if the allele frequencies are already known? I was not able to find the answer. Many thanks in advance.
if the allele frequencies are already known? I was not able to find the answer. Many thanks in advance.
It does, you can read allele frequencies using the --read-freq
flag. This is relevant when computing pair-wise genome-wide IBD on a large dataset and splitting work on mutiple processes using the --genome-lists
flag. Full details on the documentation:
http://pngu.mgh.harvard.edu/~purcell/plink/strat.shtml#cluster
Are you running something like --genome? If you are running on the ped/map type files PLINK should detect the allele frequencies based on your data. If your data isn't representative then the allele frequencies will be skewed anyway.
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