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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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書誌詳細
出版年:PLoS Comput Biol
主要な著者: Bendl, Jaroslav, Musil, Miloš, Štourač, Jan, Zendulka, Jaroslav, Damborský, Jiří, Brezovský, Jan
フォーマット: Artigo
言語:Inglês
出版事項: Public Library of Science 2016
主題:
オンライン・アクセス: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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