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 in | Journal of magnetic resonance imaging Vol. 19; no. 4; pp. 397 - 402 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.04.2004
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Subjects | |
Online Access | Get full text |
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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. |
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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 |