# A comparison of design algorithms for choosing the training population in genomic models

**Authors:** Alexandra Stadler, Werner G. Müller, Andreas Futschik

PMC · DOI: 10.3389/fgene.2024.1462855 · Frontiers in Genetics · 2025-02-13

## TL;DR

This paper compares different algorithms for selecting training populations in genomic models to improve breeding program efficiency.

## Contribution

The paper introduces and evaluates adapted classical design algorithms for genomic models, focusing on runtime and efficiency.

## Key findings

- Adapting classical algorithms reduces runtime while maintaining efficiency.
- Different design criteria show varying performance across sample sizes.
- Brute-force approaches are less efficient compared to optimized algorithms.

## Abstract

In contemporary breeding programs, typically genomic best linear unbiased prediction (gBLUP) models are employed to drive decisions on artificial selection. Experiments are performed to obtain responses on the units in the breeding program. Due to restrictions on the size of the experiment, an efficient experimental design must usually be found in order to optimize the training population. Classical exchange-type algorithms from optimal design theory can be employed for this purpose. This article suggests several variants for the gBLUP model and compares them to brute-force approaches from the genomics literature for various design criteria. Particular emphasis is placed on evaluating the computational runtime of algorithms along with their respective efficiencies over different sample sizes. We find that adapting classical algorithms from optimal design of experiments can help to decrease runtime, while maintaining efficiency.

## Full-text entities

- **Diseases:** CD (MESH:D003643)
- **Chemicals:** CD (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11865072/full.md

## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC11865072/full.md

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Source: https://tomesphere.com/paper/PMC11865072