Scientific
Showing 49–60 of 90 results
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Stability of Polygenic Scores Across Discovery GWAS
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Stakeholders’ Views on Returning Polygenic Risk Scores
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Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding
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The impact of clinical genome sequencing in a global population with suspected rare genetic disease
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The Impact of CNVs on Complex Human Traits
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Towards Health Equity: Prioritizing Community Partnerships in Human Genetics Research
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Tracing decision points in the use of race, ethnicity and genetic ancestry as population descriptors in genomics research
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Trainee Research Excellence Award Winners Session: Genetics and Genomics Digital Forum
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Trainee Research Excellence Awards Available On-Demand
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Updates and Applications of the Human Pangenome Reference
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Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number
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Workshop: Accessing and analyzing All of Us biomedical and genomic data via the Researcher Workbench
$55.00 View Product