driver genes per sample or per group?

Question

[whb]

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?

[rohitsatyam102]

Did you get an answer to your query? I have the same question in mind.