Uniform libraries, precision genotyping – DNA-seq powered by QIAseq

Reliable solutions for high-quality, complex libraries with uniform coverage

Top-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. If you’re performing whole genome and exome hybrid capture sequencing applications, our complete, all-enzymatic library prep solution, the QIAseq FX DNA Library Kit  ensures:

  • High library complexity
  • Even coverage
  • NGS-ready fragments in just 2.5 hours

Working with single cells? Our latest innovation – the REPLI-g Advanced DNA Single Cell Kit – ensures:

  • Highly uniform amplification across the entire genome
  • Negligible sequence bias
  • Suitability for use with single cells or nanograms of DNA

Detect low-frequency variants with confidence using expert panel design

Designing custom panels for your project can be difficult. Researchers can experience challenges with high GC content or low-quality DNA samples and question whether to target entire genomic regions, or just hotspots, and whether to design from scratch or boost coverage of existing content. Whether you’re targeting genes, specific exons, hotspots or genomic regions, take advantage of our QIAseq DNA panels and achieve:

  • Fail proof designs
  • Accurate results
  • Reliable detection of low-frequency variants with QIAGEN’s Unique Molecular Index (UMI) and Single Primer Extension (SPE) technologies

Visit us at ASHG 2018, booth #1339

Register for a demo
Social Sharing