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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 Mahidol University launch first Centre of Excellence in Southeast Asia | Oxford Nanopore Technologies
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Oxford Nanopore Technologies and Dubai Health to collaborate on genetic screening
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Oxford Nanopore launches a 24-hour whole genome sequencing workflow for rare disease research
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Oxford Nanopore and UK Biobank to create world's first epigenetic dataset targeting the causes of cancer, dementia, complex disease | Oxford Nanopore Technologies
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Mayo Clinic and Oxford Nanopore announce collaboration to advance precision medicine for cancer and genetic disorders
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Interview: Parent-of-origin genome analysis presents the potential to improve future genetic testing
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Interview: Advancing long-read de novo genome assembly methods in clinical research
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Blog: Resolving structural variants causing antithrombin deficiency
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Blog: Copy number variation analysis from plasma: is it feasible using nanopore sequencing?
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bioMérieux makes strategic investment in Oxford Nanopore
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Breakthrough towards protein sequencing using Oxford Nanopore holds promise for disease research and drug development
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Bio-Techne and Oxford Nanopore expand agreement to accelerate development of genetics portfolio through 2032
Company news APAC Rare Disease Consortium launched to advance genomic innovation and rare disease diagnosis
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Al Jalila Children’s Hospital advances rare disease identification through Oxford Nanopore sequencing, a new study shows | Oxford Nanopore Technologies