snp-sites 1.5.0-1ubuntu1 source package in Ubuntu

Changelog

snp-sites (1.5.0-1ubuntu1) trusty; urgency=low

  * Fix linking order for Ubuntu 14.04, resolving FTBFS.
 -- Daniel T Chen <email address hidden>   Fri, 28 Mar 2014 13:39:28 -0400

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Uploaded by:
Daniel T Chen on 2014-03-28
Uploaded to:
Trusty
Original maintainer:
Ubuntu Developers
Architectures:
any
Section:
misc
Urgency:
Low Urgency

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Series Pocket Published Component Section
Trusty release on 2014-03-28 universe misc

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File Size SHA-256 Checksum
snp-sites_1.5.0.orig.tar.gz 41.0 KiB e2fbd41892f59a2fbd3c6f8152ab1b9b70bab7d899c4da31661362878bb6e21c
snp-sites_1.5.0-1ubuntu1.debian.tar.gz 3.7 KiB 28c187a311c0735203bd120b2acd0d0e967a4c161eeeb1c1d4244582deef04ee
snp-sites_1.5.0-1ubuntu1.dsc 1.9 KiB bbc67a33930128bc25151270a84b7323b084b50e4c9e84cdd75fd213ab3e1a0f

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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-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.