Figure 5
From: MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing
Confident hypotheses of the underlying splicing mechanism disrupted for predicted exonic SAVs in Inherited disease and somatic variants in Cancer. Significant enrichment (+) or depletion (-) for a specific hypothesis is shown for the Cancer versus Inherited disease datasets (Fisher’s exact test with a Bonferroni-corrected threshold of P < 0.05).
