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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...
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| 主要な著者: | , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2012
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3580414/ https://ncbi.nlm.nih.gov/pubmed/22830651 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gm359 |
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