How to Install and Uninstall plink Package on Ubuntu 21.10 (Impish Indri)

Last updated: November 05,2024

1. Install "plink" package

Please follow the guidance below to install plink on Ubuntu 21.10 (Impish Indri)


    
        
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                sudo apt update
            
                    
    
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                sudo apt install
            
                        
                plink
            
                    
    
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2. Uninstall "plink" package

Please follow the guidance below to uninstall plink on Ubuntu 21.10 (Impish Indri):


    
        
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                sudo apt remove
            
                        
                plink
            
                    
    
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                sudo apt autoclean && sudo apt autoremove
            
                    
    
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3. Information about the plink package on Ubuntu 21.10 (Impish Indri)

Package: plink
Architecture: amd64
Version: 1.07+dfsg-3build1
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: 3317
Depends: libc6 (>= 2.29), libcrypt1 (>= 1:4.1.0), libgcc-s1 (>= 3.0), libstdc++6 (>= 9), zlib1g (>= 1:1.1.4)
Recommends: med-config (>= 2.1)
Filename: pool/universe/p/plink/plink_1.07+dfsg-3build1_amd64.deb
Size: 1155396
MD5sum: 6ce264718f7a0bc962f612cb0d748795
SHA1: 3063885f274d8fa227d446da63114c9ee495ec98
SHA256: 78a0b39f2a677a5a92af1626a86a54fb4128f8ea31b46b9db3b42a4d7247c8ee
SHA512: f0cac85edc901460b4ea05f76951a3a19215b538bb908a3719c842661060e51a8b9f8a4c4194924c52499774f59301aad88f74c5facf48c306f58561d042e5d3
Homepage: http://zzz.bwh.harvard.edu/plink/
Description-en: whole-genome association analysis toolset
plink expects as input the data from SNP (single
nucleotide polymorphism) chips of many individuals
and their phenotypical description of a disease.
It finds associations of single or pairs of DNA
variations with a phenotype and can retrieve
SNP annotation from an online source.
.
SNPs can evaluated individually or as pairs for their
association with the disease phenotypes. The joint
investigation of copy number variations is supported.
A variety of statistical tests have been implemented.
.
Please note: The executable was renamed to plink1
because of a name clash. Please read more about this
in /usr/share/doc/plink/README.Debian.
Description-md5: 0b2b918c34eb1b80efe9854bb4994923