For labs in North and South America interested in learning more about QCI Interpret for Hereditary, QIAGEN’s clinical decision support software for variant interpretation and reporting, we are hosting an exclusive, interactive virtual workshop where you can access and demo the software for free. Each attendee will be given a temporary license and a VCF file to run a case on the industry-leading software. Through a guided session, you will be able to see first-hand how QCI Interpret works, with full exploration of the software’s capabilities and features.
In this workshop, you will see how QCI Interpret:
✔ Automatically computes variant pathogenicity and actionability based on the ACMG/AMP guidelines with full transparency
✔ Enables users 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
✔ Uses AI-trained phenotype driven ranking tested on a dataset of thousands of solved cases to provides superior overall candidate ranking for causative variants in rare diseases
✔ Supports CNV interpretation and reporting with bibliographic coverage of over 60,000 CNV case reports
✔ Offers performance and scalability optimization, including enhanced filtering capabilities, addition of new annotation sources and efficiency improvements to reduce turnaround time.
Thank you for your interest in the 2024 Annual QIAGEN Digital Insights Training and Certification Courses. One of our representatives will soon be in touch. In the meantime, learn more about how QIAGEN Ingenuity Pathway Analysis (IPA) and QIAGEN CLC Genomics Workbench can support your NGS and 'omics data analysis and interpretation.
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