FOCUS ON: The Generation Study: Sequencing 100,000 Newborns
2nd April 2025
Time: 12:00–13:00 BST
Location: Online, free access
Presented by: Professor Emma Baple and Amanda Pichini
About the Generation Study
The Generation Study aims to sequence the genomes of 100,000 newborns to improve the diagnosis of genetic conditions.
- Conducted within the NHS setting, the study involves sequencing the genomes of 100,000 newborn babies.
- Objectives: Understand the benefits of newborn genome sequencing and explore clinical, scientific, ethical, and societal implications.
- Focus Areas: Study design, recruitment progress, results return, and discussion on potential impacts.
Meet the Speakers
Professor Emma Baple
- Professor of Genomic Medicine at the University of Exeter.
- Consultant Clinical Geneticist and medical lead for the NHS rapid genome sequencing service for acutely unwell children.
- Principal interest: Using genetic technologies to identify the causes of rare genetic disorders and translating that knowledge into improved clinical diagnostic testing and treatment strategies.
Amanda Pichini
- Clinical Director at Genomics England
- Leads the Generation Study with a focus on integrating genomic research into clinical care, addressing ethical considerations, and educating healthcare professionals.
REGISTER FOR THE WEBINAR HERE
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