2010
DOI: 10.1534/genetics.109.113183
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Bayesian Quantitative Trait Locus Mapping Using Inferred Haplotypes

Abstract: We describe a fast hierarchical Bayesian method for mapping quantitative trait loci by haplotype-based association, applicable when haplotypes are not observed directly but are inferred from multiple marker genotypes. The method avoids the use of a Monte Carlo Markov chain by employing priors for which the likelihood factorizes completely. It is parameterized by a single hyperparameter, the fraction of variance explained by the quantitative trait locus, compared to the frequentist fixed-effects model, which re… Show more

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Cited by 21 publications
(23 citation statements)
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“…Larger sample sizes are clearly needed to support a regression model with that many degrees of freedom. Alternative implementations that retain some degree of parsimony and, at the same time, allow for nonadditive intralocus effects are the subject of current research (Durrant and Mott 2010;Lenarcic et al 2012). The additive genetic model provides a robust compromise for detecting genetic loci that have a marginal effect.…”
Section: Discussionmentioning
confidence: 99%
“…Larger sample sizes are clearly needed to support a regression model with that many degrees of freedom. Alternative implementations that retain some degree of parsimony and, at the same time, allow for nonadditive intralocus effects are the subject of current research (Durrant and Mott 2010;Lenarcic et al 2012). The additive genetic model provides a robust compromise for detecting genetic loci that have a marginal effect.…”
Section: Discussionmentioning
confidence: 99%
“…The anti-PON3 antibody was generated by inoculating rabbits with the peptide CRVNASQEVEPVEPEN, which is specifi c to ma- with the EM algorithm ( 29 ) and the Markov Chain Monte Carlo method ( 30 ). Results are shown as means and SD in parentheses (parametric) or as medians and 95% CI (non-parametric).…”
Section: Reagents For the Pon3 Elisamentioning
confidence: 99%
“…One approach to obtaining stable estimates of allele effects is to constrain the values can take by penalization or formal hierarchical modeling. Until now, this has been achieved only for simple additive effect models that exclude covariate or random effects: specifically in inbred plants lines or the mouse Collaborative Cross using multiple imputation (17,39), or in the mouse Diversity Outbred population (akin to a rodent HS) using ridge regression (67).…”
Section: Discussionmentioning
confidence: 99%