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Webinar

Resolving vector insertion sites and cell line characterization: insights from PRINT

Watch on demand to learn how long-read sequencing is transforming vector insertion site mapping and cell-line characterization.

August 12, 2026

Publication

How ‘Sturgeon’ guides the surgeon

Authors: Mariska Sie, Oscar H.J. Eelkman Rooda, et al.

August 10, 2026

Publication

Beyond bisulfite sequencing: resolving 5-hmC with nanopore sequencing unmasks the true-5mC methylation entropy landscape

Authors: Uri Bertocchi, Eyal Katz, Jonathan Jeffet, Assaf Grunwald, Neiv Gabay, Jasline Deek, Sujal Verma, Amit Shwartz, Gali Umschweif–Nevo, Bernard Lerer, Yael Roichman, Yuval Ebenstein

August 7, 2026

Webinar

MinION Essentials: Everything you need to know about the world’s most cost-effective and accessible sequencer

Unlock the full potential of MinION with this on-demand webinar designed for researchers at every stage of their nanopore sequencing journey.

August 6, 2026

Publication

Validation of a long-read 16S rRNA-gene sequencing approach for analysis of clinical samples and bacterial identification in a clinical laboratory

Authors: Otto Van de gaer, Reinoud Cartuyvels, Timo Froyen, Petra Hilskens, Koen Magerman, Steven Martens, Britt Van Meensel, Jozef Dingemans

July 30, 2026

Publication

Nanopore sequencing identifies parent-of-origin specific age-associated methylation changes at imprinted loci in the human genome

Authors: Brynja Sigurpalsdottir, Guillaume Holley, Sverrir Þ. Sverrisson, Droplaug N. Magnusdottir, Pall I. Olafsson, Arnaldur Gylfason, Olafur Þ. Magnusson, Gisli Masson, Olafur A. Stefansson, Bjarni V. Halldorsson

July 29, 2026

Case study

Case study: pan-microbial pathogen detection in hours using metagenomic sequencing

In this case study, discover how the UK NHS Respiratory Metagenomics Network have developed a rapid Oxford Nanopore sequencing workflow that can detect the bacteria, viruses, fungi, and parasitic pathogens ...

July 29, 2026

Long read de novo sequencing from blood using SQK-LSK114 – scalable (near) telomere-to-telomere method

This protocol describes an end-to-end workflow for long read de novo sequencing of human samples. For Research Use Only

July 29, 2026

Long read de novo sequencing from blood and cells using SQK-ULK114 – expert telomere-to-telomere method

This protocol describes an end-to-end workflow for long read de novo sequencing of human samples. For Research Use Only

July 29, 2026

Webinar

Decoding complex disease through multiomics

In this webinar, our expert speakers will discuss how multiomic Oxford Nanopore sequencing supports a deeper understanding of disease mechanisms, by integrating DNA, RNA, and epigenetic analysis — all on a ...

July 22, 2026

Publication

The planktonic microbiome of the Great Barrier Reef

Authors: Steven Robbins, Marko Terzin, Katherine Dougan, Julian Zaugg, Sara C. Bell, Patrick W. Laffy, J. Pamela Engelberts, Kim-Anh Lê Cao, Renee K. Gruber, Nicole S. Webster, David G ...

July 22, 2026

Webinar

Rapid and accurate pan-cancer subtyping using RNA-sequencing

Watch this on-demand webinar exploring how RNA sequencing is transforming childhood cancer diagnosis. Dr. Adam Shlien presents a multiscale transcriptomic atlas that matched or clarified diagnoses for 85% of ...

July 20, 2026

Publication

From culture to clarity in four hours: accelerating clinical management of bloodstream infections using metagenomics

Authors: Jawad Ali, Anurag Basavaraj Bellankimath, Silje Therese Opgård, Emil Varman Manivannan, Gunnar Skov Simonsen, Rafi Ahmad

July 20, 2026

Application note

Application note: library preparation using the Ligation Sequencing Kit XL V14 from Oxford Nanopore Technologies on epMotion

In this application note, explore how the Oxford Nanopore Ligation Sequencing Kit XL V14 can be seamlessly automated on the Eppendorf epMotion systems.

July 15, 2026

Application note

Application note: library preparation using epMotion and Oxford Nanopore Technologies Native Barcoding Kit 96 V14

In this application note, discover an automated solution for preparing up to 96 sequencing libraries with the Oxford Nanopore Native Barcoding Kit 96 V14 on the Eppendorf epMotion systems.

July 15, 2026

Case study

Case study: cell-free DNA sequencing and methylation detection — promising potential for non-invasive cancer monitoring

In this case study, find out how researchers are using nanopore technology to analyse cfDNA for cancer monitoring.

July 14, 2026

Workflow overview

Workflow overview: direct RNA sequencing

This end-to-end workflow provides a simple method to characterise RNA modifications from a human blood research sample using direct RNA sequencing.

July 9, 2026

Workflow overview

Workflow overview: bulk transcriptomics

This end-to-end workflow provides a flexible method to sequence full-length transcripts for isoform-level expression analysis.

July 9, 2026

Publication

Nanopore metagenomic sequencing links clinically relevant resistance determinants to pathogens

Authors: Harika Ürel, Ela Sauerborn, Michael Biggel, Friedemann Gebhardt, Ebenezer Foster-Nyarko, Silvio D Brugger, Rhys T White, Søren Heidelbach, Mads Albertsen, Francis Muchaamba, Tim Reska, Marc J A Stevens ...

July 8, 2026

Publication

Targeted long-read sequencing enables comprehensive analysis of the genetic and epigenetic landscape of inherited myopathies

Authors: Dennis Yeow, Andre L. M. Reis, Igor Stevanovski, et al.

July 4, 2026

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Document repository

Resolving vector insertion sites and cell line characterization: insights from PRINT

How ‘Sturgeon’ guides the surgeon

Beyond bisulfite sequencing: resolving 5-hmC with nanopore sequencing unmasks the true-5mC methylation entropy landscape

MinION Essentials: Everything you need to know about the world’s most cost-effective and accessible sequencer

Validation of a long-read 16S rRNA-gene sequencing approach for analysis of clinical samples and bacterial identification in a clinical laboratory

Nanopore sequencing identifies parent-of-origin specific age-associated methylation changes at imprinted loci in the human genome

Case study: pan-microbial pathogen detection in hours using metagenomic sequencing

Long read de novo sequencing from blood using SQK-LSK114 – scalable (near) telomere-to-telomere method

Long read de novo sequencing from blood and cells using SQK-ULK114 – expert telomere-to-telomere method

Decoding complex disease through multiomics

The planktonic microbiome of the Great Barrier Reef

Rapid and accurate pan-cancer subtyping using RNA-sequencing

From culture to clarity in four hours: accelerating clinical management of bloodstream infections using metagenomics

Application note: library preparation using the Ligation Sequencing Kit XL V14 from Oxford Nanopore Technologies on epMotion

Application note: library preparation using epMotion and Oxford Nanopore Technologies Native Barcoding Kit 96 V14

Case study: cell-free DNA sequencing and methylation detection — promising potential for non-invasive cancer monitoring

Workflow overview: direct RNA sequencing

Workflow overview: bulk transcriptomics

Nanopore metagenomic sequencing links clinically relevant resistance determinants to pathogens

Targeted long-read sequencing enables comprehensive analysis of the genetic and epigenetic landscape of inherited myopathies

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