'%20transform='translate(-1229%20-954)'%3e%3cg%20clip-path='url(%23kg9jt4e4eb)'%20transform='translate(1229%20954)'%3e%3cpath%20fill='%23FFF'%20d='M0%200h28.313v58.624H0V0z'/%3e%3c/g%3e%3c/g%3e%3c/svg%3e)
'%20transform='translate(-130%20-954)'%3e%3cg%20clip-path='url(%23vjs606norb)'%20transform='rotate(-180%2079.5%20506.5)'%3e%3cpath%20fill='%23FFF'%20d='M0%200h28.313v58.624H0V0z'/%3e%3c/g%3e%3c/g%3e%3c/svg%3e)
Offering short to ultra-long native DNA and RNA reads,
only nanopore sequencing delivers…
Richer insights: Highly-accurate genomic data captures more types of genetic variation
Faster results: Near-sample, real-time workflows that don’t require batching
Accessible and affordable: Scalability that enables every application
A new generation of molecular sensing technology
Explore the nanopore portfolio of flow cells, compatible devices, manual and automated library prep, and data analysis solutions.
Use of the technology
The platform is used by scientific researchers to solve real-world challenges through answering questions about the biology of people, plants, animals, pathogens and environments. It is also increasingly being used in ‘applied’ settings such as healthcare and food safety.
Environmental
How is the microbial composition of this river changing? What is this species? Is it endangered? What can we understand about the biodiversity within this area?
Pathogens & Microbiology
What is this virus / bacteria / fungus? What makes it pathogenic? Is it resistant to antimicrobial drugs? How could we use this information to prevent or treat the disease that it causes?
Whole genome sequencing
Generate and complete microbial, human, animal, and plant genome assemblies with long nanopore sequencing reads (reads in excess of 4 Mb have been demonstrated).
Cancer research
What are the genetic changes that are causing this cancer, and the mechanism of those changes in broader cell pathways? Can knowledge of these changes influence choices on treatment? Can new therapeutics be developed as a result of this knowledge?
Clinical research
How can we use sequence data to personalise medicine? How can we integrate sequence data into clinical decision making? How does a person’s genome influence how they may respond to a disease or an infection?