Education Session by Fabric Genomics

Best of both worlds: monogenic and polygenic analysis built on the backbone of clinical genetic disease testing
In this session, speakers from organizations at the forefront of combined monogenic and polygenic research will present their work leveraging emerging knowledge and their vision for providing genomic medicine care at population scale. They will share updates on developing tools, establishing large cohorts with high diversity, and putting a “rare and common” paradigm into clinical practice.

Moderator:
Samuel Strom, PhD, FACMG; Fabric Genomics; VP Clinical Operations and Clinical Genomics
Speakers:
Francisco M. De La Vega, PhD; Galatea Bio; Chief Technology Officer
“Exploring the Genetic Architecture of Familial Hypercholesterolemia in a Mexican Cohort Using AI-Driven Genomics”
Niall J. Lennon, PhD; Broad Clinical Labs; CSO and Chair
“A new clinical assay at Broad Clinical Labs for cost-effective population screening and combined monogenic/polygenic disease risk assessment”
Robert Green, MD MPH; Harvard Medical School; Professor of Medicine (Genetics)
"Nurture Genomics: A Platform for AI-driven Newborn and Childhood Genomic Screening"