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

PLoS computational biology - 1 May 2016

Bendl Jaroslav, Musil Miloš, Štourač Jan, Zendulka Jaroslav, Damborský Jiří, Brezovský Jan

Abstract excerpt

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 causal variants plays a key role in providing accurate personalized diagnosis, prognosis, and treatment of inherited...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 27224906
DOI: 10.1371/journal.pcbi.1004962
PMCID: PMC4880439

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