Hi,Chaogan,
I came across an error when I was using CWAS in DPARSF2.3, How to solve this problem?
Looking forward to your reply. Thank you in advance.
Hello everyone,
Hi everyone!
I'm trying to run a single subject rsfmri analysis. I run DPARSF and get my 2 zFC maps , one for each of the 2 sessions (pre and post treatment). The maps look good in the viewer! I put these 2 zFC maps in the stat analysis tool by selecting a paired t test modality, in order to to get a comparison-t-map between the two. Is this right so far? The stat analysis tool look running fine and provide me with a map. However, this map cannot be seen in the viewer. When trying to upload it, matlab provides me with the following error:
严老师您好，我最近在尝试着用dpasfa进行数据分析，但是每
Hello,
I preproceed the T1 images for the VBM analysis using DPABI, and I have some inquiries regarding the output files.
I chose the "New Segment + DARTEL" option, and I got files whose prefix are "smwc", "mwc","wc1".
According to the naming convention of output files introduced in the VBM8 manual, "mwc1" seems to mean "modulated warped gray matter segments", and "smwc1" seems the smoothed "mwc1". Here, I am wondering why the smoothed files (smwc1) were generated eariler than the "mwc" files.
Hi all,
I just have a quick query, so I extracted ROI time course from 6 region. At the define ROI stage I added 6 masks and DPARSFA listed in alphabetical order. Whwn i got the results in the ROI signal folder I have 6 list (6 time course from the masks I defined). My question is are these timecourse columns in order of the the way the mask were listed, so would my first time course be the signals for the first mask of the 6 and so on).
严老师：
您好！我想看实验组和对照组治疗前后ALFF差异，是不是应该用mixed effect analysis？我用DPABI做mixed effect analysis后，得出的Interaction_F.nii在Viewer里显示的图像同ANOVA图像，只能看出哪些区域有差异，但是不能看出具体哪些是升高的，哪些是降低的。假设实验组治疗后壳核ALFF升高，而对照组治疗后壳核ALFF不变或降低，请问如果我想看两个组在壳核ALFF的变化不同，我该用什么方法呢？
希望您能在百忙中帮忙解答，谢谢您！
米涛免
Hi,
I'm trying to generate the interface and montage pictures automatically via a script. That is, I want to
1. Load a nifti file (blobs) onto a T1 anatomical image (like in the viewer)
2. Load a colormap for the blobs
3. Specify an x/y/z coordinate
4. Specify an overlay transparency value (i.e. want to set it to 0 )
5. Create the interface pictures automatically (and save to a folder) at the specified coordinates (just like it can be done with the "save interface as Picture" button only via a function/script)
------
Hi all,
So after processing and extracting roi signals, the next step is for me to analyze the roi signals of my subjects using SPSS. Does anyone know what type of analyisis I should carry out on SPSS as I have two groups, one healthy and the other have Alzheimers.
Whic do I use rregression or corellation.
Also what does the different type of file mean in the results folder for roi extraction. does Z mean zett?
much appreciation, really benefiting from this program!!