Resource Centre
Workflow )
Workflow overview: large cohort sequencing
Video )
Scalable nanopore sequencing for Alzheimer’s research
Case study )
Wastewater sequencing — an early warning system for infectious disease outbreaks
Publication )
Visualisation and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR
Video )
Using long-read sequencing for translational health research
Video )
Unlocking the banana pangenome: harnessing genetic diversity
Video )
Uncovering global genetic diversity for equitable precision medicine
Video )
Ultra-rich human data — variant analysis with EPI2ME
Video )
Towards personalised medicine for breast cancer in the Caribbean: a pilot study
Publication )
The correlation between CpG methylation and gene expression is driven by sequence variants
Poster )
Targeted nanopore sequencing using hybridisation probes reveals immune escape polymorphisms in malaria vaccine candidates
Video )
Targeted adaptive sampling for pharmacogenomics and genome-wide variant analysis
Bioinformatics tool )
Supporting data for "de novo assembly and population genomic survey of natural yeast isolates with the Oxford Nanopore MinION sequencer"
Poster )
Structural variation in All of Us analyzed with long-read sequencing at a scale
Events )
Structural variants in the French-Canadian population
Publication )
Structural variants in Chinese population and their impact on phenotypes, diseases and population adaptation
Video )
Showcase: Carrier screening
Video )
Shining light on a dark mystery: melanoma in bullhead benthic fish in Lake Memphremagog
Publication )
Scalable nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
Video )
Real-time targeted sequencing with adaptive sampling
