Join us for a live webinar to learn about a software application that can take your genome research to the next level. See first-hand how to accelerate discovery from germline or somatic tumor analyses. Plus, learn how to rapidly identify associations between gene variants and diseases.
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. Every day, one new gene is discovered to be associated with a disease. QCI Interpret Translational can get your genome 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. In addition, speed-up your discoveries by using a streamlined NGS analysis workflow in a user-friendly interface without needing bioinformatics expertise.
In this webinar, attendees will have the opportunity to:
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QCI Interpret Translational is a NGS variant assessment software solution that enables rapid, evidence-powered variant annotation, filtering, and triage for human exome, genome, and large cohort sequencing data. Learn more here.
