update plink
This page describes specialized PLINK input and output file formats which are ... Variant identifier; Expected allele #1 (from --update-alleles input file); Expected ... ,We have designed this to match PLINK 1.07's order of operations (mostly ... by ID (--snps, --exclude-snps); Update variant information (--cm-map, --update-cm, ...
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 update plink 相關參考資料
Data management - PLINK 1.9 - cog-genomics.org
--update-alleles updates variant allele codes. Its input should have the following five fields: Variant ID; One of the old allele codes; The other old allele code; New ... https://www.cog-genomics.org File format reference - PLINK 1.9 - cog-genomics.org
This page describes specialized PLINK input and output file formats which are ... Variant identifier; Expected allele #1 (from --update-alleles input file); Expected ... https://www.cog-genomics.org Order of operations - PLINK 1.9 - cog-genomics.org
We have designed this to match PLINK 1.07's order of operations (mostly ... by ID (--snps, --exclude-snps); Update variant information (--cm-map, --update-cm, ... https://www.cog-genomics.org plink --file data - PLINK: Whole genome data analysis toolset
./plink --bfile mydata --update-map chr-codes.txt --update-chr --make-bed --out mydata2. In both case, the format of the input file should be two ... https://zzz.bwh.harvard.edu PLINK 1.90 beta - cog-genomics.org
This is a comprehensive update to Shaun Purcell's PLINK command-line program, developed by Christopher Chang with support from the NIH-NIDDK's ... https://www.cog-genomics.org PLINK 2.00 alpha - cog-genomics.org
--update-map... --update-ids... --ref-allele · --ref-from-fa · --normalize · --indiv-sort · --write-covar · --variance-standardize · --quantile-normalize &mid... https://www.cog-genomics.org plink合并文件并更新SNP位置（merge file, update SNP position ...
如果是二进制文件和ped,map格式文件，则用以下命令： ? 1. plink --bfile data1 --merge data2.ped data2. https://www.cnblogs.com Standard data input - PLINK 2.0 - cog-genomics.org
--update-alleles updates variant allele codes. Its input should have the following five fields: Variant ID; One of the old allele codes; The other old allele code; New ... https://www.cog-genomics.org |