Resource Centre
Publication 
Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications
Getting started guide 
Getting started guide: targeted sequencing
Publication 
Long-read genome sequencing enhances diagnostics of paediatric neurological disorders
Video 
AMP 2025: Epigenomic diagnosis and prognosis of Acute Myeloid Leukemia
Publication 
Nanopore-based RNA methylation profiling of a circulating lung cancer biomarker
Publication 
CRISPR-Cas9-induced double-strand breaks disrupt maintenance of epigenetic information
Publication 
Reproducibility and accuracy of bacterial methylome profiling using Oxford Nanopore Technologies nanopore sequencing platform
Poster 
Scalable pharmacogenomics (PGx) using targeted long-read genotyping panels
Publication DNA methylation reprogramming in marsupial embryos is restricted to the extraembryonic lineage
Publication 
Nanopore direct RNA sequencing reveals METTL2A-mediated m3C sites in poly(A) RNA
Publication 
Enriching for answers in rare diseases
Publication 
Nanopore long-read sequencing for the critically ill facilitates ultrarapid diagnostics and urgent clinical decision-making
Publication 
Long-read genome sequencing and multi-omics in ageing and neurodegeneration
Poster 
An end-to-end workflow for pharmacogenomic target enrichment, star allele annotation, and CYP2D6 resolution using nanopore sequencing
Publication 
Single-workflow nanopore whole-genome sequencing with adaptive sampling for accelerated and comprehensive paediatric cancer profiling
Publication Long-read epigenetic clocks identify improved brain ageing predictions
Publication 
Integrating long-read nanopore sequencing for precision resolution of genomic variants in dystonia
Publication 
How ‘Sturgeon’ guides the surgeon
Publication Rapid epigenomic classification of acute leukaemia
Publication 
A complete diploid human genome benchmark for personalised genomics
