Thank you, I saw the suggestions But I think that my problem is a little different. In that suggestion he wants to remove the SNP that are common in all 32 samples, I'm interested to remove the SNPs that are present in at least 2 of my 5 samples, for example
A B C
1 2 1
2 3 3
5 5 5
7 8 9
99 99 99
where A, B and C are three different VCF files and I'd like to obtain 7, 8 e 9.
Any suggestion?