NOTEWORTHY: ISNI Assignments Top 6.5 Million; NFAIS Issues Recommended Practice on Discovery Services; W3C Launches Web and Mobile Interest Group; Find the Registration Agency for any DOI; Thomson Reuters Whitepaper Tackles Issues of Uniform Access to Global Scholarly Data; ORCID Project to Develop Use Cases and Best Practices; Research Data Alliance Formed to Facilitate Research Data Sharing and Exchange

2013 ◽  
Vol 25 (3) ◽  
pp. 37
Author(s):  
Cynthia Hodgson
2021 ◽  
Author(s):  
Kevin B Read ◽  
Heather Ganshorn ◽  
Sarah Rutley ◽  
David R. Scott

Background:As Canada increases requirements for research data management (RDM) and sharing, there is value in identifying how research data are shared, and what has been done to make them findable and reusable. This study aims to understand Canada’s data sharing landscape by reviewing how Canadian Institutes of Health Research (CIHR) funded data are shared, and comparing researchers’ data sharing practices to RDM and sharing best practices. Methods:We performed a descriptive analysis of CIHR-funded publications from PubMed and PubMed Central that were published between 1946 and Dec 31, 2019 and that indicated the research data underlying the results of the publication were shared. Each publication was analyzed to identify how and where data were shared, who shared data, and what documentation was included to support data reuse.Results:Of 4,144 CIHR-funded publications, 45.2% (n=1,876) included accessible data, 21.9% (n=909) stated data were available by request, 7.3% (n=304) stated data sharing was not applicable/possible, and we found no evidence of data sharing in 37.6% (n=1,558) of publications. Frequent data sharing methods included via a repository (n=1,549, 37.3%), within supplementary files (n=1,048, 25.2%), and by request (n=919, 22.1%). 13.1% (n=554) of publications included documentation that would facilitate data reuse.Interpretation:Our findings reveal that CIHR-funded publications largely lack the metadata, access instructions, and documentation to facilitate data discovery and reuse. Without measures to address these concerns, and enhanced support for researchers seeking to implement RDM and sharing best practices, most CIHR-funded research data will remain hidden, inaccessible, and unusable.


Author(s):  
Mike Fortun ◽  
Lindsay Poirier ◽  
Alli Morgan ◽  
Brian Callahan ◽  
Kim Fortun

This chapter points out different ways involvement with collaborative projects share form, shape, or style, and may be imagined as nested within each other, like matryoshka dolls. It deals with the Platform for Experimental Collaborative Ethnography (PECE), the digital infrastructure that support new collaborative projects in anthropology. It also cites the long-standing collaboration of The Asthma Files (TAF), which is an experimental ethnographic research project that eventually led to the conceptualization and development of PECE. The chapter mentions the Digital Practices in History and Ethnography Interest Group (DPHE-IG) that was organized within the Research Data Alliance (RDA), a global collaboration of individuals and institutions working to make data more easily and openly shareable. It emphasizes how the collaborative form is the experimental form analyzed by Hans-Jorg Rheinberger as essential to a modern scientific style.


2021 ◽  
Vol 6 ◽  
pp. 214
Author(s):  
Jude O. Igumbor ◽  
Edna N. Bosire ◽  
Marta Vicente-Crespo ◽  
Ehimario U. Igumbor ◽  
Uthman A. Olalekan ◽  
...  

Background: The rising digitisation and proliferation of data sources and repositories cannot be ignored. This trend expands opportunities to integrate and share population health data. Such platforms have many benefits, including the potential to efficiently translate information arising from such data to evidence needed to address complex global health challenges. There are pockets of quality data on the continent that may benefit from greater integration. Integration of data sources is however under-explored in Africa. The aim of this article is to identify the requirements and provide practical recommendations for developing a multi-consortia public and population health data-sharing framework for Africa. Methods: We conducted a narrative review of global best practices and policies on data sharing and its optimisation. We searched eight databases for publications and undertook an iterative snowballing search of articles cited in the identified publications. The Leximancer software © enabled content analysis and selection of a sample of the most relevant articles for detailed review. Themes were developed through immersion in the extracts of selected articles using inductive thematic analysis. We also performed interviews with public and population health stakeholders in Africa to gather their experiences, perceptions, and expectations of data sharing. Results: Our findings described global stakeholder experiences on research data sharing. We identified some challenges and measures to harness available resources and incentivise data sharing.  We further highlight progress made by the different groups in Africa and identified the infrastructural requirements and considerations when implementing data sharing platforms. Furthermore, the review suggests key reforms required, particularly in the areas of consenting, privacy protection, data ownership, governance, and data access. Conclusions: The findings underscore the critical role of inclusion, social justice, public good, data security, accountability, legislation, reciprocity, and mutual respect in developing a responsive, ethical, durable, and integrated research data sharing ecosystem.


2018 ◽  
Vol 12 (2) ◽  
pp. 107-115 ◽  
Author(s):  
Minna Ahokas ◽  
Mari Elisa Kuusniemi ◽  
Jari Friman

Many research funders have requirements for data sharing and data management plans (DMP). DMP tools are services built to help researchers to create data management plans fitting their needs and based on funder and/or organisation guidelines. Project Tuuli (2015–2017) has provided DMPTuuli, a data management planning tool for Finnish researchers and research organisations offering DMP templates and guidance. In this paper we describe how project has helped both Finnish researchers and research organisations adopt research data management best practices. As a result of the project we have also created a national Tuuli network. With growing competence and collaboration of the network, the project has reached most of its goals. The project has also actively promoted DMP support and training in Finnish research organisations.


2013 ◽  
Vol 11 (3) ◽  
pp. 157-157
Author(s):  
L. McFarland ◽  
J. Richter ◽  
C. Bredfeldt

2018 ◽  
Vol 19 (1) ◽  
Author(s):  
Phaik Yeong Cheah ◽  
Nattapat Jatupornpimol ◽  
Borimas Hanboonkunupakarn ◽  
Napat Khirikoekkong ◽  
Podjanee Jittamala ◽  
...  

2018 ◽  
Vol 37 (4) ◽  
Author(s):  
Heidi Enwald

Open research data is data that is free to access, reuse, and redistribute. This study focuses on the perceptions, opinions and experiences of staff and researchers of research institutes on topics related to open research data. Furthermore, the differences across gender, role in the research organization and research field were investigated. An international questionnaire survey, translated into Finnish and Swedish, was used as the data collection instrument. An online survey was distributed through an open science related network to Finnish research organizations. In the end, 469 responded to all 24 questions of the survey. Findings indicate that many are still unaware or uncertain about issues related to data sharing and long-term data storage. Women as well as staff and researchers of medical and health sciences were most concerned about the possible problems associated with data sharing. Those in the beginning of their scientific careers, hesitated about sharing their data.


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