To uncover meaningful biological insights from your targeted NGS data, you may be faced with several challenges, from choosing an appropriate library preparation method that covers specific targets of interest to connecting disparate informatics tools for sequence analysis and variant interpretation. These issues can be particularly critical when using custom NGS panel designs.

QIAGEN has developed an integrated workflow approach to address these NGS challenges.  In this live two-part webinar series, we will describe the latest QIAseq DNA Panel kits, which include:
• QIAseq Targeted DNA Panels: Generate uniform NGS libraries for low-frequency variant detection using Unique Molecular Indices (UMIs), and improve coverage of GC-rich regions using Single Primer Extension (SPE) technology
• CLC Genomics Workbench: Use pre-built sequence analysis workflows that can run in a push-button mode for all off-the-shelf QIAseq DNA panels, and that are easily configured for use with your custom QIAseq panel designs
• QIAGEN Clinical Insight-Interpret for QIAseq: Perform comprehensive variant interpretation with software that provides an easy-to-understand report for each variant detected in your sample, powered by the QIAGEN Knowledge Base, the industry’s most complete and up-to-date repository of curated scientific information