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Tools for Predicting the Functional Impact of Nonsynonymous Genetic Variation

As personal genome sequencing becomes a reality, understanding the effects of genetic variants on phenotype—particularly the impact of germline variants on disease risk and the impact of somatic variants on cancer development and treatment—continues to increase in importance. Because of their clear...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Genetics
Päätekijät: Tang, Haiming, Thomas, Paul D.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Genetics Society of America 2016
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4896183/
https://ncbi.nlm.nih.gov/pubmed/27270698
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.116.190033
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