Resource Centre
Brochure 
Brochure: Oxford Nanopore products
Publication 
Ultra-fast sample-to-sequencing workflow for clinical diagnostics using micropillars
Publication 
Feasibility of long-read nanopore sequencing for methylation-based classification of posterior fossa ependymomas
Workflow 
Workflow overview: Hereditary Cancer Panel
Publication 
Long-read spatial transcriptomics of patient-derived ccRCC organoids identifies heterogeneity and transcriptional remodelling following treatment
Publication 
Transcriptome-wide profiling of alternative splicing regulators with CRISPore-seq
Publication 
Novel multiplex family-wide PCR and nanopore sequencing of amplicons (FP-NSA) approach for surveillance of influenza- and coronaviruses
Getting started guide 
Getting started guide: biopharma
Publication 
Integrating long-read nanopore sequencing for precision resolution of genomic variants in dystonia
Workflow 
Workflow overview: microbial amplicon barcoding
Workflow 
Workflow overview: 24-hour human whole-genome sequencing
Getting started guide 
Getting started guide: human genomics
Workflow 
Protocol overview: interaction-free whole-genome sequencing
Publication Long-read genomic and epigenomic profiling enhances timely comprehensive variant discovery in hypotonia and muscle weakness
Publication 
Swine influenza-modified pulmonary microbiota
Publication 
Epigenomic diagnosis and prognosis of acute myeloid leukaemia
Workflow 
Workflow overview: mpox virus sequencing
Workflow 
Workflow overview: AAV sequencing
Publication 
Evaluating the diagnostic utility of 16S ONT sequencing in patients with central nervous system infections and its usefulness in antimicrobial
Poster 
Validation and quality control of a molecular cloning experiment using de novo assembly of Oxford Nanopore reads
