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
