Our goal is to enable
the analysis of anything,
by anyone, anywhere.
Clinical research and sequencing
“We're in the midst of a genomic revolution” Gavin Arno, University College London
Q20+ chemistry for raw read accuracy of 99% and higher
Highest accuracy provided by Kit V14 and R10.4.1 pore combination • Duplex-enabled for Q30+ accuracy • Solutions optimised for yield, speed, multiplexing and more.Understanding the drivers of oncogenesis
This case study highlights how a wide range of tumour-specific variation that can be captured within a single nanopore sequencing assay — from complex structural variants to epigenetic modifications.Oxford Nanopore technology update
Hear about the latest technology performance and innovations in the pipeline.Accelerating cancer research through comprehensive genomic analysis
Learn how nanopore technology can accurately resolve complex structural variants to provide new insight into the mechanisms of health and disease.- PromethION 2 devices offer flexible, high-yield nanopore sequencing, in a compact, accessible design utilising flow cells that generate hundreds of gigabases.
Oxford Nanopore at ASHG 2023
Join us for on-booth product demonstrations, Data for Breakfast, and our Industry Education Session which will showcase how nanopore technology can resolve even the most complex genetic variation.Workflow: Tumour-normal
Here we present an end-to-end workflow to detect somatic variation between tumour-normal paired research samples.NCM 2023 Houston: buy 3 tickets, get 1 free
If you're looking to attend the Nanopore Community Meeting with colleagues you can now purchase three tickets and get one ticket free.- “This was almost a year of clinical testing, and it took about 24 hours to figure this out in our lab.”Danny Miller, University of Washington, US
Accelerating cancer research through comprehensive genomic analysis
Discover the unique attributes of nanopore sequencing that are enabling researchers to characterise cancer at unprecedented resolution, unlocking previously hidden variation and accelerating research.- “…structural variant calls were highly accurate and complete, showing improvement over the current short-read and long-read methods.”Mikhail Kolmogorov et al., NIH
Q20+ chemistry for raw read accuracy of 99% and higher
Highest accuracy provided by Kit V14 and R10.4.1 pore combination • Duplex-enabled for Q30+ accuracy • Solutions optimised for yield, speed, multiplexing and more.Understanding the drivers of oncogenesis
This case study highlights how a wide range of tumour-specific variation that can be captured within a single nanopore sequencing assay — from complex structural variants to epigenetic modifications.Oxford Nanopore technology update
Hear about the latest technology performance and innovations in the pipeline.Accelerating cancer research through comprehensive genomic analysis
Learn how nanopore technology can accurately resolve complex structural variants to provide new insight into the mechanisms of health and disease.- PromethION 2 devices offer flexible, high-yield nanopore sequencing, in a compact, accessible design utilising flow cells that generate hundreds of gigabases.
Oxford Nanopore at ASHG 2023
Join us for on-booth product demonstrations, Data for Breakfast, and our Industry Education Session which will showcase how nanopore technology can resolve even the most complex genetic variation.Workflow: Tumour-normal
Here we present an end-to-end workflow to detect somatic variation between tumour-normal paired research samples.NCM 2023 Houston: buy 3 tickets, get 1 free
If you're looking to attend the Nanopore Community Meeting with colleagues you can now purchase three tickets and get one ticket free.- “This was almost a year of clinical testing, and it took about 24 hours to figure this out in our lab.”Danny Miller, University of Washington, US
Accelerating cancer research through comprehensive genomic analysis
Discover the unique attributes of nanopore sequencing that are enabling researchers to characterise cancer at unprecedented resolution, unlocking previously hidden variation and accelerating research.- “…structural variant calls were highly accurate and complete, showing improvement over the current short-read and long-read methods.”Mikhail Kolmogorov et al., NIH
Q20+ chemistry for raw read accuracy of 99% and higher
Highest accuracy provided by Kit V14 and R10.4.1 pore combination • Duplex-enabled for Q30+ accuracy • Solutions optimised for yield, speed, multiplexing and more.Understanding the drivers of oncogenesis
This case study highlights how a wide range of tumour-specific variation that can be captured within a single nanopore sequencing assay — from complex structural variants to epigenetic modifications.Oxford Nanopore technology update
Hear about the latest technology performance and innovations in the pipeline.Accelerating cancer research through comprehensive genomic analysis
Learn how nanopore technology can accurately resolve complex structural variants to provide new insight into the mechanisms of health and disease.- PromethION 2 devices offer flexible, high-yield nanopore sequencing, in a compact, accessible design utilising flow cells that generate hundreds of gigabases.
Oxford Nanopore at ASHG 2023
Join us for on-booth product demonstrations, Data for Breakfast, and our Industry Education Session which will showcase how nanopore technology can resolve even the most complex genetic variation.Workflow: Tumour-normal
Here we present an end-to-end workflow to detect somatic variation between tumour-normal paired research samples.NCM 2023 Houston: buy 3 tickets, get 1 free
If you're looking to attend the Nanopore Community Meeting with colleagues you can now purchase three tickets and get one ticket free.- “This was almost a year of clinical testing, and it took about 24 hours to figure this out in our lab.”Danny Miller, University of Washington, US
Accelerating cancer research through comprehensive genomic analysis
Discover the unique attributes of nanopore sequencing that are enabling researchers to characterise cancer at unprecedented resolution, unlocking previously hidden variation and accelerating research.- “…structural variant calls were highly accurate and complete, showing improvement over the current short-read and long-read methods.”Mikhail Kolmogorov et al., NIH
Nanopore sequencing is the only technology that offers scientific researchers…
Full biology
A new generation of molecular sensing technology
Only nanopore sequencing offers portable to ultra-high throughput scalability with real-time data delivery and the ability to reveal accurate, rich biological data through the analysis of short to ultra-long fragments of native DNA or RNA.
Use of the technology
The platform is used by scientific researchers to solve real-world challenges through answering questions about the biology of people, plants, animals, pathogens and environments. It is also increasingly being used in ‘applied’ settings such as healthcare and food safety.
Find out moreEnvironmental
How is the microbial composition of this river changing? What is this species? Is it endangered? What can we understand about the biodiversity within this area?
Learn morePathogens & Microbiology
What is this virus / bacteria / fungus? What makes it pathogenic? Is it resistant to antimicrobial drugs? How could we use this information to prevent or treat the disease that it causes?
Learn moreWhole genome sequencing
Generate and complete microbial, human, animal, and plant genome assemblies with long nanopore sequencing reads (reads in excess of 4 Mb have been demonstrated).
Learn moreCancer research
What are the genetic changes that are causing this cancer, and the mechanism of those changes in broader cell pathways? Can knowledge of these changes influence choices on treatment? Can new therapeutics be developed as a result of this knowledge?
Learn moreClinical research
How can we use sequence data to personalise medicine? How can we integrate sequence data into clinical decision making? How does a person’s genome influence how they may respond to a disease or an infection?
Learn more