Insight into Neutral and Disease-Associated Human Genetic Variants through Interpretable Predictors

A variety of methods that predict human nonsynonymous single nucleotide polymorphisms (SNPs) to be neutral or disease-associated have been developed over the last decade. These methods are used for pinpointing disease-associated variants in the many variants obtained with next-generation sequencing...

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Detalles Bibliográficos
Autores principales: van den Berg, Bastiaan A., Reinders, Marcel J. T., de Ridder, Dick, de Beer, Tjaart A. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380319/
https://www.ncbi.nlm.nih.gov/pubmed/25826299
http://dx.doi.org/10.1371/journal.pone.0120729

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380319/
https://www.ncbi.nlm.nih.gov/pubmed/25826299
http://dx.doi.org/10.1371/journal.pone.0120729

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