Discovery of new genes implicated in hereditary diseases or cancer progression is challenging and advancing rapidly with an increase in the amount of cohort data to analyze. It is estimated that every day one new gene is discovered to be associated with a disease. QCI Interpret Translational can get your research to the next level by providing you all the necessary analysis tools with the world’s most comprehensive and up-to-date curated scientific evidence. Get valuable and reliable insights for your research project and speed up your discoveries by using a streamlined NGS analysis workflow in a user-friendly interface without needing bioinformatics expertise.

In this webinar, viewers will have the opportunity to:

Explore capabilities which can enable them to accelerate discoveries from hereditary or tumor cohort analyses
Discover interactive tools with current and comprehensive associations between gene variants and diseases
Learn how these resources are supported by unique curated content among other integrated scientific evidence