Zero-inflated generalized Poisson regression mixture model for mapping quantitative trait loci underlying count trait with many zeros

被引:22
|
作者
Cui, Yuehua [1 ]
Yang, Wenzhao [1 ]
机构
[1] Michigan State Univ, Dept Stat & Probabil, E Lansing, MI 48824 USA
基金
美国国家科学基金会;
关键词
EM algorithm; Quantitative trait loci; Zero-inflated count data; Zero-inflated generalized Poisson regression model; CHOLESTEROL GALLSTONE FORMATION; ESTIMATING EQUATIONS; NONNORMAL TRAITS; MOUSE STRAINS; INTERCROSS; QTL; IDENTIFICATION; FRAMEWORK; CAST/EI; MICE;
D O I
10.1016/j.jtbi.2008.10.003
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Phenotypes measured in counts are commonly observed in nature. Statistical methods for mapping quantitative trait loci (QTL) underlying count traits are documented in the literature. The majority of them assume that the count phenotype follows a Poisson distribution with appropriate techniques being applied to handle data dispersion. When a count trait has a genetic basis, "naturally occurring" zero Status also reflects the underlying gene effects. Simply ignoring or miss-handling the zero data may lead to wrong QTL inference. In this article, we propose an interval mapping approach for mapping QTL underlying count phenotypes containing many zeros. The effects of QTLs; on the zero-inflated count trait are modelled through the zero-inflated generalized Poisson regression mixture model, which can handle the zero inflation and Poisson dispersion in the same distribution. We implement the approach using the EM algorithm with the Newton-Raphson algorithm embedded in the M-step, and provide a genome-wide scan for testing and estimating the QTL effects. The performance of the proposed method is evaluated through extensive simulation studies. Extensions to composite and multiple interval mapping are discussed. The utility of the developed approach is illustrated through a Mouse F(2) intercross data set. Significant QTLs are detected to control mouse cholesterol gallstone formation. Published by Elsevier Ltd.
引用
收藏
页码:276 / 285
页数:10
相关论文
共 50 条
  • [31] MISSING MARKERS WHEN ESTIMATING QUANTITATIVE TRAIT LOCI USING REGRESSION MAPPING
    MARTINEZ, O
    CURNOW, RN
    HEREDITY, 1994, 73 : 198 - 206
  • [32] Zero-inflated generalized Dirichlet multinomial regression model for microbiome compositional data analysis
    Tang, Zheng-Zheng
    Chen, Guanhua
    BIOSTATISTICS, 2019, 20 (04) : 698 - 713
  • [33] Functional mapping of quantitative trait loci underlying growth trajectories using a transform-both-sides logistic model
    Wu, RL
    Ma, CX
    Lin, M
    Wang, ZH
    Casella, G
    BIOMETRICS, 2004, 60 (03) : 729 - 738
  • [34] Estimation and Hypothesis Testing for the Parameters of Multivariate Zero Inflated Generalized Poisson Regression Model
    Sari, Dewi Novita
    Purhadi, Purhadi
    Rahayu, Santi Puteri
    Irhamah, Irhamah
    SYMMETRY-BASEL, 2021, 13 (10):
  • [35] Estimation of a zero-inflated Poisson regression model with missing covariates via nonparametric multiple imputation methods
    Lee, Shen-Ming
    Lukusa, T. Martin
    Li, Chin-Shang
    COMPUTATIONAL STATISTICS, 2020, 35 (02) : 725 - 754
  • [36] Model for mapping imprinted quantitative trait loci in an inbred F2 design
    Cui, YH
    Lu, Q
    Cheverud, JM
    Littell, RC
    Wu, RL
    GENOMICS, 2006, 87 (04) : 543 - 551
  • [37] Mapping quantitative trait loci in autotetraploids under a genuine tetrasomic model
    Luo, Zewei
    NEW PHYTOLOGIST, 2024, 242 (01) : 21 - 22
  • [38] Expression Quantitative Trait Loci Mapping With Multivariate Sparse Partial Least Squares Regression
    Chun, Hyonho
    Keles, Suenduez
    GENETICS, 2009, 182 (01) : 79 - 90
  • [39] Mapping of multiple quantitative trait loci by simple regression in half-sib designs
    de Koning, DJ
    Schulman, NF
    Elo, K
    Moisio, S
    Kinos, R
    Vilkki, J
    Mäki-Tanila, A
    JOURNAL OF ANIMAL SCIENCE, 2001, 79 (03) : 616 - 622
  • [40] Interval mapping of quantitative trait loci for time-to-event data with the proportional hazards mixture cure model
    Liu, Mengling
    Lu, Wenbin
    Shao, Yongzhao
    BIOMETRICS, 2006, 62 (04) : 1053 - 1061