Hi I have 50 DNA whole genome seq(bam file) that these samples produced separately (until re calibration step) and Then for variant calling using Unified Genotyper ,I produced one vcf file for all of these samples. I want to know is it a true method ? or I should merge all samples together in a bam file from realignment step until end of variant calling step?
Question: I want to know is it a true method ?
9 months ago by
siyavash_damdar • 20
siyavash_damdar • 20 wrote:
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