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Hereditary Cancer Panel: targeted sequencing via adaptive sampling


Flyer: Hereditary Cancer Panel — 2 pages

Accurately resolve complex structural variants (SVs), single nucleotide variants (SNVs), and insertions/deletions (indels) with the Oxford Nanopore Hereditary Cancer Panel — a comprehensive sequencing assay.

In this flyer, discover how to utilise the Hereditary Cancer Panel to investigate 258 key genes associated with hereditary cancer risk.

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