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NHS to Offer Whole Genome Sequencing for All Newborns Within a Decade

A £650 million genomics boost underpins a decade-long strategy to transform the NHS through prevention, community-based care, digital diagnostics.

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Overview

  • Health Secretary Wes Streeting announced a goal for whole genome sequencing to be available for every baby in England by 2035 to enable early disease prediction.
  • The Government will allocate £650 million to expand genomics infrastructure as part of its life sciences sector plan.
  • The upcoming 10-year NHS strategy will redirect care from hospitals to community teams and virtual hospitals, leveraging digital platforms.
  • The NHS has already screened 100,000 newborns for over 200 genetic conditions in a pilot scheme, storing DNA in the National Genomic Research Library under strict access controls.
  • Ethical and privacy advocates warn that lifelong genetic records may expose children to unwanted risk information and data security threats.