Environmental research and conservation

Made with multiple projects and teams in mind, GridION gives you the freedom to start, stop, and scale your sequencing experiments without impacting others. Meanwhile, onboard compute keeps your real-time data optimised. Discover more.

Discover how the portable yet powerful MinION Mk1D sequencing device can take your insights further afield. Start generating rapid, real-time results without compromise.

Discover the Oxford Nanopore sequencing techniques that can achieve comprehensive microbial genome characterisation.

This end-to-end workflow provides a rapid solution for whole-genome Oxford Nanopore sequencing of bacterial and fungal isolates.

This end-to-end workflow provides a rapid solution for species-level bacterial identification.

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.

Explore how reads with unrestricted length are revealing unprecedented insight into microbial communities.

In this masterclass, find the right microbial community sequencing workflow to meet your experimental goals. We’ll cover microbial identification from full-length 16S/ITS sequencing through to comprehensive metagenomic assembly. In this masterclass, discover: • How Oxford Nanopore sequencing deliver

In this beginner-friendly masterclass, discover how to analyse your Oxford Nanopore sequencing data. Find out how basecalling works, the common file formats you’ll encounter, and how to use MinKNOW to set up and monitor your sequencing run. Then, discover how to analyse your data with EPI2ME — no pr

Whether you’re sequencing DNA, RNA, or cDNA, a single sample or many in multiplex, there’s an Oxford Nanopore library prep kit for you. In this masterclass, discover how to choose the right one for your workflow. In this masterclass, discover: • The range of Oxford Nanopore library prep solutions av

This protocol: Uses genomic DNA Has a low input requirement Has a method involving tagmentation, barcoding and PCR amplification Allows multiplexing of 1–24 samples Is compatible with R10.4.1 flow cells For Research Use Only

Learn how to perform rapid genomic DNA barcoding using the Rapid Barcoding Kit V14 (SQK‑RBK114.24 / SQK‑RBK114.96). This fast, high‑yield library preparation workflow enables multiplexing of up to 96 gDNA samples with ~60‑minute prep time and compatibility with R10.4.1 flow cells.

- このプロトコールではゲノムDNAを使用します。 - 調製時間は約６０分です。 - フラグメンテーションは任意としています。 - PCR無し - R10.4.1フローセルとの互換性 研究用のみ この翻訳は英語バージョン「X」をもとに翻訳されています。 新しいバージョンが出ている可能性があるので、この翻訳を使用する前にコミュニティーで今の英語のバージョンをご確認ください。

This protocol describes how to carry out native barcoding of genomic DNA (gDNA) using the Native Barcoding Kit 24 V14 (SQK-NBD114.24).

This document describes the barcoding of native genomic DNA libraries. For Research Use Only

This workflow can be used for the taxonomic classification of metagenomic sequencing data.

This workflow is primarily used to assemble genomes from bacterial reads and provide information on features of interest within those assemblies through annotations.

This Nextflow workflow provides a simple way to analyse Oxford Nanopore reads generated from haploid amplicons.

This workflow provides an easy way to align Oxford Nanopore reads and gather mapping stats either locally for small amounts of data or at scale in a distributed environment such as a cluster or the cloud.

This workflow can be used for taxonomic classification of single reads from amplicon-targeted sequencing.

​Publication: Decoding the Peruvian Amazon with in situ DNA barcoding of vertebrate and plant taxa

Publication: Barcode 100K specimens: in a single nanopore run

Publications: Borg extrachromosomal elements of methane-oxidizing archaea have conserved and expressed genetic repertoires