Predicting functional effect of missense variants using graph attention neural networks | bioRxiv
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ROC analysis of the CADD, FATHMM, M-CAP, Polyphen and SIFT prediction... | Download Scientific Diagram
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MISTIC: A prediction tool to reveal disease-relevant deleterious missense variants | PLOS ONE
Predicting deleterious missense genetic variants via integrative supervised nonnegative matrix tri-factorization | Scientific Reports
![PDF] Improved pathogenicity prediction for rare human missense variants | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/5533674ee39dafedbae3c4186f012dcca0a5d3e1/10-Figure5-1.png "PDF] Improved pathogenicity prediction for rare human missense variants | Semantic Scholar")
PDF] Improved pathogenicity prediction for rare human missense variants | Semantic Scholar
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MVP: predicting pathogenicity of missense variants by deep learning | bioRxiv
Distribution of predicted scores of de novo missense variants by MVP... | Download Scientific Diagram
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ROC analysis of the CADD, FATHMM, M-CAP, Polyphen and SIFT prediction... | Download Scientific Diagram
mvPPT: A highly efficient and sensitive pathogenicity prediction tool for missense variants - ScienceDirect
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MetaRNN: Differentiating Rare Pathogenic and Rare Benign Missense SNVs and InDels Using Deep Learning | bioRxiv
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MVP predicts the pathogenicity of missense variants by deep learning | Nature Communications
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The performance comparison of KGGSeq's pathogenic prediction with REVEL... | Download Scientific Diagram
Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions | Genetics in Medicine
Genome interpretation using in silico predictors of variant impact | SpringerLink
ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants. | Semantic Scholar
Predicting deleterious missense genetic variants via integrative supervised nonnegative matrix tri-factorization | Scientific Reports
ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants. | Semantic Scholar
