This package is for version 3.8 of Bioconductor; for the stable, up-to-date release version, see GenomicAlignments.
Bioconductor version: 3.8
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.
Author: Hervé Pagès, Valerie Obenchain, Martin Morgan
Maintainer: Bioconductor Package Maintainer <maintainer at bioconductor.org>
Citation (from within R,
enter citation("GenomicAlignments")
):
To install this package, start R (version "3.5") and enter:
if (!requireNamespace("BiocManager", quietly = TRUE)) install.packages("BiocManager") BiocManager::install("GenomicAlignments")
For older versions of R, please refer to the appropriate Bioconductor release.
To view documentation for the version of this package installed in your system, start R and enter:
browseVignettes("GenomicAlignments")
R Script | An Introduction to the GenomicAlignments Package | |
R Script | Counting reads with summarizeOverlaps | |
R Script | Overlap encodings | |
R Script | Working with aligned nucleotides | |
Reference Manual | ||
Text | NEWS | |
Video | Reading from a BAM file - Part 1 | |
Video | Reading from a BAM file - Part 2 |
Follow Installation instructions to use this package in your R session.
Source Package | GenomicAlignments_1.18.1.tar.gz |
Windows Binary | GenomicAlignments_1.18.1.zip (32- & 64-bit) |
Mac OS X 10.11 (El Capitan) | GenomicAlignments_1.18.1.tgz |
Source Repository | git clone https://git.bioconductor.org/packages/GenomicAlignments |
Source Repository (Developer Access) | git clone git@git.bioconductor.org:packages/GenomicAlignments |
Package Short Url | http://bioconductor.org/packages/GenomicAlignments/ |
Package Downloads Report | Download Stats |
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