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Möls, M.

Publications and source records attributed to Möls, M..

2 recordsLinked to original sources

Bias in genome-wide association test statistics due to omitted interactions

Over the past two decades, genome-wide association studies (GWAS) enabled the discovery of thousands of variants associated with many complex human traits. However, conventional GWAS are still widely performed with linear models with the assumption that the genetic effects are predominantly additive. In this work, we investigate the test statistic behavior when linear models are used to obtain significant genotype-phenotype associations without accounting for epistasis. We first algebraically derive mean and variance shift in the null statistic due to the omitted interaction term, and define the boundary between conservative (i.e., deflated statistic tail) and anti-conservative (i.e., inflated statistic tail) regimes for the common GWAS significance threshold. We then perform phenotype simulation analyses using the Estonian Biobank genotypes and validate the mathematical model. We demonstrate that the anti-conservative regime is plausible under realistic parameter settings and models omitting interaction terms can produce spurious significance. Our findings suggest caution when interpreting statistically significant signals reported in the literature based on linear models, especially for large-scale GWAS.

bioinformatics↗

Analysis of follow-up data in large biobank cohorts: a review of methodology

This study focuses on key methodological challenges in genome-wide association studies (GWAS) of biobank data with time-to-event outcomes, analyzed using the Cox proportional hazards (CPH) model. We address four primary issues: left-truncation of the data, com-putational inefficiency of standard model-fitting algorithms, related-ness among individuals, and model misspecification. To manage left-truncation, the common practice is to use age as the timescale, with individuals entering the risk set at their age of recruitment. We assess how this choice of timescale influences bias and statistical power, under realistic GWAS conditions of varying effect sizes and censoring rates. In addition, to alleviate the computational burden typical in large-scale data, we propose and evaluate a two-step martingale residual (MR) approach for high-dimensional CPH modeling. Our results show that the timescale choice has minimal effect on accuracy for small hazard ratios, though using birth age as the timescale-ignoring recruitment age-yields the highest power for association detection. We find that relatedness, when ignored, does not substantially bias effect size estimates, while omitting key covariates introduces significant bias. The two-step MR approach proves to be computationally efficient, retaining power for detecting small effect sizes, making it suitable for large-scale association studies. However, when precise effect size estimates are critical, particularly for moderate or larger effect sizes, we recommend recalculating these estimates using the conventional CPH model, with careful attention to left-truncation and relatedness. These conclusions are drawn from simulations and illustrated with data from the Estonian Biobank cohort.

genomics↗