My gene of interest has counts ranging from 20,000 to over 100,000 reads in my "case" samples, where as the same gene has counts only in the 50-200 reads in my "control" sample. I have 4 biological replicates in each group. The log2 fold change is nearly 4 but the p-value is "NA". I'm guessing that the calculation has reached some sort of a limit in this case but would like to know how to interpret/report this value?
Thanks
Thanks
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