Abstract

Public involvement in research occurs when the public, patients, or research participants are actively contributing to the research process. Public involvement has been acknowledged as a key priority for prominent human genomics research initiatives in many different countries. However, to date, there has been no detailed analysis or review of the features, methods, and impacts of public involvement occurring in human genomics research projects worldwide. Here, we review the reported public involvement in 96 human genomics projects (initiatives), based on a database of initiatives hosted by the Global Alliance for Genomics and Health, according to information reported on public domain websites. To conduct the scoping review, we applied a structured categorization of criteria to all information extracted from the search. We found that only a third of all initiatives reported public involvement in any capacity (32/96, 33%). In those reporting public involvement, we found considerable variation in both the methods and tasks of involvement. Some noteworthy initiatives reported diverse and comprehensive ways of involving the public, occurring through different stages of the research project cycle. Three notable initiatives reported a total of eight distinct impacts as a result of involving people. Our findings suggest there would be intrinsic value in having more public involvement occur in human genomics research worldwide. We also suggest that more systematic ways of reporting and evaluating involvement would be highly beneficial, to help develop best practices.

Highlights

  • In human genomics, there is a growing need to increase involvement of the public in research and policy development

  • Using a list of human genomics research projects from a database hosted by the GA4GH, we systematically searched public domain websites for information reported on involving the public in research

  • This review provides an overview of reported public involvement occurring in prominent human genomics projects worldwide, during a period of rapid growth for genomics research

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Summary

Introduction

There is a growing need to increase involvement of the public in research and policy development. This has been identified as a crucial aspect of responsible research practice [1, 2]. The concept of “public involvement” in research is defined as research that is carried out “with” people rather than “on” them [3]. Public involvement can be defined as when the public, patients or research participants actively contribute to the research or policy development process [4]. The number of people involved in genomics research is predicted to grow substantially in coming years [5, 6]. By 2025, it is estimated that nearly 2 billion people worldwide will have had their DNA sequenced, creating a global imperative for responsible and effective

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