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ALL PRODUCTS

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CONSUMABLES

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SERVICES

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Products MinIONGridIONPromethION 2 & 2 SoloPromethION 24 &
48FlongleVolTRAXQ-Line


CONSUMABLES

Flow cellsManual & automated library prep


SERVICES

CertificationTrainingDevice warranty
Applications

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.

Learn about applications


RESEARCH AREAS

 * Microbiology
 * Human genetics
 * Microbiome
 * Clinical research
 * Cancer
 * Plant
 * Transcriptome
 * Animal
 * Population genomics
 * COVID-19
 * Environmental research & conservation
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INVESTIGATIONS

 * Structural variation
 * SNVs and phasing
 * Gene expression
 * Identification
 * Splice variation
 * Assembly
 * Fusion transcripts
 * Epigenetics
 * Single cell
 * Chromatin conformation


TECHNIQUES

 * Whole genome
 * Targeted
 * Whole transcriptome
 * Metagenomics
 * Short fragment mode

Applications


RESEARCH AREAS

MicrobiologyHuman geneticsMicrobiomeClinical
researchCancerPlantTranscriptomeAnimalPopulation genomicsCOVID-19Environmental
research & conservationInfectious disease


INVESTIGATIONS

Structural variationSNVs and phasingGene expressionIdentificationSplice
variationAssemblyFusion transcriptsEpigeneticsSingle cellChromatin conformation


TECHNIQUES

Whole genomeTargetedWhole transcriptomeMetagenomicsShort fragment modeView all
Applications
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SUPPORT & DOCUMENTATION

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LEARNING

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SUPPORT & DOCUMENTATION

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protocolsExtraction protocols


LEARNING

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analysis
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About


ABOUT

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historySustainabilityCareersMedia resources


NEWS & EVENTS

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GLOBAL PARTNERS

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LONDON CALLING 2023

17th - 19th May
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Our goal is to enable
the analysis of anything,
by anyone, anywhere.

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CANCER RESEARCH AND SEQUENCING

> “Without nanopore sequencing, our work wouldn’t be possible” Alberto Magi,
> University of Florence, Italy

Learn more


 1.  Q20+ CHEMISTRY FOR RAW READ ACCURACY OF 99% AND HIGHER
     
     
     HIGHEST ACCURACY PROVIDED BY KIT V14 AND R10.4.1 PORE COMBINATION •
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     MULTIPLEXING AND MORE
     
     Find out more
 2.  > “Using nanopore sequencing data, we generated base level maps of the most
     > complete human methylome ever produced”
     > Ariel Gershman, Johns Hopkins University
     
     Read the publication


 3.  PROMETHION 2 DEVICES OFFER FLEXIBLE, HIGH-YIELD NANOPORE SEQUENCING, IN A
     COMPACT, ACCESSIBLE DESIGN UTILISING FLOW CELLS THAT GENERATE HUNDREDS OF
     GIGABASES.
     
     Find out more
 4.  > “Long reads improve genomic assemblies by spanning repetitive regions and
     > structural variation within the genome”
     > Trent Prall, University of Wisconsin
     
     Read the publication
 5.  > “Targeted long-read sequencing … allowed us to simultaneously assay
     > repeat length, sequence content, and methylation”
     > Danny Miller, University of Washington, US
     
     Read the publication


 6.  NANOPORE COMMUNITY MEETING
     
     
     EVENT CONTENT NOW AVAILABLE TO WATCH ON DEMAND
     
     Find out more
 7.  > “We identified over 22,636 SVs per individual, three to five times more
     > than those found in short-read sequencing data”
     > Doruk Beyter, deCODE genetics
     
     Read the publication


 8.  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
     
     Find out more
 9.  > “Using nanopore sequencing data, we generated base level maps of the most
     > complete human methylome ever produced”
     > Ariel Gershman, Johns Hopkins University
     
     Read the publication


 10. PROMETHION 2 DEVICES OFFER FLEXIBLE, HIGH-YIELD NANOPORE SEQUENCING, IN A
     COMPACT, ACCESSIBLE DESIGN UTILISING FLOW CELLS THAT GENERATE HUNDREDS OF
     GIGABASES.
     
     Find out more
 11. > “Long reads improve genomic assemblies by spanning repetitive regions and
     > structural variation within the genome”
     > Trent Prall, University of Wisconsin
     
     Read the publication
 12. > “Targeted long-read sequencing … allowed us to simultaneously assay
     > repeat length, sequence content, and methylation”
     > Danny Miller, University of Washington, US
     
     Read the publication


 13. NANOPORE COMMUNITY MEETING
     
     
     EVENT CONTENT NOW AVAILABLE TO WATCH ON DEMAND
     
     Find out more
 14. > “We identified over 22,636 SVs per individual, three to five times more
     > than those found in short-read sequencing data”
     > Doruk Beyter, deCODE genetics
     
     Read the publication


 15. 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
     
     Find out more
 16. > “Using nanopore sequencing data, we generated base level maps of the most
     > complete human methylome ever produced”
     > Ariel Gershman, Johns Hopkins University
     
     Read the publication


 17. PROMETHION 2 DEVICES OFFER FLEXIBLE, HIGH-YIELD NANOPORE SEQUENCING, IN A
     COMPACT, ACCESSIBLE DESIGN UTILISING FLOW CELLS THAT GENERATE HUNDREDS OF
     GIGABASES.
     
     Find out more
 18. > “Long reads improve genomic assemblies by spanning repetitive regions and
     > structural variation within the genome”
     > Trent Prall, University of Wisconsin
     
     Read the publication
 19. > “Targeted long-read sequencing … allowed us to simultaneously assay
     > repeat length, sequence content, and methylation”
     > Danny Miller, University of Washington, US
     
     Read the publication


 20. NANOPORE COMMUNITY MEETING
     
     
     EVENT CONTENT NOW AVAILABLE TO WATCH ON DEMAND
     
     Find out more
 21. > “We identified over 22,636 SVs per individual, three to five times more
     > than those found in short-read sequencing data”
     > Doruk Beyter, deCODE genetics
     
     Read the publication

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NANOPORE SEQUENCING IS THE ONLY TECHNOLOGY THAT OFFERS SCIENTIFIC RESEARCHERS…

Sequence any DNA/RNA fragment length from short to ultra-long
Sequencing yield scalable to fit your needs, up to 14Tb
Analysis data available in real time
Simple & rapid, or automated workflows
No capital investment required


FULL BIOLOGY

SNP & INDEL
Methylation
Structural Variation
Phasing
Assembly

Find out more


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.


SEQUENCING
DEVICES

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FLOW CELLS

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MANUAL &
AUTOMATED
LIBRARY PREP

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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 more


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?

Learn more


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?

Learn more


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).

Learn more


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?

Learn more


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?

Learn more
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Nanopore technology
   
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About Oxford Nanopore
   
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 * Working at Oxford Nanopore
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Contact us
   
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 * New York (NY), USA
 * Lexington (MA), USA
 * San Francisco (CA), USA
 * Shanghai, China
 * Tokyo, Japan
 * Singapore, Singapore
   

Getting started
   
 * Buy a MinION starter pack
 * Nanopore store
 * Sequencing service providers
 * Global distributors
 * Japanese dealers
   

Nanopore technology
   
 * Subscribe to Nanopore updates
 * Resources and publications
 * What is the Nanopore Community
   

About Oxford Nanopore
   
 * News
 * Company timeline
 * Sustainability
 * Leadership team
 * Media resources & contacts
 * For investors
 * For partners
 * Working at Oxford Nanopore
 * Current vacancies
   

Contact us
   
 * Oxford (Head Office), UK
 * Cambridge, UK
 * Harwell, UK
 * New York (NY), USA
 * Lexington (MA), USA
 * San Francisco (CA), USA
 * Shanghai, China
 * Tokyo, Japan
 * Singapore, Singapore
   


   
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