Resource Centre
85 results
Workflow: large cohort sequencing
- Workflow
- Human genomics
- Clinical research
- Population genomics
- Whole genome
- Structural variation
- Variant calling
- Assembly
- Sample prep
- Library prep
- Methylation
- SNVs
October 12 2023
Scalable nanopore sequencing for Alzheimer’s research
- Human genomics
- Neuroscience
- Population genomics
May 3 2023
Wastewater sequencing — an early warning system for infectious disease outbreaks
- Bioinformatics
- Microbiology
- Microbiome
- Environment
- Plant
- Animal
- Human genomics
- Clinical research
- Cancer research
- Population genomics
- Transcriptome
- Infectious disease
November 10 2022
Visualisation and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR
- Long-read
- Population genomics
- MinION
- PromethION
- Guppy
- MinKNOW
August 15 2024
Using long nanopore reads to delineate structural variants (SVs) in the human genome
- MinION
- Structural variation
- Long-read
- Human genomics
- Cancer research
- Clinical research
- Population genomics
May 24 2018
Unlocking the banana pangenome: harnessing genetic diversity
- Plant
- Population genomics
- Variant calling
- Phasing
- Assembly
- Bioinformatics
- PromethION
- Q20+
May 24 2024
Targeted nanopore sequencing using hybridisation probes reveals immune escape polymorphisms in malaria vaccine candidates
- Infectious disease
- Population genomics
- London Calling
May 19 2023
Supporting data for "de novo assembly and population genomic survey of natural yeast isolates with the Oxford Nanopore MinION sequencer"
- MinION
- Bioinformatics
- Population genomics
- Whole genome
- Assembly
- Structural variation
December 23 2016
White paper: advantages of long reads for structural variation analysis
- Structural variation
- Human genomics
- Plant
- Clinical research
- Cancer research
- Population genomics
September 7 2021
Structural variation in All of Us analyzed with long-read sequencing at a scale
- Nanopore Community
- Human genomics
- Population genomics
- SNVs
- Phasing
- Long-read
- Whole genome
- Nanopore Community Meeting
December 11 2023
Structural variants in the French-Canadian population
- Structural variation
- Population genomics
October 22 2020
Structural variants in Chinese population and their impact on phenotypes, diseases and population adaptation
- Human genomics
- Population genomics
- Whole genome
- Structural variation
- Variant calling
- Long-read
- gDNA
- DNA
- PromethION
February 10 2021
Shining light on a dark mystery: melanoma in bullhead benthic fish in Lake Memphremagog
- London Calling
- Animal
- Bioinformatics
- Assembly
- Variant calling
- Cancer research
- Population genomics
May 24 2024
Scalable nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
- Human genomics
- Population genomics
- PromethION
- Variant calling
- SNVs
- Structural variation
September 14 2023
Real-time genomic surveillance with nanopore sequencing
- Bioinformatics
- Clinical research
- Population genomics
- MinION Mk1B
- London Calling
May 24 2024
Rapid surveillance of monkeypox virus from complex metagenomic samples
- Bioinformatics
- Microbiology
- Microbiome
- Environment
- Plant
- Animal
- Human genomics
- Clinical research
- Cancer research
- Population genomics
- Transcriptome
- Infectious disease
November 10 2022
A rapid CRISPR/Cas9-mediated, amplification-free target enrichment method for native-strand sequencing*
- Cancer research
- Clinical research
- Epigenetics
- Human genomics
- Population genomics
- Structural variation
- Animal
February 22 2019
PromethION brochure | Oxford Nanopore Technologies
- PromethION
- Plant
- Population genomics
February 29 2024
Population Genomics Showcase stage at NCM 2023 Singapore
- Assembly
- Bioinformatics
- Human genomics
- Population genomics
- SNVs
- Structural variation
- Long-read
- Whole genome
- PromethION
- Nanopore Community Meeting
September 27 2023
Personalised genomics and transcriptomics: using a portable sequencer to obtain genomic information
- Human genomics
- Whole genome
- Transcriptome
- Methylation
- gDNA
- RNA
- cDNA
- Assembly
- Cancer research
- Clinical research
- Population genomics
- SNVs
May 22 2019