Resource Centre
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Workflow overview: large cohort sequencing
- Population genomics
- Workflow
- Human genomics
- Clinical research
- Whole genome
- Structural variation
July 28 2025
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Scalable nanopore sequencing for Alzheimer’s research
- Population genomics
- Human genomics
- Neuroscience
May 3 2023
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Wastewater sequencing — an early warning system for infectious disease outbreaks
- Population genomics
- Bioinformatics
- Microbiology
- Microbiome
- Environment
- Plant
November 10 2022
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Visualisation and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR
- Population genomics
- Long-read
- MinION
- PromethION
- Guppy
- MinKNOW
August 15 2024
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Using long-read sequencing for translational health research
- Population genomics
- PromethION 2
- Single cell
- Bioinformatics
- Clinical research
- Single cell
May 19 2025
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Unlocking the banana pangenome: harnessing genetic diversity
- Population genomics
- Plant
- Variant calling
- Phasing
- Assembly
- Bioinformatics
May 24 2024
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Uncovering global genetic diversity for equitable precision medicine
- Population genomics
- Human genomics
July 1 2025
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Ultra-rich human data — variant analysis with EPI2ME
- Population genomics
- Bioinformatics
- Human genomics
- EPI2ME
- Epigenetics
- SNVs
September 17 2024
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Towards personalised medicine for breast cancer in the Caribbean: a pilot study
- Population genomics
- Variant calling
- Cancer research
- PromethION
- EPI2ME
- London Calling
May 24 2024
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The correlation between CpG methylation and gene expression is driven by sequence variants
- Population genomics
- Methylation
- Human genomics
- PromethION 24/48
July 24 2024
)
Targeted nanopore sequencing using hybridisation probes reveals immune escape polymorphisms in malaria vaccine candidates
- Population genomics
- Infectious disease
- London Calling
May 19 2023
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Targeted adaptive sampling for pharmacogenomics and genome-wide variant analysis
- Population genomics
- PromethION 2
- Pharmacogenomics
- Bioinformatics
- Clinical research
- Human genomics
May 19 2025
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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
December 23 2016
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Structural variation in All of Us analyzed with long-read sequencing at a scale
- Population genomics
- Nanopore Community
- Human genomics
- SNVs
- Phasing
- Long-read
December 11 2023
)
Structural variants in the French-Canadian population
- Population genomics
- Structural variation
October 22 2020
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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
February 10 2021
)
Showcase: Carrier screening
- Population genomics
- Cancer research
- Clinical research
- Bioinformatics
- Human genomics
- MinION
September 17 2024
)
Shining light on a dark mystery: melanoma in bullhead benthic fish in Lake Memphremagog
- Population genomics
- London Calling
- Animal
- Bioinformatics
- Assembly
- Variant calling
May 24 2024
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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
September 14 2023
)
Real-time targeted sequencing with adaptive sampling
- Population genomics
- PromethION 24/48
- Epigenetics
- Structural variation
- Human genomics
- PromethION 24/48
May 19 2025
