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