How to Install and Uninstall plink2 Package on Ubuntu 21.10 (Impish Indri)

Last updated: November 26,2024

1. Install "plink2" package

This is a short guide on how to install plink2 on Ubuntu 21.10 (Impish Indri)


    
        
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                sudo apt update
            
                    
    
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            $
        

        
            
                sudo apt install
            
                        
                plink2
            
                    
    
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2. Uninstall "plink2" package

Please follow the instructions below to uninstall plink2 on Ubuntu 21.10 (Impish Indri):


    
        
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                sudo apt remove
            
                        
                plink2
            
                    
    
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                sudo apt autoclean && sudo apt autoremove
            
                    
    
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3. Information about the plink2 package on Ubuntu 21.10 (Impish Indri)

Package: plink2
Architecture: amd64
Version: 2.00~a3-210203+dfsg-1
Built-Using: simde (= 0.7.2-3)
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: 14257
Depends: libblas3 | libblas.so.3, libc6 (>= 2.29), libdeflate0 (>= 1.0), liblapack3 | liblapack.so.3, libzstd1 (>= 1.4.4), zlib1g (>= 1:1.1.4)
Filename: pool/universe/p/plink2/plink2_2.00~a3-210203+dfsg-1_amd64.deb
Size: 1815372
MD5sum: 6a0f62819f27ad2005c405bec06ce8c2
SHA1: f3041dc8e67ac61fbef717a7cf67b4e32b195b78
SHA256: be8491933e401054100d941227294ca4b400bba117b0ba2cb6f46fbd71d2281b
SHA512: 582722ead394b6a54111aa86d3f38a9eaa5b4ce46f7383c3654f082f587c1628dcd91eb473eb82d87c4235bad43c377d312f863ee601ae582060dfb0ebea14a5
Homepage: https://www.cog-genomics.org/plink/2.0/
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.
.
plink2 is a comprehensive update of plink and plink1.9 with new algorithms
and new methods, faster and less memory consumer than the first plink.
Description-md5: 8bf29787d12baeabb31572ed571bfb04