Resource Centre
Publication )
Transcriptome-wide profiling of alternative splicing regulators with CRISPore-seq
Video )
Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing
Publication )
Transcriptional readthrough precedes alternative splicing programs triggered in CML cells by imatinib
Webinar )
Transforming hereditary cancer sequencing with adaptive sampling target enrichment
Publication )
Nanopore direct RNA sequencing reveals METTL2A-mediated m3C sites in poly(A) RNA
Publication )
Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomatic
Publication )
Nanopore sequencing reveals novel alternative splice variants of EZH2 in paediatric medulloblastoma
White paper )
White paper: human and clinical research
Publication )
Single-workflow nanopore whole-genome sequencing with adaptive sampling for accelerated and comprehensive paediatric cancer profiling
Case study )
Testimonial: Yaw Bediako
Publication )
How ‘Sturgeon’ guides the surgeon
Knowledge exchange Adaptive sampling explained: the future of flexible target enrichment
Publication Rapid epigenomic classification of acute leukaemia
Application note Application note: Comprehensive genomic and epigenomic profiling with the Oxford Nanopore Hereditary Cancer Panel
Publication DNA methylation influences human centromere positioning and function
Publication )
The landscape of microbial associations in human cancer
Brochure Flyer: Hereditary Cancer Panel
Publication )
Cross-platform methylation-based site of origin classification for squamous cell carcinomas
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
