Oxford Nanopore Technologies

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Getting started guide

Getting started guide: bulk transcriptomics

This guide introduces cDNA and direct RNA Oxford Nanopore sequencing, for ultra-rich transcriptomic data without compromise.

July 3, 2026

Case study

Case study: large-cohort cDNA sequencing advances multiomic insights into neurodegenerative disease

In this case study, discover how Kimberley Billingsley and her colleagues at the National Institutes of Health are using Oxford Nanopore large-cohort cDNA sequencing to research the human brain ...

July 3, 2026

Publication

Epigenetic liquid biopsy enables universal mutation-agnostic molecular surveillance for high-risk neuroblastoma

Publication: Epigenetic liquid biopsy enables universal mutation-agnostic molecular surveillance for high-risk neuroblastoma

July 1, 2026

Publication

Intact and single-molecule analysis of heparan sulfate

Publication: Intact and single-molecule analysis of heparan sulfate

June 29, 2026

Publication

Comparison of nanopore sequencing, Methylation EPIC array, and EM-Seq for DNA methylation detection

Publication: Comparison of nanopore sequencing, Methylation EPIC array, and EM-Seq for DNA methylation detection

June 25, 2026

Publication

Female-specific m6A remodelling in the liver correlates with post transcriptional metabolic adaptation to high fat diet

Publication: Female-specific m6A remodelling in the liver correlates with post transcriptional metabolic adaptation to high fat diet

June 22, 2026

Webinar

Unlocking high-resolution, strain-resolved microbiome analyses

During this video we learn how full length Oxford Nanopore sequencing is unlocking high-resolution microbiome analyses

June 19, 2026

Publication

Long-read nanopore sequencing enhances BRCA1/2 variant detection compared to Ion Torrent analysis

Publication: Long-read nanopore sequencing enhances BRCA1/2 variant detection compared to Ion Torrent analysis

June 19, 2026

Webinar

NIHR BioResource: Advancing translational research with Omics technologies

Dr Kathy Stirrups discusses her work on eating disorders and how multiomic analysis can be used to identify new variants and their function. She also presents results from the rare ...

June 15, 2026

Event video

Development and assessment of a standardised nanopore sequencing workflow for clinical application

Dr Koen Van Gassen shares how the University Medical Center in Utrecht is implementing Oxford Nanopore whole-genome sequencing into their work.

June 15, 2026

Brochure

Specification sheet: PromethION 2 Integrated

Explore sequencing performance data, example end-to-end workflows, technical specifications, and purchasing information to help you understand how the PromethION 2 Integrated can deliver richer insights for your laboratory.

June 12, 2026

Publication

AviNP-Seq: a blindspot-free single-molecule framework for unmasking AAV genome heterogeneity and determining packaging limits

Publication: AviNP-Seq: a blindspot-free single-molecule framework for unmasking AAV genome heterogeneity and determining packaging limits

June 12, 2026

Publication

Diagnostic value of nanopore-based targeted sequencing technology for subclinical tuberculosis

Publication: Diagnostic value of nanopore-based targeted sequencing technology for subclinical tuberculosis

June 11, 2026

Webinar

Democratising Genomic Diagnostics: A New Model for Global Childhood Cancer Care

In this talk, Dr. Nickhill Bhakta describes how the St. Jude-led DIVIA consortium is developing and evaluating approaches to expand access to high-quality diagnostic testing through a global ...

June 10, 2026

Webinar

Exploring microbial methylation

In this webinar we learn how to advance microbial genomics and epigenomics research with authenticated reference resources.

June 10, 2026

Publication

Implementing portable, real-time 16S rRNA sequencing in the healthcare sector enhances antimicrobial stewardship

Publication: Implementing portable, real-time 16S rRNA sequencing in the healthcare sector enhances antimicrobial stewardship

June 10, 2026

Analysis of scalable DNA extraction using the Promega Maxwell RSC for human blood, saliva and buccal swab processing

June 10, 2026

Publication

Identification of a novel intergenic EPCAM-MSH2 deletion causing EPCAM-associated Lynch syndrome by long-read nanopore sequencing

Publication: Identification of a novel intergenic EPCAM-MSH2 deletion causing EPCAM-associated Lynch syndrome by long-read nanopore sequencing

June 5, 2026

Publication

Sensitive long-read amplicon sequence variant recovery with savont

Publication: Sensitive long-read amplicon sequence variant recovery with savont

May 29, 2026

Publication

Third-generation nanopore sequencing for post-transplant chimerism monitoring

Publication: Third-generation nanopore sequencing for post-transplant chimerism monitoring

May 28, 2026

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Document repository

Getting started guide: bulk transcriptomics

Case study: large-cohort cDNA sequencing advances multiomic insights into neurodegenerative disease

Epigenetic liquid biopsy enables universal mutation-agnostic molecular surveillance for high-risk neuroblastoma

Intact and single-molecule analysis of heparan sulfate

Comparison of nanopore sequencing, Methylation EPIC array, and EM-Seq for DNA methylation detection

Female-specific m6A remodelling in the liver correlates with post transcriptional metabolic adaptation to high fat diet

Unlocking high-resolution, strain-resolved microbiome analyses

Long-read nanopore sequencing enhances BRCA1/2 variant detection compared to Ion Torrent analysis

NIHR BioResource: Advancing translational research with Omics technologies

Development and assessment of a standardised nanopore sequencing workflow for clinical application

Specification sheet: PromethION 2 Integrated

AviNP-Seq: a blindspot-free single-molecule framework for unmasking AAV genome heterogeneity and determining packaging limits

Diagnostic value of nanopore-based targeted sequencing technology for subclinical tuberculosis

Democratising Genomic Diagnostics: A New Model for Global Childhood Cancer Care

Exploring microbial methylation

Implementing portable, real-time 16S rRNA sequencing in the healthcare sector enhances antimicrobial stewardship

Analysis of scalable DNA extraction using the Promega Maxwell RSC for human blood, saliva and buccal swab processing

Identification of a novel intergenic EPCAM-MSH2 deletion causing EPCAM-associated Lynch syndrome by long-read nanopore sequencing

Sensitive long-read amplicon sequence variant recovery with savont

Third-generation nanopore sequencing for post-transplant chimerism monitoring

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