GeneReader NGS System 3 Clonal Amplification Next-Generation Sequencing Data Analysis & Interpretation NGS has the potential to help labs create valuable insights, but many barriers still exist, such as high cost, fragmented workflow and ensuring actionable data. From Sample to Insight, QIAGEN’s GeneReader NGS System standardizes your workflow to quickly and accurately identify the genetic markers associated with approved therapies, leading professional guidelines and active clinical trials. With the GeneReader NGS System, every lab can benefit from the experience of QIAGEN, the diversified global leader in molecular science. Whether you’re entering NGS or expanding your existing environment, GeneReader offers the efficiency of a completely connected NGS workflow focused on actionable reports. • The world’s first truly complete NGS workflow: Rely on one partner to provide a seamlessly integrated workflow offering ease of use and efficiency from Sample to Insight. • Actionable insights: Create relevant reports using QIAGEN’s proven gene panels and bioinformatics. • Flexibility to fit your needs: Scalable batch sizes and continuous loading of multiple flow cells enable you to adapt and scale the GeneReader NGS System to match your needs and grow. • Guaranteed results with predictable costs: Innovative commercial models such as price- per-insight options offer better cost management and low initial investment hurdles. • Proven expertise and service for our customers: Our teams at QIAGEN are ready to support you in efficiently implementing, validating and operating GeneReader in your lab. The GeneReader NGS System is the first complete Sample to Insight NGS solution designed for any research lab to deliver actionable results. GeneReader NGS System