Clinical Research Insights from the GeneReader NGS System
While next-generation sequencing has proven to be a very useful tool in basic research, two major hurdles remain for its broad adoption in the clinical research setting: lack of seamless workflow for routine clinical research use and truly relevant content to guide clinical research activities.
This webinar discussed Qiagen's approach to address these two issues. The Qiagen proprietary Knowledge Base was used to design a tumor panel to identify aberrations of value for clinical research. The GeneReader NGS System was then used to deliver clinical research insights in a laboratory setting. Testing was conducted with a set of colorectal cancer samples, and results confirmed with alternative testing platforms.
Our first speaker, Yassmine Akkari, Scientific Director of Molecular Pathology at Legacy Health, shared her experience of NGS panel-based testing, and some of the challenges. She also spoke about the Qiagen Actionable Insights Panel design process, and how this unique process led to robust content focused on variants of clinical significance.
Yi Kong, Product Director, NGS, Qiagen, shared some of the data generated using the Actionable Insights Tumor Panel and the GeneReader NGS System, as part of a collaboration between Qiagen and the Broad Institute.
The Qiagen GeneReader NGS System is a fully integrated sequencing workflow, engineered specifically for clinical research purposes. This turnkey solution is purpose-built, focusing on the assays that matter most. Learn more about the GeneReader NGS System here.