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Fig. 2 | BMC Genomics

Fig. 2

From: Development of pathogenicity predictors specific for variants that do not comply with clinical guidelines for the use of computational evidence

Fig. 2

Success rate of predictions obtained following the coincidence rule. In the coincidence rule (see main text) computational information is accepted as supporting evidence in clinical settings only when the pathogenicity predictions of different methods agree. Here we describe how the success rate of this rule depends on the chosen in silico predictors. a Violin plots for the Matthews Correlation Coefficients (MCC) grouped by method. Each violin plot corresponds to all possible combinations of reference predictors that include the method shown at the bottom. For example, the first plot to the left represents all combinations of five reference predictors (SIFT, PolyPhen-2, PON-P2, CADD and MutationTaster2) that include MutationTaster2. The thick lines at the bottom of each violin plot represent the individual performance of the reference predictors. b Dependence of MCC values on the number of predictors used to implement the coincidence rule

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