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Package: plink2 (2.00~a3-220218+dfsg-1)

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.

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Download plink2

Download for all available architectures
Architecture Package Size Installed Size Files
amd64 2,108.2 kB13059 kB [list of files]
arm64 921.5 kB1956 kB [list of files]
armhf 884.3 kB1690 kB [list of files]
ppc64el 1,056.9 kB2448 kB [list of files]