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Population genomics

Workflow
Workflow overview: large cohort sequencing
July 28 2025
Video
Scalable nanopore sequencing for Alzheimer’s research
May 3 2023
Case study
Wastewater sequencing — an early warning system for infectious disease outbreaks
November 10 2022
Publication
Visualisation and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR
August 15 2024
Video
Using long-read sequencing for translational health research
May 19 2025
Video
Unlocking the banana pangenome: harnessing genetic diversity
May 24 2024
Video
Uncovering global genetic diversity for equitable precision medicine
July 1 2025
Video
Ultra-rich human data — variant analysis with EPI2ME
September 17 2024
Video
Towards personalised medicine for breast cancer in the Caribbean: a pilot study
May 24 2024
Publication
The correlation between CpG methylation and gene expression is driven by sequence variants
July 24 2024
Poster
Targeted nanopore sequencing using hybridisation probes reveals immune escape polymorphisms in malaria vaccine candidates
May 19 2023
Video
Targeted adaptive sampling for pharmacogenomics and genome-wide variant analysis
May 19 2025
Bioinformatics tool
Supporting data for "de novo assembly and population genomic survey of natural yeast isolates with the Oxford Nanopore MinION sequencer"
December 23 2016
Poster
Structural variation in All of Us analyzed with long-read sequencing at a scale
December 11 2023
Publication
Structural variants in the French-Canadian population
October 22 2020
Publication
Structural variants in Chinese population and their impact on phenotypes, diseases and population adaptation
February 10 2021
Video
Showcase: Carrier screening
September 17 2024
Video
Shining light on a dark mystery: melanoma in bullhead benthic fish in Lake Memphremagog
May 24 2024
Publication
Scalable nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
September 14 2023
Video
Real-time targeted sequencing with adaptive sampling
May 19 2025

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Resource Centre

Workflow overview: large cohort sequencing

Scalable nanopore sequencing for Alzheimer’s research

Wastewater sequencing — an early warning system for infectious disease outbreaks

Visualisation and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR

Using long-read sequencing for translational health research

Unlocking the banana pangenome: harnessing genetic diversity

Uncovering global genetic diversity for equitable precision medicine

Ultra-rich human data — variant analysis with EPI2ME

Towards personalised medicine for breast cancer in the Caribbean: a pilot study

The correlation between CpG methylation and gene expression is driven by sequence variants

Targeted nanopore sequencing using hybridisation probes reveals immune escape polymorphisms in malaria vaccine candidates

Targeted adaptive sampling for pharmacogenomics and genome-wide variant analysis

Supporting data for "de novo assembly and population genomic survey of natural yeast isolates with the Oxford Nanopore MinION sequencer"

Structural variation in All of Us analyzed with long-read sequencing at a scale

Structural variants in the French-Canadian population

Structural variants in Chinese population and their impact on phenotypes, diseases and population adaptation

Showcase: Carrier screening

Shining light on a dark mystery: melanoma in bullhead benthic fish in Lake Memphremagog

Scalable nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation

Real-time targeted sequencing with adaptive sampling

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