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Nanopore sequencing offers advantages in all areas of research. Our offering includes DNA sequencing, as well as RNA and gene expression analysis and future technology for analysing proteins.

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EPI2ME SV caller workflow: real-time identification of human structural variants

The cloud-based or local data analysis platform EPI2ME provides easy access to a growing number of real-time data analysis workflows.

The SV caller workflow utilises the benefits of long, real-time nanopore sequencing reads to rapidly identify human structural variation — including insertions, deletions, and duplications.

All results are provided in an intuitive graphical interface, with no bioinformatics experience required. Data can be downloaded for further downstream analysis and all reports can be shared in real-time with collaborators.

Discover more about the advantages of long-read, real-time nanopore sequencing for structural variation detection on our dedicated resource page

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