Abstract
BackgroundCitizen science is increasingly prevalent in the biomedical sciences, including the field of human genomics. Genomic citizen science initiatives present new opportunities to engage individuals in scientific discovery, but they also are provoking new questions regarding who owns the outputs of the research, including intangible ideas and discoveries and tangible writings, tools, technologies, and products. The legal and ethical claims of participants to research outputs become stronger—and also more likely to conflict with those of institution-based researchers and other stakeholders—as participants become more involved, quantitatively and qualitatively, in the research process. It is not yet known, however, how genomic citizen science initiatives are managing the interests of their participants in accessing and controlling research outputs in practice. To help fill this gap, we conducted an in-depth review of relevant policies and practices of U.S.-based genomic citizen science initiatives.MethodsWe queried the peer-reviewed literature and grey literature to identify 22 genomic citizen science initiatives that satisfied six inclusion criteria. A data collection form was used to capture initiative features, policies, and practices relevant to participants’ access to and control over research outputs.ResultsThis analysis revealed that the genomic citizen science landscape is diverse and includes many initiatives that do not have institutional affiliations. Two trends that are in apparent tension were identified: commercialization and operationalization of a philosophy of openness. While most initiatives supported participants’ access to research outputs, including datasets and published findings, none supported participants’ control over results via intellectual property, licensing, or commercialization rights. However, several initiatives disclaimed their own rights to profit from outputs.ConclusionsThere are opportunities for citizen science initiatives to incorporate more features that support participants’ access to and control over research outputs, consistent with their specific objectives, operations, and technical capabilities.
Highlights
Citizen science is increasingly prevalent in the biomedical sciences, including the field of human genomics
The definition of citizen science is contested and evolving [2,3,4,5], but it generally refers to an approach to scientific inquiry in which members of the public participate in one or more steps of the research process other than, or in addition to, allowing personal data or biospecimens
Citizen science is deeply rooted in ecology and the environmental sciences, it is increasingly prevalent in the biomedical sciences, including the field of human genomics [7]
Summary
Citizen science is increasingly prevalent in the biomedical sciences, including the field of human genomics. The legal and ethical claims of participants to research outputs become stronger—and more likely to conflict with those of institution-based researchers and other stakeholders—as participants become more involved, quantitatively and qualitatively, in the research process. It is not yet known, how genomic citizen science initiatives are managing the interests of their participants in accessing and controlling research outputs in practice. That genomic citizen science is flourishing should not be surprising given growing public interest in the genetic bases of health, traits, and habits and the development of new tools and services that facilitate personal genetic discovery and data sharing [8]
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