News
Pioneering European collaboration to advance genetic diagnostics: introducing the European Long Read Innovation Network (ELRIN)
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- Whole genome
- Oncology
- Multiomics
- Human genomics
- Identification
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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- Clinical research
- Clinical
- DNA
- Whole genome
Oxford Nanopore Technologies collaborates with Twist Bioscience to launch Pharmacogenomics Beta Programme and advance personalised medicine
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- Biopharma
- Clinical research
Oxford Nanopore Technologies and UMC Utrecht collaborate on 1,000 human genome sequencing project
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- Clinical research
- Direct analysis
- Metagenomics
- PromethION
- Real-time
Oxford Nanopore Technologies and Plasmidsaurus announce strategic collaboration to advance plasmid sequencing
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- Plasmid
- Real-time
- Microbiology
Oxford Nanopore and Kaust collaborate to advance multi-omic discovery
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- DNA
- Environment
- High-throughput
- Identification
- Microbiology
Oxford Nanopore’s ORG.one hits milestone, announces new focus on endangered species
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- Whole genome
Oxford Nanopore expands Compatible Products Programme and strengthens multi-omics ecosystem
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- Multiomics
- Workflow
- Sample prep
- Structural variation
- Infectious disease
Oxford Nanopore expands compatibility with 10x Genomics to unlock deeper insights in single-cell transcriptomic
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- Transcriptomics
- Transcriptome
- Single cell
- EPI2ME
- Isoforms
Oxford Nanopore announces landmark UK Government partnership to advance genomics-driven healthcare innovation in the UK | Oxford Nanopore Technologies
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- Bioinformatics
- Data storage
- Epigenetics
- Cancer research
- Human genomics
Oxford Nanopore, Action for ME, and University of Edinburgh launch groundbreaking study into the genetics of ME
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- Whole genome
- DNA
Your Oxford Nanopore guide to ASHG 2020 online
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- Structural variation
- Targeted
- Event highlight
Innovations with ultra-long reads
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- Methylation
- PromethION
- London Calling
- Structural variation
- Phasing
Blog: Resolving structural variants causing antithrombin deficiency
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- Human genomics
- Clinical research
- Structural variation
- Variant calling
- PromethION
Blog: cuteSV - a powerful tool to uncover the full spectrum of genomic structural variants
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- Structural variation
- PromethION
- DNA
- gDNA
- Whole genome
Blog: Copy number variation analysis from plasma: is it feasible using nanopore sequencing?
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- Cancer research
- Clinical research
- Structural variation
- MinION
- Flongle
London Calling 2025 Technology Update: Oxford Nanopore unveils path to a true multiomics future
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- London Calling
- Development
- Flow cell
- Workflow
- Adaptive sampling