hero image
Webinar

How to translate complex genomic data

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

On-demand
icon_0085_cc_gen_calendar-s
Jan 5, 2023
icon_0310_cc_gen_timeinterval-s
30 minutes
Biomedical Research
Cancer (other / various)
Next Generation Sequencing
Cancer Research

Attendees will:

icon_0153_cc_gen_source_okay-s

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

icon_0153_cc_gen_source_okay-s

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

icon_0153_cc_gen_source_okay-s

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

Fill out the form to take part in the event