EPI2ME: bioinformatics for all levels of expertise

EPI2ME breaks the bioinformatics paradigm by enabling anyone to analyse their own data.

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EPI2ME 25.05-01 Release
Software Releases
EPI2ME 25.05-01 Release
Stephen Rudd
May 21, 2025
3 min
Teloseq 12-plex Human and Cow cell lines
Data Releases
Teloseq 12-plex Human and Cow cell lines
May 21, 2025
1 min
Phasing of small insertions and deletions
Articles
Phasing of small insertions and deletions
May 14, 2025
1 min

EPI2ME provides best practice bioinformatics analyses for nanopore sequencing

  • Simply and easily analyse your sequencing data
  • Transparent: all our analyses are open source
  • No need to upload your data to the cloud
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Phasing of small insertions and deletions
Phasing of small insertions and deletions
One of the major advantages of long-read sequencing is its ability to resolve phasing — identifying…
May 14, 2025
1 min
The variant delusion: calling variants in a mixed-up world
The variant delusion: calling variants in a mixed-up world
In the previous post , we explored a simple but powerful Bayesian model of variant calling. This…
Chris Wright
May 05, 2025
13 min
Singularity for bioinformatics
Singularity for bioinformatics
Have you ever tried downloading a new shiny software tool from GitHub, keen to run your test dataset…
Neil Horner
February 26, 2024
7 min
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