snp-sites 2.4.1-1 source package in Ubuntu

Changelog

snp-sites (2.4.1-1) unstable; urgency=medium

  * New upstream release.

 -- Sascha Steinbiss <email address hidden>  Sat, 06 Oct 2018 17:54:44 +0200

Upload details

Uploaded by:
Debian Med on 2018-10-06
Uploaded to:
Sid
Original maintainer:
Debian Med
Architectures:
any
Section:
misc
Urgency:
Medium Urgency

See full publishing history Publishing

Series Pocket Published Component Section
Eoan release on 2019-04-18 universe misc
Disco release on 2018-11-11 universe misc

Downloads

File Size SHA-256 Checksum
snp-sites_2.4.1-1.dsc 2.2 KiB f385bbab4e149594ccb4e284933973a913034a8240b81535cb34ef168605c784
snp-sites_2.4.1.orig.tar.gz 14.9 MiB 9f37bf30bcbdb52b6c8b201410a9e232b33a105f3197765f51b1b434ae851de3
snp-sites_2.4.1-1.debian.tar.xz 7.7 KiB df96831404dfb899a249be01b35da4ff6dccbf4a8c9803aafbd9acec5b0e9c77

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