ArticleeLife2025
Trade-offs in modeling context dependency in complex trait genetics.
Article in eLife, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Pervasive interactions between exposures and polygenic risk can inform more effective clinical and behavioral interventions.Nature genetics · 2026Article
- Private QTLs and the genetic architecture of hierarchical size traits: from body size to sex-specific plasticity.G3 (Bethesda, Md.) · 2026Article
- A biobank-scale method for learning modulators of gene-environment interaction underlying human complex traits from multiple environmental exposures.bioRxiv : the preprint server for biology · 2026Article
- When does accounting for gene-environment interactions improve complex trait prediction? A case study with Drosophila lifespan.G3 (Bethesda, Md.) · 2026Article
- When does accounting for gene-environment interactions improve complex trait prediction? A case study withbioRxiv : the preprint server for biology · 2025Article
- Improvement of polygenic modeling of blood pressure traits using lifestyle information in the UK Biobank.Genetics · 2025Article
- MegaLMM improves genomic predictions in new environments using environmental covariates.Genetics · 2025Article
- Dual exposure-by-polygenic score interactions highlight disparities across social groups in the proportion needed to benefit.medRxiv : the preprint server for health sciences · 2024Article
- Calibrated prediction intervals for polygenic scores across diverse contexts.Nature genetics · 2024Article
- Calibrated prediction intervals for polygenic scores across diverse contexts.medRxiv : the preprint server for health sciences · 2023Article
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4 authors.
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Abstract
Genetic effects on complex traits may depend on context, such as age, sex, environmental exposures, or social settings. However, it remains often unclear if the extent of context dependency, or gene-by-environment interaction (GxE), merits more involved models than the additive model typically used to analyze data from genome-wide association studies (GWAS). Here, we suggest considering the utility of GxE models in GWAS as a trade-off between bias and variance parameters. In particular, we derive a decision rule for choosing between competing models for the estimation of allelic effects. The rule weighs the increased estimation noise when context is considered against the potential bias when context dependency is ignored. In the empirical example of GxSex in human physiology, the increased noise of context-specific estimation often outweighs the bias reduction, rendering GxE models less useful when variants are considered independently. However, for complex traits, we argue that the joint consideration of context dependency across many variants mitigates both noise and bias. As a result, polygenic GxE models can improve both estimation and trait prediction. Finally, we exemplify (using GxDiet effects on longevity in fruit flies) how analyses based on independently ascertained 'top hits' alone can be misleading, and that considering polygenic patterns of GxE can improve interpretation.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.