From Information Overload to Actionable Insights: How a National Cancer Research Center Identifies Meaningful Mutations in Somatic Tumor Testing Free Webinar

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"From Information Overload to Actionable Insights: How a National Cancer Research Center Identifies Meaningful Mutations in Somatic Tumor Testing"

Free Webinar: "From Information Overload to Actionable Insights: How a National Cancer Research Center Identifies Meaningful Mutations in Somatic Tumor Testing"

Precision medicine is transforming cancer care, with next-generation sequencing (NGS) enabling the simultaneous analysis of multiple genomic alterations with therapeutic implications. However, due to the sporadic nature of somatic cancers and the increasing uptake of NGS testing, the number of detected variants is exponentially growing, challenging labs to confidently identify meaningful mutations that could influence or improve decisions at the point of care.
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