Genomics

The Human Pangenome Project: a global resource to map genomic diversity

Genomics and justice: mitigating the potential harms and inequities that arise from the implementation of genomics in medicine

Cost-effectiveness of exome and genome sequencing for children with rare and undiagnosed conditions

Prospective genomically-guided identification of ‘early/evolving’ and ‘undersampled’ IDH-wildtype glioblastoma leads to improved clinical outcomes

Integration of stakeholder engagement from development to dissemination in genomic medicine research: Approaches and outcomes from the CSER Consortium

Development of an Open Database of Genes Included in Hereditary Cancer Genetic Testing Panels Available From Major Sources in the US

The promise and pitfalls of gene testing for cancer risk

US private payers’ perspectives on insurance coverage for genome sequencing versus exome sequencing: A study by the Clinical Sequencing Evidence-Generating Research Consortium (CSER)

The difficulties of broad data sharing in genomic medicine: Empirical evidence from diverse participants in prenatal and pediatric clinical genomics research

Progress With the All of Us Research Program: Opening Access for Researchers

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