Hi Brent, I am using Peddy to get ancestry from VCF files from RNA-seq samples which have 5-15 million uniquely mapped reads, so the quality is not great. My question is, how do I know how many snps were used in the PCA ? This is quite important in my analysis.
Thanks.
Yusuph.
Hi Brent, I am using Peddy to get ancestry from VCF files from RNA-seq samples which have 5-15 million uniquely mapped reads, so the quality is not great. My question is, how do I know how many snps were used in the PCA ? This is quite important in my analysis. Thanks. Yusuph.