WEBINAR

Filling the gaps in rare disease research with long-read sequencing: stories from undiagnosed cohorts

Thursday, May 21, 8:00 AM PDT | 11:00 AM EDT | 5:00 PM CEST
Friday, May 22, 9:00 AM SGT | 11:00 AM AEST
Register here

Join Pacbio‘s webinar and learn how long-read sequencing is helping researchers find explanations in rare disease cases that remain unresolved with traditional approaches.

Register to:

• Understand the key advantages of long-read HiFi sequencing for rare disease research
• Learn from real-world examples where HiFi sequencing uncovered structural variants and multi-omic variation underlying rare disease
• Gain perspective on how HiFi sequencing can consolidate multiple assays and help enable adoption in clinical and translational workflows.

Speakers:

Nina Gonzaludo, PhD
Global Segment Lead – Clinical, Rare Disease @PacBio
Host + moderator

Ramakrishnan Rajagopalan, PhD
­Director of Translational Bioinformatics, Division of Genomic Diagnostics @Children’s Hospital of Philadelphia