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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Yearb Med Inform
Egile Nagusiak: Frey, L. J., Lenert, L., Lopez-Campos, G.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Schattauer GmbH 2014
Gaiak:
Sarrera elektronikoa: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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