The RP Genome Project
Research type
Research Study
Full title
The UK Inherited Retinal Disease Consortium RP Genome Project
IRAS ID
176953
Contact name
Graeme Black
Contact email
Clinicaltrials.gov Identifier
a1265, University of Manchester grant reference
Duration of Study in the UK
2 years, 4 months, 31 days
Research summary
New technology is revolutionising our understanding of the genetic causes of eye disease, but it produces large amount of complicated data, and to understand the data properly we need to start working in partnerships.
This research will involve genetic testing of DNA from patients and their relatives. Children and adults would be recruited and there could also be family members affected, but only those with the condition would be directly recruited. the research will be carried out across a group of four sites, and has three main objectives:
1. Finding new disease causing genes
2. Increasing the number of patients we can diagnose
3. Improved data sharing - We aim to work towards a national database for genetic eye diseaseThis will lead to a number of other benefits, including, improving the ways that genetic eye disease is diagnosed and helping to give more people access to genetic testing. Sharing of data will lead to the development of a database of patients with a known genetic cause for their eye disease, making it easier to recruit to future clinical trials, which may in the future include treatments
The research will also strengthen links with other research active groups working in eye disease, including the UK Eye Genetics Group (EGG), Genomics England Clinical Interpretation Partnerships (GECIPs), and aims to provide a UK hub for this type of research.
REC name
Yorkshire & The Humber - Bradford Leeds Research Ethics Committee
REC reference
15/YH/0365
Date of REC Opinion
30 Sep 2015
REC opinion
Further Information Favourable Opinion