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correction across seeds in seed to voxel connectivity

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Hi all,
How can I select several seeds for a seed to voxel connectivity and correct the results for multiple comparisons across seeds? Does this make sense? Is it possible?

RE: Using Freesurfer ROIs in Surface-based analysis

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Hi Alfonso,

Thanks for your reply - this worked perfectly!

For the first level analysis, I noticed that the Freesurfer ROIs (i.e., aparc+aseg.mgz) for each subject did NOT include a brain region name as other default atlases in CONN do. Each of the regions in the Freesurfer ROIs were named "cluster001", "cluster002", etc. Is there a way to find the regions that correspond to each cluster?

Thanks!
Kaitlin

Confusion about +ve / -ve group-level connectivity differences

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[color=#888888]Hello again,[/color]

[color=#888888]I am a bit confused about interpreting my resting-state ROI-to-ROI connectivity results hence here I'm posting in hope of getting valuable response from CONN community, would be really appreciable if someone can enlighten.[/color]

[color=#888888]I have created two second-level covariates under CONN setup tab to split the data into two groups (with alternating 1s and 0s). When I try to look at the between-subjects contrast ([1 -1] and [-1 1]) in ROI-to-ROI group level results explorer to study difference between two groups, the two-sided results appear exactly same except the red/blue colours switched for both contrasts. Will it be right to assume that connectivity patterns in blue on one contrast is negative/anti-correlation in group 1 and positive correlations in second group (as reflected by the z-score signs in the table). [/color][color=#888888]Comparatively, looking at one-sided results for the same contrasts appear to show some additional +ve / -ve ROI connections which I believe at indeed positive/negative correlations as the tag labels read. I'm not sure how to interpret this difference between one/two sided ROI-to-ROI connectivity results, any suggestion / literature referral would be helpful.[/color]

[color=#888888]On another results related note; is is possible to save the ROI-to-ROI connectivity results as .nii 3D image? Or overlay another .nii 3d MNI space normalised mask in CONN results explorer (like the overlay function within SPM12 Display). I tried using "add used-define surface" function in 3D conn results explorer window with default intensity/smoothing thresholds but the overlay somehow appears blown out and huge. Any suggestion on this would be quite helpful too.[/color]

[color=#888888]Best wishes,[/color]
[color=#888888]Dilip[/color]

reference or general info on the functional atlas in conn

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Hello!

I couldn't find more comprehensive info on functional atlas in conn. It's build on results from 500 subjects from HCP and there are several "traidtional" networks identified. 

However, I'm wondering about several issues:
1) were those subjects performing some tasks, as described on the HCP website, or were those data resting state?
2a) is there a reference I can cite in my paper if I decide to use the functional atlas? :)
2b) and in general read more about methods and theory behind this atlas? :)  
3) There is dorsal-attention network and fronto-parietal/central executive network. I am wondering if any of the rest of the provided networks is somewhat similar to the ventral attention network. Or its hubs are covered by the fronto-parietal network? 

I'll be very grateful for help!

preprocessing error

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ERROR DESCRIPTION:

Error using cellstr (line 49)
Conversion to cellstr from double is not possible.
Error in conn_datasetcopy (line 44)
existf=conn_existfile(cellstr(f1));
Error in conn_setup_preproc (line 2727)
conn_datasetcopy(sets,'original data',subjects);
Error in conn (line 1081)
ok=conn_setup_preproc('',varargin{2:end});
Error in conn_menumanager (line 120)
feval(CONN_MM.MENU{n0}.callback{n1}{1},CONN_MM.MENU{n0}.callback{n1}{2:end});
CONN18.b
SPM12 + DEM FieldMap MEEGtools
Matlab v.2017b
project: CONN18.b
storage: 437.8Gb available

Load Error in CONN

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Hi all,

After rerunning my preprocessing steps to add another ROI into my dataset, I have been unable to load the .mat file in CONN. It gives me the following erorr: 
Error using conn (line 740)
Failed to load file *file name*

Error in conn (line 4055)
conn('load',filename,true);
Error in conn_menumanager (line 120)
feval(CONN_MM.MENU{n0}.callback{n1}{1},CONN_MM.MENU{n0}.callback{n1}{2:end});

Does anyone know how to fix this?

RE: Lesion Masks

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Hi all,
I'm also running into this problem. Did anyone find a solution to this question yet?
Best regards,
Wouter
[i]Originally posted by Matthew Heard:[/i][quote]Hi Giuliana,

Any luck solving this problem? I also need advice on how to modify the TPM.nii file. So far, all I have found is a paper demonstrating that masking a lesion is crucial to analyzing functional connectivity in a brain with a lesion: https://journals.sagepub.com/doi/abs/10.1177/0271678X17709198

Thanks,
Matthew[/quote]

Diffusion steps for smoothing

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Hi,

I'm trying to run a surface-based functional connectivity analysis through a conn_batch script, and I received a prompt for entering the "number of diffusion steps for smoothing". The number is set to 10 by default, but what exactly does this number correspond to and under what circumstances should it be changed?

Thanks in advance, 
Leland

RE: Compcor threshold

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Hi, Alfonso,

I am curious about how many components should be set for CSF and WM with aCompCor in Denoising step?
Though, the default is 5 both for CSF and WM, but is there a quantifed critiera?

Thanks!

Data quality tools

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Dear experts,

I need to know if, after applying the ArtRepair toolbox, it is appropriate to correct the physiological and movement artefacts (for example, with movement, cardiac and respiratory information in the denoising step of CONN or adding these parameters as a regressor in the first level of SPM). I am worried because I don't know if applying both corrections I would be eliminating too much signal, because after applying art_global Repair (a function of ArtRepair), theoretically the artifacts are already reduced. What do you think? Should I apply both or only one? If it is only one, which of them?

On the other hand, I am doing tests to obtain the most optimal protocol. Do you suggest any parameter that allows me to compare the quality of the different tests I am doing? For example, something that allows me to observe the variability of the BOLD signal, the noise signal that the images have or any other parameter that you consider appropriate.

Thank you very much in advance.

Best regards,

Marina Fernández Álvarez, PhD-student.

Laboratory of Functional Neuroscience
Ctra. de Utrera, Km.1
41013 - Seville (Spain)

loading in previously denoised data

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Hello,

I am working on a pipeline to go from fmriprep to CONN. Currently I want to set it up to do all the preprocessing and denoising outside of conn using afni's 3dTproject. We want to be able to orthogonalize all the confounds (aCompCor, realignment parameters, fd, bandpass, and spatial smoothing). I understand that CONN can do the denoising and bandpass filtering concurrently (or with orthogonality), but is there any way to also include the spatial smoothing in this step? 

I had two thoughts about how to go about this:

1) Load in fmriprep-processed data into CONN along with seeds. Then load in confound file(s) including those created for spatial smoothing and run all together in CONN's denoising step.

2) Denoise the data first and then load into CONN. But this also requires loading in the denoised seed timecourses, and I'm not exactly sure how to do that. Would I just load in denoised ROI files for each subject, rather than loading in a set of ROIs? 


I understand the argument to extract seed timecourses from the unsmoothed data to avoid "spillage," but does that create any sort of bias in comparing a timecourse derived from unsmoothed data to that of smoothed data? How does the relationship between seed radius and whole brain smoothing affect the results? 

Best,
- Harris

RE: second level ROI-to-ROI "import values"

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Hi -

I have a related question. I submitted an article where we examined changes in 14 network correlations before and after an intervention. The reviewer now asks for the values of the pairwise correlations. I am assuming that the z-transformed Person correlations would suffice. How do I extract those values from the CONN interface?

Thank you for your help.

P.S. I am not sure how to go back to this particular post. So if someone answers would you please send the reply also directly to my work e-mail which is mfroelich@uabmc.edu.
Thanks

RE: Freesurfer's Brainmask preprocessing

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[color=#000000]Hi Oliver,[/color]

[color=#000000]Those are interesting questions. Briefly:[/color]

[color=#000000](1) that should be fine (but see (3) below)[/color]
(2) yes (and it will switch the Gray/White/CSF ROIs to point to those new tissue class masks)

(3) none of the existing pipelines will apply the normalization spatial-transformation encoded in the y_*.nii files generated during normalization to your externally-defined Gray/White/CSF ROIs (the "Segmentation&Normalization" steps will create new Gray/White/CSF ROI files as part of the segmentation step, while the "Normalization" step only normalizes the functional or structural data leaving your Gray/White/CSF ROIs unchanged; see below for some alternative options)

(4) that should work perfectly fine but your Gray/White/CSF ROIs will remain unchanged (in subject-space) so you would need to manually (e.g. using SPM gui or batch commands) transform those files to MNI-space using the y_*.nii files generated during the normalization step. 

Because (4) is somewhat time-consuming (and I imagine there would be other scenarios where users may want to use externally-defined tissue masks) I am also attaching a patch that includes a new "Structural Normalization with user-defined Gray/White/CSF masks" and "Functional Indirect Normalization with user-defined Gray/White/CSF masks" steps. These work just the same as the original "Structural Normalization" and "Functional Indirect Normalization" steps, respectively, but they will also keep any user-defined Gray/White/CSF ROIs (e.g. those that were imported from FreeSurfer) in the same space as your structural data. Internally they will simply apply in both cases the same non-linear transformations that is applied to the structural data to your Gray/White/CSF ROIs as well. Note that the assumption in both of these cases is that your externally-defined Gray/White/CSF masks will be in the same space as your structural data (which makes sense when importing FreeSurfer data). Let me know if you run into any issues with this patch (this patch is for release 18b, to install it simply copy the attached file to your conn distribution folder overwriting the file with the same name there)

Hope this helps
Alfonso

[i]Originally posted by Olivier Roy:[/i][quote]Hello,
Because I had trouble with skull-stripping with my raw T1 images (some skull often left in the posterior aspect of the brain), I decided to use the brainmask.mgz from Freesurfer which was properly skull-stripped. By using the brainmask, I also allowed Conn to import the segmentation files from Freesurfer. I then ran a modified version of the second volume-based preprocessing pipeline in Conn (see attached image): in brief, I just removed the "functional Creation of voxel-displacement map (VDM) for distortion correction" and replaced the realignment step with "functional Realignment & unwarp (subject motion estimation and correction)", effectively getting rid of the distortion correction part.

My questions are:
1. Since I used the brainmask.mgz which is already skull-stripped, will the skull-stripping part of the "functional Indirect Segmentation & Normalization" step have altered the image too much with the second skull-stripping step? So that I lose GM or CSF information for instance?

2. From what I understand, the "functional Indirect Segmentation & Normalization" step also resegment the Grey/White/CSF and overwrite those from Freesurfer. Is that true?

3. I want to co-register functional and structural volumes and then normalize to MNI while also keeping (and normalizing) the Grey/White/CSF segmentation from Freesurfer. If instead of the step "functional Indirect Segmentation & Normalization" I use the step "functional Indirect Normalization" (which also coregister structural and functional), will it also normalize the Grey/White/CSF segmentation from Freesurfer?
<span style="white-space: pre;"> </span>- I am asking this question because the "[u]functional Indirect Segmentation & Normalization[/u]" step gives as output the skull-stripped normalized structural volume, [b]normalized Grey/White/CSF masks[/b] and normalized functional volumes (all in MNI space) [u]whereas[/u] the "functional Indirect Normalization" step gives the [b]same thing (also seems to skull-strips; normal?) [/b][u]less the normalized Grey/White/CSF masks[/u]. 

4. Finally, if the answer to question #1 is that the second skull-stripping is problematic. Can I replace the step "functional Indirect Segmentation & Normalization" which skull-strips with the "functional Direct Coregistration to structural without reslicing" and subsequently "functional Direct Normalization" which do not seem to skull-strip again. How should I arrange the steps in the sequence in this case? Also in this case, how could I make sure that the Grey/White/CSF masks from Freesurfer get normalized to MNI?

Thank you and sorry for the long post,
Olivier[/quote]

Weighted GLM functional connectivity or gPPI

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Greetings, 

I am currently assessing whether a cue reactivity task modulates functional connectivity. I ran weighted GLM functional connectivity analyses at the first-level, and at the second-level, I fail to see any differences between my two task conditions (from two different sessions). Each task condition is associated with functional connectivity maps that overlap. Would it have been more beneficial to run a gPPI analysis to assess differences between conditions, or would it yield similar results? 

Thank you for your assistance, 

William Denomme

Conditions for groups with different number of scans

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Hello all,

I have a question regarding conditions setup for a project with patient and control groups. The patient group has 2 resting state scans (pre and post) while the control group only has one resting state scan.

I have already created "pre" and "post" conditions in the Setup.Conditions tab. I have affiliated "Session 1" in all subjects with the "pre" condition, and have affiliated "Session 2" in the patient group with the "post" condition (as in this post: https://www.nitrc.org/forum/message.php?msg_id=12762).

My dilemma is how to compare the post scan in patients with the single control scan once I reach 2nd level analyses. Previous posts have recommended entering the pre and post scans in patients as if they were individual scans (https://www.nitrc.org/forum/message.php?msg_id=10754). I'm wondering whether it would also be feasible to simply create a new condition in which:[list=1][*] Session 1/pre scans for the patients are not present (i.e., leave onset/duration fields empty) while[*]Session 2/post scans for the patients are present (i.e. onset of 0 and duration inf) and[*]Session 1 scans for the controls are present.[/list]If I understand correctly, this will create one condition that I can use in 2nd level analyses that compares the post scan in patients to the single control scan. Is this feasible/appropriate?


Thanks in advance for any help!
Tessa

RE: HCP data and conn

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I have the same question. Has someone encountered this and knows how to properly concatenate AP PA rest nii files before CONN processing ?

CONN v.18a Abd File Failed to Load

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We have an issue that arises from time to time with CONN v.18a. When it's trying to load a file we get a failed to load file message.

There's a patch for this we have tried. But, this did not fix the issue that has occurred again.

The specific error is as follows.

Error using conn(line 740)
Failed to load file path_to.mat file

Error in conn(line 4055)
conn('load',filename,true);

We are using CONN with spm 12 and Matlab v. 2018b.

RE: CONN TROUBLESHOOTING

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I had the same problem. I analyzed 15 subjects 2 sessions each and 4 subjects had problem.

If anyone knows something about it, please leave a comment!

Using the BETA_denoising_Subject*.nii for activity differences in another tool

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Hi Alfonso,
I would like to examine the activity differences between two conditions using GLM Flex (http://mrtools.mgh.harvard.edu/index.php?title=GLM_Flex_Fast2). For that I would need the preprocessed images. As I read on the forum, I created the BETA_denoising_Subject*.nii files by clicking on the relevant button ('Create confound-corrected time series' option in Setup.Options CONN). When I look into this nifti, it consists out of 60 sessions (constant term, realignment, fixation, each condition). How can I create subject-specific nifti files for just the conditions, so that I can compare activity between two conditions across the subjects it in GLM_Flex_Fast2?

Many thanks!
Heidi

Baseline required for task-based functional connectivity analysis?

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Hello,

I have performed a task-based functional connectivity. For this purpose, I largely followed the manual and the forum. In retrospect, I noticed that I have specified epochs for conditions that I was interested in but no baseline. While I understand that this is not necessary for resting-state functional connectivity, I imagine that it is for task-based connectivity.

Could you please advise me how to go about this? 

Thank you very much,
Leonie
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