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Dealing with the input of multiple samples #126

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b-niu opened this issue Jul 22, 2020 · 0 comments

b-niu commented Jul 22, 2020

Dear author, I'd like to ask about:

For example, if a mutation EGFR.p.L858R is in the VCFs of sample NO. 1 and 2 of a patient, but not sample NO.3. Should we leave it blank in the ssm_data.txt of sample 3?
phylowgs can handle indels, is it right?.

Thanks a lot.

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