News
)
Oxford Nanopore, Yemaachi Biotech, and Global Partners Collaborate to Improve Childhood Leukemia Outcomes in Ghana
- Human genomics
- Cancer research
- Clinical
- High-throughput
- Population genomics
- Structural variation
September 9 2024
)
Oxford Nanopore announces landmark UK Government partnership to advance genomics-driven healthcare innovation in the UK | Oxford Nanopore Technologies
- Human genomics
- Bioinformatics
- Data storage
- Epigenetics
- Cancer research
- Infectious disease
November 5 2024
)
Oxford Nanopore and UK Biobank to create world's first epigenetic dataset targeting the causes of cancer, dementia, complex disease | Oxford Nanopore Technologies
- Human genomics
- Epigenetics
- Clinical research
- Direct analysis
- High-throughput
- Methylation
November 27 2024
)
Structural variation in human genomics: 6 things to read right now
- Human genomics
- Structural variation
November 3 2020
)
Oxford Nanopore at ASHG 2021: find out how you can use nanopore technology to gain comprehensive, scalable, accurate insights in human genomics
- Human genomics
- Structural variation
- Methylation
- Assembly
October 19 2021
)
Oxford Nanopore announces multiple releases, for high-accuracy, content-rich, high-throughput whole-genome sequencing, and dynamic targeted sequencing
- Human genomics
- Structural variation
October 28 2020
)
Interview: Using PromethION for Cancer, Collaborations and more
- Human genomics
- Interview
- PromethION
- Cancer research
- Methylation
- Structural variation
June 25 2021
Interview: Scalable nanopore sequencing for Alzheimer’s research
- Human genomics
- Neuroscience
- Scalable
June 15 2023
Interview: The PromethION Experts at VIB
- Human genomics
- Interview
- PromethION
- Methylation
- Structural variation
July 2 2021
Interview: Exploring complex disease in Asian populations with PromethION
- Human genomics
- Interview
- PromethION
August 6 2021
Interview: Assembly and annotation of reference-quality human genomes
- Human genomics
- Assembly
August 13 2021
Interview: Advancing long-read de novo genome assembly methods in clinical research
- Human genomics
- Clinical research
- Interview
October 14 2022
Innovations with ultra-long reads
- Human genomics
- Long-read
- Methylation
- PromethION
- London Calling
- Structural variation
June 18 2021
)
Epigenetics, Cas9-mediated enrichment and novel insights in transcriptome variation: catch up on talks from ASHG 2020
- Human genomics
- Cancer research
- Epigenetics
- Transcriptome
- Event highlight
October 30 2020
Blog: Resolving structural variants causing antithrombin deficiency
- Human genomics
- Clinical research
- Structural variation
- Variant calling
- Long-read
- PromethION
September 14 2020