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Optimization of Sparse Phenotyping Strategies in Multi-Environmental Trials in Maize

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Abstract The phenotyping needs to be optimized and aims to achieve desired precision at low costs because selection decisions are mainly based on multi-environmental trials. Optimization of sparse phenotyping is possible in plant breeding by applying relationship measurements and genomic prediction. Our research utilized genomic data and relationship measurements between the training (full testing genotypes) and testing set (sparse testing genotypes) to optimize the allocation of genotypes to subsets in sparse testing. Different sparse phenotyping designs were mimicked based on the percentage (%) of lines in the full set, the number of partially tested lines, the number of tested environments, balanced and unbalanced methods for allocating the lines among the environments. The eight relationship measurements were utilized to calculate the relatedness between full and sparse set genotypes. The results demonstrate that balanced and allocating 50% of lines to the full set designs have shown a higher Pearson correlation in terms of accuracy measurements than assigning the 30% of lines to the full set and balanced sparse methods. By reducing untested environments per sparse set, results enhance the accuracy of measurements. The relationship measurements exhibit a low significant Pearson correlation ranging from 0.20 to 0.31 using the accuracy measurements in sparse phenotyping experiments. The positive Pearson correlation shows that the maximization of the accuracy measurements can be helpful to the optimization of the line allocation on sparse phenotyping designs.
Title: Optimization of Sparse Phenotyping Strategies in Multi-Environmental Trials in Maize
Description:
Abstract The phenotyping needs to be optimized and aims to achieve desired precision at low costs because selection decisions are mainly based on multi-environmental trials.
Optimization of sparse phenotyping is possible in plant breeding by applying relationship measurements and genomic prediction.
Our research utilized genomic data and relationship measurements between the training (full testing genotypes) and testing set (sparse testing genotypes) to optimize the allocation of genotypes to subsets in sparse testing.
Different sparse phenotyping designs were mimicked based on the percentage (%) of lines in the full set, the number of partially tested lines, the number of tested environments, balanced and unbalanced methods for allocating the lines among the environments.
The eight relationship measurements were utilized to calculate the relatedness between full and sparse set genotypes.
The results demonstrate that balanced and allocating 50% of lines to the full set designs have shown a higher Pearson correlation in terms of accuracy measurements than assigning the 30% of lines to the full set and balanced sparse methods.
By reducing untested environments per sparse set, results enhance the accuracy of measurements.
The relationship measurements exhibit a low significant Pearson correlation ranging from 0.
20 to 0.
31 using the accuracy measurements in sparse phenotyping experiments.
The positive Pearson correlation shows that the maximization of the accuracy measurements can be helpful to the optimization of the line allocation on sparse phenotyping designs.

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