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
Learning )
Which library prep workflow is right for my experiment?
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
