Blog
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Unravelling the complexity of cancer genomics and predisposition: nanopore sequencing and the potential for personalised care | Oxford Nanopore Technologies
- Structural variation
- Cancer research
- Clinical research
- Human genomics
- Gene fusions
- Methylation
October 17 2024
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Short, long, or ultra-long: which read length is right for you?
- Structural variation
- Education
- Short-read
- Long-read
- DNA
- RNA
March 19 2025
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Science unlocked: publication picks from September 2024 | Oxford Nanopore Technologies
- Structural variation
- Adaptive sampling
- AMR
- Cancer research
- Clinical research
- Epigenetics
October 2 2024
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Science unlocked: publication picks from October 2024 | Oxford Nanopore Technologies
- Structural variation
- Human genomics
- Single cell
- Chromatin conformation
- Methylation
- Animal
November 5 2024
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Science unlocked: publication picks from May 2025
- Structural variation
- RNA
- AMR
- Methylation
- Virus
- Bacteria
June 11 2025
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Science unlocked: publication picks from June 2025
- Structural variation
- RNA
- Human genomics
- Infectious disease
- Single cell
- Neuroscience
July 9 2025
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Science unlocked: publication picks from July 2025
- Structural variation
- Human genomics
- Infectious disease
- Neuroscience
- Cancer research
August 13 2025
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Science unlocked: publication picks from January 2025
- Structural variation
- AMR
- Cancer research
- Methylation
- Adaptive sampling
- SNVs
February 10 2025
Science unlocked: publication picks from February 2025
- Structural variation
- Cancer research
- Biopharma
- Clinical research
- Adaptive sampling
- Animal
March 5 2025
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Rapid identification of MSK-IMPACT cancer variants with real-time targeted nanopore sequencing
- Structural variation
- Cancer research
- Adaptive sampling
- Targeted
- SNVs
- PromethION
November 28 2024
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Uncovering pathogenic variants with the founding president of the Thai Society of Human Genetics
- Structural variation
- Clinical research
- Human genomics
March 11 2024
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Revealing hidden genetic variants in rare disease with nanopore sequencing
- Structural variation
- Clinical research
- Variant calling
- Human genomics
- Epigenetics
- SNVs
October 26 2023
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Pushing the boundaries of rare disease research
- Structural variation
- Clinical research
- Human genomics
- Whole genome
- Targeted
- PromethION
June 6 2023
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Liquid biopsies — multi-modal cell-free DNA assays using nanopore sequencing for potential cancer detection
- Structural variation
- London Calling
- Clinical research
- Cancer research
- Whole genome
- Methylation
July 14 2023
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From finding flavonoids to the ‘dark matter’ of T-DNA insertions — investigating plant genomes with nanopore sequencing
- Structural variation
- Plant
- MinION
- Whole genome
- Assembly
October 5 2022
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The Nanopore Community Meeting 2024 in Boston showcases 'a new frontier — multiomic single-molecule sensing’ of genomics
- Structural variation
- Bacteria
- Assembly
- Cancer research
- DNA
- Epigenetics
September 17 2024
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10 ways the Nanopore Community redefined genomics in 2024
- Structural variation
- Adaptive sampling
- Animal
- Bacteria
- Basecalling
- Biopharma
December 20 2024
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At London Calling 2024, the Nanopore Community showcases how ‘nanopore sequencing can drive new discoveries in biology’
- Structural variation
- Bacteria
- Cancer research
- Clinical research
- Conservation
- DNA
May 23 2024
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Adaptive sampling: redefining targeted sequencing
- Structural variation
- Education
- Short-read
- Long-read
- DNA
- RNA
June 25 2025
