Resource Centre
Brochure )
Brochure: PromethION 24
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
Brochure )
Brochure: Oxford Nanopore products
Publication )
Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications
Publication )
Efficient near telomere-to-telomere assembly of nanopore simplex reads
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
Publication )
Contaminating plasmid sequences and disrupted vector genomes in the liver following adeno-associated virus gene therapy
Publication )
Long-read genome sequencing enhances diagnostics of paediatric neurological disorders
Case study )
Case study: unlocking the abundance of information within environmental microbiomes
Case study )
Case study: bringing genomics to the forefront of biodiversity conservation
Publication )
Transcriptome-wide profiling of alternative splicing regulators with CRISPore-seq
Publication )
Single-cell long-read whole-genome sequencing reveals somatic transposon activity in human brain
Video Revealing hidden genomic variation in Parkinson’s disease
Publication )
DNA methylation reprogramming in marsupial embryos is restricted to the extraembryonic lineage
Publication )
Proof-of-principle: Nanopore adaptive sampling enables full blood group genome analysis and resolution of hybrid alleles
Video cfDNA methylation sequencing: a precision tool for early detection of neurodegenerative disorders
Publication )
Ensilication preserves high-molecular-weight native DNA for clinical long-read sequencing
Publication )
Enriching for answers in rare diseases
