Mixed Model Association with Family-Biased Case-Control Ascertainment
Tristan Hayeck, Noah A. Zaitlen, Po-Ru Loh, Samuela Pollack, Alexander Gusev, Nick Patterson, Alkes L. Price
Abstract
Mixed models have become the tool of choice for genetic association studies; however, standard mixed model methods may be poorly calibrated or underpowered under family sampling bias and/or case-control ascertainment. Previously, we introduced a liability threshold based mixed model association statistic (LTMLM) to address case-control ascertainment in unrelated samples. Here, we consider family-biased case-control ascertainment, where cases and controls are ascertained non-randomly with respect to family relatedness. Previous work has shown that this type of ascertainment can severely bias heritability estimates; we show here that it also impacts mixed model association statistics. We introduce a family-based association statistic (LT-Fam) that is robust to this problem. Similar to LTMLM, LT-Fam is computed from posterior mean liabilities (PML) under a liability threshold model; however, LT-Fam uses published narrow-sense heritability estimates to avoid the problem of biased heritability estimation, enabling correct calibration. In simulations with family-biased case-control ascertainment, LT-Fam was correctly calibrated (average{chi} 2 = 1.00), whereas Armitage Trend Test (ATT) and standard mixed model association (MLM) were mis-calibrated (e.g. average{chi} 2 = 0.50-0.67 for MLM). LT-Fam also attained higher power in these simulations, with increases of up to 8% vs. ATT and 3% vs. MLM after correcting for mis-calibration. In 1,269 type 2 diabetes cases and 5,819 controls from the CARe cohort, downsampled to induce family-biased ascertainment, LT-Fam was correctly calibrated whereas ATT and MLM were again mis-calibrated (e.g. average{chi} 2 = 0.60-0.82 for MLM). Our results highlight the importance of modeling family sampling bias in case-control data sets with related samples.
02 /Specification & Classification
Click any tag to browse matching papersReproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Mixed Model with Correction for Case-Control Ascertainment Increases Association Power
tristan hayeck, Noah Zaitlen, … Alkes Price·The American Journal of Human GeneticsPeer-reviewed·May 1, 2015
- Combining case-control status and family history of disease increases association power
Margaux L.A. Hujoel, Steven Gazal, … Alkes L. Price·Nature GeneticsPeer-reviewed·Apr 20, 2020
- Genetic association models are robust to common population kinship estimation biases
Zhuoran Hou, Alejandro Ochoa·GeneticsPeer-reviewed·Feb 27, 2023
- Incorporating family disease history and controlling case-control imbalance for population based genetic association studies
Yongwen Zhuang, Brooke N. Wolford, … Seunggeun Lee·BioinformaticsPeer-reviewed·Jul 25, 2022
- Fast and accurate construction of confidence intervals for heritability
Regev Schweiger, Shachar Kaufman, … Eran Halperin·The American Journal of Human GeneticsPeer-reviewed·Jun 1, 2016
- On a Unifying ‘Reverse’ Regression for Robust Association Studies and Allele Frequency Estimation with Related Individuals