How to Install and Uninstall r-bioc-genomicranges Package on Ubuntu 21.10 (Impish Indri)

Last updated: November 23,2024

1. Install "r-bioc-genomicranges" package

This tutorial shows how to install r-bioc-genomicranges on Ubuntu 21.10 (Impish Indri)

$ sudo apt update $ sudo apt install r-bioc-genomicranges

2. Uninstall "r-bioc-genomicranges" package

This guide let you learn how to uninstall r-bioc-genomicranges on Ubuntu 21.10 (Impish Indri):

$ sudo apt remove r-bioc-genomicranges $ sudo apt autoclean && sudo apt autoremove

3. Information about the r-bioc-genomicranges package on Ubuntu 21.10 (Impish Indri)

Package: r-bioc-genomicranges
Architecture: amd64
Version: 1.42.0+dfsg-1
Priority: optional
Section: universe/gnu-r
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian R Packages Maintainers
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 2675
Depends: r-base-core (>= 4.0.2-1build1), r-api-4.0, r-api-bioc-3.12, r-bioc-biocgenerics (>= 0.25.3), r-bioc-s4vectors (>= 0.27.12), r-bioc-iranges (>= 2.23.9), r-bioc-genomeinfodb (>= 1.15.2), r-bioc-xvector (>= 0.29.2), libc6 (>= 2.4)
Recommends: r-cran-runit, r-cran-digest, r-bioc-annotate, r-bioc-summarizedexperiment
Suggests: r-cran-matrix, r-bioc-biobase, r-bioc-annotationdbi, r-bioc-biostrings (>= 2.25.3), r-bioc-rsamtools (>= 1.13.53), r-bioc-genomicalignments, r-bioc-rtracklayer, r-bioc-bsgenome, r-bioc-genomicfeatures, r-bioc-gviz, r-bioc-variantannotation, r-bioc-annotationhub, r-bioc-deseq2, r-bioc-dexseq, r-bioc-edger, r-cran-knitr, r-bioc-biocstyle
Filename: pool/universe/r/r-bioc-genomicranges/r-bioc-genomicranges_1.42.0+dfsg-1_amd64.deb
Size: 1860660
MD5sum: 29e0cdcfc60fa4de84d12f413bbba6d8
SHA1: ae8ff7b60a956c147ccea9dbf3e69f2f37a9087e
SHA256: acfbc5f9ccf3e1ee15cfed2ed082d23ec7688cd7a1efbbf5377bc37a65ff296c
SHA512: 19e295554badb7885845521be3871c2b0402ea11dfc35d5cd2c43a63ba114d49709f62dda3b5b77f9b6997eb181a2300fb0fd10692133b0c71474cc18baabb30
Homepage: https://bioconductor.org/packages/GenomicRanges/
Description-en: BioConductor representation and manipulation of genomic intervals
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.
Description-md5: 3f662bd13374fbb5b4494cefe3dcaf66