snp-sites-dbgsym binary package in Ubuntu Xenial armhf
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).
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The software has been developed at the Wellcome Trust Sanger Institute.
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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.
Publishing history
Date | Status | Target | Component | Section | Priority | Phased updates | Version | ||
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2016-01-30 18:19:05 UTC | Published | Ubuntu Xenial armhf | release | universe | science | Optional | 2.1.3-2 | ||
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Deleted | Ubuntu Xenial armhf | proposed | universe | science | Optional | 2.1.3-2 | |||
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2016-01-30 18:19:21 UTC | Superseded | Ubuntu Xenial armhf | release | universe | science | Optional | 2.1.1-1 | ||
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2016-02-01 00:10:09 UTC | Deleted | Ubuntu Xenial armhf | proposed | universe | science | Optional | 2.1.1-1 | ||
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