velvet 1.2.10+dfsg1-6 source package in Ubuntu

Changelog

velvet (1.2.10+dfsg1-6) unstable; urgency=medium

  * Use 2to3 to port to Python3
    Closes: #945743
  * debhelper-compat 12
  * Standards-Version: 4.4.1
  * Secure URI in copyright format
  * Remove trailing whitespace in debian/changelog
  * Remove trailing whitespace in debian/control
  * autopkgtest: s/ADTTMP/AUTOPKGTEST_TMP/g
  * Use secure URI in Homepage field.
  * Set upstream metadata fields: Repository-Browse.
  * Remove obsolete fields Contact, Name from debian/upstream/metadata.

 -- Andreas Tille <email address hidden>  Mon, 02 Dec 2019 13:40:35 +0100

Upload details

Uploaded by:
Debian Med
Uploaded to:
Sid
Original maintainer:
Debian Med
Architectures:
any all
Section:
science
Urgency:
Medium Urgency

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File Size SHA-256 Checksum
velvet_1.2.10+dfsg1-6.dsc 2.2 KiB 2a0cb9b128936070b4870994ecd55aecee33961cfe36865db9b8c5de9b8a6903
velvet_1.2.10+dfsg1.orig.tar.xz 13.0 MiB 368d760ad56ffa010a2ae72b25d46680ecb7ad8cc573cf6c389848c87b32ee26
velvet_1.2.10+dfsg1-6.debian.tar.xz 16.4 KiB 68b0d97e2a6751fc34bcafca9a4f3e5db8c90334b0e05138f40d50dc0064c2bf

Available diffs

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Binary packages built by this source

velvet: Nucleic acid sequence assembler for very short reads

 Velvet is a de novo genomic assembler specially designed for short read
 sequencing technologies, such as Solexa or 454, developed by Daniel Zerbino and
 Ewan Birney at the European Bioinformatics Institute (EMBL-EBI), near
 Cambridge, in the United Kingdom.
 .
 Velvet currently takes in short read sequences, removes errors then produces
 high quality unique contigs. It then uses paired read information, if
 available, to retrieve the repeated areas between contigs.

velvet-dbgsym: debug symbols for velvet
velvet-example: Example data for the Velvet sequence assembler

 Velvet is a de novo genomic assembler specially designed for short read
 sequencing technologies, such as Solexa or 454, developed by Daniel Zerbino and
 Ewan Birney at the European Bioinformatics Institute (EMBL-EBI), near
 Cambridge, in the United Kingdom.
 .
 Velvet currently takes in short read sequences, removes errors then produces
 high quality unique contigs. It then uses paired read information, if
 available, to retrieve the repeated areas between contigs.
 .
 This package contains the example data distributed in the sources of Velvet,
 a de novo genomic assembler.

velvet-long: Nucleic acid sequence assembler for very short reads, long version

 Velvet is a de novo genomic assembler specially designed for short read
 sequencing technologies, such as Solexa or 454, developed by Daniel Zerbino and
 Ewan Birney at the European Bioinformatics Institute (EMBL-EBI), near
 Cambridge, in the United Kingdom.
 .
 Velvet currently takes in short read sequences, removes errors then produces
 high quality unique contigs. It then uses paired read information, if
 available, to retrieve the repeated areas between contigs.
 .
 This package installs special long-mode versions of Velvet, as recommended
 in the Velvet tutorials.

velvet-long-dbgsym: debug symbols for velvet-long
velvet-tests: Test data for the Velvet sequence assembler

 Velvet is a de novo genomic assembler specially designed for short read
 sequencing technologies, such as Solexa or 454, developed by Daniel Zerbino and
 Ewan Birney at the European Bioinformatics Institute (EMBL-EBI), near
 Cambridge, in the United Kingdom.
 .
 Velvet currently takes in short read sequences, removes errors then produces
 high quality unique contigs. It then uses paired read information, if
 available, to retrieve the repeated areas between contigs.
 .
 This package contains the test data to run the unit tests of Velvet, a de novo
 genomic assembler, that could be used as additional set of examples.