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Highlights from London Calling

Discover how researchers are using Oxford Nanopore sequencing to generate new insights across diverse applications.


Latest protocols

使用 SQK-NBD114.24 进行简化甲基化测序(RRMS)

仅供研究使用。

遗传性肿瘤相关基因检测(HCP)

本指南概述了从样本提取、文库制备到测序与数据分析的完整端到端流程。 本实验指南: - 使用从全血中提取的基因组 DNA - 无需 PCR 扩增 - 与 R10.4.1 测序芯片兼容 仅供研究使用

Influenza virus sequencing from RNA using SQK-NBD114 (.24 or .96)

This document describes the sequencing of the influenza virus. For Research Use Only
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ONT Logo wheel blackWorkflow

Ligation sequencing amplicons - Native Barcoding Kit 96 V14 (SQK-NBD114.96)

Ligation sequencing amplicons - Native Barcoding Kit 96 V14 (SQK-NBD114.96)
ONT Logo wheel blackWorkflow

Ligation sequencing amplicons - Native Barcoding Kit 24 V14 (SQK-NBD114.24)

Ligation sequencing amplicons - Native Barcoding Kit 24 V14 (SQK-NBD114.24)

基因组DNA连接法测序 - 免扩增条形码测序试剂盒-96(SQK-NBD114.96)

本文档描述了基因组 DNA 的免扩增条形码建库流程。 实验指南: - 使用免扩增条形码测序试剂盒-96 V14 (SQK-NBD114.96) - 无需PCR扩增 - 支持多达96种条形码 - 可分析天然DNA - 与R10.4.1 测序芯片兼容 仅供研究使用
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Webinars and events

plasmidWebinar

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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mRNAEvent

Oxford Nanopore at AMP 2026

Oxford Nanopore Technologies are exhibiting and presenting at AMP 2026 in November.

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White papers

Preview image for the plant, animal, and environmental sequencing white paper, 'Genomics for a changing planet'.White paper

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.

Clinical research white paper coverWhite paper

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

cancer researchCase 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.

Visualisation of an RNA strand with glowing orange sections in the backgroundCase 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 transcriptome, enhancing understanding of the drivers of neurodegenerative diseases.

Getting started guides

Preview image for the bulk transcriptomics getting started guideGetting started guide

A guide to transcriptomics with Oxford Nanopore

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

Preview of the microbial getting sequencing getting started guideGetting started guide

A guide to microbial sequencing with Oxford Nanopore

A guide to get started with sequencing microbial samples with Oxford Nanopore.

Workflow overviews

Flyer from Oxford Nanopore Technologies detailing RNA extraction and library preparation for full-length isoform sequencing, with images of test tubes.Workflow overview

Sequencing full-length transcripts for isoform-level expression analysis

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

A document from Oxford Nanopore Technologies detailing workflow for PCR-free, direct RNA sequencing, featuring diagrams, text, and lab tools.Workflow overview

Detecting isoforms and modifications with PCR-free, direct RNA nanopore sequencing

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

Brochures

Flyer for Oxford Nanopore Technologies' cDNA-PCR Sequencing Kits, featuring graphs, diagrams, and key product benefits for transcriptome analysis.Brochure

cDNA-PCR Sequencing Kits

In this flyer, discover how you can sequence full-length transcripts and annotate the transcriptome with confidence.

Flyer: Direct RNA Sequencing Kits — 2 pagesBrochure

Direct RNA Sequencing Kits

In this flyer, discover how you can sequence RNA in its native form. Plus, learn how the new Direct RNA Barcoding Kit unlocks multiplexed sequencing of up to 24 samples in a single run.

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Browse document repository

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