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EHR Big Data Deep Phenotyping: Contribution of the IMIA Genomic Medicine Working Group

OBJECTIVES: Given the quickening speed of discovery of variant disease drivers from combined patient genotype and phenotype data, the objective is to provide methodology using big data technology to support the definition of deep phenotypes in medical records. METHODS: As the vast stores of genomic...

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Bibliografiske detaljer
Udgivet i:Yearb Med Inform
Main Authors: Frey, L. J., Lenert, L., Lopez-Campos, G.
Format: Artigo
Sprog:Inglês
Udgivet: Schattauer GmbH 2014
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4287080/
https://ncbi.nlm.nih.gov/pubmed/25123744
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15265/IY-2014-0006
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