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Rare Genomics is a nonprofit focused on helping undiagnosed rare disease patients access genomic sequencing and reanalysis through no-cost programs and partnerships. It collaborates with patient advocacy groups, researchers, and tech partners to accelerate diagnosis, treatment, and, hopefully, a cure, by linking patients to sequencing opportunities and new scientific findings. The organization also offers patient resources and communities (RareWear, RareShare) and relies on volunteers and donations to support its mission.
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