Blog
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Unravelling the complexity of cancer genomics and predisposition: nanopore sequencing and the potential for personalised care | Oxford Nanopore Technologies
- Human genomics
- Cancer research
- Clinical research
- Structural variation
- Gene fusions
- Methylation
October 17 2024
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Top topics at ESHG 2024 | Oxford Nanopore Technologies
- Human genomics
- Cancer research
- Clinical research
- Event highlight
June 12 2024
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Science unlocked: publication picks from September 2024 | Oxford Nanopore Technologies
- Human genomics
- 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
- Human genomics
- Single cell
- Chromatin conformation
- Methylation
- Animal
- Variant calling
November 5 2024
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Science unlocked: publication picks from May 2024 | Oxford Nanopore Technologies
- Human genomics
- Animal
- Neuroscience
- Whole genome
- Bioinformatics
- Microbiology
June 5 2024
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Science unlocked: publication picks from March 2024 | Oxford Nanopore Technologies
- Human genomics
- Epigenetics
- Plant
- Microbiology
- Infectious disease
April 4 2024
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Science unlocked: publication picks from June 2024 | Oxford Nanopore Technologies
- Human genomics
- Animal
- Agriculture: animal
- P2 Solo
- MinION
- PromethION
July 3 2024
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Science unlocked: publication picks from August 2024 | Oxford Nanopore Technologies
- Human genomics
- Long-read
- Cancer research
- Animal
- Infectious disease
- Whole genome
September 6 2024
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Science unlocked: publication picks from April 2024 | Oxford Nanopore Technologies
- Human genomics
- Biodefence
- Cancer research
- Clinical research
- Clinical
May 7 2024
PrecisionMed International: the future of population health
- Human genomics
- Population genomics
- Clinical research
- Interview
May 31 2024
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Uncovering pathogenic variants with the founding president of the Thai Society of Human Genetics
- Human genomics
- Clinical research
- Structural variation
March 11 2024
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Uncovering new genetic modifiers of monogenic Parkinson’s disease and parkinsonism-related disorders
- Human genomics
- Variant calling
- mtDNA
- Neuroscience
- GridION
- MinION
August 7 2023
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Science unlocked: publication picks from Feb 2024 | Oxford Nanopore Technologies
- Human genomics
- AMR
- Infectious disease
- Cancer research
- Single cell
- Plant
March 5 2024
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Revealing hidden genetic variants in rare disease with nanopore sequencing
- Human genomics
- Clinical research
- Variant calling
- Structural variation
- Epigenetics
- SNVs
October 26 2023
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Recognising the transformative research of the Nanopore Community on Rare Disease Day
- Human genomics
- Clinical research
- MinION
- GridION
- PromethION
February 29 2024
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Pushing the boundaries of rare disease research
- Human genomics
- Clinical research
- Whole genome
- Targeted
- PromethION
- MinION
June 6 2023
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Pioneering single-cell sequencing approaches to understand the 'dark matter' of our genome
- Human genomics
- Single cell
- Epigenetics
- Methylation
- Development
- Cancer research
October 2 2023
A new benchmark: discussing telomere-to-telomere assemblies with the founder of GrandOmics
- Human genomics
- Whole genome
- Assembly
- Plant
- Animal
November 24 2023
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My research in 60 seconds — Addressing the unmet needs in Alzheimer’s research through scalable nanopore sequencing
- Human genomics
- High-throughput
- PromethION
September 8 2023