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Curating clinically relevant interpretations of genetic variants can be challenging. Velsera's Clinical Genomics Workspace (CGW) is here to assist you! Our software equips your team with the latest medical data to ensure reliable interpretations and the best therapeutic options for the patient. CGW saves you time when analyzing genomic interpretations by: 🔸Structuring interpretations systematically for convenient review and modification. 🔸Remembering your decisions about past biomarker from previous cases to enable faster sign-out time. Interested in learning more? Watch the recording: https://lnkd.in/gBe6kBkD #NGS #PrecisionMedicine #EraOfVelsera #Genomics

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