Resource Centre
Workflow 
Workflow overview: tumour-normal sequencing
Workflow 
Workflow overview: 24-hour human whole-genome sequencing
Workflow 
Workflow overview: pharmacogenomics with adaptive sampling
Workflow 
Workflow overview: large cohort sequencing
Workflow 
Workflow overview: human variant calling
Publication 
Whole-genome sequencing of SARS-CoV-2 in the Republic of Ireland during waves 1 and 2 of the pandemic
Publication 
Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer
Poster 
Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation
Publication 
Whole genome sequencing and phylogenetic classification of Tunisian SARS-CoV-2 strains from patients of the Military Hospital in Tunis
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 
Viral sequencing reveals US healthcare personnel rarely become infected with SARS-CoV-2 through patient contact
Publication 
Viral genetic sequencing identifies staff transmission of COVID-19 is important in a community hospital outbreak
Publication 
Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis
Publication 
Utilizing nanopore sequencing technology for the rapid and comprehensive characterization of eleven HLA loci
Video 
Using Targeted Nanopore Technologies
Video 
Using long-read nanopore sequencing to unravel structural genomic variations in plants
Poster 
Unprecedented access to haplotype-resolved biology enabled by ultra-long reads and Pore-C
Poster 
Unlocking the power of haplotype-based molecular breeding using long read DNA sequencing
Publication 
Unique mutational changes in SARS-CoV2 genome of different state of India
