Shortcut to success? Negotiating genetic uniqueness in global biomedicine

Since the sequencing of the human genome, as well as the completion of the first Human Genome Diversity Project, the benefits of studying one human population over another has been an ongoing debate relating to the replicability of findings in other populations. The leveraging of specific population...

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Bibliographic Details
Published in:Social Studies of Science
Main Authors: Tarkkala, Heta, Tupasela, Aaro
Other Authors: Suomen Akatemia, H2020 European Research Council, Helsingin Yliopisto
Format: Article in Journal/Newspaper
Language:English
Published: SAGE Publications 2018
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Online Access:http://dx.doi.org/10.1177/0306312718801165
http://journals.sagepub.com/doi/pdf/10.1177/0306312718801165
http://journals.sagepub.com/doi/full-xml/10.1177/0306312718801165
Description
Summary:Since the sequencing of the human genome, as well as the completion of the first Human Genome Diversity Project, the benefits of studying one human population over another has been an ongoing debate relating to the replicability of findings in other populations. The leveraging of specific populations into research markets has made headlines in cases such as deCode in Iceland, Quebec Founder Population, and Generation Scotland. In such cases, researchers and policy makers have used the genetic and historical uniqueness of their populations to attract scientific, commercial and political interest. In this article, we explore how in countries with population isolates, such as Finland, the researchers balance considerations relating to the generalization and replicability of findings in small yet unique research populations to global biomedical research interests. This highlights challenges related to forms of competition associated with genetics research markets, as well as what counts as the ‘right’ population for genetic research.