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Fig. 3 | BMC Bioinformatics

Fig. 3

From: Using variant databases for variant prioritization and to detect erroneous genotype-phenotype associations

Fig. 3

Relation between disease prevalence and proportion of the variant database available for filtering. The proposed mode of inheritance is autosomal recessive, the disease prevalence is expressed as 1/n (with n ranging from 1000 to 100,000). Both the variable quantile-based approach and the static 1%-approach are depicted. By definition, for the absence-approach all variants (100%) are available (not shown)

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