Mixed Effects Models for Quantitative Trait Loci Mapping With Inbred Strains

Fixed effects models have dominated the statistical analysis of genetic crosses between inbred strains. In spite of their popularity, the traditional models ignore polygenic background and must be tailored to each specific cross. We reexamine the role of random effect models in gene mapping with inbred strains. The biggest difficulty in implementing random effect models is the lack of a coherent way of calculating trait covariances between relatives. The standard model for outbred populations is based on premises of genetic equilibrium that simply do not apply to crosses between inbred strains since every animal in a strain is genetically identical and completely homozygous. We fill this theoretical gap by introducing novel combinatorial entities called strain coefficients. With an appropriate theory, it is possible to reformulate QTL mapping and QTL association analysis as an application of mixed models involving both fixed and random effects. After developing this theory, our first example compares the mixed effects model to a standard fixed effects model using simulated advanced intercross line (AIL) data. Our second example deals with hormone data. Here multivariate traits and parameter identifiability questions arise. Our final example involves random mating among eight strains and vividly demonstrates the versatility of our models.

[1]  J. Blangero Update to Blangero's “Statistical Genetic Approaches to Human Adaptability” (1993): A Unified Theory of Genotype × Environment Interaction , 2009, Human biology.

[2]  John D. Storey The optimal discovery procedure: a new approach to simultaneous significance testing , 2007 .

[3]  Jeffrey T Leek,et al.  The optimal discovery procedure for large-scale significance testing, with applications to comparative microarray experiments. , 2007, Biostatistics.

[4]  Mohammad Fallahi,et al.  An Integrated in Silico Gene Mapping Strategy in Inbred Mice , 2007, Genetics.

[5]  William Valdar,et al.  Simulating the Collaborative Cross: Power of Quantitative Trait Loci Detection and Mapping Resolution in Large Sets of Recombinant Inbred Strains of Mice , 2006, Genetics.

[6]  L. Almasy,et al.  A comparison of discrete versus continuous environment in a variance components-based linkage analysis of the COGA data , 2005, BMC Genetics.

[7]  K. Lange,et al.  Fishing for Pleiotropic QTLs in a Polygenic Sea , 2005, Annals of human genetics.

[8]  I. Hoeschele,et al.  Approximating Identity-by-Descent Matrices Using Multiple Haplotype Configurations on Pedigrees , 2005, Genetics.

[9]  Mark Kirkpatrick,et al.  Up hill, down dale: quantitative genetics of curvaceous traits , 2005, Philosophical Transactions of the Royal Society B: Biological Sciences.

[10]  Kenneth Lange,et al.  Association testing with Mendel , 2005, Genetic epidemiology.

[11]  William Valdar,et al.  Strategies for mapping and cloning quantitative trait genes in rodents , 2005, Nature Reviews Genetics.

[12]  G. Churchill,et al.  Combining Data From Multiple Inbred Line Crosses Improves the Power and Resolution of Quantitative Trait Loci Mapping , 2005, Genetics.

[13]  Serge Batalov,et al.  Use of a Dense Single Nucleotide Polymorphism Map for In Silico Mapping in the Mouse , 2004, PLoS biology.

[14]  Ina Hoeschele,et al.  Conditional Probability Methods for Haplotyping in Pedigrees , 2004, Genetics.

[15]  Ahmed Rebai,et al.  Power of tests for QTL detection using replicated progenies derived from a diallel cross , 1993, Theoretical and Applied Genetics.

[16]  Y. Yamada,et al.  Relationships between genotype x environment interaction and genetic correlation of the same trait measured in different environments , 1990, Theoretical and Applied Genetics.

[17]  A. Galecki,et al.  Quantitative trait loci for insulin-like growth factor I, leptin, thyroxine, and corticosterone in genetically heterogeneous mice. , 2003, Physiological genomics.

[18]  Hao Wu,et al.  R/qtl: QTL Mapping in Experimental Crosses , 2003, Bioinform..

[19]  Robert W. Williams,et al.  A Collaborative Cross for High-Precision Complex Trait Analysis CTC Workgroup Report , 2003 .

[20]  P. Sham,et al.  Variance components models for gene-environment interaction in quantitative trait locus linkage analysis. , 2002, Twin research : the official journal of the International Society for Twin Studies.

[21]  Shaun Purcell,et al.  Variance components models for gene-environment interaction in twin analysis. , 2002, Twin research : the official journal of the International Society for Twin Studies.

[22]  J. Flint,et al.  Multiple Cross Mapping (MCM) markedly improves the localization of a QTL for ethanol‐induced activation , 2002, Genes, brain, and behavior.

[23]  Florence Jaffrézic,et al.  Generalized character process models: estimating the genetic basis of traits that cannot be observed and that change with age or environmental conditions. , 2002, Biometrics.

[24]  George Seaton,et al.  QTL Express: mapping quantitative trait loci in simple and complex pedigrees , 2002, Bioinform..

[25]  Y. Benjamini,et al.  Controlling the false discovery rate in behavior genetics research , 2001, Behavioural Brain Research.

[26]  G. Churchill,et al.  A statistical framework for quantitative trait mapping. , 2001, Genetics.

[27]  Mariza de Andrade,et al.  Comparison of Multivariate Tests for Genetic Linkage , 2001, Human Heredity.

[28]  R Jansen,et al.  Mapping epistatic quantitative trait loci with one-dimensional genome searches. , 2001, Genetics.

[29]  A. C. Collins,et al.  A method for fine mapping quantitative trait loci in outbred animal stocks. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[30]  S. Pletcher,et al.  Statistical models for estimating the genetic basis of repeated measures and other function-valued traits. , 2000, Genetics.

[31]  Z. Zeng,et al.  A general mixture model approach for mapping quantitative trait loci from diverse cross designs involving multiple inbred lines. , 2000, Genetical research.

[32]  L Kruglyak,et al.  Exact multipoint quantitative-trait linkage analysis in pedigrees by variance components. , 2000, American journal of human genetics.

[33]  P. Sham,et al.  Variance‐components QTL linkage analysis of selected and non‐normal samples: Conditioning on trait values , 2000, Genetic epidemiology.

[34]  L. Almasy,et al.  Robust LOD scores for variance component‐based linkage analysis , 2000, Genetic epidemiology.

[35]  C. Geyer,et al.  The genetic analysis of age-dependent traits: modeling the character process. , 1999, Genetics.

[36]  N. Schork,et al.  Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure. , 1999, American journal of human genetics.

[37]  Z. Zeng,et al.  Multiple interval mapping for quantitative trait loci. , 1999, Genetics.

[38]  D. Schaid Mathematical and Statistical Methods for Genetic Analysis , 1999 .

[39]  Pletcher Model fitting and hypothesis testing for age‐specific mortality data , 1999 .

[40]  Kenneth F. Manly,et al.  Overview of QTL mapping software and introduction to Map Manager QT , 1999, Mammalian Genome.

[41]  S. Xu,et al.  Combining different line crosses for mapping quantitative trait loci using the identical by descent-based variance component method. , 1998, Genetics.

[42]  M. Sillanpää,et al.  Bayesian mapping of multiple quantitative trait loci from incomplete inbred line cross data. , 1998, Genetics.

[43]  J. Blangero,et al.  Effects of genotype‐by‐sex interaction on quantitative trait linkage analysis , 1997, Genetic epidemiology.

[44]  L. Almasy,et al.  Multipoint oligogenic linkage analysis of quantitative traits , 1997, Genetic epidemiology.

[45]  K Lange,et al.  Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics. , 1996, American journal of human genetics.

[46]  L Kruglyak,et al.  Parametric and nonparametric linkage analysis: a unified multipoint approach. , 1996, American journal of human genetics.

[47]  M. Soller,et al.  Advanced intercross lines, an experimental population for fine genetic mapping. , 1995, Genetics.

[48]  R. Doerge,et al.  Empirical threshold values for quantitative trait mapping. , 1994, Genetics.

[49]  Z. Zeng Precision mapping of quantitative trait loci. , 1994, Genetics.

[50]  C. Amos Robust variance-components approach for assessing genetic linkage in pedigrees. , 1994, American journal of human genetics.

[51]  N. Schork,et al.  Extended multipoint identity-by-descent analysis of human quantitative traits: efficiency, power, and modeling considerations. , 1993, American journal of human genetics.

[52]  Z B Zeng,et al.  Theoretical basis for separation of multiple linked gene effects in mapping quantitative trait loci. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[53]  C. Haley,et al.  A simple regression method for mapping quantitative trait loci in line crosses using flanking markers , 1992, Heredity.

[54]  D. Goldgar Multipoint analysis of human quantitative genetic variation. , 1990, American journal of human genetics.

[55]  E. Lander,et al.  Mapping mendelian factors underlying quantitative traits using RFLP linkage maps. , 1989, Genetics.

[56]  K. Lange Cohabitation, convergence, and environmental covariances. , 1986, American journal of medical genetics.

[57]  T. Beaty,et al.  Use of robust variance components models to analyse triglyceride data in families , 1985, Annals of human genetics.

[58]  R. Elston,et al.  A bivariate problem in human genetics: ascertainment of families through a correlated trait. , 1984, American journal of medical genetics.

[59]  K. Lange,et al.  Extensions to pedigree analysis. IV. Covariance components models for multivariate traits. , 1983, American journal of medical genetics.

[60]  J. Mathews,et al.  Extensions to multivariate normal models for pedigree analysis , 1982, Annals of human genetics.

[61]  K. Lange Central limit theorems of pedigrees , 1978 .