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sga 0.10.15-4
  • links: PTS, VCS
  • area: main
  • in suites: buster
  • size: 62,932 kB
  • sloc: cpp: 48,538; ansic: 2,035; python: 1,037; perl: 744; makefile: 349; sh: 185
file content (39 lines) | stat: -rw-r--r-- 1,396 bytes parent folder | download
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Source: sga
Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
Uploaders: Michael R. Crusoe <michael.crusoe@gmail.com>,
           Andreas Tille <tille@debian.org>
Section: science
Priority: optional
Build-Depends: debhelper (>= 11~),
               libsparsehash-dev,
               zlib1g-dev | libz-dev,
               libbamtools-dev,
               gawk,
               help2man,
# Run-Time Depends
# (to prevent building on architectures where it won't be installable)
               samtools,
               python,
               python-ruffus,
               python-pysam
Standards-Version: 4.2.1
Vcs-Browser: https://salsa.debian.org/med-team/sga
Vcs-Git: https://salsa.debian.org/med-team/sga.git
Homepage: https://github.com/jts/sga

Package: sga
Architecture: any
Depends: ${shlibs:Depends},
         ${misc:Depends},
         samtools,
         python,
         python-ruffus,
         python-pysam
Recommends: abyss (>= 2.0.2-1)
Description: de novo genome assembler that uses string graphs
 The major goal of SGA is to be very memory efficient, which is achieved by
 using a compressed representation of DNA sequence reads.
 .
 SGA is a de novo assembler for DNA sequence reads. It is based on Gene Myers'
 string graph formulation of assembly and uses the FM-index/Burrows-Wheeler
 transform to efficiently find overlaps between sequence reads.