Resource Centre
Publication 
Yaniv Erlich: A vision for Ubiquitous Sequencing
Workflow 
Workflow overview: pathogen metagenomics
Workflow 
Workflow overview: microbial amplicon barcoding
Workflow 
Workflow overview: AAV sequencing
Bioinformatics tool 
Whole Human Genome Sequencing Project
Publication 
The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematology
Publication 
Whole genome sequencing for rapid characterization of rabies virus using nanopore technology
Video 
Whole-genome sequencing in PulseNet foodborne molecular surveillance systems
Bioinformatics tool 
Whole-Genome Sequencing of a Human Clinical Isolate of emm28 Streptococcus pyogenes Causing Necrotizing Fasciitis Acquired Contemporaneously with Hurricane Harvey
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 
Visualisation and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR
Video 
Variant segregation in rare disease singletons and duos using nanopore adaptive sampling
Publication 
Validation of HPV genotyping by Oxford Nanopore sequencing in FFPE tissues and ThinPrep anal and gynaecological samples
Poster 
Validation and application of multiplex nanopore MinION sequencing for molecular typing of human adenoviruses in clinical samples: a cost effective sequencing strategy
Poster 
Validation and quality control of a molecular cloning experiment using de novo assembly of Oxford Nanopore reads
Publication 
Utilizing nanopore sequencing technology for the rapid and comprehensive characterization of eleven HLA loci
Publication 
Utilising nanopore direct RNA sequencing of blood from patients with sepsis for discovery of co- and post-transcriptional disease biomarkers
Video 
Using ultra-long-read Oxford Nanopore sequencing to detect complex structural variants in leukaemia
