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hello,
My shell is
plink --vcf GWAS.23chr.vcf \ --a2-allele GWAS.23chr.vcf.ref \ --keep-allele-order \ --double-id \ --set-missing-var-ids @:# \ --allow-no-sex \ --update-sex pheno.gender.txt 3 \ --pheno pheno.gender.txt --mpheno 4 \ --recode \ --make-bed \ --out vcf2plink && \ plink --file vcf2plink --maf 0.05 --geno 0.1 --hwe 0.000005 --mind 0.2 --make-bed --recode --out plink.filter &&\ plink --bfile plink.filter --assoc --out plink_asso --allow-no-sex
The pheno.gender.txt file contains gender information, how dose PLINK consider male and female samples for chromosome X results?
thank you best
The text was updated successfully, but these errors were encountered:
--assoc is based on allele counts. Males have only 1 allele per variant on chrX, while females have 2.
Sorry, something went wrong.
so we calculate the number of allele1 in the case cohort like this: female het_mut * 1 + female hom_mut * 2 + male mut * 1 is it right?
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hello,
My shell is
The pheno.gender.txt file contains gender information, how dose PLINK consider male and female samples for chromosome X results?
thank you
best
The text was updated successfully, but these errors were encountered: