How to Install and Uninstall varscan Package on Ubuntu 20.10 (Groovy Gorilla)
Last updated: November 22,2024
1. Install "varscan" package
Please follow the step by step instructions below to install varscan on Ubuntu 20.10 (Groovy Gorilla)
$
sudo apt update
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$
sudo apt install
varscan
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2. Uninstall "varscan" package
Please follow the steps below to uninstall varscan on Ubuntu 20.10 (Groovy Gorilla):
$
sudo apt remove
varscan
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$
sudo apt autoclean && sudo apt autoremove
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3. Information about the varscan package on Ubuntu 20.10 (Groovy Gorilla)
Package: varscan
Architecture: amd64
Version: 2.4.3+dfsg-3
Priority: optional
Section: multiverse/science
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 161
Filename: pool/multiverse/v/varscan/varscan_2.4.3+dfsg-3_amd64.deb
Size: 137764
MD5sum: aad3ae3fec33bc027f1075e125ce1082
SHA1: 15f23f64b88df82fbbb6e176a4481417d083cb86
SHA256: 90a92ffa3a135c953db246918e2e9a6dae9711c66ef99fdbc2d6a7c9b4f94dec
SHA512: 08dfb3b1c89a80c98d3d77fc3f4bf58ff09c90869f196aeb466ba372a72b698208ab7aef35a07cc47349cb718bcae4692e4abae3911ba1a19bee01806fc76bed
Homepage: https://dkoboldt.github.io/varscan/
Description-en: variant detection in next-generation sequencing data
Variant detection in massively parallel sequencing. For one sample,
calls SNPs, indels, and consensus genotypes. For tumor-normal pairs,
further classifies each variant as Germline, Somatic, or LOH, and also
detects somatic copy number changes.
Description-md5: db5aab57fa1c709b6f3f8edc023eda41
Architecture: amd64
Version: 2.4.3+dfsg-3
Priority: optional
Section: multiverse/science
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 161
Filename: pool/multiverse/v/varscan/varscan_2.4.3+dfsg-3_amd64.deb
Size: 137764
MD5sum: aad3ae3fec33bc027f1075e125ce1082
SHA1: 15f23f64b88df82fbbb6e176a4481417d083cb86
SHA256: 90a92ffa3a135c953db246918e2e9a6dae9711c66ef99fdbc2d6a7c9b4f94dec
SHA512: 08dfb3b1c89a80c98d3d77fc3f4bf58ff09c90869f196aeb466ba372a72b698208ab7aef35a07cc47349cb718bcae4692e4abae3911ba1a19bee01806fc76bed
Homepage: https://dkoboldt.github.io/varscan/
Description-en: variant detection in next-generation sequencing data
Variant detection in massively parallel sequencing. For one sample,
calls SNPs, indels, and consensus genotypes. For tumor-normal pairs,
further classifies each variant as Germline, Somatic, or LOH, and also
detects somatic copy number changes.
Description-md5: db5aab57fa1c709b6f3f8edc023eda41