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Integrating molecular networks with genetic variant interpretation for precision medicine

More reliable and cheaper sequencing technologies have revealed the vast mutational landscapes characteristic of many phenotypes. The analysis of such genetic variants has led to successful identification of altered proteins underlying many Mendelian disorders. Nevertheless the simple one‐variant on...

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Détails bibliographiques
Publié dans:Wiley Interdiscip Rev Syst Biol Med
Auteurs principaux: Capriotti, Emidio, Ozturk, Kivilcim, Carter, Hannah
Format: Artigo
Langue:Inglês
Publié: John Wiley & Sons, Inc. 2018
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6450710/
https://ncbi.nlm.nih.gov/pubmed/30548534
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/wsbm.1443
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