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Complete Genomics and Velsera Partner to Integrate Sequencing and Analysis Platforms

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Complete Genomics and Velsera are collaborating 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 at the AACR annual meeting in Chicago, will accelerate and streamline the path from sample to clinical report, promises Lisa Weingartner, MBA, head of global partnerships at Velsera.

“By integrating variant interpretation, tertiary analysis, reporting, and decision support into a unified workflow, we are helping labs expand genomic testing with greater accuracy, consistency, and confidence,” continued Velsera.

Velsera will offer plug-in workflows within the CGW to support 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 and lab automation platforms.

“Through our partnership with Velsera, Complete Genomics is expanding our ability to serve clinical laboratories with an end-to-end solution from sample to insight,” said Rob Tarbox, VP of product and marketing at Complete Genomics.

The post Complete Genomics and Velsera Partner to Integrate Sequencing and Analysis Platforms appeared first on GEN - Genetic Engineering and Biotechnology News.
 
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