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Integrating Genomics and Clinical Data for Statistical Analysis by Using GEnome MINIng (GEMINI) and Fast Healthcare Interoperability Resources (FHIR): System Design and Implementation

BACKGROUND: The introduction of next-generation sequencing (NGS) into molecular cancer diagnostics has led to an increase in the data available for the identification and evaluation of driver mutations and for defining personalized cancer treatment regimens. The meaningful combination of omics data,...

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Detalhes bibliográficos
Publicado no:J Med Internet Res
Main Authors: Gruendner, Julian, Wolf, Nicolas, Tögel, Lars, Haller, Florian, Prokosch, Hans-Ulrich, Christoph, Jan
Formato: Artigo
Idioma:Inglês
Publicado em: JMIR Publications 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7578821/
https://ncbi.nlm.nih.gov/pubmed/33026356
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2196/19879
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