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[ 原始碼: plink2  ]

套件: plink2 (2.00~a3-200217+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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下載 plink2

下載可用於所有硬體架構的
硬體架構 套件大小 安裝後大小 檔案
amd64 834.2 kB2255 kB [文件列表]