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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Shranjeno v:
Bibliografske podrobnosti
izdano v:J Med Internet Res
Main Authors: Gruendner, Julian, Wolf, Nicolas, Tögel, Lars, Haller, Florian, Prokosch, Hans-Ulrich, Christoph, Jan
Format: Artigo
Jezik:Inglês
Izdano: JMIR Publications 2020
Teme:
Original Paper
Online dostop: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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