I recently ran MutSigCV on 6 tumor-germline pairs for esophageal adenocarcinoma (EAC), but MutsigCV could not find any significantly mutated genes. For example, TP53 which has previously been implicated in EAC wasn't significantly mutated according to Mutsig, even though TP53 was mutated across all the tumors.
What could probably be causing this? Small sample size? The way the data was filtered before running Mutsig?
I filtered the data as follows :
- Tumor sample minus corresponding Normal sample
- esp, 1000genomes set at 0.01
- var % > 0.2
- exonic, exonic;splicing, splicing
- minimum of 10 reads covering a site in the tumor and normal sample
Please, I really could use someone's help right now.