Impact of scale parameter for marker variance prior in some Bayesian whole-genome regression methods.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Özge Kozakli, Ayhan Ceyhan
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引用次数: 0

Abstract

In this study, traditional single-trait Bayesian whole-genome regression methods (BayesA, BayesB, and BayesCπ), which treat the scale parameter of the marker variance prior as fixed, were compared to alternative versions (BayesSA, BayesSB, and BayesSCπ) that estimate this parameter from the data using a Gamma prior. Analyses were conducted using a publicly available dataset of 3,534 animals from a commercial PIC pig population with genotypic and phenotypic records. Model performance for each trait was evaluated through six-fold cross-validation, using the correlation between genomic estimated breeding values (GEBV) and pseudo estimated breeding values (pEBV) as the measure of predictive accuracy. The alternative BayesSA model achieved higher accuracy than BayesA, whereas BayesSB showed no improvement, likely because its estimated scale parameters were similar to the fixed values in BayesB. For BayesCπ, results confirmed that the limited influence of the prior on marker variance led to similar performance between the classical and alternative versions. Heritability was estimated for five traits (T1–T5), and model specification affected these estimates slightly. The alternative models, which estimate prior variance parameters from the data rather than assuming them as fixed, generally produced lower heritability estimates than their classical counterparts. Considering that the reference heritability values from the original PIC study were based on extensive pedigree and high-density genotype data, the alternative models’ estimates can be regarded as reasonably consistent. These findings indicate that hyperparameter estimation in Bayesian models can improve prediction accuracy and the reliability of heritability estimates, providing a more suitable framework for traits with complex genetic architectures.

一些贝叶斯全基因组回归方法中尺度参数对标记方差先验的影响。
在这项研究中,将传统的单性状贝叶斯全基因组回归方法(BayesA, BayesB和bayescc π)与使用Gamma先验从数据中估计该参数的替代版本(BayesSA, BayesSB和bayesscc π)进行了比较,这些方法将标记方差先验的尺度参数视为固定的。使用公开的数据集进行分析,该数据集包括来自商业PIC猪群的3534头动物,具有基因型和表型记录。利用基因组估计育种值(GEBV)和伪估计育种值(pEBV)之间的相关性作为预测准确性的度量,通过6倍交叉验证对每个性状的模型性能进行评估。替代BayesSA模型的准确率高于BayesA模型,而BayesSB模型没有提高,可能是因为其估计的尺度参数与BayesB中的固定值相似。对于bayescc π,结果证实了先验对标记方差的有限影响导致经典版本和替代版本之间的表现相似。估计了5个性状(T1-T5)的遗传力,模型规格对这些估计影响较小。替代模型从数据中估计先验方差参数,而不是假设它们是固定的,通常比经典模型产生更低的遗传力估计。考虑到原始PIC研究的参考遗传力值是基于广泛的家系和高密度的基因型数据,可认为替代模型的估计是合理一致的。这些结果表明,贝叶斯模型中的超参数估计可以提高遗传力估计的预测精度和可靠性,为具有复杂遗传结构的性状提供更合适的预测框架。
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来源期刊
Mammalian Genome
Mammalian Genome 生物-生化与分子生物学
CiteScore
4.00
自引率
0.00%
发文量
33
审稿时长
6-12 weeks
期刊介绍: Mammalian Genome focuses on the experimental, theoretical and technical aspects of genetics, genomics, epigenetics and systems biology in mouse, human and other mammalian species, with an emphasis on the relationship between genotype and phenotype, elucidation of biological and disease pathways as well as experimental aspects of interventions, therapeutics, and precision medicine. The journal aims to publish high quality original papers that present novel findings in all areas of mammalian genetic research as well as review articles on areas of topical interest. The journal will also feature commentaries and editorials to inform readers of breakthrough discoveries as well as issues of research standards, policies and ethics.
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