Blog
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Unravelling the complexity of cancer genomics and predisposition: nanopore sequencing and the potential for personalised care | Oxford Nanopore Technologies
- Cancer research
- Clinical research
- Human genomics
- Structural variation
- Gene fusions
- Methylation
October 17 2024
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Top topics at ESHG 2024 | Oxford Nanopore Technologies
- Cancer research
- Human genomics
- Clinical research
- Event highlight
June 12 2024
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Science unlocked: publication picks from September 2024 | Oxford Nanopore Technologies
- Cancer research
- Adaptive sampling
- AMR
- Clinical research
- Epigenetics
- Human genomics
October 2 2024
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Science unlocked: publication picks from October 2024 | Oxford Nanopore Technologies
- Cancer research
- Human genomics
- Single cell
- Chromatin conformation
- Methylation
- Animal
November 5 2024
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Science unlocked: publication picks from January 2025
- Cancer research
- AMR
- Methylation
- Structural variation
- Adaptive sampling
- SNVs
February 10 2025
Science unlocked: publication picks from February 2025
- Cancer research
- Biopharma
- Structural variation
- Clinical research
- Adaptive sampling
- Animal
March 5 2025
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Science unlocked: publication picks from December 2024
- Cancer research
- Biopharma
- Clinical research
- Bioinformatics
- Epigenetics
January 8 2025
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Science unlocked: publication picks from August 2024 | Oxford Nanopore Technologies
- Cancer research
- Long-read
- Human genomics
- Animal
- Infectious disease
- Whole genome
September 6 2024
Science unlocked: publication picks from April 2024 | Oxford Nanopore Technologies
- Cancer research
- Biodefence
- Human genomics
- Clinical research
- Clinical
May 7 2024
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Rapid identification of MSK-IMPACT cancer variants with real-time targeted nanopore sequencing
- Cancer research
- Adaptive sampling
- Targeted
- SNVs
- Structural variation
- PromethION
November 28 2024
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Science unlocked: publication picks from Feb 2024 | Oxford Nanopore Technologies
- Cancer research
- AMR
- Infectious disease
- Single cell
- Human genomics
- Plant
March 5 2024
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Pioneering single-cell sequencing approaches to understand the 'dark matter' of our genome
- Cancer research
- Single cell
- Epigenetics
- Methylation
- Human genomics
- Development
October 2 2023
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My research in 60 seconds — Improvements in direct RNA sequencing and its potential to transform clinical research
- Cancer research
- RNA
- Transcriptome
- PromethION
October 24 2023
Multiomic single-cell cancer analysis — from mutation detection to understanding disease mechanisms
- Cancer research
- Clinical 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
- Cancer research
- London Calling
- Clinical research
- Whole genome
- Methylation
- Epigenetics
July 14 2023
Applying single-cell long nanopore sequencing reads to identify the genetic basis underlying resistance in leukaemia treatment
- Cancer research
- Single cell
- Transcriptome
October 20 2022
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The Nanopore Community Meeting 2024 in Boston showcases 'a new frontier — multiomic single-molecule sensing’ of genomics
- Cancer research
- Bacteria
- Assembly
- DNA
- Epigenetics
- Food safety
September 17 2024
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London Calling 2024 opens with a day of masterclasses delivering everything you need to know for sample-to-answer nanopore sequencing
- Cancer research
- 16S
- Adaptive sampling
- Amplicons
- AMR
- Assembly
May 21 2024