Assessing enrichment
Working on a set of RNA-seq of AML patient samples, I stumble on gene X. When its expression is high, 50% of the samples are mutated on gene Y, a mutation that has a prevalence of only 20% in the rest of the dataset. Is there a link between these two observations? Let's put some numbers on this: among the 131 samples of the dataset, 28 show mutations on gene Y, 6 have high expression of X and 3 have both "features". The table below is [...]