Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencing
Author(s) -
Adam Nishimura,
Brian H. Shirts,
Michael O. Dorschner,
Laura M. Amendola,
Joe W. Smith,
Gail P. Jarvik,
Peter TarczyHornoch
Publication year - 2015
Publication title -
genetics in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.509
H-Index - 128
eISSN - 1530-0366
pISSN - 1098-3600
DOI - 10.1038/gim.2015.5
Subject(s) - pharmacogenomics , clinical decision support system , exome sequencing , exome , workflow , decision support system , medicine , pipeline (software) , medical emergency , data science , computer science , data mining , database , genetics , biology , gene , pharmacology , mutation , programming language
Electronic health records (EHRs) and their associated decision support tools are potentially important means of disseminating a patient's pharmacogenomic profile to his or her health-care providers. We sought to create a proof-of-concept decision support alert system generated from pharmacogenomic incidental findings from exome sequencing.
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