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
