Resource Centre
Publication 
ZCWPW1 loss-of-function variants in Alzheimer’s Disease
Workflow 
Workflow overview: tumour-normal sequencing
Workflow 
Workflow overview: pharmacogenomics with adaptive sampling
Workflow 
Workflow overview: large cohort sequencing
Workflow 
Workflow overview: human variant calling
Publication 
The WIPE assay for selection and elimination of HIV-1 provirus in vitro using latency-reversing agents
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 of rare disease patients in a national healthcare system
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
Bioinformatics tool 
Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment
Bioinformatics tool 
VIRUSBreakend: viral integration recognition using single breakends
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 
Utilizing nanopore sequencing technology for the rapid and comprehensive characterization of eleven HLA loci
Publication 
Using de novo assembly to identify structural variation of complex immune system gene regions
Publication 
Unraveling the features of somatic transposition in the Drosophila intestine
Video 
Unlocking the banana pangenome: harnessing genetic diversity
Publication 
Unique mutational changes in SARS-CoV2 genome of different state of India
Bioinformatics tool 
Unique K-mer sequences for validating cancer-related substitution, insertion and deletion mutations
