Complete Genomics, a leading innovator in genomic sequencing, has announced a collaboration with Velsera, a leading global healthcare technology company, to deliver an end-to-end genetic testing solution that integrates DNBSEQ sequencing technology with Velsera's Clinical Genomics Workspace (CGW) data analysis solution.
The partnership, announced this week at the American Association for Cancer Research (AACR) Annual Meeting in Chicago, will accelerate and streamline the path from sample to clinical report, enabling faster, more accurate, and cost-efficient genetic testing for clinical oncology laboratories and assay developers for better patient care.
"This partnership enables clinical laboratories and assay developers to accelerate the path from raw sequencing data to actionable clinical insights," said Lisa Weingartner, Head of Global Partnerships at Velsera. "By integrating variant interpretation, tertiary analysis, reporting, and decision support into a unified workflow, we are helping laboratories expand genomic testing with greater accuracy, consistency, and confidence."
Velsera will offer plug-in workflows within the CGW to support streamlined implementation of standard off-the-shelf assays using post-secondary analysis and secondary analysis integration models. Complete Genomics will contribute a range of low- to high-throughput DNBSEQ genetic sequencing solutions lab automation platforms.
"Through our partnership with Velsera, Complete Genomics is expanding our ability to serve clinical laboratories with a truly end-to-end solution from sample to insight," said Rob Tarbox, Vice President of Product and Marketing at Complete Genomics. "By combining our advanced sequencing and laboratory automation with Velsera's Clinical Genomics Workspace for data analysis and reporting, we're empowering laboratories to deliver high-quality, actionable results with greater efficiency and confidence."