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Brochure: Multiomic nanopore sequencing solutions


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 that aren’t compatible with disease research based on valuable tissue samples that are a scarce resource.

Download this brochure to find out how multiomic nanopore sequencing – spanning genomics, bulk and single-cell transcriptomics, epigenetics and proteomics – on a single platform, can maximize the data generated from your valuable research samples.

What you’re missing matters.

Download Brochure


 


 

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