Package: plink2 (2.00~a5.8-231123+dfsg-1 and others)

[ Source: plink2  ]

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	Version	Package Size	Installed Size	Files
armel	2.00~a5.8-231123+dfsg-1+b2	966.3 kB	2,770.0 kB	[list of files]