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partners.compatible_products_services

  • partners.product_title:
    VarSeq Suite
    partners.product_description:

    A comprehensive platform for clinical variant analysis, interpretation, and reporting. Automate your NGS workflows from raw VCF to signed reports. Incorporate long-read phasing, CNV, structural variants, and tandem repeats into a unified variant annotation, filtering, visualization, and interpretation interface.

    partners.compatible_ont_products:

    Epi2me workflows, for example:
    Wf-human-variation (rare diseases)
    Wf-hereditary-cancer (hereditary cancer)

    partners.specific_use_application:
    Rare disease diagnosis, precision oncology, hereditary disease risk, prenatal & carrier screening, pharmacogenomics
    partners.territory:
    Worldwide

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Products labelled/branded as Oxford Nanopore Diagnostics may be RUO or may be regulated as in‐vitro diagnostic devices in some jurisdictions, please check individual product labelling.
Oxford Nanopore Technologies present the materials of third parties within the user community acknowledging that those materials belong to and are the true statements and representations of those third parties. Oxford Nanopore Technologies make no endorsements of the materials shown and the statements made.

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