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
