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Webinar

How to translate complex genomic data

to clinically-oriented personalized cancer care: a real-world experience

On-demand
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Jan 5, 2023
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30 minutes
Biomedical Research
Cancer (other / various)
Next Generation Sequencing
Cancer Research

Attendees will:

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Explore the challenges of variant classification, including the limitations of manual curation, handling of VUS, and incorporating guideline recommendations.

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Learn how the IORS uses QCI Interpret to evaluate genomic profiles of hereditary cancers and identify variants with clinical utility.

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Receive a demonstration of how QCI Interpret filters and prioritizes variants, transparently computes ACMG/AMP classifications, and auto-generates clinical reports with the latest evidence.

About this webinar

Next-generation sequencing (NGS) tests encompassing multi-gene panels, whole-exome (WES), and whole-genome sequencing (WGS) are becoming an integral part of clinical diagnostics for hereditary cancers. However, analyzing and interpreting these panels can be incredibly time-consuming and complex.

Join Dr. Ana Krivokuca as she presents a use-case of how the Institute for Oncology and Radiology Serbia (IORS), a National Cancer Research Center, uses QCI Interpret, a clinical decision support software, in their NGS testing pipeline to annotate, assess, and interpret the clinical significance of germline variants in hereditary cancers.

Speakers