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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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A guide to characterising structural variants with Oxford Nanopore

Download our Getting Started guide for sample-to-answer guidance on calling SVs using nanopore sequencing.

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Overview

Structural variants (SVs) are genomic variants ranging from 50 bp to the megabase scale, and are significant in understanding both healthy variation and disease. Using long nanopore sequencing reads, SVs can now be characterised with unprecedented resolution.

SV-Getting-Started-Guide
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