Defining Rare Disease Data Models

Our rare disease meeting in May 2015 brought together researchers and clinicians to help inform the rare disease data models used in the 100,000 Genomes Project.

The morning segment of this event will be focused on Genomics England giving an update on the rationale behind the generation of rare disease data models and how they have been developed. In the afternoon, there will be optional breakout sessions aimed at addressing challenges in the generation of data models and providing individuals with the opportunity to learn about the data model development and curation process and to provide specific feedback. The optional Data Model Clinic will be an opportunity to discuss specific data models in detail with us on a 1-1 basis.

This event is open to scientists and clinicians in the rare disease research community, particularly those from NHS Genomic Medicine Centres or belonging to a GeCIP Domain.

Click here to view the event agenda.