Resource Centre
Workflow 
Workflow overview: single-cell transcriptomics
Workflow 
Workflow overview: 24-hour human whole-genome sequencing
Workflow 
Workflow overview: pharmacogenomics with adaptive sampling
Workflow 
Workflow overview: Hereditary Cancer Panel
Workflow 
Workflow overview: large cohort sequencing
Workflow 
Workflow overview: human variant calling
Workflow 
Workflow overview: direct RNA sequencing
Workflow 
Workflow overview: bacterial isolate sequencing
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 
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
Video 
Nanopore sequencing: insights from neonatal intensive care to cancer
Knowledge exchange 
Adaptive sampling explained: the future of flexible target enrichment
Case study 
Wastewater sequencing — an early warning system for infectious disease outbreaks
Video 
Cancer WGS on the PromethION
Video 
Variant segregation in rare disease singletons and duos using nanopore adaptive sampling
Publication 
Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis
Poster 
Validation and application of multiplex nanopore MinION sequencing for molecular typing of human adenoviruses in clinical samples: a cost effective sequencing strategy
Publication 
Utilizing nanopore sequencing technology for the rapid and comprehensive characterization of eleven HLA loci
