Resource Centre
Bioinformatics tool )
Yanocomp: robust prediction of m6A modifications in individual nanopore direct RNA reads
Bioinformatics tool )
yacrd and fpa: upstream tools for long-read genome assembly
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
Bioinformatics tool )
Whole Human Genome Sequencing Project
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 Nanopore DNA analysis shows that chronic corticosterone supplementation results in altered sperm DNA methylation.
Poster )
Whole-genome analysis of VREfm isolates with daptomycin resistance using Oxford Nanopore and Illumina sequencing
Bioinformatics tool )
Wengan: Efficient and high quality hybrid de novo assembly of human genomes
Bioinformatics tool )
WeFaceNano: a user-friendly pipeline for complete ONT sequence assembly and detection of antibiotic resistance in multi-plasmid bacterial isolates
Case study )
Wastewater sequencing — an early warning system for infectious disease outbreaks
Publication Wakhan: reconstruction of chromosome-scale copy number profiles of tumour genomes with long-read sequencing
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 )
Verkko2: integrating proximity ligation data with long-read De Bruijn graphs for efficient telomere-to-telomere genome assembly, phasing, and scaffold
Bioinformatics tool )
Verkko: telomere-to-telomere assembly of diploid chromosomes
