Learn more about adaptive sampling in our Nanopore Know-How: https://nanoporetech.com/blog/guided-by-data-adaptive-sampling-for-targeted-sequencing?utm_campaign=OmicsTech+25&utm_content=1771441621&utm_medium=social&utm_source=bluesky

In neonatal intensive care units, speed is vital. Oxford Nanopore’s workflow delivers whole-genome sequencing in 24 hours, offering rapid variant insights that could transform clinical care — through faster answers & reduced costs. Learn more: https://bit.ly/4rR9jCy

We are now into our third phase of London Calling tickets. Find out more: https://nanoporetech.com/about/events/conferences/lc26?utm_campaign=London+Calling+26&utm_content=1771265641&utm_medium=social&utm_source=bluesky

As one part of our many international collaborations, our team of the Biodiversity Genomics Center Cologne, BioC2 @unicologne.bsky.social, conducted a @nanoporetech.com workshop at the UNAM in Windhoek last week. Big thanks to Tarja Hoffmeyer and Joseph Kirangwa for running this. Long-reads rule!

Learn more about adaptive sampling in our latest #Nanopore Know-How. Learn more here: https://nanoporetech.com/blog/guided-by-data-adaptive-sampling-for-targeted-sequencing?utm_campaign=Platform+%2F+Omics+26&utm_content=1770985380&utm_medium=social&utm_source=bluesky

Researchers detected a salmonellosis outbreak 5 weeks before food recall was triggered. By combining wastewater sequencing with AI, researchers have shown how outbreaks could be spotted sooner, with the potential to save lives. Find out more: https://bit.ly/4b8Dal8

Critically ill patients need rapid genomic diagnosis. Don’t miss Mark Drost at #AGBT where he’ll share how his team reached disease insights 3x faster than standard methods, with the potential to support more timely clinical decisions. https://bit.ly/4qlkIK5

EXCITING day in our Lab! SI HS Ss have been learning how to use @nanoporetech.com DNA sequencing technology We've tried & failed many times We just got our longest high quality read @ 73,000 bases! It's 100% coverage & 100% similarity to staphlococcus aureus! @nysmtp.bsky.social @dnalc.bsky.social

Announcing the #banana pangenome generated by @keygene.com using @nanoporetech.com long PromethION read platform. www.linkedin.com/posts/alexan...

Are we a step closer to safer blood transfusions? Using adaptive sampling, researchers demonstrate how more comprehensive nanopore data could transform donor-patient matching, reducing the risks of rejection. https://bit.ly/4qqbRr3

Analysing sequencing data has a reputation for being complex, but is that still true? In this interview, Dr Anthony Doran dives into how recent advances are transforming analysis, making it faster, richer, and accessible to researchers everywhere. Learn more: https://bit.ly/4tb7bHE

New hifiasm-ONT assembly method delivers high-quality, cost-efficient near T2T assemblies using standard Oxford Nanopore Simplex reads, broadening access to comprehensive genome assemblies across research and clinical applications. https://bit.ly/4awzU15

Join Marilyn Li, who will kick off the talks at #AGBT, sharing how the simultaneous detection of genetic and epigenetic landscapes in cancer is enabling deeper characterisation and uncovering insights that were previously out of reach. https://bit.ly/45sPARe

Joanne and her team’s research gained ‘exponential’ growth when they moved from the #MinION to the #PromethION. Watch how this enabled them to build a large database of whole-genome sequences to better understand Parkinson’s disease. https://bit.ly/45ON7R2

In critical moments, every hour counts. See how researchers found previously undetected variants within 24 hours, showcasing how Oxford Nanopore technology has the potential to support urgent cases in the future. https://bit.ly/4sNSGZV

Remarkable insights, even decades after samples were taken. Alimat and Tilda are sequencing 400 human genomes per week. They are gaining high-quality data, even on low-quality samples, without bias. Learn more about scalable sequencing here: https://bit.ly/4q8H3uf

In case you missed it, the recording of the BugSeq + @nanoporetech.com webinar is now available on demand! Discover how Dr. Georgios Kitsios used BugSeq for respiratory metagenomics in the @upmc.com ICU: nanoporetech.com/resource-cen...

This week is your last week to get phase two tickets for London Calling. Join us to hear from a fantastic line-up of speakers who are using Oxford #Nanopore technology to gain new insights across a broad range of research areas. Get your ticket now: https://bit.ly/3ZHEYdC

Researchers delivered rapid, accurate methylome profiles with Oxford Nanopore sequencing alone. Read how this showcases an accessible, reliable approach for bacterial epigenomic analysis and has the potential to boost pathogen monitoring. https://bit.ly/4qfTncG

Javeria shares how she uses the #MinION to unify techniques to characterise cancer. This has enabled comprehensive sequencing with low capital costs, reducing the barrier to genomic data. https://bit.ly/4quP1yM

Are we a step closer to safer blood transfusions? Using adaptive sampling researchers demonstrate how more comprehensive nanopore data could transform donor-patient matching, reducing the risks of rejection. https://bit.ly/4t14tV1

We’re excited to confirm Fritz Sedlazeck as our first speaker for #nanoporeconf! His research confronts genomic inequity, identifying novel variants that could influence disease risk, gene regulation and healthcare in Hispanic populations. https://bit.ly/4sOxMKd

Current protein analysis is costly, complex & risks damaging proteins. We’re developing a protein barcoding method that's scalable, accessible & protein-friendly. Find out more: https://bit.ly/4pzmIhI

From a neonatal ICU in Wellington to clinics in Africa & Europe: a new Global Health Now feature shows how onsite @nanoporetech.com sequencing is shaping #InfectionPrevention… helping deliver answers in hours not weeks - turning #Genomic into real-world action 🖥️🧬💻 #AcademicSky #MicroSky #IDSky 🧪🧫🦠

Seeing the full picture of infection, from ICU to surveillance, requires richer data, delivered faster. Join our webinar to learn how new approaches rapidly turn insight into action. Join here: https://bit.ly/4szzhfl

In neonatal intensive care units, speed is vital. Oxford Nanopore’s new workflow delivers whole-genome sequencing in 24 hours, offering rapid variant insights that could transform clinical care — through faster answers & reduced costs. Learn more: https://bit.ly/4orVKYs

#Metagenomics is changing how infections are detected and tracked. Join our webinar to learn how it’s enabling faster, smarter care — from the ICU to global surveillance. Register here: https://bit.ly/4srSnDM

Discover how to streamline your biopharma workflows — from discovery to QC — combining multiple assays on a single, Oxford Nanopore platform, for faster, more confident decisions. Read the guide. https://bit.ly/4pIe4NOh

Looking forward to attending #PAG33 in San Diego (if flights allow…) to present @nanoporetech.com industry workshop. Some background in the link below. www.keygene.com/single-nucle...

Are you gaining deeper insights into human disease? If so, we want to hear about it! Submit an abstract before 16th January to be in with a chance to speak at this year’s London Calling. https://bit.ly/49E5I4G

Finally reveal the roots of complex disease. Unlock complete genome assemblies, variant calling, and methylation analysis — In One Go — with Oxford Nanopore sequencing. Read the guide: https://bit.ly/48jwrSm

Are you attending #PAG? Enter our raffle to get the chance to win a #GridION cow print skin! Stop by booth #211 to enter. https://nanoporetech.com/about/events/conferences/pag-2026?utm_campaign=PAG+2026&utm_content=1767710160&utm_medium=social&utm_source=bluesky

If you’ve developed an adaptive sampling panel, apply to share your work at the biggest #nanopore sequencing event of the year. Hurry, abstract submission closes on 16th January. https://bit.ly/49E5AC6 #nanoporeconf

Before CRISPR took centre stage, other clever tools made gene editing possible. Now, scientists are revisiting them to push boundaries further. Hear Frank Buchholz share how these innovations could change the future of gene editing. Find out more: https://bit.ly/43ZpmFd

With its expanding capabilities, Oxford Nanopore sequencing is detecting genetic variants that could explain long-unsolved medical mysteries. Read here: https://bit.ly/43NmLOA

Alex Zaccaron is unlocking how organisms evolve to overcome host resistance. Join his talk at #PAG to learn how he is doing this by comparative genomics and transcriptomics using Oxford Nanopore sequencing of fungal plant pathogens. https://bit.ly/3Xt9RS7

Many SVs behind neurodegenerative disease remain uncharacterised. Using Oxford Nanopore sequencing, researchers have uncovered rare variants linking to Alzheimer’s and Parkinson’s — providing deeper insights with potential for new treatment options. https://bit.ly/4rccjKm

The early bird catches the worm! This is your last chance to get an early bird ticket, get ahead of the curve and reserve your spot at London Calling 2026! Price increases soon – so act fast! Grab your ticket here: https://bit.ly/4af4Vbl #nanoporeconf

Xiaojun Su’s role focuses on optimising Oxford Nanopore workflows for complex and challenging samples. Don’t miss her talk at #PAG to discover how this is enabling high-quality assemblies and integrative analysis across diverse species. https://bit.ly/4onPgcT

Season’s greetings! 🎄 Thank you to our incredible global community for an inspiring year. Wishing you joy and rest over the festive period.

Early-stage cancer classified with 100% sensitivity, using cell-free RNA. Read how researchers detected cancer early using Oxford Nanopore sequencing as a non-invasive tool, with the potential to inform cancer care more rapidly and accurately than before. https://bit.ly/4rqvHDH

Gain an end-to-end solution for rapid and comprehensive microbial community analysis in this webinar. Join experts on Oxford Nanopore technology to learn about the Microbial Amplicon Barcoding Kit for real-time, high-resolution taxonomic identification. https://bit.ly/43UDnE5

Season’s greetings! 🎄 Thank you to our incredible global community for an inspiring year. Wishing you joy and rest over the festive period.

By sequencing entirely in situ, Sánchez-Vendizú and team showed that advanced genomics can be done locally. Their work reduces the need to export samples abroad and empowers researchers to drive biodiversity studies within their own countries. Read more: https://go.nature.com/4ilJfMA

Join Alexander Wittenberg at #PAG to uncover how he is utilising Oxford Nanopore technology to develop high-quality reference genomes and uncover genetic and phenotypic variants, which will help develop methods to improve crops. https://bit.ly/48tzBDa

Read the full blog here: https://www.technologynetworks.com/cancer-research/blog/improving-detection-and-interpretation-in-hereditary-cancer-testing-405230

Sergey Koren’s work led to the first truly complete human genomic sequencing. Join him at #PAG to learn how he is utilising Oxford Nanopore technology to build on this success so that complete and accurate genomes can become routine. https://bit.ly/49PeNIp

Discover how to generate gapless genomes without reliance on multiple platforms. Join our industry workshop at #PAG to learn how Oxford Nanopore sequencing is democratizing access to reference-quality data all over the world. Register here: https://bit.ly/4iwcJra

Gene editing can reshape more than just DNA. Mo Li and team found that CRISPR-Cas9 breaks trigger profound epigenetic changes, an overlooked complexity, underscoring the need to recognise these effects to improve safety and inform novel treatment options. https://bit.ly/4rDRmZ7

In gene therapy manufacturing, accuracy is non-negotiable. Kathleen is identifying mis-splicing or unwanted variants that could compromise safety. Using direct RNA Oxford Nanopore sequencing for vector integrity checks, this method can improve QC. https://bit.ly/4oyCj11