Bioconductor version: 2.7
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: Biocore Team c/o BioC user list <bioconductor at stat.math.ethz.ch>
To install this package, start R and enter:
source("http://bioconductor.org/biocLite.R")
biocLite("GenomicRanges")
To cite this package in a publication, start R and enter:
citation("GenomicRanges")
| An Introduction to GenomicRanges | ||
| R Script | GenomicRanges Use Cases | |
| Reference Manual |
| biocViews | Genetics, Sequencing, HighThroughputSequencing, Annotation |
| Depends | R (>= 2.8.0), methods, IRanges(>= 1.7.31) |
| Imports | methods, IRanges |
| Suggests | RUnit, BSgenome, GenomicFeatures, Rsamtools, EatonEtAlChIPseq, leeBamViews, org.Sc.sgd.db, BSgenome.Scerevisiae.UCSC.sacCer2 |
| System Requirements | |
| License | Artistic-2.0 |
| URL | |
| Depends On Me | BSgenome, chipseq, GenomicFeatures, GGtools, PICS, Rsamtools, ShortRead, SNPlocs.Hsapiens.dbSNP.20100427, SNPlocs.Hsapiens.dbSNP.20101109 |
| Imports Me | chipseq, ChIPseqR, GenomicFeatures, leeBamViews, PICS, Rsamtools, rtracklayer, ShortRead, SNPlocs.Hsapiens.dbSNP.20100427, SNPlocs.Hsapiens.dbSNP.20101109 |
| Suggests Me | |
| Version | 1.2.3 |
| Since | Bioconductor 2.6 (R-2.11) |
| Package Source | GenomicRanges_1.2.3.tar.gz |
| Windows Binary | GenomicRanges_1.2.3.zip (32- & 64-bit) |
| MacOS 10.5 (Leopard) binary | GenomicRanges_1.2.3.tgz |
| Package Downloads Report | Download Stats |
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