Despite incredible advances in genomics, the NGS data interpretation workflow for hereditary diseases remains challenging. The field is rapidly evolving, and novel findings are uncovered daily, resulting in thousands of new articles on human genetic variants being added each week to PubMed. For genetic testing labs, missing even one article among millions can mean the difference between a diagnosis or an inconclusive result.
This on-demand webinar from Qiagen shows, through a series of use cases, how to maximize the diagnostic yield of hereditary disorders with QCI Interpret, a clinical decision support platform that can streamline the interpretation workflow using a comprehensive collection of up-to-date, manually curated molecular knowledge and bibliography evidence.
In this webinar, you will:
Offered Free by: Qiagen
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