AlphaGenome Atlas helps solve rare epilepsy case and surface non-coding associations
anshulkundaje · x · 2026-09-08
AlphaGenome Atlas collaborators are already driving discoveries: with the Broad Institute, the AVI score pinpointed a DNM1 variant that helped solve an epileptic encephalopathy case prior research had missed. In population genetics, grouping UK Biobank variants by predicted effects increased rare non-coding associations, and Exeter's Gareth Hawkes isolated regulatory variants driving proteins like PLA2G7 and BMI.
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