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5.3 years ago
otokha
•
0
I have three affected and one unaffected VCF and annotated files from exome analysis. I want to compare the variants present in the affecteds and absent in unaffected data.
How can I pull out the variants unique to affected individuals from all the four files?
Kindly help.
Thanks for the help. GT[1] == "AA" represents the missing variants among the affecteds data, is it?
AA = "alt+alt" homozygous for the alternative allele(s)
Thanks for timely help.
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