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In this webinar we will explore the challenges and opportunities associated with rare disease diagnosis – with a focus on ongoing initiatives that are helping accelerate the identification of rare genetic disorders. Over the course of the 60-minute session our speakers discuss the following topics: 
The value of genomic diagnosis Expanding diagnosis and enabling precision … Continued

Following on from our recent announcement that we would be working with the Foundation for Angelman Syndrome Therapeutics (FAST) to find new treatments for Angelman Syndrome, we interviewed Dr Allyson Berent, Chief Scientific Officer at FAST, to learn more about the organisation and the ways in which AI is being used to speed up drug discovery … Continued