Resource Centre
Workflow overview: large cohort sequencing
- Population genomics
- Workflow
- Human genomics
- Clinical research
- Whole genome
- Structural variation
Scalable nanopore sequencing for Alzheimer’s research
- Population genomics
- Human genomics
- Neuroscience
Wastewater sequencing — an early warning system for infectious disease outbreaks
- Population genomics
- Bioinformatics
- Microbiology
- Microbiome
- Environment
- Plant
Visualisation and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR
- Population genomics
- Long-read
- MinION
- PromethION
- Guppy
- MinKNOW
Using long-read sequencing for translational health research
- Population genomics
- PromethION 2
- Single cell
- Bioinformatics
- Clinical research
- Single cell
Unlocking the banana pangenome: harnessing genetic diversity
- Population genomics
- Plant
- Variant calling
- Phasing
- Assembly
- Bioinformatics
Uncovering global genetic diversity for equitable precision medicine
- Population genomics
- Human genomics
Ultra-rich human data — variant analysis with EPI2ME
- Population genomics
- Bioinformatics
- Human genomics
- EPI2ME
- Epigenetics
- SNVs
Towards personalised medicine for breast cancer in the Caribbean: a pilot study
- Population genomics
- Variant calling
- Cancer research
- PromethION
- EPI2ME
- London Calling
The correlation between CpG methylation and gene expression is driven by sequence variants
- Population genomics
- Methylation
- Human genomics
- PromethION 24/48
Targeted nanopore sequencing using hybridisation probes reveals immune escape polymorphisms in malaria vaccine candidates
- Population genomics
- Infectious disease
- London Calling
Targeted adaptive sampling for pharmacogenomics and genome-wide variant analysis
- Population genomics
- PromethION 2
- Pharmacogenomics
- Bioinformatics
- Clinical research
- Human genomics
Supporting data for "de novo assembly and population genomic survey of natural yeast isolates with the Oxford Nanopore MinION sequencer"
- Population genomics
- MinION
- Bioinformatics
- Whole genome
- Assembly
- Structural variation
Structural variation in All of Us analyzed with long-read sequencing at a scale
- Population genomics
- Nanopore Community
- Human genomics
- SNVs
- Phasing
- Long-read
Structural variants in the French-Canadian population
- Population genomics
- Structural variation
Structural variants in Chinese population and their impact on phenotypes, diseases and population adaptation
- Population genomics
- Human genomics
- Whole genome
- Structural variation
- Variant calling
- Long-read
Showcase: Carrier screening
- Population genomics
- Cancer research
- Clinical research
- Bioinformatics
- Human genomics
- MinION
Shining light on a dark mystery: melanoma in bullhead benthic fish in Lake Memphremagog
- Population genomics
- London Calling
- Animal
- Bioinformatics
- Assembly
- Variant calling
Scalable nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
- Population genomics
- Human genomics
- PromethION
- Variant calling
- SNVs
- Structural variation
Real-time targeted sequencing with adaptive sampling
- Population genomics
- PromethION 24/48
- Epigenetics
- Structural variation
- Human genomics
- PromethION 24/48