In this month's The Genomics Landscape, details the strategic visioning meeting in March to launch the GLEE Initiative - a national campaign to enhance genomic literacy while keeping pace with the advances in genomics. Also included: The Genomics and Health Disparities Lecture Series welcomes its sixth speaker, Dr. Mark Cullen, from the Stanford Center for Population Health Sciences and Dr. Cynthia Tifft receives the National Organization for Rare Disorders 2017 Rare Impact Award.
A collection of oral histories released today by the National Human Genome Research Institute (NHGRI) features candid conversations with pioneering scientists involved in the Human Genome Project and a rare discussion with all three institute directors since the organization was established in 1989. In each oral history, influential scientists offer extensive insight into science and medicine, as well as biographical details and commentary on the inner workings of NHGRI and its foundational initiatives that transformed the way people think about the human genome.
NHGRI believes that broadly sharing research data will result in maximum public benefit, and we're committed to providing researchers with access to genomic data. The National Institutes of Health (NIH) Genomic Data Sharing Policy establishes a system to promote data sharing, while also protecting research participants involved in genomics studies. We need your help to improve one of NIH's central data sharing tools for human genomic data: the database of Genotypes and Phenotypes, or dbGaP.
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