Product Specifications
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Full Biology from a single experiment
Nanopore sequencing is a universal technology capable of resolving small to large genomic variants and aberrations in single loci to whole genomes, from individual samples to population-scale analyses. By sequencing native DNA fragments, from 20 bases in length to millions of bases, this single, accurate, and accessible technology provides a more comprehensive insight into the true biology present than any other sequencing technology. Follow the links below to read more
One platform. Any scale.
Three flow cells.
Versatile applications
Users can choose how to run their experiments to generate the data type they need to answer their biological question. Regardless of the way users choose to buy and run the technology, high data outputs with transparent consumable pricing delivers great value.
A universal technology
Short fragment mode
Highest read counts
Best for:
- Fragments down to 20 bases in length
- Applications such as cDNA
- Modified base information as standard
Standard fragment mode
Highest yields
Best for:
- Maximising total Gbase output
- Read N50s 5-30kb
- Flexible and adaptable applications
- Modified base information as standard
Ultra-long sequencing
Longest reads
Best for:
- The most complete assemblies of large genomes
- Read N50s > 50kb, reads up to 4 Mbases
- Modified base information as standard
RNA sequencing
Full-length transcripts
Best for:
- Single cell sequencing
- Known and novel transcript ID
- Isoform detection
![table-showing-short-fragment](https://a.storyblok.com/f/196663/2990x850/c4d467c098/shortfragment-mode.png/m/2990x850/filters:format(webp))