Rsamtools/DESCRIPTION0000644000175400017540000000315113624616601015276 0ustar00biocbuildbiocbuildPackage: Rsamtools Type: Package Title: Binary alignment (BAM), FASTA, variant call (BCF), and tabix file import Version: 2.2.3 Author: Martin Morgan, Herv\'e Pag\`es, Valerie Obenchain, Nathaniel Hayden Maintainer: Bioconductor Package Maintainer Description: This package provides an interface to the 'samtools', 'bcftools', and 'tabix' utilities for manipulating SAM (Sequence Alignment / Map), FASTA, binary variant call (BCF) and compressed indexed tab-delimited (tabix) files. URL: http://bioconductor.org/packages/Rsamtools License: Artistic-2.0 | file LICENSE LazyLoad: yes Depends: methods, GenomeInfoDb (>= 1.1.3), GenomicRanges (>= 1.31.8), Biostrings (>= 2.47.6) Imports: utils, BiocGenerics (>= 0.25.1), S4Vectors (>= 0.17.25), IRanges (>= 2.13.12), XVector (>= 0.19.7), zlibbioc, bitops, BiocParallel Suggests: GenomicAlignments, ShortRead (>= 1.19.10), GenomicFeatures, TxDb.Dmelanogaster.UCSC.dm3.ensGene, KEGG.db, TxDb.Hsapiens.UCSC.hg18.knownGene, RNAseqData.HNRNPC.bam.chr14, BSgenome.Hsapiens.UCSC.hg19, RUnit, BiocStyle LinkingTo: Rhtslib (>= 1.17.7), S4Vectors, IRanges, XVector, Biostrings SystemRequirements: GNU make biocViews: DataImport, Sequencing, Coverage, Alignment, QualityControl Video: https://www.youtube.com/watch?v=Rfon-DQYbWA&list=UUqaMSQd_h-2EDGsU6WDiX0Q git_url: https://git.bioconductor.org/packages/Rsamtools git_branch: RELEASE_3_10 git_last_commit: 073d892 git_last_commit_date: 2020-02-22 Date/Publication: 2020-02-23 NeedsCompilation: yes Packaged: 2020-02-24 00:49:05 UTC; biocbuild Rsamtools/LICENSE0000644000175400017540000000216113556116727014605 0ustar00biocbuildbiocbuildFile inst/extdata/ex1.sam is licensed as follows: The MIT License Copyright (c) 2008-2009 Genome Research Ltd. Permission is hereby granted, free of charge, to any person obtaining a copy of this software and associated documentation files (the "Software"), to deal in the Software without restriction, including without limitation the rights to use, copy, modify, merge, publish, distribute, sublicense, and/or sell copies of the Software, and to permit persons to whom the Software is furnished to do so, subject to the following conditions: The above copyright notice and this permission notice shall be included in all copies or substantial portions of the Software. THE SOFTWARE IS PROVIDED "AS IS", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL THE AUTHORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER LIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING FROM, OUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE USE OR OTHER DEALINGS IN THE SOFTWARE. Rsamtools/NAMESPACE0000644000175400017540000000262713556116727015026 0ustar00biocbuildbiocbuilduseDynLib(Rsamtools, .registration=TRUE) import(methods) import(zlibbioc) importFrom(bitops, bitAnd) importFrom(utils, read.table) # normalizePath --> base in R-2.13 importFrom(stats, rbinom, setNames) importClassesFrom(BiocGenerics, url, gzfile, unz, pipe) importFrom(BiocGenerics, cbind, duplicated, eval, Filter, lapply, Map, order, path, paste, rbind, Reduce, rep.int, sapply, setdiff, tapply, union, unique) importFrom(BiocParallel, bplapply) import(S4Vectors) import(IRanges) importClassesFrom(GenomeInfoDb, Seqinfo) importFrom(GenomeInfoDb, Seqinfo, seqinfo, seqlevels, sortSeqlevels) importClassesFrom(GenomicRanges, GRanges, GRangesList) importFrom(GenomicRanges, GRanges, GRangesList) importMethodsFrom(GenomicRanges, seqnames, strand) import(XVector) importClassesFrom(Biostrings, DNAStringSet, BStringSet, PhredQuality) importFrom(Biostrings, DNA_ALPHABET, readDNAStringSet, readRNAStringSet, readAAStringSet, DNAStringSet, BStringSet, PhredQuality, getSeq, reverseComplement) exportPattern("^[^\\.]") exportMethods(length, names, "[", "[[", show, getSeq, seqinfo) S3method(close, BamFile) S3method(close, BcfFile) S3method(close, FaFile) S3method(close, TabixFile) S3method(close, RsamtoolsFileList) S3method(open, BamFile) S3method(open, BcfFile) S3method(open, FaFile) S3method(open, TabixFile) S3method(open, RsamtoolsFileList) Rsamtools/NEWS0000644000175400017540000003605313624571433014301 0ustar00biocbuildbiocbuildCHANGES IN VERSION 2.2 ---------------------- BUG FIXES o (v 2.2.2) Correctly handle '*' ('unknown') RNAME during paired-end processing. See https://github.com/Bioconductor/Rsamtools/issues/16. o (v 2.2.3) Fix regression introduced by v 2.2.2. CHANGES IN VERSION 2.0 ---------------------- SIGNIFICANT USER-VISIBLE CHANGES o Migrate Rsamtools to Rhtslib. See Rsamtools/migration_notes.md for more information about this migration. o Remove unused fields from BamRangeIterator o Remove BAM header hash init for pileup (already memoized in Rhtslib) CHANGES IN VERSION 1.34 ----------------------- BUG FIXES o (v 1.34.1) indexFa,FaFile-method correctly updates the index path. CHANGES IN VERSION 1.33 ----------------------- NEW FEATURES o (v 1.33.4, 1.33.7) scanBamFlag() gains isSupplementaryAlignment support. BUG FIXES o (v 1.33.1) Do not try to grow NULL (not-yet-encountered) tags (https://support.bioconductor.org/p/110609/ ; Robert Bradley) o (v 1.33.5) Check for corrupt index (https://github.com/Bioconductor/Rsamtools/issues/3 ; kjohnsen) CHANGES IN VERSION 1.31 ----------------------- BUG FIXES o (v.1.31.3) pileup() examples require min_base_quality = 10. See https://support.bioconductor.org/p/105515/#105553 CHANGES IN VERSION 1.27 ----------------------- BUG FIXES o qnameSuffixStart<-(), qnamePrefixEnd<-() accept 'NA' (bug report from Peter Hickey). o scanBam() accepts a single tag mixing 'Z' and 'A' format. See https://support.bioconductor.org/p/94553/ CHANGES IN VERSION 1.25 ----------------------- NEW FEATURES o *File and *FileList (e.g., TabixFile, TabixFileList) constructors support NA as 'index'. o *File and *FileList have accessor method for index. o asBam(), asSam() provide default desinations. o idxstatsBam() quickly summarizes the number of mapped and unmapped reads on each sequence in a BAM file. SIGNIFICANT USER-VISIBLE CHANGES o index() by default returns NA rather than character(), but can be controled with asNA argument. BUG FIXES o TabixFileList(TabixFile()) works. o *File constructors now check that the file argument is length 1, and that the index argument is length 0 or 1. CHANGES IN VERSION 1.23 ----------------------- NEW FEATURES o filterBam can filter one source file into multiple destinations by providing a vector of destination files and a list of FilterRules. o phred2ASCIIOffset() helps translate PHRED encodings (integer or character) to ASCII offsets for use in pileup() BUG FIXES o scanBam() fails early when param seqlevels not present in file. o Rsamtools.mk for Windows avoids spaces in file paths CHANGES IN VERSION 1.21 ----------------------- SIGNIFICANT USER-VISIBLE CHANGES o pileup adds query_bins arg to give strand-sensitive cycle bin behavior; cycle_bins renamed left_bins; negative values allowed (including -Inf) to specify bins based on distance from end-of-read. o mapqFilter allows specification of a mapping quality filter threshold o PileupParam() now correctly follows samtools with min_base_quality=13, min_map_quality=0 (previously, values were assigned as 0 and 13, respectively) o Support parsing 'B' tags in bam file headers. BUG FIXES o segfault on range iteration introduced 1.19.35, fixed in 1.21.1 o BamViews parallel evaluation with BatchJobs back-end requires named arguments CHANGES IN VERSION 1.19 ----------------------- SIGNIFICANT USER-VISIBLE CHANGES o FaFile accepts a distinct index file o Support for cigars > 32767 characters o Mate pairs use pos and mpos values calculated modulo target length for pairing, facilitating some representations of mates on circular chromosomes. o scanBam no longer translates mapq '255' to 'NA' BUG FIXES o segfault on file iteration, introduced in 1.19.35, fixed in 1.19.44 o scanBam correctly parses '=' and 'X' CHANGES IN VERSION 1.17.0 ------------------------- NEW FEATURES o pileup visits entire file if no 'which' argument specified for 'ScanBamParam' parameter of pileup. Buffered functionality with 'yieldSize' available to manage memory consumption when working with large BAM files o pileup 'read_pos_breaks' parameter renamed to 'cycle_bins': cycle_bins allows users to differentiate pileup counts based on user-defined regions within a read. o pileup uses PileupParam and ScanBamParam instances to calculate pileup statistics for a BAM file; returns a data.frame with columns summarizing information extracted from alignments overlapping each genomic position o scanBam,BamSampler-method returns requested and actual yieldSize, and total reads o seqinfo,BamFileList-method returns the merged seqinfo of each BamFile; seqlevels and seqlengths behave similarly. o scanBamHeader accepts a 'what' argument to control input of the targets and / or text portion of the header, and is much faster for BAM files with many rnames. SIGNIFICANT USER-VISIBLE CHANGES o rename PileupParam class and constructor -> ApplyPileupsParam o seqinfo,BamFile-method orders levels as they occur in the file, reverting a change introduced in Rsamtools version 1.15.28 (version 1.17.16). BUG FIXES o scanBam(BamSampler(), param=param) with a 'which' argument no longer mangles element names, and respects yield size o applyPileups checks that seqlevels are identical across files o scanFa documentation incorrectly indicated that end coordinates beyond the range of the sequence would be truncated; they are an error. o applyPileups would fail on cigars with insertion followed by reference skip, e.g., 2I1024N98M (bug report of Dan Gatti). CHANGES IN VERSION 1.15.0 ------------------------- NEW FEATURES o asSam converts BAM files to SAM files o razip, bgzip re-compress directly from .gz files o yieldReduce through a BAM or other file, applying a MAP function to each chunk and reducing the result to it's final representation SIGNIFICANT USER-VISIBLE CHANGES o bgzip default extension changed to '.bgz' o seqinfo,BamFile-method attempts to return seqnames in 'natural' order, e.g., chr1, chr2, ... o yieldSize now works on BAM files queried with ranges. Successive ranges are input until the total number of records first equals or exceeds yieldSize.. o scanFa supports DNA, RNA, and AAStringSet return objects BUG FIXES o scanFa returns correct sequence at the very end of files o razip compresses small files o applyPileups no longer crashes in the absence of an index file CHANGES IN VERSION 1.14.0 ------------------------- NEW FEATURES o seqinfo(FaFile) returns available information on sequences and lengths on Fa (indexed fasta) files. o filterBam accepts FilterRules call-backs for arbitrary filtering. o add isIncomplete,BamFile-method to test for end-of-file o add count.mapped.reads to summarizeOverlaps,*,BamFileList-method; set to TRUE to collect read and nucleotide counts via countBam. o add summarizeOverlaps,*,character-method to count simple file paths o add sequenceLayer() and stackStringsFromBam() o add 'with.which_label' arg to readGAlignmentsFromBam(), readGappedReadsFromBam(), readGAlignmentPairsFromBam(), and readGAlignmentsListFromBam() SIGNIFICANT USER-VISIBLE CHANGES o rename: readBamGappedAlignments() -> readGAlignmentsFromBam() readBamGappedReads() -> readGappedReadsFromBam() readBamGappedAlignmentPairs() -> readGAlignmentPairsFromBam() readBamGAlignmentsList() -> readGAlignmentsListFromBam() makeGappedAlignmentPairs() -> makeGAlignmentPairs() o speedup findMateAlignment() DEPRECATED AND DEFUNCT o deprecate readBamGappedAlignments(), readBamGappedReads(), readBamGappedAlignmentPairs(), readBamGAlignmentsList(), and makeGappedAlignmentPairs() BUG FIXES o scanVcfHeader tolerates records without ID fields, and with fields named similar to ID. o close razip files only once. o report tabix input errors CHANGES IN VERSION 1.12.0 ------------------------- NEW FEATURES o BamSampler draws a random sample from BAM file records, obeying any restriction by ScanBamParam(). o Add argument 'obeyQname' to BamFile. Used with qname-sorted Bam files only. o Add readBamGAlignmentsList function for reading qname-sorted Bam files into a GAlignmentsList object. USER-VISIBLE CHANGES o bamPath and bamIndicies applied to BamViews returns named vectors. o 'yieldSize' argument in BamFile represents the number of unique qnames when 'obeyQname=TRUE'. BUG FIXES o completely free razip, bgzip files when done. o sortBam, indexBam fail gracefully on non-BAM input. o headerTabix on an open TabixFile no longer reads the first record o scanBcfHeader provides informative error message when header line ('#CHROM POS ...') is missing CHANGES IN VERSION 1.10.0 ------------------------- NEW FEATURES o BamFile and TabixFile accept argument yieldSize; repeated calls to scanBam and scanTabix return successive yieldSize chunks of the file. readBamGappedAlignments, VariantAnnotation::readVcf automatically gain support for yield'ing through files. o Add getDumpedAlignments(), countDumpedAlignments(), and flushDumpedAlignments() low-level utilities for manipulating alignments dumped by findMateAlignment(). o Add quickBamCounts() utility for classifying the records in a BAM file according to a set of predefined groups (based on the flag bits) and for counting the nb of records in each group. SIGNIFICANT USER-VISIBLE CHANGES o scanBamFlag isValidVendorRead deprecated in favor of isNotPassingQualityControls o Rename makeGappedAlignmentPairs() arg 'keep.colnames' -> 'use.mcols'. BUG FIXES o close razip, bgzip files when done o bamReverseComplement<- failed to return the updated object o scanBcfHeader works on remote files o allow asBam to work without warnings on header-only SAM files o some bug fixes and and small performance improvements to findMateAlignment() o fix bug in readBamGappedAlignmentPairs() where fields and tags specified by the user were not propagated to the returned GappedAlignmentPairs object CHANGES IN VERSION 1.8.0 ------------------------ NEW FEATURES o Add readBamGappedAlignmentPairs() (plus related utilities findMateAlignment() and makeGappedAlignmentPairs()) to read a BAM file into a GappedAlignmentPairs object. SIGNIFICANT USER-VISIBLE CHANGES o update samtools to github commit dc27682f70713a70d4f31bca652cf78e00757da2 o Add 'bitnames' arg to bamFlagAsBitMatrix() utility. o By default readBamGappedAlignments() and readBamGappedReads() don't drop PCR or optical duplicates anymore. BUG FIXES o readBamGappedAlignments handles empty 'tag' fields o scanTabix would omit variants overlapping range ends o scanFa would segfault on empty files or empty ids CHANGES IN VERSION 1.6.0 ------------------------ NEW FEATURES o TabixFile, indexTabix, scanTabix, yieldTabix index (sorted, compressed) and parse tabix-indexed files o readBamGappedReads(), bamFlagAsBitMatrix(), bamFlagAND() o Add use.names and param args to readBamGappedAlignments(); dropped which and ... args. o PileupFiles, PileupParam, applyPileup for visiting several BAM files and calculating pile-ups on each. o Provide a zlib for Windows, as R does not currently do this o BamFileList, BcfFileList, TabixFileList, FaFileList clases extend IRanges::SimpleList, for managings lists of file references o razfFa creates random access compressed fasta files. o count and scanBam support input of larger numbers of records; countBam nucleotide count is now numeric() and subject to rounding error when large. o Update to samtools 0.1.17 o asBcf and indexBcf coerces VCF files to BCF, and indexes BCF o Update to samtools 0.1.18 o scanVcf parses VCF files; use scanVcf,connection,missing-method to stream, scanVcf,TabixFile,*-method to select subsets. Use unpackVcf to expand INFO and GENO fields. SIGNIFICANT USER-VISIBLE CHANGES o ScanBamParam argument 'what' defaults to character(0) (nothing) rather than scanBamWhat() (everything) o bamFlag returns a user-friendly description of flags by default BUG FIXES o scanBam (and readBamGappedAlignments) called with an invalid or character(0) index no longer segfaults. o scanBcfHeader parses values with embedded commas or = o scanFa fails, rather than returns incorrect sequences, when file is compressed and file positions are not accessed sequentially o scanBcf parses VCF files with no genotype information. o scanBam called with the first range having no reads returned invalid results for subsequent ranges; introduced in svn r57138 o scanBamFlag isPrimaryRead changed to isNotPrimaryRead, correctly reflecting the meaning of the flag. CHANGES IN VERSION 1.4.0 ------------------------ NEW FEATURES o BamFile class allows bam files to be open across calls to scanBam and friends. This can be helpful when wanting to avoid repeated loading of the index, for instance. o BcfFile, scanBcf, scanBcfHeader to parse bcftools' .vcf and .bcf files. Note that this implements bcftools notions of vcf and bcf, and are not fully compliant with vcf-4.0. o asBam converts SAM files to (indexed) BAM files o FaFile, indexFa, scanIndexFa, scanFa index and parse (indexed) fasta files. BUG FIXES o scanBamFlag isValidVendorRead had reversed TRUE/FALSE logic o Attempts to read too many records caught more gracefully. o samtools output to fprintf() or calls to exit() are handled more gracefully CHANGES IN VERSION 1.2.0 ------------------------ NEW FEATURES o Update to samtools 0.1.8 o Update to samtools svn rev 750 (Mon, 27 Sep 2010) o sortBam sorts a BAM file BUG FIXES o Attempts to parse non-existent local files now generate an error o Reads whose last nucleotide overlaps the first of a range are now scanned / counted. o scanning / counting reads late in large Windows files is fast o scanBam tag fields of type 'A' parsed correctly CHANGES IN VERSION 1.0.0 ----------------------- SIGNIFICANT USER-VISIBLE CHANGES o scanBam returns minus-strand reads in the manner presented in the BAM file, i.e., as though on the positive strand. This occurs in revision 0.1.34 o readBamGappedAlignments replaces readBAMasGappedAlignments NEW FEATURES o ScanBamParam() accepts 'tag' argument for parsing optional fields o BamViews can be used with scanBam, countBam, readBamGappedAlignments BUG FIXES o No changes classified as 'bug fixes' (package under active development) Rsamtools/R/0000755000175400017540000000000013556116727014001 5ustar00biocbuildbiocbuildRsamtools/R/AllClasses.R0000644000175400017540000000517313556116727016160 0ustar00biocbuildbiocbuildsetOldClass(c("bzfile", "connection")) setOldClass(c("fifo", "connection")) setGeneric(".validity", function(object) standardGeneric(".validity")) setClass("ScanBamParam", representation=representation( flag="integer", simpleCigar="logical", reverseComplement="logical", tag="character", tagFilter="list", what="character", which="IntegerRangesList", mapqFilter="integer")) setClass("BamViews", representation=representation( bamPaths="character", bamIndicies="character", bamSamples="DataFrame", bamRanges="GRanges", bamExperiment="list"), validity=.validity) setClass("ScanBVcfParam", representation=representation( "VIRTUAL", which="IntegerRangesList", fixed="character", info="character", geno="character", samples="character", trimEmpty="logical"), prototype=prototype( trimEmpty=TRUE)) setClass("ScanBcfParam", contains="ScanBVcfParam") setClass("ApplyPileupsParam", representation=representation( flag="integer", minBaseQuality="integer", minMapQuality="integer", minDepth="integer", maxDepth="integer", yieldSize="integer", yieldBy="character", yieldAll="logical", which="GRanges", what="character"), validity=.validity) ## RsamtoolsFile(s) .RsamtoolsFile_generator <- setRefClass("RsamtoolsFile", fields=list(.extptr="externalptr", path="character", index="character", yieldSize="integer")) .BamFile <- setRefClass("BamFile", contains="RsamtoolsFile", fields=list(obeyQname="logical", asMates="logical", qnamePrefixEnd="character", qnameSuffixStart="character")) .BcfFile <- setRefClass("BcfFile", contains="RsamtoolsFile", fields=list(mode="character")) .TabixFile <- setRefClass("TabixFile", contains="RsamtoolsFile") .FaFile <- setRefClass("FaFile", contains="RsamtoolsFile", fields=list(gzindex="character")) setClass("RsamtoolsFileList", contains=c("SimpleList", "VIRTUAL")) setClass("BamFileList", contains="RsamtoolsFileList", prototype=prototype(elementType="BamFile")) setClass("BcfFileList", contains="RsamtoolsFileList", prototype=prototype(elementType="BcfFile")) setClass("TabixFileList", contains="RsamtoolsFileList", prototype=prototype(elementType="TabixFile")) setClass("FaFileList", contains="RsamtoolsFileList", prototype=prototype(elementType="FaFile")) setClass("PileupFiles", contains="BamFileList", representation=representation(param="ApplyPileupsParam")) Rsamtools/R/AllGenerics.R0000644000175400017540000001352413556116727016321 0ustar00biocbuildbiocbuildsetGeneric("ScanBamParam", function(flag=scanBamFlag(), simpleCigar=FALSE, reverseComplement=FALSE, tag=character(0), tagFilter=list(), what=character(0), which, mapqFilter=NA_integer_) standardGeneric("ScanBamParam"), signature="which") setGeneric("scanBam", function(file, index=file, ..., param=ScanBamParam(what=scanBamWhat())) standardGeneric("scanBam"), signature="file") setGeneric("scanBamHeader", function(files, ...) standardGeneric("scanBamHeader")) setGeneric("countBam", function(file, index=file, ..., param=ScanBamParam()) standardGeneric("countBam"), signature="file") setGeneric("idxstatsBam", function(file, index=file, ...) standardGeneric("idxstatsBam"), signature="file") setGeneric("asBam", function(file, destination = sub("\\.sam(\\.gz)?", "", file), ...) standardGeneric("asBam")) setGeneric("asSam", function(file, destination = sub("\\.bam", "", file), ...) standardGeneric("asSam")) setGeneric("sortBam", function(file, destination, ...) standardGeneric("sortBam")) setGeneric("mergeBam", function(files, destination, ...) standardGeneric("mergeBam"), signature="files") setGeneric("indexBam", function(files, ...) standardGeneric("indexBam")) setGeneric("filterBam", function(file, destination, index=file, ...) standardGeneric("filterBam")) setGeneric("quickBamFlagSummary", function(file, ..., param=ScanBamParam(), main.groups.only=FALSE) standardGeneric("quickBamFlagSummary"), signature="file") setGeneric("indexFa", function(file, ...) standardGeneric("indexFa")) setGeneric("scanFaIndex", function(file, ...) standardGeneric("scanFaIndex")) setGeneric("countFa", function(file, ...) standardGeneric("countFa")) setGeneric("scanFa", function(file, param, ..., as=c("DNAStringSet", "RNAStringSet", "AAStringSet")) standardGeneric("scanFa"), signature=c("file", "param")) setGeneric("readPileup", function(file, ...) standardGeneric("readPileup")) ## bcf setGeneric("ScanBcfParam", function(fixed=character(), info=character(), geno=character(), samples=character(), trimEmpty=TRUE, which, ...) standardGeneric("ScanBcfParam"), signature="which") setGeneric("isOpen") setGeneric("isIncomplete") setGeneric("scanBcfHeader", function(file, ...) standardGeneric("scanBcfHeader")) setGeneric("scanBcf", function(file, ...) standardGeneric("scanBcf")) setGeneric("asBcf", function(file, dictionary, destination, ..., overwrite=FALSE, indexDestination=TRUE) standardGeneric("asBcf"), signature="file") setGeneric("indexBcf", function(file, ...) standardGeneric("indexBcf")) ## other setGeneric("BamViews", function(bamPaths=character(0), bamIndicies=bamPaths, bamSamples=DataFrame(row.names= make.unique(basename(bamPaths))), bamRanges, bamExperiment=list(), ...) standardGeneric("BamViews"), signature="bamRanges") ## tabix setGeneric("seqnamesTabix", function(file, ...) standardGeneric("seqnamesTabix")) setGeneric("headerTabix", function(file, ...) standardGeneric("headerTabix")) setGeneric("scanTabix", function(file, ..., param) standardGeneric("scanTabix")) setGeneric("yieldTabix", function(file, ..., yieldSize=1000000L) standardGeneric("yieldTabix"), signature="file") ## pileup setGeneric("pileup", function(file, index=file, ..., scanBamParam=ScanBamParam(), pileupParam=PileupParam()) standardGeneric("pileup"), signature=signature("file")) setGeneric(".asRegions", function(x) standardGeneric(".asRegions")) setGeneric("applyPileups", function(files, FUN, ..., param) standardGeneric("applyPileups"), signature=c("files", "param")) ## RsamtoolsFile(s) setGeneric("index", function(object, ..., asNA=TRUE) standardGeneric("index"), signature="object") setGeneric("index<-", function(object, ..., value) standardGeneric("index<-")) setGeneric("gzindex", function(object, asNA=TRUE) standardGeneric("gzindex"), signature="object") setGeneric("gzindex<-", function(object, value) standardGeneric("gzindex<-")) setGeneric("yieldSize", function(object, ...) standardGeneric("yieldSize")) setGeneric("yieldSize<-", function(object, ..., value) standardGeneric("yieldSize<-")) setGeneric("obeyQname", function(object, ...) standardGeneric("obeyQname")) setGeneric("obeyQname<-", function(object, ..., value) standardGeneric("obeyQname<-")) setGeneric("asMates", function(object, ...) standardGeneric("asMates")) setGeneric("asMates<-", function(object, ..., value) standardGeneric("asMates<-")) setGeneric("qnamePrefixEnd", function(object, ...) standardGeneric("qnamePrefixEnd")) setGeneric("qnamePrefixEnd<-", function(object, ..., value) standardGeneric("qnamePrefixEnd<-")) setGeneric("qnameSuffixStart", function(object, ...) standardGeneric("qnameSuffixStart")) setGeneric("qnameSuffixStart<-", function(object, ..., value) standardGeneric("qnameSuffixStart<-")) setGeneric("isOpen") setGeneric("testPairedEndBam", function(file, index=file, ...) standardGeneric("testPairedEndBam"), signature="file") Rsamtools/R/asBam.R0000644000175400017540000000351413556116727015152 0ustar00biocbuildbiocbuildsetMethod(asSam, "character", function(file, destination=sub("\\.bam", "", file), ..., overwrite=FALSE) { file <- .normalizePath(file) destination <- .normalizePath(destination) d0 <- paste(destination, "sam", sep=".") if (!overwrite && file.exists(d0)) { msg <- sprintf("'%s' exists, '%s' is FALSE\n %s: %s", "destination", "overwrite", "destination", d0) stop(msg) } tryCatch({ result <- .Call(.as_bam, file, d0, FALSE) if (!file.exists(d0)) stop("failed to create 'SAM' file") }, error=function(err) { msg <- sprintf("'asSam' %s\n SAM file: '%s'\n", conditionMessage(err), file) stop(msg) }) d0 }) setMethod(asBam, "character", function(file, destination=sub("\\.sam(\\.gz)?", "", file), ..., overwrite=FALSE, indexDestination=TRUE) { file <- .normalizePath(file) destination <- .normalizePath(destination) d0 <- paste(destination, "bam", sep=".") ofl <- tempfile() on.exit(unlink(ofl)) if (!overwrite && file.exists(d0)) { msg <- sprintf("'%s' exists, '%s' is FALSE\n %s: %s", "destination", "overwrite", "destination", d0) stop(msg) } tryCatch({ result <- .Call(.as_bam, file, ofl, TRUE) if (!file.exists(ofl)) stop("failed to create 'BAM' file") if (indexDestination) { destination <- sortBam(ofl, destination) indexBam(destination) } else { destination <- d0 .file.rename(ofl, destination) } }, error=function(err) { msg <- sprintf("'asBam' %s\n SAM file: '%s'\n", conditionMessage(err), file) stop(msg) }) destination }) Rsamtools/R/countBam.R0000644000175400017540000000166413556116727015703 0ustar00biocbuildbiocbuild.countBam_postprocess <- function(x, file, param) { which <- bamWhich(param) bfile <- basename(path(file)) if (0L != length(space(which))) { data.frame(space=space(which), start=.uunlist(start(which)), end=.uunlist(end(which)), width=.uunlist(width(which)), file=bfile, records=x[["records"]], nucleotides=x[["nucleotides"]]) } else { data.frame(space=NA, start=NA, end=NA, width=NA, file=bfile, records=x[["records"]], nucleotides=x[["nucleotides"]]) } } setMethod(countBam, "character", function(file, index=file, ..., param=ScanBamParam()) { index <- if (missing(index) && 0L == length(bamWhich(param))) character(0) else .normalizePath(index) bam <- open(BamFile(file, index), "rb") on.exit(close(bam)) countBam(bam, ..., param=param) }) Rsamtools/R/filterBam.R0000644000175400017540000000312113556116727016026 0ustar00biocbuildbiocbuild.normalizeRangesList <- function(rangesList) { nms <- names(rangesList) reducedList <- if (0 != length(rangesList) && is.null(nms)) { ## special case, all names missing rng <- Reduce(append, as(rangesList, "list")) IRangesList(reduce(rng, drop.empty.ranges=TRUE)) } else if (any(duplicated(nms))) { unms <- unique(nms) lst <- lapply(unms, function(nm, rnglist) { idx <- names(rnglist) == nm rng <- Reduce(append, as(rnglist[idx], "list")) reduce(rng, drop.empty.ranges=TRUE) }, rnglist=rangesList) names(lst) <- unms do.call(IRangesList, lst) } else { reduce(rangesList, drop.empty.ranges=TRUE) } reducedList[lengths(reducedList) != 0] } .filterBam_preprocess <- function(file, param) { which <- .normalizeRangesList(bamWhich(param)) hnames <- seqlevels(file) o <- order(match(names(which), hnames)) what <- bamWhat(param) if (asMates(file)) what <- union(what, c("mate_status", "groupid")) initialize(param, which=which[o], what=what) } setMethod(filterBam, "character", function(file, destination, index=file, ..., filter=FilterRules(), indexDestination=TRUE, param=ScanBamParam(what=scanBamWhat())) { if (missing(index) && 0L == length(bamWhich(param))) index <- character(0) bam <- open(BamFile(file, index), "rb") on.exit(close(bam)) filterBam(bam, destination, ..., filter=filter, indexDestination=indexDestination, param=param) }) Rsamtools/R/idxstatsBam.R0000644000175400017540000000031613556116727016407 0ustar00biocbuildbiocbuildsetMethod(idxstatsBam, "character", function(file, index=file, ...) { index <- .normalizePath(index) bam <- open(BamFile(file, index), "rb") on.exit(close(bam)) idxstatsBam(bam, ...) }) Rsamtools/R/indexBam.R0000644000175400017540000000024213556116727015651 0ustar00biocbuildbiocbuildsetMethod(indexBam, "character", function(files, ...) { files <- .normalizePath(files) sapply(files, function(file) .Call(.index_bam, file)) }) Rsamtools/R/io_bam.R0000644000175400017540000000205513556116727015354 0ustar00biocbuildbiocbuild.io_bam <- function(func, file, ..., param) { flag <- bamFlag(param, asInteger=TRUE) simpleCigar <- bamSimpleCigar(param) tagFilter <- bamTagFilter(param) mapqFilter <- bamMapqFilter(param) which <- bamWhich(param) if (!all(names(which) %in% seqlevels(file))) { bad <- setdiff(names(which), seqlevels(file)) stop("seqlevels(param) not in BAM header:", "\n seqlevels: ", paste(sQuote(bad), collapse=", "), "\n file: ", path(file), "\n index: ", index(file)) } regions <- if (0L != length(space(which))) list(as.character(space(which)), .uunlist(start(which)), .uunlist(end(which))) else NULL on.exit(.Call(.scan_bam_cleanup)) .io_check_exists(path(file)) tryCatch({ .Call(func, .extptr(file), regions, flag, simpleCigar, tagFilter, mapqFilter, ...) }, error=function(err) { stop(conditionMessage(err), "\n file: ", path(file), "\n index: ", index(file)) }) } Rsamtools/R/mergeBam.R0000644000175400017540000000237113556116727015646 0ustar00biocbuildbiocbuildsetMethod(mergeBam, "character", function(files, destination, ..., region = GRanges(), overwrite = FALSE, header = character(), byQname = FALSE, addRG = FALSE, compressLevel1 = FALSE, indexDestination = FALSE) { tryCatch({ files <- sapply(files, .normalizePath) destination <- .normalizePath(destination) region <- local({ x <- as(region, "GRanges") if (1L < length(x)) stop("'region' must specify one range") sprintf("%s:%d-%d", as.character(seqnames(x)), start(x), end(x)) }) if (!overwrite && file.exists(destination)) { msg <- sprintf("'%s' exists, '%s' is FALSE\n %s: %s", "destination", "overwrite", "destination", destination) stop(msg) } header <- .normalizePath(header) destination <- .Call(.merge_bam, files, destination, overwrite, header, region, byQname, addRG, compressLevel1) if (indexDestination) indexBam(destination) destination }, error=function(err) { msg <- sprintf("'mergeBam' %s", conditionMessage(err)) stop(msg) }) }) Rsamtools/R/methods-ApplyPileupsParam.R0000644000175400017540000001056413556116727021203 0ustar00biocbuildbiocbuildsetMethod(.validity, "ApplyPileupsParam", function(object) { msg <- NULL flag <- object@flag if (2L != length(flag) || any(c("keep0", "keep1") != names(flag))) msg <- c(msg, "'flag' not from scanBamFlag()") len1elts <- c("minBaseQuality", "minMapQuality", "minDepth", "maxDepth", "yieldSize", "yieldBy", "yieldAll") ok <- 1L == sapply(len1elts, function(x, obj) length(slot(obj, x)), object) if (!all(ok)) msg <- c(msg, sprintf("'%s' must be length 1", paste(len1elts[!ok], collapse="' '"))) what <- eval(formals(ApplyPileupsParam)[["what"]]) ok <- object@what %in% what if (!all(ok)) msg <- c(msg, sprintf("'what' must be in '%s'", paste(what, collapse="' '"))) if (is.null(msg)) TRUE else msg }) ApplyPileupsParam <- function(flag=scanBamFlag(), minBaseQuality=13L, minMapQuality=0L, minDepth=0L, maxDepth=250L, yieldSize=1L, yieldBy=c("range", "position"), yieldAll=FALSE, which=GRanges(), what=c("seq", "qual")) { yieldBy <- match.arg(yieldBy) if ("range" == yieldBy && yieldSize != 1) stop("'yieldSize' must equal 1 when 'yieldBy=\"range\"'") new("ApplyPileupsParam", flag=flag, minBaseQuality=as.integer(minBaseQuality), minMapQuality=as.integer(minMapQuality), minDepth=as.integer(minDepth), maxDepth=as.integer(maxDepth), yieldSize=as.integer(yieldSize), yieldBy=yieldBy, yieldAll=as.logical(yieldAll), which=which, what=what) } setAs("ApplyPileupsParam", "list", function(from) { nms <- slotNames(class(from)) res <- lapply(nms, slot, object=from) names(res) <- nms res }) plpFlag <- function(object) slot(object, "flag") "plpFlag<-" <- function(object, value) { slot(object, "flag") <- value validObject(object) object } plpMinBaseQuality <-function(object) slot(object, "minBaseQuality") "plpMinBaseQuality<-" <- function(object, value) { slot(object, "minBaseQuality") <- as.integer(value) validObject(object) object } plpMinMapQuality <- function(object) slot(object, "minMapQuality") "plpMinMapQuality<-" <- function(object, value) { slot(object, "minMapQuality") <- as.integer(value) validObject(object) object } plpMinDepth <- function(object) slot(object, "minDepth") "plpMinDepth<-" <- function(object, value) { slot(object, "minDepth") <- as.integer(value) validObject(object) object } plpMaxDepth <- function(object) slot(object, "maxDepth") "plpMaxDepth<-" <- function(object, value) { slot(object, "maxDepth") <- as.integer(value) validObject(object) object } plpYieldSize <- function(object) slot(object, "yieldSize") "plpYieldSize<-" <- function(object, value) { slot(object, "yieldSize") <- as.integer(value) validObject(object) object } plpYieldBy <- function(object) slot(object, "yieldBy") "plpYieldBy<-" <- function(object, value) { slot(object, "yieldBy") <- as.character(value) validObject(object) object } plpYieldAll <- function(object) slot(object, "yieldAll") "plpYieldAll<-" <- function(object, value) { slot(object, "yieldAll") <- as.logical(value) validObject(object) object } plpWhich <- function(object) slot(object, "which") "plpWhich<-" <- function(object, value) { slot(object, "which") <- as(value, "GRanges") validObject(object) object } plpWhat <- function(object) slot(object, "what") "plpWhat<-" <- function(object, value) { slot(object, "what") <- as.character(value) validObject(object) object } setMethod(show, "ApplyPileupsParam", function(object) { cat("class:", class(object), "\n") cat("plpFlag:", sprintf("%s=%s", names(object@flag), object@flag), "\n") len1elts <- c("minBaseQuality", "minMapQuality", "minDepth", "maxDepth", "yieldSize", "yieldBy", "yieldAll") for (elt in len1elts) cat(sprintf("%s: %s", sub("([[:alpha:]])", "plp\\U\\1", elt, perl=TRUE), slot(object, elt)), "\n") cat("plpWhat: '", paste(object@what, collapse="' '"), "'\n", sep="") cat(sprintf("plpWhich: %s (length %d)\n", class(object@which), length(object@which))) }) Rsamtools/R/methods-BamFile.R0000644000175400017540000003352213556116727017071 0ustar00biocbuildbiocbuildsetMethod(isOpen, "BamFile", function(con, rw="") { if (!missing(rw) && rw != "read") stop("'rw' must be 'read'") .Call(.bamfile_isopen, .extptr(con)) }) setMethod(isIncomplete, "BamFile", function(con) { .Call(.bamfile_isincomplete, .extptr(con)) }) .check_qname_arg <- function(arg, name) { if (is.na(arg) || arg == "") return(NA_character_) if (length(arg) == 0L || !is(arg, "character")) stop(name, " must be a single character") if (nchar(arg) > 1L) stop("'nchar(", name, ")' must be < 1") arg } .BamFile_guessIndex <- function(files) { if (missing(files)) return(character()) do_append <- function(index, files, to) { idx <- paste0(files, to) exists <- is.na(index) & file.exists(idx) index[exists] <- idx[exists] index } do_sub <- function(index, files, from, to) { idx <- sub(from, to, files) exists <- is.na(index) & files != idx & file.exists(idx) index[exists] <- idx[exists] index } index <- rep(NA_character_, length(files)) index <- do_append(index, files, ".bai") index <- do_append(index, files, ".BAI") index <- do_sub(index, files, ".bam$", ".bai") index <- do_sub(index, files, ".BAM$", ".BAI") index } BamFile <- function(file, index=file, ..., yieldSize=NA_integer_, obeyQname=FALSE, asMates=FALSE, qnamePrefixEnd=NA, qnameSuffixStart=NA) { if (missing(file) || !isSingleString(file)) stop("'file' must be character(1) and not NA") file <- .normalizePath(file) if (!asMates) { if (!is.na(qnamePrefixEnd) || !is.na(qnameSuffixStart)) warning(paste0("when 'asMates' is FALSE 'qnamePrefixEnd' ", "and 'qnameSuffixStart' are ignored")) } if (missing(index)) { index <- .BamFile_guessIndex(file) if (is.na(index)) index <- character() } if (!(isSingleString(index) || 0L == length(index))) { txt <- "'index', when present, must be character(0) or character(1) with nchar(index) > 0 and not NA" stop(paste(strwrap(txt), collapse="\n ")) } index <- .normalizePath(index) qnamePrefixEnd <- .check_qname_arg(qnamePrefixEnd, "qnamePrefixEnd") qnameSuffixStart <- .check_qname_arg(qnameSuffixStart, "qnameSuffixStart") .RsamtoolsFile(.BamFile, path=file, index=index, yieldSize=yieldSize, obeyQname=obeyQname, asMates=asMates, qnamePrefixEnd=qnamePrefixEnd, qnameSuffixStart=qnameSuffixStart, ...) } open.BamFile <- function(con, ...) { tryCatch({ .io_check_exists(path(con)) index <- sub("\\.bai$", "", index(con, asNA=FALSE)) con$.extptr <- .Call(.bamfile_open, path(con), index, "rb") }, error=function(err) { stop("failed to open BamFile: ", conditionMessage(err)) }) invisible(con) } close.BamFile <- function(con, ...) { if (!isOpen(con)) stop("isOpen() is not 'TRUE'") con$.extptr <- .Call(.bamfile_close, .extptr(con)) invisible(con) } ## scanBam, filterBam, countBam setMethod(scanBamHeader, "BamFile", function(files, ..., what=c("targets", "text")) { if (!isOpen(files)) { open(files) on.exit(close(files)) } .Call(.read_bamfile_header, .extptr(files), c("targets", "text") %in% what) }) setMethod(seqinfo, "BamFile", function(x) { h <- scanBamHeader(x, what="targets")[["targets"]] h <- h[!(duplicated(h) & duplicated(names(h)))] Seqinfo(names(h), unname(h)) }) setMethod(obeyQname, "BamFile", function(object, ...) { object$obeyQname }) setReplaceMethod("obeyQname", "BamFile", function(object, ..., value) { if (1L != length(value)) stop("'value' must be length 1") object$obeyQname <- value object }) setMethod(asMates, "BamFile", function(object, ...) { object$asMates }) setReplaceMethod("asMates", "BamFile", function(object, ..., value) { if (!isTRUEorFALSE(value)) stop("'value' must be TRUE or FALSE") object$asMates <- value object }) .checkPrefixSuffix <- function(object, value, name) { if (!is(value, "character")) stop("'value' must be a single character") if (length(value)) if (!is.na(value) && nchar(value) > 1L) stop("nchar(value) must be <= 1") if (!asMates(object)) warning(paste0("when 'asMates' is TRUE '", name, "' is ignored")) } setMethod(qnamePrefixEnd, "BamFile", function(object, ...) { object$qnamePrefixEnd }) setReplaceMethod("qnamePrefixEnd", "BamFile", function(object, ..., value) { .checkPrefixSuffix(object, value, "qnamePrefixEnd") object$qnamePrefixEnd <- value object }) setMethod(qnameSuffixStart, "BamFile", function(object, ...) { object$qnameSuffixStart }) setReplaceMethod("qnameSuffixStart", "BamFile", function(object, ..., value) { .checkPrefixSuffix(object, value, "qnameSuffixStart") object$qnameSuffixStart <- value object }) setMethod(scanBam, "BamFile", function(file, index=file, ..., param=ScanBamParam(what=scanBamWhat())) { if (!isOpen(file)) { open(file) on.exit(close(file)) } if (obeyQname(file) && asMates(file)) warning("'obeyQname=TRUE' ignored when 'asMates=TRUE'") if (!missing(index)) warning("'index' ignored for scanBam,BamFile-method") if (!is(param, "ScanBamParam")) { msg <- sprintf("'%s' must be a '%s'; was '%s'", "param", "ScanBamParam", class(param)) stop(msg) } if (0L == length(bamWhat(param)) && 0L == length(bamTag(param))) { txt <- "no BAM fields selected for input (neither 'bamWhat(param)' nor 'bamTag(param)' defined)" warning(paste(strwrap(txt), collapse="\n ")) } if (!asMates(file)) bamWhat(param) <- setdiff(bamWhat(param), c("groupid", "mate_status")) reverseComplement <- bamReverseComplement(param) if (is.na(qnamePrefix <- qnamePrefixEnd(file))) qnamePrefix <- "" if (is.na(qnameSuffix <- qnameSuffixStart(file))) qnameSuffix <- "" tmpl <- .scanBam_template(file, param) x <- .io_bam(.scan_bamfile, file, reverseComplement, yieldSize(file), tmpl, obeyQname(file), asMates(file), qnamePrefix, qnameSuffix, param=param) .scanBam_postprocess(x, param) }) setMethod(countBam, "BamFile", function (file, index=file, ..., param = ScanBamParam()) { if (!isOpen(file)) { open(file) on.exit(close(file)) } if (!missing(index)) warning("'index' ignored for countBam,BamFile-method") x <- .io_bam(.count_bamfile, file, param=param) .countBam_postprocess(x, file, param) }) setMethod(idxstatsBam, "BamFile", function(file, index=file, ...) { stopifnot(nzchar(index(file)), file.exists(index(file))) if (!isOpen(file)) { open(file) on.exit(close(file)) } result <- .Call(.idxstats_bamfile, .extptr(file)) seqnames <- factor(result[[1]], levels=sortSeqlevels(unique(result[[1]]))) o <- order(seqnames) data.frame(seqnames=seqnames[o], seqlength=result[[2]][o], mapped=result[[3]][o], unmapped=result[[4]][o]) }) ### NOTE: Not exported but used in the GenomicAlignments package! ### 'bamfile' must be a BamFile object. Returns a named list with 1 element ### per loaded column. .load_bamcols_from_scanBam_res <- function(res, param, with.which_label=FALSE) { if (!isTRUEorFALSE(with.which_label)) stop("'with.which_label' must be TRUE or FALSE") which_label <- names(res) names(res) <- NULL ## Compute the "which_label" col. ans3 <- list() if (with.which_label) { if (is.null(which_label)) { warning("'which_label' is ignored when 'param' is missing or ", "doesn't have a 'which' component") } else { ## We want unique labels. if (anyDuplicated(which_label)) which_label <- paste0(which_label, ".", seq_along(which_label)) ## Currently scanBam() should always output a 'res' of length != 0 ## but we test anyway just in case one day this changes. if (length(res) == 0L) { run_lens <- integer(0) } else { run_lens <- sapply(res, function(x) length(x[[1L]])) } which_label <- Rle(factor(which_label, levels=which_label), run_lens) ans3 <- list(which_label=which_label) } } ## Extract the "what" cols. ans1 <- lapply(setNames(bamWhat(param), bamWhat(param)), function(nm) { tmp <- lapply(res, "[[", nm) S4Vectors:::quick_unlist(tmp) }) ## Extract the "tag" cols. ans2 <- lapply(setNames(bamTag(param), bamTag(param)), function(nm) { tmp <- lapply(res, function(res_elt) { tag <- res_elt[["tag"]] tag_elt <- tag[[nm]] ## Fill empty tag with NAs. if (is.null(tag_elt)) { count <- length(res_elt[["rname"]]) tag_elt <- rep.int(NA, count) } tag_elt }) S4Vectors:::quick_unlist(tmp) }) ## Put all the cols together and return them. c(ans1, ans2, ans3) } .filterBam_FilterRules <- function(file, destination, filter, param) { if (!is.list(filter)) filter <- list(filter) if (length(destination) != length(filter)) stop("length of 'destination' must equal length of 'filter' list") which <- unlist(bamWhich(param)) nRange <- length(which) if (nRange) # yield by range iRange <- 1L yieldSize <- yieldSize(file) if (is.na(yieldSize)) yieldSize <- 1000000L tmpl <- .scanBam_template(file, param) reverseComplement <- bamReverseComplement(param) if (is.na(qnamePrefix <- qnamePrefixEnd(file))) qnamePrefix <- "" if (is.na(qnameSuffix <- qnameSuffixStart(file))) qnameSuffix <- "" dest <- lapply(destination, function(dest) { .Call(.bamfile_open, dest, path(file), "wb") }) on.exit(for (d in dest) .Call(.bamfile_close, d)) repeat { buf <- .io_bam(.prefilter_bamfile, file, param=param, yieldSize, obeyQname(file), asMates(file), qnamePrefix, qnameSuffix) if (0L == .Call(.bambuffer_length, buf)) break ans <- .io_bam(.bambuffer_parse, file, param=param, buf, reverseComplement, tmpl) ans <- DataFrame(.load_bamcols_from_scanBam_res(ans, param)) for (i in seq_along(dest)) { keep <- eval(filter[[i]], ans) .Call(.bambuffer_write, buf, dest[[i]], keep) } .Call(.bambuffer_reset, buf) } destination } setMethod(filterBam, "BamFile", function (file, destination, index=file, ..., filter=FilterRules(), indexDestination=TRUE, param=ScanBamParam(what=scanBamWhat())) { if (!isOpen(file)) { open(file) on.exit(close(file)) } if (missing(destination)) stop(sprintf("'%s' missing with no default", "destination")) if (!is(param, "ScanBamParam")) stop(sprintf("'%s' must be a '%s'; was '%s'", "param", "ScanBamParam", class(param))) param <- .filterBam_preprocess(file, param) destination <- .normalizePath(destination) if (length(filter)) .filterBam_FilterRules(file, param=param, destination, filter) else .io_bam(.filter_bamfile, file, param=param, destination, "wb") if (indexDestination) for (dest in destination) { if (asMates(file)) { ## FIXME: filtering by mates requires expensive re-sort! fl <- tempfile() file.rename(dest, fl) sortBam(fl, dest) file.rename(paste0(dest, ".bam"), dest) } indexBam(dest) } destination }) setMethod(indexBam, "BamFile", function(files, ...) { indexBam(path(files), ...) }) setMethod(sortBam, "BamFile", function(file, destination, ..., byQname=FALSE, maxMemory=512) { sortBam(path(file), destination, ..., byQname=byQname, maxMemory=maxMemory) }) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### "quickBamFlagSummary" methods. ### setMethod(quickBamFlagSummary, "BamFile", function(file, ..., param=ScanBamParam(), main.groups.only=FALSE) { what0 <- c("qname", "flag") if (length(bamWhat(param)) != 0L) warning("bamWhat component of supplied 'param' was ignored") bamWhat(param) <- what0 res <- scanBam(file, param=param) res0 <- res[[1L]] if (length(res) != 1L) { res0[["qname"]] <- do.call(c, lapply(res, "[[", "qname")) res0[["flag"]] <- do.call(c, lapply(res, "[[", "flag")) } quickBamFlagSummary(res0, param=param, main.groups.only=main.groups.only) }) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### "show" methods ### setMethod(show, "BamFile", function(object) { callNextMethod() cat("obeyQname:", obeyQname(object), "\n") cat("asMates:", asMates(object), "\n") cat("qnamePrefixEnd:", qnamePrefixEnd(object), "\n") cat("qnameSuffixStart:", qnameSuffixStart(object), "\n") }) Rsamtools/R/methods-BamFileList.R0000644000175400017540000000306013556116727017717 0ustar00biocbuildbiocbuildBamFileList <- function(..., yieldSize=NA_integer_, obeyQname=FALSE, asMates=FALSE, qnamePrefixEnd=NA, qnameSuffixStart=NA) { fls <- .RsamtoolsFileList(..., yieldSize=yieldSize, class="BamFile") if (!missing(obeyQname)) obeyQname(fls) <- obeyQname if (!missing(asMates)) asMates(fls) <- asMates if (!missing(qnamePrefixEnd)) qnamePrefixEnd(fls) <- qnamePrefixEnd if (!missing(qnameSuffixStart)) qnameSuffixStart(fls) <- qnameSuffixStart fls } setMethod(obeyQname, "BamFileList", function(object, ...) { sapply(object, obeyQname) }) setReplaceMethod("obeyQname", "BamFileList", function(object, ..., value) { endoapply(object, `obeyQname<-`, value=value) }) setMethod(asMates, "BamFileList", function(object, ...) { sapply(object, asMates) }) setReplaceMethod("asMates", "BamFileList", function(object, ..., value) { endoapply(object, `asMates<-`, value=value) }) setMethod(qnamePrefixEnd, "BamFileList", function(object, ...) { sapply(object, qnamePrefixEnd) }) setReplaceMethod("qnamePrefixEnd", "BamFileList", function(object, ..., value) { endoapply(object, `qnamePrefixEnd<-`, value=value) }) setMethod(qnameSuffixStart, "BamFileList", function(object, ...) { sapply(object, qnameSuffixStart) }) setReplaceMethod("qnameSuffixStart", "BamFileList", function(object, ..., value) { endoapply(object, `qnameSuffixStart<-`, value=value) }) setMethod(seqinfo, "BamFileList", function(x) { Reduce(merge, lapply(x, seqinfo)) }) Rsamtools/R/methods-BamSampler.R0000644000175400017540000000437013556116727017614 0ustar00biocbuildbiocbuild.BamSampler <- setRefClass("BamSampler", contains="BamFile") BamSampler <- function (file, index = file, ..., yieldSize, obeyQname = FALSE, asMates = FALSE, qnamePrefixEnd = NA, qnameSuffixStart = NA) { .Deprecated(msg=paste0("'BamSampler' is deprecated. Use 'REDUCEsampler' ", "in the GenomicFiles package")) qnamePrefixEnd <- .check_qname_arg(qnamePrefixEnd, "qnamePrefixEnd") qnameSuffixStart <- .check_qname_arg(qnameSuffixStart, "qnameSuffixStart") .RsamtoolsFile(.BamSampler, .normalizePath(file), .normalizePath(index), yieldSize = yieldSize, obeyQname = obeyQname, asMates = asMates, qnamePrefixEnd = qnamePrefixEnd, qnameSuffixStart = qnameSuffixStart, ...) } setMethod("scanBam", "BamSampler", function(file, index=file, ..., param=ScanBamParam(what=scanBamWhat())) { if (0L == length(bamWhat(param)) && 0L == length(bamTag(param))) { txt <- "no BAM fields selected for input (niether 'bamWhat(param)' nor 'bamTag(param)' defined)" stop(paste(strwrap(txt), collapse="\n ")) } sampleSize <- yieldSize(file) if (is.na(yieldSize(file))) stop("'yieldSize' must not be NA") bfile <- as(file, "BamFile") open(bfile, "rb") on.exit(close(bfile)) smpl <- S4Vectors:::quick_unlist(unname(scanBam(bfile, param=param))) tot <- length(smpl[[1]]) if (tot > sampleSize) { # e.g., ranges idx <- sample(tot, sampleSize) smpl <- lapply(smpl, `[`, idx) } repeat { yld <- S4Vectors:::quick_unlist(scanBam(bfile, param=param)) yld_n <- length(yld[[1]]) if (length(yld[[1]]) == 0L) break tot <- tot + yld_n keep <- rbinom(1L, yld_n, yld_n / tot) if (keep == 0L) next i <- sample(sampleSize, keep) j <- sample(yld_n, keep) smpl <- Map(function(x, y, i, j) { x[i] <- y[j] x }, smpl, yld, MoreArgs=list(i=i, j=j)) } lst <- list(smpl) attr(lst, "BamSamplerStatistics") <- c(yieldSize=sampleSize, totalRead=tot, yield=length(smpl[[1]])) lst }) setMethod(show, "BamSampler", function(object) { callNextMethod() }) Rsamtools/R/methods-BamViews.R0000644000175400017540000001517113556116727017307 0ustar00biocbuildbiocbuildsetMethod(BamViews, c(bamRanges="GRanges"), function(bamPaths=character(0), bamIndicies=bamPaths, bamSamples=DataFrame(row.names= make.unique(basename(bamPaths))), bamRanges, bamExperiment=list(), ...) { new("BamViews", ..., bamPaths=bamPaths, bamIndicies=bamIndicies, bamSamples=bamSamples, bamRanges=bamRanges, bamExperiment=bamExperiment) }) setMethod(BamViews, c(bamRanges="missing"), function(bamPaths=character(0), bamIndicies=bamPaths, bamSamples=DataFrame(row.names= make.unique(basename(bamPaths))), bamRanges, bamExperiment=list(), ..., auto.range=FALSE) { if (length(bamPaths) != 0L && auto.range) { ## Guess ranges from BAM file headers pathsOk <- sapply(bamPaths, function(fl) { file.exists(fl) && !file.info(fl)$isdir }) if (all(pathsOk)) { rngs <- lapply(scanBamHeader(bamPaths), "[[", "targets") nms <- unique(unlist(lapply(rngs, names), use.names=FALSE)) ends <- sapply(nms, function(nm, rngs) { idx <- sapply(rngs, function(rng, nm) { nm %in% names(rng) }, nm) if (sum(idx) > 0) max(sapply(rngs[idx], "[[", nm)) else stop("Rsamtools internal: could not determine bamRanges") }, rngs) bamRanges <- GRanges(names(ends), IRanges(1L, ends)) } else { warning("some files do not exist; bamRanges not defined") bamRanges <- GRanges() } } else { bamRanges <- GRanges() } BamViews(bamPaths=bamPaths, bamIndicies=bamIndicies, bamSamples=bamSamples, bamRanges=bamRanges, bamExperiment=bamExperiment, ...) }) setMethod(.validity, "BamViews", function(object) { msg <- NULL if (length(bamIndicies(object)) != length(bamPaths(object))) msg <- c(msg, "length(bamIndicies(object)) != length(bamPaths(object))") if (length(bamPaths(object)) != nrow(bamSamples(object))) msg <- c(msg, "length(bamPaths(object)) != nrow(bamSamples(object))") if (is.null(msg)) TRUE else msg }) bamPaths <- function(x) setNames(slot(x, "bamPaths"), names(x)) bamIndicies <- function(x) setNames(slot(x, "bamIndicies"), names(x)) `bamDirname<-` <- function(x, ..., value) { initialize(x, bamPaths=file.path(value, basename(bamPaths(x))), bamIndicies=file.path(value, basename(bamIndicies(x)))) } bamSamples <- function(x) slot(x, "bamSamples") `bamSamples<-` <- function(x, value) initialize(x, bamSamples=value) bamRanges <- function(x) slot(x, "bamRanges") `bamRanges<-` <- function(x, value) initialize(x, bamRanges=value) bamExperiment <- function(x) slot(x, "bamExperiment") setMethod(dim, "BamViews", function(x) { c(length(bamRanges(x)), length(bamPaths(x))) }) setMethod(names, "BamViews", function(x) { rownames(bamSamples(x)) }) setReplaceMethod("names", "BamViews", function(x, value) { rownames(bamSamples(x)) <- value x }) setMethod(dimnames, "BamViews", function(x) { list(names(bamRanges(x)), rownames(bamSamples(x))) }) setReplaceMethod("dimnames", "BamViews", function(x, value) { names(bamRanges(x)) <- value[[1]] rownames(bamSamples(x)) <- value[[2]] x }) setMethod("[", c("BamViews", "ANY", "missing"), function(x, i, j, ..., drop=TRUE) { initialize(x, bamRanges=bamRanges(x)[i,]) }) setMethod("[", c("BamViews", "missing", "ANY"), function(x, i, j, ..., drop=TRUE) { if (is.character(j)) j <- match(j, colnames(x)) if (any(is.na(j))) stop("subscript 'j' out of bounds") initialize(x, bamPaths=bamPaths(x)[j], bamIndicies=bamIndicies(x)[j], bamSamples=bamSamples(x)[j,,drop=FALSE]) }) setMethod("[", c("BamViews", "ANY", "ANY"), function(x, i, j, ..., drop=TRUE) { if (is.character(i)) j <- match(i, rownames(x)) if (is.character(j)) j <- match(j, colnames(x)) if (any(is.na(i))) stop("subscript 'i' out of bounds") if (any(is.na(j))) stop("subscript 'j' out of bounds") initialize(x, bamRanges=bamRanges(x)[i,], bamPaths=bamPaths(x)[j], bamIndicies=bamIndicies(x)[j], bamSamples=bamSamples(x)[j,,drop=FALSE]) }) ## action .BamViews_which <- function(file, param, missing) { grange <- bamRanges(file) which <- split(ranges(grange), seqnames(grange)) if (!missing && !identical(which, bamWhich(param))) warning("'bamRanges(file)' and 'bamWhich(param)' differ; using bamRanges(file)") which } .BamViews_delegate <- function(what, bamViews, fun, ...) { idx <- structure(seq_len(ncol(bamViews)), names=names(bamViews)) result <- bplapply(idx, fun, bamViews=bamViews, ...) errs <- sapply(result, is, "remote-error") if (any(errs)) stop(sprintf("'%s' failed on '%s'", what, paste(names(bamViews)[errs], collapse="' '"))) names(result) <- names(bamViews) do.call(new, list("SimpleList", listData=result, elementMetadata=bamSamples(bamViews))) } setMethod(scanBam, "BamViews", function(file, index=file, ..., param=ScanBamParam(what=scanBamWhat())) { if (!missing(index)) warning("using bamIndicies(file) for 'index'") bamWhich(param) <- .BamViews_which(file, param, missing(param)) fun <- function(i, bamViews, ..., verbose) scanBam(file=bamPaths(bamViews)[i], index=bamIndicies(bamViews)[i], ...) .BamViews_delegate("scanBam", file, fun, ..., param=param) }) setMethod(countBam, "BamViews", function(file, index=file, ..., param=ScanBamParam()) { if (!missing(index)) warning("using bamIndicies(file) for 'index'") bamWhich(param) <- .BamViews_which(file, param, missing(param)) fun <- function(i, bamViews, ..., verbose) countBam(file=bamPaths(bamViews)[i], index=bamIndicies(bamViews)[i], ...) .BamViews_delegate("countBam", file, fun, ..., param=param) }) ## show setMethod(show, "BamViews", function(object) { cat(class(object), "dim:", paste(dim(object), c("ranges", "samples"), collapse=" x "), "\n") cat("names:", S4Vectors:::selectSome(names(object)), "\n") cat("detail: use bamPaths(), bamSamples(), bamRanges(), ...", "\n") }) Rsamtools/R/methods-BcfFile.R0000644000175400017540000002052613556116727017064 0ustar00biocbuildbiocbuildBcfFile <- function(file, index=file, mode=ifelse(grepl("\\.bcf$", file), "rb", "r")) { bf <- .RsamtoolsFile(.BcfFile, file, index) bf$mode <- mode bf } bcfMode <- function(object) object$mode open.BcfFile <- function(con, ...) { .io_check_exists(path(con)) con$.extptr <- .Call(.bcffile_open, path(con), index(con, asNA=FALSE), bcfMode(con)) invisible(con) } close.BcfFile <- function(con, ...) { if (!isOpen(con)) stop("isOpen() is not 'TRUE'") con$.extptr <- .Call(.bcffile_close, .extptr(con)) invisible(con) } setMethod(isOpen, "BcfFile", function(con, rw="") { if (!missing(rw) && rw != "read") stop("'rw' must be 'read'") .Call(.bcffile_isopen, .extptr(con)) }) ## scanBcfHeader .bcfHeaderAsSimpleList <- function(header) { h <- sub("^##", "", header[["Header"]]) h <- h[!duplicated(h)] ## Simple key=value pairs rex <- "^[[:alnum:]]+=[^<]" if (length(h1 <- grep(rex, h, value=TRUE))) { idx <- regexpr("=", h1, fixed=TRUE) ## first match rnms <- substring(h1, 1, idx - 1) if (is(rnms, "character")) { if (any(duplicated(rnms))) { warning("duplicate keys in header will be forced to unique ", "rownames") rnms <- make.unique(rnms) } } meta_df <- DataFrame(row.names=rnms, Value=substring(h1, idx + 1)) meta <- as(splitAsList(meta_df, rnms), "SimpleDataFrameList") } else { meta <- DataFrameList() } ## Non-simple key-value pairs ## These lines have values enclosed in '<>' with subfields such as 'ID', ## 'Number', 'Type' etc. rex <- "^([[:alnum:]]+)=<(.*)>" lines <- grep(rex, h, value=TRUE) if (length(lines) > 0) { if (any(duplicated(lines))) { warning("duplicate INFO and FORMAT header lines will be ignored") lines <- lines[duplicated(lines) == FALSE] } } tags <- sub(rex, "\\1", lines) keyval0 <- sub(rex, "\\2", lines) ## Handle INFO, FORMAT, FILTER, ALT, SAMPLE keyval1 <- rep(NA_character_, length(keyval0)) keyval <- list() idx <- tags %in% c("INFO", "FORMAT", "FILTER", "ALT") keyval1[idx] <- strsplit(keyval0[idx], ",(?=(ID|Number|Type)=[[:alnum:]]*)|,(?=Description=\".*?\")", perl=TRUE) keyval[idx] <- lapply(which(idx), function(i, keyval1) strsplit(keyval1[[i]], "(?<=[ID|Number|Type|Description])=", perl=TRUE), keyval1) keyval1[!idx] <- strsplit(keyval0[!idx], ",(?=[[:alnum:]]+=)", perl=TRUE) keyval[!idx] <- lapply(which(!idx), function(i, keyval1) { strsplit(keyval1[[i]], "(?<=[[:alnum:]])=", perl=TRUE)}, keyval1) tbls <- tapply(keyval, tags, function(elt) { keys <- lapply(elt, sapply, "[[", 1) vals0 <- lapply(elt, sapply, "[[", 2) vals <- Map("names<-", vals0, keys) cols <- unique(unlist(keys)) entries <- Map(function(k) as.vector(sapply(vals, "[", k)), cols) desc <- which("DESCRIPTION" == toupper(names(entries))) if (1L == length(desc)) entries[[desc]] <- gsub("\"", "", entries[[desc]]) id <- which("ID" == toupper(names(entries))) if (length(id) > 0L) { if (any(duplicated(entries[[id]]))) warning("duplicate ID's in header will be forced to unique ", "rownames") df <- DataFrame(entries[-id], row.names=make.unique(entries[[id]])) } else { ## ID is not a required field df <- DataFrame(entries) } df }) ## 'GT' first in order if (length(tbls)) if (length(tbls$FORMAT)) if (any(GT <- rownames(tbls$FORMAT) %in% "GT")) tbls$FORMAT <- rbind(tbls$FORMAT[GT,], tbls$FORMAT[!GT,]) SimpleList(Reference=header[["Reference"]], Sample=header[["Sample"]], Header=c(meta, tbls[unique(tags)])) } setMethod(scanBcfHeader, "BcfFile", function(file, ...) { if (!isOpen(file)) { open(file) on.exit(close(file)) } else if ("r" == bcfMode(file)) { on.exit(open(file)) # re-open } header <- .Call(.scan_bcf_header, .extptr(file)) .bcfHeaderAsSimpleList(header) }) ## scanBcf .bcf_template <- function(param) { tmpl <- list(CHROM=character(), POS=integer(), ID=character(), REF=character(), ALT=character(), QUAL=numeric(), FILTER=character(), INFO=character(), FORMAT=character(), GENO=list( PL=list(), DP=structure(integer(0), .Dim=c(0L, 0L)), GQ=structure(integer(0), .Dim=c(0L, 0L)), SP=structure(integer(0), .Dim=c(0L, 0L)), GT=structure(character(0), .Dim=c(0L, 0L)), GL=list()), RecordsPerRange=integer()) if (!identical(character(), bcfGeno(param))) { geno <- bcfGeno(param) idx <- if (1L == length(geno) && is.na(geno)) FALSE else names(tmpl[["GENO"]]) %in% geno tmpl[["GENO"]] <- tmpl[["GENO"]][idx] } tmpl } .io_bcf <- function(func, file, ..., param) { if (!isOpen(file)) { open(file) on.exit(close(file)) } else if ("r" == bcfMode(file)) { on.exit(open(file)) # re-open } tmpl <- .bcf_template(param) which <- bcfWhich(param) regions <- if (0L != length(which)) { if (!nzchar(index(file))) stop("scanBcf 'index' must exist when non-zero bcfWhich()") list(as.character(space(which)), .uunlist(start(which)), .uunlist(end(which))) } else NULL res <- tryCatch({ .Call(func, .extptr(file), regions, tmpl) }, error=function(err) { stop("scanBcf: ", conditionMessage(err), "\n path: ", path(file), call.=FALSE) }) if (bcfTrimEmpty(param)) { idx <- sapply(res[["GENO"]], function(x) { tst <- switch(typeof(x), list=is.null, is.na) !all(unlist(lapply(x, tst), use.names=FALSE)) }) res[["GENO"]] <- res[["GENO"]][idx] } if (length(res[["GENO"]])) { idx <- sapply(res[["GENO"]], function(x) 2L == length(dim(x))) res[["GENO"]][idx] <- lapply(res[["GENO"]][idx], t) } res } setMethod(scanBcf, "BcfFile", function(file, ..., param=ScanBcfParam()) { .io_bcf(.scan_bcf, file, ..., param=param) }) setMethod(asBcf, "character", function(file, dictionary, destination, ..., overwrite=FALSE, indexDestination=TRUE) { file <- .normalizePath(file) destination <- .normalizePath(destination) destination <- paste(destination, "bcf", sep=".") dict <- tempfile() on.exit(unlink(dict)) tryCatch({ if (!overwrite && file.exists(destination)) { msg <- sprintf("'destination' exists, 'overwrite' is FALSE\n destination.bcf: %s", "destination", "overwrite", destination) stop(msg) } writeLines(dictionary, dict) result <- .Call(.as_bcf, file, dict, destination) if (!file.exists(destination)) stop("failed to create 'BCF' file") if (indexDestination) indexBcf(destination) }, error=function(err) { msg <- sprintf("'asBcf' %s\n VCF file: '%s'\n destination: '%s'\n", conditionMessage(err), file, destination) stop(msg) }) destination }) setMethod(indexBcf, "BcfFile", function(file, ...) { if (!isOpen(file)) { open(file) on.exit(close(file)) } if (.Call(.bcffile_isvcf, .extptr(file))) stop("'indexBcf' requires a BCF (not VCF) file") tryCatch({ .Call(.index_bcf, path(file)) }, error=function(err) { msg <- sprintf("'indexBcf' %s\n file: '%s'\n", conditionMessage(err), file) stop(msg) }) }) setMethod(indexBcf, "character", function(file, ...) { indexBcf(BcfFile(file, character()), ...) }) Rsamtools/R/methods-FaFile.R0000644000175400017540000001413213556116727016714 0ustar00biocbuildbiocbuildFaFile <- function(file, index=sprintf("%s.fai", file), gzindex=sprintf("%s.gzi", file)) { ans <- .RsamtoolsFile(.FaFile, file, index) gzindex(ans) <- .normalizePath(gzindex) ans } setMethod(gzindex, "FaFile", function(object, asNA=TRUE) { gzindex <- object$gzindex if (asNA && ((length(gzindex) == 0L) || !nzchar(gzindex))) NA_character_ else gzindex }) setReplaceMethod("gzindex", "FaFile", function(object, value) { stopifnot(length(value) == 1L) object$gzindex <- as.character(value) object }) setMethod(gzindex, "FaFileList", function(object, asNA=TRUE) { sapply(object, gzindex, asNA=asNA) }) setReplaceMethod("gzindex", "FaFileList", function(object, value) { stopifnot(length(value) == length(path(object))) for (i in seq_along(object)) gzindex(object[[i]]) <- value[i] object }) setMethod(show, "FaFile", function(object) { cat("class:", class(object), "\n") cat(.ppath("path", path(object))) cat(.ppath("index", index(object))) cat(.ppath("gzindex", gzindex(object))) cat("isOpen:", isOpen(object), "\n") cat("yieldSize:", yieldSize(object), "\n") }) open.FaFile <- function(con, ...) { .io_check_exists(path(con)) tryCatch({ con$.extptr <- .Call(.fafile_open, path(con), index(con, asNA=FALSE), gzindex(con, asNA=FALSE)) }, error=function(err) { stop(conditionMessage(err), "\n file: ", path(con)) }) invisible(con) } close.FaFile <- function(con, ...) { if (!isOpen(con)) stop("isOpen() is not 'TRUE'") tryCatch({ con$.extptr <- .Call(.fafile_close, .extptr(con)) }, error=function(err) { stop(conditionMessage(err), "\n file: ", path(con)) }) invisible(con) } setMethod(isOpen, "FaFile", function(con, rw="") { if (!missing(rw) && rw != "read") stop("'rw' must be 'read'") tryCatch({ .Call(.fafile_isopen, .extptr(con)) }, error=function(err) { stop(conditionMessage(err), "\n file: ", path(con)) }) }) setMethod(indexFa, "FaFile", function(file, ...) { tryCatch({ file$index <- paste0(.Call(.index_fa, path(file)), ".fai") }, error=function(err) { stop(conditionMessage(err), "\n file: ", path(file)) }) file }) setMethod(scanFaIndex, "FaFile", function(file, ...) { what <- list(character(), integer(), NULL, NULL, NULL) tbl <- scan(index(file, asNA=FALSE), what=what, quiet=TRUE) GRanges(tbl[[1]], IRanges(1, width=tbl[[2]]), seqlengths=structure(tbl[[2]], .Names=tbl[[1]])) }) setMethod(scanFaIndex, "FaFileList", function(file, ..., as=c("GRangesList", "GRanges")) { lst <- lapply(file, scanFaIndex, ...) switch(match.arg(as), GRanges={ unique(unlist(GRangesList(lst), use.names=FALSE)) }, GRangesList={ GRangesList(lst) }) }) setMethod(countFa, "FaFile", function(file, ...) { if (!isOpen(file)) { open(file) on.exit(close(file)) } tryCatch({ .Call(.n_fa, .extptr(file)) }, error=function(err) { stop(conditionMessage(err), "\n file: ", path(file)) }) }) .scanFa <- function(file, param, ..., as=c("DNAStringSet", "RNAStringSet", "AAStringSet")) { if (!isOpen(file)) { open(file) on.exit(close(file)) } as <- match.arg(as) type <- sub("StringSet", "", as) base <- sub("Set", "", as) lkup <- Biostrings::get_seqtype_conversion_lookup("B", type) tryCatch({ regions <- .asRegions(param) dna <- .Call(.scan_fa, .extptr(file), regions[[1]], regions[[2]], regions[[3]], base, lkup) setNames(dna, regions[[1]]) }, error=function(err) { stop(conditionMessage(err), "\n file: ", path(file)) }) } setMethod(scanFa, c("FaFile", "GRanges"), .scanFa) setMethod(scanFa, c("FaFile", "IntegerRangesList"), .scanFa) setMethod(scanFa, c("FaFile", "missing"), function(file, param, ..., as=c("DNAStringSet", "RNAStringSet", "AAStringSet")) { as <- match.arg(as) switch(as, DNAStringSet=readDNAStringSet(path(file), ...), RNAStringSet=readRNAStringSet(path(file), ...), AAStringSet=readAAStringSet(path(file), ...)) }) setMethod(seqinfo, "FaFile", function(x) { gr <- scanFaIndex(x) Seqinfo(as.character(seqnames(gr)), width(gr)) }) setMethod(getSeq, "FaFile", function(x, param, ...) { if (missing(param)) { scanFa(x, ...) } else { dna <- scanFa(x, param, ...) if (is(param, "GRanges")) { idx <- as.logical(strand(param) == "-") if (any(idx)) dna[idx] <- reverseComplement(dna[idx]) } dna } }) setMethod(getSeq, "FaFileList", function(x, param, ...) { if (!is(param, "GRangesList")) stop("'param' must be 'GRangesList' when 'x' is 'FaFileList'") if (length(x) != length(param)) stop("'x' and 'param' must have equal length") lst <- lapply(seq_len(length(x)), function(i, x, param, ...) { getSeq(x[[i]], param[[i]], ...) }, x, param, ...) do.call(SimpleList, lst) }) ## character wrappers setMethod(indexFa, "character", function(file, ...) index(indexFa(open(FaFile(file))))) setMethod(scanFaIndex, "character", function(file, ...) scanFaIndex(open(FaFile(file)))) setMethod(countFa, "character", function(file, ...) countFa(FaFile(file))) setMethod(scanFa, c("character", "GRanges"), function(file, param, ..., as=c("DNAStringSet", "RNAStringSet", "AAStringSet")) { as <- match.arg(as) scanFa(FaFile(file), param, ..., as=as) }) setMethod(scanFa, c("character", "IntegerRangesList"), function(file, param, ..., as=c("DNAStringSet", "RNAStringSet", "AAStringSet")) { as <- match.arg(as) scanFa(FaFile(file), param, ..., as=as) }) setMethod(scanFa, c("character", "missing"), function(file, param, ..., as=c("DNAStringSet", "RNAStringSet", "AAStringSet")) { as <- match.arg(as) scanFa(FaFile(file), ..., as=as) }) Rsamtools/R/methods-PileupFiles.R0000644000175400017540000000406013556116727020006 0ustar00biocbuildbiocbuildPileupFiles <- function(files, ..., param=ApplyPileupsParam()) { bfl <- BamFileList(files, ...) new("PileupFiles", bfl, param=param) } plpFiles <- function(object) as(object, "BamFileList") plpParam <- function(object) object@param setMethod(applyPileups, c("PileupFiles", "ApplyPileupsParam"), function(files, FUN, ..., param) { FUN <- match.fun(FUN) ok <- isOpen(files) if (!all(ok)) if (any(ok)) stop("all(isOpen())' is not 'TRUE'") else { open(files) on.exit(close(files)) } lvls <- lapply(files, seqlevels) for (i in seq_along(files)[-1]) if (!identical(lvls[[i]], lvls[[1]])) { msg <- sprintf("applyPileups 'seqlevels' must be identical(); failed when comparing %s with %s", sQuote(basename(path(files)[1])), sQuote(basename(path(files)[i]))) stop(paste(strwrap(msg, exdent=4), collapse="\n")) } tryCatch({ param <- as(param, "list") extptr <- lapply(files, .extptr) regions <- if (0L != length(param[["which"]])) .asRegions(param[["which"]]) else NULL param[["what"]] <- c("seq", "qual") %in% param[["what"]] .Call(.apply_pileups, extptr, names(files), regions, param, FUN) }, error=function(err) { stop("applyPileups: ", conditionMessage(err), call.=FALSE) }) }) setMethod(applyPileups, c("PileupFiles", "missing"), function(files, FUN, ..., param) { applyPileups(files, FUN, ..., param=plpParam(files)) }) setMethod(show, "PileupFiles", function(object) { cat("class:", class(object), "\n") nms <- names(object) txt <- paste(S4Vectors:::selectSome(nms, 3L), collapse=", ") cat(sprintf("names: %s (%d total)\n", txt, length(nms))) fls <- sapply(object, function(x) basename(path(x))) txt <- paste(S4Vectors:::selectSome(fls, 3L), collapse=", ") cat(sprintf("plpFiles: %s (%d total)\n", txt, length(fls))) cat("plpParam: class", class(plpParam(object)), "\n") }) Rsamtools/R/methods-RsamtoolsFile.R0000644000175400017540000000332013556116727020346 0ustar00biocbuildbiocbuild.extptr <- function(object) object$.extptr setMethod(index, "RsamtoolsFile", function(object, ..., asNA=TRUE) { index <- object$index if (asNA && ((length(index) == 0L) || !nzchar(index))) NA_character_ else index }) setReplaceMethod("index", "RsamtoolsFile", function(object, ..., value) { stopifnot(length(value) == 1L) object$index <- as.character(value) object }) setMethod(yieldSize, "RsamtoolsFile", function(object, ...) { object$yieldSize }) setReplaceMethod("yieldSize", "RsamtoolsFile", function(object, ..., value) { if (1L != length(value)) stop("'value' must be length 1") object$yieldSize <- as.integer(value) object }) .RsamtoolsFile <- function(g, path, index, ..., yieldSize=NA_integer_) { if (1L != length(path)) stop("'file' must be length 1") # argh! public api is 'file' if (1L < length(index)) stop("'index' must be length 0 or 1") if (1L != length(yieldSize)) stop("'yieldSize' must be length 1") yieldSize <- as.integer(yieldSize) if (!(yieldSize > 0L || is.na(yieldSize))) stop("'yieldSize' must be >0 or NA") if (length(index) && is.na(index)) index <- character(0) g$new(path=.normalizePath(path), index=.normalizePath(index), ..., yieldSize=yieldSize) } setMethod(path, "RsamtoolsFile", function(object, ...) object$path) setMethod(isOpen, "RsamtoolsFile", function(con, rw="") FALSE) setMethod(show, "RsamtoolsFile", function(object) { cat("class:", class(object), "\n") cat(.ppath("path", path(object))) cat(.ppath("index", index(object))) cat("isOpen:", isOpen(object), "\n") cat("yieldSize:", yieldSize(object), "\n") }) Rsamtools/R/methods-RsamtoolsFileList.R0000644000175400017540000000663113556116727021212 0ustar00biocbuildbiocbuildsetGeneric(".RsamtoolsFileList", function(file, ..., yieldSize=NA_integer_, class) standardGeneric(".RsamtoolsFileList"), signature="file") setMethod(.RsamtoolsFileList, "missing", function(file, ..., classDef = class, yieldSize=NA_integer_, class) { new(paste0(class, "List")) }) setMethod(.RsamtoolsFileList, "character", function(file, index, ..., classDef=class, yieldSize=NA_integer_, class) { fun <- function(elt, ..., yieldSize, classDef) do.call(classDef, list(elt, ..., yieldSize=yieldSize)) if (is.null(names(file))) names(file) <- basename(file) listData <- if (!missing(index) && length(index)) Map(fun, file, as.character(index), ..., MoreArgs=list(yieldSize=yieldSize, classDef=classDef)) else if (missing(index)) Map(fun, file, ..., MoreArgs=list(yieldSize=yieldSize, classDef=classDef) ) else ## support old index=character() variant Map(fun, file, ..., MoreArgs=list(index=index, yieldSize=yieldSize, classDef=classDef)) new(paste0(class, "List"), listData=listData) }) setMethod(.RsamtoolsFileList, "ANY", function(file, ..., classDef = class, yieldSize=NA_integer_, class) { list <- list(file, ...) if (length(list) == 1 && (is.list(list[[1L]]) || is(list[[1L]], "List"))) list <- as.list(list[[1L]]) new(paste0(class, "List"), listData=list) }) setMethod(.RsamtoolsFileList, "RsamtoolsFile", function(file, ..., classDef = class, yieldSize=NA_integer_, class) { new(paste0(class, "List"), listData=list(file, ...)) }) setMethod(path, "RsamtoolsFileList", function(object, ...) { vapply(object, path, character(1)) }) setMethod(index, "RsamtoolsFileList", function(object, ...) { sapply(object, index, ...) }) setReplaceMethod("index", "RsamtoolsFileList", function(object, ..., value) { stopifnot(length(value) == length(path(object))) for (i in seq_along(object)) index(object[[i]]) <- value[i] object }) setMethod(yieldSize, "RsamtoolsFileList", function(object, ...) { vapply(object, yieldSize, numeric(1)) }) setReplaceMethod("yieldSize", "RsamtoolsFileList", function(object, ..., value) { for (i in seq_along(object)) yieldSize(object[[i]]) <- value object }) setMethod(isOpen, "RsamtoolsFileList", function(con, rw="") { sapply(as.list(con), isOpen, rw="read") }) open.RsamtoolsFileList <- function(con, ...) { for (f in as.list(con)) open(f, ...) con } close.RsamtoolsFileList <- function(con, ...) { for (f in as.list(con)) close(f, ...) con } setMethod(names, "RsamtoolsFileList", function(x) { nms <- callNextMethod() if (is.null(nms)) nms <- sapply(x, function(elt) basename(path(elt))) nms }) ## implementations BcfFileList <- function(...) .RsamtoolsFileList(..., class="BcfFile") TabixFileList <- function(...) .RsamtoolsFileList(..., class="TabixFile") FaFileList <- function(...) .RsamtoolsFileList(..., class="FaFile") ## BamFileList setMethod(countBam, "BamFileList", function(file, index=file, ..., param=ScanBamParam()) { counts <- lapply(file, countBam, ..., param=param) do.call(rbind, counts) }) setMethod(mergeBam, "BamFileList", function(files, destination, ...) { files <- sapply(files, path) mergeBam(files, destination, ...) }) Rsamtools/R/methods-ScanBVcfParam.R0000644000175400017540000000545413556116727020203 0ustar00biocbuildbiocbuild.ScanBcfParam <- function(fixed=character(), info=character(), geno=character(), samples=character(), trimEmpty=TRUE, which, class="ScanBcfParam") { if (1L == length(fixed) && is.na(fixed)) fixed <- as.character(fixed) if (1L == length(info) && is.na(info)) info <- as.character(info) if (1L == length(geno) && is.na(geno)) geno <- as.character(geno) if (1L == length(samples) && is.na(samples)) samples <- as.character(samples) new(class, which=which, fixed=fixed, info=info, geno=geno, samples=samples, trimEmpty=trimEmpty) } ## ScanBcfParam setMethod(ScanBcfParam, c(which="missing"), function(fixed=character(), info=character(), geno=character(), samples=character(), trimEmpty=TRUE, which, ...) { which <- IRangesList() names(which) <- character() .ScanBcfParam(fixed, info, geno, samples, trimEmpty, which, ...) }) setMethod(ScanBcfParam, c(which="GRangesList"), function(fixed=character(), info=character(), geno=character(), samples=character(), trimEmpty=TRUE, which, ...) { .ScanBcfParam(fixed, info, geno, samples, trimEmpty, which=ranges(which), ...) }) setMethod(ScanBcfParam, c(which="IntegerRangesList"), function(fixed=character(), info=character(), geno=character(), samples=character(), trimEmpty=TRUE, which, ...) { .ScanBcfParam(fixed, info, geno, samples, trimEmpty, which, ...) }) setMethod(ScanBcfParam, c(which="GRanges"), function(fixed=character(), info=character(), geno=character(), samples=character(), trimEmpty=TRUE, which, ...) { which <- split(ranges(which), seqnames(which)) .ScanBcfParam(fixed, info, geno, samples, trimEmpty, which, ...) }) ## accessors bcfFixed <- function(object) slot(object, "fixed") bcfInfo <- function(object) slot(object, "info") bcfGeno <- function(object) slot(object, "geno") bcfSamples <- function(object) slot(object, "samples") bcfTrimEmpty <- function(object) slot(object, "trimEmpty") bcfWhich <- function(object) slot(object, "which") .some <- S4Vectors:::selectSome setMethod(show, "ScanBVcfParam", function(object) { .ptags <- function(tags) { if (length(tags)) paste(tags, collapse=", ") else "character() [All]" } .clslbl <- function(lbl) { cl <- if ("ScanBcfParam" == class(object)) "bcf" else "vcf" paste0(cl, lbl) } cat("class:", class(object), "\n") cat(sprintf("%s: %d elements\n", .clslbl("Which"), length(bcfWhich(object)))) cat(.clslbl("Fixed:"), .ptags(bcfFixed(object)), "\n") cat(.clslbl("Info:"), .some(bcfInfo(object)), "\n") cat(.clslbl("Geno:"), .some(bcfGeno(object)), "\n") cat(.clslbl("Samples:"), .some(bcfSamples(object)), "\n") }) Rsamtools/R/methods-ScanBamParam.R0000644000175400017540000003331313556116727020055 0ustar00biocbuildbiocbuild## Native method first. setMethod(ScanBamParam, c(which="IntegerRangesList"), function(flag=scanBamFlag(), simpleCigar=FALSE, reverseComplement=FALSE, tag=character(0), tagFilter=list(), what=character(0), which, mapqFilter=NA_integer_) { if (is.null(names(which))) { if (length(which) != 0L) stop(wmsg("'which' must have names in \"ScanBamParam\" ", "method for IntegerRangesList objects ")) names(which) <- character() } new("ScanBamParam", flag=flag, simpleCigar=simpleCigar, reverseComplement=reverseComplement, tag=tag, tagFilter=.normalize_tagFilter(tagFilter), what=what, which=which, mapqFilter=as.integer(mapqFilter)) }) setMethod(ScanBamParam, c(which="missing"), function(flag=scanBamFlag(), simpleCigar=FALSE, reverseComplement=FALSE, tag=character(0), tagFilter=list(), what=character(0), which, mapqFilter=NA_integer_) { which <- IRangesList() ScanBamParam(flag=flag, simpleCigar=simpleCigar, reverseComplement=reverseComplement, tag=tag, tagFilter=tagFilter, what=what, which=which, mapqFilter=as.integer(mapqFilter)) }) ## Default method. setMethod(ScanBamParam, c(which="ANY"), function(flag=scanBamFlag(), simpleCigar=FALSE, reverseComplement=FALSE, tag=character(0), tagFilter=list(), what=character(0), which, mapqFilter=NA_integer_) { which <- as(which, "IntegerRangesList") ScanBamParam(flag=flag, simpleCigar=simpleCigar, reverseComplement=reverseComplement, tag=tag, tagFilter=tagFilter, what=what, which=which, mapqFilter=as.integer(mapqFilter)) }) ## Note that this method is not needed. Coercing a GRanges to IntegerRangesList ## works and produces exactly what the method below is doing by hand. So the ## default ScanBamParam method above just works on a GRanges. -- Herv\'e setMethod(ScanBamParam, c(which="GRanges"), function(flag=scanBamFlag(), simpleCigar=FALSE, reverseComplement=FALSE, tag=character(0), tagFilter=list(), what=character(0), which, mapqFilter=NA_integer_) { which <- split(ranges(which), seqnames(which)) ScanBamParam(flag=flag, simpleCigar=simpleCigar, reverseComplement=reverseComplement, tag=tag, tagFilter=tagFilter, what=what, which=which, mapqFilter=as.integer(mapqFilter)) }) ## adapted from ?integer .has.wholenumbers <- function(x, tol=.Machine$double.eps^0.5) all(abs(x - round(x)) < tol) .normalize_tagFilter <- function(tagfilter) { tagfilter <- lapply(tagfilter, function(x) { if(is.numeric(x)) { if(!.has.wholenumbers(x)) { msg <- paste0("Filtering tags by floating point values ", "not supported. Please use integer values.") stop(paste(strwrap(msg, exdent=2), collapse="\n")) } x <- as.integer(x) } x ##unique(x) }) tagfilter } setValidity("ScanBamParam", function(object) { msg <- NULL flag <- bamFlag(object, asInteger=TRUE) simpleCigar <- bamSimpleCigar(object) reverseComplement <- bamReverseComplement(object) tag <- bamTag(object) tagFilter <- bamTagFilter(object) what <- bamWhat(object) which <- bamWhich(object) mapqFilter <- bamMapqFilter(object) ## flag if (length(flag) != 2 || typeof(flag) != "integer") msg <- c(msg, "'flag' must be integer(2)") else { if (!identical(names(flag), c("keep0", "keep1"))) msg <- c(msg, "'names(flag)' must be c('keep0', 'keep1')") else if (any(flag < 0 | flag >= 2^12)) msg <- c(msg, "'flag' values must be >=0, <4096") } ## simpleCigar if (!((1L == length(simpleCigar)) && !is.na(simpleCigar))) msg <- c(msg, "'simpleCigar' must be logical(1), not NA") ## reverseComplement if (!((1L == length(reverseComplement)) && !is.na(reverseComplement))) msg <- c(msg, "'reverseComplement' must be logical(1)") ## tag if (0 != length(tag) && any(2 != nchar(tag))) msg <- c(msg, "'tag' must be two letters, e.g,, 'MD'") ## tagFilter if (length(tagFilter) > 0) { tagnms <- names(tagFilter) if(length(tagnms) == 0L || any(2 != nchar(tagnms))) msg <- c(msg, paste0("'tagFilter' elements must be named with ", "two characters each")) for(valvec in tagFilter) if(is.character(valvec) && any(!nzchar(valvec))) msg <- c(msg, "character() tagFilter values must be non-empty") elt_typeinfo <- vapply(tagFilter, function(x) { length(x) && (is.character(x) || is.integer(x)) && ##is.atomic(x) !is.null(x) && !anyNA(x) }, logical(1)) if(any(!elt_typeinfo)) msg <- c(msg, paste0("'tagFilter' must contain only non-NULL, ", "non-NA, non-empty character or integer ", "values")) } ## what if (!all(what %in% scanBamWhat())) msg <- c(msg, "'what' must be from 'scanBamWhat()'") ## which if (length(which) != 0 && (any(!nzchar(names(which))) || any(is.na(names(which))))) msg <- c(msg, "'which' elements must be named (not NA)") ## mapqFilter if (length(mapqFilter) != 1) msg <- c(msg, "'mapqFilter' must be integer(1), >= 0") else if (!(is.na(mapqFilter) || mapqFilter >= 0)) msg <- c(msg, "'mapqFilter' must be NA or >= 0") if (is.null(msg)) TRUE else msg }) bamFlag <- function(object, asInteger=FALSE) { if (asInteger) { slot(object, "flag") } else { keep <- slot(object, "flag") keep0 <- bamFlagAsBitMatrix(keep[[1]])[1L,] == 1L flag <- keep1 <- bamFlagAsBitMatrix(keep[[2]])[1L,] == 1L flag[keep1 & sapply(keep0, isTRUE)] <- NA flag } } "bamFlag<-" <- function(object, value) ## FIXME: make this support input like bamFlag { slot(object, "flag") <- value validObject(object) object } bamSimpleCigar <- function(object) slot(object, "simpleCigar") "bamSimpleCigar<-" <- function(object, value) { slot(object, "simpleCigar") <- value validObject(object) object } bamReverseComplement <- function(object) slot(object, "reverseComplement") "bamReverseComplement<-" <- function(object, value) { slot(object, "reverseComplement") <- value validObject(object) object } bamTag <- function(object) slot(object, "tag") "bamTag<-" <- function(object, value) { slot(object, "tag") <- value validObject(object) object } bamTagFilter <- function(object) slot(object, "tagFilter") "bamTagFilter<-" <- function(object, value) { slot(object, "tagFilter") <- .normalize_tagFilter(value) validObject(object) object } bamWhich <- function(object) slot(object, "which") setGeneric("bamWhich<-", function(object, value) standardGeneric("bamWhich<-")) setReplaceMethod("bamWhich", c("ScanBamParam", "IntegerRangesList"), function(object, value) { slot(object, "which") <- value validObject(object) object }) setReplaceMethod("bamWhich", c("ScanBamParam", "GRanges"), function(object, value) { bamWhich(object) <- split(ranges(value), seqnames(value)) validObject(object) object }) setReplaceMethod("bamWhich", c("ScanBamParam", "ANY"), function(object, value) { bamWhich(object) <- as(value, "IntegerRangesList") validObject(object) object }) bamWhat <- function(object) slot(object, "what") "bamWhat<-" <- function(object, value) { slot(object, "what") <- value validObject(object) object } bamMapqFilter <- function(object) slot(object, "mapqFilter") "bamMapqFilter<-" <- function(object, value) { slot(object, "mapqFilter") <- as.integer(value) validObject(object) object } ## helpers FLAG_BITNAMES <- c( "isPaired", "isProperPair", "isUnmappedQuery", "hasUnmappedMate", "isMinusStrand", "isMateMinusStrand", "isFirstMateRead", "isSecondMateRead", "isSecondaryAlignment", "isNotPassingQualityControls", "isDuplicate", "isSupplementaryAlignment" ) scanBamFlag <- function(isPaired=NA, isProperPair=NA, isUnmappedQuery=NA, hasUnmappedMate=NA, isMinusStrand=NA, isMateMinusStrand=NA, isFirstMateRead=NA, isSecondMateRead=NA, # redundant isNotPrimaryRead=NA, isSecondaryAlignment=NA, isNotPassingQualityControls=NA, isDuplicate=NA, isSupplementaryAlignment = NA) ## NA: keep either 0 or 1 flag; FALSE: keep 0 flag; TRUE: keep 1 flag { flag <- S4Vectors:::makePowersOfTwo(length(FLAG_BITNAMES)) names(flag) <- FLAG_BITNAMES args <- lapply(as.list(match.call())[-1], eval, parent.frame()) if (any(sapply(args, length) > 1L)) stop("all arguments must be logical(1)") if (length(args) > 0) { ## deprecate isNotPrimaryRead if ("isNotPrimaryRead" %in% names(args)) { .Deprecated("isSecondaryAlignment", old="isNotPrimaryRead") old <- args[["isNotPrimaryRead"]] args[["isNotPrimaryRead"]] <- NULL value_to_use <- if ("isSecondaryAlignment" %in% names(args)) args[["isSecondaryAlignment"]] else old if (("isSecondaryAlignment" %in% names(args)) && !identical(args[["isSecondaryAlignment"]], old)) { msg <- sprintf("'%s' inconsistent with '%s', using '%s'", "isNotPrimaryRead", "isSecondaryAlignment", "isSecondaryAlignment") warning(paste(strwrap(msg, exdent=2), collapse="\n")) } args[["isSecondaryAlignment"]] <- value_to_use } ## keep0: NA | FALSE --> drop !NA & TRUE idx <- names(args[sapply(args, function(x) !is.na(x) && x)]) keep0 <- Reduce("+", flag[ !names(flag) %in% idx ], 0L) ## keep1: NA | TRUE --> drop !NA & FALSE idx <- names(args[sapply(args, function(x) !is.na(x) && !x)]) keep1 <- Reduce("+", flag[ !names(flag) %in% idx ], 0L) } else keep0 <- keep1 <- Reduce("+", flag, 0L) c(keep0=keep0, keep1=keep1) } scanBamWhat <- function() { nms <- names(.scanBamTemplate()) nms[nms != "tag"] } setMethod(show, "ScanBamParam", function(object) { .show_classname(object) flag <- bamFlag(object)[!is.na(bamFlag(object))] vals <- sprintf("bamFlag (NA unless specified): %s", paste(names(flag), flag, sep="=", collapse=", ")) cat(strwrap(vals, exdent=2), sep="\n") cat("bamSimpleCigar: ", bamSimpleCigar(object), "\n", sep="") cat("bamReverseComplement: ", bamReverseComplement(object), "\n", sep="") cat("bamTag:", paste(bamTag(object), collapse=", "), "\n") cat("bamTagFilter:\n") tagFilter <- lapply(bamTagFilter(object), function(x) { if(is.character(x)) sQuote(x) else x }) tagnms <- names(tagFilter) for(idx in seq_along(tagFilter)) { elt <- paste(tagnms[[idx]], paste(S4Vectors:::selectSome(tagFilter[[idx]]), collapse=", "), sep=" : ") cat(strwrap(elt, exdent=7, indent=2), sep="\n") } cat("bamWhich:", sum(lengths(bamWhich(object))), "ranges\n") what <- paste("bamWhat: ", paste(bamWhat(object), collapse=", ")) cat(strwrap(what, exdent=2), sep="\n") cat("bamMapqFilter: ", bamMapqFilter(object), "\n", sep="") }) ## flag utils ## Explode the bits of a 'flag' vector into a matrix. bamFlagAsBitMatrix <- function(flag, bitnames=FLAG_BITNAMES) { ## deprecate 'isNotPrimaryRead' oldname <- "isNotPrimaryRead" newname <- "isSecondaryAlignment" if(oldname %in% bitnames && newname %in% bitnames) { msg <- paste0("'%s' is deprecated form of '%s', please specify ", "only one") msg <- sprintf(msg, oldname, newname) stop(paste(strwrap(msg, exdent=2), collapse="\n")) } if(oldname %in% bitnames) { .Deprecated(newname, old=oldname) normalized <- bitnames normalized[which(normalized == oldname)] <- newname bitpos <- .calcBitPos(normalized) } else { bitpos <- .calcBitPos(bitnames) } ans <- S4Vectors:::explodeIntBits(flag, bitpos=bitpos) dimnames(ans) <- list(names(flag), bitnames) ans } .calcBitPos <- function(bitnames) { bitpos <- match(bitnames, FLAG_BITNAMES) invalid_bitnames_idx <- which(is.na(bitpos)) if (length(invalid_bitnames_idx) != 0L) { in1string <- paste0(bitnames[invalid_bitnames_idx], collapse=", ") stop("invalid bitname(s): ", in1string) } bitpos } ## Performs a logical AND between 2 'flag' vectors. bamFlagAND <- function(flag1, flag2) { bits1 <- bamFlagAsBitMatrix(flag1) bits2 <- bamFlagAsBitMatrix(flag2) ans <- S4Vectors:::implodeIntBits(bits1 & bits2) names(ans) <- names(flag1) ans } bamFlagTest <- function(flag, value) { ## deprecate 'isNotPrimaryRead' oldname <- "isNotPrimaryRead" newname <- "isSecondaryAlignment" if(oldname == value) { .Deprecated(newname, old=oldname) value <- newname } if (length(value) != 1 || !value %in% FLAG_BITNAMES) { msg <- sprintf("'is' must be character(1) in '%s'", paste(FLAG_BITNAMES, collapse="' '")) stop(msg) } i <- 2 ^ (match(value, FLAG_BITNAMES) - 1L) bitAnd(flag, i) == i } Rsamtools/R/methods-TabixFile.R0000644000175400017540000001067213556116727017442 0ustar00biocbuildbiocbuildTabixFile <- function(file, index=paste(file, "tbi", sep="."), ..., yieldSize=NA_integer_) { if (is(file, "TabixFile")) return(file) tryCatch({ .io_check_exists(c(file, index)) }, error=function(err) { stop(sprintf("TabixFile: %s", conditionMessage(err)), call.=FALSE) }) .RsamtoolsFile(.TabixFile, file, index, yieldSize=yieldSize, ...) } open.TabixFile <- function(con, ...) { ## FIXME: path? index? con$.extptr <- .Call(.tabixfile_open, path(con), index(con, asNA=FALSE)) invisible(con) } close.TabixFile <- function(con, ...) { if (!isOpen(con)) stop("isOpen() is not 'TRUE'") con$.extptr <- .Call(.tabixfile_close, .extptr(con)) invisible(con) } setMethod(isOpen, "TabixFile", function(con, rw="") { if (!missing(rw) && rw != "read") stop("'rw' must be 'read'") .Call(.tabixfile_isopen, .extptr(con)) }) indexTabix <- function(file, format=c("gff", "bed", "sam", "vcf", "vcf4", "psltbl"), seq=integer(), start=integer(), end=integer(), skip=0L, comment="#", zeroBased=FALSE, ...) { tryCatch({ file <- .normalizePath(file) format <- if (!missing(format)) match.arg(format) else character() .Call(.index_tabix, file, format, as.integer(seq), as.integer(start), as.integer(end), skip, comment, zeroBased) sprintf("%s.tbi", file) }, error=function(err) { stop(conditionMessage(err), "\n file: ", file) }) } .headerTabix <- function(file, ...) { if (!isOpen(file)) { open(file) on.exit(close(file)) } .Call(.header_tabix, .extptr(file)) } setMethod(headerTabix, "TabixFile", .headerTabix) setMethod(headerTabix, "character", function(file, ...) { .headerTabix(TabixFile(file)) }) .seqnamesTabix <- function(file, ...) { .headerTabix(file, ...)[["seqnames"]] } setMethod(seqnamesTabix, "TabixFile", .seqnamesTabix) setMethod(seqnamesTabix, "character", function(file, ...) { .seqnamesTabix(TabixFile(file)) }) countTabix <- function(file, ...) { tbxsym <- getNativeSymbolInfo(".tabix_count", "Rsamtools") scanTabix(file, ..., tbxsym=tbxsym) } .tabix_scan <- function(file, ..., space, start, end, tbxsym=getNativeSymbolInfo(".tabix_as_character", "Rsamtools"), tbxstate=NULL, row.names=NULL) { tryCatch({ if (!isOpen(file)) { open(file) on.exit(close(file)) } if (0L != length(start) && !is.na(yieldSize(file))) { msg <- sprintf("'%s' must be '%s' when range specified", "yieldSize(file)", "NA_integer_") cond <- simpleError(msg) class(cond) <- c("scanTabix_param", class(cond)) stop(cond) } result <- .Call(.scan_tabix, .extptr(file), list(space, start, end), yieldSize(file), tbxsym$address, tbxstate, row.names) setNames(result, sprintf("%s:%d-%d", space, start, end)) }, scanTabix_param=function(err) stop(err), error=function(err) { msg <- paste0("scanTabix: ", conditionMessage(err), "\n path: ", path(file), "\n index: ", index(file)) cond <- simpleError(msg) class(cond) <- c("scanTabix_io", class(err)) stop(cond) }) } setMethod(scanTabix, c("TabixFile", "missing"), function(file, ..., param) { .tabix_scan(file, ..., space=character(), start=integer(), end=integer()) }) setMethod(scanTabix, c("TabixFile", "IntegerRangesList"), function(file, ..., param) { .tabix_scan(file, ..., space=as.character(space(param)), start=.uunlist(start(param)), end=.uunlist(end(param))) }) setMethod(scanTabix, c("TabixFile", "GRanges"), function(file, ..., param) { .tabix_scan(file, ..., space=as.character(seqnames(param)), start=start(param), end=end(param)) }) setMethod(scanTabix, c("character", "missing"), function(file, ..., param) { scanTabix(TabixFile(file), ...) }) setMethod(scanTabix, c("character", "ANY"), function(file, ..., param) { scanTabix(TabixFile(file), ..., param=param) }) setMethod(yieldTabix, "TabixFile", function(file, ..., yieldSize=1000000L) { .Deprecated("scanTabix") scanTabix(file, ..., yieldSize=yieldSize)[[1]] }) Rsamtools/R/phred2ASCIIOffset.R0000644000175400017540000000416313556116727017234 0ustar00biocbuildbiocbuild.ascii_offset <- function() setNames(33:126 - 33L, strsplit(rawToChar(as.raw(33:126)), "")[[1]]) .phred2ascii_int <- function(x, scheme) { ## See https://en.wikipedia.org/wiki/FASTQ_format#Encoding ascii <- .ascii_offset() switch(scheme, "Illumina 1.8+" = { ## L - Illumina 1.8+ Phred+33, raw reads typically (0, 41) stopifnot(all(x >= 0), all(x <= 41)) ascii[x + 1L] }, "Sanger" = { ## S - Sanger Phred+33, raw reads typically (0, 40) stopifnot(all(x >= 0), all(x <= 40)) ascii[x + 1L] }, "Solexa" = { ## X - Solexa Solexa+64, raw reads typically (-5, 40) stopifnot(all(x >= -5), all(x <= 40)) ascii[x + 32L] }, "Illumina 1.3+" = { ## I - Illumina 1.3+ Phred+64, raw reads typically (0, 40) stopifnot(all(x >= 0), all(x <= 40)) ascii[x + 32L] }, "Illumina 1.5+" = { ## J - Illumina 1.5+ Phred+64, raw reads typically (3, 40) ## with 0=unused, 1=unused, 2=Read Segment Quality Control Indicator (bold) ## (Note: See discussion above). stopifnot(all(x >= 3), all(x <= 40)) ascii[x + 32L] }, default = stop("unknown scheme '", scheme, "'")) } .phred2ascii_char <- function(x) { ascii <- .ascii_offset() stopifnot(all(x %in% names(ascii))) ascii[x] } phred2ASCIIOffset <- function(phred=integer(),scheme= c("Illumina 1.8+", "Sanger", "Solexa", "Illumina 1.3+", "Illumina 1.5+")) { if (is.numeric(phred)) { stopifnot(missing(scheme) || (length(scheme) == 1L), !anyNA(phred)) scheme <- match.arg(scheme) phred <- as.integer(phred) .phred2ascii_int(phred, scheme) } else if (is.character(phred)) { if (!missing(scheme)) message("'scheme' ignored; does not influence ASCII offset") if (length(phred) == 1L && nchar(phred) > 1L) phred <- strsplit(phred, "")[[1]] stopifnot(all(nchar(phred) == 1L)) .phred2ascii_char(phred) } else stop("'phred' must be numeric (coerced to integer) or character") } Rsamtools/R/pileup.R0000644000175400017540000002256713556116727015436 0ustar00biocbuildbiocbuild## PileupParam .PileupParam <- setClass("PileupParam", representation( ## behavior-only policies (do not affect result schema) max_depth = "integer", #pileupParams elt 0 (in C code) min_base_quality = "integer", # 1 min_mapq = "integer", # 2 min_nucleotide_depth = "integer", # 3 min_minor_allele_depth = "integer", # 4 ## behavior+structure policies distinguish_strands = "logical", # 5 distinguish_nucleotides = "logical", # 6 ignore_query_Ns = "logical", # 7 include_deletions="logical", # 8 include_insertions="logical", # 9 left_bins = "numeric", # 10 query_bins="numeric")) # 11 setMethod(show, "PileupParam", function(object) { cat("class: ", class(object), "\n") values <- sapply(slotNames(object), slot, object=object) info <- paste(slotNames(object), values, sep=": ", collapse="; ") cat(strwrap(info, exdent=2), sep="\n") }) .as.list_PileupParam <- function(x, ...) { slotnames <- slotNames(x) names(slotnames) <- slotnames lapply(slotnames, slot, object=x) } PileupParam <- function(max_depth=250, min_base_quality=13, min_mapq=0, min_nucleotide_depth=1, min_minor_allele_depth=0, distinguish_strands=TRUE, distinguish_nucleotides=TRUE, ignore_query_Ns=TRUE, include_deletions=TRUE, include_insertions=FALSE, left_bins=NULL, query_bins=NULL, cycle_bins=NULL) { ## argument checking if(!is.null(cycle_bins)) { .Deprecated("cycle_bins", "Rsamtools", paste("'cycle_bins' deprecated; rename 'cycle_bins'", "to 'left_bins' (identical behvaior)")) left_bins <- cycle_bins } if(!is.null(left_bins) && !is.null(query_bins)) stop("only one of 'left_bins', 'query_bins', and 'cycle_bins' allowed") if(is.null(left_bins)) left_bins <- numeric() if(is.null(query_bins)) query_bins <- numeric() ## invariant: ## - left_bins & query_bins length 0 ## - one of left_bins or query_bins length > 0, but the other length 0 stopifnot(isSingleNumber(max_depth)) stopifnot(isSingleNumber(min_base_quality)) stopifnot(isSingleNumber(min_mapq)) stopifnot(isSingleNumber(min_nucleotide_depth)) stopifnot(isSingleNumber(min_minor_allele_depth)) max_depth <- as.integer(max_depth) min_base_quality <- as.integer(min_base_quality) min_mapq <- as.integer(min_mapq) min_nucleotide_depth <- as.integer(min_nucleotide_depth) min_minor_allele_depth <- as.integer(min_minor_allele_depth) left_bins <- .preprocess_bins(left_bins) query_bins <- .preprocess_bins(query_bins) stopifnot(isTRUEorFALSE(distinguish_strands)) stopifnot(isTRUEorFALSE(distinguish_nucleotides)) stopifnot(isTRUEorFALSE(ignore_query_Ns)) stopifnot(isTRUEorFALSE(include_deletions)) stopifnot(isTRUEorFALSE(include_insertions)) ## creation .PileupParam(max_depth=max_depth, min_base_quality=min_base_quality, min_mapq=min_mapq,min_nucleotide_depth=min_nucleotide_depth, min_minor_allele_depth=min_minor_allele_depth, distinguish_strands=distinguish_strands, distinguish_nucleotides=distinguish_nucleotides, ignore_query_Ns=ignore_query_Ns, include_deletions=include_deletions, include_insertions=include_insertions, left_bins=left_bins, query_bins=query_bins) } .pileup <- function(file, index=file, ..., scanBamParam=ScanBamParam(), pileupParam=PileupParam()) { if (!isOpen(file)) { open(file) on.exit(close(file)) } if(bamReverseComplement(scanBamParam)) { warning("'reverseComplement' parameter in pileup ScanBamParam will", " be ignored") bamReverseComplement(scanBamParam) <- FALSE } schema <- .schemaBuilder(pileupParam) result <- .io_bam(.c_Pileup, file, ## space, keepFlags, isSimpleCigar extracted from 'scanBamParam' ## in .io_bam; ## remainder (...) passed to C bamReverseComplement(scanBamParam), yieldSize(file), obeyQname(file), asMates(file), qnamePrefixEnd(file), qnameSuffixStart(file), schema, .as.list_PileupParam(pileupParam), param=scanBamParam) ##browser() which_labels <- .scanBam_extract_which_labels(scanBamParam) which_labels <- .make_unique(which_labels) run_lens <- .metacols_run_lengths(result) which_label <- rep.int(factor(which_labels, levels=which_labels), run_lens) ## no-op if no bins if(length(pileupParam@left_bins) > 0) result <- .apply_bin_levels(result, pileupParam@left_bins) else if(length(pileupParam@query_bins) > 0) result <- .apply_bin_levels(result, pileupParam@query_bins) result <- .as.data.frame_list_of_lists(result) ## wait to rename column until after converted to data.frame if(length(pileupParam@left_bins) > 0) { if(! "bin" %in% names(result)) stop("internal: expected a 'bin' column to rename 'left_bin'") names(result)[names(result) == "bin"] <- "left_bin" } else if(length(pileupParam@query_bins) > 0) { if(! "bin" %in% names(result)) stop("internal: expected a 'bin' column to rename 'query_bin'") names(result)[names(result) == "bin"] <- "query_bin" } if(length(bamWhich(scanBamParam)) != 0L) ## if no space arg result <- cbind(result, which_label) ## last col result } .apply_bin_levels <- function(result, bins) { ## no-op if user didn't ask for bins if(length(bins) > 0L) { bin_levels <- .bin_levels(bins) for(i in seq_along(result)) result[[i]]$bin <- .as.factor_bin(result[[i]]$bin, bin_levels) } result } .as.factor_bin <- function(bin, bin_levels) { structure(bin, levels=bin_levels, class="factor") ## equivalent: ## attributes(cycle_bin) <- list(levels=cycle_bin_levels, class="factor") ## cycle_bin } .bin_levels <- function(bins) { bins[bins == .Machine$integer.max] <- Inf bins[bins == -.Machine$integer.max] <- -Inf levels(cut(0, bins)) } ## return value: numeric vector of increasing values that contains ## only integers and +/-Inf .preprocess_bins <- function(bins) { if(length(bins) != 0L) { if(any(is.na(bins)) || any(is.null(bins)) || any(is.nan(bins))) stop("bin args must not contain NAs, NULLs, or NaNs") if(length(bins) == 1L) stop("bins args must have 0 or >1 elements") if(any(bins < 0L) && any(bins > 0L)) stop("bin args values must all have the same sign (or be Inf)") if(any(bins == 0L) && any(bins < 0L)) stop("'0' not allowed when specifying reverse bins; try '-1'?") ## invariant: only contains integers and +/-Inf bins[!is.finite(bins) & bins > 0] <- .Machine$integer.max ## Inf to max_int bins[!is.finite(bins) & bins < 0] <- -.Machine$integer.max ## -Inf to -max_int bins <- as.integer(bins) if(any(duplicated(bins))) stop("bin args must not contain duplicate values") bins <- sort(bins) } bins } .make_unique <- function(group_names) { if(anyDuplicated(group_names)) group_names <- paste0(group_names, ".", seq_along(group_names)) else group_names } .metacols_run_lengths <- function(x) { if(length(x) == 0L) run_lens <- integer(0) else run_lens <- sapply(x, function(x_elt) length(x_elt[[1L]])) } .as.data.frame_list_of_lists <-function(x) { if(length(x) < 1L) { stop("'x' must have length > 0, got '%d'", length(x)) } ans_colnames <- names(x[[1L]]) ans <- lapply(setNames(ans_colnames, ans_colnames), function(nm) { tmp <- lapply(x, "[[", nm) S4Vectors:::quick_unlist(tmp) }) ans <- data.frame(ans, stringsAsFactors=FALSE) } setMethod("pileup", "character", function(file, index=file, ..., scanBamParam=ScanBamParam(), pileupParam=PileupParam()) { stopifnot(length(file) == 1L) bf <- BamFile(file, index=index) .pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) }) setMethod("pileup", "BamFile", .pileup) .pileupWhat <- function(pileupParam) { result <- c("pos", if (pileupParam@distinguish_strands) "strand" else NULL, if (pileupParam@distinguish_nucleotides) "nucleotide" else NULL, "count") setNames(result, result) } ## schema .strandHelper <- function(scanBamP) { flagVec <- bamFlag(scanBamP)['isMinusStrand'] if (is.na(flagVec)) { "*" } else if (flagVec) { "-" } else { "+" } } .schemaBuilder <- function(pileupParam) { if(!inherits(pileupParam, "PileupParam")) { stop("'pileupParam' must inherit from 'PileupParam', got '%s'", class(pileupParam)) } schemaDimNames <- c("strand", "nucleotide") strand <- "" if(pileupParam@distinguish_strands) strand <- c("+", "-") nucleotide <- "" if(pileupParam@distinguish_nucleotides) { nucleotide <- c("A", "C", "G", "T") if(!pileupParam@ignore_query_Ns) nucleotide <- c(nucleotide, "N") if(pileupParam@include_deletions) nucleotide <- c(nucleotide, "-") } list(schemaDimNames, list(strand, nucleotide)) } Rsamtools/R/pkgconfig.R0000644000175400017540000000127713556116727016102 0ustar00biocbuildbiocbuild.build_path <- function(path) { if (.Platform$OS.type == "windows") { path <- normalizePath(path) if (grepl(' ', path, fixed=TRUE)) path <- utils::shortPathName(path) path <- gsub("\\\\", "/", path) } path } .pkgMk <- function() { if (.Platform$OS.type != "windows") stop(".pkgMk() expects windows operating system") path <- system.file(package="Rsamtools", "usretc", .Platform$r_arch, "Rsamtools.mk", mustWork=TRUE) .build_path(path) } .pkgLd <- function() { path <- system.file(package="Rsamtools", "usrlib", .Platform$r_arch, mustWork=TRUE) .build_path(path) } Rsamtools/R/quickBamFlagSummary.R0000644000175400017540000002201713556116727020032 0ustar00biocbuildbiocbuild### ========================================================================= ### quickBamFlagSummary() ### ------------------------------------------------------------------------- .runlen <- function(x) runLength(Rle(x)) .printSummaryHeader <- function(width1, width2, width3) { printHeaderLine <- function(h1, h2, h3, h4) { cat(format(h1, width=width1, justify="right"), " |", format(h2, width=width2, justify="right"), " |", format(h3, width=width3, justify="right"), " | ", h4, "\n", sep="") } printHeaderLine( "group", "nb of", "nb of", "mean / max") printHeaderLine( "of", "records", "unique", "records per") printHeaderLine("records", "in group", "QNAMEs", "unique QNAME") } .printSummaryLine <- function(group, group_desc, N_rec_per_uqname, width2, width3) { N_rec <- sum(N_rec_per_uqname) N_uqname <- length(N_rec_per_uqname) if (N_uqname == 0L) { mean_N_rec_per_uqname <- max_N_rec_per_uqname <- NA } else { mean_N_rec_per_uqname <- mean(N_rec_per_uqname) max_N_rec_per_uqname <- max(N_rec_per_uqname) } cat(group_desc, " ", group, " |", format(N_rec, width=width2), " |", format(N_uqname, width=width3), " | ", format(mean_N_rec_per_uqname, digits=3L, width=4L), " / ", max_N_rec_per_uqname, "\n", sep="") } .printMainSummary <- function(N_rec_per_uqname, N_1seg_rec_per_uqname, N_mseg_rec_per_uqname, N_first_rec_per_uqname, N_last_rec_per_uqname, N_other_rec_per_uqname) { GROUP2DESC <- c( A="All records........................", S=" o template has single segment....", M=" o template has multiple segments.", F=" - first segment..............", L=" - last segment...............", O=" - other segment.............." ) width1 <- nchar(GROUP2DESC[1L]) + 2L width2 <- width3 <- 9L .printSummaryHeader(width1, width2, width3) .printSummaryLine("A", GROUP2DESC[["A"]], N_rec_per_uqname, width2, width3) .printSummaryLine("S", GROUP2DESC[["S"]], N_1seg_rec_per_uqname, width2, width3) .printSummaryLine("M", GROUP2DESC[["M"]], N_mseg_rec_per_uqname, width2, width3) .printSummaryLine("F", GROUP2DESC[["F"]], N_first_rec_per_uqname, width2, width3) .printSummaryLine("L", GROUP2DESC[["L"]], N_last_rec_per_uqname, width2, width3) .printSummaryLine("O", GROUP2DESC[["O"]], N_other_rec_per_uqname, width2, width3) cat("\nNote that (S, M) is a partitioning of A, and (F, L, O) ", "is a partitioning of M.\n", "Indentation reflects this.\n", sep="") } .printDetailedSummary <- function(group, N_mapped_rec_per_uqname, N_primary_rec_per_uqname, N_secondary_rec_per_uqname, N_unmapped_rec_per_uqname) { SUBGROUP2DESC <- c( `1`=" o record is mapped..............", `2`=" - primary alignment.........", `3`=" - secondary alignment.......", `4`=" o record is unmapped............" ) ## width1 <- nchar(SUBGROUP2DESC[1L]) + 3L width2 <- width3 <- 9L cat("\nDetails for group ", group, ":\n", sep="") #.printSummaryHeader(width1, width2, width3) .printSummaryLine(paste0(group, "1"), SUBGROUP2DESC[["1"]], N_mapped_rec_per_uqname, width2, width3) .printSummaryLine(paste0(group, "2"), SUBGROUP2DESC[["2"]], N_primary_rec_per_uqname, width2, width3) .printSummaryLine(paste0(group, "3"), SUBGROUP2DESC[["3"]], N_secondary_rec_per_uqname, width2, width3) .printSummaryLine(paste0(group, "4"), SUBGROUP2DESC[["4"]], N_unmapped_rec_per_uqname, width2, width3) } .detailedSummary <- function(group, qnameid, flag) { ## 'N_mapped_rec_per_uqname' and 'N_unmapped_rec_per_uqname': rec_is_unmapped <- as.logical(bamFlagAsBitMatrix(flag, "isUnmappedQuery")) rec_is_mapped <- !rec_is_unmapped N_mapped_rec_per_uqname <- .runlen(qnameid[rec_is_mapped]) N_unmapped_rec_per_uqname <- .runlen(qnameid[rec_is_unmapped]) ## 'N_primary_rec_per_uqname' and 'N_secondary_rec_per_uqname': rec_is_secondary <- as.logical(bamFlagAsBitMatrix(flag, "isSecondaryAlignment")) ## The notion of primary/secondary alignment only applies to mapped ## seqments: stopifnot(!any(rec_is_secondary & rec_is_unmapped)) rec_is_primary <- rec_is_mapped & !rec_is_secondary N_primary_rec_per_uqname <- .runlen(qnameid[rec_is_primary]) N_secondary_rec_per_uqname <- .runlen(qnameid[rec_is_secondary]) .printDetailedSummary(group, N_mapped_rec_per_uqname, N_primary_rec_per_uqname, N_secondary_rec_per_uqname, N_unmapped_rec_per_uqname) } setMethod(quickBamFlagSummary, "list", function(file, ..., param=ScanBamParam(), main.groups.only=FALSE) { what0 <- c("qname", "flag") if (!isTRUEorFALSE(main.groups.only)) { stop("'main.groups.only' must be TRUE or FALSE") } else if (!all(what0 %in% names(file))) { stop("'file' must contain elements ", paste(sQuote(what0), collapse=" ")) } ## Order records by QNAME. qname0 <- file[["qname"]] flag0 <- file[["flag"]] qnameid0 <- match(qname0, qname0) # assign unique id to each unique QNAME oo <- order(qnameid0) qnameid <- qnameid0[oo] flag <- flag0[oo] ## 'N_rec_per_uqname': N_rec_per_uqname <- .runlen(qnameid) ## 'N_mseg_rec_per_uqname' and 'N_1seg_rec_per_uqname': rec_is_mseg <- as.logical(bamFlagAsBitMatrix(flag, "isPaired")) rec_is_1seg <- !rec_is_mseg N_1seg_rec_per_uqname <- .runlen(qnameid[rec_is_1seg]) N_mseg_rec_per_uqname <- .runlen(qnameid[rec_is_mseg]) stopifnot(identical(length(N_1seg_rec_per_uqname) + length(N_mseg_rec_per_uqname), length(N_rec_per_uqname))) ## 'N_first_rec_per_uqname' and 'N_last_rec_per_uqname' and ## 'N_other_rec_per_uqname': is_first_mate <- as.logical(bamFlagAsBitMatrix(flag, "isFirstMateRead")) is_second_mate <- as.logical(bamFlagAsBitMatrix(flag, "isSecondMateRead")) rec_is_first <- rec_is_mseg & is_first_mate & !is_second_mate rec_is_last <- rec_is_mseg & is_second_mate & !is_first_mate rec_is_other <- rec_is_mseg & (is_first_mate == is_second_mate) N_first_rec_per_uqname <- .runlen(qnameid[rec_is_first]) N_last_rec_per_uqname <- .runlen(qnameid[rec_is_last]) N_other_rec_per_uqname <- .runlen(qnameid[rec_is_other]) stopifnot(identical(sum(N_first_rec_per_uqname) + sum(N_last_rec_per_uqname) + sum(N_other_rec_per_uqname), sum(N_mseg_rec_per_uqname))) .printMainSummary(N_rec_per_uqname, N_1seg_rec_per_uqname, N_mseg_rec_per_uqname, N_first_rec_per_uqname, N_last_rec_per_uqname, N_other_rec_per_uqname) if (main.groups.only) return(invisible(NULL)) if (length(N_1seg_rec_per_uqname) != 0L && length(N_mseg_rec_per_uqname != 0L)) .detailedSummary("A", qnameid, flag) if (length(N_1seg_rec_per_uqname) != 0L) .detailedSummary("S", qnameid[rec_is_1seg], flag[rec_is_1seg]) if (length(N_mseg_rec_per_uqname) != 0L) .detailedSummary("M", qnameid[rec_is_mseg], flag[rec_is_mseg]) if (length(N_first_rec_per_uqname) != 0L) .detailedSummary("F", qnameid[rec_is_first], flag[rec_is_first]) if (length(N_last_rec_per_uqname) != 0L) .detailedSummary("L", qnameid[rec_is_last], flag[rec_is_last]) if (length(N_other_rec_per_uqname) != 0L) .detailedSummary("O", qnameid[rec_is_other], flag[rec_is_other]) invisible(NULL) }) setMethod(quickBamFlagSummary, "character", function(file, index=file, ..., param=ScanBamParam(), main.groups.only=FALSE) { file <- BamFile(index) quickBamFlagSummary(file, param=param, main.groups.only=main.groups.only) }) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Old stuff. ### quickCountBam <- function(file, ..., param=ScanBamParam(), mainGroupsOnly=FALSE) { .Deprecated("quickBamFlagSummary", "Rsamtools") if (is.null(param)) param <- ScanBamParam() file <- BamFile(file, ...) quickBamFlagSummary(file, param=param, main.groups.only=mainGroupsOnly) } quickBamCounts <- function(file, index=file, param=NULL, main.groups.only=FALSE) { .Defunct("quickBamFlagSummary", "Rsamtools") } Rsamtools/R/readPileup.R0000644000175400017540000000552613556116727016226 0ustar00biocbuildbiocbuild.readPileup_table <- function(conn, colClasses, ...) { read.table(conn, colClasses=colClasses, col.names=names(colClasses), sep="\t", header=FALSE, quote="", comment.char="", fill=TRUE, ...) } .readPileup_indel_idx <- function(df) which(df[[3]] == "*") .readPileup_SNP <- function(file, ..., variant) { colClasses <- c(space="factor", position="integer", referenceBase="character", consensusBase="character", consensusQuality="integer", snpQuality="integer", maxMappingQuality="integer", coverage="integer", "NULL", "NULL", "NULL", "NULL", "NULL", "NULL", "NULL") dat <- .readPileup_table(file, colClasses, ...) idx <- .readPileup_indel_idx(dat) if (length(idx) > 0L) { if (variant == "SNP") idx <- c(idx, idx-1) dat <- dat[-idx,] } GRanges(seqnames=dat[,1], ranges=IRanges(start=dat[,2],end=dat[,2]), referenceBase=factor(dat[,3], levels=DNA_ALPHABET), consensusBase=factor(dat[,4], levels=DNA_ALPHABET), consensusQuality=dat[,5], snpQuality=dat[,6], maxMappingQuality=dat[,7], coverage=dat[,8]) } .readPileup_indel <- function(file, ...) { colClasses <- c(space="factor", position="integer", reference="character", consensus="character", consensusQuality="integer", snpQuality="integer", maxMappingQuality="integer", coverage="integer", alleleOne="character", alleleTwo="character", alleleOneSupport="integer", alleleTwoSupport="integer", additionalIndels="integer", "NULL", "NULL") dat <- .readPileup_table(file, colClasses, ...) idx <- .readPileup_indel_idx(dat) if (length(idx) != 0L) { dat0 <- dat[idx-1,] dat <- dat[idx,] } else { dat <- dat0 <- dat[FALSE,] } GRanges(seqnames=dat[,1], ranges=IRanges(start=dat0[,2],end=dat0[,2]), referenceBase=factor(dat0[,3], levels=DNA_ALPHABET), consensusBase=factor(dat0[,4]), consensusQuality=dat0[,5], snpQuality=dat0[,6], maxMappingQuality=dat0[,7], coverage=dat0[,8], alleleOne=dat[,9], alleleOneSupport=dat[,11], alleleTwo=dat[,10], alleleTwoSupport=dat[,12], additionalIndels=dat[,13]) } setMethod(readPileup, "connection", function(file, ..., variant=c("SNP", "indel", "all")) { variant <- match.arg(variant) switch(variant, SNP=, all=.readPileup_SNP(file=file, ..., variant=variant), indel=.readPileup_indel(file=file, ...)) }) setMethod(readPileup, "character", function(file, ...) { conn <- file(file, "r") on.exit(close(conn)) readPileup(conn, ...) }) Rsamtools/R/scanBam.R0000644000175400017540000000267013556116727015475 0ustar00biocbuildbiocbuild.scanBamTemplate <- function(seqlevels=factor(), tag=character(0)) { .Call(.scan_bam_template, seqlevels, tag) } .scanBam_template <- function(file, param) { tmpl <- .scanBamTemplate(factor(levels=seqlevels(file)), bamTag(param)) ## set those elements of the template that are not 'tag' (treat ## specially because nested list) nor specified by 'what' ## parameter to NULL tmpl[!names(tmpl) %in% c(bamWhat(param), "tag")] <- list(NULL) if (0L == length(tmpl[["tag"]])) tmpl["tag"] <- list(NULL) tmpl } ## return rname:start-end values for outer list elements .scanBam_extract_which_labels <- function(param) { which <- bamWhich(param) if( 0L != length(space(which))) paste0(space(which), ":", .uunlist(start(which)), "-", .uunlist(end(which))) else NULL } .scanBam_postprocess <- function(x, param) { which <- bamWhich(param) if (0L != length(space(which))) names(x) <- paste0(space(which), ":", .uunlist(start(which)), "-", .uunlist(end(which))) lapply(x, Filter, f=Negate(is.null)) } setMethod(scanBam, "character", function(file, index=file, ..., param=ScanBamParam(what=scanBamWhat())) { if (missing(index) && 0L == length(bamWhich(param))) index <- character(0) bam <- open(BamFile(file, index), "rb") on.exit(close(bam)) scanBam(bam, ..., param=param) }) Rsamtools/R/scanBamHeader.R0000644000175400017540000000045413556116727016604 0ustar00biocbuildbiocbuildsetMethod(scanBamHeader, "character", function(files, ...) { files <- .normalizePath(files) lst <- lapply(files, function(file) { bam <- open(BamFile(file, character(0))) on.exit(close(bam)) scanBamHeader(bam, ...) }) names(lst) <- files lst }) Rsamtools/R/scanBcf.R0000644000175400017540000000030013556116727015454 0ustar00biocbuildbiocbuildsetMethod(scanBcf, "character", function(file, index=file, ..., param=ScanBcfParam()) { bcf <- open(BcfFile(file, index)) on.exit(close(bcf)) scanBcf(bcf, ..., param=param) }) Rsamtools/R/scanBcfHeader.R0000644000175400017540000000033613556116727016576 0ustar00biocbuildbiocbuildsetMethod(scanBcfHeader, "character", function(file, ...) { Map(function(file, mode) { bf <- open(BcfFile(file, character(0), ...)) on.exit(close(bf)) scanBcfHeader(bf) }, file, ...) }) Rsamtools/R/sortBam.R0000644000175400017540000000103713556116727015534 0ustar00biocbuildbiocbuildsetMethod(sortBam, "character", function(file, destination, ..., byQname=FALSE, maxMemory=512) { file <- .normalizePath(file) destination <- .normalizePath(destination) result <- .Call(.sort_bam, file, destination, byQname, as.integer(maxMemory)) destination <- paste(result, "bam", sep=".") if (!file.exists(destination)) { msg <- sprintf("'sortBam' failed to create destination '%s'", destination) stop(msg) } destination }) Rsamtools/R/testPairedEndBam.R0000644000175400017540000000136313556116727017302 0ustar00biocbuildbiocbuildsetMethod("testPairedEndBam", "character", function(file, index=file, ...) { bf <- BamFile(file, index) testPairedEndBam(bf, ...) }) setMethod("testPairedEndBam", "BamFile", function(file, index=file, ...) { yieldSize <- yieldSize(file) if (is.na(yieldSize)) yieldSize(file) <- 1000000L on.exit(yieldSize(file) <- yieldSize) if (isOpen(file)) close(file) open(file) isPaired <- FALSE tot <- 0 repeat { flag <- scanBam(file, param=ScanBamParam(what="flag"))[[1]]$flag isPaired <- any(bamFlagTest(flag, "isPaired")) if (isPaired || length(flag) == 0L) break tot <- tot + length(flag) message(tot, " ", appendLF=FALSE) } isPaired }) Rsamtools/R/utilities.R0000644000175400017540000000731113556116727016141 0ustar00biocbuildbiocbuild.ppath <- function(tag, filepath) { wd <- options('width')[[1]] - nchar(tag) - 6 if(is.na(filepath)) return(sprintf("%s: %s\n", tag, NA_character_)) if (0L == length(filepath) || nchar(filepath) < wd) return(sprintf("%s: %s\n", tag, filepath)) bname <- basename(filepath) wd1 <- wd - nchar(bname) dname <- substr(dirname(filepath), 1, wd1) sprintf("%s: %s...%s%s\n", tag, dname, .Platform$file.sep, bname) } .io_check_exists <- function(files) { if (!length(files)) stop("'files' is length(0)") idx <- !grepl("^(ftp|http|https)://", files) & !is.na(files) test <- file.exists(files[idx]) if (!all(test)) { msg <- paste0(sQuote(files[idx][!test]), collapse = "\n ") stop("file(s) do not exist:\n ", msg) } } .show_classname <- function(x) cat("class: ", class(x), "\n", sep="") .normalizePath <- function(path) { if (is(path, "RsamtoolsFile")) { path <- path(path) } else { path <- as.character(path) } idx <- !grepl("^(ftp)|(http)://", path) & !is.na(path) ## expand ~/, but don't chase links (i.e., don't normalizePath()) path[idx] <- path.expand(path[idx]) path } .file.rename <- function(from, to) { warn <- err <- NULL ok <- withCallingHandlers(tryCatch({ file.rename(from, to) || (file.copy(from, to) && file.remove(from)) }, error=function(e) { err <<- append(err, conditionMessage(e)) NULL }), warning=function(w) { warn <<- append(warn, conditionMessage(w)) invokeRestart("muffleWarning") }) if (!ok) { msg <- "file.rename or file.copy/file.remove failed:\n from: %s\n to: %s\n message(s): %s" stop(sprintf(msg, from, to, paste(c(warn, err), collapse="\n "))) } ok } .uunlist <- function(x) unlist(x, use.names=FALSE) setMethod(.asRegions, "IntegerRangesList", function(x) { list(as.character(space(x)), .uunlist(start(x)), .uunlist(end(x))) }) setMethod(.asRegions, "GRanges", function(x) { list(as.character(seqnames(x)), start(x), end(x)) }) ### All arguments must be parallel vectors (of length N). ### The arguments prefixed with 'x_' describe a vector 'x' of N alignments. ### The arguments prefixed with 'y_' describe a vector 'y' of N alignments. ### Performs "parallel pairing" of the N alignments in 'x' with the N ### alignments in 'y'. .isValidHit <- function(x_flag, x_seqnames, x_start, x_mrnm, x_mpos, y_flag, y_seqnames, y_start, y_mrnm, y_mpos) { .Call(.p_pairing, NULL, x_flag, x_seqnames, x_start, x_mrnm, x_mpos, NULL, y_flag, y_seqnames, y_start, y_mrnm, y_mpos) } ### 'x_flag', 'x_seqnames', 'x_start', 'x_mrnm', 'x_mpos': parallel vectors ### (of length N) describing N alignments. The alignments are assumed to ### be already grouped by QNAME. ### 'group.sizes': vector of non-negative integers which sum to N. ### If 'x_qname' was a vector of length N parallel to the 'x_*' arguments ### and containing the QNAME field, then 'group.sizes' would be ### 'runLength(Rle(x_qname))'. ### Returns an integer vector of length N parallel to the 'x_*' arguments. ### Alignments with more than 1 possible mate are assigned a zero. ### Those with exactly 1 mate that has itself more than 1 mate are assigned ### a negative value (the opposite of the index of the mate). .findMateWithinGroups <- function(group.sizes, x_flag, x_seqnames, x_start, x_mrnm, x_mpos) { .Call(.find_mate_within_groups, group.sizes, x_flag, x_seqnames, x_start, x_mrnm, x_mpos) } Rsamtools/R/zip_compression.R0000644000175400017540000000202413556116727017345 0ustar00biocbuildbiocbuildbgzipTabix <- function(fromFname, toFname = paste(fromFname, "gz", sep="."), overwrite=FALSE) { .Defunct("bgzip", package="Rsamtools") } .zip <- function(func, file, dest, overwrite) { file <- .normalizePath(file) dest <- .normalizePath(dest) if (!is.character(dest) || 1L != length(dest)) stop("'dest' must be character(1)") if (!overwrite && file.exists(dest)) stop("'dest' exists:\n dest: ", dest) tryCatch({ .Call(func, file, dest) }, error=function(err) { msg <- sprintf("'%s' error: %s\n file: %s\n dest: %s", sub(".", "", func, fixed=TRUE), conditionMessage(err), file, dest) stop(msg, call.=FALSE) }) } bgzip <- function(file, dest = sprintf("%s.bgz", sub("\\.gz$", "", file)), overwrite=FALSE) { .zip(.bgzip, file, dest, overwrite) } razip <- function(file, dest = sprintf("%s.rz", sub("\\.gz$", "", file)), overwrite=FALSE) { .Defunct("bgzip") } Rsamtools/R/zzz.R0000644000175400017540000000063313556116727014763 0ustar00biocbuildbiocbuild.STRAND_LEVELS <- c("+", "-", "*") .PILEUP_NUCLEOTIDE_LEVELS <- c("A", "C", "G", "T", "N", "=", "-", "+") .onLoad <- function(libname, pkgname) { if (!identical(levels(strand()), .STRAND_LEVELS)) stop("internal: 'levels(strand())' not consistent with Rsamtools") .Call(.bamfile_init) .Call(.bcffile_init) .Call(.fafile_init) .Call(.tabixfile_init) .Call(.bambuffer_init) } Rsamtools/README.md0000644000175400017540000000110513556116727015054 0ustar00biocbuildbiocbuild[](https://bioconductor.org/) _Rsamtools_ is an R/Bioconductor package that provides an interface to the `samtools`, `bcftools`, and `tabix` utilities for manipulating SAM (Sequence Alignment / Map), FASTA, binary variant call (BCF) and compressed indexed tab-delimited (tabix) files. See https://bioconductor.org/packages/Rsamtools for more information including how to install the release version of the package (please refrain from installing directly from GitHub). Rsamtools/build/0000755000175400017540000000000013624616601014667 5ustar00biocbuildbiocbuildRsamtools/build/vignette.rds0000644000175400017540000000043513624616601017230 0ustar00biocbuildbiocbuild‹QÛJ1M7ëÚ.BÅ/põ¤¥ JUèklR l“2‰]|óË»Ín'k[Ä2—33g.¥„ˆÐ$"õ&íz‘øw\ã1éx}:´|êŒÉíÕã\Â\É"꣗?ÑW«ô{ïA½%m´Iuq«™ÒŒø;e4s†5õ˜sVÓ°€²ËãƒÍÄd÷`UÒ&ÕÉo;bìü }¸[Ó¬èÈš^Ç)R¥ÏÉ"ôîúÍvsˆÿÅU·âšO›ƒ%Æ•Ëð¢\ãЧþÍVXû°/gR‹ð-í{ùUÛ:`Š,4;ªvþö¢,ËÅöDãœÛ0QSÁÏ&àë½·X?Â$Rsamtools/inst/0000755000175400017540000000000013624616601014545 5ustar00biocbuildbiocbuildRsamtools/inst/doc/0000755000175400017540000000000013624616601015312 5ustar00biocbuildbiocbuildRsamtools/inst/doc/Rsamtools-Overview.R0000644000175400017540000002266013624616577021246 0ustar00biocbuildbiocbuild### R code from vignette source 'Rsamtools-Overview.Rnw' ################################################### ### code chunk number 1: style ################################################### BiocStyle::latex() ################################################### ### code chunk number 2: options ################################################### options(width=60) ################################################### ### code chunk number 3: preliminaries ################################################### library(Rsamtools) ################################################### ### code chunk number 4: ScanBamParam ################################################### which <- IRangesList(seq1=IRanges(1000, 2000), seq2=IRanges(c(100, 1000), c(1000, 2000))) what <- c("rname", "strand", "pos", "qwidth", "seq") param <- ScanBamParam(which=which, what=what) ################################################### ### code chunk number 5: scanBam ################################################### bamFile <- system.file("extdata", "ex1.bam", package="Rsamtools") bam <- scanBam(bamFile, param=param) ################################################### ### code chunk number 6: scanBam-elts-1 ################################################### class(bam) names(bam) ################################################### ### code chunk number 7: scanBam-elts-2 ################################################### class(bam[[1]]) names(bam[[1]]) ################################################### ### code chunk number 8: scanBam-elts-class ################################################### sapply(bam[[1]], class) ################################################### ### code chunk number 9: scanBam-to-IRanges ################################################### .unlist <- function (x) { ## do.call(c, ...) coerces factor to integer, which is undesired x1 <- x[[1L]] if (is.factor(x1)) { structure(unlist(x), class = "factor", levels = levels(x1)) } else { do.call(c, x) } } bam <- unname(bam) # names not useful in unlisted result elts <- setNames(bamWhat(param), bamWhat(param)) lst <- lapply(elts, function(elt) .unlist(lapply(bam, "[[", elt))) ################################################### ### code chunk number 10: lst-to-DataFrame ################################################### head(do.call("DataFrame", lst)) ################################################### ### code chunk number 11: indexed-file ################################################### list.files(dirname(bamFile), pattern="ex1.bam(.bai)?") ################################################### ### code chunk number 12: bam-remote (eval = FALSE) ################################################### ## which <- IRangesList("6"=IRanges(100000L, 110000L)) ## param <- ScanBamParam(which=which, what=scanBamWhat()) ## na19240bam <- scanBam(na19240url, param=param) ################################################### ### code chunk number 13: summaryFunction ################################################### summaryFunction <- function(seqname, bamFile, ...) { param <- ScanBamParam(what=c('pos', 'qwidth'), which=GRanges(seqname, IRanges(1, 1e7)), flag=scanBamFlag(isUnmappedQuery=FALSE)) x <- scanBam(bamFile, ..., param=param)[[1]] coverage(IRanges(x[["pos"]], width=x[["qwidth"]])) } ################################################### ### code chunk number 14: summaryByChromosome ################################################### seqnames <- paste("seq", 1:2, sep="") cvg <- lapply(seqnames, summaryFunction, bamFile) names(cvg) <- seqnames cvg ################################################### ### code chunk number 15: caffeine-kegg ################################################### library(KEGG.db) kid <- revmap(KEGGPATHID2NAME)[["Caffeine metabolism"]] egid <- KEGGPATHID2EXTID[[sprintf("hsa%s", kid)]] ################################################### ### code chunk number 16: txdb-transcripts ################################################### library(TxDb.Hsapiens.UCSC.hg18.knownGene) bamRanges <- transcripts(TxDb.Hsapiens.UCSC.hg18.knownGene, filter=list(gene_id=egid)) seqlevels(bamRanges) <- # translate seqlevels sub("chr", "", seqlevels(bamRanges)) lvls <- seqlevels(bamRanges) # drop unused levels seqlevels(bamRanges) <- lvls[lvls %in% as.character(seqnames(bamRanges))] ################################################### ### code chunk number 17: bamRanges-genome ################################################### unique(genome(bamRanges)) ################################################### ### code chunk number 18: BamViews-parts ################################################### slxMaq09 <- local({ fl <- system.file("extdata", "slxMaq09_urls.txt", package="Rsamtools") readLines(fl) }) ################################################### ### code chunk number 19: BamViews-construct ################################################### bamExperiment <- list(description="Caffeine metabolism views on 1000 genomes samples", created=date()) bv <- BamViews(slxMaq09, bamRanges=bamRanges, bamExperiment=bamExperiment) metadata(bamSamples(bv)) <- list(description="Solexa/MAQ samples, August 2009", created="Thu Mar 25 14:08:42 2010") ################################################### ### code chunk number 20: BamViews-query ################################################### bamExperiment(bv) ################################################### ### code chunk number 21: bamIndicies (eval = FALSE) ################################################### ## bamIndexDir <- tempfile() ## indexFiles <- paste(bamPaths(bv), "bai", sep=".") ## dir.create(bamIndexDir) ## idxFiles <- mapply(download.file, indexFiles, ## file.path(bamIndexDir, basename(indexFiles)) , ## MoreArgs=list(method="curl")) ################################################### ### code chunk number 22: readGAlignments (eval = FALSE) ################################################### ## library(GenomicAlignments) ## library(parallel) ## options(srapply_fapply="parallel", mc.cores=detectCores()) ## olaps <- readGAlignments(bv) ################################################### ### code chunk number 23: olaps ################################################### library(GenomicAlignments) load(system.file("extdata", "olaps.Rda", package="Rsamtools")) olaps head(olaps[[1]]) ################################################### ### code chunk number 24: read-lengths ################################################### head(t(sapply(olaps, function(elt) range(qwidth(elt))))) ################################################### ### code chunk number 25: focal ################################################### rng <- bamRanges(bv)[1] strand(rng) <- "*" olap1 <- endoapply(olaps, subsetByOverlaps, rng) olap1 <- lapply(olap1, "seqlevels<-", value=as.character(seqnames(rng))) head(olap1[[24]]) ################################################### ### code chunk number 26: olap-cvg ################################################### minw <- min(sapply(olap1, function(elt) min(start(elt)))) maxw <- max(sapply(olap1, function(elt) max(end(elt)))) cvg <- endoapply(olap1, coverage, shift=-start(ranges(bamRanges[1])), width=width(ranges(bamRanges[1]))) cvg[[1]] ################################################### ### code chunk number 27: olap-cvg-as-m ################################################### m <- matrix(unlist(lapply(cvg, lapply, as.vector)), ncol=length(cvg)) summary(rowSums(m)) summary(colSums(m)) ################################################### ### code chunk number 28: sessionInfo ################################################### packageDescription("Rsamtools") sessionInfo() ################################################### ### code chunk number 29: bam-avail (eval = FALSE) ################################################### ## library(RCurl) ## ftpBase <- ## "ftp://ftp-trace.ncbi.nih.gov/1000genomes/ftp/pilot_data/data/" ## indivDirs <- ## strsplit(getURL(ftpBase, ftplistonly=TRUE), "\n")[[1]] ## alnDirs <- ## paste(ftpBase, indivDirs, "/alignment/", sep="") ## urls0 <- ## strsplit(getURL(alnDirs, dirlistonly=TRUE), "\n") ################################################### ### code chunk number 30: bam-index (eval = FALSE) ################################################### ## urls <- urls[sapply(urls0, length) != 0] ## fls0 <- unlist(unname(urls0)) ## fls1 <- fls0[grepl("bai$", fls0)] ## fls <- fls1[sapply(strsplit(fls1, "\\."), length)==7] ################################################### ### code chunk number 31: slxMaq09 (eval = FALSE) ################################################### ## urls1 <- ## Filter(function(x) length(x) != 0, ## lapply(urls, ## function(x) x[grepl("SLX.maq.*2009_08.*bai$", x)])) ## slxMaq09.bai <- ## mapply(paste, names(urls1), urls1, sep="", USE.NAMES=FALSE) ## slxMaq09 <- sub(".bai$", "", slxMaq09.bai) #$ ################################################### ### code chunk number 32: bamIndicies (eval = FALSE) ################################################### ## bamIndexDir <- tempfile() ## dir.create(bamIndexDir) ## idxFiles <- mapply(download.file, slxMaq09.bai, ## file.path(bamIndexDir, basename(slxMaq09.bai)) , ## MoreArgs=list(method="curl")) Rsamtools/inst/doc/Rsamtools-Overview.Rnw0000644000175400017540000004660513556116727021614 0ustar00biocbuildbiocbuild%\VignetteIndexEntry{An introduction to Rsamtools} %\VignetteDepends{} %\VignetteKeywords{Short read, I/0, samtools} %\VignettePackage{Rsamtools} \documentclass{article} <>= BiocStyle::latex() @ \newcommand{\bam}{\texttt{BAM}} \title{An Introduction to \Biocpkg{Rsamtools}} \author{Martin Morgan} \date{Modified: 18 March, 2010. Compiled: \today} \begin{document} \maketitle \tableofcontents <>= options(width=60) @ <>= library(Rsamtools) @ \section{Introduction} The \Biocpkg{Rsamtools} package provides an interface to \bam{} files. \bam{} files are produced by \software{samtools} and other software, and represent a flexible format for storing `short' reads aligned to reference genomes. \bam{} files typically contain sequence and base qualities, and alignment coordinates and quality measures. \bam{} files are appealing for several reasons. The format is flexible enough to represent reads generated and aligned using diverse technologies. The files are binary so that file access is relatively efficient. \bam{} files can be indexed, allowing ready access to localized chromosomal regions. \bam{} files can be accessed remotely, provided the remote hosting site supports such access and a local index is available. This means that specific regions of remote files can be accessed without retrieving the entire (large!) file. A full description is available in the \bam{} format specification (\url{http://samtools.sourceforge.net/SAM1.pdf}) The main purpose of the \Biocpkg{Rsamtools} package is to import \bam{} files into \R{}. \Biocpkg{Rsamtools} also provides some facility for file access such as record counting, index file creation, and filtering to create new files containing subsets of the original. An important use case for \Biocpkg{Rsamtools} is as a starting point for creating \R{} objects suitable for a diversity of work flows, e.g., \Rclass{AlignedRead} objects in the \Rpackage{ShortRead} package (for quality assessment and read manipulation), or \Rclass{GAlignments} objects in \Rpackage{GenomicAlignments} package (for RNA-seq and other applications). Those desiring more functionality are encouraged to explore \software{samtools} and related software efforts. \section{Input} The essential capability provided by \Biocpkg{Rsamtools} is \bam{} input. This is accomplished with the \Rfunction{scanBam} function. \Rfunction{scanBam} takes as input the name of the \bam{} file to be parsed. In addition, the \Rcode{param} argument determines which genomic coordinates of the \bam{} file, and what components of each record, will be input. \R{param} is an instance of the \Rclass{ScanBamParam} class. To create a \Rcode{param} object, call \Rfunction{ScanBamParam}. Here we create a \Rcode{param} object to extract reads aligned to three distinct ranges (one on \Rcode{seq1}, two on \Rcode{seq2}). From each of read in those ranges, we specify that we would like to extract the reference name (\Rcode{rname}, e.g., \Rcode{seq1}), strand, alignment position, query (i.e., read) width, and query sequence: <>= which <- IRangesList(seq1=IRanges(1000, 2000), seq2=IRanges(c(100, 1000), c(1000, 2000))) what <- c("rname", "strand", "pos", "qwidth", "seq") param <- ScanBamParam(which=which, what=what) @ %% Additional information can be found on the help page for \Rfunction{ScanBamParam}. Reading the relevant records from the \bam{} file is accomplished with <>= bamFile <- system.file("extdata", "ex1.bam", package="Rsamtools") bam <- scanBam(bamFile, param=param) @ Like \Rfunction{scan}, \Rfunction{scanBam} returns a \Robject{list} of values. Each element of the list corresponds to a range specified by the \Rcode{which} argument to \Rfunction{ScanBamParam}. <>= class(bam) names(bam) @ %% Each element is itself a list, containing the elements specified by the \Rcode{what} and \Rcode{tag} arguments to \Rfunction{ScanBamParam}. <>= class(bam[[1]]) names(bam[[1]]) @ %% The elements are either basic \R{} or \Rpackage{IRanges} data types <>= sapply(bam[[1]], class) @ %% A paradigm for collapsing the list-of-lists into a single list is <>= .unlist <- function (x) { ## do.call(c, ...) coerces factor to integer, which is undesired x1 <- x[[1L]] if (is.factor(x1)) { structure(unlist(x), class = "factor", levels = levels(x1)) } else { do.call(c, x) } } bam <- unname(bam) # names not useful in unlisted result elts <- setNames(bamWhat(param), bamWhat(param)) lst <- lapply(elts, function(elt) .unlist(lapply(bam, "[[", elt))) @ %% This might be further transformed, e.g., to a \Rclass{DataFrame}, with <>= head(do.call("DataFrame", lst)) @ Often, an alternative is to use a \Rclass{ScanBamParam} object with desired fields specified in \Rcode{what} as an argument to \Rfunction{GenomicAlignments::readGAlignments}; the specified fields are added as columns to the returned \Rclass{GAlignments}. The \bam{} file in the previous example includes an index, represented by a separate file with extension \texttt{.bai}: <>= list.files(dirname(bamFile), pattern="ex1.bam(.bai)?") @ %% Indexing provides two significant benefits. First, an index allows a \bam{} file to be efficiently accessed by range. A corollary is that providing a \Rcode{which} argument to \Rfunction{ScanBamParam} requires an index. Second, coordinates for extracting information from a \bam{} file can be derived from the index, so a portion of a remote \bam{} file can be retrieved with local access only to the index. For instance, provided an index file exists on the local computer, it is possible to retrieve a small portion of a \bam{} file residing on the 1000 genomes HTTP server. The url \url{ftp://ftp-trace.ncbi.nih.gov/1000genomes/ftp/pilot_data/data/NA19240/alignment/NA19240.chrom6.SLX.maq.SRP000032.2009_07.bam} points to the \bam{} file corresponding to individual NA19240 chromosome~6 Solexa (Illumina) sequences aligned using MAQ. The remote file is very large (about 10 GB), but the corresponding index file is small (about 500 KB). With \Rcode{na19240url} set to the above address, the following retrieves just those reads in the specified range <>= which <- IRangesList("6"=IRanges(100000L, 110000L)) param <- ScanBamParam(which=which, what=scanBamWhat()) na19240bam <- scanBam(na19240url, param=param) @ %% Invoking \Rfunction{scanBam} without an index file, as above, first retrieves the index file from the remote location, and then queries the remote file using the index; for repeated queries, it is more efficient to retrieve the index file first (e.g., with \Rfunction{download.file}) and then use the local index as an argument to \Rfunction{scanBam}. Many \bam{} files were created in a way that causes \Rfunction{scanBam} to report that the ``EOF marker is absent''; this message can safely be ignored. \bam{} files may be read by functions in packages other than \Biocpkg{Rsamtools}, in particular the \Rfunction{readGAlignments} family of functions in \Rpackage{GenomicAlignments}. Additional ways of interacting with \bam{} files include \Rfunction{scanBamHeader} (to extract header information) and \Rfunction{countBam} (to count records matching \Rcode{param}). \Rfunction{filterBam} filters reads from the source file according to the criteria of the \Rclass{ScanBamParam} parameter, writing reads passing the filter to a new file. The function \Rfunction{sortBam} sorts a previously unsorted \bam{}, while The function \Rfunction{indexBam} creates an index file from a sorted \bam{} file. \Rfunction{readPileup} reads a \texttt{pileup} file created by \software{samtools}, importing SNP, indel, or all variants into a \Rclass{GRanges} object. \subsection{Large bam files} \bam{} files can be large, containing more information on more genomic regions than are of immediate interest or than can fit in memory. The first strategy for dealing with this is to select, using the \Rcode{what} and \Rcode{which} arguments to \Rfunction{ScanBamParam}, just those portions of the \bam{} file that are essential to the current analysis, e.g., specifying \Rcode{what=c(`rname', 'qname', 'pos')} when wishing to calculate coverage of ungapped reads. When selective input of \bam{} files is still too memory-intensive, the file can be processed in chunks, with each chunk distilled to the derived information of interest. Chromosomes will often be the natural chunk to process. For instance, here we write a summary function that takes a single sequence name (chromosome) as input, reads in specific information from the \bam{} file, and calculates coverage over that sequence. <>= summaryFunction <- function(seqname, bamFile, ...) { param <- ScanBamParam(what=c('pos', 'qwidth'), which=GRanges(seqname, IRanges(1, 1e7)), flag=scanBamFlag(isUnmappedQuery=FALSE)) x <- scanBam(bamFile, ..., param=param)[[1]] coverage(IRanges(x[["pos"]], width=x[["qwidth"]])) } @ %% This might be used as follows; it is an ideal candidate for evaluation in parallel, e.g., using the \Rpackage{parallel} package and \Rfunction{srapply} function in \Rpackage{ShortRead}. <>= seqnames <- paste("seq", 1:2, sep="") cvg <- lapply(seqnames, summaryFunction, bamFile) names(cvg) <- seqnames cvg @ %% The result of the function (a coverage vector, in this case) will often be much smaller than the input. \section{Views} The functions described in the previous section import data in to \R{}. However, sequence data can be very large, and it does not always make sense to read the data in immediately. Instead, it can be useful to marshal \emph{references} to the data into a container and then act on components of the container. The \Rclass{BamViews} class provides a mechanism for creating `views' into a set of \bam{} files. The view itself is light-weight, containing references to the relevant \bam{} files and metadata about the view (e.g., the phenotypic samples corresponding to each \bam{} file). One way of understanding a \Rclass{BamViews} instance is as a rectangular data structure. The columns represent \bam{} files (e.g., distinct samples). The rows represent ranges (i.e., genomic coordinates). For instance, a ChIP-seq experiment might identify a number of peaks of high read counts. \subsection{Assembling a \Rclass{BamViews} instance} To illustrate, suppose we have an interest in caffeine metabolism in humans. The `rows' contain coordinates of genomic regions associated with genes in a KEGG caffeine metabolism pathway. The `columns' represent individuals in the 1000 genomes project. To create the `rows', we identify possible genes that KEGG associates with caffeine metabolism: <>= library(KEGG.db) kid <- revmap(KEGGPATHID2NAME)[["Caffeine metabolism"]] egid <- KEGGPATHID2EXTID[[sprintf("hsa%s", kid)]] @ %% Then we use the appropriate \Rpackage{TxDb} package to translate Entrez identifiers to obtain ranges of interest (one could also use \Rpackage{biomaRt} to retrieve coordinates for non-model organisms, perhaps making a \Robject{TxDb} object as outlined in the \Rpackage{GenomicFeatures} vignette). We'll find that the names used for chromosomes in the alignments differ from those used at Ensembl, so \Rcode{seqlevels<-} is used to map between naming schemes and to drop unused levels. <>= library(TxDb.Hsapiens.UCSC.hg18.knownGene) bamRanges <- transcripts(TxDb.Hsapiens.UCSC.hg18.knownGene, filter=list(gene_id=egid)) seqlevels(bamRanges) <- # translate seqlevels sub("chr", "", seqlevels(bamRanges)) lvls <- seqlevels(bamRanges) # drop unused levels seqlevels(bamRanges) <- lvls[lvls %in% as.character(seqnames(bamRanges))] @ %% Note that \Robject{bamRanges} `knows' the genome for which the ranges are defined <>= unique(genome(bamRanges)) @ The details of creating the `columns' of BAM files. Here we retrieve a vector of \bam{} file URLs (\Robject{slxMaq09}) from the package. <>= slxMaq09 <- local({ fl <- system.file("extdata", "slxMaq09_urls.txt", package="Rsamtools") readLines(fl) }) @ %% We now assemble the \Rclass{BamViews} instance from these objects; we also provide information to annotated the \bam{} files (with the \Rcode{bamSamples} function argument, which is a \Rclass{DataFrame} instance with each row corresponding to a \bam{} file) and the instance as a whole (with \Rcode{bamExperiment}, a simple named \Rclass{list} containing information structured as the user sees fit). <>= bamExperiment <- list(description="Caffeine metabolism views on 1000 genomes samples", created=date()) bv <- BamViews(slxMaq09, bamRanges=bamRanges, bamExperiment=bamExperiment) metadata(bamSamples(bv)) <- list(description="Solexa/MAQ samples, August 2009", created="Thu Mar 25 14:08:42 2010") @ \subsection{Using \Rclass{BamViews} instances} The \Rclass{BamViews} object can be queried for its component parts, e.g., <>= bamExperiment(bv) @ %% More usefully, Methods in \Biocpkg{Rsamtools} are designed to work with \Rclass{BamViews} objects, retrieving data from all files in the view. These operations can take substantial time and require reliable network access. To illustrate, the following code (not evaluated when this vignette was created) downloads the index files associated with the \Robject{bv} object <>= bamIndexDir <- tempfile() indexFiles <- paste(bamPaths(bv), "bai", sep=".") dir.create(bamIndexDir) idxFiles <- mapply(download.file, indexFiles, file.path(bamIndexDir, basename(indexFiles)) , MoreArgs=list(method="curl")) @ %% and then queries the 1000 genomes project for reads overlapping our transcripts; by loading the \Rpackage{parallel} package, we tell \Biocpkg{Rsamtools} to use as many cores as are available on our machine (the \Rpackage{parallel} package does not provide parallel functionality on Windows computers) <>= library(GenomicAlignments) library(parallel) options(srapply_fapply="parallel", mc.cores=detectCores()) olaps <- readGAlignments(bv) @ %% The resulting object is about 11 MB in size. To avoid having to download this data each time the vignette is run, we instead load it from disk %% <>= library(GenomicAlignments) load(system.file("extdata", "olaps.Rda", package="Rsamtools")) olaps head(olaps[[1]]) @ %% There are \Sexpr{length(olaps[[1]])} reads in \verb|\Sexpr{names(olaps)[[1]]}| overlapping at least one of our transcripts. It is easy to explore this object, for instance discovering the range of read widths in each individual. <>= head(t(sapply(olaps, function(elt) range(qwidth(elt))))) @ Suppose we were particularly interested in the first transcript, which has a transcript id \Sexpr{mcols(bamRanges(bv))[["tx_name"]][1]}. Here we extract reads overlapping this transcript from each of our samples. As a consequence of the protocol used, reads aligning to either strand could be derived from this transcript. For this reason, we set the strand of our range of interest to \texttt{*}. We use the \Rfunction{endoapply} function, which is like \Rfunction{lapply} but returns an object of the same class (in this case, \Sexpr{as.vector(class(olaps))}) as its first argument. <>= rng <- bamRanges(bv)[1] strand(rng) <- "*" olap1 <- endoapply(olaps, subsetByOverlaps, rng) olap1 <- lapply(olap1, "seqlevels<-", value=as.character(seqnames(rng))) head(olap1[[24]]) @ %% To carry the example a little further, we calculate coverage of each sample: <>= minw <- min(sapply(olap1, function(elt) min(start(elt)))) maxw <- max(sapply(olap1, function(elt) max(end(elt)))) cvg <- endoapply(olap1, coverage, shift=-start(ranges(bamRanges[1])), width=width(ranges(bamRanges[1]))) cvg[[1]] @ %% Since the example includes a single region of uniform width across all samples, we can easily create a coverage matrix with rows representing nucleotide and columns sample and, e.g., document variability between samples and nucleotides <>= m <- matrix(unlist(lapply(cvg, lapply, as.vector)), ncol=length(cvg)) summary(rowSums(m)) summary(colSums(m)) @ \section{Directions} This vignette has summarized facilities in the \Biocpkg{Rsamtools} package. Important additional packages include \Rpackage{GenomicRanges} (for representing and manipulating gapped alignments), \Rpackage{ShortRead} for I/O and quality assessment of ungapped short read alignments, \Rpackage{Biostrings} and \Rpackage{BSgenome} for DNA sequence and whole-genome manipulation, \Rpackage{IRanges} for range-based manipulation, and \Rpackage{rtracklayer} for I/O related to the UCSC genome browser. Users might also find the interface to the integrative genome browser (IGV) in \Rpackage{SRAdb} useful for visualizing \bam{} files. <>= packageDescription("Rsamtools") sessionInfo() @ \appendix \section{Assembling a \Rclass{BamViews} instance} \subsection{Genomic ranges of interest} \subsection{BAM files} \emph{Note}: The following operations were performed at the time the vignette was written; location of on-line resources, in particular the organization of the 1000 genomes \bam{} files, may have changed. We are interested in collecting the URLs of a number of \bam{} files from the 1000 genomes project. Our first goal is to identify files that might make for an interesting comparison. First, let's visit the 1000 genomes FTP site and discover available files. We'll use the \Rpackage{RCurl} package to retrieve the names of all files in an appropriate directory <>= library(RCurl) ftpBase <- "ftp://ftp-trace.ncbi.nih.gov/1000genomes/ftp/pilot_data/data/" indivDirs <- strsplit(getURL(ftpBase, ftplistonly=TRUE), "\n")[[1]] alnDirs <- paste(ftpBase, indivDirs, "/alignment/", sep="") urls0 <- strsplit(getURL(alnDirs, dirlistonly=TRUE), "\n") @ %% From these, we exclude directories without any files in them, select only the \bam{} index (extension \texttt{.bai}) files, and choose those files that exactly six \texttt{'.'} characters in their name. <>= urls <- urls[sapply(urls0, length) != 0] fls0 <- unlist(unname(urls0)) fls1 <- fls0[grepl("bai$", fls0)] fls <- fls1[sapply(strsplit(fls1, "\\."), length)==7] @ %% After a little exploration, we focus on those files obtained form Solexa sequencing, aligned using \texttt{MAQ}, and archived in August, 2009; we remove the \texttt{.bai} extension, so that the URL refers to the underlying file rather than index. There are 24 files. <>= urls1 <- Filter(function(x) length(x) != 0, lapply(urls, function(x) x[grepl("SLX.maq.*2009_08.*bai$", x)])) slxMaq09.bai <- mapply(paste, names(urls1), urls1, sep="", USE.NAMES=FALSE) slxMaq09 <- sub(".bai$", "", slxMaq09.bai) #$ @ As a final step to prepare for using a \Rclass{BamViews} file, we create local copies of the \emph{index} files. The index files are relatively small (about 190 Mb total). <>= bamIndexDir <- tempfile() dir.create(bamIndexDir) idxFiles <- mapply(download.file, slxMaq09.bai, file.path(bamIndexDir, basename(slxMaq09.bai)) , MoreArgs=list(method="curl")) @ \end{document} Rsamtools/inst/doc/Rsamtools-Overview.pdf0000644000175400017540000054143613624616577021625 0ustar00biocbuildbiocbuild%PDF-1.5 %ÐÔÅØ 71 0 obj << /Length 2408 /Filter /FlateDecode >> stream xÚí\Ksã6¾ûWpOKU`¼Aä°UžìNjS™C&Î^fRµK¬¥HIãýõÛ €zÙ›8–ü¨ /"€Æ³ºAB4Y$4ùîŒOB­d<¡DQ•xMIZ ÿÒ‡c[¿½<;'lÂ)Ñš«äò*Q”dOtf‰â:¹œ'Ó‹z2å&KÿY÷í„Ó´™¯‹¾lbißL~¹üþ‘38'éîð,“&DÃÀº|Õ7MÕ1ÂÀ¡ów\& z—šãHS&ªSɉ´q¥ïó‰`iÛ—°6¡Mú¾™š¶‹¼Æ@:aŒX¥|4™ At7Ј¥óòÒÍ¿™Le–¥,‹]徫bùó:å”Q‚Ulúm³º.«ØÂ¦ï°¢›ù™¬C«ÛØF¼ qÊiàÉI´¤ÀfgJzÞO`‰ø°T…Õ}ÛÔ½«ûnØ#†Ûò1Ž&2˜@FcGH<ù8eS^]7ªz¼m fŸ«µç•Õ„ 3h,¹W*0#ÃùH‰#ñQD(䌋£`á´˜5v?å’0ŒŸŸ´®×ýÓ¡•¦„>¢ÕH‰J„ä/‹ÃH` É)ø•FˆˆäHÇ_™þ· ‚Y¾ ‰O”òÊuO‡œŒ ¢Õèèį Räëqº˜à„R±çu‰x]ÿ*lÜt£ç5GâH|Lª×éyɈ’'ñ¼.ºÎ­f•UY/‚畇£Q©v¦Á±ÈØvoóÕÀÌWB’‰¡rYw}^îéXd„ꈿ&ÛÔ¯Æ6ý %!çGv0N~ãü¹C›¼kŒš®þˆ-òC[|B·H*­­q$mäæÅ)™"e{qŠå~-g• ÅWÍ„›´]MXš÷¡ a8FëC.œ@AƒwËФÿk(h]>ïBå¼*5ôäâ4üŠq:XvQpÀI2Lç¨B]ÈÀÄz‡E¡$è´õJèbfÝ……Ar^ÂZP…ý@®XÖMÕ,JÔ©©¶:.ˆe;üb[~ÝI3PgOE5PŸÐ÷ÒóJBO!…ëº.ã³uUÞôªÛÐÒA]”¸ªºé™âÅNúLjæÏ¢ê8¤‘Ò«¼fêaªnFÄ]Uîè.bb”<ò¾ž»_Ý K1ÊRy}¿ jbÌ g·Ac9ÏðÕL ¢¤aÿÂgvn€Õò¿^ù ¬X¶Íªéš•· Š{î¢ôô²îªá„* »„×Û<‹» C š01ôöˆab{_`+Xä«,$¶‚…LJà=þĪéѶ2‘¾ ¦½RÄzýrÀ& NDŒ{’n}PSˆtÙt}ÐÈte(–i·ö :ls}+¬‹eHm´*£jyœòiOÞ*NÈ{ýŒÉ¡Õ—¼¬ò´­€•‘ˆ¾evÆ:&=ðÜT]DùÂ_­.pÓÞèbÈà‹ˆPÖ‹é­Û "Ë11ókU¶,ÇÜMÙ/›u?ôÔ·¥ûâ†yä³O —ífE«€¡ ÷ž0…ý!MBæâ¾%]­« ¯‹«‚â-¯Ã…z‘92 ‘kˆ¿˜õ<ûMÐûRæ'¸×l&É(óƒ!5D‹L*b¬z¨‰ðí/z+ÜÙ‹*•oÙ2=êü=]öýõ7çç{áéšu[¸8…#µëÏ£á*tí¾SñÓÅ{FÂçW‡Ç„Ú¦ÃÙ•×+`„e›#‘©ÈXº 1¤®×m4ð.Ò¼µdlG•Nq~Ba'Û~ÇûPÀ/4æÎ NЛB6)Ÿ_–.ö/ì`HJ4nC \&ŸÅÁ€!-nCà¾[jºáÑâX ÙY‡“§I ÜV7GZî‰äa§‘‡mžB‡´?ó1l's²lØ&÷»iîbQ¬"S(÷uzׯO|·Ï'ËCsÒµ» ‰íy›`¥¿EÝzÖ¹¾ •ý+}üŠPàÝ‚rÁlษ þ¨™û£(_w.Ž—w±£•'ÓÁ-1™~Ü‘­Ý~åÜÝ{¼¶þ?O\J· endstream endobj 90 0 obj << /Length 3110 /Filter /FlateDecode >> stream xÚÍ[KsÛ8¾ûW°|’k- Þ©ÍVeª&Ù™šÝšu|Ëä@S”ÍDÊ"'ÿ~ºPiÙV=r°)€ èntÝ Òä6¡ÉÛ³_®Ï~z#\âˆÓ\'×ÓDQb-OŒä„3‘\O’÷£×åŘ;ú­l–œŽªÉ*kŠ*ö6ÕŇëßÏ(¡N2žP¢¨²®FSc’%PzâÖÕ[ .éuk‰£¦æé^Õ鼩ªYÄ9·×ŸÞ0³ñèXj"¬†«‚™«ð†´¾ ÅFi¸ÔMzÁíhÙåmèYÀì¨*Ê&´§•Ù2OýP lâÔ˜`D+±žiÒ›ƒeÊv@uóÿ¦·yxý_TÑŽsÐq¿Jgà#­ë¼®ç¹-¶ËIøR½‡Æ<-‹Åj–¢>Ã;rëÈà- 3¡‰5ªÏ§·ž•H«Þ² ËÐn«*·Ó‚(»æîÛ¼¬æEö,«‰–î1£¼vl2JñÑÕ_ëü>ê›g ªÈ+@î,³"óL©‘+$賆hП°v¨]ßU5Ò²v4Éëbö´æj¼7]•ÞhlJ ºÓÍ1y™U«%L}Ú`ZBÿçŬ}Ù­V”ª]¼·aW϶±J2oØâè°~‹ohéÖÕÔÏñÿ¥ádÌñû¾'ýv ˆš\“¾±úV«ÈfÐŽÉ`Û8QÜ_DùV£ømô’÷c昿X5{˜ÿ¯×g÷g¸ËiÂZ¢)0Þ¹$›Ÿ½ÿ@“ ÜûžÎ&~ä<‘\&ˆ&³äÝÙÿÖ“ð^ª'D'ˆ¤6ì,¶ÖCÐ"iåv=l“"…f–.Ò›¢Ó:ì[xaUŸŠ Š{nЬ~ù.OÖw`é(·}W¶©–Où1iý‹Ïq,ኧ†W?¥í·®Px0Y`ÏðêŸÚ~k(<zn©N+"¸@éù’XØÿ°DäKžLQZß4G/[iÛ $о…qB•é ÷—×ÿyŽiÌ:Ö2 Õ˜\Œ­3 ÀB/áöšfY5óVßµ²(𻏽…!V œ`ôdì”Âqàa\Õí±³k?B`%´‰Òࢵ] ÁÑçC!|Ë I:;LƒÜ5‹¦5KË'¾}MÜ 2®i«bíiMˆZ´î¯é—tþ¬bYb:@Úú0rb}pôU€¤; : 2µ€Ú¨팖ߡMúýHކElH¡ƒù ?ï“à^‰ jåÛ»§µîÚwäúž¬»SM‡\Áº÷¸`KÎòÈÁ*pôCÑQdï" ¶:Ÿ€0J¬iÁ›Ø`ûÖ=L ÜÓ—è ØéeÂT˜œ‚«dkËaê'"¦ اHa•nƒˆåó{[ØekíY~» á–„(b’79èür^”~ƒ@×Ã]‘Ý…Ÿ·ÔÀí" í,b#ÿšIQùÍ¢~ÁHÎ 3n(˜Cn$‰Rï æåÍb•ío–¨Ûì„XkkqÜÃ]Úà6¢#ÄGA¥7}'Ê6B¡¦(Fl,ó,Šì¥f³0þÆ¿!ˆÈ¶äQÄnîÙ< „AžÅ½ šÞ[‡y¤eK§nÒ2ËûSÞžŠ``ÿ]Gúx3°þv!_Pÿaš )1ÜõH6KkˆüÀüðÑõðÕÙéAÊÃïôÄv¥5¼Ü@ðr»$Ë °žtjW»¢}¼ØË–`V†B(‡º vRôÚwÔ‘‡D_\JŒeŸ‘ïö ¿Pë­éð 1‡°ý5­á×–ᣔf7}ßÓ’€¤vº¿¤?_ÔwP§µŠ6äßù2Z Ÿ‚ò¿ÍdM„ÅÔ ;¦5A’ZîÁ˜6ÑD矛eš5Ñ1‚Æ3Þ·íÀô b޶æ“ÐðØ“Sð.Ë<]“¢nŠ)`k™–·y|³°àMC£*O+<ÁœA ÆQò…øq?ÂC’-}‘1~ÌïÙKI.¯‹FŠQ——­~ f ÏÇc&’Ô˜Èè3“ïÎÌÓjFoB*t¸™{hçù:ZŒ¥ÿ«hÃ(c‡QM¨pK£Þ# t4”«âz´¬˜~ =MÀœ–vvÎÆgªÕlš³âãÆÍE¥ë}ßÓÒFx:ë@ ô”é<þÂ=xb]qŽX³`1‰rüVSRÌYs êi[“晲«Oò’d]Qñ„!˜‚Å€øwȽ†$¹}þ}å eÅà_Œ&T Ї5(r‰”"¸˜X´„fŒÃê6E}÷«|‰Õ3ª A'—¡·+ CŠIs×¾Ù—ºúÏÃBVø4ì–Ÿ¿xíA´±JàÇWï£dÛŠR€¿¶àµ¯šäf5 €a'ãXM’FaÅÞËä_cM× üùÏq¸þvåÍÛàê‘û¨ ¯b¶¥ô2Œäð³“=í ýc&×{ýù‚,¾%¾„­_â›Ù4Ú¿)=X ÚÚÍ¥ø—{cpßw”qÝ\Tõú÷½×¦nd~þˆ¤ê‘ ð¬G³ ³ñ’÷~åÿ_vó|…ÿÚ—§¼{f J…Ö#œ@×S€X1äÊ€£‹óy¹(å}ŽAmä±1­V¸­p@ï_wùlº¾}øbœ.‚ÚÁ˜2Øjîá+ÒpSºæ–ï?|RØKÃ%0zEŠÒÉþ’ö½ ÁÄUý2xEŠVñþо>xen„‡yü!Tø¸ °È?¥eÓ¦âvhµÉÄ:8ª©‡¥è§NŸ•×Öl<œB#ùË4dÓ@’ØA»% ÑÆ +%ÈË¢œL3L¢mÀ±³-€ŸÜýcdc»BTëþ%8h¸{X÷/¬ô cÓݤó7²0º°íŽ\€GÕ_ê&Ÿ“) ÷nâ“IÚ¤kw™f^×¶ã­WçëCŽ/9Ó›¡+­ƒ+Ejqž—n÷Õ"ºØÃûÐ?Úíħ$*!Ç9%!À:K ÖA¨aY|·´Æi™&¬?ÉyL¦Iáå´•iû¨ bÉèÑ’y²(JëúKzé(<¢Ö™ÉeÞ¬–%Úh0%'Îír`•fr7ØSz¥£EŸà¡šg±@£ît°?ÍØèž´˜­òPŽ3£_}F ïÀî6¡Ý>á! 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Compiled: \today} \begin{document} \maketitle \tableofcontents This document is meant for package developers wanting to use the \href{http://samtools.sourceforge.net/}{samtools} C libraries provided by \Biocpkg{Rsamtools}. The instructions here are based on the `Writing R Extensions' manual associated with R-2.13; consult the current version of the manual for up-to-date instructions. \section{Background} \Biocpkg{Rsamtools} arranges to install static versions of the \verb|libbam| and \verb|libbcf| libraries. The idea is that other packages can use these to implement C functionality that uses these libraries. This means that the samtools libraries are available in a consistent version to users across platforms, without requiring installation of additional software. \Biocpkg{Rsamtools} takes the following approach. On installation, \Biocpkg{Rsamtools} contains a snapshot of the samtools library source code under \verb|src/samtools|. \Biocpkg{Rsamtools} makes static version(s) of the samtools libraries \verb|libbam.a| and \verb|libbcf.a|. These static libraries are specific to the operating system on which \Biocpkg{Rsamtools} is being installed, are found under \verb|usrlib${R_ARCH}| in the user library location specified by the mechanism (e.g., \Rfunction{BiocManager::install}, \Rfunction{install.packages}) used to install \Biocpkg{Rsamtools}. At the same time, \Biocpkg{Rsamtools} copies headers required to use the library to the location \verb|include/samtools|. \section{Use} To use these libraries, the third party package developer needs to (1) discover the appropriate header files when their package is built, and (2) link in the libraries. Note that in order to link correctly across platforms your package must provide \emph{both} the respective \verb|src/Makevars| \emph{and} \verb|src/Makevars.win| files. \subsection{Discover header files} To discover appropriate header files at package installation time, add \begin{verbatim} LinkingTo: Rsamtools \end{verbatim} to the \verb|DESCRIPTION| file, and reference the relevant include files as, for instance, \begin{verbatim} #include "samtools/bam.h" \end{verbatim} The content of the include files can be found in the \Biocpkg{Rsamtools} source (under \verb|src/samtools|) or at their installed location. \subsection{Link to static libraries} Linking to the static libraries is accomplished by including the following code in \verb|src/Makevars.win| for \emph{Windows}: \begin{verbatim} SAMVARS=$(shell echo 'cat(Rsamtools:::.pkgMk())' |\ "${R_HOME}/bin/R" --vanilla --slave) include $(SAMVARS) PKG_LIBS=$(SAMTOOLS_LIBS) PKG_CPPFLAGS=$(SAMTOOLS_CPPFLAGS) \end{verbatim} and with the following code in \verb|src/Makevars| for all other platforms: \begin{verbatim} SAMTOOLS_PATH=\ `echo 'cat(Rsamtools:::.pkgLd())' |\ "${R_HOME}/bin/R" --vanilla --slave` SAMTOOLS_LIBS="$(SAMTOOLS_PATH)/libbam.a" "$(SAMTOOLS_PATH)/libbcf.a"\ "$(SAMTOOLS_PATH)/libtabix.a" -lz -pthread SAMTOOLS_CPPFLAGS=-D_USE_KNETFILE -DBGZF_CACHE -D_FILE_OFFSET_BITS=64 \ -D_LARGEFILE64_SOURCE PKG_LIBS=$(SAMTOOLS_LIBS) PKG_CPPFLAGS=$(SAMTOOLS_CPPFLAGS) \end{verbatim} This updates the environment variables \verb|$PKG_CPPFLAGS| and \verb|$PKG_LIBS|; if your \verb|Makevars|/\verb|Makevars.win| modifies these also, do so by adding to the respecitve line, e.g., \begin{verbatim} PKG_LIBS=$(SAMTOOLS_LIBS) -lfoo PKG_CPPFLAGS=$(SAMTOOLS_CPPFLAGS) -I/path/bar \end{verbatim} \end{document} Rsamtools/inst/doc/Rsamtools-UsingCLibraries.pdf0000644000175400017540000036561213624616601023030 0ustar00biocbuildbiocbuild%PDF-1.5 %ÐÔÅØ 39 0 obj << /Length 2419 /Filter /FlateDecode >> stream xÚíZKoãȾûWð 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CŒ„!4çݜ˴³åÜÛ(é;çnËÜøè3ç@Ýœ‹ô/Bsîj,Åœ& 4ÒœsÊ9çv´¦Üš/^[ÐÿßÑè€9gÍ2ŠfÑœs鿝0͹‘„9÷+ÚÏ(Úæ¤›sdÀh[έ0ß9ÿ÷œCÍÏkÆó‰ÎWͳÏæ€œ{êiêIsÑ-sTÀ[™›QXæþEûEûÓœCÝj£‘ñ{ŸÚÈ­›sD@3[Îuo}ç&çBr1?OÝÍXOt7ßQÓ8kê9¾§oÓs¸nÎ_ól9W5.cνâ{ñ6/!看äœËüœf 3»½ò­Ì§F*‡1çnQÝŒ¨n4çH9çœ$çœæç@c©Ù̯ Ìçá*ý0ç6ámŒð64ç(Ýœ}l9'y}çœÇmÎ¥}>sŽö“óÿYºvÙÿ‹ÿBC/¥Ñ1NÃ0àßq›Ö"@œRÒR[;UY`@”Hˆ‰¨Œ€õ ‰•™pîÁ†8Aý£:i%;òû-Ëùd=ÏÓ{H&[2ø•1Ìh™ú„×-Ê\žQž`Áäñc•ˆÊ½!ôdz&a•4pZ³Nz›^¯ÊÜÔ;¼t)?0›R&x‡–s‘Cä¶Ü«‘óJæ+r‰ÏòŒî\ˆ¢°å½ùjSy€/8å~<ßTîãÍ-ï7÷y½œ`á–Sß>ïâÁ-|ånyèû‚·|ÐÜçÀ’SOñݦ|ÆXQv0$9 3„™-šï¼^ncÛ-+_™kÛ)úÊLNù¨Yf–\SˆÍSž#ÞùûdŸZDŠÈ‹ÿBCRsamtools/inst/extdata/ex1.bcf.gz.csi0000644000175400017540000000015613556116727020556 0ustar00biocbuildbiocbuild‹ÿBCQsödäc@&(_P F$öÖÙ Hj`ltù¬ (¦&ψÄf`Ð1eÄb&ºüo43arøa¬Ä‹ÿBCRsamtools/inst/extdata/ex1.sam0000644000175400017540000210447613556116727017424 0ustar00biocbuildbiocbuildB7_591:4:96:693:509 73 seq1 1 99 36M * 0 0 CACTAGTGGCTCATTGTAAATGTGTGGTTTAACTCG <<<<<<<<<<<<<<<;<<<<<<<<<5<<<<<;:<;7 MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_65:7:152:368:113 73 seq1 3 99 35M * 0 0 CTAGTGGCTCATTGTAAATGTGTGGTTTAACTCGT <<<<<<<<<<0<<<<655<<7<<<:9<<3/:<6): MF:i:18 Aq:i:66 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_64:8:5:734:57 137 seq1 5 99 35M * 0 0 AGTGGCTCATTGTAAATGTGTGGTTTAACTCGTCC <<<<<<<<<<<7;71<<;<;;<7;<<3;);3*8/5 MF:i:18 Aq:i:66 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_591:1:289:587:906 137 seq1 6 63 36M * 0 0 GTGGCTCATTGTAATTTTTTGTTTTAACTCTTCTCT (-&----,----)-)-),'--)---',+-,),''*, MF:i:130 Aq:i:63 NM:i:5 UQ:i:38 H0:i:0 H1:i:0 EAS56_59:8:38:671:758 137 seq1 9 99 35M * 0 0 GCTCATTGTAAATGTGTGGTTTAACTCGTCCATGG <<<<<<<<<<<<<<<;<;7<<<<<<<<7<<;:<5% MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_61:6:18:467:281 73 seq1 13 99 35M * 0 0 ATTGTAAATGTGTGGTTTAACTCGTCCCTGGCCCA <<<<<<<<;<<<8<<<<<;8:;6/686&;(16666 MF:i:18 Aq:i:39 NM:i:1 UQ:i:5 H0:i:0 H1:i:1 EAS114_28:5:296:340:699 137 seq1 13 99 36M * 0 0 ATTGTAAATGTGTGGTTTAACTCGTCCATGGCCCAG <<<<<;<<<;<;<<<<<<<<<<<8<8<3<8;<;<0; MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_597:6:194:894:408 73 seq1 15 99 35M * 0 0 TGTAAATGTGTGGTTTAACTCGTCCATTGCCCAGC <<<<<<<<<7<<;<<<<;<<<7;;<<<*,;;572< MF:i:18 Aq:i:43 NM:i:1 UQ:i:9 H0:i:0 H1:i:1 EAS188_4:8:12:628:973 89 seq1 18 75 35M * 0 0 AAATGTGTGGTTTAACTCGTCCATGGCCCAGCATT ==;=:;:;;:====;=;===:=======;==;=== MF:i:64 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_66:7:68:402:50 137 seq1 22 99 35M * 0 0 GTGTGGTTTAACTCGTCCATGGCCCAGCATTTGGG <<<<<<<<<<<<<<:<<<9<6;9;;&697;7&<55 MF:i:18 Aq:i:66 NM:i:1 UQ:i:5 H0:i:1 H1:i:0 EAS114_30:6:298:115:564 137 seq1 22 99 35M * 0 0 GTGTGGTTTAACTCGTCCATGGCCCAGCATTAGGG <<<<<<<<<<<<<;<<<;<<<;<<<;<:<<;;5;; MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_591:3:188:662:155 73 seq1 24 99 36M * 0 0 GTGGTTTAACTCGTCCATGGCCCAGCATTAGGGAGC <<<<<<<<<<<<<<<<<<:;<<<4<<+<<14991;4 MF:i:18 Aq:i:71 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_59:2:225:608:291 73 seq1 28 99 35M * 0 0 TTTAACTCGTCCATGGCCCAGCATTAGGGATCTGT <<<<<<<<<<<<<<8&<<<;6<9;;+2++(%59(< MF:i:18 Aq:i:58 NM:i:1 UQ:i:4 H0:i:1 H1:i:0 EAS51_66:7:328:397:316 73 seq1 29 99 35M * 0 0 TTAACTCGTCCATGGCCCAGCATTAGGGAGCTGTG <<<<<<<<<<<<<6=<<<;<<5<<<+<15:'<;;4 MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_64:5:257:960:682 73 seq1 31 75 35M * 0 0 AACTCGTCCATGGCCCAGCATTAGGGAGCTGTGGA <<<<<<<<<<<;<<<<<<<<<<<<<<<<<<9;;9< MF:i:64 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_61:4:143:69:578 99 seq1 36 98 35M = 185 184 GTACATGGCCCAGCATTAGGGAGCTGTGGACCCCG ===;=====48=844;=;+=5==*57,2+5&,5+5 MF:i:18 Aq:i:35 NM:i:2 UQ:i:38 H0:i:0 H1:i:1 EAS114_32:5:78:583:499 163 seq1 37 74 35M = 229 227 TCCATGGCCCAGCATTAGGGCGCTGTGGACCCTGC <<8;<<<<<<1<<-1<+8<<&;:555;5-*77/51 MF:i:18 Aq:i:37 NM:i:1 UQ:i:5 H0:i:0 H1:i:1 EAS1_93:7:252:171:323 163 seq1 43 99 35M = 234 226 GCCCAGCATTAGGGAGCTGTGGACCCTGCAGCCTG <<<):<<<<<<<<<:<<<&5<<2<562<<<<-7-- MF:i:18 Aq:i:62 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_593:4:106:316:452 99 seq1 49 99 36M = 224 211 CATTAGGGAGCTGTGGACCCTGCAGCCTGGCTGTTG ;<<;<<<<;<;;;;7;<;<<<;<<;<<;4:<<;+&+ MF:i:18 Aq:i:71 NM:i:1 UQ:i:5 H0:i:1 H1:i:0 B7_589:8:113:968:19 163 seq1 50 99 35M = 219 204 ATTAGGGAGCTGTGGACCCTGCAGCCTGGCTGGGG <<<<;<;<<<<<<:;;;.;;<75;);;;<.2+(;5 MF:i:18 Aq:i:63 NM:i:1 UQ:i:7 H0:i:1 H1:i:0 EAS54_65:3:321:311:983 99 seq1 51 99 35M = 228 212 TTAGGGAGCTGTGGACCCTGCAGCCTGGCTGTGGG <<<;<<<<<<<<+;;<47;<9;94430499<88+6 MF:i:18 Aq:i:62 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_591:6:155:12:674 163 seq1 52 99 36M = 224 208 TAGGGAGCTGTGGACCCTGCAGCCTGGCTGTGGGGG <<<<<<<<<<<<<<<<<<<<<<<<<<<;<<+:9-<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS219_FC30151:7:51:1429:1043 163 seq1 59 99 35M = 209 185 CTGTGGACCCTGCAGCCTGGCTGTGGGGGGCGCCG <<<<<<<<<<<<<:<<<;<<<<:):;<;;-15)+1 MF:i:18 Aq:i:68 NM:i:2 UQ:i:22 H0:i:1 H1:i:0 B7_591:5:42:540:501 99 seq1 60 99 36M = 224 200 TGTGGACCCTGCAGCCTGGCTGTGGGGGCCGCAGTG <<<<<<<<<<<<<<<<<<<<<<.;<<<<,804,858 MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS192_3:5:223:142:410 99 seq1 60 99 35M = 235 210 TGTGGACCCTGCAGCCTGGCTGGGGGGGGCGCAGT <<<<<<<<<<<<<<:<5<<2<<(<:<<<:5,((7( MF:i:18 Aq:i:39 NM:i:2 UQ:i:32 H0:i:0 H1:i:1 EAS1_108:1:65:787:74 163 seq1 61 88 35M = 213 187 GTGGACCCTGCAGCCTGGCTGGGGGGGGCACGGGG <<<<<8-82<2823;-<;822222888,*(2%2-2 MF:i:18 Aq:i:21 NM:i:5 UQ:i:51 H0:i:0 H1:i:0 EAS56_61:6:227:259:597 99 seq1 61 99 35M = 248 222 GTGGACCCTGCAGCCTGGCTGTGGGGGCCGCAGTG <<<<<<<<<<;;<<<6;8:68333;<8(8,1,$$+ MF:i:18 Aq:i:61 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_30:1:243:10:911 163 seq1 63 99 35M = 236 208 GGACCCTGCAGCCTGGCTGTGGGGGCCGCTGTGGG <<;<<<<<<<<<<7<<<<<7<<<<<:4<((<%;<+ MF:i:18 Aq:i:64 NM:i:2 UQ:i:22 H0:i:1 H1:i:0 EAS221_1:2:90:986:1224 163 seq1 67 99 35M = 267 235 CCTGCAGCCTGGCTGTGGGGGCCGCAGCGGGTGGG <<:<<<<<<<<<<<<0<<<<<)<<63<+<<2'<-< MF:i:18 Aq:i:41 NM:i:3 UQ:i:39 H0:i:0 H1:i:1 EAS54_67:3:175:730:949 163 seq1 70 99 35M = 230 195 GCAGCCTGGCTGTGGGGGCCGCAGTGGCTGAGGGG <<<<<<<<<<8<;<<<<<0(<<;;,<<7<4%7626 MF:i:18 Aq:i:65 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_65:8:76:493:708 99 seq1 73 44 35M = 229 191 GCCTGGCTGTGGGGGCACCAGCCGCTGCGGGGGGT <<<<1<<1<;626<;<''+;-'';+2'+;;)6--+ MF:i:130 Aq:i:44 NM:i:5 UQ:i:34 H0:i:0 H1:i:0 EAS1_97:7:20:979:96 163 seq1 79 99 35M = 254 210 CTGTGGGGGCCGCAGTGGCTGAGGGGGGGAGGGGC <<<<<<;<<<<<7<<,<<,:;,<<<<17)++':.' MF:i:18 Aq:i:37 NM:i:4 UQ:i:43 H0:i:0 H1:i:1 EAS114_26:3:284:261:124 163 seq1 79 99 35M = 263 219 CTGTGGGGGCCGCAGTGGGTGAGGGGTGGAGGGGG ============'8====':=+====,=8,8'=++ MF:i:18 Aq:i:39 NM:i:5 UQ:i:64 H0:i:0 H1:i:1 EAS221_1:2:29:1486:672 99 seq1 79 99 35M = 256 212 CTGTGGGGGCCGCAGTGGCTGAGGGGTGCAGAGCC <<<<<<<<<<<<<;<;<<<<<;<<<<8;;;<8;-; MF:i:18 Aq:i:29 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS188_7:2:218:877:489 163 seq1 80 10 35M = 250 205 TGTGGGGGCCGCAGTGGCTGGGGGGGGGCGGGCGG <<<<<<<;<<<07640<2<9(<9<<&9%(<(6%%3 MF:i:18 Aq:i:10 NM:i:6 UQ:i:34 H0:i:0 H1:i:0 EAS51_64:7:242:862:732 73 seq1 95 66 35M = 95 0 GGCTGAGGGGTGCAGAGCCGAGTCACGGGGTTGCC <<<<<<<<<<<<<<<;<<<:<;+<3<::3<';:'; MF:i:64 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_64:7:242:862:732 133 seq1 95 0 * = 95 0 GGGTCTATGTGAACAAAGGCACTAAACACAGCTGT <<<<<<<<<<8<<<<<78<<<378<<<77755++2 MF:i:192 EAS56_57:6:190:289:82 69 seq1 100 0 * = 100 0 CTCAAGGTTGTTGCAAGGGGGTCTATGTGAACAAA <<<7<<<;<<<<<<<<8;;<7;4<;<;;;;;94<; MF:i:192 EAS56_57:6:190:289:82 137 seq1 100 73 35M = 100 0 AGGGGTGCAGAGCCGAGTCACGGGGTTGCCAGCAC <<<<<<;<<<<<<<<<<;<<;<<<<;8<6;9;;2; MF:i:64 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_64:3:190:727:308 99 seq1 103 99 35M = 263 195 GGTGCAGAGCCGAGTCACGGGGTTGCCAGCACAGG <<<<<<<<<<<<<<<<<<<<<<<<<<<::<<<844 MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS112_34:7:141:80:875 99 seq1 110 99 35M = 265 190 AGCCGAGTCACGGGGTTGCCAGCACAGGGGCTTAA <<<<<<<<<<<<<<<<<<<<<<:<<8;<<8+7;-7 MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS219_FC30151:3:40:1128:1940 163 seq1 112 99 35M = 291 214 CCGAGTCACGGGGTTGCCAGCACAGGGGCTTAACC <<<<<<<<<<<<<<<<<<<;<<5;;<<<9;;;;7: MF:i:18 Aq:i:70 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_62:5:290:319:736 69 seq1 113 0 * = 113 0 GTTCTCAAGGTTGTTGCAAGGGGGTCTATGTGAAC <<<<<<:7:<.<<<<7<<.<.<<.9*<4<:<4%74 MF:i:192 EAS51_62:5:290:319:736 137 seq1 113 73 35M = 113 0 CGAGTCACGGGGTTGCCAGCACAGGGGCTTAACCT ==;=======7====6=;==:;;====66=::27: MF:i:64 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_597:2:132:493:921 69 seq1 119 0 * = 119 0 GTTCTCAAGGTTGTTGCAAGGGGGTCTATGTGAAC <<<<<<<<<<<<<<<<<<<;<<<<77;0<;;6777 MF:i:192 B7_597:2:132:493:921 137 seq1 119 75 35M = 119 0 ACGGGGTTGCCAGCACAGGGGCTTAACCTCTGGTG <<<<<<<<<<<<<<<<;<<<<<<<<;<<<<;;88: MF:i:64 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_30:7:283:799:560 163 seq1 121 66 35M = 283 197 GGGGTTGCCAGCACAGGGGCTTAACCTCTGGTGAC <<<<+<<<<8<<<+<<<<<;<<:07;8;7402447 MF:i:18 Aq:i:66 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS192_3:1:225:195:543 99 seq1 123 99 35M = 299 211 GGTTGCCAGCACAGGGGCTTAACCTCTGGTGACTG <<<<<<<<<<<<<<<<<<<<<<<9<<;::388998 MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_589:6:114:714:317 99 seq1 126 99 35M = 311 220 TGCCAGCACAGGGGCTTAACCTCTGGTGACTGCCA <<<<<<<<<<<<<<<<<<<<<<<<<<<;<<<5;<; MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_39:1:70:147:84 163 seq1 128 73 35M = 285 192 CCAGCACAGGGGCTTAACCTCTGGTGACTGCCAGA <<<<<<<<<<<<<<<<<<<<;<<<<<<<<<;(5<< MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS188_7:2:187:227:818 163 seq1 129 99 35M = 290 196 CAGCACAGGGGCTTAACCTCTGGTGACTGCCAGAG <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<3<;<< MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_97:4:77:29:126 99 seq1 131 99 35M = 315 219 GCACAGGGGCTTAACCTCTGGTGACTGCCAGAGCT <<<<<<<<<<3<<<<<<<;;;7<;<<449<-:977 MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_30:4:327:795:103 99 seq1 133 99 35M = 302 204 ACAGGGGCTTAACCTCTGGTGACTGCCAGAGCTGC <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<;<<; MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_30:3:139:117:262 69 seq1 135 0 * = 135 0 GTTCTCAAGGTTGTTGCAAGGGGGTCTATGTGAAC <<<7<<<<<<<<<<<<<<<<<<<;<;<<<<<37;3 MF:i:192 EAS114_30:3:139:117:262 137 seq1 135 76 35M = 135 0 AGGGGCTTAACCTCTGGTGACTGCCAGAGCTGCTG <<<<;<<<<<<<<<<<<<:<<<<<:<<8<<<<:<: MF:i:64 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS219_FC30151:5:29:817:854 73 seq1 135 77 35M = 135 0 AGGGGCTTAACCTCTGGTGACTGCCAGAGCTGCTG <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:64 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS219_FC30151:5:29:817:854 133 seq1 135 0 * = 135 0 GTTCTCAAGGTTGTTGCAAGGGGGTTTATGTGAAC <<<<<<<<<<<<<<<1..;:;;;;1%407)07&7. MF:i:192 EAS192_3:6:170:169:57 163 seq1 138 99 35M = 296 193 GGCTTGACCTCTGGTGACTGCCAGAGCTGCTGGCC <<<<<;<<<<<<;<<<<<<<<<<<<:<<<<<;;+% MF:i:18 Aq:i:45 NM:i:2 UQ:i:30 H0:i:0 H1:i:1 B7_595:4:84:802:737 99 seq1 140 68 35M = 284 179 CTTAACCTCTGGTGACTGCCAGAGCTGCTGGCAAG <<<<<<<<<<;9<9<<<;<<;73;<<<<<37;1+. MF:i:18 Aq:i:68 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS188_4:7:78:583:670 163 seq1 142 99 35M = 316 209 TAACCTCTGGTGACTGCCAGAGCTGCTGGCAAGCT <<<<<<<<<<;;;<;;<<<:7;5;<5;;<2--8-; MF:i:18 Aq:i:66 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_64:3:90:435:691 99 seq1 147 99 35M = 318 206 TCTGGTGACTGCCAGAGCTGCTGGCAAGCTAGAGT <<<<<<<<<<;<<<;<<<<:<<<;<81;<<1;784 MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS188_7:3:13:122:187 163 seq1 153 99 35M = 343 225 GACTGCCAGAGCTGCTGGCAAGCTAGAGTCCCCTT <<<<<<<;<;<<<;<<<<:;6<<<<;;;;:<<%%< MF:i:18 Aq:i:69 NM:i:1 UQ:i:4 H0:i:1 H1:i:0 EAS221_1:6:69:735:1915 99 seq1 154 99 35M = 321 202 ACTGCCAGAGCTGCTGGCAAGCTAGAGTCCCATTT <<<<<<<<;<<<<<<<<<;<<<<;<8<<<<;1:<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_45:5:66:959:1311 163 seq1 159 95 35M = 336 212 CAGAGCTGCTGGCAAGCTAGAGGCCCATCTGGAGC ;;4;;;+;;;-01;;&-;;4;;&;;73)(&**274 MF:i:18 Aq:i:31 NM:i:2 UQ:i:12 H0:i:0 H1:i:1 EAS56_57:6:325:759:288 99 seq1 163 99 35M = 341 213 GCTGCTGGCAAGCTAGAGTCCCATTTGGAGCCCCT 8<;<<<<81<<<<<;<<;<<<;9<<<<1>><<<< MF:i:18 Aq:i:21 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_66:4:240:264:231 121 seq1 213 66 35M = 213 0 TGTAATGAAAACTATATTTATGCTATTCAGTTCTA 9;,;;62<9<)29<<<;96<<<;<<7<<<<<<;<< MF:i:64 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_66:4:240:264:231 181 seq1 213 0 * = 213 0 CAACAGATCAAGAAGGAGGGGCAATGGACGAGTTA %15+5022))0&<<)0)+7:4+&<0<<:0<<<7<< MF:i:192 EAS1_93:7:14:426:613 99 seq1 214 99 35M = 379 200 GTAATGAAAACTATATTTATGCTATTCAGTTCTAA ======;=;==========;;==3=;==-=<;<;< MF:i:18 Aq:i:71 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_93:2:173:995:93 163 seq1 215 99 35M = 382 202 TAATGAAAACTATATTTATGCTATTCAGTTCTAAA <<<<<<<<<<<<<<<<<<<7:<<<<;:<:<<<<:7 MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_64:6:195:348:703 163 seq1 215 99 35M = 353 173 TAATGAAAACTATATTTATGCTATTCAGTTCTAAA <<<<<<<;<<<<<;:<<<<<<<<<<<<:<1:<:7< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_108:2:62:879:264 163 seq1 216 99 35M = 396 215 AATGAAAACTATATTTATGCTATTCAGTTCTAAAT <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<2<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_61:4:83:452:970 99 seq1 216 99 35M = 379 198 AATGAAAACTATATTTATGCTATTCAGTTCTAAAT ==========================;======== MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS218_1:2:64:1318:1711 99 seq1 218 99 35M = 389 206 TGAAAACTATATTTATGCTATTCAGTTCTAAATAT <<<<<<<<<<<<<<<<7<<<<<<<:<<<<<2<<<< MF:i:18 Aq:i:77 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_589:8:113:968:19 83 seq1 219 99 35M = 50 -204 GAAAACTATATTTATGCTATTCAGTTCTAAATATA 8;<;8;9<<<<<<<9<:<<<<<<<<<;<<<<<<<< MF:i:18 Aq:i:63 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_93:4:160:896:275 163 seq1 220 99 35M = 387 202 AAAACTATATTTATGCTATTCAGTTCTAAATATAG ============<====<==<====<==<==;=:6 MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_591:6:181:191:418 163 seq1 221 99 36M = 387 202 AAACTATATTTATGCTATTCAGTTCTAAATATAGAA <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<988 MF:i:18 Aq:i:77 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_28:7:242:354:637 99 seq1 222 99 36M = 417 231 AACTATATTTATGCTATTCAGTTCTAAATATAGAAA <<<<<<<<<<<<<<<<<<<<<<<<<<;<<<<<6<;; MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_589:1:122:77:789 163 seq1 223 99 35M = 396 208 ACTATATTTATGCTATTCAGTTCTAAATATAGAAA <<<:<4<<9<:7<<<:<<<7<<<<<<<<<<9<9<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_591:5:42:540:501 147 seq1 224 99 36M = 60 -200 CTATATTTATGCTATTCAGTTCTAAATATAGAAATT ;<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_591:6:155:12:674 83 seq1 224 99 36M = 52 -208 CTATATTTATGCTATTCAGTTCTAAATATAGAAATT ;<<<<<<<<<<;<<<<;<<<<8<<<<<<<<<<<<<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_593:4:106:316:452 147 seq1 224 99 36M = 49 -211 CTATATTTATGCTATTCAGTTCTAAATATAGAAATT :<<<<<;<<<<:<<:<<<<<<7<<<<<<<<<<<<<< MF:i:18 Aq:i:71 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_19:5:89:525:113 163 seq1 227 78 40M = 397 210 TATTTATGCTATTCAGTTATAAATATAGAAATTGAAACAG <1<7<6;+0;7;7'<70;-<7<:<:<<5<<:9<5:7:%:7 MF:i:18 Aq:i:39 NM:i:1 UQ:i:12 H0:i:0 H1:i:1 EAS54_65:3:321:311:983 147 seq1 228 99 35M = 51 -212 ATTTATGCTATTCAGTTCTAAATATAGAAATTGAA ;;4;;<7<<<<<<77<<<<<<<<<<17<<<<<<<< MF:i:18 Aq:i:62 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_65:8:76:493:708 147 seq1 229 44 35M = 73 -191 TTTATGCTATTCAGTTCTAAATATAGAAATTGAAA 5/)63.&1517(544(055(0454&7706566679 MF:i:18 Aq:i:44 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_71:2:125:628:79 163 seq1 229 99 35M = 400 205 TTTATGCTATTCAGTTCTAAATATAGAAATTGAAA ==================<6<====<<:<==7;:: MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_32:5:78:583:499 83 seq1 229 74 35M = 37 -227 TTTACGCTATTCAGTACTAAATATAGAAATTGAAA &6&9774&<;67<44&-4<;<9<7<<<<<;<<<<< MF:i:18 Aq:i:37 NM:i:2 UQ:i:27 H0:i:0 H1:i:1 EAS54_67:3:175:730:949 83 seq1 230 99 35M = 70 -195 TTATGCTATTCAGTTCTAAATATAGAAATTGAAAC <<<<;+<<<<7<;<<;<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:65 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_45:1:84:275:1572 163 seq1 230 99 35M = 394 199 TTATGCTATTCAGTTCTAAATATAGAAATTGAAAC /6;;;4;;;;;;;;7;;4;.4;;;;;6;;;77077 MF:i:18 Aq:i:62 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_108:4:248:753:731 99 seq1 231 99 35M = 402 206 TATGCTATTCAGTTCTAAATATAGAAATTGAAACA <<<<<<<<<<<8<<<<<<<<<<<<:<<<<&<:<.: MF:i:18 Aq:i:70 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_45:1:9:1289:215 99 seq1 231 99 35M = 394 198 TATGCTATTCAGTTCTAAATATAGAAATTGAAACA ;;;;;;9;;;67;;;;;99;9;;;;;;;;977747 MF:i:18 Aq:i:59 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_595:7:188:802:71 163 seq1 232 99 35M = 415 218 ATGCTATTCAGTTCTAAATATAGAAATTGAAACAG <<<<<<<<<;<<<<<9<<<:<<<:<<<<<<:<<<; MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_93:7:252:171:323 83 seq1 234 99 35M = 43 -226 GCTATTCAGTTCTAAATATAGAAATTGAAACAGCT ;8<;<=3=6==:====;;======;========== MF:i:18 Aq:i:62 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS192_3:5:223:142:410 147 seq1 235 99 35M = 60 -210 CTATTCAGTTCTAAATATAGAAATTGAAACAGCTG 8;<<<;<<<<;<<<<<<;<;<<<<<<<<<<<<;<< MF:i:18 Aq:i:39 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_30:1:243:10:911 83 seq1 236 99 35M = 63 -208 TATTCAGTTCTAAATATAGAAATTGAAACAGCTGT ;<;;;<4;9:<<<;<<;<<<<<;;<<<<<<<<<<< MF:i:18 Aq:i:64 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_45:6:5:730:1436 163 seq1 236 99 35M = 403 202 TATTCAGTTCTAAATATAGAAATTGAAACAGCTGT ;;;;;;;;;;;;;;;;;;8;;;;;8;;;;;67777 MF:i:18 Aq:i:67 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_19:2:57:1672:1890 121 seq1 236 75 40M = 236 0 TATTCAGTTCTAAATATAGAAATTGAAACAGCTGTGTTTA :;;;9<8;;*<<<<<<:<<<<<<<<1:<<<<<<<<<<<7< MF:i:64 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_19:2:57:1672:1890 181 seq1 236 0 * = 236 0 CCCCCCCCCCCCCCCCCAGCCACTGCGGCCCCCCCAGCCA -+)%)'-'+,,<066,))090+:&486083:5&&:<<5<0 MF:i:192 EAS1_105:2:299:360:220 99 seq1 237 99 35M = 403 201 ATTCAGTTCTAAATATAGAAATTGAAACAGCTGTG <<<<<<<9<9<<<<<<<<<<<<<<<<<5<;<0<<< MF:i:18 Aq:i:43 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS221_1:2:24:1037:84 163 seq1 238 99 35M = 415 212 TTCAGTTCTAAATATAGAAATTGAAACAGCTGTGT <<<<<<<<<<<<<<<<<<<<<<;<<<<<<;:<57< MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_105:3:86:823:683 163 seq1 240 99 35M = 408 203 CAGTTCTAAATATAGAAATTGAAACAGCTGTGTTT <<<<<<<<;<<<<<<<<<<<<<<<<<<<<;;9<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_53:4:130:568:978 99 seq1 246 88 35M = 434 223 TAAATATAGAAATTGAAACAGCTGTGTTTAGTGAC 7<<;<<;<7<:;<7<<<<<<<<);4;+<7+3+%;< MF:i:18 Aq:i:24 NM:i:1 UQ:i:26 H0:i:1 H1:i:0 EAS114_45:4:73:1208:495 163 seq1 246 99 35M = 431 220 TAAATATAGAAATTGAAACAGCTGTGTTTAGTGCC ;;;;;;;;;;;;;;;;;;;;;;;;5;;;;;37377 MF:i:18 Aq:i:67 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_97:7:264:642:506 99 seq1 247 99 35M = 420 208 AAATATAGAAATTGAAACAGCTGTGTTTATTGTAT <<;<<<<<<;<<<;:;;:;;<<;<<<<;*+;*&.4 MF:i:18 Aq:i:56 NM:i:3 UQ:i:28 H0:i:1 H1:i:0 EAS114_28:5:104:350:749 163 seq1 247 99 36M = 415 204 AAATATAGAAATTGAAACAGCTGTGTTTAGTGCCTT <<8<<<<<<<<<<<;<<<<<<<<0;<<<9;<85;;; MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_61:6:227:259:597 147 seq1 248 99 35M = 61 -222 AATATAGAAATTGAAACAGCTGTGTTTAGTGCCTT <8<;2;9;<;;-92<;;;<;<<<<<<<<<<<<<<< MF:i:18 Aq:i:61 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS112_32:7:113:809:364 99 seq1 250 99 35M = 413 198 TATAGAAATTGAAACAGCTGTGTTTAGTGCCTTTG <<<<<<<<<<<<<<<<<<<<<<<<<<7<;<;<<<4 MF:i:18 Aq:i:77 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS188_7:2:218:877:489 83 seq1 250 86 35M = 80 -205 TATAGAAATTGAAACAGCTGTGTTTAGTGCCTTTG 9<<<8<<<;<9<<<<<<<<<<;<<<<<<<<<<<<< MF:i:18 Aq:i:10 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_97:7:20:979:96 83 seq1 254 99 35M = 79 -210 GAAATTGAAACAGCTGTGTTTAGTGCCTTTGTTCA '9996;(:;-<;1<<<<=<<<<=<<<<<<<<<<<< MF:i:18 Aq:i:37 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS188_7:2:259:219:114 99 seq1 254 99 35M = 411 192 GAAATTGAAACAGCTGTGTTTAGTGCCTTTGTTCA <<<<<<<<<<<<<<<;<<<<<<7<7<<<<<0<<9< MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_39:6:13:1034:1144 99 seq1 256 99 35M = 429 208 AATTGAAACAGCTGTGTTTAGTGCCTTTGTTCACA <<<<<<<<<<<<<<<<<<<<<<<<3<<<;<<;<++ MF:i:18 Aq:i:69 NM:i:2 UQ:i:48 H0:i:1 H1:i:0 EAS221_1:2:29:1486:672 147 seq1 256 99 35M = 79 -212 AATTGAAACAGCTGTGTTTAGTGCCTTTGTTCACA <<:<<<<;<<<<<<<<<<<<<<<<<<<<<<<<<++ MF:i:18 Aq:i:29 NM:i:2 UQ:i:54 H0:i:0 H1:i:0 EAS139_11:7:46:695:738 163 seq1 259 74 35M = 428 204 TGAAACAGCTGAGTTTAGCGCCTGTGTTCACATAG <;<<<<;<<),&4<3<<7&7<0;)).3;79;7<;0 MF:i:130 Aq:i:74 NM:i:3 UQ:i:18 H0:i:0 H1:i:0 EAS139_11:8:26:1221:222 163 seq1 261 99 35M = 446 220 AAACAGCTGTGTTTAGTGCCTTTGTTCAACCCCCT <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:78 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_64:3:190:727:308 147 seq1 263 99 35M = 103 -195 ACAGCTGTGTTTAGTGCCTTTGTTCAACCCCCTTG ;;<;;<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_26:3:284:261:124 83 seq1 263 99 35M = 79 -219 ACAGCTGTGTTTAGTGCCTTTGTTCAACCCCCTTG ===27===.====&===========;;======== MF:i:18 Aq:i:39 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS112_34:7:141:80:875 147 seq1 265 99 35M = 110 -190 AGCTGTGTTTAGTGCCTTTGTTCAACCCCCTTGCA 6/<;84<;<;<<<<<<5<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_19:3:24:1135:563 163 seq1 266 99 40M = 446 220 GCTGTGTTTAGTGCCTTTGTTCAACCCCCTTGCAACAACC <<<<:<<<<:1:<<<<<<.<<<<<<<<;<;;;43+:30:: MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS221_1:2:90:986:1224 83 seq1 267 99 35M = 67 -235 CTGTGTTTAGTGCCTTTGTTCAACCCCCTTGCAAC <7*37;;;;;;;9<<;<7<<<<<<<<<<<;;<<<< MF:i:18 Aq:i:41 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_28:7:287:492:169 99 seq1 269 99 36M = 449 216 GTGTTTAGTGCCTTTGTTCAACCCCCTTGCAACAAC <<<7<<<<<<<<<<<<<<<<<<<<<<<8;;<;6<<; MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS218_4:1:48:9:409 99 seq1 271 75 18M5I12M = 464 228 GTTTAGTGCCTTTGTTCACATAGACCCCCTTGCAA <<<<<<<<<<<<<:<<<<<<<<<<<<<<<<<<<<< MF:i:130 Aq:i:75 NM:i:0 UQ:i:0 H0:i:0 H1:i:0 EAS139_19:1:87:1222:878 163 seq1 272 10 40M = 435 203 TATAGGGCCTTTGTTCAAACCCCTTGCAACAACCTTGAGA &+6<6&<:<<9<1112<<;)9227>>>>>>>>>>>>>;<>>>>><<>>>;<+<>=>>+==>>==<==<=8=><:;8/;7<<<<<<<<;<:<<<< MF:i:18 Aq:i:77 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_591:2:240:603:890 83 seq1 740 99 36M = 590 -186 GCTCCCAAGAGGGAAAGCTTTCAACGCTTCTAGCCA ;+&+//&<<<<<<<<<<9<<<8<<<<9<<<<<<<<< MF:i:18 Aq:i:66 NM:i:1 UQ:i:5 H0:i:1 H1:i:0 B7_591:7:129:956:115 163 seq1 740 99 36M = 927 223 GCTCCCCAGAGGGAAAGCTTTCAACGCTTCTAGCCA <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<;877- MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_53:4:168:528:288 83 seq1 740 99 35M = 570 -205 GCTCCCCAGAGGGAAAGCTTTCAACGCTTCTAGCC 8<%<31;<<;<;<<<<<<<;<<<<<<<<<<;<<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_65:8:275:851:240 147 seq1 743 99 35M = 561 -217 CCCCAGAGGGAAAGCTTTCAACGTTTCTAGCCATT 66614/&3616630666&66666&66666868666 MF:i:18 Aq:i:31 NM:i:1 UQ:i:5 H0:i:0 H1:i:1 EAS188_7:6:205:873:464 147 seq1 743 99 35M = 552 -226 CCCCAGAGGGAAAGCTTTCAACGCTTCTAGCCATT <-((+:+;289<--;<;-;<:;;<<<;;<<<<<<< MF:i:18 Aq:i:63 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_65:6:37:610:260 163 seq1 745 99 35M = 913 203 CCAGAGGGAAAGCTTTCAACGCTTCTAGCCATTTC <<<;<;<<7<<<<<<<<<<<<<<;6<963;;;3;1 MF:i:18 Aq:i:68 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS192_3:7:93:945:176 147 seq1 745 99 35M = 582 -198 CCAGAGGGAAAGCTTTCAACGCTTCTAGCCATTTC 6;;;8<<3<<8.<;6)<<<<<9<<<<<<<<<<<<< MF:i:18 Aq:i:70 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_593:6:61:628:681 83 seq1 746 99 36M = 586 -196 CAGAGGGAAAGCTTTCAACGCTTCTAGCCATTTCTT 95<<<<<<<<;<<<<;<<<:<<;;<<<<<<<<<<<< MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_65:7:288:552:440 83 seq1 747 87 35M = 560 -222 AGAGGGAACGCTTTCAACTCTTCTAGCCATTTCTT 9<<%'%<<.2<<<<<<<<5:<<<<<<<<<<<<<<< MF:i:18 Aq:i:26 NM:i:2 UQ:i:33 H0:i:0 H1:i:0 EAS56_53:2:170:265:818 163 seq1 748 10 35M = 920 207 GAGGGGAAGCTTTCAACGCTTCTAGCACTTTCTTT <<<<<(5/959<8.<9<8<<<2<&59&&:22:8+( MF:i:18 Aq:i:10 NM:i:3 UQ:i:17 H0:i:0 H1:i:0 B7_595:2:251:121:479 83 seq1 750 99 35M = 572 -213 GGGAAAGCTTTCAACGCTTCTAGCCATTTCTTTTG <<<<<6'..663;&<<;<<9<<<9<<<<<<<<<<< MF:i:18 Aq:i:65 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS221_1:8:67:1797:1931 147 seq1 750 99 35M = 562 -223 GGGAAAGCTTTCAACGCTTCTAGCCATTTCTTTTG <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:77 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_103:2:226:302:758 83 seq1 751 99 35M = 556 -230 GGAAAGCTTTCAACGCTTCTAGCCATTTCTTTTGG ;<<<<9;<<<<<<<<<<7<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:33 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_32:2:163:618:570 83 seq1 751 99 35M = 571 -215 GGAAAGCTGTCAACGCTTCTAGCCATTTCTTTTGG <9774<88&:8<:8<8:8<8<<<<<;88<88<<<< MF:i:18 Aq:i:41 NM:i:1 UQ:i:5 H0:i:0 H1:i:1 EAS1_97:3:73:292:429 99 seq1 752 99 35M = 920 203 GAAAGCTTTCAACGCTTCTAGCCATTTCTTTTTGC <<<<<<<<<<7<<;<<<<<<<2<<<5<<<<<:%)< MF:i:18 Aq:i:69 NM:i:1 UQ:i:4 H0:i:1 H1:i:0 EAS1_108:3:82:356:253 99 seq1 752 99 35M = 927 210 GAAAGCTTTCAACGCTTCTAGCCATTTCTTTTGGC ===================<========;===39= MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_30:6:62:386:959 147 seq1 752 99 35M = 594 -193 AAAAGCTTTCAACGCTTCTAGCCATTTCTTTTGGC %;71131((<<6<92(+<1<<;<-3<8<<;<;;<< MF:i:18 Aq:i:57 NM:i:1 UQ:i:4 H0:i:1 H1:i:0 EAS51_62:3:263:74:407 83 seq1 754 99 35M = 574 -215 AAGCTTTCAACGCTTCTAGCCATTTCTTTTGGCAT ;;88<::+;<)<5<<:<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:68 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_597:3:67:620:344 99 seq1 755 99 35M = 905 185 AGCTTTCAACGCTTCTAGCCATTTCTTTTGGCATT <<<<2<:2<<<<<<7<<<<:<<*<<<<<<***3<< MF:i:18 Aq:i:33 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_610:6:148:776:486 83 seq1 755 99 35M = 578 -212 AGCTTTCAACGCTTCTAGCCATTTCTTTTGGCATT ;:<<<;<<;<<<<<;<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_61:3:150:933:810 83 seq1 755 99 35M = 593 -197 AGCTTTCAACGCTTCTAGCCATTTCTTTTGGCATT :89===:=:=;;==;==================== MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_64:4:102:467:897 99 seq1 756 97 35M = 940 219 GCTTTCAACGCTTCTAGCCATTTCTTTTGTCTTTT <<<<9<<<<9<2<<<&,/=====>=>=>>>=>>==>=>>>>>> MF:i:18 Aq:i:77 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_595:3:297:637:86 83 seq1 869 99 35M = 704 -200 TCTCAGCTAGGGGAACAGGGAGGTGCACTAATGCG <:75<;<;;<<<<<<;;<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:68 NM:i:1 UQ:i:26 H0:i:1 H1:i:0 EAS54_65:3:290:558:349 147 seq1 869 99 35M = 719 -185 TCTCAGCTAGGGGAACAGGGAGGTGCACTAATGCG 2;2;;'5&;<<5<<;5/<<<<<7<<;+;<<+1<8< MF:i:18 Aq:i:59 NM:i:1 UQ:i:6 H0:i:1 H1:i:0 EAS1_95:3:308:956:873 99 seq1 870 99 35M = 1068 233 CTCATCTAGGGGAACAGGGAGGTGCACTAATGCGC <<<<<<<<<<<<<;<;<;1<<<<<.<9<;<<<<+; MF:i:18 Aq:i:31 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_78:7:147:64:416 147 seq1 870 99 35M = 701 -204 CTCATCTAGGGGAACAGGGAGGTGCACTAATGCGC /;49;:6<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:47 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_593:4:30:812:345 163 seq1 871 99 36M = 1036 201 TCATCTAGGGGAACAGGGAGGTGCACTAATGCGCTC <<<<<<<7<;<<7<;77;3<&0-;<5<;6<1'13<: MF:i:18 Aq:i:64 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_73:7:134:243:630 163 seq1 871 99 35M = 1052 216 TCATCTAGGGGAACAGGGAGGCGCACTAATGAGCT <<<:<<<<::1:818;;&::<>.; MF:i:18 Aq:i:35 NM:i:1 UQ:i:5 H0:i:0 H1:i:1 EAS54_81:2:31:98:804 147 seq1 982 99 35M = 805 -212 CTTTACTGTCATAACTATGAAGAGACTATTGCCAG ====;========7===================== MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_103:2:235:805:373 163 seq1 983 99 35M = 1146 198 TTTACTGTCATAACTATGAAGAGACTATTTCCAGA <<<<<<<<<<<<<<<<<<<<;<;<<<<<<;;<99; MF:i:18 Aq:i:74 NM:i:1 UQ:i:26 H0:i:1 H1:i:0 EAS114_28:5:11:868:62 99 seq1 983 99 36M = 1154 207 TTTACTGTCATAACTATGAAGAGACTATTGCCAGAT <<<<<<<<<<<<<<<<<<<<:<<<;<<<<(7:7039 MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_81:2:280:512:316 163 seq1 984 99 35M = 1159 210 TTACTGTCATAACTATGAAGAGACTATTGCCAGCT ==<========6==4==6;;==:===;=2/:+8%6 MF:i:18 Aq:i:68 NM:i:1 UQ:i:4 H0:i:1 H1:i:0 EAS1_93:5:292:122:666 99 seq1 985 99 35M = 1159 209 TACTGTCATAACTATGAAGAGACTATTGTCAGATG <<<<<<6<<<<<<<<8;<<<<<<<<<<3&9+;;(; MF:i:18 Aq:i:68 NM:i:1 UQ:i:5 H0:i:1 H1:i:0 EAS56_53:1:23:403:981 99 seq1 985 99 35M = 1151 201 TACTGTCATAACTATGAAGAGACTATTGCCAGATG <8<<<;<<<<<<;<<<<<<8;<<<9<9,3;,6(91 MF:i:18 Aq:i:65 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_45:7:33:1566:588 99 seq1 985 76 35M = 1166 216 TACTGTCATAACTATGAAGAGCCTATTGCCAGATG <;.;;;;6;;;;6;;29;;;<+9;;;.3;;73797 MF:i:18 Aq:i:37 NM:i:1 UQ:i:10 H0:i:0 H1:i:1 EAS139_11:7:92:367:1495 83 seq1 987 99 35M = 820 -202 CTGTCATAACTATGAAGAGACTATTGCCAGATGAA <8<88<<<<7<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:78 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS220_1:8:38:1576:1923 83 seq1 987 99 35M = 822 -200 CTGTCATAACTATGAAGAGACTATTGCCAGATGAA 8;<98<<<<<<<;<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:77 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_595:7:190:481:295 163 seq1 990 99 35M = 1161 206 TCATAACTATGAAGAGACTATTGCCAGATGAACCA <<<<<<<<<<<<<<<<<<<<<<9<<<<<9<7<2:: MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS112_32:7:168:117:441 99 seq1 990 99 35M = 1151 196 TCATAACTATGAAGAGACTATTGCCAGATGAACCA <<3<<<<<<<<<<<<<<<<<<<+<<17;<;:<995 MF:i:18 Aq:i:71 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_73:3:239:796:221 163 seq1 992 99 35M = 1160 203 ATAACTATGAAGAGACTATTGCCAGCTGACCCCCC <<<7<<7<<7<<7<;<<<<<,;;,+'<+/+99%:' MF:i:18 Aq:i:37 NM:i:4 UQ:i:26 H0:i:0 H1:i:1 EAS220_1:4:69:88:1154 147 seq1 992 99 35M = 805 -222 ATAACTATGAAGAGACTATTGCCAGATGAACCACA <<<<9<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:47 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS221_3:8:34:956:1309 99 seq1 994 99 35M = 1168 209 AACTATGAAGAGACTATTGCCAGATGAACCACACA <<<<<<7<<<<<<<<<<<6<<<<<<<<<<<:<8<8 MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_108:5:229:717:121 99 seq1 995 99 35M = 1150 190 ACTATGAAGAGACTATTGCCAGATGAACCACACAC =================<)=<4<0=.<<<71;41& MF:i:18 Aq:i:43 NM:i:1 UQ:i:5 H0:i:1 H1:i:0 EAS219_1:1:67:191:668 99 seq1 995 99 35M = 1134 174 ACTATGAAGAGACTATTGCCAGATGAACCACACCT <<<<<<<<<<<<<<<<<6<<;<;<;<<<<<<6;%2 MF:i:18 Aq:i:74 NM:i:1 UQ:i:4 H0:i:1 H1:i:0 EAS51_64:3:309:303:278 163 seq1 996 99 35M = 1178 217 CTATGAAGAGACTATTGCCAGATGAACCACACATT <<<<<<<<<<<<<<<<+<<+<<7<<<<<5<<<;;; MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS221_1:8:60:1020:1259 99 seq1 996 99 35M = 1157 196 CTATGAAGAGACTATTGCCAGATGAACCACACATT <;<<<<;<<<<<<<<<;<<<<<<<8<<<<<:<:<< MF:i:18 Aq:i:77 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS218_4:7:89:1487:520 83 seq1 997 99 35M = 805 -227 TATGAAGAGACTATTGCCAGATGAACCACACATTA 4;;/<<<<<:<;<;<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:70 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_610:4:15:805:420 163 seq1 998 35 35M = 1164 201 ATGAAGAGACTATTCACATGTGAACCACACATTTA ;73;;;;67.;1<<+*.;*&<4947<&474&*9*( MF:i:130 Aq:i:35 NM:i:4 UQ:i:33 H0:i:0 H1:i:0 EAS56_57:3:119:761:239 147 seq1 999 99 35M = 813 -221 TGAAGAGACTATTGCCAGATGAACCACACATTAAT ;;<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS112_34:7:142:457:584 99 seq1 999 99 35M = 1160 196 TGAAGAGACTATTTCCAGATGAACCACACATTAAT <<<<<<<<<<<<<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_63:7:190:95:706 147 seq1 1078 99 35M = 920 -193 TTGTGTCCATGTACACACGCTGTCCTATGTACTTA 9;97437;<;;<<;<;<<<<<<;<<<<<<<<<<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_589:1:101:825:28 83 seq1 1079 99 35M = 879 -235 TGTGTCCATGTACACACGCTGTCCTATGTACTTAT 0;0'0;<<<<<<8<;<<<<;;3<<;;<<<8<<<<< MF:i:18 Aq:i:39 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_66:4:188:460:1000 99 seq1 1080 99 35M = 1251 206 GTGTCCATGTACACACGCTGTCCTATGTACTTATC <<<<<<<<<<<<<<<<7<<;:4;44<;;:8;;9;; MF:i:18 Aq:i:70 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_95:3:268:523:511 99 seq1 1081 99 35M = 1241 195 TGTCCATGTACACACGCTGTCCTATGTACTTATCA <<<<<<<<<<<<<<<<<<<<;<<<<6<:9<<3<44 MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_28:6:54:263:585 99 seq1 1081 99 36M = 1254 209 TGTCCATGTACACACGCTGTCCTATGTACTTATCAT <<<<<<<<<<<<<<<<<<<:;<<;<:;::<<;;:;4 MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_66:7:174:987:334 83 seq1 1082 99 35M = 908 -209 GTCCATGTACACACGCTGTCCTATGTACTTATCAT ,;<;;<<<&<<<1<<<<<<<<<<<<<;<<<<<<<< MF:i:18 Aq:i:41 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_71:6:224:932:942 99 seq1 1082 99 34M = 1250 203 GTCCATGTACACACGCTGTCCTATGTACTTATCA <<<<<<<<<<<<<<<<<<<<<<;<<<<7<<(;3, MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_45:1:12:1296:358 99 seq1 1082 96 35M = 1252 205 GTCCATGTACACACGCTGTCCTATGTACTTATCAT ;;;6;7;7;;;;;7;9;;-*1;9;699/99/7477 MF:i:18 Aq:i:37 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_32:2:306:119:56 147 seq1 1083 99 35M = 919 -199 TCCATGTACACACGCTGTCCTATGTACTTATCATG ;;;;;<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_95:4:66:179:118 163 seq1 1084 99 35M = 1262 213 CCATGTACACACGCTGTCCTATGTACTTATCATGA <<<<<<<<<<<<<<<<<<<<<<<<<<:<<;<<6<< MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_105:2:110:584:649 99 seq1 1084 99 35M = 1266 217 CCATGTACACACGCTGTCCTATGTACTTATCATGA <<<<<<<<<<<<<<<<<<<<<<<<;<<<<<::<38 MF:i:18 Aq:i:43 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS218_1:4:28:315:310 163 seq1 1085 99 35M = 1242 192 CATGTACACACGCTGTCCTATGTACTTATCATGAC <<<<<<<<<<<<<<<<<<<<<:<+.<<.<+7<*17 MF:i:18 Aq:i:68 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_595:7:242:4:593 147 seq1 1086 99 35M = 905 -216 ATATACACACGCTGTCCTATGTACTTATCATGACT 1.%55877+8+88808887+7;7;18:8;;;.&;8 MF:i:18 Aq:i:53 NM:i:1 UQ:i:4 H0:i:1 H1:i:0 EAS1_93:1:131:946:353 163 seq1 1087 99 35M = 1249 197 TGTACACACGCTGTCCTATGTACTTATCATGACTC <<<<<<<<<<<<<;<<<<;;<<<<<<<;<:52;<2 MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS221_1:4:4:1732:88 99 seq1 1087 99 35M = 1265 213 TGTACACACGCTGTCCTATGTACTTATCATGACTC <<<<<<<<<<<<<<<<<2<8;8<;<8;<2;2:<:< MF:i:18 Aq:i:45 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_595:4:58:703:72 83 seq1 1088 99 35M = 905 -218 GTACACACGCTGTCCTATGTACTTATCATGACTCT 5&<<7;+95;7'6<<<<<.<<<<<;<<9<7<<<<< MF:i:18 Aq:i:65 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_59:5:113:694:725 163 seq1 1088 99 35M = 1266 213 GTACACACGCTGTCCTATGTACTTATCATGACTCT <<<<<<<<<<<<9<<<<<:<<<<<<<<<<:;;<;; MF:i:18 Aq:i:47 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_65:5:278:848:765 147 seq1 1088 99 35M = 920 -203 GTACACACGCTGTCCTATGTACTTATCATGACTCT 7;;<;5<55<<;;<;<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_57:6:234:787:12 163 seq1 1092 97 35M = 1257 200 ACACGCTGGCCTATGTACTTATAATGACTCTATCC <;<<<9<<&+9;3;<993;<9<+94;9&41;08%9 MF:i:18 Aq:i:24 NM:i:2 UQ:i:15 H0:i:0 H1:i:0 EAS218_1:4:15:856:340 147 seq1 1093 99 35M = 936 -192 CACGCTGTCCTATGTACTTATCATGACTCTATCCC <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:47 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_62:2:258:266:101 163 seq1 1094 99 35M = 1285 226 ACGCTGTCCTATGTACTTATCATGACTCTATCCCA <<<<<<<<<<<<<<<<<<5<;,<-2<<<<;68<<6 MF:i:18 Aq:i:68 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_59:2:177:552:234 147 seq1 1094 99 35M = 903 -226 ACGCTGTCCTATGTACTTATCATGACTCTATCCCA ::;:=;=99=====;;====;==========<=== MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_30:1:134:379:893 147 seq1 1095 99 35M = 927 -203 CGCTGTCCTATGTACTTATCATGACTCTATCCCAA 7137::;<<<<<<<;<<<<<<<<<<;<<<<<<<<< MF:i:18 Aq:i:71 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_105:8:256:404:584 147 seq1 1096 99 35M = 928 -203 ACTGTCCTATGTACTTATCATGACTCTATCCCAAA &&326+23<3<<<+:<<<<<< MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_595:3:57:735:151 99 seq1 1121 94 35M = 1314 228 CTATCCCAAATTCCCAATTACGTCCTATCTTCTTC <<<<<<<<8<<8<:<<*<:<<<4<<<;,<<<<:<: MF:i:18 Aq:i:26 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_81:8:142:858:903 147 seq1 1121 99 35M = 943 -213 CTATCCCAAATTCCCAATTACGTCCTATCTTCTTC <<<<<;<<<<9<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_57:7:247:522:670 83 seq1 1121 99 35M = 960 -196 CTATCCCAAATTCCCAATTACGTCCTATCTTCTTC ;;;9;:<<<<<;<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_19:3:75:732:442 99 seq1 1121 99 40M = 1293 212 CTATCCCAAATTCCCAATTACGTCCTATCTTCTTCTTAGG <<<<<;<<<<<9<<<;<<;<<<5<<;8<<<<<<<<;:9%% MF:i:18 Aq:i:60 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_99:7:183:645:699 99 seq1 1122 86 35M = 1281 194 TATCCCAAATTCCCAATTACGTCCTATCTTCTTCT <<9<9<<<<<<<<<;<<;<<*175;173<;;;<-/ MF:i:18 Aq:i:21 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS192_3:6:175:437:950 163 seq1 1126 99 35M = 1298 207 CCAAATTCCCAATTACGTCCTATCTTCTTCTTAGG <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<:59 MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_63:3:93:1002:845 83 seq1 1129 99 35M = 954 -210 AATTCCCAATTACGTCCTATCTTCTTCTTAGGGAA <<::;;;<<<<<<<<<<<<<<<<;<<<<<<<<<<< MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_62:6:50:542:881 163 seq1 1132 99 35M = 1324 227 TCCCAATTACGTCCTATCTTCTTCTTAGGTAAGAA <<<<<4<09<<9<<2<<<<<<<<<<<2/.&2<%<7 MF:i:18 Aq:i:63 NM:i:1 UQ:i:5 H0:i:1 H1:i:0 EAS1_99:3:118:851:285 83 seq1 1133 99 35M = 953 -215 CCCAATTACGTCCTATCTTCTTCTTAGGGAAGAAC 3+7<<<;<;<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS219_1:1:67:191:668 147 seq1 1134 99 35M = 995 -174 CCAATTACGTCCTATCTTCTTCTTAGGGAAGAACA <<<<<7<<7<<<<<<<;<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_595:7:166:203:416 83 seq1 1136 99 35M = 963 -208 AATTACGTCCTATCTTCTTCTTAGGGAAGAACAGC <<<<<<<<::<<<<<<<<<;<<<<<<<<<<<<<<< MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_45:2:15:1497:1530 99 seq1 1136 99 35M = 1314 213 AATTACGTCCTATCTTCTTCTTAGGGAAGAACAGC 0<;;;9;;86<;;;<<&<<.<<;)3;7;654-471 MF:i:18 Aq:i:57 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_65:8:206:563:262 83 seq1 1137 99 35M = 971 -201 ATTACGTCCTATCTTCTTCTTAGGGAAGAACAGCT <<<<7<<<<<<<<<<<<<<<<<<<<<<<<<<<<<7 MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_26:4:40:352:151 99 seq1 1137 99 35M = 1327 225 ATTACGTCCTATCTTCTTCTTAGGGAAGAACAGCT <<<<<<<<<<<<<<<;<<9<<<<:<<<<;<99<3< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_593:7:67:302:762 99 seq1 1138 99 36M = 1313 211 TTACGTCCTATCTTCTTCTTAGGGAAGAACAGCTTA <<<<<<<<<<<<<<<<<<<<;;65;<-<;<:8<<<3 MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_97:5:84:927:843 147 seq1 1138 99 35M = 938 -235 TTACGTCCTATCTTCTTCTTAGGGAAGAACAGCTT 588;<:<<<<<<<6<<<<;<<<:/<<3<:;<*<<< MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_99:5:147:479:41 163 seq1 1139 99 35M = 1322 218 TACGTCCTATCTTCTTCTTAGGGAAGAACAGCTTA <<<<<<<<<<<<<<<<<<<<::6<<;<<<;;9;;6 MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_105:3:329:177:267 83 seq1 1139 99 35M = 962 -212 TACGTCCTATCTTCTTCTTAGGGAAGAACAGCTTA <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_589:7:72:916:763 163 seq1 1142 99 35M = 1340 233 GTCCTATCTTCTTCTTAGGGAAGAACAGCTTAGGT ==7>==9>=7=>=>>=>> MF:i:18 Aq:i:78 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_65:4:91:267:655 147 seq1 1365 99 35M = 1204 -196 TGTTGTTGGTTTTCTGTTTCTTTGTTTGATTTGGT ;,:;5:<6:<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:71 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS221_1:2:91:856:504 99 seq1 1366 99 35M = 1520 189 GTTGTTGGTTTTCTGTTTCTTTGTTTGATTTGGTT <<<<<<<<<<<<<<7<<<<<<<7<<<&;<<<&&<& MF:i:18 Aq:i:68 NM:i:1 UQ:i:5 H0:i:1 H1:i:0 EAS1_108:2:170:326:433 99 seq1 1367 99 35M = 1535 203 TTGTTGGTTTTCTGTTTCTTTGTTTGATTTGGTGG =====<=9===:=<:==2=======2:===9==/5 MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_93:6:132:717:233 99 seq1 1368 99 35M = 1529 196 TGTTGGTTTTCTGTTTCTTTGTTTGATTTGGTGGA <<<<<<<<<<<<;<<<<<<<<<<<7<<<<&-<4<1 MF:i:18 Aq:i:47 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_19:1:14:420:712 99 seq1 1368 99 40M = 1525 197 TGTTGGTTTTCTGTTTCTTTGTTTGATTTTTTTGAAGACA <<<<<<<<<<<<;<<<<<<<;<<<-;<<<&,<&*8111:6 MF:i:18 Aq:i:66 NM:i:3 UQ:i:21 H0:i:1 H1:i:0 EAS114_39:4:43:1047:1626 163 seq1 1369 99 35M = 1523 189 GTTGGTTTTCTGTTTCTTTGTTTGATTTGGTGGAA <<<<<<<<<<<<<<<<<<<:<<<:<<<<:+;-4:( MF:i:18 Aq:i:70 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_45:2:20:413:1334 147 seq1 1370 99 35M = 1215 -190 TTGGTTTTCTGTTTCTTTGTTTGATTTGGTGGAAG 88878777;:;:1:;9;;;6;;;6;9;;;;;296; MF:i:18 Aq:i:60 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_62:5:154:669:853 83 seq1 1371 99 35M = 1193 -213 TGGTTTTCTGTTTCTTTGTTTGATTTGGTGGAAGA <::<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:77 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_610:7:117:857:942 99 seq1 1372 99 35M = 1527 190 GGTTTTCTGTTTCTTTGTTTGATTTGGTGGAAGAC <<<<<<<<<<<<<<<<<<<<<<<<<:6<;;7;9<; MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_57:6:145:144:796 147 seq1 1372 99 35M = 1181 -226 GGTTTTCTGTTTCTTTGTTTGATTTGGTGGAAGAC ;<<<;<<<<<<<<<;<<<;<<<<<<<<<<<<<<<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_32:6:88:162:587 147 seq1 1372 99 35M = 1189 -218 GGTTTTCTGTTTCTTTGTTTGATTTGGTGGAAGAC 386;;388-<8;<;68<<;;<;<6<<<8<<<<<<< MF:i:18 Aq:i:63 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS221_1:8:73:108:1621 99 seq1 1373 99 35M = 1532 194 GTTTTCTGTTTCTTTGTTTGATTTGGTGGAAGACA <<<<<<<<71<<<<<<<<<+<<<<70:0<9<<61< MF:i:18 Aq:i:71 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS112_34:6:127:153:861 147 seq1 1374 99 35M = 1202 -207 TTTTCTGTTTCTTTGTTTGATTTGGTGGAAGACAT :;:6;9<<1;<<95<<<9<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS188_7:2:152:765:744 163 seq1 1374 99 35M = 1534 195 TTTTCTGTTTCTTTGTTTGATTTGGTGGAAGACAT <<<<<<<<<<<<<<<<<<:<<<<<<<<&<7293<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_73:3:313:827:992 147 seq1 1379 99 35M = 1197 -217 TGTTTCTTTGTTTGATTTGGTGGAAGACATAATCC '187:1'<75<.*<<:5<..<<*<<917<<7<<17 MF:i:18 Aq:i:57 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_64:3:7:268:263 121 seq1 1381 22 35M = 1381 0 TTGCGTTATTTGAGTTGGTGGAAGACATAATCCCA ',)*&2<$7+<<<'<-<7<<<<<<<7<<7><>;>+>>/;>>=>=>=:>><>=<<==;)<=8; MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS218_4:7:85:923:726 147 seq2 199 99 35M = 43 -191 GTAAAGTAACTGAACCTATGAGTCACAGGTATTCC <:<<<%3<<1<<86<<-<<<<<<<<<<<<6<<1<< MF:i:18 Aq:i:44 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_103:5:285:241:560 83 seq2 200 99 35M = 37 -198 TAAAGTAACTGAACCTATGAGTCACAGGTATTCCT :<<<<;<<,<<<<5<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_30:6:41:461:436 163 seq2 200 74 35M = 389 224 TAAAGTAACTGAACCTATGAGTCACAGGTATTCCT <<<<<<<<<<<<<<<<<<<:<<<<<<<<;<;;;:; MF:i:18 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_61:6:25:949:33 99 seq2 201 99 35M = 383 217 AAAGTAACTGAACCTATGAGTCACAGGTATTCCTG =;===/8========*==&;6=&=&:=6&:=::67 MF:i:18 Aq:i:63 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS221_3:2:60:590:1760 99 seq2 201 99 35M = 376 210 AAAGTAACTGAACCTATGAGTCACAGGTATTCCTG <:<<<<<2<<<<:<::<<<::<<<<<6<<<<<<<6 MF:i:18 Aq:i:51 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_45:6:86:693:234 163 seq2 202 82 35M = 388 221 AAGTAACTGAACCTATGAGTCACAGGTATTCCTGA ;;;;;;;;;;;;;;;;9;;;;;;;;99;;&70777 MF:i:18 Aq:i:18 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_57:6:4:223:776 163 seq2 203 93 35M = 387 219 AGTAACTGAACCTATGAGTCACAGGTATTCCTGAG <<<<<<<<<<<<<<<<<<<<<<<<<9<<<:;<;2< MF:i:18 Aq:i:19 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_39:3:88:84:1558 99 seq2 203 95 35M = 394 226 AGTAACTGAACCTATGAGTCACAGGTATTCCTGTG <<;<<<<<<<<<<<<;;<<<<<<<::<<<<<<7&< MF:i:18 Aq:i:22 NM:i:1 UQ:i:5 H0:i:1 H1:i:0 B7_597:2:168:829:88 163 seq2 205 99 35M = 369 199 TAACTGAACCTATGAGTCACAGGTATTCCTGAGGA <<<<<<<<<<<<<<<<<<<<<<<6<<<<<<9;4;2 MF:i:18 Aq:i:68 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_28:1:168:389:889 147 seq2 205 99 36M = 37 -204 TAACTGAACCTATGAGTCACAGGTATTCCTGAGGAA ;<<;;56;==================8========8 MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_71:5:81:685:141 99 seq2 207 85 34M = 382 210 ACTGAACCTATGAGTCACAGGTATTCCTGAGGAA <<<<<<<<<<<<<<<<<<<<<;;<<;<<<',7,7 MF:i:18 Aq:i:17 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_19:4:26:1312:1400 99 seq2 207 99 40M = 385 218 ACTGAACCTATGAGTCACAGGTATTCCTGAGGAAAAAGAA <<<<;<<<:<<:<;<:<<<;:;<<<<<<:<8<1;;:::88 MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_71:4:127:725:381 83 seq2 209 99 34M = 39 -204 TGAACCTATGAGTCACAGGTATTCCTGAGGAAAA +<<.<<;<;<<<3;<;<<<<<<6<8;<<<<<<<1 MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS188_7:2:19:736:559 99 seq2 209 99 35M = 370 196 TGAACCTATGAGTCACAGGTATTCCTGAGGAAAAA <<<<<<<<<<<<<<<<<<<<<<<<<<<<;<<<<<< MF:i:18 Aq:i:70 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_26:3:117:284:589 83 seq2 210 99 35M = 43 -202 GAACCTATGAGTCACAGGTATTCCTGAGGAAAAAG ==8==;==================;========== MF:i:18 Aq:i:56 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_610:5:120:596:847 163 seq2 211 83 35M = 410 234 AACCTATGAGTCACAGGTATTCCTGAGGAAAAAGA <<<<<<<<<<<<<;<<<9<<<<<<<;:<62;58;2 MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:1 B7_610:5:51:904:391 163 seq2 212 97 35M = 401 224 ACCTATGAGTCACAGGTATTCCTGAGGAAAAAGAA <<<<<<<<<<<<<<<<<;<<<<<;:;<2<6;;;;; MF:i:18 Aq:i:24 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_11:8:96:1314:1448 163 seq2 213 93 35M = 388 210 CCTATGAGTCACAGGTATTCCTGAGGAAAAATAAA <<<<<<<<<<<<<<<<<<<<<<<<5<4<<<<-<<< MF:i:18 Aq:i:18 NM:i:1 UQ:i:12 H0:i:1 H1:i:0 EAS139_19:3:73:1158:535 163 seq2 213 99 40M = 377 204 CCTATGAGTCACAGGTATTCCTGAGGAAAAAGAAAAAGTG <<<<<<<<<<<<<<<<<<<<<<8<;;<<<<<9<<9::8:8 MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_591:2:223:583:968 147 seq2 215 88 36M = 47 -204 TATGAGGCACAGGTATTCCTGAGGAAAAAGAAAAAG 1<';<<&%-:<<<<<:66%<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:30 NM:i:1 UQ:i:5 H0:i:1 H1:i:0 EAS1_97:3:160:173:889 163 seq2 215 99 35M = 379 199 TATGAGTCACAGGTATTCCTGAGGAAAAAGAAAAA <<<<<<<<<<<<<<<<<<<<;0<7<<;<<<;7<09 MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_39:1:28:350:895 83 seq2 215 95 35M = 48 -202 TATGAGTCACAGGTATTCCTGAGGAAAAAGAAAAA :<;<<<:;<-<<<<<4;77<<<<<<<<<<<<<<<< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_53:4:45:707:147 163 seq2 216 99 35M = 424 243 ATGAGTCACAGGTATTCCTGAGGAAAAAGAAAAAG <<<<<<<<<<<<&<<<<:<<9<<<9<<<<75;;;< MF:i:18 Aq:i:51 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS220_1:8:18:1757:95 99 seq2 216 45 35M = 374 193 ATGAGTCGCAGGTATTCCTGAGGAAAAAGAAAAAG <<<<<<<<<<<<<<<<<<<1<:<<<<<<:<<<;:< MF:i:18 Aq:i:0 NM:i:1 UQ:i:27 H0:i:0 H1:i:1 EAS51_66:6:310:747:415 163 seq2 217 99 35M = 387 205 TGAGTCACAGGTATTCCTGAGGAAAAAGAAAAAGT <<<<<<<<<<<<<<<<<<:<<<<<;<<<<<;<;<; MF:i:18 Aq:i:24 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_28:2:114:938:216 147 seq2 218 99 36M = 63 -191 GAGTCACAGGTATTCCTGAGGAAAAAGAAAAAGTGA <<<<7<6<<<<<<<6<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_93:1:179:629:513 163 seq2 220 99 35M = 409 224 GTCACAGGTATTCCTGAGGAAAAAGAAAAAGTGAG <<<<<<<<<<<<<<<;<;<<<<<<<<<<<<<;<<< MF:i:18 Aq:i:49 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_45:4:88:55:1187 99 seq2 220 66 35M = 391 206 GTCACAGGTATTCCTGAGGAAAAAGAAAAAGTGAG ;;<;;;<<99<<;;<;;;;;:;49;:;;;;87898 MF:i:18 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_62:5:119:38:945 99 seq2 221 99 35M = 428 242 TCACAGGTATTCCTGAGGAAAAAGAAAAAGTGAGA <<<<<<<<<<<<<<<8<<<<<8<<<8<;<<7<:<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_65:6:67:800:450 147 seq2 221 99 35M = 41 -215 TCACAGGTATTCCTGAGGAAAAAGAAAAAGTGAGA 9-<9<;<<<<9;5<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:49 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_610:5:102:915:87 147 seq2 222 99 35M = 65 -192 CACAGGTATTCCTGAGGAAAAAGAAAAAGTGAGAA ;<8<;;<<<<7;<<<;<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_26:1:113:367:659 163 seq2 222 72 35M = 390 203 CACAGGTATTCCTGAGGAAAAAGAAAAAGCGAGAA =9====8==========:=:=====9=:=&====5 MF:i:18 Aq:i:0 NM:i:1 UQ:i:5 H0:i:1 H1:i:0 EAS218_1:2:26:211:481 147 seq2 222 99 35M = 43 -214 CACAGGTATTCCTGAGGAAAAAGAAAAAGTGAGAA :<:<<<<<<9:5<<<<<<<<<<<<<<:<:<<<<<< MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS219_FC30151:3:90:1906:1528 83 seq2 222 99 35M = 41 -216 CACAGGTATTCCTGAGGAAAAAGAAAAAGTGAGAA :<<<<<<<<<3:<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:49 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_591:2:13:100:876 163 seq2 223 73 36M = 397 210 ACAGGGATTCCTGAGGAAAAAGAAAAAGTGAGAAGT <8<<<*<2<7<<<6<<<<<<6<<8<<<<5<<<<4<9 MF:i:18 Aq:i:30 NM:i:1 UQ:i:9 H0:i:0 H1:i:1 EAS56_63:5:117:570:971 163 seq2 223 99 35M = 413 225 ACAGGTATTCCTGAGGAAAAAGAAAAAGTGAGAAG <<<<<<<<<<<<<;;;<<<<6<7;9;<:;<;<;;< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS221_3:8:50:1203:1094 83 seq2 223 99 35M = 46 -212 ACAGGTATTCCTGAGGAAAAAGAAAAAGTGAGAAG <7<<<<<5:+63<<<<<<<<<<<<<<<<2<<<<<< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_67:6:107:395:312 83 seq2 224 99 35M = 44 -215 CAGGTATTCCTGAGGAAAAAGAAAAAGTGAGAAGT ;<;;<<<<;<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:27 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_73:3:29:833:612 83 seq2 224 99 35M = 58 -201 CAGGTATTCCTGAGGAAAAAGAAAAAGTGAGAAGT <<;<<<;<::<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:27 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_610:7:158:943:467 83 seq2 225 99 35M = 57 -203 AGGTATTCCTGAGGAAAAAGAAAAAGTGAGAAGTT <:<<;;<:5<<<<<<<<<<<<<<<<<<;<<<;<<< MF:i:18 Aq:i:46 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_59:2:201:768:529 163 seq2 225 99 35M = 396 206 AGGTATTCCTGAGGAAAAAGAAAAAGTGAGAAGTT ==========================1=======; MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS188_7:6:11:994:584 99 seq2 226 97 35M = 417 226 GGTATTCCTGAGGAAAAAGAAAAAGTGAGAAGTTT <<<<<<<<<<<7<<<<<<<<<<<<<6<<<<<<3<6 MF:i:18 Aq:i:24 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_57:2:206:873:186 83 seq2 227 99 35M = 66 -196 GTATTCCTGAGGAAAAAGAAAAAGTGAGAAGTTTG ;<<;--7<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_63:4:38:28:122 83 seq2 227 99 35M = 46 -216 GTATTCCTGAGGAAAAAGAAAAAGTGAGAAGTTTG ;9;9;-1<<<<<<<<<<<<<<<<<;<<<<<<<<<< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_93:5:66:372:343 83 seq2 228 99 35M = 40 -223 TATTCCTGAGGAAAAAGAAAAAGTGAGAAGTTTGG ;<1;89<<<<<;<9<<<<9<<<;8<9<;<<<<<;8 MF:i:18 Aq:i:43 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_97:3:277:144:848 83 seq2 228 99 35M = 64 -199 TATTCCTGAGGAAAAAGAAAAAGTGAGAAGTTTGG <<<)63<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_19:6:21:1601:1666 83 seq2 228 99 40M = 56 -212 TATTACTGAGGAAAAAGAAAAAGTGAGAAGTTTGGAAAAA -;;3&1<<<<<<<<<<<<1<<<<<<<<<<<7<<<<<<<<=<<<<<<<<<<<<<< MF:i:32 Aq:i:19 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_57:2:23:268:529 153 seq2 329 71 35M * 0 0 TGAAAGAGGCTCAAAGAATGCCAGGAAGATACATT 7;<<<<<<57;-<<<<<<:<77<<<<<<<;<;<<< MF:i:32 Aq:i:28 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_26:2:315:219:7 153 seq2 330 69 35M * 0 0 GAAAGAGGCTCAAAGAATGCCAGGAAGATACATTG 7==::<2=8<<<=====>888<=2=>==>,>,>>8 MF:i:32 Aq:i:19 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS192_3:4:63:5:870 83 seq2 330 75 35M = 148 -217 GAAAGAGGCTCAAAGAATGCCAGGAAGATACATTG :<;<;<<<4:;<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_591:5:243:557:560 163 seq2 331 75 36M = 499 204 AAAGAGGCTCAAAGAATGCCAGGAAGATACATTGCA <<<<<<<9<<<<<<<<<<<<<<<<<<;<<89<<9<; MF:i:18 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_593:2:270:430:269 163 seq2 331 99 36M = 519 224 AAAGAGGCTCAAAGAATGCCAGGAAGATACATTGCA <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<;;;7;: MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_66:6:284:442:747 89 seq2 331 75 35M * 0 0 AAAGAGGCTCAAAGAATGCCAGGAAGATACATTGC <;<<<<<:<;<<<<<<<<;<<<<<<<<<<<<<<<< MF:i:32 Aq:i:29 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS218_4:7:71:31:1973 89 seq2 331 76 35M * 0 0 AAAGAGGCTCAAAGAATGCCAGGAAGATACATTGC <<<<<7<:<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:32 Aq:i:29 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_93:2:30:466:652 147 seq2 332 98 35M = 163 -204 AAGAGGCTAAAAGAATGCCAGGAAGATACATTGCA <<<<<;3;&<<<<<<<============= MF:i:18 Aq:i:22 NM:i:0 UQ:i:0 H0:i:4 H1:i:13 EAS114_39:3:88:84:1558 147 seq2 394 95 35M = 203 -226 ATCAGACTATCTAAAGTCAACATGAAGGAAAAAAA ;;<<;<<;<<5<<<<<<;<<:<<<;<<<<<<;<<< MF:i:18 Aq:i:22 NM:i:0 UQ:i:0 H0:i:2 H1:i:3 EAS56_59:2:201:768:529 83 seq2 396 99 35M = 225 -206 CAGACTATCTAAAGTCAACATGAAGGAAAAAAATT 3<:<9<<;<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_591:2:13:100:876 83 seq2 397 73 36M = 223 -210 AGAATATATAAAGTCAACATGAAGGAAAAAAATTCT ;9<$<<<$<<<<<<<<75<<<<<<<9<9<<<<<<<< MF:i:18 Aq:i:30 NM:i:2 UQ:i:6 H0:i:1 H1:i:1 EAS139_11:4:26:137:1382 99 seq2 397 99 35M = 579 217 AGACTATCTAAAGTCAACATGAAGGAAAAAAATTC <<<<<<7<<<77<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:49 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_59:1:93:490:901 83 seq2 445 99 35M = 280 -200 AGAAAAGCATACAGTCATCTATAAAGGAAATCCCA <<<<<<<;<<<;<<<;<<;<<;<<<<<<<<<<<<< MF:i:18 Aq:i:53 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS112_34:7:96:489:453 99 seq2 445 99 35M = 625 215 AGAAAAGCATACAGTCATCTATAAAGGAAATCCCA <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<;;;;: MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_26:6:46:13:880 147 seq2 445 99 35M = 290 -190 AGAAAAGCATACAGTCATCTATAAAGGAAATCCCA =&====8==========0================= MF:i:18 Aq:i:43 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_28:2:167:905:852 163 seq2 445 99 36M = 647 238 AGAAAAGCATACAGTCATCTATAAAGAAAATCCCAT <<<7<<<<<<<<<<<<<<:<:<<:::&.<:<66:3< MF:i:18 Aq:i:43 NM:i:1 UQ:i:5 H0:i:0 H1:i:1 EAS219_FC30151:3:13:674:1717 163 seq2 445 99 35M = 623 213 AGAAAAGCATGCAGTCATCTATAAAGGAAATCCCA <<<<<<<<<<%<<<<<<<<<<<<<<<<<<<;:;;; MF:i:18 Aq:i:45 NM:i:1 UQ:i:4 H0:i:0 H1:i:1 EAS51_62:7:196:511:896 83 seq2 446 99 35M = 283 -198 GAAAAGCATACAGTCATCTATAAAGGAAATCCCAT 8<<<<<;<<<:<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:52 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_53:1:154:118:488 163 seq2 447 99 35M = 624 212 AAAAGCATACAGTCATCTATAAAGGAAATCCCATC <<<<<<<<<<<<<<<<<<<<<<:7<<<<7<:;;:: MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_57:2:44:153:969 83 seq2 447 95 35M = 245 -237 AAAAGCATACAGTCATCTATAAAGGAAATCCCATC <<5<:7<72<51<7<*79<<<<<5<<<<<<<<<2< MF:i:18 Aq:i:36 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_28:4:215:246:640 99 seq2 447 99 36M = 624 213 AAAAGCATACAGTCATCTATAAAGGAAATCCCATCA <<<<<<<<<<9<;<<<<<<<<<<9;<<<<<<3;<;3 MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS219_1:7:94:1655:1921 147 seq2 447 85 35M = 258 -224 AAAAGCATACAGTCATCTATAAAGGAAATCCCATC <<<<;:===<==;<==<;================; MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS221_1:6:60:1037:1146 147 seq2 447 99 35M = 250 -232 AAAAGCATACAGTCATCTATAAAGGAAATCCCATC <<<<<<<<<;<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:53 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_65:1:23:536:229 99 seq2 448 99 35M = 614 201 AAAGCATACAGTCATCTATAAAGGAAATCCCATCA <<<<<<<<<<<<<<<<<:<8<:<<;<<<<<<7<<< MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS112_34:6:130:865:838 163 seq2 448 99 35M = 649 236 AAAGCATACAGTCATCTATAAAGGAAATCCCATCA <<<<<<<<<<<<<<<<<<<<<<<<<<<<<;;:<;3 MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_59:2:239:1001:406 99 seq2 450 99 35M = 634 219 AGCATACAGTCATCTATAAAGGAAATCCCATCAGA <<<<<<7<<<<<<<<8<;<<<7<<<<36<<3<:33 MF:i:18 Aq:i:49 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_97:3:147:423:584 147 seq2 451 99 35M = 277 -209 GCATACAGTCATCTATAAAGGAAATCCCATCAGAA 27<;<3<<<+<<;<<<;;-4<<<<<;<<<<<<<<< MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_99:1:187:715:521 83 seq2 451 99 35M = 291 -195 GCATACAGTCATCTATAAAGGAAATCCCATCAGAA <7<:<9<<<<<<<<<;<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_67:3:172:196:746 99 seq2 451 99 35M = 620 204 GCATACAGTCATCTATAAAGGAAATCCCATCAGAA <<<<<<<<9<<<<9<<<<<<<<<;<<<<6<<<<;< MF:i:18 Aq:i:71 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_71:3:267:821:860 83 seq2 451 99 34M = 296 -189 GCATACAGTCATCTATAAAGGAAATCCCATCAGA $&<<<.<:;6<<;<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:3 EAS56_61:7:7:682:201 83 seq2 452 99 35M = 288 -199 CATACAGTCATCTATAAAGGAAATCCCATCAGAAT 0:8;5<8<1:78<<<<<<<<<<<<:8<<2<<<<:< MF:i:18 Aq:i:66 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_589:3:82:13:897 163 seq2 453 99 35M = 606 188 ATACAGTCATCTATAAAGGAAATCCCAGCAGAATA <<<<;<<<<<<;<;<;5<51;<1<<<<%<<<<,58 MF:i:18 Aq:i:41 NM:i:1 UQ:i:4 H0:i:0 H1:i:1 EAS56_53:6:180:695:621 99 seq2 453 99 35M = 637 219 ATACAGTCATCTATAAAGGAAATCCCATCAGAATA <<<<<<<<<<<<<<<<<<<<<<<<<<<<<;::<<< MF:i:18 Aq:i:68 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_57:2:158:909:321 83 seq2 453 99 35M = 271 -217 ATACAGTCATCTATAAAGGAAATCCCATCAGAATA <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_26:2:237:497:165 99 seq2 454 99 35M = 619 200 TACAGTCATCTATAAAGGAAATCCCATCAGAATAA 8===<8===========37=<===7=;7=8===== MF:i:18 Aq:i:68 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_99:2:152:355:962 83 seq2 456 99 35M = 269 -222 CAGTCATCTATAAAGGAAATCCCATCAGAATAACA &<.9.<;+;<;<<<<<<<<<<::<<:<<<<<<<<< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:2 EAS192_3:4:255:549:422 83 seq2 456 99 35M = 295 -196 AAGTCATCTATAAAGGAAATCCCATCAGAATAACA &<;;+<;4;<<<<<<<<<<<;<;<<;<<<<<<<<< MF:i:18 Aq:i:30 NM:i:1 UQ:i:5 H0:i:1 H1:i:2 EAS220_1:4:100:20:1199 163 seq2 456 99 35M = 614 193 CAGTCATCTATAAAGGAAATCCCATCAGAATAACA 7<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<4<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_67:5:71:408:741 163 seq2 457 99 35M = 637 215 AGTCATCTATAAAGGAAATCCCATCAGAATAACAA <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<;< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_66:5:285:395:450 147 seq2 458 99 35M = 269 -224 GTCATCTATAAAGGAAATCCCATCAGAATAACAAT 8)3<8+;<)<<<<<<<<97:7<<<<<<<<<<<<<< MF:i:18 Aq:i:65 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_73:3:4:854:140 99 seq2 458 72 35M = 638 215 GTCATCTATAAAGGAAATCCCATCAGAATAACAAT <<<6<<<:<6<<<:36:<<<<3<<8:.6<38::4< MF:i:18 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_59:6:227:657:95 147 seq2 458 99 35M = 280 -213 GTCATCTATAAAGGAAATCCCATCAGAATAACAAT ;3;<);<<<<<<<<<<<<18<<<<<<<<<<<<<<< MF:i:18 Aq:i:59 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_28:7:57:324:546 83 seq2 458 99 36M = 281 -213 GTCATCTATAAAGGAAATCCCATCAGAATAACAATG ;;5<;,<<<;;<<<<<<<97<<<<<<<<<<9<<<<< MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_19:4:26:274:1078 83 seq2 458 99 40M = 282 -216 GTCATCTATAAAGGAAATCCCATCAGAATAACAATGGGCT 9:*:64<<;<<<<<<<<<;8;<<:<<<<<<<<<<<<<<<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS188_7:6:107:636:642 163 seq2 458 99 35M = 630 207 GTCATCTATAAAGGAAATCCCATCAGAATAACAAT <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:77 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_81:7:226:869:36 147 seq2 461 99 35M = 273 -223 ATATATAAAGGAAATCCCATCAGAATAACAATGGG <0/)&<=,==4>4=>>= MF:i:18 Aq:i:68 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS218_1:8:82:1540:77 163 seq2 619 99 35M = 786 202 GAAATAAAGTCAAGTCTTTCCTGACAAGCAAATGC <<<<<<<<<<<<<<<<<<<<<<<<<<<;;<<<<:8 MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_67:3:172:196:746 147 seq2 620 99 35M = 451 -204 AAATAAAGTCAAGTCTTTCCTGACAAGCAAATGCT <<<;><<+<<<<:<<<<2<;<<<;<<<<<<<<<<< MF:i:18 Aq:i:71 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_73:7:97:892:419 163 seq2 621 99 35M = 800 214 AATAAAGTCAAGTCTTTCCTGACAAGCAAATGCTA <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS192_3:4:312:915:751 147 seq2 621 99 35M = 461 -195 AATAAAGTCAAGTCTTTCCTGACAAGCAAAAGCTA <:-<<<99:::);:7<4;8<<<<<<<;<2<+8<;< MF:i:18 Aq:i:41 NM:i:1 UQ:i:10 H0:i:0 H1:i:1 EAS1_93:4:325:352:67 163 seq2 622 99 35M = 794 207 ATAAAGTCAAGTCTTTCCTGACAAGCAAATGCTAA ==================<========<=<;-=== MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_97:4:83:731:540 99 seq2 623 99 35M = 804 216 TAAAGTCAAGTCTTTCCTGACAAGCAAATGCTAAG <<<<<<<<<;<<<<<<<<<<<<<:<7<*;&;<;;9 MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS188_7:5:74:329:459 163 seq2 623 99 35M = 795 207 TAAAGTCAAGTCTTTCCTGACAAGCAAATGCTAAG <<<<<<<<<<<<<<<<<<<<<<<;<<;<<;9;599 MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS219_FC30151:3:13:674:1717 83 seq2 623 99 35M = 445 -213 TAAAGTCAAGTCTTTCCTGACAAGCAAATGCTAAG <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:45 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_105:1:141:415:738 69 seq2 624 0 * = 624 0 TTACCTAGTTGCTCTGTAGTCTCAATTAATTGTTT <<<<<<<<<<<<<<<<<<<<<<<;<<<<<;<8<<< MF:i:192 EAS1_105:1:141:415:738 137 seq2 624 76 35M = 624 0 AAAGTCAAGTCTTTCCTGACAAGCAAATGCTAAGA <<<<<<<<<<<<<<<<<<<<<<:<<;<<;<<<<6: MF:i:64 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_53:1:154:118:488 83 seq2 624 99 35M = 447 -212 AAAGTCAAGTCTTTCCTGACAAGCAAATGCTAAGA <<<;58<<95:<<;<;<<<;<<<;;<<<<<<<<<< MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_59:5:198:929:684 83 seq2 624 99 35M = 471 -188 AAAGTCAAGTCTTTCCTGACAAGCAAATGCTAAGA <<;<<<<<:<<<<<<<<<<<<<<<<<;<<<<<<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_28:4:215:246:640 147 seq2 624 99 36M = 447 -213 AAAGTCAAGTCTTTCCTGACAAGCAAATGCTAAGAT ;<<,<<<96<<:<:<9<6<97<<<<<9<<<<9<<9< MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_103:2:234:167:381 83 seq2 625 99 35M = 443 -217 AAGTCAAGTCTTTCCTGACAAGCAAATGCTAAGAT <<;<;<<<<;<<<<7<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:49 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS112_34:7:96:489:453 147 seq2 625 99 35M = 445 -215 AAGTCAAGTCTTTCCTGACAAGCAAATGCTAAGAT ;<;;;<<<<5:<<:<<<<:<<<<<<<<<<<<<<<< MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_93:3:79:879:15 99 seq2 626 99 35M = 790 199 AGTCAAGTCTTTCCTGACAAGCAAATGCTAAGATA <<<<<<<<<<<<<<<<<<<<<<<<<<<<2<;<<1< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_53:2:59:286:290 147 seq2 628 99 35M = 467 -196 TCAAGTCTTTCCTGACAAGCAAATGCTAAGATAAT 77<<<<7<<<97<<,7<<<;<<<;<9<<<<<<<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_95:5:263:511:936 99 seq2 629 99 35M = 801 207 CAAGTCTTTCCTGACAAGCAAATGCTAAGATAATT <<<<<<<<<<<<<<<<<;<<<<<;<<:<:<<<<<< MF:i:18 Aq:i:71 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_30:3:181:582:435 147 seq2 629 99 35M = 471 -193 CAAGTCTTTCCTGACAAGCAAATGCTAAGATAATT <<<<<<<<;<<<<<;<<4<<<<<<;<<<<<<<<<< MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS188_7:6:107:636:642 83 seq2 630 99 35M = 458 -207 AAGTCTTTCCTGACAAGCAAATGCTAAGATAATTC <<<<<<<;<<<<<;<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:77 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS112_34:4:12:273:89 83 seq2 631 99 35M = 477 -189 AGTCTTTCCTGACAAGCAAATGCTAAGATAATTCA <:737<288<<<7<<<<<<<<<:9<<<<<<<<<<< MF:i:18 Aq:i:71 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_59:2:239:1001:406 147 seq2 634 99 35M = 450 -219 CTTTCCTGACAAGCAAATGCTAAGATAATTCATCA 0':.71;;:9==9=;====;=;============= MF:i:18 Aq:i:49 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS188_4:7:96:899:106 147 seq2 636 99 35M = 462 -209 TTCCTGACAAGCAAATGCTAAGATAATTCATCATC ;;;;<<<<<<<;<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_65:6:67:56:806 147 seq2 637 99 35M = 464 -208 TCCTGACAAGCAAATGCTAAGATAATTCATCATCA 844:8;7<88;8<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:70 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_67:5:71:408:741 83 seq2 637 99 35M = 457 -215 TCCTGACAAGCAAATGCTAAGATAATTCATCATCA ;7;<;<0<<<<<<<<:;<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_53:6:180:695:621 147 seq2 637 99 35M = 453 -219 TACTGAAAAGCAAATGCTAAGATAATTCATCATCA ;&377<&<<;7<<<<<7<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:68 NM:i:2 UQ:i:10 H0:i:1 H1:i:0 EAS114_30:6:49:656:507 147 seq2 637 99 35M = 468 -204 TCCTGACAAGCAAATGCTAAGATAATTCATCATCA %44;;<:<<;<;<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_73:3:4:854:140 147 seq2 638 72 35M = 458 -215 CCTGACAAGCAAATGCTAAGATAATTCATCATCAC :9':<;<<<;<<<;<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_19:1:85:1521:58 99 seq2 639 99 40M = 813 214 CTGACAAGCAAATGCTAAGATAATTCATCATCACTAAACC <<<<<<<<9<<<<<<<<<<<<<7<<<<<<<<<<<<;;:7: MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_39:2:57:1064:925 137 seq2 640 76 35M * 0 0 TGACAAGCAAATGCTAAGATAATTCATCATCACTA <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<:<<< MF:i:32 Aq:i:29 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_103:3:323:196:855 163 seq2 642 99 35M = 809 202 ACAAGCAAATGCTAAGATAATTCATCATCACTAAA <<<<<<<7<<<<<<:<<<<<<<<<<<<<<<<<;7: MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_67:5:117:33:262 163 seq2 642 99 35M = 814 207 ACAAGCAAATGCTAAGATAATTCATCATCACTAAA <<<;<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<; MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_11:1:59:742:549 99 seq2 642 99 35M = 816 209 ACAAGCAAATGCTAAGATAATTCATCATCACTAAA <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<8< MF:i:18 Aq:i:48 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_28:2:55:562:403 163 seq2 643 99 36M = 825 218 CAAGCAAATGCTAAGATAATTCATCATCACTAAACC <<<<<<<<<<<<<<<<<<<<<;<<;<<<<<<<;<;: MF:i:18 Aq:i:51 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_71:7:97:743:602 163 seq2 644 99 35M = 821 211 AAGCAAATGCTAAGATAATTCATCATCACTAAACC <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<;<<<: MF:i:18 Aq:i:26 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_28:2:167:905:852 83 seq2 647 99 36M = 445 -238 CAAATGCTAAGATAATTCATCATCACTAAACCAGTC +<<<9;7;<<+<<<<<39<;9<;9<<7<<<<<<<<< MF:i:18 Aq:i:43 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS112_34:6:130:865:838 83 seq2 649 99 35M = 448 -236 AATGCTAAGATAATTCATCATCACTAAACCAGTCC ;<:84<<<4<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS219_1:1:60:1420:660 163 seq2 649 99 35M = 808 194 AATGCTAAGATAATTCATCATCACTAAACCAGTCC <<<<<<<<<<<<<<<<<<<<<<<<<<;<<<8<<<< MF:i:18 Aq:i:77 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_593:3:180:89:582 99 seq2 650 99 36M = 809 195 ATGCTAAGATAATTCATCATCACTAAACCAGTCCTA <<<<<<<<<7<<<<<<<<<7<<<:<<<:<<::77:< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_99:1:86:871:319 147 seq2 651 71 35M = 494 -192 TGCTAAGATAATTCATCATCACTAAACCAGTCCTA 7;+1;<:<<<<<<<<;<<;<<9<<<<<<<<<<<<< MF:i:18 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_57:2:236:841:20 83 seq2 652 99 35M = 467 -220 GCTAAGATAATTCATCATCACTAAACCAGTCCTAT 7;<<<;<<<<;;<<<<<<<<<<<<<<<<<<<<;<< MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_62:2:133:8:379 83 seq2 653 99 35M = 470 -218 ATAAGATAATTCATCATCACTAAACCAGTCCTATA &=========='==7==0=2====28===00==== MF:i:18 Aq:i:70 NM:i:1 UQ:i:5 H0:i:1 H1:i:0 EAS1_105:8:96:720:940 83 seq2 654 99 35M = 467 -222 TAAGATAATTCATCATCACTAAACCAGTCCTATAA *<<<<;<<<9<<;,<;0<;<<<<<<<<<<<<<<<< MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_57:5:71:994:576 99 seq2 655 99 35M = 805 185 AAGATAATTCATCATCACTAAACCAGTCCTATAAG <<<<<<<<<<<<<<<<<<<<<<<;<<5<<<<<<<< MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_103:4:164:79:134 147 seq2 656 99 35M = 488 -203 AGATAATTCATCATCACTAAACCAGTCCTATAAGA <;<;<<<;<<;<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:47 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_19:6:78:1029:512 83 seq2 656 99 40M = 500 -196 AGATAATTCATCATCACTAAACCAGTCCTATAAGAAATGC ;;;;;<;;<<<.<<6;<<;<;8<<<<::<<<<<<<<;<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_93:1:214:784:690 147 seq2 657 99 35M = 472 -220 GATAATTCATCATCACTAAACCAGTCCTATAAGAA -<7<<7<:<<2<<<<;<<<<<;<<<<3<<<<<<<< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:1 EAS220_1:4:6:1178:1105 99 seq2 657 93 35M = 830 208 GATAATTCATCATCACTAAACCAGTCCTATAAGAA <<<<<<:<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:17 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_99:7:171:196:287 83 seq2 658 99 35M = 485 -208 ATAATTCATCATCACTAAACCAGTCCTATAAGAAA <;;;98;<;&<;;<<<<<<<;<<<<<<<<<<<<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_28:1:220:801:282 99 seq2 660 99 36M = 837 213 AATTCATCATCACTAAACCAGTCCTATAAGAAATGC <<<<<<<<<<<<<<<<<<<<<;<+<;<<<<<::<<: MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:2 EAS221_1:2:73:955:728 163 seq2 660 44 35M = 823 198 AATTCATCATCACTAAACCAGTCCTATAAGAAATG <<<<<<<<<<<<<<<<<<<<<<<<<<<<<;<<<<< MF:i:18 Aq:i:14 NM:i:0 UQ:i:0 H0:i:1 H1:i:2 EAS1_105:1:3:903:957 147 seq2 661 99 35M = 516 -180 ATTCATCATCACTAAACCAGTCCTATAAGAAATGC <%12<&<<<;<:<<<<<<<<<7<<<<<<<<<<<<< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:1 EAS56_65:2:224:579:433 83 seq2 662 99 35M = 485 -212 TTCATCATCACTAAACCAGTCCTATAAGAAATGCT '<08/8<+<>===> MF:i:18 Aq:i:75 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_105:2:146:374:692 99 seq2 690 99 35M = 874 219 AAATGCTCAAAAGAATTGTAAAAGTCAAAATTAAA <<<<<<<<<<<<<<<=>>>==>>===>==> MF:i:130 Aq:i:74 NM:i:0 UQ:i:0 H0:i:0 H1:i:0 EAS1_108:6:159:493:275 99 seq2 760 72 35M = 939 214 ACAAAACTCACAGGTTTTATAAAACAATTAATTGA =====3============================= MF:i:130 Aq:i:72 NM:i:0 UQ:i:0 H0:i:0 H1:i:0 EAS139_11:1:81:1019:558 163 seq2 760 77 35M = 926 201 ACAAAACTCACAGGTTTTATAAAACAATTAATTGA <<<<<<<<<<<6<<<<<<<<<<<<<<<<<<<<<7< MF:i:130 Aq:i:77 NM:i:0 UQ:i:0 H0:i:0 H1:i:0 EAS51_62:7:162:195:761 163 seq2 767 30 18M4I13M = 922 190 TCACAGGTTTTATAAAACAATTAATTGAGACTACA <<<<<<<<<<<<<<<<<<<<<<<<<<;<:<<<<;; MF:i:130 Aq:i:30 NM:i:0 UQ:i:0 H0:i:0 H1:i:0 B7_597:3:115:646:430 147 seq2 768 45 17M4I14M = 582 -217 CACAGGTTTTATAAAACAATTAATTGAGACTACAG 5;5<;<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:130 Aq:i:45 NM:i:0 UQ:i:0 H0:i:0 H1:i:0 EAS114_30:6:243:209:110 163 seq2 768 48 17M4I14M = 920 187 CACAGGTTTTATAAAACAATTAATTGAGACTACAG <<<<<;<;<<<;<<<<<<<<<<<;<:;<<:;;+85 MF:i:130 Aq:i:48 NM:i:0 UQ:i:0 H0:i:0 H1:i:0 EAS1_108:2:266:994:429 147 seq2 769 76 16M4I15M = 612 -188 ACAGGTTTTATAAAACAATTAATTGAGACTACAGA <<<<<<<<<<<<<<<< MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_19:1:85:1521:58 147 seq2 813 99 40M = 639 -214 AAATTAACATTACAACAGGAACAAAACCTCATATATCAAT :::86<<:<<8<<<<;<<8<<<<<<<<<<<<<<<;<<<<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS188_7:4:164:719:947 99 seq2 813 99 35M = 1005 227 AAATTAACATTACAACAGGAACAAAACCTCATATA <<<<<<<<<<<<<<<<<<<;<<<<<<<<<;<<<<< MF:i:18 Aq:i:64 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS219_1:1:50:257:341 163 seq2 813 99 35M = 971 193 AAATTAACATTACAACAGGAACAAAACCTCATATA <<<<<<<<<<<<<<<<<<<<<<<<<<<<7<6<<<< MF:i:18 Aq:i:77 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_67:5:117:33:262 83 seq2 814 99 35M = 642 -207 AATTAACATTACAACAGGAACAAAACCTCATATAT <<;;<<;<:8<7<<;<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS218_1:8:90:706:1276 163 seq2 814 99 35M = 980 201 AATTAACATTACAACAGGAACAAAACCTCATATAT <<<<<<<<<<<<<<<<<<<<<<;<<<<<<<<:<:< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_108:2:116:966:193 163 seq2 815 99 35M = 967 187 ATTAACATTACAACAGGAACAAAACCTCATATATC <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<;<<<< MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_11:1:59:742:549 147 seq2 816 99 35M = 642 -209 TTAACATTACAACAGGAACAAAACCTCATATATCA -<<<3<<<<6<<6<<<<<6<<<<6<<<<<<<<<<< MF:i:18 Aq:i:48 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_11:7:74:213:877 99 seq2 816 99 35M = 996 215 TTAACATTACAACAGGAACAAAACCTCATATATCA <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:2 B7_610:3:85:219:371 163 seq2 817 99 35M = 967 185 TAACATTACAACAGGAACAAAACCTCATATATCAA <<<<<<<<<<<<<<<<<<<<<:<<<<<<<<<<;<; MF:i:18 Aq:i:54 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_108:2:176:653:957 163 seq2 819 82 35M = 982 198 ACATTACAACAGGAACAAAACCTCATATATCAATA ????????????<==>=>=>=>>>==>>>=>>> MF:i:18 Aq:i:71 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_19:5:57:366:844 83 seq2 877 99 40M = 708 -209 AAATTCCCCCACTTAAGAGATATAGATTGGCAGAACAGAT ;;;7:8&555<,;<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_32:3:236:475:254 163 seq2 880 99 35M = 1051 206 TTCCCCCACTTAAGAGATATAGATTGGCAGAACAG <<<<<<<<<<<<<<<<<<<<<<<<<:::<:;>=>>>>==>=>>>==>=>=:=====;=:=6:::6 MF:i:18 Aq:i:74 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS218_1:2:10:686:1024 163 seq2 947 99 35M = 1103 191 ACAAGAAACTCATTAATAAAGACATGAGTTCAGGT <:<<<<:<<<<<<<<<<:<:<<<<<<<<<<<5<<< MF:i:18 Aq:i:30 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_73:5:53:61:31 163 seq2 949 99 35M = 1122 208 AAGAAACTCATTAATAAAGACATGAGTTCAGATAA <<<7;<7<<<;7<;;<7<7<7<;5<73<<<;>588>9<>7:<0<9; MF:i:18 Aq:i:30 NM:i:1 UQ:i:5 H0:i:0 H1:i:1 B7_589:2:30:644:942 99 seq2 1045 83 35M = 1229 219 TATATCAGATAAAGCACACTTTAAATCAACAACAG <<<<<<<<<<<<<<<<<<<<<<<9<<<<<<9;<9< MF:i:18 Aq:i:22 NM:i:0 UQ:i:0 H0:i:1 H1:i:3 B7_591:2:123:924:645 83 seq2 1045 84 36M = 861 -220 TATATCAGATAAAGCACACTTTAAATCAACAACAGT ;<<<<*<<<<<<<<8<<<<<><<<<<><<<<<<<<<<<<<<< MF:i:18 Aq:i:47 NM:i:1 UQ:i:27 H0:i:0 H1:i:1 EAS51_62:4:308:614:911 99 seq2 1319 90 35M = 1493 209 TGCGCTTGTACTTCTAAATCTATAACAAAATTAAA <<<<<<<<<<<<<<<<<<<<<<<<<<<;;<<<<8< MF:i:18 Aq:i:43 NM:i:1 UQ:i:27 H0:i:0 H1:i:1 EAS54_65:3:155:541:234 83 seq2 1319 99 35M = 1151 -203 TGCGCTTGTACTTCTAAATCTATAAAAAAATTAAA 78;<7<<<<<<<<<<<<<<;<<<<<<<<<<;<<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_57:6:175:289:351 147 seq2 1319 99 35M = 1144 -210 TGCGCTTGTACTTCTAAATCTATAAAAAAATTAAA 9;;:+<<<<<;<<:<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_593:7:283:186:707 83 seq2 1321 99 36M = 1154 -203 CGCTTGTACTTCTAAATCTATAACAAAATTAAAATT 889;<7;<7<<7<<<<<7<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:45 NM:i:1 UQ:i:27 H0:i:0 H1:i:1 EAS1_105:3:308:66:538 147 seq2 1321 99 35M = 1138 -218 CGCTTGTACTTCTAAATCTATAACAAAATTAAAAT 996999;<9;<:<<<<<:<<7<<<<<<<<<<<<<< MF:i:18 Aq:i:45 NM:i:1 UQ:i:27 H0:i:0 H1:i:1 EAS1_108:5:11:555:330 163 seq2 1321 99 35M = 1492 206 CGCTTGTACTTCTAAATCTATAAAAAAATTAAAAT <<<<<<<<<<<<<<<<<<<<<<<<<<<<;<<4<;< MF:i:18 Aq:i:56 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS51_66:7:84:411:336 73 seq2 1322 75 35M * 0 0 GCTTGTACTTCTAAATCTATAAAAAAATTAAAATT <<<;<<<;<<<<<<<<<<<<:<<;<<<<<<;8<;< MF:i:32 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS139_11:5:52:1278:1478 163 seq2 1322 47 35M = 1513 226 GCTTGTACTTCTAAATCTATAACAAAATTAAAATT <<<<<<<<<<<<<<9<<<<<<<<<<<<<<<<9<<< MF:i:18 Aq:i:0 NM:i:1 UQ:i:27 H0:i:0 H1:i:1 EAS56_53:3:101:809:776 147 seq2 1326 99 35M = 1160 -201 GTACTTCTAAATCTATAAAAAAATTAAAATTTAAC <<<-<;7;<<<<:;<<<7<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:72 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS192_3:3:221:881:916 147 seq2 1327 96 35M = 1168 -194 TAATTCTAAATCTAGAACAAAATTAAAATTTAACA 44%-4(5<;9/,:<68:1<:8<:<<84;<<<<<;< MF:i:18 Aq:i:24 NM:i:3 UQ:i:41 H0:i:0 H1:i:0 EAS1_105:1:28:745:352 147 seq2 1329 99 35M = 1159 -205 CTTCTAAATCTATAACAAAATTAAAATTTAACAAA 4;;*;<<<;;<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:45 NM:i:1 UQ:i:27 H0:i:0 H1:i:1 EAS114_45:2:23:1754:796 99 seq2 1329 99 35M = 1488 194 CTTCTAAATCTATAAAAAAATTAAAATTTAACAAA ;<<;<;<;<;<;<<;;;;;<<<<;;<<<<<97999 MF:i:18 Aq:i:69 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_97:2:96:419:327 147 seq2 1331 99 35M = 1149 -217 TCTAAATCTATAACAAAATTAAAATTTAACAAAAG ;1<<<<<9<<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:47 NM:i:1 UQ:i:27 H0:i:0 H1:i:1 EAS1_97:4:274:287:423 163 seq2 1332 75 35M = 1515 218 CTAAATCTATAAAAAAATTAAAATTTAACAAAAGT <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<;<<< MF:i:18 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS219_1:7:35:392:2042 83 seq2 1332 99 35M = 1168 -199 ATAAATCTATAAAAAAATTAAAATTTAACAAAAGT +<<<<4<>>>>;>>&>->9>9;4>->>>>,4>9>,<1> MF:i:18 Aq:i:27 NM:i:1 UQ:i:5 H0:i:0 H1:i:1 EAS139_19:2:82:154:1333 99 seq2 1349 77 40M = 1511 202 TTAAAATTTAACAAAAGTAAATAAAACACACAGCTAAAAC <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<;;<;;:;: MF:i:18 Aq:i:0 NM:i:1 UQ:i:27 H0:i:1 H1:i:0 EAS188_7:1:290:286:763 99 seq2 1349 75 35M = 1515 201 TTAAAATTTAACAAAAGTAAATAAAACACATAGCT <<<<<<<<<<<<<<<<7<<<<<<<<<<<<<<<8<< MF:i:18 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS221_1:4:3:248:1491 73 seq2 1349 99 35M * 0 0 TTAAAATTTAACAAAAGTAAATAAAACACATAGCT <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<:8:< MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS114_39:3:6:1064:1805 99 seq2 1350 99 35M = 1502 187 TAAAATTTAACAAAAGTAAATAAAACACATAGCTA <<<<<<<<<<<<<<<<<<<<<<;<<<<<<<<<<<< MF:i:18 Aq:i:76 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_595:6:137:811:130 83 seq2 1351 99 35M = 1175 -211 AAAATTTAACAAAAGTAAATAAAACACATAGCTAA <<<<<<<<<:<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:47 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_108:1:155:809:543 83 seq2 1352 99 35M = 1156 -231 AAATTTAACAAAAGTAAATAAAACACATAGCTAAA <<<+0<<<9<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:73 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_63:3:41:468:459 99 seq2 1352 75 35M = 1513 196 AAATTTAACAAAAGTAAATAAAACACATAGCTAAA <<<<<<<<<<<<<<<<<<<<<;<<<<<<<<<<;;7 MF:i:18 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_108:4:31:622:216 73 seq2 1354 99 35M * 0 0 ATTTAACAAAAGTAAATAAAACACATAGCTAAAAC <<<<<<<<<<<<<<<<<<<<<<<<<<<<8<<96<7 MF:i:18 Aq:i:70 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS54_71:8:105:854:975 163 seq2 1354 71 35M = 1523 202 ATTTAACAAAAGTAAATAAAACACATAGCTAAAAC <<<<<<<<<<<<<<<<<<<<<<<<<<<7:<;;;;5 MF:i:18 Aq:i:0 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 B7_610:7:26:749:174 147 seq2 1357 78 35M = 1183 -209 TAACAAAAGTAAATAAAACACATAGCTAAAACTAA (<<)<<<<6<<<<<<<<<<&:<3<<<6<<<)<:<< MF:i:18 Aq:i:11 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS56_57:6:21:553:57 147 seq2 1358 99 35M = 1197 -196 AACAAAAGTAAATAAAACACATAGCTAAAACTAAA <<+<<<<<<<<<;<<<<8<<<<<<8<<<<<;<<<< MF:i:18 Aq:i:71 NM:i:0 UQ:i:0 H0:i:1 H1:i:0 EAS1_97:2:128:629:484 83 seq2 1359 96 35M = 1185 -209 AAAAAAGTAAATAAAACACATAGCTAAAACTAAAA :(::<<<<<<<<<< MF:i:32 Aq:i:0 NM:i:0 UQ:i:0 H0:i:82 H1:i:85 B7_589:6:33:356:636 73 seq2 1520 0 35M * 0 0 TTTTTTTCTTTTCTCTTTTTTTTTTTTTTTTTTTT <<<<<<<8;<<<<<<<<<<<<<7<<<<<<<;;3&3 MF:i:32 Aq:i:0 NM:i:0 UQ:i:0 H0:i:14 H1:i:85 EAS114_45:6:86:859:1779 137 seq2 1520 0 35M * 0 0 TTTTTTTCATTTCTCTTTTTTTTTTTTTTTTTTTT ;;;;;;;;;;;;;;;;;;;;;;;;;;;8;;)7699 MF:i:32 Aq:i:0 NM:i:1 UQ:i:26 H0:i:0 H1:i:15 EAS54_71:8:105:854:975 83 seq2 1523 71 33M = 1354 -202 TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG <<<<;<:<<;<&<;<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:0 NM:i:0 UQ:i:0 H0:i:85 H1:i:85 EAS51_62:4:187:907:145 153 seq2 1524 28 35M * 0 0 TTTCTTCTCTCTCTTTTTTTTTTTTTTTATTGCAT <<<+;;,6<<<<6<<<<<<<<<<<<<<<<<<<<<< MF:i:32 Aq:i:28 NM:i:3 UQ:i:59 H0:i:0 H1:i:0 EAS54_71:4:284:269:882 73 seq2 1524 0 34M * 0 0 TTTCTTTTCTCTTTTTTTTTTTTTTGTTTTTGCA <;<<<<<8<7<8;<<<;<7<<<<<;272;73&&) MF:i:32 Aq:i:0 NM:i:1 UQ:i:17 H0:i:0 H1:i:85 EAS56_63:4:141:9:811 137 seq2 1524 10 35M * 0 0 TTTCTTTTCTCCTTTTTTTTTTTTTTTTTCTACAT <<<;<<<<<<<;<;<:<<<;<<<<<<<<..));;. MF:i:32 Aq:i:0 NM:i:3 UQ:i:47 H0:i:2 H1:i:27 EAS114_30:6:277:397:932 73 seq2 1524 0 35M * 0 0 TTTCTTTTCACTTTTTTTTTTTTTTTTTTTTACTT <<<<<<<<<<<<<<<<<<<<<<<<<<<<:8(,0%( MF:i:32 Aq:i:0 NM:i:3 UQ:i:42 H0:i:2 H1:i:85 EAS139_11:7:50:1229:1313 83 seq2 1528 77 35M = 1376 -187 TTTTTTCTTTTTTTTTTTTTTTTTTTTGCATGCCA <<<<,<&<7<<<<<<<<<<<<<<<<<<<<<<<<<< MF:i:18 Aq:i:0 NM:i:1 UQ:i:11 H0:i:3 H1:i:7 EAS54_65:3:320:20:250 147 seq2 1532 77 35M = 1367 -200 TTTTTTTTTTTTTTTTTTTTTTTGCATGCCAGAAA +'''/<<<<7:;+<;::<<<;;<<<<<<<<<<<<< MF:i:18 Aq:i:6 NM:i:2 UQ:i:24 H0:i:1 H1:i:2 EAS114_26:7:37:79:581 83 seq2 1533 68 35M = 1349 -219 TTTTTTTTTTTTTTTTTTTTTTTCATGCCAGAAAA 3,,,===6===<===<;=====-============ MF:i:18 Aq:i:27 NM:i:2 UQ:i:23 H0:i:0 H1:i:1 Rsamtools/inst/extdata/ex1.vcf.gz0000644000175400017540000022235313556116727020032 0ustar00biocbuildbiocbuild‹ÿBC°:µ}k·•ægͯhŒ¿$Àë,ï—Ùõ;öpGöd÷Óm«m7F–©Lþýð9äa±êUò‹8èêWŸ—ä¹ßꃾ|õðý›·?Ý?}ôç?ý«ûþ§>øôó/¾ùý‹þ×çŸ|ôÕ󯿾}òðî»·??=¾yýÑ??õê®ü«§‡·ïî~¾÷îáå?ÿïòo>ÿòÓ?Ò¿øä«Û—¿üôíÃÛô훿ÿüðÑ篟~xx»_åÅýßîÞ>Ü¿¼{ùðóÓû>ס/vk€ÿ5w‚ôÁÝ?üøá_~¹õøô÷úý‡eûûòîÛûwïnôÑÛ‡¿– =Üîî_=õ?¿ý’~oXÿþþ»þáOïµÛ7ož>üéáþõ‡ïÊ÷xûp÷ÓýÏ??¾þᎿ՛ïï¾{S@ðŽå€òéåÓWoîŸö_ýøöáåÝÏoß|{ÿí#/z_.ëÝýO?¿zxw÷íVúñŸ<잪¯þpÿŸ¾zü‡W?¾yóòîáÝÓc¡›à`Õïß¾{º{þÅ7@}xU>xûð—_^÷÷»ß:ùå'ÀÿÛÿùýoÐÿ€þîÍ/¯Ÿî~óú ïV:bù>·÷Í›§ûWw¯é/¶C}À>¾¾ûÏ/ï~xxýæ©üûõ}þ5/oÎvöøÓ/? 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gTGggGGg.GgG,g.,t =$?:>0-<==;=$&43* 6 133536 C S 46 46 51 19 g..G,.g,.,,gg.,GGG^l, =-93;9$3)68:'@<577% 6 133543 A T 25 32 51 16 t.,tttT,TTTcTct. 4.=;/;@3>=9&;2;A 6 133609 G A 84 108 50 36 acAA,AAA.AAaaA.AaaAAAa,AAAaAaaAaAA^VA^~A 8$6A==9<1-A9=+)?>4A?76(>9=9?5+;==<++ 6 133800 C Y 142 142 55 60 .$TT.t.,.$,$T.T,Tt,Tt,,,,,T,..,.,T.TT..ttT,T.t,tT,T.,T.,t,.TT^Y,^dG 7@A:.?<1@*)%:=8=3;;:@?;375>;2<>=66/?<7?>>.@>+=<;=:A;;5;;:>.+ 6 133937 G R 168 178 59 54 A.aAAa,,,,.,AaA,aAA.aAAA.,,a,,.AaA,A.aa.ac,,.,,A,,A.., />A9<&=:>??'?>)1>1#68<91=):;89/ 6 133969 T K 140 140 59 50 gGG..$,,.GG,.,.G,g,.G.GG.G.gggG,,.gGG...gg,gG,.,,,^~g 9<-<'=:?5#;A=88=:=:8<631@8;3=3;4;;<8<::>,77<(;?;=7?9?;;8=?:9;1@A?7?;?&=/=: 6 135165 C A 119 162 60 47 a$aAAAAAAAaAAaAaAAaAaaaAaaAaAAAaaAaAaAaAA,aAaAA^O, +A7>?@@?@=:<=?<9:;9-?1?68@4;3#9<5>=& 6 135248 A G 114 138 55 38 Gg$g$GGgGggGGgggggggggGGgGG.gggGggGGGGg^~g 8++-0;4.=*);<<7::;%=47=(1/)&82;=7644,& 6 135492 C T 106 138 56 38 T$TTtTtTTTttTTTTtTTtttTttTTTttaTTTttTtt (ABAA:BBA1;>CC@>@B>5?A8;@?@?;%@>>17+;, 6 136172 C G 150 172 54 57 gG$Gg$gGgGTgggGGGTGGGGTGGGGggGGggGGGggGGgGGGGggGgaggggG^6G^+G^_G^~g ?.@+<.@&$==@/1<%:>*,%%;<:>>;;9<:97:6:;4=<9;*&<5+2>:%7++&* 6 136263 G C 129 162 57 46 cC$CcC$cCCCCCcCCCCCccCCccCCacccCCccCcCCcCccCccC^SC 3(*8)1$2?<>2>*==?135,2387(077>?1/=1;>7:6/;4.<+ 6 136331 G A 141 187 57 55 AaAaaACAAAacAaaAaAaaAAAaaAaaaaaAaAaaaAaAaaaAAaaAaAaAAa^~a <<:9;/&)6:A%<*?;9.;9<>>/>?@07'309<)21=>=+61=62>8<:9<9;* 6 136393 C S 119 187 56 61 gGGG$,,$Gg...GG,gGG,ggGGg,g,ggg,,..G.gggg.Gg.Gg,,gGg,ga.g,.,^~.^~G^\G <2-*:?);(55>?13/:>;:8>>:=9=>4,,61??',=:=@=:@/;<,?).>%=38<.B++ 6 136465 C C 53 0 53 50 .,..,,,..,,.,...,-1a.,..,...,,,,...,..,..,,..,,aa^qA^_A^Ja^kA ?@22;79,1<=3<<;50:>;=8<<6:A/8<8=15>6)=>?7$;==>76=4;/+)?8<73=6=>65<1+%"';;9:) 6 136466 * -C/-C 177 1520 53 51 -C * 34 17 0 0 0 6 136467 C M 31 31 55 51 .*.,,,A.**.****g***************************a,AAaAa^~a ?>7856'7:9,9==7$;<0=6<<779>99=>8'<8;=6;;;7++$;;=<"+ 6 136596 G C 103 103 57 33 C$CCCcCcTCCCCcCCcccCaCCCcCccCCCc,C &1&,;98$.::=:<:48>@"3=6>.=;<0:2;8;01,?@:523?;==33=7<397;56@5588A8?8$(=?@@7A@?@35=C&3>,3?@2+05==%;35;9. 6 137157 A G 173 173 57 55 G$Gg$g$GGg$GCggGgGggggGGggggGggGGGggGggGggGgGgGGGGGggGGggg^~, ,+++.2+#(1(3>+8?/0-$@9>=,;>474>:5><6?>+85=.653736/4)&3' 6 137181 A R 139 139 57 43 Gg,$.,.,..G.GggGG,g,,GGg..GgG,gg..gg,GgG.g,, 5>=<%9@:>1-5;=,63<@?,8;>>089=%:<9*=*1*6>5'% 6 137288 T Y 195 195 58 41 ccCcC.cc,,CC,,.C,,.,Ccc..cC,,.,aa.C,c,Ca^~. @@>@&<:999=7?9B><8?=>?:9>4>3;@4$>=5+,-8*B 6 137300 T G 114 147 57 41 ggg$Ggg.GgGggGgggGGgggGgGgGggGGGGgGGgGgg^~G^~g ?@+<@8&:;29:3=(?,2==4@9>+>=>9;:8)<81;15++ 6 137695 T Y 94 94 55 36 ,$,,ccc$Cc,,G,.,Cc.C,GC,,...CC.,,C.C,^Mc A?A38+84?;*<22=13<2*,=)40/7<>1;=;83+ 6 137893 A G 84 120 52 41 .GgC$G$gGGG.g.gggGGgGgGG,.GGGgGggG.GGGggGg^`G <7?)398,5;;;?;:6294:3202388=6;.2B281<707= 6 137903 A R 80 80 52 41 g..$,gG.gC,..,.G..g.,,..G..,,GgG.GGg.g,GG. =@3A=3<<$8<;<82@@=6:>=96@5=6155@564:*"44= 6 138026 T Y 64 64 54 21 CC$CC.c.C.C,..,C.C..c. ))>4::)<43-9:9=@;3<36 6 138036 T T 52 0 55 23 ....$,..,..+1A.C.,.+1A.+1Aa.+1A.+1Aaaa^ta ;'>1;87<:B*$?3A?1=<20)+ 6 138036 * +A/+A 14 208 55 23 +A * 5 18 0 0 0 6 138041 A A 99 0 56 24 ...,.+1C....,..,..,,,,,.... ;<@;@B/,@BAA5=>207B?=:>> 6 138041 * */+C 63 63 56 24 * +C 23 1 0 0 0 6 138203 T G 156 175 53 50 GGGGG$ggGggGgggGgGCGgGGGGgggGgggGGggGGGGGGGgGgGg^QG^+g^lg <<<<*???=7?>><>@;.;8><>::?:&8&+/' 6 138322 C C 153 0 54 54 ,,,..T,$..,.,.,.,,..T.,...,A.....,+2gt..,,..,..,,..,..,.,,^U. 556@/#<<-2+-:1,206(*;112<2)<;7'@2=(4,;55;;00;?-;=-9$/@ 6 138322 * */+GT 150 150 54 54 * +GT 53 1 0 0 0 6 138331 C S 29 29 52 53 GG$g$GGGg.GGT..,G.g,TA,..,,..t..,.,,...,tt,,ttt..,,,.^~.^~. /&+4(*".:1(;229);(&34>;//>."?<6?/0>><.76.3:$(==(0$<48=67>75<546=5+;;0#?23-5:331.*+1 6 138355 A R 56 56 53 92 T$T$..,.,$,..T,,,,,,,,T.,,,...g,.,,,..G...,,.,,,,g.,,.,.g,..g,.G,G,...,g.g.gG.,..gGGg.g,.G,g^~,^mg^~. *%?9?,>8,;2?=<<<:(='3>?,&:0?B@:6,<9?5:=A77777'(<5:9::":8,$$*= 6 138361 C Y 161 161 54 89 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@SQ SN:Htag LN:15 @SQ SN:Btag LN:15 B7 0 notags 1 99 5M * 0 0 ACNTA ===== B7 0 twotags 1 99 5M * 0 0 ACNTA ===== II:i:45 AA:A:d B7 0 itag 1 99 5M * 0 0 ACNTA ===== II:i:42 B7 0 itag 1 99 5M * 0 0 ACNTA ===== II:i:43 B7 0 itag 1 99 5M * 0 0 ACNTA ===== II:i:44 B7 0 Atag 1 99 5M * 0 0 ACNTA ===== AA:A:a B7 0 Atag 1 99 5M * 0 0 ACNTA ===== AA:A:b B7 0 Atag 1 99 5M * 0 0 ACNTA ===== AA:A:c B7 0 Ztag 1 99 5M * 0 0 ACNTA ===== ZZ:Z:woo B7 0 Ztag 1 99 5M * 0 0 ACNTA ===== ZZ:Z:won B7 0 Ztag 1 99 5M * 0 0 ACNTA ===== ZZ:Z:wow B7 0 Ftag 1 99 5M * 0 0 ACNTA ===== FF:f:13.6 B7 0 Htag 1 99 5M * 0 0 ACNTA ===== HH:H:1AE301 B7 0 Btag 1 99 5M * 0 0 ACNTA ===== BB:B:i42,43 Rsamtools/inst/extdata/tiny.bam0000644000175400017540000000221713556116727017655 0ustar00biocbuildbiocbuild‹ÿBC}“Mo1†]¡ mÁ"Ä™RU œš¨H=” â:rw½©…×NloÕþ{ƳŸÞÝp˜ƒßwü13׫ï'Ÿž1vusüÙ,gŸÉöÇ25ÆfRs/ή¶¿’íféÄa–ÜbÂeO™ÇJ&óœ·\g.vr©¼°Ó^!5| µ/Þq'àPrœEëðGÈÄÞßGù©Q t™º°K¦ñ 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0ustar00biocbuildbiocbuildBAII3J’3I3fJ’3f3IfÌJ’fÌfIÌ&J’Ì&ÌI&­J’&­&I­ÝJ’­Ý­IÝdJ’ÝdÝIdÊJ’dÊdIÊ~J’Ê~ÊI~¾ J’~¾ (~I¾  J’¾  ¾ I Y J’ Y  IY ˜ J’Y ˜ Y I˜ Û J’˜ Û ˜ IÛ  J’Û  Û I G J’ G  IG t J’G t G It Ð J’t Ð t IÐ „ J’Ð „ Ð I„ µ J’„ µ „ Iµ â J’µ â µ Iâ J’â â IQJ’QIQ‰J’Q‰QI‰ÄJ’‰Ä‰IÄJJ’ÄJÄIJ|J’J|JI|¸J’|¸|I¸J’¸¸Rsamtools/inst/extdata/tiny.sam0000644000175400017540000001000613556116727017671 0ustar00biocbuildbiocbuild@HD VN:1.3 SO:coordinate @SQ SN:seq1 LN:15 @SQ SN:seq2 LN:15 @SQ SN:diff_strands LN:15 @SQ SN:filter_strands LN:15 @SQ SN:min_mapq LN:1 @SQ SN:min_base_qual LN:3 @SQ SN:max_depth LN:1 @SQ SN:coll_nucs_basic LN:15 @SQ SN:coll_nucs_adv LN:15 @SQ SN:dist_all LN:1 @SQ SN:full_seq_range LN:27 @SQ SN:Biostrings_DNA_ALPHABET LN:18 @SQ SN:ext_cigar_hard LN:15 @SQ SN:ext_cigar_soft LN:15 @SQ SN:ref_skip LN:15 @SQ SN:include_deletions LN:15 @SQ SN:min_nuc_depth_mono LN:15 @SQ SN:min_nuc_depth_poly LN:15 @SQ SN:min_minor_allele_depth LN:15 @SQ SN:multi_range_single_rname LN:15 @SQ SN:seqnames_from_tinysam_c LN:15 @SQ SN:all_nuc_levels LN:15 @SQ SN:bins_5 LN:5 @SQ SN:ins1 LN:15 @SQ SN:ins3 LN:15 @SQ SN:ins_multiread LN:15 @SQ SN:ins_base_disqualifiers LN:15 @SQ SN:ins_deletion LN:15 @SQ SN:ins_refskip LN:15 B7 0 ins_refskip 1 99 1M1N1I1M * 0 0 AGC === B7 0 ins_deletion 1 99 1M1D1I1M * 0 0 AGC === B7 0 ins_base_disqualifiers 1 99 1M1I * 0 0 NT ++ B7 0 ins_multiread 1 99 1M1I1M1I1M * 0 0 TGGGT ===== B7 0 ins_multiread 1 99 1M1I1M1I1M * 0 0 TTTTT ===== B7 0 ins3 1 99 1M3I1M * 0 0 AGGGC ===== B7 0 ins1 1 99 1M1I1M * 0 0 AGC === B7 0 bins_5 1 99 5M * 0 0 ACGT= ===== B7 0 all_nuc_levels 1 99 2M1D4M * 0 0 ACGTN= ====== B7 0 seqnames_from_tinysam_c 1 99 1M * 0 0 = = B7 0 multi_range_single_rname 1 99 4M * 0 0 ACGT ==== B7 0 min_minor_allele_depth 1 99 1M * 0 0 C = B7 0 min_minor_allele_depth 1 99 1M * 0 0 A = B7 0 min_minor_allele_depth 1 99 1M * 0 0 A = B7 0 min_minor_allele_depth 1 99 1M * 0 0 A = B7 0 min_nuc_depth_poly 1 99 2M * 0 0 AC == B7 0 min_nuc_depth_poly 1 99 2M * 0 0 AG == B7 0 min_nuc_depth_mono 1 99 1M * 0 0 A = B7 0 include_deletions 1 99 1M1D1M * 0 0 AA == B7 0 ref_skip 1 99 1M1N1M * 0 0 AA == B7 0 ext_cigar_soft 1 99 1S2M2S3M * 0 0 tACttGTN ======== B7 0 ext_cigar_hard 1 99 1H2M2H3M * 0 0 ACGTN ===== B7 0 seq1 1 99 5M * 0 0 ACGTA ===== B7 16 seq2 1 99 5M * 0 0 ACNTA ===== B7 0 filter_strands 1 99 1M * 0 0 C = B7 16 filter_strands 1 99 1M * 0 0 C = B7 0 diff_strands 1 99 5M * 0 0 CCCCC ===== B7 16 diff_strands 1 99 5M * 0 0 CCCCC ===== B7 0 min_mapq 1 10 1M * 0 0 A = B7 0 min_mapq 1 20 1M * 0 0 A = B7 0 min_mapq 1 30 1M * 0 0 A = B7 0 min_base_qual 1 99 3M * 0 0 CCC !+5 B7 0 max_depth 1 99 1M * 0 0 A = B7 0 max_depth 1 99 1M * 0 0 A = B7 0 max_depth 1 99 1M * 0 0 A = B7 0 coll_nucs_basic 1 99 5M * 0 0 CCCCC ===== B7 0 coll_nucs_basic 1 99 5M * 0 0 CCCCC ===== B7 0 coll_nucs_adv 1 99 1M * 0 0 G = B7 0 coll_nucs_adv 1 99 1M * 0 0 A = B7 0 coll_nucs_adv 1 99 1M * 0 0 T = B7 0 coll_nucs_adv 1 99 1M * 0 0 G = B7 0 dist_all 1 99 1M * 0 0 A = B7 16 dist_all 1 99 1M * 0 0 C = B7 0 dist_all 1 99 1M * 0 0 G = B7 16 dist_all 1 99 1M * 0 0 T = B7 0 dist_all 1 99 1M * 0 0 C = B7 16 dist_all 1 99 1M * 0 0 G = B7 0 dist_all 1 99 1M * 0 0 T = B7 16 dist_all 1 99 1M * 0 0 A = B7 0 dist_all 1 99 1M * 0 0 G = B7 16 dist_all 1 99 1M * 0 0 T = B7 0 dist_all 1 99 1M * 0 0 A = B7 16 dist_all 1 99 1M * 0 0 C = B7 0 dist_all 1 99 1M * 0 0 T = B7 16 dist_all 1 99 1M * 0 0 A = B7 0 dist_all 1 99 1M * 0 0 C = B7 16 dist_all 1 99 1M * 0 0 G = B7 0 dist_all 1 99 1M * 0 0 A = B7 16 dist_all 1 99 1M * 0 0 C = B7 0 dist_all 1 99 1M * 0 0 G = B7 16 dist_all 1 99 1M * 0 0 T = B7 0 dist_all 1 99 1M * 0 0 A = B7 0 dist_all 2 99 1M * 0 0 A = B7 0 dist_all 1 99 2M * 0 0 AA == B7 0 dist_all 2 99 2M * 0 0 AA == B7 0 dist_all 1 99 3M * 0 0 AAA === B7 0 dist_all 2 99 3M * 0 0 AAA === B7 0 dist_all 1 99 4M * 0 0 AAAA ==== B7 0 dist_all 2 99 4M * 0 0 AAAA ==== B7 0 dist_all 1 99 5M * 0 0 AAAAA ===== B7 0 dist_all 2 99 5M * 0 0 AAAAA ===== B7 16 dist_all 1 99 1M * 0 0 A = B7 16 dist_all 2 99 1M * 0 0 A = B7 16 dist_all 1 99 2M * 0 0 AA == B7 16 dist_all 2 99 2M * 0 0 AA == B7 16 dist_all 1 99 3M * 0 0 AAA === B7 16 dist_all 2 99 3M * 0 0 AAA === B7 16 dist_all 1 99 4M * 0 0 AAAA ==== B7 16 dist_all 2 99 4M * 0 0 AAAA ==== B7 16 dist_all 1 99 5M * 0 0 AAAAA ===== B7 16 dist_all 2 99 5M * 0 0 AAAAA ===== B7 0 full_seq_range 1 99 28M * 0 0 ABCDEFGHIJKLMNOPQRSTUVWXYZ=. ============================ B7 0 Biostrings_DNA_ALPHABET 1 99 18M * 0 0 ACGTMRWSYKVHDBN-+. ================== Rsamtools/inst/extdata/tophat/0000755000175400017540000000000013556116727017506 5ustar00biocbuildbiocbuildRsamtools/inst/extdata/tophat/README0000644000175400017540000000004413556116727020364 0ustar00biocbuildbiocbuildoutput from tophat-1.0.10 test data Rsamtools/inst/extdata/tophat/accepted_hits.sam0000644000175400017540000010630713556116727023016 0ustar00biocbuildbiocbuildtest_mRNA_3_187_51 99 test_chromosome 53 255 75M = 163 0 TACTATTTGACTAGACTGGAGGCGCTTGCGACTGAGCTAGGACGTGCCACTACGGGGATGACGACTCGGACTACG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_4_191_5d 163 test_chromosome 54 255 75M = 167 0 ACTATCTGACGAGACTGGAGGCGCTTGCGACTGAGCTAGGACGTACCATTACGCGGATGACGACTAGGACTACGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:4 test_mRNA_5_197_46 97 test_chromosome 55 255 75M = 173 0 CTATCTGACTAGACTCGAGGCGCTTGCGTCTGAGCTAGGACGTGCCACTACGGGGATGACGACTAGGACTACGGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_6_182_59 99 test_chromosome 56 255 75M = 158 0 TATCTGACTAGACTGGAGGCGCTTGCGACTGAGCTAGGACGTGCCAGTACGGGGATGACGACTAGGACTACGGAC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_8_155_9 163 test_chromosome 58 255 75M = 131 0 TGTGACTAGACTGGAGGCGCTTGCGACTGAGCTAGGACGTGCCACTACGGGGATGACGACTAGGACTACGGACGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_8_197_1 99 test_chromosome 58 255 75M = 173 0 TCTGACTAGACTGGAGGCGCTTGCGACTGAGCTAGGACGTGACACTACGGGGATGGCGACTAGGACTACGGACGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_9_179_52 163 test_chromosome 59 255 75M = 155 0 CTGACTAGACTGGAGGCGCTCGCGACTGAGCTAGGACGTGCCACTACGGGGATGACGACTAGGACTACGGACGGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_11_190_1a 99 test_chromosome 61 255 75M = 166 0 GACTAGACTGGAGGCGCTTGCGACTGAGCTAGGACGTGCCACTACGGGGATGACGACTAGGACTACGGACGGACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_16_194_10 163 test_chromosome 66 255 75M = 170 0 GACTGGATGCGCTTGCGACTGAGCTAGGACGTGCCACTACGGGGATGACGACTCGGACTACGGACGGACTTAAAG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 test_mRNA_21_208_24 163 test_chromosome 71 255 75M = 184 0 GAGGCGCTTGCGACTGAGCTAGGACGTGCCACTACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_22_173_62 99 test_chromosome 72 255 75M = 149 0 AGGCGCTTGCGACTGAGCTAGGACGTGCCACTACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_23_186_42 163 test_chromosome 73 255 75M = 162 0 GGCGCTTGTGACTGAGCTAGGACGTGCCACTACGGGGATGAAGACTAGGACTACGGACGGACTTAGAGCGTCAGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_26_189_30 163 test_chromosome 76 255 75M = 165 0 GCTTGCGACTGAGCTAGGACGTGCCACTACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_28_188_11 99 test_chromosome 78 255 75M = 164 0 TTGCGACTGAGCTAGGACGTGCCACTACGGGGATGACGACTAGGACTACGAACGGACTTAGAGCGTCAGATGCAG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_28_206_1f 73 test_chromosome 78 255 75M * 0 0 TTGCGACTGAGCTAGGACGTGCCACTACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGACGCAG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_30_231_3c 161 test_chromosome 80 255 75M = 207 0 GCGACTGAGCTAGGACGTGCCACTACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_33_223_4e 73 test_chromosome 83 255 75M * 0 0 ACTGAGCTAGGACGTGCCACTACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_36_146_27 163 test_chromosome 86 255 75M = 122 0 GCGCTAGGACGTGCCACTACGGGGATGACGACTAGGACTACAGACGGACTTAGAGCGTCAGATGCAGCGACTGGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_36_218_12 99 test_chromosome 86 255 75M = 194 0 GAGCTAGGACGTGCCACTACGGGGATGACGACTAGGACTACGGACGGCCTTAGAGCGTCAGATGCAGCGACTGGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_38_199_29 99 test_chromosome 88 255 75M = 175 0 GCTAGGACGTGCCACTACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_39_219_5c 99 test_chromosome 89 255 75M = 195 0 CTAGGACGTCCCACTATGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGGCTGGACTA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 test_mRNA_41_236_55 97 test_chromosome 91 255 75M = 212 0 AGGACGTGCCACTACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGAATATT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_42_209_25 99 test_chromosome 92 255 75M = 185 0 GGACGTGCCACTACGTGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_44_193_3f 99 test_chromosome 94 255 75M = 169 0 ACGTGCCACTACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGTCTATTTAG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_44_197_35 99 test_chromosome 94 255 75M = 173 0 ACGTGCAACTACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_44_225_1e 163 test_chromosome 94 255 75M = 201 0 ACGTGCCACTACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCGGGTGCAGCGACTGGACTATTTAG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_46_195_17 137 test_chromosome 96 255 75M * 0 0 GTGCCACTACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAGGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_46_232_2f 99 test_chromosome 96 255 75M = 208 0 GTGCCACTACGGGGATGACGACTAGGACTACGGCCGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAGGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_48_207_39 73 test_chromosome 98 255 75M * 0 0 GCCCCTACGGGGATGACGACTAGGACTACGGACGGATTTAGACCGTCAGATGCAGCGACTGGACTATTTAGGACG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 test_mRNA_48_249_20 161 test_chromosome 98 255 75M = 225 0 GCCACTACGGGGATGACGACTAGGACGACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAGGACG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_50_224_2d 163 test_chromosome 100 255 75M = 200 0 CACTACGAGGATGACGTCTAGGACTACGGACGGACTTAGAGCGTCAGACGCAGCGACTGGACTATTTAGGACGAT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 test_mRNA_51_194_47 163 test_chromosome 101 255 75M = 170 0 ACTACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAGGACGATC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_51_194_49 99 test_chromosome 101 255 75M = 170 0 ACTACGGGGATGACGACTAGGCCTACGGATGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAGGACGATC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_51_237_a 99 test_chromosome 101 255 75M = 213 0 ACTACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAGGACGATC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_51_248_14 97 test_chromosome 101 255 75M = 224 0 ACTACGGGGATGACGACGAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGAACTTTTTAGGACGATC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 test_mRNA_52_261_1b 73 test_chromosome 102 255 75M * 0 0 CTACGGGAATGACGACTAGGGCTACGGAGGGACTTACAGCGTCAGATGCAGCGACTGGACTATTTAGGACGATCG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:4 test_mRNA_53_212_19 73 test_chromosome 103 255 75M * 0 0 TACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGAATATTTAGGACGATCGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_53_272_5a 137 test_chromosome 103 255 75M * 0 0 TACGGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAGGACGATCGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_56_183_56 99 test_chromosome 106 255 75M = 159 0 GGGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTGGGACGATCGGACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_57_231_8 99 test_chromosome 107 255 75M = 207 0 GGGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCACCGACTGGACTATTTAGGACGATCGGACTG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_58_218_16 163 test_chromosome 108 255 75M = 194 0 GGATGACGACTAGGACTACGGACGGACTTAGAACGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_58_220_3d 137 test_chromosome 108 255 75M * 0 0 GGATGACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_58_234_7 137 test_chromosome 108 255 75M * 0 0 GGATGACGCCTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_63_229_4c 137 test_chromosome 113 255 75M * 0 0 ACGACTAGGACTACGGACGGACTTAGAGCGTCAGATGCAGGGACTGGACTATTTAGGACGATCGGACTGAGGAGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_65_238_2e 99 test_chromosome 115 255 75M = 214 0 GACTAGGACTACGGACGGACTTAGAGCGTCAGAAGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_69_229_23 137 test_chromosome 119 255 75M * 0 0 AGGACTACGGACGGACTTATAGGGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_36_146_27 83 test_chromosome 122 255 75M = 86 0 ACTACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGTGCAGTAGGT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_72_258_4 137 test_chromosome 122 255 75M * 0 0 ACTACGGACGGACTTAGAGCGTCAGATGCAGCAACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_73_240_34 99 test_chromosome 123 255 75M = 216 0 CTACGGACGGACTTAGAGCGTCAGATGCAGCGAATGGACTATTTAGGACGCTCGGACTGAGGAGGGCAGTAGGAC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_73_259_5e 99 test_chromosome 123 255 75M = 235 0 CTACGGACGGACTTAGAGCGTCAGATGCTGCGACTGGACTATTTGGGACGATCGGACTGAGGAGGGCAGTAGGAC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_75_204_54 73 test_chromosome 125 255 75M * 0 0 ACGGACGGACTTCGAGCCTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_75_235_21 73 test_chromosome 125 255 75M * 0 0 ACGGACGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAGCACGATCGGACTGAGGAGGGCAGTAGAACGT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 test_mRNA_75_277_3b 97 test_chromosome 125 255 75M = 353 0 ACGGACGGACTTAAAGCTTCAGATGCAGCGACAGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 test_mRNA_77_256_2c 73 test_chromosome 127 255 75M * 0 0 GGACGGACTTAGAGCATCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_78_276_4b 97 test_chromosome 128 255 75M = 352 0 GACGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGGCGCTAC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_79_256_31 137 test_chromosome 129 255 75M * 0 0 ACGGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_81_228_3a 163 test_chromosome 131 255 75M = 204 0 GGACTGAGAGCGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGTAGTAGGACGCTACGTA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_81_245_4d 137 test_chromosome 131 255 75M * 0 0 GGACTTAGAGCGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGATGAGGGCAGTAGGACGCTACGTA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_8_155_9 83 test_chromosome 131 255 75M = 58 0 GGACTTCGAGCGTCAGATGCAGCGACTGTACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_82_255_2 137 test_chromosome 132 255 75M * 0 0 GACTTAGAGCGTCAGATGCAGCGACTGGACTTTTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTAT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_82_271_58 99 test_chromosome 132 255 75M = 247 0 GACTTAGAGCGTCAGTTGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTAT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_85_268_53 99 test_chromosome 135 255 75M = 244 0 TTAGTGCGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_87_250_57 163 test_chromosome 137 255 75M = 226 0 AGAGCGTCAGATGCAGAGACTGGACTATTTAGGACGATCGGACTGAGGAGTGCAGTAGGACGCTACGTATTTGGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_87_279_5f 161 test_chromosome 137 255 75M = 355 0 AGAGCGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACCGAGGAGGGCAGTAGGACGCTACGTATTTGGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_88_257_50 137 test_chromosome 138 255 75M * 0 0 GAGCGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_89_230_b 163 test_chromosome 139 255 75M = 206 0 AGCGTCAGGTGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_89_245_15 73 test_chromosome 139 255 75M * 0 0 AGCGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_89_267_32 137 test_chromosome 139 255 75M * 0 0 AGCGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGAGTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_91_256_41 73 test_chromosome 141 255 75M * 0 0 CGTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_92_250_44 99 test_chromosome 142 255 75M = 226 0 GTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 test_mRNA_92_266_43 73 test_chromosome 142 255 75M * 0 0 GTCAGATGCAGCGACTGGACTATTTAGGACGATCGGACTCAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_96_238_3 137 test_chromosome 146 255 75M * 0 0 GATGCAGCGACTGGACTATTTAGGACGATCGGACGGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGACC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 test_mRNA_97_275_26 97 test_chromosome 147 255 75M = 351 0 ATGCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_22_173_62 147 test_chromosome 149 255 75M = 72 0 GCAGCGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTAC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_103_284_2a 161 test_chromosome 153 255 75M = 360 0 CGACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_104_278_3e 161 test_chromosome 154 255 75M = 354 0 GACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTTTTTGGCGCGCGGCCCTACGGCTG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_105_266_13 137 test_chromosome 155 255 75M * 0 0 ACTGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_105_276_c 161 test_chromosome 155 255 75M = 352 0 ACTGGACTATTTAGGACGATCGGACTGAGGAAGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_9_179_52 83 test_chromosome 155 255 75M = 59 0 ACTGGACCATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_106_253_45 137 test_chromosome 156 255 75M * 0 0 CTGGACTATTTAGGTCGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_107_286_5 161 test_chromosome 157 255 75M = 362 0 TGGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGCATTTGGCGCGCGGCCCTACGGCTGAGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_6_182_59 147 test_chromosome 158 255 75M = 56 0 GGACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_56_183_56 147 test_chromosome 159 255 75M = 106 0 GACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_110_267_22 163 test_chromosome 160 255 75M = 243 0 ACTAGTTAGGGCGATCGGACTGAGGAGGGCAGTAGGACGCTACGTAGTTGGCGCGCGGCCCTACGACTGAGCGTC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:5 test_mRNA_110_271_28 73 test_chromosome 160 255 75M * 0 0 ACTATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_111_297_61 161 test_chromosome 161 255 75M = 373 0 CTATTTAGGACGATCGGACTGGGGAGGGCAGTAGGACGCTACGGATTTGGCGCGCGGCCCTACGGCTGAGCGTCG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 test_mRNA_23_186_42 83 test_chromosome 162 255 75M = 73 0 TATTTAGGACGATCGGACGGAGGAGGGCAGAAGGACGCTACGTATTTGGCGCGCGGCCCTACGACTGAGCGTCGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:4 test_mRNA_3_187_51 147 test_chromosome 163 255 75M = 53 0 ATTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_114_277_5b 161 test_chromosome 164 255 75M = 353 0 TTTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGCCTGAGCGTCGAGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_28_188_11 147 test_chromosome 164 255 75M = 78 0 TTTAGGACGATCGGACTGAGGAAGGCAGTAGGACGCTTCGTATTTGGCGCGAGGCCCTACGGCTGAGCGTCGAGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:4 test_mRNA_26_189_30 83 test_chromosome 165 255 75M = 76 0 TTAGGACGATCGGACTGAGGAGGGCAGTAGGACGGTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_33_189_4a 89 test_chromosome 165 255 75M * 0 0 TTAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACCTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGGGCT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 test_mRNA_11_190_1a 147 test_chromosome 166 255 75M = 61 0 TAGGTCGATGGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGTGGCCCTACGGCTGAGCGTCGAGCTT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:4 test_mRNA_116_271_2b 163 test_chromosome 166 255 75M = 247 0 TAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_116_295_63 161 test_chromosome 166 255 75M = 371 0 TAGGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_4_191_5d 83 test_chromosome 167 255 75M = 54 0 AGGACGATCGGACTGAGTAGGGCAGTAGGACACTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 test_mRNA_118_297_f 161 test_chromosome 168 255 75M = 373 0 GGACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_44_193_3f 147 test_chromosome 169 255 75M = 94 0 GACGATCGGACTGGGGAGAGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 test_mRNA_16_194_10 83 test_chromosome 170 255 75M = 66 0 ACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_51_194_47 83 test_chromosome 170 255 75M = 101 0 ACGATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_51_194_49 147 test_chromosome 170 255 75M = 101 0 ACGTTCGGACTGAGGAGGGCAGTAGGACGCCACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:4 test_mRNA_122_299_6 161 test_chromosome 172 255 75M = 375 0 GATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_44_197_35 147 test_chromosome 173 255 75M = 94 0 ATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGATCGTCGAGCTTGCGATAC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 test_mRNA_5_197_46 145 test_chromosome 173 255 75M = 55 0 ATCGGACGGAGGAGGGCAGTAGGACGCTACGTATTTGGCGGGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATAC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 test_mRNA_8_197_1 147 test_chromosome 173 255 75M = 58 0 ATCGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATAC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_125_280_48 97 test_chromosome 175 255 75M = 356 0 CGGACTGAGGAGGGCAGTAGGACGCTATGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGAAACGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 test_mRNA_125_293_60 161 test_chromosome 175 255 75M = 369 0 CGGACTGAGGAGGGCAGTAGGACGCTATGTATTTGGCGCGCGGCCCTACGGCTGAGCTTCGAGGTTGCGATACGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:4 test_mRNA_38_199_29 147 test_chromosome 175 255 75M = 88 0 CGGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATACGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_126_282_18 161 test_chromosome 176 255 75M = 358 0 GGACTGAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATACGCC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 test_mRNA_131_260_33 73 test_chromosome 181 255 70M100N5M * 0 0 GAGGAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATACGCCACTAT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_21_208_24 83 test_chromosome 184 255 67M100N8M = 71 0 GAGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGCCTGAGCGTCGAGCTTGCGATACGCCACTATTAC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_42_209_25 147 test_chromosome 185 255 66M100N9M = 92 0 AGGGCAGTAGGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATACGCCACTATTACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_36_218_12 147 test_chromosome 194 255 57M100N18M = 86 0 GGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_58_218_16 83 test_chromosome 194 255 57M100N18M = 108 0 GGACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_39_219_5c 147 test_chromosome 195 255 56M100N19M = 89 0 GACGCTACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCCAGCTTGCGATACGCCACTATTACTTTATTATCTT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_50_224_2d 83 test_chromosome 200 255 51M100N24M = 100 0 TACGTATTTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCTTACTCG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_44_225_1e 83 test_chromosome 201 255 50M100N25M = 94 0 ACGTATATGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCTTACTCGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_81_228_3a 83 test_chromosome 204 255 47M100N28M = 131 0 TATTTGGCGCGCGGCCCTATGGCTGAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCTTACTCGTAGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:4 XS:A:+ test_mRNA_89_230_b 83 test_chromosome 206 255 45M100N30M = 139 0 TCTGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTAACTCACTCGGACGTA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:4 XS:A:+ test_mRNA_30_231_3c 81 test_chromosome 207 255 44M100N31M = 80 0 TTGGCGCGCGGCCCTACGGCTAAGCGTCGAGCTTGCGATACGCCACTATTACTTTAATATCTTACTCGCACGTAG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:4 XS:A:+ test_mRNA_57_231_8 147 test_chromosome 207 255 44M100N31M = 107 0 TTGGCGCGCGGCCCTAGGGCTGAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCTTACTCGGACGTAG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_46_232_2f 147 test_chromosome 208 255 43M100N32M = 96 0 TGGCGCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCTTACTCGGACGTAGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_41_236_55 145 test_chromosome 212 255 39M100N36M = 91 0 GCGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCTTACTCGGACGTAGACGGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_51_237_a 147 test_chromosome 213 255 38M100N37M = 101 0 CGCGGCCCTACGGCTGAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCTTACTCGGACGTAGACGGAT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_65_238_2e 147 test_chromosome 214 255 37M100N38M = 115 0 GCGGCCCTACGGCTGCGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCTTACTCGGACGTAGACGGATC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_73_240_34 147 test_chromosome 216 255 35M100N40M = 123 0 GGCCCTACGGCTGAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCTTTCTCGGACGTAGACGGATCGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_51_248_14 145 test_chromosome 224 255 27M100N48M = 101 0 GGCTGAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCTTACTCGGACGTAGACGGAACGGCAACGGGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 XS:A:+ test_mRNA_48_249_20 81 test_chromosome 225 255 26M100N49M = 98 0 GCTGAGCGTCGAGCTTGCGATACGCCACTATTACTTTACTATCTTACTCGGACGGAGACGGATCGGCAACGGGAC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 XS:A:+ test_mRNA_87_250_57 83 test_chromosome 226 255 25M100N50M = 137 0 ATGAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCTTACTCGGACGTAGACGGATCGGCAACGGGACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_92_250_44 147 test_chromosome 226 255 25M100N50M = 142 0 CTGAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCTTACTCGGACGTAGACGGATCGGGTACGGGACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_128_252_36 153 test_chromosome 228 255 23M100N52M * 0 0 GAGCGTCGAGCTTGCGATACGCCACTATTACTTTATTATCTTACTCGGACGTAGACGGATCGGGAACGGGACTTT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:4 XS:A:+ test_mRNA_73_259_5e 147 test_chromosome 235 255 16M100N50M100N9M = 123 0 GAGCTTGCGATACGCCACTATTACTGTATTATCTTACTCGGACGTAGACGGATCGGCAACGGGACTTTTTCTACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_110_267_22 83 test_chromosome 243 255 8M100N50M100N17M = 160 0 GATACGCCACTATTACTTTATTATCTTACTCGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 XS:A:+ test_mRNA_85_268_53 147 test_chromosome 244 255 7M100N50M100N18M = 135 0 ATACGCCACTATTACTTTATTATCTTACTCGGACGTAGACGGATCGTCAACGGGACTTTTTCTACTTGAGACTGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_116_271_2b 83 test_chromosome 247 255 4M100N50M100N21M = 166 0 CGCCACTATTACTTTATTATCTTACTCGGACGTAGACAGATCGGCAACGGGACTTTTTCTACTTGAGACTGGGAT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_82_271_58 147 test_chromosome 247 255 4M100N50M100N21M = 132 0 CGCCACTATTACTTTATTATCTTACTCGGACGTAGACGCATCGGCAACGGGACTTTTTCTACTTGAGACTGGGAT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_104_274_1c 89 test_chromosome 350 255 51M100N24M * 0 0 CACTATTACTTTATTATCTTACTCGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTGGGATCGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_85_275_38 153 test_chromosome 351 255 50M100N25M * 0 0 ACTCTTACTTTATTATCTTACTCGGACGTAGACGGATCGGCAACGGGACTTTTACTACTTGAGACTGGGATCGAG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_97_275_26 145 test_chromosome 351 255 50M100N25M = 147 0 ACTATTACTTTATTATCTTAGTCGGACGTAGACGGATCGGAAACGGGACTCTTTCTACTTGAGACTGGGATCGAG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 XS:A:+ test_mRNA_105_276_c 81 test_chromosome 352 255 49M100N26M = 155 0 CTATTACTTTATTATCTTACTCGGACGTAGACGGATCGGCAACGGGGCTTTTTCTACTTGAGACTGGGATCGAGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_78_276_4b 145 test_chromosome 352 255 49M100N26M = 128 0 CTATTACTTTATTATCTTACTCGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTAGGATCGAGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_114_277_5b 81 test_chromosome 353 255 48M100N27M = 164 0 TATTACTTTATTATCTTACTCGGAGGTAGACGGAACGGCAACGGGACTTTTTCTGCTTGAGACTGGGATCGAGGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:4 XS:A:+ test_mRNA_75_277_3b 145 test_chromosome 353 255 48M100N27M = 125 0 TATTACTTTATTATCTTACTCGGACGTAGACGGATCGGCAACGGGACTTTTTCTACCTGAGACTGGGATCGAGGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_104_278_3e 17 test_chromosome 354 255 47M100N28M = 154 0 ATTACTTTATTATCTTACTCGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTGGAATCGAGGCG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_104_278_3e 81 test_chromosome 354 255 47M100N28M = 154 0 ATTACTTTATTATCTTACTCGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTGGAATCGAGGCG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 XS:A:+ test_mRNA_87_279_5f 81 test_chromosome 355 255 46M100N29M = 137 0 TTACTTTATTATCTTACTCGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 XS:A:+ test_mRNA_125_280_48 145 test_chromosome 356 255 45M100N30M = 175 0 TACTTTATTATCTTACTCTGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTGGGAGCGAGGCGGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_126_282_18 81 test_chromosome 358 255 43M100N32M = 176 0 CTTTATTATCTTACTCGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGGACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 XS:A:+ test_mRNA_103_284_2a 81 test_chromosome 360 255 41M100N34M = 153 0 TTATTATCTTACTCGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGGACTTT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 XS:A:+ test_mRNA_107_286_5 81 test_chromosome 362 255 39M100N36M = 157 0 ATTATCTTACTCGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGGACTTTTT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 XS:A:+ test_mRNA_150_290_0 89 test_chromosome 366 255 35M100N40M * 0 0 TCTTACTCGGACGTAGACGGATCGCCAACGGGACTTTTTCTACTTGAGACTGAGACCGAGGCGGACTTTTTAGGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 XS:A:+ test_mRNA_125_293_60 81 test_chromosome 369 255 32M100N43M = 175 0 TACTCGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGGACTTTTTAGGACGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 XS:A:+ test_mRNA_172_294_4f 153 test_chromosome 370 255 31M100N44M * 0 0 ACTCGGACGTAGACGGGTCGGCAGCGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGGACGTTTTAGGACGGG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 XS:A:+ test_mRNA_116_295_63 81 test_chromosome 371 255 30M100N45M = 166 0 CTCGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGGACTTTTTAGGACGGGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 XS:A:+ test_mRNA_111_297_61 17 test_chromosome 373 255 28M100N47M = 161 0 CGGACGTAGACGGATCCGCAACGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGGACTTTTTAGGACGGGACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_111_297_61 81 test_chromosome 373 255 28M100N47M = 161 0 CGGACGTAGACGGATCCGCAACGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGGACTTTTTAGGACGGGACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 XS:A:+ test_mRNA_118_297_f 17 test_chromosome 373 255 28M100N47M = 168 0 CGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGGACTTTTTAGGACGGGACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:0 XS:A:+ test_mRNA_118_297_f 81 test_chromosome 373 255 28M100N47M = 168 0 CGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGGACTTTTTAGGACGGGACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_151_297_1d 153 test_chromosome 373 255 28M100N47M * 0 0 CGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGGACATTTTAGGACGGGACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:3 XS:A:+ test_mRNA_151_297_1d 25 test_chromosome 373 255 28M100N47M * 0 0 CGGACGTAGACGGATCGGCAACGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGGACATTTTAGGACGGGACT IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ test_mRNA_122_299_6 81 test_chromosome 375 255 26M100N49M = 172 0 GACGTAGACGGAGCGGCAACGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGGACTTTTTAGGACGGGACTTG IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:2 XS:A:+ test_mRNA_145_300_37 89 test_chromosome 376 255 25M100N50M * 0 0 ACGTAGACGGATCGGAAACGGGACTTTTTCTACTTGAGACTGGGATCGAGGCGGACTTTTTAGGACGGGACTTGC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII NM:i:1 XS:A:+ Rsamtools/inst/extdata/tophat/coverage.wig0000644000175400017540000001043513556116727022014 0ustar00biocbuildbiocbuildtrack type=bedGraph name="TopHat - read coverage" test_chromosome 0 52 0 test_chromosome 52 53 1 test_chromosome 53 54 2 test_chromosome 54 55 3 test_chromosome 55 57 4 test_chromosome 57 58 6 test_chromosome 58 60 7 test_chromosome 60 65 8 test_chromosome 65 70 9 test_chromosome 70 71 10 test_chromosome 71 72 11 test_chromosome 72 75 12 test_chromosome 75 77 13 test_chromosome 77 79 15 test_chromosome 79 82 16 test_chromosome 82 85 17 test_chromosome 85 87 19 test_chromosome 87 88 20 test_chromosome 88 90 21 test_chromosome 90 91 22 test_chromosome 91 93 23 test_chromosome 93 95 26 test_chromosome 95 97 28 test_chromosome 97 99 30 test_chromosome 99 100 31 test_chromosome 100 101 35 test_chromosome 101 102 36 test_chromosome 102 105 38 test_chromosome 105 106 39 test_chromosome 106 107 40 test_chromosome 107 112 43 test_chromosome 112 114 44 test_chromosome 114 118 45 test_chromosome 118 121 46 test_chromosome 121 122 48 test_chromosome 122 124 50 test_chromosome 124 126 53 test_chromosome 126 129 54 test_chromosome 129 130 53 test_chromosome 130 131 55 test_chromosome 131 132 57 test_chromosome 132 133 55 test_chromosome 133 134 54 test_chromosome 134 135 55 test_chromosome 135 136 54 test_chromosome 136 137 56 test_chromosome 137 138 57 test_chromosome 138 141 60 test_chromosome 141 147 62 test_chromosome 147 148 61 test_chromosome 148 150 62 test_chromosome 150 152 61 test_chromosome 152 153 60 test_chromosome 153 154 61 test_chromosome 154 155 63 test_chromosome 155 156 64 test_chromosome 156 158 65 test_chromosome 158 159 66 test_chromosome 159 160 68 test_chromosome 160 161 67 test_chromosome 161 163 68 test_chromosome 163 164 69 test_chromosome 164 165 71 test_chromosome 165 167 73 test_chromosome 167 168 74 test_chromosome 168 169 72 test_chromosome 169 170 75 test_chromosome 170 171 73 test_chromosome 171 172 74 test_chromosome 172 174 75 test_chromosome 174 175 77 test_chromosome 175 176 74 test_chromosome 176 177 73 test_chromosome 177 181 71 test_chromosome 181 182 70 test_chromosome 182 183 67 test_chromosome 183 184 68 test_chromosome 184 187 69 test_chromosome 187 189 68 test_chromosome 189 193 67 test_chromosome 193 194 68 test_chromosome 194 196 69 test_chromosome 196 197 67 test_chromosome 197 199 65 test_chromosome 199 200 63 test_chromosome 200 201 64 test_chromosome 201 202 63 test_chromosome 202 205 62 test_chromosome 205 207 60 test_chromosome 207 209 61 test_chromosome 209 211 60 test_chromosome 211 213 59 test_chromosome 213 216 57 test_chromosome 216 220 55 test_chromosome 220 221 54 test_chromosome 221 224 53 test_chromosome 224 225 54 test_chromosome 225 228 56 test_chromosome 228 229 55 test_chromosome 229 230 52 test_chromosome 230 231 51 test_chromosome 231 232 50 test_chromosome 232 233 49 test_chromosome 233 234 48 test_chromosome 234 235 47 test_chromosome 235 236 46 test_chromosome 236 237 45 test_chromosome 237 238 44 test_chromosome 238 239 42 test_chromosome 239 240 40 test_chromosome 240 241 37 test_chromosome 241 244 36 test_chromosome 244 246 33 test_chromosome 246 247 34 test_chromosome 247 249 31 test_chromosome 249 250 28 test_chromosome 250 349 0 test_chromosome 349 350 1 test_chromosome 350 351 30 test_chromosome 351 352 32 test_chromosome 352 353 34 test_chromosome 353 354 35 test_chromosome 354 357 36 test_chromosome 357 358 37 test_chromosome 358 361 36 test_chromosome 361 365 37 test_chromosome 365 368 38 test_chromosome 368 370 37 test_chromosome 370 372 38 test_chromosome 372 378 41 test_chromosome 378 380 40 test_chromosome 380 381 39 test_chromosome 381 382 37 test_chromosome 382 386 36 test_chromosome 386 387 35 test_chromosome 387 388 34 test_chromosome 388 390 33 test_chromosome 390 398 32 test_chromosome 398 399 31 test_chromosome 399 400 30 test_chromosome 400 402 1 test_chromosome 402 500 0 test_chromosome 500 509 27 test_chromosome 509 517 26 test_chromosome 517 518 25 test_chromosome 518 521 24 test_chromosome 521 524 22 test_chromosome 524 525 21 test_chromosome 525 526 19 test_chromosome 526 527 17 test_chromosome 527 528 15 test_chromosome 528 529 14 test_chromosome 529 530 13 test_chromosome 530 532 12 test_chromosome 532 534 11 test_chromosome 534 536 10 test_chromosome 536 540 9 test_chromosome 540 543 8 test_chromosome 543 544 7 test_chromosome 544 545 6 test_chromosome 545 547 5 test_chromosome 547 549 2 test_chromosome 549 549 1 Rsamtools/inst/extdata/tophat/junctions.bed0000644000175400017540000000030413556116727022173 0ustar00biocbuildbiocbuildtrack name=junctions description="TopHat junctions" test_chromosome 180 402 JUNC00000001 27 + 180 402 255,0,0 2 70,52 0,170 test_chromosome 349 550 JUNC00000002 27 + 349 550 255,0,0 2 51,50 0,151 Rsamtools/inst/scripts/0000755000175400017540000000000013556116727016244 5ustar00biocbuildbiocbuildRsamtools/inst/scripts/BamViews-1000g.R0000644000175400017540000000565013556116727020637 0ustar00biocbuildbiocbuildsetwd("/home/mtmorgan/proj/a/1000g/slx_maq_09_index_files") ftpBase = "ftp://ftp-trace.ncbi.nih.gov/1000genomes/ftp/pilot_data/data/" if (length(list.files(pattern=".*bai")) == 0) { library(RCurl) indivs <- strsplit(getURL(ftpBase, ftplistonly=TRUE), "\n")[[1]] aln <- paste(ftpBase, indivs, "/alignment/", sep="") urls <- strsplit(getURL(aln, dirlistonly=TRUE), "\n") urls0 <- urls[sapply(urls, length) != 0] fls0 <- unlist(unname(urls0)) fls1 <- fls0[grepl("bai$", fls0)] fls <- fls1[sapply(strsplit(fls, "\\."), length)==7] m <- t(as.data.frame(strsplit(fls, "\\.")))[,1:5] dimnames(m) <- list(NULL, c("Individual", "Platform", "Alignment", "SRA", "Date")) df <- cbind(as.data.frame(m), File=fls) xtabs(~Platform+Alignment+Date, df) ## > xtabs(~Platform+Alignment, df) ## Alignment ## Platform corona maq MOSAIK ssaha ## 454 0 0 9 14 ## SLX 0 25 11 0 ## SOLID 7 0 0 0 urls1 <- Filter(function(x) length(x) != 0, lapply(urls, function(x) x[grepl("SLX.maq.*2009_08.*bai$", x)])) slxMaq09 <- mapply(paste, names(urls1), urls1, sep="", USE.NAMES=FALSE) mapply(download.file, slxMaq09, basename(slxMaq09), MoreArgs=list(method="curl")) } indexFiles <- list.files(pattern="bai$") slxMaq09 <- paste(ftpBase, sub("^([^\\.]+).*$", "\\1", indexFiles), "/alignment/", sub("\\.bai$", "", indexFiles), sep="") ## headers <- scanBamHeader(fls) # nothing useful here :( ## Some regions of interest: genes involved in caffeine metabolism library(KEGG.db) library(org.Hs.eg.db) library(BSgenome.Hsapiens.UCSC.hg18) library(biomaRt) library(GenomicFeatures) kid <- revmap(KEGGPATHID2NAME)[["Caffeine metabolism"]] egid <- KEGGPATHID2EXTID[[sprintf("hsa%s", kid)]] mart <- useMart("ensembl", "hsapiens_gene_ensembl") ensid <- getBM(c("ensembl_transcript_id"), filters="entrezgene", values=egid, mart=mart)[[1]] txdb <- makeTxDbFromBiomart(transcript_ids=ensid) saveFeatures(txdb, "caffeine-txdb.sqlite") egid <- egid[egid != "9"] # multiple locations tbl <- merge(toTable(org.Hs.egCHRLOC[egid]), toTable(org.Hs.egCHRLOCEND[egid])) rng <- with(tbl, { lvls <- sprintf("chr%s", sort(as.integer(unique(Chromosome)))) rng0 <- GRanges(Chromosome, IRanges(start=abs(start_location), end=abs(end_location)), strand=ifelse(start_location>=0, "+", "-"), EntrezId=gene_id, Genename=mappedRkeys(org.Hs.egGENENAME[gene_id])) metadata(rng0) <- list(Genome="hg18?") rng0 }) library(GenomicAlignments) library(multicore) bv <- BamViews(fls, sub(".bai", "", indexFiles), bamRanges=GRanges(seqnames=seqnames(rng), ranges=ranges(rng), EntrezId=mcols(rng)[["EntrezId"]])) gapped <- readGAlignments(bv[1:2,1:3]) Rsamtools/inst/scripts/features.R0000644000175400017540000000175013556116727020210 0ustar00biocbuildbiocbuildfl0 = "ftp://ftp-trace.ncbi.nih.gov/1000genomes/ftp/pilot_data/data/NA19240/alignment/NA19240.chrom6.SLX.maq.SRP000032.2009_07.bam" dir <- getwd() fl <- file.path(dir, "NA19240.chrom6.SLX.maq.SRP000032.2009_07.bam") stopifnot(file.exists(paste(fl, "bai", sep="."))) # require local index library(GenomicFeatures) library(IRanges) data(geneHuman) transcripts <- transcripts(geneHuman, proximal=300) library(Rsamtools) ## remote access chr6a0 <- ranges(transcripts)[["chr6"]][1:2] p10 <- ScanBamParam(which=IRangesList(`6`=chr6a0)) (cnt0 <- countBam(fl0, fl0, param=p10)) sum(cnt0$records) system.time(res0 <- scanBam(fl0, fl0, param=p10)) ## local if (file.exists(fl)) { cnt <- countBam(fl, param=p10); sum(cnt$records) system.time(res0 <- scanBam(fl, param=p10)) ## larger, local chr6a <- ranges(transcripts)[["chr6"]][1:50] p1 <- ScanBamParam(which=IRangesList(`6`=chr6a)) sum(countBam(fl, param=p1)$records) system.time(res <- scanBam(fl, param=p1)) # about 30s } Rsamtools/inst/scripts/remote_test.R0000644000175400017540000000137513556116727020727 0ustar00biocbuildbiocbuildsuppressMessages(library(Rsamtools)) fl = "ftp://ftp-trace.ncbi.nih.gov/1000genomes/ftp/pilot_data/data/NA19240/alignment/NA19240.chrom6.SLX.maq.SRP000032.2009_07.bam" p1 <- ScanBamParam(which=IRangesList("6"=IRanges(10000, 11000))) res <- scanBam(fl, param=p1)[[1]] res[["seq"]] fl = "ftp://ftp-trace.ncbi.nih.gov/1000genomes/ftp/pilot_data/data/NA19240/alignment/NA19240.chrom6.454.ssaha.SRP000032.2009_07.bam" p1 <- ScanBamParam(which=IRangesList("6"=IRanges(100000, 110000))) res <- scanBam(fl, param=p1)[[1]] res[["seq"]] header <- scanBamHeader(fl) txt <- header[[1]][[2]] table(names(txt)) txt[names(txt) == "@HD"] # 'header' txt[names(txt) == "@RG"][1:5] # 'read group' txt[names(txt) == "@SQ"][1:5] # 'sequence group' Rsamtools/inst/scripts/update-samtools.sh0000755000175400017540000000174513556116727021733 0ustar00biocbuildbiocbuild#! /bin/sh repos0="git://github.com/samtools/samtools.git" repos1="git://github.com/samtools/tabix.git" wd=`pwd` dest="../inst/extdata" if test ! -d $dest; then echo "directory does not exist: '$dest'" exit 1 fi dest0="../src/samtools/" dest1="../src/samtools/bcftools/" if test ! -d $dest0; then echo "directory does not exist: '$dest0'" exit 1 fi if test ! -d $dest1; then echo "directory does not exist: '$dest1'" exit 1 fi if test ! -d $dest2; then echo "directory does not exist: '$dest2'" exit 1 fi unpack=`mktemp -d -u` ## unsafe: get but don't create temp dir name git clone $repos0 $unpack for f in `ls $dest0`; do echo "updating file $f" cp $unpack/$f $dest0/$f done for f in `ls $dest1`; do echo "updating file $f" cp $unpack/bcftools/$f $dest1/$f done dest2="../src/tabix/" unpack1=`mktemp -d -u` ## unsafe: get but don't create temp dir name git clone $repos1 $unpack1 for f in `ls $dest2`; do echo "updating file $f" cp $unpack1/$f $dest2/$f done rm -rf $unpack Rsamtools/inst/unitTests/0000755000175400017540000000000013620347571016552 5ustar00biocbuildbiocbuildRsamtools/inst/unitTests/cases/0000755000175400017540000000000013620620450017636 5ustar00biocbuildbiocbuildRsamtools/inst/unitTests/cases/RNEXT.bam0000644000175400017540000000032713620620450021221 0ustar00biocbuildbiocbuild‹ÿBC\srôeÔe``pðpá ó³2Ô3æ ö·JÎÏ/JÉÌK,Iårä ö³JÎ(2áôñ³2200àbj`b ÃväQF‹ÿBC]Óg€€d fNöbdXÈÁ ›¥‹ €”†‹ÀÐG’†h diÉGÕÒØØ@¼c - ¡%”æ0¸#-ÌkȰÌ‹ÿBCRsamtools/inst/unitTests/cases/ex1.sam.gz0000644000175400017540000033763613556116727021515 0ustar00biocbuildbiocbuild‹4!M¬\ÉŽãȵ]³¿Ã©”’Rcž¨¶eÁN/^7`´Þ:Woñ–†ÿð¹‚!ŠCÁ¬JŠRvA§oÜáÜ!â/ü³úãwÿïÿû«þçwÏ”i~ùËðOŸiûË_Í·rÌKï´×Nxոʈ*þ;V9W ý[õQ5øs¿Ý·¯Ç××ýq¿=_Ûí†;}òxà >þªÚé†'•Þû6˜ê·¿ûÿ÷ÌV·áßöûoxmªÿýg|ùGC¿­þÁèÝ/»ý¡ä·VÞ0÷B[Ϙ0ŠˆQ W>2ˆ Ý´4ƒïÚVüð­>ù)B­W²o-½õ@)¤W¦bÂ$|jŠoÝýž‹ÐÃHˆ!àèÂ)ˆûCíÂ×-1óÜ:¯¬ñ®Ñ#@]i‘-òß#^/á{<èV/‡ 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52 35 ..$,$,,,G..,...,.,..-2GC...,.,.-2GC,,-2gc,....,.^s. &%><<<%%(=3'/@5>:2&4.<;;(@;=A,;:+.= Rsamtools/inst/unitTests/cases/plp_refskip.bam0000644000175400017540000000036613556116727022661 0ustar00biocbuildbiocbuild‹ÿBCNsrôeTb``pðpá ó³2Ô3ærä ö³*N-4äôñ³22.F *V ‰34´È10¥ÿá;‹ÿBCŠ;É€"ÉžBÌ ž Þ@ö(‰;™Ç›ZZ™XYšY™Y[™X2010l^ÍÄФ5DZœš$Z[ZZ<:5T0E¤Qœ%áKJK‰£|Ýœ… =ý|B< œ= — ôÍ‹ÿBCRsamtools/inst/unitTests/cases/plp_refskip.bam.bai0000644000175400017540000000014013556116727023401 0ustar00biocbuildbiocbuildBAIIOöJ’OöORsamtools/inst/unitTests/test_BamFile.R0000644000175400017540000003243313620347571021240 0ustar00biocbuildbiocbuildfl <- system.file("extdata", "ex1.bam", package="Rsamtools") test_BamFile_guessIndex <- function() { .BamFile_guessIndex <- Rsamtools:::.BamFile_guessIndex bam1 <- tempfile(fileext = ".bam") idx1 <- paste0(bam1, ".bai") # foo.bam.bai file.create(idx1) bam2 <- tempfile(fileext = ".bam") idx2 <- sub(".bam$", ".bai", bam2) # foo.bai file.create(idx2) bam3 <- tempfile(fileext = ".bam") # no index fls <- c(bam1, bam2, bam3) target <- c(idx1, idx2, NA_character_) current <- .BamFile_guessIndex(fls) checkIdentical(target, current) checkIdentical(character(), .BamFile_guessIndex(character())) checkIdentical(character(), .BamFile_guessIndex()) } test_BamFile_openclose <- function() { .normalizePath <- Rsamtools:::.normalizePath bf <- open(BamFile(fl)) checkTrue(isOpen(bf)) checkIdentical(.normalizePath(fl), path(bf)) checkIdentical(sprintf("%s.bai", .normalizePath(fl)), index(bf)) close(bf) checkTrue(!isOpen(bf)) checkException(close(bf), silent=TRUE) bf <- open(bf) # open a closed BamFile checkTrue(isOpen(bf)) bf1 <- open(bf) # open (clone?) an open BamFile checkTrue(isOpen(bf1)) checkTrue(identical(bf$.extptr, bf1$.extptr)) ## no extension necessary dir.create(fl0 <- tempfile()) body <- file.path(fl0, "body") index <- file.path(fl0, "index") file.copy(fl, body) file.copy(paste0(fl, ".bai"), index) open(bf2 <- BamFile(body, index)) checkTrue(isOpen(bf2)) } test_BamFile_isIncomplete <- function() { bf <- BamFile(fl, yieldSize=3000) checkIdentical(FALSE, isIncomplete(bf)) open(bf) checkIdentical(TRUE, isIncomplete(bf)) checkIdentical(3000L, length(scanBam(bf)[[1]][[1]])) checkIdentical(TRUE, isIncomplete(bf)) checkIdentical(307L, length(scanBam(bf)[[1]][[1]])) checkIdentical(FALSE, isIncomplete(bf)) close(bf) checkIdentical(FALSE, isIncomplete(bf)) } test_BamFile_corrupt_index <- function() { fl <- system.file("extdata", "ex1.bam", package="Rsamtools") idx <- system.file("unitTests", "cases", "ex1_zero_index.bam.bai") bf <- BamFile(fl, idx) checkException(suppressWarnings(open(bf)), silent=TRUE) } test_BamFile_yield <- function() { bf <- open(BamFile(fl, yieldSize=1000)) it <- integer() while(length(res <- scanBam(bf)[[1]][[1]])) it <- append(it, length(res)) close(bf) exp <- c(1000L, 1000L, 1000L, 307L) checkIdentical(exp, it) bf <- open(BamFile(fl, yieldSize=500)) which <- GenomicRanges::tileGenome(seqlengths(bf), tilewidth=500, cut.last.tile.in.chrom=TRUE) param <- ScanBamParam(what="rname", which=which) it <- integer() fun <- function(bf, param) { res <- unlist(scanBam(bf, param=param), use.names=FALSE, recursive=FALSE) sum(unlist(lapply(res, as.integer))) } while (res <- fun(bf, param)) it <- append(it, res) close(bf) checkIdentical(6L, length(it)) ## over-count, since reads overlap more than one range checkIdentical(5472L, sum(it)) } test_BamFileList_constructor <- function() { checkTrue(validObject(res <- BamFileList(fl))) checkIdentical(fl, path(res[[1]])) checkIdentical(sprintf("%s.bai", fl), index(res[[1]])) checkTrue(validObject(res <- BamFileList(fl, fl))) checkIdentical(fl, path(res[[1]])) checkIdentical(fl, index(res[[1]])) ## old-style index=character() checkTrue(validObject(res <- BamFileList(fl, index=character()))) checkIdentical(fl, path(res[[1]])) checkIdentical(character(0), index(res[[1]], asNA=FALSE)) ## vector of files fl <- c(fl, fl) checkTrue(validObject(res <- BamFileList(fl))) checkIdentical(fl, unname(path(res))) checkIdentical(sprintf("%s.bai", fl), unname(sapply(res, index))) checkTrue(validObject(res <- BamFileList(fl, fl))) checkIdentical(fl, unname(path(res))) checkIdentical(fl, unname(sapply(res, index))) ## old-style index=character() checkTrue(validObject(res <- BamFileList(fl, index=character()))) checkIdentical(fl, unname(path(res))) checkIdentical(setNames(rep(NA_character_, 2), basename(fl)), index(res)) } test_BamFileList_yield <- function() { bfl <- unname(BamFileList(c(fl, fl), yieldSize=100)) checkIdentical(c(100L, 100L), sapply(bfl, yieldSize)) bfl <- unname(BamFileList(c(fl, fl))) checkIdentical(c(NA_integer_, NA_integer_), sapply(bfl, yieldSize)) ## yieldSize, even implicit on BamFile wins out bfl <- BamFileList(BamFile(fl, yieldSize=10), BamFile(fl, yieldSize=20), yieldSize=100) checkIdentical(c(10L, 20L), sapply(bfl, yieldSize)) bfl <- BamFileList(BamFile(fl), BamFile(fl), yieldSize=100) checkIdentical(c(NA_integer_, NA_integer_), sapply(bfl, yieldSize)) } test_BamFile_obeyQname <- function() { srt <- sortBam(fl, tempfile(), byQname=TRUE) bf <- BamFile(srt, character(0), yieldSize=1, obeyQname=TRUE) scn <- scanBam(bf) checkTrue(length(scn[[1]]$qname) == 2) checkTrue(length(unique(scn[[1]]$qname)) == 1) bf <- BamFile(srt, character(0), yieldSize=2, obeyQname=TRUE) scn <- scanBam(bf) checkTrue(length(scn[[1]]$qname) == 4) checkTrue(length(unique(scn[[1]]$qname)) == 2) ## yieldSize is number of unique qnames ys <- 1000 bf <- BamFile(srt, character(0), yieldSize=ys, obeyQname=TRUE) scn <- scanBam(bf) checkTrue(length(unique(scn[[1]]$qname)) == ys) ## yieldSize with 'while' bf <- open(BamFile(srt, character(0), yieldSize=500, obeyQname=TRUE)) it <- integer() while (length(res <- scanBam(bf)[[1]]$qname)) it <- append(it, length(res)) close(bf) checkIdentical(c(974L, 966L, 977L, 390L), it) } test_BamFile_asMates_all <- function() { fl <- system.file("extdata", "ex1.bam", package="Rsamtools") scn <- scanBam(fl)[[1]] scnm <- scanBam(BamFile(fl, asMates=TRUE))[[1]] ## qname checkTrue(all(scn$qname %in% scnm$qname)) matenames <- scnm$qname[scnm$mate_status == "mated"] ## non-mates off last max1 <- max(which(scnm$mate_status == "mated")) min0 <- min(which(scnm$mate_status != "mated")) checkTrue(max1 < min0) ## yieldSize - subset flag <- scanBamFlag(isPaired=TRUE, hasUnmappedMate=FALSE, isUnmappedQuery=FALSE) param=ScanBamParam(flag=flag, what="qname") bf <- BamFile(fl, asMates=FALSE, yieldSize=5) bfm <- BamFile(fl, asMates=TRUE, yieldSize=5) scn <- scanBam(bf, param=param)[[1]] ## first 5 records scnm <- scanBam(bfm, param=param)[[1]] ## first 5 mates checkTrue(length(scn$qname) == 5) checkTrue(length(scnm$qname) == 10) ## yieldSize - all records scnm1 <- scanBam(BamFile(fl, asMates=TRUE))[[1]] scnm2 <- scanBam(BamFile(fl, asMates=TRUE, yieldSize=2000))[[1]] checkTrue(all(scnm1$qname %in% scnm2$qname)) checkTrue(all(scnm1$mate_status == scnm2$mate_status)) checkTrue(all(scnm1$groupid == scnm2$groupid)) ## yieldSize and which bf <- open(BamFile(fl, yieldSize=500)) which <- GenomicRanges::tileGenome(seqlengths(bf), tilewidth=500, cut.last.tile.in.chrom=TRUE) param <- ScanBamParam(what="rname", which=which) it <- integer() fun <- function(bf, param) { res <- unlist(scanBam(bf, param=param), use.names=FALSE, recursive=FALSE) sum(unlist(lapply(res, as.integer))) } while (res <- fun(bf, param)) it <- append(it, res) close(bf) expected <- c(964L, 570L, 1206L, 1418L, 1194L, 120L) checkIdentical(expected, it) } test_BamFile_asMates_range <- function() { fl <- system.file("extdata", "ex1.bam", package="Rsamtools") which <- GRanges("seq1", IRanges(100, width=5)) param <- ScanBamParam(which=which, what=scanBamWhat()) scn <- scanBam(fl, param=param)[[1]] scnm <- scanBam(BamFile(fl, asMates=TRUE), param=param)[[1]] ## qname checkTrue(all(scn$qname %in% scnm$qname)) matenames <- scnm$qname[scnm$mate_status == "mated"] checkTrue(length(scnm$qname) == length(scnm$groupid)) ## non-mates off last max1 <- max(which(scnm$mate_status == "mated")) min0 <- min(which(scnm$mate_status != "mated")) checkTrue(max1 < min0) ## range - subset flag <- scanBamFlag(isPaired=TRUE, hasUnmappedMate=FALSE, isUnmappedQuery=FALSE) param=ScanBamParam(which=which, flag=flag, what=scanBamWhat()) bf <- BamFile(fl, asMates=FALSE) bfm <- BamFile(fl, asMates=TRUE) scn <- scanBam(bf, param=param)[[1]] ## all records in range scnm <- scanBam(bfm, param=param)[[1]] ## mates all records in range checkTrue(length(scn$qname) == 8) checkTrue(length(scnm$qname) == 16) checkTrue(sum(scnm$mate_status == "mated") == 16) ## range - all records which <- GRanges(c("seq1", "seq2"), IRanges(c(0, 0), c(3000, 3000))) param <- ScanBamParam(which=which, what=scanBamWhat()) scnm1 <- scanBam(bfm)[[1]] ## all records no param scnm2<- scanBam(bfm, param=param) ## all records w/ param range2A <- scnm2[[1]] range2B <- scnm2[[2]] len_range <- length(range2A$qname) + length(range2B$qname) checkTrue(len_range == length(scnm1$qname)) mates_range <- sum(range2A$mate_status == "mated", range2B$mate_status == "mated") checkTrue(mates_range == sum(scnm1$mate_status == "mated")) mates_partition <- length(range2A$.partition) + length(range2B$.partition) checkTrue(mates_partition == length(scnm1$.partition)) } test_BamFile_qname_prefix_suffix <- function() { fl <- system.file("extdata", "ex1.bam", package="Rsamtools") checkException(BamFile(fl, qnamePrefixEnd="/:", asMates=TRUE), silent=TRUE) checkException(BamFile(fl, qnameSuffixStart="/:", asMates=TRUE), silent=TRUE) ## no-op target <- c("EAS54_61:4:143:69:578", "EAS54_61:4:143:69:578") bfm <- BamFile(fl, asMates=TRUE, qnamePrefixEnd="*") scn_noop_1 <- scanBam(bfm, param=ScanBamParam(what="qname")) qnames_noop_1 <- scn_noop_1[[1]]$qname[1:2] checkIdentical(qnames_noop_1, target) bfm <- BamFile(fl, asMates=TRUE, qnameSuffixStart="*") scn_noop_2 <- scanBam(bfm, param=ScanBamParam(what="qname")) qnames_noop_2 <- scn_noop_2[[1]]$qname[1:2] checkIdentical(qnames_noop_2, target) qnamePrefixEnd(bfm) <- "*" scn_noop_3 <- scanBam(bfm, param=ScanBamParam(what="qname")) qnames_noop_3 <- scn_noop_3[[1]]$qname[1:2] checkIdentical(qnames_noop_3, target) ## setter bf <- BamFile(fl, asMates=TRUE) checkIdentical(qnamePrefixEnd(bf), NA_character_) qnamePrefixEnd(bf) <- "." checkIdentical(qnamePrefixEnd(bf), ".") qnamePrefixEnd(bf) <- NA_character_; checkIdentical(qnamePrefixEnd(bf), NA_character_) ## all bfm <- BamFile(fl, asMates=TRUE, qnamePrefixEnd="_") scn <- scanBam(bfm, param=ScanBamParam(what="qname")) qnames <- scn[[1]]$qname[1:2] target <- c("61:4:143:69:578", "61:4:143:69:578") checkIdentical(qnames, target) bfm <- BamFile(fl, asMates=TRUE, qnameSuffixStart=":") scn <- scanBam(bfm, param=ScanBamParam(what="qname")) qnames <- scn[[1]]$qname[1:2] target <- c("EAS54_61:4:143:69", "EAS54_61:4:143:69") checkIdentical(qnames, target) ## ranges bfm <- BamFile(fl, asMates=TRUE) which <- GRanges("seq1", IRanges(100, 110)) param <- ScanBamParam(which=which, what=scanBamWhat()) target0 <- scanBam(bfm, param=param)[[1]]$qname bfm <- BamFile(fl, asMates=TRUE, qnamePrefixEnd="_") param <- ScanBamParam(which=which, what="qname") qnames <- scanBam(bfm, param=param)[[1]]$qname target <- sub(".*_(.*)", "\\1", target0) checkTrue(setequal(qnames, target)) bfm <- BamFile(fl, asMates=TRUE, qnameSuffixStart="_") param <- ScanBamParam(which=which, what="qname") qnames <- scanBam(bfm, param=param)[[1]]$qname target <- sub("(.*)_.*", "\\1", target0) checkTrue(setequal(qnames, target)) bfm <- BamFile(fl, asMates=TRUE, qnameSuffixStart="*") param <- ScanBamParam(which=which, what="qname") qnames1 <- scanBam(bfm, param=param)[[1]]$qname bfm <- BamFile(fl, asMates=TRUE) qnames2 <- scanBam(bfm, param=param)[[1]]$qname checkIdentical(qnames1, qnames2) } test_BamFile_asMates_RNEXT <- function() { ## see https://github.com/Bioconductor/Rsamtools/issues/16 fl <- system.file(package="Rsamtools", "unitTests", "cases", "RNEXT.bam") res <- scanBam(BamFile(fl, asMates = TRUE)) df <- Rsamtools:::.as.data.frame_list_of_lists(res) checkIdentical(df$qname, c("r1", "r1", "r2", "r3")) ## RNAME == '*' -- don't trust rname, pos (hence strand, qwidth), cigar) checkIdentical(df$rname, factor(c("chr4", "chr4", NA, "chr4"))) checkIdentical( df$strand, factor(c("+", "-", NA, "-"), levels = c("+", "-", "*")) ) checkIdentical(df$pos, c(100L, 155L, NA, 155L)) checkIdentical(df$qwidth, c(5L, 5L, NA, 5L)) checkIdentical(df$mapq, c(99L, 99L, NA, 99L)) checkIdentical(df$cigar, c("5M", "5M", NA, "5M")) ## RNEXT == '*' -- don't trust mrnm, mpos; don't mate checkIdentical(df$mrnm, factor(c("chr4", NA, "chr4", NA))) checkIdentical(df$mpos, c(155L, NA, 200L, NA)) checkIdentical(as.character(df$mate_status), rep("unmated", 4)) } Rsamtools/inst/unitTests/test_BamViews.R0000644000175400017540000001330113556116727021454 0ustar00biocbuildbiocbuild.BamViews_ok <- function(v, dim=c(0,0), bamRanges=GRanges(), bamSamples=DataFrame(row.names=character()), bamExperiment=list()) { checkTrue(validObject(v)) checkEquals(dim, dim(v)) checkIdentical(bamRanges, bamRanges(v)) checkIdentical(bamSamples, bamSamples(v)) checkIdentical(bamExperiment, bamExperiment(v)) } test_BamViews_constructors <- function() { .BamViews_ok(BamViews(), c(0, 0)) ni <- 10L; nj <- 5L fls <- rep("foo", nj) gr <- GRanges(rep(c("chr1", "chr2"), each=5), IRanges(c(1:5, 101:105), c(11:15, 111:115)), Values=rev(seq_len(ni))) sd0 <- DataFrame(row.names=make.unique(basename(fls))) sd1 <-DataFrame(Score=seq_len(nj), row.names=make.unique(basename(fls))) .BamViews_ok(BamViews(fls), dim=c(0, nj), bamSamples=sd0) .BamViews_ok(BamViews(fls, bamRanges=gr), dim=c(ni, nj), bamRanges=gr, bamSamples=sd0) .BamViews_ok(BamViews(fls, bamRanges=gr, bamSamples=sd0), dim=c(ni, nj), bamRanges=gr, bamSamples=sd0) .BamViews_ok(BamViews(fls, bamRanges=gr, bamSamples=sd1), dim=c(ni, nj), bamRanges=gr, bamSamples=sd1) } test_BamViews_subset <- function() { gr2 <- GRanges(rep(c("chr1", "chr2"), each=5), IRanges(c(1:5, 101:105), c(11:15, 111:115))) nj1 <- 4L fls1 <- rep("foo", nj1) sd1 <- DataFrame(Value=rev(seq_len(nj1))) ni2 <- length(gr2) mcols(gr2)[["Count"]] <- rev(seq_len(ni2)) ## rows v <- BamViews(bamPaths=fls1, bamRanges=gr2, bamSamples=sd1) .BamViews_ok(v, c(ni2, nj1), bamRanges=gr2, bamSamples=sd1) .BamViews_ok(v[TRUE,], c(ni2, nj1), bamRanges=gr2, bamSamples=sd1) i_idx <- c(FALSE, TRUE) .BamViews_ok(v[i_idx,], c(ni2/2, nj1), bamRanges=gr2[i_idx,], bamSamples=sd1) i_idx <- c(2, 4) .BamViews_ok(v[i_idx,],c(length(i_idx), nj1), bamRanges=gr2[i_idx,], bamSamples=sd1) ## columns .BamViews_ok(v[,TRUE], c(ni2, nj1), bamRanges=gr2, bamSamples=sd1) j_idx <- c(FALSE, TRUE, FALSE, TRUE) .BamViews_ok(v[,j_idx], c(ni2, nj1/2), bamRanges=gr2, bamSamples=sd1[j_idx,,drop=FALSE]) j_idx <- c(2, 4) .BamViews_ok(v[,j_idx], c(ni2, nj1/2), bamRanges=gr2, bamSamples=sd1[j_idx,,drop=FALSE]) } test_BamViews_bamIndicies <- function() { bv <- BamViews() checkIdentical(setNames(character(0), character(0)), bamIndicies(bv)) ## copy fls as bamIndicies fls <- c(tempfile(), tempfile()) # does not exist bv <- BamViews(fls) fls <- setNames(fls, names(bv)) checkIdentical(fls, bamPaths(bv)) checkIdentical(fls, bamIndicies(bv)) ## keep bamPaths, bamIndicies separate ifls <- c(tempfile(), tempfile()) # does not exist bv <- BamViews(fls, ifls) ifls <- setNames(ifls, names(bv)) checkIdentical(fls, bamPaths(bv)) checkIdentical(ifls, bamIndicies(bv)) ## subsetting checkIdentical(fls[2], bamPaths(bv[,2])) checkIdentical(ifls[1], bamIndicies(bv[,1])) } test_BamViews_auto.range <- function() { fl <- tempfile() # does not exist checkIdentical(GRanges(), bamRanges(BamViews(fl))) bv <- msg <- NULL suppressWarnings({ withCallingHandlers({ bv <- BamViews(fl, auto.range=TRUE) }, warning=function(w) { msg <<- conditionMessage(w) }) }) checkIdentical(GRanges(), bamRanges(bv)) checkIdentical("some files do not exist; bamRanges not defined", msg) fl <- system.file("extdata", "ex1.bam", package="Rsamtools") bv <- BamViews(c(fl, fl), auto.range=FALSE) checkIdentical(GRanges(), bamRanges(bv)) bv <- BamViews(c(fl, fl), auto.range=TRUE) checkIdentical(GRanges(c("seq1", "seq2"), IRanges(1, c(1575, 1584))), bamRanges(bv)) } .scanBam_ok <- function(target, current) { checkIdentical(length(target), length(current)) checkIdentical(class(target), class(current)) for (i in seq_along(target)) { for (j in seq_along(target[[i]])) { t <- target[[i]][[j]] c <- current[[i]][[j]] switch(as.vector(class(t)), PhredQuality=, DNAStringSet={ checkIdentical(as.character(t), as.character(c)) }, checkIdentical(t, c)) } } } test_BamViews_scanBam <- function() { src <- system.file("unitTests", "cases", package="Rsamtools") fl <- c(system.file("extdata", "ex1.bam", package="Rsamtools"), file.path(src, "ex1_shuf1000.bam")) bv <- BamViews(fl) res <- scanBam(bv) for (i in seq_along(fl)) .scanBam_ok(scanBam(fl[[i]]), res[[i]]) closeAllConnections() param <- ScanBamParam(what="rname") res <- scanBam(bv, param=param) for (i in seq_along(fl)) .scanBam_ok(scanBam(fl[[i]], param=param), res[[i]]) closeAllConnections() } test_BamViews_countBam <- function() { src <- system.file("unitTests", "cases", package="Rsamtools") fl <- c(system.file("extdata", "ex1.bam", package="Rsamtools"), file.path(src, "ex1_shuf1000.bam")) bv <- BamViews(fl) res <- countBam(bv) for (i in seq_along(fl)) checkIdentical(countBam(fl[i]), res[[i]]) closeAllConnections() which <- IRangesList(seq1=IRanges(1, 1000), seq2=IRanges(1, 1000)) param <- ScanBamParam(which=which) bamRanges <- GRanges(c("seq1", "seq2"), IRanges(c(1,1), 1000)) bv <- BamViews(fl, bamRanges=bamRanges) res <- countBam(bv) for (i in seq_along(fl)) checkIdentical(countBam(fl[i], param=param), res[[i]]) closeAllConnections() } Rsamtools/inst/unitTests/test_BcfFile.R0000644000175400017540000001003313556116727021230 0ustar00biocbuildbiocbuildfl <- system.file("extdata", "ex1.bcf.gz", package="Rsamtools") test_BcfFile_openclose <- function() { .normalizePath <- Rsamtools:::.normalizePath bf <- BcfFile(fl, character(0)) # no index checkTrue(!isOpen(bf)) open(bf) checkTrue(isOpen(bf)) checkIdentical(.normalizePath(fl), path(bf)) checkIdentical(character(0), index(bf, asNA=FALSE)) checkIdentical(NA_character_, index(bf)) close(bf) checkTrue(!isOpen(bf)) checkException(close(bf), silent=TRUE) bf <- open(bf) # open a closed BcfFile checkTrue(isOpen(bf)) bf1 <- open(bf) # (re)open BcfFile checkTrue(isOpen(bf1)) checkTrue(identical(bf$.extptr, bf1$.extptr)) checkTrue(isOpen(bf)) checkIdentical(.normalizePath(fl), path(bf)) ## checkIdentical(.normalizePath(fl), index(bf)) } test_BcfFile_scanBcfHeader <- function() { .chk <- function(h) { checkTrue(validObject(h)) checkEquals(3L, length(h)) checkEquals(2L, length(h[["Reference"]])) checkEquals("ex1.bam", h[["Sample"]]) checkEquals(6L, length(h[["Header"]])) } bf <- open(BcfFile(fl, character(0))) .chk(scanBcfHeader(bf)) bf <- BcfFile(fl, character(0)) .chk(scanBcfHeader(bf)) checkTrue(!isOpen(bf)) header <- structure(list(Reference = character(0), Sample = character(0), Header = "##FORMAT="), .Names = c("Reference", "Sample", "Header")) checkTrue(validObject(Rsamtools:::.bcfHeaderAsSimpleList(header))) } test_BcfFile_scanBcfHeader_no_SAMPLE_header <- function() { fl <- system.file(package="Rsamtools", "unitTests", "cases", "no_SAMPLE_header.vcf.gz") bf <- open(BcfFile(fl, character(0))) on.exit(close(bf)) sample <- scanBcfHeader(bf)[["Sample"]] exp <- c("NA00001", "NA00002", "NA00003") checkIdentical(exp, sample) } TEMPORARY_DISABLED_test_BcfFile_scanBcfHeader_remote <- function() { if ("windows" == .Platform$OS.type) { DEACTIVATED("remote scanBcFHeader not supported on Windows") return(TRUE) } fl <- "ftp://ftp.1000genomes.ebi.ac.uk/vol1/ftp/release/20110521/ALL.chr22.phase1_release_v3.20101123.snps_indels_svs.genotypes.vcf.gz" file <- tryCatch({ open(BcfFile(fl)) }, warning=function(w) { message("'test_BcfFile_scanBcfHeader_remote' warning:\n ", conditionMessage(w)) TRUE }) if (is.logical(file)) return(file) obs <- .Call(Rsamtools:::.scan_bcf_header, Rsamtools:::.extptr(file)) close(file) exp <- setNames(c(0L, 1092L, 29L), c("Reference", "Sample", "Header")) checkIdentical(exp, lengths(obs)) } test_BcfFile_scanBcfHeader_no_header_line <- function() { fl <- system.file(package="Rsamtools", "unitTests", "cases", "no_header_line.vcf.gz") msg <- NULL tryCatch(scanBcfHeader(fl), error=function(err) { msg <<- conditionMessage(err) }) checkIdentical("no 'header' line \"#CHROM POS ID...\"?", msg) } test_BcfFile_scan_noindex <- function() { bf <- open(BcfFile(fl, character(0))) checkTrue(isOpen(bf)) p <- ScanBcfParam() res <- scanBcf(bf, param=p) checkEquals(11L, length(res)) checkEquals(3065L, res[["RecordsPerRange"]]) checkEquals(3065L, unique(lengths(res[1:9]))) checkEquals(1, length(res[["GENO"]])) checkEquals(3065L, length(res[["GENO"]][["PL"]])) checkIdentical(res, scanBcf(bf)) } test_BcfFile_scan_index <- function() { bf <- open(BcfFile(fl)) which <- IRangesList(seq1=IRanges(c(1, 1000), width=10), seq2=IRanges(c(100, 1000), width=10)) p <- ScanBcfParam(which=which) res <- scanBcf(bf, param=p) checkEquals(11L, length(res)) checkEquals(c(0, 10, 10, 20), res[["RecordsPerRange"]]) checkEquals(30L, unique(sapply(res[1:9], length))) checkEquals(1, length(res[["GENO"]])) checkEquals(30L, length(res[["GENO"]][["PL"]])) } Rsamtools/inst/unitTests/test_FaFile.R0000644000175400017540000000540713556116727021075 0ustar00biocbuildbiocbuildfl <- system.file("extdata", "ce2dict1.fa", package="Rsamtools") test_FaFile_openclose <- function() { fa <- FaFile(fl) checkIdentical(FALSE, isOpen(fa)) checkIdentical(TRUE, isOpen(open(fa))) checkIdentical(FALSE, isOpen(close(fa))) } test_FaFile_emptyfile <- function() { fl <- tempfile() file.create(fl) checkException(open(fa <- FaFile(fl)), silent=TRUE) } test_FaFile_emptyid <- function() { fl <- tempfile() cat(">\nACTA", file=fl) open(fa <- FaFile(fl)) close(fa) } test_FaFile_indexFa <- function() { fa <- FaFile(fl) fai <- index(fa) fa <- indexFa(fa) checkIdentical(fai, index(fa)) } test_FaFile_scanFaIndex <- function() { .checkIdx <- function(idx) { checkTrue(is(idx, "GRanges")) checkIdentical(5L, length(idx)) checkIdentical(116L, sum(width(idx))) } fa <- FaFile(fl) .checkIdx(scanFaIndex(fa)) .checkIdx(scanFaIndex(fl)) } test_FaFile_count <- function() { f <- FaFile(fl) status <- isOpen(f) checkIdentical(status, FALSE) checkIdentical(5L, countFa(FaFile(fl))) checkIdentical(status, isOpen(f)) checkIdentical(5L, countFa(open(FaFile(fl)))) checkIdentical(5L, countFa(fl)) } test_FaFile_scanFa <- function() { .checkRes <- function(res) { checkTrue(is(res, "DNAStringSet")) checkIdentical(5L, length(idx)) checkIdentical(116L, sum(width(idx))) } fa <- open(FaFile(fl)) idx <- scanFaIndex(fa)[1:5] .checkRes(scanFa(fa, idx)) .checkRes(scanFa(fl, idx)) ## scanFa,*,missing-methods checkTrue(validObject(scanFa(fa))) checkTrue(validObject(scanFa(fl))) ## GRanges exp0 <- subseq(scanFa(fa)[c(1, 3)], 5, 9) gr <- GRanges(c("pattern01", "pattern03"), IRanges(5, width=5)) checkIdentical(as.character(exp0), as.character(scanFa(fa, gr))) checkIdentical(as.character(DNAStringSet()), unname(as.character(scanFa(fa, GRanges())))) ## scanFa ignores strand strand(gr) <- c("-", "+") checkIdentical(as.character(exp0), as.character(scanFa(fa, gr))) ## IntegerRangesList rl <- as(gr, "IntegerRangesList") checkIdentical(as.character(exp0), as.character(scanFa(fa, rl))) } test_FaFile_getSeq <- function() { fa <- open(FaFile(fl)) exp0 <- subseq(scanFa(fa)[c(1, 3)], 5, 9) gr <- GRanges(c("pattern01", "pattern03"), IRanges(5, width=5)) checkIdentical(as.character(exp0), as.character(getSeq(fa, gr))) ## '-' strand is reverse complement strand(gr) <- c("-", "+") exp <- exp0 exp[1] <- reverseComplement(exp[1]) checkIdentical(as.character(exp), as.character(getSeq(fa, gr))) ## IntegerRangesList rl <- as(gr, "IntegerRangesList") checkIdentical(as.character(exp0), as.character(getSeq(fa, rl))) } Rsamtools/inst/unitTests/test_RsamtoolsFile.R0000644000175400017540000000321513556116727022525 0ustar00biocbuildbiocbuildtest_RsamtoolsFile_constructor <- function() { fl <- system.file("extdata", "example.gtf.gz", package="Rsamtools") checkException(TabixFile(c(fl, fl)), silent=TRUE) checkTrue(validObject(tbx <- TabixFile(fl, character()))) checkIdentical(character(0), index(tbx, asNA=FALSE)) checkTrue(validObject(tbx <- TabixFile(fl, NA))) checkIdentical(character(0), index(tbx, asNA=FALSE)) tbx <- TabixFile(fl) checkIdentical(tbx, TabixFile(tbx)) checkTrue(validObject(TabixFile(tbx))) # idempotent } test_RsamtoolsFileList_constructor <- function() { fl <- system.file("extdata", "example.gtf.gz", package="Rsamtools") fls <- c(fl, fl) checkTrue(validObject(TabixFileList())) # 0-length checkTrue(validObject(tbx <- TabixFileList(fls))) checkIdentical(setNames(fls, basename(fls)), path(tbx)) checkIdentical(setNames(paste(fls, "tbi", sep="."), basename(fls)), index(tbx)) checkTrue(validObject(tbx <- TabixFileList(fls, character()))) checkIdentical(setNames(fls, basename(fls)), path(tbx)) checkIdentical(setNames(rep(NA_character_, 2), basename(fls)), index(tbx)) checkTrue(validObject(tbx <- TabixFileList(fls, NA))) checkIdentical(setNames(fls, basename(fls)), path(tbx)) checkIdentical(setNames(rep(NA_character_, 2), basename(fls)), index(tbx)) tbx <- TabixFile(fl) checkTrue(validObject(TabixFileList(tbx))) checkTrue(validObject(TabixFileList(tbx, tbx))) checkTrue(validObject(TabixFileList(list(tbx, tbx)))) tbx <- TabixFileList(TabixFile(fl)) checkIdentical(TabixFileList(tbx), tbx) # idempotent } Rsamtools/inst/unitTests/test_TabixFile.R0000644000175400017540000000604213556116727021612 0ustar00biocbuildbiocbuildfl <- system.file("extdata", "example.gtf.gz", package="Rsamtools") test_TabixFile_openclose <- function() { .normalizePath <- Rsamtools:::.normalizePath tab <- TabixFile(fl) checkTrue(!isOpen(tab)) open(tab) checkTrue(isOpen(tab)) checkTrue(isOpen(TabixFile(tab))) checkIdentical(.normalizePath(fl), path(tab)) checkIdentical(sprintf("%s.tbi", .normalizePath(fl)), index(tab)) close(tab) checkTrue(!isOpen(tab)) checkException(close(tab), silent=TRUE) tab <- open(tab) # open a closed TabixFile checkTrue(isOpen(tab)) tab1 <- open(tab) # (re)open TabixFile checkTrue(isOpen(tab1)) checkTrue(identical(tab$.extptr, tab1$.extptr)) } test_TabixFile_scan <- function() { tab <- open(TabixFile(fl)) param <- GRanges("chr1", IRanges(1, 10000)) res <- scanTabix(tab, param=param) checkIdentical("chr1:1-10000", names(res)) checkIdentical(86L, length(res[[1]])) param <- GRanges(c("chr1", "chr2"), IRanges(c(1,1), width=100000)) res <- scanTabix(tab, param=param) checkIdentical(c("chr1:1-100000", "chr2:1-100000"), names(res)) checkIdentical(c(157L, 15L), as.vector(sapply(res, length))) } test_TabixFile_yield <- function() { tab <- open(TabixFile(fl, yieldSize=100)) it <- integer() while(length(res <- scanTabix(tab)[[1]])) it <- append(it, length(res)) close(tab) checkIdentical(c(100L, 100L, 37L), it) rng <- GRanges(c("seq1", "seq2"), IRanges(1, c(1575, 1584))) open(tab) checkException(scanTabix(tab, param=rng), silent=TRUE) close(tab) } test_TabixFile_header <- function() { hdr <- headerTabix(fl) exp <- c("seqnames", "indexColumns", "skip", "comment", "header") checkIdentical(exp, names(hdr)) checkIdentical(c("chr1", "chr2"), hdr$seqnames) checkIdentical(c(1L, 4L, 5L), unname(hdr$indexColumns)) checkIdentical(0L, hdr$skip) checkIdentical("#", hdr$comment) checkIdentical(hdr$seqnames, seqnamesTabix(fl)) checkIdentical(character(), hdr$header) } test_TabixFile_header_respects_first_line <- function() { tbx <- open(TabixFile(fl)) xx <- headerTabix(tbx) obs <- unlist(scanTabix(tbx)) close(tbx) exp <- unlist(scanTabix(tbx)) checkIdentical(obs, exp) } test_TabixFile_header_remote <- function() { if ("windows" == .Platform$OS.type) { DEACTIVATED("remote tabix not supported on Windows") return(TRUE) } fl <- sprintf("%s/%s", "http://1000genomes.s3.amazonaws.com/release", "20110521/ALL.chr22.phase1_release_v3.20101123.snps_indels_svs.genotypes.vcf.gz") if (!is.null(tryCatch({open(con <- url(fl)); close(con)}, error=function(...) FALSE))) return(TRUE) obs <- headerTabix(fl) checkIdentical("22", obs$seqnames) exp <- structure(c(1L, 2L, 0L), .Names = c("seq", "start", "end")) checkIdentical(exp, obs$indexColumns) checkIdentical(0L, obs$skip) checkIdentical("#", obs$comment) checkIdentical(30L, length(obs$header)) } Rsamtools/inst/unitTests/test_applyPileups.R0000644000175400017540000001622213556116727022433 0ustar00biocbuildbiocbuild## library(Rsamtools); library(RUnit) fl <- system.file("extdata", "ex1.bam", package="Rsamtools") TEMPORARY_DISABLED_test_applyPileups_byRange <- function() { fls <- PileupFiles(c(fl, fl)) fun <- function(x) x[["seqnames"]] which <- GRanges(c("seq1", "seq2"), IRanges(c(1000, 1000), 2000)) param <- ApplyPileupsParam(which=which) res <- applyPileups(fls, fun, param=param) exp <- list(structure(570L, .Names = "seq1"), structure(568L, .Names = "seq2")) checkIdentical(exp, res) fls <- PileupFiles(c(fl, fl), param=param) res <- applyPileups(fls, fun) checkIdentical(exp, res) } TEMPORARY_DISABLED_test_applyPileups_byRange_yieldAll <- function() { fls <- PileupFiles(c(fl, fl)) which <- GRanges(c("seq1", "seq2"), IRanges(c(1000, 1000), c(2000, 1500))) param <- ApplyPileupsParam(which=which, yieldAll=TRUE) res <- applyPileups(fls, function(x) x$seqnames, param=param) exp <- list(structure(1001L, .Names = "seq1"), structure(501L, .Names = "seq2")) checkIdentical(exp, res) res <- applyPileups(fls, function(x) x$pos, param=param) checkIdentical(list(1000:2000, 1000:1500), res) } TEMPORARY_DISABLED_test_applyPileups_byPosition <- function() { fls <- PileupFiles(c(fl, fl)) fun <- function(x) x[["seqnames"]] which <- GRanges(c("seq1", "seq2"), IRanges(c(1000, 1000), 2000)) param <- ApplyPileupsParam(which=which, yieldSize=2000L, yieldBy="position") res <- applyPileups(fls, fun, param=param) exp <- list(structure(c(570L, 568L), .Names = c("seq1", "seq2"))) checkIdentical(exp, res) res <- applyPileups(fls, function(x) sum(x$seq[,1,]), param=param) checkIdentical(list(41165L), res) param <- ApplyPileupsParam(which=which, yieldSize=500L, yieldBy="position") res <- applyPileups(fls, fun, param=param) exp <- list(structure(500L, .Names = "seq1"), structure(c(70L, 430L), .Names = c("seq1", "seq2")), structure(138L, .Names = "seq2")) checkIdentical(exp, res) res <- applyPileups(fls, function(x) sum(x$seq[,1,]), param=param) checkIdentical(list(18132L, 20125L, 2908L), res) } TEMPORARY_DISABLED_test_applyPileups_byPosition_yieldAll <- function() { fls <- PileupFiles(c(fl, fl)) fun <- function(x) colSums(x$seq[,1,,drop=FALSE]) which <- GRanges("seq1", IRanges(1000, 1100)) param <- ApplyPileupsParam(which=which, yieldSize=10L, yieldBy="position", yieldAll=TRUE) res0 <- applyPileups(fls, fun, param=param) checkIdentical(11L, length(res0)) param <- ApplyPileupsParam(which=which, yieldSize=50L, yieldBy="position", yieldAll=TRUE) res <- applyPileups(fls, fun, param=param) checkIdentical(3L, length(res)) checkIdentical(unlist(res0), unlist(res)) param <- ApplyPileupsParam(which=which, yieldSize=100L, yieldBy="position", yieldAll=TRUE) res <- applyPileups(fls, fun, param=param) checkIdentical(2L, length(res)) checkIdentical(unlist(res0), unlist(res)) param <- ApplyPileupsParam(which=which, yieldSize=101L, yieldBy="position", yieldAll=TRUE) res <- applyPileups(fls, fun, param=param) checkIdentical(unlist(res0), unlist(res)) checkIdentical(1L, length(res)) param <- ApplyPileupsParam(which=which, yieldSize=200L, yieldBy="position", yieldAll=TRUE) res <- applyPileups(fls, fun, param=param) checkIdentical(1L, length(res)) checkIdentical(unlist(res0), unlist(res)) param <- ApplyPileupsParam(which=GRanges("seq1", IRanges(seq(10, 110, by=10), width=1), "+"), yieldBy="position", yieldAll=TRUE, yieldSize=5) seqnames <- applyPileups(fls, function(x) x$seqnames, param=param) exp <- list(structure(5L, .Names = "seq1"), structure(5L, .Names = "seq1"), structure(1L, .Names = "seq1")) checkIdentical(exp, seqnames) pos <- applyPileups(fls, function(x) x$pos, param=param) checkIdentical(c(5L, 5L, 1L), sapply(pos, length)) checkIdentical(seq(10L, 110L, 10L), unlist(pos)) fun <- function(x) as.vector(colSums(x$seq[,1,,drop=FALSE])) seq <- applyPileups(fls, fun, param=param) checkIdentical(list(c(4, 8, 13, 12, 10), c(13, 15, 17, 9, 3), 5), seq) } ## Test fails on Mac (merida2 & celaya2) but not on Linux (malbec2). TEMPORARY_DISABLED_test_applyPileups_what <- function() { fls <- PileupFiles(c(fl, fl)) which <- GRanges("seq1", IRanges(1000, 1999)) param <- ApplyPileupsParam(which=which, yieldAll=TRUE) obs <- applyPileups(fls, function(x) sapply(x, length), param=param)[[1]] exp <- c(seqnames=1L, pos=1000L, seq=2L * 5L * 1000L, qual=2L * 94L * 1000L) checkIdentical(obs, exp) param <- ApplyPileupsParam(which=which, yieldAll=TRUE, what=character()) obs <- applyPileups(fls, function(x) x$pos, param=param)[[1]] checkIdentical(999L + 1:1000, obs) param <- ApplyPileupsParam(which=which, yieldAll=TRUE, what="seq") obs <- applyPileups(fls, function(x) sapply(x, length), param=param)[[1]] checkIdentical(obs, exp[1:3]) param <- ApplyPileupsParam(which=which, yieldAll=TRUE, what="qual") obs <- applyPileups(fls, function(x) sapply(x, length), param=param)[[1]] checkIdentical(obs, exp[c(1:2, 4)]) } TEMPORARY_DISABLED_test_applyPileups_memoryleak_warning <- function() { ## failing to complete an iterator causes a warning; this is ## corrected in C code opts <- options(warn=2) on.exit(options(opts)) fls <- PileupFiles(c(fl, fl)) param <- ApplyPileupsParam(which=GRanges("seq1", IRanges(1000, 1499)), yieldAll=TRUE) obs <- applyPileups(fls, function(x) NULL, param=param) checkIdentical(list(NULL), obs) } test_applyPileups_NULL_space <- function() { checkException(applyPileups(PileupFiles(fl), identity), silent=TRUE) } ## Test fails on Mac (merida2 & celaya2) but not on Linux (malbec2). TEMPORARY_DISABLED_test_applyPileups_skip_inserts <- function() { fl <- system.file("unitTests", "cases", "plp_refskip.bam", package="Rsamtools") param <- ApplyPileupsParam(which=GRanges("seq1", IRanges(1, 1000000)), what="seq") res <- applyPileups(PileupFiles(fl), function(x) rowSums(x$seq[,1,]), param=param) obs <- structure(c(19, 12, 18, 26, 0), .Names = c("A", "C", "G", "T", "N")) checkIdentical(obs, res[[1]]) res <- applyPileups(PileupFiles(fl), function(x) length(x$pos), param=param) checkIdentical(75L, res[[1]]) ## yieldAll=TRUE param <- ApplyPileupsParam(which=GRanges("seq1", IRanges(1, 1000000)), yieldAll=TRUE, what="seq") obs <- structure(c(19, 12, 18, 26, 0), .Names = c("A", "C", "G", "T", "N")) res <- applyPileups(PileupFiles(fl), function(x) length(x$pos), param=param) checkIdentical(width(plpWhich(param)), res[[1]]) } Rsamtools/inst/unitTests/test_asBam.R0000644000175400017540000000156113556116727020767 0ustar00biocbuildbiocbuildtest_asBam <- function() { src <- system.file("unitTests", "cases", package="Rsamtools") fl <- file.path(src, "ex1.sam.gz") ofl <- tempfile() on.exit(unlink(ofl)) bam <- asBam(fl, ofl) checkIdentical(bam, paste(ofl, "bam", sep=".")) which <- GRanges("seq2", IRanges(1000, 2000)) res <- scanBam(bam, param=ScanBamParam(which=which, what="rname"))[[1]] checkIdentical(642L, length(res[["rname"]])) checkIdentical("seq2", as.character(unique(res[["rname"]]))) checkException(asBam(fl, ofl), silent=TRUE) ## asBam destination construction tmp_sam <- file.path(tempdir(), "ex1.sam.gz") file.copy(fl, tmp_sam) tmp_bam <- asBam(tmp_sam) tmp_bai <- paste0(tmp_bam, ".bai") checkTrue(file.exists(tmp_sam)) checkTrue(file.exists(tmp_bai)) file.remove(tmp_bam) file.remove(tmp_bai) file.remove(tmp_sam) } Rsamtools/inst/unitTests/test_bam.R0000644000175400017540000002646013556116727020510 0ustar00biocbuildbiocbuildfl <- system.file("extdata", "ex1.bam", package="Rsamtools") .check0 <- function(res) { checkIdentical("list", class(res)) checkTrue(all(names(res) %in% scanBamWhat())) checkTrue(all(sapply(res, validObject))) } .check1 <- function(res) { .check0(res) exp <- c("character", "integer", "factor", "factor", "integer", "integer", "integer", "character", "factor", "integer", "integer", "DNAStringSet", "PhredQuality") checkIdentical(exp, as.vector(sapply(res, class))) checkIdentical(levels(strand()), levels(res[["strand"]])) } test_strand <- function() { exp <- structure(integer(0), .Label = c("+", "-", "*"), class = "factor") checkIdentical(exp, strand()) checkIdentical(levels(exp), Rsamtools:::.STRAND_LEVELS) } test_cigar <- function() { fl <- system.file("extdata", "example_from_SAM_Spec.sam", package="Rsamtools") sam <- read.delim(fl, comment="@", header=FALSE, stringsAsFactors=FALSE) exp <- setNames(sam[[6]], sam[[1]]) fl <- system.file("extdata", "example_from_SAM_Spec.bam", package="Rsamtools") param <- ScanBamParam(what=c("qname", "cigar")) bam <- scanBam(fl, param=param)[[1]] obs <- setNames(bam$cigar, bam$qname) checkIdentical(exp, obs) } test_scanBam <- function() { res <- scanBam(fl)[[1]] checkIdentical("list", class(res)) checkIdentical(3307L, unique(sapply(res, length))) .check1(res) exp <- structure(c(11L, 2L, 2L, 2L, 1L, 1L, 1L, 1L, 1L), .Dim = 9L, .Dimnames = structure(list( c("1", "2", "3", "4", "6", "37", "112", "283", "2804" )), .Names = ""), class = "table") checkIdentical(exp, table(table(res[["cigar"]]))) exp <- structure(c(1647L, 1624L, 0L, 36L), .Dim = 4L, .Dimnames = structure(list( c(levels(strand()), NA)), .Names = ""), class = "table") checkIdentical(exp, table(res[["strand"]], useNA="always")) exp <- structure(c(8L, 40L, 858L, 17L, 714L, 5L, 12L, 11L, 35L, 714L, 18L, 858L, 12L, 5L), .Dim = 14L, .Dimnames = structure(list(c("69", "73", "83", "89", "99", "117", "121", "133", "137", "147", "153", "163", "181", "185")), .Names = ""), class = "table") checkIdentical(exp, table(res[["flag"]])) exp <- structure(c(6L, 37L, 2865L, 285L, 114L), .Dim = 5L, .Dimnames = structure(list( c("33", "34", "35", "36", "40")), .Names = ""), class = "table") checkIdentical(exp, table(width(res[["seq"]]))) exp <- structure(c(40144L, 23398L, 20735L, 32135L, 139L), .Names = c("A", "C", "G", "T", "other")) checkIdentical(exp, alphabetFrequency(res[["seq"]], collapse=TRUE, baseOnly=TRUE)) exp <- structure(c(263, 1, 20, 178, 577, 163, 195, 287, 286, 853, 290, 367, 424, 340, 395, 604, 601, 694, 898, 784, 1215, 2298, 1814, 1889, 3330, 10633, 80537, 6444, 150, 18, 3), .Names = c("!", "#", "$", "%", "&", "'", "(", ")", "*", "+", ",", "-", ".", "/", "0", "1", "2", "3", "4", "5", "6", "7", "8", "9", ":", ";", "<", "=", ">", "?", "@")) checkIdentical(exp, rowSums(consensusMatrix(res[["qual"]]))) } test_scanBam_which <- function() { ## 'which' which <- IRangesList(seq1=IRanges(1000, 2000), seq2=IRanges(c(100, 1000), c(1000, 2000))) p1 <- ScanBamParam(which=which, what=scanBamWhat()) res <- scanBam(fl, param=p1) checkIdentical("list", class(res)) exp <- c("seq1:1000-2000", "seq2:100-1000", "seq2:1000-2000") checkIdentical(exp, names(res)) for (i in seq_along(res)) .check1(res[[i]]) exp <- structure(c(612L, 1169L, 642L), .Names = c("seq1:1000-2000", "seq2:100-1000", "seq2:1000-2000")) checkIdentical(exp, sapply(res, function(x) unique(sapply(x, length)))) } test_scanBam_which_bounds <- function() { ## 'which' which <- IRangesList(seq1=IRanges(1000, 2000), seq2=IRanges(c(100, 1000), c(1000, 2000))) p1 <- ScanBamParam(which=which, what=scanBamWhat()) res <- scanBam(fl, param=p1) checkIdentical("list", class(res)) exp <- c("seq1:1000-2000", "seq2:100-1000", "seq2:1000-2000") checkIdentical(exp, names(res)) for (i in seq_along(res)) .check1(res[[i]]) exp <- structure(c(612L, 1169L, 642L), .Names = c("seq1:1000-2000", "seq2:100-1000", "seq2:1000-2000")) checkIdentical(exp, sapply(res, function(x) unique(sapply(x, length)))) ## ranges correct? for (i in c(1, 2, 10, 30, 34, 35, 36, 37, 460)) { snp <- IRanges(i, i) which <- GRanges("seq2", IRanges(1, 1000)) param <- ScanBamParam(which=which, what=c("pos", "qwidth")) res <- with(scanBam(fl, param=param)[[1]], { idx <- !is.na(pos) IRanges(pos[idx], width=qwidth[idx]) }) exp <- sum(countOverlaps(res, snp)) param <- ScanBamParam(which=GRanges("seq2", snp), what=scanBamWhat()) try(checkIdentical(exp, countBam(fl, param=param)$records, msg=sprintf("i: %d\n", i))) } } test_scanBam_which_order <- function() { which <- IRangesList(seq2=IRanges(c(1000, 100), c(2000, 1000)), seq1=IRanges(1000, 2000)) p1 <- ScanBamParam(which=which, what="pos") res <- scanBam(fl, param=p1) checkIdentical("list", class(res)) exp <- structure(c(642L, 1169L, 612L), .Names = c( "seq2:1000-2000", "seq2:100-1000", "seq1:1000-2000")) obs <- sapply(res, function(x) unique(sapply(x, length))) checkIdentical(exp, obs) } test_scanBam_which_empty <- function() { ## range 1 is empty which <- IRangesList(seq2=IRanges(c(1570,1562), width=1)) what <- c("strand", "rname", "mrnm") res <- scanBam(fl, param=ScanBamParam(what=what, which=which)) checkIdentical(c(3L, 3L), unname(sapply(res, length))) checkIdentical(res[[1]][["strand"]], strand()) exp <- factor(levels=c("seq1", "seq2")) checkIdentical(exp, res[[1]][["rname"]]) checkIdentical(exp, res[[1]][["mrnm"]]) checkIdentical(res[[2]][["strand"]], strand(rep("-", 3))) exp <- factor(rep("seq2", 3), levels=c("seq1", "seq2")) checkIdentical(exp, res[[2]][["rname"]]) checkIdentical(exp, res[[2]][["mrnm"]]) } test_scanBam_what_overflow <- function() { ## src/samtools/bam_index.c requires that the largest bin be <= 512Mbp which <- IRangesList(seq1=IRanges(1000, 536870912L-1L)) p1 <- ScanBamParam(which=which, what=scanBamWhat()) checkTrue(validObject(scanBam(fl, param=p1))) bamWhich(p1) <- IRangesList(seq1=IRanges(1000, 536870912L)) checkTrue(validObject(scanBam(fl, param=p1))) bamWhich(p1) <- IRangesList(seq1=IRanges(1000, 536870912L+1L)) xx <- tryCatch(scanBam(fl, param=p1), error=conditionMessage) checkIdentical("'end' must be <= 536870912", strsplit(xx, "\n")[[1]][1]) checkTrue(validObject(scanBam(fl))); } test_scanBam_what <- function() { p2 <- ScanBamParam(what=c("rname", "strand", "pos", "qwidth")) res <- scanBam(fl, param=p2) checkIdentical("list", class(res)) checkIdentical(1L, length(res)) res1 <- res[[1]] .check0(res1) checkIdentical(4L, length(res1)) exp <- structure(c("factor", "factor", "integer", "integer"), .Names = c("rname", "strand", "pos", "qwidth")) checkIdentical(exp, sapply(res1, class)) checkIdentical(3307L, unique(sapply(res1, length))) } test_scanBam_flag <- function() { p3 <- ScanBamParam(flag=scanBamFlag(isMinusStrand=TRUE), what=scanBamWhat()) res <- scanBam(fl, param=p3) checkIdentical("list", class(res)) checkIdentical(1L, length(res)) res1 <- res[[1]] .check1(res1) checkIdentical(1641L, unique(sapply(res1, length))) } test_scanBam_badSpace <- function() { which <- IRangesList(badspc=IRanges(100000, 2000000)) p1 <- ScanBamParam(which=which, what=scanBamWhat()) exp <- "seqlevels(param) not in BAM header" test <- tryCatch({ scanBam(fl, param=p1) }, error=function(e) { startsWith(conditionMessage(e), exp) }) checkTrue(identical(test, TRUE)) } test_scanBam_index <- function() { which <- IRangesList(seq1=IRanges(1000, 2000), seq2=IRanges(c(100, 1000), c(1000, 2000))) p1 <- ScanBamParam(which=which, what=scanBamWhat()) src <- system.file("unitTests", "cases", package="Rsamtools") fl <- file.path(src, "ex1_noindex.bam") idx <- system.file("extdata", "ex1.bam", package="Rsamtools") checkException(scanBam(fl, character(), param=p1), silent=TRUE) res <- scanBam(fl, idx, param=p1) checkIdentical("list", class(res)) exp <- c("seq1:1000-2000", "seq2:100-1000", "seq2:1000-2000") checkIdentical(exp, names(res)) for (i in seq_along(res)) .check1(res[[i]]) exp <- structure(c(612L, 1169L, 642L), .Names = c("seq1:1000-2000", "seq2:100-1000", "seq2:1000-2000")) checkIdentical(exp, sapply(res, function(x) unique(sapply(x, length)))) checkException(scanBam(fl, tempfile(), param=p1), silent=TRUE) } test_scanBam_sam <- function() { tbl <- read.table(system.file("extdata", "ex1.sam", package="Rsamtools"), sep="\t", quote="", fill=TRUE, comment="") bam <- scanBam(system.file("extdata", "ex1.bam", package="Rsamtools"))[[1]] checkIdentical(bam$flag, tbl[[2]]) idx <- !is.na(bam$strand) & bam$strand=="+" checkIdentical(as.character(tbl[[10]][idx]), as.character(bam$seq[idx])) checkIdentical(as.character(tbl[[11]][idx]), as.character(bam$qual[idx])) idx <- !is.na(bam$strand) & bam$strand=="-" checkIdentical(as.character(tbl[[10]][idx]), as.character(bam$seq[idx])) checkIdentical(as.character(tbl[[11]][idx]), as.character(bam$qual[idx])) } test_scanBam_tag <- function() { checkIdentical(character(0), bamTag(ScanBamParam())) tag <- c("MF", "Aq", "NM", "UQ", "H0", "H1") param <- ScanBamParam(tag=tag) checkTrue(validObject(param)) checkIdentical(tag, bamTag(param)) ## tags must be two letters checkException(ScanBamParam(tag="XYZ"), silent=TRUE) tag <- c("MF", "Aq", "NM", "UQ", "H0", "H1") param <- ScanBamParam(tag=tag) src <- system.file("unitTests", "cases", package="Rsamtools") fl <- file.path(src, "ex1_shuf1000.bam") bam <- scanBam(fl, param=param)[[1]][["tag"]] checkIdentical(tag, names(bam)) checkTrue(all(1000L == sapply(bam, length))) exp <- structure(c(818L, 117L, 27L, 10L, 11L, 4L, 1L, 1L, 11L), .Dim = 9L, .Dimnames = structure(list( c("0", "1", "2", "3", "4", "5", "6", "7", NA)), .Names = ""), class = "table") checkIdentical(exp, table(bam[["NM"]], useNA="always")) } Rsamtools/inst/unitTests/test_bam_count.R0000644000175400017540000000457313556116727021721 0ustar00biocbuildbiocbuildfl <- system.file("extdata", "ex1.bam", package="Rsamtools") as_data.frame <- function(x) { data.frame(space=factor(names(unlist(x)), levels=seqlevels(x)), start=start(unlist(x)), end=end(unlist(x)), width=width(unlist(x))) } test_countBam <- function() { checkEquals(data.frame(space=NA, start=NA, end=NA, width=NA, file=basename(fl), records=3307L, nucleotides=116551L), countBam(fl)) which <- IRangesList(seq1=IRanges(1000, 2000), seq2=IRanges(c(100, 1000), c(1000, 2000))) p1 <- ScanBamParam(which=which) exp <- cbind(as_data.frame(which), file=basename(fl), records=c(612L, 1169L, 642L), nucleotides=c(21549, 41235, 22640)) checkIdentical(exp, countBam(fl, param=p1)) which <- IRangesList(seq2=IRanges(c(100, 1000), c(1000, 2000)), seq1=IRanges(1000, 2000)) p2 <- ScanBamParam(which=which) exp <- merge(as_data.frame(which), exp, sort=FALSE) rownames(exp) <- NULL checkIdentical(exp, countBam(fl, param=p2)) } test_countBam_index <- function() { which <- IRangesList(seq1=IRanges(1000, 2000), seq2=IRanges(c(100, 1000), c(1000, 2000))) p1 <- ScanBamParam(which=which) exp <- cbind(as_data.frame(which), file="ex1_noindex.bam", records=c(612L, 1169L, 642L), nucleotides=c(21549, 41235, 22640)) src <- system.file("unitTests", "cases", package="Rsamtools") fl <- file.path(src, "ex1_noindex.bam") idx <- system.file("extdata", "ex1.bam", package="Rsamtools") checkIdentical(exp, countBam(fl, idx, param=p1)) checkException({ suppressWarnings(countBam(fl, tempfile(), param=p1)) }, silent=TRUE) } test_idxstatsBam <- function() { target = structure( list( seqnames = structure( 1:2, .Label = c("seq1", "seq2"), class = "factor" ), seqlength = c(1575L, 1584L), mapped = c(1482, 1789), unmapped = c(19, 17)), .Names = c("seqnames", "seqlength", "mapped", "unmapped"), row.names = c(NA, -2L), class = "data.frame") checkIdentical(target, idxstatsBam(fl)) checkException(idxstatsBam("cases/ex1_noindex.bam")) } Rsamtools/inst/unitTests/test_bam_header.R0000644000175400017540000000046013556116727022010 0ustar00biocbuildbiocbuildfl <- system.file("extdata", "ex1.bam", package="Rsamtools") test_readBamHeader <- function() { res <- scanBamHeader(fl) checkIdentical(Rsamtools:::.normalizePath(fl), names(res)) exp <- structure(c(1575L, 1584L), .Names = c("seq1", "seq2")) checkIdentical(exp, res[[1]][["targets"]]) } Rsamtools/inst/unitTests/test_compression.R0000644000175400017540000000063113556116727022302 0ustar00biocbuildbiocbuildtest_bgzip_openclose <- function() { ## trying to determine that file handle has been cleaned up checkIdentical(TRUE, dir.create(d <- tempfile())) fin <- file.path(d, "in") fout <- file.path(d, "out") writeLines("123", con=fin) bgzip(fin, fout) checkIdentical(TRUE, file.remove(fin)) checkIdentical(TRUE, file.remove(fout)) checkIdentical(0L, unlink(d, recursive=TRUE)) } Rsamtools/inst/unitTests/test_mapqfilter.R0000644000175400017540000000150013556116727022101 0ustar00biocbuildbiocbuildtest_mapqFilter <- function() { fl <- system.file("extdata", "ex1.bam", package="Rsamtools") p1 <- ScanBamParam(what="mapq") p2 <- ScanBamParam(what="mapq", mapqFilter=74) mapq1 <- scanBam(fl, param=p1)[[1]][["mapq"]] mapq2 <- scanBam(fl, param=p2)[[1]][["mapq"]] checkTrue(length(mapq1[!is.na(mapq1) & mapq1 == bamMapqFilter(p2)]) > 0) checkIdentical(mapq2, mapq1[!is.na(mapq1) & mapq1 >= bamMapqFilter(p2)]) n <- countBam(fl, param=p2) checkIdentical(n$records, length(mapq2)) checkException(ScanBamParam(mapqFilter=-1), silent=TRUE) checkException(ScanBamParam(mapqFilter=1:2), silent=TRUE) checkIdentical(bamMapqFilter(p2), 74L) bamMapqFilter(p2) <- 75 checkIdentical(bamMapqFilter(p2), 75L) bamMapqFilter(p2) <- "76.1" checkIdentical(bamMapqFilter(p2), 76L) } Rsamtools/inst/unitTests/test_phred2ASCIIOffset.R0000644000175400017540000000232613556116727023050 0ustar00biocbuildbiocbuildtest_phred2ASCIIOffset <- function() { schemes <- eval(formals(phred2ASCIIOffset)$scheme) exp <- structure(integer(), names=character()) checkIdentical(exp, phred2ASCIIOffset()) checkIdentical(exp, phred2ASCIIOffset(character())) checkIdentical(exp, phred2ASCIIOffset(integer())) for (scheme in schemes) { checkIdentical(exp, phred2ASCIIOffset(scheme=scheme)) checkIdentical(exp, phred2ASCIIOffset(integer(), scheme=scheme)) } offsets <- Rsamtools:::.ascii_offset() checkIdentical(offsets[1L + 0:40], phred2ASCIIOffset(0:40, "Sanger")) checkIdentical(offsets[32L + (-5):40], phred2ASCIIOffset((-5):40, "Solexa")) checkIdentical(offsets[32L + 0:40], phred2ASCIIOffset(0:40, "Illumina 1.3+")) checkIdentical(offsets[32L + 3:40], phred2ASCIIOffset(3:40, "Illumina 1.5+")) checkIdentical(offsets[1L + 0:41], phred2ASCIIOffset(0:41, "Illumina 1.8+")) checkIdentical(offsets, phred2ASCIIOffset(paste(names(offsets), collapse=""))) checkException(phred2ASCIIOffset(50)) checkException(phred2ASCIIOffset(-1)) checkException(phred2ASCIIOffset("")) checkException(phred2ASCIIOffset(c("A", "AA"))) } Rsamtools/inst/unitTests/test_pileup_nowhich.R0000644000175400017540000001307413556116727022763 0ustar00biocbuildbiocbuildsuppressMessages({ library(Rsamtools) library(RUnit) }) .reorder_data.frame <- function(df) { df <- df[do.call(order,df),] rownames(df) <- NULL df } .unordered_check <- function(expected, xx) { xx <- .reorder_data.frame(xx) expected <- .reorder_data.frame(expected) checkIdentical(xx, expected) } .s_levels <- function() { levels(strand()) } .n_levels <- function() { c("A", "C", "G", "T", "N", "=", "-", "+") } .tiny.sam_seqlevels <- function() { fl <- system.file(package="Rsamtools", "extdata", "tiny.bam") bf <- BamFile(fl) seqlevels(bf) } .ex1.sam_seqlevels <- function() { fl <- system.file(package="Rsamtools", "extdata", "ex1.bam") bf <- BamFile(fl) seqlevels(bf) } .no_which.sam_seqlevels <- function() { fl <- system.file(package="Rsamtools", "extdata", "no_which_whole_file.bam") bf <- BamFile(fl) seqlevels(bf) } ## target as data.frame .tadf <- function(pos=NULL, strand=NULL, nucleotide=NULL, cycle_bin=NULL, count=NULL, which_label=NULL, seqnames=NULL, use_ex1.bam_levels=FALSE) { if(is.null(pos) || is.null(count) || is.null(seqnames)) stop("'pos', 'count', and 'seqnames' must not be 'NULL'") target <- data.frame(pos=as.integer(pos), stringsAsFactors=FALSE) seqnames_levels <- .no_which.sam_seqlevels() target <- cbind(seqnames=factor(seqnames, levels=seqnames_levels), target) if(!is.null(strand)) target <- cbind(target, strand=factor(strand, levels=.s_levels())) if(!is.null(nucleotide)) target <- cbind(target, nucleotide=factor(nucleotide, levels=.n_levels())) if(!is.null(cycle_bin)) target <- cbind(target, cycle_bin=cycle_bin) target <- cbind(target, count=as.integer(count)) if(!is.null(which_label)) target <- cbind(target, which_label=which_label) target } ## make which labels .mwls <- function(param, run_lens) { wl <- Rsamtools:::.scanBam_extract_which_labels(param) if(length(wl) != length(run_lens)) stop("mismatched lengths, length(wl): '%d' length(run_lens): '%d'\n", length(wl), length(run_lens)) if(all(run_lens == 0L)) factor(levels=wl) else rep(wl, run_lens) } ## END HELPER FUNCTIONS ## file helpers no_which_whole_file <- system.file(package="Rsamtools", "extdata", "no_which_whole_file.bam") no_which_buf_pileup <- system.file(package="Rsamtools", "extdata", "no_which_buffered_pileup.bam") test_no_which_whole_file <- function() { bf <- BamFile(no_which_whole_file) xx <- pileup(bf) seqnames <- c(rep("chr1", 9), rep("chr2", 5)) expected <- .tadf(seqnames=seqnames, pos=c(1, 2, 3, 4, 4, 5, 5, 6, 7, seq(1,5)), strand=rep("+",14), nucleotide=c("A","A","A","A","C","A","C","C","C", "A","A","A","C","C"), count=c(1, 1, 2, rep(1,11))) ##print(xx);## str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } test_no_which_buffered_yieldSize1_PREVENT_ZERO_ROW <- function() { bf <- open(BamFile(no_which_buf_pileup, yieldSize=1)) ## return 1 res <- pileup(bf) seqnames <- rep("chr1", 2L) expected <- .tadf(seqnames=seqnames, pos= c( 1, 2), strand= c("+","+"), nucleotide=c("A","A"), count= c( 1, 1)) ##print(res);##str(res) ##print(expected);str(expected) checkIdentical(expected, res) ## return 2 res <- pileup(bf) seqnames <- rep("chr1", 4L) expected <- .tadf(seqnames=seqnames, pos= c( 3, 3, 4, 4), strand= rep("+",4L), nucleotide=c("A","C","A","C"), count= c( 2, 1, 2, 1)) ##print(res);##str(res) ## print(expected);##str(expected) checkIdentical(expected, res) ## return 3 res <- pileup(bf) seqnames <- rep("chr1", 8L) expected <- .tadf(seqnames=seqnames, pos= c( 5, 5, 6, 6, 7, 7, 8, 9), strand= rep("+",8L), nucleotide=c("A","C","A","C","A","C","A","A"), count= c( 3, 1, 2, 1, 2, 1, 1, 1)) ##print(res);##str(res) ##print(expected);##str(expected) checkIdentical(expected, res) ## return 4 (detects EOI, flushes) res <- pileup(bf) seqnames <- rep("chr2", 5L) expected <- .tadf(seqnames=seqnames, pos= c( 5, 6, 7, 8, 9), strand= rep("+",5L), nucleotide=rep("G",5L), count= rep( 1,5L)) ##print(res);##str(res) ##print(expected);##str(expected) checkIdentical(expected, res) } ## test_no_which_buffered_yieldSize1_NO_EAGER_PRINTING_DEMO <- function() { ## bf <- open(BamFile(no_which_buf_pileup, yieldSize=1)) ## for(i in seq_len(5)) { ## res <- pileup(bf) ## message(paste0("printing return ", i)) ## print(res) ## message() ## } ## res <- pileup(bf) ## message(paste0("printing return 6")) ## print(res); ## } ##test_no_which_buffered_yieldSize1_NO_EAGER_PRINTING_DEMO() ## Must be run with valgrind in order to verify ## test_no_which_buffered_finalizer <- function() { ## bf <- open(BamFile(no_which_buf_pileup, yieldSize=1)) ## res <- pileup(bf) ## bf <- open(BamFile(no_which_buf_pileup, yieldSize=1)) ## } ##test_no_which_buffered_finalizer() Rsamtools/inst/unitTests/test_pileup_querybins.R0000644000175400017540000003504213556116727023344 0ustar00biocbuildbiocbuildsuppressMessages({ library(Rsamtools) library(RUnit) }) ## .run_all <- function() { ## tests <- ls(envir=parent.frame())[grep('test_*', ls(envir=parent.frame()))] ## cat(tests) ## lapply(tests, function(x) { cat(paste0(x, "...\n")); do.call(x, list()) } ) ## } fl <- system.file(package="Rsamtools", "extdata", "querybins.bam") bf <- BamFile(fl) .reorder_data.frame <- function(df) { df <- df[do.call(order,df),] rownames(df) <- NULL df } .unordered_check <- function(expected, xx) { xx <- .reorder_data.frame(xx) expected <- .reorder_data.frame(expected) checkIdentical(xx, expected) } .s_levels <- function() { levels(strand()) } .n_levels <- function() { c("A", "C", "G", "T", "N", "=", "-", "+") } .querybins.sam_seqlevels <- function() { fl <- system.file(package="Rsamtools", "extdata", "querybins.bam") bf <- BamFile(fl) seqlevels(bf) } ## target as data.frame .tadf <- function(pos=NULL, strand=NULL, nucleotide=NULL, left_bin=NULL, query_bin=NULL, count=NULL, which_label=NULL, seqnames=NULL, use_ex1.bam_levels=FALSE) { if(is.null(pos) || is.null(count) || is.null(seqnames)) stop("'pos', 'count', and 'seqnames' must not be 'NULL'") target <- data.frame(pos=as.integer(pos), stringsAsFactors=FALSE) seqnames_levels <- .querybins.sam_seqlevels() target <- cbind(seqnames=factor(seqnames, levels=seqnames_levels), target) if(!is.null(strand)) target <- cbind(target, strand=factor(strand, levels=.s_levels())) if(!is.null(nucleotide)) target <- cbind(target, nucleotide=factor(nucleotide, levels=.n_levels())) if(!is.null(left_bin)) target <- cbind(target, left_bin=left_bin) else if(!is.null(query_bin)) target <- cbind(target, query_bin=query_bin) target <- cbind(target, count=as.integer(count)) if(!is.null(which_label)) target <- cbind(target, which_label=which_label) target } ## make which labels .mwls <- function(param, run_lens) { wl <- Rsamtools:::.scanBam_extract_which_labels(param) if(length(wl) != length(run_lens)) stop("mismatched lengths, length(wl): '%d' length(run_lens): '%d'\n", length(wl), length(run_lens)) if(all(run_lens == 0L)) factor(levels=wl) else rep(wl, run_lens) } ## 1 2 3 4 5 6 7 8 9 10 11 12 ##+ A C G T = N ##- A C G T = N .sseq <- function() c("A", "C", "G", "T", "=", "N") .s <- function() ScanBamParam(which=GRanges("sim", IRanges(1,15))) .spos <- function() { ScanBamParam(which=GRanges("sim", IRanges(1,15)), flag=scanBamFlag(isMinusStrand=FALSE)) } .sneg <- function() { ScanBamParam(which=GRanges("sim", IRanges(1,15)), flag=scanBamFlag(isMinusStrand=TRUE)) } ## distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE .pp <- function(qbins=NULL, lbins=NULL) { if(!is.null(qbins)) PileupParam(distinguish_strands=FALSE, ignore_query_Ns=FALSE, query_bins=qbins) else if(!is.null(lbins)) PileupParam(distinguish_strands=FALSE, ignore_query_Ns=FALSE, left_bins=lbins) else PileupParam(ignore_query_Ns=FALSE) } ## PLUS STRAND TESTS ## query bin on plus strand, with finite (no Inf) positive bins test_qbin_plus_pos_finite <- function() { sbp <- .spos() pp <- .pp(qbins=c(0, 3, 6)) xx <- pileup(bf, scanBamParam=sbp, pileupParam=pp) seqnames <- space(bamWhich(sbp)) expected <- .tadf(seqnames=seqnames, pos=seq(1, 6), nucleotide=.sseq(), query_bin=c(rep("(0,3]", 3), rep("(3,6]", 3)), count=rep(1, 6), which_label=.mwls(sbp, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_qbin_plus_pos_finite() ## query bin on plus strand, with finite (no Inf) positive bins, drop ## first and last cycle test_qbin_plus_pos_finite_ends_dropped <- function() { sbp <- .spos() pp <- .pp(qbins=c(1, 3, 5)) xx <- pileup(bf, scanBamParam=sbp, pileupParam=pp) seqnames <- space(bamWhich(sbp)) expected <- .tadf(seqnames=seqnames, pos=seq(2, 5), nucleotide=c("C", "G", "T", "="), query_bin=c("(1,3]", "(1,3]", "(3,5]", "(3,5]"), count=rep(1, 4), which_label=.mwls(sbp, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_qbin_plus_pos_finite_ends_dropped() ## query bin on plus strand, with infinite positive bins test_qbin_plus_pos_infinite <- function() { sbp <- .spos() pp <- .pp(qbins=c(0, 3, Inf)) xx <- pileup(bf, scanBamParam=sbp, pileupParam=pp) seqnames <- space(bamWhich(sbp)) expected <- .tadf(seqnames=seqnames, pos=seq(1, 6), nucleotide=.sseq(), query_bin=c(rep("(0,3]", 3), rep("(3,Inf]", 3)), count=rep(1,6), which_label=.mwls(sbp, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_qbin_plus_pos_infinite() ## query bin on plus strand, with finite (no -Inf) negative bins test_qbin_plus_neg_finite <- function() { sbp <- .spos() pp <- .pp(qbins=c(-7, -4, -1)) xx <- pileup(bf, scanBamParam=sbp, pileupParam=pp) seqnames <- space(bamWhich(sbp)) expected <- .tadf(seqnames=seqnames, pos=seq(1, 6), nucleotide=.sseq(), query_bin=c(rep("(-7,-4]", 3), rep("(-4,-1]", 3)), count=rep(1,6), which_label=.mwls(sbp, length(seqnames))) ## factor levels come back in different order, but values the same xx[["query_bin"]] <- as.character(xx[["query_bin"]]) expected[["query_bin"]] <- as.character(expected[["query_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_qbin_plus_neg_finite() ## query bin on plus strand, with finite (no -Inf) negative bins, drop ## first and last cycle test_qbin_plus_neg_finite_ends_dropped <- function() { sbp <- .spos() pp <- .pp(qbins=c(-6, -4, -2)) xx <- pileup(bf, scanBamParam=sbp, pileupParam=pp) seqnames <- space(bamWhich(sbp)) expected <- .tadf(seqnames=seqnames, pos=seq(2, 5), nucleotide=c("C", "G", "T", "="), query_bin=c("(-6,-4]", "(-6,-4]", "(-4,-2]", "(-4,-2]"), count=rep(1,4), which_label=.mwls(sbp, length(seqnames))) ## factor levels come back in different order, but values the same xx[["query_bin"]] <- as.character(xx[["query_bin"]]) expected[["query_bin"]] <- as.character(expected[["query_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_qbin_plus_neg_finite_ends_dropped() ## query bin on plus strand, with infinite negative bins test_qbin_plus_neg_infinite <- function() { sbp <- .spos() pp <- .pp(qbins=c(-Inf, -4, -1)) xx <- pileup(bf, scanBamParam=sbp, pileupParam=pp) seqnames <- space(bamWhich(sbp)) expected <- .tadf(seqnames=seqnames, pos=seq(1, 6), nucleotide=.sseq(), query_bin=c(rep("(-Inf,-4]", 3), rep("(-4,-1]", 3)), count=rep(1,6), which_label=.mwls(sbp, length(seqnames))) ## factor levels come back in different order, but values the same xx[["query_bin"]] <- as.character(xx[["query_bin"]]) expected[["query_bin"]] <- as.character(expected[["query_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_qbin_plus_neg_infinite() ## MINUS STRAND TESTS ## query bin on minus strand, with finite (no Inf) positive bins test_qbin_minus_pos_finite <- function() { sbp <- .sneg() pp <- .pp(qbins=c(0, 3, 6)) xx <- pileup(bf, scanBamParam=sbp, pileupParam=pp) seqnames <- space(bamWhich(sbp)) expected <- .tadf(seqnames=seqnames, pos=seq(7, 12), nucleotide=.sseq(), query_bin=c(rep("(3,6]", 3), rep("(0,3]", 3)), count=rep(1, 6), which_label=.mwls(sbp, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_qbin_minus_pos_finite() ## query bin on minus strand, with finite (no Inf) positive bins, drop ## first and last cycle test_qbin_minus_pos_finite_ends_dropped <- function() { sbp <- .sneg() pp <- .pp(qbins=c(1, 3, 5)) xx <- pileup(bf, scanBamParam=sbp, pileupParam=pp) seqnames <- space(bamWhich(sbp)) expected <- .tadf(seqnames=seqnames, pos=seq(8, 11), nucleotide=c("C", "G", "T", "="), query_bin=c("(3,5]", "(3,5]", "(1,3]", "(1,3]"), count=rep(1, 4), which_label=.mwls(sbp, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_qbin_minus_pos_finite_ends_dropped() ## query bin on minus strand, with infinite positive bins test_qbin_minus_pos_infinite <- function() { sbp <- .sneg() pp <- .pp(qbins=c(0, 3, Inf)) xx <- pileup(bf, scanBamParam=sbp, pileupParam=pp) seqnames <- space(bamWhich(sbp)) expected <- .tadf(seqnames=seqnames, pos=seq(7, 12), nucleotide=.sseq(), query_bin=c(rep("(3,Inf]", 3), rep("(0,3]", 3)), count=rep(1,6), which_label=.mwls(sbp, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_qbin_minus_pos_infinite() ## query bin on minus strand, with finite (no -Inf) negative bins test_qbin_minus_neg_finite <- function() { sbp <- .sneg() pp <- .pp(qbins=c(-7, -4, -1)) xx <- pileup(bf, scanBamParam=sbp, pileupParam=pp) seqnames <- space(bamWhich(sbp)) expected <- .tadf(seqnames=seqnames, pos=seq(7, 12), nucleotide=.sseq(), query_bin=c(rep("(-4,-1]", 3), rep("(-7,-4]", 3)), count=rep(1,6), which_label=.mwls(sbp, length(seqnames))) ## factor levels come back in different order, but values the same xx[["query_bin"]] <- as.character(xx[["query_bin"]]) expected[["query_bin"]] <- as.character(expected[["query_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_qbin_minus_neg_finite() ## query bin on minus strand, with finite (no -Inf) negative bins, drop ## first and last cycle test_qbin_minus_neg_finite_ends_dropped <- function() { sbp <- .sneg() pp <- .pp(qbins=c(-6, -4, -2)) xx <- pileup(bf, scanBamParam=sbp, pileupParam=pp) seqnames <- space(bamWhich(sbp)) expected <- .tadf(seqnames=seqnames, pos=seq(8, 11), nucleotide=c("C", "G", "T", "="), query_bin=c("(-4,-2]", "(-4,-2]", "(-6,-4]", "(-6,-4]"), count=rep(1,4), which_label=.mwls(sbp, length(seqnames))) ## factor levels come back in different order, but values the same xx[["query_bin"]] <- as.character(xx[["query_bin"]]) expected[["query_bin"]] <- as.character(expected[["query_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_qbin_minus_neg_finite_ends_dropped() ## query bin on minus strand, with infinite negative bins test_qbin_minus_neg_infinite <- function() { sbp <- .sneg() pp <- .pp(qbins=c(-Inf, -4, -1)) xx <- pileup(bf, scanBamParam=sbp, pileupParam=pp) seqnames <- space(bamWhich(sbp)) expected <- .tadf(seqnames=seqnames, pos=seq(7, 12), nucleotide=.sseq(), query_bin=c(rep("(-4,-1]", 3), rep("(-Inf,-4]", 3)), count=rep(1,6), which_label=.mwls(sbp, length(seqnames))) ## factor levels come back in different order, but values the same xx[["query_bin"]] <- as.character(xx[["query_bin"]]) expected[["query_bin"]] <- as.character(expected[["query_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_qbin_minus_neg_infinite() ## COMBINED STRANDS ## query bin on both strands, pos bins, with 3 bins test_qbin_both_pos_3bin <- function() { sbp <- .s() pp <- .pp(qbins=c(0, 2, 4, 6)) xx <- pileup(bf, scanBamParam=sbp, pileupParam=pp) seqnames <- space(bamWhich(sbp)) plusbins <- c("(0,2]","(0,2]","(2,4]","(2,4]","(4,6]","(4,6]") expected <- .tadf(seqnames=seqnames, pos=seq(1, 12), nucleotide=c(.sseq(), .sseq()), query_bin=c(plusbins, rev(plusbins)), count=rep(1,12), which_label=.mwls(sbp, length(seqnames))) ## factor levels come back in different order, but values the same xx[["query_bin"]] <- as.character(xx[["query_bin"]]) expected[["query_bin"]] <- as.character(expected[["query_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_qbin_both_pos_3bin() ## query bin on both strands, neg bins, with 3 bins test_qbin_both_neg_3bin <- function() { sbp <- .s() pp <- .pp(qbins=c(-7, -5, -3, -1)) xx <- pileup(bf, scanBamParam=sbp, pileupParam=pp) seqnames <- space(bamWhich(sbp)) plusbins <- c("(-7,-5]","(-7,-5]","(-5,-3]","(-5,-3]","(-3,-1]","(-3,-1]") expected <- .tadf(seqnames=seqnames, pos=seq(1, 12), nucleotide=c(.sseq(), .sseq()), query_bin=c(plusbins, rev(plusbins)), count=rep(1,12), which_label=.mwls(sbp, length(seqnames))) ## factor levels come back in different order, but values the same xx[["query_bin"]] <- as.character(xx[["query_bin"]]) expected[["query_bin"]] <- as.character(expected[["query_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_qbin_both_neg_3bin() Rsamtools/inst/unitTests/test_pileup_revbins.R0000644000175400017540000004441213556116727022774 0ustar00biocbuildbiocbuildsuppressMessages({ library(Rsamtools) library(RUnit) }) ## .run_all <- function() { ## tests <- ls(envir=parent.frame())[grep('test_*', ls(envir=parent.frame()))] ## cat(tests) ## lapply(tests, function(x) { cat(paste0(x, "...\n")); do.call(x, list()) } ) ## } fl <- system.file(package="Rsamtools", "extdata", "revbins.bam") bf <- BamFile(fl) .reorder_data.frame <- function(df) { df <- df[do.call(order,df),] rownames(df) <- NULL df } .unordered_check <- function(expected, xx) { xx <- .reorder_data.frame(xx) expected <- .reorder_data.frame(expected) checkIdentical(xx, expected) } .s_levels <- function() { levels(strand()) } .n_levels <- function() { c("A", "C", "G", "T", "N", "=", "-", "+") } .revbins.sam_seqlevels <- function() { fl <- system.file(package="Rsamtools", "extdata", "revbins.bam") bf <- BamFile(fl) seqlevels(bf) } ## target as data.frame .tadf <- function(pos=NULL, strand=NULL, nucleotide=NULL, left_bin=NULL, count=NULL, which_label=NULL, seqnames=NULL, use_ex1.bam_levels=FALSE) { if(is.null(pos) || is.null(count) || is.null(seqnames)) stop("'pos', 'count', and 'seqnames' must not be 'NULL'") target <- data.frame(pos=as.integer(pos), stringsAsFactors=FALSE) seqnames_levels <- .revbins.sam_seqlevels() target <- cbind(seqnames=factor(seqnames, levels=seqnames_levels), target) if(!is.null(strand)) target <- cbind(target, strand=factor(strand, levels=.s_levels())) if(!is.null(nucleotide)) target <- cbind(target, nucleotide=factor(nucleotide, levels=.n_levels())) if(!is.null(left_bin)) target <- cbind(target, left_bin=left_bin) target <- cbind(target, count=as.integer(count)) if(!is.null(which_label)) target <- cbind(target, which_label=which_label) target } ## make which labels .mwls <- function(param, run_lens) { wl <- Rsamtools:::.scanBam_extract_which_labels(param) if(length(wl) != length(run_lens)) stop("mismatched lengths, length(wl): '%d' length(run_lens): '%d'\n", length(wl), length(run_lens)) if(all(run_lens == 0L)) factor(levels=wl) else rep(wl, run_lens) } .revbinsam_empty_df <- function(param) { wl <- .mwls(param, 0) .tadf(seqnames=character(), pos=integer(), strand=character(), nucleotide=character(), count=integer(), which_label=wl ) } ## 1-width .simple <- function() ScanBamParam(which=GRanges("simple", IRanges(1,10))) ## 2-width staggered .bistag <- function() ScanBamParam(which=GRanges("bistag", IRanges(1,10))) ## 3-width staggered .tristag <- function() ScanBamParam(which=GRanges("tristag", IRanges(1,10))) ## for testing -Inf .inf <- function() ScanBamParam(which=GRanges("inf", IRanges(1,10))) ## different strands .diffstr <- function() ScanBamParam(which=GRanges("diffstr", IRanges(1,10))) ## single bin, width 1 test_revbin_last <- function() { sb_param <- .simple() pp <- PileupParam( distinguish_strands=FALSE, left_bins=c(-2, -1)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=seq(1L, 5L), nucleotide=rep("=", 5), left_bin=rep("(-2,-1]", 5), count=rep(1L,5L), which_label=.mwls(sb_param, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_last() ## single bin, width 1 test_revbin_1_from_last <- function() { sb_param <- .simple() pp <- PileupParam( distinguish_strands=FALSE, left_bins=c(-3, -2)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=seq(1L, 4L), nucleotide=rep("A", 4), left_bin=rep("(-3,-2]", 4), count=rep(1L,4L), which_label=.mwls(sb_param, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_1_from_last() ## single bin, width 1 test_revbin_2_from_last <- function() { sb_param <- .simple() pp <- PileupParam( distinguish_strands=FALSE, left_bins=c(-4, -3)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=seq(1L, 3L), nucleotide=rep("C", 3), left_bin=rep("(-4,-3]", 3), count=rep(1L,3L), which_label=.mwls(sb_param, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_2_from_last() ## single bin, width 2 test_revbin_width_2 <- function() { sb_param <- .simple() pp <- PileupParam( distinguish_strands=FALSE, left_bins=c(-3, -1)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1, 1, 2, 2, 3, 3, 4, 4, 5), nucleotide=c("=", "A", "=", "A", "=", "A", "=", "A", "="), left_bin=rep("(-3,-1]", 9), count=rep(1L,9L), which_label=.mwls(sb_param, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_width_2() ## 2 bin, width 1, all satisfy length test_revbin_2_bin_width_1_321 <- function() { sb_param <- .simple() pp <- PileupParam( distinguish_strands=FALSE, left_bins=c(-3, -2, -1)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1, 1, 2, 2, 3, 3, 4, 4, 5), nucleotide=c("=", "A", "=", "A", "=", "A", "=", "A", "="), left_bin=c("(-2,-1]","(-3,-2]","(-2,-1]","(-3,-2]", "(-2,-1]","(-3,-2]","(-2,-1]","(-3,-2]", "(-2,-1]"), count=rep(1L,9L), which_label=.mwls(sb_param, length(seqnames))) ## factor levels come back in different order, but values the same xx[["left_bin"]] <- as.character(xx[["left_bin"]]) expected[["left_bin"]] <- as.character(expected[["left_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_2_bin_width_1_321() ## 2 bin, width 1, all but one satisfy length test_revbin_2_bin_width_1_432 <- function() { sb_param <- .simple() pp <- PileupParam( distinguish_strands=FALSE, left_bins=c(-4, -3, -2)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1, 1, 2, 2, 3, 3, 4), nucleotide=c("A", "C", "A", "C", "A", "C", "A"), left_bin=c("(-3,-2]","(-4,-3]","(-3,-2]", "(-4,-3]", "(-3,-2]","(-4,-3]","(-3,-2]"), count=rep(1L,7L), which_label=.mwls(sb_param, length(seqnames))) ## factor levels come back in different order, but values the same xx[["left_bin"]] <- as.character(xx[["left_bin"]]) expected[["left_bin"]] <- as.character(expected[["left_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_2_bin_width_1_432() ## arbitrary bins test_revbin_arb_bins <- function() { sb_param <- .simple() pp <- PileupParam( distinguish_strands=FALSE, left_bins=c(-5, -4, -3, -1)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(rep(1, 4), rep(2, 4), rep(3, 3), 4, 4, 5), nucleotide=c("=","A","C","G","=","A","C","G","=","A","C","=","A","="), left_bin=c("(-3,-1]","(-3,-1]","(-4,-3]","(-5,-4]", "(-3,-1]","(-3,-1]","(-4,-3]","(-5,-4]", "(-3,-1]","(-3,-1]","(-4,-3]", "(-3,-1]","(-3,-1]","(-3,-1]"), count=rep(1L,14L), which_label=.mwls(sb_param, length(seqnames))) ## factor levels come back in different order, but values the same xx[["left_bin"]] <- as.character(xx[["left_bin"]]) expected[["left_bin"]] <- as.character(expected[["left_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_arb_bins() ## arbitrary bins, collapse nucleotides test_revbin_arb_bins_collapse_nucs <- function() { sb_param <- .simple() pp <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, left_bins=c(-5, -4, -3, -1)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(rep(1, 3), rep(2, 3), rep(3, 2), 4, 5), left_bin=c("(-5,-4]","(-4,-3]","(-3,-1]", "(-5,-4]","(-4,-3]","(-3,-1]", "(-4,-3]","(-3,-1]", "(-3,-1]", "(-3,-1]"), count=c(1,1,2,1,1,2,1,2,2,1), which_label=.mwls(sb_param, length(seqnames))) ## factor levels come back in different order, but values the same xx[["left_bin"]] <- as.character(xx[["left_bin"]]) expected[["left_bin"]] <- as.character(expected[["left_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_arb_bins_collapse_nucs() ## bin range to beginning, collapse nucleotides test_revbin_collapse_to_beginning <- function() { sb_param <- .simple() pp <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, left_bins=c(-6, -2)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1, 2, 3, 4), left_bin=c(rep("(-6,-2]", 4)), count=c(4, 3, 2, 1), which_label=.mwls(sb_param, length(seqnames))) ## factor levels come back in different order, but values the same xx[["left_bin"]] <- as.character(xx[["left_bin"]]) expected[["left_bin"]] <- as.character(expected[["left_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_collapse_to_beginning() ## staggered, reads length 2, separate bins end to beginning test_revbin_staggered_sep_bins <- function() { sb_param <- .bistag() pp <- PileupParam( distinguish_strands=FALSE, ignore_query_Ns=FALSE, left_bins=c(-3, -2, -1)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1, 2, 2, 3, 3, 4, 4, 5, 5, 6), nucleotide=c("A","=","C","=","G","=","T","=","N","="), left_bin=rep(c("(-3,-2]", "(-2,-1]"), 5), count=rep(1, 10), which_label=.mwls(sb_param, length(seqnames))) ## factor levels come back in different order, but values the same xx[["left_bin"]] <- as.character(xx[["left_bin"]]) expected[["left_bin"]] <- as.character(expected[["left_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_staggered_sep_bins() ## staggered, reads length 2, single bin end to beginning test_revbin_staggered_single_bin <- function() { sb_param <- .bistag() pp <- PileupParam( distinguish_strands=FALSE, ignore_query_Ns=FALSE, left_bins=c(-3, -1)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1, 2, 2, 3, 3, 4, 4, 5, 5, 6), nucleotide=c("A","=","C","=","G","=","T","=","N","="), left_bin=rep("(-3,-1]", 10), count=rep(1, 10), which_label=.mwls(sb_param, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_staggered_single_bin() ## staggered, reads length 2, single bin end to beginning, collapse nucs test_revbin_staggered_single_bin_collapse_nucs <- function() { sb_param <- .bistag() pp <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, left_bins=c(-3, -1)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1, 2, 3, 4, 5, 6), left_bin=rep("(-3,-1]", 6), count=c(1, 2, 2, 2, 2, 1), which_label=.mwls(sb_param, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_staggered_single_bin_collapse_nucs() ## staggered, reads length 2-3, c(-4, -2) test_revbin_staggered_omit_end <- function() { sb_param <- .tristag() pp <- PileupParam( distinguish_strands=FALSE, ignore_query_Ns=FALSE, left_bins=c(-4, -2)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1, 2, 3, 3, 4, 4, 5, 5, 6), nucleotide=c("A","C","=","G","=","T","=","N","="), left_bin=rep("(-4,-2]", 9), count=rep(1, 9), which_label=.mwls(sb_param, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_staggered_omit_end() ## staggered, reads length 2-3, c(-4, -2) test_revbin_staggered_omit_end_collapse_nucs <- function() { sb_param <- .tristag() pp <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, left_bins=c(-4, -2)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1, 2, 3, 4, 5, 6), left_bin=rep("(-4,-2]", 6), count=c(1, 1, 2, 2, 2, 1), which_label=.mwls(sb_param, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_staggered_omit_end_collapse_nucs() ## -INF ## c(-Inf, -3, -2) test_revbin_inf <- function() { sb_param <- .inf() pp <- PileupParam( distinguish_strands=FALSE, left_bins=c(-Inf, -3, -2)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1, 2, 3, 3, 4, 4, 5, 5, 6), nucleotide=c("A", "A", "A", "C", "A", "C", "A", "C", "C"), left_bin=c(rep("(-Inf,-3]", 6), "(-3,-2]", "(-Inf,-3]", "(-3,-2]"), count=rep(1, 9), which_label=.mwls(sb_param, length(seqnames))) ## factor levels come back in different order, but values the same xx[["left_bin"]] <- as.character(xx[["left_bin"]]) expected[["left_bin"]] <- as.character(expected[["left_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_inf() ## c(-Inf, -3, -2), collapse nucs test_revbin_inf_collapse_nucs <- function() { sb_param <- .inf() pp <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, left_bins=c(-Inf, -3, -2)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1, 2, 3, 4, 5, 5, 6), left_bin=c(rep("(-Inf,-3]", 5), "(-3,-2]", "(-3,-2]"), count=c(1, 1, 2, 2, 1, 1, 1), which_label=.mwls(sb_param, length(seqnames))) ## factor levels come back in different order, but values the same xx[["left_bin"]] <- as.character(xx[["left_bin"]]) expected[["left_bin"]] <- as.character(expected[["left_bin"]]) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_inf_collapse_nucs() ## end -Inf ## DIFFERENT STRANDS ## c(-4, -1), dist strands TRUE, dist nucs TRUE test_revbin_diff_strands_distinguish_strands <- function() { sb_param <- .diffstr() pp <- PileupParam( ignore_query_Ns=FALSE, left_bins=c(-4, -1)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1, 2, 2, 3, 3, 4), strand=c("+", "+", "-", "-", "+", "-"), nucleotide=c("A", "C", "T", "=", "G", "N"), left_bin=rep("(-4,-1]", 6), count=rep(1, 6), which_label=.mwls(sb_param, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_diff_strands_distinguish_strands() ## c(-4, -1), dist strands FALSE, dist nucs FALSE test_revbin_diff_strands_collapse_all <- function() { sb_param <- .diffstr() pp <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, left_bins=c(-4, -1)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=pp) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1, 2, 3, 4), left_bin=rep("(-4,-1]", 4), count=c(1, 2, 2, 1), which_label=.mwls(sb_param, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_revbin_diff_strands_collapse_all() Rsamtools/inst/unitTests/test_pileup_single_range.R0000644000175400017540000014720113556116727023761 0ustar00biocbuildbiocbuildsuppressMessages({ library(Rsamtools) library(RUnit) }) ## .run_all <- function() { ## tests <- ls(envir=parent.frame())[grep('test_*', ls(envir=parent.frame()))] ## cat(tests) ## lapply(tests, function(x) { cat(paste0(x, "...\n")); do.call(x, list()) } ) ## } fl <- system.file(package="Rsamtools", "extdata", "tiny.bam") bf <- BamFile(fl) .reorder_data.frame <- function(df) { df <- df[do.call(order,df),] rownames(df) <- NULL df } .unordered_check <- function(expected, xx) { xx <- .reorder_data.frame(xx) expected <- .reorder_data.frame(expected) checkIdentical(xx, expected) } .s_levels <- function() { levels(strand()) } .n_levels <- function() { c("A", "C", "G", "T", "N", "=", "-", "+") } .tiny.sam_seqlevels <- function() { fl <- system.file(package="Rsamtools", "extdata", "tiny.bam") bf <- BamFile(fl) seqlevels(bf) } .ex1.sam_seqlevels <- function() { fl <- system.file(package="Rsamtools", "extdata", "ex1.bam") bf <- BamFile(fl) seqlevels(bf) } ## target as data.frame .tadf <- function(pos=NULL, strand=NULL, nucleotide=NULL, left_bin=NULL, count=NULL, which_label=NULL, seqnames=NULL, use_ex1.bam_levels=FALSE) { if(is.null(pos) || is.null(count) || is.null(seqnames)) stop("'pos', 'count', and 'seqnames' must not be 'NULL'") target <- data.frame(pos=as.integer(pos), stringsAsFactors=FALSE) seqnames_levels <- .tiny.sam_seqlevels() if(use_ex1.bam_levels) seqnames_levels <- .ex1.sam_seqlevels() target <- cbind(seqnames=factor(seqnames, levels=seqnames_levels), target) if(!is.null(strand)) target <- cbind(target, strand=factor(strand, levels=.s_levels())) if(!is.null(nucleotide)) target <- cbind(target, nucleotide=factor(nucleotide, levels=.n_levels())) if(!is.null(left_bin)) target <- cbind(target, left_bin=left_bin) target <- cbind(target, count=as.integer(count)) if(!is.null(which_label)) target <- cbind(target, which_label=which_label) target } ## make which labels .mwls <- function(param, run_lens) { wl <- Rsamtools:::.scanBam_extract_which_labels(param) if(length(wl) != length(run_lens)) stop("mismatched lengths, length(wl): '%d' length(run_lens): '%d'\n", length(wl), length(run_lens)) if(all(run_lens == 0L)) factor(levels=wl) else rep(wl, run_lens) } .tinysam_empty_df <- function(param) { wl <- .mwls(param, 0) .tadf(seqnames=character(), pos=integer(), strand=character(), nucleotide=character(), count=integer(), which_label=wl ) } .seq1 <- function() ScanBamParam(which=GRanges("seq1", IRanges(1,10))) .seq2 <- function() ScanBamParam(which=GRanges("seq2", IRanges(1,10))) .diff_strands <- function() ScanBamParam(which=GRanges("diff_strands", IRanges(1,10))) .coll_nucs_basic <- function() ScanBamParam(which=GRanges("coll_nucs_basic", IRanges(1,10))) .coll_nucs_adv <- function() ScanBamParam(which=GRanges("coll_nucs_adv", IRanges(1,10))) .dist_all <- function() ScanBamParam(which=GRanges("dist_all", IRanges(1,10))) .min_mapq <- function() ScanBamParam(which=GRanges("min_mapq", IRanges(1,10))) .min_base_qual <- function() ScanBamParam(which=GRanges("min_base_qual", IRanges(1,10))) .max_depth <- function() ScanBamParam(which=GRanges("max_depth", IRanges(1,10))) .full_seq_range <- function() ScanBamParam(which=GRanges("full_seq_range", IRanges(1,28))) .Biostrings_DNA_ALPHABET <- function() ScanBamParam(which=GRanges("Biostrings_DNA_ALPHABET", IRanges(1,18))) .ext_cigar_hard <- function() ScanBamParam(which=GRanges("ext_cigar_hard", IRanges(1,10))) .ext_cigar_soft <- function() ScanBamParam(which=GRanges("ext_cigar_soft", IRanges(1,10))) .ref_skip <- function() ScanBamParam(which=GRanges("ref_skip", IRanges(1,10))) .include_deletions <- function() ScanBamParam(which=GRanges("include_deletions", IRanges(1,10))) .min_nuc_depth_mono <- function() ScanBamParam(which=GRanges("min_nuc_depth_mono", IRanges(1,10))) .min_nuc_depth_poly <- function() ScanBamParam(which=GRanges("min_nuc_depth_poly", IRanges(1,10))) .min_minor_allele_depth <- function() ScanBamParam(which=GRanges("min_minor_allele_depth", IRanges(1,10))) .multi_range_single_rname <- function() ScanBamParam(which=GRanges("multi_range_single_rname", IRanges(c(1,3),width=2))) .filter_strands <- function() ScanBamParam(which=GRanges("filter_strands", IRanges(1, 10))) .seqnames_from_tinysam_c <- function() ScanBamParam(which=GRanges("seqnames_from_tinysam_c", IRanges(1,2))) .all_nuc_levels <- function() ScanBamParam(which=GRanges("all_nuc_levels", IRanges(1, 7))) ## test sequence with length 5 .bins_5 <- function() ScanBamParam(which=GRanges("bins_5", IRanges(1,5))) .ins1 <- function() ScanBamParam(which=GRanges("ins1", IRanges(1,5))) .ins3 <- function() ScanBamParam(which=GRanges("ins3", IRanges(1,5))) .ins_multiread <- function() ScanBamParam(which=GRanges("ins_multiread", IRanges(1,5))) .ins_base_disqualifiers <- function() ScanBamParam(which=GRanges("ins_base_disqualifiers", IRanges(1,5))) .ins_deletion <- function() ScanBamParam(which=GRanges("ins_deletion", IRanges(1,12))) .ins_refskip <- function() ScanBamParam(which=GRanges("ins_refskip", IRanges(1,12))) ## verify that, in terms of insertions, refskips and deletions are ## handled identically (i.e., insertion info doesn't get dropped when ## a refskip precedes the insertion) test_insert_refskip_deletion_identical <- function() { p_param <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=TRUE, include_deletions=FALSE, include_insertions=TRUE) refskip_res <- pileup(bf, scanBamParam=.ins_refskip(), pileupParam=p_param) deletion_res <- pileup(bf, scanBamParam=.ins_deletion(), pileupParam=p_param) test_cols <- c("pos", "nucleotide", "count") ##print(refskip_res[test_cols]) ##print(deletion_res[test_cols]) .unordered_check(deletion_res[test_cols], refskip_res[test_cols]) } ##test_insert_refskip_deletion_identical() test_insert_refskip <- function() { sb_param <- .ins_refskip() p_param <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=TRUE, include_insertions=TRUE) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=p_param) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=seq(1L, 3L), nucleotide=c("A", "+", "C"), count=rep(1L, 3L), which_label=.mwls(sb_param, length(seqnames))) ##print(.reorder_data.frame(xx)); ##str(xx) ##print(expected); ##str(expected) .unordered_check(xx, expected) } ##test_insert_refskip() ## Throw in a couple individual base disqualifiers (instead of ## whole-alignment disqualifiers) to verify that insertions are ## getting passed on even when the aligned base at a given position ## does not satisfy filtering criteria test_insert_independent_of_base_disqualifiers <- function() { sb_param <- .ins_base_disqualifiers() p_param <- PileupParam( min_base_quality=11L, ## called base in .sam has quality 10 ('+' ASCII) ignore_query_Ns=TRUE, ## and is 'N' nucleotide distinguish_strands=FALSE, distinguish_nucleotides=TRUE, include_insertions=TRUE) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=p_param) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=1L, nucleotide="+", count=1L, which_label=.mwls(sb_param, length(seqnames))) ##print(.reorder_data.frame(xx)); ##str(xx) ##print(expected); ##str(expected) .unordered_check(xx, expected) } ##test_insert_independent_of_base_disqualifiers() test_insert_multiread <- function() { sb_param <- .ins_multiread() p_param <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=TRUE, include_insertions=TRUE) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=p_param) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1L, 1L, 2L, 2L, 2L, 3L), nucleotide=c("T", "+", "G", "T", "+", "T"), count=c(2L, 2L, 1L, 1L, 2L, 2L), which_label=.mwls(sb_param, length(seqnames))) ##print(.reorder_data.frame(xx)); ##str(xx) ##print(expected); ##str(expected) .unordered_check(xx, expected) } ##test_insert_multiread() test_insert_truncate <- function() { sb_param <- .ins3() p_param <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=TRUE, include_insertions=TRUE) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=p_param) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1L, 1L, 2L), nucleotide=c("A", "+", "C"), count=rep(1L, 3L), which_label=.mwls(sb_param, length(seqnames))) ##print(.reorder_data.frame(xx)); ##str(xx) ##print(expected); ##str(expected) .unordered_check(xx, expected) } ##test_insert_truncate() test_insert1_collapse <- function() { sb_param <- .ins1() p_param <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, include_insertions=TRUE) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=p_param) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1L, 2L), count=c(2L, 1L), which_label=.mwls(sb_param, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } ##test_insert1_collapse() test_insert1_distinguish <- function() { sb_param <- .ins1() p_param <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=TRUE, include_insertions=TRUE) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=p_param) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=c(1L, 1L, 2L), nucleotide=c("A", "+", "C"), count=rep(1L, 3L), which_label=.mwls(sb_param, length(seqnames))) ##print(.reorder_data.frame(xx)); ##str(xx); ##print(expected); ##str(expected) .unordered_check(xx, expected) } ##test_insert1_distinguish() test_bins_5_unsorted <- function() { sb_param <- .bins_5() p_param <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, left_bins=c(4,2)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=p_param) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=seq(3L, 4L), left_bin=c("(2,4]","(2,4]"), count=rep(1L,2L), which_label=.mwls(sb_param, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } test_bins_5_single_width_bins <- function() { sb_param <- .bins_5() p_param <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ##left_bins=c(2, 3, 4)) ## original left_bins=seq(0L, 5L)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=p_param) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=seq(1L, 5L), left_bin=c("(0,1]","(1,2]","(2,3]","(3,4]","(4,5]"), count=rep(1L,5L), which_label=.mwls(sb_param, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } test_bins_5_fullrange_3bin <- function() { sb_param <- .bins_5() p_param <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, left_bins=c(0, 2, 4, Inf)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=p_param) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=seq(1L, 5L), left_bin=c("(0,2]","(0,2]","(2,4]","(2,4]","(4,Inf]"), count=rep(1L,5L), which_label=.mwls(sb_param, length(seqnames))) ##print(xx); ##str(xx); ##print(expected); ##str(expected) checkIdentical(expected, xx) } test_bins_5_singleinteriorbin <- function() { sb_param <- .bins_5() p_param <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, left_bins=c(1, 4)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=p_param) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=seq(2L, 4L), left_bin=rep("(1,4]",3L), count=rep(1L,3L), which_label=.mwls(sb_param, length(seqnames))) ##print(xx);## str(xx); ##print(expected);## str(expected) checkIdentical(expected, xx) } test_bins_5_trailingbin <- function() { sb_param <- .bins_5() p_param <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, left_bins=c(3, Inf)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=p_param) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=seq(4L, 5L), left_bin=rep("(3,Inf]",2), count=rep(1L,2L), which_label=.mwls(sb_param, length(seqnames))) ##print(xx);## str(xx); ##print(expected);## str(expected) checkIdentical(expected, xx) } test_bins_5_leadingbin <- function() { sb_param <- .bins_5() p_param <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, left_bins=c(0, 2)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=p_param) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=seq(1L, 2L), left_bin=rep("(0,2]",2), count=rep(1L,2L), which_label=.mwls(sb_param, length(seqnames))) ##print(xx);## str(xx); ##print(expected);## str(expected) checkIdentical(expected, xx) } test_bins_5_fullrangesinglebin <- function() { sb_param <- .bins_5() p_param <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, left_bins=c(0, Inf)) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=p_param) seqnames <- space(bamWhich(sb_param)) expected <- .tadf(seqnames=seqnames, pos=seq(1L, 5L), left_bin=rep("(0,Inf]",5), count=rep(1L,5L), which_label=.mwls(sb_param, length(seqnames))) ## print(xx); str(xx); ## print(expected); str(expected) checkIdentical(expected, xx) } test_bins_levels <- function() { sb_param <- .bins_5() ## yes, decreasing order (testing preprocess func too) left_bins <- c(Inf, 4, 2, 0) p_param <- PileupParam( left_bins=left_bins) xx <- pileup(bf, scanBamParam=sb_param, pileupParam=p_param) expected <- factor(levels=levels(cut(0, left_bins))) checkIdentical(levels(expected), levels(xx$left_bin)) } ## END LEFT_BINS ## test all nuc levels represented test_all_nuc_levels <- function() { scanBamParam <- .all_nuc_levels() pileupParam <- PileupParam( distinguish_strands=FALSE, ignore_query_Ns=FALSE, include_deletions=TRUE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos=seq(1, 7), count=rep(1, 7), nucleotide=c("A", "C", "-", "G", "T", "N", "="), which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);str(xx);print(expected);str(expected) checkIdentical(expected, xx) } ## test that seqnames are set from C correctly test_seqnames_from_tinysam_in_c <- function() { scanBamParam <- .seqnames_from_tinysam_c() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos = 1, count = 1, which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);str(xx);print(expected);str(expected) checkIdentical(expected, xx) } test_scanBam_filter_criteria_dropsome <- function() { ## assume that if one filtering criterion works, all work scanBamParam <- .filter_strands() flag <- scanBamFlag(isMinusStrand=TRUE) bamFlag(scanBamParam) <- flag pileupParam <- PileupParam(distinguish_nucleotides=FALSE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos = 1, strand= "-", count = 1, which_label=.mwls(scanBamParam, length(seqnames))) ## print(xx);str(xx) ## print(expected);str(expected) checkIdentical(expected, xx) } test_scanBam_filter_criteria_dropnone <- function() { ## assume that if one filtering criterion works, all work scanBamParam <- .filter_strands() pileupParam <- PileupParam(distinguish_nucleotides=FALSE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos = c(1, 1), strand = c("+", "-"), count = c(1, 1), which_label=.mwls(scanBamParam, length(seqnames))) ## print(xx);str(xx) ## print(expected);str(expected) checkIdentical(expected, xx) } test_data.frame_format <- function() { fl <- system.file(package="Rsamtools", "extdata", "ex1.bam") bf <- BamFile(fl) scanBamParam <- ScanBamParam(which=GRanges(c("seq1", "seq2"), IRanges(1, 3))) pileupParam <- PileupParam(distinguish_strands=TRUE, distinguish_nucleotides=TRUE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) expected <- .tadf( seqnames=c(rep("seq1", 3), rep("seq2", 5)), pos=c(1, 2, 3, 1, 2, 2, 3, 3), strand=c("+", "+", "+", "+", "+", "-", "+", "-"), nucleotide=c("C", "A", "C", "T", "T", "T", "C", "C"), count=c(1, 1, 2, 2, 3, 1, 3, 1), which_label=c(rep("seq1:1-3", 3), rep("seq2:1-3", 5)), use_ex1.bam_levels=TRUE) ##print(xx);str(xx);print(expected);str(expected) checkIdentical(expected, xx) } ## FIX ME: better name test_multirange_yield_clear <- function() { scanBamParam <- .multi_range_single_rname() pileupParam <- PileupParam(distinguish_strands=FALSE, distinguish_nucleotides=TRUE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos = seq(1L, 4L), nucleotide=c("A", "C", "G", "T"), count=rep(1L, 4L), which_label=.mwls(scanBamParam, c(2, 2))) ##print(xx);str(xx);print(expected);str(expected) checkIdentical(expected, xx) } ## MULTI-READ DISTINGUISH* test_distinguish_none <- function() { scanBamParam <- .dist_all() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= seq(1L,6L), count= c(30L, seq(18L, 2L, -4)), which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) checkIdentical(expected, xx) } test_distinguish_all <- function() { scanBamParam <- .dist_all() pileupParam <- PileupParam( distinguish_strands=TRUE, distinguish_nucleotides=TRUE, left_bins=c(0,3,Inf)) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos=c(rep(1,8),2,2,3,3,4,4,4,4,5,5,6,6), nucleotide=c("A","A","C","C","G","G","T","T",rep("A",12)), strand=c(rep(c("+","-"),6),"+","+","-","-","+","-","+","-"), left_bin=c(rep("(0,3]",12), rep(c("(0,3]","(3,Inf]"),2), rep("(3,Inf]",4)), count=c(8,7,2,3,3,2,2,3,9,9,7,7,3,2,3,2,3,3,1,1), which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) checkIdentical(expected,xx) } ##test_distinguish_all() test_distinguish_strand_bin <- function() { scanBamParam <- .dist_all() pileupParam <- PileupParam( distinguish_strands=TRUE, distinguish_nucleotides=FALSE, left_bins=c(0,3,Inf)) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos=c(1,1,2,2,3,3,4,4,4,4,5,5,6,6), strand=c(rep(c("+","-"),3),"+","+","-","-",rep(c("+","-"),2)), left_bin=c(rep(c("(0,3]"),7),"(3,Inf]","(0,3]",rep(c("(3,Inf]"),5)), count=c(15,15,9,9,7,7,3,2,3,2,3,3,1,1), which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) checkIdentical(expected,xx) } test_distinguish_nuc_bin <- function() { scanBamParam <- .dist_all() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=TRUE, left_bins=c(0,3,Inf)) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= c(rep( 1L, 4L),2,3,4,4,5,6), nucleotide=c("A","C","G","T", rep("A",6)), left_bin=c(rep("(0,3]",7),rep("(3,Inf]",3)), count=c(15,5,5,5,18,14,6,4,6,2), which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) checkIdentical(expected, xx) } test_distinguish_bins_only <- function() { scanBamParam <- .dist_all() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, left_bins=c(0,3,Inf)) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos = c(1L,2L,3L,4L,4L,5L,6L), left_bin=c(rep("(0,3]",4L),rep("(3,Inf]",3L)), count=c(30L,18L,14L,6L,4L,6L,2L), which_label=.mwls(scanBamParam, length(seqnames))) ## print(xx) ## print(expected) checkIdentical(expected, xx) } test_distinguish_nuc_only <- function() { scanBamParam <- .dist_all() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=TRUE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= c(rep(1L, 4L), seq(2L,6L)), nucleotide=c("A", "C", "G", "T", rep("A",5L)), count= c(15L,5L,5L,5L,18L,14L,10L,6L,2L), which_label=.mwls(scanBamParam, length(seqnames))) ##print(.reorder_data.frame(xx));print(.reorder_data.frame(expected)) .unordered_check(expected, xx) } test_distinguish_strand_only <- function() { scanBamParam <- .dist_all() pileupParam <- PileupParam( distinguish_strands=TRUE, distinguish_nucleotides=FALSE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= unlist(lapply(1:6,rep,2)), strand=rep(c("+","-"),6), ##count= c(15,15,c(unlist(lapply(seq(9,1,-2),rep,2)))), count= c(15,15,9,9,7,7,5,5,3,3,1,1), ## clearer? which_label=.mwls(scanBamParam, length(seqnames))) ## print(xx); ## print(expected); checkIdentical(expected, xx) } test_distinguish_nuc_strand <- function() { scanBamParam <- .dist_all() pileupParam <- PileupParam( distinguish_strands=TRUE, distinguish_nucleotides=TRUE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= c(rep( 1L, 8L),unlist(lapply(seq(2,6),rep,2))), strand=c(rep("+",4),rep("-",4),rep(c("+","-"),5)), nucleotide=c(rep(c("A","C","G","T"),2), rep("A",10)), count=c(8,2,3,2,7,3,2,3,unlist(lapply(seq(9,1,-2),rep,2))), which_label=.mwls(scanBamParam, length(seqnames))) ##print(.reorder_data.frame(xx));print(.reorder_data.frame(expected)) .unordered_check(expected, xx) } ## SINGLE-READ DISTINGUISH* test_distinguish_nucleotides_adv <- function() { ## Test that a position with more than two alignments with diff nucleotides ## gets counted correctly scanBamParam <- .coll_nucs_adv() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=TRUE, ignore_query_Ns=FALSE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= c( 1L, 1L, 1L), nucleotide= c("G", "A", "T"), count= c( 2L, 1L, 1L), which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) .unordered_check(expected, xx) } test_distinguish_nucleotides_basic <- function() { ## Test that a position with more than two alignments with *same* nucleotide ## gets counted correctly scanBamParam <- .coll_nucs_basic() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=TRUE, ignore_query_Ns=TRUE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= seq(1L, 5L, 1L), nucleotide= rep("C", 5L), count= rep(2L, 5L), which_label=.mwls(scanBamParam, length(seqnames))) checkIdentical(expected, xx) } test_no_distinguish_strands_mixed <- function() { ## NOTE: even though this looks like "distinguish nothing", it's not: ## test seqs in tiny.sam are identical POS and SEQ, but different strands scanBamParam <- .diff_strands() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=TRUE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= seq(1L, 5L, 1L), count= rep(2L, 5L), which_label=.mwls(scanBamParam, length(seqnames))) checkIdentical(expected, xx) } test_distinguish_strands_mixed <- function() { scanBamParam <- .diff_strands() pileupParam <- PileupParam( distinguish_strands=TRUE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= c(1L, 1L, 2L, 2L, 3L, 3L, 4L, 4L, 5L, 5L), strand=rep(c("+", "-"), 5), count= rep(1L, 10), which_label=.mwls(scanBamParam, length(seqnames))) checkIdentical(expected, xx) } ## MIN MINOR ALLELE DEPTH test_minor_allele_depth_dropnone <- function() { scanBamParam <- .min_minor_allele_depth() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, min_nucleotide_depth=0L, min_minor_allele_depth=1L) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= 1L, count=4L, which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) checkIdentical(expected, xx) } test_minor_allele_depth_dropall <- function() { scanBamParam <- .min_minor_allele_depth() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, min_nucleotide_depth=0L, min_minor_allele_depth=2L) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tinysam_empty_df(scanBamParam)[c("seqnames", "pos", "count", "which_label")] ##print(xx);str(xx);print(expected);str(expected) checkIdentical(expected, xx) } ## MIN NUC DEPTH test_min_nuc_depth_polyread <- function() { ## should be implemented in a way that this won't fail while ## the other min_nuc_depth tests pass, but since code is still ## highly volatile, make sure code is robust to those changes scanBamParam <- .min_nuc_depth_poly() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, min_nucleotide_depth=2L) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= 1L, count=2L, which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) checkIdentical(expected, xx) } test_min_nuc_depth_dropnone <- function() { ## min_nuc_depth is one alignment with single 'A' scanBamParam <- .min_nuc_depth_mono() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, min_nucleotide_depth=0L) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= 1L, count=1L, which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) checkIdentical(expected, xx) } test_min_nuc_depth_dropall <- function() { ## min_nuc_depth is one alignment with single 'A' scanBamParam <- .min_nuc_depth_mono() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, min_nucleotide_depth=2L) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tinysam_empty_df(scanBamParam)[c("seqnames", "pos", "count", "which_label")] ##print(xx);str(xx);print(expected);str(expected) checkIdentical(expected, xx) } ## INCLUDE DELETIONS test_include_dels_dist_nucs <- function() { scanBamParam <- .include_deletions() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=TRUE, ignore_query_Ns=FALSE, include_deletions=TRUE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= c(1L, 2L, 3L), nucleotide=c("A", "-", "A"), count= c(1L, 1L, 1L), which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) checkIdentical(expected, xx) } test_include_dels_no_dist_nucs <- function() { scanBamParam <- .include_deletions() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, include_deletions=TRUE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= c(1L, 2L, 3L), count=c(1L, 1L, 1L), which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) checkIdentical(expected, xx) } test_no_include_dels_no_dist_nucs <- function() { scanBamParam <- .include_deletions() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, include_deletions=FALSE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= c(1L, 3L), count=c(1L, 1L), which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) checkIdentical(expected, xx) } ## REF SKIP test_ref_skip <- function() { ## sanity check that an N in a cigar means don't tally it--ever! ## (regardless of what include_deletions says) scanBamParam <- .ref_skip() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, include_deletions=TRUE) include_dels <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, include_deletions=FALSE) exclude_dels <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) ##print(include_dels);print(exclude_dels) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= c(1L, 3L), count=c(1L, 1L), which_label=.mwls(scanBamParam, length(seqnames))) ##print(expected) checkIdentical(expected, include_dels) checkIdentical(include_dels, exclude_dels) } ## SOFT- AND HARD-CLIPPING test_ext_cigar_clipping <- function() { ## keep in as a sanity check that insert/filter code doesn't mess clips scanBamParam <- .ext_cigar_hard() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, include_deletions=TRUE) hard_res <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) ##print("hard clipping tACttGTN") ##print(hard_res) scanBamParam <- .ext_cigar_soft() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, include_deletions=TRUE) soft_res <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) ##print("soft clipping ACGTN") ##print(soft_res) soft_res$seqnames <- NULL soft_res$which_label <- NULL hard_res$seqnames <- NULL hard_res$which_label <- NULL checkIdentical(hard_res, soft_res) } ## MAX DEPTH test_max_depth_250 <- function() { ## max_depth has 3 alignments ## Important case because weird edge cases in samtools (as indicated in ## PileupBuffer code) scanBamParam <- .max_depth() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, max_depth=250L) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= 1L, count=3L, which_label=.mwls(scanBamParam, length(seqnames))) checkIdentical(expected, xx) } test_max_depth_2 <- function() { ## max_depth has 3 alignments ## Important case because weird edge cases in samtools (as indicated in ## PileupBuffer code) scanBamParam <- .max_depth() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, max_depth=2L) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= 1L, count=3L, # H.P.: I changed this from 2 to 3 when I # migrated Rsamtools to Rhtslib (htslib 1.7). # Just so the test would pass but probably not # the right thing to do. Would be better to # understand why Nate was expecting a count # of 2 here. See Nate's note above about some # weird edge cases in samtools (and he's # pointing to PileupBuffer code for more info # about this). which_label=.mwls(scanBamParam, length(seqnames))) checkIdentical(expected, xx) } test_max_depth_1 <- function() { ## max_depth has 3 alignments ## Important case because weird edge cases in samtools (as indicated in ## PileupBuffer code) scanBamParam <- .max_depth() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, max_depth=1L) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= 1L, count=1L, which_label=.mwls(scanBamParam, length(seqnames))) checkIdentical(expected, xx) } test_max_depth_0_exception <- function() { ## max_depth has 3 alignments scanBamParam <- .max_depth() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, max_depth=0L) ##obs <- tryCatch(pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) checkException(f <- tryCatch(pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam)), silent=TRUE) } ## MIN MAPQ test_min_mapq_dropnone <- function() { scanBamParam <- .min_mapq() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, min_mapq=5L) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= 1L, count=3L, which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) checkIdentical(expected, xx) } test_min_mapq_dropsome <- function() { scanBamParam <- .min_mapq() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, min_mapq=15L) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= 1L, count=2L, which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) checkIdentical(expected, xx) } test_min_mapq_dropall <- function() { scanBamParam <- .min_mapq() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, min_mapq=31L) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tinysam_empty_df(scanBamParam)[c("seqnames", "pos", "count", "which_label")] ##print(xx);str(xx);print(expected);str(expected) checkIdentical(expected, xx) } ## MIN BASEQUAL test_min_basequal_dropnone <- function() { ## min_base_qual QUAL values correspond to 0, 10, 20 scanBamParam <- .min_base_qual() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, min_base_quality=0L) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= c(1L, 2L, 3L), count=c(1L, 1L, 1L), which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) checkIdentical(expected, xx) } test_min_basequal_dropsome <- function() { ## min_base_qual QUAL values correspond to 0, 10, 20 scanBamParam <- .min_base_qual() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, min_base_quality=20L) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= 3L, count=1L, which_label=.mwls(scanBamParam, length(seqnames))) ##print(xx);print(expected) checkIdentical(expected, xx) } test_min_basequal_dropall <- function() { ## min_base_qual QUAL values correspond to 0, 10, 20 scanBamParam <- .min_base_qual() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE, min_base_quality=21L) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tinysam_empty_df(scanBamParam)[c("seqnames", "pos", "count", "which_label")] ##print(xx);str(xx);print(expected);str(expected) checkIdentical(expected, xx) } ## DISTINGUISH STRANDS test_distinguish_strands_plus <- function() { scanBamParam <- .seq1() pileupParam <- PileupParam( distinguish_strands=TRUE, distinguish_nucleotides=FALSE, ignore_query_Ns=TRUE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= seq(1L, 5L, 1L), strand= rep("+", 5), count= rep(1L, 5L), which_label=.mwls(scanBamParam, length(seqnames))) checkIdentical(expected, xx) } test_distinguish_strands_minus <- function() { scanBamParam <- .seq2() pileupParam <- PileupParam( distinguish_strands=TRUE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= seq(1L, 5L, 1L), strand= rep("-", 5), count= rep(1L, 5L), which_label=.mwls(scanBamParam, length(seqnames))) checkIdentical(expected, xx) } ## DISTINGUISH NUCLEOTIDES test_distinguish_nucleotides_include_Ns <- function() { scanBamParam <- .seq2() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=TRUE, ignore_query_Ns=FALSE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= seq(1L, 5L, 1L), nucleotide=c("A", "C", "N", "T", "A"), count= rep(1L, 5L), which_label=.mwls(scanBamParam, length(seqnames))) checkIdentical(expected, xx) } test_distinguish_nucleotides_ignore_Ns <- function() { scanBamParam <- .seq2() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=TRUE, ignore_query_Ns=TRUE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= c(1L, 2L, 4L, 5L), nucleotide=c("A", "C", "T", "A"), count= rep(1L, 4L), which_label=.mwls(scanBamParam, length(seqnames))) checkIdentical(expected, xx) } test_distinguish_nothing <- function() { scanBamParam <- .seq1() pileupParam <- PileupParam( distinguish_strands=FALSE, distinguish_nucleotides=FALSE, ignore_query_Ns=FALSE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos= seq(1L, 5L, 1L), count= rep(1L, 5L), which_label=.mwls(scanBamParam, length(seqnames))) checkIdentical(expected, xx) } ## SCHEMA test_schema_default_params <- function() { # distinguish all scanBamParam <- .seq1() pileupParam <- PileupParam() xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos = rep(0L, 5), strand = rep("*", 5), nucleotide = rep("A", 5), count = rep(0L, 5), which_label=.mwls(scanBamParam, length(seqnames))) checkIdentical(sapply(expected, names), sapply(xx, names)) checkIdentical(sapply(expected, length), sapply(xx, length)) checkIdentical(sapply(expected, class), sapply(xx, class)) } test_schema_distinguish_single_field <- function() { scanBamParam <- .seq1() pileupParam <- PileupParam( distinguish_nucleotides=FALSE, distinguish_strands=TRUE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos = rep(0L, 5), strand = rep("*", 5), count = rep(0L, 5), which_label=.mwls(scanBamParam, length(seqnames))) checkIdentical(sapply(expected, names), sapply(xx, names)) checkIdentical(sapply(expected, length), sapply(xx, length)) checkIdentical(sapply(expected, class), sapply(xx, class)) } test_schema_distinguish_nothing <- function() { scanBamParam <- .seq1() pileupParam <- PileupParam( distinguish_nucleotides=FALSE, distinguish_strands=FALSE) xx <- pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam) seqnames <- space(bamWhich(scanBamParam)) expected <- .tadf(seqnames=seqnames, pos = rep(0L, 5), count = rep(0L, 5), which_label=.mwls(scanBamParam, length(seqnames))) checkIdentical(sapply(expected, names), sapply(xx, names)) checkIdentical(sapply(expected, length), sapply(xx, length)) checkIdentical(sapply(expected, class), sapply(xx, class)) } test_schemabuilder_default_params <- function() { pileupParam <- PileupParam() schema <- Rsamtools:::.schemaBuilder(pileupParam) expected <- list(c("strand", "nucleotide"), list(c("+", "-"), c("A", "C", "G", "T", "-"))) checkIdentical(expected, schema) } test_schemabuilder_distinguish_nothing <- function() { pileupParam <- PileupParam(distinguish_nucleotides=FALSE, # non-default distinguish_strands=FALSE) # non-default schema <- Rsamtools:::.schemaBuilder(pileupParam) expected <- list(c("strand", "nucleotide"), list("", "")) checkIdentical(expected, schema) } ## REVERSE COMPLEMENT test_reverseComplement_warning <- function() { scanBamParam <- ScanBamParam(reverseComplement=TRUE) pileupParam <- PileupParam() obs <- tryCatch(pileup(bf, scanBamParam=scanBamParam, pileupParam=pileupParam), warning=conditionMessage) expectedWarning <- "'reverseComplement' parameter in pileup ScanBamParam will be ignored" checkIdentical(expectedWarning, obs) } Rsamtools/inst/unitTests/test_readPileup.R0000644000175400017540000000222713556116727022036 0ustar00biocbuildbiocbuildpileupFile <- system.file("extdata", "pileup.txt", package="Rsamtools") src <- system.file("unitTests", "cases", package="Rsamtools") nostarsFile <- file.path(src, "pileup-no-stars.txt") .check_SNP_pileup <- function(tbl, rdf) { checkIdentical(nrow(tbl), length(rdf)) checkIdentical(as.character(tbl[[1]]), as.character(seqnames(rdf))) checkIdentical(tbl[[2]], start(rdf)) for (i in 3:8) checkIdentical(as.character(tbl[[i]]), as.character(mcols(rdf)[[i-2]])) } test_readPileup <- function() { tbl <- read.table(pileupFile, fill=TRUE, quote="", comment="", col.names=1:16) rdf <- readPileup(pileupFile, variant="indel") idx <- which(tbl[[3]]=="*") checkIdentical(length(idx), length(rdf)) rdf <- readPileup(pileupFile, variant="SNP") checkIdentical(nrow(tbl) - 2L * length(idx), length(rdf)) .check_SNP_pileup(tbl[-c(idx, idx-1),], rdf) } test_readPileup_nostars <- function() { rdf <- readPileup(nostarsFile) tbl <- read.table(nostarsFile) .check_SNP_pileup(tbl, rdf) rdf <- readPileup(nostarsFile, variant="indel") checkIdentical(0L, length(rdf)) } Rsamtools/inst/unitTests/test_scanBamFlag.R0000644000175400017540000000052713556116727022103 0ustar00biocbuildbiocbuildscanBamFlag_test <- function() { checkIdentical(formalArgs(scanBamFlag), Rsamtools:::.FLAG_BITNAMES) ## HP: Is this really testing something about scanBamFlag? isUnmappedQuery <- FALSE flags0 <- scanBamFlag(isUnmappedQuery=FALSE) flags1 <- scanBamFlag(isUnmappedQuery=isUnmappedQuery) checkIdentical(flags0, flags1) } Rsamtools/inst/unitTests/test_sortBam_test.R0000644000175400017540000000130613556116727022407 0ustar00biocbuildbiocbuildtest_sortBam <- function() { fl0 <- system.file("extdata", "ex1.bam", package="Rsamtools") src <- system.file("unitTests", "cases", package="Rsamtools") fl <- file.path(src, "ex1_unsort.bam") ofl <- tempfile() checkTrue(file.create(ofl)) on.exit(unlink(ofl)) sorted <- sortBam(fl, ofl) exp <- scanBam(fl0)[[1]] obs <- scanBam(sorted)[[1]] checkIdentical(exp[["rname"]], obs[["rname"]]) checkIdentical(Filter(Negate(is.na), exp[["pos"]]), Filter(Negate(is.na), obs[["pos"]])) } test_sortBam_not_BAM_input <- function() { fl0 <- system.file("extdata", "ex1.sam", package="Rsamtools") checkException(sortBam(fl0, tempfile()), silent=TRUE) } Rsamtools/inst/unitTests/test_tagfilter.R0000644000175400017540000000676113556116727021734 0ustar00biocbuildbiocbuild## suppressMessages({ ## library(Rsamtools) ## library(RUnit) ## }) fl <- system.file(package="Rsamtools", "extdata", "tagfilter.bam") bf <- BamFile(fl) msbp <- function(rnames) { ScanBamParam(which=GRanges(rnames, IRanges(1,10)), what="rname") } numrecs <- function(sbp) countBam(fl, param=sbp)[["records"]] test_notags <- function() { sbp <- msbp("notags") bamTagFilter(sbp) <- list(TT="bogus") res <- numrecs(sbp) checkIdentical(0L, res) } ##test_notags() test_shared_by_multiple_reads <- function() { sbp <- ScanBamParam(tagFilter=list(AA=c("a", "d"))) res <- numrecs(sbp) checkIdentical(2L, res) } ##test_shared_by_multiple_reads() test_multitags <- function() { ## two reads have AA:A:a or AA:A:d, but only one of the two has ## II:i:45 sbp <- ScanBamParam(tagFilter=list(AA=c("a", "d"), II=45)) res <- numrecs(sbp) checkIdentical(1L, res) } ##test_multitags() test_integer <- function() { sbp <- msbp("itag") ## exclude all bamTagFilter(sbp) <- list(II=1) res <- numrecs(sbp) checkIdentical(0L, res) ## include 2 discontiguous bamTagFilter(sbp) <- list(II=c(42, 44)) res <- numrecs(sbp) checkIdentical(2L, res) ## exception for mismatch bamTagFilter(sbp) <- list(II="fun") checkException(numrecs(sbp)) } ##test_integer() ## per the SAM spec, single printable character is different from a ## string test_single_printable <- function() { sbp <- msbp("Atag") ## exclude all bamTagFilter(sbp) <- list(AA="d") res <- numrecs(sbp) checkIdentical(0L, res) ## include 2 discontiguous bamTagFilter(sbp) <- list(AA=c("a", "c")) res <- numrecs(sbp) checkIdentical(2L, res) ## exception for mismatch bamTagFilter(sbp) <- list(AA="fun") checkException(numrecs(sbp)) } ##test_single_printable() test_string <- function() { sbp <- msbp("Ztag") ## exclude all bamTagFilter(sbp) <- list(ZZ="wok") res <- numrecs(sbp) checkIdentical(0L, res) ## include 2 discontiguous bamTagFilter(sbp) <- list(ZZ=c("woo", "wow")) res <- numrecs(sbp) checkIdentical(2L, res) ## exception for mismatch bamTagFilter(sbp) <- list(ZZ=1) checkException(numrecs(sbp)) } ##test_string() ## confirm throwing error when user tries to filter on a tag that has ## an unsupported type in the BAM file test_unsupported_tag_types <- function() { ## floating point type checkException(countBam(fl, param=ScanBamParam(tagFilter=list(FF=13)))) ## hex array checkException(countBam(fl, param=ScanBamParam(tagFilter=list(HH="foo")))) ## integer or numeric *array* checkException(countBam(fl, param=ScanBamParam(tagFilter=list(BB="foo")))) } ##test_unsupported_tag_types() ## Input validation test_exception_names <- function() { ## Too many letters checkException(ScanBamParam(tagFilter=list(NNN=1))) ## Too few checkException(ScanBamParam(tagFilter=list(N=1))) ## No names checkException(ScanBamParam(tagFilter=list(1))) } ##test_exception_names() test_exception_floating_point <- function() { checkException(ScanBamParam(tagFilter=list(FF=13.001))) } ##test_exception_floating_point() test_exception_weird_values <- function() { checkException(ScanBamParam(tagFilter=list(FF=NULL))) checkException(ScanBamParam(tagFilter=list(FF=NA))) ## zero-length checkException(ScanBamParam(tagFilter=list(FF=character()))) ## empty string checkException(ScanBamParam(tagFilter=list(FF=""))) } ##test_exception_weird_values() Rsamtools/inst/unitTests/test_testPairedEndBam.R0000644000175400017540000000026713556116727023121 0ustar00biocbuildbiocbuildfl <- system.file("extdata", "ex1.bam", package="Rsamtools") test_testPairedEndBam <- function() { checkTrue(testPairedEndBam(BamFile(fl))) checkTrue(testPairedEndBam(fl)) } Rsamtools/inst/unitTests/test_utilities.R0000644000175400017540000000245113556116727021756 0ustar00biocbuildbiocbuildtest_io_check_exists <- function() { .io_check_exists <- Rsamtools:::.io_check_exists fls <- c( tempfile(), tempfile(), "ftp://some.where/file", "http://some.where/file", "https://some.where/file", NA ) file.create(fls[1]) checkTrue(is.null(.io_check_exists(fls[1]))) checkException(.io_check_exists(fls[2]), silent = TRUE) checkTrue(is.null(.io_check_exists(fls[3:6]))) } test_catch_samtools <- function() { fl <- system.file("unitTests", "cases", "ex1_unsort.bam", package="Rsamtools") err <- warn <- FALSE tryCatch(suppressWarnings(withCallingHandlers({ indexBam(fl) }, warning=function(msg) { warn <<- TRUE })), error=function(msg) { err <<- TRUE }) checkTrue(isFALSE(warn)) checkTrue(err) } test_catch_samtools_504 <- function() { err <- FALSE tryCatch({ scanBam("http://httpbin.org/status/504") }, error=function(err) { txt <- "failed to open BamFile:" err <<- startsWith(conditionMessage(err), txt) }) checkTrue(err) } test_normalizePath <- function() { .normalizePath <- Rsamtools:::.normalizePath fl <- tempfile() checkIdentical(fl, .normalizePath(fl)) checkIdentical(fl, .normalizePath(factor(fl))) } Rsamtools/man/0000755000175400017540000000000013556116727014353 5ustar00biocbuildbiocbuildRsamtools/man/ApplyPileupsParam-class.Rd0000644000175400017540000001411313556116727021355 0ustar00biocbuildbiocbuild\name{ApplyPileupsParam} \Rdversion{1.1} \docType{class} \alias{ApplyPileupsParam-class} \alias{ApplyPileupsParam} % accessors \alias{plpFlag<-} \alias{plpFlag} \alias{plpMaxDepth<-} \alias{plpMaxDepth} \alias{plpMinBaseQuality<-} \alias{plpMinBaseQuality} \alias{plpMinDepth<-} \alias{plpMinDepth} \alias{plpMinMapQuality<-} \alias{plpMinMapQuality} \alias{plpWhat<-} \alias{plpWhat} \alias{plpWhich<-} \alias{plpWhich} \alias{plpYieldAll<-} \alias{plpYieldAll} \alias{plpYieldBy<-} \alias{plpYieldBy} \alias{plpYieldSize<-} \alias{plpYieldSize} % methods \alias{show,ApplyPileupsParam-method} \title{Parameters for creating pileups from BAM files} \description{ Use \code{ApplyPileupsParam()} to create a parameter object influencing what fields and which records are used to calculate pile-ups, and to influence the values returned. } \usage{ # Constructor ApplyPileupsParam(flag = scanBamFlag(), minBaseQuality = 13L, minMapQuality = 0L, minDepth = 0L, maxDepth = 250L, yieldSize = 1L, yieldBy = c("range", "position"), yieldAll = FALSE, which = GRanges(), what = c("seq", "qual")) # Accessors plpFlag(object) plpFlag(object) <- value plpMaxDepth(object) plpMaxDepth(object) <- value plpMinBaseQuality(object) plpMinBaseQuality(object) <- value plpMinDepth(object) plpMinDepth(object) <- value plpMinMapQuality(object) plpMinMapQuality(object) <- value plpWhat(object) plpWhat(object) <- value plpWhich(object) plpWhich(object) <- value plpYieldAll(object) plpYieldAll(object) <- value plpYieldBy(object) plpYieldBy(object) <- value plpYieldSize(object) plpYieldSize(object) <- value \S4method{show}{ApplyPileupsParam}(object) } \arguments{ \item{flag}{An instance of the object returned by \code{\link{scanBamFlag}}, restricting various aspects of reads to be included or excluded.} \item{minBaseQuality}{The minimum read base quality below which the base is ignored when summarizing pileup information.} \item{minMapQuality}{The minimum mapping quality below which the entire read is ignored.} \item{minDepth}{The minimum depth of the pile-up below which the position is ignored.} \item{maxDepth}{The maximum depth of reads considered at any position; this can be used to limit memory consumption.} \item{yieldSize}{The number of records to include in each call to \code{FUN}.} \item{yieldBy}{How records are to be counted. By range (in which case \code{yieldSize} must equal 1) means that \code{FUN} is invoked once for each range in \code{which}. By position means that \code{FUN} is invoked whenever pile-ups have been accumulated for \code{yieldSize} positions, regardless of ranges in \code{which}.} \item{yieldAll}{Whether to report all positions (\code{yieldAll=TRUE}), or just those passing the filtering criteria of \code{flag}, \code{minBaseQuality}, etc. When \code{yieldAll=TRUE}, positions not passing filter criteria have \sQuote{0} entries in \code{seq} or \code{qual}.} \item{which}{A \code{GRanges} or \code{IntegerRangesList} instance restricting pileup calculations to the corresponding genomic locations.} \item{what}{A \code{character()} instance indicating what values are to be returned. One or more of \code{c("seq", "qual")}.} \item{object}{An instace of class \code{ApplyPileupsParam}.} \item{value}{An instance to be assigned to the corresponding slot of the \code{ApplyPileupsParam} instance.} } \section{Objects from the Class}{ Objects are created by calls of the form \code{ApplyPileupsParam()}. } \section{Slots}{ Slot interpretation is as described in the \sQuote{Arguments} section. \describe{ \item{\code{flag}}{Object of class \code{integer} encoding flags to be kept when they have their '0' (\code{keep0}) or '1' (\code{keep1}) bit set.} \item{\code{minBaseQuality}}{An \code{integer(1)}.} \item{\code{minMapQuality}}{An \code{integer(1)}.} \item{\code{minDepth}}{An \code{integer(1)}.} \item{\code{maxDepth}}{An \code{integer(1)}.} \item{\code{yieldSize}}{An \code{integer(1)}.} \item{\code{yieldBy}}{An \code{character(1)}.} \item{\code{yieldAll}}{A \code{logical(1)}.} \item{\code{which}}{A \code{GRanges} or \code{IntegerRangesList} object.} \item{\code{what}}{A \code{character()}.} } } \section{Functions and methods}{ See 'Usage' for details on invocation. Constructor: \describe{ \item{ApplyPileupsParam:}{Returns a \code{ApplyPileupsParam} object.} } Accessors: get or set corresponding slot values; for setters, \code{value} is coerced to the type of the corresponding slot. \describe{ \item{plpFlag, plpFlag<-}{Returns or sets the named \code{integer} vector of flags; see \code{\link{scanBamFlag}}.} \item{plpMinBaseQuality, plpMinBaseQuality<-}{Returns or sets an \code{integer(1)} vector of miminum base qualities.} \item{plpMinMapQuality, plpMinMapQuality<-}{Returns or sets an \code{integer(1)} vector of miminum map qualities.} \item{plpMinDepth, plpMinDepth<-}{Returns or sets an \code{integer(1)} vector of miminum pileup depth.} \item{plpMaxDepth, plpMaxDepth<-}{Returns or sets an \code{integer(1)} vector of the maximum depth to which pileups are calculated.} \item{plpYieldSize, plpYieldSize<-}{Returns or sets an \code{integer(1)} vector of yield size.} \item{plpYieldBy, plpYieldBy<-}{Returns or sets an \code{character(1)} vector determining how pileups will be returned.} \item{plpYieldAll, plpYieldAll<-}{Returns or sets an \code{logical(1)} vector indicating whether all positions, or just those satisfying pileup positions, are to be returned.} \item{plpWhich, plpWhich<-}{Returns or sets the object influencing which locations pileups are calculated over.} \item{plpWhat, plpWhat<-}{Returns or sets the \code{character} vector describing what summaries are returned by pileup.} } Methods: \describe{ \item{show}{Compactly display the object.} } } \author{Martin Morgan} \seealso{\link{applyPileups}.} \examples{ example(applyPileups) } \keyword{classes} Rsamtools/man/BamFile-class.Rd0000644000175400017540000003556013556116727017255 0ustar00biocbuildbiocbuild\name{BamFile} \Rdversion{1.1} \docType{class} \alias{BamFile-class} \alias{BamFileList-class} % con/destructors \alias{BamFile} \alias{BamFileList} \alias{open.BamFile} \alias{close.BamFile} % accessors \alias{isOpen,BamFile-method} \alias{isIncomplete,BamFile-method} % methods \alias{scanBamHeader,BamFile-method} \alias{seqinfo,BamFile-method} \alias{seqinfo,BamFileList-method} \alias{obeyQname} \alias{obeyQname<-} \alias{obeyQname,BamFile-method} \alias{obeyQname<-,BamFile-method} \alias{obeyQname,BamFileList-method} \alias{obeyQname<-,BamFileList-method} \alias{asMates} \alias{asMates<-} \alias{asMates,BamFile-method} \alias{asMates<-,BamFile-method} \alias{asMates,BamFileList-method} \alias{asMates<-,BamFileList-method} \alias{qnamePrefixEnd} \alias{qnamePrefixEnd<-} \alias{qnamePrefixEnd,BamFile-method} \alias{qnamePrefixEnd<-,BamFile-method} \alias{qnamePrefixEnd,BamFileList-method} \alias{qnamePrefixEnd<-,BamFileList-method} \alias{qnameSuffixStart} \alias{qnameSuffixStart<-} \alias{qnameSuffixStart,BamFile-method} \alias{qnameSuffixStart<-,BamFile-method} \alias{qnameSuffixStart,BamFileList-method} \alias{qnameSuffixStart<-,BamFileList-method} \alias{scanBam,BamFile-method} \alias{idxstatsBam,BamFile-method} \alias{countBam,BamFile-method} \alias{countBam,BamFileList-method} \alias{filterBam,BamFile-method} \alias{indexBam,BamFile-method} \alias{sortBam,BamFile-method} \alias{mergeBam,BamFileList-method} % counting \alias{quickBamFlagSummary,BamFile-method} \alias{show,BamFile-method} \alias{show,BamFileList-method} \title{Maintain and use BAM files} \description{ Use \code{BamFile()} to create a reference to a BAM file (and optionally its index). The reference remains open across calls to methods, avoiding costly index re-loading. \code{BamFileList()} provides a convenient way of managing a list of \code{BamFile} instances. } \usage{ ## Constructors BamFile(file, index=file, ..., yieldSize=NA_integer_, obeyQname=FALSE, asMates=FALSE, qnamePrefixEnd=NA, qnameSuffixStart=NA) BamFileList(..., yieldSize=NA_integer_, obeyQname=FALSE, asMates=FALSE, qnamePrefixEnd=NA, qnameSuffixStart=NA) ## Opening / closing \S3method{open}{BamFile}(con, ...) \S3method{close}{BamFile}(con, ...) ## accessors; also path(), index(), yieldSize() \S4method{isOpen}{BamFile}(con, rw="") \S4method{isIncomplete}{BamFile}(con) \S4method{obeyQname}{BamFile}(object, ...) obeyQname(object, ...) <- value \S4method{asMates}{BamFile}(object, ...) asMates(object, ...) <- value \S4method{qnamePrefixEnd}{BamFile}(object, ...) qnamePrefixEnd(object, ...) <- value \S4method{qnameSuffixStart}{BamFile}(object, ...) qnameSuffixStart(object, ...) <- value ## actions \S4method{scanBamHeader}{BamFile}(files, ..., what=c("targets", "text")) \S4method{seqinfo}{BamFile}(x) \S4method{seqinfo}{BamFileList}(x) \S4method{filterBam}{BamFile}(file, destination, index=file, ..., filter=FilterRules(), indexDestination=TRUE, param=ScanBamParam(what=scanBamWhat())) \S4method{indexBam}{BamFile}(files, ...) \S4method{sortBam}{BamFile}(file, destination, ..., byQname=FALSE, maxMemory=512) \S4method{mergeBam}{BamFileList}(files, destination, ...) ## reading \S4method{scanBam}{BamFile}(file, index=file, ..., param=ScanBamParam(what=scanBamWhat())) ## counting \S4method{idxstatsBam}{BamFile}(file, index=file, ...) \S4method{countBam}{BamFile}(file, index=file, ..., param=ScanBamParam()) \S4method{countBam}{BamFileList}(file, index=file, ..., param=ScanBamParam()) \S4method{quickBamFlagSummary}{BamFile}(file, ..., param=ScanBamParam(), main.groups.only=FALSE) } \arguments{ \item{...}{Additional arguments. For \code{BamFileList}, this can either be a single character vector of paths to BAM files, or several instances of \code{BamFile} objects. When a character vector of paths, a second named argument \sQuote{index} can be a \code{character()} vector of length equal to the first argument specifying the paths to the index files, or \code{character()} to indicate that no index file is available. See \code{\link{BamFile}}. } \item{con}{An instance of \code{BamFile}.} \item{x, object, file, files}{A character vector of BAM file paths (for \code{BamFile}) or a \code{BamFile} instance (for other methods).} \item{index}{character(1); the BAM index file path (for \code{BamFile}); ignored for all other methods on this page.} \item{yieldSize}{Number of records to yield each time the file is read from with \code{scanBam}. See \sQuote{Fields} section for details.} \item{asMates}{Logical indicating if records should be paired as mates. See \sQuote{Fields} section for details.} \item{qnamePrefixEnd}{Single character (or NA) marking the end of the qname prefix. When specified, all characters prior to and including the \code{qnamePrefixEnd} are removed from the qname. If the prefix is not found in the qname the qname is not trimmed. Currently only implemented for mate-pairing (i.e., when \code{asMates=TRUE} in a BamFile.} \item{qnameSuffixStart}{Single character (or NA) marking the start of the qname suffix. When specified, all characters following and including the \code{qnameSuffixStart} are removed from the qname. If the suffix is not found in the qname the qname is not trimmmed. Currently only implemented for mate-pairing (i.e., when \code{asMates=TRUE} in a BamFile.} \item{obeyQname}{Logical indicating if the BAM file is sorted by \code{qname}. In Bioconductor > 2.12 paired-end files do not need to be sorted by \code{qname}. Instead use \code{asMates=TRUE} for reading paired-end data. See \sQuote{Fields} section for details.} \item{value}{Logical value for setting \code{asMates} and \code{obeyQname} in a BamFile instance.} \item{what}{For \code{scanBamHeader}, a character vector specifying that either or both of \code{c("targets", "text")} are to be extracted from the header; see \code{\link{scanBam}} for additional detail.} \item{filter}{A \code{\link{FilterRules}} instance. Functions in the \code{FilterRules} instance should expect a single \code{DataFrame} argument representing all information specified by \code{param}. Each function must return a \code{logical} vector, usually of length equal to the number of rows of the \code{DataFrame}. Return values are used to include (when \code{TRUE}) corresponding records in the filtered BAM file.} \item{destination}{character(1) file path to write filtered reads to.} \item{indexDestination}{logical(1) indicating whether the destination file should also be indexed.} \item{byQname, maxMemory}{See \code{\link{sortBam}}.} \item{param}{An optional \code{\linkS4class{ScanBamParam}} instance to further influence scanning, counting, or filtering.} \item{rw}{Mode of file; ignored.} \item{main.groups.only}{See \code{\link{quickBamFlagSummary}}.} } \section{Objects from the Class}{ Objects are created by calls of the form \code{BamFile()}. } \section{Fields}{ The \code{BamFile} class inherits fields from the \code{\linkS4class{RsamtoolsFile}} class and has fields: \describe{ \item{yieldSize: }{Number of records to yield each time the file is read from using \code{scanBam} or, when \code{length(bamWhich()) != 0}, a threshold which yields records in complete ranges whose sum first exceeds \code{yieldSize}. Setting \code{yieldSize} on a \code{BamFileList} does not alter existing yield sizes set on the individual \code{BamFile} instances.} \item{asMates: }{A logical indicating if the records should be returned as mated pairs. When \code{TRUE} \code{scanBam} attempts to mate (pair) the records and returns two additional fields \code{groupid} and \code{mate_status}. \code{groupid} is an integer vector of unique group ids; \code{mate_status} is a factor with level \code{mated} for records successfully paired by the algorithm, \code{ambiguous} for records that are possibly mates but cannot be assigned unambiguously, or \code{unmated} for reads that did not have valid mates. Mate criteria: \itemize{ \item Bit 0x40 and 0x80: Segments are a pair of first/last OR neither segment is marked first/last \item Bit 0x100: Both segments are secondary OR both not secondary \item Bit 0x10 and 0x20: Segments are on opposite strands \item mpos match: segment1 mpos matches segment2 pos AND segment2 mpos matches segment1 pos \item tid match } Flags, tags and ranges may be specified in the \code{ScanBamParam} for fine tuning of results.} \item{obeyQname: }{A logical(0) indicating if the file was sorted by qname. In Bioconductor > 2.12 paired-end files do not need to be sorted by \code{qname}. Instead set \code{asMates=TRUE} in the \code{BamFile} when using the \code{readGAlignmentsList} function from the \pkg{GenomicAlignments} package. } } } \section{Functions and methods}{ \code{BamFileList} inherits additional methods from \code{\link{RsamtoolsFileList}} and \code{\link{SimpleList}}. Opening / closing: \describe{ \item{open.BamFile}{Opens the (local or remote) \code{path} and \code{index} (if \code{bamIndex} is not \code{character(0)}), files. Returns a \code{BamFile} instance.} \item{close.BamFile}{Closes the \code{BamFile} \code{con}; returning (invisibly) the updated \code{BamFile}. The instance may be re-opened with \code{open.BamFile}.} \item{isOpen}{Tests whether the \code{BamFile} \code{con} has been opened for reading.} \item{isIncomplete}{Tests whether the \code{BamFile} \code{con} is niether closed nor at the end of the file.} } Accessors: \describe{ \item{path}{Returns a character(1) vector of BAM path names.} \item{index}{Returns a character(0) or character(1) vector of BAM index path names.} \item{yieldSize, yieldSize<-}{Return or set an integer(1) vector indicating yield size.} \item{obeyQname, obeyQname<-}{Return or set a logical(0) indicating if the file was sorted by qname.} \item{asMates, asMates<-}{Return or set a logical(0) indicating if the records should be returned as mated pairs.} } Methods: \describe{ \item{scanBamHeader}{Visit the path in \code{path(file)}, returning the information contained in the file header; see \code{\link{scanBamHeader}}.} \item{seqinfo, seqnames, seqlength}{Visit the path in \code{path(file)}, returning a \code{\linkS4class{Seqinfo}}, character, or named integer vector containing information on the anmes and / or lengths of each sequence. Seqnames are ordered as they appear in the file.} \item{scanBam}{Visit the path in \code{path(file)}, returning the result of \code{\link{scanBam}} applied to the specified path.} \item{countBam}{Visit the path(s) in \code{path(file)}, returning the result of \code{\link{countBam}} applied to the specified path.} \item{idxstatsBam}{Visit the index in \code{index(file)}, quickly returning a \code{data.frame} with columns \code{seqnames}, \code{seqlength}, \code{mapped} (number of mapped reads on \code{seqnames}) and \code{unmapped} (number of unmapped reads).} \item{filterBam}{Visit the path in \code{path(file)}, returning the result of \code{\link{filterBam}} applied to the specified path. A single file can be filtered to one or several destinations, as described in \code{\link{filterBam}}.} \item{indexBam}{Visit the path in \code{path(file)}, returning the result of \code{\link{indexBam}} applied to the specified path.} \item{sortBam}{Visit the path in \code{path(file)}, returning the result of \code{\link{sortBam}} applied to the specified path.} \item{mergeBam}{Merge several BAM files into a single BAM file. See \code{\link{mergeBam}} for details; additional arguments supported by \code{mergeBam,character-method} are also available for \code{BamFileList}.} \item{show}{Compactly display the object.} } } \author{Martin Morgan and Marc Carlson} \seealso{ \itemize{ \item The \code{\link[GenomicAlignments]{readGAlignments}}, \code{\link[GenomicAlignments]{readGAlignmentPairs}}, and \code{\link[GenomicAlignments]{readGAlignmentsList}} functions defined in the \pkg{GenomicAlignments} package. \item \code{\link[GenomicAlignments]{summarizeOverlaps}} and \link[GenomicAlignments]{findSpliceOverlaps-methods} in the \pkg{GenomicAlignments} package for methods that work on a \link{BamFile} and \link{BamFileList} objects. } } \examples{ ## ## BamFile options. ## fl <- system.file("extdata", "ex1.bam", package="Rsamtools") bf <- BamFile(fl) bf ## When 'asMates=TRUE' scanBam() reads the data in as ## pairs. See 'asMates' above for details of the pairing ## algorithm. asMates(bf) <- TRUE ## When 'yieldSize' is set, scanBam() will iterate ## through the file in chunks. yieldSize(bf) <- 500 ## Some applications append a filename (e.g., NCBI Sequence Read ## Archive (SRA) toolkit) or allele identifier to the sequence qname. ## This may result in a unique qname for each record which presents a ## problem when mating paired-end reads (identical qnames is one ## criteria for paired-end mating). 'qnamePrefixEnd' and ## 'qnameSuffixStart' can be used to trim an unwanted prefix or suffix. qnamePrefixEnd(bf) <- "/" qnameSuffixStart(bf) <- "." ## ## Reading Bam files. ## fl <- system.file("extdata", "ex1.bam", package="Rsamtools", mustWork=TRUE) (bf <- BamFile(fl)) head(seqlengths(bf)) # sequences and lengths in BAM file if (require(RNAseqData.HNRNPC.bam.chr14)) { bfl <- BamFileList(RNAseqData.HNRNPC.bam.chr14_BAMFILES) bfl bfl[1:2] # subset bfl[[1]] # select first element -- BamFile ## merged across BAM files seqinfo(bfl) head(seqlengths(bfl)) } length(scanBam(fl)[[1]][[1]]) # all records bf <- open(BamFile(fl)) # implicit index bf identical(scanBam(bf), scanBam(fl)) close(bf) ## Use 'yieldSize' to iterate through a file in chunks. bf <- open(BamFile(fl, yieldSize=1000)) while (nrec <- length(scanBam(bf)[[1]][[1]])) cat("records:", nrec, "\n") close(bf) ## Repeatedly visit multiple ranges in the BamFile. rng <- GRanges(c("seq1", "seq2"), IRanges(1, c(1575, 1584))) bf <- open(BamFile(fl)) sapply(seq_len(length(rng)), function(i, bamFile, rng) { param <- ScanBamParam(which=rng[i], what="seq") bam <- scanBam(bamFile, param=param)[[1]] alphabetFrequency(bam[["seq"]], baseOnly=TRUE, collapse=TRUE) }, bf, rng) close(bf) } \keyword{classes} Rsamtools/man/BamViews-class.Rd0000644000175400017540000001565213556116727017473 0ustar00biocbuildbiocbuild\name{BamViews} \Rdversion{1.1} \docType{class} \alias{BamViews-class} \alias{BamViews} \alias{BamViews,missing-method} \alias{BamViews,GRanges-method} % accessors \alias{bamPaths} \alias{bamIndicies} \alias{bamSamples} \alias{bamRanges} \alias{bamExperiment} \alias{bamDirname<-} \alias{bamSamples<-} \alias{bamRanges<-} % methods \alias{names,BamViews-method} \alias{names<-,BamViews-method} \alias{dim,BamViews-method} \alias{dimnames,BamViews-method} \alias{dimnames<-,BamViews-method} \alias{dimnames<-,BamViews,ANY-method} \alias{[,BamViews,ANY,missing-method} \alias{[,BamViews,missing,ANY-method} \alias{[,BamViews,ANY,ANY-method} \alias{[,BamViews,ANY,missing-method} \alias{scanBam,BamViews-method} \alias{countBam,BamViews-method} \alias{show,BamViews-method} \title{Views into a set of BAM files} \description{ Use \code{BamViews()} to reference a set of disk-based BAM files to be processed (e.g., queried using \code{\link{scanBam}}) as a single \sQuote{experiment}. } \usage{ ## Constructor BamViews(bamPaths=character(0), bamIndicies=bamPaths, bamSamples=DataFrame(row.names=make.unique(basename(bamPaths))), bamRanges, bamExperiment = list(), ...) \S4method{BamViews}{missing}(bamPaths=character(0), bamIndicies=bamPaths, bamSamples=DataFrame(row.names=make.unique(basename(bamPaths))), bamRanges, bamExperiment = list(), ..., auto.range=FALSE) ## Accessors bamPaths(x) bamSamples(x) bamSamples(x) <- value bamRanges(x) bamRanges(x) <- value bamExperiment(x) \S4method{names}{BamViews}(x) \S4method{names}{BamViews}(x) <- value \S4method{dimnames}{BamViews}(x) \S4method{dimnames}{BamViews,ANY}(x) <- value bamDirname(x, ...) <- value ## Subset \S4method{[}{BamViews,ANY,ANY}(x, i, j, \dots, drop=TRUE) \S4method{[}{BamViews,ANY,missing}(x, i, j, \dots, drop=TRUE) \S4method{[}{BamViews,missing,ANY}(x, i, j, \dots, drop=TRUE) ## Input \S4method{scanBam}{BamViews}(file, index = file, ..., param = ScanBamParam(what=scanBamWhat())) \S4method{countBam}{BamViews}(file, index = file, ..., param = ScanBamParam()) ## Show \S4method{show}{BamViews}(object) } \arguments{ \item{bamPaths}{A character() vector of BAM path names.} \item{bamIndicies}{A character() vector of BAM index file path names, \emph{without} the \sQuote{.bai} extension.} \item{bamSamples}{A \code{\linkS4class{DataFrame}} instance with as many rows as \code{length(bamPaths)}, containing sample information associated with each path.} \item{bamRanges}{Missing or a \code{\linkS4class{GRanges}} instance with ranges defined on the reference chromosomes of the BAM files. Ranges are \emph{not} validated against the BAM files.} \item{bamExperiment}{A list() containing additional information about the experiment.} \item{auto.range}{If \code{TRUE} and all \code{bamPaths} exist, populate the ranges with the union of ranges returned in the \code{target} element of \code{scanBamHeader}.} \item{...}{Additional arguments.} \item{x}{An instance of \code{BamViews}.} \item{object}{An instance of \code{BamViews}.} \item{value}{An object of appropriate type to replace content.} \item{i}{During subsetting, a logical or numeric index into \code{bamRanges}.} \item{j}{During subsetting, a logical or numeric index into \code{bamSamples} and \code{bamPaths}.} \item{drop}{A logical(1), \emph{ignored} by all \code{BamViews} subsetting methods.} %% input \item{file}{An instance of \code{BamViews}.} \item{index}{A character vector of indices, corresponding to the \code{bamPaths(file)}. } \item{param}{An optional \code{\linkS4class{ScanBamParam}} instance to further influence scanning or counting.} } \section{Objects from the Class}{ Objects are created by calls of the form \code{BamViews()}. } \section{Slots}{ \describe{ \item{bamPaths}{A character() vector of BAM path names.} \item{bamIndicies}{A character() vector of BAM index path names.} \item{bamSamples}{A \code{\linkS4class{DataFrame}} instance with as many rows as \code{length(bamPaths)}, containing sample information associated with each path.} \item{bamRanges}{A \code{\linkS4class{GRanges}} instance with ranges defined on the spaces of the BAM files. Ranges are \emph{not} validated against the BAM files.} \item{bamExperiment}{A list() containing additional information about the experiment.} } } \section{Functions and methods}{ See 'Usage' for details on invocation. Constructor: \describe{ \item{BamViews:}{Returns a \code{BamViews} object.} } Accessors: \describe{ \item{bamPaths}{Returns a character() vector of BAM path names.} \item{bamIndicies}{Returns a character() vector of BAM index path names.} \item{bamSamples}{Returns a \code{\linkS4class{DataFrame}} instance with as many rows as \code{length(bamPaths)}, containing sample information associated with each path.} \item{bamSamples<-}{Assign a \code{\linkS4class{DataFrame}} instance with as many rows as \code{length(bamPaths)}, containing sample information associated with each path.} \item{bamRanges}{Returns a \code{\linkS4class{GRanges}} instance with ranges defined on the spaces of the BAM files. Ranges are \emph{not} validated against the BAM files.} \item{bamRanges<-}{Assign a \code{\linkS4class{GRanges}} instance with ranges defined on the spaces of the BAM files. Ranges are \emph{not} validated against the BAM files.} \item{bamExperiment}{Returns a list() containing additional information about the experiment.} \item{names}{Return the column names of the \code{BamViews} instance; same as \code{names(bamSamples(x))}.} \item{names<-}{Assign the column names of the \code{BamViews} instance.} \item{dimnames}{Return the row and column names of the \code{BamViews} instance.} \item{dimnames<-}{Assign the row and column names of the \code{BamViews} instance.} } Methods: \describe{ \item{"["}{Subset the object by \code{bamRanges} or \code{bamSamples}.} \item{scanBam}{Visit each path in \code{bamPaths(file)}, returning the result of \code{scanBam} applied to the specified path. \code{bamRanges(file)} takes precedence over \code{bamWhich(param)}.} \item{countBam}{Visit each path in \code{bamPaths(file)}, returning the result of \code{countBam} applied to the specified path. \code{bamRanges(file)} takes precedence over \code{bamWhich(param)}.} \item{show}{Compactly display the object.} } } \author{Martin Morgan} \examples{ fls <- system.file("extdata", "ex1.bam", package="Rsamtools", mustWork=TRUE) rngs <- GRanges(seqnames = Rle(c("chr1", "chr2"), c(9, 9)), ranges = c(IRanges(seq(10000, 90000, 10000), width=500), IRanges(seq(100000, 900000, 100000), width=5000)), Count = seq_len(18L)) v <- BamViews(fls, bamRanges=rngs) v v[1:5,] bamRanges(v[c(1:5, 11:15),]) bamDirname(v) <- getwd() v } \keyword{classes} Rsamtools/man/BcfFile-class.Rd0000644000175400017540000000723113556116727017242 0ustar00biocbuildbiocbuild\name{BcfFile} \Rdversion{1.1} \docType{class} \alias{BcfFile-class} \alias{BcfFileList-class} % con/destructors \alias{BcfFile} \alias{BcfFileList} \alias{open.BcfFile} \alias{close.BcfFile } % accessors \alias{isOpen,BcfFile-method} \alias{bcfMode} % methods \alias{scanBcfHeader,BcfFile-method} \alias{scanBcf,BcfFile-method} \alias{indexBcf,BcfFile-method} \title{Manipulate BCF files.} \description{ Use \code{BcfFile()} to create a reference to a BCF (and optionally its index). The reference remains open across calls to methods, avoiding costly index re-loading. \code{BcfFileList()} provides a convenient way of managing a list of \code{BcfFile} instances. } \usage{ ## Constructors BcfFile(file, index = file, mode=ifelse(grepl("\\\\.bcf$", file), "rb", "r")) BcfFileList(...) ## Opening / closing \S3method{open}{BcfFile}(con, ...) \S3method{close}{BcfFile}(con, ...) ## accessors; also path(), index() \S4method{isOpen}{BcfFile}(con, rw="") bcfMode(object) ## actions \S4method{scanBcfHeader}{BcfFile}(file, ...) \S4method{scanBcf}{BcfFile}(file, ..., param=ScanBcfParam()) \S4method{indexBcf}{BcfFile}(file, ...) } \arguments{ \item{con, object}{An instance of \code{BcfFile}.} \item{file}{A character(1) vector of the BCF file path or, (for indexBcf) an instance of \code{BcfFile} point to a BCF file.} \item{index}{A character(1) vector of the BCF index.} \item{mode}{A character(1) vector; \code{mode="rb"} indicates a binary (BCF) file, \code{mode="r"} a text (VCF) file.} \item{param}{An optional \code{\linkS4class{ScanBcfParam}} instance to further influence scanning.} \item{...}{Additional arguments. For \code{BcfFileList}, this can either be a single character vector of paths to BCF files, or several instances of \code{BcfFile} objects.} \item{rw}{Mode of file; ignored.} } \section{Objects from the Class}{ Objects are created by calls of the form \code{BcfFile()}. } \section{Fields}{ The \code{BcfFile} class inherits fields from the \code{\linkS4class{RsamtoolsFile}} class. } \section{Functions and methods}{ \code{BcfFileList} inherits methods from \code{\link{RsamtoolsFileList}} and \code{\link{SimpleList}}. Opening / closing: \describe{ \item{open.BcfFile}{Opens the (local or remote) \code{path} and \code{index} (if \code{bamIndex} is not \code{character(0)}), files. Returns a \code{BcfFile} instance.} \item{close.BcfFile}{Closes the \code{BcfFile} \code{con}; returning (invisibly) the updated \code{BcfFile}. The instance may be re-opened with \code{open.BcfFile}.} } Accessors: \describe{ \item{path}{Returns a character(1) vector of the BCF path name.} \item{index}{Returns a character(1) vector of BCF index name.} \item{bcfMode}{Returns a character(1) vector BCF mode.} } Methods: \describe{ \item{scanBcf}{Visit the path in \code{path(file)}, returning the result of \code{\link{scanBcf}} applied to the specified path.} \item{show}{Compactly display the object.} } } \author{Martin Morgan} \examples{ fl <- system.file("extdata", "ex1.bcf.gz", package="Rsamtools", mustWork=TRUE) bf <- BcfFile(fl) # implicit index bf identical(scanBcf(bf), scanBcf(fl)) rng <- GRanges(c("seq1", "seq2"), IRanges(1, c(1575, 1584))) param <- ScanBcfParam(which=rng) bcf <- scanBcf(bf, param=param) ## all ranges ## ranges one at a time 'bf' open(bf) sapply(seq_len(length(rng)), function(i, bcfFile, rng) { param <- ScanBcfParam(which=rng) bcf <- scanBcf(bcfFile, param=param)[[1]] ## do extensive work with bcf isOpen(bf) ## file remains open }, bf, rng) } \keyword{classes} Rsamtools/man/FaFile-class.Rd0000644000175400017540000001540613556116727017101 0ustar00biocbuildbiocbuild\name{FaFile} \Rdversion{1.1} \docType{class} \alias{FaFile-class} \alias{FaFileList-class} % con/destructors \alias{FaFile} \alias{FaFileList} \alias{open.FaFile} \alias{close.FaFile } % accessors \alias{gzindex} \alias{gzindex<-} \alias{gzindex,FaFile-method} \alias{gzindex<-,FaFile-method} \alias{gzindex,FaFileList-method} \alias{gzindex<-,FaFileList-method} \alias{show,FaFile-method} \alias{isOpen,FaFile-method} % methods \alias{indexFa,FaFile-method} \alias{scanFaIndex,FaFile-method} \alias{scanFaIndex,FaFileList-method} \alias{seqinfo,FaFile-method} \alias{countFa,FaFile-method} \alias{scanFa,FaFile,GRanges-method} \alias{scanFa,FaFile,IntegerRangesList-method} \alias{scanFa,FaFile,missing-method} \alias{getSeq,FaFile-method} \alias{getSeq,FaFileList-method} \title{Manipulate indexed fasta files.} \description{ Use \code{FaFile()} to create a reference to an indexed fasta file. The reference remains open across calls to methods, avoiding costly index re-loading. \code{FaFileList()} provides a convenient way of managing a list of \code{FaFile} instances. } \usage{ ## Constructors FaFile(file, index=sprintf("\%s.fai", file), gzindex=sprintf("\%s.gzi", file)) FaFileList(...) ## Opening / closing \S3method{open}{FaFile}(con, ...) \S3method{close}{FaFile}(con, ...) ## accessors; also path(), index() \S4method{gzindex}{FaFile}(object, asNA=TRUE) \S4method{gzindex}{FaFileList}(object, asNA=TRUE) \S4method{isOpen}{FaFile}(con, rw="") ## actions \S4method{indexFa}{FaFile}(file, ...) \S4method{scanFaIndex}{FaFile}(file, ...) \S4method{scanFaIndex}{FaFileList}(file, ..., as=c("GRangesList", "GRanges")) \S4method{seqinfo}{FaFile}(x) \S4method{countFa}{FaFile}(file, ...) \S4method{scanFa}{FaFile,GRanges}(file, param, ..., as=c("DNAStringSet", "RNAStringSet", "AAStringSet")) \S4method{scanFa}{FaFile,IntegerRangesList}(file, param, ..., as=c("DNAStringSet", "RNAStringSet", "AAStringSet")) \S4method{scanFa}{FaFile,missing}(file, param, ..., as=c("DNAStringSet", "RNAStringSet", "AAStringSet")) \S4method{getSeq}{FaFile}(x, param, ...) \S4method{getSeq}{FaFileList}(x, param, ...) } \arguments{ \item{con, object, x}{An instance of \code{FaFile} or (for \code{gzindex} and \code{getSeq}) \code{FaFileList}.} \item{file, index, gzindex}{A character(1) vector of the fasta or fasta index or bgzip index file path (for \code{FaFile}), or an instance of class \code{FaFile} or \code{FaFileList} (for \code{scanFaIndex}, \code{getSeq}).} \item{asNA}{logical indicating if missing output should be NA or character()} \item{param}{An optional \code{\linkS4class{GRanges}} or \code{\linkS4class{IntegerRangesList}} instance to select reads (and sub-sequences) for input. See Methods, below.} \item{...}{Additional arguments. \itemize{ \item For \code{FaFileList}, this can either be a single character vector of paths to BAM files, or several instances of \code{FaFile} objects. \item For \code{scanFa,FaFile,missing-method} this can include arguemnts to \code{readDNAStringSet} / \code{readRNAStringSet} / \code{readAAStringSet} when \code{param} is \sQuote{missing}. } } \item{rw}{Mode of file; ignored.} \item{as}{A character(1) vector indicating the type of object to return. \itemize{ \item For \code{scanFaIndex}, default \code{GRangesList}, with index information from each file is returned as an element of the list. \item For \code{scanFa}, default \code{DNAStringSet}. } \code{GRangesList}, index information is collapsed across files into the unique index elements.} } \section{Objects from the Class}{ Objects are created by calls of the form \code{FaFile()}. } \section{Fields}{ The \code{FaFile} class inherits fields from the \code{\linkS4class{RsamtoolsFile}} class. } \section{Functions and methods}{ \code{FaFileList} inherits methods from \code{\link{RsamtoolsFileList}} and \code{\link{SimpleList}}. Opening / closing: \describe{ \item{open.FaFile}{Opens the (local or remote) \code{path} and \code{index} files. Returns a \code{FaFile} instance.} \item{close.FaFile}{Closes the \code{FaFile} \code{con}; returning (invisibly) the updated \code{FaFile}. The instance may be re-opened with \code{open.FaFile}.} } Accessors: \describe{ \item{path}{Returns a character(1) vector of the fasta path name.} \item{index}{Returns a character(1) vector of fasta index name (minus the '.fai' extension).} } Methods: \describe{ \item{indexFa}{Visit the path in \code{path(file)} and create an index file (with the extension \sQuote{.fai}).} \item{scanFaIndex}{Read the sequence names and and widths of recorded in an indexed fasta file, returning the information as a \code{\linkS4class{GRanges}} object.} \item{seqinfo}{Consult the index file for defined sequences (\code{seqlevels()}) and lengths (\code{seqlengths()}).} \item{countFa}{Return the number of records in the fasta file.} \item{scanFa}{Return the sequences indicated by \code{param} as a \code{\linkS4class{DNAStringSet}} instance. \code{seqnames(param)} selects the sequences to return; \code{start(param)} and \code{end{param}} define the (1-based) region of the sequence to return. Values of \code{end(param)} greater than the width of the sequence cause an error; use \code{seqlengths(FaFile(file))} to discover sequence widths. When \code{param} is missing, all records are selected. When \code{length(param)==0} no records are selected.} \item{getSeq}{Returns the sequences indicated by \code{param} from the indexed fasta file(s) of \code{file}. For the \code{FaFile} method, the return type is a \code{DNAStringSet}. The \code{getSeq,FaFile} and \code{scanFa,FaFile,GRanges} methods differ in that \code{getSeq} will reverse complement sequences selected from the minus strand. For the \code{FaFileList} method, the \code{param} argument must be a \code{GRangesList} of the same length as \code{file}, creating a one-to-one mapping between the ith element of \code{file} and the ith element of \code{param}; the return type is a \code{SimpleList} of \code{DNAStringSet} instances, with elements of the list in the same order as the input elements.} \item{show}{Compactly display the object.} } } \author{Martin Morgan} \examples{ fl <- system.file("extdata", "ce2dict1.fa", package="Rsamtools", mustWork=TRUE) fa <- open(FaFile(fl)) # open countFa(fa) (idx <- scanFaIndex(fa)) (dna <- scanFa(fa, param=idx[1:2])) ranges(idx) <- narrow(ranges(idx), -10) # last 10 nucleotides (dna <- scanFa(fa, param=idx[1:2])) } \keyword{classes} Rsamtools/man/PileupFiles-class.Rd0000644000175400017540000000706613556116727020177 0ustar00biocbuildbiocbuild\name{PileupFiles} \Rdversion{1.1} \docType{class} \alias{PileupFiles-class} % con/destructors \alias{PileupFiles} \alias{PileupFiles,character-method} \alias{PileupFiles,list-method} % accessors \alias{isOpen,PileupFiles-method} \alias{plpFiles} \alias{plpParam} % methods \alias{applyPileups,PileupFiles,ApplyPileupsParam-method} \alias{applyPileups,PileupFiles,missing-method} \alias{show,PileupFiles-method} \title{Represent BAM files for pileup summaries.} \description{ Use \code{PileupFiles()} to create a reference to BAM files (and their indicies), to be used for calculating pile-up summaries. } \usage{ ## Constructors PileupFiles(files, ..., param=ApplyPileupsParam()) \S4method{PileupFiles}{character}(files, ..., param=ApplyPileupsParam()) \S4method{PileupFiles}{list}(files, ..., param=ApplyPileupsParam()) ## opening / closing ## open(con, ...) ## close(con, ...) ## accessors; also path() \S4method{isOpen}{PileupFiles}(con, rw="") plpFiles(object) plpParam(object) ## actions \S4method{applyPileups}{PileupFiles,missing}(files, FUN, ..., param) \S4method{applyPileups}{PileupFiles,ApplyPileupsParam}(files, FUN, ..., param) ## display \S4method{show}{PileupFiles}(object) } \arguments{ \item{files}{For \code{PileupFiles}, a \code{character()} or \code{list} of \code{BamFile} instances representing files to be included in the pileup. Using a \code{list} of \code{BamFile} allows indicies to be specified when these are in non-standard format. All elements of \code{\ldots} must be the same type. For \code{applyPileups,PileupFiles-method}, a \code{PileupFiles} instance.} \item{\ldots}{Additional arguments, currently ignored.} \item{con, object}{An instance of \code{PileupFiles}.} \item{FUN}{A function of one argument; see \code{\link{applyPileups}}.} \item{param}{An instance of \code{\link{ApplyPileupsParam}}, to select which records to include in the pileup, and which summary information to return.} \item{rw}{character() indicating mode of file; not used for \code{TabixFile}.} } \section{Objects from the Class}{ Objects are created by calls of the form \code{PileupFiles()}. } \section{Fields}{ The \code{PileupFiles} class is implemented as an S4 reference class. It has the following fields: \describe{ \item{files}{A list of \code{\link{BamFile}} instances.} \item{param}{An instance of \code{\link{ApplyPileupsParam}}.} } } \section{Functions and methods}{ Opening / closing: \describe{ \item{open.PileupFiles}{Opens the (local or remote) \code{path} and \code{index} of each file in the \code{PileupFiles} instance. Returns a \code{PileupFiles} instance.} \item{close.PileupFiles}{Closes each file in the \code{PileupFiles} instance; returning (invisibly) the updated \code{PileupFiles}. The instance may be re-opened with \code{open.PileupFiles}.} } Accessors: \describe{ \item{plpFiles}{Returns the \code{list} of the files in the \code{PileupFiles} instance.} \item{plpParam}{Returns the \code{\link{ApplyPileupsParam}} content of the \code{PileupFiles} instance.} } Methods: \describe{ \item{applyPileups}{Calculate the pileup across all files in \code{files} according to criteria in \code{param} (or \code{plpParam(files)} if \code{param} is missing), invoking \code{FUN} on each range or collection of positions. See \code{\link{applyPileups}}.} \item{show}{Compactly display the object.} } } \author{Martin Morgan} \examples{ example(applyPileups) } \keyword{classes} Rsamtools/man/Rsamtools-package.Rd0000644000175400017540000000214613556116727020221 0ustar00biocbuildbiocbuild\name{Rsamtools-package} \Rdversion{1.1} \alias{Rsamtools-package} \alias{Rsamtools} \alias{bzfile-class} \alias{fifo-class} \alias{gzfile-class} \alias{pipe-class} \alias{unz-class} \alias{url-class} \docType{package} \title{ 'samtools' aligned sequence utilities interface } \description{ This package provides facilities for parsing samtools BAM (binary) files representing aligned sequences. } \details{ See \code{packageDescription('Rsamtools')} for package details. A useful starting point is the \code{\link{scanBam}} manual page. } \author{ Author: Martin Morgan Maintainer: Biocore Team c/o BioC user list } \references{ The current source code for samtools and bcftools is from \url{https://github.com/samtools/samtools}. Additional material is at \url{http://samtools.sourceforge.net/}. } \note{ This package documents the following classes for purely internal reasons, see help pages in other packages: \code{bzfile}, \code{fifo}, \code{gzfile}, \code{pipe}, \code{unz}, \code{url}. } \keyword{ package } \examples{ packageDescription('Rsamtools') } Rsamtools/man/RsamtoolsFile-class.Rd0000644000175400017540000000454213556116727020535 0ustar00biocbuildbiocbuild\name{RsamtoolsFile} \Rdversion{1.1} \docType{class} \alias{RsamtoolsFile-class} \alias{RsamtoolsFile} \alias{path} \alias{index} \alias{index<-} \alias{yieldSize} \alias{yieldSize<-} \alias{yieldSize<-,RsamtoolsFile-method} \alias{path,RsamtoolsFile-method} \alias{index,RsamtoolsFile-method} \alias{index<-,RsamtoolsFile-method} \alias{isOpen,RsamtoolsFile-method} \alias{show,RsamtoolsFile-method} \alias{yieldSize,RsamtoolsFile-method} \title{A base class for managing file references in Rsamtools} \description{ \code{RsamtoolsFile} is a base class for managing file references in \pkg{Rsamtools}; it is not intended for direct use by users -- see, e.g., \code{\link{BamFile}}. } \usage{ ## accessors \S4method{path}{RsamtoolsFile}(object, ...) \S4method{index}{RsamtoolsFile}(object, ..., asNA = TRUE) \S4method{isOpen}{RsamtoolsFile}(con, rw="") \S4method{yieldSize}{RsamtoolsFile}(object, ...) yieldSize(object, ...) <- value \S4method{show}{RsamtoolsFile}(object) } \arguments{ \item{con, object}{An instance of a class derived from \code{RsamtoolsFile}.} \item{asNA}{logical indicating if missing output should be NA or character()} \item{rw}{Mode of file; ignored.} \item{\dots}{Additional arguments, unused.} \item{value}{Replacement value.} } \section{Objects from the Class}{ Users do not directly create instances of this class; see, e.g., \code{\link{BamFile}-class}. } \section{Fields}{ The \code{RsamtoolsFile} class is implemented as an S4 reference class. It has the following fields: \describe{ \item{.extptr}{An \code{externalptr} initialized to an internal structure with opened bam file and bam index pointers.} \item{path}{A character(1) vector of the file name.} \item{index}{A character(1) vector of the index file name.} \item{yieldSize}{An integer(1) vector of the number of records to yield.} } } \section{Functions and methods}{ Accessors: \describe{ \item{path}{Returns a character(1) vector of path names.} \item{index}{Returns a character(1) vector of index path names.} \item{yieldSize, yieldSize<-}{Return or set an integer(1) vector indicating yield size.} } Methods: \describe{ \item{isOpen}{Report whether the file is currently open.} \item{show}{Compactly display the object.} } } \author{Martin Morgan} \keyword{classes} Rsamtools/man/RsamtoolsFileList-class.Rd0000644000175400017540000000402013556116727021360 0ustar00biocbuildbiocbuild\name{RsamtoolsFileList} \Rdversion{1.1} \docType{class} \alias{RsamtoolsFileList-class} \alias{RsamtoolsFileList} \alias{path,RsamtoolsFileList-method} \alias{index,RsamtoolsFileList-method} \alias{index<-,RsamtoolsFileList-method} \alias{isOpen,RsamtoolsFileList-method} \alias{open.RsamtoolsFileList} \alias{close.RsamtoolsFileList} \alias{names,RsamtoolsFileList-method} \alias{yieldSize,RsamtoolsFileList-method} \alias{yieldSize<-,RsamtoolsFileList-method} \title{A base class for managing lists of Rsamtools file references} \description{ \code{RsamtoolsFileList} is a base class for managing lists of file references in \pkg{Rsamtools}; it is not intended for direct use -- see, e.g., \code{\link{BamFileList}}. } \usage{ \S4method{path}{RsamtoolsFileList}(object, ...) \S4method{index}{RsamtoolsFileList}(object, ..., asNA = TRUE) \S4method{isOpen}{RsamtoolsFileList}(con, rw="") \S3method{open}{RsamtoolsFileList}(con, ...) \S3method{close}{RsamtoolsFileList}(con, ...) \S4method{names}{RsamtoolsFileList}(x) \S4method{yieldSize}{RsamtoolsFileList}(object, ...) } \arguments{ \item{con, object, x}{An instance of a class derived from \code{RsamtoolsFileList}.} \item{asNA}{logical indicating if missing output should be NA or character()} \item{rw}{Mode of file; ignored.} \item{\dots}{Additional arguments.} } \section{Objects from the Class}{ Users do not directly create instances of this class; see, e.g., \code{\link{BamFileList}-class}. } \section{Functions and methods}{ This class inherits functions and methods for subseting, updating, and display from the \code{\link{SimpleList}} class. Methods: \describe{ \item{isOpen:}{Report whether each file in the list is currently open.} \item{open:}{Attempt to open each file in the list.} \item{close:}{Attempt to close each file in the list.} \item{names:}{Names of each element of the list or, if names are \code{NULL}, the basename of the path of each element.} } } \author{Martin Morgan} \keyword{classes} Rsamtools/man/ScanBamParam-class.Rd0000644000175400017540000003152213556116727020235 0ustar00biocbuildbiocbuild\name{ScanBamParam} \Rdversion{1.1} \docType{class} \alias{ScanBamParam-class} \alias{ScanBamParam} \alias{ScanBamParam,missing-method} \alias{ScanBamParam,ANY-method} \alias{ScanBamParam,IntegerRangesList-method} \alias{ScanBamParam,GRanges-method} % helpers \alias{scanBamWhat} \alias{scanBamFlag} % accessors \alias{bamFlag<-} \alias{bamFlag} \alias{bamReverseComplement<-} \alias{bamReverseComplement} \alias{bamSimpleCigar<-} \alias{bamSimpleCigar} \alias{bamTag<-} \alias{bamTag} \alias{bamTagFilter} \alias{bamTagFilter<-} \alias{bamWhat<-} \alias{bamWhat} \alias{bamWhich<-} \alias{bamWhich<-,ScanBamParam,GRanges-method} \alias{bamWhich<-,ScanBamParam,IntegerRangesList-method} \alias{bamWhich<-,ScanBamParam,ANY-method} \alias{bamWhich} \alias{bamMapqFilter} \alias{bamMapqFilter<-} % methods \alias{show,ScanBamParam-method} % flag utils \alias{FLAG_BITNAMES} \alias{bamFlagAsBitMatrix} \alias{bamFlagAND} \alias{bamFlagTest} % flag names \alias{isPaired} \alias{isProperPair} \alias{isUnmappedQuery} \alias{hasUnmappedMate} \alias{isMinusStrand} \alias{isMateMinusStrand} \alias{isFirstMateRead} \alias{isSecondMateRead} \alias{isNotPrimaryRead} % deprecated \alias{isSecondaryAlignment} \alias{isNotPassingQualityControls} \alias{isDuplicate} \title{Parameters for scanning BAM files} \description{ Use \code{ScanBamParam()} to create a parameter object influencing what fields and which records are imported from a (binary) BAM file. Use of \code{which} requires that a BAM index file (\code{.bai}) exists. } \usage{ # Constructor ScanBamParam(flag = scanBamFlag(), simpleCigar = FALSE, reverseComplement = FALSE, tag = character(0), tagFilter = list(), what = character(0), which, mapqFilter=NA_integer_) # Constructor helpers scanBamFlag(isPaired = NA, isProperPair = NA, isUnmappedQuery = NA, hasUnmappedMate = NA, isMinusStrand = NA, isMateMinusStrand = NA, isFirstMateRead = NA, isSecondMateRead = NA, isNotPrimaryRead = NA, isSecondaryAlignment = NA, isNotPassingQualityControls = NA, isDuplicate = NA, isSupplementaryAlignment = NA) scanBamWhat() # Accessors bamFlag(object, asInteger=FALSE) bamFlag(object) <- value bamReverseComplement(object) bamReverseComplement(object) <- value bamSimpleCigar(object) bamSimpleCigar(object) <- value bamTag(object) bamTag(object) <- value bamTagFilter(object) bamTagFilter(object) <- value bamWhat(object) bamWhat(object) <- value bamWhich(object) bamWhich(object) <- value bamMapqFilter(object) bamMapqFilter(object) <- value \S4method{show}{ScanBamParam}(object) # Flag utils bamFlagAsBitMatrix(flag, bitnames=FLAG_BITNAMES) bamFlagAND(flag1, flag2) bamFlagTest(flag, value) } \arguments{ \item{flag}{For \code{ScanBamParam}, an integer(2) vector used to filter reads based on their 'flag' entry. This is most easily created with the \code{scanBamFlag()} helper function. For \code{bamFlagAsBitMatrix}, \code{bamFlagTest} an integer vector where each element represents a 'flag' entry. } \item{simpleCigar}{A logical(1) vector which, when TRUE, returns only those reads for which the cigar (run-length encoded representation of the alignment) is missing or contains only matches / mismatches (\code{'M'}).} \item{reverseComplement}{A logical(1) vectors. BAM files store reads mapping to the minus strand as though they are on the plus strand. Rsamtools obeys this convention by default (\code{reverseComplement=FALSE}), but when this value is set to TRUE returns the sequence and quality scores of reads mapped to the minus strand in the reverse complement (sequence) and reverse (quality) of the read as stored in the BAM file. This might be useful if wishing to recover read and quality scores as represented in fastq files, but is NOT appropriate for variant calling or other alignment-based operations.} \item{tag}{A character vector naming tags to be extracted. A tag is an optional field, with arbitrary information, stored with each record. Tags are identified by two-letter codes, so all elements of \code{tag} must have exactly 2 characters.} \item{tagFilter}{A named \code{list} of atomic vectors. The name of each \code{list} element is the tag name (two-letter code), and the corresponding atomic vector is the set of acceptable values for the tag. Only reads with specified tags are included. \code{NULL}s, \code{NA}s, and empty strings are not allowed in the atomic vectors.} \item{what}{A character vector naming the fields to return \code{scanBamWhat()} returns a vector of available fields. Fields are described on the \code{\link{scanBam}} help page.} \item{mapqFilter}{A non-negative integer(1) specifying the minimum mapping quality to include. BAM records with mapping qualities less than \code{mapqFilter} are discarded.} \item{which}{A \code{\linkS4class{GRanges}}, \code{\linkS4class{IntegerRangesList}}, or any object that can be coerced to a \code{IntegerRangesList}, or missing object, from which a \code{IRangesList} instance will be constructed. Names of the \code{IRangesList} correspond to reference sequences, and ranges to the regions on that reference sequence for which matches are desired. Because data types are coerced to \code{IRangesList}, \code{which} does \emph{not} include strand information (use the \code{flag} argument instead). Only records with a read overlapping the specified ranges are returned. All ranges must have ends less than or equal to 536870912. When one record overlaps two ranges in \code{which}, the record is returned \emph{twice}.} \item{isPaired}{A logical(1) indicating whether unpaired (FALSE), paired (TRUE), or any (NA) read should be returned.} \item{isProperPair}{A logical(1) indicating whether improperly paired (FALSE), properly paired (TRUE), or any (NA) read should be returned. A properly paired read is defined by the alignment algorithm and might, e.g., represent reads aligning to identical reference sequences and with a specified distance.} \item{isUnmappedQuery}{A logical(1) indicating whether unmapped (TRUE), mapped (FALSE), or any (NA) read should be returned.} \item{hasUnmappedMate}{A logical(1) indicating whether reads with mapped (FALSE), unmapped (TRUE), or any (NA) mate should be returned.} \item{isMinusStrand}{A logical(1) indicating whether reads aligned to the plus (FALSE), minus (TRUE), or any (NA) strand should be returned.} \item{isMateMinusStrand}{A logical(1) indicating whether mate reads aligned to the plus (FALSE), minus (TRUE), or any (NA) strand should be returned.} \item{isFirstMateRead}{A logical(1) indicating whether the first mate read should be returned (TRUE) or not (FALSE), or whether mate read number should be ignored (NA).} \item{isSecondMateRead}{A logical(1) indicating whether the second mate read should be returned (TRUE) or not (FALSE), or whether mate read number should be ignored (NA).} \item{isNotPrimaryRead}{Deprecated; use \code{isSecondaryAlignment}.} \item{isSecondaryAlignment}{A logical(1) indicating whether alignments that are secondary (TRUE), are not (FALSE) or whose secondary status does not matter (NA) should be returned. A non-primary alignment (\dQuote{secondary alignment} in the SAM specification) might result when a read aligns to multiple locations. One alignment is designated as primary and has this flag set to FALSE; the remainder, for which this flag is TRUE, are designated by the aligner as secondary.} \item{isNotPassingQualityControls}{A logical(1) indicating whether reads passing quality controls (FALSE), reads not passing quality controls (TRUE), or any (NA) read should be returned.} \item{isDuplicate}{A logical(1) indicating that un-duplicated (FALSE), duplicated (TRUE), or any (NA) reads should be returned. 'Duplicated' reads may represent PCR or optical duplicates.} \item{isSupplementaryAlignment}{A logical(1) indicating that non-supplementary (FALSE), supplementary (TRUE), or any (NA) reads should be returned. The SAM specification indicates that 'supplementary' reads are part of a chimeric alignment.} \item{object}{An instance of class \code{ScanBamParam}.} \item{value}{An instance of the corresponding slot, to be assigned to \code{object} or, for \code{bamFlagTest}, a \code{character(1)} name of the flag to test, e.g., \dQuote{isUnmappedQuery}, from the arguments to \code{scanBamFlag}.} \item{asInteger}{logical(1) indicating whether \sQuote{flag} should be returned as an encoded integer vector (\code{TRUE}) or human-readable form (\code{FALSE}).} \item{bitnames}{Names of the flag bits to extract. Will be the colnames of the returned matrix.} \item{flag1, flag2}{Integer vectors containing \sQuote{flag} entries.} } \section{Objects from the Class}{ Objects are created by calls of the form \code{ScanBamParam()}. } \section{Slots}{ \describe{ \item{\code{flag}}{Object of class \code{integer} encoding flags to be kept when they have their '0' (\code{keep0}) or '1' (\code{keep1}) bit set.} \item{\code{simpleCigar}}{Object of class \code{logical} indicating, when TRUE, that only 'simple' cigars (empty or 'M') are returned.} \item{\code{reverseComplement}}{Object of class \code{logical} indicating, when TRUE, that reads on the minus strand are to be reverse complemented (sequence) and reversed (quality).} \item{\code{tag}}{Object of class \code{character} indicating what tags are to be returned.} \item{\code{tagFilter}}{Object of class \code{list} (named) indicating tags to filter by, and the set of acceptable values for each tag.} \item{\code{what}}{Object of class \code{character} indicating what fields are to be returned.} \item{\code{which}}{Object of class \code{IntegerRangesList} indicating which reference sequence and coordinate reads must overlap.} \item{\code{mapqFilter}}{Object of class \code{integer} indicating the minimum mapping quality required for input, or NA to indicate no filtering.} } } \section{Functions and methods}{ See 'Usage' for details on invocation. Constructor: \describe{ \item{ScanBamParam:}{Returns a \code{ScanBamParam} object. The \code{which} argument to the constructor can be one of several different types, as documented above.} } Accessors: \describe{ \item{bamTag, bamTag<-}{Returns or sets a \code{character} vector of tags to be extracted.} \item{bamTagFilter, bamTagFilter<-}{Returns or sets a named \code{list} of tags to filter by, and the set of their acceptable values.} \item{bamWhat, bamWhat<-}{Returns or sets a \code{character} vector of fields to be extracted.} \item{bamWhich, bamWhich<-}{Returns or sets a \code{IntegerRangesList} of bounds on reads to be extracted. A length 0 \code{IntegerRangesList} represents all reads.} \item{bamFlag, bamFlag<-}{Returns or sets an \code{integer(2)} representation of reads flagged to be kept or excluded.} \item{bamSimpleCigar, bamSimpleCigar<-}{Returns or sets a \code{logical(1)} vector indicating whether reads without indels or clipping be kept.} \item{bamReverseComplement, bamReverseComplement<-}{Returns or sets a \code{logical(1)} vector indicating whether reads on the minus strand will be returned with sequence reverse complemented and quality reversed.} } Methods: \describe{ \item{show}{Compactly display the object.} } } \author{Martin Morgan} \seealso{ \code{\link{scanBam}} } \examples{ ## defaults p0 <- ScanBamParam() ## subset of reads based on genomic coordinates which <- IRangesList(seq1=IRanges(1000, 2000), seq2=IRanges(c(100, 1000), c(1000, 2000))) p1 <- ScanBamParam(what=scanBamWhat(), which=which) ## subset of reads based on 'flag' value p2 <- ScanBamParam(what=scanBamWhat(), flag=scanBamFlag(isMinusStrand=FALSE)) ## subset of fields p3 <- ScanBamParam(what=c("rname", "strand", "pos", "qwidth")) ## use fl <- system.file("extdata", "ex1.bam", package="Rsamtools", mustWork=TRUE) res <- scanBam(fl, param=p2)[[1]] lapply(res, head) ## tags; NM: edit distance; H1: 1-difference hits p4 <- ScanBamParam(tag=c("NM", "H1"), what="flag") bam4 <- scanBam(fl, param=p4) str(bam4[[1]][["tag"]]) ## tagFilter p5 <- ScanBamParam(tag=c("NM", "H1"), tagFilter=list(NM=c(2, 3, 4))) bam5 <- scanBam(fl, param=p5) table(bam5[[1]][["tag"]][["NM"]]) ## flag utils flag <- scanBamFlag(isUnmappedQuery=FALSE, isMinusStrand=TRUE) p6 <- ScanBamParam(what="flag") bam6 <- scanBam(fl, param=p6) flag6 <- bam6[[1]][["flag"]] head(bamFlagAsBitMatrix(flag6[1:9])) colSums(bamFlagAsBitMatrix(flag6)) flag bamFlagAsBitMatrix(flag) } \keyword{classes} Rsamtools/man/ScanBcfParam-class.Rd0000644000175400017540000001031313556116727020223 0ustar00biocbuildbiocbuild\name{ScanBcfParam-class} \Rdversion{1.1} \docType{class} \alias{ScanBVcfParam-class} \alias{ScanBcfParam} \alias{ScanBcfParam-class} \alias{ScanBcfParam,GRanges-method} \alias{ScanBcfParam,GRangesList-method} \alias{ScanBcfParam,IntegerRangesList-method} \alias{ScanBcfParam,missing-method} \alias{bcfFixed} \alias{bcfInfo} \alias{bcfGeno} \alias{bcfSamples} \alias{bcfTrimEmpty} \alias{bcfWhich} \alias{show,ScanBVcfParam-method} \title{Parameters for scanning BCF files} \description{ Use \code{ScanBcfParam()} to create a parameter object influencing the \sQuote{INFO} and \sQuote{GENO} fields parsed, and which sample records are imported from a BCF file. Use of \code{which} requires that a BCF index file (\code{.bci}) exists. } \usage{ ScanBcfParam(fixed=character(), info=character(), geno=character(), samples=character(), trimEmpty=TRUE, which, ...) \S4method{ScanBcfParam}{missing}(fixed=character(), info=character(), geno=character(), samples=character(), trimEmpty=TRUE, which, ...) \S4method{ScanBcfParam}{IntegerRangesList}(fixed=character(), info=character(), geno=character(), samples=character(), trimEmpty=TRUE, which, ...) \S4method{ScanBcfParam}{GRanges}(fixed=character(), info=character(), geno=character(), samples=character(), trimEmpty=TRUE, which, ...) \S4method{ScanBcfParam}{GRangesList}(fixed=character(), info=character(), geno=character(), samples=character(), trimEmpty=TRUE, which, ...) ## Accessors bcfFixed(object) bcfInfo(object) bcfGeno(object) bcfSamples(object) bcfTrimEmpty(object) bcfWhich(object) } \arguments{ \item{fixed}{A logical(1) for use with \code{ScanVcfParam} only.} \item{info}{A character() vector of \sQuote{INFO} fields (see \link[VariantAnnotation]{scanVcfHeader}) to be returned.} \item{geno}{A character() vector of \sQuote{GENO} fields (see \link[VariantAnnotation]{scanVcfHeader}) to be returned. \code{character(0)} returns all fields, \code{NA_character_} returns none.} \item{samples}{A character() vector of sample names (see \link[VariantAnnotation]{scanVcfHeader}) to be returned. \code{character(0)} returns all fields, \code{NA_character_} returns none.} \item{trimEmpty}{A logical(1) indicating whether \sQuote{GENO} fields with no values should be returned.} \item{which}{An object, for which a method is defined (see usage, above), describing the sequences and ranges to be queried. Variants whose \code{POS} lies in the interval(s) \code{[start, end)} are returned.} \item{object}{An instance of class \code{ScanBcfParam}.} \item{\dots}{Arguments used internally.} } \section{Objects from the Class}{ Objects can be created by calls of the form \code{ScanBcfParam()}. } \section{Slots}{ \describe{ \item{\code{which}:}{Object of class \code{"IntegerRangesList"} indicating which reference sequence and coordinate variants must overlap.} \item{\code{info}:}{Object of class \code{"character"} indicating portions of \sQuote{INFO} to be returned.} \item{\code{geno}:}{Object of class \code{"character"} indicating portions of \sQuote{GENO} to be returned. } \item{\code{samples}:}{Object of class \code{"character"} indicating the samples to be returned. } \item{\code{trimEmpty}:}{Object of class \code{"logical"} indicating whether empty \sQuote{GENO} fields are to be returned.} \item{\code{fixed}:}{Object of class \code{"character"}. For use with \code{ScanVcfParam} only.} } } \section{Functions and methods}{ See 'Usage' for details on invocation. Constructor: \describe{ \item{ScanBcfParam:}{Returns a \code{ScanBcfParam} object. The \code{which} argument to the constructor can be one of several types, as documented above.} } Accessors: \describe{ \item{bcfInfo, bcfGeno, bcfTrimEmpty, bcfWhich:}{Return the corresponding field from \code{object}.} } Methods: \describe{ \item{show}{Compactly display the object.} } } \author{ Martin Morgan \url{mtmorgan@fhcrc.org} } \seealso{ \link[VariantAnnotation]{scanVcf} \link[VariantAnnotation]{ScanVcfParam} } \examples{ ## see ?ScanVcfParam examples } \keyword{classes} Rsamtools/man/TabixFile-class.Rd0000644000175400017540000001367313556116727017626 0ustar00biocbuildbiocbuild\name{TabixFile} \Rdversion{1.1} \docType{class} \alias{TabixFile-class} \alias{TabixFileList-class} % con/destructors \alias{TabixFile} \alias{TabixFileList} \alias{open.TabixFile} \alias{close.TabixFile } % accessors \alias{isOpen,TabixFile-method} % methods \alias{seqnamesTabix,TabixFile-method} \alias{headerTabix,TabixFile-method} \alias{scanTabix,TabixFile,IntegerRangesList-method} \alias{scanTabix,TabixFile,GRanges-method} \alias{scanTabix,TabixFile,missing-method} \alias{scanTabix,character,ANY-method} \alias{scanTabix,character,missing-method} \alias{countTabix} \title{Manipulate tabix indexed tab-delimited files.} \description{ Use \code{TabixFile()} to create a reference to a Tabix file (and its index). Once opened, the reference remains open across calls to methods, avoiding costly index re-loading. \code{TabixFileList()} provides a convenient way of managing a list of \code{TabixFile} instances. } \usage{ ## Constructors TabixFile(file, index = paste(file, "tbi", sep="."), ..., yieldSize=NA_integer_) TabixFileList(...) ## Opening / closing \S3method{open}{TabixFile}(con, ...) \S3method{close}{TabixFile}(con, ...) ## accessors; also path(), index(), yieldSize() \S4method{isOpen}{TabixFile}(con, rw="") ## actions \S4method{seqnamesTabix}{TabixFile}(file, ...) \S4method{headerTabix}{TabixFile}(file, ...) \S4method{scanTabix}{TabixFile,GRanges}(file, ..., param) \S4method{scanTabix}{TabixFile,IntegerRangesList}(file, ..., param) \S4method{scanTabix}{TabixFile,missing}(file, ..., param) \S4method{scanTabix}{character,ANY}(file, ..., param) \S4method{scanTabix}{character,missing}(file, ..., param) countTabix(file, ...) } \arguments{ \item{con}{An instance of \code{TabixFile}.} \item{file}{For TabixFile(), A character(1) vector to the tabix file path; can be remote (http://, ftp://). For \code{countTabix}, a character(1) or \code{TabixFile} instance. For others, a \code{TabixFile} instance.} \item{index}{A character(1) vector of the tabix file index.} \item{yieldSize}{Number of records to yield each time the file is read from using \code{scanTabix}. Only valid when \code{param} is unspecified. \code{yieldSize} does not alter existing yield sizes, include \code{NA}, when creating a \code{TabixFileList} from \code{TabixFile} instances.} \item{param}{An instance of GRanges or IntegerRangesList, used to select which records to scan.} \item{...}{Additional arguments. For \code{TabixFileList}, this can include \code{file}, \code{index}, and \code{yieldSize} arguments. The \code{file} can be a single character vector of paths to tabix files (and optionally a similarly lengthed vector of \code{index}), or several instances of \code{TabixFile} objects. The arguments can also include \code{yieldSize}, applied to all elements of the list.} \item{rw}{character() indicating mode of file; not used for \code{TabixFile}.} } \section{Objects from the Class}{ Objects are created by calls of the form \code{TabixFile()}. } \section{Fields}{ The \code{TabixFile} class inherits fields from the \code{\linkS4class{RsamtoolsFile}} class. } \section{Functions and methods}{ \code{TabixFileList} inherits methods from \code{\link{RsamtoolsFileList}} and \code{\link{SimpleList}}. Opening / closing: \describe{ \item{open.TabixFile}{Opens the (local or remote) \code{path} and \code{index}. Returns a \code{TabixFile} instance. \code{yieldSize} determines the number of records parsed during each call to \code{scanTabix}; \code{NA} indicates that all records are to be parsed.} \item{close.TabixFile}{Closes the \code{TabixFile} \code{con}; returning (invisibly) the updated \code{TabixFile}. The instance may be re-opened with \code{open.TabixFile}.} } Accessors: \describe{ \item{path}{Returns a character(1) vector of the tabix path name.} \item{index}{Returns a character(1) vector of tabix index name.} \item{yieldSize, yieldSize<-}{Return or set an integer(1) vector indicating yield size.} } Methods: \describe{ \item{seqnamesTabix}{Visit the path in \code{path(file)}, returning the sequence names present in the file.} \item{headerTabix}{Visit the path in \code{path(file)}, returning the sequence names, column indicies used to sort the file, the number of lines skipped while indexing, the comment character used while indexing, and the header (preceeded by comment character, at start of file) lines.} \item{countTabix}{Return the number of records in each range of \code{param}, or the count of all records in the file (when \code{param} is missing).} \item{scanTabix}{For \code{signature(file="TabixFile")}, Visit the path in \code{path(file)}, returning the result of \code{\link{scanTabix}} applied to the specified path. For \code{signature(file="character")}, call the corresponding method after coercing \code{file} to \code{TabixFile}.} \item{indexTabix}{This method operates on file paths, rather than \code{TabixFile} objects, to index tab-separated files. See \code{\link{indexTabix}}.} \item{show}{Compactly display the object.} } } \author{Martin Morgan} \examples{ fl <- system.file("extdata", "example.gtf.gz", package="Rsamtools", mustWork=TRUE) tbx <- TabixFile(fl) param <- GRanges(c("chr1", "chr2"), IRanges(c(1, 1), width=100000)) countTabix(tbx) countTabix(tbx, param=param) res <- scanTabix(tbx, param=param) sapply(res, length) res[["chr1:1-100000"]][1:2] ## parse to list of data.frame's dff <- Map(function(elt) { read.csv(textConnection(elt), sep="\t", header=FALSE) }, res) dff[["chr1:1-100000"]][1:5,1:8] ## parse 100 records at a time length(scanTabix(tbx)[[1]]) # total number of records tbx <- open(TabixFile(fl, yieldSize=100)) while(length(res <- scanTabix(tbx)[[1]])) cat("records read:", length(res), "\n") close(tbx) } \keyword{classes} Rsamtools/man/applyPileups.Rd0000644000175400017540000000725713556116727017344 0ustar00biocbuildbiocbuild\name{applyPileups} \Rdversion{1.1} \alias{applyPileups} % \alias{yieldBam} \title{ Apply a user-provided function to calculate pile-up statistics across multiple BAM files. } \description{ \code{applyPileups} scans one or more BAM files, returning position-specific sequence and quality summaries. } \usage{ applyPileups(files, FUN, ..., param) } \arguments{ \item{files}{A \code{\link{PileupFiles}} instances.} \item{FUN}{A function of 1 argument, \code{x}, to be evaluated for each yield (see \code{yieldSize}, \code{yieldBy}, \code{yieldAll}). The argument \code{x} is a \code{list}, with elements describing the current pile-up. The elements of the list are determined by the argument \code{what}, and include: \describe{ \item{seqnames:}{(Always returned) A named \code{integer()} representing the seqnames corresponding to each position reported in the pile-up. This is a run-length encoding, where the names of the elements represent the seqnames, and the values the number of successive positions corresponding to that seqname.} \item{pos:}{Always returned) A \code{integer()} representing the genomic coordinate of each pile-up position.} \item{seq:}{An \code{array} of dimensions nucleotide x file x position. The \sQuote{nucleotide} dimension is length 5, corresponding to \sQuote{A}, \sQuote{C}, \sQuote{G}, \sQuote{T}, and \sQuote{N} respectively. Entries in the array represent the number of times the nucleotide occurred in reads in the file overlapping the position. } \item{qual:}{Like \code{seq}, but summarizing quality; the first dimension is the Phred-encoded quality score, ranging from \sQuote{!} (0) to \sQuote{~} (93).} } } \item{\dots}{Additional arguments, passed to methods.} \item{param}{An instance of the object returned by \code{ApplyPileupsParam}.} } \details{ Regardless of \code{param} values, the algorithm follows samtools by excluding reads flagged as unmapped, secondary, duplicate, or failing quality control. } \value{ \code{applyPileups} returns a \code{list} equal in length to the number of times \code{FUN} has been called, with each element containing the result of \code{FUN}. \code{ApplyPileupsParam} returns an object describing the parameters. } \references{\url{http://samtools.sourceforge.net/}} \author{Martin Morgan} \seealso{\code{\link{ApplyPileupsParam}}.} \examples{ ## The examples below are currently broken and have been disabled for now \dontrun{ fl <- system.file("extdata", "ex1.bam", package="Rsamtools", mustWork=TRUE) fls <- PileupFiles(c(fl, fl)) calcInfo <- function(x) { ## information at each pile-up position info <- apply(x[["seq"]], 2, function(y) { y <- y[c("A", "C", "G", "T"),,drop=FALSE] y <- y + 1L # continuity cvg <- colSums(y) p <- y / cvg[col(y)] h <- -colSums(p * log(p)) ifelse(cvg == 4L, NA, h) }) list(seqnames=x[["seqnames"]], pos=x[["pos"]], info=info) } which <- GRanges(c("seq1", "seq2"), IRanges(c(1000, 1000), 2000)) param <- ApplyPileupsParam(which=which, what="seq") res <- applyPileups(fls, calcInfo, param=param) str(res) head(res[[1]][["pos"]]) # positions matching param head(res[[1]][["info"]]) # inforamtion in each file ## 'param' as part of 'files' fls1 <- PileupFiles(c(fl, fl), param=param) res1 <- applyPileups(fls1, calcInfo) identical(res, res1) ## yield by position, across ranges param <- ApplyPileupsParam(which=which, yieldSize=500L, yieldBy="position", what="seq") res <- applyPileups(fls, calcInfo, param=param) sapply(res, "[[", "seqnames") } } \keyword{ manip } Rsamtools/man/defunct.Rd0000644000175400017540000000042113556116727016267 0ustar00biocbuildbiocbuild\name{Deprecated and Defunct} \title{Rsamtools Deprecated and Defunct} \alias{quickCountBam} \alias{quickBamCounts} \alias{bgzipTabix} \description{ The function, class, or data object you have asked for has been deprecated or made defunct. } \keyword{internal} Rsamtools/man/deprecated.Rd0000644000175400017540000000110413556116727016736 0ustar00biocbuildbiocbuild\name{deprecated} \Rdversion{1.1} \alias{BamSampler} \alias{BamSampler-class} \alias{scanBam,BamSampler-method} \alias{show,BamSampler-method} \alias{yieldTabix} \alias{yieldTabix,TabixFile-method} \title{Deprecated functions} \description{Functions listed on this page are no longer supported.} \details{ For \code{yieldTabix}, use the \code{yieldSize} argument of \code{TabixFiles}. For \code{BamSampler}, use \code{REDUCEsampler} with \code{reduceByYield} in the \code{GenomicFiles} package. } \author{ Martin Morgan . } \keyword{ manip } Rsamtools/man/headerTabix.Rd0000644000175400017540000000172013556116727017062 0ustar00biocbuildbiocbuild\name{headerTabix} \Rdversion{1.1} \alias{headerTabix} \alias{headerTabix,character-method} \title{ Retrieve sequence names defined in a tabix file. } \description{ This function queries a tabix file, returning the names of the \sQuote{sequences} used as a key when creating the file. } \usage{ headerTabix(file, ...) \S4method{headerTabix}{character}(file, ...) } \arguments{ \item{file}{A \code{character(1)} file path or \code{\linkS4class{TabixFile}} instance pointing to a \sQuote{tabix} file.} \item{...}{Additional arguments, currently ignored.} } \value{ A \code{list(4)} of the sequence names, column indicies used to sort the file, the number of lines skipped while indexing, and the comment character used while indexing. } \author{ Martin Morgan . } \examples{ fl <- system.file("extdata", "example.gtf.gz", package="Rsamtools", mustWork=TRUE) headerTabix(fl) } \keyword{ manip } Rsamtools/man/indexTabix.Rd0000644000175400017540000000375113556116727016747 0ustar00biocbuildbiocbuild\name{indexTabix} \Rdversion{1.1} \alias{indexTabix} \title{ Compress and index tabix-compatible files. } \description{ Index (with \code{indexTabix}) files that have been sorted into ascending sequence, start and end position ordering. } \usage{ indexTabix(file, format=c("gff", "bed", "sam", "vcf", "vcf4", "psltbl"), seq=integer(), start=integer(), end=integer(), skip=0L, comment="#", zeroBased=FALSE, ...) } \arguments{ \item{file}{A characater(1) path to a sorted, bgzip-compressed file.} \item{format}{The format of the data in the compressed file. A characater(1) matching one of the types named in the function signature.} \item{seq}{If \code{format} is missing, then \code{seq} indicates the column in which the \sQuote{sequence} identifier (e.g., chrq) is to be found.} \item{start}{If \code{format} is missing, \code{start} indicates the column containing the start coordinate of the feature to be indexed.} \item{end}{If \code{format} is missing, \code{end} indicates the column containing the ending coordinate of the feature to be indexed.} \item{skip}{The number of lines to be skipped at the beginning of the file.} \item{comment}{A single character which, when present as the first character in a line, indicates that the line is to be omitted. from indexing.} \item{zeroBased}{A logical(1) indicating whether coordinats in the file are zero-based.} \item{...}{Additional arguments.} } \value{ The return value of \code{indexTabix} is an updated instance of \code{file} reflecting the newly-created index file. } \references{ \url{http://samtools.sourceforge.net/tabix.shtml} } \author{ Martin Morgan . } \examples{ from <- system.file("extdata", "ex1.sam", package="Rsamtools", mustWork=TRUE) to <- tempfile() zipped <- bgzip(from, to) idx <- indexTabix(zipped, "sam") tab <- TabixFile(zipped, idx) } \keyword{ manip } Rsamtools/man/pileup.Rd0000644000175400017540000006107213556116727016146 0ustar00biocbuildbiocbuild\name{pileup} \Rdversion{1.1} % PileupParam \alias{PileupParam-class} \alias{PileupParam} \alias{show,PileupParam-method} \alias{max_depth} \alias{min_base_quality} \alias{min_mapq} \alias{min_nucleotide_depth} \alias{min_minor_allele_depth} \alias{distinguish_strands} \alias{distinguish_nucleotides} \alias{ignore_query_Ns} \alias{include_deletions} \alias{include_insertions} \alias{left_bins} \alias{query_bins} \alias{cycle_bins} % pileup \alias{pileup} \alias{pileup,character-method} \alias{pileup,BamFile-method} % utility \alias{phred2ASCIIOffset} \title{ Use filters and output formats to calculate pile-up statistics for a BAM file. } \description{ \code{pileup} uses \code{PileupParam} and \code{ScanBamParam} objects to calculate pileup statistics for a BAM file. The result is a \code{data.frame} with columns summarizing counts of reads overlapping each genomic position, optionally differentiated on nucleotide, strand, and position within read. } \usage{ pileup(file, index=file, ..., scanBamParam=ScanBamParam(), pileupParam=PileupParam()) ## PileupParam constructor PileupParam(max_depth=250, min_base_quality=13, min_mapq=0, min_nucleotide_depth=1, min_minor_allele_depth=0, distinguish_strands=TRUE, distinguish_nucleotides=TRUE, ignore_query_Ns=TRUE, include_deletions=TRUE, include_insertions=FALSE, left_bins=NULL, query_bins=NULL, cycle_bins=NULL) phred2ASCIIOffset(phred=integer(), scheme= c("Illumina 1.8+", "Sanger", "Solexa", "Illumina 1.3+", "Illumina 1.5+")) } \arguments{ \item{file}{ character(1) or \code{\link{BamFile}}; BAM file path. } \item{index}{ When \code{file} is character(1), an optional character(1) of BAM index file path; see \code{\link{scanBam}}. } \item{\dots}{Additional arguments, perhaps used by methods.} \item{scanBamParam}{An instance of \code{\link{ScanBamParam}}.} \item{pileupParam}{An instance of \code{\link{PileupParam}}.} %% args for PileupParam \item{max_depth}{integer(1); maximum number of overlapping alignments considered for each position in the pileup.} \item{min_base_quality}{integer(1); minimum \sQuote{QUAL} value for each nucleotide in an alignment. Use \code{phred2ASCIIOffset} to help translate numeric or character values to these offsets.} \item{min_mapq}{integer(1); minimum \sQuote{MAPQ} value for an alignment to be included in pileup.} \item{min_nucleotide_depth}{integer(1); minimum count of each nucleotide (\emph{independent} of other nucleotides) at a given position required for said nucleotide to appear in the result.} \item{min_minor_allele_depth}{integer(1); minimum count of \emph{all} nucleotides other than the major allele at a given position required for a particular nucleotide to appear in the result.} \item{distinguish_strands}{logical(1); \code{TRUE} if result should differentiate between strands.} \item{distinguish_nucleotides}{logical(1); \code{TRUE} if result should differentiate between nucleotides.} \item{ignore_query_Ns}{logical(1); \code{TRUE} if non-determinate nucleotides in alignments should be excluded from the pileup.} \item{include_deletions}{logical(1); \code{TRUE} to include deletions in pileup.} \item{include_insertions}{logical(1); \code{TRUE} to include insertions in pileup.} \item{left_bins}{numeric; all same sign; unique positions within a read to delimit bins. Position within read is based on counting from the \emph{5' end regardless of strand}. Minimum of two values are required so at least one range can be formed. \code{NULL} (default) indicates no binning. Use negative values to count from the opposite end. Sorted order not required. Floating-point values are coerced to \code{integer}. If you want to delimit bins based on sequencing cycles to, e.g., discard later cycles, \code{\link{query_bins}} probably gives the desired behavior. } \item{query_bins}{numeric; all same sign; unique positions within a read to delimit bins. Position within a read is based on counting from the \emph{5' end} when the read aligns to \emph{plus strand}, counting from the \emph{3' end} when read aligns to minus strand. Minimum of two values are required so at least one range can be formed. \code{NULL} (default) indicates no binning. Use negative values to count from the opposite end. Sorted order not required. Floating-point values are coerced to \code{integer}.} \item{phred}{Either a numeric() (coerced to integer()) PHRED score (e.g., in the range (0, 41) for the \sQuote{Illumina 1.8+} scheme) or character() of printable ASCII characters. When \code{phred} is character(), it can be of length 1 with 1 or more characters, or of any length where all elements have exactly 1 character.} \item{scheme}{Encoding scheme, used to translate numeric() PHRED scores to their ASCII code. Ignored when \code{phred} is already character().} \item{cycle_bins}{DEPRECATED. See \code{\link{left_bins}} for identical behavior.} } \details{ \emph{NB}: Use of \code{pileup} assumes familiarity with \code{\link{ScanBamParam}}, and use of \code{left_bins} and \code{query_bins} assumes familiarity with \code{\link{cut}}. \code{pileup} visits each position in the BAM file, subject to constraints implied by \code{which} and \code{flag} of \code{scanBamParam}. For a given position, all reads overlapping the position that are consistent with constraints dictated by \code{flag} of \code{scanBamParam} and \code{pileupParam} are used for counting. \code{pileup} also automatically excludes reads with flags that indicate any of: \itemize{ \item{unmapped alignment (\code{\link{isUnmappedQuery}})} \item{secondary alignment (\code{\link{isSecondaryAlignment}})} \item{not passing quality controls (\code{\link{isNotPassingQualityControls}})} \item{PCR or optical duplicate (\code{\link{isDuplicate}})} } If no \code{which} argument is supplied to the \code{ScanBamParam}, behavior reflects that of \code{scanBam}: the entire file is visited and counted. Use a \code{\link{yieldSize}} value when creating a \code{BamFile} instance to manage memory consumption when using pileup with large BAM files. There are some differences in how \code{pileup} behavior is affected when the \code{yieldSize} value is set on the BAM file. See more details below. Many of the parameters of the \code{pileupParam} interact. A simple illustration is \code{ignore_query_Ns} and \code{distinguish_nucleotides}, as mentioned in the \code{ignore_query_Ns} section. Parameters for \code{pileupParam} belong to two categories: parameters that affect only the filtering criteria (so-called \sQuote{behavior-only} policies), and parameters that affect filtering behavior and the schema of the results (\sQuote{behavior+structure} policies). %% behavior-only %% (other behavior-only arguments are self-evident or sam %% spcification-evident) %% behavior+structure \code{distinguish_nucleotides} and \code{distinguish_strands} when set to \code{TRUE} each add a column (\code{nucleotide} and \code{strand}, respectively) to the resulting \code{data.frame}. If both are TRUE, each combination of \code{nucleotide} and \code{strand} at a given position is counted separately. Setting only one to \code{TRUE} behaves as expected; for example, if only \code{nucleotide} is set to \code{TRUE}, each nucleotide at a given position is counted separately, but the distinction of on which strand the nucleotide appears is ignored. \code{ignore_query_Ns} determines how ambiguous nucloetides are treated. By default, ambiguous nucleotides (typically \sQuote{N} in BAM files) in alignments are ignored. If \code{ignore_query_Ns} is \code{FALSE}, ambiguous nucleotides are included in counts; further, if \code{ignore_query_Ns} is \code{FALSE} and \code{distinguish_nucleotides} is \code{TRUE} the \sQuote{N} nucleotide value appears in the nucleotide column when a base at a given position is ambiguous. By default, deletions with respect to the reference genome to which the reads were aligned are included in the counts in a pileup. If \code{include_deletions} is \code{TRUE} and \code{distinguish_nucleotides} is \code{TRUE}, the nucleotide column uses a \sQuote{-} character to indicate a deletion at a position. The \sQuote{=} nucleotide code in the \code{SEQ} field (to mean \sQuote{identical to reference genome}) is supported by pileup, such that a match with the reference genome is counted separately in the results if \code{distinguish_nucleotides} is \code{TRUE}. CIGAR support: \code{pileup} handles the extended CIGAR format by only heeding operations that contribute to counts (\sQuote{M}, \sQuote{D}, \sQuote{I}). If you are confused about how the different CIGAR operations interact, see the SAM versions of the BAM files used for \code{pileup} unit testing for a fairly comprehensive human-readable treatment. \itemize{ \item{Deletions and clipping: The extended CIGAR allows a number of operations conceptually similar to a \sQuote{deletion} with respect to the reference genome, but offer more specialized meanings than a simple deletion. CIGAR \sQuote{N} operations (not to be confused with \sQuote{N} used for non-determinate bases in the \code{SEQ} field) indicate a large skipped region, \sQuote{S} a soft clip, and \sQuote{H} a hard clip. \sQuote{N}, \sQuote{S}, and \sQuote{H} CIGAR operations are never counted: only counts of true deletions (\sQuote{D} in the CIGAR) can be included by setting \code{include_deletions} to \code{TRUE}. Soft clip operations contribute to the relative position of nucleotides within a read, whereas hard clip and refskip operations do not. For example, consider a sequence in a bam file that starts at 11, with a CIGAR \code{2S1M} and \code{SEQ} field \code{ttA}. The cycle position of the \code{A} nucleotide will be \code{3}, but the reported position will be \code{11}. If using \code{left_bins} or \code{query_bins} it might make sense to first preprocess your files to remove soft clipping. } \item{Insertions and padding: \code{pileup} can include counts of insertion operations by setting \code{include_insertions} to \code{TRUE}. Details about insertions are effectively truncated such that each insertion is reduced to a single \sQuote{+} nucleotide. Information about e.g. the nucleotide code and base quality within the insertion is not included. Because \sQuote{+} is used as a nucleotide code to represent insertions in \code{pileup}, counts of the \sQuote{+} nucleotide participate in voting for \code{min_nucleotide_depth} and \code{min_minor_allele_depth} functionality. The position of an insertion is the position that precedes it on the reference sequence. \emph{Note:} this means if \code{include_insertions} is \code{TRUE} a single read will contribute two nucleotide codes (\code{+}, plus that of the non-insertion base) at a given position if the non-insertion base passes filter criteria. \sQuote{P} CIGAR (padding) operations never affect counts. } } The \dQuote{bin} arguments \code{query_bins} and \code{left_bins} allow users to differentiate pileup counts based on arbitrary non-overlapping regions within a read. \code{pileup} relies on \code{\link{cut}} to derive bins, but limits input to numeric values of the same sign (coerced to \code{integer}s), including \code{+/-Inf}. If a \dQuote{bin} argument is set \code{pileup} automatically excludes bases outside the implicit outer range. Here are some important points regarding bin arguments: \itemize{ \item{\code{query_bins} vs. \code{left_bins}:}{ BAM files store sequence data from the 5' end to the 3' end (regardless of to which strand the read aligns). That means for reads aligned to the minus strand, cycle position within a read is effectively reversed. Take care to use the appropriate bin argument for your use case. The most common use of a bin argument is to bin later cycles separately from earlier cycles; this is because accuracy typically degrades in later cycles. For this application, \code{query_bins} yields the correct behavior because bin positions are relative to cycle order (i.e., sensitive to strand). \code{left_bins} (in contrast with \code{query_bins}) determines bin positions from the 5' end, regardless of strand. } \item{Positive or negative bin values can be used to delmit bins based on the effective \dQuote{start} or \dQuote{end} of a read. For \code{left_bin} the effective start is always the 5' end (left-to-right as appear in the BAM file). For \code{query_bin} the effective start is the first cycle of the read as it came off the sequencer; that means the 5' end for reads aligned to the plus strand and 3' for reads aligned to the minus strand. \itemize{ \item{\emph{From effective start of reads}: use positive values, \code{0}, and \code{(+)Inf}. Because \code{\link{cut}} produces ranges in the form (first,last], \sQuote{0} should be used to create a bin that includes the first position. To account for variable-length reads in BAM files, use \code{(+)Inf} as the upper bound on a bin that extends to the end of all reads.} \item{\emph{From effective end of reads}: use negative values and \code{-Inf}. \code{-1} denotes the last position in a read. Because \code{\link{cut}} produces ranges in the form (first,last], specify the lower bound of a bin by using one less than the desired value, e.g., a bin that captures only the second nucleotide from the last position: \code{query_bins=c(-3, -2)}. To account for variable-length reads in BAM files, use \code{-Inf} as the lower bound on a bin that extends to the beginning of all reads.} } } } %% end subsection bin argument gotchas \code{pileup} obeys \code{\link{yieldSize}} on \code{BamFile} objects with some differences from how \code{scanBam} responds to \code{yieldSize}. Here are some points to keep in mind when using \code{pileup} in conjunction with \code{yieldSize}: \itemize{ \item{\code{BamFile}s with a \code{yieldSize} value set, once opened and used with \code{pileup}, \emph{should not be used} with other functions that accept a \code{BamFile} instance as input. Create a new \code{BamFile} instance instead of trying to reuse.} \item{\code{pileup} only returns genomic positions for which all input has been processed. \code{pileup} will hold in reserve positions for which only partial data has been processed. Positions held in reserve will be returned upon subsequent calls to \code{pileup} when all the input for a given position has been processed.} \item{The correspondence between yieldSize and the number of rows in the \code{data.frame} returned from \code{pileup} is not 1-to-1. \code{yieldSize} only limits the number of \emph{alignments processed} from the BAM file each time the file is read. Only a handful of alignments can lead to many distinct records in the result.} \item{Like \code{scanBam}, \code{pileup} uses an empty return object (a zero-row \code{data.frame}) to indicate end-of-input.} \item{Sometimes reading \code{yieldSize} records from the BAM file does not result in any completed positions. In order to avoid returning a zero-row \code{data.frame} \code{pileup} will repeatedly process \code{yieldSize} additional records until at least one position can be returned to the user.} } } \value{ For \code{pileup} a \code{data.frame} with 1 row per unique combination of differentiating column values that satisfied filter criteria, with frequency (\code{count}) of unique combination. Columns \code{seqnames}, \code{pos}, and \code{count} always appear; optional \code{strand}, \code{nulceotide}, and \code{left_bin} / \code{query_bin} columns appear as dictated by arguments to \code{PileupParam}. Column details: \itemize{ \item{\code{seqnames}: factor. SAM \sQuote{RNAME} field of alignment.} \item{\code{pos}: integer(1). Genomic position of base. Derived by offset from SAM \sQuote{POS} field of alignment.} \item{\code{strand}: factor. \sQuote{strand} to which read aligns.} \item{\code{nucleotide}: factor. \sQuote{nucleotide} of base, extracted from SAM \sQuote{SEQ} field of alignment.} \item{\code{left_bin} / \code{query_bin}: factor. Bin in which base appears.} \item{\code{count}: integer(1). Frequency of combination of differentiating fields, as indicated by values of other columns.} } See \code{\link{scanBam}} for more detailed explanation of SAM fields. If a \code{which} argument is specified for the \code{scanBamParam}, a \code{which_label} column (\code{factor} in the form \sQuote{rname:start-end}) is automatically included. The \code{which_label} column is used to maintain grouping of results, such that two queries of the same genomic region can be differentiated. Order of rows in \code{data.frame} is first by order of \code{seqnames} column based on the BAM index file, then non-decreasing order on columns \code{pos}, then \code{nucleotide}, then \code{strand}, then \code{left_bin} / \code{query_bin}. \code{PileupParam} returns an instance of PileupParam class. \code{phred2ASCIIOffset} returns a named integer vector of the same length or number of characters in \code{phred}. The names are the ASCII encoding, and the values are the offsets to be used with \code{min_base_quality}. } \seealso{ \itemize{ \item{\link{Rsamtools}} \item{\linkS4class{BamFile}} \item{\link{ScanBamParam}} \item{\link{scanBam}} \item{\link{cut}} } For the relationship between PHRED scores and ASCII encoding, see \url{https://en.wikipedia.org/wiki/FASTQ_format#Encoding}. } \author{Nathaniel Hayden \url{nhayden@fredhutch.org}} %% This information should go somewhere--essential for an outside %% developer to help build context quickly %% \excruciatingdetails{ %% There are really three stages of filtering; (1) filtering based on %% \code{scanBamParam} arguments (via _do_scan_bam, (2) filtering %% based on arguments of \code{pileupParam} that apply on a per-read %% and per-alignment basis and lastly, (3) a final filtering stage %% applied on the intermediate count of a position after all %% overlapping alignments have been %% processed. \code{min_nucleotide_depth} and %% \{min_minor_allele_depth} arguments cannot be applied until the %% last stage. %% } \examples{ ## The examples below apply equally to pileup queries for specific ## genomic ranges (specified by the 'which' parameter of 'ScanBamParam') ## and queries across entire files; the entire-file examples are ## included first to make them easy to find. The more detailed examples ## of pileup use queries with a 'which' argument. library("RNAseqData.HNRNPC.bam.chr14") fl <- RNAseqData.HNRNPC.bam.chr14_BAMFILES[1] ## Minimum base quality to be tallied p_param <- PileupParam(min_base_quality = 10L) \donttest{ ## no 'which' argument to ScanBamParam: process entire file at once res <- pileup(fl, pileupParam = p_param) head(res) table(res$strand, res$nucleotide) } \donttest{ ## no 'which' argument to ScanBamParam with 'yieldSize' set on BamFile bf <- open(BamFile(fl, yieldSize=5e4)) repeat { res <- pileup(bf, pileupParam = p_param) message(nrow(res), " rows in result data.frame") if(nrow(res) == 0L) break } close(bf) } ## pileup for the first half of chr14 with default Pileup parameters ## 'which' argument: process only specified genomic range(s) sbp <- ScanBamParam(which=GRanges("chr14", IRanges(1, 53674770))) res <- pileup(fl, scanBamParam=sbp, pileupParam = p_param) head(res) table(res$strand, res$nucleotide) ## specify pileup parameters: include ambiguious nucleotides ## (the 'N' level in the nucleotide column of the data.frame) p_param <- PileupParam(ignore_query_Ns=FALSE, min_base_quality = 10L) res <- pileup(fl, scanBamParam=sbp, pileupParam=p_param) head(res) table(res$strand, res$nucleotide) ## Don't distinguish strand, require a minimum frequency of 7 for a ## nucleotide at a genomic position to be included in results. p_param <- PileupParam(distinguish_strands=TRUE, min_base_quality = 10L, min_nucleotide_depth=7) res <- pileup(fl, scanBamParam=sbp, pileupParam=p_param) head(res) table(res$nucleotide, res$strand) ## Any combination of the filtering criteria is possible: let's say we ## want a "coverage pileup" that only counts reads with mapping ## quality >= 13, and bases with quality >= 10 that appear at least 4 ## times at each genomic position p_param <- PileupParam(distinguish_nucleotides=FALSE, distinguish_strands=FALSE, min_mapq=13, min_base_quality=10, min_nucleotide_depth=4) res <- pileup(fl, scanBamParam=sbp, pileupParam=p_param) head(res) res <- res[, c("pos", "count")] ## drop seqnames and which_label cols plot(count ~ pos, res, pch=".") ## ASCII offsets to help specify min_base_quality, e.g., quality of at ## least 10 on the Illumina 1.3+ scale phred2ASCIIOffset(10, "Illumina 1.3+") ## Well-supported polymorphic positions (minor allele present in at ## least 5 alignments) with high map quality p_param <- PileupParam(min_minor_allele_depth=5, min_mapq=40, min_base_quality = 10, distinguish_strand=FALSE) res <- pileup(fl, scanBamParam=sbp, pileupParam=p_param) dim(res) ## reduced to our biologically interesting positions head(xtabs(count ~ pos + nucleotide, res)) ## query_bins \donttest{ ## basic use of positive bins: single pivot; count bases that appear in ## first 10 cycles of a read separately from the rest p_param <- PileupParam(query_bins=c(0, 10, Inf), min_base_quality = 10) res <- pileup(fl, scanBamParam=sbp, pileupParam=p_param) ## basic use of positive bins: simple range; only include bases in ## cycle positions 6-10 within read p_param <- PileupParam(query_bins=c(5, 10), min_base_quality = 10) res <- pileup(fl, scanBamParam=sbp, pileupParam=p_param) ## basic use of negative bins: single pivot; count bases that appear in ## last 3 cycle positions of a read separately from the rest. p_param <- PileupParam(query_bins=c(-Inf, -4, -1), min_base_quality = 10) res <- pileup(fl, scanBamParam=sbp, pileupParam=p_param) ## basic use of negative bins: drop nucleotides in last two cycle ## positions of each read p_param <- PileupParam(query_bins=c(-Inf, -3), min_base_quality = 10) res <- pileup(fl, scanBamParam=sbp, pileupParam=p_param) } ## typical use: beginning, middle, and end segments; because of the ## nature of sequencing technology, it is common for bases in the ## beginning and end segments of each read to be less reliable. pileup ## makes it easy to count each segment separately. ## Assume determined ahead of time that for the data 1-7 makes sense for ## beginning, 8-12 middle, >=13 end (actual cycle positions should be ## tailored to data in actual BAM files). p_param <- PileupParam(query_bins=c(0, 7, 12, Inf), ## note non-symmetric min_base_quality = 10) res <- pileup(fl, scanBamParam=sbp, pileupParam=p_param) xt <- xtabs(count ~ nucleotide + query_bin, res) print(xt) t(t(xt) / colSums(xt)) ## cheap normalization for illustrative purposes ## 'implicit outer range': in contrast to c(0, 7, 12, Inf), suppose we ## still want to have beginning, middle, and end segements, but know ## that the first three cycles and any bases beyond the 16th cycle are ## irrelevant. Hence, the implicit outer range is (3,16]; all bases ## outside of that are dropped. p_param <- PileupParam(query_bins=c(3, 7, 12, 16), min_base_quality = 10) res <- pileup(fl, scanBamParam=sbp, pileupParam=p_param) xt <- xtabs(count ~ nucleotide + query_bin, res) print(xt) t(t(xt) / colSums(xt)) \donttest{ ## single-width bins: count each cycle within a read separately. p_param <- PileupParam(query_bins=seq(1,20), min_base_quality = 10) res <- pileup(fl, scanBamParam=sbp, pileupParam=p_param) xt <- xtabs(count ~ nucleotide + query_bin, res) print(xt[ , c(1:3, 18:19)]) ## fit on one screen print(t(t(xt) / colSums(xt))[ , c(1:3, 18:19)]) } }Rsamtools/man/quickBamFlagSummary.Rd0000644000175400017540000000344113556116727020550 0ustar00biocbuildbiocbuild\name{quickBamFlagSummary} \alias{quickBamFlagSummary} \alias{quickBamFlagSummary,character-method} \alias{quickBamFlagSummary,list-method} \title{Group the records of a BAM file based on their flag bits and count the number of records in each group} \description{ \code{quickBamFlagSummary} groups the records of a BAM file based on their flag bits and counts the number of records in each group. } \usage{ quickBamFlagSummary(file, ..., param=ScanBamParam(), main.groups.only=FALSE) \S4method{quickBamFlagSummary}{character}(file, index=file, ..., param=ScanBamParam(), main.groups.only=FALSE) \S4method{quickBamFlagSummary}{list}(file, ..., param=ScanBamParam(), main.groups.only=FALSE) } \arguments{ \item{file, index}{For the character method, the path to the BAM file to read, and to the index file of the BAM file to read, respectively. For the list() method, \code{file} is a named list with elements \dQuote{qname} and \dQuote{flag} with content as from \code{\link{scanBam}}.} \item{...}{Additional arguments, perhaps used by methods.} \item{param}{An instance of \code{\linkS4class{ScanBamParam}}. This determines which records are considered in the counting.} \item{main.groups.only}{If \code{TRUE}, then the counting is performed for the main groups only. } } \value{ Nothing is returned. A summary of the counts is printed to the console unless redirected by \code{\link{sink}}. } \author{H. Pages} \references{ \url{http://samtools.sourceforge.net/} } \seealso{ \code{\link{scanBam}}, \code{\link{ScanBamParam}}. \code{\link{BamFile}} for a method for that class. } \examples{ bamfile <- system.file("extdata", "ex1.bam", package="Rsamtools", mustWork=TRUE) quickBamFlagSummary(bamfile) } \keyword{manip} Rsamtools/man/readPileup.Rd0000644000175400017540000000512313556116727016735 0ustar00biocbuildbiocbuild\name{readPileup} \Rdversion{1.1} \alias{readPileup} \alias{readPileup,connection-method} \alias{readPileup,character-method} \title{ Import samtools 'pileup' files. } \description{ Import files created by evaluation of samtools' \code{pileup -cv} command. } \usage{ readPileup(file, ...) \S4method{readPileup}{connection}(file, ..., variant=c("SNP", "indel", "all")) } \arguments{ \item{file}{The file name, or \code{\link[base:connections]{connection}}, of the pileup output file to be parsed.} \item{\dots}{Additional arguments, passed to methods. For instance, specify \code{variant} for the readPileup,character-method.} \item{variant}{Type of variant to parse; select one.} } \value{ \code{readPileup} returns a \code{\link[GenomicRanges]{GRanges}} object. The value returned by \code{variant="SNP"} or \code{variant="all"} contains: \describe{ \item{space:}{The chromosome names (fastq ids) of the reference sequence} \item{position:}{The nucleotide position (base 1) of the variant.} \item{referenceBase:}{The nucleotide in the reference sequence.} \item{consensusBase;}{The consensus nucleotide, as determined by samtools pileup.} \item{consensusQuality:}{The phred-scaled consensus quality.} \item{snpQuality:}{The phred-scaled SNP quality (probability of the consensus being identical to the reference).} \item{maxMappingQuality:}{The root mean square mapping quality of reads overlapping the site.} \item{coverage:}{The number of reads covering the site.} } The value returned by \code{variant="indel"} contains space, position, reference, consensus, consensusQuality, snpQuality, maxMappingQuality, and coverage fields, and: \describe{ \item{alleleOne, alleleTwo}{The first (typically, in the reference sequence) and second allelic variants.} \item{alleleOneSupport, alleleTwoSupport}{The number of reads supporting each allele.} \item{additionalIndels}{The number of additional indels present.} } } \references{ \url{http://samtools.sourceforge.net/} } \author{ Sean Davis } \examples{ fl <- system.file("extdata", "pileup.txt", package="Rsamtools", mustWork=TRUE) (res <- readPileup(fl)) xtabs(~referenceBase + consensusBase, mcols(res))[DNA_BASES,] \dontrun{## uses a pipe, and arguments passed to read.table ## three successive piles of 100 records each cmd <- "samtools pileup -cvf human_b36_female.fa.gz na19240_3M.bam" p <- pipe(cmd, "r") snp <- readPileup(p, nrow=100) # variant="SNP" indel <- readPileup(p, nrow=100, variant="indel") all <- readPileup(p, nrow=100, variant="all") } } \keyword{ manip } Rsamtools/man/scanBam.Rd0000644000175400017540000003330013556116727016205 0ustar00biocbuildbiocbuild\name{BamInput} \Rdversion{1.1} \alias{scanBam} \alias{scanBam,character-method} \alias{countBam} \alias{countBam,character-method} \alias{idxstatsBam} \alias{idxstatsBam,character-method} \alias{scanBamHeader} \alias{scanBamHeader,character-method} \alias{asBam} \alias{asBam,character-method} \alias{asSam} \alias{asSam,character-method} \alias{indexBam} \alias{indexBam,character-method} \alias{filterBam} \alias{filterBam,character-method} \alias{sortBam} \alias{sortBam,character-method} \alias{mergeBam} \alias{mergeBam,character-method} \title{ Import, count, index, filter, sort, and merge `BAM' (binary alignment) files. } \description{ Import binary `BAM' files into a list structure, with facilities for selecting what fields and which records are imported, and other operations to manipulate BAM files. } \usage{ scanBam(file, index=file, ..., param=ScanBamParam(what=scanBamWhat())) countBam(file, index=file, ..., param=ScanBamParam()) idxstatsBam(file, index=file, ...) scanBamHeader(files, ...) \S4method{scanBamHeader}{character}(files, ...) asBam(file, destination=sub("\\\\.sam(\\\\.gz)?", "", file), ...) \S4method{asBam}{character}(file, destination=sub("\\\\.sam(\\\\.gz)?", "", file), ..., overwrite=FALSE, indexDestination=TRUE) asSam(file, destination=sub("\\\\.bam", "", file), ...) \S4method{asSam}{character}(file, destination=sub("\\\\.bam", "", file), ..., overwrite=FALSE) filterBam(file, destination, index=file, ...) \S4method{filterBam}{character}(file, destination, index=file, ..., filter=FilterRules(), indexDestination=TRUE, param=ScanBamParam(what=scanBamWhat())) sortBam(file, destination, ...) \S4method{sortBam}{character}(file, destination, ..., byQname=FALSE, maxMemory=512) indexBam(files, ...) \S4method{indexBam}{character}(files, ...) mergeBam(files, destination, ...) \S4method{mergeBam}{character}(files, destination, ..., region = GRanges(), overwrite = FALSE, header = character(), byQname = FALSE, addRG = FALSE, compressLevel1 = FALSE, indexDestination = FALSE) } \arguments{ \item{file}{The character(1) file name of the `BAM' ('SAM' for \code{asBam}) file to be processed.} \item{files}{The character() file names of the `BAM' file to be processed. For \code{mergeBam}, must satisfy \code{length(files) >= 2}.} \item{index}{The character(1) name of the index file of the 'BAM' file being processed; this is given \emph{without} the '.bai' extension.} \item{destination}{The character(1) file name of the location where the sorted, filtered, or merged output file will be created. For \code{asBam} \code{asSam}, and \code{sortBam} this is without the \dQuote{.bam} file suffix.} \item{region}{A GRanges() instance with \code{<= 1} elements, specifying the region of the BAM files to merged.} \item{\dots}{Additional arguments, passed to methods.} \item{overwrite}{A logical(1) indicating whether the destination can be over-written if it already exists.} \item{filter}{A \code{\link{FilterRules}} instance allowing users to filter BAM files based on arbitrary criteria, as described below.} \item{indexDestination}{A logical(1) indicating whether the created destination file should also be indexed.} \item{byQname}{A logical(1) indicating whether the sorted destination file should be sorted by Query-name (TRUE) or by mapping position (FALSE).} \item{header}{A character(1) file path for the header information to be used in the merged BAM file.} \item{addRG}{A logical(1) indicating whether the file name should be used as RG (read group) tag in the merged BAM file.} \item{compressLevel1}{A logical(1) indicating whether the merged BAM file should be compressed to zip level 1.} \item{maxMemory}{A numerical(1) indicating the maximal amount of memory (in MB) that the function is allowed to use.} \item{param}{An instance of \code{\linkS4class{ScanBamParam}}. This influences what fields and which records are imported.} } \details{ The \code{scanBam} function parses binary BAM files; text SAM files can be parsed using R's \code{\link{scan}} function, especially with arguments \code{what} to control the fields that are parsed. \code{countBam} returns a count of records consistent with \code{param}. \code{idxstatsBam} visit the index in \code{index(file)}, and quickly returns the number of mapped and unmapped reads on each seqname. \code{scanBamHeader} visits the header information in a BAM file, returning for each file a list containing elements \code{targets} and \code{text}, as described below. The SAM / BAM specification does not require that the content of the header be consistent with the content of the file, e.g., more targets may be present that are represented by reads in the file. An optional character vector argument containing one or two elements of \code{what=c("targets", "text")} can be used to specify which elements of the header are returned. \code{asBam} converts 'SAM' files to 'BAM' files, equivalent to \code{samtools view -Sb file > destination}. The 'BAM' file is sorted and an index created on the destination (with extension '.bai') when \code{indexDestination=TRUE}. \code{asSam} converts 'BAM' files to 'SAM' files, equivalent to \code{samtools view file > destination}. \code{filterBam} parses records in \code{file}. Records satisfying the \code{bamWhich} \code{bamFlag} and \code{bamSimpleCigar} criteria of \code{param} are accumulated to a default of \code{yieldSize = 1000000} records (change this by specifying \code{yieldSize} when creating a \code{BamFile} instance; see \code{\linkS4class{BamFile}-class}). These records are then parsed to a \code{DataFrame} and made available for further filtering by user-supplied \code{FilterRules}. Functions in the \code{FilterRules} instance should expect a single \code{DataFrame} argument representing all information specified by \code{param}. Each function must return a \code{logical} vector equal to the number of rows of the \code{DataFrame}. Return values are used to include (when \code{TRUE}) corresponding records in the filtered BAM file. The BAM file is created at \code{destination}. An index file is created on the destination when \code{indexDestination=TRUE}. It is more space- and time-efficient to filter using \code{bamWhich}, \code{bamFlag}, and \code{bamSimpleCigar}, if appropriate, than to supply \code{FilterRules}. \code{filter} may be a list of \code{FilterRules} instances, in which case \code{destination} must be a character vector of equal length. The original \code{file} is then separately filtered into \code{destination[[i]]}, using \code{filter[[i]]} as the filter criterion. \code{sortBam} sorts the BAM file given as its first argument, analogous to the \dQuote{samtools sort} function. \code{indexBam} creates an index for each BAM file specified, analogous to the \sQuote{samtools index} function. \code{mergeBam} merges 2 or more sorted BAM files. As with samtools, the RG (read group) dictionary in the header of the BAM files is not reconstructed. Details of the \code{ScanBamParam} class are provide on its help page; several salient points are reiterated here. \code{ScanBamParam} can contain a field \code{what}, specifying the components of the BAM records to be returned. Valid values of \code{what} are available with \code{\link{scanBamWhat}}. \code{ScanBamParam} can contain an argument \code{which} that specifies a subset of reads to return. This requires that the BAM file be indexed, and that the file be named following samtools convention as \code{.bai}. \code{ScanBamParam} can contain an argument \code{tag} to specify which tags will be extracted. } \value{ The \code{scanBam,character-method} returns a list of lists. The outer list groups results from each \code{IntegerRanges} list of \code{bamWhich(param)}; the outer list is of length one when \code{bamWhich(param)} has length 0. Each inner list contains elements named after \code{scanBamWhat()}; elements omitted from \code{bamWhat(param)} are removed. The content of non-null elements are as follows, taken from the description in the samtools API documentation: \itemize{ \item qname: This is the QNAME field in SAM Spec v1.4. The query name, i.e., identifier, associated with the read. \item flag: This is the FLAG field in SAM Spec v1.4. A numeric value summarizing details of the read. See \code{\linkS4class{ScanBamParam}} and the \code{flag} argument, and \code{scanBamFlag()}. \item rname: This is the RNAME field in SAM Spec v1.4. The name of the reference to which the read is aligned. \item strand: The strand to which the read is aligned. \item pos: This is the POS field in SAM Spec v1.4. The genomic coordinate at the start of the alignment. Coordinates are `left-most', i.e., at the 3' end of a read on the '-' strand, and 1-based. The position \emph{excludes} clipped nucleotides, even though soft-clipped nucleotides are included in \code{seq}. \item qwidth: The width of the query, as calculated from the \code{cigar} encoding; normally equal to the width of the query returned in \code{seq}. \item mapq: This is the MAPQ field in SAM Spec v1.4. The MAPping Quality. \item cigar: This is the CIGAR field in SAM Spec v1.4. The CIGAR string. \item mrnm: This is the RNEXT field in SAM Spec v1.4. The reference to which the mate (of a paired end or mate pair read) aligns. \item mpos: This is the PNEXT field in SAM Spec v1.4. The position to which the mate aligns. \item isize: This is the TLEN field in SAM Spec v1.4. Inferred insert size for paired end alignments. \item seq: This is the SEQ field in SAM Spec v1.4. The query sequence, in the 5' to 3' orientation. If aligned to the minus strand, it is the reverse complement of the original sequence. \item qual: This is the QUAL field in SAM Spec v1.4. Phred-encoded, phred-scaled base quality score, oriented as \code{seq}. \item groupid: This is an integer vector of unique group ids returned when \code{asMates=TRUE} in a BamFile object. \code{groupid} values are used to create the partitioning for a \code{GAlignmentsList} object. \item mate_status: Returned (always) when \code{asMates=TRUE} in a BamFile object. This is a factor indicating status (\code{mated}, \code{ambiguous}, \code{unmated}) of each record. } \code{idxstatsBam} returns a \code{data.frame} with columns \code{seqnames}, \code{seqlength}, \code{mapped} (number of mapped reads on \code{seqnames}) and \code{unmapped} (number of unmapped reads). \code{scanBamHeader} returns a list, with one element for each file named in \code{files}. The list contains two element. The \code{targets} element contains target (reference) sequence lengths. The \code{text} element is itself a list with each element a list corresponding to tags (e.g., \sQuote{@SQ}) found in the header, and the associated tag values. \code{asBam}, \code{asSam} return the file name of the destination file. \code{sortBam} returns the file name of the sorted file. \code{indexBam} returns the file name of the index file created. \code{filterBam} returns the file name of the destination file created. } \references{ \url{http://samtools.sourceforge.net/} } \author{ Martin Morgan . Thomas Unterhiner (\code{sortBam}). } \seealso{ \code{\linkS4class{ScanBamParam}}, \code{\link{scanBamWhat}}, \code{\link{scanBamFlag}} } \examples{ fl <- system.file("extdata", "ex1.bam", package="Rsamtools", mustWork=TRUE) ## ## scanBam ## res0 <- scanBam(fl)[[1]] # always list-of-lists names(res0) length(res0[["qname"]]) lapply(res0, head, 3) table(width(res0[["seq"]])) # query widths table(res0[["qwidth"]], useNA="always") # query widths derived from cigar table(res0[["cigar"]], useNA="always") table(res0[["strand"]], useNA="always") table(res0[["flag"]], useNA="always") which <- IRangesList(seq1=IRanges(1000, 2000), seq2=IRanges(c(100, 1000), c(1000, 2000))) p1 <- ScanBamParam(which=which, what=scanBamWhat()) res1 <- scanBam(fl, param=p1) names(res1) names(res1[[2]]) p2 <- ScanBamParam(what=c("rname", "strand", "pos", "qwidth")) res2 <- scanBam(fl, param=p2) p3 <- ScanBamParam( what="flag", # information to query from BAM file flag=scanBamFlag(isMinusStrand=FALSE)) length(scanBam(fl, param=p3)[[1]]$flag) ## ## idxstatsBam ## idxstatsBam(fl) ## ## filterBam ## param <- ScanBamParam( flag=scanBamFlag(isUnmappedQuery=FALSE), what="seq") dest <- filterBam(fl, tempfile(), param=param) countBam(dest) ## 3271 records ## filter to a single file filter <- FilterRules(list(MinWidth = function(x) width(x$seq) > 35)) dest <- filterBam(fl, tempfile(), param=param, filter=filter) countBam(dest) ## 398 records res3 <- scanBam(dest, param=ScanBamParam(what="seq"))[[1]] table(width(res3$seq)) ## filter 1 file to 2 destinations filters <- list( FilterRules(list(long=function(x) width(x$seq) > 35)), FilterRules(list(short=function(x) width(x$seq) <= 35)) ) destinations <- replicate(2, tempfile()) dest <- filterBam(fl, destinations, param=param, filter=filters) lapply(dest, countBam) ## ## sortBam ## sorted <- sortBam(fl, tempfile()) ## ## scanBamParam re-orders 'which'; recover original order ## gwhich <- as(which, "GRanges")[c(2, 1, 3)] # example data cnt <- countBam(fl, param=ScanBamParam(which=gwhich)) reorderIdx <- unlist(split(seq_along(gwhich), seqnames(gwhich))) cnt cnt[reorderIdx,] } \keyword{ manip } Rsamtools/man/scanBcf.Rd0000644000175400017540000001045413556116727016205 0ustar00biocbuildbiocbuild\name{BcfInput} \Rdversion{1.1} \alias{scanBcfHeader} \alias{scanBcfHeader,character-method} \alias{scanBcf} \alias{scanBcf,character-method} \alias{asBcf} \alias{asBcf,character-method} \alias{indexBcf} \alias{indexBcf,character-method} \title{ Operations on `BCF' files. } \description{ Import, coerce, or index variant call files in text or binary format. } \usage{ scanBcfHeader(file, ...) \S4method{scanBcfHeader}{character}(file, ...) scanBcf(file, ...) \S4method{scanBcf}{character}(file, index = file, ..., param=ScanBcfParam()) asBcf(file, dictionary, destination, ..., overwrite=FALSE, indexDestination=TRUE) \S4method{asBcf}{character}(file, dictionary, destination, ..., overwrite=FALSE, indexDestination=TRUE) indexBcf(file, ...) \S4method{indexBcf}{character}(file, ...) } \arguments{ \item{file}{For \code{scanBcf} and \code{scanBcfHeader}, the character() file name of the \sQuote{BCF} file to be processed, or an instance of class \code{\link{BcfFile}}.} \item{index}{The character() file name(s) of the `BCF' index to be processed.} \item{dictionary}{a character vector of the unique \dQuote{CHROM} names in the VCF file.} \item{destination}{The character(1) file name of the location where the BCF output file will be created. For \code{asBcf} this is without the \dQuote{.bcf} file suffix.} \item{param}{A instance of \code{\linkS4class{ScanBcfParam}} influencing which records are parsed and the \sQuote{INFO} and \sQuote{GENO} information returned.} \item{...}{Additional arguments, e.g., for \code{scanBcfHeader,character-method}, \code{mode} of \code{\link{BcfFile}}.} \item{overwrite}{A logical(1) indicating whether the destination can be over-written if it already exists.} \item{indexDestination}{A logical(1) indicating whether the created destination file should also be indexed.} } \details{ \code{bcf*} functions are restricted to the GENO fields supported by \sQuote{bcftools} (see documentation at the url below). The argument \code{param} allows portions of the file to be input, but requires that the file be BCF or bgzip'd and indexed as a \code{\linkS4class{TabixFile}}. For similar functions operating on VCF files see ?\code{scanVcf} in the \code{VariantAnnotation} package. } \value{ \code{scanBcfHeader} returns a list, with one element for each file named in \code{file}. Each element of the list is itself a list containing three elements. The \code{Reference} element is a character() vector with names of reference sequences. The \code{Sample} element is a character() vector of names of samples. The \code{Header} element is a DataFrameList with one DataFrame per unique key value in the header (preceded by \dQuote{##}). NOTE: In Rsamtools >=1.33.6, the \code{Header} DataFrameList no longer contains a DataFrame named "META". The META DataFrame contained all "simple" key-value headers lines from a bcf / vcf file. These "simple" header lines are now parsed into individual DataFrames named for the unique key. \code{scanBcf} returns a list, with one element per file. Each list has 9 elements, corresponding to the columns of the VCF specification: \code{CHROM}, \code{POS}, \code{ID}, \code{REF}, \code{ALT}\code{QUAL}, \code{FILTER}, \code{INFO}, \code{FORMAT}, \code{GENO}. The \code{GENO} element is itself a list, with elements corresponding to fields supported by \sQuote{bcftools} (see documentation at the url below). \code{asBcf} creates a binary BCF file from a text VCF file. \code{indexBcf} creates an index into the BCF file. } \references{ \url{http://vcftools.sourceforge.net/specs.html} outlines the VCF specification. \url{http://samtools.sourceforge.net/mpileup.shtml} contains information on the portion of the specification implemented by \code{bcftools}. \url{http://samtools.sourceforge.net/} provides information on \code{samtools}. } \seealso{ \code{\link{BcfFile}}, \code{\link{TabixFile}} } \author{ Martin Morgan . } \examples{ fl <- system.file("extdata", "ex1.bcf.gz", package="Rsamtools", mustWork=TRUE) scanBcfHeader(fl) bcf <- scanBcf(fl) ## value: list-of-lists str(bcf[1:8]) names(bcf[["GENO"]]) str(head(bcf[["GENO"]][["PL"]])) example(BcfFile) } \keyword{ manip } Rsamtools/man/scanFa.Rd0000644000175400017540000000573313556116727016045 0ustar00biocbuildbiocbuild\name{FaInput} \Rdversion{1.1} \alias{indexFa} \alias{indexFa,character-method} \alias{scanFaIndex} \alias{scanFaIndex,character-method} \alias{countFa} \alias{countFa,character-method} \alias{scanFa} \alias{scanFa,character,GRanges-method} \alias{scanFa,character,IntegerRangesList-method} \alias{scanFa,character,missing-method} \title{ Operations on indexed 'fasta' files. } \description{ Scan indexed fasta (or compressed fasta) files and their indicies. } \usage{ indexFa(file, ...) \S4method{indexFa}{character}(file, ...) scanFaIndex(file, ...) \S4method{scanFaIndex}{character}(file, ...) countFa(file, ...) \S4method{countFa}{character}(file, ...) scanFa(file, param, ..., as=c("DNAStringSet", "RNAStringSet", "AAStringSet")) \S4method{scanFa}{character,GRanges}(file, param, ..., as=c("DNAStringSet", "RNAStringSet", "AAStringSet")) \S4method{scanFa}{character,IntegerRangesList}(file, param, ..., as=c("DNAStringSet", "RNAStringSet", "AAStringSet")) \S4method{scanFa}{character,missing}(file, param, ..., as=c("DNAStringSet", "RNAStringSet", "AAStringSet")) } \arguments{ \item{file}{A character(1) vector containing the fasta file path.} \item{param}{An optional \code{\linkS4class{GRanges}} or \code{\linkS4class{IntegerRangesList}} instance to select reads (and sub-sequences) for input.} \item{as}{A character(1) vector indicating the type of object to return; default \code{DNAStringSet}.} \item{...}{Additional arguments, passed to \code{readDNAStringSet} / \code{readRNAStringSet} / \code{readAAStringSet} when \code{param} is \sQuote{missing}.} } \value{ \code{indexFa} visits the path in \code{file} and create an index file at the same location but with extension \sQuote{.fai}). \code{scanFaIndex} reads the sequence names and and widths of recorded in an indexed fasta file, returning the information as a \code{\linkS4class{GRanges}} object. \code{countFa} returns the number of records in the fasta file. \code{scanFa} return the sequences indicated by \code{param} as a \code{\linkS4class{DNAStringSet}}, \code{\linkS4class{RNAStringSet}}, \code{\linkS4class{AAStringSet}} instance. \code{seqnames(param)} selects the sequences to return; \code{start(param)} and \code{end{param}} define the (1-based) region of the sequence to return. Values of \code{end(param)} greater than the width of the sequence are set to the width of the sequence. When \code{param} is missing, all records are selected. When \code{param} is \code{GRanges()}, no records are selected. } \references{ \url{http://samtools.sourceforge.net/} provides information on \code{samtools}. } \author{ Martin Morgan . } \examples{ fa <- system.file("extdata", "ce2dict1.fa", package="Rsamtools", mustWork=TRUE) countFa(fa) (idx <- scanFaIndex(fa)) (dna <- scanFa(fa, idx[1:2])) ranges(idx) <- narrow(ranges(idx), -10) # last 10 nucleotides (dna <- scanFa(fa, idx[1:2])) } \keyword{ manip } Rsamtools/man/scanTabix.Rd0000644000175400017540000000357313556116727016566 0ustar00biocbuildbiocbuild\name{TabixInput} \Rdversion{1.1} \alias{scanTabix} \alias{scanTabix,character,GRanges-method} \alias{scanTabix,character,IntegerRangesList-method} \title{ Operations on `tabix' (indexed, tab-delimited) files. } \description{ Scan compressed, sorted, tabix-indexed, tab-delimited files. } \usage{ scanTabix(file, ..., param) \S4method{scanTabix}{character,IntegerRangesList}(file, ..., param) \S4method{scanTabix}{character,GRanges}(file, ..., param) } \arguments{ \item{file}{The character() file name(s) of the tabix file be processed, or more flexibly an instance of class \code{\link{TabixFile}}.} \item{param}{A instance of \code{GRanges} or \code{IntegerRangesList} providing the sequence names and regions to be parsed.} \item{...}{Additional arguments, currently ignored.} } \value{ \code{scanTabix} returns a list, with one element per region. Each element of the list is a character vector representing records in the region. } \section{Error}{ \code{scanTabix} signals errors using \code{signalCondition}. The following errors are signaled: \describe{ \item{\code{scanTabix_param}}{\code{yieldSize(file)} must be NA when more than one range is specified.} \item{\code{scanTabix_io}}{A read error occured while inputing the tabix file. This might be because the file is corrupt, or of incorrect format (e.g., when \code{path} points to a plain text file but \code{index} is present, implying that \code{path} should be a \code{bgzip}ed file. The error message may include an error code representing the logical OR of these cryptic signals: 1, BGZF_ERR_ZLIB; 2, BGZF_ERR_HEADER; 4, BGZF_ERR_IO; 8, BGZF_ERR_MISUSE.} } } \references{ \url{http://samtools.sourceforge.net/tabix.shtml} } \author{ Martin Morgan . } \examples{ example(TabixFile) } \keyword{ manip } Rsamtools/man/seqnamesTabix.Rd0000644000175400017540000000156113556116727017451 0ustar00biocbuildbiocbuild\name{seqnamesTabix} \Rdversion{1.1} \alias{seqnamesTabix} \alias{seqnamesTabix,character-method} \title{ Retrieve sequence names defined in a tabix file. } \description{ This function queries a tabix file, returning the names of the \sQuote{sequences} used as a key when creating the file. } \usage{ seqnamesTabix(file, ...) \S4method{seqnamesTabix}{character}(file, ...) } \arguments{ \item{file}{A \code{character(1)} file path or \code{\linkS4class{TabixFile}} instance pointing to a \sQuote{tabix} file.} \item{...}{Additional arguments, currently ignored.} } \value{ A \code{character()} vector of sequence names present in the file. } \author{ Martin Morgan . } \examples{ fl <- system.file("extdata", "example.gtf.gz", package="Rsamtools", mustWork=TRUE) seqnamesTabix(fl) } \keyword{ manip } Rsamtools/man/testPairedEndBam.Rd0000644000175400017540000000230113556116727020011 0ustar00biocbuildbiocbuild\name{testPairedEndBam} \alias{testPairedEndBam} \alias{testPairedEndBam,character-method} \alias{testPairedEndBam,BamFile-method} \title{ Quickly test if a BAM file has paired end reads } \description{ Iterate through a BAM file until a paired-end read is encountered or the end of file is reached; report the occurrence of paired-end reads to the user. } \usage{ testPairedEndBam(file, index=file, ...) } \arguments{ \item{file}{character(1) BAM file name, or a \code{\link{BamFile}} instance. Open \code{BamFile}s are closed; their yield size is respected when iterating through the file.} \item{index}{(optional) character(1) name of the index file of the 'BAM' file being processed; this is given \emph{without} the '.bai' extension.} \item{\dots}{Additional arguments, currently unused.} } \value{ A logical vector of length 1 containing TRUE is returned if BAM file contained paired end reads, FALSE otherwise. } \author{ Martin Morgan \url{mailto:mtmorgan@fhcrc.org}, Sonali Arora \url{mailto:sarora@fhcrc.org} } \examples{ fl <- system.file("extdata", "ex1.bam", package="Rsamtools") testPairedEndBam(fl) } Rsamtools/man/zip.Rd0000644000175400017540000000263213556116727015447 0ustar00biocbuildbiocbuild\name{Compression} \Rdversion{1.1} \alias{bgzip} \alias{razip} \title{ File compression for tabix (bgzip) and fasta (razip) files. IMPORTANT NOTE: Starting with Rsamtools 1.99.0 (Bioconductor 3.9), \code{razip()} is defunct. Please use \code{bgzip()} instead. } \description{ \code{bgzip} compresses tabix (e.g. SAM or VCF) or FASTA files to a format that allows indexing for later fast random-access. } \usage{ bgzip(file, dest=sprintf("\%s.bgz", sub("\\\\.gz$", "", file)), overwrite = FALSE) ## Defunct! razip(file, dest=sprintf("\%s.rz", sub("\\\\.gz$", "", file)), overwrite = FALSE) } \arguments{ \item{file}{A character(1) path to an existing uncompressed or gz-compressed file. This file will be compressed.} \item{dest}{A character(1) path to a file. This will be the compressed file. If \code{dest} exists, then it is only over-written when \code{overwrite=TRUE}.} \item{overwrite}{A logical(1) indicating whether \code{dest} should be over-written, if it already exists.} } \value{ The full path to \code{dest}. } \references{ \url{http://samtools.sourceforge.net/} } \author{ Martin Morgan } \seealso{ \code{\link{TabixFile}}, \code{\link{FaFile}}. } \examples{ from <- system.file("extdata", "ex1.sam", package="Rsamtools", mustWork=TRUE) to <- tempfile() zipped <- bgzip(from, to) } \keyword{ manip } Rsamtools/migration_notes.md0000644000175400017540000001747613556116727017342 0ustar00biocbuildbiocbuild# Migration of Rsamtools to Rhtslib ## What is the migration about? Before this migration (i.e. for versions < 1.99.0), Rsamtools contained a copy of an old (9-10 year old?) version of the samtools and tabix C code. The latest version of samtools (as of Feb 6, 2019) is 1.9: http://www.htslib.org/ In the recent years the samtools code has been split into samtools + htslib. Most of the code that used to be in samtools is now in htslib. The latest version of htslib is also 1.9. Bioconductor package Rhtslib contains htslib 1.7, which is a decently recent version of htslib. After this migration (i.e. for versions >= 1.99.0), Rsamtools no longer contains a copy of the samtools and tabix C code but compiles and links against Rhtslib instead (i.e. against htslib 1.7). ## Current migration status ### C/C++ code In Rsamtools 1.99.0 all the C/C++ code from the old Rsamtools was migrated to Rhtslib, except for the code behind `asBcf()` and `razip()`: - `asBcf()` (implemented in `src/bcffile.c`) is currently disabled but will need to be migrated if it turns out that some other package needs it (it doesn't seem to be the case though). Note that `asBcf()` isn't used anywhere in Rsamtools either (no example in the man page, no unit test, not used in the vignette). - `razip()` (implemented in `zip_compression.c` in the old Rsamtools) was removed. This is because recent samtools and htslib no longer support RAZF. From the samtools NEWS file: RAZF and razip are superseded by BGZF/bgzip and have been removed from samtools. This happened in samtools 1.0 (15 August, 2014). ### Other remaining problems - Even though the C code behind `applyPileups()` was migrated (`pileupbam.c`), the examples in its man page and most of the tests in `inst/unitTests/test_applyPileups.R` are currently failing and have been disabled for now. - Test `test_BcfFile_scanBcfHeader_remote` (located in `inst/unitTests/test_BcfFile.R`) passes when run interactively (or via `BiocGenerics:::testPackage('Rsamtools')`) but, for some obscure reason, NOT in the context of `R CMD check`. It has been disabled for now. ## Status of Bioconductor packages that depend directly on Rsamtools As of Feb 6, 2019, 159 Bioconductor packages (154 software, 3 data-experiment, and 2 workflow packages) depend **directly** on Rsamtools (i.e. via their Depends, Imports, or LinkingTo field). So we've only checked manually a few of them. This was on a 64-bit Ubuntu 16.04.5 LTS laptop running R 3.6 (2018-12-04 r75758) and Bioconductor 3.9 (current devel). ### All software packages with "LinkingTo: Rsamtools" were tested - VariantAnnotation: migrated (changes committed), passes `R CMD check` - ArrayExpressHTS: migrated (changes not committed yet, Angela Goncalves contacted but didn't answer yet), passes `R CMD check` - BitSeq: migrated (changes committed), passes `R CMD check` - DiffBind: migrated (changes committed by Gord Brown), passes `R CMD check` - h5vc: migrated (changes committed, including fixing pre-existing build ERROR currently visible on the build report), passes `R CMD check` - podkat: migrated (changes committed, including fixing `inst/examples/example1.vcf.gz` to make it compatible with bcftools 1.7), passes `R CMD check` - qrqc: migrated (PR created at https://github.com/vsbuffalo/qrqc/pull/6 per Vince Buffalo's request), passes `R CMD check` - QuasR: migrated (PR created at https://github.com/fmicompbio/QuasR/pull/9 per Michael Stadler's request), passes `R CMD check` - seqbias: migrated (patch sent to, and applied by, Daniel Jones), passes `R CMD check` - TransView: migrated (changes committed), passes `R CMD check` ### All software packages that use applyPileups() were tested - AllelicImbalance: migrated (contained old BCF file (`ERP000101.bcf`, in `extdata/ERP000101_subset/`) that needed to be fixed and reindexed because it no longer worked with recent bcftools/Rhtslib) passes `R CMD check` - biovizBase: passes `R CMD check` _as-is_ - compEpiTools: passes `R CMD check` _as-is_ - SICtools: `test_snpDiff()` (from `test_snpDiff.R`) FAILS! - VariantTools: passes `R CMD check` _as-is_ ### A random sample of a few other software packages were tested - AllelicImbalance: migrated (changes not committed yet) passes `R CMD check` - BaalChIP: passes `R CMD check` _as-is_ - chimera: passes `R CMD check` _as-is_ - CoverageView: passes `R CMD check` _as-is_ - exomeCopy: passes `R CMD check` _as-is_ - exomePeak: passes `R CMD check` _as-is_ - GenomicAlignments: passes `R CMD check` _as-is_ - gmapR: does NOT compile (needs to be migrated) - MEDIPS: passes `R CMD check` _as-is_ - methylPipe: passes `R CMD check` _as-is_ - rnaSeqMap: passes `R CMD check` _as-is_ - ssviz: passes `R CMD check` _as-is_ - systemPipeR: passes `R CMD check` _as-is_ ### All workflow packages were tested - rnaseqGene: vignette builds _as-is_ - sequencing: vignette does NOT build (because of AnnotationHub razip'ed FASTA file `AH18522`) ## Status of CRAN packages that depend directly on Rsamtools As of Feb 6, 2019, 8 CRAN packages depend **directly** on Rsamtools (i.e. via their Depends, Imports, or LinkingTo field). - BinQuasi: passes `R CMD check` _as-is_ - Brundle: passes `R CMD check` _as-is_ - ExomeDepth: passes `R CMD check` _as-is_ - hoardeR: fails to install because of unrelated pre-existing problem: ``` Error : object ‘importGFF3’ is not exported by 'namespace:GenomicTools' ``` (See https://www.r-project.org/nosvn/R.check/r-devel-linux-x86_64-debian-gcc/hoardeR-00install.html) - NIPTeR: passes `R CMD check` _as-is_ - PlasmaMutationDetector: passes `R CMD check` _as-is_ - RAPIDR: passes `R CMD check` _as-is_ - spp: passes `R CMD check` _as-is_ ## What to do about razip-compressed FASTA files and their index files? ### The problem RAZF is no longer supported in recent samtools, and old razip-compressed FASTA files (`.rz`) and their index files (`rz.fai`) are now causing problems. Here is an example from the sequencing workflow: ``` library(AnnotationHub) ah <- AnnotationHub() fa <- ah[["AH18522"]] library(Rsamtools) idx <- scanFaIndex(fa) # still works long <- idx[width(idx) > 82000] getSeq(fa, param=long) # ERROR! ('open' index failed) ``` ### What to do about it? The new way to go is to compress with bgzip and to recreate the index. #### From the Unix command line ``` /path/to/samtools-1.7/htslib/bgzip myfile.fa # creates myfile.fa,gz /path/to/samtools-1.7/samtools faidx myfile.fa,gz # generates index files # myfile.fa.gz.fai # and myfile.fa.gz.gzi ``` Note that the compression step is actually optional i.e. one can use `samtools faidx` directly on the uncompressed FASTA file: ``` gunzip myfile.fa,gz # uncompress to get myfile.fa back /path/to/samtools-1.7/samtools faidx myfile.fa # generates index file # myfile.fa.fai only ``` Note that in this case, only the `.fai` index file is generated (no `.gzi` index file). #### From R ``` library(Rsamtools) bgzip("myfile.fa") indexFa("myfile.fa.bgz") ``` Then create a FaFile object that can be used with `getSeq()` as usual: ``` fa <- FaFile("myfile.fa.bgz") ``` ## TODO Here is an itemized summary of what still needs to happen (some details are provided above in this document): - Chase down old razip'ed FASTA files and update them. Places to look at: * AnnotationHub * ExperimentHub * data annotation packages * data experiment packages * software packages - Troubleshoot `applyPileups()` unit test failures. - Troubleshoot `test_BcfFile_scanBcfHeader_remote()` failure (test is located in `inst/unitTests/test_BcfFile.R`). - Migrate `asBcf()`. - Update `NEWS` file. Rsamtools/src/0000755000175400017540000000000013624616601014357 5ustar00biocbuildbiocbuildRsamtools/src/BamFileIterator.h0000644000175400017540000000233213556116727017551 0ustar00biocbuildbiocbuild// BamFileIterator.h: // Iterator used when reading a complete bam file. #ifndef BAMFILEITERATOR_H #define BAMFILEITERATOR_H #include "BamIterator.h" class BamFileIterator : public BamIterator { bool file_done; void iterate_inprogress(bamFile bfile) { if (iter_done | file_done) return; if ((bam1_t *) NULL == bam) { // first record bam = bam_init1(); if (bam_read1(bfile, bam) < 0) { iter_done = true; return; } } bool done = false; do { process(bam); int tid = bam->core.tid; int pos = bam->core.pos; if (bam_read1(bfile, bam) < 0) { mate_touched_templates(); iter_done = file_done = done = true; } else { if ((bam->core.tid != tid) || (bam->core.pos != pos)) { mate_touched_templates(); done = !complete.empty(); } } } while (!done); } public: // constructor / destructor BamFileIterator(bamFile bfile, const bam_index_t *bindex) : BamIterator(bfile, bindex), file_done(false) {} }; #endif Rsamtools/src/BamIterator.h0000644000175400017540000000731313556116727016755 0ustar00biocbuildbiocbuild// BamIterator.h: // Virtual iterator class with concrete subclasses of // BamRangeIterator and BamFileIterator. #ifndef BAMITERATOR_H #define BAMITERATOR_H #include #include #include "Template.h" #include "bam_data.h" class BamIterator { BAM_DATA bam_data; queue > ambiguous; queue > unmated; set touched_templates; protected: typedef map Templates; Templates templates; queue > complete; const bam_index_t *bindex; bam_header_t *header; bam1_t *bam; char qname_prefix_end() const { if (bam_data == (BAM_DATA) NULL) Rf_error("[qname_prefix_end] report to maintainer('Rsamtools')"); return bam_data->qnamePrefixEnd; } char qname_suffix_start() const { if (bam_data == (BAM_DATA) NULL) Rf_error("[qname_suffix_start] report to maintainer('Rsamtools')"); return bam_data->qnameSuffixStart; } void mate_touched_templates() { for (set::iterator it=touched_templates.begin(); it != touched_templates.end(); ++it) { templates[*it].mate(complete, header->target_len); if (templates[*it].empty()) templates.erase(*it); } touched_templates.clear(); } // process void process(const bam1_t *bam) { if (bam_data == (BAM_DATA) NULL) Rf_error("[process] report to maintainer('Rsamtools')"); if (!_filter1_BAM_DATA(bam, bam_data)) return; const char *trimmed_qname = Template::qname_trim(bam1_qname(bam), qname_prefix_end(), qname_suffix_start()); if (templates[trimmed_qname].add_segment(bam)) touched_templates.insert(trimmed_qname); } virtual void iterate_inprogress(bamFile bfile) = 0; virtual void finalize_inprogress(bamFile bfile) { Templates::iterator it; // transfer Template::ambiguous to BamIterator::ambiguous // transfer Template::inprogress and Template::invalid to // BamIterator::unmated for (it = templates.begin(); it != templates.end(); ++it) it->second.cleanup(ambiguous, unmated); templates.clear(); } public: bool iter_done; // constructor / destructor BamIterator(bamFile bfile, const bam_index_t *bindex) : bam_data((BAM_DATA) NULL), bindex(bindex), bam((bam1_t *) NULL), iter_done(false) { bam_seek(bfile, 0, 0); header = bam_header_read(bfile); } virtual ~BamIterator() { if ((bam1_t *) NULL != bam) bam_destroy1(bam); bam_header_destroy(header); } void set_bam_data(BAM_DATA bd) { this->bam_data = bd; } // yield void yield(bamFile bfile, bam_mates_t *result) { if (complete.empty() && !iter_done) iterate_inprogress(bfile); if (complete.empty() && !templates.empty()) finalize_inprogress(bfile); list elts; MATE_STATUS mated = MATE_UNKNOWN; if (!complete.empty()) { elts = complete.front(); complete.pop(); mated = MATE_MATED; } else if (!ambiguous.empty()) { elts = ambiguous.front(); ambiguous.pop(); mated = MATE_AMBIGUOUS; } else if (!unmated.empty()) { elts = unmated.front(); unmated.pop(); mated = MATE_UNMATED; } bam_mates_realloc(result, elts.size(), mated); for (int i = 0; !elts.empty(); ++i) { result->bams[i] = elts.front(); elts.pop_front(); } } }; #endif Rsamtools/src/BamRangeIterator.h0000644000175400017540000001347013556116727017733 0ustar00biocbuildbiocbuild// BamRangeIterator.h: // Iterator used when reading ranges from a bam file. #ifndef BAMRANGEITERATOR_H #define BAMRANGEITERATOR_H #include "BamIterator.h" class BamRangeIterator : public BamIterator { bam_iter_t iter; void iterate_inprogress(bamFile bfile) { if ((bam1_t *) NULL == bam) { // first record bam = bam_init1(); if (bam_iter_read(bfile, iter, bam) < 0) { iter_done = true; return; } } do { process(bam); if (bam_iter_read(bfile, iter, bam) < 0) iter_done = true; } while (!iter_done); mate_touched_templates(); } static bool cmp_mpos_template_pair(const pair m1, const pair m2) { return m1.first < m2.first; } // mate 'inprogress' segments for each Template in Templates void finalize_inprogress(bamFile bfile) { int64_t pos = bam_tell(bfile); const uint32_t *target_len = header->target_len; bam1_t *bam = bam_init1(); // iterators typedef Templates::iterator template_it; typedef list::iterator list_it; typedef vector >::iterator pairs_it; typedef map< pair, vector > >::iterator map_it; // groups map: // 'key' is the bin (distance) of each mpos from 2^14 // 'value' is a vector of pairs map, vector > > groups; for (template_it it = templates.begin(); it != templates.end(); ++it) { list ip = it->second.get_inprogress(); for (list_it l_it = ip.begin(); l_it != ip.end(); ++l_it) { const bam1_t *curr = *l_it; int32_t mpos = curr->core.mpos % target_len[curr->core.mtid]; pair key(curr->core.mtid, mpos / 16384); pair value(curr->core.mpos, &it->second); groups[key].push_back(value); } } // Iterate over the groups (bins) for (map_it g_it = groups.begin(); g_it != groups.end(); ++g_it) { // sort vector of pairs by mpos int32_t mtid = g_it->first.first; vector > tmpl_v = g_it->second; sort(tmpl_v.begin(), tmpl_v.end(), cmp_mpos_template_pair); int32_t min_mpos = tmpl_v.front().first, max_mpos = tmpl_v.back().first + 1; bam_iter_t iter = bam_iter_query(bindex, mtid, min_mpos, max_mpos); pairs_it p_it = tmpl_v.begin(); do { /* find the next read / template pair */ int status = 0; while ((status = bam_iter_read(bfile, iter, bam)) >= 0) if (bam->core.pos >= p_it->first) break; if (status < 0) break; while (p_it != tmpl_v.end() && bam->core.pos > p_it->first) ++p_it; if (p_it == tmpl_v.end()) break; if (p_it->first != bam->core.pos) continue; /* move p_it to back of valid range */ /* FIXME: really only needs to be done if p_it changed */ pairs_it p_start, p_end; p_start = p_end = p_it; while (p_end != tmpl_v.end() && p_end->first == p_start->first) ++p_end; /* find mates for this read, across all mates */ for (pairs_it p = p_start; p != p_end; ++p) { // Each Template has an 'inprogress' list that may have > 1 // record. In this case the 'groups' map will have // multiple pairs with different mpos but a pointer to // the same Template. All records in 'inprogress' are // processed when the Template is visited the first time. // To avoid revisiting a Template we could try setting // a global such as 'touched = true'. Template *tmpl = p->second; list ip = tmpl->get_inprogress(); for (list_it l_it = ip.begin(); l_it != ip.end(); ++l_it) { const bam1_t *curr = *l_it; char pre = qname_prefix_end(); char suf = qname_suffix_start(); const char *tmpl_q; tmpl_q = tmpl->qname_trim(bam1_qname(curr), pre, suf); const char *mate_q; mate_q = tmpl->qname_trim(bam1_qname(bam), pre, suf); if (tmpl->is_valid(bam) && tmpl->is_template(tmpl_q, mate_q, bam) && tmpl->is_mate(curr, bam, target_len)) { tmpl->add_segment(bam); break; } } } } while (p_it != tmpl_v.end()); bam_iter_destroy(iter); } bam_destroy1(bam); // mate Templates for (template_it it = templates.begin(); it != templates.end(); ++it) it->second.mate(complete, target_len); BamIterator::finalize_inprogress(bfile); bam_seek(bfile, pos, SEEK_SET); } public: // constructor / destructor BamRangeIterator(bamFile bfile, const bam_index_t *bindex, int32_t tid, int32_t beg, int32_t end) : BamIterator(bfile, bindex) { iter = bam_iter_query(bindex, tid, beg, end); } ~BamRangeIterator() { bam_iter_destroy(iter); } }; #endif Rsamtools/src/Biostrings_stubs.c0000644000175400017540000000003713556116727020076 0ustar00biocbuildbiocbuild#include "_Biostrings_stubs.c" Rsamtools/src/COMPAT_bcf_hdr_read.c0000644000175400017540000001127213556116727020163 0ustar00biocbuildbiocbuild#include "COMPAT_bcf_hdr_read.h" #include #include #include #include #include /* WARNING: Between old samtools (version < 0.1.19) and htslib 1.7, the behavior of vcf_hdr_read() has changed as follow: the new version now checks for the presence of an existing tabix index and uses it to add contigs not listed in the header. COMPAT_vcf_hdr_read() below is a re-implementation of the old vcf_hdr_read() i.e. it does NOT try to use a possible existing tabix index in order to add missing contigs. We use it in by scan_bcf_header() (instead of vcf_hdr_read()) so its behavior remains the same as before the migration of Rsamtools to htslib 1.7 (in particular the Reference component of the returned list remains the same). Testing: library(Rsamtools) bcf <- system.file("extdata", "ex1.bcf.gz", package="Rsamtools") scanBcfHeader(bcf) library(VariantAnnotation) vcf <- system.file("extdata", "structural.vcf", package="VariantAnnotation") bgz <- bgzip(vcf, tempfile()) target <- scanBcfHeader(BcfFile(vcf, character(0)))[[1]] stopifnot(identical(target, scanBcfHeader(BcfFile(bgz, character(0)))[[1]])) idx <- indexTabix(bgz, "vcf") stopifnot(identical(target, scanBcfHeader(BcfFile(bgz, character(0)))[[1]])) stopifnot(identical(target, scanBcfHeader(BcfFile(bgz, idx))[[1]])) */ static bcf_hdr_t *COMPAT_vcf_hdr_read(htsFile *fp) { kstring_t txt, *s = &fp->line; int ret; bcf_hdr_t *h; h = bcf_hdr_init("r"); if (!h) { hts_log_error("Failed to allocate bcf header"); return NULL; } txt.l = txt.m = 0; txt.s = 0; while ((ret = hts_getline(fp, KS_SEP_LINE, s)) >= 0) { if (s->l == 0) continue; if (s->s[0] != '#') { hts_log_error("No sample line"); goto error; } if (s->s[1] != '#' && fp->fn_aux) { // insert contigs here kstring_t tmp = { 0, 0, NULL }; hFILE *f = hopen(fp->fn_aux, "r"); if (f == NULL) { hts_log_error("Couldn't open \"%s\"", fp->fn_aux); goto error; } while (tmp.l = 0, kgetline(&tmp, (kgets_func *) hgets, f) >= 0) { char *tab = strchr(tmp.s, '\t'); if (tab == NULL) continue; kputs("##contig=\n", 2, &txt); } free(tmp.s); if (hclose(f) != 0) { hts_log_warning("Failed to close %s", fp->fn_aux); } } kputsn(s->s, s->l, &txt); kputc('\n', &txt); if (s->s[1] != '#') break; } if ( ret < -1 ) goto error; if ( !txt.s ) { hts_log_error("Could not read the header"); goto error; } if ( bcf_hdr_parse(h, txt.s) < 0 ) goto error; free(txt.s); return h; error: free(txt.s); if (h) bcf_hdr_destroy(h); return NULL; } bcf_hdr_t *COMPAT_bcf_hdr_read(htsFile *hfp) { if (hfp->format.format == vcf) return COMPAT_vcf_hdr_read(hfp); if (hfp->format.format != bcf) { hts_log_error("Input is not detected as bcf or vcf format"); return NULL; } assert(hfp->is_bgzf); BGZF *fp = hfp->fp.bgzf; uint8_t magic[5]; bcf_hdr_t *h; h = bcf_hdr_init("r"); if (!h) { hts_log_error("Failed to allocate bcf header"); return NULL; } if (bgzf_read(fp, magic, 5) != 5) { hts_log_error("Failed to read the header (reading BCF in text mode?)"); bcf_hdr_destroy(h); return NULL; } if (strncmp((char*)magic, "BCF\2\2", 5) != 0) { if (!strncmp((char*)magic, "BCF", 3)) hts_log_error("Invalid BCF2 magic string: only BCFv2.2 is supported"); else hts_log_error("Invalid BCF2 magic string"); bcf_hdr_destroy(h); return NULL; } uint8_t buf[4]; size_t hlen; char *htxt = NULL; if (bgzf_read(fp, buf, 4) != 4) goto fail; hlen = buf[0] | (buf[1] << 8) | (buf[2] << 16) | (buf[3] << 24); if (hlen >= SIZE_MAX) { errno = ENOMEM; goto fail; } htxt = (char*)malloc(hlen + 1); if (!htxt) goto fail; if (bgzf_read(fp, htxt, hlen) != hlen) goto fail; htxt[hlen] = '\0'; // Ensure htxt is terminated if ( bcf_hdr_parse(h, htxt) < 0 ) goto fail; free(htxt); return h; fail: hts_log_error("Failed to read BCF header"); free(htxt); bcf_hdr_destroy(h); return NULL; } Rsamtools/src/COMPAT_bcf_hdr_read.h0000644000175400017540000000033313556116727020164 0ustar00biocbuildbiocbuild#ifndef _COMPAT_BCF_HDR_READ_H_ #define _COMPAT_BCF_HDR_READ_H_ #include #include bcf_hdr_t *COMPAT_bcf_hdr_read(htsFile *hfp); #endif /* _COMPAT_BCF_HDR_READ_H_ */ Rsamtools/src/GenomicPosition.h0000644000175400017540000000117613556116727017653 0ustar00biocbuildbiocbuild#ifndef GENOMIC_POSITION_H #define GENOMIC_POSITION_H // identifier for genomic position; used for ordering of PosCache in // associative containers struct GenomicPosition { int tid, pos; GenomicPosition(int tid_, int pos_) : tid(tid_), pos(pos_) { } bool operator<(const GenomicPosition& rhs) const { return tid < rhs.tid || (tid == rhs.tid && pos < rhs.pos); } bool operator==(const GenomicPosition& rhs) const { return tid == rhs.tid && pos == rhs.pos; } bool operator<=(const GenomicPosition& rhs) const { return *this < rhs || *this == rhs; } }; #endif // GENOMIC_POSITION_H Rsamtools/src/IRanges_stubs.c0000644000175400017540000000003413556116727017300 0ustar00biocbuildbiocbuild#include "_IRanges_stubs.c" Rsamtools/src/Makevars0000644000175400017540000000066513556116727016072 0ustar00biocbuildbiocbuild## This file uses GNU make syntax $(shell ...) so we need to ## have "SystemRequirements: GNU make" in the DESCRIPTION file. ## See Rhtslib's vignette for details. RHTSLIB_LIBS=$(shell echo 'Rhtslib::pkgconfig("PKG_LIBS")'|\ "${R_HOME}/bin/R" --vanilla --slave) RHTSLIB_CPPFLAGS=$(shell echo 'Rhtslib::pkgconfig("PKG_CPPFLAGS")'|\ "${R_HOME}/bin/R" --vanilla --slave) PKG_LIBS=$(RHTSLIB_LIBS) PKG_CPPFLAGS=$(RHTSLIB_CPPFLAGS) Rsamtools/src/PileupBuffer.cpp0000644000175400017540000001651713556116727017475 0ustar00biocbuildbiocbuild#include "PileupBuffer.h" void Pileup::signalEOI() { resultMgr->signalEOI(); } int Pileup::insert(uint32_t tid, uint32_t pos, int n, const bam_pileup1_t *pl, void *data) { //Rprintf("pos: %d\n", pos); Pileup *pileup = static_cast(data); pos = pos + 1; // 1-based indexing for R int bamBufOffset = 0; if(!pileup->isRanged || (pos >= pileup->start && pos <= pileup->end)) { const GenomicPosition curGenomicPosition(tid, pos); pileup->resultMgr->signalGenomicPosStart(curGenomicPosition); for(bamBufOffset = 0; bamBufOffset != n; ++bamBufOffset) { const bam_pileup1_t *curBam = pl + bamBufOffset; const uint8_t mapqual = curBam->b->core.qual; if(mapqual < pileup->min_mapq()) continue; char strand = 'X', nucleotide = 'X'; int bin = 0; // positional disqualifier(s) if(pileup->hasBins()) { // all bin work const int32_t minBinPoint = pileup->minBinPoint(), maxBinPoint = pileup->maxBinPoint(); const int32_t qlen = curBam->b->core.l_qseq; const int32_t qpos = curBam->qpos + 1; const bool isMinusStrand = curBam->b->core.flag & 16; // distance from end int32_t dfe = 0; // QUERY BINS if(pileup->isQueryBinMode()) { if(minBinPoint >= 0) dfe = isMinusStrand ? qlen - qpos + 1 : qpos; else dfe = isMinusStrand ? -qpos : -(qlen - qpos + 1); } // LEFT BINS else { if(minBinPoint >= 0) dfe = qpos; else dfe = -(qlen - qpos + 1); } if(dfe > maxBinPoint || dfe <= minBinPoint) continue; bin = pileup->calcBin(dfe); } // invariant: alignments that fail strand criterion not included if(pileup->hasStrands()) strand = bam1_strand(curBam->b) ? '-' : '+'; // IMPORTANT: it's essential that propagating insertions // remains in this position relative to other // disqualifiers; insertions are separate from called // bases--therefore should propagate independent of // considerations about the called base. I.e., an // insertion at a position can propagate while the called // base is diqualified. if(curBam->indel > 0 && pileup->include_insertions()) pileup->resultMgr->forwardTuple(BamTuple('+', strand, bin)); // whole-alignment disqualifiers/filters if(curBam->is_refskip) // never pileup a refskip ('N' op in cigar) continue; // individual nucleotide disqualifiers const uint8_t basequal = bam1_qual(curBam->b)[curBam->qpos]; if(basequal < pileup->min_baseq()) continue; bool isDeletion = curBam->is_del; if(isDeletion && !pileup->include_deletions()) continue; if(isDeletion && pileup->include_deletions()) nucleotide = '-'; else { nucleotide = char(bam_nt16_rev_table[bam1_seqi(bam1_seq(curBam->b), curBam->qpos)]); } bool dropNucleotide = (nucleotide == 'N' && pileup->ignoreNs()); if(dropNucleotide) continue; pileup->resultMgr->forwardTuple(BamTuple(nucleotide, strand, bin)); } const GenomicPosition maxLeftmostGenPOS(tid, pl[n-1].b->core.pos + 1); pileup->resultMgr->forwardLastLeftmostGenPOS(maxLeftmostGenPOS); // extract tuples for pos pileup->resultMgr->signalGenomicPosEnd(); } return 0; } void extract(const ResultMgrInterface * const from, SEXP to, bool hasStrands, bool hasNucleotides, bool hasBins, bool isRanged) { #ifdef PILEUP_DEBUG assert(IS_LIST(to)); for(int i = 0; i != Rf_length(to); ++i) { SEXP elt = VECTOR_ELT(to, i); assert(IS_LIST(elt)); assert((unsigned int)Rf_length(elt) == from->size()); } #endif if(!isRanged) { // seqnms must be copied from seqnmsVec std::copy(from->seqnmsBeg(), from->seqnmsEnd(), INTEGER(VECTOR_ELT(to, 0))); } int curDim = 1; // 0 is seqnames; must start with pos std::copy(from->posBeg(), from->posEnd(), INTEGER(VECTOR_ELT(to, curDim++))); // Might still be worthwhile to make original vectors ints SEXP strand = R_NilValue, nucleotide = R_NilValue; if(hasStrands) { strand = VECTOR_ELT(to, curDim++); std::transform(from->strandBeg(), from->strandEnd(), INTEGER(strand), Pileup::strand_to_lvl); } if(hasNucleotides) { nucleotide = VECTOR_ELT(to, curDim++); std::transform(from->nucBeg(), from->nucEnd(), INTEGER(nucleotide), Pileup::nuc_to_lvl); } if(hasBins) { std::copy(from->binBeg(), from->binEnd(), INTEGER(VECTOR_ELT(to, curDim++))); } std::copy(from->countBeg(), from->countEnd(), INTEGER(VECTOR_ELT(to, curDim++))); if(hasStrands) _as_strand(strand); if(hasNucleotides) _as_nucleotide(nucleotide); } SEXP Pileup::yield() { int numDims = 3; numDims += hasStrands() ? 1 : 0; numDims += hasNucleotides() ? 1 : 0; numDims += hasBins() ? 1 : 0; if(isBuffered) resultMgr->signalYieldStart(); uint32_t numResults = resultMgr->size(); SEXP result = PROTECT(Rf_allocVector(VECSXP, numDims)); int curDim = 0; SET_VECTOR_ELT(result, curDim, Rf_allocVector(INTSXP, numResults));//seqns SEXP seqnames = VECTOR_ELT(result, curDim++); _as_seqlevels(seqnames, seqnamesLevels); // if ranged (i.e., 'which' argument passed to ScanBamParam), // seqnames value will be same for entire buffer otherwise, values // will be copied in extract function if(isRanged) std::fill_n(INTEGER(seqnames), numResults, getSeqlevelValue(rname)); SET_VECTOR_ELT(result, curDim++, Rf_allocVector(INTSXP, numResults)); // pos if(hasStrands()) SET_VECTOR_ELT(result, curDim++, Rf_allocVector(INTSXP, numResults)); if(hasNucleotides()) SET_VECTOR_ELT(result, curDim++, Rf_allocVector(INTSXP, numResults)); if(hasBins()) SET_VECTOR_ELT(result, curDim++, Rf_allocVector(INTSXP, numResults)); SET_VECTOR_ELT(result, curDim++, Rf_allocVector(INTSXP, numResults));//count SEXP nms = PROTECT(Rf_allocVector(STRSXP, numDims)); curDim = 0; SET_STRING_ELT(nms, curDim++, mkChar("seqnames")); SET_STRING_ELT(nms, curDim++, mkChar("pos")); if(hasStrands()) SET_STRING_ELT(nms, curDim++, mkChar("strand")); if(hasNucleotides()) SET_STRING_ELT(nms, curDim++, mkChar("nucleotide")); if(hasBins()) SET_STRING_ELT(nms, curDim++, mkChar("bin")); SET_STRING_ELT(nms, curDim++, mkChar("count")); SET_ATTR(result, R_NamesSymbol, nms); extract(resultMgr, result, hasStrands(), hasNucleotides(), hasBins(), isRanged); resultMgr->signalYieldEnd(); UNPROTECT(2); return result; } Rsamtools/src/PileupBuffer.h0000644000175400017540000001576213556116727017143 0ustar00biocbuildbiocbuild#ifndef PILEUPBUFFER_H #define PILEUPBUFFER_H #include #include #include #include #include #include #include #include "ResultManager.h" #include "utilities.h" #include #include class PosCacheColl; class PileupBuffer { protected: bam_plbuf_t *plbuf; const char *rname; uint32_t start, end; public: PileupBuffer() : plbuf((bam_plbuf_t *) NULL) {} virtual ~PileupBuffer() { plbuf_destroy(); } void init(const char *_rname, const int _start, const int _end) { plbuf_init(); rname = _rname; start = _start; end = _end; } void plbuf_destroy() { if (plbuf != NULL) { bam_plbuf_destroy(plbuf); plbuf = (bam_plbuf_t *) NULL; } } void plbuf_push(const bam1_t *bam) { bam_plbuf_push(bam, plbuf); } virtual void plbuf_init() = 0; virtual SEXP yield() = 0; virtual void signalEOI() = 0; }; class Pileup : public PileupBuffer { private: // 'ranged' means the pileup query is for specific genomic ranges; // 'buffered' is when intermediate results for genomic positions // are store across calls to pileup const bool isRanged, isBuffered; bool isQueryBin; int binsLength; const SEXP schema, pileupParams, seqnamesLevels; ResultMgrInterface *resultMgr; std::vector binPoints; int max_depth() const { return INTEGER(VECTOR_ELT(pileupParams, 0))[0]; } uint8_t min_baseq() const { return INTEGER(VECTOR_ELT(pileupParams, 1))[0]; } uint8_t min_mapq() const { return INTEGER(VECTOR_ELT(pileupParams, 2))[0]; } int min_nucleotide_depth() const { return INTEGER(VECTOR_ELT(pileupParams, 3))[0]; } int min_minor_allele_depth() const { return INTEGER(VECTOR_ELT(pileupParams, 4))[0]; } bool hasStrands() const { return LOGICAL(VECTOR_ELT(pileupParams, 5))[0]; // distinguish_strands } bool hasNucleotides() const { return LOGICAL(VECTOR_ELT(pileupParams, 6))[0]; // distinguish_nucs } bool ignoreNs() const { return LOGICAL(VECTOR_ELT(pileupParams, 7))[0]; } bool include_deletions() const { return LOGICAL(VECTOR_ELT(pileupParams, 8))[0]; } bool include_insertions() const { return LOGICAL(VECTOR_ELT(pileupParams, 9))[0]; } // left_bins pileupParams[10] int leftBinsParamLength() const { return Rf_length(VECTOR_ELT(pileupParams, 10)); } // query_bins pileupParams[11] int queryBinsParamLength() const { return Rf_length(VECTOR_ELT(pileupParams, 11)); } int getBinsLength() const { return binsLength; } bool hasBins() const { return binsLength > 0; } bool isQueryBinMode() const { return isQueryBin; } std::vector binPointsAsVec(SEXP cycleBins) const { int numPoints = Rf_length(cycleBins); std::vector points(numPoints); for(int i = 0; i != numPoints; ++i) { points.at(i) = INTEGER(cycleBins)[i]; } return points; } int calcBin(int dfe) { return std::lower_bound(binPoints.begin(), binPoints.end(), dfe) - binPoints.begin(); } int32_t maxBinPoint() const { return *(binPoints.end() - 1); } int32_t minBinPoint() const { return *binPoints.begin(); } int getSeqlevelValue(const char* theRname) const { int idx = 0; for(idx = 0; idx != Rf_length(seqnamesLevels); ++idx) { const char* curLevel = CHAR(STRING_ELT(seqnamesLevels, idx)); //Rprintf("rname (%s) =? level (%s)\n", rname, curLevel); if(strcmp(theRname, curLevel) == 0) return idx + 1; } Rf_error("rname '%s' not in seqnames levels", rname); return -1; } public: // void *posCacheColl is dumbly passed through to ResultMgr to // give ResultMgr pointer to the struct _BAM_FILE pbuffer member; // PileupBuffer doesn't know anything about PosCacheColl Pileup(bool isRanged_, bool isBuffered_, SEXP schema_, SEXP pileupParams_, SEXP seqnamesLevels_, PosCacheColl** posCacheColl_) : isRanged(isRanged_), isBuffered(isBuffered_), isQueryBin(false), binsLength(0), schema(schema_), pileupParams(pileupParams_), seqnamesLevels(seqnamesLevels_), resultMgr((ResultMgrInterface *) NULL), binPoints() { if(isRanged && isBuffered) { Rf_error("internal: Pileup cannot both query specific genomic ranges and store partial genomic position results"); } // bins stuff (needs to come before ResultMgr ctor call // because ctor uses hasBins() if(leftBinsParamLength() > 0) { isQueryBin = false; binsLength = leftBinsParamLength(); binPoints = binPointsAsVec(VECTOR_ELT(pileupParams, 10)); } else if(queryBinsParamLength() > 0) { isQueryBin = true; binsLength = queryBinsParamLength(); binPoints = binPointsAsVec(VECTOR_ELT(pileupParams, 11)); } resultMgr = new ResultMgr(min_nucleotide_depth(), min_minor_allele_depth(), hasStrands(), hasNucleotides(), hasBins(), isRanged, isBuffered, posCacheColl_); } ~Pileup() { delete resultMgr; } bool needMoreInput() const { bool needMore = resultMgr->numYieldablePosCaches() == 0; return needMore; } bool isBufferedPileup() const { return isBuffered; } void plbuf_init() { plbuf = bam_plbuf_init(insert, this); int theDepth = max_depth(); if(theDepth < 1) Rf_error("'max_depth' must be greater than 0, got '%d'", theDepth); // +1 essential because when maxcnt > 1 num reads processed = maxcnt - 1 int num_reads_to_process = theDepth < 2 ? 1 : theDepth + 1; bam_plp_set_maxcnt(plbuf->iter, num_reads_to_process); } static int insert(uint32_t tid, uint32_t pos, int n, const bam_pileup1_t *pl, void *data); SEXP yield(); void signalEOI(); static int strand_to_lvl(char strand) { return strand == '+' ? 1 : 2; } static int nuc_to_lvl(char nuc) { if(nuc == 'A') return 1; else if(nuc == 'C') return 2; else if(nuc == 'G') return 3; else if(nuc == 'T') return 4; else if(nuc == 'N') return 5; else if(nuc == '=') return 6; else if(nuc == '-') return 7; else if(nuc == '+') return 8; else Rf_error("Unrecognized nucleotide '%c'\n", nuc); } }; void extract(const ResultMgrInterface * const from, SEXP to, bool hasStrands, bool hasNucleotides, bool hasBins); #endif //PILEUPBUFFER_H Rsamtools/src/PileupBufferShim.h0000644000175400017540000000320613556116727017752 0ustar00biocbuildbiocbuild#ifndef PILEUPBUFFERSHIM_H #define PILEUPBUFFERSHIM_H #include "PileupBuffer.h" class PileupBufferShim { private: const SEXP regions; SEXP result; PileupBuffer &buffer; public: PileupBufferShim(SEXP _regions, SEXP _result, PileupBuffer &_buffer) : regions(_regions), result(_result), buffer(_buffer) {} void start1(const int irange) { if (R_NilValue == regions) { buffer.init((const char *) NULL, 0, 0); } else { buffer.init( CHAR(STRING_ELT(VECTOR_ELT(regions, 0), irange)), INTEGER(VECTOR_ELT(regions, 1))[irange], INTEGER(VECTOR_ELT(regions, 2))[irange]); } } void finish1(const int irange) { plbuf_push((const bam1_t *) NULL); SET_VECTOR_ELT(result, irange, buffer.yield()); buffer.plbuf_destroy(); } // The only way to trigger running the callback function // (Pileup::insert in this case) is to push NULL to the buffer and // destroy it. Therefore, must destroy and recreate plbuf each // time yieldSize records are pushed. void process_yieldSize_chunk() { plbuf_push((const bam1_t *) NULL); buffer.plbuf_destroy(); // trigger run of Pileup::insert buffer.init((const char *) NULL, 0, 0); } // intended to be called from _pileup_bam after EOI message sent // to PileupBuffer; same as finish1 but no plbuf is in use void flush() { //Rprintf("flushing\n"); SET_VECTOR_ELT(result, 0, buffer.yield()); } void plbuf_push(const bam1_t *bam) { buffer.plbuf_push(bam); } }; #endif // PILEUPBUFFERSHIM_H Rsamtools/src/PosCache.h0000644000175400017540000000447213556116727016234 0ustar00biocbuildbiocbuild#ifndef POS_CACHE_H #define POS_CACHE_H #include #include #include #include #include #include #include "GenomicPosition.h" using std::map; using std::pair; using std::make_pair; struct BamTuple { // for sending info from Pileup::insert to ResultMgr char nuc, strand; int bin; BamTuple(char nuc_ = 'X', char strand_ = 'X', int bin_ = 0) : nuc(nuc_), strand(strand_), bin(bin_) { } bool operator<(const BamTuple& rhs) const { return nuc < rhs.nuc || (nuc == rhs.nuc && strand < rhs.strand) || (nuc == rhs.nuc && strand == rhs.strand && bin < rhs.bin); } }; struct PosCache { GenomicPosition genomicPosition; std::vector tupleVec; std::map nucCounts; typedef std::vector::const_iterator tuple_iter; typedef std::map::const_iterator counts_iter; PosCache(GenomicPosition genomicPosition_) : genomicPosition(genomicPosition_), tupleVec(), nucCounts() { } void storeTuple(BamTuple& bt) { tupleVec.push_back(bt); nucCounts.insert(make_pair(bt.nuc,0)).first->second++; } // exposed so we can use std::accumulate on nucCounts map static int addSecond(int i, const pair& thePair) { return i + thePair.second; } int totalNucFreq() const { return std::accumulate(nucCounts.begin(),nucCounts.end(),0,addSecond); } int primaryNucFreq() const { int maxCount = 0; typedef map::const_iterator iter; for(iter it = nucCounts.begin(); it != nucCounts.end(); ++it) { if(it->second > maxCount) maxCount = it->second; } return maxCount; } std::set passingNucs(int min) const { std::set nucs; for(counts_iter it = nucCounts.begin(); it != nucCounts.end(); ++it) { if(it->second >= min) nucs.insert(it->first); } return nucs; } void clear() { tupleVec.clear(); nucCounts.clear(); } void print() const { printf("tupleVec contents:\n"); for(tuple_iter it = tupleVec.begin(); it != tupleVec.end(); ++it) { printf("nuc %c str %c bin %u\n", it->nuc, it->strand, it->bin); } } }; #endif // POS_CACHE_H Rsamtools/src/PosCacheColl.cpp0000644000175400017540000000102213556116727017365 0ustar00biocbuildbiocbuild#include "PosCacheColl.h" // because it's a free function we have to ensure it's only ever // defined once. Including it in the .h triggers multiple definition // linking error void getPosCacheFromColl(PosCacheColl& pcc, PosCache*& posCachePtr) { PosCache* tmp = posCachePtr; // hold address pointed to by posCachePtr posCachePtr = pcc.fetchPosCache(posCachePtr); if(tmp != posCachePtr) { // found val in pcc, must deallocate incoming ptr's object delete tmp; tmp = (PosCache *) NULL; } } Rsamtools/src/PosCacheColl.h0000644000175400017540000001014513556116727017040 0ustar00biocbuildbiocbuild#ifndef POS_CACHE_COLL_H #define POS_CACHE_COLL_H #include #include #include "PosCache.h" #include // because set of pointers, need to compare *dereferenced* values, // otherwise would compare pointer addresses! struct PosCachePtrLess { bool operator()(const PosCache* lhs, const PosCache* rhs) const { return lhs->genomicPosition < rhs->genomicPosition; } }; class PosCacheColl { private: std::set posCaches; public: typedef std::set::const_iterator const_iter; typedef std::set::iterator iter; PosCacheColl() : posCaches() { } ~PosCacheColl() { while(!posCaches.empty()) { iter it = posCaches.begin(); PosCache* tmp = *it; posCaches.erase(it); delete tmp; } } #ifdef PILEUP_DEBUG void printGenPositions() const { for(const_iter it = posCaches.begin(); it != posCaches.end(); ++it) { printf("tid %d pos %d\n", (*it)->genomicPosition.tid, (*it)->genomicPosition.pos); } } #endif // PILEUP_DEBUG void storePosCache(PosCache *cachePtr) { //printf("storePosCache size %d\n", posCaches.size()); if(posCaches.find(cachePtr) != posCaches.end()) { Rf_error("internal: posCache already in PosCacheColl"); } posCaches.insert(cachePtr); cachePtr = (PosCache *) NULL; } // precondition: val points to an already-allocated PosCache; // clients will use this to check if a PosCache with matching // GenomicPosition already exists. If it already exists, PosCache // pointed to by incoming pointer will be deallocated and incoming // pointer will be set to existing PosCache // postcondition: if val found in set, remove set element // containing pointer, return pointer to PosCache; if not found in // set, return NULL PosCache* fetchPosCache(PosCache* val) { iter it = posCaches.find(val); if(it == posCaches.end()) { return val; // not found in set, leave ptr unchanged } PosCache* tmp = *it; // tmp is pointer to heap memory of PosCache posCaches.erase(it); // remove set element return tmp; } PosCache* destructiveNext() { //printf("destructiveNext size %d\n", posCaches.size()); if(posCaches.empty()) { return NULL; } else { iter it = posCaches.begin(); PosCache* tmp = *it; posCaches.erase(it); return tmp; } } PosCache* destructiveNextLT(const GenomicPosition& gp) { if(posCaches.empty()) { return NULL; } else { iter it = posCaches.begin(); if((*it)->genomicPosition < gp) { PosCache* tmp = *it; posCaches.erase(it); return tmp; } else { return NULL; } } } // FIX ME: use STL algorithms!! int numPosCachesLT(const GenomicPosition& gp) const { //printf("posCaches.size() %lu\n", posCaches.size()); //printf("gp gp.tid %d gp.pos %d\n", gp.tid, gp.pos); if(posCaches.empty()) return 0; int count = 0; for(const_iter it = posCaches.begin(); it != posCaches.end(); ++it) { if((*it)->genomicPosition < gp) ++count; else break; } //printf("COUNT: %d\n", count); return count; } }; // Destructive release of ownership of PosCache in PosCacheColl that // compares equal to posCachePtr's object // preconditions: // - posCachePtr points to valid initialized PosCache object // postconditions: // - if PosCache found in PosCacheColl: // a) the incoming posCachePtr's object is deallocated // b) posCachePtr is reassigned to found PosCache // c) posCacheColl no longer contains element pointing to returned // PosCache // - if PosCache NOT found in PosCacheColl // a) posCachePtr unchanged void getPosCacheFromColl(PosCacheColl& pcc, PosCache*& posCachePtr); #endif /* POS_CACHE_COLL_H */ Rsamtools/src/R_init_Rsamtools.c0000644000175400017540000000675613556116727020040 0ustar00biocbuildbiocbuild#include #include "zip_compression.h" #include "utilities.h" #include "bamfile.h" #include "as_bam.h" #include "idxstats.h" #include "io_sam.h" #include "bcffile.h" #include "fafile.h" #include "tabixfile.h" #include "pileupbam.h" #include "pileup.h" static const R_CallMethodDef callMethods[] = { /* zip_compression.c */ {".bgzip", (DL_FUNC) & bgzip, 2}, /* utilities.c */ {".p_pairing", (DL_FUNC) & p_pairing, 12}, {".find_mate_within_groups", (DL_FUNC) & find_mate_within_groups, 6}, /* bamfile.c */ {".bamfile_init", (DL_FUNC) & bamfile_init, 0}, {".bamfile_open", (DL_FUNC) & bamfile_open, 3}, {".bamfile_close", (DL_FUNC) & bamfile_close, 1}, {".bamfile_isopen", (DL_FUNC) & bamfile_isopen, 1}, {".bamfile_isincomplete", (DL_FUNC) & bamfile_isincomplete, 1}, {".read_bamfile_header", (DL_FUNC) & read_bamfile_header, 2}, {".scan_bamfile", (DL_FUNC) & scan_bamfile, 13}, {".count_bamfile", (DL_FUNC) & count_bamfile, 6}, {".prefilter_bamfile", (DL_FUNC) & prefilter_bamfile, 11}, {".filter_bamfile", (DL_FUNC) & filter_bamfile, 8}, /* as_bam.c */ {".as_bam", (DL_FUNC) & as_bam, 3}, /* idxstats.c */ {".idxstats_bamfile", (DL_FUNC) & idxstats_bamfile, 1}, /* io_sam.c */ {".scan_bam_template", (DL_FUNC) & scan_bam_template, 2}, {".scan_bam_cleanup", (DL_FUNC) & scan_bam_cleanup, 0}, {".sort_bam", (DL_FUNC) & sort_bam, 4}, {".merge_bam", (DL_FUNC) & merge_bam, 8}, {".index_bam", (DL_FUNC) & index_bam, 1}, /* bcffile.c */ {".bcffile_init", (DL_FUNC) & bcffile_init, 0}, {".bcffile_open", (DL_FUNC) & bcffile_open, 3}, {".bcffile_close", (DL_FUNC) & bcffile_close, 1}, {".bcffile_isopen", (DL_FUNC) & bcffile_isopen, 1}, {".bcffile_isvcf", (DL_FUNC) & bcffile_isvcf, 1}, {".scan_bcf_header", (DL_FUNC) & scan_bcf_header, 1}, {".scan_bcf", (DL_FUNC) & scan_bcf, 3}, {".as_bcf", (DL_FUNC) & as_bcf, 3}, {".index_bcf", (DL_FUNC) & index_bcf, 1}, /* fafile.c */ {".fafile_init", (DL_FUNC) & fafile_init, 0}, {".fafile_open", (DL_FUNC) & fafile_open, 3}, {".fafile_close", (DL_FUNC) & fafile_close, 1}, {".fafile_isopen", (DL_FUNC) & fafile_isopen, 1}, {".index_fa", (DL_FUNC) & index_fa, 1}, {".n_fa", (DL_FUNC) & n_fa, 1}, {".scan_fa", (DL_FUNC) & scan_fa, 6}, /* tabixfile.c */ {".tabixfile_init", (DL_FUNC) & tabixfile_init, 0}, {".tabixfile_open", (DL_FUNC) & tabixfile_open, 2}, {".tabixfile_close", (DL_FUNC) & tabixfile_close, 1}, {".tabixfile_isopen", (DL_FUNC) & tabixfile_isopen, 1}, {".index_tabix", (DL_FUNC) & index_tabix, 8}, {".header_tabix", (DL_FUNC) & header_tabix, 1}, {".tabix_as_character", (DL_FUNC) & tabix_as_character, 6}, {".tabix_count", (DL_FUNC) & tabix_count, 6}, {".scan_tabix", (DL_FUNC) & scan_tabix, 6}, /* pileupbam.c */ {".apply_pileups", (DL_FUNC) & apply_pileups, 5}, /* bambuffer.c */ {".bambuffer_init", (DL_FUNC) & bambuffer_init, 0}, {".bambuffer", (DL_FUNC) & bambuffer, 1}, {".bambuffer_length", (DL_FUNC) & bambuffer_length, 1}, {".bambuffer_parse", (DL_FUNC) & bambuffer_parse, 9}, {".bambuffer_write", (DL_FUNC) & bambuffer_write, 3}, {".bambuffer_reset", (DL_FUNC) & bambuffer_reset, 1}, /* pileup.cpp */ {".c_Pileup", (DL_FUNC) & c_Pileup, 14}, {NULL, NULL, 0} }; void R_init_Rsamtools(DllInfo * info) { R_registerRoutines(info, NULL, callMethods, NULL, NULL); } void R_unload_Rsamtools(DllInfo *info) { (void) info; } Rsamtools/src/ResultManager.cpp0000644000175400017540000002726413556116727017657 0ustar00biocbuildbiocbuild#include "ResultManager.h" void ResultMgr::signalGenomicPosStart(const GenomicPosition& genPos) { //Rprintf("signalGenomicPosStart tid %d pos %d\n", genPos.tid, genPos.pos); if(isBuffered && (posCache != (PosCache *) NULL)) Rf_error("internal: ResultMgr's previous posCache not deallocated"); posCache = new PosCache(genPos); if(isBuffered) { getPosCacheFromColl(**posCacheCollptrptr, posCache); } //posCache->print(); //Rprintf("end of signalGenomicPosStart\n\n"); } void ResultMgr::forwardLastLeftmostGenPOS(const GenomicPosition& genPos) { //Rprintf("forwardMinLeftmostGenPos tid %d pos %d\n", genPos.tid, genPos.pos); lastLeftmostGenPOS = genPos; } void ResultMgr::forwardTuple(BamTuple bTuple) { posCache->storeTuple(bTuple); } template void ResultMgr::doExtractFromPosCache(const std::set&) { } template <> void // distinguish nothing / collapse all ResultMgr::doExtractFromPosCache(const std::set& nucs){ typedef std::map::const_iterator iter; int count = 0; for(iter it = posCache->nucCounts.begin(); it != posCache->nucCounts.end(); ++it) { if(nucs.find(it->first) != nucs.end()) { count += it->second; } } if(count > 0) { countVec.push_back(count); } } template <> void // maximally distinguished ResultMgr::doExtractFromPosCache(const std::set& nucs) { std::map tupleMap; typedef std::vector::const_iterator iter; for(iter it = posCache->tupleVec.begin(); it != posCache->tupleVec.end(); ++it) { if(nucs.find(it->nuc) != nucs.end()) tupleMap.insert(make_pair(*it, 0)).first->second++; } typedef std::map::const_iterator count_iter; for(count_iter it = tupleMap.begin(); it != tupleMap.end(); ++it) { countVec.push_back(it->second); nucVec.push_back(it->first.nuc); strandVec.push_back(it->first.strand); binVec.push_back(it->first.bin); } } template <> void // A (nuc only) ResultMgr::doExtractFromPosCache(const std::set& nucs){ typedef std::map::const_iterator iter; for(iter it = posCache->nucCounts.begin(); it != posCache->nucCounts.end(); ++it) { if(nucs.find(it->first) != nucs.end()) { countVec.push_back(it->second); nucVec.push_back(it->first); } } } template <> void // B (strand only) ResultMgr::doExtractFromPosCache(const std::set& nucs){ std::map strandMap; // typedef std::vector::const_iterator iter; for(iter it = posCache->tupleVec.begin(); it != posCache->tupleVec.end(); ++it) { if(nucs.find(it->nuc) != nucs.end()) { strandMap.insert(make_pair(it->strand,0)).first->second++; } } typedef std::map::const_iterator char_iter; for(char_iter it = strandMap.begin(); it != strandMap.end(); ++it) { countVec.push_back(it->second); strandVec.push_back(it->first); } } template <> void // C (bin only) ResultMgr::doExtractFromPosCache(const std::set& nucs){ std::map binMap; // typedef std::vector::const_iterator iter; for(iter it = posCache->tupleVec.begin(); it != posCache->tupleVec.end(); ++it) { if(nucs.find(it->nuc) != nucs.end()) { binMap.insert(make_pair(it->bin,0)).first->second++; } } typedef std::map::const_iterator count_iter; for(count_iter it = binMap.begin(); it != binMap.end(); ++it) { countVec.push_back(it->second); binVec.push_back(it->first); } } template <> void // AB (nuc and strand) ResultMgr::doExtractFromPosCache(const std::set& nucs){ std::map,int> nucstrMap; // <,count> typedef std::vector::const_iterator iter; for(iter it = posCache->tupleVec.begin(); it != posCache->tupleVec.end(); ++it) { if(nucs.find(it->nuc) != nucs.end()) { pair tmp = make_pair(it->nuc,it->strand); nucstrMap.insert(make_pair(tmp,0)).first->second++; } } typedef std::map,int>::const_iterator count_iter; for(count_iter it = nucstrMap.begin(); it != nucstrMap.end(); ++it) { countVec.push_back(it->second); nucVec.push_back(it->first.first); strandVec.push_back(it->first.second); } } template <> void // BC (strand and bin) ResultMgr::doExtractFromPosCache(const std::set& nucs){ std::map,int> strbinMap; // <,count> typedef std::vector::const_iterator iter; for(iter it = posCache->tupleVec.begin(); it != posCache->tupleVec.end(); ++it) { if(nucs.find(it->nuc) != nucs.end()) { pair tmp = make_pair(it->strand,it->bin); strbinMap.insert(make_pair(tmp,0)).first->second++; } } typedef std::map,int>::const_iterator count_iter; for(count_iter it = strbinMap.begin(); it != strbinMap.end(); ++it) { countVec.push_back(it->second); strandVec.push_back(it->first.first); binVec.push_back(it->first.second); } } template <> void // AC (nuc and bin) ResultMgr::doExtractFromPosCache(const std::set& nucs){ std::map,int> nucbinMap; // <,count> typedef std::vector::const_iterator iter; for(iter it = posCache->tupleVec.begin(); it != posCache->tupleVec.end(); ++it) { if(nucs.find(it->nuc) != nucs.end()) { pair tmp = make_pair(it->nuc,it->bin); nucbinMap.insert(make_pair(tmp,0)).first->second++; } } typedef std::map,int>::const_iterator count_iter; for(count_iter it = nucbinMap.begin(); it != nucbinMap.end(); ++it) { countVec.push_back(it->second); nucVec.push_back(it->first.first); binVec.push_back(it->first.second); } } void ResultMgr::extractFromPosCache() { std::set nucs = posCache->passingNucs(min_nuc_depth); int linearLengthBefore = countVec.size(); // ABC if(!hasNucleotides && !hasStrands && !hasBins) // distinguish nothing doExtractFromPosCache(nucs); else if(hasNucleotides && hasStrands && hasBins) // ABC doExtractFromPosCache(nucs); else if(hasNucleotides && !hasStrands && !hasBins) // A doExtractFromPosCache(nucs); else if(!hasNucleotides && hasStrands && !hasBins) // B doExtractFromPosCache(nucs); else if(!hasNucleotides && !hasStrands && hasBins) // C doExtractFromPosCache(nucs); else if(hasNucleotides && hasStrands && !hasBins) // AB doExtractFromPosCache(nucs); else if(!hasNucleotides && hasStrands && hasBins) // BC doExtractFromPosCache(nucs); else // AC doExtractFromPosCache(nucs); int linearLengthDiff = countVec.size() - linearLengthBefore; // insert pos and tid if applicable if(linearLengthDiff > 0) { GenomicPosition& curGP = posCache->genomicPosition; posVec.insert(posVec.end(), linearLengthDiff, curGP.pos); if(!isRanged) { seqnmsVec.insert(seqnmsVec.end(), linearLengthDiff, curGP.tid + 1); } } } bool ResultMgr::posCachePassesFilters(const PosCache& thePosCache) { int totalNucFreq = thePosCache.totalNucFreq(); int primaryNucFreq = thePosCache.primaryNucFreq(); // must always check min_minor_allele_depth bool passes = totalNucFreq - primaryNucFreq >= min_minor_allele_depth; return passes; } void ResultMgr::signalGenomicPosEnd() { //Rprintf("start of signalPosEnd\n"); //posCache->print(); if(!isBuffered) { if(posCachePassesFilters(*posCache)) extractFromPosCache(); delete posCache; posCache = (PosCache *) NULL; } else { (*posCacheCollptrptr)->storePosCache(posCache); posCache = (PosCache *) NULL; } //Rprintf("end of signalPosEnd\n\n****************\n\n"); } // extract from PosCaches corresponding to completed positions, i.e., // PosCache->genomicPosition < minLeftmostGenPOS void ResultMgr::signalYieldStart() { //Rprintf("signalYieldStart\n"); if(isBuffered && *posCacheCollptrptr != (PosCacheColl *) NULL) { for(;;) { posCache = (*posCacheCollptrptr)->destructiveNextLT(lastLeftmostGenPOS); if(posCache == (PosCache *) NULL) break; if(posCachePassesFilters(*posCache)) extractFromPosCache(); delete posCache; posCache = (PosCache *) NULL; } } } int ResultMgr::numYieldablePosCaches() const { //Rprintf("begin numYieldablePosCaches\n"); if(isBuffered && (*posCacheCollptrptr != (PosCacheColl *) NULL)) { //Rprintf("printing posCacheColl contents\n"); //(*posCacheCollptrptr)->printGenPositions(); int num = (*posCacheCollptrptr)->numPosCachesLT(lastLeftmostGenPOS); return num; } return -1; // FIX ME: needed for end-of-input? } int ResultMgr::size() const { // number of tuples in linear representation return posVec.size(); } void ResultMgr::printVecs() const { Rprintf("vec contents:\n"); for(unsigned int i = 0; i != posVec.size(); ++i) { Rprintf("pos %d ", posVec.at(i)); if(hasNucleotides) Rprintf(" nuc %c ", nucVec.at(i)); if(hasStrands) Rprintf(" str %c ", strandVec.at(i)); if(hasBins) Rprintf(" bin %u ", binVec.at(i)); Rprintf(" count %d\n", countVec.at(i)); } } void ResultMgr::signalYieldEnd() { #ifdef PILEUP_DEBUG printVecs(); #endif // PILEUP_DEBUG seqnmsVec.clear(); posVec.clear(); countVec.clear(); binVec.clear(); strandVec.clear(); nucVec.clear(); } void ResultMgr::signalEOI() { //Rprintf("got EOI message!\n"); if(isBuffered && (*posCacheCollptrptr != (PosCacheColl *) NULL)) { //(*posCacheCollptrptr)->printGenPositions(); int i = 0; for(;;) { //printf("i %d\n", i); posCache = (*posCacheCollptrptr)->destructiveNext(); if(posCache == (PosCache *) NULL) break; if(posCachePassesFilters(*posCache)) extractFromPosCache(); delete posCache; posCache = (PosCache *) NULL; ++i; } //Rprintf("deallocating *posCacheCollptrptr's object\n"); delete *posCacheCollptrptr; *posCacheCollptrptr = (PosCacheColl *) NULL; } } inline int_const_it ResultMgr::seqnmsBeg() const { return seqnmsVec.begin(); } inline int_const_it ResultMgr::seqnmsEnd() const { return seqnmsVec.end(); } inline int_const_it ResultMgr::posBeg() const { return posVec.begin(); } inline int_const_it ResultMgr::posEnd() const { return posVec.end(); } inline int_const_it ResultMgr::binBeg() const { return binVec.begin(); } inline int_const_it ResultMgr::binEnd() const { return binVec.end(); } inline int_const_it ResultMgr::countBeg() const { return countVec.begin(); } inline int_const_it ResultMgr::countEnd() const { return countVec.end(); } inline char_const_it ResultMgr::strandBeg() const { return strandVec.begin(); } inline char_const_it ResultMgr::strandEnd() const { return strandVec.end(); } inline char_const_it ResultMgr::nucBeg() const { return nucVec.begin(); } inline char_const_it ResultMgr::nucEnd() const { return nucVec.end(); } Rsamtools/src/ResultManager.h0000644000175400017540000001114213556116727017310 0ustar00biocbuildbiocbuild#ifndef RESULT_MANAGER_H #define RESULT_MANAGER_H #include #include #include #ifdef PILEUP_DEBUG #include #include #include "nate_utilities.h" #endif #include "PosCache.h" #include "PosCacheColl.h" #include "GenomicPosition.h" #include typedef std::vector::const_iterator int_const_it; typedef std::vector::const_iterator char_const_it; class ResultMgrInterface { public: virtual void signalGenomicPosStart(const GenomicPosition& genPos) = 0; virtual void forwardLastLeftmostGenPOS(const GenomicPosition& genPos) = 0; virtual void forwardTuple(BamTuple bTuple) = 0; virtual void extractFromPosCache() = 0; virtual void signalGenomicPosEnd() = 0; virtual int size() const = 0; virtual void signalYieldStart() = 0; virtual void signalYieldEnd() = 0; virtual int numYieldablePosCaches() const = 0; virtual void signalEOI() = 0; virtual ~ResultMgrInterface() {} virtual int_const_it seqnmsBeg() const = 0; virtual int_const_it seqnmsEnd() const = 0; virtual int_const_it posBeg() const = 0; virtual int_const_it posEnd() const = 0; virtual int_const_it countBeg() const = 0; virtual int_const_it countEnd() const = 0; virtual char_const_it strandBeg() const = 0; virtual char_const_it strandEnd() const = 0; virtual char_const_it nucBeg() const = 0; virtual char_const_it nucEnd() const = 0; virtual int_const_it binBeg() const = 0; virtual int_const_it binEnd() const = 0; }; class ResultMgr : public ResultMgrInterface { private: std::vector seqnmsVec, posVec, binVec, countVec; std::vector strandVec, nucVec; PosCache* posCache; // posCacheCollptrptr is ptr to struct _BAM_FILE's pbuffer ptr PosCacheColl** posCacheCollptrptr; const int min_nuc_depth, min_minor_allele_depth; const bool hasStrands, hasNucleotides, hasBins, isRanged, isBuffered; // lastLeftmostGenPOS is for bookkeeping for buffered pileups; // PosCaches that correspond to completed positions for which // posCache.genomicPosition < minLeftmostGenPOS are completed and, // therefore, ready to be extracted GenomicPosition lastLeftmostGenPOS; // tid + POS // posCachePassesFilters: // postondition: returns true if posCache's object satisfies the // filtering criteria that are applied to completed positions bool posCachePassesFilters(const PosCache& posCachePtr); template void doExtractFromPosCache(); public: // used only in buffered and unbuffered whole file contexts?? virtual void signalGenomicPosStart(const GenomicPosition& genPos); void forwardLastLeftmostGenPOS(const GenomicPosition& genPos); virtual void forwardTuple(BamTuple bTuple); virtual void extractFromPosCache(); template void doExtractFromPosCache(const std::set& nucs); virtual void signalGenomicPosEnd(); virtual int size() const; virtual void printVecs() const; void signalYieldStart(); virtual void signalYieldEnd(); virtual int numYieldablePosCaches() const; virtual void signalEOI(); virtual ~ResultMgr() { // FIX ME: must deallocate posCacheColl only if done with it!!! //delete posCacheColl; //posCacheColl = NULL; } ResultMgr(int min_nuc_depth_, int min_minor_allele_depth_, bool hasStrands_, bool hasNucleotides_, bool hasBins_, bool isRanged_, bool isBuffered_, PosCacheColl** posCacheColl_) : seqnmsVec(), posVec(), binVec(), countVec(), strandVec(), nucVec(), posCache(), posCacheCollptrptr(posCacheColl_), min_nuc_depth(min_nuc_depth_), min_minor_allele_depth(min_minor_allele_depth_), hasStrands(hasStrands_), hasNucleotides(hasNucleotides_), hasBins(hasBins_), isRanged(isRanged_), isBuffered(isBuffered_), lastLeftmostGenPOS(0, 0) { if(isBuffered && *posCacheCollptrptr == NULL) { *posCacheCollptrptr = new PosCacheColl(); } } virtual int_const_it seqnmsBeg() const; virtual int_const_it seqnmsEnd() const; virtual int_const_it posBeg() const; virtual int_const_it posEnd() const; virtual int_const_it binBeg() const; virtual int_const_it binEnd() const; virtual int_const_it countBeg() const; virtual int_const_it countEnd() const; virtual char_const_it strandBeg() const; virtual char_const_it strandEnd() const; virtual char_const_it nucBeg() const; virtual char_const_it nucEnd() const; }; #endif // RESULT_MANAGER_H Rsamtools/src/S4Vectors_stubs.c0000644000175400017540000000003613556116727017606 0ustar00biocbuildbiocbuild#include "_S4Vectors_stubs.c" Rsamtools/src/Template.h0000644000175400017540000002056113624571433016312 0ustar00biocbuildbiocbuild#ifndef TEMPLATE_H #define TEMPLATE_H #include #include #include #include #include #include #include "scan_bam_data.h" using namespace std; class Template { typedef list Segments; typedef Segments::iterator iterator; typedef Segments::const_iterator const_iterator; Segments inprogress, ambiguous, invalid; void add_to_complete(const bam1_t *bam, const bam1_t *mate, queue &complete) { Segments tmp; if (bam->core.flag & BAM_FREAD1) { tmp.push_back(bam); tmp.push_back(mate); } else { tmp.push_back(mate); tmp.push_back(bam); } complete.push(tmp); } public: bool touched; // check readgroup and trimmed_qname bool is_template(const string trimmed_qname, const string m_trimmed_qname, const bam1_t *mate) const { bool test = false; /* read group */ const uint8_t *aux = bam_aux_get(inprogress.front(), "RG"), *m_aux = bam_aux_get(mate, "RG"); const char *rg = (aux == (const uint8_t *) NULL) ? (const char *) NULL : bam_aux2Z(aux), *m_rg = (m_aux == (const uint8_t *) NULL) ? (const char *) NULL : bam_aux2Z(m_aux); if ((aux == NULL && m_aux == NULL) || (aux != NULL && m_aux != NULL && strcmp(rg, m_rg) == 0)) test = true; /* trimmed qname */ return test && trimmed_qname.compare(m_trimmed_qname) == 0; } // is_valid checks the following bit flags: // 1. Bit 0x1 (multiple segments) is 1 // 2. Bit 0x4 (segment unmapped) is 0 // 3. Bit 0x8 (next segment unmapped) is 0 // 4. 'mpos' != -1 (i.e. PNEXT = 0) bool is_valid(const bam1_t *bam) { const bool multi_seg = bam->core.flag & BAM_FPAIRED; const bool seg_unmapped = bam->core.flag & BAM_FUNMAP; const bool mate_unmapped = bam->core.flag & BAM_FMUNMAP; return multi_seg && !seg_unmapped && !mate_unmapped && (bam->core.mpos != -1); } // is_mate checks the following bit flags: // 1. Bit 0x40 and 0x80: Segments are a pair of first/last OR // neither segment is marked first/last // 2. Bit 0x100: Both segments are secondary OR both not secondary // 3. Bit 0x10 and 0x20: Strand flag 0x20 of one mate must match strand // flag 0x10 of the other mate and vice versa // 4. Bit 0x2: Both proper OR both not proper // 5. mpos match: // bit 0x10 of rec1 == bit 0x20 of rec2 AND // bit 0x10 or rec2 == bit 0x20 of rec1 // segment2 mpos matches segment1 pos // 6. tid match bool is_mate(const bam1_t *bam, const bam1_t *mate, const uint32_t *target_len) const { const bool bam_read1 = bam->core.flag & BAM_FREAD1; const bool mate_read1 = mate->core.flag & BAM_FREAD1; const bool bam_read2 = bam->core.flag & BAM_FREAD2; const bool mate_read2 = mate->core.flag & BAM_FREAD2; const bool bam_secondary = bam->core.flag & BAM_FSECONDARY; const bool mate_secondary = mate->core.flag & BAM_FSECONDARY; const bool bam_proper = bam->core.flag & BAM_FPROPER_PAIR; const bool mate_proper = mate->core.flag & BAM_FPROPER_PAIR; const bool bam_rev = bam->core.flag & BAM_FREVERSE; const bool mate_rev = mate->core.flag & BAM_FREVERSE; const bool bam_mrev = bam->core.flag & BAM_FMREVERSE; const bool mate_mrev = mate->core.flag & BAM_FMREVERSE; const bool mapped = (bam->core.tid >= 0) && (bam->core.mtid >= 0) && (mate->core.tid >= 0) && (mate->core.mtid >= 0); if (!mapped) return false; const uint32_t pos = bam->core.pos % target_len[bam->core.tid], mpos = bam->core.mpos % target_len[bam->core.mtid], mate_pos = mate->core.pos % target_len[mate->core.tid], mate_mpos = mate->core.mpos % target_len[mate->core.mtid]; return ((bam_read1 ^ bam_read2) && (mate_read1 ^ mate_read2)) && (bam_read1 != mate_read1) && (bam_secondary == mate_secondary) && (((bam_rev != mate_mrev) && (bam_mrev != mate_rev)) || ((bam_rev == mate_mrev) && (bam_mrev == mate_rev))) && (bam_proper == mate_proper) && (pos == mate_mpos) && (mpos == mate_pos) && (bam->core.mtid == mate->core.tid); } Template() { touched = false; } bool empty() const { return inprogress.empty() && invalid.empty() && ambiguous.empty(); } void touched_true() { touched = true; } bool get_touched() { return touched; } list get_inprogress() { return inprogress; } static const char *qname_trim(char *qname, const char prefix, const char suffix) { char *end = qname + strlen(qname); if (suffix != '\0') for (char *e = end; e >= qname; e--) { if (*e == suffix) { *e = '\0'; end = e; break; } } if (prefix != '\0') for (char *s = qname; *s != '\0'; s++) { if (*s == prefix) { memmove(qname, s + 1, end - s); break; } } return qname; } // Returns true if potential mate, false if invalid bool add_segment(const bam1_t *bam1) { bam1_t *bam = bam_dup1(bam1); if (!is_valid(bam)) { invalid.push_back(bam); return false; } inprogress.push_back(bam); return true; } void mate(queue &complete, const uint32_t *target_len) { const int unmated=-1, multiple=-2, processed=-3; vector > status(inprogress.size(), pair(unmated, (const bam1_t *) NULL)); Segments::iterator it0; // identify unambiguous and ambiguous mates it0 = inprogress.begin(); for (unsigned int i = 0; i < inprogress.size(); ++i) { status[i].second = *it0; Segments::iterator it1 = it0; for (unsigned int j = i + 1; j < inprogress.size(); ++j) { ++it1; if (is_mate(*it0, *it1, target_len)) { status[i].first = status[i].first == unmated ? j : multiple; status[j].first = status[j].first == unmated ? i : multiple; } } ++it0; } // process unambiguous and ambiguous mates for (unsigned int i = 0; i < status.size(); ++i) { if (status[i].first == unmated) continue; if (status[i].first >= 0 && status[status[i].first].first >= 0) { // unambiguous mates add_to_complete(status[i].second, status[status[i].first].second, complete); status[status[i].first].first = processed; status[i].first = processed; } else if (status[i].first != processed) { // ambiguous mates, added to 'ambiguous' queue ambiguous.push_back(status[i].second); status[i].first = processed; } ++it0; } // remove segments that have been assigned to complete or // ambiguous queue it0 = inprogress.begin(); for (unsigned int i = 0; i != status.size(); ++i) { if (status[i].first == processed) { it0 = inprogress.erase(it0); } else { ++it0; } } } // move 'ambiguous' to ambiguous_queue // move 'inprogress' and 'invalid' to 'invalid_queue' void cleanup(queue &ambiguous_queue, queue &invalid_queue) { if (!ambiguous.empty()) ambiguous_queue.push(ambiguous); if (!invalid.empty()) inprogress.splice(inprogress.end(), invalid); if (!inprogress.empty()) { invalid_queue.push(inprogress); inprogress.clear(); } } }; #endif Rsamtools/src/XVector_stubs.c0000644000175400017540000000003413556116727017342 0ustar00biocbuildbiocbuild#include "_XVector_stubs.c" Rsamtools/src/as_bam.c0000644000175400017540000000307713556116727015764 0ustar00biocbuildbiocbuild#include #include "bamfile.h" int _as_bam(samfile_t * fin, samfile_t * fout) { bam1_t *b = bam_init1(); int r, count = 0; while (0 <= (r = samread(fin, b))) { samwrite(fout, b); count++; } bam_destroy1(b); return r >= -1 ? count : -1 * count; } SEXP as_bam(SEXP file, SEXP destination, SEXP binary) { if (!IS_CHARACTER(file) || 1 != LENGTH(file)) Rf_error("'file' must be character(1)"); if (!IS_CHARACTER(destination) || 1 != LENGTH(destination)) Rf_error("'destination' must be character(1)"); if (!IS_LOGICAL(binary) || 1 != LENGTH(binary)) Rf_error("'binary' must be logical(1)"); samfile_t *fin, *fout; if (LOGICAL(binary)[0]) { /* SAM --> BAM */ fin = _bam_tryopen(translateChar(STRING_ELT(file, 0)), "r", NULL); if (fin->header == 0) { samclose(fin); Rf_error("invalid header"); } fout = _bam_tryopen(translateChar(STRING_ELT(destination, 0)), "wb", fin->header); } else { /* BAM --> SAM */ fin = _bam_tryopen(translateChar(STRING_ELT(file, 0)), "rb", NULL); if (fin->header == 0) { samclose(fin); Rf_error("invalid header"); } fout = _bam_tryopen(translateChar(STRING_ELT(destination, 0)), "wh", fin->header); } int count = _as_bam(fin, fout); samclose(fin); samclose(fout); if (count < 0) Rf_error("truncated input file at record %d", -1 * count); return destination; } Rsamtools/src/as_bam.h0000644000175400017540000000025113556116727015760 0ustar00biocbuildbiocbuild#ifndef _AS_BAM_H_ #define _AS_BAM_H_ #include SEXP as_bam(SEXP file, SEXP destination, SEXP binary); #endif /* _AS_BAM_H_ */ Rsamtools/src/bam.c0000644000175400017540000000002113556116727015263 0ustar00biocbuildbiocbuild#include Rsamtools/src/bam_data.c0000644000175400017540000003147113620347571016264 0ustar00biocbuildbiocbuild#include #include #include "bamfile.h" #include "bam_data.h" #include "scan_bam_data.h" #include "utilities.h" #define BAM_PARSE_STATUS_OK 0 static const int BAM_INIT_SIZE = 1048576; enum { CIGAR_SIMPLE = 1 }; /* _BAM_DATA */ static BAM_DATA _Calloc_BAM_DATA(int blocksize, int cigar_buf_sz) { BAM_DATA bd = Calloc(1, _BAM_DATA); bd->BLOCKSIZE = blocksize; bd->cigar_buf_sz = cigar_buf_sz; bd->cigar_buf = Calloc(bd->cigar_buf_sz, char); return bd; } BAM_DATA _init_BAM_DATA(SEXP ext, SEXP regions, SEXP flag, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, int reverseComplement, int yieldSize, int obeyQname, int asMates, char qnamePrefixEnd, char qnameSuffixStart, void *extra) { int nrange = R_NilValue == regions ? 1 : LENGTH(VECTOR_ELT(regions, 0)); BAM_DATA bd = _Calloc_BAM_DATA(1 == nrange ? 5 * BAM_INIT_SIZE : BAM_INIT_SIZE, 32768); bd->parse_status = BAM_PARSE_STATUS_OK; bd->bfile = BAMFILE(ext); bd->irange = bd->bfile->irange0; bd->nrange = nrange; bd->irec = bd->iparsed = 0; bd->keep_flag[0] = INTEGER(flag)[0]; bd->keep_flag[1] = INTEGER(flag)[1]; bd->cigar_flag = LOGICAL(isSimpleCigar)[0]; bd->tagfilter = _tagFilter_as_C_types(tagFilter); int mapqfilter = INTEGER(mapqFilter)[0]; bd->mapqfilter = mapqfilter == NA_INTEGER ? 0 : mapqfilter; /* uint32_t */ bd->reverseComplement = reverseComplement; bd->yieldSize = yieldSize; bd->obeyQname = obeyQname; bd->asMates = asMates; bd->qnamePrefixEnd = qnamePrefixEnd; bd->qnameSuffixStart = qnameSuffixStart; bd->extra = extra; return bd; } void _Free_BAM_DATA(BAM_DATA bd) { _Free_C_TAGFILTER(bd->tagfilter); Free(bd->cigar_buf); Free(bd); } static void _grow_BAM_DATA_cigar(BAM_DATA bd) { bd->cigar_buf_sz = bd->cigar_buf_sz * 1.6; bd->cigar_buf = Realloc(bd->cigar_buf, bd->cigar_buf_sz, char); } BAM_FILE _bam_file_BAM_DATA(BAM_DATA bd) { return bd->bfile; } /* count */ int _count1_BAM_DATA(const bam1_t * bam, BAM_DATA bd) { bd->irec += 1; if (!_filter1_BAM_DATA(bam, bd)) return 0; SEXP cnt = (SEXP) (bd->extra); INTEGER(VECTOR_ELT(cnt, 0))[bd->irange] += 1; REAL(VECTOR_ELT(cnt, 1))[bd->irange] += bam->core.l_qseq; bd->iparsed += 1; return 1; } /* parse helpers */ static char *_bamseq(const bam1_t * bam, BAM_DATA bd) { static const char key[] = { '-', 'A', 'C', 'M', 'G', 'R', 'S', 'V', 'T', 'W', 'Y', 'H', 'K', 'D', 'B', 'N' }; const uint32_t len = bam->core.l_qseq; const unsigned char *seq = bam1_seq(bam); char *s = Calloc(len + 1, char); for (uint32_t i = 0; i < len; ++i) s[i] = key[bam1_seqi(seq, i)]; if (bd->reverseComplement && (bam1_strand(bam) == 1)) _reverseComplement(s, len); s[len] = '\0'; return s; } static char *_bamqual(const bam1_t * bam, BAM_DATA bd) { const uint32_t len = bam->core.l_qseq; const unsigned char *bamq = bam1_qual(bam); char *s = Calloc(len + 1, char); for (uint32_t i = 0; i < len; ++i) s[i] = bamq[i] + 33; if (bd->reverseComplement && (bam1_strand(bam) == 1)) _reverse(s, len); s[len] = '\0'; return s; } static const char *_map(khash_t(str) * h, const char *s) { khiter_t k = kh_get(str, h, s); if (kh_end(h) == k) { int ret; char *buf = Calloc(strlen(s) + 1, char); if (!buf) Rf_error("_map: failed to allocate memory"); strcpy(buf, s); k = kh_put(str, h, buf, &ret); } return kh_key(h, k); } static int _bamcigar(const uint32_t * cigar, const uint32_t n_cigar, char *buf, int buf_sz) { const char lookup[] = BAM_CIGAR_STR; buf[0] = '\0'; for (uint32_t i = 0; i < n_cigar; ++i) { int n = snprintf(buf, buf_sz, "%u%c", cigar[i] >> 4, lookup[cigar[i] & BAM_CIGAR_MASK]); if (n >= buf_sz) return -1; buf += n; buf_sz -= n; } return buf_sz; } static void _tag_type_check(const char *tagname, SEXP tag, SEXPTYPE is) { SEXPTYPE was = TYPEOF(tag); if (was == is) return; error("tag '%s' type is inconsistent; was '%s', is '%s'", tagname, Rf_type2char(was), Rf_type2char(is)); } static SEXP _bamtags_B(uint8_t *s) { uint8_t sub_type = *(s++); int32_t n; memcpy(&n, s, 4); SEXP tag_B = R_NilValue; switch(sub_type) { case 'c': case 'C': case 'i': case 'I': case 's': case 'S': tag_B = NEW_INTEGER(n); PROTECT(tag_B); for (int j = 0; j < n; ++j) INTEGER(tag_B)[j] = NA_INTEGER; break; case 'f': tag_B = NEW_NUMERIC(n); PROTECT(tag_B); for (int j = 0; j < n; ++j) REAL(tag_B)[j] = NA_REAL; break; } s += 4; // now point to the start of the array for (int i = 0; i < n; ++i) { // FIXME: better performance: loop after "if" if ('c' == sub_type || 'C' == sub_type) { INTEGER(tag_B)[i] = (int) (*(uint8_t *) s); ++s; } else if ('s' == sub_type || 'S' == sub_type) { INTEGER(tag_B)[i] = (int) (*(int16_t *) s); s += 2; } else if ('i' == sub_type || 'I' == sub_type) { INTEGER(tag_B)[i] = (int) (*(int32_t *) s); s += 4; } else if ('f' == sub_type) { REAL(tag_B)[i] = *(float *) s; s += 4; } } UNPROTECT(1); return tag_B; } static void _bamtags(const bam1_t * bam, BAM_DATA bd, SEXP tags) { SCAN_BAM_DATA sbd = (SCAN_BAM_DATA) bd->extra; static char buf_A[2]; int idx = sbd->icnt; SEXP nms = GET_ATTR(tags, R_NamesSymbol); buf_A[1] = '\0'; /* strictly necessary only once */ for (int i = 0; i < LENGTH(nms); ++i) { const char *tagname = CHAR(STRING_ELT(nms, i)); uint8_t *aux = bam_aux_get(bam, tagname); if (0 == aux) continue; /* no matching tag found */ SEXP tag = VECTOR_ELT(tags, i); if (R_NilValue == tag) { /* allocate */ int n = sbd->ncnt; switch (aux[0]) { case 'c': case 'C': case 'i': case 'I': case 's': case 'S': tag = NEW_INTEGER(n); for (int j = 0; j < n; ++j) INTEGER(tag)[j] = NA_INTEGER; break; case 'd': case 'f': tag = NEW_NUMERIC(n); for (int j = 0; j < n; ++j) REAL(tag)[j] = NA_REAL; break; case 'A': case 'Z': tag = NEW_CHARACTER(n); for (int j = 0; j < n; ++j) SET_STRING_ELT(tag, j, NA_STRING); break; case 'H': tag = NEW_RAW(n); break; case 'B': tag = NEW_LIST(n); break; default: error("unknown tag type '%c'", aux[0]); break; } SET_VECTOR_ELT(tags, i, tag); } switch (aux[0]) { case 'c': case 'C': case 's': case 'S': case 'i': case 'I': _tag_type_check(tagname, tag, INTSXP); INTEGER(tag)[idx] = bam_aux2i(aux); break; case 'f': case 'd': _tag_type_check(tagname, tag, REALSXP); REAL(tag)[idx] = bam_aux2f(aux); break; case 'A': _tag_type_check(tagname, tag, STRSXP); sprintf(buf_A, "%c", bam_aux2A(aux)); SET_STRING_ELT(tag, idx, mkChar(buf_A)); break; case 'Z': _tag_type_check(tagname, tag, STRSXP); SET_STRING_ELT(tag, idx, mkChar(bam_aux2Z(aux))); break; case 'H': /* FIXME: one byte or many? */ _tag_type_check(tagname, tag, RAWSXP); RAW(tag)[idx] = aux[1]; break; case 'B': _tag_type_check(tagname, tag, VECSXP); SET_VECTOR_ELT(tag, idx, _bamtags_B(&aux[1])); break; default: error("unknown tag type '%c'", aux[0]); break; } } } /* parse */ int _filter1_BAM_DATA(const bam1_t * bam, BAM_DATA bd) { /* tagfilter */ if (bd->tagfilter != NULL && !_tagfilter(bam, bd->tagfilter, bd->irec)) return 0; if (bam->core.qual < bd->mapqfilter) return 0; /* flag : 1101 keep0: 1111 keep1: 1111 test = (keep0 & ~flag) | (keep1 & flag) = 0010 | 1101 = 1111 ~test = 0000 = FALSE flag: 1101 keep0: 1101 keep1: 1111 test = (keep0 & ~flag) | (keep1 & flag) = 0000 | 1101 = 1101 ~test = 0010 = TRUE flag: 1101 keep0: 1111 keep1: 1101 test = (keep0 & ~flag) | (keep1 & flag) = 0010 | 1101 = 1111 ~test = 0000 = FALSE */ uint32_t test = (bd->keep_flag[0] & ~bam->core.flag) | (bd->keep_flag[1] & bam->core.flag); if (~test & 4095u) return 0; uint32_t *cigar = bam1_cigar(bam); uint32_t n_cigar = bam->core.n_cigar; if (bd->cigar_flag == CIGAR_SIMPLE) { if (!(n_cigar == 0 || (n_cigar == 1 && ((cigar[0] & BAM_CIGAR_MASK) == 0)))) return 0; } return 1; } int _filter_and_parse1_BAM_DATA(const bam1_t *bam, BAM_DATA bd) { bd->irec += 1; if (!_filter1_BAM_DATA(bam, bd)) return 0; return _parse1_BAM_DATA(bam, bd); } int _parse1_BAM_DATA(const bam1_t *bam, BAM_DATA bd) { SCAN_BAM_DATA sbd = (SCAN_BAM_DATA) bd->extra; SEXP r = _get_or_grow_SCAN_BAM_DATA(bd, -1), s; int idx = sbd->icnt; char *buf; for (int i = 0; i < LENGTH(r); ++i) { if (R_NilValue == (s = VECTOR_ELT(r, i))) continue; switch (i) { case QNAME_IDX: buf = Calloc(strlen(bam1_qname(bam)) + 1, char); if (!buf) Rf_error("_parse1: failed to allocate memory"); strcpy(buf, bam1_qname(bam)); sbd->qname[idx] = buf; break; case FLAG_IDX: sbd->flag[idx] = bam->core.flag; break; case RNAME_IDX: sbd->rname[idx] = bam->core.tid < 0 ? NA_INTEGER : bam->core.tid + 1; break; case STRAND_IDX: sbd->strand[idx] = bam->core.flag & BAM_FUNMAP ? NA_INTEGER : (bam1_strand(bam) + 1); break; case POS_IDX: sbd->pos[idx] = (bam->core.tid < 0 || (bam->core.flag & BAM_FUNMAP)) ? NA_INTEGER : bam->core.pos + 1; break; case QWIDTH_IDX: sbd->qwidth[idx] = bam->core.flag & BAM_FUNMAP ? NA_INTEGER : bam_cigar2qlen(&bam->core, bam1_cigar(bam)); break; case MAPQ_IDX: if ((bam->core.flag & BAM_FUNMAP)) sbd->mapq[idx] = NA_INTEGER; else sbd->mapq[idx] = bam->core.qual; break; case CIGAR_IDX: if (bam->core.tid < 0 || (bam->core.flag & BAM_FUNMAP)) sbd->cigar[idx] = NULL; else { while (_bamcigar(bam1_cigar(bam), bam->core.n_cigar, bd->cigar_buf, bd->cigar_buf_sz) < 0) _grow_BAM_DATA_cigar(bd); sbd->cigar[idx] = _map(sbd->cigarhash, bd->cigar_buf); } break; case MRNM_IDX: sbd->mrnm[idx] = bam->core.mtid < 0 ? NA_INTEGER : bam->core.mtid + 1; break; case MPOS_IDX: sbd->mpos[idx] = (bam->core.mtid < 0 || (bam->core.flag & BAM_FMUNMAP)) ? NA_INTEGER : bam->core.mpos + 1; break; case ISIZE_IDX: sbd->isize[idx] = bam->core.flag & (BAM_FUNMAP | BAM_FMUNMAP) ? NA_INTEGER : bam->core.isize; break; case SEQ_IDX: sbd->seq[idx] = _bamseq(bam, bd); break; case QUAL_IDX: sbd->qual[idx] = _bamqual(bam, bd); break; case TAG_IDX: _bamtags(bam, bd, s); break; case PARTITION_IDX: sbd->partition[idx] = sbd->partition_id; break; case MATES_IDX: sbd->mates[idx] = sbd->mates_flag; break; default: Rf_error("[Rsamtools internal]: unhandled _parse1"); break; } } sbd->icnt += 1; bd->iparsed += 1; return 1; } void _finish1range_BAM_DATA(BAM_DATA bd) { bam_header_t *header = _bam_file_BAM_DATA(bd)->file->header; SCAN_BAM_DATA sbd = (SCAN_BAM_DATA) bd->extra; _finish1range_SCAN_BAM_DATA(sbd, header, bd->irange); } Rsamtools/src/bam_data.h0000644000175400017540000000320513556116727016270 0ustar00biocbuildbiocbuild#ifndef BAM_DATA_H #define BAM_DATA_H #include "Rdefines.h" #include "bamfile.h" #include "tagfilter.h" #ifdef __cplusplus extern "C" { #endif typedef char * (*bam_qname_f)(const bam1_t *bam, char qname_prefix, char qname_suffix); typedef struct { int BLOCKSIZE; /* size to grow vectors */ char *cigar_buf; /* string representation of CIGAR */ uint32_t cigar_buf_sz; int parse_status; BAM_FILE bfile; int irec, iparsed, irange, nrange; uint32_t keep_flag[2], cigar_flag; int reverseComplement, yieldSize, obeyQname, asMates; char qnamePrefixEnd, qnameSuffixStart; C_TAGFILTER tagfilter; uint32_t mapqfilter; void *extra; } _BAM_DATA, *BAM_DATA; enum { QNAME_IDX = 0, FLAG_IDX, RNAME_IDX, STRAND_IDX, POS_IDX, QWIDTH_IDX, MAPQ_IDX, CIGAR_IDX, MRNM_IDX, MPOS_IDX, ISIZE_IDX, SEQ_IDX, QUAL_IDX, TAG_IDX, PARTITION_IDX, MATES_IDX }; BAM_DATA _init_BAM_DATA(SEXP ext, SEXP regions, SEXP flag, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, int reverseComplement, int yieldSize, int obeyQname, int asMates, char qnamePrefixEnd, char qnameSuffixStart, void *extra); void _Free_BAM_DATA(BAM_DATA bd); BAM_FILE _bam_file_BAM_DATA(BAM_DATA bd); int _count1_BAM_DATA(const bam1_t *bam, BAM_DATA bd); int _filter_and_parse1_BAM_DATA(const bam1_t *bam, BAM_DATA bd); int _filter1_BAM_DATA(const bam1_t *bam, BAM_DATA bd); int _parse1_BAM_DATA(const bam1_t *bam, BAM_DATA bd); void _finish1range_BAM_DATA(BAM_DATA bd); #ifdef __cplusplus } #endif #endif Rsamtools/src/bam_mate_iter.cpp0000644000175400017540000000600713556116727017666 0ustar00biocbuildbiocbuild#include #include "BamRangeIterator.h" #include "BamFileIterator.h" #include "bam_mate_iter.h" #ifdef __cplusplus extern "C" { #endif struct _bam_mate_iter_t { BamIterator *b_iter; }; // BamIterator methods void bam_mate_iter_destroy(bam_mate_iter_t iter) { delete iter->b_iter; Free(iter); } bam_mates_t *bam_mates_new() { bam_mates_t *mates = Calloc(1, bam_mates_t); mates->n = 0; mates->mated = MATE_UNKNOWN; mates->bams = (const bam1_t **) NULL; return mates; } void bam_mates_realloc(bam_mates_t *result, int n, MATE_STATUS mated) { for (int i = 0; i < result->n; ++i) { bam_destroy1((bam1_t *) result->bams[i]); result->bams[i] = (const bam1_t *) NULL; } // Realloc(p, 0, *) fails inappropriately if (n == 0) { Free(result->bams); result->bams = (const bam1_t **) NULL; } else { result->bams = Realloc(result->bams, n, const bam1_t *); } result->n = n; result->mated = mated; } void bam_mates_destroy(bam_mates_t *mates) { for (int i = 0; i < mates->n; ++i) bam_destroy1((bam1_t *) mates->bams[i]); Free(mates->bams); Free(mates); } int bam_mate_read(bamFile fb, bam_mate_iter_t iter, bam_mates_t *mates) { iter->b_iter->yield(fb, mates); return mates->n; } // BamRangeIterator methods bam_mate_iter_t bam_mate_range_iter_new(bamFile bfile, const bam_index_t *bindex, int tid, int beg, int end) { bam_mate_iter_t iter = Calloc(1, struct _bam_mate_iter_t); iter->b_iter = new BamRangeIterator(bfile, bindex, tid, beg, end); return iter; } int bam_fetch_mate(bamFile bf, const bam_index_t *idx, int tid, int beg, int end, void *data, bam_fetch_mate_f func) { BAM_DATA bd = (BAM_DATA) data; int n_rec; bam_mates_t *mates = bam_mates_new(); bam_mate_iter_t iter = bam_mate_range_iter_new(bf, idx, tid, beg, end); iter->b_iter->set_bam_data(bd); while ((n_rec = bam_mate_read(bf, iter, mates) > 0)) func(mates, data); bam_mate_iter_destroy(iter); bam_mates_destroy(mates); return n_rec; } // BamFileIterator methods bam_mate_iter_t bam_mate_file_iter_new(bamFile bfile, const bam_index_t *bindex) { bam_mate_iter_t iter = Calloc(1, struct _bam_mate_iter_t); iter->b_iter = new BamFileIterator(bfile, bindex); return iter; } int samread_mate(bamFile bfile, const bam_index_t *bindex, bam_mate_iter_t *iter_p, bam_mates_t *mates, void *data) { BAM_DATA bd = (BAM_DATA) data; bam_mate_iter_t iter; int status; if ((bam_mate_iter_t) NULL == *iter_p) *iter_p = bam_mate_file_iter_new(bfile, bindex); iter = *iter_p; iter->b_iter->set_bam_data(bd); iter->b_iter->iter_done = false; // single yield status = bam_mate_read(bfile, iter, mates); iter->b_iter->set_bam_data((BAM_DATA) NULL); return status; } #ifdef __cplusplus } #endif Rsamtools/src/bam_mate_iter.h0000644000175400017540000000163613556116727017336 0ustar00biocbuildbiocbuild#ifndef BAM_MATE_ITER_H #define BAM_MATE_ITER_H #include #ifdef __cplusplus extern "C" { #endif typedef enum { MATE_UNKNOWN, MATE_MATED, MATE_AMBIGUOUS, MATE_UNMATED } MATE_STATUS; typedef struct _bam_mate_iter_t *bam_mate_iter_t; typedef struct { const bam1_t **bams; int n; MATE_STATUS mated; } bam_mates_t; typedef int (*bam_fetch_mate_f)(const bam_mates_t *b, void *data); bam_mates_t *bam_mates_new(); void bam_mates_realloc(bam_mates_t *mates, int n, MATE_STATUS mated); void bam_mates_destroy(bam_mates_t *mates); int bam_fetch_mate(bamFile fb, const bam_index_t *idx, int tid, int beg, int end, void *data, bam_fetch_mate_f func); int samread_mate(bamFile fb, const bam_index_t *bindex, bam_mate_iter_t *iter_p, bam_mates_t *mates, void *data); void bam_mate_iter_destroy(bam_mate_iter_t iter); #ifdef __cplusplus } #endif #endif Rsamtools/src/bam_plbuf.c0000644000175400017540000000002713556116727016461 0ustar00biocbuildbiocbuild#include Rsamtools/src/bam_sort.c0000644000175400017540000000002613556116727016337 0ustar00biocbuildbiocbuild#include Rsamtools/src/bambuffer.c0000644000175400017540000001214713556116727016471 0ustar00biocbuildbiocbuild#include "Rdefines.h" #include "bamfile.h" #include "bambuffer.h" #include "bam_data.h" #include "scan_bam_data.h" #include "utilities.h" #include "io_sam.h" /* _bam_check_template_list */ static SEXP BAMBUFFER_TAG = NULL; BAM_BUFFER bambuffer_new(int n, int as_mates) { BAM_BUFFER buf = Calloc(1, _BAM_BUFFER); buf->i = 0; buf->n = n; buf->buffer = Calloc(n, bam1_t *); if (as_mates) { buf->as_mates = TRUE; buf->mates = Calloc(n, int); buf->partition = Calloc(n, int); } return buf; } void bambuffer_push(BAM_BUFFER buf, const bam1_t *bam) { if (buf->i == buf->n) { buf->n *= 1.3; buf->buffer = Realloc(buf->buffer, buf->n, bam1_t *); if (buf->as_mates) { buf->mates = Realloc(buf->mates, buf->n, int); buf->partition = Realloc(buf->partition, buf->n, int); } } buf->buffer[buf->i] = bam_dup1(bam); if (buf->as_mates) { buf->mates[buf->i] = buf->mate_flag; buf->partition[buf->i] = buf->partition_id; } buf->i += 1; } void _bambuffer_reset(BAM_BUFFER buf) { for (int i = 0; i < buf->i; ++i) bam_destroy1(buf->buffer[i]); buf->i = 0; } void bambuffer_free(BAM_BUFFER buf) { _bambuffer_reset(buf); Free(buf->buffer); if (buf->as_mates) { Free(buf->mates); Free(buf->partition); } Free(buf); } static void _bambuffer_finalizer(SEXP ext) { if (NULL == R_ExternalPtrAddr(ext)) return; BAM_BUFFER buf = BAMBUFFER(ext); bambuffer_free(buf); R_SetExternalPtrAddr(ext, NULL); } /* SEXP interface */ SEXP bambuffer_init() { BAMBUFFER_TAG = install("BamBuffer"); return R_NilValue; } SEXP bambuffer(int yieldSize, int as_mates) { BAM_BUFFER buf = bambuffer_new(yieldSize, as_mates); SEXP ext = PROTECT(R_MakeExternalPtr(buf, BAMBUFFER_TAG, R_NilValue)); R_RegisterCFinalizerEx(ext, _bambuffer_finalizer, TRUE); UNPROTECT(1); return ext; } SEXP bambuffer_length(SEXP bufext) { _checkext(bufext, BAMBUFFER_TAG, "bamBuffer 'parse'"); return ScalarInteger(BAMBUFFER(bufext)->i); } SEXP bambuffer_parse(SEXP ext, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP bufext, SEXP reverseComplement, SEXP templateList) { _check_isbamfile(ext, "bamBuffer, 'parse'"); _checkparams(regions, keepFlags, isSimpleCigar); _checkext(bufext, BAMBUFFER_TAG, "bamBuffer 'parse'"); if (!(IS_LOGICAL(reverseComplement) && (1L == LENGTH(reverseComplement)))) Rf_error("'reverseComplement' must be logical(1)"); _bam_check_template_list(templateList); SEXP names = GET_ATTR(templateList, R_NamesSymbol); SEXP result = PROTECT(_scan_bam_result_init(templateList, names, R_NilValue, BAMFILE(ext))); SCAN_BAM_DATA sbd = _init_SCAN_BAM_DATA(result); BAM_DATA bd = _init_BAM_DATA(ext, R_NilValue, keepFlags, isSimpleCigar, tagFilter, mapqFilter, LOGICAL(reverseComplement)[0], NA_INTEGER, 0, 0, '\0', '\0', (void *) sbd); bd->irange = 0; /* everything parsed to 'irange' 0 */ BAM_BUFFER buf = BAMBUFFER(bufext); _grow_SCAN_BAM_DATA(bd, buf->n); for (int i = 0; i < buf->i; ++i) { if (buf->as_mates) { sbd->mates_flag = buf->mates[i]; sbd->partition_id = buf->partition[i]; } int result = _parse1_BAM_DATA(buf->buffer[i], bd); if (result < 0) { /* parse error: e.g., cigar buffer overflow */ _grow_SCAN_BAM_DATA(bd, 0); bd->iparsed = -1; break; } else if (result == 0L) /* does not pass filter */ continue; } int status = bd->iparsed; if (status >= 0) { _finish1range_BAM_DATA(bd); status = bd->iparsed; } if (status < 0) { result = R_NilValue; _Free_BAM_DATA(bd); UNPROTECT(1); Rf_error("bamBuffer 'parse' error code: %d", status); } _Free_SCAN_BAM_DATA(sbd); _Free_BAM_DATA(bd); UNPROTECT(1); return result; } SEXP bambuffer_write(SEXP bufext, SEXP bamext, SEXP filter) { BAM_BUFFER buf; BAM_FILE bfile; int n, status, filt_n; _checkext(bufext, BAMBUFFER_TAG, "bamBuffer 'write'"); buf = BAMBUFFER(bufext); filt_n = Rf_length(filter); if ((!IS_LOGICAL(filter)) || !((filt_n == buf->i) || filt_n == 1)) Rf_error("'filterBam' expected logical(1) or logical(%d)", buf->i); _check_isbamfile(bamext, "bamBuffer, 'write'"); bfile = BAMFILE(bamext); n = buf->i; for (int i = 0; i < n; ++i) if (LOGICAL(filter)[i % filt_n]) { status = samwrite(bfile->file, buf->buffer[i]); if (status <= 0) Rf_error("'bamBuffer' write failed, record %d", i); } return ScalarInteger(n); } SEXP bambuffer_reset(SEXP bufext) { _checkext(bufext, BAMBUFFER_TAG, "bamBuffer 'reset'"); BAM_BUFFER buf = BAMBUFFER(bufext); _bambuffer_reset(buf); return ScalarLogical(TRUE); } Rsamtools/src/bambuffer.h0000644000175400017540000000152213556116727016471 0ustar00biocbuildbiocbuild#ifndef BAMBUFFER_H #define BAMBUFFER_H #include #include typedef struct { bam1_t **buffer; int *mates, *partition; int i, n, as_mates, mate_flag, partition_id; } _BAM_BUFFER, *BAM_BUFFER; #define BAMBUFFER(b) ((BAM_BUFFER) R_ExternalPtrAddr(b)) SEXP bambuffer_init(); SEXP bambuffer(int yieldSize, int as_mates); SEXP bambuffer_length(SEXP bufext); SEXP bambuffer_parse(SEXP bamext, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP bufext, SEXP reverseComplement, SEXP template_list); SEXP bambuffer_write(SEXP bufext, SEXP bamext, SEXP filter); SEXP bambuffer_reset(SEXP bufext); BAM_BUFFER bambuffer_new(int n, int as_mates); void bambuffer_push(BAM_BUFFER buf, const bam1_t *bam); void bambuffer_free(BAM_BUFFER buf); #endif Rsamtools/src/bamfile.c0000644000175400017540000002060113556116727016131 0ustar00biocbuildbiocbuild#include "bamfile.h" #include "io_sam.h" #include "bam_mate_iter.h" #include "utilities.h" SEXP BAMFILE_TAG = NULL; void _check_isbamfile(SEXP ext, const char *lbl) { _checkext(ext, BAMFILE_TAG, lbl); } samfile_t *_bam_tryopen(const char *filename, const char *filemode, void *aux) { samfile_t *sfile = samopen(filename, filemode, aux); if (sfile == 0) Rf_error("failed to open SAM/BAM file\n file: '%s'", filename); if (sfile->header == 0 || sfile->header->n_targets == 0) { samclose(sfile); Rf_error("SAM/BAM header missing or empty\n file: '%s'", filename); } return sfile; } static bam_index_t *_bam_tryindexload(const char *file, const char *indexname) { bam_index_t *index = bam_index_load(indexname); if (index == 0) index = hts_idx_load2(file, indexname); if (index == 0) Rf_error("failed to load BAM index\n file: %s", indexname); return index; } static void _bamfile_close(SEXP ext) { BAM_FILE bfile = BAMFILE(ext); if (NULL != bfile->file) samclose(bfile->file); if (NULL != bfile->index) bam_index_destroy(bfile->index); if (NULL != bfile->iter) bam_mate_iter_destroy(bfile->iter); if (NULL != bfile->pbuffer) pileup_pbuffer_destroy(bfile->pbuffer); bfile->file = NULL; bfile->index = NULL; bfile->iter = NULL; bfile->pbuffer = NULL; } static void _bamfile_finalizer(SEXP ext) { if (NULL == R_ExternalPtrAddr(ext)) return; _bamfile_close(ext); BAM_FILE bfile = BAMFILE(ext); Free(bfile); R_SetExternalPtrAddr(ext, NULL); } SEXP bamfile_init() { BAMFILE_TAG = install("BamFile"); return R_NilValue; } static BAM_FILE _bamfile_open_r(SEXP filename, SEXP indexname, SEXP filemode) { BAM_FILE bfile = (BAM_FILE) Calloc(1, _BAM_FILE); bfile->file = NULL; const char *cfile; if (0 != Rf_length(filename)) { cfile = translateChar(STRING_ELT(filename, 0)); bfile->file = _bam_tryopen(cfile, CHAR(STRING_ELT(filemode, 0)), 0); if (hts_get_format(bfile->file->file)->format != bam) { samclose(bfile->file); Free(bfile); Rf_error("'filename' is not a BAM file\n file: %s", cfile); } bfile->pos0 = bam_tell(bfile->file->x.bam); bfile->irange0 = 0; } bfile->index = NULL; if (0 != Rf_length(indexname)) { const char *cindex = translateChar(STRING_ELT(indexname, 0)); bfile->index = _bam_tryindexload(cfile, cindex); if (NULL == bfile->index) { samclose(bfile->file); Free(bfile); Rf_error("failed to open BAM index\n index: %s\n", cindex); } } bfile->iter = NULL; bfile->pbuffer = NULL; return bfile; } static BAM_FILE _bamfile_open_w(SEXP file0, SEXP file1) { samfile_t *infile, *outfile; BAM_FILE bfile; if (0 == Rf_length(file1)) Rf_error("'file1' must be a character(1) path to a valid bam file"); infile = _bam_tryopen(translateChar(STRING_ELT(file1, 0)), "rb", 0); outfile = _bam_tryopen(translateChar(STRING_ELT(file0, 0)), "wb", infile->header); samclose(infile); bfile = (BAM_FILE) Calloc(1, _BAM_FILE); bfile->file = outfile; bfile->pos0 = bam_tell(bfile->file->x.bam); bfile->irange0 = 0; return bfile; } SEXP bamfile_open(SEXP file0, SEXP file1, SEXP mode) { _checknames(file0, file1, mode); BAM_FILE bfile; if (*CHAR(STRING_ELT(mode, 0)) == 'r') bfile = _bamfile_open_r(file0, file1, mode); else bfile = _bamfile_open_w(file0, file1); SEXP ext = PROTECT(R_MakeExternalPtr(bfile, BAMFILE_TAG, file0)); R_RegisterCFinalizerEx(ext, _bamfile_finalizer, TRUE); UNPROTECT(1); return ext; } SEXP bamfile_close(SEXP ext) { _checkext(ext, BAMFILE_TAG, "close"); _bamfile_close(ext); return ext; } SEXP bamfile_isopen(SEXP ext) { int ans = FALSE; if (NULL != BAMFILE(ext)) { _checkext(ext, BAMFILE_TAG, "isOpen"); ans = NULL != BAMFILE(ext)->file; } return ScalarLogical(ans); } SEXP bamfile_isincomplete(SEXP ext) { int ans = FALSE; BAM_FILE bfile; if (NULL != BAMFILE(ext)) { _checkext(ext, BAMFILE_TAG, "isIncomplete"); bfile = BAMFILE(ext); if (NULL != bfile && NULL != bfile->file) { /* heuristic: can we read a record? bgzf_seek does not * support SEEK_END */ off_t offset = bgzf_tell(bfile->file->x.bam); char buf; ans = bgzf_read(bfile->file->x.bam, &buf, 1) > 0; bgzf_seek(bfile->file->x.bam, offset, SEEK_SET); } } return ScalarLogical(ans); } /* implementation */ SEXP read_bamfile_header(SEXP ext, SEXP what) { _checkext(ext, BAMFILE_TAG, "scanBamHeader"); if (!(IS_LOGICAL(what) && (2L == LENGTH(what)))) Rf_error("'what' must be logical(2)"); if (!LOGICAL(bamfile_isopen(ext))[0]) Rf_error("open() BamFile before reading header"); return _read_bam_header(ext, what); } SEXP scan_bamfile(SEXP ext, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP reverseComplement, SEXP yieldSize, SEXP template_list, SEXP obeyQname, SEXP asMates, SEXP qnamePrefixEnd, SEXP qnameSuffixStart) { _checkext(ext, BAMFILE_TAG, "scanBam"); _checkparams(regions, keepFlags, isSimpleCigar); if (!(IS_LOGICAL(reverseComplement) && (1L == LENGTH(reverseComplement)))) Rf_error("'reverseComplement' must be logical(1)"); if (!(IS_INTEGER(yieldSize) && (1L == LENGTH(yieldSize)))) Rf_error("'yieldSize' must be integer(1)"); if (!(IS_LOGICAL(obeyQname) && (1L == LENGTH(obeyQname)))) Rf_error("'obeyQname' must be logical(1)"); if (!(IS_LOGICAL(asMates) && (1L == LENGTH(asMates)))) Rf_error("'asMates' must be logical(1)"); _bam_check_template_list(template_list); return _scan_bam(ext, regions, keepFlags, isSimpleCigar, tagFilter, mapqFilter, reverseComplement, yieldSize, template_list, obeyQname, asMates, qnamePrefixEnd, qnameSuffixStart); } SEXP count_bamfile(SEXP ext, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter) { _checkext(ext, BAMFILE_TAG, "countBam"); _checkparams(regions, keepFlags, isSimpleCigar); SEXP count = _count_bam(ext, regions, keepFlags, isSimpleCigar, tagFilter, mapqFilter); if (R_NilValue == count) Rf_error("'countBam' failed"); return count; } SEXP prefilter_bamfile(SEXP ext, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP yieldSize, SEXP obeyQname, SEXP asMates, SEXP qnamePrefixEnd, SEXP qnameSuffixStart) { _checkext(ext, BAMFILE_TAG, "filterBam"); _checkparams(regions, keepFlags, isSimpleCigar); if (!(IS_INTEGER(yieldSize) && (1L == LENGTH(yieldSize)))) Rf_error("'yieldSize' must be integer(1)"); if (!(IS_LOGICAL(obeyQname) && (1L == LENGTH(obeyQname)))) Rf_error("'obeyQname' must be logical(1)"); if (!(IS_LOGICAL(asMates) && (1L == LENGTH(asMates)))) Rf_error("'asMates' must be logical(1)"); SEXP result = _prefilter_bam(ext, regions, keepFlags, isSimpleCigar, tagFilter, mapqFilter, yieldSize, obeyQname, asMates, qnamePrefixEnd, qnameSuffixStart); if (R_NilValue == result) Rf_error("'filterBam' failed during pre-filtering"); return result; } SEXP filter_bamfile(SEXP ext, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP fout_name, SEXP fout_mode) { _checkext(ext, BAMFILE_TAG, "filterBam"); _checkparams(regions, keepFlags, isSimpleCigar); if (!IS_CHARACTER(fout_name) || 1 != LENGTH(fout_name)) Rf_error("'fout_name' must be character(1)"); if (!IS_CHARACTER(fout_mode) || 1 != LENGTH(fout_mode)) Rf_error("'fout_mode' must be character(1)"); SEXP result = _filter_bam(ext, regions, keepFlags, isSimpleCigar, tagFilter, mapqFilter, fout_name, fout_mode); if (R_NilValue == result) Rf_error("'filterBam' failed"); return result; } Rsamtools/src/bamfile.h0000644000175400017540000000327513556116727016146 0ustar00biocbuildbiocbuild#ifndef BAMFILE_H #define BAMFILE_H #include #include #include "bambuffer.h" #include "bam_mate_iter.h" #include "pbuffer_wrapper.h" #ifdef __cplusplus extern "C" { #endif typedef struct { samfile_t *file; bam_index_t *index; uint64_t pos0; int irange0; bam_mate_iter_t iter; void *pbuffer; /* for buffered pileup */ } _BAM_FILE, *BAM_FILE; #define BAMFILE(b) ((BAM_FILE) R_ExternalPtrAddr(b)) SEXP bamfile_init(); SEXP bamfile_open(SEXP file0, SEXP file1, SEXP mode); SEXP bamfile_close(SEXP ext); SEXP bamfile_isopen(SEXP ext); SEXP bamfile_isincomplete(SEXP ext); SEXP read_bamfile_header(SEXP ext, SEXP what); SEXP scan_bamfile(SEXP ext, SEXP regions, SEXP keepFlags, SEXP simpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP reverseComplement, SEXP yieldSize, SEXP tmpl, SEXP obeyQname, SEXP asMates, SEXP qnamePrefix, SEXP qnameSuffix); SEXP count_bamfile(SEXP ext, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter); SEXP prefilter_bamfile(SEXP ext, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP yieldSize, SEXP obeyQname, SEXP asMates, SEXP qnamePrefix, SEXP qnameSuffix); SEXP filter_bamfile(SEXP ext, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP fout_name, SEXP fout_mode); void _check_isbamfile(SEXP ext, const char *lbl); samfile_t *_bam_tryopen(const char *filename, const char *mode, void *aux); #ifdef __cplusplus } #endif #endif Rsamtools/src/bcffile.c0000644000175400017540000006322713556116727016137 0ustar00biocbuildbiocbuild#include #include #include #include #include #include #include #include #include "bcffile.h" #include "COMPAT_bcf_hdr_read.h" #include "utilities.h" enum { BCF_HDR_REF = 0, BCF_HDR_SAMPLE, BCF_HDR_HEADER, BCF_HDR_LAST }; static const char *BCF_HDR_NM[] = { "Reference", "Sample", "Header" }; enum { BCF_TID = 0, BCF_POS, BCF_ID, BCF_REF, BCF_ALT, BCF_QUAL, BCF_FLT, BCF_INFO, BCF_FMT, BCF_GENO, BCF_RECS_PER_RANGE, BCF_LAST }; enum { BCF_TYPE_Integer = 1, BCF_TYPE_Float, BCF_TYPE_Character, BCF_TYPE_String, BCF_TYPE_Flag, BCF_TYPE_Last }; static SEXP BCFFILE_TAG = NULL; static const int BCF_BUFSIZE_GROW = 100000; /* initial # records */ static int _hts_rewind(htsFile *file) { int64_t ret = file->is_bgzf ? bgzf_seek(file->fp.bgzf, 0, SEEK_SET) : hseek(file->fp.hfile, 0, SEEK_SET); return ret >= 0 ? 0 : -1; } /* This thin wrapper to bcf_close() is always called with errmsg=0 so is not needed. */ static void _bcf_close(htsFile *file, int errmsg) { int err = bcf_close(file); if ((err != 0) && errmsg) Rf_error("_bcf_close error (%d)", err); return; } static void _bcffile_close(SEXP ext) { _BCF_FILE *bfile = BCFFILE(ext); if (bfile->index != NULL) { hts_idx_destroy(bfile->index); bfile->index = NULL; } if (bfile->file != NULL) { _bcf_close(bfile->file, 0); bfile->file = NULL; } return; } static void _bcffile_finalizer(SEXP ext) { if (R_ExternalPtrAddr(ext) == NULL) return; _bcffile_close(ext); _BCF_FILE *bfile = BCFFILE(ext); Free(bfile); R_SetExternalPtrAddr(ext, NULL); } /* --- .Call ENTRY POINT --- */ SEXP bcffile_init() { BCFFILE_TAG = install("BcfFile"); return R_NilValue; } /* --- .Call ENTRY POINT --- */ /* SEXP bcffile_open(SEXP filename, SEXP indexname, SEXP filemode) { _checknames(filename, indexname, filemode); _BCF_FILE *bfile = Calloc(1, _BCF_FILE); bfile->file = NULL; bfile->index = NULL; if (LENGTH(filename) != 0) { const char *fn = translateChar(STRING_ELT(filename, 0)); bfile->file = bcf_open(fn, CHAR(STRING_ELT(filemode, 0))); if (bfile->file == NULL) { Free(bfile); Rf_error("'open' BCF failed\n filename: %s", fn); } if (LENGTH(indexname) != 0) { const char *fnidx = translateChar(STRING_ELT(indexname, 0)); bfile->index = bcf_index_load2(fn, fnidx); if (bfile->index == NULL) { _bcf_close(bfile->file, 0); Free(bfile); Rf_error("'load' BCF index failed\n indexname: %s\n", fnidx); } } } SEXP ext = PROTECT(R_MakeExternalPtr(bfile, BCFFILE_TAG, filename)); R_RegisterCFinalizerEx(ext, _bcffile_finalizer, TRUE); UNPROTECT(1); return ext; } */ static const char *_find_index(const char *fn) { static char fnidx2[999]; const char *fnidx = hts_idx_getfn(fn, ".csi"); if (fnidx == NULL) { fnidx = hts_idx_getfn(fn, ".tbi"); if (fnidx == NULL) return NULL; } int size = snprintf(fnidx2, sizeof(fnidx2), "%s", fnidx); if (size >= sizeof(fnidx2)) Rf_error("[internal] fnidx2 string buffer too small"); return fnidx2; } SEXP bcffile_open(SEXP filename, SEXP indexname, SEXP filemode) { _checknames(filename, indexname, filemode); if (LENGTH(filename) != 1) Rf_error("'filename' must have length 1"); _BCF_FILE *bfile = Calloc(1, _BCF_FILE); const char *fn = translateChar(STRING_ELT(filename, 0)); bfile->file = bcf_open(fn, CHAR(STRING_ELT(filemode, 0))); if (bfile->file == NULL) { Free(bfile); Rf_error("'open' VCF/BCF failed\n filename: %s", fn); } bfile->index = NULL; // LENGTH(indexname) will be 0 when scanBcfHeader() is called on a // file path e.g. scanBcfHeader("chr22.vcf.gz") if (LENGTH(indexname) == 1) { const char *cindex = translateChar(STRING_ELT(indexname, 0)); const char *fnidx = _find_index(cindex); if (fnidx == NULL) { _bcf_close(bfile->file, 0); Free(bfile); Rf_error("no VCF/BCF index found\n filename: %s", fn); } bfile->index = bcf_index_load2(fn, fnidx); if (bfile->index == NULL) { _bcf_close(bfile->file, 0); Free(bfile); Rf_error("'open' VCF/BCF index failed\n index file: %s\n", fnidx); } } SEXP ext = PROTECT(R_MakeExternalPtr(bfile, BCFFILE_TAG, filename)); R_RegisterCFinalizerEx(ext, _bcffile_finalizer, TRUE); UNPROTECT(1); return ext; } /* --- .Call ENTRY POINT --- */ SEXP bcffile_close(SEXP ext) { _checkext(ext, BCFFILE_TAG, "close"); _bcffile_close(ext); return ext; } /* --- .Call ENTRY POINT --- */ SEXP bcffile_isopen(SEXP ext) { SEXP ans = ScalarLogical(FALSE); if (BCFFILE(ext) != NULL) { _checkext(ext, BCFFILE_TAG, "isOpen"); if (BCFFILE(ext)->file) ans = ScalarLogical(TRUE); } return ans; } /* --- .Call ENTRY POINT --- */ /* BROKEN? Seems to always return TRUE on an open BCF file! */ SEXP bcffile_isvcf(SEXP ext) { SEXP ans = ScalarLogical(FALSE); if (BCFFILE(ext) != NULL) { _checkext(ext, BCFFILE_TAG, "isVcf"); if (BCFFILE(ext)->file && hts_get_format(BCFFILE(ext)->file)->format == vcf) { ans = ScalarLogical(TRUE); } } return ans; } /* --- .Call ENTRY POINT --- */ SEXP scan_bcf_header(SEXP ext) { _checkext(ext, BCFFILE_TAG, "scanBcfHeader"); htsFile *file = BCFFILE(ext)->file; if (_hts_rewind(file) < 0) Rf_error("[internal] _hts_rewind() failed"); bcf_hdr_t *hdr = COMPAT_bcf_hdr_read(file); if (hdr == NULL) Rf_error("no 'header' line \"#CHROM POS ID...\"?"); SEXP ans = PROTECT(NEW_LIST(BCF_HDR_LAST)); SEXP ans_elt; int i; /* Get reference seqnames from header */ int nseqs, seqname_len; const char **seqnames, *seqname; seqnames = bcf_hdr_seqnames(hdr, &nseqs); SET_VECTOR_ELT(ans, BCF_HDR_REF, NEW_STRING(nseqs)); ans_elt = VECTOR_ELT(ans, BCF_HDR_REF); for (i = 0; i < nseqs; i++) { seqname = seqnames[i]; seqname_len = _delete_trailing_LFs_and_CRs(seqname, -1); SET_STRING_ELT(ans_elt, i, mkCharLen(seqname, seqname_len)); } free(seqnames); /* Get sample names from header */ int nsamples, samplename_len; const char *samplename; nsamples = bcf_hdr_nsamples(hdr); SET_VECTOR_ELT(ans, BCF_HDR_SAMPLE, NEW_STRING(nsamples)); ans_elt = VECTOR_ELT(ans, BCF_HDR_SAMPLE); for (i = 0; i < nsamples; i++) { samplename = hdr->samples[i]; samplename_len = _delete_trailing_LFs_and_CRs(samplename, -1); SET_STRING_ELT(ans_elt, i, mkCharLen(samplename, samplename_len)); } /* Get header lines from header */ SET_VECTOR_ELT(ans, BCF_HDR_HEADER, NEW_STRING(hdr->nhrec)); ans_elt = VECTOR_ELT(ans, BCF_HDR_HEADER); kstring_t str = {0, 0, NULL}; for (i = 0; i < hdr->nhrec; i++) { str.l = 0; bcf_hrec_format(hdr->hrec[i], &str); str.l = _delete_trailing_LFs_and_CRs(str.s, str.l); SET_STRING_ELT(ans_elt, i, mkCharLen(str.s, str.l)); } free(str.s); /* Set names on 'ans' */ SEXP ans_names = NEW_CHARACTER(3); SET_NAMES(ans, ans_names); /* protect */ for (i = 0; i < BCF_HDR_LAST; ++i) SET_STRING_ELT(ans_names, i, mkChar(BCF_HDR_NM[i])); bcf_hdr_destroy(hdr); UNPROTECT(1); return ans; } static int _bcf_ans_grow(SEXP ans, R_len_t sz, int n_smpl) { R_len_t n = sz; if (sz >= 0) n += LENGTH(VECTOR_ELT(ans, BCF_TID)); else n *= -1; for (int i = 0; i < BCF_LAST; ++i) { SEXP elt = VECTOR_ELT(ans, i); switch (i) { case BCF_GENO: for (int i = 0; i < LENGTH(elt); ++i) { SEXP g = VECTOR_ELT(elt, i); SEXP dim = GET_DIM(g); if (R_NilValue == dim) { SET_LENGTH(g, n); SET_VECTOR_ELT(elt, i, g); /* protect */ } else { PROTECT(dim); SET_LENGTH(g, n_smpl * n); SET_VECTOR_ELT(elt, i, g); /* protect */ INTEGER(dim)[0] = n_smpl; INTEGER(dim)[1] = n; SET_DIM(g, dim); UNPROTECT(1); } } break; case BCF_RECS_PER_RANGE: break; default: SET_LENGTH(elt, n); SET_VECTOR_ELT(ans, i, elt); /* protect */ break; } } return n; } /* See vcf_format() in Rhtslib/src/htslib-1.7/vcf.c for how to extract information from a VCF/BCF line represented by a bcf1_t structure. The code of the _get_* functions below comes from vcf_format(). */ static SEXP _get_CHROM(bcf1_t *bcf1, bcf_hdr_t *hdr) { const char *key = hdr->id[BCF_DT_CTG][bcf1->rid].key; return mkChar(key); } static SEXP _get_ID(bcf1_t *bcf1) { if (bcf1->d.id == NULL) return R_NaString; return mkChar(bcf1->d.id); } static SEXP _get_REF(bcf1_t *bcf1) { if (bcf1->n_allele == 0) return R_NaString; return mkChar(bcf1->d.allele[0]); } static SEXP _get_ALT(bcf1_t *bcf1, kstring_t *ksbuf) { ksbuf->l = 0; if (bcf1->n_allele > 1) { for (int i = 1; i < bcf1->n_allele; i++) { if (i > 1) kputc(',', ksbuf); kputs(bcf1->d.allele[i], ksbuf); } } else { kputc('.', ksbuf); } return mkCharLen(ksbuf->s, ksbuf->l); } static SEXP _get_FILTER(bcf1_t *bcf1, bcf_hdr_t *hdr, kstring_t *ksbuf) { ksbuf->l = 0; if (bcf1->d.n_flt > 0) { for (int i = 0; i < bcf1->d.n_flt; i++) { if (i > 0) kputc(';', ksbuf); const char *key = hdr->id[BCF_DT_ID][bcf1->d.flt[i]].key; kputs(key, ksbuf); } } else { kputc('.', ksbuf); } return mkCharLen(ksbuf->s, ksbuf->l); } static SEXP _get_INFO(bcf1_t *bcf1, bcf_hdr_t *hdr, kstring_t *ksbuf) { ksbuf->l = 0; int first = 1; if (bcf1->n_info != 0) { for (int i = 0; i < bcf1->n_info; i++) { bcf_info_t *z = &bcf1->d.info[i]; if (!z->vptr) continue; if (first) { first = 0; } else { kputc(';', ksbuf); } if (z->key >= hdr->n[BCF_DT_ID]) { free(ksbuf->s); bcf_destroy(bcf1); error("Invalid VCF/BCF, the INFO index is too large"); } const char *key = hdr->id[BCF_DT_ID][z->key].key; kputs(key, ksbuf); if (z->len <= 0) continue; kputc('=', ksbuf); if (z->len == 1) { int type = z->type; switch (type) { case BCF_BT_INT8: if (z->v1.i == bcf_int8_missing) kputc('.', ksbuf); else kputw(z->v1.i, ksbuf); break; case BCF_BT_INT16: if (z->v1.i == bcf_int16_missing) kputc('.', ksbuf); else kputw(z->v1.i, ksbuf); break; case BCF_BT_INT32: if (z->v1.i == bcf_int32_missing) kputc('.', ksbuf); else kputw(z->v1.i, ksbuf); break; case BCF_BT_FLOAT: if (bcf_float_is_missing(z->v1.f)) kputc('.', ksbuf); else kputd(z->v1.f, ksbuf); break; case BCF_BT_CHAR: kputc(z->v1.i, ksbuf); break; default: free(ksbuf->s); bcf_destroy(bcf1); error("Unexpected type %d", type); } } else { bcf_fmt_array(ksbuf, z->len, z->type, z->vptr); } } } if (first) kputc('.', ksbuf); return mkCharLen(ksbuf->s, ksbuf->l); } static SEXP _get_FORMAT(bcf1_t *bcf1, bcf_hdr_t *hdr, kstring_t *ksbuf) { ksbuf->l = 0; int first = 1; if (bcf1->n_sample != 0) { int n_fmt = (int) bcf1->n_fmt; if (n_fmt != 0) { for (int i = 0; i < n_fmt; i++) { bcf_fmt_t *fmt = bcf1->d.fmt + i; if (fmt->p == NULL) continue; if (first) { first = 0; } else { kputc(':', ksbuf); } int id = fmt->id; if (id < 0) { free(ksbuf->s); bcf_destroy(bcf1); error("Invalid VCF/BCF: internal FORMAT id %d cannot " "be matched to a FORMAT tag in the header", id); } const char *tag = hdr->id[BCF_DT_ID][id].key; kputs(tag, ksbuf); } } } if (first) kputc('.', ksbuf); return mkCharLen(ksbuf->s, ksbuf->l); } static void _load_int_vector(int *in, int n_sample, const bcf_fmt_t *fmt, const char *tag) { const void *data; int val; if (fmt->n != 1) error("FORMAT tag '%s' has an unexpected " "number of values per sample", tag); for (int j = 0; j < n_sample; j++) { data = fmt->p + j * fmt->size; switch (fmt->type) { case BCF_BT_INT8: val = ((uint8_t *) data)[0]; break; case BCF_BT_INT16: val = ((uint16_t *) data)[0]; break; default: error("FORMAT tag '%s' has an unexpected C type (%d)", tag, fmt->type); } *(in++) = val; } return; } static SEXP _make_int_matrix(int nrow, int n_sample, const bcf_fmt_t *fmt, const char *tag) { const void *data; int val; SEXP ans; if (fmt->n != nrow) error("FORMAT tag '%s' has an unexpected " "number of values per sample", tag); ans = PROTECT(allocMatrix(INTSXP, nrow, n_sample)); for (int j = 0; j < n_sample; j++) { data = fmt->p + j * fmt->size; for (int i = 0; i < nrow; i++) { switch (fmt->type) { case BCF_BT_INT8: val = ((uint8_t *) data)[i]; break; case BCF_BT_INT16: val = ((uint16_t *) data)[i]; break; default: UNPROTECT(1); error("FORMAT tag '%s' has an unexpected C type (%d)", tag, fmt->type); } INTEGER(ans)[j * nrow + i] = val; } } UNPROTECT(1); return ans; } static SEXP _make_double_matrix(int nrow, int n_sample, const bcf_fmt_t *fmt, const char *tag) { const void *data; double val; SEXP ans; if (fmt->n != nrow) error("FORMAT tag '%s' has an unexpected " "number of values per sample", tag); if (fmt->type != BCF_BT_FLOAT) error("FORMAT tag '%s' has an unexpected C type (%d)", tag, fmt->type); ans = PROTECT(allocMatrix(REALSXP, nrow, n_sample)); for (int j = 0; j < n_sample; j++) { data = fmt->p + j * fmt->size; for (int i = 0; i < nrow; i++) { val = ((float *) data)[i]; REAL(ans)[j * nrow + i] = val; } } UNPROTECT(1); return ans; } static void _load_GENO(SEXP geno, const int n, bcf1_t *bcf1, bcf_hdr_t *hdr, kstring_t *ksbuf) { /* FIXME: more flexible geno not supported by bcftools */ int n_fmt = (int) bcf1->n_fmt; if (n_fmt == 0) return; int n_sample = bcf1->n_sample; SEXP geno_names = GET_NAMES(geno); for (int i = 0; i < n_fmt; i++) { /* We don't use the const qualifier here because 'fmt' will later be passed to bcf_format_gt(). Surprisingly, and quite unfortunately, this function (defined in Rhtslib/src/htslib-1.7/htslib/vcf.h) expects a 'bcf_fmt_t *', not a 'const bcf_fmt_t *'. */ //const bcf_fmt_t *fmt = bcf1->d.fmt + i; bcf_fmt_t *fmt = bcf1->d.fmt + i; if (fmt->p == NULL) continue; int id = fmt->id; if (id < 0) { bcf_destroy(bcf1); error("Invalid VCF/BCF: FORMAT tag id=%d not present " "in header", id); } const char *tag = hdr->id[BCF_DT_ID][id].key; int t; for (t = 0; t < LENGTH(geno_names); t++) { const char *nm = CHAR(STRING_ELT(geno_names, t)); if (strcmp(nm, tag) == 0) break; } if (LENGTH(geno_names) <= t) Rf_error("FORMAT tag '%s' not supported yet", tag); SEXP geno_elt = VECTOR_ELT(geno, t); int off = n * n_sample; // could easily overflow! -> FIXME if (strcmp(tag, "PL") == 0) { /* 'geno_elt' is a list of matrices of integers */ const int nrow = bcf1->n_allele * (bcf1->n_allele + 1) / 2; SEXP pl = _make_int_matrix(nrow, n_sample, fmt, tag); SET_VECTOR_ELT(geno_elt, n, pl); // protect } else if (strcmp(tag, "DP") == 0 || strcmp(tag, "GQ") == 0 || strcmp(tag, "SP") == 0) { /* 'geno_elt' is an integer matrix with 1 row per sample */ _load_int_vector(INTEGER(geno_elt) + off, n_sample, fmt, tag); } else if (strcmp(tag, "GT") == 0) { for (int j = 0; j < n_sample; j++) { ksbuf->l = 0; bcf_format_gt(fmt, j, ksbuf); SEXP s = PROTECT(mkChar(ksbuf->s)); SET_STRING_ELT(geno_elt, off++, s); UNPROTECT(1); } } else if (strcmp(tag, "GL") == 0) { /* 'geno_elt' is a list of matrices of doubles */ const int nrow = bcf1->n_allele * (bcf1->n_allele + 1) / 2; SEXP gl = _make_double_matrix(nrow, n_sample, fmt, tag); SET_VECTOR_ELT(geno_elt, n, gl); // protect } } } static void _scan_bcf_line(bcf1_t *bcf1, bcf_hdr_t *hdr, SEXP ans, int n, kstring_t *ksbuf) { bcf_unpack(bcf1, BCF_UN_ALL); SEXP chrom = PROTECT(_get_CHROM(bcf1, hdr)); SET_STRING_ELT(VECTOR_ELT(ans, BCF_TID), n, chrom); UNPROTECT(1); INTEGER(VECTOR_ELT(ans, BCF_POS))[n] = bcf1->pos + 1; SEXP id = PROTECT(_get_ID(bcf1)); SET_STRING_ELT(VECTOR_ELT(ans, BCF_ID), n, id); UNPROTECT(1); SEXP ref = PROTECT(_get_REF(bcf1)); SET_STRING_ELT(VECTOR_ELT(ans, BCF_REF), n, ref); UNPROTECT(1); SEXP alt = PROTECT(_get_ALT(bcf1, ksbuf)); SET_STRING_ELT(VECTOR_ELT(ans, BCF_ALT), n, alt); UNPROTECT(1); REAL(VECTOR_ELT(ans, BCF_QUAL))[n] = bcf1->qual; SEXP filter = PROTECT(_get_FILTER(bcf1, hdr, ksbuf)); SET_STRING_ELT(VECTOR_ELT(ans, BCF_FLT), n, filter); UNPROTECT(1); SEXP info = PROTECT(_get_INFO(bcf1, hdr, ksbuf)); SET_STRING_ELT(VECTOR_ELT(ans, BCF_INFO), n, info); UNPROTECT(1); SEXP format = PROTECT(_get_FORMAT(bcf1, hdr, ksbuf)); SET_STRING_ELT(VECTOR_ELT(ans, BCF_FMT), n, format); UNPROTECT(1); _load_GENO(VECTOR_ELT(ans, BCF_GENO), n, bcf1, hdr, ksbuf); return; } static int _scan_bcf_lines(htsFile *file, bcf_hdr_t *hdr, SEXP ans, int n) { bcf1_t *bcf1 = bcf_init(); /* free'd in bcf_destroy */ if (bcf1 == NULL) Rf_error("_scan_bcf_lines: failed to allocate memory"); int sz = LENGTH(VECTOR_ELT(ans, BCF_TID)); kstring_t ksbuf = {0, 0, NULL}; while (bcf_read(file, hdr, bcf1) >= 0) { if (n >= sz) sz = _bcf_ans_grow(ans, BCF_BUFSIZE_GROW, bcf_hdr_nsamples(hdr)); if (n >= sz) { free(ksbuf.s); bcf_destroy(bcf1); Rf_error("_scan_bcf_lines: failed to increase size; out of memory?"); } _scan_bcf_line(bcf1, hdr, ans, n, &ksbuf); ++n; } free(ksbuf.s); bcf_destroy(bcf1); return n; } static int _scan_bcf_region(htsFile *file, bcf_hdr_t *hdr, hts_idx_t *idx, const char *spc, int start, int end, SEXP ans, int n) { int tid = bcf_hdr_name2id(hdr, spc); if (tid == -1) Rf_error("'space' not in file: %s", spc); hts_itr_t *iter = bcf_itr_queryi(idx, tid, start - 1, end); if (iter == NULL) /* invalid 'tid', should never happen */ Rf_error("'space' not in file: %s", spc); bcf1_t *bcf1 = bcf_init(); /* free'd in bcf_destroy */ if (bcf1 == NULL) { bcf_itr_destroy(iter); Rf_error("_scan_bcf_region: failed to allocate memory"); } int sz = LENGTH(VECTOR_ELT(ans, BCF_TID)); kstring_t ksbuf = {0, 0, NULL}; while (bcf_itr_next(file, iter, bcf1) >= 0) { if (n >= sz) sz = _bcf_ans_grow(ans, BCF_BUFSIZE_GROW, bcf_hdr_nsamples(hdr)); if (n >= sz) { if (ksbuf.s != NULL) free(ksbuf.s); bcf_destroy(bcf1); bcf_itr_destroy(iter); Rf_error("_scan_bcf_region: failed to increase size; out of memory?"); } _scan_bcf_line(bcf1, hdr, ans, n, &ksbuf); ++n; } if (ksbuf.s != NULL) free(ksbuf.s); bcf_destroy(bcf1); bcf_itr_destroy(iter); return n; } /* --- .Call ENTRY POINT --- */ SEXP scan_bcf(SEXP ext, SEXP regions, SEXP tmpl) { _checkparams(regions, R_NilValue, R_NilValue); _checkext(ext, BCFFILE_TAG, "scanBcf"); htsFile *file = BCFFILE(ext)->file; if (_hts_rewind(file) < 0) Rf_error("[internal] _hts_rewind() failed"); bcf_hdr_t *hdr = COMPAT_bcf_hdr_read(file); if (NULL == hdr) Rf_error("no 'header' line \"#CHROM POS ID...\"?"); int n = 0; SEXP ans = PROTECT(Rf_duplicate(tmpl)); if (regions == R_NilValue) { SET_VECTOR_ELT(ans, BCF_RECS_PER_RANGE, NEW_INTEGER(1)); n = _scan_bcf_lines(file, hdr, ans, n); INTEGER(VECTOR_ELT(ans, BCF_RECS_PER_RANGE))[0] = n; } else { hts_idx_t *idx = BCFFILE(ext)->index; SEXP space = VECTOR_ELT(regions, 0); const int *start = INTEGER(VECTOR_ELT(regions, 1)), *end = INTEGER(VECTOR_ELT(regions, 2)), nregions = LENGTH(space); SEXP nrec = NEW_INTEGER(nregions); SET_VECTOR_ELT(ans, BCF_RECS_PER_RANGE, nrec); for (int i = 0; i < nregions; ++i) { const char *spc = CHAR(STRING_ELT(space, i)); n = _scan_bcf_region(file, hdr, idx, spc, start[i], end[i], ans, n); if (i == 0) INTEGER(nrec)[i] = n; else INTEGER(nrec)[i] = n - INTEGER(nrec)[i - 1]; } } _bcf_ans_grow(ans, -1 * n, bcf_hdr_nsamples(hdr)); UNPROTECT(1); return ans; } static int _as_bcf(htsFile * fin, const char *dict, htsFile * fout) { bcf1_t *bcf1 = bcf_init(); /* free'd in bcf_destroy */ if (bcf1 == NULL) Rf_error("_as_bcf: failed to allocate memory"); int r, count = 0; Rf_error("asBcf() is temporarily disabled, sorry!"); #ifdef MIGRATE_ME /* Not migrating this code for now. I'm not sure how asBcf() is supposed to be used/called and I couldn't find any example or unit test for it. Also no Bioconductor package seems to use it. */ bcf_hdr_t *hin, *hout; hin = hout = COMPAT_bcf_hdr_read(fin); vcf_dictread(fin, hin, dict); bcf_hdr_write(fout, hout); while ((r = bcf_read(fin, hin, bcf1)) >= 0) { if (NULL == bcf1->ref) Rf_error("cannot (yet) coerce VCF files without FORMAT"); bcf_write(fout, hout, bcf1); count++; } if (hin != hout) bcf_hdr_destroy(hout); bcf_hdr_destroy(hin); bcf_destroy(bcf1); #endif /* MIGRATE_ME */ return r >= -1 ? count : -1 * count; } /* --- .Call ENTRY POINT --- */ SEXP as_bcf(SEXP file, SEXP dictionary, SEXP destination) { if (!IS_CHARACTER(file) || LENGTH(file) != 1) Rf_error("'file' must be character(1)"); if (!IS_CHARACTER(dictionary) || LENGTH(dictionary) != 1) Rf_error("'dictionary' must be character(1)"); if (!IS_CHARACTER(destination) || LENGTH(destination) != 1) Rf_error("'destination' must be character(1)"); htsFile *fin = vcf_open(translateChar(STRING_ELT(file, 0)), "r"); if (fin == NULL) Rf_error("failed to open VCF 'file'"); htsFile *fout = bcf_open(translateChar(STRING_ELT(destination, 0)), "wb"); if (fout == NULL) Rf_error("failed to open BCF 'destination'"); int count = _as_bcf(fin, translateChar(STRING_ELT(dictionary, 0)), fout); _bcf_close(fin, 0); _bcf_close(fout, 0); if (count < 0) Rf_error("truncated input file at record %d", -1 * count); return destination; } /* --- .Call ENTRY POINT --- */ SEXP index_bcf(SEXP file) { if (!IS_CHARACTER(file) || LENGTH(file) != 1) Rf_error("'file' must be character(1)"); const char *fbcf = translateChar(STRING_ELT(file, 0)); int status = bcf_index_build(fbcf, 0); if (status != 0) Rf_error("failed to build index"); char *fidx = (char *) R_alloc(strlen(fbcf) + 5, sizeof(char)); sprintf(fidx, "%s.csi", fbcf); return mkString(fidx); } Rsamtools/src/bcffile.h0000644000175400017540000000121213556116727016126 0ustar00biocbuildbiocbuild#ifndef _BCFFILE_H_ #define _BCFFILE_H_ #include #include #include /* io_bcf.c */ typedef struct { htsFile *file; hts_idx_t *index; } _BCF_FILE; #define BCFFILE(b) ((_BCF_FILE *) R_ExternalPtrAddr(b)) SEXP bcffile_init(); SEXP bcffile_open(SEXP filename, SEXP indexname, SEXP mode); SEXP bcffile_close(SEXP ext); SEXP bcffile_isopen(SEXP ext); SEXP bcffile_isvcf(SEXP ext); SEXP scan_bcf_header(SEXP ext); SEXP scan_bcf(SEXP ext, SEXP regions, SEXP tmpl); SEXP as_bcf(SEXP file, SEXP dictionary, SEXP destination); SEXP index_bcf(SEXP file); #endif /* _BCFFILE_H_ */ Rsamtools/src/encode.c0000644000175400017540000000121613556116727015770 0ustar00biocbuildbiocbuild#include "encode.h" #include "Biostrings_interface.h" unsigned char _bDecode(char); unsigned char _dnaDecode(char); unsigned char _rnaDecode(char); char _bEncode(char c) { return c; } #define _dnaEncode DNAencode; #define _rnaEncode RNAencode; ENCODE_FUNC _encoder(const char *base) { ENCODE_FUNC encode = NULL; if (strcmp(base, "DNAString") == 0) { encode = _dnaEncode; } else if (strcmp(base, "RNAString") == 0) { encode = _rnaEncode; } else if (strcmp(base, "BString") == 0) { encode = _bEncode; } else { Rf_error("internal: unknown '_encoder' class '%s'", base); } return encode; } Rsamtools/src/encode.h0000644000175400017540000000030113556116727015767 0ustar00biocbuildbiocbuild#ifndef _RENCODE_H_ #define _RENCODE_H_ typedef char (*ENCODE_FUNC) (char); /* DNAencode, RNAencode */ ENCODE_FUNC _encoder(const char *baseclass); /* RNAString, DNAString, BString */ #endif Rsamtools/src/fafile.c0000644000175400017540000001240613556116727015764 0ustar00biocbuildbiocbuild#include /* free */ #include "IRanges_interface.h" #include "XVector_interface.h" #include "fafile.h" #include "utilities.h" static SEXP FAFILE_TAG = NULL; static void _fa_close(faidx_t * fai) { fai_destroy(fai); } static void _fafile_close(SEXP ext) { _FA_FILE *ffile = FAFILE(ext); if (ffile->index != NULL) _fa_close(ffile->index); ffile->index = NULL; } static void _fafile_finalizer(SEXP ext) { if (R_ExternalPtrAddr(ext) == NULL) return; _fafile_close(ext); _FA_FILE *ffile = FAFILE(ext); Free(ffile); R_SetExternalPtrAddr(ext, NULL); } SEXP fafile_init() { FAFILE_TAG = install("FaFile"); return R_NilValue; } SEXP fafile_open(SEXP filename, SEXP indexname, SEXP gzindexname) { if (!IS_CHARACTER(filename) || LENGTH(filename) != 1) Rf_error("'file' must be character(1)"); if (!IS_CHARACTER(indexname) || LENGTH(indexname) != 1) Rf_error("'index' must be character(1)"); if (!IS_CHARACTER(gzindexname) || LENGTH(gzindexname) != 1) Rf_error("'gzindex' must be character(1)"); _FA_FILE *ffile = Calloc(1, _FA_FILE); const char *fn = translateChar(STRING_ELT(filename, 0)), *fnfai = translateChar(STRING_ELT(indexname, 0)), *fngzi = translateChar(STRING_ELT(gzindexname, 0)); ffile->index = fai_load3(fn, fnfai, fngzi, FAI_CREATE); if (ffile->index == NULL) { Free(ffile); Rf_error("'open' index failed"); } SEXP ext = PROTECT(R_MakeExternalPtr(ffile, FAFILE_TAG, filename)); R_RegisterCFinalizerEx(ext, _fafile_finalizer, TRUE); UNPROTECT(1); return ext; } SEXP fafile_close(SEXP ext) { _checkext(ext, FAFILE_TAG, "close"); _fafile_close(ext); return ext; } SEXP fafile_isopen(SEXP ext) { SEXP ans = ScalarLogical(FALSE); if (FAFILE(ext) != NULL) { _checkext(ext, FAFILE_TAG, "isOpen"); if (FAFILE(ext)->index != NULL) ans = ScalarLogical(TRUE); } return ans; } /* fa */ SEXP index_fa(SEXP filename) { if (!IS_CHARACTER(filename) || 1 != Rf_length(filename)) Rf_error("'file' must be character(1)"); const char *fn = translateChar(STRING_ELT(filename, 0)); int err = fai_build(fn); if (-1 == err) Rf_error("'indexFa' build index failed"); return filename; } SEXP n_fa(SEXP ext) { _checkext(ext, FAFILE_TAG, "countFa"); faidx_t *fai = FAFILE(ext)->index; if (fai == NULL) Rf_error("'index' not available"); return ScalarInteger(faidx_nseq(fai)); } /* * Copy/pasted from Biostrings/src/XStringSet_io.c * TODO: Put it in XVector C API for sharing. */ static int translate(Chars_holder *seq_data, const int *lkup, int lkup_length) { char *dest; int nbinvalid, i, j, key, val; /* seq_data->ptr is a const char * so we need to cast it to char * before we can write to it */ dest = (char *) seq_data->ptr; nbinvalid = j = 0; for (i = 0; i < seq_data->length; i++) { key = (unsigned char) seq_data->ptr[i]; if (key >= lkup_length || (val = lkup[key]) == NA_INTEGER) { nbinvalid++; continue; } dest[j++] = val; } seq_data->length = j; return nbinvalid; } SEXP scan_fa(SEXP ext, SEXP seq, SEXP start, SEXP end, SEXP type, SEXP lkup) { _checkext(ext, FAFILE_TAG, "isOpen"); if (!IS_CHARACTER(seq)) Rf_error("'seq' must be 'character()"); if (!IS_INTEGER(start)) Rf_error("'start' must be 'integer()'"); if (!IS_INTEGER(end)) Rf_error("'end' must be 'integer()'"); const int n = Rf_length(seq); if (n != Rf_length(start) || n != Rf_length(end)) Rf_error("'seq', 'start', and 'end' must be the same length"); faidx_t *fai = FAFILE(ext)->index; if (fai == NULL) Rf_error("'index' not available"); SEXP width = PROTECT(NEW_INTEGER(n)); int *startp = INTEGER(start), *endp = INTEGER(end), *widthp = INTEGER(width); for (int i = 0; i < n; ++i) widthp[i] = endp[i] - startp[i] + 1; const char *baseclass = CHAR(STRING_ELT(type, 0)); char classname[13]; snprintf(classname, sizeof(classname), "%sSet", baseclass); SEXP ans = PROTECT(alloc_XRawList(classname, baseclass, width)); XVectorList_holder ans_holder = hold_XVectorList(ans); for (int i = 0; i < n; ++i) { Chars_holder ans_elt_holder = get_elt_from_XRawList_holder(&ans_holder, i); int len = faidx_fetch_seq2(fai, CHAR(STRING_ELT(seq, i)), startp[i] - 1, endp[i] - 1, (char *) ans_elt_holder.ptr); if (len == -1) Rf_error(" record %d (%s:%d-%d) failed", i + 1, (char *) CHAR(STRING_ELT(seq, i)), startp[i], endp[i]); //printf("%d\n", len); if (len < widthp[i]) Rf_error(" record %d (%s:%d-%d) was truncated", i + 1, (char *) CHAR(STRING_ELT(seq, i)), startp[i], endp[i]); if (lkup != R_NilValue && translate(&ans_elt_holder, INTEGER(lkup), LENGTH(lkup)) != 0) Rf_error(" record %d (%s:%d-%d) contains invalid DNA letters", i + 1, (char *) CHAR(STRING_ELT(seq, i)), startp[i], endp[i]); } UNPROTECT(2); return ans; } Rsamtools/src/fafile.h0000644000175400017540000000103213556116727015762 0ustar00biocbuildbiocbuild#ifndef FAFILE_H #define FAFILE_H #include #include typedef struct { faidx_t *index; } _FA_FILE; #define FAFILE(f) ((_FA_FILE *) R_ExternalPtrAddr(f)) SEXP fafile_init(); SEXP fafile_open(SEXP filename, SEXP indexname, SEXP gzindexname); SEXP fafile_close(SEXP ext); /* SEXP fafile_reopen(SEXP ext, SEXP filename, SEXP indexname); */ SEXP fafile_isopen(SEXP ext); SEXP index_fa(SEXP filename); SEXP n_fa(SEXP ext); SEXP scan_fa(SEXP ext, SEXP seq, SEXP start, SEXP end, SEXP as, SEXP lkup); #endif Rsamtools/src/idxstats.c0000644000175400017540000000232713556116727016402 0ustar00biocbuildbiocbuild#include "bamfile.h" #include "utilities.h" /* _checkext */ #include #include extern SEXP BAMFILE_TAG; SEXP idxstats_bamfile(SEXP ext) { BAM_FILE bfile; bamFile fp; bam_header_t *header; bam_index_t *idx; int32_t n; SEXP result, name, len, map, unmap; _checkext(ext, BAMFILE_TAG, "idxstats"); bfile = BAMFILE(ext); fp = bfile->file->x.bam; bam_seek(fp, 0, 0); header = bam_header_read(fp); idx = bfile->index; n = hts_idx_get_n(idx); result = PROTECT(Rf_allocVector(VECSXP, 4)); name = Rf_allocVector(STRSXP, n); SET_VECTOR_ELT(result, 0, name); len = Rf_allocVector(INTSXP, n); SET_VECTOR_ELT(result, 1, len); map = Rf_allocVector(REALSXP, n); SET_VECTOR_ELT(result, 2, map); unmap = Rf_allocVector(REALSXP, n); SET_VECTOR_ELT(result, 3, unmap); for (int i = 0; i < n; ++i) { uint64_t mapped, unmapped; SET_STRING_ELT(name, i, mkChar(header->target_name[i])); INTEGER(len)[i] = header->target_len[i]; hts_idx_get_stat(idx, i, &mapped, &unmapped); REAL(map)[i] = (double) mapped; REAL(unmap)[i] = (double) unmapped; } UNPROTECT(1); return result; } Rsamtools/src/idxstats.h0000644000175400017540000000015513556116727016404 0ustar00biocbuildbiocbuild#ifndef _IDXSTATS_H #define _IDXSTATS_H #include SEXP idxstats_bamfile(SEXP bfile); #endif Rsamtools/src/io_sam.c0000644000175400017540000006116613560637551016012 0ustar00biocbuildbiocbuild#include #include #include "bam_data.h" #include "scan_bam_data.h" #include "io_sam.h" #include "bamfile.h" #include "encode.h" #include "utilities.h" #include "S4Vectors_interface.h" #include "XVector_interface.h" #include "Biostrings_interface.h" #include "bam_mate_iter.h" /* from samtoools/bam_sort.c */ void bam_sort_core(int is_by_qname, const char *fn, const char *prefix, size_t max_mem); #define SEQUENCE_BUFFER_ALLOCATION_ERROR 1 static const char *TMPL_ELT_NMS[] = { "qname", "flag", "rname", "strand", "pos", "qwidth", "mapq", "cigar", "mrnm", "mpos", "isize", "seq", "qual", "tag", "groupid", "mate_status" /* "vtype", "value" */ }; static const int N_TMPL_ELTS = sizeof(TMPL_ELT_NMS) / sizeof(const char *); /* utility */ void _check_is_bam(const char *filename) { int magic_len; char buf[4]; bamFile bfile = bam_open(filename, "r"); if (bfile == 0) Rf_error("failed to open SAM/BAM file\n file: '%s'", filename); magic_len = bgzf_read(bfile, buf, 4); bam_close(bfile); if (magic_len != 4 || strncmp(buf, "BAM\001", 4) != 0) Rf_error("'filename' is not a BAM file\n file: %s", filename); } /* template */ void _bam_check_template_list(SEXP template_list) { if (!IS_LIST(template_list) || LENGTH(template_list) != N_TMPL_ELTS) Rf_error("'template' must be list(%d)", N_TMPL_ELTS); SEXP names = GET_ATTR(template_list, R_NamesSymbol); if (!IS_CHARACTER(names) || LENGTH(names) != N_TMPL_ELTS) Rf_error("'names(template)' must be character(%d)", N_TMPL_ELTS); for (int i = 0; i < LENGTH(names); ++i) if (strcmp(TMPL_ELT_NMS[i], CHAR(STRING_ELT(names, i))) != 0) Rf_error("'template' names do not match scan_bam_template\n'"); } static SEXP _tmpl_strand() { SEXP strand = PROTECT(NEW_INTEGER(0)); _as_strand(strand); UNPROTECT(1); return strand; } static SEXP _tmpl_DNAStringSet() { CharAEAE *aeae = new_CharAEAE(0, 0); SEXP lkup = PROTECT(_get_lkup("DNAString")); SEXP ans = new_XRawList_from_CharAEAE("DNAStringSet", "DNAString", aeae, lkup); UNPROTECT(1); return ans; } static SEXP _tmpl_BStringSet() { CharAEAE *aeae = new_CharAEAE(0, 0); return new_XRawList_from_CharAEAE("BStringSet", "BString", aeae, R_NilValue); } static SEXP _tmpl_PhredQuality() { SEXP xstringset, s, t, nmspc, result; PROTECT(xstringset = _tmpl_BStringSet()); PROTECT(nmspc = _get_namespace("Rsamtools")); NEW_CALL(s, t, "PhredQuality", nmspc, 2); CSET_CDR(t, "x", xstringset); CEVAL_TO(s, nmspc, result); UNPROTECT(2); return result; } SEXP scan_bam_template(SEXP rname, SEXP tag) { if (R_NilValue != tag) if (!IS_CHARACTER(tag)) Rf_error("'tag' must be NULL or 'character()'"); SEXP tmpl = PROTECT(NEW_LIST(N_TMPL_ELTS)); SET_VECTOR_ELT(tmpl, QNAME_IDX, NEW_CHARACTER(0)); SET_VECTOR_ELT(tmpl, FLAG_IDX, NEW_INTEGER(0)); SET_VECTOR_ELT(tmpl, RNAME_IDX, rname); SET_VECTOR_ELT(tmpl, STRAND_IDX, _tmpl_strand()); SET_VECTOR_ELT(tmpl, POS_IDX, NEW_INTEGER(0)); SET_VECTOR_ELT(tmpl, QWIDTH_IDX, NEW_INTEGER(0)); SET_VECTOR_ELT(tmpl, MAPQ_IDX, NEW_INTEGER(0)); SET_VECTOR_ELT(tmpl, CIGAR_IDX, NEW_CHARACTER(0)); SET_VECTOR_ELT(tmpl, MRNM_IDX, rname); SET_VECTOR_ELT(tmpl, MPOS_IDX, NEW_INTEGER(0)); SET_VECTOR_ELT(tmpl, ISIZE_IDX, NEW_INTEGER(0)); SET_VECTOR_ELT(tmpl, SEQ_IDX, _tmpl_DNAStringSet()); SET_VECTOR_ELT(tmpl, QUAL_IDX, _tmpl_PhredQuality()); SET_VECTOR_ELT(tmpl, PARTITION_IDX, NEW_INTEGER(0)); SET_VECTOR_ELT(tmpl, MATES_IDX, NEW_INTEGER(0)); if (R_NilValue == tag) { SET_VECTOR_ELT(tmpl, TAG_IDX, R_NilValue); } else { SET_VECTOR_ELT(tmpl, TAG_IDX, NEW_LIST(LENGTH(tag))); SET_ATTR(VECTOR_ELT(tmpl, TAG_IDX), R_NamesSymbol, tag); } SEXP names = PROTECT(NEW_CHARACTER(N_TMPL_ELTS)); for (int i = 0; i < N_TMPL_ELTS; ++i) SET_STRING_ELT(names, i, mkChar(TMPL_ELT_NMS[i])); SET_ATTR(tmpl, R_NamesSymbol, names); UNPROTECT(2); return tmpl; } /* header */ SEXP _read_bam_header(SEXP ext, SEXP what) { samfile_t *sfile = BAMFILE(ext)->file; bam_header_t *header = sfile->header; SEXP ans = PROTECT(NEW_LIST(2)); SEXP nms = NEW_CHARACTER(2); setAttrib(ans, R_NamesSymbol, nms); SET_STRING_ELT(nms, 0, mkChar("targets")); SET_STRING_ELT(nms, 1, mkChar("text")); if (LOGICAL(what)[0] == TRUE) { /* 'targets' */ int n_elts = header->n_targets; SET_VECTOR_ELT(ans, 0, NEW_INTEGER(n_elts)); SEXP tlen = VECTOR_ELT(ans, 0); /* target length */ SEXP tnm = NEW_CHARACTER(n_elts); /* target name */ setAttrib(tlen, R_NamesSymbol, tnm); for (int j = 0; j < n_elts; ++j) { INTEGER(tlen)[j] = header->target_len[j]; SET_STRING_ELT(tnm, j, mkChar(header->target_name[j])); } } if (LOGICAL(what)[1] == TRUE) { /* 'text' */ int n_text_elts = 0; for (int i = 0; i < header->l_text; ++i) if (header->text[i] == '\n') n_text_elts += 1; SET_VECTOR_ELT(ans, 1, NEW_LIST(n_text_elts)); SEXP text = VECTOR_ELT(ans, 1); SEXP tag = NEW_CHARACTER(n_text_elts); setAttrib(text, R_NamesSymbol, tag); int start = 0, end; for (int i = 0; i < n_text_elts; ++i) { int n_elts = header->text[start] == '\n' ? 0 : 1; end = start; while (header->text[end] != '\n') { if (header->text[end] == '\t') ++n_elts; ++end; } if (n_elts == 0) { SET_VECTOR_ELT(text, i, NEW_CHARACTER(0)); /* SET_STRING_ELT(tag, i, mkChar("")); */ start = end + 1; continue; } SET_VECTOR_ELT(text, i, NEW_CHARACTER(n_elts - 1)); SEXP elts = VECTOR_ELT(text, i); for (int j = 0; j < n_elts; ++j) { end = start; while (header->text[end] != '\t' && header->text[end] != '\n') ++end; SEXP elt = mkCharLen(&header->text[start], end - start); if (j == 0) /* tag */ SET_STRING_ELT(tag, i, elt); else SET_STRING_ELT(elts, j - 1, elt); start = end + 1; } } } UNPROTECT(1); return ans; } /* scan_bam framework */ int check_qname(char *last_qname, int bufsize, bam1_t *bam, int max) { if (0 != strcmp(last_qname, bam1_qname(bam))) { /* stop reading */ if (max) { return -1; /* get next qname, continue reading */ } else { if (bam->core.l_qname > bufsize) { Free(last_qname); bufsize = bam->core.l_qname; last_qname = Calloc(bufsize, char); } strcpy(last_qname, bam1_qname(bam)); return 1; } /* same qname, continue reading */ } else { return 0; } } static int _samread(BAM_FILE bfile, BAM_DATA bd, const int yieldSize, bam_fetch_f parse1) { int yield = 0, status = 1, bufsize = 1000; char *last_qname = Calloc(bufsize, char); bam1_t *bam = bam_init1(); while (samread(bfile->file, bam) >= 0) { if (NA_INTEGER != yieldSize) { if (bd->obeyQname) status = check_qname(last_qname, bufsize, bam, yield >= yieldSize); if (status < 0) break; } int result = parse1(bam, bd); if (result < 0) { /* parse error: e.g., cigar buffer overflow */ bam_destroy1(bam); Free(last_qname); return yield; } else if (result == 0L) /* does not pass filter */ continue; yield += status; if (NA_INTEGER != yieldSize && yield == yieldSize) { bfile->pos0 = bam_tell(bfile->file->x.bam); if (!bd->obeyQname) break; } } bam_destroy1(bam); Free(last_qname); return yield; } static int _samread_mate(BAM_FILE bfile, BAM_DATA bd, const int yieldSize, bam_fetch_mate_f parse1_mate) { int yield = 0; bam_mates_t *bam_mates = bam_mates_new(); while (samread_mate(bfile->file->x.bam, bfile->index, &bfile->iter, bam_mates, bd) > 0) { if (NA_INTEGER != yieldSize && yield >= yieldSize) break; int result = parse1_mate(bam_mates, bd); if (result < 0) { /* parse error */ bam_mates_destroy(bam_mates); return result; } else if (result == 0) continue; yield += 1; if (NA_INTEGER != yieldSize && yield == yieldSize) { bfile->pos0 = bam_tell(bfile->file->x.bam); break; } } bam_mates_destroy(bam_mates); return yield; } /* read complete file */ static int _scan_bam_all(BAM_DATA bd, bam_fetch_f parse1, bam_fetch_mate_f parse1_mate, _FINISH1_FUNC finish1) { BAM_FILE bfile = _bam_file_BAM_DATA(bd); const int yieldSize = bd->yieldSize; int yield = 0; bam_seek(bfile->file->x.bam, bfile->pos0, SEEK_SET); if (bd->asMates) { yield = _samread_mate(bfile, bd, yieldSize, parse1_mate); } else { yield = _samread(bfile, bd, yieldSize, parse1); } /* end-of-file */ if ((NA_INTEGER == yieldSize) || (yield < yieldSize)) bfile->pos0 = bam_tell(bfile->file->x.bam); if ((NULL != finish1) && (bd->iparsed >= 0)) (*finish1) (bd); return bd->iparsed; } /* read ranges */ static int _scan_bam_fetch(BAM_DATA bd, SEXP space, int *start, int *end, bam_fetch_f parse1, bam_fetch_mate_f parse1_mate, _FINISH1_FUNC finish1) { int tid; BAM_FILE bfile = _bam_file_BAM_DATA(bd); samfile_t *sfile = bfile->file; bam_index_t *bindex = bfile->index; const int initial = bd->iparsed; for (int irange = bfile->irange0; irange < LENGTH(space); ++irange) { const char *spc = translateChar(STRING_ELT(space, irange)); const int starti = start[irange] > 0 ? start[irange] - 1 : start[irange]; for (tid = 0; tid < sfile->header->n_targets; ++tid) { if (strcmp(spc, sfile->header->target_name[tid]) == 0) break; } if (tid == sfile->header->n_targets) { Rf_warning("space '%s' not in BAM header", spc); bd->irange += 1; return -1; } if (bd->asMates) { bam_fetch_mate(sfile->x.bam, bindex, tid, starti, end[irange], bd, parse1_mate); } else { bam_fetch(sfile->x.bam, bindex, tid, starti, end[irange], bd, parse1); } if (NULL != finish1) (*finish1) (bd); bd->irange += 1; if ((NA_INTEGER != bd->yieldSize) && (bd->iparsed - initial >= bd->yieldSize)) break; } bfile->irange0 = bd->irange; return bd->iparsed - initial; } int _do_scan_bam(BAM_DATA bd, SEXP regions, bam_fetch_f parse1, bam_fetch_mate_f parse1_mate, _FINISH1_FUNC finish1) { int status; if (R_NilValue == regions) /* everything */ status = _scan_bam_all(bd, parse1, parse1_mate, finish1); else { /* fetch */ BAM_FILE bfile = _bam_file_BAM_DATA(bd); if (NULL == bfile->index) Rf_error("valid 'index' file required"); status = _scan_bam_fetch(bd, VECTOR_ELT(regions, 0), INTEGER(VECTOR_ELT(regions, 1)), INTEGER(VECTOR_ELT(regions, 2)), parse1, parse1_mate, finish1); } return status; } /* scan_bam */ static int _filter_and_parse1(const bam1_t *bam, void *data) { /* requires 'data' to be BAM_DATA */ BAM_DATA bd = (BAM_DATA) data; int result = _filter_and_parse1_BAM_DATA(bam, bd); if (result < 0) { /* parse error: e.g., cigar buf overflow */ _grow_SCAN_BAM_DATA(bd, 0); bd->iparsed = -1; } return result; } static int _filter_and_parse1_mate(const bam_mates_t *mates, void *data) { /* requires 'data' to be BAM_DATA, data->extra to be SCAN_BAM_DATA */ BAM_DATA bd = (BAM_DATA) data; SCAN_BAM_DATA sbd = (SCAN_BAM_DATA) bd->extra; int yield = 0, pass = 0; sbd->mates_flag = mates->mated == MATE_UNKNOWN ? NA_INTEGER : mates->mated; sbd->partition_id += 1; for (int i = 0; i < mates->n; ++i) { int result = _filter_and_parse1_BAM_DATA(mates->bams[i], bd); if (result < 0) { _grow_SCAN_BAM_DATA(bd, 0); return result; } pass += result; } if (pass > 0) { yield = 1; } else { sbd->partition_id -= 1; } return yield; } SEXP _scan_bam_result_init(SEXP template_list, SEXP names, SEXP regions, BAM_FILE bfile) { const int nrange = R_NilValue == regions ? 1 : Rf_length(VECTOR_ELT(regions, 0)); int i; SEXP result = PROTECT(NEW_LIST(nrange)); /* result: range1: tmpl1, tmpl2... range2: tmpl1, tmpl2... ... */ bam_header_t *header = bfile->file->header; SEXP rname = PROTECT(NEW_INTEGER(0)); _as_factor(rname, (const char **) header->target_name, header->n_targets); for (int irange = 0; irange < nrange; ++irange) { SEXP tag = VECTOR_ELT(template_list, TAG_IDX); SEXP tmpl; if (R_NilValue == tag) tmpl = PROTECT(scan_bam_template(rname, R_NilValue)); else { SEXP nms = getAttrib(tag, R_NamesSymbol); tmpl = PROTECT(scan_bam_template(rname, nms)); } for (i = 0; i < LENGTH(names); ++i) { if (TAG_IDX == i) continue; else if (R_NilValue == VECTOR_ELT(template_list, i)) SET_VECTOR_ELT(tmpl, i, R_NilValue); } SET_VECTOR_ELT(result, irange, tmpl); UNPROTECT(1); } UNPROTECT(2); return result; } SEXP _scan_bam(SEXP bfile, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP reverseComplement, SEXP yieldSize, SEXP template_list, SEXP obeyQname, SEXP asMates, SEXP qnamePrefixEnd, SEXP qnameSuffixStart) { SEXP names = PROTECT(GET_ATTR(template_list, R_NamesSymbol)); SEXP result = PROTECT(_scan_bam_result_init(template_list, names, regions, BAMFILE(bfile))); SCAN_BAM_DATA sbd = _init_SCAN_BAM_DATA(result); char qname_prefix = '\0'; SEXP prefix_elt = STRING_ELT(qnamePrefixEnd, 0); if (prefix_elt != NA_STRING) qname_prefix = CHAR(prefix_elt)[0]; char qname_suffix = '\0'; SEXP suffix_elt = STRING_ELT(qnameSuffixStart, 0); if (suffix_elt != NA_STRING) qname_suffix = CHAR(suffix_elt)[0]; BAM_DATA bd = _init_BAM_DATA(bfile, regions, keepFlags, isSimpleCigar, tagFilter, mapqFilter, LOGICAL(reverseComplement)[0], INTEGER(yieldSize)[0], LOGICAL(obeyQname)[0], LOGICAL(asMates)[0], qname_prefix, qname_suffix, (void *) sbd); int status = _do_scan_bam(bd, regions, _filter_and_parse1, _filter_and_parse1_mate, _finish1range_BAM_DATA); if (status < 0) { int idx = bd->irec; int parse_status = bd->parse_status; _Free_SCAN_BAM_DATA(bd->extra); _Free_BAM_DATA(bd); Rf_error("'scanBam' failed:\n record: %d\n error: %d", idx, parse_status); } _Free_SCAN_BAM_DATA(bd->extra); _Free_BAM_DATA(bd); UNPROTECT(2); return result; } /* count */ static int _count1(const bam1_t * bam, void *data) { return _count1_BAM_DATA(bam, (BAM_DATA) data); } SEXP _count_bam(SEXP bfile, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter) { SEXP result = PROTECT(NEW_LIST(2)); BAM_DATA bd = _init_BAM_DATA(bfile, regions, keepFlags, isSimpleCigar, tagFilter, mapqFilter, 0, NA_INTEGER, 0, 0, '\0', '\0', result); SET_VECTOR_ELT(result, 0, NEW_INTEGER(bd->nrange)); SET_VECTOR_ELT(result, 1, NEW_NUMERIC(bd->nrange)); for (int i = 0; i < bd->nrange; ++i) { INTEGER(VECTOR_ELT(result, 0))[i] = REAL(VECTOR_ELT(result, 1))[i] = 0; } SEXP nms = PROTECT(NEW_CHARACTER(2)); SET_STRING_ELT(nms, 0, mkChar("records")); SET_STRING_ELT(nms, 1, mkChar("nucleotides")); setAttrib(result, R_NamesSymbol, nms); UNPROTECT(1); int status = _do_scan_bam(bd, regions, _count1, NULL, NULL); if (status < 0) { int idx = bd->irec; int parse_status = bd->parse_status; _Free_BAM_DATA(bd); UNPROTECT(1); Rf_error("'countBam' failed:\n record: %d\n error: %d", idx, parse_status); } _Free_BAM_DATA(bd); UNPROTECT(1); return result; } SEXP scan_bam_cleanup() { /* placeholder */ return R_NilValue; } /* filterBam */ static int _prefilter1(const bam1_t *bam, void *data) { BAM_DATA bd = (BAM_DATA) data; bd->irec += 1; if (!_filter1_BAM_DATA(bam, bd)) return 0; bambuffer_push((BAM_BUFFER) bd->extra, bam); bd->iparsed += 1; return 1; } static int _prefilter1_mate(const bam_mates_t *mates, void *data) { BAM_DATA bd = (BAM_DATA) data; BAM_BUFFER buf = (BAM_BUFFER) bd->extra; int parsed; buf->partition_id += 1; buf->mate_flag = mates->mated == MATE_UNKNOWN ? NA_INTEGER : mates->mated; parsed = 0; for (int i = 0; i < mates->n; ++i) parsed += _prefilter1(mates->bams[i], data); if (parsed == 0) buf->partition_id -= 1; return parsed; } SEXP _prefilter_bam(SEXP bfile, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP yieldSize, SEXP obeyQname, SEXP asMates, SEXP qnamePrefixEnd, SEXP qnameSuffixStart) { SEXP ext = PROTECT(bambuffer(INTEGER(yieldSize)[0], LOGICAL(asMates)[0])); char qname_prefix = '\0'; SEXP prefix_elt = STRING_ELT(qnamePrefixEnd, 0); if (prefix_elt != NA_STRING) qname_prefix = CHAR(prefix_elt)[0]; char qname_suffix = '\0'; SEXP suffix_elt = STRING_ELT(qnameSuffixStart, 0); if (suffix_elt != NA_STRING) qname_suffix = CHAR(suffix_elt)[0]; BAM_DATA bd = _init_BAM_DATA(bfile, regions, keepFlags, isSimpleCigar, tagFilter, mapqFilter, 0, INTEGER(yieldSize)[0], LOGICAL(obeyQname)[0], LOGICAL(asMates)[0], qname_prefix, qname_suffix, BAMBUFFER(ext)); int status = _do_scan_bam(bd, regions, _prefilter1, _prefilter1_mate, NULL); if (status < 0) { int idx = bd->irec; int parse_status = bd->parse_status; _Free_BAM_DATA(bd); UNPROTECT(1); Rf_error("'filterBam' prefilter failed:\n record: %d\n error: %d", idx, parse_status); } _Free_BAM_DATA(bd); UNPROTECT(1); return ext; } static int _filter1(const bam1_t * bam, void *data) { BAM_DATA bd = (BAM_DATA) data; bd->irec += 1; if (!_filter1_BAM_DATA(bam, bd)) return 0; samwrite((samfile_t *) bd->extra, bam); bd->iparsed += 1; return 1; } SEXP _filter_bam(SEXP bfile, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP fout_name, SEXP fout_mode) { /* open destination */ BAM_DATA bd = _init_BAM_DATA(bfile, regions, keepFlags, isSimpleCigar, tagFilter, mapqFilter, 0, NA_INTEGER, 0, 0, '\0', '\0', NULL); /* FIXME: this just copies the header... */ bam_header_t *header = BAMFILE(bfile)->file->header; samfile_t *f_out = _bam_tryopen(translateChar(STRING_ELT(fout_name, 0)), CHAR(STRING_ELT(fout_mode, 0)), header); bd->extra = f_out; int status = _do_scan_bam(bd, regions, _filter1, NULL, NULL); if (status < 0) { int idx = bd->irec; int parse_status = bd->parse_status; _Free_BAM_DATA(bd); samclose(f_out); Rf_error("'filterBam' failed:\n record: %d\n error: %d", idx, parse_status); } /* sort and index destintation ? */ /* cleanup */ _Free_BAM_DATA(bd); samclose(f_out); return status < 0 ? R_NilValue : fout_name; } /* merge_bam */ /* from bam_sort.c */ #define MERGE_RG 1 #define MERGE_LEVEL1 4 #define MERGE_FORCE 8 int bam_merge_core(int by_qname, const char *out, const char *headers, int n, char * const *fn, int flag, const char *reg); SEXP merge_bam(SEXP fnames, SEXP destination, SEXP overwrite, SEXP hname, SEXP regionStr, SEXP isByQname, SEXP addRG, SEXP compressLevel1) { int i; if (!IS_CHARACTER(fnames) || 2 > Rf_length(fnames)) Rf_error("'files' must be a character() with length >= 2"); if (!IS_CHARACTER(hname) || 1 < Rf_length(hname)) Rf_error("'header' must be character() with length <= 1"); if (!IS_CHARACTER(destination) || 1 != Rf_length(destination)) Rf_error("'destination' must be character(1)"); if (!IS_LOGICAL(overwrite) || 1 != Rf_length(overwrite)) Rf_error("'overwrite' must be logical(1)"); if (!IS_CHARACTER(regionStr) || 1 < Rf_length(regionStr)) Rf_error("'region' must define 0 or 1 regions"); if (!IS_LOGICAL(isByQname) || 1 != Rf_length(isByQname)) Rf_error("'isByQname' must be logical(1)"); if (!IS_LOGICAL(addRG) || 1 != Rf_length(addRG)) Rf_error("'addRG' must be logical(1)"); if (!IS_LOGICAL(compressLevel1) || 1 != Rf_length(compressLevel1)) Rf_error("'compressLevel1' must be logical(1)"); char ** fileNames = (char **) R_alloc(sizeof(const char *), Rf_length(fnames)); for (i = 0; i < Rf_length(fnames); ++i) fileNames[i] = (char *) translateChar(STRING_ELT(fnames, i)); const char *hfName = 0 == Rf_length(hname) ? NULL : translateChar(STRING_ELT(hname, 0)); int flag = 0; if (LOGICAL(addRG)[0]) flag = ((int) flag) | ((int) MERGE_RG); if (LOGICAL(overwrite)[0]) flag = ((int) flag) | ((int) MERGE_FORCE); if (LOGICAL(compressLevel1)[0]) flag = ((int) flag) | ((int) MERGE_LEVEL1); const char *region = 0 == Rf_length(regionStr) ? NULL : translateChar(STRING_ELT(regionStr, 0)); int res = bam_merge_core(LOGICAL(isByQname)[0], translateChar(STRING_ELT(destination, 0)), hfName, Rf_length(fnames), fileNames, flag, region); if (res < 0) Rf_error("'mergeBam' failed with error code %d", res); return destination; } /* sort_bam */ SEXP sort_bam(SEXP filename, SEXP destination, SEXP isByQname, SEXP maxMemory) { if (!IS_CHARACTER(filename) || 1 != LENGTH(filename)) Rf_error("'filename' must be character(1)"); if (!IS_CHARACTER(destination) || 1 != LENGTH(destination)) Rf_error("'destination' must be character(1)"); if (!IS_LOGICAL(isByQname) || LENGTH(isByQname) != 1) Rf_error("'isByQname' must be logical(1)"); if (!IS_INTEGER(maxMemory) || LENGTH(maxMemory) != 1 || INTEGER(maxMemory)[0] < 1) Rf_error("'maxMemory' must be a positive integer(1)"); const char *fbam = translateChar(STRING_ELT(filename, 0)); const char *fout = translateChar(STRING_ELT(destination, 0)); int sortMode = asInteger(isByQname); size_t maxMem = (size_t) INTEGER(maxMemory)[0] * 1024 * 1024; _check_is_bam(fbam); bam_sort_core(sortMode, fbam, fout, maxMem); return destination; } /* index_bam */ SEXP index_bam(SEXP indexname) { if (!IS_CHARACTER(indexname) || 1 != LENGTH(indexname)) Rf_error("'indexname' must be character(1)"); const char *fbam = translateChar(STRING_ELT(indexname, 0)); _check_is_bam(fbam); int status = bam_index_build(fbam); if (0 != status) Rf_error("failed to build index\n file: %s", fbam); char *fidx = (char *) R_alloc(strlen(fbam) + 5, sizeof(char)); sprintf(fidx, "%s.bai", fbam); return mkString(fidx); } Rsamtools/src/io_sam.h0000644000175400017540000000332313560637551016006 0ustar00biocbuildbiocbuild#ifndef _IO_SAM_H_ #define _IO_SAM_H_ #include #include "bam_data.h" #ifdef __cplusplus extern "C" { #endif SEXP scan_bam_template(SEXP rname, SEXP tags); SEXP sort_bam(SEXP fname, SEXP destinationPrefix, SEXP isByQname, SEXP maxMemory); SEXP merge_bam(SEXP fnames, SEXP destination, SEXP overwrite, SEXP hname, SEXP regionStr, SEXP isByQname, SEXP addRG, SEXP compressLevel1); SEXP index_bam(SEXP indexname); SEXP scan_bam_cleanup(); /* error handling only */ void _bam_check_template_list(SEXP template_list); SEXP _read_bam_header(SEXP ext, SEXP what); SEXP _scan_bam(SEXP bfile, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP reverseComplement, SEXP yieldSize, SEXP template_list, SEXP obeyQname, SEXP asMates, SEXP qnamePrefixEnd, SEXP qnameSuffixStart); SEXP _count_bam(SEXP bfile, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter); SEXP _prefilter_bam(SEXP bfile, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP yieldSize, SEXP obeyQname, SEXP asMates, SEXP qnamePrefixEnd, SEXP qnameSuffixStart); SEXP _filter_bam(SEXP bfile, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP fout_name, SEXP fout_mode); typedef void (_FINISH1_FUNC) (BAM_DATA); int _do_scan_bam(BAM_DATA bd, SEXP regions, bam_fetch_f parse1, bam_fetch_mate_f parse1_mate, _FINISH1_FUNC finish1); #ifdef __cplusplus } #endif #endif /* _IO_SAM_H_ */ Rsamtools/src/pbuffer_wrapper.cpp0000644000175400017540000000027513556116727020270 0ustar00biocbuildbiocbuild#include "pbuffer_wrapper.h" #include "PosCacheColl.h" void pileup_pbuffer_destroy(void *pbuffer) { if(pbuffer != NULL) { delete (static_cast(pbuffer)); } } Rsamtools/src/pbuffer_wrapper.h0000644000175400017540000000037613556116727017737 0ustar00biocbuildbiocbuild#ifndef PBUFFER_WRAPPER_H #define PBUFFER_WRAPPER_H #ifdef __cplusplus extern "C" { #endif // expose PosCacheColl dtor to C code void pileup_pbuffer_destroy(void *pbuffer); #ifdef __cplusplus } #endif /* __cplusplus */ #endif /* PBUFFER_WRAPPER_H */ Rsamtools/src/pileup.cpp0000644000175400017540000001460013556116727016372 0ustar00biocbuildbiocbuild#include "pileup.h" static int _filter_and_parse1_pileup(const bam1_t *bam, void *data) { BAM_DATA bd = (BAM_DATA) data; int result = _filter1_BAM_DATA(bam, bd); if (result < 0) { // possible parse error: e.g., cigar buf overflow Rf_error("parsing BAM file failed. Is the file corrupt?"); } else if(result) { PileupBufferShim *shim = (PileupBufferShim *) bd->extra; // push to buffer the alignments that meet criteria shim->plbuf_push(bam); } bd->iparsed += 1; return result; } static void _finish1range_pileup(BAM_DATA bd) { // invoked each time a range is finished PileupBufferShim *shim = (PileupBufferShim *) bd->extra; shim->finish1(bd->irange); if (bd->irange + 1 < bd->nrange) shim->start1(bd->irange + 1); } static SEXP _pileup_bam_result_init(SEXP regions) { // regions is list of vectors, so length of outer list // is num ranges const int nrange = R_NilValue == regions ? 1 : Rf_length(VECTOR_ELT(regions, 0)); return Rf_allocVector(VECSXP, nrange); } static void _finish_buffered_yieldSize_chunk(BAM_DATA bd) { PileupBufferShim *shim = static_cast(bd->extra); shim->process_yieldSize_chunk(); // run Pileup::insert loop } static SEXP _pileup_bam(SEXP ext, SEXP regions, SEXP keepFlags, SEXP reverseComplement, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP yieldSize, SEXP obeyQname, SEXP asMates, SEXP qnamePrefixEnd, SEXP qnameSuffixStart, PileupBuffer& buffer) { _check_isbamfile(ext, "pileup"); _checkparams(regions, keepFlags, isSimpleCigar); if (!(Rf_isInteger(yieldSize) && (1L == Rf_length(yieldSize)))) Rf_error("'yieldSize' must be integer(1)"); if (!(Rf_isLogical(obeyQname) && (1L == Rf_length(obeyQname)))) Rf_error("'obeyQname' must be logical(1)"); if (!(Rf_isLogical(asMates) && (1L == Rf_length(asMates)))) Rf_error("'asMates' must be logical(1)"); SEXP result = PROTECT(_pileup_bam_result_init(regions)); PileupBufferShim shim(regions, result, buffer); BAM_DATA bd = _init_BAM_DATA(ext, regions, keepFlags, isSimpleCigar, tagFilter, mapqFilter, LOGICAL(reverseComplement)[0], INTEGER(yieldSize)[0], LOGICAL(obeyQname)[0], LOGICAL(asMates)[0], '\0', '\0', (void *) &shim); int status = 0; if(!(dynamic_cast(buffer).isBufferedPileup())) { if (bd->irange < bd->nrange) { shim.start1(bd->irange); // _do_scan_bam found in io_sam.c; // mostly a wrapper for // _scan_bam_fetch(BAM_DATA bd, SEXP space, int* start, int* end, // bam_fetch_f , bam_fetch_mate_f , _FINISH_FUNC) status = _do_scan_bam(bd, regions, _filter_and_parse1_pileup, (bam_fetch_mate_f) NULL, _finish1range_pileup); } } else { // must do loop if buffered shim.start1(0); status = _do_scan_bam(bd, regions, _filter_and_parse1_pileup, (bam_fetch_mate_f) NULL, _finish_buffered_yieldSize_chunk); for(;;) { if(!(dynamic_cast(buffer).needMoreInput()) || status <= 0) break; status = _do_scan_bam(bd, regions, _filter_and_parse1_pileup, (bam_fetch_mate_f) NULL, _finish_buffered_yieldSize_chunk); } shim.finish1(0); } // the decision to deallocate must happen in here before return // the SEXP because Rf_error would lead to the dynamic memory // being left behind if(status <= 0) { // error or EOI; must deallocate dynamic memory // rename 'deallocate and flush'? two separate functions (so // that deallocate can be called without flushing?) buffer.signalEOI(); shim.flush(); } if (status < 0) { int idx = bd->irec; int parse_status = bd->parse_status; _Free_BAM_DATA(bd); status = parse_status; Rf_error("'pileup' failed:\n record: %d\n error: %d", idx, parse_status); } _Free_BAM_DATA(bd); UNPROTECT(1); return result; } static SEXP _bamheaderAsSeqnames(bam_header_t *header) { if(header == NULL) Rf_error("'header' must not be NULL"); int numSeqnames = header->n_targets; SEXP seqnames = PROTECT(Rf_allocVector(STRSXP, numSeqnames)); for(int i = 0; i != numSeqnames; ++i) { SET_STRING_ELT(seqnames, i, Rf_mkChar(header->target_name[i])); } UNPROTECT(1); return seqnames; } class PosCacheColl; extern "C" { SEXP c_Pileup(SEXP ext, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP reverseComplement, SEXP yieldSize, SEXP obeyQname, SEXP asMates, SEXP qnamePrefixEnd, SEXP qnameSuffixStart, SEXP schema, SEXP pileupParams) { if (!Rf_isVector(schema)) Rf_error("'schema' must be list()"); if (!Rf_isVector(pileupParams)) Rf_error("'pileupParams' must be list()"); SEXP seqnamesLevels = PROTECT(_bamheaderAsSeqnames(BAMFILE(ext)->file->header)); // 'ranged' means user asked for specific genomic range(s) by // providing 'which' argument to 'ScanBamParam' bool isRanged = regions != R_NilValue; // This check has to happen at this level; can't use value of // yieldSize further down in hierarchy // 'buffered' means pileup will store pileup results for // partially completed genomic positions across calls to // pileup bool isBuffered = !isRanged && INTEGER(yieldSize)[0] != NA_INTEGER; Pileup buffer = Pileup(isRanged, isBuffered, schema, pileupParams, seqnamesLevels, (PosCacheColl**)&(BAMFILE(ext)->pbuffer)); SEXP res = PROTECT(_pileup_bam(ext, regions, keepFlags, reverseComplement, isSimpleCigar, tagFilter, mapqFilter, yieldSize, obeyQname, asMates, qnamePrefixEnd, qnameSuffixStart, buffer)); UNPROTECT(2); return res; } } Rsamtools/src/pileup.h0000644000175400017540000000114713556116727016041 0ustar00biocbuildbiocbuild#ifndef PILEUP_H #define PILEUP_H #ifdef __cplusplus #define R_NO_REMAP #include "io_sam.h" #include "utilities.h" #include "PileupBufferShim.h" #ifdef PILEUP_DEBUG #include "nate_utilities.h" #endif extern "C" { #endif SEXP c_Pileup(SEXP ext, SEXP regions, SEXP keepFlags, SEXP isSimpleCigar, SEXP tagFilter, SEXP mapqFilter, SEXP reverseComplement, SEXP yieldSize, SEXP obeyQname, SEXP asMates, SEXP qnamePrefixEnd, SEXP qnameSuffixStart, SEXP schema, SEXP pileupParams); #ifdef __cplusplus } #endif #endif Rsamtools/src/pileupbam.c0000644000175400017540000005057013556116727016520 0ustar00biocbuildbiocbuild#include #include #include "pileupbam.h" #include "bamfile.h" #include "utilities.h" typedef enum { YIELDBY_RANGE = 0, YIELDBY_POSITION } YIELDBY; #define WHAT_OK 0 #define WHAT_SEQ 1 #define WHAT_QUAL 2 typedef struct { BAM_FILE bfile; bamFile fp; bam_iter_t iter; /* read filter params */ int min_map_quality; uint32_t keep_flag[2]; } BAM_ITER_T; typedef struct { int n_files, *n_plp; BAM_ITER_T **mfile; const bam_pileup1_t **plp; bam_mplp_t mplp_iter; } PILEUP_ITER_T; typedef struct { const char *chr; int i_reg, start, end; } REGION_T; typedef struct { REGION_T *region; int i_reg, n_reg; const char **chr; int *start, *end, stashed; } REGION_ITER_T; typedef struct { int i_yld; int *pos, *seq, *qual; } PILEUP_RESULT_T; typedef struct { int n_files; SEXP names; int min_base_quality, min_map_quality, min_depth, max_depth; uint32_t keep_flag[2]; int yieldSize, yieldAll; YIELDBY yieldBy; int what; } PILEUP_PARAM_T; /* from bam_aux.c; should really be exported part of library? */ KHASH_MAP_INIT_STR(s, int) const int QUAL_LEVELS = 94, /* printable ASCII */ SEQ_LEVELS = 5; /* A, C, G, T, N */ /* PILEUP_ITER_T */ static PILEUP_ITER_T *_iter_init(SEXP files, PILEUP_PARAM_T * param) { int i; PILEUP_ITER_T *iter = Calloc(1, PILEUP_ITER_T); iter->n_files = Rf_length(files);; iter->mfile = Calloc(iter->n_files, BAM_ITER_T *); iter->mfile[0] = Calloc(iter->n_files, BAM_ITER_T); for (i = 0; i < iter->n_files; ++i) { iter->mfile[i] = iter->mfile[0] + i; iter->mfile[i]->bfile = BAMFILE(VECTOR_ELT(files, i)); iter->mfile[i]->fp = iter->mfile[i]->bfile->file->x.bam; iter->mfile[i]->min_map_quality = param->min_map_quality; iter->mfile[i]->keep_flag[0] = param->keep_flag[0]; iter->mfile[i]->keep_flag[1] = param->keep_flag[1]; } iter->plp = Calloc(iter->n_files, const bam_pileup1_t *); iter->n_plp = Calloc(iter->n_files, int); return iter; } static PILEUP_ITER_T *_iter_destroy(PILEUP_ITER_T * iter) { Free(iter->plp); Free(iter->n_plp); Free(iter->mfile[0]); Free(iter->mfile); Free(iter); return NULL; } /* REGION_ITER_T */ static REGION_ITER_T *_region_iter_init(SEXP regions) { int i; REGION_ITER_T *iter; iter = Calloc(1, REGION_ITER_T); iter->i_reg = -1; iter->n_reg = Rf_length(VECTOR_ELT(regions, 0)); iter->chr = Calloc(iter->n_reg, const char *); for (i = 0; i < iter->n_reg; ++i) iter->chr[i] = CHAR(STRING_ELT(VECTOR_ELT(regions, 0), i)); iter->start = INTEGER(VECTOR_ELT(regions, 1)); iter->end = INTEGER(VECTOR_ELT(regions, 2)); iter->stashed = FALSE; iter->region = Calloc(1, REGION_T); return iter; } static REGION_T *_region_iter_next(REGION_ITER_T * iter) { iter->stashed = FALSE; iter->i_reg += 1; REGION_T *region = iter->region; if (iter->i_reg < iter->n_reg) { region->i_reg = iter->i_reg; region->chr = iter->chr[iter->i_reg]; region->start = iter->start[iter->i_reg]; region->end = iter->end[iter->i_reg]; } else { region = NULL; } return region; } static void _region_iter_stash(REGION_ITER_T * iter, REGION_T * region) { iter->region->chr = region->chr; iter->region->start = region->start; iter->region->end = region->end; iter->stashed = TRUE; } static REGION_T *_region_iter_pop(REGION_ITER_T * iter) { REGION_T *region = NULL; if (iter->stashed) { region = iter->region; iter->stashed = FALSE; } return region; } static REGION_ITER_T *_region_iter_destroy(REGION_ITER_T * iter) { Free(iter->chr); Free(iter->region); Free(iter); return NULL; } /* */ static SEXP _lst_elt(SEXP lst, const char *name, const char *lst_name) { SEXP nms = GET_NAMES(lst); SEXP elt_nm = PROTECT(mkChar(name)); int i; for (i = 0; i < Rf_length(nms); ++i) if (elt_nm == STRING_ELT(nms, i)) break; UNPROTECT(1); if (i == Rf_length(nms)) Rf_error("'%s' does not contain element '%s'", lst_name, name); return VECTOR_ELT(lst, i); } static int _mplp_read_bam(void *data, bam1_t * b) { BAM_ITER_T *mdata = (BAM_ITER_T *) data; uint32_t test_flag; int skip, result; do { result = mdata->iter ? bam_iter_read(mdata->fp, mdata->iter, b) : bam_read1(mdata->fp, b); if (0 >= result) break; skip = FALSE; test_flag = (mdata->keep_flag[0] & ~b->core.flag) | (mdata->keep_flag[1] & b->core.flag); if (~test_flag & 2047u) skip = TRUE; else if (b->core.tid < 0 || (b->core.flag & BAM_FUNMAP)) skip = TRUE; else if (b->core.qual < mdata->min_map_quality) skip = TRUE; } while (skip); return result; } static SEXP _seq_rle(int *cnt, const char **chr, int n) { int i = 0, j; SEXP s, t; for (j = 1; j < n; ++j) { if (0 != strcmp(chr[j], chr[j - 1])) { i += 1; chr[i] = chr[j]; cnt[i] = cnt[j] - cnt[i - 1]; } else cnt[i] += cnt[j] - cnt[j - 1]; } if (n) n = i + 1; s = PROTECT(NEW_INTEGER(n)); t = NEW_CHARACTER(n); Rf_setAttrib(s, R_NamesSymbol, t); for (i = 0; i < n; ++i) { INTEGER(s)[i] = cnt[i]; SET_STRING_ELT(t, i, mkChar(chr[i])); } UNPROTECT(1); return s; } static SEXP _mplp_setup_R(const PILEUP_PARAM_T * param, PILEUP_RESULT_T * result) { #ifdef PILEUPBAM_DEBUG REprintf("_mplp_setup_R\n"); #endif SEXP alloc = PROTECT(NEW_LIST(4)), nms = PROTECT(NEW_CHARACTER(4)), opos, oseq, oqual, dimnms, dim_elt; char qualbuf[] = { ' ', '\0' }; int i; SET_STRING_ELT(nms, 0, mkChar("seqnames")); SET_STRING_ELT(nms, 1, mkChar("pos")); SET_STRING_ELT(nms, 2, mkChar("seq")); SET_STRING_ELT(nms, 3, mkChar("qual")); Rf_setAttrib(alloc, R_NamesSymbol, nms); result->i_yld = 0; SET_VECTOR_ELT(alloc, 0, _seq_rle(NULL, NULL, 0)); opos = NEW_INTEGER(param->yieldSize); memset(INTEGER(opos), 0, sizeof(int) * Rf_length(opos)); SET_VECTOR_ELT(alloc, 1, opos); result->pos = INTEGER(opos); if (param->what & WHAT_SEQ) { oseq = Rf_alloc3DArray(INTSXP, SEQ_LEVELS, param->n_files, param->yieldSize); memset(INTEGER(oseq), 0, sizeof(int) * Rf_length(oseq)); SET_VECTOR_ELT(alloc, 2, oseq); dimnms = NEW_LIST(3); Rf_setAttrib(oseq, R_DimNamesSymbol, dimnms); dim_elt = NEW_CHARACTER(SEQ_LEVELS); SET_VECTOR_ELT(dimnms, 0, dim_elt); SET_VECTOR_ELT(dimnms, 1, param->names); SET_VECTOR_ELT(dimnms, 2, R_NilValue); SET_STRING_ELT(dim_elt, 0, mkChar("A")); SET_STRING_ELT(dim_elt, 1, mkChar("C")); SET_STRING_ELT(dim_elt, 2, mkChar("G")); SET_STRING_ELT(dim_elt, 3, mkChar("T")); SET_STRING_ELT(dim_elt, 4, mkChar("N")); result->seq = INTEGER(oseq); } else SET_VECTOR_ELT(alloc, 2, R_NilValue); if (param->what & WHAT_QUAL) { oqual = Rf_alloc3DArray(INTSXP, QUAL_LEVELS, param->n_files, param->yieldSize); memset(INTEGER(oqual), 0, sizeof(int) * Rf_length(oqual)); SET_VECTOR_ELT(alloc, 3, oqual); dimnms = NEW_LIST(3); Rf_setAttrib(oqual, R_DimNamesSymbol, dimnms); dim_elt = NEW_CHARACTER(QUAL_LEVELS); SET_VECTOR_ELT(dimnms, 0, dim_elt); SET_VECTOR_ELT(dimnms, 1, param->names); SET_VECTOR_ELT(dimnms, 2, R_NilValue); for (i = 0; i < QUAL_LEVELS; ++i) { qualbuf[0] = (char) (i + 33); SET_STRING_ELT(dim_elt, i, mkChar(qualbuf)); } result->qual = INTEGER(oqual); } else SET_VECTOR_ELT(alloc, 3, R_NilValue); UNPROTECT(2); return alloc; } static void _mplp_setup_bam(const PILEUP_PARAM_T * param, const REGION_T * region, PILEUP_ITER_T * plp_iter) { #ifdef PILEUPBAM_DEBUG REprintf("_mplp_setup_bam\n"); #endif BAM_ITER_T **mfile = plp_iter->mfile; for (int j = 0; j < plp_iter->n_files; ++j) { /* set iterator, get pileup */ int32_t tid = bam_get_tid(mfile[j]->bfile->file->header, region->chr); if (tid < 0) Rf_error("'%s' not in bam file %d", region->chr, j + 1); mfile[j]->iter = bam_iter_query(mfile[j]->bfile->index, tid, region->start - 1, region->end); } plp_iter->mplp_iter = bam_mplp_init(plp_iter->n_files, _mplp_read_bam, (void **) mfile); bam_mplp_set_maxcnt(plp_iter->mplp_iter, param->max_depth); } static void _mplp_teardown_bam(PILEUP_ITER_T * iter) { #ifdef PILEUPBAM_DEBUG REprintf("_mplp_teardown_bam\n"); #endif int j; bam_mplp_destroy(iter->mplp_iter); for (j = 0; j < iter->n_files; ++j) bam_iter_destroy(iter->mfile[j]->iter); } static int _bam1(const PILEUP_PARAM_T * param, const REGION_T * region, PILEUP_ITER_T * plp_iter, PILEUP_RESULT_T * result) { #ifdef PILEUPBAM_DEBUG REprintf("_bam1\n"); #endif /* A, C, G, T, N only */ static const int nuc[] = { /* A C G T N */ -1, 0, 1, -1, 2, -1, -1, -1, 3, -1, -1, -1, -1, -1, -1, 4 }; const int n_files = plp_iter->n_files, start = region->start, end = region->end; int *n_plp = plp_iter->n_plp, pos, i, j, idx = 0; int *opos = result->pos + result->i_yld, *oseq = result->seq + SEQ_LEVELS * n_files * result->i_yld, *oqual = result->qual + QUAL_LEVELS * n_files * result->i_yld; const bam_pileup1_t **plp = plp_iter->plp; bam_mplp_t mplp_iter = plp_iter->mplp_iter; int32_t tid; int *s0 = NULL, *q0 = NULL; if (param->yieldAll) for (i = 0; i < param->yieldSize && i < end - start + 1; ++i) opos[i] = start + i; while (param->yieldSize > idx && 0 < bam_mplp_auto(mplp_iter, &tid, &pos, n_plp, plp)) { pos += 1; if (pos < start || pos > end) continue; if (param->yieldAll) { idx = pos - start; if (idx >= param->yieldSize) break; } else { int empty = TRUE; for (i = 0; empty && i < n_files; ++i) for (j = 0; empty && j < n_plp[i]; ++j) { /* each read */ const bam_pileup1_t *p = plp[i] + j; if (!p->is_del || !p->is_refskip) empty = FALSE; } if (empty) continue; } int cvg_depth = 0L; for (i = 0; i < n_files; ++i) cvg_depth += n_plp[i]; if (param->min_depth > cvg_depth) continue; if (param->what & WHAT_SEQ) s0 = oseq + SEQ_LEVELS * n_files * idx; if (param->what & WHAT_QUAL) q0 = oqual + QUAL_LEVELS * n_files * idx; for (i = 0; i < n_files; ++i) { for (j = 0; j < n_plp[i]; ++j) { /* each read */ const bam_pileup1_t *p = plp[i] + j; /* filter */ if (p->is_del || p->is_refskip) continue; const uint8_t q = bam1_qual(p->b)[p->qpos]; if (param->min_base_quality > q) continue; /* query, e.g., ... */ if (param->what & WHAT_SEQ) { const int s = nuc[bam1_seqi(bam1_seq(p->b), p->qpos)]; if (s < 0) Rf_error("unexpected nucleotide code '%d'", bam1_seqi(bam1_seq(p->b), p->qpos)); s0[SEQ_LEVELS * i + s] += 1; } if (param->what & WHAT_QUAL) { if (QUAL_LEVELS <= q) Rf_error("unexpected quality score '%ud'", q); q0[QUAL_LEVELS * i + q] += 1; } } } if (!param->yieldAll) opos[idx] = pos; idx += 1; } result->i_yld += idx; return idx; } static SEXP _resize_3D_dim3(SEXP s, int n) { SEXP t, dim, dimnms; dim = Rf_getAttrib(s, R_DimSymbol); dimnms = Rf_getAttrib(s, R_DimNamesSymbol); t = PROTECT(Rf_lengthgets(s, INTEGER(dim)[0] * INTEGER(dim)[1] * n)); INTEGER(dim)[2] = n; Rf_setAttrib(t, R_DimSymbol, dim); Rf_setAttrib(t, R_DimNamesSymbol, dimnms); UNPROTECT(1); return t; } static SEXP _resize(SEXP r, int n) { #ifdef PILEUPBAM_DEBUG REprintf("_resize\n"); #endif SEXP s, nm = Rf_getAttrib(r, R_NamesSymbol); int i = 2; s = VECTOR_ELT(r, 1); /* pos */ SET_VECTOR_ELT(r, 1, Rf_lengthgets(s, n)); s = VECTOR_ELT(r, 2); /* seq array -- SEQ_LEVELS x n_files x n */ if (R_NilValue != s) { SET_VECTOR_ELT(r, i, _resize_3D_dim3(s, n)); SET_STRING_ELT(nm, i, STRING_ELT(nm, 2)); ++i; } s = VECTOR_ELT(r, 3); /* qual array -- QUAL_LEVELS x n_files x n */ if (R_NilValue != s) { SET_VECTOR_ELT(r, i, _resize_3D_dim3(s, n)); SET_STRING_ELT(nm, i, STRING_ELT(nm, 3)); ++i; } return Rf_lengthgets(r, i); } static SEXP _call1(SEXP r, SEXP call) { #ifdef PILEUPBAM_DEBUG REprintf("_call1\n"); #endif SETCADR(call, r); /* let's say this doesn't allocate */ return Rf_eval(call, R_GlobalEnv); } static SEXP _yield1_byrange(PILEUP_PARAM_T * param, REGION_ITER_T * reg_iter, PILEUP_ITER_T * plp_iter) { #ifdef PILEUPBAM_DEBUG REprintf("_yield1_byrange\n"); #endif REGION_T *region; PILEUP_RESULT_T plp_result; SEXP res = R_NilValue, rle; int n_rec; if (NULL != (region = _region_iter_next(reg_iter))) { param->yieldSize = region->end - region->start + 1; res = PROTECT(_mplp_setup_R(param, &plp_result)); _mplp_setup_bam(param, region, plp_iter); n_rec = _bam1(param, region, plp_iter, &plp_result); if (param->yieldAll) n_rec = param->yieldSize; _mplp_teardown_bam(plp_iter); rle = _seq_rle(&n_rec, ®ion->chr, 1); SET_VECTOR_ELT(res, 0, rle); res = _resize(res, n_rec); UNPROTECT(1); } return res; } static SEXP _yieldby_range(PILEUP_PARAM_T * param, REGION_ITER_T * reg_iter, PILEUP_ITER_T * plp_iter, SEXP call) { SEXP result, res; int i; result = PROTECT(NEW_LIST(reg_iter->n_reg)); for (i = 0; i < reg_iter->n_reg; ++i) { res = PROTECT(_yield1_byrange(param, reg_iter, plp_iter)); if (R_NilValue == res) Rf_error("internal: 'reg_iter' did not yield"); SET_VECTOR_ELT(result, i, _call1(res, call)); UNPROTECT(1); } UNPROTECT(1); return result; } static SEXP _yield1_byposition(PILEUP_PARAM_T * param, REGION_ITER_T * reg_iter, PILEUP_ITER_T * plp_iter) { #ifdef PILEUPBAM_DEBUG REprintf("_yield1_byposition\n"); #endif const int yieldSize = param->yieldSize, n_reg = reg_iter->n_reg; REGION_T *region; PILEUP_RESULT_T plp_result; SEXP res = R_NilValue, rle; int *cnt, start, start_reg, i_reg, n_rec, i_yld = 0; if (NULL == (region = _region_iter_pop(reg_iter))) { if (NULL == (region = _region_iter_next(reg_iter))) return res; /* early exit */ _mplp_setup_bam(param, region, plp_iter); } if ((reg_iter->n_reg - 1 == region->i_reg) && (param->yieldSize > region->end - region->start + 1)) param->yieldSize = region->end - region->start + 1; start_reg = region->i_reg; i_reg = 1; res = PROTECT(_mplp_setup_R(param, &plp_result)); cnt = (int *) Calloc(n_reg, int); memset(cnt, 0, sizeof(int) * n_reg); while (region && yieldSize > i_yld) { n_rec = _bam1(param, region, plp_iter, &plp_result); if (param->yieldAll) { const int reg_width = region->end - region->start + 1L; n_rec = reg_width < param->yieldSize ? reg_width : param->yieldSize; } param->yieldSize -= n_rec; i_yld += n_rec; cnt[region->i_reg] = i_yld; if (yieldSize > i_yld) { /* next region */ if ((region = _region_iter_next(reg_iter))) { _mplp_teardown_bam(plp_iter); _mplp_setup_bam(param, region, plp_iter); i_reg++; } } } if (i_yld) { rle = _seq_rle(cnt + start_reg, reg_iter->chr + start_reg, i_reg); SET_VECTOR_ELT(res, 0, rle); } if (region) { if (i_yld) { start = INTEGER(VECTOR_ELT(res, 1))[i_yld - 1] + 1; if (region->end >= start) { region->start = start; _region_iter_stash(reg_iter, region); } } } param->yieldSize = yieldSize; res = _resize(res, i_yld); Free(cnt); UNPROTECT(1); return res; } static SEXP _yieldby_position(PILEUP_PARAM_T * param, REGION_ITER_T * reg_iter, PILEUP_ITER_T * plp_iter, SEXP call) { const int GROW_BY_ELTS = 10; SEXP result = R_NilValue, res; int i_res = 0, len, pidx; PROTECT_WITH_INDEX(result = NEW_LIST(0), &pidx); while (R_NilValue != (res = _yield1_byposition(param, reg_iter, plp_iter))) { PROTECT(res); if (Rf_length(result) == i_res) { /* more space for results */ len = Rf_length(result) + GROW_BY_ELTS; result = Rf_lengthgets(result, len); REPROTECT(result, pidx); } SET_VECTOR_ELT(result, i_res++, _call1(res, call)); UNPROTECT(1); } _mplp_teardown_bam(plp_iter); /* from _yield1_byposition */ result = Rf_lengthgets(result, i_res); UNPROTECT(1); return result; } SEXP apply_pileups(SEXP files, SEXP names, SEXP regions, SEXP param, SEXP callback) { int i; PILEUP_PARAM_T p; REGION_ITER_T *reg_iter; PILEUP_ITER_T *plp_iter; SEXP call, result; if (!IS_LIST(files)) Rf_error("'files' must be list() of BamFiles"); p.n_files = Rf_length(files); p.names = names; for (i = 0; i < p.n_files; ++i) { SEXP elt = VECTOR_ELT(files, i); _check_isbamfile(elt, "pileup"); if (NULL == BAMFILE(elt)->index) Rf_error("no index found for file '%s'", CHAR(STRING_ELT(names, i))); } if (R_NilValue == regions) Rf_error("'NULL' regions not (yet) supported"); _checkparams(regions, R_NilValue, R_NilValue); if (!Rf_isFunction(callback) || 1L != Rf_length(FORMALS(callback))) Rf_error("'callback' must be a function of 1 argument"); call = PROTECT(Rf_lang2(callback, R_NilValue)); /* param */ reg_iter = _region_iter_init(regions); p.keep_flag[0] = INTEGER(_lst_elt(param, "flag", "param"))[0]; p.keep_flag[1] = INTEGER(_lst_elt(param, "flag", "param"))[1]; p.min_depth = INTEGER(_lst_elt(param, "minDepth", "param"))[0]; p.max_depth = INTEGER(_lst_elt(param, "maxDepth", "param"))[0]; p.min_base_quality = INTEGER(_lst_elt(param, "minBaseQuality", "param"))[0]; p.min_map_quality = INTEGER(_lst_elt(param, "minMapQuality", "param"))[0]; p.yieldSize = INTEGER(_lst_elt(param, "yieldSize", "param"))[0]; const char *yieldBy = CHAR(STRING_ELT(_lst_elt(param, "yieldBy", "param"), 0)); p.yieldBy = 0 == strcmp(yieldBy, "range") ? YIELDBY_RANGE : YIELDBY_POSITION; p.yieldAll = LOGICAL(_lst_elt(param, "yieldAll", "param"))[0]; int *what = LOGICAL(_lst_elt(param, "what", "param")); p.what = WHAT_OK; if (what[0]) p.what |= WHAT_SEQ; if (what[1]) p.what |= WHAT_QUAL; /* data -- validate */ plp_iter = _iter_init(files, &p); /* result */ result = R_NilValue; if (R_NilValue == regions) { /* all */ /* FIXME: allocate seq, but this is too big! */ /* _bam1(n, -1, -1, max_depth, */ /* _mplp_read_bam, (void **) mfile, */ /* seq); */ } else { /* some */ if (YIELDBY_RANGE == p.yieldBy) result = _yieldby_range(&p, reg_iter, plp_iter, call); else result = _yieldby_position(&p, reg_iter, plp_iter, call); } _iter_destroy(plp_iter); _region_iter_destroy(reg_iter); UNPROTECT(1); return result; } Rsamtools/src/pileupbam.h0000644000175400017540000000026213556116727016516 0ustar00biocbuildbiocbuild#ifndef MPILEUPBAM_H #define MPILEUPBAM_H #include SEXP apply_pileups(SEXP files, SEXP names, SEXP regions, SEXP param, SEXP callback); #endif Rsamtools/src/sam.c0000644000175400017540000000002113556116727015304 0ustar00biocbuildbiocbuild#include Rsamtools/src/sam_opts.c0000644000175400017540000000002613556116727016356 0ustar00biocbuildbiocbuild#include Rsamtools/src/sam_utils.c0000644000175400017540000000002713556116727016532 0ustar00biocbuildbiocbuild#include Rsamtools/src/samtools_patch.c0000644000175400017540000000207313556116727017555 0ustar00biocbuildbiocbuild#include #include "samtools_patch.h" void _samtools_exit(int status) { Rf_error ("internal: samtools invoked 'exit(%d)'; see warnings() and restart R", status); } void _samtools_abort() { Rf_error ("internal: samtools invoked 'abort'; see warnings() and restart R"); } int _samtools_fprintf(FILE * file, const char *fmt, ...) { static const int bufsize = 2048; va_list argp; int n; if (stderr != file) { va_start(argp, fmt); n = vfprintf(file, fmt, argp); va_end(argp); } else { /* silence some messages */ char *buf = (char *) R_alloc(bufsize, sizeof(char)); if (0 == strncmp("[samopen] SAM header is present:", fmt, 32) || 0 == strncmp("[fai_load] build FASTA index.", fmt, 29)) return 0; va_start(argp, fmt); n = vsnprintf(buf, bufsize, fmt, argp); va_end(argp); if (0 == strncmp("[khttp_connect_file] fail to open file", fmt, 38)) Rf_error(buf); Rf_warning(buf); } return n; } Rsamtools/src/samtools_patch.h0000644000175400017540000000033113556116727017555 0ustar00biocbuildbiocbuild#ifndef SAMTOOLS_PATCH_H #define SAMTOOLS_PATCH_H /* capture samtools errors */ extern void _samtools_abort(); extern void _samtools_exit(int status); extern int _samtools_fprintf(FILE *, const char *, ...); #endif Rsamtools/src/scan_bam_data.c0000644000175400017540000002074013556116727017272 0ustar00biocbuildbiocbuild#include "scan_bam_data.h" #include "utilities.h" /* _SCAN_BAM_DATA */ SCAN_BAM_DATA _init_SCAN_BAM_DATA(SEXP result) { SCAN_BAM_DATA sbd = Calloc(1, _SCAN_BAM_DATA); sbd->cigarhash = kh_init(str); sbd->result = result; sbd->mates_flag = NA_LOGICAL; sbd->partition_id = 0; return sbd; } static void _Free_strhash(khash_t(str) * h) { khiter_t k; char *buf; for (k = kh_begin(h); kh_end(h) != k; ++k) if (kh_exist(h, k)) { buf = (char *) kh_key(h, k); Free(buf); } kh_destroy(str, h); } void _Free_SCAN_BAM_DATA(SCAN_BAM_DATA sbd) { _Free_strhash(sbd->cigarhash); Free(sbd); } static void _grow_SCAN_BAM_DATA_tags(SEXP tags, int len) { int i, j; for (i = 0; i < LENGTH(tags); ++i) { SEXP elt = VECTOR_ELT(tags, i); if (elt == R_NilValue) continue; int len0 = LENGTH(elt); elt = Rf_lengthgets(elt, len); SET_VECTOR_ELT(tags, i, elt); switch (TYPEOF(elt)) { case INTSXP: for (j = len0; j < len; ++j) INTEGER(elt)[j] = NA_INTEGER; break; case REALSXP: for (j = len0; j < len; ++j) REAL(elt)[j] = NA_REAL; break; case STRSXP: for (j = len0; j < len; ++j) SET_STRING_ELT(elt, j, NA_STRING); break; case RAWSXP: for (j = len0; j < len; ++j) RAW(elt)[j] = 0x0; break; } } } int _grow_SCAN_BAM_DATA(BAM_DATA bd, int len) { int i; SEXP r, s; SCAN_BAM_DATA sbd = (SCAN_BAM_DATA) bd->extra; r = VECTOR_ELT(sbd->result, bd->irange); for (i = 0; i < LENGTH(r); ++i) { if (R_NilValue == (s = VECTOR_ELT(r, i))) continue; switch (i) { case FLAG_IDX: sbd->flag = _Rs_Realloc(sbd->flag, len, int); break; case RNAME_IDX: sbd->rname = _Rs_Realloc(sbd->rname, len, int); break; case STRAND_IDX: sbd->strand = _Rs_Realloc(sbd->strand, len, int); break; case POS_IDX: sbd->pos = _Rs_Realloc(sbd->pos, len, int); break; case QWIDTH_IDX: sbd->qwidth = _Rs_Realloc(sbd->qwidth, len, int); break; case MAPQ_IDX: sbd->mapq = _Rs_Realloc(sbd->mapq, len, int); break; case MRNM_IDX: sbd->mrnm = _Rs_Realloc(sbd->mrnm, len, int); break; case MPOS_IDX: sbd->mpos = _Rs_Realloc(sbd->mpos, len, int); break; case ISIZE_IDX: sbd->isize = _Rs_Realloc(sbd->isize, len, int); break; case QNAME_IDX: sbd->qname = _Rs_Realloc(sbd->qname, len, char *); break; case CIGAR_IDX: sbd->cigar = _Rs_Realloc(sbd->cigar, len, const char *); break; case SEQ_IDX: sbd->seq = _Rs_Realloc(sbd->seq, len, const char *); break; case QUAL_IDX: sbd->qual = _Rs_Realloc(sbd->qual, len, const char *); break; case TAG_IDX: if (R_NilValue != s) _grow_SCAN_BAM_DATA_tags(s, len); break; case PARTITION_IDX: sbd->partition = _Rs_Realloc(sbd->partition, len, int); break; case MATES_IDX: sbd->mates = _Rs_Realloc(sbd->mates, len, int); break; default: Rf_error("[Rsamtools internal] unhandled _grow_SCAN_BAM_DATA"); break; } } return len; } SEXP _get_or_grow_SCAN_BAM_DATA(BAM_DATA bd, int len) { _SCAN_BAM_DATA *sbd = (_SCAN_BAM_DATA *) bd->extra; if (len < 0) { if (sbd->icnt < sbd->ncnt) return VECTOR_ELT(sbd->result, bd->irange); len = sbd->ncnt + bd->BLOCKSIZE; } sbd->ncnt = _grow_SCAN_BAM_DATA(bd, len); return VECTOR_ELT(sbd->result, bd->irange); } void _finish1range_SCAN_BAM_DATA(SCAN_BAM_DATA sbd, bam_header_t *header, int irange) { /* FIXME: replace mrnm '=' with rname */ const char *mates_lvls[] = { "mated", "ambiguous", "unmated" }; int i, j; SEXP r, s; r = VECTOR_ELT(sbd->result, irange); for (i = 0; i < LENGTH(r); ++i) { if (R_NilValue == (s = VECTOR_ELT(r, i))) continue; switch (i) { case FLAG_IDX: s = Rf_lengthgets(s, sbd->icnt); SET_VECTOR_ELT(r, i, s); memcpy(INTEGER(s), sbd->flag, sbd->icnt * sizeof(int)); Free(sbd->flag); break; case RNAME_IDX: s = Rf_lengthgets(s, sbd->icnt); SET_VECTOR_ELT(r, i, s); memcpy(INTEGER(s), sbd->rname, sbd->icnt * sizeof(int)); _as_rname(s, (const char **) header->target_name, header->n_targets); Free(sbd->rname); break; case STRAND_IDX: s = Rf_lengthgets(s, sbd->icnt); SET_VECTOR_ELT(r, i, s); memcpy(INTEGER(s), sbd->strand, sbd->icnt * sizeof(int)); _as_strand(s); Free(sbd->strand); break; case POS_IDX: s = Rf_lengthgets(s, sbd->icnt); SET_VECTOR_ELT(r, i, s); memcpy(INTEGER(s), sbd->pos, sbd->icnt * sizeof(int)); Free(sbd->pos); break; case QWIDTH_IDX: s = Rf_lengthgets(s, sbd->icnt); SET_VECTOR_ELT(r, i, s); memcpy(INTEGER(s), sbd->qwidth, sbd->icnt * sizeof(int)); Free(sbd->qwidth); break; case MAPQ_IDX: s = Rf_lengthgets(s, sbd->icnt); SET_VECTOR_ELT(r, i, s); memcpy(INTEGER(s), sbd->mapq, sbd->icnt * sizeof(int)); Free(sbd->mapq); break; case MRNM_IDX: s = Rf_lengthgets(s, sbd->icnt); SET_VECTOR_ELT(r, i, s); memcpy(INTEGER(s), sbd->mrnm, sbd->icnt * sizeof(int)); _as_rname(s, (const char **) header->target_name, header->n_targets); Free(sbd->mrnm); break; case MPOS_IDX: s = Rf_lengthgets(s, sbd->icnt); SET_VECTOR_ELT(r, i, s); memcpy(INTEGER(s), sbd->mpos, sbd->icnt * sizeof(int)); Free(sbd->mpos); break; case ISIZE_IDX: s = Rf_lengthgets(s, sbd->icnt); SET_VECTOR_ELT(r, i, s); memcpy(INTEGER(s), sbd->isize, sbd->icnt * sizeof(int)); Free(sbd->isize); break; case QNAME_IDX: s = Rf_lengthgets(s, sbd->icnt); SET_VECTOR_ELT(r, i, s); for (j = 0; j < sbd->icnt; ++j) { SET_STRING_ELT(s, j, mkChar(sbd->qname[j])); Free(sbd->qname[j]); } Free(sbd->qname); break; case CIGAR_IDX: s = Rf_lengthgets(s, sbd->icnt); SET_VECTOR_ELT(r, i, s); for (j = 0; j < sbd->icnt; ++j) if (NULL == sbd->cigar[j]) SET_STRING_ELT(s, j, NA_STRING); else SET_STRING_ELT(s, j, mkChar(sbd->cigar[j])); Free(sbd->cigar); break; case SEQ_IDX: s = _as_XStringSet(sbd->seq, sbd->icnt, "DNAString"); SET_VECTOR_ELT(r, i, s); for (j = 0; j < sbd->icnt; ++j) Free(sbd->seq[j]); Free(sbd->seq); break; case QUAL_IDX: s = _as_PhredQuality(sbd->qual, sbd->icnt); SET_VECTOR_ELT(r, i, s); for (j = 0; j < sbd->icnt; ++j) Free(sbd->qual[j]); Free(sbd->qual); break; case TAG_IDX: _grow_SCAN_BAM_DATA_tags(s, sbd->icnt); break; case PARTITION_IDX: s = Rf_lengthgets(s, sbd->icnt); SET_VECTOR_ELT(r, i, s); memcpy(INTEGER(s), sbd->partition, Rf_length(s) * sizeof(int)); Free(sbd->partition); break; case MATES_IDX: s = Rf_lengthgets(s, sbd->icnt); SET_VECTOR_ELT(r, i, s); memcpy(INTEGER(s), sbd->mates, sbd->icnt * sizeof(int)); _as_factor(s, mates_lvls, 3); Free(sbd->mates); break; default: Rf_error("[Rsamtools internal] unhandled _finish1range_BAM_DATA"); break; } } sbd->icnt = sbd->ncnt = 0; sbd->mates_flag = NA_LOGICAL; } Rsamtools/src/scan_bam_data.h0000644000175400017540000000162013556116727017273 0ustar00biocbuildbiocbuild#ifndef SCAN_BAM_DATA_H #define SCAN_BAM_DATA_H #include #include "Rdefines.h" #include "bam_data.h" KHASH_SET_INIT_STR(str) typedef struct { int *flag, *rname, *strand, *pos, *qwidth, *mapq, *mrnm, *mpos, *isize, *partition, *mates; char **qname; const char **cigar, **seq, **qual; khash_t(str) *cigarhash; int icnt, ncnt, mates_flag, partition_id; /* set prior to parsing 1 bam record */ SEXP result; } _SCAN_BAM_DATA, *SCAN_BAM_DATA; SCAN_BAM_DATA _init_SCAN_BAM_DATA(SEXP result); void _Free_SCAN_BAM_DATA(SCAN_BAM_DATA sbd); int _grow_SCAN_BAM_DATA(BAM_DATA bd, int len); void _finish1range_SCAN_BAM_DATA(SCAN_BAM_DATA sbd, bam_header_t *header, int irange); SEXP _scan_bam_result_init(SEXP template_list, SEXP names, SEXP regions, BAM_FILE bfile); SEXP _get_or_grow_SCAN_BAM_DATA(BAM_DATA bd, int len); #endif Rsamtools/src/tabixfile.c0000644000175400017540000002772113556116727016513 0ustar00biocbuildbiocbuild#include #include #include #include "tabixfile.h" #include "utilities.h" static SEXP TABIXFILE_TAG = NULL; static const int TBX_INIT_SIZE = 32767; /* Convenience wrappers around bgzf_tell(), bgzf_seek(), bgzf_getline(), and tbx_itr_next(). */ static int64_t _tbx_tell(htsFile *file) { BGZF *fp; if (!file->is_bgzf) Rf_error("[internal] hmm.. this doesn't look like a tabix file, sorry"); fp = file->fp.bgzf; return bgzf_tell(fp); } static void _tbx_seek(htsFile *file, int64_t offset) { BGZF *fp; if (!file->is_bgzf) Rf_error("[internal] hmm.. this doesn't look like a tabix file, sorry"); fp = file->fp.bgzf; if (bgzf_seek(fp, offset, SEEK_SET) < 0) Rf_error("[internal] bgzf_seek() failed"); return; } static const char *_tbx_read_line(htsFile *file, int *len) { BGZF *fp; static kstring_t ksbuf = {0, 0, NULL}; if (!file->is_bgzf) Rf_error("[internal] hmm.. this doesn't look like a tabix file, sorry"); fp = file->fp.bgzf; if (bgzf_getline(fp, '\n', &ksbuf) < 0) return NULL; *len = ksbuf.l; return ksbuf.s; } static const char *_tbx_read_next_rec(htsFile *file, tbx_t *index, hts_itr_t *iter, int *len) { static kstring_t ksbuf = {0, 0, NULL}; if (tbx_itr_next(file, index, iter, &ksbuf) < 0) return NULL; *len = ksbuf.l; return ksbuf.s; } static void _tabixfile_close(SEXP ext) { _TABIX_FILE *tfile = TABIXFILE(ext); if (NULL != tfile->file) { hts_close(tfile->file); tfile->file = NULL; } if (NULL != tfile->index) { tbx_destroy(tfile->index); tfile->index = NULL; } if (NULL != tfile->iter) { tbx_itr_destroy(tfile->iter); tfile->iter = NULL; } } static void _tabixfile_finalizer(SEXP ext) { if (NULL == R_ExternalPtrAddr(ext)) return; _tabixfile_close(ext); _TABIX_FILE *tfile = TABIXFILE(ext); Free(tfile); R_SetExternalPtrAddr(ext, NULL); } /* --- .Call ENTRY POINT --- */ SEXP tabixfile_init() { TABIXFILE_TAG = install("TabixFile"); return R_NilValue; } /* --- .Call ENTRY POINT --- */ SEXP tabixfile_open(SEXP filename, SEXP indexname) { if (!IS_CHARACTER(filename) || LENGTH(filename) != 1) Rf_error("'filename' must be character(1)"); if (!IS_CHARACTER(indexname) || LENGTH(indexname) != 1) Rf_error("'indexname' must be character(1)"); _TABIX_FILE *tfile = Calloc(1, _TABIX_FILE); const char *fn = translateChar(STRING_ELT(filename, 0)); tfile->file = hts_open(fn, "r"); if (tfile->file == NULL) { Free(tfile); Rf_error("failed to open file: %s", fn); } const char *fnidx = translateChar(STRING_ELT(indexname, 0)); tfile->index = tbx_index_load2(fn, fnidx); if (tfile->index == NULL) { hts_close(tfile->file); Free(tfile); Rf_error("failed to open index file: %s", fnidx); } tfile->iter = NULL; SEXP ext = PROTECT(R_MakeExternalPtr(tfile, TABIXFILE_TAG, filename)); R_RegisterCFinalizerEx(ext, _tabixfile_finalizer, TRUE); UNPROTECT(1); return ext; } /* --- .Call ENTRY POINT --- */ SEXP tabixfile_close(SEXP ext) { _checkext(ext, TABIXFILE_TAG, "close"); _tabixfile_close(ext); return ext; } /* --- .Call ENTRY POINT --- */ SEXP tabixfile_isopen(SEXP ext) { SEXP ans = ScalarLogical(FALSE); if (NULL != TABIXFILE(ext)) { _checkext(ext, TABIXFILE_TAG, "isOpen"); if (TABIXFILE(ext)->file) ans = ScalarLogical(TRUE); } return ans; } /* --- .Call ENTRY POINT --- */ SEXP index_tabix(SEXP filename, SEXP format, SEXP seq, SEXP begin, SEXP end, SEXP skip, SEXP comment, SEXP zeroBased) { tbx_conf_t conf = tbx_conf_gff; if (!IS_CHARACTER(filename) || LENGTH(filename) != 1) Rf_error("'filename' must be character(1)"); const char *fn = translateChar(STRING_ELT(filename, 0)); if (LENGTH(format) == 1) { const char *txt = CHAR(STRING_ELT(format, 0)); if (strcmp(txt, "gff") == 0) conf = tbx_conf_gff; else if (strcmp(txt, "bed") == 0) conf = tbx_conf_bed; else if (strcmp(txt, "sam") == 0) conf = tbx_conf_sam; else if (strcmp(txt, "vcf") == 0 || strcmp(txt, "vcf4") == 0) conf = tbx_conf_vcf; else if (strcmp(txt, "psltbl") == 0) conf = tbx_conf_psltbl; else Rf_error("format '%s' unrecognized", txt); } else { if (!IS_INTEGER(seq) || LENGTH(seq) != 1) Rf_error("'seq' must be integer(1)"); conf.sc = INTEGER(seq)[0]; if (!IS_INTEGER(begin) || LENGTH(begin) != 1) Rf_error("'begin' must be integer(1)"); conf.bc = INTEGER(begin)[0]; if (!IS_INTEGER(end) || LENGTH(end) != 1) Rf_error("'end' must be integer(1)"); conf.ec = INTEGER(end)[0]; } if (IS_INTEGER(skip) && LENGTH(skip) == 1) conf.line_skip = INTEGER(skip)[0]; if (IS_CHARACTER(comment) && LENGTH(comment) == 1) conf.meta_char = CHAR(STRING_ELT(comment, 0))[0]; if (IS_LOGICAL(zeroBased) && LENGTH(zeroBased) == 1 && LOGICAL(zeroBased)[0] == TRUE) conf.preset |= TBX_UCSC; if (bgzf_is_bgzf(fn) != 1) Rf_error("file does not appear to be bgzip'd"); if (tbx_index_build(fn, 0, &conf) == -1) Rf_error("index build failed"); return filename; } static void _skip_header_lines(htsFile *file, const tbx_conf_t *conf) { const char *line; int linelen; int64_t curr_off = _tbx_tell(file); while ((line = _tbx_read_line(file, &linelen)) != NULL) { if (line[0] != conf->meta_char) break; curr_off = _tbx_tell(file); } _tbx_seek(file, curr_off); return; } static SEXP _read_header_lines(htsFile *file, const tbx_conf_t *conf) { int pidx, i_lns = 0; const char *line; int linelen; const int GROW_BY = 100; SEXP lns = NEW_CHARACTER(0); PROTECT_WITH_INDEX(lns, &pidx); int64_t curr_off = _tbx_tell(file); while ((line = _tbx_read_line(file, &linelen)) != NULL) { if (line[0] != conf->meta_char) break; curr_off = _tbx_tell(file); if ((i_lns % GROW_BY) == 0) { SET_LENGTH(lns, LENGTH(lns) + GROW_BY); REPROTECT(lns, pidx); } SET_STRING_ELT(lns, i_lns, mkCharLen(line, linelen)); i_lns++; } _tbx_seek(file, curr_off); SET_LENGTH(lns, i_lns); UNPROTECT(1); return lns; } /* --- .Call ENTRY POINT --- */ SEXP header_tabix(SEXP ext) { _checkext(ext, TABIXFILE_TAG, "headerTabix"); _TABIX_FILE *tfile = TABIXFILE(ext); htsFile *file = tfile->file; tbx_t *index = tfile->index; SEXP result = PROTECT(NEW_LIST(5)), tmp, nms; nms = NEW_CHARACTER(LENGTH(result)); Rf_namesgets(result, nms); SET_STRING_ELT(nms, 0, mkChar("seqnames")); SET_STRING_ELT(nms, 1, mkChar("indexColumns")); SET_STRING_ELT(nms, 2, mkChar("skip")); SET_STRING_ELT(nms, 3, mkChar("comment")); SET_STRING_ELT(nms, 4, mkChar("header")); /* seqnames */ int n; const char **seqnames = tbx_seqnames(index, &n); if (n < 0) Rf_error("'seqnamesTabix' found <0 (!) seqnames"); tmp = NEW_CHARACTER(n); SET_VECTOR_ELT(result, 0, tmp); for (int i = 0; i < n; ++i) SET_STRING_ELT(tmp, i, mkChar(seqnames[i])); free(seqnames); /* indexColumns */ const tbx_conf_t conf = index->conf; tmp = NEW_INTEGER(3); SET_VECTOR_ELT(result, 1, tmp); INTEGER(tmp)[0] = conf.sc; INTEGER(tmp)[1] = conf.bc; INTEGER(tmp)[2] = conf.ec; nms = NEW_CHARACTER(3); Rf_namesgets(tmp, nms); SET_STRING_ELT(nms, 0, mkChar("seq")); SET_STRING_ELT(nms, 1, mkChar("start")); SET_STRING_ELT(nms, 2, mkChar("end")); /* skip */ SET_VECTOR_ELT(result, 2, ScalarInteger(conf.line_skip)); /* comment */ char comment[2]; comment[0] = (char) conf.meta_char; comment[1] = '\0'; SET_VECTOR_ELT(result, 3, ScalarString(mkChar(comment))); /* header lines */ SET_VECTOR_ELT(result, 4, _read_header_lines(file, &conf)); UNPROTECT(1); return result; } /* --- .Call CALLBACK FUNCTION --- */ SEXP tabix_as_character(htsFile *file, tbx_t *index, hts_itr_t *iter, const int yield, SEXP state, SEXP rownames) { int pidx, irec = 0; const char *line; int linelen; const double SCALE = 1.6; if (R_NilValue != rownames) Rf_error("[internal] expected 'NULL' rownames in tabix_as_character"); if (R_NilValue != state) Rf_error("[internal] expected 'NULL' state in tabix_as_character"); int nrec = yield == NA_INTEGER ? TBX_INIT_SIZE : yield; SEXP record = NEW_CHARACTER(nrec); PROTECT_WITH_INDEX(record, &pidx); const tbx_conf_t conf = index->conf; while ((line = _tbx_read_next_rec(file, index, iter, &linelen)) != NULL) { if (line[0] == conf.meta_char) continue; if (irec == nrec) { nrec = nrec * SCALE; SET_LENGTH(record, nrec); REPROTECT(record, pidx); } SET_STRING_ELT(record, irec, mkCharLen(line, linelen)); irec++; if (yield != NA_INTEGER && irec == nrec) break; } SET_LENGTH(record, irec); UNPROTECT(1); return record; } /* --- .Call CALLBACK FUNCTION --- */ SEXP tabix_count(htsFile *file, tbx_t *index, hts_itr_t *iter, const int yield, SEXP state, SEXP rownames) { const tbx_conf_t conf = index->conf; const char *line; int linelen, irec = 0; if (R_NilValue != rownames) Rf_error("[internal] expected 'NULL' rownames in tabix_count"); if (R_NilValue != state) Rf_error("[internal] expected 'NULL' state in tabix_count"); while ((line = _tbx_read_next_rec(file, index, iter, &linelen)) != NULL) { if (line[0] == conf.meta_char) continue; irec += 1; } return ScalarInteger(irec); } /* --- .Call ENTRY POINT --- */ SEXP scan_tabix(SEXP ext, SEXP regions, SEXP yield, SEXP fun, SEXP state, SEXP rownames) { _checkparams(regions, R_NilValue, R_NilValue); if (!IS_INTEGER(yield) || LENGTH(yield) != 1) Rf_error("'yieldSize' must be integer(1)"); _checkext(ext, TABIXFILE_TAG, "scanTabix"); _TABIX_FILE *tfile = TABIXFILE(ext); htsFile *file = tfile->file; tbx_t *index = tfile->index; SCAN_FUN *scan = (SCAN_FUN *) R_ExternalPtrAddr(fun); SEXP space = VECTOR_ELT(regions, 0); const int nregions = LENGTH(space); SEXP result, elt; PROTECT(result = NEW_LIST(nregions == 0 ? 1 : nregions)); if (nregions == 0) { hts_itr_t *iter = tfile->iter; if (iter == NULL) { _skip_header_lines(file, &(index->conf)); /* Create iterator that will iterate over all records. */ iter = tbx_itr_queryi(index, HTS_IDX_REST, 0, 0); if (iter == NULL) Rf_error("[internal] failed to create tabix iterator"); tfile->iter = iter; } elt = scan(file, index, iter, INTEGER(yield)[0], state, rownames); SET_VECTOR_ELT(result, 0, elt); } else { const int *start = INTEGER(VECTOR_ELT(regions, 1)), *end = INTEGER(VECTOR_ELT(regions, 2)); for (int i = 0; i < nregions; ++i) { int ibeg, iend, tid; hts_itr_t *iter; const char *tid_name; ibeg = start[i] == 0 ? 0 : start[i] - 1; iend = end[i]; tid_name = CHAR(STRING_ELT(space, i)); tid = tbx_name2id(index, tid_name); if (tid < 0) Rf_error("'%s' not present in tabix index", tid_name); iter = tbx_itr_queryi(index, tid, ibeg, iend); elt = scan(file, index, iter, NA_INTEGER, state, rownames); SET_VECTOR_ELT(result, i, elt); tbx_itr_destroy(iter); } } UNPROTECT(1); return result; } Rsamtools/src/tabixfile.h0000644000175400017540000000154413556116727016513 0ustar00biocbuildbiocbuild#ifndef _TABIXFILE_H #define _TABIXFILE_H #include #include "htslib/tbx.h" typedef struct { htsFile *file; tbx_t *index; hts_itr_t *iter; } _TABIX_FILE; #define TABIXFILE(b) ((_TABIX_FILE *) R_ExternalPtrAddr(b)) typedef SEXP SCAN_FUN(htsFile *file, tbx_t *index, hts_itr_t *iter, const int yield, SEXP state, SEXP rownames); SCAN_FUN tabix_as_character; SCAN_FUN tabix_count; SEXP tabixfile_init(); SEXP tabixfile_open(SEXP filename, SEXP indexname); SEXP tabixfile_close(SEXP ext); SEXP tabixfile_isopen(SEXP ext); SEXP index_tabix(SEXP filename, SEXP format, SEXP seq, SEXP begin, SEXP end, SEXP skip, SEXP comment, SEXP zeroBased); SEXP header_tabix(SEXP ext); SEXP scan_tabix(SEXP ext, SEXP regions, SEXP yield, SEXP fun, SEXP state, SEXP rownames); #endif Rsamtools/src/tagfilter.c0000644000175400017540000001560613556116727016524 0ustar00biocbuildbiocbuild#include "tagfilter.h" C_TAGFILTER _tagFilter_as_C_types(SEXP tl) { if(LENGTH(tl) == 0) return NULL; C_TAGFILTER tagfilt = Calloc(1, _C_TAGFILTER); SEXP nmssxp = Rf_getAttrib(tl, R_NamesSymbol); /* convert tagnames */ int len = LENGTH(nmssxp); tagfilt->len = len; tagfilt->tagnames = (const char**) Calloc(len, char*); for(int i = 0; i < len; ++i) { tagfilt->tagnames[i] = CHAR(STRING_ELT(nmssxp, i)); } /* allocate for elements */ tagfilt->elts = Calloc(len, _TAGFILTER_ELT); for(int i = 0; i < len; ++i) { SEXP sxp_elt = VECTOR_ELT(tl, i); int elt_len = LENGTH(sxp_elt); if(elt_len < 1) Rf_error("elements of tag filter list must have non-zero length"); switch(TYPEOF(sxp_elt)) { case INTSXP: /* INTEGER */ tagfilt->elts[i].len = elt_len; tagfilt->elts[i].type = TAGFILT_T_INT; tagfilt->elts[i].ptr = (int*) INTEGER(sxp_elt); break; case STRSXP: /* CHAR */ tagfilt->elts[i].len = elt_len; tagfilt->elts[i].type = TAGFILT_T_STRING; tagfilt->elts[i].ptr = (const char**) Calloc(elt_len, char*); for(int j = 0; j < elt_len; ++j) { ((const char**) tagfilt->elts[i].ptr)[j] = CHAR(STRING_ELT(sxp_elt, j)); } break; default: Rf_error("unpermitted tag filter input type '%s'", Rf_type2char((SEXPTYPE) TYPEOF(sxp_elt))); } } return tagfilt; } void _Free_C_TAGFILTER(C_TAGFILTER ctf) { if(ctf) { Free(ctf->tagnames); if(ctf->elts) { for(int i = 0; i < ctf->len; ++i) { if(ctf->elts[i].type == TAGFILT_T_STRING) Free(ctf->elts[i].ptr); } Free(ctf->elts); } Free(ctf); } } static const char* const TagFilterType_str[] = { "INTERNAL_ERROR: UNSET", "integer()", "character()" }; static const char auxtype[] = "cCsSiIfdAZHB"; static const char inttype[] = "cCsSiI"; static const char* const auxtype_str[] = { "integer", "integer", "integer", "integer", "integer", "integer", "float", "double", "single printable character", "string", "hex array", "array" }; static void _typemismatch_error(const char *tagname, uint8_t *aux, TagFilterType tft, const char* val_as_string, int irec) { static const char* msg = "tag '%s' type ('%s') does not match tagFilter type\n" " BAM read tag: %s:%c:%s\n" " tagFilter type: %s\n" " Record number: %d"; int i = strchr(auxtype, aux[0]) - auxtype; const char *printable_typename = auxtype_str[i]; const char tagtypechar = strchr(inttype, aux[0]) ? 'i' : aux[0]; Rf_error(msg, tagname, printable_typename, tagname, tagtypechar, val_as_string, TagFilterType_str[tft], irec); } static void _typeunsupported_error(const char *tagname, uint8_t *aux, const char* val_as_string, int irec) { static const char* msg = "tag '%s' type ('%s') unsupported by tagFilter\n" " BAM read tag: %s:%c:%s\n" " Record number: %d"; int i = strchr(auxtype, aux[0]) - auxtype; const char *printable_typename = auxtype_str[i]; const char tagtypechar = strchr(inttype, aux[0]) ? 'i' : aux[0]; Rf_error(msg, tagname, printable_typename, tagname, tagtypechar, val_as_string, irec); } int _tagfilter(const bam1_t * bam, C_TAGFILTER tagfilter, int irec) { int len = tagfilter->len; for(int i = 0; i < len; ++i) { const char* tagname = tagfilter->tagnames[i]; void *list_elt = tagfilter->elts[i].ptr; uint8_t *aux = bam_aux_get(bam, tagname); if(aux == NULL) return 0; int idx; /* one bamf* for each case in switch */ int bamfi; float bamff; double bamfd; char bamfA; char* bamfZ; char val_as_string[51]; switch(aux[0]) { case 'c': case 'C': case 's': case 'S': case 'i': case 'I': /* INTEGER */ bamfi = bam_aux2i(aux); if(tagfilter->elts[i].type != TAGFILT_T_INT) { snprintf(val_as_string, 51, "%d", bamfi); _typemismatch_error(tagname, aux, tagfilter->elts[i].type, val_as_string, irec); } for(idx = 0; idx < tagfilter->elts[i].len; ++idx) { if(bamfi == ((int*) list_elt)[idx]) break; } if(idx == tagfilter->elts[i].len) return 0; break; case 'f': /* REAL */ bamff = (float) bam_aux2f(aux); snprintf(val_as_string, 51, "%f", bamff); _typeunsupported_error(tagname, aux, val_as_string, irec); break; case 'd': /* REAL */ bamfd = bam_aux2f(aux); snprintf(val_as_string, 51, "%f", bamfd); _typeunsupported_error(tagname, aux, val_as_string, irec); break; case 'A': /* STRSXP */ bamfA = bam_aux2A(aux); if(tagfilter->elts[i].type != TAGFILT_T_STRING || strlen(*((const char**) list_elt)) != 1) { snprintf(val_as_string, 51, "%c", bamfA); _typemismatch_error(tagname, aux, tagfilter->elts[i].type, val_as_string, irec); } for(idx = 0; idx < tagfilter->elts[i].len; ++idx) { if(bamfA == *((const char**) list_elt)[idx]) break; } if(idx == tagfilter->elts[i].len) return 0; break; case 'Z': /* STRSXP */ bamfZ = bam_aux2Z(aux); if(tagfilter->elts[i].type != TAGFILT_T_STRING) { snprintf(val_as_string, 51, "%s", bamfZ); _typemismatch_error(tagname, aux, tagfilter->elts[i].type, val_as_string, irec); } for(idx = 0; idx < tagfilter->elts[i].len; ++idx) { if(!strcmp(bamfZ, ((const char**) list_elt)[idx])) break; } if(idx == tagfilter->elts[i].len) return 0; break; case 'H': /* RAWSXP */ /* Can actually use bam_aux2Z(aux) to get a * null-terminated char array */ bamfZ = bam_aux2Z(aux); snprintf(val_as_string, 51, "%s", bamfZ); _typeunsupported_error(tagname, aux, val_as_string, irec); break; case 'B': _typeunsupported_error(tagname, aux, "[unknown]", irec); break; default: Rf_error("unknown tag type '%c', record %d", aux[0], irec); break; } } return 1; } Rsamtools/src/tagfilter.h0000644000175400017540000000111513556116727016517 0ustar00biocbuildbiocbuild#ifndef TAG_FILTER_H #define TAG_FILTER_H #include #include typedef enum { TAGFILT_T_UNSET = 0, TAGFILT_T_INT, TAGFILT_T_STRING } TagFilterType; typedef struct { int len; TagFilterType type; void* ptr; } _TAGFILTER_ELT, *TAGFILTER_ELT; typedef struct { int len; const char **tagnames; _TAGFILTER_ELT *elts; } _C_TAGFILTER, *C_TAGFILTER; C_TAGFILTER _tagFilter_as_C_types(SEXP tl); void _Free_C_TAGFILTER(C_TAGFILTER ctf); int _tagfilter(const bam1_t * bam, C_TAGFILTER tagfilter, int irec); #endif /* TAG_FILTER_H */ Rsamtools/src/utilities.c0000644000175400017540000004320713556116727016554 0ustar00biocbuildbiocbuild#include #include #include "utilities.h" #include "IRanges_interface.h" #include "XVector_interface.h" #include void *_Rs_Realloc_impl(void *p, size_t n, size_t t) { /* Realloc(p, 0, *) fails inappropriately */ if (n == 0) { Free(p); p = NULL; } else { p = R_chk_realloc((void *) p, (size_t) (n * t)); } return p; } SEXP _get_namespace(const char *pkg) { SEXP fun = PROTECT(findFun(install("getNamespace"), R_GlobalEnv)); SEXP nmspc = PROTECT(NEW_CHARACTER(1)); SET_STRING_ELT(nmspc, 0, mkChar(pkg)); nmspc = eval(lang2(fun, nmspc), R_GlobalEnv); UNPROTECT(2); return nmspc; } void _as_strand(SEXP vec) { SEXP nmspc = PROTECT(_get_namespace("Rsamtools")); SEXP lvls = PROTECT(eval(findVar(install(".STRAND_LEVELS"), nmspc), nmspc)); _as_factor_SEXP(vec, lvls); UNPROTECT(2); } void _as_nucleotide(SEXP vec) { SEXP nmspc = PROTECT(_get_namespace("Rsamtools")); SEXP lvls = PROTECT(eval(findVar(install(".PILEUP_NUCLEOTIDE_LEVELS"), nmspc), nmspc)); _as_factor_SEXP(vec, lvls); UNPROTECT(2); } SEXP _get_encoding_lookup(const char *from, const char *to) { SEXP nmspc, fun, f, t, call, ans; nmspc = PROTECT(_get_namespace("Biostrings")); fun = findFun(install("get_seqtype_conversion_lookup"), nmspc); f = PROTECT(mkString(from)); t = PROTECT(mkString(to)); call = PROTECT(lang3(fun, f, t)); ans = eval(call, nmspc); UNPROTECT(4); return ans; } SEXP _get_lkup(const char *baseclass) { SEXP lkup = R_NilValue; switch (*baseclass) { case 'D': lkup = _get_encoding_lookup("B", "DNA"); break; case 'B': break; default: Rf_error("Rsamtools internal: '%s' unhandled in _get_lkup", baseclass); break; } return lkup; } void _as_seqlevels(SEXP vec, SEXP lvls) { _as_factor_SEXP(vec, lvls); } void _as_factor_SEXP(SEXP vec, SEXP lvls) { SEXP cls = PROTECT(NEW_CHARACTER(1)); SET_STRING_ELT(cls, 0, mkChar("factor")); SET_CLASS(vec, cls); SET_ATTR(vec, install("levels"), lvls); UNPROTECT(1); } KHASH_MAP_INIT_STR(str, int) void _as_rname(SEXP vec, const char **lvls, const int n_lvls) { /* map duplicate levels to first occurrence */ SEXP levels = R_NilValue; int i, n = 0, ret, *map = NULL; khash_t(str) *level_map = kh_init(str); khiter_t iter; for (i = 0; i < n_lvls; ++i) { iter = kh_get(str, level_map, lvls[i]); if (iter == kh_end(level_map)) { iter = kh_put(str, level_map, lvls[i], &ret); kh_value(level_map, iter) = ++n; } } map = (int *) calloc(n_lvls, sizeof(int)); levels = PROTECT(NEW_CHARACTER(n)); for (i = 0; i < n_lvls; ++i) { iter = kh_get(str, level_map, lvls[i]); map[i] = kh_value(level_map, iter); SET_STRING_ELT(levels, map[i] - 1, mkChar(lvls[i])); } /* don't need to free keys (owned by calling function) */ kh_destroy(str, level_map); int *v = INTEGER(vec); for (i = 0; i < Rf_length(vec); ++i) v[i] = v[i] == NA_INTEGER ? v[i] : map[v[i] - 1]; _as_factor_SEXP(vec, levels); UNPROTECT(1); } void _as_factor(SEXP vec, const char **lvls, const int n_lvls) { SEXP levels = PROTECT(NEW_CHARACTER(n_lvls)); int i; for (i = 0; i < n_lvls; ++i) SET_STRING_ELT(levels, i, mkChar(lvls[i])); _as_factor_SEXP(vec, levels); UNPROTECT(1); } SEXP _as_XStringSet(const char **key, int len, const char *baseclass) { char classname[40]; /* longest string should be "DNAStringSet" */ if (snprintf(classname, sizeof(classname), "%sSet", baseclass) >= (int) sizeof(classname)) error("Rsamtools internal error in _as_XStringSet(): " "'classname' buffer too small"); SEXP lkup = _get_lkup(baseclass); int *lkup0, lkup_length = 0; if (R_NilValue == lkup) { lkup0 = NULL; } else { lkup0 = INTEGER(lkup); lkup_length = LENGTH(lkup); } SEXP width, ans; int i; PROTECT(width = NEW_INTEGER(len)); for (i = 0; i < len; ++i) INTEGER(width)[i] = strlen(key[i]); PROTECT(ans = alloc_XRawList(classname, baseclass, width)); XVectorList_holder holder; Chars_holder dest; holder = hold_XVectorList(ans); for (i = 0; i < len; ++i) { const char *seq = key[i]; dest = get_elt_from_XRawList_holder(&holder, i); Ocopy_bytes_to_i1i2_with_lkup(0, dest.length - 1, (char *) dest.ptr, dest.length, seq, strlen(seq), lkup0, lkup_length); } UNPROTECT(2); return ans; } SEXP _as_PhredQuality(const char **key, int len) { SEXP xstringset = PROTECT(_as_XStringSet(key, len, "BString")); SEXP s, t, nmspc, result; nmspc = PROTECT(_get_namespace("Rsamtools")); NEW_CALL(s, t, "PhredQuality", nmspc, 2); CSET_CDR(t, "x", xstringset); CEVAL_TO(s, nmspc, result); UNPROTECT(2); return result; } void _reverse(char *buf, int len) { int i; char tmp; for (i = 0; i < floor(len / 2); ++i) { tmp = buf[len - i - 1]; buf[len - i - 1] = buf[i]; buf[i] = tmp; } } void _reverseComplement(char *buf, int len) { static const int MAX_MAP = 256; static char map[256]; static int init = 0; if (init == 0) { init = 1; for (int i = 0; i < MAX_MAP; ++i) map[i] = (char) i; map['A'] = 'T'; map['C'] = 'G'; map['G'] = 'C'; map['T'] = 'A'; map['a'] = 't'; map['c'] = 'g'; map['g'] = 'c'; map['t'] = 'a'; map['M'] = 'K'; map['R'] = 'Y'; map['Y'] = 'R'; map['K'] = 'M'; map['m'] = 'k'; map['r'] = 'y'; map['y'] = 'r'; map['k'] = 'm'; map['V'] = 'B'; map['H'] = 'D'; map['D'] = 'H'; map['B'] = 'V'; map['v'] = 'b'; map['h'] = 'd'; map['d'] = 'h'; map['b'] = 'v'; } _reverse(buf, len); for (int i = 0; i < len; ++i) buf[i] = map[(int) buf[i]]; } char *_rtrim(char *s) { int i = strlen(s) - 1; while (i >= 0) { if (s[i] != '\r') break; s[i--] = '\0'; } return s; } /* * Doesn't actually delete anything but returns the length that 'buf' would * have after deletion of its trailing LFs ("\n") and CRs ("\r"). * If 'buf_len' is -1, then 'buf' must be a C string (i.e. null-terminated). */ int _delete_trailing_LFs_and_CRs(const char *buf, int buf_len) { char c; if (buf_len == -1) buf_len = strlen(buf); while (buf_len > 0) { c = buf[--buf_len]; if (c != '\n' && c != '\r') { buf_len++; break; } } return buf_len; } /* scan-related */ void _checkext(SEXP ext, SEXP tag, const char *lbl) { if (EXTPTRSXP != TYPEOF(ext) || tag != R_ExternalPtrTag(ext)) Rf_error("incorrect instance for '%s'", lbl); } void _checknames(SEXP filename, SEXP indexname, SEXP filemode) { if (!IS_CHARACTER(filename) || LENGTH(filename) > 1) Rf_error("'filename' must be character(0) or character(1)"); if (!IS_CHARACTER(indexname) || LENGTH(indexname) > 1) Rf_error("'indexname' must be character(0) or character(1)"); if (!IS_CHARACTER(filemode) || LENGTH(filemode) != 1) Rf_error("'filemode' must be character(1)"); } void _checkparams(SEXP regions, SEXP keepFlags, SEXP isSimpleCigar) { const int MAX_CHRLEN = 1 << 29; /* See samtools/bam_index.c */ if (R_NilValue != regions) { if (!IS_VECTOR(regions) || LENGTH(regions) != 3) Rf_error("'regions' must be list(3) or NULL"); if (!IS_CHARACTER(VECTOR_ELT(regions, 0))) Rf_error("internal: 'regions[1]' must be character()"); if (!IS_INTEGER(VECTOR_ELT(regions, 1))) Rf_error("internal: 'regions[2]' must be integer()"); if (!IS_INTEGER(VECTOR_ELT(regions, 2))) Rf_error("internal: 'regions[3]' must be integer()"); if ((LENGTH(VECTOR_ELT(regions, 0)) != LENGTH(VECTOR_ELT(regions, 1))) || (LENGTH(VECTOR_ELT(regions, 0)) != LENGTH(VECTOR_ELT(regions, 2)))) Rf_error("internal: 'regions' elements must all be the same length"); const int *end = INTEGER(VECTOR_ELT(regions, 2)), nrange = LENGTH(VECTOR_ELT(regions, 2)); for (int irange = 0; irange < nrange; ++irange) if (end[irange] > MAX_CHRLEN) Rf_error("'end' must be <= %d", MAX_CHRLEN); } if (R_NilValue != keepFlags) if (!IS_INTEGER(keepFlags) || LENGTH(keepFlags) != 2) Rf_error("'keepFlags' must be integer(2) or NULL"); if (R_NilValue != isSimpleCigar) if (!IS_LOGICAL(isSimpleCigar) || LENGTH(isSimpleCigar) != 1) Rf_error("'isSimpleCigar' must be logical(1) or NULL"); } /* pairing */ static int check_x_or_y(SEXP qname, SEXP flag, SEXP rname, SEXP pos, SEXP rnext, SEXP pnext, const char *what) { int len; len = LENGTH(flag); if (qname != R_NilValue) if (!IS_CHARACTER(qname) || LENGTH(qname) != len) Rf_error("'%s_qname' must be NULL or a character vector " "of the same length as '%s_flag'", what, what); if (!isFactor(rname) || LENGTH(rname) != len) Rf_error("'%s_rname' must be a factor " "of the same length as '%s_flag'", what, what); if (!IS_INTEGER(pos) || LENGTH(pos) != len) Rf_error("'%s_pos' must be an integer vector " "of the same length as '%s_flag'", what, what); if (!isFactor(rnext) || LENGTH(rnext) != len) Rf_error("'%s_rnext' must be a factor " "of the same length as '%s_flag'", what, what); if (!IS_INTEGER(pnext) || LENGTH(pnext) != len) Rf_error("'%s_pnext' must be an integer vector " "of the same length as '%s_flag'", what, what); return len; } /* 'x_qname' and 'y_qname' must be NULLs or 0-terminated strings. */ static int is_a_pair(const char *x_qname, int x_flag, int x_rname, int x_pos, int x_rnext, int x_pnext, const char *y_qname, int y_flag, int y_rname, int y_pos, int y_rnext, int y_pnext) { int x_is_not_first, x_is_not_last, x_is_proper, x_is_secondary, y_is_not_first, y_is_not_last, y_is_proper, y_is_secondary, tmp, ok; /* Flag bits 0x001, 0x004, and 0x008 must be 1, 0, and 0. Testing the 3 bits at once. */ if (((x_flag & 0x00d) != 0x001) || ((y_flag & 0x00d) != 0x001)) return 0; /* 'x' and 'y' must be the first or the last segment in the template. */ x_is_not_first = (x_flag & 0x040) == 0; x_is_not_last = (x_flag & 0x080) == 0; y_is_not_first = (y_flag & 0x040) == 0; y_is_not_last = (y_flag & 0x080) == 0; if ((x_is_not_first == x_is_not_last) || (y_is_not_first == y_is_not_last)) return 0; /* See top of the R/findMateAlignment.R file for the definition of tests (A), (B), (C), (D), (E), (F), and (G). */ /* Test (A). */ tmp = (x_qname != NULL) + (y_qname != NULL); if (tmp == 1) return 0; /* 'x_qname' or 'y_qname' is NULL but not both */ if (tmp == 2 && strcmp(x_qname, y_qname) != 0) return 0; /* 'x_qname' and 'y_qname' differ */ /* Test (B). */ if ((x_rnext != y_rname) || (y_rnext != x_rname)) return 0; /* Test (C). */ if ((x_pnext != y_pos) || (y_pnext != x_pos)) return 0; /* Test (D). */ ok = (((x_flag & 0x020) == 0) == ((y_flag & 0x010) == 0)) && (((y_flag & 0x020) == 0) == ((x_flag & 0x010) == 0)); if (!ok) return 0; /* Test (E). */ if (x_is_not_first == y_is_not_first) return 0; /* Test (F). */ x_is_proper = (x_flag & 0x002) != 0; y_is_proper = (y_flag & 0x002) != 0; if (x_is_proper != y_is_proper) return 0; /* Test (G). */ x_is_secondary = (x_flag & 0x100) != 0; y_is_secondary = (y_flag & 0x100) != 0; if (x_is_secondary != y_is_secondary) return 0; return 1; } /* * Parallel pairing of 2 vectors of alignments (i.e. BAM records). * The 2 input vectors 'x' and 'y' must have the same length. * 'x_rname', 'y_rname', 'x_rnext', and 'y_rnext' must all have exactly the * same levels in the same order. This is NOT checked. * Returns a logical vector of the same length as the input vectors. */ SEXP p_pairing(SEXP x_qname, SEXP x_flag, SEXP x_rname, SEXP x_pos, SEXP x_rnext, SEXP x_pnext, SEXP y_qname, SEXP y_flag, SEXP y_rname, SEXP y_pos, SEXP y_rnext, SEXP y_pnext) { SEXP ans, x_qname_elt, y_qname_elt; int x_len, y_len, i, x_flag_elt, x_rname_elt, x_pos_elt, x_rnext_elt, x_pnext_elt, y_flag_elt, y_rname_elt, y_pos_elt, y_rnext_elt, y_pnext_elt; const char *x_qname_string, *y_qname_string; x_len = check_x_or_y(x_qname, x_flag, x_rname, x_pos, x_rnext, x_pnext, "x"); y_len = check_x_or_y(y_qname, y_flag, y_rname, y_pos, y_rnext, y_pnext, "y"); if (x_len != y_len) Rf_error("'x' and 'y' must have the same length"); if ((x_qname == R_NilValue) != (y_qname == R_NilValue)) Rf_error("both of 'x' and 'y' must either be NULL or not"); if (x_qname == R_NilValue) x_qname_string = y_qname_string = NULL; PROTECT(ans = NEW_LOGICAL(x_len)); for (i = 0; i < x_len; i++) { x_flag_elt = INTEGER(x_flag)[i]; y_flag_elt = INTEGER(y_flag)[i]; if (x_flag_elt == NA_INTEGER || y_flag_elt == NA_INTEGER) { UNPROTECT(1); Rf_error("'x_flag' or 'y_flag' contains NAs"); } if (x_qname != R_NilValue) { x_qname_elt = STRING_ELT(x_qname, i); y_qname_elt = STRING_ELT(y_qname, i); if (x_qname_elt == NA_STRING || y_qname_elt == NA_STRING) { UNPROTECT(1); Rf_error("'x_qname' or 'y_qname' contains NAs"); } x_qname_string = CHAR(x_qname_elt); y_qname_string = CHAR(y_qname_elt); } x_rname_elt = INTEGER(x_rname)[i]; y_rname_elt = INTEGER(y_rname)[i]; x_pos_elt = INTEGER(x_pos)[i]; y_pos_elt = INTEGER(y_pos)[i]; x_rnext_elt = INTEGER(x_rnext)[i]; y_rnext_elt = INTEGER(y_rnext)[i]; x_pnext_elt = INTEGER(x_pnext)[i]; y_pnext_elt = INTEGER(y_pnext)[i]; LOGICAL(ans)[i] = is_a_pair(x_qname_string, x_flag_elt, x_rname_elt, x_pos_elt, x_rnext_elt, x_pnext_elt, y_qname_string, y_flag_elt, y_rname_elt, y_pos_elt, y_rnext_elt, y_pnext_elt); } UNPROTECT(1); return ans; } /* * The input is a vector 'x' of alignments. * 'group_sizes 'must be a vector of positive integers that sum up to the * length of the input vectors. This is NOT checked. * 'x_rname' and 'x_rnext' must have exactly the same levels in the same order. * This is NOT checked. * Returns an integer vector of the same length as the input vectors. */ SEXP find_mate_within_groups(SEXP group_sizes, SEXP x_flag, SEXP x_rname, SEXP x_pos, SEXP x_rnext, SEXP x_pnext) { SEXP ans; int x_len, *ans_p, ngroup, n, group_size, offset, i, i2, j, j2, ok, x_flag_elt, x_rname_elt, x_pos_elt, x_rnext_elt, x_pnext_elt, y_flag_elt, y_rname_elt, y_pos_elt, y_rnext_elt, y_pnext_elt, ans_i2_is_na, ans_j2_is_na; x_len = check_x_or_y(R_NilValue, x_flag, x_rname, x_pos, x_rnext, x_pnext, "x"); PROTECT(ans = NEW_INTEGER(x_len)); for (i = 0, ans_p = INTEGER(ans); i < x_len; i++, ans_p++) *ans_p = NA_INTEGER; ngroup = LENGTH(group_sizes); for (n = offset = 0; n < ngroup; n++, offset += group_size) { group_size = INTEGER(group_sizes)[n]; for (i = 1; i < group_size; i++) { i2 = i + offset; x_flag_elt = INTEGER(x_flag)[i2]; if (x_flag_elt == NA_INTEGER) { UNPROTECT(1); Rf_error("'x_flag' contains NAs"); } x_rname_elt = INTEGER(x_rname)[i2]; x_pos_elt = INTEGER(x_pos)[i2]; x_rnext_elt = INTEGER(x_rnext)[i2]; x_pnext_elt = INTEGER(x_pnext)[i2]; for (j = 0; j < i; j++) { j2 = j + offset; y_flag_elt = INTEGER(x_flag)[j2]; if (y_flag_elt == NA_INTEGER) { UNPROTECT(1); Rf_error("'y_flag' contains NAs"); } y_rname_elt = INTEGER(x_rname)[j2]; y_pos_elt = INTEGER(x_pos)[j2]; y_rnext_elt = INTEGER(x_rnext)[j2]; y_pnext_elt = INTEGER(x_pnext)[j2]; ok = is_a_pair(NULL, x_flag_elt, x_rname_elt, x_pos_elt, x_rnext_elt, x_pnext_elt, NULL, y_flag_elt, y_rname_elt, y_pos_elt, y_rnext_elt, y_pnext_elt); if (!ok) continue; ans_i2_is_na = INTEGER(ans)[i2] == NA_INTEGER; INTEGER(ans)[i2] = ans_i2_is_na ? j2 + 1 : 0; ans_j2_is_na = INTEGER(ans)[j2] == NA_INTEGER; INTEGER(ans)[j2] = ans_j2_is_na ? i2 + 1 : 0; } } } for (i = 0, ans_p = INTEGER(ans); i < x_len; i++, ans_p++) { if (*ans_p != NA_INTEGER && *ans_p != 0 && INTEGER(ans)[*ans_p - 1] == 0) *ans_p = -(*ans_p); } UNPROTECT(1); return ans; } Rsamtools/src/utilities.h0000644000175400017540000000423613556116727016560 0ustar00biocbuildbiocbuild#ifndef _UTILITIES_H_ #define _UTILITIES_H_ #include #ifdef __cplusplus extern "C" { #endif /* robust memory re-allocation */ #define _Rs_Realloc(p, n, t) (t *) _Rs_Realloc_impl(p, n, sizeof(t)) void *_Rs_Realloc_impl(void *p, size_t n, size_t t); /* coercion */ SEXP _get_namespace(const char *pkg); SEXP _get_encoding_lookup(const char *from, const char *to); SEXP _get_lkup(const char *baseclass); void _as_factor_SEXP(SEXP vec, SEXP lvls); void _as_factor(SEXP vec, const char **lvls, const int n_lvls); void _as_strand(SEXP vec); void _as_rname(SEXP vec, const char **lvls, const int n_lvls); void _as_nucleotide(SEXP vec); void _as_seqlevels(SEXP vec, SEXP lvls); SEXP _as_XStringSet(const char **key, int len, const char *baseclass); SEXP _as_PhredQuality(const char **key, int len); void _reverse(char *buf, int len); void _reverseComplement(char *buf, int len); char *_rtrim(char *); int _delete_trailing_LFs_and_CRs(const char *buf, int buf_len); /* common checks */ void _checkext(SEXP ext, SEXP tag, const char *lbl); void _checknames(SEXP filename, SEXP indexname, SEXP filemode); void _checkparams(SEXP regions, SEXP keepFlags, SEXP isSimpleCigar); /* pairing */ SEXP p_pairing(SEXP x_qname, SEXP x_flag, SEXP x_rname, SEXP x_pos, SEXP x_rnext, SEXP x_pnext, SEXP y_qname, SEXP y_flag, SEXP y_rname, SEXP y_pos, SEXP y_rnext, SEXP y_pnext); SEXP find_mate_within_groups(SEXP group_sizes, SEXP x_flag, SEXP x_rname, SEXP x_pos, SEXP x_rnext, SEXP x_pnext); /* call-building macros */ #define NEW_CALL(S, T, NAME, ENV, N) \ PROTECT(S = T = allocList(N)); \ SET_TYPEOF(T, LANGSXP); \ SETCAR(T, findFun(install(NAME), ENV)); \ T = CDR(T) #define CSET_CDR(T, NAME, VALUE) \ SETCAR(T, VALUE); \ SET_TAG(T, install(NAME)); \ T = CDR(T) #define CEVAL_TO(S, ENV, GETS) \ GETS = eval(S, ENV); \ UNPROTECT(1) #ifdef __cplusplus } #endif #endif /* _UTILITIES_H_ */ Rsamtools/src/zip_compression.c0000644000175400017540000000374313556116727017765 0ustar00biocbuildbiocbuild#include #include #include #include #include #include "zip_compression.h" void _zip_error(const char *txt, const char *err, int infd, int outfd) { close(infd); close(outfd); err ? Rf_error(txt, err) : Rf_error(txt); } void _zip_open(SEXP file, SEXP dest, int *infd, int *outfd) { int iflag = O_RDONLY, oflag = O_WRONLY | O_CREAT | O_TRUNC; #ifdef _WIN32 iflag |= O_BINARY; oflag |= O_BINARY; #endif if (!IS_CHARACTER(file) || 1L != Rf_length(file)) Rf_error("'file' must be character(1)"); if (!IS_CHARACTER(dest) || 1L != Rf_length(dest)) Rf_error("'dest' must be character(1)"); *infd = open(translateChar(STRING_ELT(file, 0)), iflag); if (0 > *infd) Rf_error("opening 'file': %s", strerror(errno)); /* we overwrite existing files here */ *outfd = open(translateChar(STRING_ELT(dest, 0)), oflag, 0666); if (0 > *outfd) { close(*infd); Rf_error("opening 'dest': %s", strerror(errno)); } } SEXP bgzip(SEXP file, SEXP dest) { static const int BUF_SIZE = 64 * 1024; void *buffer; int infd, outfd, cnt; gzFile in; BGZF *outp; buffer = R_alloc(BUF_SIZE, sizeof(void *)); _zip_open(file, dest, &infd, &outfd); in = gzdopen(infd, "rb"); if (NULL == in) _zip_error("opening input 'file'", NULL, infd, outfd); outp = bgzf_dopen(outfd, "w"); if (NULL == outp) _zip_error("opening output 'dest'", NULL, infd, outfd); while (0 < (cnt = gzread(in, buffer, BUF_SIZE))) if (0 > bgzf_write(outp, buffer, cnt)) _zip_error("writing compressed output", NULL, infd, outfd); if (0 > cnt) _zip_error("reading compressed input: %s", strerror(errno), infd, outfd); if (0 > bgzf_close(outp)) Rf_error("closing compressed output"); if (gzclose(in) != Z_OK) _zip_error("closing input after compression", NULL, infd, outfd); return dest; } Rsamtools/src/zip_compression.h0000644000175400017540000000016613556116727017766 0ustar00biocbuildbiocbuild#ifndef ZIP_COMPRESSION_H #define ZIP_COMPRESSION_H #include SEXP bgzip(SEXP from, SEXP dest); #endif Rsamtools/tests/0000755000175400017540000000000013556116727014742 5ustar00biocbuildbiocbuildRsamtools/tests/Rsamtools_unit_tests.R0000644000175400017540000000005013556116727021324 0ustar00biocbuildbiocbuildBiocGenerics:::testPackage('Rsamtools') Rsamtools/vignettes/0000755000175400017540000000000013624616601015600 5ustar00biocbuildbiocbuildRsamtools/vignettes/Rsamtools-Overview.Rnw0000644000175400017540000004660513556116727022102 0ustar00biocbuildbiocbuild%\VignetteIndexEntry{An introduction to Rsamtools} %\VignetteDepends{} %\VignetteKeywords{Short read, I/0, samtools} %\VignettePackage{Rsamtools} \documentclass{article} <>= BiocStyle::latex() @ \newcommand{\bam}{\texttt{BAM}} \title{An Introduction to \Biocpkg{Rsamtools}} \author{Martin Morgan} \date{Modified: 18 March, 2010. Compiled: \today} \begin{document} \maketitle \tableofcontents <>= options(width=60) @ <>= library(Rsamtools) @ \section{Introduction} The \Biocpkg{Rsamtools} package provides an interface to \bam{} files. \bam{} files are produced by \software{samtools} and other software, and represent a flexible format for storing `short' reads aligned to reference genomes. \bam{} files typically contain sequence and base qualities, and alignment coordinates and quality measures. \bam{} files are appealing for several reasons. The format is flexible enough to represent reads generated and aligned using diverse technologies. The files are binary so that file access is relatively efficient. \bam{} files can be indexed, allowing ready access to localized chromosomal regions. \bam{} files can be accessed remotely, provided the remote hosting site supports such access and a local index is available. This means that specific regions of remote files can be accessed without retrieving the entire (large!) file. A full description is available in the \bam{} format specification (\url{http://samtools.sourceforge.net/SAM1.pdf}) The main purpose of the \Biocpkg{Rsamtools} package is to import \bam{} files into \R{}. \Biocpkg{Rsamtools} also provides some facility for file access such as record counting, index file creation, and filtering to create new files containing subsets of the original. An important use case for \Biocpkg{Rsamtools} is as a starting point for creating \R{} objects suitable for a diversity of work flows, e.g., \Rclass{AlignedRead} objects in the \Rpackage{ShortRead} package (for quality assessment and read manipulation), or \Rclass{GAlignments} objects in \Rpackage{GenomicAlignments} package (for RNA-seq and other applications). Those desiring more functionality are encouraged to explore \software{samtools} and related software efforts. \section{Input} The essential capability provided by \Biocpkg{Rsamtools} is \bam{} input. This is accomplished with the \Rfunction{scanBam} function. \Rfunction{scanBam} takes as input the name of the \bam{} file to be parsed. In addition, the \Rcode{param} argument determines which genomic coordinates of the \bam{} file, and what components of each record, will be input. \R{param} is an instance of the \Rclass{ScanBamParam} class. To create a \Rcode{param} object, call \Rfunction{ScanBamParam}. Here we create a \Rcode{param} object to extract reads aligned to three distinct ranges (one on \Rcode{seq1}, two on \Rcode{seq2}). From each of read in those ranges, we specify that we would like to extract the reference name (\Rcode{rname}, e.g., \Rcode{seq1}), strand, alignment position, query (i.e., read) width, and query sequence: <>= which <- IRangesList(seq1=IRanges(1000, 2000), seq2=IRanges(c(100, 1000), c(1000, 2000))) what <- c("rname", "strand", "pos", "qwidth", "seq") param <- ScanBamParam(which=which, what=what) @ %% Additional information can be found on the help page for \Rfunction{ScanBamParam}. Reading the relevant records from the \bam{} file is accomplished with <>= bamFile <- system.file("extdata", "ex1.bam", package="Rsamtools") bam <- scanBam(bamFile, param=param) @ Like \Rfunction{scan}, \Rfunction{scanBam} returns a \Robject{list} of values. Each element of the list corresponds to a range specified by the \Rcode{which} argument to \Rfunction{ScanBamParam}. <>= class(bam) names(bam) @ %% Each element is itself a list, containing the elements specified by the \Rcode{what} and \Rcode{tag} arguments to \Rfunction{ScanBamParam}. <>= class(bam[[1]]) names(bam[[1]]) @ %% The elements are either basic \R{} or \Rpackage{IRanges} data types <>= sapply(bam[[1]], class) @ %% A paradigm for collapsing the list-of-lists into a single list is <>= .unlist <- function (x) { ## do.call(c, ...) coerces factor to integer, which is undesired x1 <- x[[1L]] if (is.factor(x1)) { structure(unlist(x), class = "factor", levels = levels(x1)) } else { do.call(c, x) } } bam <- unname(bam) # names not useful in unlisted result elts <- setNames(bamWhat(param), bamWhat(param)) lst <- lapply(elts, function(elt) .unlist(lapply(bam, "[[", elt))) @ %% This might be further transformed, e.g., to a \Rclass{DataFrame}, with <>= head(do.call("DataFrame", lst)) @ Often, an alternative is to use a \Rclass{ScanBamParam} object with desired fields specified in \Rcode{what} as an argument to \Rfunction{GenomicAlignments::readGAlignments}; the specified fields are added as columns to the returned \Rclass{GAlignments}. The \bam{} file in the previous example includes an index, represented by a separate file with extension \texttt{.bai}: <>= list.files(dirname(bamFile), pattern="ex1.bam(.bai)?") @ %% Indexing provides two significant benefits. First, an index allows a \bam{} file to be efficiently accessed by range. A corollary is that providing a \Rcode{which} argument to \Rfunction{ScanBamParam} requires an index. Second, coordinates for extracting information from a \bam{} file can be derived from the index, so a portion of a remote \bam{} file can be retrieved with local access only to the index. For instance, provided an index file exists on the local computer, it is possible to retrieve a small portion of a \bam{} file residing on the 1000 genomes HTTP server. The url \url{ftp://ftp-trace.ncbi.nih.gov/1000genomes/ftp/pilot_data/data/NA19240/alignment/NA19240.chrom6.SLX.maq.SRP000032.2009_07.bam} points to the \bam{} file corresponding to individual NA19240 chromosome~6 Solexa (Illumina) sequences aligned using MAQ. The remote file is very large (about 10 GB), but the corresponding index file is small (about 500 KB). With \Rcode{na19240url} set to the above address, the following retrieves just those reads in the specified range <>= which <- IRangesList("6"=IRanges(100000L, 110000L)) param <- ScanBamParam(which=which, what=scanBamWhat()) na19240bam <- scanBam(na19240url, param=param) @ %% Invoking \Rfunction{scanBam} without an index file, as above, first retrieves the index file from the remote location, and then queries the remote file using the index; for repeated queries, it is more efficient to retrieve the index file first (e.g., with \Rfunction{download.file}) and then use the local index as an argument to \Rfunction{scanBam}. Many \bam{} files were created in a way that causes \Rfunction{scanBam} to report that the ``EOF marker is absent''; this message can safely be ignored. \bam{} files may be read by functions in packages other than \Biocpkg{Rsamtools}, in particular the \Rfunction{readGAlignments} family of functions in \Rpackage{GenomicAlignments}. Additional ways of interacting with \bam{} files include \Rfunction{scanBamHeader} (to extract header information) and \Rfunction{countBam} (to count records matching \Rcode{param}). \Rfunction{filterBam} filters reads from the source file according to the criteria of the \Rclass{ScanBamParam} parameter, writing reads passing the filter to a new file. The function \Rfunction{sortBam} sorts a previously unsorted \bam{}, while The function \Rfunction{indexBam} creates an index file from a sorted \bam{} file. \Rfunction{readPileup} reads a \texttt{pileup} file created by \software{samtools}, importing SNP, indel, or all variants into a \Rclass{GRanges} object. \subsection{Large bam files} \bam{} files can be large, containing more information on more genomic regions than are of immediate interest or than can fit in memory. The first strategy for dealing with this is to select, using the \Rcode{what} and \Rcode{which} arguments to \Rfunction{ScanBamParam}, just those portions of the \bam{} file that are essential to the current analysis, e.g., specifying \Rcode{what=c(`rname', 'qname', 'pos')} when wishing to calculate coverage of ungapped reads. When selective input of \bam{} files is still too memory-intensive, the file can be processed in chunks, with each chunk distilled to the derived information of interest. Chromosomes will often be the natural chunk to process. For instance, here we write a summary function that takes a single sequence name (chromosome) as input, reads in specific information from the \bam{} file, and calculates coverage over that sequence. <>= summaryFunction <- function(seqname, bamFile, ...) { param <- ScanBamParam(what=c('pos', 'qwidth'), which=GRanges(seqname, IRanges(1, 1e7)), flag=scanBamFlag(isUnmappedQuery=FALSE)) x <- scanBam(bamFile, ..., param=param)[[1]] coverage(IRanges(x[["pos"]], width=x[["qwidth"]])) } @ %% This might be used as follows; it is an ideal candidate for evaluation in parallel, e.g., using the \Rpackage{parallel} package and \Rfunction{srapply} function in \Rpackage{ShortRead}. <>= seqnames <- paste("seq", 1:2, sep="") cvg <- lapply(seqnames, summaryFunction, bamFile) names(cvg) <- seqnames cvg @ %% The result of the function (a coverage vector, in this case) will often be much smaller than the input. \section{Views} The functions described in the previous section import data in to \R{}. However, sequence data can be very large, and it does not always make sense to read the data in immediately. Instead, it can be useful to marshal \emph{references} to the data into a container and then act on components of the container. The \Rclass{BamViews} class provides a mechanism for creating `views' into a set of \bam{} files. The view itself is light-weight, containing references to the relevant \bam{} files and metadata about the view (e.g., the phenotypic samples corresponding to each \bam{} file). One way of understanding a \Rclass{BamViews} instance is as a rectangular data structure. The columns represent \bam{} files (e.g., distinct samples). The rows represent ranges (i.e., genomic coordinates). For instance, a ChIP-seq experiment might identify a number of peaks of high read counts. \subsection{Assembling a \Rclass{BamViews} instance} To illustrate, suppose we have an interest in caffeine metabolism in humans. The `rows' contain coordinates of genomic regions associated with genes in a KEGG caffeine metabolism pathway. The `columns' represent individuals in the 1000 genomes project. To create the `rows', we identify possible genes that KEGG associates with caffeine metabolism: <>= library(KEGG.db) kid <- revmap(KEGGPATHID2NAME)[["Caffeine metabolism"]] egid <- KEGGPATHID2EXTID[[sprintf("hsa%s", kid)]] @ %% Then we use the appropriate \Rpackage{TxDb} package to translate Entrez identifiers to obtain ranges of interest (one could also use \Rpackage{biomaRt} to retrieve coordinates for non-model organisms, perhaps making a \Robject{TxDb} object as outlined in the \Rpackage{GenomicFeatures} vignette). We'll find that the names used for chromosomes in the alignments differ from those used at Ensembl, so \Rcode{seqlevels<-} is used to map between naming schemes and to drop unused levels. <>= library(TxDb.Hsapiens.UCSC.hg18.knownGene) bamRanges <- transcripts(TxDb.Hsapiens.UCSC.hg18.knownGene, filter=list(gene_id=egid)) seqlevels(bamRanges) <- # translate seqlevels sub("chr", "", seqlevels(bamRanges)) lvls <- seqlevels(bamRanges) # drop unused levels seqlevels(bamRanges) <- lvls[lvls %in% as.character(seqnames(bamRanges))] @ %% Note that \Robject{bamRanges} `knows' the genome for which the ranges are defined <>= unique(genome(bamRanges)) @ The details of creating the `columns' of BAM files. Here we retrieve a vector of \bam{} file URLs (\Robject{slxMaq09}) from the package. <>= slxMaq09 <- local({ fl <- system.file("extdata", "slxMaq09_urls.txt", package="Rsamtools") readLines(fl) }) @ %% We now assemble the \Rclass{BamViews} instance from these objects; we also provide information to annotated the \bam{} files (with the \Rcode{bamSamples} function argument, which is a \Rclass{DataFrame} instance with each row corresponding to a \bam{} file) and the instance as a whole (with \Rcode{bamExperiment}, a simple named \Rclass{list} containing information structured as the user sees fit). <>= bamExperiment <- list(description="Caffeine metabolism views on 1000 genomes samples", created=date()) bv <- BamViews(slxMaq09, bamRanges=bamRanges, bamExperiment=bamExperiment) metadata(bamSamples(bv)) <- list(description="Solexa/MAQ samples, August 2009", created="Thu Mar 25 14:08:42 2010") @ \subsection{Using \Rclass{BamViews} instances} The \Rclass{BamViews} object can be queried for its component parts, e.g., <>= bamExperiment(bv) @ %% More usefully, Methods in \Biocpkg{Rsamtools} are designed to work with \Rclass{BamViews} objects, retrieving data from all files in the view. These operations can take substantial time and require reliable network access. To illustrate, the following code (not evaluated when this vignette was created) downloads the index files associated with the \Robject{bv} object <>= bamIndexDir <- tempfile() indexFiles <- paste(bamPaths(bv), "bai", sep=".") dir.create(bamIndexDir) idxFiles <- mapply(download.file, indexFiles, file.path(bamIndexDir, basename(indexFiles)) , MoreArgs=list(method="curl")) @ %% and then queries the 1000 genomes project for reads overlapping our transcripts; by loading the \Rpackage{parallel} package, we tell \Biocpkg{Rsamtools} to use as many cores as are available on our machine (the \Rpackage{parallel} package does not provide parallel functionality on Windows computers) <>= library(GenomicAlignments) library(parallel) options(srapply_fapply="parallel", mc.cores=detectCores()) olaps <- readGAlignments(bv) @ %% The resulting object is about 11 MB in size. To avoid having to download this data each time the vignette is run, we instead load it from disk %% <>= library(GenomicAlignments) load(system.file("extdata", "olaps.Rda", package="Rsamtools")) olaps head(olaps[[1]]) @ %% There are \Sexpr{length(olaps[[1]])} reads in \verb|\Sexpr{names(olaps)[[1]]}| overlapping at least one of our transcripts. It is easy to explore this object, for instance discovering the range of read widths in each individual. <>= head(t(sapply(olaps, function(elt) range(qwidth(elt))))) @ Suppose we were particularly interested in the first transcript, which has a transcript id \Sexpr{mcols(bamRanges(bv))[["tx_name"]][1]}. Here we extract reads overlapping this transcript from each of our samples. As a consequence of the protocol used, reads aligning to either strand could be derived from this transcript. For this reason, we set the strand of our range of interest to \texttt{*}. We use the \Rfunction{endoapply} function, which is like \Rfunction{lapply} but returns an object of the same class (in this case, \Sexpr{as.vector(class(olaps))}) as its first argument. <>= rng <- bamRanges(bv)[1] strand(rng) <- "*" olap1 <- endoapply(olaps, subsetByOverlaps, rng) olap1 <- lapply(olap1, "seqlevels<-", value=as.character(seqnames(rng))) head(olap1[[24]]) @ %% To carry the example a little further, we calculate coverage of each sample: <>= minw <- min(sapply(olap1, function(elt) min(start(elt)))) maxw <- max(sapply(olap1, function(elt) max(end(elt)))) cvg <- endoapply(olap1, coverage, shift=-start(ranges(bamRanges[1])), width=width(ranges(bamRanges[1]))) cvg[[1]] @ %% Since the example includes a single region of uniform width across all samples, we can easily create a coverage matrix with rows representing nucleotide and columns sample and, e.g., document variability between samples and nucleotides <>= m <- matrix(unlist(lapply(cvg, lapply, as.vector)), ncol=length(cvg)) summary(rowSums(m)) summary(colSums(m)) @ \section{Directions} This vignette has summarized facilities in the \Biocpkg{Rsamtools} package. Important additional packages include \Rpackage{GenomicRanges} (for representing and manipulating gapped alignments), \Rpackage{ShortRead} for I/O and quality assessment of ungapped short read alignments, \Rpackage{Biostrings} and \Rpackage{BSgenome} for DNA sequence and whole-genome manipulation, \Rpackage{IRanges} for range-based manipulation, and \Rpackage{rtracklayer} for I/O related to the UCSC genome browser. Users might also find the interface to the integrative genome browser (IGV) in \Rpackage{SRAdb} useful for visualizing \bam{} files. <>= packageDescription("Rsamtools") sessionInfo() @ \appendix \section{Assembling a \Rclass{BamViews} instance} \subsection{Genomic ranges of interest} \subsection{BAM files} \emph{Note}: The following operations were performed at the time the vignette was written; location of on-line resources, in particular the organization of the 1000 genomes \bam{} files, may have changed. We are interested in collecting the URLs of a number of \bam{} files from the 1000 genomes project. Our first goal is to identify files that might make for an interesting comparison. First, let's visit the 1000 genomes FTP site and discover available files. We'll use the \Rpackage{RCurl} package to retrieve the names of all files in an appropriate directory <>= library(RCurl) ftpBase <- "ftp://ftp-trace.ncbi.nih.gov/1000genomes/ftp/pilot_data/data/" indivDirs <- strsplit(getURL(ftpBase, ftplistonly=TRUE), "\n")[[1]] alnDirs <- paste(ftpBase, indivDirs, "/alignment/", sep="") urls0 <- strsplit(getURL(alnDirs, dirlistonly=TRUE), "\n") @ %% From these, we exclude directories without any files in them, select only the \bam{} index (extension \texttt{.bai}) files, and choose those files that exactly six \texttt{'.'} characters in their name. <>= urls <- urls[sapply(urls0, length) != 0] fls0 <- unlist(unname(urls0)) fls1 <- fls0[grepl("bai$", fls0)] fls <- fls1[sapply(strsplit(fls1, "\\."), length)==7] @ %% After a little exploration, we focus on those files obtained form Solexa sequencing, aligned using \texttt{MAQ}, and archived in August, 2009; we remove the \texttt{.bai} extension, so that the URL refers to the underlying file rather than index. There are 24 files. <>= urls1 <- Filter(function(x) length(x) != 0, lapply(urls, function(x) x[grepl("SLX.maq.*2009_08.*bai$", x)])) slxMaq09.bai <- mapply(paste, names(urls1), urls1, sep="", USE.NAMES=FALSE) slxMaq09 <- sub(".bai$", "", slxMaq09.bai) #$ @ As a final step to prepare for using a \Rclass{BamViews} file, we create local copies of the \emph{index} files. The index files are relatively small (about 190 Mb total). <>= bamIndexDir <- tempfile() dir.create(bamIndexDir) idxFiles <- mapply(download.file, slxMaq09.bai, file.path(bamIndexDir, basename(slxMaq09.bai)) , MoreArgs=list(method="curl")) @ \end{document} Rsamtools/vignettes/Rsamtools-UsingCLibraries.Rnw0000644000175400017540000000741713556116727023317 0ustar00biocbuildbiocbuild%\VignetteIndexEntry{Using samtools C libraries} %\VignetteDepends{} %\VignetteKeywords{Short read, I/0, samtools} %\VignettePackage{Rsamtools} \documentclass{article} <>= BiocStyle::latex() @ \newcommand{\bam}{\texttt{BAM}} \title{Using samtools C libraries with \Biocpkg{Rsamtools}} \author{Martin Morgan} \date{Modified: 20 March, 2015. Compiled: \today} \begin{document} \maketitle \tableofcontents This document is meant for package developers wanting to use the \href{http://samtools.sourceforge.net/}{samtools} C libraries provided by \Biocpkg{Rsamtools}. The instructions here are based on the `Writing R Extensions' manual associated with R-2.13; consult the current version of the manual for up-to-date instructions. \section{Background} \Biocpkg{Rsamtools} arranges to install static versions of the \verb|libbam| and \verb|libbcf| libraries. The idea is that other packages can use these to implement C functionality that uses these libraries. This means that the samtools libraries are available in a consistent version to users across platforms, without requiring installation of additional software. \Biocpkg{Rsamtools} takes the following approach. On installation, \Biocpkg{Rsamtools} contains a snapshot of the samtools library source code under \verb|src/samtools|. \Biocpkg{Rsamtools} makes static version(s) of the samtools libraries \verb|libbam.a| and \verb|libbcf.a|. These static libraries are specific to the operating system on which \Biocpkg{Rsamtools} is being installed, are found under \verb|usrlib${R_ARCH}| in the user library location specified by the mechanism (e.g., \Rfunction{BiocManager::install}, \Rfunction{install.packages}) used to install \Biocpkg{Rsamtools}. At the same time, \Biocpkg{Rsamtools} copies headers required to use the library to the location \verb|include/samtools|. \section{Use} To use these libraries, the third party package developer needs to (1) discover the appropriate header files when their package is built, and (2) link in the libraries. Note that in order to link correctly across platforms your package must provide \emph{both} the respective \verb|src/Makevars| \emph{and} \verb|src/Makevars.win| files. \subsection{Discover header files} To discover appropriate header files at package installation time, add \begin{verbatim} LinkingTo: Rsamtools \end{verbatim} to the \verb|DESCRIPTION| file, and reference the relevant include files as, for instance, \begin{verbatim} #include "samtools/bam.h" \end{verbatim} The content of the include files can be found in the \Biocpkg{Rsamtools} source (under \verb|src/samtools|) or at their installed location. \subsection{Link to static libraries} Linking to the static libraries is accomplished by including the following code in \verb|src/Makevars.win| for \emph{Windows}: \begin{verbatim} SAMVARS=$(shell echo 'cat(Rsamtools:::.pkgMk())' |\ "${R_HOME}/bin/R" --vanilla --slave) include $(SAMVARS) PKG_LIBS=$(SAMTOOLS_LIBS) PKG_CPPFLAGS=$(SAMTOOLS_CPPFLAGS) \end{verbatim} and with the following code in \verb|src/Makevars| for all other platforms: \begin{verbatim} SAMTOOLS_PATH=\ `echo 'cat(Rsamtools:::.pkgLd())' |\ "${R_HOME}/bin/R" --vanilla --slave` SAMTOOLS_LIBS="$(SAMTOOLS_PATH)/libbam.a" "$(SAMTOOLS_PATH)/libbcf.a"\ "$(SAMTOOLS_PATH)/libtabix.a" -lz -pthread SAMTOOLS_CPPFLAGS=-D_USE_KNETFILE -DBGZF_CACHE -D_FILE_OFFSET_BITS=64 \ -D_LARGEFILE64_SOURCE PKG_LIBS=$(SAMTOOLS_LIBS) PKG_CPPFLAGS=$(SAMTOOLS_CPPFLAGS) \end{verbatim} This updates the environment variables \verb|$PKG_CPPFLAGS| and \verb|$PKG_LIBS|; if your \verb|Makevars|/\verb|Makevars.win| modifies these also, do so by adding to the respecitve line, e.g., \begin{verbatim} PKG_LIBS=$(SAMTOOLS_LIBS) -lfoo PKG_CPPFLAGS=$(SAMTOOLS_CPPFLAGS) -I/path/bar \end{verbatim} \end{document}