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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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Bibliographische Detailangaben
Veröffentlicht in:Wiley Interdiscip Rev Syst Biol Med
Hauptverfasser: Capriotti, Emidio, Ozturk, Kivilcim, Carter, Hannah
Format: Artigo
Sprache:Inglês
Veröffentlicht: John Wiley & Sons, Inc. 2018
Schlagworte:
Online Zugang: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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