Closed Rashesh7 closed 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.
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.