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arXiv 2408.00237stat.MLcs.LGstat.ME

经验贝叶斯关联矩阵分解

Empirical Bayes Linked Matrix Decomposition

University of Minnesota(明尼苏达大学)

Eric F. Lock

AI总结:

本文提出一种经验变分贝叶斯关联矩阵分解方法,支持二维整合、自动收缩且无需调参,在低秩信号恢复、共享与特定信号分解及缺失数据插补上表现优异,并在乳腺癌多组学数据中验证有效。

摘要:

多个不同领域应用中的数据可以表示为在行或列上相互关联的多个矩阵。这在分子生物医学研究中尤为常见,其中多种分子“组学”技术可能捕获不同的特征集(例如,对应矩阵中的行)和/或不同的样本群体(对应列)。这促使了大量关于整合矩阵分解方法的研究,这些方法识别并分解跨多个矩阵共享或特定于某个矩阵的低维信号。我们提出了一种经验变分贝叶斯方法来解决该问题,与现有技术相比具有若干优势,包括能够灵活地容纳任意数量的行或列集合上的共享信号(即二维整合)、一个直观的基于模型的目标函数,能够为推断信号提供适当的收缩,以及一个相对高效且无需调参的估计算法。一个一般性结果为一类广泛的方法(包括所提出的方法)建立了底层分解唯一性的条件。针对存在缺失数据的场景,我们描述了一种相关的迭代插补方法,该方法在单矩阵情境下是新颖的,并且在各种关联矩阵情境下是一种强大的“分块”插补方法(其中整行或整列缺失)。大量模拟表明,该方法在不同场景下在恢复底层低秩信号、准确分解共享信号和特定信号以及准确插补缺失数据方面表现非常好。该方法被应用于乳腺癌组织和正常乳腺组织的基因表达和miRNA数据,给出了信息丰富的变异分解,并在缺失数据插补方面优于替代策略。

英文摘要:

Data for several applications in diverse fields can be represented as multiple matrices that are linked across rows or columns. This is particularly common in molecular biomedical research, in which multiple molecular "omics" technologies may capture different feature sets (e.g., corresponding to rows in a matrix) and/or different sample populations (corresponding to columns). This has motivated a large body of work on integrative matrix factorization approaches that identify and decompose low-dimensional signal that is shared across multiple matrices or specific to a given matrix. We propose an empirical variational Bayesian approach to this problem that has several advantages over existing techniques, including the flexibility to accommodate shared signal over any number of row or column sets (i.e., bidimensional integration), an intuitive model-based objective function that yields appropriate shrinkage for the inferred signals, and a relatively efficient estimation algorithm with no tuning parameters. A general result establishes conditions for the uniqueness of the underlying decomposition for a broad family of methods that includes the proposed approach. For scenarios with missing data, we describe an associated iterative imputation approach that is novel for the single-matrix context and a powerful approach for "blockwise" imputation (in which an entire row or column is missing) in various linked matrix contexts. Extensive simulations show that the method performs very well under different scenarios with respect to recovering underlying low-rank signal, accurately decomposing shared and specific signals, and accurately imputing missing data. The approach is applied to gene expression and miRNA data from breast cancer tissue and normal breast tissue, for which it gives an informative decomposition of variation and outperforms alternative strategies for missing data imputation.

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