ACMG 2025

Details

Get the most out of your genome.

Illumina is excited to be exhibiting at ACMG in Los Angeles. We will be featuring a dynamic program of end-to-end solutions, technologies and talks that can support labs who are eager to embrace genomics or simply looking to scale and optimize their workflows.

This year’s highlights include constellation mapped read technology, a new approach to whole-genome sequencing that generates long-range insights using standard SBS sequencing. In addition, we will be providing live demos of our interpretation software, to move your research and understanding of disease forward.

Visit Illumina booth 409 to meet with our specialists and to learn more about sequencing and informatics solutions in addition to how we can support your implementation strategies or questions.

Schedule of Illumina events
Wednesday, March 19, 2025

12:15 PM – 1:15 PM (PT)
ACMG Foundation Corporate Partner Insights Session
Getting the most out of your genome
Location: Los Angeles Convention Center, Room 403B

Vaidehi Jobanputra

Vaidehi Jobanputra, PhD, FACMG
Professor of Pathology and Cell Biology
Co-Director of Laboratory of Personalized Genomic Medicine
CUIMC Department Of Pathology

Kyle Kai-How Farh

Kyle Kai-How Farh, MD, PhD
Vice President and Distinguished Scientist
Illumina Artificial Intelligence Lab 

Friday, March 21, 2025

10:45 AM – 11:15 AM (PT)
Exhibit theater presentation
Genomics unleashed: Informatics integration at the heart of healthcare
Location: Exhibit Hall Floor, Theater 1

Alisa Gaskell

Alisa Gaskell, PhD
Scientific Director, Precision Medicine Institute
Section Director, Precision Diagnostic Laboratory
Children’s Hospital Colorado


12:30 PM – 1 PM (PT)
Exhibit theater presentation
Constellation: The next generation of whole-genome sequencing (WGS)
Location: Exhibit Hall Floor, Theater 2

Ali Crawford

Ali Crawford, PhD
Sr. Director of Scientific Research
Illumina

Date & Time
18 Mar. 2025 – 22 Mar. 2025
Location
Los Angeles Convention Center
Illumina booth 409
Los Angeles, California
Topic
Complex disease genomics, Genetic & rare diseases
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