GeneReader NGS System (ROW) - Actionable insights – Create relevant reports using QIAGEN’s proven gene panels and bioinformatics tools

GeneReader NGS System 5 One of the biggest challenges of NGS is content selection. With ever-expanding genomic information and increasingly complex medical knowledge, how can you ensure your tests target all of the right genes and variants, and can provide you with the answers you need for your clinical research? QIAGEN NGS Target Enrichment panels are purpose- built for clinical research labs, designed to identify critical and meaningful variants in actionable genes. Our panel content is carefully selected and purposefully designed, targeting only genes and variants that are important to specific diseases. The QIAGEN Knowledge Base is a comprehensive biomedical information resource, built to help labs interpret variants in their clinical research context. Here is it also used to direct panel design by focusing only on actionable genes and variants. The QIAGEN Knowledge Base includes clinically relevant findings from approved drug labels, professional association practice guidelines, active clinical trials, primary literature and curated clinical cases. Our database contains over 10 million findings, 2 million ontology classes and 50 thousand disease-to-phenotype links. The QIAGEN Clinical Insight platform allows you to access the regularly updated content in the QIAGEN Knowledge Base and links variant interpretation and reporting to original panel design. Actionable insights – Create relevant reports using QIAGEN’s proven gene panels and bioinformatics tools Library Preparation Clonal Amplification Next-Generation Sequencing Data Analysis & Interpretation Nucleic Acid Extraction Target Enrichment External databases Professional guidelines Drug labels Clinical Trials Scientific literature Clinical Case Counts QCI Interpret QIAGEN Knowledge Base

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