Turn millions of DNA bases into insights — without bioinformatics experience.
In the latest Nanopore Know-How, uncover how EPI2ME delivers powerful bioinformatics at your fingertips with preconfigured workflows, giving you confidence in data analysis. nanoporetech.com/blog/epi2me-...
In the latest Nanopore Know-How, uncover how EPI2ME delivers powerful bioinformatics at your fingertips with preconfigured workflows, giving you confidence in data analysis. nanoporetech.com/blog/epi2me-...
September 24, 2025 at 12:20 PM
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Regarding that last bioinformatics point, I think ONT would be better off concentrating on creating a good sequencing technology, and leaving the analysis component to the community. In other words, drop Epi2ME; shift all that stuff to Galaxy, Bioconductor, or other existing toolkits.
December 15, 2024 at 11:15 AM
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I think EPI2ME is a waste of time and effort, seemingly only existing to match a "not-invented-here" attitude.
It would be far better for ONT to encourage the use & development of existing well-used bioinformatics platforms for nanopore workflows, such as Galaxy.
galaxyproject.org/use/nanogala...
It would be far better for ONT to encourage the use & development of existing well-used bioinformatics platforms for nanopore workflows, such as Galaxy.
galaxyproject.org/use/nanogala...
NanoGalaxy - Galaxy Community Hub
All about Galaxy and its community.
galaxyproject.org
January 22, 2025 at 11:02 AM
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#nanopore for people who rely on software as a [web] service:
In line with the publicised timelines the legacy EPI2ME platform accessible through the EPI2ME Agent client program and epi2me.nanoporetech.com is no longer in service. New workflows cannot be started and data is no longer downloadable.
In line with the publicised timelines the legacy EPI2ME platform accessible through the EPI2ME Agent client program and epi2me.nanoporetech.com is no longer in service. New workflows cannot be started and data is no longer downloadable.
epi2me.nanoporetech.com
February 3, 2025 at 6:16 PM
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New for 2025 in EPI2ME - Teloseq, trio and pharmacogenomics workflows
May 22, 2025 at 12:04 PM
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Improve Oxford Nanopore's EPI2ME for non-experts 🧬💻
NextSprints shows how to tackle this product challenge!
#ProductManagement #NextSprints #Biotech
NextSprints shows how to tackle this product challenge!
#ProductManagement #NextSprints #Biotech
July 16, 2025 at 7:15 PM
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July 16, 2025 at 7:15 PM
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EPI2ME free to download and runs on Windows, Mac and Linux
May 22, 2025 at 11:59 AM
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GitHub - epi2me-labs/wf-metagenomics: Metagenomic classification of long-read sequencing data
Metagenomic classification of long-read sequencing data - epi2me-labs/wf-metagenomics
github.com
December 6, 2024 at 1:54 AM
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The @nanoporetech.com #EPI2ME team is hiring!
If you want to build workflows to analyse @nanoporetech.com sequencing data for end to end applications then this job is for you!
ejnh.fa.em2.oraclecloud.com/hcmUI/Candid...
If you want to build workflows to analyse @nanoporetech.com sequencing data for end to end applications then this job is for you!
ejnh.fa.em2.oraclecloud.com/hcmUI/Candid...
Bioinformatics Software Developer
We are looking for talented Bioinformatics Software Engineer to work within the Customer Analysis Workflows group who will be responsible for developing coherent bioinformatic software tools for end u...
ejnh.fa.em2.oraclecloud.com
May 3, 2025 at 6:32 AM
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This sort of thing is disturbingly common. Cellranger, epi2me (at least the workflows I’ve seen), even blast sends back usage info unless you block it.
November 26, 2024 at 7:11 AM
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EPI2ME workflows are next flow based you can upload your own
May 22, 2025 at 12:01 PM
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Attending #AACR25?
Don’t miss Sergey Aganezov’s on-booth talk describing the EPI2ME workflow using Oxford Nanopore technology to deliver unprecedented insight into tumour-normal research samples by characterising genomic and epigenomic variants. nanoporetech.com/about/events...
Don’t miss Sergey Aganezov’s on-booth talk describing the EPI2ME workflow using Oxford Nanopore technology to deliver unprecedented insight into tumour-normal research samples by characterising genomic and epigenomic variants. nanoporetech.com/about/events...
April 24, 2025 at 8:34 AM
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@nanoporetech.com #EPI2ME Christmas party tonight!!!
December 14, 2024 at 1:14 AM
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We had a great turnout for yesterday's data for breakfast at #ASHG25. Sean McKenzie shared insights on solving complex genetic architectures with state-of-the-art de novo Oxford Nanopore assembly. Stop by booth #619 today at 10:15 am to join Matt Parker with the latest #EPI2ME updates.
October 16, 2025 at 1:00 PM
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We are hosting a Knowledge exchange on data analysis for rare diseases using EPI2ME and our data interpretation partners @geneyx.bsky.social and @fabricgenomics at the end of the month register: nanoporetech.com/about/events...
Webinar: Intuitive discovery and prioritisation of variants in rare diseases with EPI2ME and partners
Learn more learn how EPI2ME simplifies genomic and epigenomic analysis of your rare disease samples, and how partners Geneyx and Fabric offer solutions for variant prioritisation to guide insights for...
nanoporetech.com
March 11, 2025 at 12:00 PM
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June 3, 2025 at 3:07 PM
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Thought it was time I joined @nanoporetech.com on here - follow me for the latest #EPI2ME tweets… probably the odd smattering of trains and travel too.
December 8, 2024 at 3:22 PM
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trying out the EPI2ME cloud genome assembly pipeline...
May 13, 2025 at 3:26 PM
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But we have an EPI2ME cloud genome assembly pipeline at home!
May 13, 2025 at 4:01 PM
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