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
- Uploaded to:
- Sid
- Original maintainer:
- Debian Med
- Architectures:
- any
- Section:
- misc
- Urgency:
- Medium Urgency
See full publishing history Publishing
| Series | Published | Component | Section |
|---|
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
- diff from 2.4.0-1 to 2.4.1-1 (1.2 KiB)
No changes file available.
Binary packages built by this source
- libsnp-sites1: No summary available for libsnp-sites1 in ubuntu disco.
No description available for libsnp-sites1 in ubuntu disco.
- libsnp-sites1-dbgsym: No summary available for libsnp-sites1-dbgsym in ubuntu disco.
No description available for libsnp-
sites1- dbgsym in ubuntu disco.
- 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
