Ask bolder questions.
Make no compromises.
What you’re missing matters.
Any-length sequencing. Ultra-rich datasets. Real-time insights. You'll never see sequencing the same way again.

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Oxford Nanopore meets Apple’s M3 silicon chip

Apple showcased Oxford Nanopore at its M3 silicon chip launch event — highlighting how it increases access to powerful compute and makes it easier for anyone, anywhere to use nanopore sequencing.
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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.
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Capturing global genomic diversity in the human pangenome with long

This case study outlines how PromethION was used to sequence 47 genomes from diverse backgrounds contributing to the first draft of the human pangenome.
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Oxford Nanopore technology update

Hear about the latest technology performance and innovations in the pipeline.
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What you're missing matters

Find out how you can generate ultra-rich data for answers with impact.
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A guide to investigating methylation in the human genome

Discover how nanopore sequencing provides unbiased and unprecedented resolution to study base modifications in the human genome.
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PromethION 2 | PromethION 2 Solo
PromethION 2 devices offer flexible, high-yield nanopore sequencing, in a compact, accessible design utilising flow cells that generate hundreds of gigabases.
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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.
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Characterising methylation markers in imprinting disorders

Learn how nanopore long reads can assess methylation status in imprinting disorders, and provide greater resolution of epigenetic changes across the genome.
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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.
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“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
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Workflow: large cohort sequencing

Here we present an end-to-end workflow for genome-wide analysis of genomic and epigenomic variants across a large cohort of human clinical research samples.
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“…structural variant calls were highly accurate and complete, showing improvement over the current short-read and long-read methods.”
Mikhail Kolmogorov et al., NIH
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Advancing human genomics with nanopore sequencing

Learn how researchers are utilising nanopore technology, including whole genome, targeted, & RNA sequencing to provide unprecedented insight into human genetic diversity.
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Offering short to ultra-long native DNA and RNA reads,
only nanopore sequencing delivers…

Richer insights: Highly-accurate genomic data captures more types of genetic variation

Faster results from near-sample, real-time workflows that don’t require batching

Accessible and affordable, with scalability that enables more use cases

A new generation of molecular sensing technology

Explore the nanopore portfolio of flow cells, compatible devices, manual and automated library prep, and data analysis solutions.

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Prepare

your library

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Preparation vials
Preparation kits
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Sequence

with flow cells & devices

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Nanopore sequencing devices
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Analyse

your data

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GridION data analysis

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.

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Environmental

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?

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Pathogens & 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?

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Whole 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).

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Cancer 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?

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Clinical 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?

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