QCI Interpret for Hereditary
Shed light on Hereditary Disorders with QCI Interpret
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Learning objectives:
Learn about QCI Interpret’s analysis and interpretation workflow for hereditary diseases using targeted and extended gene panels, including WES/WGS
Learn about QCI Interpret and QIAGEN’s expert curation process based on the latest ACMG carrier screening guidelines
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 and triage mode of variant assessment.
Learn how QCI Interpret supports CNV interpretation and reporting with bibliographic coverage of over 60,000 CNV case reports”
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