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NHGRI Bold Predictions Seminar #7
Bold Predictions for Human Genomics by 2030

Bold Prediction #7: The clinical relevance of all encountered genomic variants will be readily predictable, rendering the diagnostic designation “variant of uncertain significance (VUS)” obsolete.

On September 16, 2021, NHGRI will host the seventh seminar in a series focused on the “Bold Predictions for Human Genomics by 2030” that are described in NHGRI’s “Strategic Vision for Improving Human Health at the Forefront of Genomics.” For each session, two speakers will use a specific bold prediction as an aspirational theme to discuss their own research and speculate about next decade of genomic advancements. A moderated question and answer session will follow the speakers.

Closed captioning will be provided for this event. Individuals with disabilities who need reasonable accommodation to participate in this event should contact Susan Vasquez (susan.vasquez@nih.gov, 301-503-9790) and/or the Federal Relay Service at 800-877-8339. Requests should be made five days in advance of the event.

Sep 16, 2021 03:00 PM in Eastern Time (US and Canada)

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