Literature DB >> 28017371

Mixed Model Association with Family-Biased Case-Control Ascertainment.

Tristan J Hayeck1, Po-Ru Loh2, Samuela Pollack2, Alexander Gusev2, Nick Patterson3, Noah A Zaitlen4, Alkes L Price5.   

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 case and control subjects 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 χ2 = 1.00-1.02 for null SNPs), whereas the Armitage trend test (ATT), standard mixed model association (MLM), and case-control retrospective association test (CARAT) were mis-calibrated (e.g., average χ2 = 0.50-1.22 for MLM, 0.89-2.65 for CARAT). LT-Fam also attained higher power than other methods in some settings. In 1,259 type 2 diabetes-affected case subjects and 5,765 control subjects from the CARe cohort, downsampled to induce family-biased ascertainment, LT-Fam was correctly calibrated whereas ATT, MLM, and CARAT were again mis-calibrated. Our results highlight the importance of modeling family sampling bias in case-control datasets with related samples.
Copyright © 2017 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 28017371      PMCID: PMC5223022          DOI: 10.1016/j.ajhg.2016.11.015

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  26 in total

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3.  Mixed model with correction for case-control ascertainment increases association power.

Authors:  Tristan J Hayeck; Noah A Zaitlen; Po-Ru Loh; Bjarni Vilhjalmsson; Samuela Pollack; Alexander Gusev; Jian Yang; Guo-Bo Chen; Michael E Goddard; Peter M Visscher; Nick Patterson; Alkes L Price
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