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Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs?

BACKGROUND: Citizen 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 outpu...

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Autores principales: Guerrini, Christi J., Lewellyn, Meaganne, Majumder, Mary A., Trejo, Meredith, Canfield, Isabel, McGuire, Amy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868686/
https://www.ncbi.nlm.nih.gov/pubmed/31752834
http://dx.doi.org/10.1186/s12910-019-0419-1
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author Guerrini, Christi J.
Lewellyn, Meaganne
Majumder, Mary A.
Trejo, Meredith
Canfield, Isabel
McGuire, Amy L.
author_facet Guerrini, Christi J.
Lewellyn, Meaganne
Majumder, Mary A.
Trejo, Meredith
Canfield, Isabel
McGuire, Amy L.
author_sort Guerrini, Christi J.
collection PubMed
description BACKGROUND: Citizen 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. METHODS: We 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. RESULTS: This 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. CONCLUSIONS: There 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.
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spelling pubmed-68686862019-12-12 Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs? Guerrini, Christi J. Lewellyn, Meaganne Majumder, Mary A. Trejo, Meredith Canfield, Isabel McGuire, Amy L. BMC Med Ethics Research Article BACKGROUND: Citizen 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. METHODS: We 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. RESULTS: This 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. CONCLUSIONS: There 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. BioMed Central 2019-11-21 /pmc/articles/PMC6868686/ /pubmed/31752834 http://dx.doi.org/10.1186/s12910-019-0419-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Guerrini, Christi J.
Lewellyn, Meaganne
Majumder, Mary A.
Trejo, Meredith
Canfield, Isabel
McGuire, Amy L.
Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs?
title Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs?
title_full Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs?
title_fullStr Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs?
title_full_unstemmed Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs?
title_short Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs?
title_sort donors, authors, and owners: how is genomic citizen science addressing interests in research outputs?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868686/
https://www.ncbi.nlm.nih.gov/pubmed/31752834
http://dx.doi.org/10.1186/s12910-019-0419-1
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