News
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Singapore’s National Precision Medicine (NPM) programme engages Oxford Nanopore to advance understanding of the genetics of Singapore’s multi-ethnic p
- Structural variation
- PromethION
- DNA
- RNA
August 3 2024
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Oxford Nanopore and Kaust collaborate to advance multi-omic discovery
- Structural variation
- DNA
- Environment
- High-throughput
- Identification
- Long-read
September 25 2024
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Oxford Nanopore Technologies and Dubai Health to collaborate on genetic screening
- Structural variation
- Population genomics
- Adaptive sampling
- Clinical research
- DNA
- Epigenetics
March 13 2025
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Oxford Nanopore launches a 24-hour whole genome sequencing workflow for rare disease research
- Structural variation
- Clinical research
- Flow cell
- Human genomics
- Metagenomics
- Whole genome
September 30 2025
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Oxford Nanopore expands Compatible Products Programme and strengthens multi-omics ecosystem
- Structural variation
- Multiomics
- Workflow
- Sample prep
- Infectious disease
- Human genomics
April 14 2025
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Oxford Nanopore, Yemaachi Biotech, and Global Partners Collaborate to Improve Childhood Leukemia Outcomes in Ghana
- Structural variation
- Cancer research
- Clinical
- Human genomics
- High-throughput
- Population genomics
September 9 2024
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Your Oxford Nanopore guide to ASHG 2020 online
- Structural variation
- Long-read
- Targeted
- Event highlight
October 26 2020
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Structural variation in human genomics: 6 things to read right now
- Structural variation
- Human genomics
November 3 2020
Structural variation & cancer: top 7 things to read right now
- Structural variation
- Cancer research
November 20 2020
Oxford Nanopore at ASHG 2021: find out how you can use nanopore technology to gain comprehensive, scalable, accurate insights in human genomics
- Structural variation
- Human genomics
- Methylation
- Assembly
October 19 2021
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Oxford Nanopore announces multiple releases, for high-accuracy, content-rich, high-throughput whole-genome sequencing, and dynamic targeted sequencing
- Structural variation
- Human genomics
October 28 2020
Interview: Using PromethION for Cancer, Collaborations and more
- Structural variation
- Interview
- PromethION
- Human genomics
- Cancer research
- Methylation
June 25 2021
Interview: The PromethION Experts at VIB
- Structural variation
- Interview
- PromethION
- Human genomics
- Methylation
July 2 2021
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Interview: Nanopore sequencing: the mobile methylome
- Structural variation
- Bioinformatics
- Interview
November 17 2020
Interview: Improving structural variant interpretation for hereditary cancer susceptibility
- Structural variation
- Cancer research
- Bioinformatics
- Interview
October 5 2020
Interview: Identification of structural variation in chimpanzees using optical mapping and nanopore sequencing
- Structural variation
- Interview
July 10 2020
Innovations with ultra-long reads
- Structural variation
- Long-read
- Methylation
- PromethION
- London Calling
- Phasing
June 18 2021
Blog: Resolving structural variants causing antithrombin deficiency
- Structural variation
- Human genomics
- Clinical research
- Variant calling
- Long-read
- PromethION
September 14 2020
Blog: cuteSV - a powerful tool to uncover the full spectrum of genomic structural variants
- Structural variation
- PromethION
- DNA
- gDNA
- Whole genome
- Long-read
October 19 2020
Blog: Copy number variation analysis from plasma: is it feasible using nanopore sequencing?
- Structural variation
- Cancer research
- Clinical research
- MinION
- Flongle
- GridION
September 29 2020
