Bioconductor version: 2.9
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>
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")
R Script | An Introduction to GenomicRanges | |
R Script | GenomicRanges Use Cases | |
R Script | Overview of summarizeOverlaps | |
summarizeOverlaps-modes.pdf | ||
Reference Manual | ||
Text | NEWS |
Package Source | GenomicRanges_1.6.7.tar.gz |
Windows Binary | GenomicRanges_1.6.7.zip (32- & 64-bit) |
MacOS 10.5 (Leopard) binary | GenomicRanges_1.6.7.tgz |
Package Downloads Report | Download Stats |
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