This article aims to explore the ethical issues arising from attempts to diversify genomic data and include individuals from underserved groups in studies exploring the relationship between genomics and health. Diverse data are not ethical in and of themselves, and without being attentive to the social, historical and political contexts that shape the lives of potential participants, endeavours to diversify genomic data run the risk of worsening existing inequities.
Understanding this could lead to better treatments, improved diagnostics, or a deeper grasp of how the human body works — benefiting patient care globally.
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| Category | 🧬 Medicine & Biology |
| Published | Jan 01, 2024 |
| Journal | Cambridge prisms. Precision medicine |
| Authors | Hardcastle Faranak, Lyle Kate, Horton Rachel, Samuel Gabrielle, Weller Susie |
| DOI | 10.1017/pcm.2023.20 |
| Source | PubMed |