ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants
Author:
Funder
Genome Canada
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference38 articles.
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3. REVEL: an ensemble method for predicting the pathogenicity of rare missense variants;Ioannidis;Am. J. Hum. Genet.,2016
4. Improving the assessment of the outcome of nonsynonymous SNVs with a consensus deleteriousness score, Condel;González-Pérez;Am. J. Hum. Genet.,2011
5. dbNSFP: a lightweight database of human nonsynonymous SNPs and their functional predictions;Liu;Hum. Mutat.,2011
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