Invited Sessions	CME | P.A.C.E.® | NSGC
Wednesday, October 28
Session 021 – Variant-to-Function Coupling: Understanding Non-coding Variation in Human Disease	1.50
Session 022 – Re-evaluating Penetrance: Modifiers, Mechanisms and Implications for Genetic Testing
Session 023 – Asthma in Diverse Populations
Session 024 – Underrepresented Populations in Genomics: Health, Evolutionary, and Ethical Aspects
Session 020 – ASHG/ESHG Building Bridges Symposium: ASHG/ESHG Reconciling U.S. and European Guidelines on Variant Interpretation and Secondary Findings
Thursday, October 29
Session 033 – The History and Future of Protections Against Genetic Discrimination	1.50
Session 034 – Scalable Functional Genomics Approaches to Dissect Genetic Architecture
Session 035 – Extending Phenotype-Genotype Correlations to the Fetus: Integrating Genetics, Imaging, and the Electric Health Record
Session 037 – Evolutionary Genomic Medicine
Friday, October 30
Session 046 – Indigenous Biobanking: Global Perspectives on Keeping Our Genomic Data Local	1.50
Session 047 – Using Novel Analytical Approaches to Identify High-Risk Genes in Next-Generation Sequencing of Multiplex Pedigrees
Session 048 – Epi-Phenotyping of Neurodevelopmental Disabilities
Session 049 – Advances in Functional Transcriptomics: Linking Genetic Variation to RNA Processing
Session 050 – Application of Long Read Methods to Cancer Genomics
Platform Presentations	CME | P.A.C.E.® | NSGC
Wednesday, October 28
Session 013 – Machine Learning	1.50
Session 014 – Genetics and Functional Insights into Cardiovascular Disease
Session 015 – Disorders of Brain Development
Session 016 – Mechanisms of Gene Regulation in Cis and Trans
Session 017 – Novel Statistical Genetics Methods for Complex Traits
Session 018 – Strength in Diversity: Improving representation in study populations
Thursday, October 29
Session 026 – Insights into Structural Variation Features in Constitutional Diseases and Cancer Genomes	1.50
Session 027 – Novel Genetic Factors for Cancer and Related Phenotypes
Session 028 – Rare Variants and Complex Disease
Session 029 – Natural Selection on Polygenic Traits and Omics
Session 030 – Single Cell Profiling in Disease, Development, and Distribution of Mutations
Session 031 – From Genes to Therapeutic Targets and Clinical Traits
Friday, October 30
Session 039 – Computational approaches for disease diagnosis and variant effect determination	1.50
Session 040 – Improving our understanding of the causes and consequences of cardiometabolic dysfunction
Session 041 – Molecular Mechanisms in Mendelian Disorders
Session 042 – Methods to Connect Gene Expression and Disease
Session 043 – Matchmaking and Mechanisms in Mendelian Disorders
Session 044 – Genetic Insights from Diverse Cohorts
Friday, October 30
Session 051 – Novel Biology from Large-Scale Genome Sequencing	1.50
Session 052 – Genome Discoveries from Long-Read Sequencing
Session 053 – Molecular Insights into Risk Factors and Mechanisms of Alzheimer Disease
Session 054 – Insights from Pediatric and Rare Disease Cohorts
Session 055 – Diverse Approaches in Analyses of Complex Disease
Session 056 – The Public Genome
Plenary Presentations	CME | P.A.C.E.® | NSGC
Tuesday, October 27
Session 001 – Presidential Address: The Big Tent of Genetics/Genomics and Our World	0.50
Session 008 – Featured Plenary Session I	1.25
Wednesday, October 28
Session 019 – Featured Plenary Session II	1.25
Thursday, October 29
Session 032 – Featured Plenary Session III	1.25
Friday, October 30
Session 045 – Featured Plenary Session IV	1.25

16.0

**Please Note: Workshops can be viewed On-Demand to acquire an additional 10 hours of CME credit or 1 CEU

Presenters

To see the session presenters, please visit the online program planner. To view a list of speaker/moderator disclosures click here.