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Assessing the capability of massively parallel sequencing for opportunistic pharmacogenetic screening
PURPOSE: To assess exome data for pre-emptive pharmacogenetic screening for 203 clinically-relevant pharmacogenetic variant positions from the Pharmacogenomics Knowledgebase and Clinical Pharmacogenetics Implementation Consortium and identify copy number variants (CNVs) in CYP2D6. METHODS: We examin...
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Publicado no: | Genet Med |
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Main Authors: | , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
2016
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5316383/ https://ncbi.nlm.nih.gov/pubmed/27537706 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2016.105 |
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