Evren Gokcen, Anna I Jasper, Adam Kohn, Christian K Machens, Byron M Yu
{"title":"Fast Multigroup Gaussian Process Factor Models.","authors":"Evren Gokcen, Anna I Jasper, Adam Kohn, Christian K Machens, Byron M Yu","doi":"10.1162/neco.a.22","DOIUrl":null,"url":null,"abstract":"<p><p>Gaussian processes are now commonly used in dimensionality-reduction approaches tailored to neuroscience, especially to describe changes in high-dimensional neural activity over time. As recording capabilities expand to include neuronal populations across multiple brain areas, cortical layers, and cell types, interest in extending gaussian process factor models to characterize multipopulation interactions has grown. However, the cubic run-time scaling of current methods with the length of experimental trials and the number of recorded populations (groups) precludes their application to large-scale multipopulation recordings. Here, we improve this scaling from cubic to linear in both trial length and group number. We present two approximate approaches to fitting multigroup gaussian process factor models based on inducing variables and the frequency domain. Empirically, both methods achieved orders of magnitude speed-up with minimal impact on statistical performance, in simulation and on neural recordings of hundreds of neurons across three brain areas. The frequency domain approach, in particular, consistently provided the greatest run-time benefits with the fewest trade-offs in statistical performance. We further characterize the estimation biases introduced by the frequency domain approach and demonstrate effective strategies to mitigate them. This work enables a powerful class of analysis techniques to keep pace with the growing scale of multipopulation recordings, opening new avenues for exploring brain function.</p>","PeriodicalId":54731,"journal":{"name":"Neural Computation","volume":" ","pages":"1-74"},"PeriodicalIF":2.1000,"publicationDate":"2025-07-24","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.22","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
Gaussian processes are now commonly used in dimensionality-reduction approaches tailored to neuroscience, especially to describe changes in high-dimensional neural activity over time. As recording capabilities expand to include neuronal populations across multiple brain areas, cortical layers, and cell types, interest in extending gaussian process factor models to characterize multipopulation interactions has grown. However, the cubic run-time scaling of current methods with the length of experimental trials and the number of recorded populations (groups) precludes their application to large-scale multipopulation recordings. Here, we improve this scaling from cubic to linear in both trial length and group number. We present two approximate approaches to fitting multigroup gaussian process factor models based on inducing variables and the frequency domain. Empirically, both methods achieved orders of magnitude speed-up with minimal impact on statistical performance, in simulation and on neural recordings of hundreds of neurons across three brain areas. The frequency domain approach, in particular, consistently provided the greatest run-time benefits with the fewest trade-offs in statistical performance. We further characterize the estimation biases introduced by the frequency domain approach and demonstrate effective strategies to mitigate them. This work enables a powerful class of analysis techniques to keep pace with the growing scale of multipopulation recordings, opening new avenues for exploring brain function.
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.