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Details
No rare disease will go unseen.
The ACMG Annual Meeting provides can’t-miss opportunities for industry, advocacy croups, government agencies, academic institutions, and publishers to position their organization and showcase products and services to practitioners representing the entire genetics team. Members of the medical genetics and genomics community from across the globe will come together for four days of professional growth, education, networking, and collaboration.
Visit Illumina booth 801 to learn more about our solutions for whole-genome sequencing, Illumina Complete Long Reads, and Illumina Connected Software to help uncover rare disease insights.
Exhibit theatre presentation
Preparing for a genome world: AI and informatics automation at the core
Thursday, March 14, 11:55 AM–12:25 PM (ET)
With growing evidence demonstrating the superiority of whole-genome sequencing’s (WGS) utility for evaluating genetic diseases and economic feasibility, the momentum behind policy expansion, adoption and access will likely accelerate. Navigating towards a genome world requires a sequencing and informatics strategy to prepare for data management, scalability and the versality of applications (cardiology, neurology, pediatric rare disease, hereditary cancer).
Baylor Genetics leverages their AI and informatics automation workflow developed with Illumina technology to catalyze their operability for meeting a genome world.
Speaker:
Dr. Christine Eng, MD
Chief Medical Officer, Chief Quality Officer
Baylor Genetics
- Date & Time
- Mar 12, 2024 – Mar 16, 2024
- Location
- Metro Toronto Center
Toronto - Canada
- Sponsor
- American College of Medical Genetics (ACMG)
- Topic
- Complex disease genomics, Genetic & rare diseases