Thank you very much!
I used plink to generate MAF statistics but I am not sure about the output format.
The command I used is "plink --bfile <my file=""> --freq case-control --out temp --1".
In the output file "temp.frq.cc", the column names are "CHR, SNP, A1, A2, MAF_A, MAF_U, NCHROBS_A, NCHROBS_U". I am not sure which one is case and which one is control (MAF_A and MAF_U).
Could anyone give some suggestions, please? Thank you very much.
1 answer
https://www.cog-genomics.org/plink2/formats#frq_cc
CHR Chromosome code
SNP Variant identifier
A1 Allele 1 (usually minor)
A2 Allele 2 (usually major)
MAF_A Allele 1 frequency in cases (Affected)
MAF_U Allele 1 frequency in controls (Unaffected)
NCHROBS_A Number of case allele observations
NCHROBS_U Number of control allele observations
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