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        <rdf:li rdf:resource="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1488"/>
        <rdf:li rdf:resource="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1481"/>
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    <link>http://gmane.org</link>
  </image>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1505">
    <title>error relating to opening an image file when doingroi analysis.</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1505</link>
    <description>&lt;pre&gt;To whom it may concern:

I am trying to do the roi batch analysis on my fmri data. But I encounter a 
problem. 

For some subjects data, I could not open the image file. See the error message 
below: 

MarsBaR analysis functions prepended to path
Design reporting                        :                        ...done
Fetching data                           :                         1/1   ??? 
Error using ==&amp;gt; spm_sample_vol
Cant open image file.

Error in ==&amp;gt; maroi.getdata at 103
  data = spm_sample_vol(data_imgs(i),...

Error in ==&amp;gt; maroi.get_marsy at 76
  [y vals vXYZ mat]  = getdata(o, VY);

Error in ==&amp;gt; marsbar at 985
marsY = get_marsy(o{:}, VY, sumfunc, 'v');

Error in ==&amp;gt; spm at 982
evalin('base',CBs{v-1})
 
??? Error while evaluating uicontrol Callback

I ever tried to search on the mailinglist to find some answers. But it seems 
that there are no definitive replies. 

Does anyone here know about it and how to fix it?

Thanks for your consideration in advance.

Best,
li


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&lt;/pre&gt;</description>
    <dc:creator>Yansong</dc:creator>
    <dc:date>2012-05-25T10:04:26</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1500">
    <title>Percent signal change calculation</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1500</link>
    <description>&lt;pre&gt;Hi,

When I did SPM analysis, I modeled  the events with HRF and both time derivative and dispersion derivative. Will this affect the percent signal change calculation? And we also have a default baseline (directional arrow images), will this affect the reliability of the method? Can area under the curve calculation be an alternative method for ROI analysis? Thank you!

Yan

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&lt;/pre&gt;</description>
    <dc:creator>Yan Fang</dc:creator>
    <dc:date>2012-04-27T23:09:56</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1494">
    <title>Q regarding Extract Roi (Full Options)</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1494</link>
    <description>&lt;pre&gt;Hey All,
A couple of questions regarding some of the options/functions of Extract Roi(Full Options)...

1. Is it appropriate to use this function directly on the .con files generated after running your GLM (assuming that you choose not to specify a SPM.mat)? 

2. What is the nature of the value generated when you select raw data? That is, what does the value represent with respect to the contrast I have selected. A colleague of mine suggested that it was derived from the Betas in the selected .con, but I am not so sure. Anyone have any ideas?

Thanks in advance,
Andrew Furman
Graduate Student - Johns Hopkins University

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&lt;/pre&gt;</description>
    <dc:creator>Andrew Furman</dc:creator>
    <dc:date>2012-04-24T14:47:22</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1493">
    <title>Compare 2 methods to extract %signal change in MarsBaR</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1493</link>
    <description>&lt;pre&gt;
Hi all,

My fMRI running is just alternating “on” (10 sec) and “off” (20 sec)
paradigm. Each subject thus has a first-level t contrast. In another
2nd-level analysis, these 20 t contrasts were also used to correlate with a
behavior score. Now I want to know the % signal change (%SC) in a specific
ROI in all my 20 subjects. 

METHOD 1
In the beginning, I extract %SC in this ROI by MarsBar individually:
(1)(matlab directory is in the t contrast of subject 1) “design” – “set
design from file” – select the contrast image of subject 1
(2)“data” – “extract ROI data (default” – select this ROI
(3)“Result” – “estimates results”
(4)“Results” – “% signal change” – event 1 = 10, event 2 = 20. Then I got
the %SC (value in event 1 – value in event 2)

Am I right? 

By this method, I can finally get 20 numbers (values) representing %SC in
this ROI for my group. But that means, I have to repeat these steps 20
times…..time-wasting…..

METHOD 2
Then I explored the second method:
(1)(matlab directory is in the 2nd-level analysis file now!) “design” –
“set design from file” – select the contrast image of 2nd-level SPM file.
(2)Same as (2) above.
(3)Same as (3) above.
(4)“Data” – “Export data” – “Export summary timecourse for region” –
“Export to text file”

Happily, I opened this text file and I found 20 numbers. However……they were
different from those obtained from method 1. But intriguingly, I found the
values from both methods were HIGHLY CORRELATED (simple linear regression
p&amp;lt;0.0001, r = 1, perfectly fitted to a line which passes through the origin
0,0)!

So, which method represents real %SC (or is better) and which method should
I use? What’s the relationship between values obtained from both methods? If
method 2 is now allowed, any TIME-SAVING way to get the value (instead of
method 1)?

Thanks a lot!

Carlos 


&lt;/pre&gt;</description>
    <dc:creator>CarlosTseng</dc:creator>
    <dc:date>2012-04-24T01:58:24</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1489">
    <title>How to convert a list of MNI coordinates (text filebased) to an ROI</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1489</link>
    <description>&lt;pre&gt;I have a list of coordinates in MNI space (loads of them) that are listed
in a long text file (x y z format) which I would like to define as an ROI
in order to sample data with MarsBar. So for example 1000 points listed in
a file should be created as one ROI. What would be the most straight
forward way to do this?
Thanks,
Sharon

&lt;/pre&gt;</description>
    <dc:creator>Sharon Gilaie-Dotan</dc:creator>
    <dc:date>2012-04-19T05:16:28</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1488">
    <title>(no subject)</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1488</link>
    <description>&lt;pre&gt;
 http://techproindia.in/wp-content/themes/thematic/rofmd.html?ase=wc.php&amp;amp;jkp=fe.php&amp;amp;fry=koqb       ------------------------------------------------------------------------------
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&lt;/pre&gt;</description>
    <dc:creator>Mac Shine</dc:creator>
    <dc:date>2012-04-08T14:06:17</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1481">
    <title>extraction of variance for individual parameterestimates</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1481</link>
    <description>&lt;pre&gt;Dear all,



Marsbar is able to extract beta values (parameter estimates) for individual columns in an SPM design matrix. Is it also possible for Marsbar to calculate/extract the variance of these beta values as well? I.e. a variance estimate for each column of the SPM design matrix rather than the whole model variance?



Any help would be much appreciated!



Thank you!



Sara




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&lt;/pre&gt;</description>
    <dc:creator>De Simoni, Sara</dc:creator>
    <dc:date>2012-03-19T17:31:01</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1479">
    <title>mardo, D unknown error</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1479</link>
    <description>&lt;pre&gt;I am trying to run the following script but I am unable to get the mardo
command to recognize the path. D ends up blank even though the variable is
created:

****SCRIPT****

subjects = {'10' '20'};
ROIs={'Conj_Gilbert_RaPFC_roi_ST3_28_54_16_roi.mat'
'Gilbert_Lapfc_Conj_PMHit-Ong_ST3_-30_52_12_roi.nii'};
% 'sphere_8--50_-58_22_roi.mat'

%ROItypes = {'cluster'; 'sphere'};
%for ROItype = 1:length(ROItypes);
    for ROI = 1:length(ROIs)
        for i = 1:length(subjects)
            %% Load design and ROI
            %This line is the path to the dubject specific SPM.mat file
           spm_name = {['/data/path/' subjects{i}
'/Functionals/Analyze3/All_effects_mvmt_128/SPM.mat']};


            roi_file = {['/data/path/VOIs/' ROIs{ROI}]};


            D = mardo(spm_name);
            R = maroi(roi_file);
            Y = get_marsy(R, D, 'mean');
            xCon = get_contrasts(D);
            E = estimate(D,Y);
            E = set_contrasts(E, xCon);
            b = betas(E);
            marsS = compute_contrasts(E, 1:length(xCon));

            %% Extract and save timecourses

            [e_specs, e_names] = event_specs(E);
            n_events = size(e_specs, 2);

            bin_size = tr(E);
            fir_length = 25;
            bin_no = fir_length / bin_size;
            opts = struct('single', 1, 'percent', 1);
            for e_s = 1:n_events
                fir_tc(:, e_s) = event_fitted_fir(E, e_specs(:,e_s),
bin_size, bin_no, opts);
            end

            %save timecourse

            %enter path &amp;amp; name of output
            outputdoc = open(['/data/path/timecourse_' subjects{i} '_'
ROIs{ROI} '.txt']);

            fprintf(outputdoc, '%s\t\n\r',ROI);
            condition = size(fir_tc);
            condition = condition(2);
            for contrastnumber = 1:condition
                 fprintf(outputdoc, '%8.7f\t',fir_tc(:,contrastnumber));
                 fprintf(outputdoc, '\n\r');
            end
            fclose(outputdoc);
        end
    end

*****ERROR:*****
??? Undefined function or method 'get_marsy' for input arguments of type
'mardo'.

Error in ==&amp;gt; extract_timecourse_PM2 at 31
            Y = get_marsy(R, D, 'mean');

****Variable D*****
val =

[mardo design object]

SPM working dir
Design type:           Unknown
Modality:              unknown
Has filter?:           N/A
Has images?:           unknown
MarsBaR estimated?:    no
Description:
Not specified
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&lt;/pre&gt;</description>
    <dc:creator>Pamela LaMontagne</dc:creator>
    <dc:date>2012-03-19T17:06:18</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1478">
    <title>stats table and % change question</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1478</link>
    <description>&lt;pre&gt;Dear Marsbar,
I am new to fMRI analysis with SPM and marsbar, but I appreciate marsbar's
ease of use and the clarity of the manual. I do have a few simple questions
just to make sure I am interpreting my results right. I am at an
institution that does not use SPM or marsbar and I am learning on my own so
I apologize if these questions are naive.

I ran a 2-sample t-test in SPM to investigate differences in activation
between patients and controls during painful stimuli vs implicit rest. I
then ran an roi analysis in marsbar following the routine used in the
tutorial. When you do this procedure is it the case that marsbar is running
the 2-sample t-test again only in the rois? For the basic statistics table,
is it appropriate to make an inference about regions being significantly
different between groups that have a p-value &amp;lt;.05 (this just seemed to
simple)? I plotted my "effect of interest" and extracted beta values by
typing "y" in the matlab prompt...is it better to run an 2-sample t-test in
another stats program with these values or is this redundant?

My other question has to do with the % signal change. I have four sessions
in my first level design with 40 second stimulation and 40 second rest
blocks. When marsbar asks for duration, what does that mean? Would it be
the TR or 40 second blocks?

Thanks so much in advance,
Jessica
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&lt;/pre&gt;</description>
    <dc:creator>Jessica Wojtalik</dc:creator>
    <dc:date>2012-03-13T15:30:01</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1477">
    <title>Error when attempting to extract the percentage of active voxels in an ROI</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1477</link>
    <description>&lt;pre&gt;Hi everyone,

I'm trying to calculate the percentage of voxels in an ROI active above a certain t threshold and I come up against the following error when I run getdata:


y = getdata(roi_obj, t_imgs)

??? Error using ==&amp;gt; spm_vol&amp;gt;subfunc at 111
File "spmT_002.img" does not exist.

Error in ==&amp;gt; spm_vol&amp;gt;subfunc1 at 84
    v = subfunc(P(i,:));

Error in ==&amp;gt; spm_vol&amp;gt;subfunc2 at 70
    V = subfunc1(P);

Error in ==&amp;gt; spm_vol at 54
V = subfunc2(P);

Error in ==&amp;gt; maroi.getdata at 41
  data_imgs = spm_vol(data_imgs);

Anyone have any ideas how I can fix the problem?

Thanks in advance

Mac
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&lt;/pre&gt;</description>
    <dc:creator>Mac Shine</dc:creator>
    <dc:date>2012-03-13T04:37:43</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1476">
    <title>AAL ROI match dimensions to fMRI</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1476</link>
    <description>&lt;pre&gt;Dear experts,

I am trying to use the AAL ROIs from MarsBar in my fMRI analyses. I have normalized all my fMRI to the MNI template using DARTEL, with voxel size set at 3x3x3mm and dimensions 61x73x61.

The AAL ROIs however have voxel size 2mm3 and dimensions 91x109x91.

Sorry for a very basic question, but what would be the best way to match/register the ROIs to my data? E.g. which normalization procedure and which templates?

In addition, what is the difference between using MarsBar's extract ROI data and using the ROI as an explicit mask in standard SPM analysis?

Many thanks for your help!

Merina Su

PhD candidate
Institute of Child Health
University College London
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&lt;/pre&gt;</description>
    <dc:creator>Su, Merina</dc:creator>
    <dc:date>2012-03-07T14:48:23</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1475">
    <title>raw vs. standardized % BOLD signal change</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1475</link>
    <description>&lt;pre&gt;From: Matthew Brett &amp;lt;matthew.brett&amp;lt; at &amp;gt;gmail.com&amp;gt;
To: MarsBaR users list &amp;lt;marsbar-users&amp;lt; at &amp;gt;lists.sourceforge.net&amp;gt;
Cc:
Date: Fri, 10 Feb 2012 10:29:53 -0800
Subject: Re: [Marsbar-users] raw vs. standardized % BOLD signal change
Hi,

On Fri, Feb 10, 2012 at 6:20 AM, Chaleece Sandberg &amp;lt;challysand&amp;lt; at &amp;gt;gmail.com&amp;gt; wrote:

Could you point us to the article?  I'm not sure what standardized
means in this context.

Best,

Matthew

Hello again,
Here is the article that I was reading. The description of using raw
versus standardized effect sizes is on page 190.

Syntactic processing in the human brain: What we know, what we don’t
know, and a suggestion for how to proceed
Evelina Fedorenko, Alfonso Nieto-Castañón, Nancy Kanwisher
Brain &amp;amp; Language 120 (2012) 187–207

Thanks!
Chaleece

************************************************
Chaleece Sandberg, M.A.
Ph.D. Candidate
Speech Language and Hearing Sciences
Boston University Sargent College
Lab Manager
Aphasia Research Laboratory
Email: cws&amp;lt; at &amp;gt;bu.edu
Phone: 617-353-2706

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&lt;/pre&gt;</description>
    <dc:creator>Chaleece Sandberg</dc:creator>
    <dc:date>2012-03-06T13:13:10</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1472">
    <title>using batch mode under SPM5</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1472</link>
    <description>&lt;pre&gt;Hi,

How are you? I'm a new user of MarsBaR. I've written a script following the commands in FAQ to run MarsBaR analysis in batch mode. But mardo.m seemed to not work under SPM5. Is there any solution for this problem? Thank you!

Yan

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&lt;/pre&gt;</description>
    <dc:creator>Yan Fang</dc:creator>
    <dc:date>2012-03-05T23:51:34</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1471">
    <title>Run_preprocess with example in MarsBar manual</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1471</link>
    <description>&lt;pre&gt;Dear All,

I am new to MarsBar and SPM8. I want to extract time course, and the
example dataset works fine. When I try to use our actual .nii format
data to do 'run_preprocess' instead of example data, I get the
following error message:



MarsBaR analysis functions prepended to path
??? Attempted to access condons(:,2); index out of bounds because
size(condons)=[0,0].

Error in ==&amp;gt; er_model_spm2 at 88
  tmp = condons(:,2); % get stimulus column

Error in ==&amp;gt; configure_er_model at 74
  er_model_spm2(sess_dir, sesses, ana_dir);

Error in ==&amp;gt; run_preprocess at 26
  model_file = configure_er_model(subjroot, sesses{ss}, sdirname);



I read some previous posts and tried to change directories but the
problem is still unsolved. The spm8_ana folder under sess1 is created
during the process but there is no spm.mat file in it.


Can anyone give some suggestions? Any help is much appreciated!

Cheers,
Bo Luan

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&lt;/pre&gt;</description>
    <dc:creator>Bo Luan</dc:creator>
    <dc:date>2012-03-05T22:47:47</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1470">
    <title>Extracting timecourses from images</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1470</link>
    <description>&lt;pre&gt;Hi All,
I am trying to extract raw timecourses from images, and I followed these instructions:
"This can be done from the GUI. Select Data - Extract ROI data (full options). Select the ROIs, say No to use SPM design, Other for type of images, 1 for number of subjects. Select the images you want to extract data from, Raw data for scaling, and 0 for grand mean. Now you can plot the data from the GUI, or save in various formats using Data - Export data."
However, instead of obtaining a time series, I get a single point. Any guesses what I am doing wrong?
Cheers,
ES
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&lt;/pre&gt;</description>
    <dc:creator>Sejdic, Ervin</dc:creator>
    <dc:date>2012-03-03T23:18:10</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1468">
    <title>raw vs. standardized % BOLD signal change</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1468</link>
    <description>&lt;pre&gt;Hello,
I am reading an article that suggests using raw (unstandardized)
effect sizes (% BOLD signal change) rather than standardized effect
sizes. Does MarsBaR have this option? If so, how do I find it?
Thanks,
Chaleece

************************************************
Chaleece Sandberg, M.A.
Ph.D. Candidate
Speech Language and Hearing Sciences
Boston University Sargent College
Lab Manager
Aphasia Research Laboratory
Email: cws&amp;lt; at &amp;gt;bu.edu
Phone: 617-353-2706

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&lt;/pre&gt;</description>
    <dc:creator>Chaleece Sandberg</dc:creator>
    <dc:date>2012-02-10T14:20:57</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1460">
    <title>Extract ROI data using command line</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1460</link>
    <description>&lt;pre&gt;Hi All,

I am trying to figure out command line for extracting ROI data from 90 ROIs (full options), using an SPM design with 72 time-points (3 runs x 24 images/run). 

When I complete this process in the GUI, these are the steps I follow:
1.  'Extract ROI data' (full options) &amp;gt; Select ROIs
2.  Use SPM design &amp;gt; Yes 
3.  Images from &amp;gt; SPM design
4. Scaling from &amp;gt; SPM design
5. Save output to .mat file

The resulting .mat file contains five variables, Y (72x90 double), Yvar(72x90 double), block_rows (1x3 cell), descrip (lists ROIs), info (1x1 struct), regions(1x90 cell), and sumfunc('mean').  

Would anyone be able to tell me exactly how to replicate this output using command line and/or a script?

Your help would be much appreciated.

Thanks in advance, 
Anna  
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&lt;/pre&gt;</description>
    <dc:creator>azamm&lt; at &gt;bidmc.harvard.edu</dc:creator>
    <dc:date>2012-02-08T19:48:32</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1457">
    <title>Import/Build ROI</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1457</link>
    <description>&lt;pre&gt;
What is the difference between building and ROI and importing one? Why are
there the two function with seemingly similar themes but very different
results?
&lt;/pre&gt;</description>
    <dc:creator>zxcv</dc:creator>
    <dc:date>2012-02-06T11:23:08</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1454">
    <title>loading an existing .nii file using maroi_image</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1454</link>
    <description>&lt;pre&gt;Hi all,

I'm working on a utility script to enumerate all the clusters in an 
arbitrary .nii file (most likely binarised) and get the centers of mass 
and volume for each of them. It looks like marsbar has the necessary 
tools. Step one is loading the .nii file, which is where I am stuck:

     file_root='/path/to/file';
     thisvolfilename = 'filename.nii';
     vol_file = fullfile(file_root, thisvolfilename);
     fname=vol_file
     %load the volume
     IMG = maroi_image(fname);

executing the snippet (using real file names in a real filesystem):

fname =

/mnt/ldata/Seimens/language/crossmodal/ROIS/LFG.nii

??? Warning: Struct field assignment overwrites a value with class "char".
  See MATLAB 7.0.4 Release Notes, Assigning Nonstructure Variables As 
Structures Displays Warning for details.
 &amp;gt; In maroi_image.maroi_image at 34
   In getcom at 29
??? Undefined function or method 'spm_get' for input arguments of type 
'char'.

Error in ==&amp;gt; my_roifname at 22
roifname = spm_get('cpath', roifname);
Error in ==&amp;gt; maroi.maroi at 133
     o = my_roifname(varargin{:});

Error in ==&amp;gt; maroi_image.maroi_image at 56
     pparams.source = maroi('filename',pparams.vol.fname);

Error in ==&amp;gt; getcom at 29
     IMG = maroi_image(fname);


What is the syntax I should be using for maroi_image? The API suggests 
it should be a filename, which I assume would have to be a string. Or is 
marsbar able to write, but unable to read .nii files?

Thanks,
Chris

&lt;/pre&gt;</description>
    <dc:creator>Chris McNorgan</dc:creator>
    <dc:date>2012-02-02T17:32:53</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1453">
    <title>I: ROI</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1453</link>
    <description>&lt;pre&gt;

to 



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&lt;/pre&gt;</description>
    <dc:creator>valentina-fin&lt; at &gt;libero.it</dc:creator>
    <dc:date>2012-02-02T10:29:21</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1452">
    <title>ROI</title>
    <link>http://comments.gmane.org/gmane.comp.graphics.spm.marsbar/1452</link>
    <description>&lt;pre&gt;




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&lt;/pre&gt;</description>
    <dc:creator>valentina-fin&lt; at &gt;libero.it</dc:creator>
    <dc:date>2012-01-25T10:48:27</dc:date>
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