CheckRare Panel Discussion: Data Silos Are Hindering Rare Disease Research

Data sharing is a common request in the rare disease community. Unfortunately, the realities of our current research infrastructure make it problematic for researchers to share their data. The net result is a plethora of data silos that can dramatically delay our understanding of diseases, especially ultra-rare diseases, that can lead to treatments. Watch the full discussion.

Previous
Previous

10 Crucial Years for Rare Disease Research

Next
Next

Dr. James M. Wilson and Alex Karnal Establish the Nonprofit Institute for Life Changing Medicines to Identify and Develop Next Generation Medicines for Rare Diseases