Cross-Spectral Factor Analysis

被引:0
|
作者
Gallagher, Neil M. [1 ]
Ulrich, Kyle [2 ]
Talbot, Austin [3 ]
Dzirasa, Kafui [1 ,4 ]
Carin, Lawrence [2 ]
Carlson, David E. [5 ,6 ]
机构
[1] Duke Univ, Dept Neurobiol, Durham, NC 27706 USA
[2] Duke Univ, Dept Elect & Comp Engn, Durham, NC 27706 USA
[3] Duke Univ, Dept Stat Sci, Durham, NC 27706 USA
[4] Duke Univ, Dept Psychiat & Behav Sci, Durham, NC 27706 USA
[5] Duke Univ, Dept Civil & Environm Engn, Durham, NC 27706 USA
[6] Duke Univ, Dept Biostat & Bioinformat, Durham, NC 27706 USA
基金
美国国家卫生研究院;
关键词
D O I
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中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
In neuropsychiatric disorders such as schizophrenia or depression, there is often a disruption in the way that regions of the brain synchronize with one another. To facilitate understanding of network-level synchronization between brain regions, we introduce a novel model of multisite low-frequency neural recordings, such as local field potentials (LFPs) and electroencephalograms (EEGs). The proposed model, named Cross-Spectral Factor Analysis (CSFA), breaks the observed signal into factors defined by unique spatio-spectral properties. These properties are granted to the factors via a Gaussian process formulation in a multiple kernel learning framework. In this way, the LFP signals can be mapped to a lower dimensional space in a way that retains information of relevance to neuroscientists. Critically, the factors are interpretable. The proposed approach empirically allows similar performance in classifying mouse genotype and behavioral context when compared to commonly used approaches that lack the interpretability of CSFA. We also introduce a semi-supervised approach, termed discriminative CSFA (dCSFA). CSFA and dCSFA provide useful tools for understanding neural dynamics, particularly by aiding in the design of causal follow-up experiments.
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页数:11
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