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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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