安装这个包,开始R和输入:

# #试试http://如果https:// url不支持源(“//www.anjoumacpherson.com/biocLite.R”) biocLite (“GenomicRanges”)

在大多数情况下,您不需要下载包存档。

GenomicRanges

这个包是3.2版本Bioconductor;的稳定,最新的发布版本,请参阅GenomicRanges

表示和操纵基因间隔和变量定义在一个基因组

Bioconductor版本:3.2

能够有效地表示和操纵基因注释和校准时发挥着核心作用分析高通量测序数据(或称门店数据)。GenomicRanges包定义了通用的容器存储和操纵基因间隔和变量定义在一个基因组。更专业的容器代表和操纵短对参考基因组比对,或表来总结一个实验,分别GenomicAlignments和SummarizedExperiment包中定义的。两个包之上构建GenomicRanges基础设施。

作者:p . Aboyoun h .页,和m .劳伦斯

维修工:Bioconductor包维护者<维护者bioconductor.org >

从内部引用(R,回车引用(“GenomicRanges”)):

安装

安装这个包,开始R和输入:

# #试试http://如果https:// url不支持源(“//www.anjoumacpherson.com/biocLite.R”) biocLite (“GenomicRanges”)

文档

查看文档的版本这个包安装在您的系统,开始R和输入:

browseVignettes (“GenomicRanges”)

PDF 简单介绍农庄和GRangesList对象
PDF 介绍GenomicRanges
PDF 延长GenomicRanges
PDF GenomicRanges howto
PDF 参考手册
文本 新闻

细节

biocViews 注释,报道,遗传学,GenomeAnnotation,基础设施,测序,软件
版本 1.22.4
Bioconductor自 BioC 2.6 (r - 2.11)(6年)
许可证 艺术- 2.0
取决于 R(> = 2.10),方法,BiocGenerics(> = 0.16.1),S4Vectors(> = 0.8.6),IRanges(> = 2.4.6),GenomeInfoDb(> = 1.1.20)
进口 跑龙套,统计数据,XVector
链接 S4Vectors,IRanges
建议 Biobase,AnnotationDbi(> = 1.21.1),注释,Biostrings(> = 2.25.3),Rsamtools(> = 1.13.53),SummarizedExperiment(> = 0.1.5),GenomicAlignments,rtracklayer,BSgenome,GenomicFeatures,Gviz,VariantAnnotation,AnnotationHub,DESeq,DEXSeq,刨边机,KEGGgraph,BiocStyle,消化,RUnit,BSgenome.Hsapiens.UCSC.hg19,BSgenome.Scerevisiae.UCSC.sacCer2,KEGG.db,hgu95av2.db,org.Hs.eg.db,org.Mm.eg.db,org.Sc.sgd.db,pasilla,pasillaBamSubset,TxDb.Athaliana.BioMart.plantsmart22,TxDb.Dmelanogaster.UCSC.dm3.ensGene,TxDb.Hsapiens.UCSC.hg19.knownGene
SystemRequirements
增强了
URL
取决于我 AllelicImbalance,annmap,AnnotationHubData,Basic4Cseq,baySeq,biomvRCNS,BiSeq,BSgenome,bsseq,BubbleTree,bumphunter,咖啡馆,卡斯珀,cheung2010,嵌合体,ChIPComp,ChIPpeakAnno,ChIPQC,chipseq,cleanUpdTSeq,cn.mops,CNPBayes,cnvGSA,CNVPanelizer,compEpiTools,CSAR,csaw,DASiR,deepSNV,DESeq2,DEXSeq,DiffBind,diffHic,DMRcaller,DMRcatedata,DMRforPairs,DOQTL,EatonEtAlChIPseq,EnrichedHeatmap,ensembldb,ensemblVEP,epigenomix,exomeCopy,fastseg,FourCSeq,GeneBreak,geneRxCluster,基因组,GenomicAlignments,GenomicFeatures,GenomicFiles,GenomicTuples,genoset,GenoView,geuvStore,ggtut,gmapR,哥特,GreyListChIP,groHMM,吉他,Gviz,hiAnnotator,HilbertCurve,HiTC,htSeqTools,IdeoViz,InPAS,intansv,工商管理硕士,metagene,methyAnalysis,methylPipe,minfi,MMDiff,OmicCircos,PGA,,podkat,QuasR,r3Cseq,Rariant,Rcade,地区,rfPred,rGREAT,riboSeqR,RIPSeeker,RnBeads,RnBeads.hg19,RnBeads.hg38,RnBeads.mm10,RnBeads.mm9,RnBeads.rn5,Rsamtools,RSVSim,rtracklayer,segmentSeq,seqbias,SGSeq,SigFuge,SNPhood,SNPlocs.Hsapiens.dbSNP.20090506,SNPlocs.Hsapiens.dbSNP.20100427,SNPlocs.Hsapiens.dbSNP.20101109,SNPlocs.Hsapiens.dbSNP.20110815,SNPlocs.Hsapiens.dbSNP.20111119,SNPlocs.Hsapiens.dbSNP.20120608,SNPlocs.Hsapiens.dbSNP141.GRCh38,SNPlocs.Hsapiens.dbSNP142.GRCh37,SomatiCA,SomaticSignatures,SummarizedExperiment,TarSeqQC,trackViewer,TransView,tra利用,VanillaICE,VariantAnnotation,VariantTools,vtpnet,wavClusteR,XtraSNPlocs.Hsapiens.dbSNP141.GRCh38
进口我 ALDEx2,ArrayExpressHTS,舞会礼服,bamsignals,beadarray,击败,biovizBase,BiSeq,BSgenome,篮球选手,CexoR,cgdv17,冠军,chipenrich,chipenrich.data,ChIPseeker,chipseq,ChIPseqR,chromDraw,cn,彗星,conumee,copynumber,文案,COSMIC.67,CoverageView,customProDB,DChIPRep,derfinder,derfinderPlot,DMRcate,easyRNASeq,EDASeq,埃尔默,ELMER.data,epivizr,erma,啪嗒啪嗒地响,FourCSeq,FunciSNP,genomation,genomeIntervals,GenomicAlignments,GenomicInteractions,genotypeeval,GGBase,ggbio,GGtools,GoogleGenomics,gQTLBase,gQTLstats,GUIDEseq,gwascat,h5vc,hiReadsProcessor,HTSeqGenie,检查,iva,LedPred,leeBamViews,萝拉,光民,M3D,MafDb.ALL.wgs.phase1.release.v3.20101123,MafDb.ALL.wgs.phase3.release.v5a.20130502,MafDb.ALL.wgs.phase3.release.v5b.20130502,MafDb.ESP6500SI.V2.SSA137,MafDb.ExAC.r0.3.sites,,MEDIPS,methyAnalysis,MethylSeekR,methylumi,MinimumDistance,MMDiff,motifbreakR,NarrowPeaks,诊断,oligoClasses,OrganismDbi,Pbase,pepDat,pepStat,phastCons100way.UCSC.hg19,phastCons100way.UCSC.hg38,phastCons7way.UCSC.hg38,图片,prebs,proBAMr,Pviz,pwOmics,qpgraph,R3CPET,R453Plus1Toolbox,RareVariantVis,rCGH,地区,regionReport,Repitools,rgsepd,RiboProfiling,RNAprobR,rnaSeqMap,咆哮,seq2pathway,SeqArray,seqPattern,seqplots,SeqVarTools,ShortRead,SICtools,simulatorZ,SNPchip,SNPlocs.Hsapiens.dbSNP.20090506,SNPlocs.Hsapiens.dbSNP.20100427,SNPlocs.Hsapiens.dbSNP.20101109,SNPlocs.Hsapiens.dbSNP.20110815,SNPlocs.Hsapiens.dbSNP.20111119,SNPlocs.Hsapiens.dbSNP.20120608,SNPlocs.Hsapiens.dbSNP141.GRCh38,SNPlocs.Hsapiens.dbSNP142.GRCh37,SNPlocs.Hsapiens.dbSNP144.GRCh37,SNPlocs.Hsapiens.dbSNP144.GRCh38,soGGi,SomatiCA,SomaticCancerAlterations,连接工具,SplicingGraphs,SVM2CRM,systemPipeR,TCGAbiolinks,TFBSTools,ToPASeq,tracktables,三层,VariantFiltering,waveTiling,XtraSNPlocs.Hsapiens.dbSNP141.GRCh38,XtraSNPlocs.Hsapiens.dbSNP144.GRCh37,XtraSNPlocs.Hsapiens.dbSNP144.GRCh38
建议我 AnnotationHub,BeadArrayUseCases,biobroom,BiocGenerics,BiocParallel,腰带,GenomeInfoDb,gtrellis,interactiveDisplay,IRanges,metaseqR,海市蜃楼,NarrowPeaks,NGScopy,SeqGSEA,斯坦
构建报告

包档案

遵循bob 体育网址 指示在R会话中使用这个包。

包的来源 GenomicRanges_1.22.4.tar.gz
Windows二进制 GenomicRanges_1.22.4.zip(32位和64位)
Mac OS X 10.6 (Snow Leopard) GenomicRanges_1.22.1.tgz
Mac OS X 10.9(小牛) GenomicRanges_1.22.4.tgz
Subversion源 (用户名/密码:只读的)
Git源代码 https://github.com/bioconductor - mirror/genomicranges/tree/release - 3.2
包短Url //www.anjoumacpherson.com/packages/GenomicRanges/
包下载报告 下载数据

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