Whole genome sequencing could save NHS millions of pounds, study suggests

Genomics England and NHS England findings highlight benefits of using WGS to help detect rare diseases

The use of whole genome sequencing could save the NHS millions of pounds, a study suggests, after it found a quarter of people with rare illnesses received a diagnosis for their condition through the technology.

In some cases, the findings have provided reassurance for families that they have not passed their condition on to their children, while in others they have inspired life-changing treatments.

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