Whole genome sequencing improves diagnosis of rare diseases and shortens diagnostic journeys for patients, according to world first study
London (ots/PRNewswire) - NB: SCIENCE MEDIA BRIEFING TAKING PLACE 14:00 GMT 9TH NOVEMBER 2021
- whole genome sequencing proved to be a better way to diagnose rare diseases than usual genomic testing methods
- whole genome sequencing led to new rare disease diagnoses for NHS patients in some cases ending decades-long diagnostic odysseys
- study represents significant step towards the goal of precision medicine - a transition that will have huge impact across the NHS and globally
A world-first scientific study,!-->…