Simplify your 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 all QIAseq DNA, RNA and RNA fusion panels, and custom panels
Uncover hidden knowledge with Ingenuity Pathway Analysis (IPA) and OmicSoft Array Suite 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 using IPA’s Analysis Match functionality
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
Sign up for a demonstration of these applications and speak with an expert who can help you apply our solutions to your own research!