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A Unified Bayesian Framework for Bi-overlapping-Clustering Multi-omics Data via Sparse Matrix Factorization. 基于稀疏矩阵分解的多组学数据双重叠聚类的统一贝叶斯框架
IF 1 Q2 Mathematics Pub Date : 2023-12-01 Epub Date: 2022-07-08 DOI: 10.1007/s12561-022-09350-w
Fangting Zhou, Kejun He, James J Cai, Laurie A Davidson, Robert S Chapkin, Yang Ni

The advances of modern sequencing techniques have generated an unprecedented amount of multi-omics data which provide great opportunities to quantitatively explore functional genomes from different but complementary perspectives. However, distinct modalities/sequencing technologies generate diverse types of data which greatly complicate statistical modeling because uniquely optimized methods are required for handling each type of data. In this paper, we propose a unified framework for Bayesian nonparametric matrix factorization that infers overlapping bi-clusters for multi-omics data. The proposed method adaptively discretizes different types of observations into common latent states on which cluster structures are built hierarchically. The proposed Bayesian nonparametric method is able to automatically determine the number of clusters. We demonstrate the utility of the proposed method using simulation studies and applications to a single-cell RNA-sequencing dataset, a combination of single-cell RNA-sequencing and single-cell ATAC-sequencing dataset, a bulk RNA-sequencing dataset, and a DNA methylation dataset which reveal several interesting findings that are consistent with biological literature.

现代测序技术的进步产生了前所未有的多组学数据,为从不同但互补的角度定量探索功能基因组提供了绝佳机会。然而,不同的模式/测序技术会产生不同类型的数据,这使得统计建模变得非常复杂,因为处理每种类型的数据都需要独特的优化方法。在本文中,我们提出了一种统一的贝叶斯非参数矩阵因式分解框架,可推导出多组学数据的重叠双簇。所提出的方法能自适应地将不同类型的观测数据离散为共同的潜在状态,并在此基础上分层构建聚类结构。所提出的贝叶斯非参数方法能够自动确定聚类的数量。我们通过模拟研究和应用于单细胞 RNA 序列数据集、单细胞 RNA 序列和单细胞 ATAC 序列组合数据集、批量 RNA 序列数据集和 DNA 甲基化数据集,证明了所提方法的实用性,并揭示了与生物学文献一致的一些有趣发现。
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引用次数: 0
On Estimation of the Effect Lag of Predictors and Prediction in a Functional Linear Model 预测器效应滞后的估计与函数线性模型的预测
Q2 Mathematics Pub Date : 2023-11-08 DOI: 10.1007/s12561-023-09393-7
Haiyan Liu, Georgios Aivaliotis, Vijay Kumar, Jeanine Houwing-Duistermaat
Abstract We propose a functional linear model to predict a functional response using multiple functional and longitudinal predictors and to estimate the effect lags of predictors. The coefficient functions are written as the expansion of a basis system (e.g. functional principal components, splines), and the coefficients of the basis functions are estimated via optimizing a penalization criterion. Then effect lags are determined by simultaneously searching on a prior designed grid mesh based on minimization of a proposed prediction error criterion. Mathematical properties of the estimated regression functions and predicted responses are studied. The performance of the method is evaluated by extensive simulations and a real data analysis application on chronic obstructive pulmonary disease (COPD).
摘要:我们提出了一个函数线性模型,利用多个函数和纵向预测因子来预测功能响应,并估计预测因子的效应滞后。系数函数被写成基系统的展开(如功能主成分,样条),并且基函数的系数通过优化惩罚准则来估计。然后,基于所提出的预测误差准则的最小化,通过在预先设计的网格上同时搜索来确定效应滞后。研究了估计回归函数和预测响应的数学性质。通过大量的模拟和慢性阻塞性肺疾病(COPD)的实际数据分析应用,对该方法的性能进行了评估。
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引用次数: 0
Bayesian Inference for High Dimensional Cox Models with Gaussian and Diffused-Gamma Priors: A Case Study of Mortality in COVID-19 Patients Admitted to the ICU 高斯先验和弥散先验的高维Cox模型的贝叶斯推断——以新冠肺炎ICU住院患者死亡率为例
Q2 Mathematics Pub Date : 2023-11-04 DOI: 10.1007/s12561-023-09395-5
Jiyeon Song, Subharup Guha, Yi Li
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引用次数: 0
Nonnegative Matrix Factorization with Group and Basis Restrictions 具有群和基限制的非负矩阵分解
Q2 Mathematics Pub Date : 2023-11-04 DOI: 10.1007/s12561-023-09398-2
Phillip Shreeves, Jeffrey L. Andrews, Xinchen Deng, Ramie Ali-Adeeb, Andrew Jirasek
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引用次数: 0
Introduction to Special Issue on Machine Learning Algorithms in Genomics and Genetics 基因组学和遗传学中的机器学习算法特刊导论
Q2 Mathematics Pub Date : 2023-11-03 DOI: 10.1007/s12561-023-09401-w
Yingying Wei
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引用次数: 0
Bivariate Analysis of Birth Weight and Gestational Age by Bayesian Distributional Regression with Copulas 基于copula的贝叶斯分布回归分析出生体重和胎龄的双变量分析
Q2 Mathematics Pub Date : 2023-10-27 DOI: 10.1007/s12561-023-09396-4
Jonathan Rathjens, Arthur Kolbe, Jürgen Hölzer, Katja Ickstadt, Nadja Klein
Abstract We analyze perinatal data including biometric and obstetric information as well as data on maternal smoking, among others. Birth weight is the primarily interesting response variable. Gestational age is usually an important covariate and included in polynomial form. However, in opposition to this univariate regression, bivariate modeling of birth weight and gestational age is recommended to distinguish effects on each, on both, and between them. Rather than a parametric bivariate distribution, we apply conditional copula regression, where the marginal distributions of birth weight and gestational age (not necessarily of the same form) and the dependence structure are modeled conditionally on covariates. In the resulting distributional regression model, all parameters of the two marginals and the copula parameter are observation specific. While the Gaussian distribution is suitable for birth weight, the skewed gestational age data are better modeled by the three-parameter Dagum distribution. The Clayton copula performs better than the Gumbel and the symmetric Gaussian copula, indicating lower tail dependence (stronger dependence when both variables are low), although this non-linear dependence between birth weight and gestational age is surprisingly weak and only influenced by Cesarean section. A non-linear trend of birth weight on gestational age is detected by a univariate model that is polynomial with respect to the effect of gestational age. Covariate effects on the expected birth weight are similar in our copula regression model and a univariate regression model, while distributional copula regression reveals further insights, such as effects of covariates on the association between birth weight and gestational age.
我们分析围产期数据,包括生物特征和产科信息以及产妇吸烟等数据。出生体重是最有趣的反应变量。胎龄通常是一个重要的协变量,并以多项式形式包含。然而,与这种单变量回归相反,建议对出生体重和胎龄进行双变量建模,以区分对每个、两个和它们之间的影响。而不是参数双变量分布,我们应用条件联结回归,其中出生体重和胎龄的边际分布(不一定是相同的形式)和依赖结构是有条件地在协变量上建模的。在得到的分布回归模型中,两个边际的所有参数和copula参数都是观测特有的。虽然高斯分布适合于出生体重,但偏胎龄数据更适合用三参数Dagum分布来建模。Clayton copula比Gumbel和对称高斯copula表现得更好,表明尾依赖性较低(当两个变量都较低时依赖性更强),尽管出生体重和胎龄之间的非线性依赖性令人惊讶地弱,仅受剖宫产的影响。通过对胎龄影响的多项式单变量模型检测出生体重对胎龄的非线性趋势。在我们的联合回归模型和单变量回归模型中,协变量对预期出生体重的影响是相似的,而分布联合回归揭示了进一步的见解,例如协变量对出生体重和胎龄之间关系的影响。
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引用次数: 0
AI-Powered Bayesian Statistics in Biomedicine 生物医学中的人工智能贝叶斯统计
Q2 Mathematics Pub Date : 2023-10-26 DOI: 10.1007/s12561-023-09400-x
Qiwei Li
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引用次数: 0
Efficient Estimation of Semiparametric Transformation Model with Interval-Censored Data in Two-Phase Cohort Studies 两期队列研究中具有区间截尾数据的半参数转换模型的有效估计
Q2 Mathematics Pub Date : 2023-10-25 DOI: 10.1007/s12561-023-09392-8
Fei Gao, Kwun Chuen Gary Chan
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引用次数: 0
Variable Selection for Nonlinear Covariate Effects with Interval-Censored Failure Time Data 失效时间间隔截尾非线性协变量效应的变量选择
Q2 Mathematics Pub Date : 2023-10-20 DOI: 10.1007/s12561-023-09391-9
Tian Tian, Jianguo Sun
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引用次数: 0
A Resampling Approach for Causal Inference on Novel Two-Point Time-Series with Application to Identify Risk Factors for Type-2 Diabetes and Cardiovascular Disease 新两点时间序列因果推断的重采样方法及其在2型糖尿病和心血管疾病危险因素识别中的应用
Q2 Mathematics Pub Date : 2023-10-16 DOI: 10.1007/s12561-023-09390-w
Xiaowu Dai, Saad Mouti, Marjorie Lima do Vale, Sumantra Ray, Jeffrey Bohn, Lisa Goldberg
Abstract Two-point time-series data, characterized by baseline and follow-up observations, are frequently encountered in health research. We study a novel two-point time-series structure without a control group, which is driven by an observational routine clinical dataset collected to monitor key risk markers of type-2 diabetes (T2D) and cardiovascular disease (CVD). We propose a resampling approach called “I-Rand” for independently sampling one of the two-time points for each individual and making inferences on the estimated causal effects based on matching methods. The proposed method is illustrated with data from a service-based dietary intervention to promote a low-carbohydrate diet (LCD), designed to impact risk of T2D and CVD. Baseline data contain a pre-intervention health record of study participants, and health data after LCD intervention are recorded at the follow-up visit, providing a two-point time-series pattern without a parallel control group. Using this approach we find that obesity is a significant risk factor of T2D and CVD, and an LCD approach can significantly mitigate the risks of T2D and CVD. We provide code that implements our method.
以基线和随访观察为特征的两点时间序列数据在卫生研究中经常遇到。我们研究了一种新的两点时间序列结构,没有对照组,该结构由收集的观察性常规临床数据驱动,用于监测2型糖尿病(T2D)和心血管疾病(CVD)的关键风险标志物。我们提出了一种称为“I-Rand”的重新采样方法,用于对每个个体的两个时间点中的一个进行独立采样,并根据匹配方法对估计的因果效应进行推断。通过一项以服务为基础的饮食干预来促进低碳水化合物饮食(LCD),旨在影响T2D和CVD的风险。基线数据包含研究参与者的干预前健康记录,LCD干预后的健康数据在随访时记录,提供两点时间序列模式,而不需要平行对照组。通过该方法,我们发现肥胖是T2D和CVD的重要危险因素,LCD方法可以显著降低T2D和CVD的风险。我们提供了实现方法的代码。
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引用次数: 0
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