NHS England has announced the start of their new project, the 100,000 Genomes Project, in early 2015. The project aims to sequence 100,000 genomes within three years to determine the genetic mutations that lead to various cancers and rare diseases. This will enable targeted treatments to be developed for a wide range of conditions.
Doctors will be able to refer patients with relevant diseases, who are interested in taking part, to one of 11 Genomic Medicine Centres for inclusion in the project. Samples will be collected, genetic sequencing carried out and the data analysed.
NHS England are hoping to recruit 75,000 patients and The Lake Foundation is encouraging members of the African Caribbean community to take part to ensure that minorities are well represented and any ethnic genetic differences are identified.
