GREGoR Consortium

The GREGoR Consortium’s main goal is to develop and apply new technologies, genome sequencing strategies and analytical approaches that will aid researchers to identify the cause of rare, unsolved cases with a suspected genetic cause. Funded by and working with the National Human Genome Research Institute (NHGRI) within the National Institutes of Health (NIH), the GREGoR Consortium is a group of 5 Research Centers and a Data Coordinating Center: 1. Baylor College of Medicine Research Center 2. Broad Institute 3. University of California, Irvine - GREGoR 4. GREGoR Stanford Site 5. University of Washington Center for Rare Disease Research 6. University of Washington Genetic Analysis Center - Data Coordinating Center for GREGoR While the GREGoR Consortium’s focus is on developing new tools and methods for researchers (versus providing direct clinical advice), the 5 Research Centers in the Consortium do conduct research studies. For patients, families and clinicians interested in learning more, see the Learning Hub on GREGoR’s web site. For a deeper dive into the areas of research within each of the GREGoR Research Centers, see also the GREGoR Collaboration page. Cover image by Freepik