|Attendees will not be audible or visible during this online event, but will still be able to put questions and comments to the speakers and chai|
A free-to-attend online event about whole genome sequencing at birth, asking about implications for healthcare professionals if this becomes offered routinely.
This event is produced by the Progress Educational Trust (PET), in partnership with Genomics England and its Newborn Genomes Programme.
The event will be chaired by Sarah Norcross, with speakers including Sarah-Jane Marsh, Professor Eamonn Sheridan, Professor Pali Hungin, Dr Michelle Bishop and Professor Angus Clarke.
Genomics England's Newborn Genomes Programme will explore – in an ethics-approved research pilot, due to be embedded in the NHS – whether and how whole genome sequencing might, in future, be offered routinely for newborn babies in the UK.
The Newborn Genomes Programme builds on other work, such as the creation of the NHS Genomic Medicine Service, that has already increased the prominence of genomics in healthcare. If whole genome sequencing were offered routinely for newborns, then this would further extend the use of genomics in mainstream health contexts.
At this event, experts and advocates will address questions including:
If discussing this event on social media, please use the hashtag #GenomicsConversation
If you are a journalist and are interested in reporting on this event, please email [email protected] with any queries.r, via a Q&A tool within Zoom Video Webinars.