fig5
![CCEPAS: the creation and validation of a fast and sensitive clinical whole exome analysis pipeline based on gene and variant ranking](https://image.oaes.cc/b65a3519-5c16-4399-8fa3-f36e32caa9e3/2378.fig.5.png)
Figure 5. Identification of causative gene variants by Pheno2Gene in conjunction with VarEval in100 clinical exome cases. Importantly, the causative variants were found in the top 20 for autosomal dominant, autosomal recessive and X-linked disorders for 100% of the cases. Moreover, for singleton cases all causative variants were in the top 50 variants for 100% of cases