Resource Centre
Case study )
Case study: unlocking the abundance of information within environmental microbiomes
Case study )
Case study: from seed to harvest — protecting food crops with a single platform
Case study )
Bringing genomics to the forefront of biodiversity conservation
White paper )
White paper: plant, animal, and environmental sequencing
Video )
AMP 2025: Oxford Nanopore-based structural and epigenetic profiling of D4Z4 arrays in FSHD
Knowledge exchange )
Fast answers and the most complete view: 24-hour whole-genome sequencing with Oxford Nanopore
Video )
Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing
Video )
Sequencing the wild: unlocking animal and marine metagenomes with Oxford Nanopore
Publication )
Whole-genome nanopore sequencing and automatic downstream analysis of respiratory syncytial virus using RSVTyper
Video )
Webinar: Microbes in microgravity: identifying diversity and adaptions
Publication )
A complete diploid human genome benchmark for personalised genomics
Workflow )
Workflow overview: 24-hour human whole-genome sequencing
Getting started guide )
Getting started guide: human genomics
Brochure )
Flyer: Oxford Nanopore 24-hour whole-genome sequencing for paediatric rare disease research
Workflow )
Protocol overview: interaction-free whole-genome sequencing
Workflow )
Protocol overview: influenza virus whole-genome sequencing
Case study Case study: is the end to the diagnostic odyssey within reach?
Publication )
Genomic heterogeneity and lineage-specific beta-lactamases in recurrent Achromobacter bloodstream infection patients
Case study )
Case study: expanding reference genomes with T2T assembly to reflect global diversity
Webinar )
Uncovering hidden variation in rare and complex diseases webinar
