How to Install and Uninstall r-bioc-genomicranges Package on Ubuntu 20.10 (Groovy Gorilla)

Last updated: May 03,2024

1. Install "r-bioc-genomicranges" package

This is a short guide on how to install r-bioc-genomicranges on Ubuntu 20.10 (Groovy Gorilla)

$ 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 20.10 (Groovy Gorilla):

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

3. Information about the r-bioc-genomicranges package on Ubuntu 20.10 (Groovy Gorilla)

Package: r-bioc-genomicranges
Architecture: amd64
Version: 1.40.0+dfsg-1build1
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: 2682
Depends: r-base-core (>= 4.0.0.20200528-1), r-api-4.0, r-api-bioc-3.11, r-bioc-biocgenerics (>= 0.25.3), r-bioc-s4vectors (>= 0.25.14), r-bioc-iranges (>= 2.21.6), r-bioc-genomeinfodb (>= 1.15.2), r-bioc-xvector (>= 0.27.2), 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-edger, r-cran-knitr
Filename: pool/universe/r/r-bioc-genomicranges/r-bioc-genomicranges_1.40.0+dfsg-1build1_amd64.deb
Size: 1875112
MD5sum: fe7ecbbd1a64c66409b59208cb53d5fb
SHA1: f5d9d25c94684e629211f49df9b019bdd4d1a63a
SHA256: 410861115f194996e34b374a076f1f8034c987f338393ddf20b0c30d96563927
SHA512: 5fc6fc8068092c8db85cd5c454e91011a18e2353d8a41088a061041b940b386dbf741a3d4046bfa9f403e608f29f863164dbd6068297b8577d830ca5f1f2437f
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