Abstract

Variance component (VC) approaches based on restricted maximum likelihood (REML) have been used as an attractive method for positioning of quantitative trait loci (QTL). Linkage disequilibrium (LD) information can be easily implemented in the covariance structure among QTL effects (e.g. genotype relationship matrix) and mapping resolution appears to be high. Because of the use of LD information, the covariance structure becomes much richer and denser compared to the use of linkage information alone. This makes an average information (AI) REML algorithm based on mixed model equations and sparse matrix techniques less useful. In addition, (near-) singularity problems often occur with high marker densities, which is common in fine-mapping, causing numerical problems in AIREML based on mixed model equations. The present study investigates the direct use of the variance covariance matrix of all observations in AIREML for LD mapping with a general complex pedigree. The method presented is more efficient than the usual approach based on mixed model equations and robust to numerical problems caused by near-singularity due to closely linked markers. It is also feasible to fit multiple QTL simultaneously in the proposed method whereas this would drastically increase computing time when using mixed model equation-based methods.

Highlights

  • Variance component (VC) approaches have been widely used to detect the existence of variation associated with quantitative trait loci (QTL) [1, 3, 10, 13, 15, 38]

  • QTL position can be estimated with maximum likelihood (ML) or restricted maximum likelihood (REML) at the location with the highest likelihood value across the chromosome

  • The aim of this study was to investigate the efficiency of a REML algorithm with the direct use of the V compared to the usual REML algorithm based on mixed model equations (MME) when the combined linkage disequilibrium (LD) and linkage (LDL) mapping is used with a general complex pedigree

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Summary

Introduction

Variance component (VC) approaches have been widely used to detect the existence of variation associated with quantitative trait loci (QTL) [1, 3, 10, 13, 15, 38]. QTL position can be estimated with maximum likelihood (ML) or restricted maximum likelihood (REML) at the location with the highest likelihood value across the chromosome. This idea has been extended to a fine-mapping method using linkage disequilibrium (LD) generated from closely linked markers [27, 28]. In the fine-mapping method, IBD coefficients between unrelated founders in a recorded pedigree are estimated based on haplotype similarity using the genedropping method [26] or the coalescence method This allows utilizing unknown relationships beyond the recorded pedigree as well as known relationships, possibly allowing to estimate QTL position within a smaller region, e.g. within a few cM [30]

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