Resource Centre
372 results
Workflow: tumour-normal sequencing
- Cancer research
- Workflow
- Structural variation
- SNVs
- Epigenetics
- Methylation
- Human genomics
- Whole genome
- PromethION
- Kits
- Sample prep
- Variant calling
August 4 2023
Workflow: single-cell transcriptomics
- Cancer research
- Single cell
- Transcriptome
- PromethION
- Clinical research
- cDNA
- Workflow
- Human genomics
- Splice variation
- Gene fusions
- Gene expression
- Kits
February 20 2024
Workflow: human variant calling
- Cancer research
- Human genomics
- Clinical research
- PromethION
- Whole genome
- Variant calling
- Epigenetics
- Phasing
- Methylation
- Structural variation
- SNVs
July 5 2024
Workflow: FFPE cancer research samples
- Cancer research
- Workflow
- 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 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 carcinoma
- Cancer research
- Microbiology
- Infectious disease
- Clinical research
- Bacteria
- 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 cancer
- Cancer research
- Long-read
- Whole genome
- Human genomics
- Oncology
- SNVs
- Structural variation
- Variant calling
- MinION
April 29 2021
Whole genome assembly of human papillomavirus by nanopore long-read sequencing
- Cancer research
- Oncology
- Clinical research
- Microbiology
- Infectious disease
- MinION
- DNA
- Long-read
January 4 2022
Resolving complex genomic structures and regulation patterns in cervical cancer
- Cancer research
- Epigenetics
April 11 2023
Webinar: Rapid leukemia classification using nanopore sequencing
- Cancer research
- Transcriptome
October 7 2022
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 cancer
- Cancer research
- PromethION
- Clinical research
November 15 2023
Investigating epigenomic alterations in cancer with nanopore sequencing
- Cancer research
- Epigenetics
October 11 2022
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 sequencing
- Cancer research
December 15 2022
Advancing long-read de novo genome assembly methods in clinical research
- Cancer research
- Human genomics
- Clinical research
September 15 2022
Wastewater sequencing — an early warning system for infectious disease outbreaks
- Cancer research
- Bioinformatics
- Microbiology
- Microbiome
- Environment
- Plant
- Animal
- Human genomics
- Clinical research
- Population genomics
- Transcriptome
- Infectious disease
November 10 2022
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 sequencing
- Cancer research
- MinION
- PromethION
- GridION
- VolTRAX
- SmidgION
- Flongle
- Monitoring
- Plant
- Infectious disease
November 25 2020