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9 - Mapping in practice

Published online by Cambridge University Press:  05 August 2013

J. W. Van Ooijen
Affiliation:
Kyazma B.V., Wageningen, The Netherlands
J. Jansen
Affiliation:
Biometris, Wageningen University and Research Centre, The Netherlands
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Summary

Genetic linkage mapping is a very powerful tool, but it turns out to be quite sensitive to incomplete or erroneous information. In practice, it is often impossible to record data on all loci-individual combinations. Therefore, the mapping computations have to be done with some missing observations. It also turns out that a mapping experiment is prone to errors because of the huge number of observations. In this chapter, we address some of the common problems encountered in practice.

Introduction

The preceding chapters describe the theory underlying the construction of genetic linkage maps. With suitable computer software, map construction should be straightforward. We write should, because in practice this is not always the case. There are two reasons for this. As in statistical modelling, we view map construction as a method in which observations are fitted to a model. In practice, the fit between observations and model can be far from perfect. In this case, the observations may not behave according to the model or the model is an incorrect abstraction of the way the observations behave. In our specific case of genetic map construction, this means that a poor fit may either be caused by poor quality of the marker observations or by an imperfect model of the genetics, or both.

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Chapter
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Publisher: Cambridge University Press
Print publication year: 2013

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References

Farré, A., Lacasa Benito, I., Cistué, L., De Jong, J. H., Romagosa, I. & Jansen, J. (2011). Linkage map construction involving a reciprocal translocation. Theoretical and Applied Genetics, 122, 1029–37.CrossRefGoogle ScholarPubMed
Jansen, J., De Jong, A.G. & Van Ooijen, J.W. (2001a). Constructing dense genetic linkage maps. Theoretical and Applied Genetics, 102, 1113–22.CrossRefGoogle Scholar
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Lincoln, S. E. & Lander, E. (1992). Systematic detection of errors in genetic linkage data. Genomics, 14, 604–10.CrossRefGoogle ScholarPubMed
Speed, T. P., McPeek, M. S. & Evans, S. N. (1992). Robustness of the no-interference model for ordering genetic markers. Proceedings of the National Academy of Sciences USA, 89, 3103–6.CrossRefGoogle ScholarPubMed
Van Berloo, R. (2007). GGT 2.0: versatile software for the visualization of genetic data. Journal of Heredity, 99, 232–6.CrossRefGoogle Scholar

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