Complete Genomics was established in 2005 with a vision to deliver the highest quality whole human genome sequencing and analysis as a simple outsourced service. The Complete Genomics Analysis Platform combines Complete Genomics' proprietary human genome sequencing technology with advanced informatics and data management software. Researchers using these services to conduct large-scale disease projects receive highly accurate genomic data, assembled and annotated, ready for biological interpretation.

As the world’s first company dedicated to large-scale whole human genome sequencing and bioinformatics analysis provided as a service, Complete Genomics frees researchers from purchasing and operating sequencing instruments and computing infrastructures so they can focus on making biological discoveries. By providing highly accurate, affordable large-scale whole human genome sequencing, researchers can increase their understanding of the genetic mechanisms underlying drug responses and complex diseases in order to improve human healthcare. Complete Genomics’ customers use these services in support of Mendelian disease research, family studies, and oncology work – sequencing tumour-normal pairs in particular.

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