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...

全面介紹

Saved in:
書目詳細資料
Main Authors: Gruendner, Julian (Author), Wolf, Nicolas (Author), Tögel, Lars (Author), Haller, Florian (Author), Prokosch, Hans-Ulrich (Author), Christoph, Jan (Author)
格式: 圖書
出版: JMIR Publications, 2020-10-01T00:00:00Z.
主題:
在線閱讀:Connect to this object online.
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!

因特網

Connect to this object online.

3rd Floor Main Library

持有資料詳情 3rd Floor Main Library
索引號: A1234.567
復印件 1 可用