The appropriate preservation and sharing mechanism will depend on your project and the data you generate. However, the NIH DMS Policy requires or recommends the following, which all investigators should understand and consider:
We recommend reviewing and bookmarking the NIH guidance on sharing scientific data as a first step. It will help you understand how and when NIH expects data to be shared and how to safeguard the privacy of human participants while sharing scientific data.
Using an established, quality data repository generally improves the FAIRness (Findable, Accessible, Interoperable, and Re-usable) of data. Additionally, using an established repository can reduce risks related to accidental loss and security when relevant.
When selecting a repository, NIH encourages and prioritizes the following:
As noted in the infographic above, NLM's BMIC has a searchable and filterable list of NIH-supported data repositories. You can filter it by institute or center or search the repository descriptions via relevant key terms.
If you don’t find a repository there, you can search for and evaluate additional repositories with the tools described below. OHSU Librarians librarians are available to help you navigate these resources. Contact us to schedule a consultation.
Some of the language above was adapted from Fred Hutch Biomedical Data Science Wiki.
When working with human participant data, including de-identified human data, there are additional considerations and repository characteristics that must be considered. For example, you must ensure that the consent process for data collection allows for sharing the data in the way you have planned. NIH expects that in drafting their DMS plans, researchers will attempt to maximize scientific data sharing but acknowledge that certain factors (i.e., ethical, legal, or technical) may necessitate limiting sharing to some extent.
Some of the language above was adapted from Fred Hutch Biomedical Data Science Wiki.