At Zetta Genomics our products and services are empowering the application of genomic data to improve health outcomes for millions of patients around the world. We are pioneers in genomics with over a decade of experience – handling complex and large genomic data is at the heart of what we do.
Born from the prestigious University of Cambridge and honed through our contributions to Genomics England’s landmark 100,000 Genomes Project, our genome-native platform XetaBase leverages cutting-edge, real-world tested technology to deliver powerful genomic analysis solutions.
XetaBase is revolutionising genomic analysis from the individual case level to whole populations at scale. Featuring the most advanced genomic variant database, XetaBase can index hundreds of thousands of whole genomes and trillions of variants. Our technology replaces slow and expensive legacy analysis methods which handle individual and flat VCF files. Our aggregated variant database can seamlessly scale as databases grow, enabling real-time execution of complex data queries to deliver results within seconds.
As a unified platform for both research and clinical applications, XetaBase enables us to collaborate with healthcare systems, life sciences companies, research institutions and global health-tech innovators, ensuring that the promise of precision medicine becomes a reality for all.