Provides efficient containers for storing and manipulating short genomic alignments (typically obtained by aligning short reads to a reference genome). This includes read counting, computing the coverage, junction detection, and working with the nucleotide content of the alignments.
Package details |
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Bioconductor views | Alignment Coverage DataImport Genetics ImmunoOncology Infrastructure RNASeq SNP Sequencing |
Maintainer | |
License | Artistic-2.0 |
Version | 1.41.0 |
URL | https://bioconductor.org/packages/GenomicAlignments |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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