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Extracting Complementary Insights from Molecular Phenotypes for Prioritization of Disease-Associated Mutations

Rapid advances in next-generation sequencing technology have resulted in an explosion of whole-exome/genome sequencing data, providing an unprecedented opportunity to identify disease- and trait-associated variants in humans on a large scale. To date, the long-standing paradigm has leveraged fitness...

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Detalhes bibliográficos
Publicado no:Curr Opin Syst Biol
Main Authors: Wierbowski, Shayne D., Fragoza, Robert, Liang, Siqi, Yu, Haiyuan
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6510504/
https://ncbi.nlm.nih.gov/pubmed/31086831
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.coisb.2018.09.006
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