KAPA HyperPlus Kits, our most advanced library preparation option, provide a streamlined workflow that includes fully automatable fragmentation and library preparation in a single tube. This kit is based on our DNA Hyper portfolio which offers  industry-leading library construction efficiencies. This integrated solution combines enzymatic fragmentation, similar in quality to mechanical shearing, with the speed and convenience of tagmentation-based workflows.

KAPA HyperPlus Kits offer a complete library preparation solution with KAPA Adapters and KAPA HyperPure Beads (sold separately). The kits are compatible with the Illumina sequencing platform and provide qualified automation methods.

Features and Benefits of KAPA HyperPlus Kits

• Fully automatable DNA library construction in 1.5–3 hours with low-bias enzymatic fragmentation

• Industry-leading conversion rates and library complexity,* particularly for FFPE DNA

• Now includes an additional End Repair and A-Tailing module for more sensitive applications with no change to the workflow

• PCR-free workflows from lower inputs and improved sequence coverage in workflows with PCR

• Compatibility with a wide range of sample types and inputs, and flexibility with respect to fragment size, adapter design and library amplification 

Product Highlights

Industry-leading library construction yields* with integrated workflow

  •  Low-input samples no longer require specialist library construction workflows or reagents
  •  PCR-free workflows possible from as little as 50 ng starting material
  •  Both the existing and upgraded KAPA HyperPlus chemistry produce the highest post-ligation yields

Validated with the HyperCap Workflow v2.0

 

Tunable and low-bias enzymatic fragmentation

  • Library insert sizes adjustable from 150–800 bp by varying fragmentation time or temperature
  • Robust and reproducible fragmentation across a range of GC content and DNA input amounts and sample types

Superior sequencing results with KAPA HyperPlus Kits

  • Higher post-ligation yields result in fewer amplification cycles and lower duplication rates
  •  Detect low-frequency mutations with high confidence due to decreased sequencing artifacts and increased sensitivity with the upgraded version of the KAPA HyperPlus Kit

Improved coverage depth for FFPE samples compared to Covaris-sheared DNA

  • Significant increase in coverage depth compared to KAPA HyperPrep Kits using Covaris-sheared DNA
  • Lower duplication rates, more on-target reads and more bases covered compared to KAPA HyperPrep Kits using Covaris-sheared DNA
  • Detection of variants with high degree of correlation between libraries prepared from KAPA HyperPrep Kits using  Covaris-sheared DNA versus HyperPlus Kits*

Minimal sequence coverage bias

  • Lower sequence bias when compared other enzymatic fragmentation methods
  • Less bias leads to more uniform sequencing coverage and reduced sequencing costs

Featured Webinar

NGS library preparation: Theory and practice
Part 3: A practical example—Library preparation with the KAPA HyperPlus Kit

Presenter: Dr. Maryke Appel, Roche

Watch Now

*Data on file.