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Mathematics in Independent Component Analysis

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44 Chapter 1. Statistical mach<strong>in</strong>e learn<strong>in</strong>g of biomedical data<br />

(a) general l<strong>in</strong>ear model analysis (b) one <strong>in</strong>dependent component<br />

Figure 1.22: Comparison of model-based and model-free analysis of a word-perception fMRI<br />

experiment. (a) illustrates the result of a regression-based analysis, which shows actitity mostly<br />

<strong>in</strong> the auditive cortex. (b) is a s<strong>in</strong>gle component extracted by ICA, which is corresponds to a<br />

word-detection network.<br />

with a resolution of 3 × 3 × 4 mm. A s<strong>in</strong>gle 2d-slice is analyzed, which is oriented parallel to<br />

the calcar<strong>in</strong>e fissure. Photic stimulation was performed us<strong>in</strong>g an 8 Hz alternat<strong>in</strong>g checkerboard<br />

stimulus with a central fixation po<strong>in</strong>t and a dark background.<br />

At first, we show an example result us<strong>in</strong>g spatial ICA. We perform a dimension reduction us<strong>in</strong>g<br />

PCA to n = 6 dimensions, which still conta<strong>in</strong>ed 99.77% of the eigenvalues. Then, we applied<br />

HessianICA with K = 100 Hessians evaluated at randomly chosen samples, see section 1.2.1 and<br />

Theis (2004a). The result<strong>in</strong>g 6-dimensional sources are <strong>in</strong>terpreted as the 6 component maps<br />

that encode the data set. The columns of the mix<strong>in</strong>g matrix conta<strong>in</strong> the relative contribution of<br />

each component map to the mixtures at the given time po<strong>in</strong>t, so they represent the components’<br />

time courses. The maps together with the correspond<strong>in</strong>g time courses are shown <strong>in</strong> figure 1.23.<br />

A s<strong>in</strong>gle highly task-related component (#4) is found, which after a shift of 4s has a high crosscorrelation<br />

with the block-based stimulus (cc = 0.89). Other component maps encode artifacts,<br />

e.g. <strong>in</strong> the <strong>in</strong>terstitial bra<strong>in</strong> region and other background activity.<br />

We then tested the usefulness of tak<strong>in</strong>g <strong>in</strong>to account additional <strong>in</strong>formation conta<strong>in</strong>ed <strong>in</strong><br />

the data set such as the spatiotemporal dependencies. For this, we analyzed the data us<strong>in</strong>g<br />

spatiotemporal BSS as described <strong>in</strong> section 1.3.2 and Theis et al. (2005b), Theis et al. (2007b),<br />

see chapter 9. In order to make th<strong>in</strong>gs more challeng<strong>in</strong>g, only 4 components were to be extracted<br />

from the data, with preprocess<strong>in</strong>g either by PCA only or by the slightly more general s<strong>in</strong>gular<br />

value decomposition, a necessary preprocess<strong>in</strong>g for spatiotemporal BSS. We based the algorithms<br />

on jo<strong>in</strong>t diagonalization, for which K = 10 autocorrelation matrices were used, both for spatial<br />

and temporal decorrelation, weighted equally (α = 0.5). Although the data was reduced to only<br />

4 components, stSOBI was able to extract the stimulus component very well, with a equally<br />

high crosscorrelation of cc = 0.89. We compared this result with some established algorithms<br />

for bl<strong>in</strong>d fMRI analysis by discuss<strong>in</strong>g the s<strong>in</strong>gle component that is maximally autocorrelated

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