Resource Centre
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Workflow overview: tumour-normal sequencing
- Cancer research
- Workflow
- Structural variation
- SNVs
- Epigenetics
- Methylation
July 21 2025
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Workflow overview: single-cell transcriptomics
- Cancer research
- Single cell
- Transcriptome
- PromethION 24/48
- Clinical research
- cDNA
February 24 2025
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Workflow overview: human variant calling
- Cancer research
- Human genomics
- Clinical research
- PromethION 24/48
- Whole genome
- Variant calling
April 29 2025
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Workflow overview: bulk transcriptomics
- Cancer research
- cDNA
- Exome
- Transcriptome
- Transcriptomics
July 28 2025
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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
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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
August 29 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
- Cancer research
- Long-read
- Whole genome
- Human genomics
- Oncology
- SNVs
April 29 2021
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Whole-genome insights: nanopore sequencing in neuropathology
- Cancer research
- PromethION 2
- PromethION 24/48
- EPI2ME
- Epigenetics
- Fusion transcript
May 19 2025
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Whole genome assembly of human papillomavirus by nanopore long-read sequencing
- Cancer research
- Oncology
- Clinical research
- Microbiology
- Infectious disease
- MinION
January 4 2022
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Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing
- Cancer research
- Webinar
- Epigenetics
- Real-time
- Whole genome
- Methylation
November 18 2025
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Transforming hereditary cancer sequencing with adaptive sampling target enrichment
- Cancer research
- Clinical research
- Adaptive sampling
- Webinar
November 11 2025
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Resolving complex genomic structures and regulation patterns in cervical cancer
- Cancer research
- Epigenetics
April 11 2023
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Webinar: Rapid leukemia classification using nanopore sequencing
- Cancer research
- Transcriptome
October 7 2022
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Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
- Cancer research
- Clinical research
- Human genomics
- Phasing
- Methylation
- Epigenetics
June 26 2023
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Nanopore sequencing: insights from neonatal intensive care to cancer
- Cancer research
- PromethION
- Clinical research
November 15 2023
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Investigating epigenomic alterations in cancer with nanopore sequencing
- Cancer research
- Epigenetics
October 11 2022
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Detecting, classifying, and monitoring CNS tumors with nanopore sequencing
- Cancer research
- Neuroscience
- cfDNA
- Methylation
July 14 2023
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Analysing complex somatic rearrangements in cancer using nanopore sequencing
- Cancer research
December 15 2022
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Advancing long-read de novo genome assembly methods in clinical research
- Cancer research
- Human genomics
- Clinical research
September 15 2022
Adaptive sampling explained: the future of flexible target enrichment
- Cancer research
- Clinical research
- Adaptive sampling
- Webinar
- Knowledge exchange
September 23 2025
