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Roche Sequencing & Life Science

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. We offer sample prep solutions for different sample types and sequencing applications that are proven, simple, and complete.

lab technician evaluate library prep samples

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

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Target Enrichment

Discover robust new products for 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 Roche Target Enrichment portfolio offers solutions for:

  • Human whole-exome sequencing (WES)
  • Custom-designed panels for human or nonhuman genomic regions
  • Combine the performance of hybrid-capture target enrichment with the speed and simplicity of amplicon workflows, with KAPA HyperPETE
  • Explore target enrichment technologies with our selection guide

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AVENIO Edge System

NGS Automation Solutions

Maximize the potential of your lab with a trusted NGS partner


Roche offers automated solutions across the entire next-generation sequencing (NGS) sample prep workflow, including DNA and RNA library preparation, target enrichment, and library quantification. Automation of NGS sample prep can help your lab generate more reproducible results, increase operational efficiency, and unlock more hands-off time and resources for collaborations and innovations. 

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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.

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For Research Use Only. Not for use in diagnostic procedures.