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NHS to Sequence the Genome of Every Newborn in England

The upcoming 10-year strategy features a £650 million genomics investment to screen every newborn as the NHS shifts toward predictive prevention.

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Overview

  • The NHS will roll out whole genome sequencing for all newborns in England within a decade, expanding on a 100,000-baby pilot screening for over 200 genetic conditions.
  • The government has allocated £650 million to genomics under its life sciences sector plan to fund the long-term health strategy.
  • Health Secretary Wes Streeting says personalised genome data will enable a move from reactive treatment to proactive disease prevention and tailored care.
  • The 10-year health plan, due in early July, outlines shifts from hospital to community care, analogue to digital services, and a £29 billion annual funding increase over three years.
  • Clinicians and patient advocates welcome early diagnosis but warn that ethical, privacy and data-security frameworks must keep pace with the genomic expansion.