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. 2014 Jan 13;15(1):R19. doi: 10.1186/gb-2014-15-1-r19

Figure 5.

Figure 5

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).