Topics

This NIH website details the Data Sharing and Management Plan format, discusses each element of the plan, and provides 4 sample plans.

This NIH webinar describes the applicability of the 2023 DMS policy, discusses data sharing considerations, and describes how to prepare a Data Management and Sharing Plan.

This slide deck, which defines scientific data, lists allowable justifications for limiting data sharing, reviews elements of a DMS Plan, and covers other topics, was presented in Part 1 of the…

This NIH website provides answers to frequently asked questions about the 2023 DMS policy such as those about sharing qualitative data, how noncompliance will be handled, protection of research…

This NIH webinar provides guidance on privacy protections for human subjects and considers the interaction of the 2023 DMS policy with the NIH Genomic Data Sharing Policy

"The Meaning of Eugenics: Historical and Present-Day Discussions of Eugenics and Scientific Racism" was a two-day virtual symposium convened by the NHGRI in December 2021 and led by NHGRI Historian…

A team of researchers from the Dolan DNA Learning Center of Cold Spring Harbor Laboratory created the Image Archive on the American Eugenics Movement website to host 2,500 photos, correspondence,…

The Polygenic Risk Methods in Diverse Populations (PRIMED) Consortium (comprised of NIH program staff, affiliate members, investigators at 7 study sites, and a Coordinating Center) is funded by the…

The National Center on Disability and Journalism at Arizona State University’s Walter Cronkite School of Journalism and Mass Communication provides a style guide for journalists and other…

An open-access repository of FAQs that accompany genomic research in social and behavioral genomics. This resource was developed in collaboration with researchers at the Stanford University Center…