Get started with Emedgene
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Welcome to Emedgene, where we unlock genomic insights for hereditary disease and streamline your tertiary analysis workflows.
So you've signed in and can't wait to get started? Here we will guide you through the platform architecture, case creation, and results review. You can dive a bit deeper by following the links and exploring manuals for the platform's applications:
- Genomic analysis workbench, where you can accession, interpret, curate and report on your cases, while also efficiently managing the lab workflow.
- A repository for all of your organizational curated knowledge.
The platform is operated from the .
By clicking on the corresponding buttons, you can enter:
Select file type,
Upload files,
Create a family tree,
Annotate each sample with clinical information,
Specify analysis details, and
Launch the analysis!
You'll be notified when results are ready.
page
page
menu
dropdown menu
dropdown menu
To enter the flow, click on the namesake button on the . Here:
Select a case to review on the page. You'll be directed to the that:
Showcases an AI-curated suggested to be checked first, namely and ,
Provides numerous customizable to help you by yourself, and
Documents all the case-related information like , , and used during case analysis.
On the , each variant can be thoroughly investigated and accordingly .
When you're ready to , indicate the end result of the analysis and variants to be reported in the Case interpretation widget.