Blog
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Unravelling the complexity of cancer genomics and predisposition: nanopore sequencing and the potential for personalised care | Oxford Nanopore Technologies
- Clinical research
- Cancer research
- Human genomics
- Structural variation
- Gene fusions
- Methylation
October 17 2024
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Top topics at ESHG 2024 | Oxford Nanopore Technologies
- Clinical research
- Human genomics
- Cancer research
- Event highlight
June 12 2024
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Short, long, or ultra-long: which read length is right for you?
- Clinical research
- Education
- Short-read
- Long-read
- DNA
- RNA
March 19 2025
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Science unlocked: publication picks from July 2024
- Clinical research
- Animal
- Methylation
- Epigenetics
- Infectious disease
- RNA
August 5 2024
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Science unlocked: publication picks from September 2024 | Oxford Nanopore Technologies
- Clinical research
- Adaptive sampling
- AMR
- Cancer research
- Epigenetics
- Human genomics
October 2 2024
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Science unlocked: publication picks from June 2024
- Clinical research
- Animal
- Agriculture: animal
- MinION
- PromethION 24/48
- Microbiology
July 3 2024
Science unlocked: publication picks from February 2025
- Clinical research
- Cancer research
- Biopharma
- Structural variation
- Adaptive sampling
- Animal
March 5 2025
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Science unlocked: publication picks from December 2024
- Clinical research
- Biopharma
- Cancer research
- Bioinformatics
- Epigenetics
January 8 2025
Science unlocked: publication picks from April 2024 | Oxford Nanopore Technologies
- Clinical research
- Biodefence
- Cancer research
- Human genomics
- Clinical
May 7 2024
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Reshaping rare disease diagnosis — an end to the diagnostic odyssey?
- Clinical research
- Clinical
- Human genomics
April 8 2025
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Rapid identification of MSK-IMPACT cancer variants with real-time targeted nanopore sequencing
- Clinical research
- Cancer research
- Adaptive sampling
- Targeted
- SNVs
- Structural variation
November 28 2024
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PrecisionMed International: the future of population health
- Clinical research
- Population genomics
- Human genomics
- Interview
May 31 2024
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Uncovering pathogenic variants with the founding president of the Thai Society of Human Genetics
- Clinical research
- Human genomics
- Structural variation
March 11 2024
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Revealing hidden genetic variants in rare disease with nanopore sequencing
- Clinical research
- Variant calling
- Human genomics
- Structural variation
- Epigenetics
- SNVs
October 26 2023
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Recognising the transformative research of the Nanopore Community on Rare Disease Day
- Clinical research
- Human genomics
- MinION
- GridION
- PromethION
February 29 2024
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Pushing the boundaries of rare disease research
- Clinical research
- Human genomics
- Whole genome
- Targeted
- PromethION
- MinION
June 6 2023
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Multiomic single-cell cancer analysis — from mutation detection to understanding disease mechanisms
- Clinical research
- Cancer research
- Human genomics
- Single cell
- Transcriptome
- cDNA
February 13 2024
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Liquid biopsies — multi-modal cell-free DNA assays using nanopore sequencing for potential cancer detection
- Clinical research
- London Calling
- Cancer research
- Whole genome
- Methylation
- Epigenetics
July 14 2023
Hot discussion topics from London Calling 2023 and looking forward to London Calling 2024
- Clinical research
- London Calling
- Human genomics
- Infectious disease
- Plant
- Animal
March 22 2024
