Resource Centre
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Whole-genome insights: nanopore sequencing in neuropathology
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Welcome to London Calling 2025
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Welcome back to London Calling 2025
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Variant phasing for antisense oligonucleotide design using adaptive sampling
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Utilizing nanopore long-read sequencing to simplify hereditary movement disorder diagnostics
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Using ultra-long-read Oxford Nanopore sequencing to detect complex structural variants in leukaemia
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Using long-read sequencing for translational health research
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Update from the Oxford Nanopore Technologies Applications team LC 25
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Ultra-fast deep-learned classification algorithms for diagnosing pediatric CNS and solid tumors
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Towards routine modopathy diagnostics: advances and clinical application of direct RNA sequencing
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Third-generation cytogenetic analysis
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Targeted adaptive sampling for pharmacogenomics and genome-wide variant analysis
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Studying disease-causing transposable element insertions using Oxford Nanopore sequencing
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Streamlined glioma diagnosis from FFPE tissue: one assay, lower cost, and faster turnaround time
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Stepping into the future of nanopore protein sequencing
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Stencilling accessible chromatin fibres reveals haplotype-specific regulation
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Single-molecule DNA methylation reveals unique epigenetic identity profiles of T helper cells
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Single-cell transcriptome sequencing
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Real-time targeted sequencing with adaptive sampling
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Rapid-response mobile laboratory for disease elimination, outbreak investigation, and pathogen X
