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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...
Gorde:
| Argitaratua izan da: | Yearb Med Inform |
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| Egile Nagusiak: | , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Schattauer GmbH
2014
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| 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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