Hi

> On 12 Apr 2015, at 17:15, Nomi, Jason <[email protected]> wrote:
> 
> Thank you Steve!
> 
> Yes - I was speaking about the group-ICA spatial maps.  I have noticed that I 
> can threshold the group-ICA spatial maps for each component at a much higher 
> level than other ICAs that I have done on non-HCP data.  
> 
> Your explanation about strong CNR makes sense.  
> 
> I am still a little unclear about the relationship of instantiating a strong 
> threshold on the group-ICA spatial maps relative to the time series. 

there is no thresholding in the dual-regression approach - it's a multiple 
spatial (or temporal depending on the stage) regression.   
Eg in stage 1, the multiple unthresholded spatial maps are the multiple 
regressors - with all voxels used, but the higher-valued ones "used more".

Cheers


> 
> For example, if I threshold a component's spatial map at a lower level, more 
> areas of activation will naturally show up.  Does the time series represent 
> all voxels in the spatial map when there is no thresholding?  Or, does the 
> time series represent only the strongest voxels of activation?  
> 
> Thus, when I apply a strong threshold for image presentation to "clean up" 
> the image a little, does the time series also include those voxels that are 
> not visible due to high thresholding?   
> 
> Thanks again!
> 
> Jason
> 
> 
> From: Stephen Smith <[email protected]>
> Sent: Saturday, April 11, 2015 3:29 AM
> To: Nomi, Jason
> Cc: [email protected]
> Subject: Re: [HCP-Users] Parcellated Connectome
>  
> Hi - there are many factors that affect overall scaling - more below:
> 
> 
>> On 10 Apr 2015, at 14:22, Nomi, Jason <[email protected] 
>> <mailto:[email protected]>> wrote:
>> 
>> Dear Experts,
>> 
>> I have noticed that the time-series for individual subjects from the dual 
>> regression output in the parcellated connectome (100 comp ICA) has a much 
>> larger range than I am used to seeing.
>> 
>> The range for time series values are approximately -800 to 800 while dual 
>> regression outputs that I have conducted myself are usually around -5 to 5.  
>> 
>> I also notice that I can set the threshold much higher for the independent 
>> components when isolating activation compared to dual regression analyses 
>> that I have done myself. This "cleans up" the component representation 
>> substantially.  
>> 
>> My questions are:
>> 
>> 1) Is there a particular reason for this large increase in ranges?
>> 
> 
> In this case most likely because we set the max of the group maps used in 
> dualreg stage 1 to be 1. This causes output timeseries to have larger scaling 
> - but the overall scaling is arbitrary anyway.
> 
>> 
>> 2) Does the larger threshold for component activation have any influence on 
>> the time series that is being produced?  Does the time series from the dual 
>> regression output only represent the areas from the independent component 
>> with the most intense activation?  I would like to ensure that my 
>> presentation of component images using a much higher threshold is actually 
>> representative of the time series that I am analyzing.  
>> 
> 
> Do you mean the group-ICA spatial maps or maps output by diualreg stage 2?
> 
> The group-ICA maps have high peaks (compared with the background scaling) for 
> a couple of reasons:  a) because there are so many subjects being combined 
> that  the ICA components are strong, and b) the group-PCA reduction has 
> removed a lot of unstructured noise before the PCA+ICA step.  But despite the 
> maps having strong "CNR", they are still valid maps.
> 
> Cheers, Steve.
> 
> 
> 
>> 
>> Thanks!
>> 
>> Jason
>> 
>> 
>> 
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> 
> 
> ---------------------------------------------------------------------------
> Stephen M. Smith, Professor of Biomedical Engineering
> Associate Director,  Oxford University FMRIB Centre
> 
> FMRIB, JR Hospital, Headington, Oxford  OX3 9DU, UK
> +44 (0) 1865 222726  (fax 222717)
> [email protected] <mailto:[email protected]>    
> http://www.fmrib.ox.ac.uk/~steve <http://www.fmrib.ox.ac.uk/~steve>
> ---------------------------------------------------------------------------
> 
> Stop the cultural destruction of Tibet <http://smithinks.net/>
> 
> 
> 
> 


---------------------------------------------------------------------------
Stephen M. Smith, Professor of Biomedical Engineering
Associate Director,  Oxford University FMRIB Centre

FMRIB, JR Hospital, Headington, Oxford  OX3 9DU, UK
+44 (0) 1865 222726  (fax 222717)
[email protected]    http://www.fmrib.ox.ac.uk/~steve 
<http://www.fmrib.ox.ac.uk/~steve>
---------------------------------------------------------------------------

Stop the cultural destruction of Tibet <http://smithinks.net/>





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