Multidimensional insights.
In one go.
Unlock the deepest level of multiomic insights on a single technology
You’re not just getting more data — you’re seeing how it all connects. Oxford Nanopore sequencing provides insights across multiple dimensions, powering new discoveries in human disease.
Genomics, epigenomics, and transcriptomics
Multiomic approaches are crucial to resolving the mechanisms underpinning human diseases. Using Oxford Nanopore sequencing, you can gain genomic, epigenomic, and transcriptomic data from a single platform.
Decipher biological code beyond A, C, T, and G
Reveal layers of biology other technologies leave behind. Direct, amplification-free Oxford Nanopore sequencing eliminates bias and supports simultaneous detection of DNA and RNA modifications along with structural variants and long-range phasing.
Reveal more RNA biology. In one go
Characterise full-length isoforms, identify fusions, and generate single-cell transcriptomic data. Combine rich multiomic data with scalable formats and enable new insights into human health and disease.
See your data come together on a single platform
From 50 to 4,000,000 bases and everything in between, Oxford Nanopore technology gives you the power to sequence any length fragment of DNA or RNA, capturing all the insights you need — in one go.
From the pocket-sized MinION to the high-throughput, population-scale PromethION 24 device — scale to suit any experimental needs.
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