Blog
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Unravelling the complexity of cancer genomics and predisposition: nanopore sequencing and the potential for personalised care | Oxford Nanopore Technologies
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Top topics at ESHG 2024 | Oxford Nanopore Technologies
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Short, long, or ultra-long: which read length is right for you?
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Science unlocked: publication picks from July 2024
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Science unlocked: publication picks from September 2024 | Oxford Nanopore Technologies
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Science unlocked: publication picks from October 2025
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Science unlocked: publication picks from June 2024
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Science unlocked: publication picks from February 2025
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Science unlocked: publication picks from December 2024
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Science unlocked: publication picks from April 2024 | Oxford Nanopore Technologies
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Reshaping rare disease diagnosis — an end to the diagnostic odyssey?
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Rapid identification of MSK-IMPACT cancer variants with real-time targeted nanopore sequencing
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PrecisionMed International: the future of population health
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Uncovering pathogenic variants with the founding president of the Thai Society of Human Genetics
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Revealing more to transform human health
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Revealing hidden genetic variants in rare disease with nanopore sequencing
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Recognising the transformative research of the Nanopore Community on Rare Disease Day
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Pushing the boundaries of rare disease research
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Multiomic single-cell cancer analysis — from mutation detection to understanding disease mechanisms
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Liquid biopsies — multi-modal cell-free DNA assays using nanopore sequencing for potential cancer detection