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.

 


 

This content was provided by

 


Submit Your Research to the F1000Research Cell & Molecular Biology Gateway

Contribute to advancing molecular biology by publishing your research with the F1000Research Cell & Molecular Biology Gateway. With trusted publishing, open access, and transparent peer review, your work will uphold the highest standards of rigor and integrity while driving innovation in cellular and molecular science.

Join a platform that values transparency, openness, and author control. Submit your research today at F1000Research Cell & Molecular Biology Gateway.