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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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Enregistré dans:
Détails bibliographiques
Publié dans:Per Med
Auteurs principaux: Londin, Eric R, Clark, Peter, Sponziello, Marialuisa, Kricka, Larry J, Fortina, Paolo, Park, Jason Y
Format: Artigo
Langue:Inglês
Publié: 2014
Sujets:
Accès en ligne: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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