Building databases to support clinical and research applications of long-read sequencing

In this webinar, Danny Miller and Jonas (Gus) Gustafson of the Miller Lab at the University of Washington discuss their work to develop resources to support analysis of long-read sequencing data and hasten its adoption in clinical and research spaces.

Watch this webinar to:

• Learn how Oxford Nanopore long-read sequencing has the potential to overcome limitations of prior clinical and research genetic testing approaches

• Understand barriers to implementing long-read sequencing at scale in clinical and research environments

• See how variants identified in short-read sequencing data may be less effective for filtering long-read sequencing data

Please note: This is independent, investigator-led research using Oxford Nanopore technology. Oxford Nanopore products are for research use only, and not for use in diagnostic procedures.