Resource Centre

Get startedSubscribe
555 results
Workflow: tumour-normal sequencingWorkflow

Workflow: tumour-normal sequencing

  • Workflow
  • Structural variation
  • SNVs
  • Epigenetics
  • Methylation
  • Cancer research
  • Human genomics
  • Whole genome
  • PromethION
  • Kits
  • Sample prep
  • Variant calling
August 4 2023
Workflow: structural variationWorkflow

Workflow: structural variation

  • Structural variation
  • PromethION
  • Human genomics
  • Library prep
  • Bioinformatics
  • Alignment
  • Variant calling
  • gDNA
  • Clinical research
  • Workflow
November 10 2023
Workflow: large cohort sequencingWorkflow

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
Workflow: human variant callingWorkflow

Workflow: human variant calling

  • Human genomics
  • Clinical research
  • Cancer research
  • PromethION
  • Whole genome
  • Variant calling
  • Epigenetics
  • Phasing
  • Methylation
  • Structural variation
  • SNVs
July 5 2024
William Jeck: Nanopore sequencing and rapid fusion testing – a ‘killer app’ in molecular pathologyVideo

William Jeck: Nanopore sequencing and rapid fusion testing – a ‘killer app’ in molecular pathology

  • Nanopore Community Meeting
  • Oncology
  • Structural variation
December 14 2018
The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematologyPublication

The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematology

  • Cancer research
  • Structural variation
  • Targeted
January 23 2024
Whole-genome sequencing of rare disease patients in a national healthcare systemPublication

Whole-genome sequencing of rare disease patients in a national healthcare system

  • Human genomics
  • Clinical research
  • Whole genome
  • DNA
  • gDNA
  • Structural variation
  • Variant calling
  • Long-read
February 18 2020
Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancerPublication

Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer

  • Long-read
  • Whole genome
  • Human genomics
  • Cancer research
  • Oncology
  • SNVs
  • Structural variation
  • Variant calling
  • MinION
April 29 2021
Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variationPoster

Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation

  • Clinical research
  • PromethION
  • gDNA
  • Whole genome
  • Variant calling
  • Structural variation
  • SNVs
  • Methylation
May 15 2023
Whole-genome DNA sequencing using nanopore R10.4 promises best practice for single-cell variation detection and methylation profilingPoster

Whole-genome DNA sequencing using nanopore R10.4 promises best practice for single-cell variation detection and methylation profiling

  • SNVs
  • Structural variation
  • Whole genome
  • London Calling
May 19 2023
Webinar: Structural variants in the French-Canadian populationEvents

Webinar: Structural variants in the French-Canadian population

  • Structural variation
  • Human genomics
October 30 2020
Webinar - Nanopore from 100 to 1000 genomes: towards a better understanding of phenotypesVideo

Webinar - Nanopore from 100 to 1000 genomes: towards a better understanding of phenotypes

  • Structural variation
  • Human genomics
  • Assembly
  • Bioinformatics
  • Webinar
January 10 2020
Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignmentBioinformatics tool

Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment

  • Long-read
  • Bioinformatics
  • Structural variation
  • Variant calling
  • Alignment
September 24 2021
Virus-derived variation in diverse human genomesPublication

Virus-derived variation in diverse human genomes

  • Microbiology
  • Virus
  • Targeted
  • Structural variation
  • Human genomics
  • Flongle
  • DNA
  • Amplicons
  • Evolution
November 20 2020
Virtual Nanopore Day, Australia - Rare Disease and NeurologyEvents

Virtual Nanopore Day, Australia - Rare Disease and Neurology

  • Neuroscience
  • Structural variation
February 11 2021
Virtual Nanopore Day, EdinburghVideo

Virtual Nanopore Day, Edinburgh

  • Infectious disease
  • Virus
  • Outbreak
  • GridION
  • MinION
  • Bioinformatics
  • Direct analysis
  • RNA
  • cDNA
  • Long-read
  • Structural variation
November 25 2020
Cloud computing for clinical nanopore fusion detectionVideo

Cloud computing for clinical nanopore fusion detection

  • Cancer research
  • Clinical research
  • Structural variation
September 8 2021
Variants at the *ASIP* locus contribute to coat color darkening in Nellore cattlePublication

Variants at the ASIP locus contribute to coat color darkening in Nellore cattle

  • Long-read
  • Structural variation
  • MinION
  • gDNA
  • DNA
  • Whole genome
  • Animal
April 28 2021
VACmap: an accurate long-read aligner for unravelling complex genomic rearrangementsPublication

VACmap: an accurate long-read aligner for unravelling complex genomic rearrangements

  • Bioinformatics
  • Structural variation
  • Human genomics
May 7 2024
Using Targeted Nanopore TechnologiesVideo

Using Targeted Nanopore Technologies

  • DNA
  • Targeted
  • Phasing
  • Structural variation
  • SNVs
  • Clinical research
January 27 2021

Categories

Products

Investigations

Techniques

Research areas