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:
Used together in one kit*, these best-in-class components allow you to design, execute and interpret NGS results in a single integrated workflow with the confidence that comes from the quality and support for which QIAGEN is known. By attending both webinars, you will learn how to readily execute these integrated workflows–whether using your own custom-designed QIAseq DNA panels, or pre-built catalog panels. You will also gain an understanding and appreciation of the true value that comes from using all NGS components from a single supplier, who provides support for every aspect of the NGS workflow.
Part 1: Integrated NGS workflows, from library preparation to variant interpretation
Presenter: James Caffrey, M.B.A., Ph.D., Director, Strategic Marketing, QIAGEN
This first webinar will describe the overall QIAseq integrated NGS workflow, starting with pre-designed, catalog QIAseq DNA panels. It will include an overview of CLC Genomics Workbench for sequence mapping and mutation detection, and QIAGEN Clinical Insight-Interpret for QIAseq, for biological interpretation of variants. The webinar will highlight the seamless integration between each component, comprehensive variant reporting capabilities and other time-saving functions that accelerate the pace of discovery using NGS panels.