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
See full publishing history Publishing
Series | Published | Component | Section |
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Downloads
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
No changes file available.
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.