACCCGGTTTATGATTT AAGAAACATTTGGCCTACAATATTTTATATTATGGATTTTAGTTTTAGTT AACTAAATGAAATTGTAAAAGACAGTAAAAAATTCTTAATGTATTTTTGA AGATTATCTAGAAGTGGTACAAATCATCCATCAATTGCCCAAAGGGGAGT AAGTTGTAGTAAAGTAGATTTAGGGGAACCTGAATCTAGTAATAAAACTA TTTTTAAATATGTTTTGAAAACATGTTTTGAGGTAACTCGTAGTTTTTAA GAGTTAGTTTAATATAGAATTGTTGACTGTTAATCAAAAGGTGTACCTCT TAATATAAGAGTTTAGTTTAAGTTAAAACGTTAGATTGTAAATCTAAAGA TTATTGCTCTTGATAATTTTAGTTTTACTTATAGTTATTTTAATGATGAT TTTTATTGTTCAAAGAATCGCTTTTATTACTCTATATGAGCGTCATTTAT TGGGAAGAAGACAAAATCGTCTAGGGCCCACCAAGGTTACATTTATGGGA TTAGCACAAGCTTTATTGGATGGGGTTAAACTTTTAAAAAAAGAACAAAT AACACCCTTAAATTCCTCTGAAGTATCATTTTTACTTGTACCAGGAATTT CTTTTGTTGTAATATATTTAGAATGATTTACGTTACCATATTTTTTTGAT TTTATTAGTTTTGAGTATTCAGTTTTATTTTTTTTATGTTTAATTGGATT TTCTGTTTATACAACTTTAATTAGCGGTATCGTAAGAAAATCAAAATATG GTATAATTGGGGCCATCCGTGCTAGAAGACAAAGAATTTCTTATGAAATT GCTTTTTCTTTATATGTTTTGTGTATTATTATTCATAATAATGTTTTTAA TTTTGTTTCAAAATTTAATTTGAGACTTTTAATTATTTACATCCCATTTT TAATTATAGTAATTGCTGAACTTAACCGGGCGCCATTTGATTTTTCTGAA GGTGAAAGGGAGTTAGTTAGAGGATTTAATGTGGAGTTTGCCAGAGTAGC TTTTGTTTTATTATTTTTAAGGGAATATGGAAGATTAATTTTTTTTAGGG TACTTTCTTCTGCTATATTTTTTAAATTTTCAATTTTTATAGCATTTAGT ATTTTTTCATTATTAATTTTTATTCGTAGTTCATACCCTCGTTATCGTTA TGATTTAATAATAAGTTTATTTTGATTTAAACTTTTACCAATCTCTTTAA TTATATTGTGTTTTTACGCAGTTATTTTTTATTATTAATCAAGTTTATTT TTTAGACATTTTTATATTTGTTTTTGTTTTACAATTTTTGTTTTATTTTA AAGAAAGTATATTAAATACTTTAGTGAAAAAATTTCTTAATAGGTTAGTA GGAGTATTTAGATATACAAATACTTTACCATTAAGGTCAGTAATTTCTAT TTTTACTTTTATTGTTCTTTTAACTTGTTGTTTTGGAGGTTATTTTACTT ACTCTTTTTGTCCTTGTGGAATGGTTGAATTTACTTTTGTTTATGCTGCT GTAGCGTGATTAAGTACTTTGTTAACTTTTATTTCAAGAGAAAAATTTTC AGTTTATATAAGAAAACCAGGAGACACATATTTGAAAACTCTTAGAATGC TATTAATTGAAATCGTTAGAGAATTTTCTCGTCCACTTGCTTTAACAGTG CGTTTAACAGTTAATATTACTGTTGGTCATTTAGTTAGAATAATGCTTTA TCAAGGATTAGAATTAAGAATAGGTGATCAGTATATTTGATTATCAATTT TAGCCATTATAATAGAATGTTTTGTTTTCTTCATTCAAAGTTATATTTTC TCTCGTTTAATTTTTTTATATCTTAATGAGTAATAAAAAAAAAAAGATGT TAACTTAAGTTTTAAAGTGCCAAACTTTTAATTTGGAAATGGTGGACCAC ATCTTAGTTGATATAGCATAAGAAGTGCATTTGTTTTAAGCGCAAAAGAT ATCCGTCAACTAACGAGTTCATAAAGCAAGTCTTCTAAATTTGTTCTAGG TTAAATCCTGCTCGTTTTTGATTGTTTTTATTTCTTTATTTACCTTGTTT TTAACATTATTAAGAATTTTGACTAATAACGTTATTGTTTGATGAAGAAT TTTTTTATTGATAACTGTAGTTTTTATTCTATTAAATAAAAGCAGCAAGA GATATACCAGAATTTTTAATTATTTTGTTATTCAAGAGTCTTTAGGTTTA TTATTTCTTCTTTGTAGAGGAGGTCTATTACAATTTTTTATTATTTTATT GAAAATTGGTGTAGCACCGCTCCACTTTTGAATTTTTAATGTAACAAATA ACATTTTTAATTATGGGCTAATGTGGTTTTTAACATTTCAAAAATTACCA TTTTTAACTATTTTATTACAAATTTTTTGGTTAAGATCCGTGTATATTTT GTTATTTGGTTTATTGATTTGTTATGTTCAAATTTTTGTCATAAAAAGTT ATAAAAATTTGTTAATTATTTCATCCACAGAGTCTTTTAATTGGATTGTT TTGGGAGTATTTTTTTCAATGTTTAATACATTTTATTTATTTATTTATTA CTTTGTATTAATAGTTTTATTAATTTCTAAGTTTTCTAAAACTAGGGGTT ATAATTTTATTAATTGAGAAACAACATTAGTATTTTTAAATATTCCATTT AGAGTTTCATTTTTTGTAAAAATTTTCTCATTGAGGGAAATTTTTAAATA TGATAGATTCTTTACTCTATTTTTGCTTTTTACAATATTTTTATCTGTAT TGGCATTTAGATTTTGATTAATTAACTTGAGAATGAAAAATAATGAAGAA ACTTCAAATAATAATAAAATAAATTATTTTATTATTTTTCCGTTAATAGT TATTTCTATTATTTAATTACTTTTCTAGTAAAATATATTATATTATCTTG ATAAGGTAAAGTTCCAGTTGGGAGAAGTAAGATGTAAAATAGATATTACT ATGTTTGGTTACGGTCCAAAAAGATGCACATCTTTGCGATCTAGTTTAGA AAAAATATTTGTTTTTGGTGCAAAAGAGTTTGATTGCATTTAGTTTACTC TTTTAGTTTATAATTAAAATATGGCCCTGAAGAGGCTAAGAATATTAGGA GTATTGAAAATTAATAATAGATTATTAAATTTTGTTAATGGGATGTTGGT GACATTGCCATCTAGAAAAACTTTAACATTAAGATGAAATTTTGGTAGTA TATTGGGTATAGTTTTAATCTTTCAGATTTTAACAGGTACATTTTTAGCA TTTTATTATACGCCCGATAGGTTAATAGCATTTTCAACAGTGCAGTATAT TATGTATGAGGTAAATTTTGGATGAGTATTTCGAATTTTTCATTTTAATG GGGCCAGGTTATTTTTTATTTTTTTGTATTTACATATTTTTAAAGGGTTA TTTTTTATAAGATATCGTTTAAAAAAAGTATGAATGTCTGGTTTAACAAT TTATTTATTAGTAATAATAGAAGCTTTTATAGGTTATGTTTTAGTTTGAG CTCAAATAAGATTTTGAGCAGCAGTAGTTATTACTAGACTTTTAAGAGTT ATTCCAATTTGAGGGCCAACTATTGTTACTTGAATTTGAAGAGGTTTTGG TGTTACAGGGGCAACATTAAAATTCTTTTTTGTATTACATTTTTTATTGC CGTGAGCTATTCTAGTTATTGTATTGGGGCATTTAATTTTTTTACACAGA ACTGGTAGAACATCTAGGTTATATTGCCACGGTGATTATGATAAAGTTTG TTTTAGACCTGAGTACTTAGGTAAAGATGCTTATAATATTGTTATTTGAT TATTATTTATTGTGTTAAGGTTGATTTACCCGTTTAATTTAGGTGATGCA GAGATGTTTATTGAAGCTGACCCTATAATGAGGCCAGTTCATATTGTTCC AGAGTGATATTTTTTATTTGCTTATGCAATTTTGCGTGCTATTCCAAATA AAGTCTTAGGGGTAATTGCTTTATTAATAAGGATCGTAACATTTTATTTT TTTGCTTTAGTTAATAATTATACCTCTTGTTTAACCAAATTAAATAAATT TTTAGTATTTATATTTATTATCTCATCTACTATTTTAAGATGACTAGGTC AATGCACTGTAGAAGACCCTTTTACAATTTTAAGACCTTTATTTTCTTTT ATTTATTTTGGTTTAGCTTATTTAATATTGTTTATTTTTATAAGAAGTAA ATTGTTATTTAAATAATAAAACATGTCTAGTATAAGTTAATACATTAGAT TTAGGTTCTAAAGATTTGTGATATGTTATATTTCATAATTTTCATATTTT AAGACTTTCAAGGTATGCATATAATTTATTTTTTGCCTCAGCCGGAATGT TAAGATCTTTAGTAATATTTTTTAAATTTGGACTATACGAATTATTTATT TTTACACTATTTTCTGTGTTATTTATTTCTTTTGCTTGAGGTAAGGATAT TGCTATAGAAGGTTTAAGAGGTTACCATAATTTTTTCGTTATAGACGGGT TTAAATTCGGAGTAATTTTATTTGTGTTTAGGGAGTTTATATTCTTCTTT TGTATTTTTTGAACATTTTTTGATGCTGCTCTAGTACCAGTACACGAGTT GGGAGAGACTTGATCACCTTTTGGAATGCACTTAGTTAATCCATTTGGTG TACCGTTATTAAATACAATTATTTTATTAAGGAGTGGTGTTACAGTAACT TGAGCACATCACAGATTACTTAGAAATAAAAGATGTACTAATAGTATAAT TTTAACATGTTTATTGGCAGCTTATTTTACAGGAATTCAATTAATAGAGT ATATAGAAGCTAGATTTTCTATTGCAGACGGAGTATTTGGAAGGATTTTT TATTTATCTACGGGATTTCACGGAATTCATGTCTTGTGTGGTGGTTTGTT CTTAGCATTTAATTTTTTACGTCTTCTAAAAAATCATTTTAATTATAATC ATCATCTGGGGTTGGAATTTGCTATTTTATATTGACATTTTGTTGATGTA GTGTGATTATTTTTATTTGTGTTTGTTTATTGATGATCTTACTAATATAG CTATGATAGTTTAATTTAGAATATATAACTTGTAATTATAAGGTTTCTAG TAGCTTTGTTAGAATTTCTTTTTATCTCCTTATTATGACTTTTTAAACCT ATTTATTTTTTATTATTTACAGTGATGTTTAGGTTTTTAATTTTTAATAA TTTTTCATGAGGCGGACTATTTTTAGTATTAGATTCATATAGATTTATTT TATTGATTGTTATAAGATTATTTATTTTAGGTATTATTGTTATTAGAGAA AAAAATAATAATTTATTGATTTTATCTGAAATTTTAGTATTTATTTGTAT TATTTTTTTTATTCCTAGTAATATAATAATATTATATATGTTTTTTGAAT TATCTATATTTCCAATTTTGGTTATAATTCTAGGTTATGGTTCTCAAATT GAAAAAATTAACTCCTCTTATTATTTAATATTTTATGCAGCTTTTTGTTC ATTCCCATTTTTATTTGTATATTTTAAGAGTAATTTTTTATTGGTTTTTA CTTACTATAATTTTGTTATTTCTTGAGAAATATTTTTTATTCTTAGTTTA AGATTTATAATAAAATTTCCAATTTATTTTTTACATCTTTGATTACCTAA AGCTCATGTAGAGGCTCCTACAACAGCTAGAATACTTTTAGCTGGATTAC TATTAAAATTAGGCACAGCGGGATTTTTACGTATTTTAGGTAGTTTAAGA TTTGTACACAACAATGTATGAATTTTAATTGCATTTTTAGGGATAATTTT AGGATCTTTTTGTTGTGTGTTTCAAAGAGATTCAAAGGCTTTAGCAGCTT ATTCTTCAGTCACTCATATAAGGTTTTTATTATTATCACTGGTATTTATC ACAATGAGTAGTAAAATTAGAAGAGTTATGCTTATGCTAGCACACGGTTA TACATCTACACTTATGTTTTACCTTATTGGTGAATTTTATCATACATCTG GGAGGCGTATAATTTATTTTATAAGTAGATTTTTTAGATCTAGAATAATT ATAGGTATTTTGTTTTCAGTTGTATTTTTATCAAATAGGGGTGTACCACC TTCTTTGTCATTTTTATCAGAATTTTTAGTTATTTCTAATAGTATATTAA TTAGAAAAAGTATATTTGTAATAATTTTTATTTATTTTGTAGTATCTTTT TACTATTCTTTATTTTTGATTACAAGATCTTTAATAGGAAAAGGTTACCA TAATTTTAATACTTGAAATGTAGGGTTTTCAGCACCATTAGTCTTAATAA TATATAATGTATTTTGATTAAGTGTGTTTTACTAATAATCTAGAGATCTA TCTCTTTTTTGAGCACGTTAGTACATTATTTTTAATAATGTGCTAATAAT TATGTTTAAAAGTAAAATTTTTATTTTAAGTATTCAACTTTTAAATTAAT CTTTATAAAAAATATCAAGGAGGATTGGCAGTTTGATTAGAGAGATCTAA TCATAAAGATATCGGAACTCTTTATTTTATTTTTGGACTTTGATCTGGTA TGGTTGGTACTAGATTTTCTTTATTAATTCGTTTAGAATTAGCTAAACCA GGTTTTTTTCTTAGGAATGGACAGTTGTATAATTCAGTTATTACAGCTCA TGCTATTTTAATAATTTTTTTTATGGTAATACCTACTATAATCGGTGGTT TTGGTAACTGATTATTACCACTTATGTTAGGAGCACCTGATATAAGATTT CCACGTTTAAATAATTTAAGATTTTGGTTATTACCTACATCTATATTATT AATTTTAGATGCTTGTTTTGTAGATATAGGTTGTGGGACTAGGTGAACAG TCTACCCACCTTTAAGAACAATGGGGCACCCTGGAAGTAGAGTAGATTTA GCTATTTTTAGTTTACATGCAGCAGGGTTAAGATCTATCTTAGGTGGTAT TAATTTTATGTGTACTACTAAAAATTTACGTAGAAGTTCTATTTCATTAG AACATATAACTTTATTTGTTTGAACTGTATTTGTAACAGTGTTTTTACTG GTTTTATCTCTACCGGTTTTAGCAGGGGCTATTACTATGTTGTTAACTGA TCGTAATTTAAATACTTCATTTTTTGATCCAAGAACTGGAGGTAATCCTC TTATTTATCAACATTTGTTTTGATTTTTTGGTCATCCTGAAGTATATATT TTGATTTTACCAGCTTTTGGTATTGTCAGACAATCTACACTTTATTTAAC AGGAAAAAAAGAAGTTTTTGGTGCTTTGGGTATAGTTTATGCAATTTTAA GAATTGGTTTAATTGGTTGTGTAGTATGAGCTCACCATATGTATACAGTA GGTATAGATTTGGATTCACGTGCTTATTTTTCGGCTGCTACTATAGTTAT TGCAGTGCCAACAGGTGTTAAAGTGTTTAGATGATTGGCTACATTATTTG GTATAAAAATGGTATTTAATCCACTTTTATTGTGAGTATTGGGTTTTATT TTTTTGTTTACTTTAGGTGGGTTGACAGGTGTTGTATTATCTAATTCAAG ATTGGATATTATTTTACATGATACTTATTATGTAGTTAGACATTTTCATT ATGTTTTAAGTTTAGGAGCTGTTTTTGGGATTTTCACGGGTGTTACACTA TGATGAAGATTTATTACAGGGTATGTGTTAGATAAACTTATGATATCTGC AGTATTTATTTTATTATTTATTGGGGTAAATTTAACATTTTTCCCGCTAC ATTTTGCAGGACTACACGGGTTCCCACGTAAATATTTAGATTACCCTGAT GTTTATTCGGTATGAAATATTATTGCCTCTTATGGTTCTATTATTAGAAC TGCAGGACTATTCTTATTTATTTATGTATTATTAGAGTCTTTCTTTAGTT ATCGTTTAGTAATTAGAGATTATTATTCTAATAGAAGACCTGAGTATTGT ATGAGTAATTATGTATTTGGTCACAGTTATCAGTCTGAGATTTATTTTAG AACTACTAGATTAAAAAATTAGAAACCTTAGTATAATTTTAGTATATTTA ATTGCAAATTAAATGGTATTGGTTTTTAGTAAGATAGGATAATTAAGTCT GTAAGGTTCATACCCTTGAGGTGGTTTTCTCTTATTAAAAGTTTTAGTAT AAAAAAGTATATTTTATTGTCAATAAAAAGGTAAAAACTTTAGATTCTTT AGTATAATTCAGTATGTTTGACTTCCAATCAAAAGGTTTTGAGGATTAAT TAATAATTTTTTTCAAGGATATAATTTACTATTTCAGCATAGTTTATTTG CTAGTTATATAGATTGATTTCATAGGTTTAATTGTAGTTTATTGTTGGGA GTTTTAGTGTTTGTTACTTTATTGTTTGGATATTTAATTTTTGGTACTTT TTATTTTAAAAGAAAAAAAATTGAGTATCAGTTTGGTGAATTATTGTGTA GTATTTTTCCAACTATTATTTTATTAATACAAATAGTTCCTTCACTTAGG CTTTTATATTATTACGGATTAATAAATTTAGATAGAAATTTAACAGTTAA GGTTACAGGACATCAGTGATATTGAAGATATGAATATAGAGATATTCCTG GGTTAGAATTTGACTCTTATATAAAATCACTAGATCAATTAAGTTTAGGT GAACCACGTTTATTAGAAGTTGATAATCGTTGTGTTATTCCTTGTGATAC TAACATTCGTTTTTGTATTACATCTGCTGATGTTATTCATGCTTGGGCAT TAAATTCTTTATCTGTAAAATTAGATGCTATAAGAGGAATTTTAAGAACA TTTAGTTACAGGTTTCCTATAGTGGGAGTTTTTTATGGTCAATGTTCAGA GATTTGTGGAGCAAATCATAGTTTTATACCAATTGCTTTAGAGGTAACAT TATTGGATAATTTTAAAAGATGATGTTTTGGTACTATAGAATAATTTAGC TTAATAGTTTATATTAAAATGTTTACTTGTGGTGTAAGAGAATATAGAGC TTTAAATTTTACTTGTTTAAATATTGGTATTGCATACTATTACAATAAAA TTTCATGTTAATGAAAAATAGAAACAAAGGGTAGAGTAAATATTAGTTTT ATTGTTTCATACTAAAAATTATATTTATTAGAGTTGATATGTCGACCTTT GTGATAACTGTTTTTATTTTTATATTAGAAAATTATATATTATATAATTA TTTTAGGAAATTTAAAATTTGAAGTGTTTTAAATTTATGTTTTACAACAT TTTCCTAATTTTATTTAAGTTTAATTTTTAATTTAATAAAGTTTTATTAA ATAAATAATTTGTAAATTAGTAAATTTTATAAATTTAATTTATTATTAAA ATATAATTGAAGAACTTGAAGTCTTGATCAAATGTTTTTTAAAGACTTAG GCTTTATATTAAAGCTGGCTTCTGCCCTATGATATTTAAATGGCAGTCTT AGCGTGAGGACATTAAGGTAGCAAAATAATTTGTGCTTTTATTGAGTTCC AGTATGAATGAAGTTATTGGTTAGTTCTATTTATGTTTTATGTTTGAATT TAATTTTTATTTAAGAAAAAATAAATATATTTATACAAAGATAAGTCTTC GGAAATTCTGTTATTACACAATTAAATAATTGTGTAATAAATTTTCTAGG GCAGAATATTATATAATAGTATTTCACTATATTTAATTTAAAGAATTACT CCGGAGTTAACAGAAAATCATACCTAATCTAGTACTTATAGTAAGGTAAG TTTTACATCGATGTTGTATTCAGATAATCTAAGAGAGGAGAAGGCTTAGT AGTTTAGACTGTTCTTCTATTAATTAATCTGACGTGATATTAGTTTAATT CATTGTGAGATAGAATTGTTTATCTTGATAAATATTTATATTTAATACAT TTAGTACGAAAGGAACATTGTAAAAGTTTTAAACTTTAAAGATTTTGAAA TCTTTATTTTAGTGCTATTAATAGTTTTAGTGTTTACGCTAGTTTTATTA TTTGCTTTTTATTTGATTAATTTTTTATTAAGAATTAAGGATATAGGAAA AAATAAAATTAGAGCGTTTGAATGTGGTTTTGTAAGAGTTGGAAAAATTC AAAATTCTTTTAGAATTCATTTTTTTATTATGATATTGATATTTGTTATT TTTGATTTAGAAATTGTTATGTTTTTAGGTATTTTAGTATCAGATTTAAG TTCGTATATCAGGTTTTTAATAATATTCATCTTCATCTTGGGAGGATTTT ACATAGAGTGATGATATGGTAAATTAGTTTGAGTAATTTAATTAATATTT CTATTTTTTTGATTGGATTTGTTTTTTTTATAGGTGGAATTAGTGTTTGG CTTATACCCACATTTAAATTAGGAATCTTTTTTTTAGAATGAGATTTTTT AAGGTTAAAATTTAATTTTTATTTTAATAGAATCTTATTTTCGTTTATTC TTTTTTTGGTAACGTTTAGAGTTTTAGTTTTTAGTACTTATTATTTAAAT AGTGAGTTAAACTTTAATTATTATTATTTTGTATTGTTAATTTTCGTAGG TAGAATGTTTAGGCTAAATTTTAGAAACAGTATTTTTACAATGTTACTAA GATGAGATTTATTGGGTATTTCTAGGTTTTTTTTAGTTTTATTTTATAAT AATTGAGATAGATGTAGGGGTGCAATAAATACAGCATTAACTAATCGTCT AGGTGATTATTTTATATTTGTCTTTTTTGGTTTATCGGTTTTTAGAGGTT ATTATTTTTTAAGATTTAGAATATTTAGAAGTTATATATCTTTATTATTA CTTTTAACAGCTTTTACTAAAAGAGCACAATTTCCATTTAGATCTTGGTT ACCCAAAGCTATAAGAGCCCCCACACCGGTGAGGTCTTTGGTTCATAGTA GAACTTTAGTTACAGCAGGATTAATTCTATTAATAAATTTTAATAATTTA GTAATACAGAAAGATTTTATCAGTTTTGTTCTGATTATTGGCCTATTTAC TATATTTTTTTCTAGCTTAGCAAGTTTGGTCGAAGAAGATTTGAAGAAGG TGGTAGCCTTGAGGACACTTTCACAAATAGGTTTTTCAATAGTTACTTTG GGCCTAGGGCTTAGGTTTATTTCATTTATTCATTTAGTTAGACATGCTTT GTTCAAAAGATGTTTATTTATACAAGTAGGTTACATTATTCATTGTTCAT TTGGACAACAAGATGGACGTAATTATAGGAATAATGGTAATTTACCAAAT TTTATTCAGTTACAAATATTAGTAACCCTATTTTGTTTATGTGGATTAAT TTTCTCAAGGGGTGCTGTAAGAAAAGATTTTATTTTAGAATTATTTTTTT CTAATAACTATATAATGTTTTTTAGATTAATATTTTTTGTTTCAGTGTTT TTGACTTTTGGTTACAGTTTTCGTCTTTGAAAAAGATTTTTTTTAAGGTT TAATAAAGTAATAAATCATTACAGTAGCACAGTATTTATAAATTTTTTAA GTTTAGTATTAGTTATTTTTTCTATTAGATTTTTATGATGAATAAATTTT AATCTTCTTAACATCCCAAGACTTTTCTTATACGTAGATTTTTTTGGCCC TCTAGTATTTTTATTTATAATAATTTTTTTATCTTTTTTAATTTTAAAAA TATTATTTAAGGAGTTAATATACAAGTTTTTAGTTGATTATTTGGCTAAA AATAGTATTTATAAAATAAAGAATTTAAAATTTATAGATTTATTTTTAAA TAATATTAATTCTAAGGGGTACACCTTATTTTTAAGCAGTGGTATATTTA AAAATTACTATTTAAAAAGGTTAAATTTTAATAGTGTAGTAGTTTTAATT TTTATTTTTTTTATAATTTGTTAAGGGATTTTAGTTTAATAAAAATATAT GTTTTGCATACATAAGATAATAATTCTAGATAGTTTTACACGCGCGTATA CGCGCGTTATAAATATATATATATATATATATATATATATATATATATAA TAATAATATTATATTTATATTATAAATATAATATTTATTATAAATTATAT ATTATATTTATATTATAAATATAATATTTATTATAAATTATATATTATAT TTATATTATAAATATAATATTTATTATAAATTATATATTATATTTATATT ATAAATATAATATTTATTATAAATTATATATTATATTTATATTATAAATA TAATATTTATTATATATTATATATATTATATTTATATTATAAATATAATA TTTATTATTAATAATTCATCATATTTATATTATAAATATGATGAAGTACT AAAAAAAAGATGAATATTCTATAATATATTTAGATATATTATAGAGTATT TATCTTATTATTTATAGATATATACTTTGTATATATCTATATTA BSgenome/inst/extdata/ce2dict0.fa0000644000126300012640000000307612227064204020155 0ustar00biocbuildphs_compbio>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/man/0000755000126300012640000000000012227064177014417 5ustar00biocbuildphs_compbioBSgenome/man/BSParams-class.Rd0000644000126300012640000000353512227064177017467 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000002137012227064177017513 0ustar00biocbuildphs_compbio\name{BSgenome-class} \docType{class} % Classes \alias{class:BSgenome} \alias{BSgenome-class} \alias{BSgenome} % Accessor methods: \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} % Standard generic methods: \alias{show,BSgenome-method} \alias{length,BSgenome-method} \alias{[[,BSgenome-method} \alias{[[<-,BSgenome-method} \alias{$,BSgenome-method} \title{BSgenome objects} \description{ The BSgenome class is a container for the complete genome sequence of a given organism. } \section{Accessor methods}{ In the code snippets below, \code{x} is a BSgenome object. Note that, because the BSgenome class contains the \code{\link{GenomeDescription}} class, then all the accessor methods for \code{\link{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.hg19 package, load it and see the Note section in \code{?`\link[BSgenome.Hsapiens.UCSC.hg19]{BSgenome.Hsapiens.UCSC.hg19}`}. } } } \author{H. Pages} \seealso{ \code{\link{available.genomes}}, \link{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: mseqnames(Celegans) upstream1000 <- Celegans$upstream1000 upstream1000 class(upstream1000) # a DNAStringSet instance ## Character vector containing the description lines of the first ## 4 sequences in the original FASTA file: names(upstream1000)[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(chrI, upstream1000) gc() # chrI and upstream1000 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(chrV <- Celegans[["chrV"]]) # read from disk gc()["Vcells", "(Mb)"] - mem0 # chrV occupies 20Mb in memory system.time(tmp <- Celegans[["chrV"]]) # 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 chrV): y <- subseq(chrV, 10, 8000000) gc()["Vcells", "(Mb)"] - mem0 ## We must remove all references to chrV before it can be removed from ## the cache (so the 20Mb of memory used by this sequence are freed). options(verbose=TRUE) rm(chrV, tmp) gc() ## Remember that 'y' holds a reference to chrV too: rm(y) gc() options(verbose=FALSE) gc()["Vcells", "(Mb)"] - mem0 } \keyword{methods} \keyword{classes} BSgenome/man/BSgenome-utils.Rd0000644000126300012640000001306012227064177017543 0ustar00biocbuildphs_compbio\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), asRangedData = FALSE) \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, asRangedData = 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), asRangedData = FALSE) \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. } \item{asRangedData}{ A logical value to assist in migrating output type from \link[IRanges]{RangedData} (defunct) to \link[GenomicRanges]{GRanges}. Should be \code{FALSE}. } } \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[IRanges]{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.Rd0000644000126300012640000001025012227064177017366 0ustar00biocbuildphs_compbio\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=".", masks_srcdir=".", destdir=".", verbose=TRUE) ## Low-level BSgenomeForge functions: forgeSeqlengthsFile(seqnames, prefix="", suffix=".fa", seqs_srcdir=".", seqs_destdir=".", verbose=TRUE) forgeSeqFiles(seqnames, mseqnames=NULL, prefix="", suffix=".fa", seqs_srcdir=".", seqs_destdir=".", verbose=TRUE) forgeMasksFiles(seqnames, nmask_per_seq, seqs_destdir=".", 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{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{prefix, suffix}{ See the BSgenomeForge vignette in this package for more information, in particular the description of the \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. Pages} \examples{ forgeSeqFiles("chrM", prefix="ce2", suffix=".fa", seqs_srcdir=system.file("extdata", package="BSgenome"), seqs_destdir=tempdir()) load(file.path(tempdir(), "chrM.rda")) chrM } \keyword{manip} BSgenome/man/GenomeData-class.Rd0000644000126300012640000001055612227064177020024 0ustar00biocbuildphs_compbio\name{GenomeData-class} \docType{class} \alias{GenomeData-class} % Accessors: \alias{provider,GenomeData-method} \alias{organism,GenomeData-method} \alias{providerVersion,GenomeData-method} % Constructor: \alias{GenomeData} % Show: \alias{show,GenomeData-method} % Coercion: \alias{coerce,GenomeData,data.frame-method} \alias{coerce,GenomeData,RangesList-method} \alias{coerce,GenomeData,RangedData-method} \title{Data on the genome} \description{\code{GenomeData} formally represents genomic data as a list, with one element per chromosome in the genome.} \details{ This class facilitates storing data on the genome by formalizing a set of metadata fields for storing the organism (e.g. Mmusculus), genome build provider (e.g. UCSC), and genome build version (e.g. mm9). The data is represented as a list, with one element per chromosome (or really any sequence, like a gene). There are no constraints as to the data type of the elements. Note that as a \code{\linkS4class{SimpleList}}, it is possible to store chromosome-level data (e.g. the lengths) in the \code{elementMetadata} slot. The \code{organism}, \code{provider} and \code{providerVersion} are all stored in the \code{SimpleList} \code{metadata}, so they may be retrieved in list form by calling \code{metadata(x)}. } \section{Accessor methods}{ In the code snippets below, \code{x} is a \code{GenomeData} object. \describe{ \item{}{\code{organism(x)}: Get the single string indicating the organism, if specified, otherwise \code{NULL}. } \item{}{\code{provider(x)}: Get the single string indicating the genome build provider, if specified, otherwise \code{NULL}. } \item{}{\code{providerVersion(x)}: Get the single string indicating the genome build version, if specified, otherwise \code{NULL}. } } } \section{Constructor}{ \describe{ \item{}{ \code{GenomeData(listData = list(), providerVersion = metadata[["providerVersion"]], organism = metadata[["organism"]], provider = metadata[["provider"]], metadata = list(), elementMetadata = NULL, ...)}: Creates a \code{GenomeData} with the elements from the \code{listData} parameter, a list. The other arguments correspond to the metadata fields, and, with the exception of \code{elementMetadata}, should all be either single strings or \code{NULL} (unspecified). Additional global metadata elements may be passed in \code{metadata}, in list-form, and via \code{...}. The elements in \code{metadata} are always overridden by the explicit arguments, like \code{organism} and those in \code{...}. \code{elementMetadata} should be an \code{\linkS4class{DataTable}} or \code{NULL}. } } } \section{Coercion}{ \describe{ \item{}{\code{as(from, "data.frame")}: Coerces each subelement to a data frame, and binds them into a single data frame with an additional column indicating chromosome } \item{}{\code{as(from, "RangesList")}: Coerces each subelement to a \code{\linkS4class{Ranges}} and combines them into a \code{\linkS4class{RangesList}} with the same names. The \dQuote{universe} metadata property is set to the \code{providerVersion} of \code{from}. } \item{}{\code{as(from, "RangedData")}: Coerces each subelement to a \code{\linkS4class{RangedData}} and combines them into a single \code{RangedData} with the same names. The \dQuote{universe} metadata property is set to the \code{providerVersion} of \code{from}. } } } \author{ Michael Lawrence } \seealso{ \link{GenomeDataList-class}, a container for storing a list of GenomeData objects and useful e.g. for storing data on multiple samples. \link{SimpleList-class}, the base of this class. \code{\link{gdapply}} for applying a function to elements of a GenomeData object. \code{\link{gdReduce}} for successively combining GenomeData objects into a single GenomeData objects. } \examples{ gd <- GenomeData(list(chr1 = IRanges(1, 10), chrX = IRanges(2, 5)), organism = "Mmusculus", provider = "UCSC", providerVersion = "mm9") organism(gd) providerVersion(gd) provider(gd) gd[["chr1"]] # get data for chromsome 1 } \keyword{methods} \keyword{classes} BSgenome/man/GenomeDataList-class.Rd0000644000126300012640000000361012227064177020651 0ustar00biocbuildphs_compbio\name{GenomeDataList-class} \docType{class} \alias{GenomeDataList-class} % Constructor: \alias{GenomeDataList} % Coercion: \alias{coerce,GenomeDataList,data.frame-method} \title{List of GenomeData objects} \description{\code{GenomeDataList} is a list of \code{\linkS4class{GenomeData}} objects. It could be useful for storing data on multiple experiments or samples.} \details{ This class inherits from \code{\linkS4class{SimpleList}} and requires that all of its elements to be instances of \code{GenomeData}. One should try to take advantage of the metadata storage facilities provided by \code{SimpleList}. The \code{elementMetadata} field, for example, could be used to store the experimental design, while the \code{metadata} field could store the experimental platform. } \section{Constructor}{ \describe{ \item{}{ \code{GenomeDataList(listData = list(), metadata = list(), elementMetadata = NULL)}: Creates a \code{GenomeDataList} with the elements from the \code{listData} parameter, a list of \code{GenomeData} instances. The other arguments correspond to the optional metadata stored in \code{\linkS4class{SimpleList}}. } } } \section{Coercion}{ \describe{ \item{}{\code{as(from, "data.frame")}: Coerces each subelement to a data frame, and binds them into a single data frame with an additional column indicating chromosome } } } \author{ Michael Lawrence } \seealso{ \linkS4class{GenomeData}, the type of elements stored in this class. \linkS4class{SimpleList} } \examples{ gd <- GenomeData(list(chr1 = IRanges(1, 10), chrX = IRanges(2, 5)), organism = "Mmusculus", provider = "UCSC", providerVersion = "mm9") gdl <- GenomeDataList(list(gd), elementMetadata = DataFrame(induced = TRUE)) gdl[[1]] # get first element } \keyword{methods} \keyword{classes} BSgenome/man/GenomeDescription-class.Rd0000644000126300012640000001045412227064177021433 0ustar00biocbuildphs_compbio\name{GenomeDescription-class} \docType{class} % Classes \alias{class:GenomeDescription} \alias{GenomeDescription-class} \alias{GenomeDescription} % Accessor methods: \alias{organism} \alias{organism,GenomeDescription-method} \alias{species} \alias{species,GenomeDescription-method} \alias{provider} \alias{provider,GenomeDescription-method} \alias{providerVersion} \alias{providerVersion,GenomeDescription-method} \alias{releaseDate} \alias{releaseDate,GenomeDescription-method} \alias{releaseName} \alias{releaseName,GenomeDescription-method} \alias{bsgenomeName} \alias{bsgenomeName,GenomeDescription-method} \alias{seqinfo,GenomeDescription-method} % Standard generic methods: \alias{show,GenomeDescription-method} \title{GenomeDescription objects} \description{ A GenomeDescription object holds the meta information describing a given genome. } \details{ In general the user will not need to manipulate directly a GenomeDescription instance but will manipulate instead a higher-level object that belongs to a class containing the GenomeDescription class. For example the top-level object defined in any BSgenome data package is a \link{BSgenome} object. But because the \link{BSgenome} class contains the GenomeDescription class, it is also a GenomeDescription object and can therefore be treated as such. In other words all the methods described below will work on it. } \section{Accessor methods}{ In the code snippets below, \code{x} is a GenomeDescription object. \describe{ \item{}{ \code{organism(x)}: Return the target organism for this genome e.g. \code{"Homo sapiens"}, \code{"Mus musculus"}, \code{"Caenorhabditis elegans"}, etc... } \item{}{ \code{species(x)}: Return the target species for this genome e.g. \code{"Human"}, \code{"Mouse"}, \code{"Worm"}, etc... } \item{}{ \code{provider(x)}: Return the provider of this genome e.g. \code{"UCSC"}, \code{"BDGP"}, \code{"FlyBase"}, etc... } \item{}{ \code{providerVersion(x)}: Return the provider-side version of this genome. For example UCSC uses versions \code{"hg18"}, \code{"hg17"}, etc... for the different Builds of the Human genome. } \item{}{ \code{releaseDate(x)}: Return the release date of this genome e.g. \code{"Mar. 2006"}. } \item{}{ \code{releaseName(x)}: Return the release name of this genome, which is generally made of the name of the organization who assembled it plus its Build version. For example, UCSC uses \code{"hg18"} for the version of the Human genome corresponding to the Build 36.1 from NCBI hence the release name for this genome is \code{"NCBI Build 36.1"}. } \item{}{ \code{bsgenomeName(x)}: Uses the meta information stored in \code{x} to make the name of the corresponding BSgenome data package (see \link{available.genomes} for details about the naming scheme used for those packages). Of course there is no guarantee that a package with that name actually exists. } \item{\code{seqinfo(x)}}{ Gets information about the genome sequences. This information is returned in a \link[GenomicRanges]{Seqinfo} object. Each part of the information can be retrieved separately with \code{seqnames(x)}, \code{seqlengths(x)}, and \code{isCircular(x)}, respectively, as described below. } \item{\code{seqnames(x)}}{ Gets the names of the genome sequences. \code{seqnames(x)} is equivalent to \code{seqnames(seqinfo(x))}. } \item{\code{seqlengths(x)}}{ Gets the lengths of the genome sequences. \code{seqlengths(x)} is equivalent to \code{seqlengths(seqinfo(x))}. } \item{\code{isCircular(x)}}{ Returns the circularity flags of the genome sequences. \code{isCircular(x)} is equivalent to \code{isCircular(seqinfo(x))}. } } } \author{H. Pages} \seealso{ \code{\link{available.genomes}}, \link[GenomicRanges]{Seqinfo-class}, \link{BSgenome-class} } \examples{ library(BSgenome.Celegans.UCSC.ce2) class(Celegans) is(Celegans, "GenomeDescription") provider(Celegans) seqinfo(Celegans) gendesc <- as(Celegans, "GenomeDescription") class(gendesc) gendesc provider(gendesc) seqinfo(gendesc) bsgenomeName(gendesc) } \keyword{methods} \keyword{classes} BSgenome/man/available.genomes.Rd0000644000126300012640000000455512227064177020273 0ustar00biocbuildphs_compbio\name{available.genomes} \alias{available.genomes} \alias{installed.genomes} \title{Find available/installed genomes} \description{ \code{available.genomes} gets the list of BSgenome data packages that are currently available on the Bioconductor repositories for your version of R/Bioconductor. \code{installed.genomes} gets the list of BSgenome data packages that are already installed on your machine. } \usage{ available.genomes(splitNameParts=FALSE, type=getOption("pkgType")) installed.genomes(splitNameParts=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. } \item{type}{ Character string indicating the type of package (\code{"source"}, \code{"mac.binary"} or \code{"win.binary"}) to look for. } } \details{ A BSgenome data package contains the full genome for a given organism. Its name has 4 parts separated by a dot (e.g. BSgenome.Celegans.UCSC.ce2). The 1st part is always BSgenome, the 2nd part is the name of the organism (abbreviated), the 3rd part is the name of the organisation who assembled the genome and the 4th part is the release string or number used by this organisation for this genome. A BSgenome data package contains a single top-level object (a \link[BSgenome:BSgenome-class]{BSgenome} object) named like the second part of the package name (e.g. Celegans in the case of BSgenome.Celegans.UCSC.ce2) where all the sequences for this genome are stored. } \value{ A character vector containing the names of the BSgenome data packages that are currently available (for \code{available.genomes}), or already installed (for \code{installed.genomes}). } \author{H. Pages} \seealso{ \link{BSgenome-class}, \code{\link[utils:update.packages]{available.packages}} } \examples{ # What genomes are already installed: installed.genomes() # What genomes are available: available.genomes() # Split the package names in parts: ag <- available.genomes(TRUE) table(ag$organism) table(ag$provider) # Make your choice and install with: source("http://bioconductor.org/biocLite.R") biocLite("BSgenome.Scerevisiae.UCSC.sacCer1") # Have a coffee ;-) # Load the package and display the index of sequences for this genome: library(BSgenome.Scerevisiae.UCSC.sacCer1) Scerevisiae } \keyword{manip} BSgenome/man/bsapply.Rd0000644000126300012640000000526312227064177016366 0ustar00biocbuildphs_compbio\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}, a GenomeData object is returned containing the results generated using the remaining BSParams specifications. If \code{BSParams} sets \code{simplify = TRUE}, an \code{sapply}-like simplification is used on the results. } \author{Marc Carlson} \seealso{ \link{BSParams-class}, \link{BSgenome-class}, \link{BSgenome-utils}, \link{GenomeData-class} } \examples{ ## Load the Worm genome: library("BSgenome.Celegans.UCSC.ce2") ## Count the alphabet frequencies for every chromosome but exclude ## mitochrondrial ones: params <- new("BSParams", X = Celegans, FUN = alphabetFrequency, exclude = "M") bsapply(params) ## Or we can do this same function with simplify = TRUE: params <- new("BSParams", X = Celegans, FUN = alphabetFrequency, exclude = "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.hg19") ## 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 = Hsapiens, FUN = alphabetFrequency, exclude = c(1:8,"M","X","random","hap"), 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/gdReduce.Rd0000644000126300012640000000644512227064177016441 0ustar00biocbuildphs_compbio\name{gdReduce} \Rdversion{1.1} \alias{gdReduce} \alias{gdReduce,GenomeData-method} \alias{gdReduce,GenomeDataList-method} % Deprecated \alias{gdreduce} \title{ Reduces arguments to a single GenomeData instance } \description{ This function accepts one or more objects that are reduced, with a user-specified function, to a single \code{\linkS4class{GenomeData}} instance. } \usage{ gdReduce(f, ..., init, right = FALSE, accumulate = FALSE, gdArgs = list()) } \arguments{ \item{f}{ An object of class \code{"function"}, accepting two instances of classes appropriate for the \code{...} arguments, and returning an object suitable for subsequent use in \code{f} and incorporation into \code{GenomeData}. } \item{\dots}{ Objects to be reduced. All objects should be of the same class, as dictated by methods defined on \code{gdReduce} A function to be applied to each chromosome-level sub-element of \code{X}. } \item{init}{ An R object of the same kind as the elements of \dots. } \item{right}{ A logical indicating whether to proceed from left to right (default) or right to left. } \item{accumulate}{ A logical indicating whether the successive reduce combinations should be accumulated. By default, only the final combination is used.} \item{gdArgs}{ Additional arguments passed to the \code{\linkS4class{GenomeData}} constructor used to assemble the final object. } } \details{ The \code{gdReduce} method for \link{GenomeData} objects successively combines \link{GenomeData} elements of \code{...} using \code{f}; all arguments assigned to \code{...} must be of class \link{GenomeData}. \code{f} is a function accepting two objects returned by \code{"[["} applied to the successive elements of \code{...}, returning a single \link{GenomeData} object to be used in subsequent calls to \code{f}. \code{init}, \code{right}, and \code{accumulate} are as described for \code{\link{Reduce}}. \code{gdArgs} can be used to provide metadata information to the constructor used to create the final \link{GenomeData} object. Currently the \code{gdReduce} method for \link{GenomeDataList} objects works when a single \link{GenomeDataList} object \code{x} is provided as \code{...} and it does \code{gdReduce(f, x[[1]], x[[2]] ... x[[N]], init, right, accumulate, gdArgs)} where \code{N} is the length of \code{x} i.e. the number of \link{GenomeData} objects in it. } \value{ An object of class \code{GenomeData}, containing elements corresponding to the intersection of all named elements of \code{\dots} (in the case of the method for \link{GenomeData} objects) or all elements in the single \link{GenomeDataList} object passed to it (in the case of the method for \link{GenomeDataList} objects). } \author{ Martin Morgan } \seealso{ \code{\link{Reduce}}, \link{GenomeData-class}, \link{GenomeDataList-class} } \examples{ gdReduce showMethods("gdReduce") gd <- GenomeData(list(chr1 = IRanges(1, 10), chrX = IRanges(2, 5)), organism = "Mmusculus", provider = "UCSC", providerVersion = "mm9") gdr <- gdReduce(function(x, y) { ## "[[" returns IRanges instances, construct a synthetic version IRanges(c(start(x), start(y)), c(end(x), end(y))) }, GenomeDataList(list(gd, gd[2]))) gdr[["chr1"]] gdr[["chrX"]] } \keyword{manip} BSgenome/man/gdapply.Rd0000644000126300012640000000151012227064177016343 0ustar00biocbuildphs_compbio\name{gdapply} \Rdversion{1.1} \alias{gdapply} \alias{gdapply,GenomeData,function-method} \alias{gdapply,GenomeDataList,function-method} % Defunct: \alias{gdApply} \title{ Applies a function to elements of a GenomeData } \description{ Returns a list of values obtained by applying a function to elements of a \link{GenomeData} or \link{GenomeDataList} object. } \usage{ gdapply(X, FUN, ...) } \arguments{ \item{X}{ An object of class \link{GenomeData} or \link{GenomeDataList}. } \item{FUN}{ A function to be applied to each chromosome-level sub-element of \code{X}. } \item{\dots}{ Further arguments; passed to \code{FUN} } } \value{ Typically an object of the same class as \code{X}. } \author{ Deepayan Sarkar } \seealso{ \link{GenomeData-class}, \link{GenomeDataList-class} } \keyword{manip} BSgenome/man/getSeq-methods.Rd0000644000126300012640000003104112227064177017576 0ustar00biocbuildphs_compbio\name{getSeq-methods} \alias{getSeq,BSgenome-method} \title{getSeq method for BSgenome objects} \description{ A \code{\link[Biostrings]{getSeq}} method for extracting a set of sequences (or subsequences) from a \link{BSgenome} object. } \usage{ \S4method{getSeq}{BSgenome}(x, names, start=NA, end=NA, width=NA, strand="+", as.character=FALSE) } \arguments{ \item{x}{ A \link{BSgenome} object. See the \code{\link{available.genomes}} function for how to install a genome. } \item{names}{ 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 \link[IRanges]{RangedData} 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. } \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]{RangedData}, \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, or a \link[IRanges]{RangedData} object with a strand column. } \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[IRanges]{RangedData} object then L = \code{nrow(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, or a \link[IRanges]{RangedData} object with a strand column, 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. } } \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]{RangedData}, \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. Pages; 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]{RangedData-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) ## Get the "NM_058280_up_1000" sequence (belongs to the upstream1000 ## multiple sequence) as a DNAString object: s1 <- getSeq(Celegans, "NM_058280_up_1000") stopifnot(identical(getSeq(Celegans, "NM_058280_up_5000", start=-1000), s1)) \dontrun{ ## Fails because there is more than one sequence across ## Celegans$upstream1000, Celegans$upstream2000 and Celegans$upstream5000 ## with "NM_058280" in its name: getSeq(Celegans, "NM_058280") ## Fails because there is no sequence named exactly "NM_058280": getSeq(Celegans, "^NM_058280$") } ## --------------------------------------------------------------------- ## 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), elementLengths(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() } \keyword{manip} BSgenome/man/injectSNPs.Rd0000644000126300012640000001077112227064177016734 0ustar00biocbuildphs_compbio\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} \alias{SNPcount,InjectSNPsHandler-method} \alias{SNPcount,BSgenome-method} \alias{SNPlocs} \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, SNPlocs_pkgname) SNPlocs_pkgname(x) SNPcount(x) SNPlocs(x, seqname) ## Related utilities available.SNPs(type=getOption("pkgType")) installed.SNPs() } \arguments{ \item{x}{ A \link[BSgenome:BSgenome-class]{BSgenome} object. } \item{SNPlocs_pkgname}{ The name of a SNPlocs data package containing SNP information for the single sequences contained in \code{x}. This package 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. } } \value{ \code{injectSNPs} returns a copy of the original genome \code{x} where some or all of the single sequences were altered by injecting the SNPs defined in the SNPlocs data package specified thru the \code{SNPlocs_pkgname} argument. 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:BSgenome-class]{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 data packages that are currently available on the Bioconductor repositories for your version of R/Bioconductor. A SNPlocs data package contains basic SNP information (location and alleles) for a given organism. \code{installed.SNPs} returns a character vector containing the names of the SNPlocs 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 if it's not already loaded. } \author{H. Pages} \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.dbSNP.20100427") } ## Inject SNPs from dbSNP into the Human genome: library(BSgenome.Hsapiens.UCSC.hg19) Hsapiens SNPlocs_pkgname(Hsapiens) SNP_Hsapiens <- injectSNPs(Hsapiens, "SNPlocs.Hsapiens.dbSNP.20100427") SNP_Hsapiens # note the extra "with SNPs injected from ..." line SNPlocs_pkgname(SNP_Hsapiens) SNPcount(SNP_Hsapiens) head(SNPlocs(SNP_Hsapiens, "chr1")) alphabetFrequency(Hsapiens$chr1) alphabetFrequency(SNP_Hsapiens$chr1) ## Find runs of SNPs of length at least 25 in chr1. Might require ## more memory than some platforms can handle (e.g. 32-bit Windows ## and maybe some Mac OS X machines with little memory): is_32bit_windows <- .Platform$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(SNP_Hsapiens$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/tests/0000755000126300012640000000000012227064177015006 5ustar00biocbuildphs_compbioBSgenome/tests/unit/0000755000126300012640000000000012227133625015760 5ustar00biocbuildphs_compbio