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Valid inference for machine learning-assisted GWAS
Open accessPreprint — published as 10.1038/s41588-024-01934-0 · Paper page
Abstract
Machine learning (ML) has revolutionized analytical strategies in almost all scientific disciplines including human genetics and genomics. Due to challenges in sample collection and precise phenotyping, ML-assisted genome-wide association study (GWAS) which uses sophisticated ML to impute phenotypes and then performs GWAS on imputed outcomes has quickly gained popularity in complex trait genetics research. However, the validity of associations identified from ML-assisted GWAS has not been carefully evaluated. In this study, we report pervasive risks for false positive associations in ML-assisted GWAS, and introduce POP-GWAS, a novel statistical framework that reimagines GWAS on ML-imputed outcomes. POP-GWAS provides valid statistical inference irrespective of the quality of imputation or variables and algorithms used for imputation. It also only requires GWAS summary statistics as input. We employed POP-GWAS to perform the largest GWAS of bone mineral density (BMD) derived from dual-energy X-ray absorptiometry imaging at 14 skeletal sites, identifying 89 novel loci reaching genome-wide significance and revealing skeletal site-specific genetic architecture of BMD. Our framework may fundamentally reshape the analytical strategies in future ML-assisted GWAS.
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Cites
Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764
Flagged first, then by citations
Research works printed but not linked: 57
- 2021, Genome-wide association studies, Nature Reviews Methods Primers, 1, 59, 10.1038/s43586-021-00056-9 · DOI · Paper page
- Dahl, A. et al. Phenotype integration improves power and preserves specificity in biobank-based genetic studies of major depressive disorder. Nature Genetics (2023). · DOI
- An, U. et al. Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries. Nature Genetics (2023). · DOI
- 2023, Genome-wide analysis of a model-derived binge eating disorder phenotype identifies risk loci and implicates iron metabolism, Nature Genetics, 55, 1462, 10.1038/s41588-023-01464-1 · DOI
- Cosentino, J. et al. Inference of chronic obstructive pulmonary disease with deep learning on raw spirograms identifies new genetic loci and improves risk models. Nature Genetics, 1–9 (2023). · DOI
- 2023, The genetic architecture and evolution of the human skeletal form, Science, 381, eadf8009, 10.1126/science.adf8009 · DOI
- 2023, Genetics implicates overactive osteogenesis in the development of diffuse idiopathic skeletal hyperostosis, Nature Communications, 14, 2644, 10.1038/s41467-023-38279-x · DOI
- 10.1016/j.ajhg.2021.05.004 · DOI
- 10.1038/ng.3513 · DOI
- 10.1038/s41586-018-0579-z · DOI · Paper page
- 2023, Plasma proteomic associations with genetics and health in the UK Biobank, Nature, 622, 329, 10.1038/s41586-023-06592-6 · DOI · Paper page
- 10.1126/science.abf3736 · DOI
- 10.1126/science.abn6598 · DOI
- 2021, Analysing electrocardiographic traits and predicting cardiac risk in UK biobank, JRSM Cardiovascular Disease, 10, 20480040211023664, 10.1177/20480040211023664 · DOI
- 2023, Atlas of plasma NMR biomarkers for health and disease in 118,461 individuals from the UK Biobank, Nature Communications, 14, 604, 10.1038/s41467-023-36231-7 · DOI
- He, K. , Zhang, X. , Ren, S. & Sun, J . Deep residual learning for image recognition. in Proceedings of the IEEE conference on computer vision and pattern recognition 770–778 (2016). · DOI · Paper page
- 10.1038/nature14539 · DOI · Paper page
- 10.1016/j.ajhg.2016.04.013 · DOI · Paper page
- 10.1038/s41588-017-0009-4 · DOI · Paper page
- 2010, Spectral regularization algorithms for learning large incomplete matrices, The Journal of Machine Learning Research, 11, 2287
- 10.1038/s41588-022-01058-3 · DOI · Paper page
- 10.1038/s41588-022-01200-1 · DOI
- 2017, Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis, PLoS medicine, 14, e1002383, 10.1371/journal.pmed.1002383 · DOI · Paper page
- 10.1016/j.ajhg.2019.08.010 · DOI
- 10.1900/rds.2015.12.351 · DOI
- 10.1038/s41588-021-00852-9 · DOI
- 10.1038/ng.3406 · DOI · Paper page
- 10.1038/nature14878 · DOI
- 10.1038/ng.2249 · DOI
- 10.2967/jnumed.120.256180 · DOI
- 2021, Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations, Cell, 184, 4784, 10.1016/j.cell.2021.07.038 · DOI
- 2023, An atlas of genetic determinants of forearm fracture, Nature Genetics, 55, 1820, 10.1038/s41588-023-01527-3 · DOI
- 2023, Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis, Communications Biology, 6, 691, 10.1038/s42003-023-04869-0 · DOI
- Nethander, M. , et al. Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study. Cell Reports Medicine 3(2022). · DOI
- Trajanoska, K. et al. Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study. bmj 362(2018). · DOI
- 10.1002/jbmr.3412 · DOI
- 10.1186/s13059-020-1935-5 · DOI · Paper page
- 2019, COL4A2 in the tissue-specific extracellular matrix plays important role on osteogenic differentiation of periodontal ligament stem cells, Theranostics, 9, 4265, 10.7150/thno.35914 · DOI · Paper page
- 2011, Role of the WWOX tumor suppressor gene in bone homeostasis and the pathogenesis of osteosarcoma, American journal of cancer research, 1, 585
- 10.1038/s41588-018-0302-x · DOI · Paper page
- 10.1016/j.ajhg.2017.12.005 · DOI
- 10.1126/scisignal.aaz4051 · DOI
- 2022, Role of LGR5-positive mesenchymal cells in craniofacial development, Frontiers in Cell and Developmental Biology, 10, 810527, 10.3389/fcell.2022.810527 · DOI
- 10.1128/MCB.24.22.9736-9743.2004 · DOI
- 10.1073/pnas.2001238117 · DOI
- 2023, Prediction-powered inference, Science, 382, 669, 10.1126/science.adi6000 · DOI
- McCaw, Z.R. , Gao, J.R. , Lin, X. & Gronsbell, J . Leveraging a machine learning derived surrogate phenotype to improve power for genome-wide association studies of partially missing phenotypes in population biobanks. bioRxiv, 2022.12. 12.520180 (2022). · DOI
- 10.1093/bioinformatics/btq340 · DOI · Paper page
- 10.1038/ng.3211 · DOI · Paper page
- 2020, Eliciting priors and relaxing the single causal variant assumption in colocalisation analyses, PLoS genetics, 16, e1008720, 10.1371/journal.pgen.1008720 · DOI · Paper page
- 10.1038/ng.3404 · DOI · Paper page
- 10.1038/ng.3954 · DOI · Paper page
- 2017, Systematic tissue-specific functional annotation of the human genome highlights immune-related DNA elements for late-onset Alzheimer’s disease, PLoS genetics, 13, e1006933, 10.1371/journal.pgen.1006933 · DOI · Paper page
- 2017, Functional mapping and annotation of genetic associations with FUMA, Nature communications, 8, 1826, 10.1038/s41467-017-01261-5 · DOI · Paper page
- 2015, MAGMA: generalized gene-set analysis of GWAS data, PLoS computational biology, 11, e1004219, 10.1371/journal.pcbi.1004219 · DOI · Paper page
- 10.1038/ng.3538 · DOI · Paper page
- 10.1007/s00439-011-1118-2 · DOI · Paper page
Metadata
- Authors
- Miao, J., Wu, Y., Sun, Z., Miao, X., Lu, T., Zhao, J., & Lu, Q.
- Affiliations
- University of Wisconsin–Madison (US)
- University of Toronto (CA)
- Corresponding author
- Lu, Qiongshi
- Venue
- Nature Genetics
- Publisher
- openRxiv
- Published
- 2024-01-04
- Volume
- 56
- Issue
- 11
- Pages
- 2361-2369
- ISSN
- 1061-4036 (ISSN-L)
- PMC
- PMC11972620
- OpenAlex
- W4402992718
- Cited by
- 28
- References
- 1
- Citations by year
- 2026: 5 · 2025: 20 · 2024: 3
- FWCI
- 7.43
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Licence
- cc-by-nc-nd
- Locations
- Nature Genetics (publishedVersion)
- medRxiv (acceptedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- U.S. Department of Health and Human Services (U01 HG012039, P30 AG017266)
- Wisconsin Alumni Research Foundation
- University of Wisconsin-Madison (P30 AG017266)
- National Institutes of Health
- National Institute on Aging (AG017266, P30AG017266)
- National Human Genome Research Institute (U01HG012039)
- Division of Graduate Education
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Mapping and Diversity in Plants and Animals
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and phenotypic traits in livestock
- Keywords
- false positive association, bone mineral density, complex trait genetics, statistical inference validity
- MeSH terms
- Machine Learning, Algorithms, Humans, Phenotype, Bone Density, Polymorphism, Single Nucleotide, Genome-Wide Association Study
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