CCMG Webinar – Exploring “hidden” Genomic Variation In Rare Diseases: Application Of Long-read Genomic Sequencing In The Care4rare Solve Research Project

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Presented by PacBio

In this session we will discuss long-read genome sequencing and its applications in human rare genetic diseases. We will introduce the Care4Rare-SOLVE project, provide insights from the application of long-read genome sequencing to study unsolved rare diseases in the context of our Canadian cohort, and discuss the challenges and opportunities of adding new genomic technologies to our molecular toolbelt for rare disease research.

Speaker: Dr. Kym Boycott

Click HERE to register.

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