primer3 2.4.0-2 source package in Ubuntu

Changelog

primer3 (2.4.0-2) unstable; urgency=medium

  [ Liubov Chuprikova ]
  * Team upload.
  * Skip tests that fail on big endian
    Closes: #890993
  * Added d/README.source with explanation why some tests are skipped
  * debian/patches/p3test_fix_exit_status.patch: Fix test to show correct exit
    status

  [ Andreas Tille ]
  * Point Vcs fields to salsa.debian.org
  * Standards-Version: 4.1.4

 -- Liubov Chuprikova <email address hidden>  Mon, 28 May 2018 13:44:30 +0000

Upload details

Uploaded by:
Debian Med on 2018-05-29
Uploaded to:
Sid
Original maintainer:
Debian Med
Architectures:
any all
Section:
science
Urgency:
Medium Urgency

See full publishing history Publishing

Series Pocket Published Component Section
Focal release on 2019-10-18 universe science
Eoan release on 2019-04-18 universe science
Disco release on 2018-10-30 universe science
Cosmic release on 2018-08-26 universe science

Downloads

File Size SHA-256 Checksum
primer3_2.4.0-2.dsc 2.1 KiB 541ec07c9092995dd359620326630c45135321868ee2c2350ef61e1d4d67628d
primer3_2.4.0.orig.tar.gz 30.3 MiB 6d537640c86e2b4656ae77f75b6ad4478fd0ca43985a56cce531fb9fc0431c47
primer3_2.4.0-2.debian.tar.xz 11.8 KiB 96247e4223393e0056a8886209b1bb37abfa7dc7fb00eca4e3e695daf62dd71e

No changes file available.

Binary packages built by this source

primer3: tool to design flanking oligo nucleotides for DNA amplification

 Primer3 picks primers for Polymerase Chain Reactions (PCRs), considering as
 criteria oligonucleotide melting temperature, size, GC content and
 primer-dimer possibilities, PCR product size, positional constraints within
 the source sequence, and miscellaneous other constraints. All of these
 criteria are user-specifiable as constraints, and some are specifiable as
 terms in an objective function that characterizes an optimal primer pair.

primer3-dbgsym: debug symbols for primer3
primer3-examples: tool to design flanking oligo nucleotides for DNA amplification (examples)

 Primer3 picks primers for Polymerase Chain Reactions (PCRs), considering as
 criteria oligonucleotide melting temperature, size, GC content and
 primer-dimer possibilities, PCR product size, positional constraints within
 the source sequence, and miscellaneous other constraints. All of these
 criteria are user-specifiable as constraints, and some are specifiable as
 terms in an objective function that characterizes an optimal primer pair.
 .
 This package contains example data to test the package.