GenomicRanges: Representation and manipulation of genomic intervals and variables defined along a genome
Version 1.28.3

The ability to efficiently represent and manipulate genomic annotations and alignments is playing a central role when it comes to analyzing high-throughput sequencing data (a.k.a. NGS data). The GenomicRanges package defines general purpose containers for storing and manipulating genomic intervals and variables defined along a genome. More specialized containers for representing and manipulating short alignments against a reference genome, or a matrix-like summarization of an experiment, are defined in the GenomicAlignments and SummarizedExperiment packages respectively. Both packages build on top of the GenomicRanges infrastructure.

Package details

AuthorP. Aboyoun, H. Pagès, and M. Lawrence
Bioconductor views Annotation Coverage Genetics GenomeAnnotation Infrastructure Sequencing
MaintainerBioconductor Package Maintainer <>
Package repositoryView on Bioconductor
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GenomicRanges documentation built on May 31, 2017, 2:31 p.m.