Resource Centre
Poster 
Poster: EPI2ME – an extensible product for applied bioinformatics to make sense of your sequencing
Publication 
Nanopore long-read-only genome assembly of clinical Enterobacterales isolates is complete and accurate
Publication 
DUCKS4: a comprehensive workflow for nanopore sequencing analysis of facioscapulohumeral muscular dystrophy (FSHD)
Case study 
Case study: high-quality bacterial genome without the complexity
Publication 
Wakhan: reconstruction of chromosome-scale copy number profiles of tumour genomes with long-read sequencing
Publication 
Analysis of clinically relevant large tandem repeats using nanopore sequencing
Publication 
Targeted sequencing and iterative assembly of near-complete genomes
Publication Pre-phasing long reads improves structural variant genotyping
Publication 
Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomatic
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
Publication 
Nanopore- and AI-empowered microbial viability inference
Case study Case study: is the end to the diagnostic odyssey within reach?
Case study 
Case study: expanding reference genomes with T2T assembly to reflect global diversity
Workflow Workflow overview: pharmacogenomics with adaptive sampling
Workflow 
Workflow overview: large cohort sequencing
Workflow 
Workflow overview: tumour-normal sequencing
Publication 
DeepNanoHi-C: deep learning enables accurate single-cell nanopore long-read data analysis and 3D genome interpretation
