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Understanding the mechanisms of disease requires complex data ranging from genomic data through to transcriptomics, epigenetics and proteomics. Legacy multiomic approaches require multiple platforms and complex processes, which are incompatible with disease research that utilises scarce tissue samples.

Download the brochure to learn how multiomic nanopore sequencing can generate data on:

  • Genomics
  • Bulk and single-cell transcriptomics
  • Epigenetics
  • Proteomics

All on a single platform.

What you’re missing matters: maximise the data generated from your valuable research samples.


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