Take hold of
the promise of NGS





Visit us at AMP and discover how the GeneReader NGS System is redefining the NGS workflow

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. 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: All components of the workflow, from sample prep to sequencing and data interpretation, designed together to work in synchronization.
  • Actionable Insights: Designed with the central goal of generating a simple, clear report of only the most relevant variants.
  • Flexible to fit your current and future needs: Design elements and automation solutions to match the throughput needs of your lab.
  • Guaranteed results with predictable costs: A single NGS provider means complete pricing transparency from sample to result.
  • Proven expertise and service: Our team of NGS specialists are ready to support you in efficiently implementing, validating and operating the GeneReader in your lab.

Hear how QIAGEN can help to reduce the complexity of NGS from Lab Director at Legacy Health, Dr Yassmine Akkari


The GeneReader NGS System is for Research Use Only. Not for use in diagnostic procedures. The GeneReader NGS System is currently only available with proprietary new sequencing chemistry in the US. Legacy sequencing chemistry is only available ex-US.


Visit us at AMP 2017, Booth #707

Register for a demo
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