基于门控残差变量选择神经网络的多任务基因组预测。

IF 3.3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Yuhua Fan, Patrik Waldmann
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引用次数: 0

摘要

背景:近年来高通量测序技术的发展为全基因组预测(GWP)提供了大量数据。虽然GWP本身是有效的,但将传统的多基因谱系信息纳入GWP已被证明可以进一步提高预测精度。然而,该领域开发的大多数方法要求具有基因组信息的个体可以在标准的线性混合模型框架内与多基因谱系联系起来,该框架涉及计算组合谱系的计算要求矩阵逆。将这种集成方法扩展到更灵活的机器学习方法的过程一直很缓慢。方法:采用门控残差变量选择神经网络(GRVSNN)进行多任务基因组预测,提高基因组预测能力。通过整合来自基于谱系的关系矩阵和基因组标记的低秩信息,与传统的回归和深度学习(DL)模型相比,我们寻求提高预测的准确性和可解释性。在火炬松、小鼠和猪等实际数据集上对GRVSNN模型的预测性能进行了评估。结果:实验结果表明,GRVSNN模型优于传统的表格基因组预测模型,包括贝叶斯回归方法和LassoNet。利用基因组和系谱信息,GRVSNN在测试数据中实现了较低的均方误差(MSE),以及较高的Pearson (r)和距离(dCor)相关性。此外,GRVSNN选择较少的遗传标记和谱系负载,从而提高了可解释性。结论:所提出的GRVSNN框架通过整合传统家系信息和基因组数据,为提高基因组预测精度提供了一种新颖且计算有效的方法。该模型进行多任务预测的能力强调了它在提高农业物种选择过程和在精准医学中预测多种疾病方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Multi-task genomic prediction using gated residual variable selection neural networks.

Multi-task genomic prediction using gated residual variable selection neural networks.

Multi-task genomic prediction using gated residual variable selection neural networks.

Background: The recent development of high-throughput sequencing techniques provide massive data that can be used in genome-wide prediction (GWP). Although GWP is effective on its own, the incorporation of traditional polygenic pedigree information into GWP has been shown to further improve prediction accuracy. However, most of the methods developed in this field require that individuals with genomic information can be connected to the polygenic pedigree within a standard linear mixed model framework that involves calculation of computationally demanding matrix inverses of the combined pedigrees. The extension of this integrated approach to more flexible machine learning methods has been slow.

Methods: This study aims to enhance genomic prediction by implementing gated residual variable selection neural networks (GRVSNN) for multi-task genomic prediction. By integrating low-rank information from pedigree-based relationship matrices with genomic markers, we seek to improve predictive accuracy and interpretability compared to conventional regression and deep learning (DL) models. The prediction properties of the GRVSNN model are evaluated on several real-world datasets, including loblolly pine, mouse and pig.

Results: The experimental results demonstrate that the GRVSNN model outperforms traditional tabular genomic prediction models, including Bayesian regression methods and LassoNet. Using genomic and pedigree information, GRVSNN achieves a lower mean squared error (MSE), and higher Pearson (r) and distance (dCor) correlation between predicted and true phenotypic values in the test data. Moreover, GRVSNN selects fewer genetic markers and pedigree loadings which improves interpretability.

Conclusion: The suggested GRVSNN framework provides a novel and computationally effective approach to improve genomic prediction accuracy by integrating information from traditional pedigrees with genomic data. The model's ability to conduct multi-task predictions underscores its potential to enhance selection processes in agricultural species and predict multiple diseases in precision medicine.

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来源期刊
BMC Bioinformatics
BMC Bioinformatics 生物-生化研究方法
CiteScore
5.70
自引率
3.30%
发文量
506
审稿时长
4.3 months
期刊介绍: BMC Bioinformatics is an open access, peer-reviewed journal that considers articles on all aspects of the development, testing and novel application of computational and statistical methods for the modeling and analysis of all kinds of biological data, as well as other areas of computational biology. BMC Bioinformatics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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