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,...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Med Internet Res
Egile Nagusiak: Gruendner, Julian, Wolf, Nicolas, Tögel, Lars, Haller, Florian, Prokosch, Hans-Ulrich, Christoph, Jan
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: JMIR Publications 2020
Gaiak:
Original Paper
Sarrera elektronikoa: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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