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I find set of SNPs that in 4 different population have same minor allele frequency and also same alleles. but I find that most of my alternative alleles are the alleles with major frequency! how can I genetically explain it?
Yes, it is for human genome. I find alternative allele for my data according to reference allele and I expect most of alternative alleles be minor allele but they are major allele?
In human genomes you would just be looking at heterozygous or homozygous SNPs, not major/minor. If you alternate allele is 0.9-1.0 in frequency, I would call this as a homozygous SNP. If it is 0.35-0.65, I would call it a heterozygous SNP.
This is assuming each of your datasets represents one individuals sequencing, rather then populations as you previously mentioned.