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the analysis of anything,
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Cancer research and sequencing

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

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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.
Find out more
London Calling 2023: Technology update
Hear about breakthrough technology performance and our pathway to enabling sequencing by anyone, anywhere.
Watch on demand
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
Genomics England long-read cancer whole-genome sequencing pilot
Helen Webb discussed the impact of identifying the correct variants in a fast, scalable, and cost-efficient manner, and how we can translate this research into clinical settings.
Watch on demand
“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
Watch on demand
London Calling 2023
Catch up on all the talks from this year's London Calling.
Watch on demand
“…structural variant calls were highly accurate and complete, showing improvement over the current short-read and long-read methods”
Mikhail Kolmogorov et al., NIH
Read the publication
Uncover the environmental microbial world
Unlocking the microbiome of the International Space Station, detecting previously undetected parasitising elements & borg extrachromosomal genomes were all discussed at London Calling 2023.
Watch on demand
Data analysis tools: methylation & phasing
Hear how the four researchers shared the latest tools being developed for the analysis of DNA methylation genome-wide and for methylation-based haplotype phasing at London Calling 2023
Watch on demand
“We can detect SNPs with an F1 score better than [short reads]…& can discover structural variants with an F1 score comparable to state-of-the-art methods...but obviously with a lower cost.”
Kimberley Billingsley, NIH Center for Alzheimer's and Related Dementias
Watch on demand
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
London Calling 2023: Technology update
Hear about breakthrough technology performance and our pathway to enabling sequencing by anyone, anywhere.
Watch on demand
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
Genomics England long-read cancer whole-genome sequencing pilot
Helen Webb discussed the impact of identifying the correct variants in a fast, scalable, and cost-efficient manner, and how we can translate this research into clinical settings.
Watch on demand
“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
Watch on demand
London Calling 2023
Catch up on all the talks from this year's London Calling.
Watch on demand
“…structural variant calls were highly accurate and complete, showing improvement over the current short-read and long-read methods”
Mikhail Kolmogorov et al., NIH
Read the publication
Uncover the environmental microbial world
Unlocking the microbiome of the International Space Station, detecting previously undetected parasitising elements & borg extrachromosomal genomes were all discussed at London Calling 2023.
Watch on demand
Data analysis tools: methylation & phasing
Hear how the four researchers shared the latest tools being developed for the analysis of DNA methylation genome-wide and for methylation-based haplotype phasing at London Calling 2023
Watch on demand
“We can detect SNPs with an F1 score better than [short reads]…& can discover structural variants with an F1 score comparable to state-of-the-art methods...but obviously with a lower cost.”
Kimberley Billingsley, NIH Center for Alzheimer's and Related Dementias
Watch on demand
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
London Calling 2023: Technology update
Hear about breakthrough technology performance and our pathway to enabling sequencing by anyone, anywhere.
Watch on demand
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
Genomics England long-read cancer whole-genome sequencing pilot
Helen Webb discussed the impact of identifying the correct variants in a fast, scalable, and cost-efficient manner, and how we can translate this research into clinical settings.
Watch on demand
“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
Watch on demand
London Calling 2023
Catch up on all the talks from this year's London Calling.
Watch on demand
“…structural variant calls were highly accurate and complete, showing improvement over the current short-read and long-read methods”
Mikhail Kolmogorov et al., NIH
Read the publication
Uncover the environmental microbial world
Unlocking the microbiome of the International Space Station, detecting previously undetected parasitising elements & borg extrachromosomal genomes were all discussed at London Calling 2023.
Watch on demand
Data analysis tools: methylation & phasing
Hear how the four researchers shared the latest tools being developed for the analysis of DNA methylation genome-wide and for methylation-based haplotype phasing at London Calling 2023
Watch on demand
“We can detect SNPs with an F1 score better than [short reads]…& can discover structural variants with an F1 score comparable to state-of-the-art methods...but obviously with a lower cost.”
Kimberley Billingsley, NIH Center for Alzheimer's and Related Dementias
Watch on demand

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Nanopore sequencing is the only technology that offers scientific researchers…

Sequencing of 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

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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.

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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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London Calling 2023

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Cancer research and sequencing

Q20+ chemistry for raw read accuracy of 99% and higher

London Calling 2023: Technology update

Nanopore sequencing is the only technology that offers scientific researchers…

Full biology

A new generation of molecular sensing technology

Sequencing devices

Flow cells

Manual & automated library prep

Use of the technology

Environmental

Pathogens & Microbiology

Whole genome sequencing

Cancer research

Clinical research

Sequencing
devices

Manual &
automated
library prep