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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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| Foilsithe in: | Wiley Interdiscip Rev Syst Biol Med |
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| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
John Wiley & Sons, Inc.
2018
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| Ábhair: | |
| Rochtain Ar Líne: | 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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