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Shufei Ge

Publications and source records attributed to Shufei Ge.

11 recordsLinked to original sources

A Bayesian hierarchical model for meta-analysis

Meta-analysis is a key statistical tool for synthesizing clinical trial data to evaluate treatment effects, yet traditional methods such as fixed-effect and random-effects models often fail to handle heterogeneity, study-level covariates, or hierarchical structures effectively. To overcome these limitations, we developed a Bayesian hierarchical meta-analysis framework for robust parameter estimation on small samples and utilized analytical integration for efficient inference. Simulation studies indicated robust estimation of the proposed model. We applied it to the efficacy and safety profiles of Oxcarbazepine (OXC) and Carbamazepine (CBZ) in epilepsy treatment. Gibbs sampling and analytical integration produced nearly identical results across all three clinical datasets. The results indicated no significant difference between OXC and CBZ in complete seizure control, while OXC was significantly associated with a higher probability of at least a 50% reduction in seizure frequency and a lower risk of side effects than CBZ. The code and relevant data used in this study are openly available on GitHub at https://github.com/xsjk/HierarchicalMetaAnalysis.

stat.AP

Poisson Hyperplane Processes with Rectified Linear Units

Neural networks have shown state-of-the-art performances in various classification and regression tasks. Rectified linear units (ReLU) are often used as activation functions for the hidden layers in a neural network model. In this article, we establish the connection between the Poisson hyperplane processes (PHP) and two-layer ReLU neural networks. We show that the PHP with a Gaussian prior is an alternative probabilistic representation to a two-layer ReLU neural network. In addition, we show that a two-layer neural network constructed by PHP is scalable to large-scale problems via the decomposition propositions. Finally, we propose an annealed sequential Monte Carlo algorithm for Bayesian inference. Our numerical experiments demonstrate that our proposed method outperforms the classic two-layer ReLU neural network. The implementation of our proposed model is available at https://github.com/ShufeiGe/Pois_Relu.git.

cs.LG

Bayesian Brain Edge-Based Connectivity (BBeC): a Bayesian model for brain edge-based connectivity inference

Brain connectivity analysis based on magnetic resonance imaging is crucial for understanding neurological mechanisms. However, edge-based connectivity inference faces significant challenges, particularly the curse of dimensionality when estimating high-dimensional covariance matrices. Existing methods often struggle to account for the unknown latent topological structure among brain edges, leading to inaccurate parameter estimation and unstable inference. To address these issues, this study proposes a Bayesian model based on a finite-dimensional Dirichlet distribution. Unlike non-parametric approaches, our method utilizes a finite-dimensional Dirichlet distribution to model the topological structure of brain networks, ensuring constant parameter dimensionality and improving algorithmic stability. We reformulate the covariance matrix structure to guarantee positive definiteness and employ a Metropolis-Hastings algorithm to simultaneously infer network topology and correlation parameters. Simulations validated the recovery of both network topology and correlation parameters. When applied to the Alzheimer's Disease Neuroimaging Initiative dataset, the model successfully identified structural subnetworks. The identified clusters were not only validated by composite anatomical metrics but also consistent with established findings in the literature, collectively demonstrating the model's reliability. The estimated covariance matrix also revealed that intragroup connection strength is stronger than intergroup connection strength. This study introduces a Bayesian framework for inferring brain network topology and high-dimensional covariance structures. The model configuration reduces parameter dimensionality while ensuring the positive definiteness of covariance matrices. As a result, it offers a reliable tool for investigating intrinsic brain connectivity in large-scale neuroimaging studies.

stat.ME

A near-exact linear mixed model for genome-wide association studies

Linear mixed models (LMM) are widely adopted in genome-wide association studies (GWAS) to account for population stratification and cryptic relatedness. However, the parameter estimation of LMMs imposes substantial computational burdens due to large-scale operations on genetic similarity matrices (GSM). We introduced the near-exact linear mixed model (NExt-LMM), a novel LMM framework that overcomes critical computational bottlenecks in GWAS through the following key innovations. Firstly, we exploit the inherent low-rank structure of the GSM iteratively with the Hierarchical Off-Diagonal Low-Rank (HODLR) format, which is much faster than traditional decomposition methods. Secondly, we leverage the HODLR-approximated GSM to dramatically accelerate the further maximum likelihood estimation with the shared heritability ratios. Moreover, we establish rigorous error bounds for the NExt-LMM estimator, proving that Kullback-Leibler divergence between the approximated and exact estimators can be arbitrarily small. Consequently, our proposed dual approach accelerates inference of LMMs while guaranteeing low approximation errors. We use numerical experiments to demonstrate that the NExt-LMM significantly improves inference efficiency compared to existing methods. We develop a Python package that is available at https://github.com/ZhibinPU/NExt-LMM.

stat.CO

A Mapper Algorithm with implicit intervals and its optimization

The Mapper algorithm is an essential tool for visualizing complex, high dimensional data in topology data analysis (TDA) and has been widely used in biomedical research. It outputs a combinatorial graph whose structure implies the shape of the data. However,the need for manual parameter tuning and fixed intervals, along with fixed overlapping ratios may impede the performance of the standard Mapper algorithm. Variants of the standard Mapper algorithms have been developed to address these limitations, yet most of them still require manual tuning of parameters. Additionally, many of these variants, including the standard version found in the literature, were built within a deterministic framework and overlooked the uncertainty inherent in the data. To relax these limitations, in this work, we introduce a novel framework that implicitly represents intervals through a hidden assignment matrix, enabling automatic parameter optimization via stochastic gradient descent. In this work, we develop a soft Mapper framework based on a Gaussian mixture model(GMM) for flexible and implicit interval construction. We further illustrate the robustness of the soft Mapper algorithm by introducing the Mapper graph mode as a point estimation for the output graph. Moreover, a stochastic gradient descent algorithm with a specific topological loss function is proposed for optimizing parameters in the model. Both simulation and application studies demonstrate its effectiveness in capturing the underlying topological structures. In addition, the application to an RNA expression dataset obtained from the Mount Sinai/JJ Peters VA Medical Center Brain Bank (MSBB) successfully identifies a distinct subgroup of Alzheimer's Disease.

cs.LG

A spatial-correlated multitask linear mixed-effects model for imaging genetics

Imaging genetics aims to uncover the hidden relationship between imaging quantitative traits (QTs) and genetic markers (e.g. single nucleotide polymorphism (SNP)), and brings valuable insights into the pathogenesis of complex diseases, such as cancers and cognitive disorders (e.g. the Alzheimer's Disease). However, most linear models in imaging genetics didn't explicitly model the inner relationship among QTs, which might miss some potential efficiency gains from information borrowing across brain regions. In this work, we developed a novel Bayesian regression framework for identifying significant associations between QTs and genetic markers while explicitly modeling spatial dependency between QTs, with the main contributions as follows. Firstly, we developed a spatial-correlated multitask linear mixed-effects model (LMM) to account for dependencies between QTs. We incorporated a population-level mixed effects term into the model, taking full advantage of the dependent structure of brain imaging-derived QTs. Secondly, we implemented the model in the Bayesian framework and derived a Markov chain Monte Carlo (MCMC) algorithm to achieve the model inference. Further, we incorporated the MCMC samples with the Cauchy combination test (CCT) to examine the association between SNPs and QTs, which avoided computationally intractable multi-test issues. The simulation studies indicated improved power of our proposed model compared to classic models where inner dependencies of QTs were not modeled. We also applied the new spatial model to an imaging dataset obtained from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database.

stat.ME

A distribution-guided Mapper algorithm

Motivation: The Mapper algorithm is an essential tool to explore shape of data in topology data analysis. With a dataset as an input, the Mapper algorithm outputs a graph representing the topological features of the whole dataset. This graph is often regarded as an approximation of a reeb graph of data. The classic Mapper algorithm uses fixed interval lengths and overlapping ratios, which might fail to reveal subtle features of data, especially when the underlying structure is complex. Results: In this work, we introduce a distribution guided Mapper algorithm named D-Mapper, that utilizes the property of the probability model and data intrinsic characteristics to generate density guided covers and provides enhanced topological features. Our proposed algorithm is a probabilistic model-based approach, which could serve as an alternative to non-prababilistic ones. Moreover, we introduce a metric accounting for both the quality of overlap clustering and extended persistence homology to measure the performance of Mapper type algorithm. Our numerical experiments indicate that the D-Mapper outperforms the classical Mapper algorithm in various scenarios. We also apply the D-Mapper to a SARS-COV-2 coronavirus RNA sequences dataset to explore the topological structure of different virus variants. The results indicate that the D-Mapper algorithm can reveal both vertical and horizontal evolution processes of the viruses. Availability: Our package is available at https://github.com/ShufeiGe/D-Mapper.

math.AT

Shape Modeling with Spline Partitions

Shape modelling (with methods that output shapes) is a new and important task in Bayesian nonparametrics and bioinformatics. In this work, we focus on Bayesian nonparametric methods for capturing shapes by partitioning a space using curves. In related work, the classical Mondrian process is used to partition spaces recursively with axis-aligned cuts, and is widely applied in multi-dimensional and relational data. The Mondrian process outputs hyper-rectangles. Recently, the random tessellation process was introduced as a generalization of the Mondrian process, partitioning a domain with non-axis aligned cuts in an arbitrary dimensional space, and outputting polytopes. Motivated by these processes, in this work, we propose a novel parallelized Bayesian nonparametric approach to partition a domain with curves, enabling complex data-shapes to be acquired. We apply our method to HIV-1-infected human macrophage image dataset, and also simulated datasets sets to illustrate our approach. We compare to support vector machines, random forests and state-of-the-art computer vision methods such as simple linear iterative clustering super pixel image segmentation. We develop an R package that is available at \url{https://github.com/ShufeiGe/Shape-Modeling-with-Spline-Partitions}.

stat.ML

Adaptive semiparametric Bayesian differential equations via sequential Monte Carlo

Nonlinear differential equations (DEs) are used in a wide range of scientific problems to model complex dynamic systems. The differential equations often contain unknown parameters that are of scientific interest, which have to be estimated from noisy measurements of the dynamic system. Generally, there is no closed-form solution for nonlinear DEs, and the likelihood surface for the parameter of interest is multi-modal and very sensitive to different parameter values. We propose a Bayesian framework for nonlinear DE systems. A flexible nonparametric function is used to represent the dynamic process such that expensive numerical solvers can be avoided. A sequential Monte Carlo algorithm in the annealing framework is proposed to conduct Bayesian inference for parameters in DEs. In our numerical experiments, we use examples of ordinary differential equations and delay differential equations to demonstrate the effectiveness of the proposed algorithm. We developed an R package that is available at \url{https://github.com/shijiaw/smcDE}.

stat.CO

Random Tessellation Forests

Space partitioning methods such as random forests and the Mondrian process are powerful machine learning methods for multi-dimensional and relational data, and are based on recursively cutting a domain. The flexibility of these methods is often limited by the requirement that the cuts be axis aligned. The Ostomachion process and the self-consistent binary space partitioning-tree process were recently introduced as generalizations of the Mondrian process for space partitioning with non-axis aligned cuts in the two dimensional plane. Motivated by the need for a multi-dimensional partitioning tree with non-axis aligned cuts, we propose the Random Tessellation Process (RTP), a framework that includes the Mondrian process and the binary space partitioning-tree process as special cases. We derive a sequential Monte Carlo algorithm for inference, and provide random forest methods. Our process is self-consistent and can relax axis-aligned constraints, allowing complex inter-dimensional dependence to be captured. We present a simulation study, and analyse gene expression data of brain tissue, showing improved accuracies over other methods.

stat.ML

A Bayesian Spatial Model for Imaging Genetics

We develop a Bayesian bivariate spatial model for multivariate regression analysis applicable to studies examining the influence of genetic variation on brain structure. Our model is motivated by an imaging genetics study of the Alzheimer's Disease Neuroimaging Initiative (ADNI), where the objective is to examine the association between images of volumetric and cortical thickness values summarizing the structure of the brain as measured by magnetic resonance imaging (MRI) and a set of 486 SNPs from 33 Alzheimer's Disease (AD) candidate genes obtained from 632 subjects. A bivariate spatial process model is developed to accommodate the correlation structures typically seen in structural brain imaging data. First, we allow for spatial correlation on a graph structure in the imaging phenotypes obtained from a neighbourhood matrix for measures on the same hemisphere of the brain. Second, we allow for correlation in the same measures obtained from different hemispheres (left/right) of the brain. We develop a mean-field variational Bayes algorithm and a Gibbs sampling algorithm to fit the model. We also incorporate Bayesian false discovery rate (FDR) procedures to select SNPs. We implement the methodology in a new release of the R package bgsmtr. We show that the new spatial model demonstrates superior performance over a standard model in our application. Data used in the preparation of this article were obtained from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database (adni.loni.usc.edu).

stat.ME