Resource Centre
Poster 
Validation and application of multiplex nanopore MinION sequencing for molecular typing of human adenoviruses in clinical samples: a cost effective sequencing strategy
Video 
Towards routine modopathy diagnostics: advances and clinical application of direct RNA sequencing
Video 
Stepping into the future of nanopore protein sequencing
Video 
Stencilling accessible chromatin fibres reveals haplotype-specific regulation
Publication 
Single-cell rapid capture hybridization sequencing (scRaCH-seq) to reliably detect isoform usage and coding mutations in targeted genes at a single-cell level
Poster 
A multi-omic investigation of gene dysregulation in a complex chromothripsis-like translocation event using Oxford Nanopore sequencing
Poster 
Poster: structural and epigenetic profiling of D4Z4 arrays in FSHD using Oxford Nanopore sequencing
Video 
Nanopore sequencing reveals psilocybin-induced brain 5mC/5hmC epigenetic changes
Video 
Nanopore sequencing of intact, aminoacylated tRNA
Publication 
Nanopore sequencing of DNA-barcoded probes for highly multiplexed detection of microRNA, proteins and small biomarkers
Publication 
Nanopore-based consensus sequencing enables accurate multimodal tumour cell-free DNA profiling
Poster 
Multiomic data identifies skewed X-inactivation and its role in masking Mendelian inheritance patterns
Publication 
Multi-omics analysis reveals COVID-19 vaccine induced attenuation of inflammatory responses during breakthrough disease
Publication 
Multi-omic profiling reveals epigenetic drivers of immunotherapy resistance in multiple myeloma
Video 
Masterclass: How to select the right library prep workflow for your experiment | LC25
Video 
Masterclass: How to get started with Oxford Nanopore sequencing | LC25
Video 
Masterclass: How to extract high-quality DNA and RNA | LC25
Video 
Masterclass: How to call variants and methylation across the human genome | LC25
Video 
Masterclass: How to analyse your Oxford Nanopore sequencing data | LC25
Publication 
Long-read single-cell genome, transcriptome and open chromatin profiling links genotype to phenotypes
