Comparison of TCA and ICA techniques in fMRI data processing

Purpose To make a quantitative comparison of temporal cluster analysis (TCA) and independent component analysis (ICA) techniques in detecting brain activation by using simulated data and in vivo event‐related functional MRI (fMRI) experiments. Materials and Methods A single‐slice MRI image was repli...

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Published inJournal of magnetic resonance imaging Vol. 19; no. 4; pp. 397 - 402
Main Authors Zhao, Xia, Glahn, David, Tan, Li Hai, Li, Ning, Xiong, Jinhu, Gao, Jia-Hong
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.04.2004
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Summary:Purpose To make a quantitative comparison of temporal cluster analysis (TCA) and independent component analysis (ICA) techniques in detecting brain activation by using simulated data and in vivo event‐related functional MRI (fMRI) experiments. Materials and Methods A single‐slice MRI image was replicated 150 times to simulate an fMRI time series. An event‐related brain activation pattern with five different levels of intensity and Gaussian noise was superimposed on these images. Maximum contrast‐to‐noise ratio (CNR) of the signal change ranged from 1.0 to 2.0 by 0.25 increments. In vivo visual stimulation fMRI experiments were performed on a 1.9 T magnet. Six human volunteers participated in this study. All imaging data were analyzed using both TCA and ICA methods. Results Both simulated and in vivo data have shown that no statistically significant difference exists in the activation areas detected by both ICA and TCA techniques when CNR of fMRI signal is larger than 1.75. Conclusion TCA and ICA techniques are comparable in generating functional brain maps in event‐related fMRI experiments. Although ICA has richer features in exploring the spatial and temporal information of the functional images, the TCA method has advantages in its computational efficiency, repeatability, and readiness to average data from group subjects. J. Magn. Reson. Imaging 2004;19:397–402. © 2004 Wiley‐Liss, Inc.
Bibliography:NIH - No. RR17198; No. AG19844
istex:F916EEC127A578D5E89DCE5578104F0A7E911934
Office of National Drug Control Policy, U.S. - No. DABK39-03-C-0047
National Natural Science Foundation of China - No. 30128005
ArticleID:JMRI20023
ark:/67375/WNG-3DQM8Q1W-Q
Hong Kong Research Grants Council Central Allocation Vote - No. HKU 3/02C
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:1053-1807
1522-2586
DOI:10.1002/jmri.20023