arXiv subjects

Yu-Ping Wang

Publications and source records attributed to Yu-Ping Wang.

At least 55 records · Page 3Linked to original sources

arXiv2020

Functional connectome fingerprinting: Identifying individuals and predicting cognitive function via deep learning

The dynamic characteristics of functional network connectivity have been widely acknowledged and studied. Both shared and unique information has been shown to be present in the connectomes. However, very little has been known about whether and how this common pattern can predict the individual variability of the brain, i.e. "brain fingerprinting", which attempts to reliably identify a particular individual from a pool of subjects. In this paper, we propose to enhance the individual uniqueness based on an autoencoder network. More specifically, we rely on the hypothesis that the common neural activities shared across individuals may lessen individual discrimination. By reducing contributions from shared activities, inter-subject variability can be enhanced. Results show that that refined connectomes utilizing an autoencoder with sparse dictionary learning can successfully distinguish one individual from the remaining participants with reasonably high accuracy (up to 99:5% for the rest-rest pair). Furthermore, high-level cognitive behavior (e.g., fluid intelligence, executive function, and language comprehension) can also be better predicted using refined functional connectivity profiles. As expected, the high-order association cortices contributed more to both individual discrimination and behavior prediction. The proposed approach provides a promising way to enhance and leverage the individualized characteristics of brain networks.

q-bio.NC↗

arXiv2020

Interpretable multimodal fusion networks reveal mechanisms of brain cognition

Multimodal fusion benefits disease diagnosis by providing a more comprehensive perspective. Developing algorithms is challenging due to data heterogeneity and the complex within- and between-modality associations. Deep-network-based data-fusion models have been developed to capture the complex associations and the performance in diagnosis has been improved accordingly. Moving beyond diagnosis prediction, evaluation of disease mechanisms is critically important for biomedical research. Deep-network-based data-fusion models, however, are difficult to interpret, bringing about difficulties for studying biological mechanisms. In this work, we develop an interpretable multimodal fusion model, namely gCAM-CCL, which can perform automated diagnosis and result interpretation simultaneously. The gCAM-CCL model can generate interpretable activation maps, which quantify pixel-level contributions of the input features. This is achieved by combining intermediate feature maps using gradient-based weights. Moreover, the estimated activation maps are class-specific, and the captured cross-data associations are interest/label related, which further facilitates class-specific analysis and biological mechanism analysis. We validate the gCAM-CCL model on a brain imaging-genetic study, and show gCAM-CCL's performed well for both classification and mechanism analysis. Mechanism analysis suggests that during task-fMRI scans, several object recognition related regions of interests (ROIs) are first activated and then several downstream encoding ROIs get involved. Results also suggest that the higher cognition performing group may have stronger neurotransmission signaling while the lower cognition performing group may have problem in brain/neuron development, resulting from genetic variations.

q-bio.NC↗

arXiv2020

Causal inference of brain connectivity from fMRI with $ψ$-Learning Incorporated Linear non-Gaussian Acyclic Model ($ψ$-LiNGAM)

Functional connectivity (FC) has become a primary means of understanding brain functions by identifying brain network interactions and, ultimately, how those interactions produce cognitions. A popular definition of FC is by statistical associations between measured brain regions. However, this could be problematic since the associations can only provide spatial connections but not causal interactions among regions of interests. Hence, it is necessary to study their causal relationship. Directed acyclic graph (DAG) models have been applied in recent FC studies but often encountered problems such as limited sample sizes and large number of variables (namely high-dimensional problems), which lead to both computational difficulty and convergence issues. As a result, the use of DAG models is problematic, where the identification of DAG models in general is nondeterministic polynomial time hard (NP-hard). To this end, we propose a $ψ$-learning incorporated linear non-Gaussian acyclic model ($ψ$-LiNGAM). We use the association model ($ψ$-learning) to facilitate causal inferences and the model works well especially for high-dimensional cases. Our simulation results demonstrate that the proposed method is more robust and accurate than several existing ones in detecting graph structure and direction. We then applied it to the resting state fMRI (rsfMRI) data obtained from the publicly available Philadelphia Neurodevelopmental Cohort (PNC) to study the cognitive variance, which includes 855 individuals aged 8-22 years. Therein, we have identified three types of hub structure: the in-hub, out-hub and sum-hub, which correspond to the centers of receiving, sending and relaying information, respectively. We also detected 16 most important pairs of causal flows. Several of the results have been verified to be biologically significant.

stat.ML↗

arXiv2020

A Bayesian incorporated linear non-Gaussian acyclic model for multiple directed graph estimation to study brain emotion circuit development in adolescence

Emotion perception is essential to affective and cognitive development which involves distributed brain circuits. The ability of emotion identification begins in infancy and continues to develop throughout childhood and adolescence. Understanding the development of brain's emotion circuitry may help us explain the emotional changes observed during adolescence. Our previous study delineated the trajectory of brain functional connectivity (FC) from late childhood to early adulthood during emotion identification tasks. In this work, we endeavour to deepen our understanding from association to causation. We proposed a Bayesian incorporated linear non-Gaussian acyclic model (BiLiNGAM), which incorporated our previous association model into the prior estimation pipeline. In particular, it can jointly estimate multiple directed acyclic graphs (DAGs) for multiple age groups at different developmental stages. Simulation results indicated more stable and accurate performance over various settings, especially when the sample size was small (high-dimensional cases). We then applied to the analysis of real data from the Philadelphia Neurodevelopmental Cohort (PNC). This included 855 individuals aged 8-22 years who were divided into five different adolescent stages. Our network analysis revealed the development of emotion-related intra- and inter- modular connectivity and pinpointed several emotion-related hubs. We further categorized the hubs into two types: in-hubs and out-hubs, as the center of receiving and distributing information. Several unique developmental hub structures and group-specific patterns were also discovered. Our findings help provide a causal understanding of emotion development in the human brain.

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arXiv2020

A generalized kernel machine approach to identify higher-order composite effects in multi-view datasets

In recent years, a comprehensive study of multi-view datasets (e.g., multi-omics and imaging scans) has been a focus and forefront in biomedical research. State-of-the-art biomedical technologies are enabling us to collect multi-view biomedical datasets for the study of complex diseases. While all the views of data tend to explore complementary information of a disease, multi-view data analysis with complex interactions is challenging for a deeper and holistic understanding of biological systems. In this paper, we propose a novel generalized kernel machine approach to identify higher-order composite effects in multi-view biomedical datasets. This generalized semi-parametric (a mixed-effect linear model) approach includes the marginal and joint Hadamard product of features from different views of data. The proposed kernel machine approach considers multi-view data as predictor variables to allow more thorough and comprehensive modeling of a complex trait. The proposed method can be applied to the study of any disease model, where multi-view datasets are available. We applied our approach to both synthesized datasets and real multi-view datasets from adolescence brain development and osteoporosis study, including an imaging scan dataset and five omics datasets. Our experiments demonstrate that the proposed method can effectively identify higher-order composite effects and suggest that corresponding features (genes, region of interests, and chemical taxonomies) function in a concerted effort. We show that the proposed method is more generalizable than existing ones.

stat.ML↗

arXiv2020

TZC: Efficient Inter-Process Communication for Robotics Middleware with Partial Serialization

Inter-process communication (IPC) is one of the core functions of modern robotics middleware. We propose an efficient IPC technique called TZC (Towards Zero-Copy). As a core component of TZC, we design a novel algorithm called partial serialization. Our formulation can generate messages that can be divided into two parts. During message transmission, one part is transmitted through a socket and the other part uses shared memory. The part within shared memory is never copied or serialized during its lifetime. We have integrated TZC with ROS and ROS2 and find that TZC can be easily combined with current open-source platforms. By using TZC, the overhead of IPC remains constant when the message size grows. In particular, when the message size is 4MB (less than the size of a full HD image), TZC can reduce the overhead of ROS IPC from tens of milliseconds to hundreds of microseconds and can reduce the overhead of ROS2 IPC from hundreds of milliseconds to less than 1 millisecond. We also demonstrate the benefits of TZC by integrating with TurtleBot2 that are used in autonomous driving scenarios. We show that by using TZC, the braking distance can be shortened by 16% than ROS.

cs.RO↗

arXiv2019

Brain Maturation Study during Adolescence Using Graph Laplacian Learning Based Fourier Transform

Objective: Longitudinal neuroimaging studies have demonstrated that adolescence is the crucial developmental epoch of continued brain growth and change. A large number of researchers dedicate to uncovering the mechanisms about brain maturity during adolescence. Motivated by both achievement in graph signal processing and recent evidence that some brain areas act as hubs connecting functionally specialized systems, we proposed an approach to detect these regions from spectral analysis perspective. In particular, as human brain undergoes substantial development throughout adolescence, we addressed the challenge by evaluating the functional network difference among age groups from functional magnetic resonance imaging (fMRI) observations. Methods: We treated these observations as graph signals defined on the parcellated functional brain regions and applied graph Laplacian learning based Fourier Transform (GLFT) to transform the original graph signals into frequency domain. Eigen-analysis was conducted afterwards to study the behavior of the corresponding brain regions, which enables the characterization of brain maturation. Result: We first evaluated our method on the synthetic data and further applied the method to resting and task state fMRI imaging data from Philadelphia Neurodevelopmental Cohort (PNC) dataset, comprised of normally developing adolescents from 8 to 22. The model provided a highest accuracy of 95.69% in distinguishing different adolescence stages. Conclusion: We detected 13 hubs from resting state fMRI and 16 hubs from task state fMRI that are highly related to brain maturation process. Significance: The proposed GLFT method is powerful in extracting the brain connectivity patterns and identifying hub regions with a high prediction power

q-bio.NC↗

arXiv2019

Multimodal Sparse Classifier for Adolescent Brain Age Prediction

The study of healthy brain development helps to better understand the brain transformation and brain connectivity patterns which happen during childhood to adulthood. This study presents a sparse machine learning solution across whole-brain functional connectivity (FC) measures of three sets of data, derived from resting state functional magnetic resonance imaging (rs-fMRI) and task fMRI data, including a working memory n-back task (nb-fMRI) and an emotion identification task (em-fMRI). These multi-modal image data are collected on a sample of adolescents from the Philadelphia Neurodevelopmental Cohort (PNC) for the prediction of brain ages. Due to extremely large variable-to-instance ratio of PNC data, a high dimensional matrix with several irrelevant and highly correlated features is generated and hence a pattern learning approach is necessary to extract significant features. We propose a sparse learner based on the residual errors along the estimation of an inverse problem for the extreme learning machine (ELM) neural network. The purpose of the approach is to overcome the overlearning problem through pruning of several redundant features and their corresponding output weights. The proposed multimodal sparse ELM classifier based on residual errors (RES-ELM) is highly competitive in terms of the classification accuracy compared to its counterparts such as conventional ELM, and sparse Bayesian learning ELM.

cs.LG↗

arXiv2019

A Manifold Regularized Multi-Task Learning Model for IQ Prediction from Multiple fMRI Paradigms

Multi-modal brain functional connectivity (FC) data have shown great potential for providing insights into individual variations in behavioral and cognitive traits. The joint learning of multi-modal imaging data can utilize the intrinsic association, and thus can boost the learning performance. Although several multi-task based learning models have already been proposed by viewing the feature learning on each modality as one task, most of them ignore the geometric structure information inherent in the modalities, which may play an important role in extracting discriminative features. In this paper, we propose a new manifold regularized multi-task learning model by simultaneously considering between-subject and between-modality relationships. Besides employing a group-sparsity regularizer to jointly select a few common features across multiple tasks (modalities), we design a novel manifold regularizer to preserve the structure information both within and between modalities in our model. This will make our model more adaptive for realistic data analysis. Our model is then validated on the Philadelphia Neurodevelopmental Cohort dataset, where we regard our modalities as functional MRI (fMRI) data collected under two paradigms. Specifically, we conduct experimental studies on fMRI based FC network data in two task conditions for intelligence quotient (IQ) prediction. The results demonstrate that our proposed model can not only achieve improved prediction performance, but also yield a set of IQ-relevant biomarkers.

q-bio.QM↗

arXiv2018

Alternating Diffusion Map Based Fusion of Multimodal Brain Connectivity Networks for IQ Prediction

To explain individual differences in development, behavior, and cognition, most previous studies focused on projecting resting-state functional MRI (fMRI) based functional connectivity (FC) data into a low-dimensional space via linear dimensionality reduction techniques, followed by executing analysis operations. However, linear dimensionality analysis techniques may fail to capture nonlinearity of brain neuroactivity. Moreover, besides resting-state FC, FC based on task fMRI can be expected to provide complementary information. Motivated by these considerations, we nonlinearly fuse resting-state and task-based FC networks (FCNs) to seek a better representation in this paper. We propose a framework based on alternating diffusion map (ADM), which extracts geometry-preserving low-dimensional embeddings that successfully parameterize the intrinsic variables driving the phenomenon of interest. Specifically, we first separately build resting-state and task-based FCNs by symmetric positive definite matrices using sparse inverse covariance estimation for each subject, and then utilize the ADM to fuse them in order to extract significant low-dimensional embeddings, which are used as fingerprints to identify individuals. The proposed framework is validated on the Philadelphia Neurodevelopmental Cohort data, where we conduct extensive experimental study on resting-state and fractal $n$-back task fMRI for the classification of intelligence quotient (IQ). The fusion of resting-state and $n$-back task fMRI by the proposed framework achieves better classification accuracy than any single fMRI, and the proposed framework is shown to outperform several other data fusion methods. To our knowledge, this paper is the first to demonstrate a successful extension of the ADM to fuse resting-state and task-based fMRI data for accurate prediction of IQ.

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arXiv2018

Spectral Resolution Clustering for Brain Parcellation

We take an image science perspective on the problem of determining brain network connectivity given functional activity. But adapting the concept of image resolution to this problem, we provide a new perspective on network partitioning for individual brain parcellation. The typical goal here is to determine densely-interconnected subnetworks within a larger network by choosing the best edges to cut. We instead define these subnetworks as resolution cells, where highly-correlated activity within the cells makes edge weights difficult to determine from the data. Subdividing the resolution estimates into disjoint resolution cells via clustering yields a new variation, and new perspective, on spectral clustering. This provides insight and strategies for open questions such as the selection of model order and the optimal choice of preprocessing steps for functional imaging data. The approach is demonstrated using functional imaging data, where we find the proposed approach produces parcellations which are more predictive across multiple scans versus conventional methods, as well as versus alternative forms of spectral clustering.

q-bio.NC↗

arXiv2018

FDR-Corrected Sparse Canonical Correlation Analysis with Applications to Imaging Genomics

Reducing the number of false discoveries is presently one of the most pressing issues in the life sciences. It is of especially great importance for many applications in neuroimaging and genomics, where datasets are typically high-dimensional, which means that the number of explanatory variables exceeds the sample size. The false discovery rate (FDR) is a criterion that can be employed to address that issue. Thus it has gained great popularity as a tool for testing multiple hypotheses. Canonical correlation analysis (CCA) is a statistical technique that is used to make sense of the cross-correlation of two sets of measurements collected on the same set of samples (e.g., brain imaging and genomic data for the same mental illness patients), and sparse CCA extends the classical method to high-dimensional settings. Here we propose a way of applying the FDR concept to sparse CCA, and a method to control the FDR. The proposed FDR correction directly influences the sparsity of the solution, adapting it to the unknown true sparsity level. Theoretical derivation as well as simulation studies show that our procedure indeed keeps the FDR of the canonical vectors below a user-specified target level. We apply the proposed method to an imaging genomics dataset from the Philadelphia Neurodevelopmental Cohort. Our results link the brain connectivity profiles derived from brain activity during an emotion identification task, as measured by functional magnetic resonance imaging (fMRI), to the corresponding subjects' genomic data.

stat.ME↗

arXiv2018

A Model of the Collapse and Evaporation of Charged Black Holes

In this paper, a natural generalization of KMY model is proposed for the evaporation of charged black holes. Within the proposed model, the back reaction of Hawking radiation is considered. More specifically, we consider the equation $G_{μν} = 8π\langle T_{μν}\rangle$, in which the matter content $\langle T_{μν}\rangle$ is assumed spherically symmetric. With this equation of motion, the asymptotic behavior of the model is analyzed. Two kinds of matter contents are taken into consideration in this paper. In the first case (the thin-shell model), the infalling matter is simulated by a null-like charged sphere collapsing into its center. In the second case, we consider a continuous distribution of spherical symmetric infalling null-like charged matter. It is simulated by taking the continuous limit of many co-centric spheres collapsing into the center. We find that in the thin-shell case, an event horizon forms and the shell passes through the horizon before becoming extremal, provided that it is not initially near-extremal. In the case of continuous matter distribution, we consider explicitly an extremal center covered by neutral infalling matter and find that the event horizon also forms. The black hole itself will become near-extremal eventually, leaving possibly a non-electromagnetic energy residue less than the order of $\ell_{p}^{4}/e_{0}^{3}$. The details of the behavior of these models are explicitly worked out in this paper.

gr-qc↗

arXiv2017

Kernel Method for Detecting Higher Order Interactions in multi-view Data: An Application to Imaging, Genetics, and Epigenetics

In this study, we tested the interaction effect of multimodal datasets using a novel method called the kernel method for detecting higher order interactions among biologically relevant mulit-view data. Using a semiparametric method on a reproducing kernel Hilbert space (RKHS), we used a standard mixed-effects linear model and derived a score-based variance component statistic that tests for higher order interactions between multi-view data. The proposed method offers an intangible framework for the identification of higher order interaction effects (e.g., three way interaction) between genetics, brain imaging, and epigenetic data. Extensive numerical simulation studies were first conducted to evaluate the performance of this method. Finally, this method was evaluated using data from the Mind Clinical Imaging Consortium (MCIC) including single nucleotide polymorphism (SNP) data, functional magnetic resonance imaging (fMRI) scans, and deoxyribonucleic acid (DNA) methylation data, respectfully, in schizophrenia patients and healthy controls. We treated each gene-derived SNPs, region of interest (ROI) and gene-derived DNA methylation as a single testing unit, which are combined into triplets for evaluation. In addition, cardiovascular disease risk factors such as age, gender, and body mass index were assessed as covariates on hippocampal volume and compared between triplets. Our method identified $13$-triplets ($p$-values $\leq 0.001$) that included $6$ gene-derived SNPs, $10$ ROIs, and $6$ gene-derived DNA methylations that correlated with changes in hippocampal volume, suggesting that these triplets may be important in explaining schizophrenia-related neurodegeneration. With strong evidence ($p$-values $\leq 0.000001$), the triplet ({\bf MAGI2, CRBLCrus1.L, FBXO28}) has the potential to distinguish schizophrenia patients from the healthy control variations.

stat.ML↗

arXiv2017

Influence Function and Robust Variant of Kernel Canonical Correlation Analysis

Many unsupervised kernel methods rely on the estimation of the kernel covariance operator (kernel CO) or kernel cross-covariance operator (kernel CCO). Both kernel CO and kernel CCO are sensitive to contaminated data, even when bounded positive definite kernels are used. To the best of our knowledge, there are few well-founded robust kernel methods for statistical unsupervised learning. In addition, while the influence function (IF) of an estimator can characterize its robustness, asymptotic properties and standard error, the IF of a standard kernel canonical correlation analysis (standard kernel CCA) has not been derived yet. To fill this gap, we first propose a robust kernel covariance operator (robust kernel CO) and a robust kernel cross-covariance operator (robust kernel CCO) based on a generalized loss function instead of the quadratic loss function. Second, we derive the IF for robust kernel CCO and standard kernel CCA. Using the IF of the standard kernel CCA, we can detect influential observations from two sets of data. Finally, we propose a method based on the robust kernel CO and the robust kernel CCO, called {\bf robust kernel CCA}, which is less sensitive to noise than the standard kernel CCA. The introduced principles can also be applied to many other kernel methods involving kernel CO or kernel CCO. Our experiments on synthesized data and imaging genetics analysis demonstrate that the proposed IF of standard kernel CCA can identify outliers. It is also seen that the proposed robust kernel CCA method performs better for ideal and contaminated data than the standard kernel CCA.

stat.ML↗

arXiv2016

Learning Schizophrenia Imaging Genetics Data Via Multiple Kernel Canonical Correlation Analysis

Kernel and Multiple Kernel Canonical Correlation Analysis (CCA) are employed to classify schizophrenic and healthy patients based on their SNPs, DNA Methylation and fMRI data. Kernel and Multiple Kernel CCA are popular methods for finding nonlinear correlations between high-dimensional datasets. Data was gathered from 183 patients, 79 with schizophrenia and 104 healthy controls. Kernel and Multiple Kernel CCA represent new avenues for studying schizophrenia, because, to our knowledge, these methods have not been used on these data before. Classification is performed via k-means clustering on the kernel matrix outputs of the Kernel and Multiple Kernel CCA algorithm. Accuracies of the Kernel and Multiple Kernel CCA classification are compared to that of the regularized linear CCA algorithm classification, and are found to be significantly more accurate. Both algorithms demonstrate maximal accuracies when the combination of DNA methylation and fMRI data are used, and experience lower accuracies when the SNP data are incorporated.

q-bio.QM↗

arXiv2016

Identifying Outliers using Influence Function of Multiple Kernel Canonical Correlation Analysis

Imaging genetic research has essentially focused on discovering unique and co-association effects, but typically ignoring to identify outliers or atypical objects in genetic as well as non-genetics variables. Identifying significant outliers is an essential and challenging issue for imaging genetics and multiple sources data analysis. Therefore, we need to examine for transcription errors of identified outliers. First, we address the influence function (IF) of kernel mean element, kernel covariance operator, kernel cross-covariance operator, kernel canonical correlation analysis (kernel CCA) and multiple kernel CCA. Second, we propose an IF of multiple kernel CCA, which can be applied for more than two datasets. Third, we propose a visualization method to detect influential observations of multiple sources of data based on the IF of kernel CCA and multiple kernel CCA. Finally, the proposed methods are capable of analyzing outliers of subjects usually found in biomedical applications, in which the number of dimension is large. To examine the outliers, we use the stem-and-leaf display. Experiments on both synthesized and imaging genetics data (e.g., SNP, fMRI, and DNA methylation) demonstrate that the proposed visualization can be applied effectively.

stat.ML↗

arXiv2016

Gene-Gene association for Imaging Genetics Data using Robust Kernel Canonical Correlation Analysis

In genome-wide interaction studies, to detect gene-gene interactions, most methods are divided into two folds: single nucleotide polymorphisms (SNP) based and gene-based methods. Basically, the methods based on the gene are more effective than the methods based on a single SNP. Recent years, while the kernel canonical correlation analysis (Classical kernel CCA) based U statistic (KCCU) has proposed to detect the nonlinear relationship between genes. To estimate the variance in KCCU, they have used resampling based methods which are highly computationally intensive. In addition, classical kernel CCA is not robust to contaminated data. We, therefore, first discuss robust kernel mean element, the robust kernel covariance, and cross-covariance operators. Second, we propose a method based on influence function to estimate the variance of the KCCU. Third, we propose a nonparametric robust KCCU method based on robust kernel CCA, which is designed for contaminated data and less sensitive to noise than classical kernel CCA. Finally, we investigate the proposed methods to synthesized data and imaging genetic data set. Based on gene ontology and pathway analysis, the synthesized and genetics analysis demonstrate that the proposed robust method shows the superior performance of the state-of-the-art methods.

stat.ML↗