A review study: Computational techniques for expecting the impact of non-synonymous single nucleotide variants in human diseases

Author:

Hassan Marwa S.,Shaalan A.A.,Dessouky M.I.,Abdelnaiem Abdelaziz E.,ElHefnawi Mahmoud

Funder

National Research Center in Egypt

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference98 articles.

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2. A method and server for predicting damaging missense mutations;Adzhubei;Nat. Methods,2010

3. Predicting the functional effect of human missense mutations using PolyPhen-2;Adzhubei;Curr. Protoc. Hum. Genet.,2013

4. PredictSNP: robust and accurate consensus classifier for prediction of disease-related mutations;Bendle;PLoS Comput. Biol.,2014

5. PredictSNP2: a unified platform for accurately evaluating SNP effects by exploiting the different characteristics of variants in distinct genomic regions;Bendle;PLoS Comput. Biol.,2016

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