QCI Interpret for Hereditary
Solve Every Hereditary Disorder Case for All Types of Mutations
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In this webinar, we will show you how to maximize your diagnostic yield of hereditary disorders with QCI Interpret. A clinical decision support platform powered by augmented molecular intelligence, QCI Interpret streamlines the interpretation workflow and uses the world’s most comprehensive collection of globally trusted, up-to-date, manually curated molecular knowledge and bibliography evidence to give you the best possible chance of solving any case while taking your turnaround time from hours to minutes. Through a series of use-cases, we will show you how QCI Interpret ensures a complete and thorough investigation of every case for all types of genetic variation, including CNVs, so you can deliver clear answers to patients and their families every time.
In this webinar, you will:
Learn about QCI Interpret’s analysis and interpretation workflow for hereditary diseases using targeted and extended gene panels, including WES/WGS
View demonstrations of unique features in QCI Interpret, including how to input symptoms relevant to a case and receive relationships to candidate diseases and mutated genes using the Phenotype Network Analysis feature
Learn how QCI Interpret supports CNV interpretation and reporting with bibliographic coverage of over 60,000 CNV case reports
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