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Reveal the hidden causes of rare diseases that families have been searching for. This brochure showcases how Oxford Nanopore technology resolves the full spectrum of genetic and epigenetic changes – enabling you to find the missing piece of the puzzle. bit.ly/4jwTw85

The harsh treatment of bisulfite can damage precious DNA samples. ​ Catch Claire Attwooll at booth 1553 at #AACR25 to discover how direct nanopore sequencing is providing rapid, real-time tumour methylation profiling, without the need for bisulfite. bit.ly/4j23Qou

Methylation is emerging as the missing piece of the puzzle in rare disease. In this guide, discover how to reveal what others have missed with native DNA/RNA nanopore sequencing to unlock the full spectrum of epigenetic changes behind rare disease. bit.ly/3Y2Ydy3

First time at #nanoporeconf? It’s Salvatore Benfatto’s too! Catch his talk on the potential of real-time acute leukemia classification using Oxford Nanopore sequencing. bit.ly/3Yc520t

Catch Rob King at #AACR to discover how to seamlessly integrate #multiomic insights into your cancer research. Unlock novel insights with nanopore technology that unlocks methylation, CNVs, & breakpoint-level resolution of SVs & fusion genes. bit.ly/42CC786

Attending #AACR25? Join Maddy Hartley at 3 pm (CT) today at booth #1553 as she kicks off the first of our demos. Don't miss this opportunity to gain hands-on experience loading a flow cell and initiating an Oxford Nanopore sequencing run. Come discover supercharged sequencing

Last call for London Calling Innovation Day in-person tickets! Tickets are almost sold out for this year's #nanoporeconf, moving to waitlist next week. Don’t miss out on inspiring talks, fantastic networking opportunities and a global conversation. bit.ly/449u5VA

Arianna Ceruti will showcase a mobile laboratory which enables a rapid response for outbreak investigation using Oxford Nanopore technology at this year's #nanoporeconf. Can’t attend in person? Register to attend online for free: bit.ly/4jwztH9

At #AACR25, Maddy shares her excitement for the potential of the Oxford Nanopore Hereditary Cancer Panel. Want to learn more? Don't miss Rob King at booth #1553 today, where he will share how this single assay provides comprehensive multiomic data to unlock novel cancer

In this knowledge exchange, learn how to generate a comprehensive genomic view of mixed microbial samples using #nanopore technology. Gain rapid taxonomic classification and AMR identification for quick response to public health threats. bit.ly/4in6vIp

Emma describes her path into Oxford Nanopore by finding a skill she enjoyed and applying it to her role as a Senior Development Engineer. To find out more about careers at Oxford Nanopore click here: bit.ly/3EqMuCo

Marine genomics meets Oxford Nanopore sequencing: Queen’s University Belfast publishes the first genome of Nucella lapillus — a key bioindicator species for pollution and climate change studies. A major step for environmental monitoring. nature.com/articles/s4159…

The biggest Oxford Nanopore sequencing event of the year is around the corner. Can’t make the event in person? Wherever you are in the world, you can be a part of a global conversation with our free virtual London Calling event. See what you’re missing:

There are just 3 weeks to go until London Calling 2025. Join us for the virtual event & immerse yourself in inspiring talks, dynamic breakout sessions, & exclusive content. Click here for the opportunity to learn, engage, and be a part of something bigger:

#AACR25 #nanopore come visit poster section 46 to learn more from Sergey Aganezov to learn about cancer multiomics whole genome sequencing using Oxford Nanopore Sequencing

The future is now. In this webinar, Prof. Matt Loose showcases a revolutionary tool, ROBIN, that uses Oxford Nanopore technology for rapid and comprehensive molecular profiling of central nervous system tumours. Watch the webinar here: bit.ly/3REqZSd

At #nanoporeconf, Paula Saffie will share a scalable, cost-effective approach using Oxford Nanopore technology to identify genetic causes of ataxia. Don’t miss how this method has potential to transform genetic testing for hereditary movement disorders. bit.ly/4lIXGvo

Explore the latest bioinformatics tools - from sequencing challenging genomic regions to a deeper understanding of gene expression, DNA replication, and tRNA biology, at this breakout. Learn more: bit.ly/42L0655

Find the missing piece of the rare disease puzzle. This end-to-end workflow will enable you to resolve the full spectrum of genetic & epigenetic changes using long, native nanopore reads to identify previously hidden pathogenic variants. bit.ly/3Gf879A #WYMM

In Debarshi Mustafi’s talk at #AACR25, he shared how epigenetic modifications we previously ‘glossed over’ play a vital role in cancer progression. Read how they are unlocking novel biomarkers by assigning parent of origin in retinoblastoma. bit.ly/4jX5DeU