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Singapore’s National Precision Medicine (NPM) programme engages Oxford Nanopore to advance understanding of the genetics of Singapore’s multi-ethnic p
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Oxford Nanopore Technologies and UMC Utrecht collaborate on 1,000 human genome sequencing project
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Oxford Nanopore opens genomics market with PromethION 2 Solo: the world’s first portable, high yield sequencer providing comprehensive DNA analysis for anyone, anywhere
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Oxford Nanopore launches PromethION 2 Integrated into open early access
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Oxford Nanopore at ASHG 2022: One sequencing platform for all your biology
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Oxford Nanopore and Genomics England announce new strategic research project to resolve undiagnosed rare disease cases
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Interview: Using PromethION for Cancer, Collaborations and more
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Interview: Sequencing the poplar with PromethION
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Interview: The PromethION Experts at VIB
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Interview: PromethION 24 and human disease research
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Interview: Exploring complex disease in Asian populations with PromethION
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Innovations with ultra-long reads
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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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Al Jalila Children’s Hospital advances rare disease identification through Oxford Nanopore sequencing, a new study shows | Oxford Nanopore Technologies