Resource Centre
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cfDNA methylation sequencing: a precision tool for early detection of neurodegenerative disorders
- Webinar
- PromethION 2
- PromethION 24/48
- Methylation
- Epigenetics
- Neuroscience
November 5 2025
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How to sequence full-length 16S and ITS amplicons
- 16S
- Microbiology
- Amplicons
- Webinar
- Knowledge exchange
- GridION
October 30 2025
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Sequencing from large scale to single cell — the new era of biological discovery
- Human genomics
- Clinical research
October 21 2025
Enhanced hereditary cancer screening through scalable parent-of-origin-aware genomic analysis
- Human genomics
- Clinical research
October 21 2025
Webinar: Microbes in microgravity: identifying diversity and adaptions
- 16S
- Whole genome
- Microbiology
- Microbiome
- MinION
October 13 2025
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Foodborne pathogen surveillance with Oxford Nanopore sequencing
- Food safety
- Infectious disease
- Microbiology
- Bacteria
October 1 2025
Webinar: building databases to support clinical and research applications of long-read sequencing
- Clinical research
September 15 2025
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Uncovering global genetic diversity for equitable precision medicine
- Population genomics
- Human genomics
July 1 2025
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Exploring Oxford Nanopore sequencing methods for environmental samples
- Metagenomics
- Infectious disease
- Microbiology
- Webinar
- Microbiome
- Clinical research
June 26 2025
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Integrating Nanopore Sequencing Into Clinical Research: Case Studies in Pathogen, Cancer and Genomics Analysis
- Webinar
- Cancer research
- Infectious disease
- Clinical research
- Clinical
- Microbiology
June 24 2025
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Decoding paediatric cancers: multiomic insights powered by Oxford Nanopore sequencing
- Clinical research
- Cancer research
June 6 2025
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Assessing the clinical utility of Oxford Nanopore sequencing | ESHG 2025
- Clinical research
June 2 2025
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Whole-genome insights: nanopore sequencing in neuropathology
- PromethION 2
- PromethION 24/48
- EPI2ME
- Epigenetics
- Fusion transcript
- SNVs
May 19 2025
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Variant phasing for antisense oligonucleotide design using adaptive sampling
- PromethION 24/48
- Phasing
- Targeted
- Human genomics
- PromethION 24/48
- Phasing
May 19 2025
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Utilizing nanopore long-read sequencing to simplify hereditary movement disorder diagnostics
- PromethION 24/48
- PromethION 24/48
- London Calling
May 19 2025
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Using ultra-long-read Oxford Nanopore sequencing to detect complex structural variants in leukaemia
- MinION
- PromethION 2
- Phasing
- Structural variation
- Targeted
- Whole genome
May 19 2025
