Oxford Nanopore Technologies plc. products

A versatile sequencing kit optimised for modal raw read accuracy of Q20+ (99%+) and long read singleplex samples.

Identification and quantification of full-length transcripts with highest output.

The Flow Cell Wash Kit provides the reagents required to wash and reuse MinION and PromethION Flow Cells on a higher scale.

The only portable, real-time devices for DNA and RNA sequencing, giving complete control and creativity over when, where and how often you sequence, regardless of application. Accessible from $1,000, generate up to 50 Gb in 72 hours* without capital expenditure.

Self-contained, easily deployable benchtop device designed to run and analyse up to five MinION or Flongle Flow Cells. Simple, robust scalability for all your sequencing needs. Invest with capital or consumable budget, with options to offer nanopore sequencing as a service.

Choose PromethION 2 devices for flexible, high-yield sequencing, in a compact, accessible design. Utilising flow cells that generate hundreds of gigabases, enable PromethION-scale benefits in small to medium sized labs — including cores and commercial service providers. Suitable for users with lower sample processing requirements, up to ~200 flow cells per year. The PromethION 2 devices allow users to explore their applications and projects, before scaling up to a PromethION 24 or PromethION 48 device if required.

Flongle is an adapter for MinION or GridION that enables direct, real-time DNA or RNA sequencing on smaller, single-use flow cells.

A wide range of library preparation kits are available to suit all whole genome sequencing requirements. Amplification-free kits allow direct, long-read sequencing of native DNA, eliminating the potential for PCR bias and allowing the detection of base modifications alongside nucleotide sequence. Amplification-based kits are also available, enabling whole genome sequencing from low input amounts or poor quality DNA (e.g. FFPE).

Long-read nanopore sequencing expands the application of targeted sequencing to include cost-effective, assembly-free analysis of repetitive regions, structural variants, and variant phasing across entire genes or large genomic regions of interest. Through analysis of the entire 16S rRNA gene, the long sequencing reads provided by the 16S Barcoding Kit also provide more accurate taxonomic classification of bacteria and archaea.

Confidently characterise and quantify full-length RNA transcripts, splice variants, and fusions using long-read nanopore sequencing. Accurately analyse differential gene expression and transcript usage. Sequence native RNA directly, without amplification or reverse transcription, and identify base modifications.