Resource Centre
Workflow 
Workflow overview: mpox virus sequencing
Workflow 
Workflow overview: 24-hour human whole-genome sequencing
Workflow 
Workflow overview: whole-plasmid sequencing
Workflow 
Workflow overview: pathogen metagenomics
Workflow 
Workflow overview: Hereditary Cancer Panel
Workflow 
Workflow overview: microbial amplicon barcoding
Workflow 
Workflow overview: AAV sequencing
Video 
Whole-genome insights: nanopore sequencing in neuropathology
Poster 
Whole-genome analysis of VREfm isolates with daptomycin resistance using Oxford Nanopore and Illumina sequencing
Video 
Core lab webinar series: A new 'gold standard' solution for complete plasmid sequencing
Publication 
Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis
Poster 
Validation and quality control of a molecular cloning experiment using de novo assembly of Oxford Nanopore reads
Video 
Ultra-rich human data — variant analysis with EPI2ME
Publication 
Ultra-fast sample-to-sequencing workflow for clinical diagnostics using micropillars
Publication 
Transcriptome-wide profiling of alternative splicing regulators with CRISPore-seq
Poster 
Transcriptome analysis using long nanopore reads
Poster 
Towards ultra-rapid microbial cfDNA nanopore sequencing for the identification of sepsis-causing pathogens
Video 
Towards personalised medicine for breast cancer in the Caribbean: a pilot study
Publication 
The performance of nanopore sequencing in rapid detection of pathogens and antimicrobial resistance genes in blood cultures
Publication 
TARPON - a telomere analysis and research pipeline optimised for nanopore
