- 100,000 babies to have BBC genetic code mapped
- Genome sequencing trial to test benefits of identifying genetic diseases at birth The Guardian
- UK to study DNA of 100,000 newborns looking for rare diseases Bloomberg
- More than £175m for cutting-edge genomics research GOV.UK
- New £105m scheme aims to speed up diagnosis of rare genetic diseases in newborns The Independent
- See full coverage on Google News