Library preparation to sequence any fragment length
Whether you are studying the human genome, investigating the microbiome, or exploring the diversity of life on earth, Oxford Nanopore library preparation solutions offer a flexible, cost-effective, and streamlined way to generate high-quality sequencing data.
Comprehensive library preparation solutions for genomic analysis
Oxford Nanopore library preparation solutions are tailored to specific research needs, from whole-genome to targeted sequencing and beyond. They are compatible with all nanopore sequencing devices, giving you the flexibility to select the most suitable solution for your experiment. Find out more about our library preparation options and how they can help you accelerate your research.
DNA and RNA library preparation
- From 20 bases to 4 Mb+
- Prep in just 10 minutes
- Base modifications preserved*
*when sequencing native DNA
- The only direct RNA sequencing technology
- Full-length RNA and cDNA transcripts
- Base modifications preserved*
*when sequencing native RNA
High-quality library prep: the foundation for your discoveries
Native: library preparation solution for direct sequencing of the original DNA or RNA strand eliminates PCR and the possibility of GC bias, retaining all the biological information including base modifications without extra library prep or sample manipulation, reducing costs and preparation time.
Comprehensive: library preparation solutions for any DNA and RNA fragment length (from 20 bp to 4 Mb+) to access whole genomes, targeted genomes, methylomes, structural variants, full-length transcripts, and much more.
Scalable: easily scaled library preparation solutions (automatable on various liquid handlers) to meet diverse needs, ensuring consistent and reproducible results.
Versatile: library preparation solutions compatible with a wide range of sample types, including DNA, RNA, and cDNA, allowing you to generate high-quality libraries for a variety of applications.
Streamlined: simple and robust workflows enable you to prepare high-quality libraries quickly and efficiently, typically with 5 to 20 minutes of hands-on time.
High quality: library preparation solutions designed for high output and minimal bias, enabling users to obtain reliable and accurate results.
Automated library preparation
Automation of library preparation improves the overall consistency of results, supporting robust and standardised workflows, which enables increased sample throughput for medium- and large-scale projects, such as large cohort studies. Our streamlined library preparation kits are easy to automate, and protocols are available for a range of liquid handlers.
- Increase your sample throughput
- Optimise for reproducibility
- Deliver robust and standardised workflows
Streamlined and automated nanopore sequencing
Leveraging the advantages of our technology, centred around the flow cell and the compact size of our sequencers, you can automate your sequencing workflows. Our versatile automation solutions include portable and benchtop devices that are capable of sample extraction, library prep, sequencing, and even data analysis — all within a single device.
Sample-to-answer benchtop device:
Extract, prepare, sequence, analyse
TraxION (coming soon)
Sample-to-sequence portable device:
Extract, prepare, sequence