Entering edit mode
2.7 years ago
whb
▴
50
When using driver genes prediction tools such as ONCOCLUST in maftools or dNdScv, should we input the variants of per samples? or per group (same treatment/disease)?
Both tutorials use input that were from multiple subjects. Is driver genes are usually described as per group/population instead of subject/sample?
Did you get an answer to your query? I have the same question in mind.