Enhanced Efficiency of Quantitative Trait Loci Mapping Analysis Based on Multivariate Complexes of Quantitative Traits

Genetics ◽  
2001 ◽  
Vol 157 (4) ◽  
pp. 1789-1803 ◽  
Author(s):  
Abraham B Korol ◽  
Yefim I Ronin ◽  
Alexander M Itskovich ◽  
Junhua Peng ◽  
Eviatar Nevo

AbstractAn approach to increase the efficiency of mapping quantitative trait loci (QTL) was proposed earlier by the authors on the basis of bivariate analysis of correlated traits. The power of QTL detection using the log-likelihood ratio (LOD scores) grows proportionally to the broad sense heritability. We found that this relationship holds also for correlated traits, so that an increased bivariate heritability implicates a higher LOD score, higher detection power, and better mapping resolution. However, the increased number of parameters to be estimated complicates the application of this approach when a large number of traits are considered simultaneously. Here we present a multivariate generalization of our previous two-trait QTL analysis. The proposed multivariate analogue of QTL contribution to the broad-sense heritability based on interval-specific calculation of eigenvalues and eigenvectors of the residual covariance matrix allows prediction of the expected QTL detection power and mapping resolution for any subset of the initial multivariate trait complex. Permutation technique allows chromosome-wise testing of significance for the whole trait complex and the significance of the contribution of individual traits owing to: (a) their correlation with other traits, (b) dependence on the chromosome in question, and (c) both a and b. An example of application of the proposed method on a real data set of 11 traits from an experiment performed on an F2/F3 mapping population of tetraploid wheat (Triticum durum × T. dicoccoides) is provided.

Genetics ◽  
1998 ◽  
Vol 149 (3) ◽  
pp. 1547-1555 ◽  
Author(s):  
Wouter Coppieters ◽  
Alexandre Kvasz ◽  
Frédéric Farnir ◽  
Juan-Jose Arranz ◽  
Bernard Grisart ◽  
...  

Abstract We describe the development of a multipoint nonparametric quantitative trait loci mapping method based on the Wilcoxon rank-sum test applicable to outbred half-sib pedigrees. The method has been evaluated on a simulated dataset and its efficiency compared with interval mapping by using regression. It was shown that the rank-based approach is slightly inferior to regression when the residual variance is homoscedastic normal; however, in three out of four other scenarios envisaged, i.e., residual variance heteroscedastic normal, homoscedastic skewed, and homoscedastic positively kurtosed, the latter outperforms the former one. Both methods were applied to a real data set analyzing the effect of bovine chromosome 6 on milk yield and composition by using a 125-cM map comprising 15 microsatellites and a granddaughter design counting 1158 Holstein-Friesian sires.


Genetics ◽  
2003 ◽  
Vol 165 (2) ◽  
pp. 867-883 ◽  
Author(s):  
Nengjun Yi ◽  
Shizhong Xu ◽  
David B Allison

AbstractMost complex traits of animals, plants, and humans are influenced by multiple genetic and environmental factors. Interactions among multiple genes play fundamental roles in the genetic control and evolution of complex traits. Statistical modeling of interaction effects in quantitative trait loci (QTL) analysis must accommodate a very large number of potential genetic effects, which presents a major challenge to determining the genetic model with respect to the number of QTL, their positions, and their genetic effects. In this study, we use the methodology of Bayesian model and variable selection to develop strategies for identifying multiple QTL with complex epistatic patterns in experimental designs with two segregating genotypes. Specifically, we develop a reversible jump Markov chain Monte Carlo algorithm to determine the number of QTL and to select main and epistatic effects. With the proposed method, we can jointly infer the genetic model of a complex trait and the associated genetic parameters, including the number, positions, and main and epistatic effects of the identified QTL. Our method can map a large number of QTL with any combination of main and epistatic effects. Utility and flexibility of the method are demonstrated using both simulated data and a real data set. Sensitivity of posterior inference to prior specifications of the number and genetic effects of QTL is investigated.


2010 ◽  
Vol 4 ◽  
pp. BBI.S4153 ◽  
Author(s):  
Song Wu ◽  
Jie Yang ◽  
Youjun Huang ◽  
Yao Li ◽  
Tongming Yin ◽  
...  

A pseudo-testcross pedigree is widely used for mapping quantitative trait loci (QTL) in outcrossing species, but the model for analyzing pseudo-testcross data borrowed from the inbred backcross design can only detect those QTLs that are heterozygous only in one parent. In this study, an intercross model that incorporates the high heterozygosity and phase uncertainty of outcrossing species was used to reanalyze a published data set on QTL mapping in poplar trees. Several intercross QTLs that are heterozygous in both parents were detected, which are responsible not only for biomass traits, but also for their genetic correlations. This study provides a more complete identification of QTLs responsible for economically important biomass traits in poplars.


2014 ◽  
Vol 2 (1) ◽  
Author(s):  
Rizki Amelia ◽  
Saiful Hikam ◽  
Paul Benyamin Timotiwu

Tanaman padi (Oryza sativa L.) merupakan salah satu tanaman pangan yang diusahakan di Indonesia. Salah satu usaha untuk meningkatkan produksi padi dengan metode quantitative trait loci (QTL). Tujuan penelitian adalah (1) mendapatkan kultivar QTL yang mengalami segregasi fenotipe pada tanaman padi yang ditanam pada lingkungan sawah baru; (2) mendapatkan kultivar QTL yang memiliki ragam genetik dan heritabilitas broad- sense dari tanaman padi yang diteliti di lingkungan sawah baru dan mendapatkan peubah yang dapat dijadikan parameter untuk seleksi langsung dan tidak langsung. Penelitian ini dilaksanakan pada bulan Maret - Mei 2012 di Politeknik Negeri Lampung dan Laboratorium Benih Fakultas Pertanian Universitas Lampung. Rancangan perlakuan disusun dalam kuasi Rancangan Kelompok Teracak Sempurna (RKTS) dengan 3 ulangan untuk setiap sampel. Data terlebih dahulu dicari rata-ratanya. Selanjutnya, data pengamatan diuji dengan uji Bartlett dan Levene untuk kehomogenan data. Bila homogen analisis data dilanjutkan dengan analisis ragam. Hasil penelitian menunjukkan bahwa (1) segregasi fenotipe muncul di lingkungan sawah baru pada tanaman padi varietas IR64 yang merupakan varietas nasional. Segregasi fenotipe terlihat dari parameter tinggi tanaman dan jumlah anakan yang tidak sama pada tanaman padi yang ditanam di lingkungan sawah baru; (2) Keragaman genetik dan heritabilitas yang tinggi terlihat pada semua varietas baik varietas lokal maupun varietas nasional yang ditanam di lingkungan sawah baru dan seleksi langsung ditunjukkan oleh parameter produksi, sedangkan seleksi tidak langsung ditujukkan oleh parameter bobot gabah isi, bobot gabah total, dan jumlah bulir isi pada varietas padi lokal dan nasional di lingkungan sawah baru.


Genetics ◽  
2004 ◽  
Vol 168 (3) ◽  
pp. 1737-1749 ◽  
Author(s):  
Sébastien Crepieux ◽  
Claude Lebreton ◽  
Bertrand Servin ◽  
Gilles Charmet

Genetics ◽  
1998 ◽  
Vol 148 (1) ◽  
pp. 391-399 ◽  
Author(s):  
Ritsert C Jansen ◽  
David L Johnson ◽  
Johan A M Van Arendonk

Abstract A mixture model approach is presented for the mapping of one or more quantitative trait loci (QTLs) in complex populations. In order to exploit the full power of complete linkage maps the simultaneous likelihood of phenotype and a multilocus (all markers and putative QTLs) genotype is computed. Maximum likelihood estimation in our mixture models is implemented via an Expectation-Maximization algorithm: exact, stochastic or Monte Carlo EM by using a simple and flexible Gibbs sampler. Parameters include allele frequencies of markers and QTLs, discrete or normal effects of biallelic or multiallelic QTLs, and homogeneous or heterogeneous residual variances. As an illustration a dairy cattle data set consisting of twenty half-sib families has been reanalyzed. We discuss the potential which our and other approaches have for realistic multiple-QTL analyses in complex populations.


Genetics ◽  
2003 ◽  
Vol 164 (3) ◽  
pp. 1129-1138 ◽  
Author(s):  
Nengjun Yi ◽  
Varghese George ◽  
David B Allison

AbstractIn this article, we utilize stochastic search variable selection methodology to develop a Bayesian method for identifying multiple quantitative trait loci (QTL) for complex traits in experimental designs. The proposed procedure entails embedding multiple regression in a hierarchical normal mixture model, where latent indicators for all markers are used to identify the multiple markers. The markers with significant effects can be identified as those with higher posterior probability included in the model. A simple and easy-to-use Gibbs sampler is employed to generate samples from the joint posterior distribution of all unknowns including the latent indicators, genetic effects for all markers, and other model parameters. The proposed method was evaluated using simulated data and illustrated using a real data set. The results demonstrate that the proposed method works well under typical situations of most QTL studies in terms of number of markers and marker density.


Genetics ◽  
1999 ◽  
Vol 152 (3) ◽  
pp. 1203-1216
Author(s):  
Chen-Hung Kao ◽  
Zhao-Bang Zeng ◽  
Robert D Teasdale

Abstract A new statistical method for mapping quantitative trait loci (QTL), called multiple interval mapping (MIM), is presented. It uses multiple marker intervals simultaneously to fit multiple putative QTL directly in the model for mapping QTL. The MIM model is based on Cockerham's model for interpreting genetic parameters and the method of maximum likelihood for estimating genetic parameters. With the MIM approach, the precision and power of QTL mapping could be improved. Also, epistasis between QTL, genotypic values of individuals, and heritabilities of quantitative traits can be readily estimated and analyzed. Using the MIM model, a stepwise selection procedure with likelihood ratio test statistic as a criterion is proposed to identify QTL. This MIM method was applied to a mapping data set of radiata pine on three traits: brown cone number, tree diameter, and branch quality scores. Based on the MIM result, seven, six, and five QTL were detected for the three traits, respectively. The detected QTL individually contributed from ∼1 to 27% of the total genetic variation. Significant epistasis between four pairs of QTL in two traits was detected, and the four pairs of QTL contributed ∼10.38 and 14.14% of the total genetic variation. The asymptotic variances of QTL positions and effects were also provided to construct the confidence intervals. The estimated heritabilities were 0.5606, 0.5226, and 0.3630 for the three traits, respectively. With the estimated QTL effects and positions, the best strategy of marker-assisted selection for trait improvement for a specific purpose and requirement can be explored. The MIM FORTRAN program is available on the worldwide web (http://www.stat.sinica.edu.tw/~chkao/).


Genetics ◽  
1996 ◽  
Vol 143 (4) ◽  
pp. 1831-1842 ◽  
Author(s):  
Pekka Uimari ◽  
Georg Thaller ◽  
Ina Hoeschele

Abstract Information on multiple linked genetic markers was used in a Bayesian method for the statistical mapping of quantitative trait loci (QTL). Bayesian parameter estimation and hypothesis testing were implemented via Markov chain Monte Carlo algorithms. Variables sampled were the augmented data (marker-QTL genotypes, polygenic effects), an indicator variable for linkage or nonlinkage, and the parameters. The parameter vector included allele frequencies at the markers and the QTL, map distances of the markers and the QTL, QTL substitution effect, and polygenic and residual variances. The criterion for QTL detection was the marginal posterior probability of a QTL being located on the chromosome carrying the markers, The method was evaluated empirically by analyzing simulated granddaughter designs consisting of 2000 sons, 20 related sires, and their ancestors.


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