Prepare
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Fast-track your workflows with library prep in minutes
Whether you are studying the human genome, investigating the microbiome, or exploring the diversity of life on Earth, our library prep solutions provide a fast, streamlined, and scalable way to generate rich Oxford Nanopore sequencing data.
Simplify your library prep
- Amplification-free — sequence native DNA or RNA to reveal more biology, with built-in gold-standard methylation detection
- Any fragment length — generate short to ultra-long reads (20 bp to >4 Mb) for comprehensive insights
- Streamlined protocols — prepare sequencing libraries in as little as 10 minutes, with low-input options and minimal hands-on time
- Scale to your needs — easy to automate on a range of automation systems
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Find your library prep kit
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DNA kits
Unlock genetic and epigenetic insights with Oxford Nanopore DNA sequencing.
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RNA kits
Revolutionise your RNA research with full-length sequencing of native RNA or cDNA.
Automation made simple
Automating library preparation improves consistency, supports standardised workflows, and increases sample throughput for medium- and large-scale projects. Protocols are available for a range of automation systems.
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End-to-end workflows
Simplify every step of your experiment, from sample to answer, with our end-to-end workflows.
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Sample extraction protocols
Access recommended extraction protocols for a range of sample types.
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Explore accuracy
Learn more about our platform performance and accuracy, including built-in gold-standard methylation detection.
Sample and library prep masterclasses
Sequencing and analysis solutions
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Choose your sequencing device
From palm-sized to production-scale, there’s an Oxford Nanopore sequencing device to suit you.
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Analyse your data
Easy-to-use analysis tools to help you turn data into insights.
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