In this webcast we provide an overview of our complete end-to-end clinical stack. It walks through our powerful secondary analysis pipeline which allows you to call SNVs and CNVs. It demonstrates how various types of CNVs are called and discuss metrics that express the confidence associated with each call.
We then show our powerful tertiary analysis capabilities for gene panels, exome and whole genome data. And finally, we demonstrate how our users can move seamlessly from the variant interpretation stage to a clinical report.