I am going through my list of significantly mutated genes as determined by 'genome music smg' and am puzzled by the fact that many of the genes in this list carry a single mutation in a single patient and yet have assigned a highly significant p-value. How is this explained? Isn't it a neccessity that a gene is mutated multiple times (either within one patient or between patients) such that a p-value can be meaningfully computed?
Here is one example of such a gene, taken from the output of the smg analysis:
#Gene Indels SNVs Tot Muts Covd Bps Muts pMbp P-value FCPT P-value LRT P-value CT FDR FCPT FDR LRT FDR CT
LMOD1 0 1 1 55 18181.82 0.000661479 4.91E-07 4.86E-11 0.487266065 0.000280645 1.24E-07
This is correct. Christian, in your example, notice how LMOD1 only has 55 covered bps across all your samples. You might want to loosen the minimum tumor/normal read depths, in the calc-covg step before running calc-bmr and subsequently the SMG test.