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.
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
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
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. .
Whole-genome sequencing (WGS) provides access to the wealth of information
inside every human DNA sample. Learn more about the fully integrated Roche Sequencing NGS Workflow—from automated DNA extraction through accurate
Start the RNA-seq process off the right way by making high-quality libraries through the streamlined, single-day workflow of the KAPA RNA HyperPrep Kits and achieve robust performance across different sample types and low-input amounts, including
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