Resource Centre
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
Workflow )
Workflow overview: Hereditary Cancer Panel
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
Video )
AMP 2025: Rapid comprehensive molecular profiling of CNS tumors
Video AMP 2025: Epigenomic diagnosis and prognosis of Acute Myeloid Leukemia
Publication )
Nanopore-based RNA methylation profiling of a circulating lung cancer biomarker
Publication )
Wakhan: reconstruction of chromosome-scale copy number profiles of tumour genomes with long-read sequencing
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
