Unlock literature-driven real-world evidence to accelerate development, expand disease insights, optimize trials, and bring precision therapies to patients.
Real World Evidence
Provide clinicians and researchers open access to curated genetic evidence, reducing diagnostic barriers while advancing awareness, recognition, and scientific understanding.
Genetic Disease Sponsorship
Explore our platforms for germline and somatic variant interpretation.
Access article information on more than 26 million variants, as well as curated germline variant content.
Our Cancer Knowledgebase is used to interpret cancer variants, connecting them to therapies and clinical trials.
Partner with our team of experts to create Tailored Solutions for your unique needs
Gain access to an expansive, constantly updated database of curated genomic information
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