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The Xcelerate RARE Challenge brings together academic and biopharmaceutical industry researchers
Sleep Consortium and RARE-X, the Global Genes research program and patient-owned data collection
The Huntington’s Disease Society of America (HDSA) and RARE-X, the Global Genes patient-driven
Global Genes unveils a three-pronged strategy focused on support for patients and developing
The first Xcelerate RARE challenge will launch in the spring of 2023 and will focus on rare
Partnership supports rare disease research and breaking down data silos to accelerate treatments
Global Genes/RARE-X Sr Director of Scientific Programs Karmen Trzupek explains how to upload
In this video, Christina O’Keeffe from Wiedemann-Steiner Syndrome Foundation presented their
In this video, Dr. Wendy Chung explains the importance of patients and caregivers uploading genetic
This spring, RARE-X will bring together researchers and data scientists to use patient-provided
RARE-X will kick off Xcelerate RARE: A Rare Disease Open Science Data Challenge this spring. For