Integrating Genomics and Clinical Data for Statistical Analysis by Using GEnome MINIng (GEMINI) and Fast Healthcare Interoperability Resources (FHIR): System Design and Implementation
BackgroundThe 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, i...
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Main Authors: | Gruendner, Julian (Author), Wolf, Nicolas (Author), Tögel, Lars (Author), Haller, Florian (Author), Prokosch, Hans-Ulrich (Author), Christoph, Jan (Author) |
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Format: | Book |
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JMIR Publications,
2020-10-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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