Resources
Highlights from London Calling
Discover how researchers are using Oxford Nanopore sequencing to generate new insights across diverse applications.
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Discover nanopore sequencing
- What it can do
- How it’s being used
- How to get started
Latest protocols
遗传性肿瘤相关基因检测（HCP）
Nanopore-only Microbial Isolate Sequencing Solution (NO-MISS) – automated ElysION MinION (SQK-RBK114.96)
Long read de novo sequencing from blood and cells using SQK-ULK114 – expert telomere-to-telomere method
Microbial amplicon barcoding for 16S and ITS – automated ElysION MinION (SQK-MAB114.24)
Rapid PCR barcoding DNA V14 – automated ElysION MinION (SQK-RPB114.24)
Rapid barcoding DNA V14 – automated ElysION MinION (SQK-RBK114.96)
Webinars and events
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Unlocking high-resolution, strain-resolved microbiome analyses | ASM Microbe 26
During this video we learn how full length Oxford Nanopore sequencing is unlocking high-resolution microbiome analyses
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Oxford Nanopore at AMP 2026
Oxford Nanopore Technologies are exhibiting and presenting at AMP 2026 in November.
White papers
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Genomics for a changing planet: sequencing the living world
Discover how a global community of researchers are harnessing Oxford Nanopore sequencing to study the far-reaching impacts of climate change, revealing deep insights across environmental research, agriculture, and pathogen surveillance.
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New approaches for human and clinical research
Explore the advantages of Oxford Nanopore sequencing to detect genomic and epigenomic variants in human and clinical research.
Case studies
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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 underlying respiratory infections in a matter of hours.
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Mapping RNA modifications in the human brain with full-length transcript sequencing
A single gene can produce multiple RNA isoforms through complex gene regulation mechanisms, such as alternative splicing and post-transcriptional modifications. This creates a large transcriptional diversity by generating multiple isoforms, as exhibited in the human brain, facilitating the regulatio
Getting started guides
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A guide to transcriptomics with Oxford Nanopore
This guide introduces cDNA and direct RNA Oxford Nanopore sequencing, for ultra-rich transcriptomic data without compromise.
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A guide to microbial sequencing with Oxford Nanopore
A guide to get started with sequencing microbial samples with Oxford Nanopore.
Workflow overviews
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Comprehensive characterisation of cancer predisposition genes using the Hereditary Cancer Panel
Discover the Hereditary Cancer Panel workflow and streamline your precision oncology research.
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Comprehensive human genomic variant and methylation analysis with long Oxford Nanopore reads
This end-to-end workflow provides a scalable method to identify previously hidden and potentially pathogenic variants.
Brochures
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Oxford Nanopore sequencing solutions for cell and gene therapies
Discover how Oxford Nanopore technology can support the development of your cell, gene, and RNA therapies.
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cDNA-PCR Sequencing Kits
In this flyer, discover how you can sequence full-length transcripts and annotate the transcriptome with confidence.
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Browse document repository
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