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Fig. 4 | Human Genomics

Fig. 4

From: A pipeline combining multiple strategies for prioritizing heterozygous variants for the identification of candidate genes in exome datasets

Fig. 4

Benchmarking analyses combining prioritizing strategies. Bar charts show the percentage of shared variants for hearing loss (a) and CNM (b), ranked by PAVAR + VAAST (purple), Exomiser v2 + (VAAST-Phevor) (yellow), the three systems (green) the three systems and CADD (red), and the three systems and FATHMM (blue) among the top 10, 20, or 50, after filtering by different control datasets. F = family controls exome dataset, T-F = in-house control data exome dataset without family control dataset, and T = in-house and family control datasets

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Human Genomics

ISSN: 1479-7364