Structural variants (SVs) are of high importance in both normal and aberrant phenotypes; however, their detection using traditional technologies is limited by their size, complexity, and position in the genome. Long nanopore reads can span SVs end-to-end, with no need for PCR, enabling unprecedented resolution of even highly complex variants — in any genomic context.

Span entire structural variants and repeats in single sequencing reads
Amplification-free whole genome or targeted sequencing approaches — detect base modifications as standard
Scalable to any project size, including large population-scale studies

For those that are attending the conference in person please visit the Oxford Nanopore Technologies table between sessions to meet members our team. Discuss the advantages of Oxford Nanopore's technology and how it can enhance your research. If you are attending virtually, book a call with one of our scientific support team to learn more and discuss your project.