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A university research team has collected health data from a First Peoples commun...

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A university research team has collected health data from a First Peoples community for a study on diabetes prevalence. The researchers have completed their analysis and are preparing to publish their findings in an international journal. The community council contacts the researchers asking to review the findings before publication and requesting that certain information not be included as it could stigmatise the community. How should the researchers respond according to Indigenous Data Sovereignty (IDS) principles?

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