Details

How AI and Automation Enhance Cytogenetic Array Analysis

Labs face increasing challenges with variant knowledge, sample volume, and evolving assay needs, all while maintaining operational and cost efficiencies. This 20-minute webinar and live demo will show how bioinformatic solutions can streamline data analysis and interpretation in array clinical research workflows. 

Key topics include: 

  1. Secondary Analysis with DRAGEN™ Array: Industry-leading accuracy and comprehensiveness for variant calling, including structural and complex variants. 
  2. Tertiary Analysis with Emedgene™: Streamlined variant interpretation powered by automation and variant prioritization using explainable AI (XAI), boosting review efficiency and confidence. 
  3. Unified Variant Curation: A single software ecosystem for both sequencing and array-based analyses. 
  4. Upcoming Webinar Series and Roadmaps: Future sessions on algorithms, workflows, and enterprise data strategies. 

DRAGEN and Emedgene are integrated with Illumina’s Global Diversity Array (GDA) and Global Screening Array (GSA), with customizable configurations for other array types. Join us to see the solution in action.

Want to find out more about how you can transform data into insights? Click here 

Fill Out Form to Access Webinar

Your email address is never shared with third parties.

Date & Time
27 Feb 2025
12:00 PM
Location
Europe
Register