Reviewing Analysis

Once a workflow has produced results, a clinical geneticist reviews and interprets them in the Variant Interpreter. This is the tertiary-analysis step that follows locating your outputs.

Opening the Variant Interpreter

To review a completed analysis:

1. From the Data Page, select the instrument and locate your sample.

2. Open the sample to reach its details page.

3. Select the workflow run you want to interpret. Only a run that succeeded can be reviewed.

4. Click Review analysis to open the sample in the Variant Interpreter.

You land on the Summary tab, which surfaces the priority findings for the case.

What you can do in the Variant Interpreter

• Triage the priority findings and step through the strongest candidates.

• Review each variant class on its own tab: small variants, structural variants, copy number, tandem repeats, and paralogs.

• Classify variants and add them to the report.

• Submit the report for Admin review and sign-off.

For the full walkthrough, see the Variant Interpreter documentation.

The Variant Interpreter is the interpretation surface for long-read tertiary analysis. It presents the output of a completed workflow rather than calling variants itself.