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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Dades bibliogràfiques
Publicat a:J Med Internet Res
Autors principals: Gruendner, Julian, Wolf, Nicolas, Tögel, Lars, Haller, Florian, Prokosch, Hans-Ulrich, Christoph, Jan
Format: Artigo
Idioma:Inglês
Publicat: JMIR Publications 2020
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Original Paper
Accés en línia: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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