Hello everyone,
I have a quick question and I could not have the answer from the help of varscan.
I need to know if it is possible to get all the positions of a genome in the output
of varscan, not only which have snp/indel but everything.
I tried to change the value of option --variants 1 but it does not change anything.
Any solution(s) ?
Thanks in advance,
I have a quick question and I could not have the answer from the help of varscan.
I need to know if it is possible to get all the positions of a genome in the output
of varscan, not only which have snp/indel but everything.
I tried to change the value of option --variants 1 but it does not change anything.
Any solution(s) ?
Thanks in advance,
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