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FAIR data is data which meets the FAIR principles of findability, accessibility, interoperability, and reusability (FAIR). [ 1 ] [ 2 ] The acronym and principles were defined in a March 2016 paper in the journal Scientific Data by a consortium of scientists and organizations.
The European Code of Conduct for Research Integrity 2023 states, for example, the principles that, "Researchers, research institutions, and organisations ensure that access to data is as open as possible, as closed as necessary, and where appropriate in line with the FAIR Principles (Findable, Accessible, Interoperable and Reusable) for data ...
Data management has recently become a primary focus of the policy and research debate on open scientific data. The influential FAIR principles are voluntarily centered on the key features of "good data management" in a scientific context. [44] In a research context, data management is frequently associated to data lifecycles. Various models of ...
FORCE11 is an international coalition of researchers, librarians, publishers and research funders working to reform or enhance the research publishing and communication system. Initiated in 2011 as a community of interest on scholarly communication, FORCE11 is a registered 501(c)(3) organization based in the United States but with members and ...
The abbreviation FAIR/O data is sometimes used to indicate that the dataset or database in question complies with the principles of FAIR data and carries an explicit data‑capable open license. Overview
Self-archiving by authors is permitted under green OA. Independently from publication by a publisher, the author also posts the work to a website controlled by the author, the research institution that funded or hosted the work, or to an independent central open repository, where people can download the work without paying.
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Appropriate application of the four principles requires that Stakeholder analysis must first be performed. Thorough stakeholder analysis is important to identify: the correct entity(s) from whom to seek informed consent; the party(s) who bear the burdens or face risks of research; the party(s) who will benefit from research activity; and, the party(s) who are critical to mitigation in the ...