Literature DB >> 26993820

The role of diversity in complex ICA algorithms for fMRI analysis.

Wei Du1, Yuri Levin-Schwartz2, Geng-Shen Fu1, Sai Ma1, Vince D Calhoun3, Tülay Adalı1.   

Abstract

BACKGROUND: The widespread use of data-driven methods, such as independent component analysis (ICA), for the analysis of functional magnetic resonance imaging data (fMRI) has enabled deeper understanding of neural function. However, most popular ICA algorithms for fMRI analysis make several simplifying assumptions, thus ignoring sources of statistical information, types of "diversity," and limiting their performance. NEW
METHOD: We propose the use of complex entropy rate bound minimization (CERBM) for the analysis of actual fMRI data in its native, complex, domain. Though CERBM achieves enhanced performance through the exploitation of the three types of diversity inherent to complex fMRI data: noncircularity, non-Gaussianity, and sample-to-sample dependence, CERBM produces results that are more variable than simpler methods. This motivates the development of a minimum spanning tree (MST)-based stability analysis that mitigates the variability of CERBM. COMPARISON WITH EXISTING
METHODS: In order to validate our method, we compare the performance of CERBM with the popular CInfomax as well as complex entropy bound minimization (CEBM).
RESULTS: We show that by leveraging CERBM and the MST-based stability analysis, we are able to consistently produce components that have a greater number of activated voxels in physically meaningful regions and can more accurately classify patients with schizophrenia than components generated using simpler models.
CONCLUSIONS: Our results demonstrate the advantages of using ICA algorithms that can exploit all inherent types of diversity for the analysis of fMRI data when coupled with appropriate stability analyses.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  AOD task; Complex fMRI; ICA

Mesh:

Year:  2016        PMID: 26993820      PMCID: PMC4833547          DOI: 10.1016/j.jneumeth.2016.03.012

Source DB:  PubMed          Journal:  J Neurosci Methods        ISSN: 0165-0270            Impact factor:   2.390


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