Facilitating phenotype transfer using a common data model

BACKGROUND: Implementing clinical phenotypes across a network is labor intensive and potentially error prone. Use of a common data model may facilitate the process. METHODS: Electronic Medical Records and Genomics (eMERGE) sites implemented the Observational Health Data Sciences and Informatics (OHD...

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Publicat a:J Biomed Inform
Autors principals: Hripcsak, George, Shang, Ning, Peissig, Peggy L., Rasmussen, Luke V., Liu, Cong, Benoit, Barbara, Carroll, Robert J., Carrell, David S., Denny, Joshua C., Dikilitas, Ozan, Gainer, Vivian S., Howell, Kayla Marie, Klann, Jeffrey G., Kullo, Iftikhar J., Lingren, Todd, Mentch, Frank D., Murphy, Shawn N., Natarajan, Karthik, Pacheco, Jennifer A., Wei, Wei-Qi, Wiley, Ken, Weng, Chunhua
Format: Artigo
Idioma:Inglês
Publicat: 2019
Matèries:
Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6697565/
https://ncbi.nlm.nih.gov/pubmed/31325501
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jbi.2019.103253
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