The CCGA is a global collaborative effort to describe clinical context-based knowledge for gene- and chromosome-level abnormalities observed in cancer.
- Provide a centralized resource of genetic correlates for pathologic entities, structured based on current disease-level WHO classification system, with direct links to significant internal and external site content.
- Support real-time updating and sharing of clinically relevant content that is peer-reviewed and easily searchable.
- Engage community experts and their trainees in curating, updating and utilizing content.
- Include cancer variant knowledge identified through diverse methods and across multiple disciplines.
- Facilitate building educational content that describes the latest advancements in the field.
The global hub for clinical cancer genomic aberrations.
The CCGA is a Cancer Genomics Consortium (CGC)-supported resource.