How to Install and Uninstall snp-sites Package on Ubuntu 16.04 LTS (Xenial Xerus)
Last updated: January 11,2025
1. Install "snp-sites" package
This is a short guide on how to install snp-sites on Ubuntu 16.04 LTS (Xenial Xerus)
$
sudo apt update
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$
sudo apt install
snp-sites
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2. Uninstall "snp-sites" package
Here is a brief guide to show you how to uninstall snp-sites on Ubuntu 16.04 LTS (Xenial Xerus):
$
sudo apt remove
snp-sites
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$
sudo apt autoclean && sudo apt autoremove
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3. Information about the snp-sites package on Ubuntu 16.04 LTS (Xenial Xerus)
Package: snp-sites
Priority: optional
Section: universe/science
Installed-Size: 29
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Architecture: amd64
Version: 2.1.3-2
Depends: libc6 (>= 2.4), libsnp-sites1
Filename: pool/universe/s/snp-sites/snp-sites_2.1.3-2_amd64.deb
Size: 7012
MD5sum: 9a4b428709e841fe0bb34b083263345b
SHA1: 977d39aa6ef2e28b9efa5e03d20ddc732af4517b
SHA256: 86f7326114911792494515e7c7d5bc5e19f68ac8746889cca3c5c72af68daa6f
Description-en: 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.
Description-md5: 3d6d30c82729352bdf61e8d907df5811
Homepage: https://github.com/sanger-pathogens/snp_sites
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Origin: Ubuntu
Priority: optional
Section: universe/science
Installed-Size: 29
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Architecture: amd64
Version: 2.1.3-2
Depends: libc6 (>= 2.4), libsnp-sites1
Filename: pool/universe/s/snp-sites/snp-sites_2.1.3-2_amd64.deb
Size: 7012
MD5sum: 9a4b428709e841fe0bb34b083263345b
SHA1: 977d39aa6ef2e28b9efa5e03d20ddc732af4517b
SHA256: 86f7326114911792494515e7c7d5bc5e19f68ac8746889cca3c5c72af68daa6f
Description-en: 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.
Description-md5: 3d6d30c82729352bdf61e8d907df5811
Homepage: https://github.com/sanger-pathogens/snp_sites
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Origin: Ubuntu