snp-sites 2.4.0-1 source package in Ubuntu

Changelog

snp-sites (2.4.0-1) unstable; urgency=medium

  * New upstream version.
  * Adjust watchfile to allow 'v' in version tags.
  * Update upstream metadata (thanks Steffen Moeller).
  * Remove obsolete autotools Build-Depends.
  * Use debhelper 11.
  * Bump Standards-Version.
  * Use secure copyright format URL.

 -- Sascha Steinbiss <email address hidden>  Thu, 14 Jun 2018 17:29:53 +0200

Upload details

Uploaded by:
Debian Med on 2018-06-15
Uploaded to:
Sid
Original maintainer:
Debian Med
Architectures:
any
Section:
misc
Urgency:
Medium Urgency

See full publishing history Publishing

Series Pocket Published Component Section
Cosmic release on 2018-06-15 universe misc

Downloads

File Size SHA-256 Checksum
snp-sites_2.4.0-1.dsc 1.9 KiB dcf2881bd8b2891c3bd74e5c22a9520fbfc24fbd04d34809f0858cc05abb60bb
snp-sites_2.4.0.orig.tar.gz 14.9 MiB 4ccbf6016b37ba1aae67ee8dd265537098eb9a7965186deb0b862efd7c416ae6
snp-sites_2.4.0-1.debian.tar.xz 7.7 KiB e6f14b90fdf47ec63ee6c4d87b4534072fbf5e4e6de62fee48e3a0928255005a

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: debug symbols for libsnp-sites1
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