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GWAS Study

Principled distillation of UK Biobank phenotype data reveals underlying structure in human variation.

Carey CE, Shafee R, Wedow R et al.

38965376 PubMed ID
GWAS Study Type
80058 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CC
Carey CE
SR
Shafee R
WR
Wedow R
EA
Elliott A
PD
Palmer DS
CJ
Compitello J
KM
Kanai M
AL
Abbott L
SP
Schultz P
KK
Karczewski KJ
BS
Bryant SC
CC
Cusick CM
CC
Churchhouse C
HD
Howrigan DP
KD
King D
DS
Davey Smith G
NB
Neale BM
WR
Walters RK
RE
Robinson EB
Chapter II

Abstract

Summary of the research findings

Data within biobanks capture broad yet detailed indices of human variation, but biobank-wide insights can be difficult to extract due to complexity and scale. Here, using large-scale factor analysis, we distill hundreds of variables (diagnoses, assessments and survey items) into 35 latent constructs, using data from unrelated individuals with predominantly estimated European genetic ancestry in UK Biobank. These factors recapitulate known disease classifications, disentangle elements of socioeconomic status, highlight the relevance of psychiatric constructs to health and improve measurement of pro-health behaviours. We go on to demonstrate the power of this approach to clarify genetic signal, enhance discovery and identify associations between underlying phenotypic structure and health outcomes. In building a deeper understanding of ways in which constructs such as socioeconomic status, trauma, or physical activity are structured in the dataset, we emphasize the importance of considering the interwoven nature of the human phenome when evaluating public health patterns.

80,058 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

80058
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

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