Solve Every Hereditary Disorder Case for All Types of Genetic Variation

Presented By:
Georgios Stamoulis, Ph.D.

Speaker Biography:
Georgios Stamoulis, Ph.D., holds the position of QIAGEN Digital Insights Director of Global Product Management for Hereditary diseases. Dr. Georgios Stamoulis is a Molecular Geneticist by training and he holds a Ph.D. in Human Genetics from the University of Geneva, and an MSc in Medical Genetics from University of Glasgow. Georgios has more than 12 years of experience in human genetics and genomic diagnostics & research and in product management of hereditary disease products with a focus on NGS interpretation tools. Before joining QIAGEN, Georgios served as the Global Product Manager of Hereditary diseases in SOPHiA Genetics. In 2016, he received the “Fellowship of Excellence for Young Investigators” from the European Society of Human Genetics (ESHG). He is also an author of multiple human genomics publications

Solve Every Hereditary Disorder Case for All Types of Genetic Variation

Webinar Abstract:
Despite incredible advances in genomics, the NGS data interpretation workflow for hereditary diseases remains challenging. The field is rapidly evolving, and novel findings are uncovered daily, resulting in thousands of new articles on human genetic variants being added each week to PubMed. For genetic testing labs, missing even one article among millions can mean the difference between a diagnosis or an inconclusive result.
In this webinar, we will show you how to maximize your diagnostic yield of hereditary disorders with QCI Interpret. A clinical decision support platform powered by augmented molecular intelligence, QCI Interpret streamlines the interpretation workflow and uses the world’s most comprehensive collection of globally trusted, up-to-date, manually curated molecular knowledge and bibliography evidence to give you the best possible chance of solving any case while taking your turnaround time from hours to minutes. Through a series of use-cases, we will show you how QCI Interpret ensures a complete and thorough investigation of every case for all types of genetic variation, including CNVs, so you can deliver clear answers to patients and their families every time.

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