News
18 results
Oxford Nanopore Technologies selected by Murdoch Children’s Research Institute to support landmark research into faster genetic screening for rare dis
- Long-read
- Clinical research
- Clinical
- DNA
- Whole genome
August 9 2024
Oxford Nanopore Technologies collaborates with Twist Bioscience to launch Pharmacogenomics Beta Programme and advance personalised medicine
- Long-read
- Biopharma
- Clinical research
May 22 2024
Oxford Nanopore Technologies and UMC Utrecht collaborate on 1,000 human genome sequencing project
- Long-read
- Clinical research
- Direct analysis
- Metagenomics
- PromethION
- Real-time
- Short-read
- SNVs
September 30 2024
Oxford Nanopore Technologies and Plasmidsaurus announce strategic collaboration to advance plasmid sequencing
- Long-read
- Plasmid
- Real-time
- Microbiology
July 23 2024
Oxford Nanopore and Kaust collaborate to advance multi-omic discovery
- Long-read
- DNA
- Environment
- High-throughput
- Identification
- Microbiology
- Plant
- Structural variation
- Whole genome
September 25 2024
Oxford Nanopore’s ORG.one hits milestone, announces new focus on endangered species
- Long-read
- Whole genome
May 8 2024
Oxford Nanopore announces landmark UK Government partnership to advance genomics-driven healthcare innovation in the UK | Oxford Nanopore Technologies
- Long-read
- Bioinformatics
- Data storage
- Epigenetics
- Cancer research
- Human genomics
- Infectious disease
- Metagenomics
- Monitoring
- Real-time
- Whole genome
November 5 2024
Your Oxford Nanopore guide to ASHG 2020 online
- Long-read
- Structural variation
- Targeted
- Event highlight
October 26 2020
Innovations with ultra-long reads
- Long-read
- Methylation
- PromethION
- London Calling
- Structural variation
- Phasing
- Human genomics
June 18 2021
Blog: Resolving structural variants causing antithrombin deficiency
- Long-read
- Human genomics
- Clinical research
- Structural variation
- Variant calling
- PromethION
- DNA
- gDNA
- Whole genome
- Immunology
- Research story
September 14 2020
Blog: cuteSV - a powerful tool to uncover the full spectrum of genomic structural variants
- Long-read
- Structural variation
- PromethION
- DNA
- gDNA
- Whole genome
- Human genomics
- Research story
October 19 2020
Blog: Copy number variation analysis from plasma: is it feasible using nanopore sequencing?
- Long-read
- Cancer research
- Clinical research
- Structural variation
- MinION
- Flongle
- GridION
- DNA
- Research story
September 29 2020
Breakthrough towards protein sequencing using Oxford Nanopore holds promise for disease research and drug development
- Long-read
- Protein
- Direct analysis
- Clinical research
September 12 2024
Breakthrough in aging and cancer through telomere sequencing unveiled by Oxford Nanopore Technologies and the Salk Institute
- Long-read
- Cancer research
June 21 2024
Al Jalila Children’s Hospital advances rare disease identification through Oxford Nanopore sequencing, a new study shows | Oxford Nanopore Technologies
- Long-read
- Whole genome
- Clinical research
- PromethION
November 14 2024