, Volume 101, Issue 1, pp 47–58

Mapping quantitative trait loci with dominant and missing markers in various crosses from two inbred lines

  • Changjian Jiang
  • Zhao-Bang Zeng

DOI: 10.1023/A:1018394410659

Cite this article as:
Jiang, C. & Zeng, ZB. Genetica (1997) 101: 47. doi:10.1023/A:1018394410659


Dominant phenotype of a genetic marker provides incomplete information about the marker genotype of an individual. A consequence of using this incomplete information for mapping quantitative trait loci (QTL) is that the inference of the genotype of a putative QTL flanked by a marker with dominant phenotype will depend on the genotype or phenotype of the next marker. This dependence can be extended further until a marker genotype is fully observed. A general algorithm is derived to calculate the probability distribution of the genotype of a putative QTL at a given genomic position, conditional on all observed marker phenotypes in the region with dominant and missing marker information for an individual. The algorithm is implemented for various populations stemming from two inbred lines in the context of mapping QTL. Simulation results show that if only a proportion of markers contain missing or dominant phenotypes, QTL mapping can be almost as efficient as if there were no missing information in the data. The efficiency of the analysis, however, may decrease substantially when a very large proportion of markers contain missing or dominant phenotypes and a genetic map has to be reconstructed first on the same data as well. So it is important to combine dominant markers with codominant markers in a QTL mapping study.

dominant markers genetic mapping Markov chain missing data quantitative trait loci 

Copyright information

© Kluwer Academic Publishers 1997

Authors and Affiliations

  • Changjian Jiang
    • 1
  • Zhao-Bang Zeng
    • 2
  1. 1.CIMMYT IntMexicoMexico
  2. 2.Program in Statistical Genetics, Department of StatisticsNorth Carolina State UniversityRaleighUSA

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