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PredictSNP2: A Unified Platform for Accurately Evaluating SNP Effects by Exploiting the Different Characteristics of Variants in Distinct Genomic Regions

An important message taken from human genome sequencing projects is that the human population exhibits approximately 99.9% genetic similarity. Variations in the remaining parts of the genome determine our identity, trace our history and reveal our heritage. The precise delineation of phenotypically...

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Detalhes bibliográficos
Publicado no:PLoS Comput Biol
Main Authors: Bendl, Jaroslav, Musil, Miloš, Štourač, Jan, Zendulka, Jaroslav, Damborský, Jiří, Brezovský, Jan
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4880439/
https://ncbi.nlm.nih.gov/pubmed/27224906
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pcbi.1004962
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