On Dec. 5, 2018, Genomics England announced the 100,000 Genomes Project, done in partnership with National Health Service (NHS), had reached its goal of sequencing 100,000 whole genomes from NHS patients.

The 100,000 Genomes Project has delivered life-changing results for patients with one in four participants with rare diseases receiving a diagnosis for the first time, and providing potential actionable findings in up to half of cancer patients where there is an opportunity to take part in a clinical trial or to receive a targeted therapy.