Scientific
Showing 25–36 of 85 results
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Global Perspectives and Initiatives for Large-Scale Genomics
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Identifying Disease Risk Through Newborn Genomic Sequencing
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In vivo correction of human phenylketonuria variants via base and prime editing
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Insights from Large-Scale Studies of Diverse Phenotypes and Populations
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Introduction to the GA4GH Variation Representation Specification (VRS)
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Invited Talks Available On-Demand
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Massively parallel reporter assays and variant scoring identified functional variants and target genes for melanoma loci and highlighted cell-type specificity
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New Insights Into Preeclampsia Genetic Risk Factors
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Novel delivery models to meet the demand for genetics services in primary care
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Plenary Talks Available On-Demand
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Polygenic Risk Prediction in Diverse Populations: Leveraging Ancestry and Family History
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Population-Level Study of Developmental Stuttering
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