Resource Centre
Video )
Whole-genome insights: nanopore sequencing in neuropathology
Video )
Using ultra-long-read Oxford Nanopore sequencing to detect complex structural variants in leukaemia
Video )
Using long-read sequencing for translational health research
Publication )
Transcriptome profiling of paediatric extracranial solid tumours and lymphomas enables rapid low‑cost diagnostic classification
Video )
Third-generation cytogenetic analysis
Publication )
Targeted sequencing and iterative assembly of near-complete genomes
Video )
Targeted adaptive sampling for pharmacogenomics and genome-wide variant analysis
Publication )
Targeted adaptive sampling enables clinical pharmacogenomics testing and genome-wide genotyping
Video )
Studying disease-causing transposable element insertions using Oxford Nanopore sequencing
Video )
Streamlined glioma diagnosis from FFPE tissue: one assay, lower cost, and faster turnaround time
Video )
Stencilling accessible chromatin fibres reveals haplotype-specific regulation
Video )
Single-molecule DNA methylation reveals unique epigenetic identity profiles of T helper cells
Video )
Single-cell transcriptome sequencing
Publication )
Sequencing and assembling the genome of Przewalski's horse in the classroom
Video )
Robbing the array to feed the pore: exploring ultra-fast brain tumour diagnosis
Publication )
Resolving RH and GYP hybrid alleles while accessing the entire blood group genome with nanopore adaptive sampling
Publication )
Realfreq: real-time base modification analysis for nanopore sequencing
Publication )
Real-time genomic characterisation of paediatric acute leukaemia using adaptive sampling
Video )
Rapid nephrogenomics for thrombotic microangiopathies
Publication Rapid epigenomic classification of acute leukaemia
