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Wasatch BioLabs and Oxford Nanopore Team Up to Accelerate Methylation Sequencing Towards Clinical Use
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Pioneering European collaboration to advance genetic diagnostics: introducing the European Long Read Innovation Network (ELRIN)
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Oxford Nanopore Technologies selected by Murdoch Children’s Research Institute to support landmark research into faster genetic screening for rare dis
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Oxford Nanopore and Kaust collaborate to advance multi-omic discovery
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Oxford Nanopore’s ORG.one hits milestone, announces new focus on endangered species
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Oxford Nanopore launches a 24-hour whole genome sequencing workflow for rare disease research
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Oxford Nanopore announces PromethION Plus Flow Cell and other human genetics updates at ASHG 2025
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Oxford Nanopore announces landmark UK Government partnership to advance genomics-driven healthcare innovation in the UK | Oxford Nanopore Technologies
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Oxford Nanopore, Action for ME, and University of Edinburgh launch groundbreaking study into the genetics of ME
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Interview: Tumoroids from colon cancer, including WGS-strategy
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Interview: Old is new: maximizing read lengths and yield for genome assembly
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Blog: Resolving structural variants causing antithrombin deficiency
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Blog: cuteSV - a powerful tool to uncover the full spectrum of genomic structural variants
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London Calling 2025 Technology Update: Oxford Nanopore unveils path to a true multiomics future
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Cepheid and Oxford Nanopore Technologies partner to advance automated sequencing-based solutions
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CariGenetics launches Caribbean Genome Programme with Oxford Nanopore to drive regional genomic research
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Breakthrough algorithm enables partially phased, near telomere-to-telomere assembly using standard Oxford Nanopore simplex reads
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Al Jalila Children’s Hospital advances rare disease identification through Oxford Nanopore sequencing, a new study shows | Oxford Nanopore Technologies