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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Detalles Bibliográficos
Autores principales: Gruendner, Julian, Wolf, Nicolas, Tögel, Lars, Haller, Florian, Prokosch, Hans-Ulrich, Christoph, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JMIR Publications 2020
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7578821/
https://www.ncbi.nlm.nih.gov/pubmed/33026356
http://dx.doi.org/10.2196/19879

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7578821/
https://www.ncbi.nlm.nih.gov/pubmed/33026356
http://dx.doi.org/10.2196/19879

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