Stochastic gradient descent estimation of generalized matrix factorization models with application to single-cell RNA sequencing data.

IF 2.1 3区 数学 Q3 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Cristian Castiglione, Alexandre Segers, Lieven Clement, Davide Risso
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引用次数: 0

Abstract

Single-cell RNA sequencing allows the quantification of gene expression at the individual cell level, enabling the study of cellular heterogeneity and gene expression dynamics. Dimensionality reduction is a common preprocessing step critical for the visualization, clustering, and phenotypic characterization of samples. This step, often performed using principal component analysis or closely related methods, is challenging because of the size and complexity of the data. In this work, we present a generalized matrix factorization model assuming a general exponential dispersion family distribution and we show that many of the proposed approaches in the single-cell dimensionality reduction literature can be seen as special cases of this model. Furthermore, we propose a scalable adaptive stochastic gradient descent algorithm that allows us to estimate the model efficiently, enabling the analysis of millions of cells. We benchmark the proposed algorithm through extensive numerical experiments against state-of-the-art methods and showcase its use in real-world biological applications. The proposed method systematically outperforms existing methods of both generalized and non-negative matrix factorization, demonstrating faster execution times and parsimonious memory usage, while maintaining, or even enhancing, matrix reconstruction fidelity and accuracy in biological signal extraction. On real data, we show that our method scales seamlessly to millions of cells, enabling dimensionality reduction in large single-cell datasets. Finally, all the methods discussed here are implemented in an efficient open-source R package, sgdGMF, available on CRAN.

广义矩阵分解模型的随机梯度下降估计及其在单细胞RNA测序数据中的应用。
单细胞RNA测序允许在单个细胞水平上定量基因表达,使细胞异质性和基因表达动力学的研究成为可能。降维是一个常见的预处理步骤,对样本的可视化、聚类和表型表征至关重要。这一步通常使用主成分分析或密切相关的方法来执行,由于数据的大小和复杂性,这一步具有挑战性。在这项工作中,我们提出了一个广义矩阵分解模型,假设一般指数分散族分布,我们表明,许多在单细胞降维文献中提出的方法可以被视为该模型的特殊情况。此外,我们提出了一种可扩展的自适应随机梯度下降算法,使我们能够有效地估计模型,从而能够分析数百万个细胞。我们通过广泛的数值实验对最先进的方法进行基准测试,并展示其在现实世界生物应用中的使用。该方法系统地优于现有的广义矩阵分解和非负矩阵分解方法,在保持甚至提高生物信号提取中矩阵重构保真度和准确性的同时,展示了更快的执行时间和更节省的内存使用。在实际数据中,我们证明了我们的方法可以无缝地扩展到数百万个单元格,从而可以在大型单单元格数据集中实现降维。最后,这里讨论的所有方法都是在一个高效的开源R包sgdGMF中实现的,该包可以在CRAN上获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biostatistics
Biostatistics 生物-数学与计算生物学
CiteScore
5.10
自引率
4.80%
发文量
45
审稿时长
6-12 weeks
期刊介绍: Among the important scientific developments of the 20th century is the explosive growth in statistical reasoning and methods for application to studies of human health. Examples include developments in likelihood methods for inference, epidemiologic statistics, clinical trials, survival analysis, and statistical genetics. Substantive problems in public health and biomedical research have fueled the development of statistical methods, which in turn have improved our ability to draw valid inferences from data. The objective of Biostatistics is to advance statistical science and its application to problems of human health and disease, with the ultimate goal of advancing the public''s health.
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