詳細

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.

Date:

9th April 2025, Wednesday

Time:

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)

Speakers:

Jackie Hagan
Staff Product Manager, Human Genotyping Arrays,
Illumina Inc.

 

Eithan Zand
Staff Technical Product Manager,
Illumina Inc.

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日時
2025/04/09
Topic
Clinical research products, Software & informatics, Genetic & rare diseases
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