Product Specifications
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.
Select your output
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Flongle
Adapting MinION and GridION for smaller rapid tests and analyses. Suitable applications include amplicons, targeted sequencing, quality control, and small test runs before scaling up
- Output (Gb)
- Price per GB
One flow cell for all your small projects, available with an adapter to fit into all MinION and GridION devices
Less than $90 per Flongle Flow Cell
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MinION Flow Cell
Suitable applications include whole eukaryotic genomes, metagenomics, targeted sequencing, large transcriptomes (cDNA), and small transcriptomes (direct RNA).
- Output (Gb)
- Price per GB
Choose between DNA and direct RNA flow cells
MinION Flow Cell devices provide ultimate portability — plug and play into your laptop or GridION
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PromethION Flow Cell
Suitable applications include whole mammalian genomes, complete metagenomic genomes, targeted sequencing and isoform-level whole transcriptomes at single-cell resolution
- Output (Gb)
- Price per GB
Choose between DNA, direct RNA and High Duplex Flow Cells
Compatible with all PromethION devices, delivering scalable — from portable to benchtop — high output sequencing using 2 to 48 independently addressable/operable 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
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