snp-sites 2.1.1-1 source package in Ubuntu

Changelog

snp-sites (2.1.1-1) unstable; urgency=medium

  * New upstream release

 -- Sascha Steinbiss <email address hidden>  Tue, 15 Dec 2015 22:21:56 +0000

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Uploaded by:
Debian Med
Uploaded to:
Sid
Original maintainer:
Debian Med
Architectures:
any
Section:
misc
Urgency:
Medium Urgency

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snp-sites_2.1.1-1.dsc 2.2 KiB 520ba61946aed60296bc8f51886926fa8651d968a76ccb9e72e0c254025c1810
snp-sites_2.1.1.orig.tar.gz 41.9 KiB a316e413a3033ff5570d9f44cbd46c812163929a51b118713c8a4184f14a184d
snp-sites_2.1.1-1.debian.tar.xz 7.6 KiB c839e31c87b16b61d8b935a77d7a6cd6ead36c96c551a0f522fd3c5d475c6dbb

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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-dbgsym: debug symbols for package libsnp-sites1

 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.

snp-sites-dbgsym: debug symbols for 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.