Implementation of long-read HiFi sequencing: Insights from Clinical Laboratories

What should clinical labs know as HiFi sequencing moves closer to adoption?

In this expert panel, hear how leaders from Myriad Genetics, GeneDx, Karolinska University Hospital, Radboudumc, and PacBio are thinking about HiFi sequencing across rare disease testing, carrier screening, and broader human genomics workflows.

The session offers practical perspective on where HiFi WGS and PureTarget fit, how more comprehensive sequencing can help reduce the need for multiple assays, and what laboratory teams should consider when planning for validation, adoption, and scale.

What you'll get:

✔ A clear introduction to HiFi sequencing and its role in clinical laboratory workflows
✔ Expert perspectives on evaluating, validating, and adopting HiFi sequencing
✔ Insight into where HiFi WGS and PureTarget may support rare disease and carrier screening workflows
✔ A practical look at assay consolidation through a single HiFi sequencing workflow
✔ Considerations for teams planning for workflow fit, adoption, and scale

Browse the speaker lineup below, and register to access the complete panel session.

What you'll get:

A clear introduction to HiFi sequencing and its role in clinical laboratory workflows
Expert perspectives on evaluating, validating, and implementing HiFi sequencing
Insight into where HiFi WGS and PureTarget may support rare disease and carrier screening workflows
A practical look at assay consolidation through a single HiFi sequencing workflow
Considerations for teams planning for workflow fit, adoption, and scale

Implementation of long-read HiFi sequencing

Insights from clinical laboratories

SPEAKERS AND PANELISTS