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Oxford Nanopore DNA and RNA Sequencing Devices

Sequencing platforms

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Nanopore sequencing offers advantages in all areas of research. Our offering includes DNA sequencing, as well as RNA and gene expression analysis and future technology for analysing proteins.

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Choose nanopore sequencing for:

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  • Sequencing any DNA/RNA fragment length from short to ultra-long
  • Direct sequencing of native DNA/RNA
  • Availability of data in real time
  • Simple & rapid, or automated, library prep
  • No capital investment
  • Portable devices to ultra-high throughput desktop devices

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MinION Mk1C. Fully integrated, portable sequencing and analysis.

Combining the real-time, rapid, portable sequencing of MinION with powerful computing and a high-resolution screen.

The complete, go-anywhere solution for long-read DNA and RNA sequencing and analysis.

Looking for flow cells, sample kits and consumables?

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Sequence and analyse

MinION device
Research use

From $1,000

The only portable, real-time devices for DNA and RNA sequencing, putting you in control of your sequence data. Access to sequencing for $1,000. Sequence immediately, not wait. Sequence outside a lab. Up to 50 Gb per 72 hrs*. Avoid CapEx investments.

Why choose MinION?

  • Pocket-sized, portable device for biological analysis
  • Up to 512 nanopore channels
  • Simple 10-min sample prep available
  • Real-time analysis for rapid, efficient workflows
  • Adaptable to direct DNA or RNA sequencing
  • MinIT available to support IT/software needs
GridION device
Research use Q-Line IVD Testing

From $49,955

Compact benchtop device designed to run and analyse up to five Flongle or MinION Flow Cells. Scale up from MinION. Offer nanopore sequencing as a service. Choice to invest from a capital or consumable budget.

Why choose GridION?

  • Run up to five independently addressable Flongle or MinION Flow Cells
  • As much as 250 Gb of data* — streamed in real time for immediate analysis
  • Powerful onboard data processing and analysis, minimising IT requirements
  • Small footprint, suitable for any lab
  • Pay just for consumables
PromethION device
Research use

From $195,455

Large-scale, long-read, direct DNA and RNA sequencing. Offer nanopore sequencing as a service. Very large data volumes projects (Tb). On-demand sequencing for large numbers of samples. Avoid CapEx investments.

Why choose PromethION?

  • Run up to 48 independently addressable, high-capacity PromethION Flow Cells
  • Generate terabases of data — streamed in real time for immediate analysis
  • Alleviate data analysis bottlenecks
  • Generate sub-$1,000 human genomes
  • Pay just for consumables
Research use
Flongle device

From $1,460

Flongle is an adapter for MinION or GridION that enables direct, real-time DNA sequencing, or cDNA sequencing on smaller, single-use flow cells.

Why choose Flongle?

  • Costing just $90 per flow cell, Flongle is the quickest, most accessible solution for smaller tests and experiments.
  • Immediate access to data for rapid, actionable results.
  • Rapidly assess sample quality prior to starting a larger sequencing experiment.
  • Run single samples on demand instead of multiplexing.

* Theoretical max output when system is run for 72 hours at 420 bases / second. Outputs may vary according to library type, run conditions, etc.

Nanopore analysis

From the moment data acquisition begins, analysis can be performed in real time. Find out more about analysis solutions for nanopore sequencing data.

Learn more

Prepare

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Research use
VolTRAX

From $8,150

Automatic library preparation: VolTRAX is designed as an alternative to a range of lab equipment, enabling the preparation of your biological samples, ready for analysis, hands-free.

Why choose VolTRAX?

  • Only minutes of hands-on time, even for novel/complex experiments
  • Take sample prep out of the lab
  • Develop own sample and library prep methods, including fluorescence detection and incubations
  • Select your protocol, load, and leave
A Whole genome sequencing kit

Whole genome sequencing kits

Conduct long-read sequencing of native DNA, eliminating the potential for PCR bias and allowing the detection of base modifications alongside nucleotide sequence. More
A Targeted DNA sequencing kit

Targeted DNA sequencing kits

Cost-effective, assembly-free analysis of repetitive regions, structural variants, and variant phasing across entire genes or large genomic regions of interest. More
An RNA sequencing kit

RNA sequencing kits

Confidently characterise and quantify full-length RNA transcripts, splice variants, and fusions using long-read nanopore sequencing. More
A barcoding kit

Barcoding kits

Run multiple DNA or RNA samples on a single flow cell. Buy either as dedicated kits, or to enhance your existing sequencing kit. More
An expansion pack

Expansion packs

A range of add-on packs to enhance your existing native or amplification-based nanopore sequencing kits. More

Protocol builder

Optimise your complete nanopore sequencing workflow – from extraction to analysis.

Learn more

Flow cells

Flongle with flow cell and MinION

Flongle flow cells

Flow cells designed for smaller, frequent, rapid tests and analyses. More
PromethION Flow cells

PromethION flow cells

Up to 3,000 nanopore channels for DNA or RNA sequencing in real time. More
MinION and GridION Flow cells

MinION & Gridion flow cells

Up to 512 nanopore channels for DNA or RNA sequencing in real time. More
VolTRAX Flow cell

VolTRAX Cartridges

Liquids move around the cartridge in a software programmed path, performing reactions in sequence. More

In development

Learn about nanopore technology
SmidgION
  • Designed to be our smallest sequencing device so far
  • Same nanopore sensing technology as MinION and PromethION
  • Designed for use with a smartphone in any location
Learn more
Plongle
  • High-throughput, real-time, long-read sequencing for smaller tests or experiments
  • Cost-efficient, 96-well plate format
  • Compatible with high-throughput automation
Learn more

Recommended for you

Cas9-Assisted Targeting of CHromosome segments (CATCH) for targeted nanopore sequencing and optical genome mapping Publication 1st Jan 2020

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