{"title":"Sparse Graphical Modeling for Electrophysiological Phase-Based Connectivity Using Circular Statistics.","authors":"Issey Sukeda, Takeru Matsuda","doi":"10.1162/NECO.a.1536","DOIUrl":null,"url":null,"abstract":"<p><p>Identifying phase coupling from electrophysiological signals recorded by multiple electrodes, such as electroencephalogram (EEG) and electrocorticography (ECoG), helps neuroscientists and clinicians understand underlying brain structures or mechanisms. From a statistical perspective, these signals are multidimensional circular measurements that are correlated with one another and can be effectively modeled using a torus graph model designed for circular random variables. Using the torus graph model avoids the issue of detecting spurious correlations. However, the naive estimation of this model tends to lead to a dense network structure that is difficult to interpret. Therefore, to enhance the interpretability of the brain network structure, this review proposes a sparse estimation method for the torus graph model using regularized score matching combined with information criteria. In numerical simulations, our method successfully recovered the true dependence structure from a synthetic data set. Furthermore, we present analyses of two real data sets, one involving human EEG and the other marmoset ECoG, demonstrating that our method can be widely applied to phase-coupling analysis across different types of neural data. We found that when we used our proposed method, the modularity of the estimated network structure revealed more resolved brain structures and demonstrated differences in trends among individuals.</p>","PeriodicalId":54731,"journal":{"name":"Neural Computation","volume":"38 7","pages":"1135-1179"},"PeriodicalIF":2.1000,"publicationDate":"2026-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neural Computation","FirstCategoryId":"94","ListUrlMain":"https://doi.org/10.1162/NECO.a.1536","RegionNum":4,"RegionCategory":"计算机科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"COMPUTER SCIENCE, ARTIFICIAL INTELLIGENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Identifying phase coupling from electrophysiological signals recorded by multiple electrodes, such as electroencephalogram (EEG) and electrocorticography (ECoG), helps neuroscientists and clinicians understand underlying brain structures or mechanisms. From a statistical perspective, these signals are multidimensional circular measurements that are correlated with one another and can be effectively modeled using a torus graph model designed for circular random variables. Using the torus graph model avoids the issue of detecting spurious correlations. However, the naive estimation of this model tends to lead to a dense network structure that is difficult to interpret. Therefore, to enhance the interpretability of the brain network structure, this review proposes a sparse estimation method for the torus graph model using regularized score matching combined with information criteria. In numerical simulations, our method successfully recovered the true dependence structure from a synthetic data set. Furthermore, we present analyses of two real data sets, one involving human EEG and the other marmoset ECoG, demonstrating that our method can be widely applied to phase-coupling analysis across different types of neural data. We found that when we used our proposed method, the modularity of the estimated network structure revealed more resolved brain structures and demonstrated differences in trends among individuals.
期刊介绍:
Neural Computation is uniquely positioned at the crossroads between neuroscience and TMCS and welcomes the submission of original papers from all areas of TMCS, including: Advanced experimental design; Analysis of chemical sensor data; Connectomic reconstructions; Analysis of multielectrode and optical recordings; Genetic data for cell identity; Analysis of behavioral data; Multiscale models; Analysis of molecular mechanisms; Neuroinformatics; Analysis of brain imaging data; Neuromorphic engineering; Principles of neural coding, computation, circuit dynamics, and plasticity; Theories of brain function.