Next-Generation Sequencing (NGS) Solutions

Next-generation sequencing (NGS) is driving advances in translational and clinical research. From expanding our understanding of cancer, reproductive and developmental biology to unravelling complex microbial populations, NGS is touching all facets of human disease and well­being.

Sample prep for NGS holds the key to unlocking the potential of every sample. Explore our integrated Roche Sample Preparation Solutions, encompassing all the steps required to convert a sample to a sequencing-ready library. From sample collection to library quantification, we offer sample prep solutions for different sample types and sequencing applications that are proven, simple, and complete.

Integrated Next-Generation Sequencing Workflow

Integrated Next-Generation Sequencing Workflow

Library Preparation

Explore KAPA NGS library preparation kits for the highest-quality sequencing libraries, for use on lllumina sequencing platforms. Every kit leverages high-quality enzymes selected through our directed evolution technology, and is formulated in convenient, easy-to-use master mixes. Use KAPA library preparation kits for:

  • RNA-seq libraries, including rRNA depletion, mRNA enrichment, and custom depletion
  • DNA sequencing libraries, with options for enzymatic or manual DNA fragmentation
  • Challenging, degraded RNA or DNA samples

Target Enrichment

Discover robust new products for hybridization-based target capture, with streamlined workflows that focus sequencing resources on regions of interest. Increase efficiency and depth of targeted resequencing for human genetic disease and cancer research, as well as other applications. The KAPA Target Enrichment portfolio offers solutions for:

  • Human whole-exome sequencing (WES)
  • Custom-designed panels for human or nonhuman genomic regions
  • Monitor SARS-CoV-2, including new variants, by targeting 100% of the viral genome with NEW KAPA SARS-CoV-2 Target Enrichment Panel
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Target Enrichment
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Oncology Assays

Explore the AVENIO family of NGS oncology assays comprising three ctDNA and three corresponding tumor tissue assays with matched panel content for comprehensive genomic profiling, longitudinal monitoring and concordance analysis of solid tumors from tissue and plasma samples. Detect alll four mutation classes (SNVs, indels, fusions, and CNVs) in a single DNA workflow.

Featured Application Areas

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How to Order

Register or log in to purchase KAPA NGS, PCR, and qPCR products online. Our online option includes custom quotes and pricing specific to your account, a quick order form for rapid and efficient order submission, and personalized promotions and content.

AVENIO, KAPA, and MILLISECT are trademarks of Roche.. All other product names and trademarks are the property of their respective owners.

Research Use Only. Not for use in diagnostic procedures.