A new Bayesian automatic model selection approach for mapping quantitative trait loci under variance component model

Genetica ◽  
2008 ◽  
Vol 135 (3) ◽  
pp. 429-437 ◽  
Author(s):  
Ming Fang ◽  
Dan Jiang ◽  
Huijiang Gao ◽  
Dongxiao Sun ◽  
Runqing Yang ◽  
...  



Genetics ◽  
2010 ◽  
Vol 187 (2) ◽  
pp. 611-621 ◽  
Author(s):  
Ping Wang ◽  
John A. Dawson ◽  
Mark P. Keller ◽  
Brian S. Yandell ◽  
Nancy A. Thornberry ◽  
...  


Genetics ◽  
2007 ◽  
Vol 176 (3) ◽  
pp. 1865-1877 ◽  
Author(s):  
Nengjun Yi ◽  
Daniel Shriner ◽  
Samprit Banerjee ◽  
Tapan Mehta ◽  
Daniel Pomp ◽  
...  


Genetics ◽  
2008 ◽  
Vol 181 (3) ◽  
pp. 1077-1086 ◽  
Author(s):  
Ani Manichaikul ◽  
Jee Young Moon ◽  
Śaunak Sen ◽  
Brian S. Yandell ◽  
Karl W. Broman


Genetics ◽  
2000 ◽  
Vol 156 (1) ◽  
pp. 411-422 ◽  
Author(s):  
Nengjun Yi ◽  
Shizhong Xu

AbstractVariance component analysis of quantitative trait loci (QTL) is an important strategy of genetic mapping for complex traits in humans. The method is robust because it can handle an arbitrary number of alleles with arbitrary modes of gene actions. The variance component method is usually implemented using the proportion of alleles with identity-by-descent (IBD) shared by relatives. As a result, information about marker linkage phases in the parents is not required. The method has been studied extensively under either the maximum-likelihood framework or the sib-pair regression paradigm. However, virtually all investigations are limited to normally distributed traits under a single QTL model. In this study, we develop a Bayes method to map multiple QTL. We also extend the Bayesian mapping procedure to identify QTL responsible for the variation of complex binary diseases in humans under a threshold model. The method can also treat the number of QTL as a parameter and infer its posterior distribution. We use the reversible jump Markov chain Monte Carlo method to infer the posterior distributions of parameters of interest. The Bayesian mapping procedure ends with an estimation of the joint posterior distribution of the number of QTL and the locations and variances of the identified QTL. Utilities of the method are demonstrated using a simulated population consisting of multiple full-sib families.



Genetics ◽  
2005 ◽  
Vol 170 (3) ◽  
pp. 1333-1344 ◽  
Author(s):  
Nengjun Yi ◽  
Brian S. Yandell ◽  
Gary A. Churchill ◽  
David B. Allison ◽  
Eugene J. Eisen ◽  
...  


2011 ◽  
Vol 93 (5) ◽  
pp. 333-342 ◽  
Author(s):  
XIA SHEN ◽  
LARS RÖNNEGÅRD ◽  
ÖRJAN CARLBORG

SummaryDealing with genotype uncertainty is an ongoing issue in genetic analyses of complex traits. Here we consider genotype uncertainty in quantitative trait loci (QTL) analyses for large crosses in variance component models, where the genetic information is included in identity-by-descent (IBD) matrices. An IBD matrix is one realization from a distribution of potential IBD matrices given available marker information. In QTL analyses, its expectation is normally used resulting in potentially reduced accuracy and loss of power. Previously, IBD distributions have been included in models for small human full-sib families. We develop an Expectation–Maximization (EM) algorithm for estimating a full model based on Monte Carlo imputation for applications in large animal pedigrees. Our simulations show that the bias of variance component estimates using traditional expected IBD matrix can be adjusted by accounting for the distribution and that the calculations are computationally feasible for large pedigrees.





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