vg 1.25.0+ds-2ubuntu1 source package in Ubuntu

Changelog

vg (1.25.0+ds-2ubuntu1) groovy; urgency=medium

  * Fix build by not linking anymore libebl.a

 -- Gianfranco Costamagna <email address hidden>  Tue, 28 Jul 2020 12:11:33 +0200

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Uploaded by:
Gianfranco Costamagna
Uploaded to:
Groovy
Original maintainer:
Debian Med
Architectures:
amd64 i386 arm64 ppc64el s390x riscv64 x32 all
Section:
misc
Urgency:
Medium Urgency

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vg_1.25.0+ds.orig.tar.xz 124.5 MiB 7a97f05a1ecb553dd721dce416b4fcd7efc5d50c6ba3062349bc7707073140ae
vg_1.25.0+ds-2ubuntu1.debian.tar.xz 40.9 KiB ef5c72cfecc692c0ff519539f4e8102c08a381239708853aed7f8f881ada1edf
vg_1.25.0+ds-2ubuntu1.dsc 2.9 KiB 699b697134678467a2bbea4a8e36995ce4b1a0b5f48892f317566c4537db95fc

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Binary packages built by this source

vg: tools for working with genome variation graphs

 variation graph data structures, interchange formats, alignment, genotyping,
 and variant calling methods
 .
 Variation graphs provide a succinct encoding of the sequences of many genomes.
 A variation graph (in particular as implemented in vg) is composed of:
 .
  - nodes, which are labeled by sequences and ids
  - edges, which connect two nodes via either of their respective ends
  - paths, describe genomes, sequence alignments, and annotations (such as gene
   models and transcripts) as walks through nodes connected by edges
 .
 This model is similar to a number of sequence graphs that have been used in
 assembly and multiple sequence alignment. Paths provide coordinate systems
 relative to genomes encoded in the graph, allowing stable mappings to be
 produced even if the structure of the graph is changed.

vg-dbgsym: debug symbols for vg
vg-docs: tools for working with genome variation graphs -- docs

 variation graph data structures, interchange formats, alignment, genotyping,
 and variant calling methods
 .
 Variation graphs provide a succinct encoding of the sequences of many genomes.
 A variation graph (in particular as implemented in vg) is composed of:
 .
  - nodes, which are labeled by sequences and ids
  - edges, which connect two nodes via either of their respective ends
  - paths, describe genomes, sequence alignments, and annotations (such as gene
   models and transcripts) as walks through nodes connected by edges
 .
 This model is similar to a number of sequence graphs that have been used in
 assembly and multiple sequence alignment. Paths provide coordinate systems
 relative to genomes encoded in the graph, allowing stable mappings to be
 produced even if the structure of the graph is changed.
 .
 This package provides the documentation