Rsamtools

DOI: 10.18129/B9.bioc.Rsamtools    

Binary alignment (BAM), FASTA, variant call (BCF), and tabix file import

Bioconductor version: Release (3.14)

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.

Author: Martin Morgan, Hervé Pagès, Valerie Obenchain, Nathaniel Hayden

Maintainer: Bioconductor Package Maintainer <maintainer at bioconductor.org>

Installation

To install this package, start R (version "4.1") and enter:

if (!require("BiocManager", quietly = TRUE))
    install.packages("BiocManager")

BiocManager::install("Rsamtools")

For older versions of R, please refer to the appropriate Bioconductor release.

Documentation

To view documentation for the version of this package installed in your system, start R and enter:

browseVignettes("Rsamtools")

 

PDF	R Script	An introduction to Rsamtools
PDF		Reference Manual
Text		NEWS
Text		LICENSE
Video		pileup in Rsamtools

Details

biocViews	Alignment, Coverage, DataImport, QualityControl, Sequencing, Software
Version	2.10.0
In Bioconductor since	BioC 2.6 (R-2.11) (12 years)
License	Artistic-2.0 | file LICENSE
Depends	methods, GenomeInfoDb(>= 1.1.3), GenomicRanges(>= 1.31.8), Biostrings(>= 2.47.6), R (>= 3.5.0)
Imports	utils, BiocGenerics(>= 0.25.1), S4Vectors(>= 0.17.25), IRanges(>= 2.13.12), XVector(>= 0.19.7), zlibbioc, bitops, BiocParallel, stats
LinkingTo	Rhtslib(>= 1.17.7), S4Vectors, IRanges, XVector, Biostrings
Suggests	GenomicAlignments, ShortRead(>= 1.19.10), GenomicFeatures, TxDb.Dmelanogaster.UCSC.dm3.ensGene, TxDb.Hsapiens.UCSC.hg18.knownGene, RNAseqData.HNRNPC.bam.chr14, BSgenome.Hsapiens.UCSC.hg19, RUnit, BiocStyle
SystemRequirements	GNU make
Enhances
URL	https://bioconductor.org/packages/Rsamtools
BugReports	https://github.com/Bioconductor/Rsamtools/issues
Depends On Me	ArrayExpressHTS, BaalChIP, BitSeq, CODEX, contiBAIT, CoverageView, esATAC, exomeCopy, FRASER, GenomicAlignments, GenomicFiles, girafe, gmapR, HelloRanges, IntEREst, leeBamViews, MEDIPS, methylPipe, MMDiff2, podkat, r3Cseq, Rcade, RepViz, ReQON, rfPred, RiboDiPA, SCOPE, sequencing, SGSeq, ShortRead, SICtools, SNPhood, spiky, ssviz, systemPipeR, TarSeqQC, TBX20BamSubset, TEQC, VariantAnnotation, wavClusteR
Imports Me	AllelicImbalance, alpine, AneuFinder, annmap, AnnotationHubData, APAlyzer, appreci8R, ArrayExpressHTS, ASpediaFI, ASpli, ATACseqQC, atena, BadRegionFinder, bambu, BBCAnalyzer, biovizBase, biscuiteer, breakpointR, BRGenomics, BSgenome, CAGEr, casper, cellbaseR, CexoR, cfDNAPro, ChIC, chimeraviz, ChIPComp, ChIPexoQual, ChIPpeakAnno, ChIPQC, chipseqDBData, ChromSCape, chromstaR, chromVAR, cn.mops, CNVfilteR, CNVPanelizer, CNVrd2, compEpiTools, consensusDE, CopyNumberPlots, CopywriteR, CrispRVariants, csaw, CSSQ, customProDB, DAMEfinder, DegNorm, derfinder, DEXSeq, DiffBind, diffHic, easyRNASeq, EDASeq, ensembldb, epigenomix, epigraHMM, eudysbiome, exomePeak2, FilterFFPE, FLAMES, FunChIP, gcapc, GeneGeneInteR, GenoGAM, genomation, GenomicAlignments, GenomicInteractions, GenVisR, ggbio, gmoviz, GOTHiC, GreyListChIP, GUIDEseq, Gviz, h5vc, HTSeqGenie, icetea, IMAS, INSPEcT, karyoploteR, ldblock, LungCancerLines, MACPET, MADSEQ, MDTS, metagene, metagene2, metaseqR2, methylKit, MMAPPR2, MMAPPR2data, mosaics, motifmatchr, msgbsR, NADfinder, NanoMethViz, nearBynding, nucleR, ORFik, panelcn.mops, PICS, plyranges, pram, profileplyr, PureCN, QDNAseq, qsea, QuasR, R453Plus1Toolbox, ramwas, Rbowtie2, recoup, Repitools, RiboProfiling, riboSeqR, ribosomeProfilingQC, RNAmodR, RNASeqR, Rqc, rtracklayer, scruff, segmentSeq, seqsetvis, SimFFPE, sitadela, soGGi, SplicingGraphs, srnadiff, strandCheckR, systemPipeRdata, TCseq, TFutils, tracktables, trackViewer, transcriptR, TRESS, tRNAscanImport, TSRchitect, TVTB, UMI4Cats, uncoverappLib, VariantFiltering, VariantTools, VaSP, VCFArray, VplotR
Suggests Me	AnnotationHub, bamsignals, BaseSpaceR, BiocGenerics, BiocParallel, biomvRCNS, Chicago, chipseqDB, epivizrChart, gage, GenomeInfoDb, GenomicDataCommons, GenomicFeatures, GenomicRanges, GeuvadisTranscriptExpr, gwascat, IRanges, MungeSumstats, NanoporeRNASeq, omicsPrint, parathyroidSE, RNAmodR.ML, SeqArray, seqbias, SigFuge, similaRpeak, Streamer
Links To Me
Build Report

Package Archives

Follow Installation instructions to use this package in your R session.

Source Package	Rsamtools_2.10.0.tar.gz
Windows Binary	Rsamtools_2.10.0.zip (32- & 64-bit)
macOS 10.13 (High Sierra)	Rsamtools_2.10.0.tgz
Source Repository	git clone https://git.bioconductor.org/packages/Rsamtools
Source Repository (Developer Access)	git clone git@git.bioconductor.org:packages/Rsamtools
Package Short Url	https://bioconductor.org/packages/Rsamtools/
Package Downloads Report	Download Stats
Old Source Packages for BioC 3.14	Source Archive