Although there have been remarkable improvements in genomics, interpreting NGS data for hereditary diseases remains difficult. The field is constantly changing, and numerous new articles on human genetic variants are added to PubMed each week. For genetic testing labs, overlooking even a single article among millions can make a significant difference between an inconclusive result and a diagnosis.

In this webinar, we will demonstrate how QCI Interpret can improve your diagnostic yield for hereditary disorders. QCI Interpret is a clinical decision support platform that leverages augmented molecular intelligence to streamline the interpretation workflow. It uses the most extensive, globally trusted and manually curated molecular knowledge and bibliography evidence to provide you with the best possible opportunity to solve every case. By demonstrating the different features and series of use-cases, we will show you how QCI Interpret guarantees a comprehensive and thorough investigation of every case for all types of genetic variation, including copy number variants (CNVs). This will allow you to provide precise answers to patients and their families, while also reducing test turnaround time from hours to minutes.