How to Install and Uninstall vt Package on Ubuntu 20.10 (Groovy Gorilla)
Last updated: December 23,2024
1. Install "vt" package
Please follow the instructions below to install vt on Ubuntu 20.10 (Groovy Gorilla)
$
sudo apt update
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$
sudo apt install
vt
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2. Uninstall "vt" package
This tutorial shows how to uninstall vt on Ubuntu 20.10 (Groovy Gorilla):
$
sudo apt remove
vt
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$
sudo apt autoclean && sudo apt autoremove
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3. Information about the vt package on Ubuntu 20.10 (Groovy Gorilla)
Package: vt
Architecture: amd64
Version: 0.57721+ds-2
Priority: optional
Section: universe/science
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 2561
Depends: libc6 (>= 2.29), libgcc-s1 (>= 3.0), libhts3 (>= 1.10), libpcre2-8-0 (>= 10.22), libstdc++6 (>= 5.2), r-base-core
Filename: pool/universe/v/vt/vt_0.57721+ds-2_amd64.deb
Size: 752792
MD5sum: c52f97008df194d5d55c338910c1d0b2
SHA1: c463e1b28969600c2f58020d17ee32d44cd46b72
SHA256: a388e0cbd9a515a072f284d18be7004d2c64fa912b5b7f35497375234d684787
SHA512: 2fd0ea5a85df7112fe51b6b14967c7694645bdbd68f5c350d9352e23ace1223df649294d864b902262ff447a5e444c6da1058d9d2da0ae0a3b8b7ac3a928f530
Homepage: https://genome.sph.umich.edu/wiki/Vt
Description-en: toolset for short variant discovery in genetic sequence data
vt is a variant tool set that discovers short variants from Next Generation
Sequencing data.
.
Vt-normalize is a tool to normalize representation of genetic variants in
the VCF. Variant normalization is formally defined as the consistent
representation of genetic variants in an unambiguous and concise way. In
vt a simple general algorithm to enforce this is implemented.
Description-md5: 64a323ea15dddc144c1570bf0e8f8f87
Architecture: amd64
Version: 0.57721+ds-2
Priority: optional
Section: universe/science
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 2561
Depends: libc6 (>= 2.29), libgcc-s1 (>= 3.0), libhts3 (>= 1.10), libpcre2-8-0 (>= 10.22), libstdc++6 (>= 5.2), r-base-core
Filename: pool/universe/v/vt/vt_0.57721+ds-2_amd64.deb
Size: 752792
MD5sum: c52f97008df194d5d55c338910c1d0b2
SHA1: c463e1b28969600c2f58020d17ee32d44cd46b72
SHA256: a388e0cbd9a515a072f284d18be7004d2c64fa912b5b7f35497375234d684787
SHA512: 2fd0ea5a85df7112fe51b6b14967c7694645bdbd68f5c350d9352e23ace1223df649294d864b902262ff447a5e444c6da1058d9d2da0ae0a3b8b7ac3a928f530
Homepage: https://genome.sph.umich.edu/wiki/Vt
Description-en: toolset for short variant discovery in genetic sequence data
vt is a variant tool set that discovers short variants from Next Generation
Sequencing data.
.
Vt-normalize is a tool to normalize representation of genetic variants in
the VCF. Variant normalization is formally defined as the consistent
representation of genetic variants in an unambiguous and concise way. In
vt a simple general algorithm to enforce this is implemented.
Description-md5: 64a323ea15dddc144c1570bf0e8f8f87