Filling the gaps in rare disease research with long-read sequencing: stories from undiagnosed cohorts
May 21, 2026 - May 22, 2026
In this webinar, learn how long-read sequencing is helping researchers find explanations in rare disease cases that remain unresolved with traditional approaches.
Featuring real-world examples from undiagnosed cohorts, you’ll discover how HiFi sequencing detects complex genetic variation and integrates multiomic data to help resolve challenging cases.