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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Detalles Bibliográficos
Autores principales: Bendl, Jaroslav, Musil, Miloš, Štourač, Jan, Zendulka, Jaroslav, Damborský, Jiří, Brezovský, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4880439/
https://www.ncbi.nlm.nih.gov/pubmed/27224906
http://dx.doi.org/10.1371/journal.pcbi.1004962

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4880439/
https://www.ncbi.nlm.nih.gov/pubmed/27224906
http://dx.doi.org/10.1371/journal.pcbi.1004962

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