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340 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: single-cell transcriptomicsWorkflow

Workflow: single-cell transcriptomics

  • Single cell
  • Transcriptome
  • PromethION
  • Cancer research
  • Clinical research
  • cDNA
  • Workflow
  • Human genomics
  • Splice variation
  • Gene fusions
  • Gene expression
  • Kits
February 20 2024
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
Workflow: Characterising structural variants in FFPE cancer research samplesWorkflow

Workflow: Characterising structural variants in FFPE cancer research samples

  • Workflow
  • Cancer research
  • Clinical research
  • Whole genome
  • Human genomics
  • Sample prep
  • Library prep
  • gDNA
  • DNA
  • PromethION
  • Bioinformatics
July 8 2022
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 reveals virulence potentials of *Helicobacter pylori* strain KE21 isolated from a Kenyan patient with gastric signet ring cell carcinomaPublication

Whole genome sequencing reveals virulence potentials of Helicobacter pylori strain KE21 isolated from a Kenyan patient with gastric signet ring cell carcinoma

  • Microbiology
  • Infectious disease
  • Clinical research
  • Bacteria
  • Cancer research
  • MinION
  • Whole genome
  • Assembly
August 29 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 assembly of human papillomavirus by nanopore long-read sequencingPublication

Whole genome assembly of human papillomavirus by nanopore long-read sequencing

  • Oncology
  • Cancer research
  • Clinical research
  • Microbiology
  • Infectious disease
  • MinION
  • DNA
  • Long-read
January 4 2022
Resolving complex genomic structures and regulation patterns in cervical cancerVideo

Resolving complex genomic structures and regulation patterns in cervical cancer

  • Cancer research
  • Epigenetics
April 11 2023
Webinar: Rapid leukemia classification using nanopore sequencingVideo

Webinar: Rapid leukemia classification using nanopore sequencing

  • Cancer research
  • Transcriptome
October 7 2022
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variantsVideo

Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants

  • Cancer research
  • Clinical research
  • Human genomics
  • Phasing
  • Methylation
  • Epigenetics
June 26 2023
Nanopore sequencing: insights from neonatal intensive care to cancerVideo

Nanopore sequencing: insights from neonatal intensive care to cancer

  • PromethION
  • Cancer research
  • Clinical research
November 15 2023
Investigating epigenomic alterations in cancer with nanopore sequencingVideo

Investigating epigenomic alterations in cancer with nanopore sequencing

  • Cancer research
  • Epigenetics
October 11 2022
Detecting, classifying, and monitoring CNS tumors with nanopore sequencingVideo

Detecting, classifying, and monitoring CNS tumors with nanopore sequencing

  • Cancer research
  • Neuroscience
  • cfDNA
  • Methylation
July 14 2023
Analysing complex somatic rearrangements in cancer using nanopore sequencingVideo

Analysing complex somatic rearrangements in cancer using nanopore sequencing

  • Cancer research
December 15 2022
Advancing long-read de novo genome assembly methods in clinical researchVideo

Advancing long-read de novo genome assembly methods in clinical research

  • Human genomics
  • Cancer research
  • Clinical research
September 15 2022
Wastewater sequencing — an early warning system for infectious disease outbreaksCase study

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
In vivo genetic screen identifies a SLC5A3-dependent myo-inositol auxotrophy in acute myeloid leukemiaPublication

In vivo genetic screen identifies a SLC5A3-dependent myo-inositol auxotrophy in acute myeloid leukemia

  • Cancer research
  • Oncology
  • Long-read
  • DNA
  • GridION
  • Clinical research
  • Targeted
  • Methylation
  • Epigenetics
December 22 2020
Virtual Nanopore Day, Australia. Cancer research with nanopore sequencingVideo

Virtual Nanopore Day, Australia. Cancer research with nanopore sequencing

  • MinION
  • PromethION
  • GridION
  • VolTRAX
  • SmidgION
  • Flongle
  • Monitoring
  • Cancer research
  • Plant
  • Infectious disease
November 25 2020
Rapid genomic profiling of hematologic malignancies: an updateEvents

Rapid genomic profiling of hematologic malignancies: an update

  • Cancer research
  • Clinical research
  • GridION
September 8 2021

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