Rsamtools
DOI:
10.18129 / B9.bioc.Rsamtools
此包适用于Bioconductor的3.7版;有关稳定的、最新的发布版本,请参见Rsamtools。
二进制对齐(BAM)、FASTA、变体调用(BCF)和tabix文件导入
Bioconductor版本:3.7
这个包提供了'samtools', 'bcftools'和'tabix'实用程序的接口(见'LICENCE'),用于操作SAM(序列对齐/映射),FASTA,二进制变体调用(BCF)和压缩索引tab分隔(tabix)文件。
作者:Martin Morgan, Herv\ e Pag\ ' es, Valerie Obenchain, Nathaniel Hayden
Maintainer: Bioconductor Package Maintainer < Maintainer at Bioconductor。org>
引文(从R中输入引用(“Rsamtools”)
):
安装
要安装这个软件包,请从R开始,然后输入:
##如果https:// url不支持源(“//www.anjoumacpherson.com/biocLite.R”)biocLite(“Rsamtools”)
文档
要查看系统中安装的软件包版本的文档,请启动R并输入:
browseVignettes(“Rsamtools”)
细节
biocViews |
对齐,报道,DataImport,质量控制,测序,软件 |
版本 |
1.32.3 |
Bioconductor自 |
BioC 2.6 (R-2.11)(8.5年) |
许可证 |
art -2.0 |文件许可 |
取决于 |
方法,GenomeInfoDb(> = 1.1.3),GenomicRanges(> = 1.31.8),Biostrings(> = 2.47.6) |
进口 |
跑龙套,BiocGenerics(> = 0.25.1),S4Vectors(> = 0.17.25),IRanges(> = 2.13.12),XVector(> = 0.19.7),zlibbioc,bitops,BiocParallel |
链接 |
S4Vectors,IRanges,XVector,Biostrings |
建议 |
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 |
SystemRequirements |
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增强了 |
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URL |
//www.anjoumacpherson.com/packages/release/bioc/html/Rsamtools.html |
取决于我 |
ArrayExpressHTS,BaalChIP,BitSeq,嵌合体,chipseqDB,食典委,contiBAIT,CoverageView,esATAC,exomeCopy,exomePeak,GenoGAM,GenomicAlignments,GenomicFiles,girafe,gmapR,吉他,HelloRanges,感兴趣,leeBamViews,MEDIPS,methylPipe,MMDiff2,podkat,qrqc,r3Cseq,Rcade,ReQON,rfPred,RIPSeeker,rnaseqGene,rnaSeqMap,测序,SGSeq,ShortRead,SICtools,SNPhood,ssviz,systemPipeR,TarSeqQC,TBX20BamSubset,TEQC,VariantAnnotation,wavClusteR |
进口我 |
AllelicImbalance,高山,AneuFinder,annmap,AnnotationHubData,ArrayExpressHTS,ASpli,ATACseqQC,BadRegionFinder,BBCAnalyzer,biovizBase,BSgenome,篮球选手,卡斯珀,cellbaseR,CexoR,chimeraviz,ChIPComp,ChIPexoQual,ChIPpeakAnno,ChIPQC,ChIPSeqSpike,chromstaR,chromVAR,cn.mops,CNVPanelizer,CNVrd2,compEpiTools,文案,CrispRVariants,csaw,customProDB,derfinder,DEXSeq,DiffBind,diffHic,DOQTL,easyRNASeq,EDASeq,ensembldb,epigenomix,eudysbiome,FourCSeq,FunChIP,FunciSNP,gcapc,GeneGeneInteR,genomation,GenomicAlignments,GenomicInteractions,GenVisR,ggbio,GGtools,GoogleGenomics,哥特,GreyListChIP,GUIDEseq,Gviz,gwascat,h5vc,HTSeqGenie,ima,检查,karyoploteR,ldblock,LungCancerLines,MACPET,MADSEQ,maftools,联合化疗,metagene,methylKit,马赛克,motifmatchr,msgbsR,NADfinder,诊断,ORFik,panelcn.mops,PGA,图片,plyranges,PureCN,QDNAseq,qsea,QuasR,R453Plus1Toolbox,ramwas,Rariant,Repitools,RiboProfiling,riboSeqR,RNAprobR,Rqc,rtracklayer,segmentSeq,seqplots,seqsetvis,soGGi,SplicingGraphs,srnadiff,TCseq,TFutils,TitanCNA,tracktables,trackViewer,transcriptR,TransView,TSRchitect,TVTB,VariantFiltering,VariantTools |
建议我 |
annotationhub.,bamsignals,BaseSpaceR,BiocGenerics,BiocParallel,biomvRCNS,芝加哥,计,GenomeInfoDb,GenomicDataCommons,GenomicFeatures,GenomicRanges,GeuvadisTranscriptExpr,gQTLstats,IRanges,metaseqR,omicsPrint,parathyroidSE,收回,RnaSeqTutorial,SeqArray,seqbias,SigFuge,similaRpeak,彩带 |
我的链接 |
ArrayExpressHTS,BitSeq,DiffBind,h5vc,podkat,qrqc,QuasR,seqbias,TransView,VariantAnnotation |
构建报告 |
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包档案
遵循bob 体育网址
在R会话中使用这个包的说明。