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On the future of genetic risk assessment
Next-generation sequencing (NGS) techniques have greatly accelerated the molecular elucidation of Mendelian disorders, and affordable NGS-based diagnostic tests are around the corner that promise to detect or rule out mutations in specific subsets of the known disease genes. Whole exome sequencing a...
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| Format: | Artigo |
| Jezik: | Inglês |
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Springer-Verlag
2012
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| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3419289/ https://ncbi.nlm.nih.gov/pubmed/22467181 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12687-012-0092-2 |
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