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Babies To Get New Test For Eye Cancer In The Womb To Save Their Sight
May 3 2022
A life-saving test that allows doctors to spot a rare form of eye cancer in […]
Whole Genome Sequencing Robustly Detects the Most Common Inherited Neurological Diseases and is Adopted by Healthcare
February 22 2022
Scientists have found whole genome sequencing (WGS) can quickly and accurately detect the most common […]
Whole Genome Sequencing Improves Diagnosis of Rare Diseases and Shortens Diagnostic Journeys for Patients, According to World First Study
November 11 2021
A world-first scientific study, published today in the New England Journal of Medicine, has shown that […]
NHS to Diagnose Thousands of People with Rare Diabetes
August 31 2021
Genetic testing on the NHS will spot a rare form of diabetes in thousands of […]