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Performance of exome sequencing for pharmacogenomics
AIM: We present the potential false-negative rate of exome sequencing for the detection of pharmacogenomic variants. MATERIALS & METHODS: Depth of coverage of 1928 pharmacogenomically relevant variant positions was ascertained from 62 exome-sequenced samples. RESULTS: Approximately 14% of the 19...
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| Publicat a: | Per Med |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4526024/ https://ncbi.nlm.nih.gov/pubmed/26257813 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2217/PME.14.77 |
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