The pilot study of rare undiagnosed diseases involved analysing the genes of 4,660 people from 2,183 families – all of whom were early participants in the 100,000 Genomes Project. The ground-breaking Project, led by Genomics England and NHS England and involving the University of Exeter, was established in 2013 to sequence 100,000 whole genomes from […]
University of Exeter: Whole genome sequencing improves diagnosis of rare diseases and shortens diagnostic journeys for patients
- Post author:admin
- Post published:November 11, 2021
- Post category:Uncategorized
Tags: Education News