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

dna strand

SNP Detection

methylation

Methylation Detection

dna strand

SV Detection

dna phasing

Phasing

dna strands

Assembly

One platform. Any scale.
Two flow cells.

Select your output

MinION Flow Cell

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

PromethION Flow Cell

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 and direct RNA 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