Hi all,
I'm running VarScan somatic with 2 samples. But the outputs of snp and indel only contain information of chrM, chrX, and chrY. And the log file reports,"Resetting normal file because chrY_random > chrUn_random" .
So, I'm wondering where the problem is. Does VarScan have a preferred choromosome order?
I'm running VarScan somatic with 2 samples. But the outputs of snp and indel only contain information of chrM, chrX, and chrY. And the log file reports,"Resetting normal file because chrY_random > chrUn_random" .
So, I'm wondering where the problem is. Does VarScan have a preferred choromosome order?
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