snp-sites 2.5.1-2 source package in Ubuntu

Changelog

snp-sites (2.5.1-2) unstable; urgency=medium

  * Fix watch file
  * Standards-Version: 4.6.0 (routine-update)
  * debhelper-compat 13 (routine-update)
  * Remove trailing whitespace in debian/changelog (routine-update)
  * Add salsa-ci file (routine-update)
  * Rules-Requires-Root: no (routine-update)
  * No tab in license text (routine-update)
  * Trim trailing whitespace.
  * Set upstream metadata fields: Bug-Database, Bug-Submit.
  * Apply multi-arch hints.
    + libsnp-sites1, libsnp-sites1-dev: Add Multi-Arch: same.
  * Remove *.la file which should not be installed

 -- Andreas Tille <email address hidden>  Fri, 01 Oct 2021 16:16:44 +0200

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

Series Pocket Published Component Section
Noble release universe misc
Mantic release universe misc
Lunar release universe misc
Jammy release universe misc

Downloads

File Size SHA-256 Checksum
snp-sites_2.5.1-2.dsc 2.2 KiB 19c276124488230054868878b8a089518b3ed9fe287b9ac3a4c1ece65b48065a
snp-sites_2.5.1.orig.tar.gz 14.9 MiB 913f79302e5d3127aea382756abc9ffeb05e26ce00022f43a6ea16a55cdd7a7e
snp-sites_2.5.1-2.debian.tar.xz 8.1 KiB 711f075ad6b75b0ab8a61398a86f493cd3aa2c7391d8235d99b43d886a998e61

Available diffs

No changes file available.

Binary packages built by this source

libsnp-sites1: Shared libraries of the package snp-sites

 Snp-sites finds single nucleotide polymorphism (SNP) sites from
 multi-fasta alignment input files (which might be compressed). Its
 output can be in various widely used formats (Multi Fasta Alignment,
 Vcf, phylip).
 .
 The software has been developed at the Wellcome Trust Sanger Institute.
 .
 This package contains the dynamic library uses by snp-sites.

libsnp-sites1-dbgsym: No summary available for libsnp-sites1-dbgsym in ubuntu kinetic.

No description available for libsnp-sites1-dbgsym in ubuntu kinetic.

libsnp-sites1-dev: Static libraries and header files for the package snp-sites

 Snp-sites finds single nucleotide polymorphism (SNP) sites from
 multi-fasta alignment input files (which might be compressed). Its
 output can be in various widely used formats (Multi Fasta Alignment,
 Vcf, phylip).
 .
 The software has been developed at the Wellcome Trust Sanger Institute.
 .
 This package contains the development files to include snp-sites
 into your own code. The library enables Python developers to make
 snp-sites function calls (Python bindings) through the Boost Python
 Library.

snp-sites: Binary code for the package snp-sites

 This program finds single nucleotide polymorphism (SNP) sites from
 multi-fasta alignment input files (which might be compressed). Its
 output can be in various widely used formats (Multi Fasta Alignment,
 Vcf, phylip).
 .
 The software has been developed at the Wellcome Trust Sanger Institute.
 .
 A Single Nucleotide - polymorphism (SNP, pronounced snip; plural snips)
 is a DNA sequence variation occurring when a Single Nucleotide — A, T, C
 or G — in the genome (or other shared sequence) differs between members
 of a biological species or paired chromosomes. For example, two
 sequenced DNA fragments from different individuals, AAGCCTA to AAGCTTA,
 contain a difference in a single nucleotide. In this case there are two
 alleles. Almost all common SNPs have only two alleles.

snp-sites-dbgsym: debug symbols for snp-sites