Oxford Nanopore Technologies
Oxford Nanopore has developed a new generation of DNA/RNA sequencing technology. It is the only sequencing technology that offers real-time analysis in fully scalable formats from pocket to population scale, that can analyze native DNA or RNA and sequence any length of fragment to achieve short to ultra-long read lengths.
Latest Oxford Nanopore Technologies Content
News
New RNA Liquid Biopsy Platform Improves Cancer Detection
A new liquid biopsy platform has been developed that uses RNA "dark matter" to diagnose cancer types including pancreatic, lung and esophageal, in the early stages.
Product News
Nanopore Technology Achieves Breakthrough in Protein Variant Detection
A team of scientists led by the University of Oxford have achieved a significant breakthrough in detecting modifications on protein structures.
Whitepaper
Advancing Human Genomics With Nanopore Sequencing
This whitepaper highlights specific case studies that reveal how researchers are applying nanopore technology to a variety of sequencing techniques, including whole genome, targeted, RNA sequencing and single-cell analysis.
eBook
Whole-Genome Sequencing: Small Genomes
The ability to characterize microbial genomes is advancing many fields of research. In fact, sequencing approaches now allow scientists to understand disease origins and anticipate transmission patterns with applications across human health, farming and food production industries.
News
Thousands of Unknown Viruses “Hide” in the DNA of Unicellular Organisms
During a large-scale study of complex single-celled microbes, scientists made an unexpected discovery. Built into the genome of the microbes, they found the DNA of over 30,000 previously unknown viruses. This "hidden" DNA may allow the replication of complete and functional viruses in the host cell.
App Note / Case Study
Alternative Transcript Isoform Detection With Single Cell and Spatial Resolution
The ability to study transcript isoforms in detail could have a significant impact on our understanding of health and disease. However, most commonly, bulk sequencing is the selected method that only provides an average of the transcripts expressed across your sample of cells.
Webinar
Scalable Nanopore Sequencing for Alzheimer’s Research
On-Demand
We will introduce the National Institutes of Health (NIH) Center for Alzheimer’s and Related Dementias (CARD) long-read sequencing initiative, which will generate a new genetic resource for Alzheimer’s and related dementias from thousands of human brain samples.
Webinar
Resolving Complex Genomic Structures and Regulation Patterns in Cervical Cancer
On-Demand
In this webinar, our expert speaker, Vanessa Porter, will present her research into identifying and classifying genomic perturbations arising from HPV integration.
Article
New DNA Extraction Method for Long-Read Sequencing in Plant Tissues
A novel DNA preparation protocol enables labs to isolate high molecular weight DNA from a variety of plant species cost-effectively and rapidly, opening opportunities to improve the robustness of commercially valuable plants.
Whitepaper
Delivering the Future of Genomic Pathogen Surveillance
Serious infectious disease outbreaks have been an ever-present threat throughout human history and, driven by factors such as increasing globalization, population growth, urbanization and climate change, that threat is increasing.
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