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:
- Secondary Analysis with DRAGEN™ Array: Industry-leading accuracy and comprehensiveness for variant calling, including structural and complex variants.
- Tertiary Analysis with Emedgene™: Streamlined variant interpretation powered by automation and variant prioritization using explainable AI (XAI), boosting review efficiency and confidence.
- Unified Variant Curation: A single software ecosystem for both sequencing and array-based analyses.
- Upcoming Webinar Series and Roadmaps: Future sessions on algorithms, workflows, and enterprise data strategies.
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Date:
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9th April 2025, Wednesday
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Time:
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09:00 am - 09:30 am (Cape Town)
11:00 am - 11:30 am (Dubai)
12:30 pm – 01:00 pm (Delhi)
02:00 pm - 02:30 pm (Bangkok)
03:00 pm - 03:30 pm (Singapore)
04:00 pm - 04:30 pm (Seoul / Tokyo)
05:00 pm - 05:30 pm (Melbourne)
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Speakers:
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Jackie Hagan
Staff Product Manager, Human Genotyping Arrays,
Illumina Inc.
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Eithan Zand
Staff Technical Product Manager,
Illumina Inc.
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