Embedding ethics into Genomics England’s Generation Study

The Generation Study is a large-scale research initiative led by Genomics England in partnership with the National Health Service, aiming to evaluate the use of whole genome sequencing in newborn screening, as well as ongoing research use of these genomic data. The Generation Study will sequence 100 000 newborn genomes in England to potentially identify approximately 200 rare and treatable conditions. This paper outlines the study's approach to embedding ethics from inception through implementation. A model of 'ethical embeddedness' that emphasises transparency, trustworthiness and responsiveness to uncertainty is utilised. Drawing on the deliberations of a multidisciplinary Ethics Working Group, public dialogue findings and design research, the paper presents key decisions and our approach to complex ethical challenges including consent, potential impact of the study on clinical services and navigating uncertainty. The paper also reflects on the ethical tensions inherent in balancing research ambitions with operational realities, particularly in a context of evolving genomic science and sometimes limited regulatory clarity. By embedding ethics into the study's design and delivery, we hope to foster public trust and inform future policy and practice.

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Publication Details

Journal
BMJ Open
Published
2026-02-01
DOI
https://doi.org/10.1136/bmjopen-2025-112134
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00
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article

Embedding ethics into Genomics England’s Generation Study

Harriet Etheredge, Mathilde Leblond, Natalie Banner, Joanna L. Ziff et al.
BMJ Open
Genomics and Rare Diseases
article

Embedding ethics into Genomics England’s Generation Study

Harriet Etheredge, Mathilde Leblond, Natalie Banner, Joanna L. Ziff, Alice Tuff-Lacey, Amanda Pichini, Meekai To, E Thomas, Richard Scott
article en

Abstract

The Generation Study is a large-scale research initiative led by Genomics England in partnership with the National Health Service, aiming to evaluate the use of whole genome sequencing in newborn screening, as well as ongoing research use of these genomic data. The Generation Study will sequence 100 000 newborn genomes in England to potentially identify approximately 200 rare and treatable conditions. This paper outlines the study's approach to embedding ethics from inception through implementation. A model of 'ethical embeddedness' that emphasises transparency, trustworthiness and responsiveness to uncertainty is utilised. Drawing on the deliberations of a multidisciplinary Ethics Working Group, public dialogue findings and design research, the paper presents key decisions and our approach to complex ethical challenges including consent, potential impact of the study on clinical services and navigating uncertainty. The paper also reflects on the ethical tensions inherent in balancing research ambitions with operational realities, particularly in a context of evolving genomic science and sometimes limited regulatory clarity. By embedding ethics into the study's design and delivery, we hope to foster public trust and inform future policy and practice.

BMJ OpenVol. 16(2)
Genomics England (GB)
Partnerships for the goals
Openalex Percentile: Top 65%
Genomics and Rare Diseases
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