Hi,

I've poked around a little more, and I'm wondering if L2 normalization would 
ameliorate my second issue regarding lesion size being a confounding factor in 
my classification? 
http://www.pymvpa.org/generated/mvpa.misc.transformers.l2_normed.html

At the end of the day, all I mainly want to ensure that (a) 0/1 scaling is 
correct and (b) determine how much of the CV is due to lesion size alone. If it 
were a simpler univariate regression, I could include lesion size as a 
covariate, but I'm not sure how to do something analogous in PyMVPA.

Thanks!
David


On Sep 6, 2011, at 12:52 AM, David V. Smith wrote:

> 
> Hello,
> 
> I have lesion data, and I am trying to test whether particular patterns of 
> lesions distinguish two classes of patients. I have two questions:
> 
> 1) What is the best way to scale the lesion data? Traditionally, these data 
> are represented with 1s (lesion) and 0s (no lesion). I've played around with 
> different scalings, and I've gotten different (but replicable) results using 
> the SMLR classifier in PyMVPA 0.4. See below: first column is the 
> leave-one-out CV; second column the value for the spared voxels; third column 
> is the value for the damaged voxels.
> CV    NoLesion        Lesion
> 83.571        000     001
> 75.000        001     002
> 77.143        002     004
> 81.429        100     200
> 81.429        200     400
> 
> 2.) What is the best way to control for a nuisance factor? I know there is an 
> additional variable (i.e., lesion volume) that can distinguish between my two 
> patient groups, so I would like the resulting CV and heavily weighted voxels 
> to be uncontaminated by this nuisance factor. Ideally, I would like to know 
> how much additional predictive power is gained over and above this nuisance 
> factor. 
> 
> Thanks,
> David
> 
> 
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