source("http://bioconductor.org/biocLite.R")
biocLite("GenomicRanges")

GenomicRanges

Representation and manipulation of genomic intervals

Bioconductor version: 2.13

The ability to efficiently store genomic annotations and alignments is playing a central role when it comes to analyze high-throughput sequencing data (a.k.a. NGS data). The package defines general purpose containers for storing genomic intervals as well as more specialized containers for storing alignments against a reference genome.

Author: P. Aboyoun, H. Pages and M. Lawrence

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

Installation

To install this package, start R and enter:

source("http://bioconductor.org/biocLite.R")
biocLite("GenomicRanges")

Documentation

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

browseVignettes("GenomicRanges")

 

PDF	R Script	An Introduction to GenomicRanges
PDF	R Script	Counting reads with summarizeOverlaps
PDF	R Script	GenomicRanges HOWTOs
PDF	R Script	Overlap encodings
PDF		summarizeOverlaps-modes.pdf
PDF		Reference Manual
Text		NEWS

Details

biocViews	Annotation, Genetics, HighThroughputSequencing, Sequencing, Software
Version	1.14.4
In Bioconductor since	BioC 2.6 (R-2.11)
License	Artistic-2.0
Depends	R (>= 2.10), methods, BiocGenerics(>= 0.7.7), IRanges(>= 1.20.3), XVector(>= 0.1.3)
Imports	methods, utils, stats, BiocGenerics, IRanges
Suggests	AnnotationDbi(>= 1.21.1), AnnotationHub, BSgenome, BSgenome.Hsapiens.UCSC.hg19, BSgenome.Scerevisiae.UCSC.sacCer2, BSgenome.Dmelanogaster.UCSC.dm3, Biostrings(>= 2.25.3), Rsamtools(>= 1.13.53), rtracklayer, KEGG.db, KEGGgraph, GenomicFeatures, TxDb.Dmelanogaster.UCSC.dm3.ensGene, TxDb.Hsapiens.UCSC.hg19.knownGene, seqnames.db, org.Sc.sgd.db, VariantAnnotation, edgeR, DESeq, DEXSeq, pasilla, pasillaBamSubset, RUnit, digest, BiocStyle
System Requirements
URL
Depends On Me	AllelicImbalance, annmap, baySeq, biomvRCNS, BiSeq, BSgenome, bsseq, bumphunter, casper, cheung2010, chimera, chipseq, cleanUpdTSeq, cn.mops, CSAR, DASiR, deepSNV, DESeq2, DiffBind, DREAM4, dsQTL, easyRNASeq, EatonEtAlChIPseq, ensemblVEP, epigenomix, epivizr, exomeCopy, fastseg, genomes, GenomicFeatures, genoset, GGtools, ggtut, gmapR, gwascat, HiTC, htSeqTools, intansv, methyAnalysis, minfi, MMDiff, OmicCircos, parathyroidSE, PING, QuasR, r3Cseq, Rcade, rfPred, RIPSeeker, Rsamtools, rSFFreader, RSVSim, rtracklayer, segmentSeq, seqbias, ShortRead, SigFuge, SNPlocs.Hsapiens.dbSNP.20090506, SNPlocs.Hsapiens.dbSNP.20100427, SNPlocs.Hsapiens.dbSNP.20101109, SNPlocs.Hsapiens.dbSNP.20110815, SNPlocs.Hsapiens.dbSNP.20111119, SNPlocs.Hsapiens.dbSNP.20120608, SomatiCA, SplicingGraphs, TransView, VariantAnnotation, VariantTools, vtpnet
Imports Me	AnnotationHub, ArrayExpressHTS, biovizBase, BiSeq, CAGEr, CexoR, chipenrich, chipenrich.data, chipseq, ChIPseqR, copynumber, customProDB, DEXSeq, DNaseR, epigenomix, flipflop, FunciSNP, GenomicFeatures, genoset, ggbio, gmapR, Gviz, h5vc, HTSeqGenie, HTSFilter, interactiveDisplay, leeBamViews, lumi, MEDIPS, methyAnalysis, MethylSeekR, MinimumDistance, MMDiff, NarrowPeaks, nucleR, oligoClasses, PICS, prebs, QuasR, Repitools, rnaSeqMap, rSFFreader, rtracklayer, segmentSeq, SeqArray, SeqVarTools, 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, SomatiCA, SomaticCancerAlterations, spliceR, SplicingGraphs, triplex, VanillaICE, VariantTools, waveTiling
Suggests Me	BeadArrayUseCases, BiocGenerics, IRanges, methylumi, MiRaGE, NarrowPeaks, RnaSeqTutorial

Package Archives

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

Package Source	GenomicRanges_1.14.4.tar.gz
Windows Binary	GenomicRanges_1.14.4.zip (32- & 64-bit)
Mac OS X 10.6 (Snow Leopard)	GenomicRanges_1.14.4.tgz
Browse/checkout source	(username/password: readonly)
Package Downloads Report	Download Stats