Detection, interpretation, access
Next-generation sequencing (NGS) doesn't have to be complicated. Whether your lab is new to NGS or wanting to improve your existing pipeline, QIAGEN provides complete NGS workflows for labs of all sizes, budgets and experience.
Complete out-of-the-box sample-to-report workflows ideal for labs building their first NGS pipeline. Includes library preparation, sequencing, and data analysis, interpretation and reporting. Learn more here.
Fully customizable workflow solutions for labs with a sequencer who want to improve their existing NGS pipeline. Includes library preparation and data analysis, interpretation and reporting. Learn more here.
Ideal for labs who already have panels and a sequencer. Includes data analysis, interpretation and reporting solutions for hereditary and oncology applications. Learn more here.
For labs that need to supplement their current workflow with the additional support of virtual variant scientists, QIAGEN offers professional variant interpretation services (formely N-of-One) for precision oncology testing. Learn more here.
For labs who have a sequencer but need a panel and downstream data analysis.
For labs who have a panel and sequencer and would like to improve their downstream variant analysis, interpretation and reporting.
Let us help you optimize your NGS analysis pipeline. Our services team is here to answer your questions and help you get from sample to final report in less time, for less money, with our NGS workflows and sample to data insight solutions.
