Resource Centre
Publication Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications
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Contaminating plasmid sequences and disrupted vector genomes in the liver following adeno-associated virus gene therapy
Getting started guide 
Getting started guide: biopharma
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Single-workflow nanopore whole-genome sequencing with adaptive sampling for accelerated and comprehensive paediatric cancer profiling
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Enhancing CYP2D6 genotyping with nanopore sequencing to address allele diversity P. vivax malaria elimination
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How ‘Sturgeon’ guides the surgeon
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Rapid epigenomic classification of acute leukaemia
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Bioactive molecules unearthed by terabase-scale long-read sequencing of a soil metagenome
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Swine influenza-modified pulmonary microbiota
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Nanopore- and AI-empowered microbial viability inference
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A spatial long-read approach at near-single-cell resolution reveals developmental regulation of splicing and polyadenylation sites
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Shallow shotgun metagenomic sequencing of vaginal microbiomes with the Oxford Nanopore technology enables the reliable determination of state types
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Epigenomic diagnosis and prognosis of acute myeloid leukaemia
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Structural variation in 1,019 diverse humans based on long-read sequencing
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Continental-scale genomic surveillance of Plasmodium falciparum malaria with rapid nanopore sequencing
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Precise identification of viral–host integration events in HPV-positive cervical cancers by targeted long-read sequencing
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Combining panel-based and whole-transcriptome-based gene fusion detection by long-read sequencing
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'Vivaldi': an amplicon-based whole-genome sequencing method for the four seasonal human coronaviruses, 229E, NL63, OC43 and HKU1, alongside SARS-CoV-2
Workflow 
Workflow overview: mpox virus sequencing
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Determining genotype and antimicrobial resistance of Salmonella Typhi in environmental samples by amplicon sequencing