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We conduct mpileup2somatic call variants from 17 sample(the first one is normal sample, the others are somatic samples)
Now, we want to filter the vcf using varscan , but seems the vcf file of multiple samples could not been uesd as input file directly?
The text was updated successfully, but these errors were encountered:
We conduct mpileup2somatic call variants from 17 sample(the first one is normal sample, the others are somatic samples)
Now, we want to filter the vcf using varscan , but seems the vcf file of multiple samples could not been uesd as input file directly?
The text was updated successfully, but these errors were encountered: