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 |
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Bioconductor views | Annotation Coverage DataRepresentation Genetics GenomeAnnotation Infrastructure Sequencing |
Maintainer | |
License | Artistic-2.0 |
Version | 1.59.1 |
URL | https://bioconductor.org/packages/GenomicRanges |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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