Integrating Multi-Omics to Advance Genetics and Genomic Medicine - ASHG

Integrating Multi-Omics to Advance Genetics and Genomic Medicine

$120.00

This ASHG Virtual Symposium will focus on multi-modal data. Talks will range from integrating different datasets via summary statistics to applying different technologies to the samples from the same person, or even the same cell. Attendees will be eligible to claim 6 CE.

See schedule below.

December 2 and 3, 9:30 AM–3:00 PM ET.

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Description

This ASHG Virtual Symposium will focus on multi-modal data. Talks will range from integrating different datasets via summary statistics to applying different technologies to the samples from the same person, or even the same cell. Attendees will be eligible to claim 6 CE.

Day One: December 2, 2026

This session will feature talks about multiomic resources and databases.

9:30am – 10:00am      Opening Keynote (Andrew Stergachis, MD, PhD, Division of Medical Genetics, UW Medicine; Departments of Medical Genetics and Genome Sciences, University of Washington)

10:00am – 10:30am     To be announced

10:30am – 11:00am      To be announced

11:00am – 11:30am      The MoTrPAC Data Hub: Resources for the molecular map of exercise (Daniel H Katz, MD, Stanford University)

11:30am – 12:00pm      Panel Discussion (All Speakers)

12:00pm – 1:00pm      Break

In this session, we’ll feature talks on how to combine data sources and summary statistics to generate new insights.

1:00pm – 1:30pm      3D genome rewiring and lncRNA-associated cis-regulatory disruption of the FOXL2 region underlie blepharophimosis syndrome, a rare enhanceropathy (Charlotte Matton, Center for Medical Genetics Ghent)

1:30pm – 2:00pm    Inter-individual multiomics improves subtype resolution and risk stratification in cardiovascular disease (Richard Wang, PhD, Illumina Inc.)

2:00pm – 2:30pm      Omics outlier analysis in rare cancers reveals the function of rare germline variants in predisposition genes (Ata Jadid Ahari, Technical University of Munich)

2:30pm – 3:00pm       Panel Discussion (All Speakers)

Day Two: December 3, 2026

This session will feature talks on powering multiomics discovery using large-scale datasets.

9:30am – 10:00am      Opening Keynote (Anne O’Donnell-Luria, MD, PhD, Center for Mendelian Genomics at the Broad Institute)

10:00am – 10:30am      To be announced

10:30am – 11:00am       To be announced

11:00am – 11:30am      Multi-modal Causal Gene Prioritization and Nonlinear Tissue and Cell-type Interaction Risk Modeling Reveal the Regulatory Architecture of Childhood-onset Asthma (Nan Huang, University of California, San Diego)

11:30am – 12:00pm      Panel Discussion (All Speakers)

12:00pm – 1:00pm       Break

This session will feature talks on leveraging multi-omic data to interpret genetic variant impact.

1:00pm – 1:30pm     Machine learning-based penetrance of genetic variants using metabolomics data  (Megan Wojciechowicz, Icahn School of Medicine at Mount Sinai)

1:30pm – 2:00pm      Single-cell multi-omic dissection of ASXL1-mutant clonal hematopoiesis: Integrating genotype, transcriptome, and protein in myeloid disease progression (Terra Lasho, PhD, Mayo Clinic)

2:00pm – 2:30pm      Large-scale multi-omics analyses of cardiometabolic traits in the Middle East (Mohamad Saad, PhD, Qatar Computing Research Institute, H amad Bin Khalifa University)

2:30pm – 3:00pm       Panel Discussion (All Speakers)