Source: r-bioc-rsubread
Standards-Version: 4.7.4
Maintainer: Debian R Packages Maintainers <r-pkg-team@alioth-lists.debian.net>
Uploaders:
 Steffen Moeller <moeller@debian.org>,
Section: gnu-r
Testsuite: autopkgtest-pkg-r
Build-Depends:
 debhelper-compat (= 14),
 dh-r,
 r-base-dev,
 r-cran-matrix,
 r-pkg-team-core-architecture,
Vcs-Browser: https://salsa.debian.org/r-pkg-team/r-bioc-rsubread
Vcs-Git: https://salsa.debian.org/r-pkg-team/r-bioc-rsubread.git
Homepage: https://bioconductor.org/packages/Rsubread/

Package: r-bioc-rsubread
Architecture: any
Depends:
 ${R:Depends},
 ${shlibs:Depends},
 ${misc:Depends},
 r-pkg-team-core-architecture,
Recommends:
 ${R:Recommends},
Suggests:
 ${R:Suggests},
Description: Mapping, quantification and variant analysis of sequencing data
 Alignment, quantification and analysis of RNA sequencing data
 (including both bulk RNA-seq and scRNA-seq) and DNA sequenicng data
 (including ATAC-seq, ChIP-seq, WGS, WES etc). Includes functionality
 for read mapping, read counting, SNP calling, structural variant detection
 and gene fusion discovery. Can be applied to all major sequencing techologies
 and to both short and long sequence reads.
