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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:

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