Resource Centre
Getting started guide 
Getting started guide: targeted sequencing
Video 
AMP 2025: Epigenomic diagnosis and prognosis of Acute Myeloid Leukemia
Publication 
CRISPR-Cas9-induced double-strand breaks disrupt maintenance of epigenetic information
Video 
Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing
Video 
cfDNA methylation sequencing: a precision tool for early detection of neurodegenerative disorders
Publication 
Nanopore direct RNA sequencing reveals METTL2A-mediated m3C sites in poly(A) RNA
Publication 
Long-read epigenetic clocks identify improved brain ageing predictions
Workflow 
Workflow overview: 24-hour human whole-genome sequencing
Getting started guide 
Getting started guide: human genomics
Brochure 
Flyer: Oxford Nanopore 24-hour whole-genome sequencing for paediatric rare disease research
Workflow 
Protocol overview: interaction-free whole-genome sequencing
Workflow Workflow overview: direct RNA sequencing
Case study 
Case study: is the end to the diagnostic odyssey within reach?
Publication 
Deregulating m6A regulators leads to altered RNA biology in glioma cell lines
Case study 
Case study: unravelling tumour biology with single-cell Oxford Nanopore sequencing
Webinar 
Uncovering hidden variation in rare and complex diseases webinar
Case study 
Case study: exploring the future of rapid leukaemia diagnosis with a single-platform workflow
Workflow 
Workflow overview: tumour-normal sequencing
Publication 
Direct detection of 8-oxo-dG using nanopore sequencing
Video 
Whole-genome insights: nanopore sequencing in neuropathology