In this webinar, learn how QCI Interpret, clinical decision support software for variant interpretation and reporting, can help your lab rapidly identify pathogenic variants, improve diagnostic yields, and significantly reduce test turnaround time for hereditary diseases. Attendees will receive a demonstration of QCI Interpret’s unique capabilities and advanced features for germline variant interpretation with example workflows for carrier screening and whole-exome sequencing panels. Key highlights will include how your lab can expedite variant interpretation by leveraging the most extensive, manually curated knowledge base, dynamically compute pathogenicity based on ACMG guidelines for every variant with full transparency, and leverage QCI Interpret’s proprietary augmented molecular intelligence approach to literature curation and variant classification to streamline your interpretation workflow. 

In this webinar, attendees will: 

• Receive a demonstration of QCI Interpret’s analysis and interpretation workflows for hereditary diseases using targeted and extended gene panels, including whole-genome and whole-exome sequencing. 
• Learn about QIAGEN’s proprietary expert curation process for the knowledge base in QCI Interpret.
• Explore unique time-saving features within QCI Interpret, including phenotype-driven ranking and automation of ACMG guidelines.
• Understand how QCI Interpret supports copy number variant (CNV) interpretation and reporting with bibliographic coverage of over 60,000 CNV case reports.