Resource Centre
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Workflow overview: tumour-normal sequencing
- Structural variation
- Workflow
- SNVs
- Epigenetics
- Methylation
- Cancer research
July 21 2025
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Workflow overview: structural variation
- Structural variation
- PromethION
- Human genomics
- Library prep
- Bioinformatics
- Alignment
November 10 2023
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Workflow overview: large cohort sequencing
- Structural variation
- Workflow
- Human genomics
- Clinical research
- Population genomics
- Whole genome
October 12 2023
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Workflow overview: human variant calling
- Structural variation
- Human genomics
- Clinical research
- Cancer research
- PromethION 24/48
- Whole genome
April 29 2025
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William Jeck: Nanopore sequencing and rapid fusion testing – a ‘killer app’ in molecular pathology
- Structural variation
- Nanopore Community Meeting
- Oncology
December 14 2018
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The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematology
- Structural variation
- Cancer research
- Targeted
January 23 2024
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Whole-genome sequencing of rare disease patients in a national healthcare system
- Structural variation
- Human genomics
- Clinical research
- Whole genome
- DNA
- gDNA
February 18 2020
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Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer
- Structural variation
- Long-read
- Whole genome
- Human genomics
- Cancer research
- Oncology
April 29 2021
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Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation
- Structural variation
- Clinical research
- PromethION
- gDNA
- Whole genome
- Variant calling
May 15 2023
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Whole-genome insights: nanopore sequencing in neuropathology
- Structural variation
- Structural variation
- PromethION 2
- PromethION 24/48
- EPI2ME
- Epigenetics
May 19 2025
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Whole-genome DNA sequencing using nanopore R10.4 promises best practice for single-cell variation detection and methylation profiling
- Structural variation
- SNVs
- Whole genome
- London Calling
May 19 2023
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Webinar: Structural variants in the French-Canadian population
- Structural variation
- Human genomics
October 30 2020
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Webinar - Nanopore from 100 to 1000 genomes: towards a better understanding of phenotypes
- Structural variation
- Human genomics
- Assembly
- Bioinformatics
- Webinar
January 10 2020
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Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment
- Structural variation
- Long-read
- Bioinformatics
- Variant calling
- Alignment
September 24 2021
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Virus-derived variation in diverse human genomes
- Structural variation
- Microbiology
- Virus
- Targeted
- Human genomics
- Flongle
November 20 2020
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Virtual Nanopore Day, Australia - Rare Disease and Neurology
- Structural variation
- Neuroscience
February 11 2021
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Virtual Nanopore Day, Edinburgh
- Structural variation
- Infectious disease
- Virus
- Outbreak
- GridION
- MinION
November 25 2020
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Cloud computing for clinical nanopore fusion detection
- Structural variation
- Cancer research
- Clinical research
September 8 2021
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Variants at the ASIP locus contribute to coat color darkening in Nellore cattle
- Structural variation
- Long-read
- MinION
- gDNA
- DNA
- Whole genome
April 28 2021
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Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis
- Structural variation
- Human genomics
- Bioinformatics
- Clinical research
- SNVs
- PromethION 24/48
May 2 2025