Ubuntu
brig package

brig 0.95+dfsg-3 source package in Ubuntu

Changelog

brig (0.95+dfsg-3) unstable; urgency=medium

  [ Jelmer Vernooij ]
  * Use secure copyright file specification URI.

  [ Andreas Tille ]
  * Drop blast2 completely from Build-Depends
    Closes: #952624
  * Standards-Version: 4.5.0 (routine-update)
  * debhelper-compat 12 (routine-update)
  * Remove trailing whitespace in debian/copyright (routine-update)
  * Add salsa-ci file (routine-update)
  * Set upstream metadata fields: Archive, Bug-Database, Bug-Submit,
    Repository.

 -- Andreas Tille <email address hidden>  Thu, 27 Feb 2020 15:12:22 +0100

Upload details

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

See full publishing history Publishing

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Downloads

File Size SHA-256 Checksum
brig_0.95+dfsg-3.dsc 2.0 KiB ea81cac410a4d4dec7a1b4bd3025eba5e1cd73d2f8b1cf149e9801b828c9fb43
brig_0.95+dfsg.orig.tar.xz 8.7 MiB 08d1e84d0933ce759d06fab6e7ea476cb44f1ef5953ce1698561778d2dc410d9
brig_0.95+dfsg-3.debian.tar.xz 4.8 KiB eb887be091c19dfe6425231c697d87e44774ed6c6a6405db25f40a00631bab98

Available diffs

No changes file available.

Binary packages built by this source

brig: BLAST Ring Image Generator

 BRIG can display circular comparisons between a large number of genomes,
 with a focus on handling genome assembly data.
  * Images show similarity between a central reference sequence and other
    sequences as concentric rings.
  * BRIG will perform all BLAST comparisons and file parsing automatically
    via a simple GUI.
  * Contig boundaries and read coverage can be displayed for draft genomes;
    customized graphs and annotations can be displayed.
  * Using a user-defined set of genes as input, BRIG can display gene
    presence, absence, truncation or sequence variation in a set of
    complete genomes, draft genomes or even raw, unassembled sequence data.
  * BRIG also accepts SAM-formatted read-mapping files enabling genomic
    regions present in unassembled sequence data from multiple samples to
    be compared simultaneously