A free-to-attend online event discussing the Generation Study – an NHS-embedded research study which is sequencing the whole genomes of 100,000 newborn babies, in order to understand whether we can improve our ability to diagnose and treat genetic conditions.
Wednesday, 23 October 2024, 5.30PM - 7.30PM
The study involves babies born in a number of different hospitals in England. Results of the study will help inform future decisions about using whole genome sequencing to support newborn screening.
At this event, experts and practitioners will discuss how the Generation Study is being implemented, and the benefits and risks that may be involved.
The event will be chaired by Sarah Norcross, with speakers including Amanda Pichini, Phern Adams, Dr Chinthika Piyasena and Dr Robin Lachmann.