Free genetic testing for babies

The study offers free genome sequencing for newborn babies to detect over 200 rare but treatable genetic conditions.

St George’s Hospital is proud to be part of The Generation Study, a new national research initiative led by Genomics England in partnership with the NHS. The study offers free genome sequencing for newborn babies to detect over 200 rare but treatable genetic conditions.

This is a major step forward in newborn care. By identifying conditions before symptoms appear, we can help families access treatment faster and plan care more effectively. The study aims to sequence the genomes of 100,000 newborns across England, helping to shape the future of genomic medicine.

Pregnant people who choose to have their baby at St George’s can choose to take part in this study. The test uses a small blood sample from the umbilical cord at birth. Researchers then study each baby’s genome to look for early signs of rare conditions. Early diagnosis means treatment can start sooner, improving outcomes for affected babies and families.

We need all clinical and maternity staff to help raise awareness. Please make sure pregnant patients know they can take part in The Generation Study if they wish. The research team can answer any questions and support families through the process.

We are especially keen to involve families from communities that are often underrepresented in research, so your encouragement and signposting can make a real difference.

Find out more or refer patients

For further details or to put a patient in touch with the team, please contact:

The Generation Study Research Team

Generation.Study@stgeorges.nhs.uk

07345 428496