Package: Rsubread
Version: 1.32.2
Date: 2018-12-05
Title: Subread sequence alignment and counting for R
Author: Wei Shi and Yang Liao with contributions from Gordon K Smyth, Jenny Dai
        and Timothy Triche, Jr.
Maintainer: Wei Shi <shi@wehi.edu.au>, Yang Liao <liao@wehi.edu.au> and Gordon K Smyth <smyth@wehi.EDU.AU>
Description: Rsubread is a toolbox developed for the analyses of
        second and third generation sequencing data. It can be used
        for read mapping, read counting, SNP calling, structural
        variant detection and gene fusion discovery. It can be applied
        to all major sequencing techologies and is suitable for the
        analysis of both short and long reads.
URL: http://bioconductor.org/packages/release/bioc/html/Rsubread.html
License: GPL-3
biocViews: Sequencing, Alignment, SequenceMatching, RNASeq, ChIPSeq,
        GeneExpression, GeneRegulation, Genetics, ImmunoOncology, SNP,
        GeneticVariability, Preprocessing, QualityControl,
        GenomeAnnotation, Software
git_url: https://git.bioconductor.org/packages/Rsubread
git_branch: RELEASE_3_8
git_last_commit: 041f1d9
git_last_commit_date: 2018-12-04
Date/Publication: 2018-12-05
NeedsCompilation: yes
Packaged: 2018-12-06 00:21:21 UTC; biocbuild
Built: R 3.5.1; x86_64-conda_cos6-linux-gnu; 2018-12-09 23:25:16 UTC; unix
