Nanopore sequencing is a unique, scalable technology that enables direct, real-time analysis of DNA or RNA fragments of any length. It works by monitoring changes to an electrical current as nucleic acids are passed through a protein nanopore. The resulting signal is decoded to provide the specific DNA or RNA sequence.
Library preparation
Why Oxford Nanopore technology?
Richer insights
● Highly accurate genomic data that captures more types of genetic variation
● Any read length — short to ultra long: 20 bp to >4 Mb*
● Phasing, structural variants, and isoform detection inaccessible to legacy technologies
● SNV accuracy comparable to short-read sequencing
● Built-in modification and best-in-class methylation detection
Faster results
●Near-sample, real-time workflows that don’t require batching
● Real-time sequencing for immediate access to actionable results
● On-device targeted sequencing via adaptive sampling software
● Independently controlled flow cells — run multiple applications on one device
● Rapid 10-minute (DNA) library prep and automatable kit formats
Accessible and affordable
●Scalability that enables every application
● Sequence anywhere — at the point of need, in the field or lab
● Choice of personal, project-scale, and production-scale sequencers
● From amplicons to thousands of human genomes
● End-to-end workflows and intuitive analysis software
One technology for all your biology
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