At Central and South Genomics, we work closely with the public to ensure we have a good understanding of the experiences and views of patients and their families in genomic testing, diagnosis and treatment.

Most prominently, we have a patient and public involvement (PPI) group that meets regularly to co-create a range of events and materials, and to advise us on the development of our service. We also regularly engage with the public at external events, conferences and educational meetings, as well as providing guidance and materials to other patient and public-facing organisations on the impact of genomics on our health.