Implementation of HiFi sequencing: Insights from Clinical Laboratories

Long-read sequencing is rapidly moving from research into routine workflows, driven by the need for comprehensive, accurate, and scalable testing solutions.

Traditional genotyping and short-read sequencing leave critical gaps, missing structural variants, repeat expansions, and challenging genomic regions. These limitations may reduce the ability to achieve comprehensive genomic insights and force labs to run multiple assays to comprehensively query the genome.

In this webinar, PacBio will introduce research and clinical laboratory stakeholders to HiFi long-read sequencing technology and discuss how it is being adopted by laboratories around the world. Following a brief overview, a panel of experts will share their experiences evaluating, validating, and implementing HiFi sequencing in research and translational settings.

Watch the recording to:

Learn how HiFi WGS and PureTarget are enabling rare disease testing and carrier screening, streamlining workflows, and advancing scientific understanding to inform diagnostic development and clinical applications
Discover how PacBio technology enables scalable testing and consolidates multiple assays into a single workflow
Gain practical insights from experts on evaluating and implementing HiFi sequencing in clinical laboratory workflows

SPEAKERS AND PANELISTS

Nina Gonzaludo, PhD

Senior Manager, Human Genomics Segment Marketing, PacBio
Host + moderator

Sarah Kingan, PhD

Associate Director, Product Marketing, PacBio

Dale Muzzey, PhD

Chief Scientific Officer, Myriad Genetics

Keith Nykamp, PhD

VP, Research & Innovation, GeneDx

Anna Lindstrand, MD, PhD

Director, Clinical Genetics Laboratory, Clinical Genetics and Genomics, Karolinska University Hospital

Lisenka Vissers, PhD

Professor of Translational Genomics, Radboudumc