Hi I have 50 whole genome sequence data for SNP discovery. somebody say to me you should use all samples together for realignment and if I do realignment Separately for each sample then my results of SNP discovery will be wrong. I want to know is it true?
Question: can i merge many vcfs or I should do in realignment?
3 months ago by
siyavash_damdar • 20
siyavash_damdar • 20 wrote:
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