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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 Technologies collaborates with Twist Bioscience to launch Pharmacogenomics Beta Programme and advance personalised medicine
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Oxford Nanopore Technologies and UMC Utrecht collaborate on 1,000 human genome sequencing project
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Oxford Nanopore Technologies and Plasmidsaurus announce strategic collaboration to advance plasmid sequencing
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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 expands Compatible Products Programme and strengthens multi-omics ecosystem
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Oxford Nanopore expands compatibility with 10x Genomics to unlock deeper insights in single-cell transcriptomic
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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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Your Oxford Nanopore guide to ASHG 2020 online
Company news National German initiative partners with Oxford Nanopore to advance research of rare diseases with nanopore-based genome sequencing
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"Most complete human genome assembly to date using single tech": Nature Biotech paper from consortium of nine centres use MinION to sequence human genome
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Longer and longer: DNA sequence of more than two million bases now achieved with nanopore sequencing.
Company news Innovations with ultra-long reads
Company news Blog: Resolving structural variants causing antithrombin deficiency
Company news Blog: cuteSV - a powerful tool to uncover the full spectrum of genomic structural variants
Company news Blog: Copy number variation analysis from plasma: is it feasible using nanopore sequencing?
