一种支持多源基因表达数据整合的高维线性回归鲁棒迁移学习方法。

IF 3.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS PLoS Computational Biology Pub Date : 2025-01-10 eCollection Date: 2025-01-01 DOI:10.1371/journal.pcbi.1012739
Lulu Pan, Qian Gao, Kecheng Wei, Yongfu Yu, Guoyou Qin, Tong Wang
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引用次数: 0

摘要

迁移学习旨在整合多源数据集的有用信息,以提高目标数据的学习性能。当我们了解目标组织中的基因关联时,这可以有效地应用于基因组学,并且可以整合来自其他组织的数据。然而,基因组学数据中普遍存在重尾分布和离群值,这对当前迁移学习方法的有效性提出了挑战。本文研究了具有t分布误差的高维线性模型(Trans-PtLR)下的迁移学习问题,该问题旨在通过从有用的源数据中借鉴信息,并提供鲁棒性以适应具有重尾和异常值的复杂数据,从而提高对目标数据的估计和预测。在已知可转移源数据集的oracle情况下,建立了一种基于惩罚极大似然和期望最大化的迁移学习算法。为了避免包括非信息源,我们建议选择基于交叉验证的可转移源。大量的仿真实验和应用表明,与迁移学习相比,Trans-PtLR在存在重尾和离群值的情况下具有鲁棒性和更好的估计和预测性能。数据整合,变量选择,T分布,期望最大化算法,基因型-组织表达,交叉验证。
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A robust transfer learning approach for high-dimensional linear regression to support integration of multi-source gene expression data.

Transfer learning aims to integrate useful information from multi-source datasets to improve the learning performance of target data. This can be effectively applied in genomics when we learn the gene associations in a target tissue, and data from other tissues can be integrated. However, heavy-tail distribution and outliers are common in genomics data, which poses challenges to the effectiveness of current transfer learning approaches. In this paper, we study the transfer learning problem under high-dimensional linear models with t-distributed error (Trans-PtLR), which aims to improve the estimation and prediction of target data by borrowing information from useful source data and offering robustness to accommodate complex data with heavy tails and outliers. In the oracle case with known transferable source datasets, a transfer learning algorithm based on penalized maximum likelihood and expectation-maximization algorithm is established. To avoid including non-informative sources, we propose to select the transferable sources based on cross-validation. Extensive simulation experiments as well as an application demonstrate that Trans-PtLR demonstrates robustness and better performance of estimation and prediction when heavy-tail and outliers exist compared to transfer learning for linear regression model with normal error distribution. Data integration, Variable selection, T distribution, Expectation maximization algorithm, Genotype-Tissue Expression, Cross validation.

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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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