The Generation Study is a research programme being delivered by Genomics England in partnership with the NHS. It aims to recruit 100,000 newborn babies, whose genomes will be sequenced after birth (with their parents' consent). The study aims to facilitate the earlier identification of rare genetic conditions in babies, to gather genomic data for wider research purposes and to explore the risks and benefits of storing an individual's genome over their lifetime.
More information about the study can be found at the Generation Study GeNote:
https://www.genomicseducation.hee.nhs.uk/genotes/knowledge-hub/the-generation-study
or on Genomics England's website:
https://www.genomicsengland.co.uk/initiatives/newborns
For healthcare professionals involved in delivering the study, further information can be found on the Generation Study Future NHS workspace. This includes education and training materials, confirmatory testing pathways, and result referral pack documents sent to clinical teams when a suspected condition is identified.
If you require access, or have other queries about the study please contact the Genomics England Team at: [email protected]