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QIAGEN Advances Leadership in Pre-Analytical Solutions for Next-generation Sequencing (NGS) With Launch of 14 New Cancer Gene Panels
Date:7/15/2014

fast and integrated workflows," said Peer M. Schatz, Chief Executive Officer of QIAGEN. "The new GeneRead panels incorporate sophisticated algorithms to enable analysis of many gene variants and customization for specific objectives. We continue to deliver on QIAGEN's growth driver of providing universal solutions for NGS workflows by addressing our customers' urgent needs for fast turnaround times, low DNA input requirements, and quality control to ensure accurate, reproducible results."

The 14 new GeneRead DNAseq V2 panels cover an extensive range of cancer-related genes and gene regions, including "focused" panels each targeting 8-25 genes, "disease-specific" panels for 40-50 genes, and "comprehensive" panels for as many as 160 genes. The content of the panels has been developed based on the latest recommendations from relevant medical and scientific literature. The gene panels are integrated with QIAGEN's industry-leading bioinformatics software, Ingenuity® Variant AnalysisTM, an extensive, curated database of gene variants and clinical data that enables interpretation of NGS results and delivers valuable insights from sequencing data. Laboratories also can customize GeneRead panels for specific disease pathways or research needs by tapping into QIAGEN's deep molecular content portfolio through GeneGlobe, an online portal covering more than 60,000 annotated molecular assays.

QIAGEN has been collaborating with selected customers in the development of the new gene panels to validate product performance in a wide range of applications, including translational research and clinical applications. Dr. Gregory J. Tsongalis, Professor and Director of Molecular Pathology at the Department of Pathology at Dartmouth Hitchcock Medical Center in Lebanon, New Hampshire, one of the early users of QIAGEN's GeneRead V2 panels, commented: "For focused anal
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