, Undark; For Vulnerable Populations, the Thorny Ethics of Genetic Data Collection
"Research to capture these snapshots, called genome-wide association
studies, can only draw conclusions about the data that’s been collected.
Without studies that look at each underrepresented population, genetic
tests and therapies can’t be tailored to everyone. Still, projects
intended as correctives, like All of Us and the International HapMap Project, face an ethical conundrum: Collecting that data could exploit the very people the programs intend to help."
The Paperback version of my Bloomsbury book "Ethics, Information, and Technology" will be published on Nov. 13, 2025; the Ebook on Dec. 11; and the Hardback and Cloth versions on Jan. 8, 2026. Preorders are available via Amazon and this Bloomsbury webpage: https://www.bloomsbury.com/us/ethics-information-and-technology-9781440856662/
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