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Description
View invited talks available on-demand.
Sessions with talks available include:
- To report or not to report: The quandary of variants of uncertain significance (VUSs)
- The impact of ascertainment, phenotyping, and population structure on human genetic research
- Long-read RNA-seq to illuminate splice-driven mechanisms of human genetic diseases
- Mosaicism, vascular anomalies, and emerging therapeutics: Models for using the rare to understand the common
- Novel preclinical models of Down syndrome elucidate the complex genetic etiology of neurodevelopmental phenotypes
- Genome mapping technologies – Enabling next-generation cytogenetics
- COVID-19 in the post-pandemic era: Long COVID, vaccine response, and beyond
- New advances in computational genome interpretation: From prediction to the clinics
- Demographic history, natural selection, and disease risk in diverse global biobanks
- ASHG/ESHG Building Bridges: Complete Genomes Require New Directions to Democratize Data
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