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GWAS Study

Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries.

An U, Pazokitoroudi A, Alvarez M et al.

37985819 PubMed ID
GWAS Study Type
285405 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

AU
An U
PA
Pazokitoroudi A
AM
Alvarez M
HL
Huang L
BS
Bacanu S
SA
Schork AJ
KK
Kendler K
PP
Pajukanta P
FJ
Flint J
ZN
Zaitlen N
CN
Cai N
DA
Dahl A
SS
Sankararaman S
Chapter II

Abstract

Summary of the research findings

Biobanks that collect deep phenotypic and genomic data across many individuals have emerged as a key resource in human genetics. However, phenotypes in biobanks are often missing across many individuals, limiting their utility. We propose AutoComplete, a deep learning-based imputation method to impute or 'fill-in' missing phenotypes in population-scale biobank datasets. When applied to collections of phenotypes measured across ~300,000 individuals from the UK Biobank, AutoComplete substantially improved imputation accuracy over existing methods. On three traits with notable amounts of missingness, we show that AutoComplete yields imputed phenotypes that are genetically similar to the originally observed phenotypes while increasing the effective sample size by about twofold on average. Further, genome-wide association analyses on the resulting imputed phenotypes led to a substantial increase in the number of associated loci. Our results demonstrate the utility of deep learning-based phenotype imputation to increase power for genetic discoveries in existing biobank datasets.

285,405 British ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

285405
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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