Blog
11 results
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
- DNA
- Adaptive sampling
- Targeted
- Whole genome
October 17 2024
Science unlocked: publication picks from September 2024 | Oxford Nanopore Technologies
- Structural variation
- Adaptive sampling
- AMR
- Cancer research
- Clinical research
- Epigenetics
- Human genomics
- Infectious disease
- Methylation
- Microbiology
- MinION
- Phasing
- rRNA
- Targeted
- Variant calling
October 2 2024
Science unlocked: publication picks from October 2024 | Oxford Nanopore Technologies
- Structural variation
- Human genomics
- Single cell
- Chromatin conformation
- Methylation
- Animal
- Variant calling
- Data storage
- Epigenetics
- Cancer research
- Adaptive sampling
- Targeted
- Infectious disease
- Plant
- PromethION
November 5 2024
Rapid identification of MSK-IMPACT cancer variants with real-time targeted nanopore sequencing | Oxford Nanopore Technologies | Oxford Nanopore Technologies
- Structural variation
- Cancer research
- Adaptive sampling
- Targeted
- SNVs
- PromethION
- Human genomics
- Clinical research
- DNA
- Variant calling
- EPI2ME
November 28 2024
Uncovering pathogenic variants with the founding president of the Thai Society of Human Genetics
- Structural variation
- Clinical research
- Human genomics
March 11 2024
Revealing hidden genetic variants in rare disease with nanopore sequencing
- Structural variation
- Clinical research
- Variant calling
- Human genomics
- Epigenetics
- SNVs
- Whole genome
- Targeted
- Direct analysis
- DNA
- gDNA
- London Calling
October 26 2023
Pushing the boundaries of rare disease research
- Structural variation
- Clinical research
- Human genomics
- Whole genome
- Targeted
- PromethION
- MinION
- Bioinformatics
- Assembly
- SNVs
- Phasing
- Amplicons
- Variant calling
- Splice variation
- Transcriptome
- cDNA
- RNA
June 6 2023
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
- Epigenetics
- cfDNA
July 14 2023
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
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
- Food safety
- Human genomics
- Infectious disease
- Microbiology
- Methylation
- Neuroscience
- Oncology
- Whole genome
- Water testing
September 17 2024
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
- Epigenetics
- Human genomics
- Infectious disease
- London Calling
- MinION
- PromethION
- Portable
- SNVs
- Targeted
- Whole genome
May 23 2024