Resource Centre
Poster Poster: structural and epigenetic profiling of D4Z4 arrays in FSHD using Oxford Nanopore sequencing
Poster 
Poster: DNA extraction from dried blood spots for Oxford Nanopore sequencing
Publication Nanopore metagenomic sequencing links clinically relevant resistance determinants to pathogens
Publication 
Exon skipping as a potential diagnostic biomarker in colorectal cancer: an integrated epigenomic-transcriptomic analysis
Getting started guide 
Getting started guide: targeted sequencing
Publication DUCKS4: a comprehensive workflow for nanopore sequencing analysis of facioscapulohumeral muscular dystrophy (FSHD)
Publication 
Ultra-fast sample-to-sequencing workflow for clinical diagnostics using micropillars
Publication 
Functional and epigenomic consequences of DNMT1 variants in inherited neurological disorders
Publication 
Feasibility of long-read nanopore sequencing for methylation-based classification of posterior fossa ependymomas
Publication 
Long-read genome sequencing enhances diagnostics of paediatric neurological disorders
Video 
AMP 2025: Rapid comprehensive molecular profiling of CNS tumors
Publication 
Nanopore-based RNA methylation profiling of a circulating lung cancer biomarker
Publication 
Reproducibility and accuracy of bacterial methylome profiling using Oxford Nanopore Technologies nanopore sequencing platform
Video 
Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing
Video 
Revealing hidden genomic variation in Parkinson’s disease
Poster 
Scalable pharmacogenomics (PGx) using targeted long-read genotyping panels
Publication 
DNA methylation reprogramming in marsupial embryos is restricted to the extraembryonic lineage
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 
Enriching for answers in rare diseases