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I'm curious about the output from merge multiple samples using svtyper and lmerge. It seems like different from SNP vcf from GATK. How can I understand the REF (N), ALT (<DEL>) and genotype such as 0/0, 0/1. The situations are as follows.
Thanks a lot.
The text was updated successfully, but these errors were encountered:
I'm curious about the output from merge multiple samples using svtyper and lmerge. It seems like different from SNP vcf from GATK. How can I understand the REF (N), ALT (<DEL>) and genotype such as 0/0, 0/1. The situations are as follows.
Thanks a lot.
The text was updated successfully, but these errors were encountered: