Rsamtools (original) (raw)

This is the released version of Rsamtools; for the devel version, seeRsamtools.

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

Bioconductor version: Release (3.20)

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 [aut], Hervé Pagès [aut], Valerie Obenchain [aut], Nathaniel Hayden [aut], Busayo Samuel [ctb] (Converted Rsamtools vignette from Sweave to RMarkdown / HTML.), Bioconductor Package Maintainer [cre]

Maintainer: Bioconductor Package Maintainer

Citation (from within R, enter citation("Rsamtools")):

Installation

To install this package, start R (version "4.4") 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")
An Introduction to Rsamtools HTML R Script
Reference Manual PDF
NEWS Text
LICENSE Text
Video

Details

biocViews Alignment, Coverage, DataImport, QualityControl, Sequencing, Software
Version 2.22.0
In Bioconductor since BioC 2.6 (R-2.11) (14.5 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
System Requirements GNU make
URL https://bioconductor.org/packages/Rsamtools
Bug Reports https://github.com/Bioconductor/Rsamtools/issues

See More

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, knitr
Linking To Rhtslib(>= 2.99.1), S4Vectors, IRanges, XVector, Biostrings
Enhances
Depends On Me CODEX, CoverageView, esATAC, FRASER, GenomicAlignments, GenomicFiles, girafe, gmapR, HelloRanges, IntEREst, MEDIPS, methylPipe, MMDiff2, podkat, r3Cseq, RepViz, RiboDiPA, SCOPE, SGSeq, ShortRead, SICtools, SNPhood, spiky, ssviz, systemPipeR, TEQC, VariantAnnotation, wavClusteR, leeBamViews, TBX20BamSubset, sequencing, csawBook, minimapR
Imports Me alabaster.files, alabaster.vcf, AllelicImbalance, AneuFinder, annmap, AnnotationHubData, APAlyzer, appreci8R, ASpli, ATACseqQC, ATACseqTFEA, atena, BadRegionFinder, bambu, BBCAnalyzer, biovizBase, biscuiteer, breakpointR, BSgenome, CAGEr, casper, CellBarcode, cellbaseR, CexoR, cfdnakit, cfDNAPro, chimeraviz, ChIPexoQual, ChIPpeakAnno, ChIPQC, ChromSCape, chromVAR, CircSeqAlignTk, CleanUpRNAseq, cn.mops, CNVfilteR, CNVPanelizer, CNVrd2, compEpiTools, consensusDE, CopyNumberPlots, CrispRVariants, csaw, CSSQ, customProDB, DAMEfinder, Damsel, DegNorm, derfinder, DEXSeq, DiffBind, diffHic, DNAfusion, easyRNASeq, EDASeq, ensembldb, epigenomix, epigraHMM, eudysbiome, extraChIPs, FilterFFPE, FLAMES, gcapc, gDNAx, GeneGeneInteR, genomation, GenomicAlignments, GenomicInteractions, GenomicPlot, GenVisR, ggbio, gmoviz, GOTHiC, GreyListChIP, GUIDEseq, Gviz, h5vc, icetea, IMAS, INSPEcT, karyoploteR, MADSEQ, magpie, MDTS, metagene2, metaseqR2, methylKit, mosaics, motifmatchr, msgbsR, NADfinder, NanoMethViz, nearBynding, nucleR, ORFik, panelcn.mops, PICS, plyranges, pram, profileplyr, PureCN, QDNAseq, qsea, QuasR, R453Plus1Toolbox, raer, ramwas, Rbowtie2, recoup, Repitools, rfPred, RiboProfiling, riboSeqR, ribosomeProfilingQC, RNAmodR, Rqc, rtracklayer, scDblFinder, scPipe, scRNAseqApp, scruff, segmentSeq, seqsetvis, SimFFPE, sitadela, soGGi, SplicingGraphs, strandCheckR, tadar, TCseq, TFutils, tracktables, trackViewer, transcriptR, TRESS, tRNAscanImport, TVTB, UMI4Cats, uncoverappLib, VariantFiltering, VariantTools, VaSP, VCFArray, VplotR, ZygosityPredictor, chipseqDBData, gDNAinRNAseqData, LungCancerLines, MetaScope, raerdata, GenoPop, hoardeR, iimi, kibior, MAAPER, MicroSEC, NIPTeR, noisyr, PlasmaMutationDetector, PlasmaMutationDetector2, revert, scPloidy, Signac, umiAnalyzer, VALERIE
Suggests Me AnnotationHub, bamsignals, BaseSpaceR, BiocGenerics, BiocParallel, biomvRCNS, BSgenomeForge, Chicago, epivizrChart, gage, GenomeInfoDb, GenomicDataCommons, GenomicFeatures, GenomicRanges, gwascat, HIBAG, igvShiny, IRanges, ldblock, MOSim, MungeSumstats, omicsPrint, RNAmodR.ML, SeqArray, SigFuge, similaRpeak, Streamer, TENxIO, GeuvadisTranscriptExpr, NanoporeRNASeq, parathyroidSE, systemPipeRdata, chipseqDB, karyotapR, polyRAD, seqmagick
Links To Me
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Package Archives

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

Source Package Rsamtools_2.22.0.tar.gz
Windows Binary (x86_64) Rsamtools_2.22.0.zip
macOS Binary (x86_64) Rsamtools_2.22.0.tgz
macOS Binary (arm64) Rsamtools_2.22.0.tgz
Source Repository git clone https://git.bioconductor.org/packages/Rsamtools
Source Repository (Developer Access) git clone git@git.bioconductor.org:packages/Rsamtools
Bioc Package Browser https://code.bioconductor.org/browse/Rsamtools/
Package Short Url https://bioconductor.org/packages/Rsamtools/
Package Downloads Report Download Stats