Patient-partnered research

By sharing their data, samples, and experiences, patients have the power to accelerate discoveries that could reveal new treatments for disease and improve health care. Our scientists partner with patients and their loved ones to guide research and ensure that all patients' voices are heard.

Count Me In enables anyone in the US and Canada ever diagnosed with cancer to accelerate research by sharing their samples, their clinical information, and their voices.

The Rare Genomes Project is a patient-driven research study making the latest advances in genomic sequencing accessible to families with rare and undiagnosed conditions.