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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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| Publicado en: | Curr Opin Syst Biol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2018
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| Assuntos: | |
| Acceso en liña: | 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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