Literature DB >> 24197457

Estimates of marker-associated QTL effects in Monte Carlo backcross generations using multiple regression.

J Moreno-Gonzalez1.   

Abstract

The decision of whether or not to use QTLassociated markers in breeding programs needs further information about the magnitude of the additive and dominance effects that can be estimated. The objectives of this paper are (1) to apply some of the Moreno-Gonzalez (1993) genetic models to backcross simulation data generated by the Monte Carlo method, and (2) to get simulation information about the number of testing progenies and mapping density in relation to the magnitude of gene effect estimates. Results of the Monte Carlo study show that the stepwise regression analysis was able to detect relatively small additive and dominance effects when the QTL are independently segregating. When testing selfed families derived from backcross individuals, dominance effects had a larger error standard deviation and were estimated at a lower frequency. Linked QTL require a higher marker mapping density on the genome and a larger number of progenies to detect small genetic effects. Reduction of the environmental error variance by evaluating selfed backcross families in replicate experiments increased the power of the test. Expressions of the number of progenies for detecting significant additive effects were developed for some genetic situations. The ratio of the within-backcross genetic variance to the square of a gene effect estimate is a function of the number of progenies, the heritability of the trait, the marker map density and the portion of the genetic variance explained by the model. Different values (from 0 to 1) assigned to ρ (relative position of the QTL in the marker segment) did not cause a large shift in the residual mean square of the model.

Year:  1992        PMID: 24197457     DOI: 10.1007/BF00222324

Source DB:  PubMed          Journal:  Theor Appl Genet        ISSN: 0040-5752            Impact factor:   5.699


  6 in total

1.  Genetic polymorphism in varietal identification and genetic improvement.

Authors:  M Soller; J S Beckmann
Journal:  Theor Appl Genet       Date:  1983-11       Impact factor: 5.699

2.  Mapping quantitative trait loci using molecular marker linkage maps.

Authors:  S J Knapp; W C Bridges; D Birkes
Journal:  Theor Appl Genet       Date:  1990-05       Impact factor: 5.699

3.  Genetic models to estimate additive and non-additive effects of marker-associated QTL using multiple regression techniques.

Authors:  J Moreno-Gonzalez
Journal:  Theor Appl Genet       Date:  1992-12       Impact factor: 5.699

4.  Efficiency of marker-assisted selection in the improvement of quantitative traits.

Authors:  R Lande; R Thompson
Journal:  Genetics       Date:  1990-03       Impact factor: 4.562

5.  Mapping mendelian factors underlying quantitative traits using RFLP linkage maps.

Authors:  E S Lander; D Botstein
Journal:  Genetics       Date:  1989-01       Impact factor: 4.562

6.  Molecular-marker-facilitated investigations of quantitative-trait loci in maize. I. Numbers, genomic distribution and types of gene action.

Authors:  M D Edwards; C W Stuber; J F Wendel
Journal:  Genetics       Date:  1987-05       Impact factor: 4.562

  6 in total
  2 in total

1.  Multiple regression for molecular-marker, quantitative trait data from large F2 populations.

Authors:  A J Wright; R P Mowers
Journal:  Theor Appl Genet       Date:  1994-10       Impact factor: 5.699

2.  Genetic models to estimate additive and non-additive effects of marker-associated QTL using multiple regression techniques.

Authors:  J Moreno-Gonzalez
Journal:  Theor Appl Genet       Date:  1992-12       Impact factor: 5.699

  2 in total

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