Next-Generation Sequencing

Accelerate integrated insights from NGS data with maximum ease

You’ve run your benchtop experiment and finally achieved NGS data. But what does it all mean? No matter what your research application, translating complex NGS data into meaningful insights can be complicated. Data analysis and interpretation are critical both to understanding your experimental results and planning your next steps. QIAGEN offers multiple best-in-class bioinformatics solutions to help uncover integrated insights faster and with minimal effort.

  • Biologist-friendly: No specialist knowledge of bioinformatics, computers or scripting needed. Analyze and interpret your data using our graphically-driven software tools, with results presented in viewers that make sense to molecular biologists
  • Optimized: Software solutions built with a deep understanding of the wet-lab chemistry used to power today’s DNA-seq and RNA-seq experiments and optimized to take advantage of the latest biotechnology approaches
  • Content-rich: Informatics tools that take advantage of the life science industry’s most comprehensive and up-to-date databases of curated biological content
Experimental design

Empower your journey of discovery with GeneGlobe – your resource for design and customization of NGS experiments. Seamlessly navigate knowledge, products and analyses relevant to your research.

Integrated insights solutions for targeted NGS

Make the leap from generating data to accumulating insights with greater ease and speed with our integrated, single-kit solution! Our QIAseq DNA Panels include subscription licenses for intuitive bioinformatics software.

Scientist in front of two computer sreens
Think outside the box
Think outside the box – discover QIAGEN Digital Insights

Learn how our intuitive, user-friendly bioinformatics solutions can deliver impactful insights from your data.


Learn what our customers are saying about our QIAseq DNA panels and our bioinformatics solutions for analysis and interpretation of NGS data.

Fast and easy sequencing data interpretation.

Anna Stittrich, Primary Investigator, Charité Universitätsmedizin Berlin

QCI-I saves a significant amount of time, especially for panels without common pathogenic variants.

Dr. Ansreas Rump, Institute for Clinical Genetics at Technical University Dresden
The CLC Genomics software is easy to learn and use. No need to have an extensive knowledge of computer languages to be able to analyze NGS data.
Primary Investigator, Federal Government
Dr. Fergus J Couch
"For researchers to be able to analyze very large numbers of samples at the same time, we needed a strategy which was high-throughput and cost-effective. We are running 800 samples a week in batch mode and analyzing them across 38 genes, all with the help of the QIAseq panels."

Dr. Fergus Couch, Mayo Clinic