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Patients with rare diseases give their views on genomics

 

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Patients with rare diseases give their views on genomics

Genomics England commissioned research into the views of patients and carers around the introduction of whole genome sequencing into the NHS.

They also wanted to hear about people’s experiences of taking part in the 100,000 genomes project. This information will be used by Genomics England to inform the mainstreaming of genome sequencing as part of the new genomic medicine service.