Expert panel design and uniform libraries for DNA-seq

Accelerate NGS library prep success

High-quality library preparation is fundamental to the success of your DNA-seq applications. The faster you can prepare NGS libraries, the faster you can proceed with sequencing your sample and uncovering insights that accelerate your understanding of its underlying biology.

Streamline library prep with our QIAseq FX Kits and achieve:

  • High library complexity
  • Uniform coverage across the genome
  • Negligible sequence bias
  • Superior library quality

So whether you’re working with ultralow amounts of DNA and single cells or trying to access GC-rich regions, our library prep solutions provide comprehensive genome coverage, exceptional sequence fidelity, reduced false positives and dropouts, as well as fast and easy workflows that can also be automated.

Resolve your NGS panel design dilemmas

Experiencing challenges with high GC content or low-quality DNA samples and questioning whether to target entire genomic regions or just focus on the exome? Wondering whether to design panels from scratch or boost coverage of existing content?

Our experts can help you take the fuss out of panel design – regardless of whether you’re targeting genes, specific exons, hotspots or genomic regions. QIAseq Targeted DNA catalog and custom panels enable detection of low-frequency variants with confidence by leveraging Unique Molecular Index (UMI) and Single Primer Extension (SPE) technologies for the ultimate precision. From comprehensive profiling of the immune repertoire to evaluating tumor mutational burden and microsatellite instability, our expertly designed NGS panels help you generate reliable results. For carrier screening applications, our panels include integrated bioinformatics to provide evidence-based, actionable insights, accelerating advances in hereditary disease research.

High-precision panels + intuitive, integrated bioinformatics = DNA-seq success

We’ve combined the precision of our QIAseq DNA Panels with intuitive bioinformatics tools to create a single unified solution so you can detect low-frequency variants and analyze your NGS data with confidence. QIAseq DNA panels now include subscription licenses for CLC Genomics Workbench and QIAGEN Clinical Insight (QCI)-Interpret for QIAseq software, so you can make the leap from generating data to accumulating insights with greater ease and speed. Learn more

Join us at booth 1119 to discuss your individual project requirements and find out how we can help.

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