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snp-sites

Binary code for the package snp-sites

Binary code for the package snp-sites
from version 1.5.0-1ubuntu1

Description

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.

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Homepage

https://github.com/sanger-pathogens/snp-sites


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894 other people were interested in this package here. The newest known version of this software is 2.4.1-1 (Information last updated about 18 hours ago.)