Oxford Nanopore Technologies

Take your sequencing to the next level with the recently released PromethION 2 devices. They enable flexible, high-yield sequencing, in a compact, accessible design. The devices are designed for users with sample processing requirements of up to four full-length sequencing runs per week / ~200 flow cells per year. Each flow cell can deliver hundreds of gigabases of nanopore sequencing data. With this sequencing capacity, you can obtain the data you need for completing large genomes, studying complex metagenomic samples, obtaining known and novel transcripts from single-cell sequencing, and much more.

[url][link]https://nanoporetech.com/resource-centre/promethion-2-brochure?utm_campaign=P2%202022&utm_source=tech_networks&utm_medium=video[/link][name]Download the PromethION 2 brochure[/name][/url]

[url][link]https://nanoporetech.com/products/promethion-2?utm_campaign=P2%202022&utm_source=tech_networks&utm_medium=video[/link][name]Browse the PromethION 2 page[/name][/url]


Flexible, high-yield nanopore sequencing for every lab

The genetics behind cancer are both diverse and complex, with many abnormalities causing, contributing, or indicating the disease. Using nanopore sequencing, scientists can resolve variants and epigenetic modifications across the entire genome, target large panels or single genes, and detect known and novel full-length transcripts – for the most comprehensive insight into cancer genomes.

In this short, impactful video, scientists share how nanopore sequencing has made their work possible, leading to greater understanding of cancer, and how some of their own life experiences prompted them to pursue a career in this area.

[url][link]https://nanoporetech.com/accelerating-cancer-research-through-comprehensive-genomic-analysis?utm_campaign=Cancer%202022&utm_source=tech_networks&utm_medium=video[/link][name]Download this white paper to learn more about nanopore sequencing in cancer research[/name][/url]

[url][link]https://nanoporetech.com/resource-centre/rapid-low-cost-detection-genomic-aberrations-flongle?utm_campaign=Cancer%202022&utm_source=tech_networks&utm_medium=video[/link][name]Read this case study on rapid, low-cost detection of genomic aberrations[/name][/url]

Nanopore Sequencing: The Most Comprehensive Insight Into Cancer

Oxford Nanopore sequencing devices enable direct, real-time analysis of short to ultra-long fragments of DNA/RNA in fully scalable formats. 

It’s possible to target regions of DNA in real time using adaptive sampling on nanopore devices. The nanopore has the ability to read the strand sequence in real time, if it is not the strand of interest, the strand is ejected, but if it is, the nanopore recognises this and continues to read the strand. Researchers then get more of the sequence they are interested in within a shorter period of time, allowing faster and easier analysis. 

Adaptive Sampling: Target Regions of DNA in Real Time

Loss of biodiversity is an urgent problem. Oxford Nanopore launched ORG.one to support faster, more localised sequencing of critically endangered species. Using portable nanopore sequencing, biologists can rapidly sequence species close to the sample’s origin.

Why nanopore sequencing technology?
Oxford Nanopore devices sequence DNA/RNA directly, providing rich data that can be streamed in real time for rapid insights. The technology is fully scalable, from pocket to population scale, and makes it possible to sequence short to ultra-long DNA/RNA fragments. With this new generation of high-performance nanopore-based sensing technology, Oxford Nanopore aim to bring the widest benefits to society through enabling the analysis of anything, by anyone, anywhere.

[url][link]https://org.one/oo[/link][name]Learn more about ORG.one[/name][/url]
[url][link]https://nanoporetech.com/how-it-works[/link][name]Learn how nanopore sequencing works[/name][/url]

ORG.one: supporting sequencing of critically endangered species

Flongle is an adapter (flow cell dongle) for MinION or GridION that enables direct, real-time DNA or RNA sequencing on smaller, single-use flow cells.<br/><br/>Providing access to sequence data as soon your experiment starts, Flongle is designed to be the quickest, most accessible and cost-efficient sequencing system for smaller tests and experiments.<br/>

Flongle - for rapid DNA/RNA sequencing tests in any environment

Oxford Nanopore’s long-read cDNA sequencing solutions allow researchers to sequence millions of whole transcripts end-to-end in single reads. This enables users to simultaneously perform accurate isoform-level transcriptome characterisation, and  differential gene expression profiling  without any of the compromises on cost, quantitation, computational or workflow complexity required to achieve this on other short or long read sequencing platforms.

https://store.nanoporetech.com/cdna-and-direct-rna/

Oxford Nanopore Technologies

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