Resource Centre
Publication 
Yaniv Erlich: A vision for Ubiquitous Sequencing
Workflow 
Workflow overview: mpox virus sequencing
Workflow 
Workflow overview: tumour-normal sequencing
Workflow 
Workflow overview: 24-hour human whole-genome sequencing
Workflow 
Workflow overview: plant genome assembly
Workflow 
Workflow overview: large cohort sequencing
Workflow 
Workflow overview: human variant calling
Workflow 
Workflow overview: NO-MISS
Bioinformatics tool 
Whole Human Genome Sequencing Project
Publication 
Whole genome sequencing for rapid characterization of rabies virus using nanopore technology
Publication 
Whole-genome nanopore sequencing and automatic downstream analysis of respiratory syncytial virus using RSVTyper
Poster 
Whole genome Nanopore DNA analysis shows that chronic corticosterone supplementation results in altered sperm DNA methylation.
Video 
Whole-genome insights: nanopore sequencing in neuropathology
Poster 
Whole-genome DNA sequencing using nanopore R10.4 promises best practice for single-cell variation detection and methylation profiling
Publication 
Whole genome assembly of a hybrid Trypanosoma cruzi strain assembled with nanopore sequencing alone
Poster 
Whole-genome analysis of VREfm isolates with daptomycin resistance using Oxford Nanopore and Illumina sequencing
Publication 
WGS of a cluster of MDR Shigella sonnei utilising Oxford Nanopore R10.4.1 long-read sequencing
Bioinformatics tool 
Wengan: Efficient and high quality hybrid de novo assembly of human genomes
Knowledge exchange 
Turning data into answers: Rare disease case studies from clinical researchers
Company news 
"...we need a better name than follow through"
