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Identifying disease mutations in genomic medicine settings: current challenges and how to accelerate progress
The pace of exome and genome sequencing is accelerating, with the identification of many new disease-causing mutations in research settings, and it is likely that whole exome or genome sequencing could have a major impact in the clinical arena in the relatively near future. However, the human genomi...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2012
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580414/ https://www.ncbi.nlm.nih.gov/pubmed/22830651 http://dx.doi.org/10.1186/gm359 |