Does your lab need a faster and easier way to uncover associations between gene variants, diseases, and biological pathways? As next-generation sequencing (NGS) data grows exponentially, discovering new genes implicated in hereditary diseases or cancer progression has never been more challenging or time-intensive. However, advanced bioinformatics tools and expert-curated content from QIAGEN can simplify, enrich, and accelerate your research.

Join us for an informative webinar that will provide a deep-dive into three cutting-edge solutions: QIAGEN CLC Genomics Workbench, QCI Interpret Translational, and QIAGEN Ingenuity Pathway Analysis (IPA). Attendees will learn through demonstrations how these three solutions can analyze sequencing data from a variety of NGS technologies, annotate genes using the world’s most comprehensive and up-to-date curated scientific evidence, and find biological connections in gene variants. Helping you streamline your NGS workflows from FASTQ to discovery, these three easy-to-use solutions will enable you to pinpoint disease-associated variants, uncover biological mechanisms, and turn data into breakthroughs faster than ever.

In this webinar, you’ll learn how to:

• Use the LightSpeed module of QIAGEN CLC Genomics Workbench for ultra-fast, FASTQ-to-VCF NGS data processing that can deliver whole genome or exome results in minutes.

• Leverage QCI Interpret Translational to accelerate your understanding of hereditary and tumor variants with powerful cohort analysis capabilities.

• Use QIAGEN IPA to uncover novel biological mechanisms with the world’s most comprehensive manually curated database.

This is your opportunity to speed up discoveries, gain deeper insights, and make impactful connections. Don’t miss out—your next breakthrough starts here.