Overcome common challenges in the analysis and interpretation of NGS cancer data

Visit us at booth #5113 to learn more about how QIAGEN’s innovative bioinformatics solutions

Interpret and report on NGS variants for somatic cancer testing with QIAGEN Clinical Insight (QCI) Interpret software.

  • Minimize the complexity, time and cost of determining clinical significance and actionability
  • Leverage knowledge from over 10 million relevant biomedical findings, with full transparency
  • Built-in adherence to community guidelines from AMP/ASCO/CAP and ACMG

Uncover hidden knowledge in cancer biology with Ingenuity Pathway Analysis (IPA) and OmicSoft Array Studio applications.

  • Pinpoint significant genes and differential expression associated with disease
  • Generate novel regulatory networks as hypotheses for further investigation
  • Gain additional insights by comparing your results with normalized public datasets

Simplify targeted NGS panel data analysis with Biomedical Genomics Workbench software.

  • Pre-configured, built-in point-and-click analysis workflows
  • Detect multiple types of variation – from SNVs to fusions
  • Support for off-the-shelf DNA, RNA and RNA fusion panels, and custom panels

Learn more about these and other bioinformatics solutions at www.qiagenbioinformatics.com

Sign up for a demonstration of these applications and speak with an expert who can help you apply our solutions to your own cancer research!

Visit us at the 2018 ASCO Annual Meeting, Booth #5113

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