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Expand the capabilities of your targeted sequencing assays

Enabling the generation of any length of sequencing read — from short to ultra long (50 bp to >4 Mb) — Oxford Nanopore technology expands the capabilities of targeted sequencing approaches beyond the analysis of single nucleotide variants (SNVs), to include high-coverage characterisation and phasing of structural variants (SV), repetitive regions, and base modifications.

Real-time data analysis provides faster access to results and underpins adaptive sampling — a unique on-device enrichment methodology that requires no additional wet-lab prep.

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