Discover how long-read HiFi sequencing is redefining what’s possible for clinical genomics and translational applications. In this workshop, we will highlight how labs and institutions are implementing HiFi targeted and whole genome sequencing to resolve challenging variants missed by conventional methods, including repeat expansions and complex structural variants. Learn about real-world examples spanning applications like oncology, neurology, and carrier screening. Attendees will gain insight into how researchers are leveraging HiFi sequencing to streamline genetic testing workflows, improve understanding of disease and treatment options, and support clinical interpretation and decision-making – delivering more complete, confident answers to help improve patient care.
