morrislab / phylowgs

Application for inferring subclonal composition and evolution from whole-genome sequencing data.
GNU General Public License v3.0
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Which Battenberg output file #114

Closed Rashesh7 closed 5 years ago

Rashesh7 commented 5 years ago

Hi,

I am trying to run phyloWGS on my samples. I have an output from Battenberg using https://github.com/cancerit/cgpBattenberg I was wondering which specific output should I be using as the CNV input? I could not find any description of the outputs.

You help is much appreciated

Thank you.