Join our Life Science Networking Event at the first Tuesday of every month!
Join the Novo Nordisk Foundation Center for Genomic Mechanisms of Disease at Broad Institute on Tuesday, March 19 for the Variant to Function Symposium.
Large-scale human genetic studies have succeeded in identifying hundreds of thousands of variants associated with human diseases and traits. One of the grand challenges on the frontier of human genomics and health is to pioneer new scalable paradigms and technologies to systematically link these many variants to cellular programs and gene regulation networks driving complex disorders. This will enable a deep understanding of the genetically-anchored biological programs affected in diseases, lay the foundation for a new generation of rationally designed medicines, and benefit patients and societies across the globe.
The symposium will highlight some of the important work and progress ongoing across the Broad community in this domain.
Attend in-person at Broad, or virtually. More info: https://broad.io/v2f