Resource Centre
Publication )
Nanopore long-read-only genome assembly of clinical Enterobacterales isolates is complete and accurate
Publication )
Concurrent L1 retrotransposition events promote reciprocal translocations in human tumorigenesis
Publication )
Flexible and rapid validation of structural variation using adaptive sampling
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
Publication )
Sensitive, flexible, and affordable serum RNA sequencing for pathogen detection on the Oxford Nanopore platform
Publication )
Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications
Publication DUCKS4: a comprehensive workflow for nanopore sequencing analysis of facioscapulohumeral muscular dystrophy (FSHD)
Publication )
Improving local diagnostic capacity for microbiological identification and antimicrobial resistance gene detection in Northern Nigeria using nanopore
Publication )
Efficient near telomere-to-telomere assembly of nanopore simplex reads
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 Genetic diagnosis of CYP21A2-related CAH: adaptive sampling long-read sequencing is an accurate and scalable solution
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 spatial transcriptomics of patient-derived ccRCC organoids identifies heterogeneity and transcriptional remodelling following treatment
Publication )
Clinical validation and utility of targeted nanopore sequencing for rapid pathogen diagnosis and precision therapy in lung cancer patients
Publication )
Long-read genome sequencing enhances diagnostics of paediatric neurological disorders
Publication )
Twist-ONT: combining nanopore sequencing with the Twist comprehensive viral research panel
Publication )
RAPID: a targeted long-read RNA workflow for functional resolution of splicing variants in rare disease
