Unified Database for all Genomic Data
Sequences, variations, and annotations from all sources can be unified into a single, continuous database that is accessible to all researchers and clinicians. Sources include project and company data, partnership studies, and public reference datasets – removing all silos.
Users can perform analysis and interpretation – including the generation of comprehensive variation reports – on any selection from the unified database. Bioinformatic teams can build more powerful applications through common, programmatic access to the entire collection of data.
