Translating genomic information into clinical medicine: Lung cancer as a paradigm

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 3.
Figure 3.

Screenshot visualizing tumor gene mutation results in the electronic health record linked to decision support. (A) In the provider dashboard, patients are listed in separate rows with their respective gene mutation results shown as colored indicators in each column (yellow: mutation detected; gray: mutation not detected). “H-GFR” and “H-SLP” refer to the specific diagnostic tests performed, as named by the molecular diagnostic lab, while the remaining nine columns refer to the specific genes assessed for mutations. The user clicks on a specific gene indicator to view the specific gene mutation results shown in B. Gene mutations are reported using the REFSEQ nomenclature with results reported as Detected or Not Detected. The user clicks on the specific gene mutation and is taken to C. Summary of the clinical significance for the specific gene mutation in the patient's specific cancer diagnosis.

This Article

  1. Genome Res. 22: 2101-2108

Preprint Server