Question everything

Get all the rich data you need from sequencing native DNA and RNA molecules in a single platform with access to all of your biology, so you can get a more complex and comprehensive view of the genetics of human disease.

What you’re missing matters

Ask bolder questions. Uncover novel biology.

With the ability to read any length of DNA or RNA, short to ultra-long, nanopore sequencing captures more genomic variation — including structural variation and methylation — so you can get the context and clarity you need, every time. This comprehensive view powers the bigger and bolder research questions you’ve always wanted to ask. And real-time data means rapid insight to time-critical results, all in a platform that sits on your lab bench.

Groundbreaking speed. Any-length sequencing reads. Rich datasets. You’ll never see sequencing the same way again.

Transcriptomic, genomic, and epigenomic data​

Multiomic approaches — spanning genomics, bulk and single-cell transcriptomics, epigenetics, and proteomics — are crucial to resolving the mechanisms underpinning human diseases. Using nanopore sequencing, you can gain genomic, transcriptomic, and epigenomic data from a single platform.

There's light at the end of the tunnel

Generate ultra-rich data for answers with impact.

Direct, amplification-free sequencing eliminates bias and supports simultaneous detection of epigenetic modifications. You get the rich data you need in a single platform with access to all of your biology for a more complex and comprehensive view of the genetics of human disease.

With direct reads see base modifications without extra sample prep. Stay on top of what's next.

Reveal more biology to transform complex disease

Characterise human genetic variation, close genomic gaps, and generate full-length RNA transcripts. Combining rich genetic data with scalable formats enables whole-genome sequencing, targeted sequencing, transcriptomics and other techniques for new insights into human health and disease.​

Every insight you can imagine, and then some.

What you're missing matters.

From 20 bases to 4,000,000 and everything in between, nanopore technology gives you the power to sequence any length fragment of DNA, capturing all the insights you need. Long nanopore sequencing reads confer the ability to identify and phase SNPs, structural variants, and epigenetic modifications, and fully characterise novel isoforms and fusion transcripts.

Take a wider lens on human genomics with technology that powers a more diverse range of experiments.

Nanopore sequencing is fully scalable

Scale to suit your needs

Nanopore sequencing is the only sequencing technology to enable real-time analysis in fully scalable formats. From the pocket-sized MinION to the high-throughput, population-scale PromethION — scale nanopore sequencing to suit any experimental needs.


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