snp-sites 2.3.3-2 source package in Ubuntu

Changelog

snp-sites (2.3.3-2) unstable; urgency=medium

  * Upload to unstable.

 -- Sascha Steinbiss <email address hidden>  Sun, 18 Jun 2017 17:33:33 +0000

Upload details

Uploaded by:
Debian Med on 2017-06-19
Uploaded to:
Sid
Original maintainer:
Debian Med
Architectures:
any
Section:
misc
Urgency:
Medium Urgency

See full publishing history Publishing

Series Pocket Published Component Section
Bionic release on 2017-10-24 universe misc
Artful release on 2017-06-20 universe misc

Downloads

File Size SHA-256 Checksum
snp-sites_2.3.3-2.dsc 1.9 KiB 74e35a9e32ad7b0b81ab365fa61f2a067e4ebb1d95099d14ecfc662485025789
snp-sites_2.3.3.orig.tar.gz 14.9 MiB 73210a0c1aedee54546dadd0d7e495131c6d01451fc917d98ea122d9786b838f
snp-sites_2.3.3-2.debian.tar.xz 8.4 KiB 6fb1283db2dae1a20d2ebdab52e00dc82858f7e571006da6b95bb14596546e01

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