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From: Ankeeta S. <ank...@ya...> - 2021-07-09 14:21:32
|
Dear developers I am new to use this toolbox and it says that it cannot read the directory of SPM.mat file.Please help With Regards Ankeeta Sent from Yahoo Mail on Android |
From: Joyce D. <JDi...@tr...> - 2020-03-23 15:21:29
|
Hi All, I have the following error: RFXPLOT has terminated with an error. If you want to report this error, please type ''rfx_debug = 1" at the MATLAB prompt and rerun rfxplot ERROR MESSAGE: Cant open image file. ERROR STACK: 66 rfx_get_data_img 425 rfx_main 200 rfxplot 981 spm Does anyone know how to solve this problem? It appears almost near the end of using rfx plot while plotting effect sizes. While it is asking for Xtick positions. Hope to hear from anyone. Best, Joyce Met vriendelijke groet, Joyce Dieleman Promovendus - Jeugd www.trimbos.nl<http://www.trimbos.nl> Da Costakade 45 - 3521 VS Utrecht Postbus 725 - 3500 AS Utrecht Disclaimer<http://www.trimbos.nl/emaildisclaimer> [Bezoek de Trimbos website]<http://www.trimbos.nl/> [Trimbos Neiuwsbrieven] <https://www.trimbos.nl/actueel/nieuwsbrieven> [Volg ons op Twitter!] <http://www.twitter.com/trimbos> [Volg ons op Linkedin!] <https://www.linkedin.com/company/trimbos-instituut/> [Volg ons op Facebook!] <http://www.facebook.com/Trimbos.instituut> |
From: Katharina V. <kat...@mo...> - 2019-09-25 06:12:31
|
Hi all, I’m currently trying to plot the interaction effect sizes for each of my conditions of a factorial design. Unfortunately I get an error saying 'the field ‘u’ does not exist” . Could you please let me know what might go wrong and how I can fix it? Thank you, Kati ___________________________________ Katharina Voigt BSc(Hons), MSc, PhD Postdoctoral Research Fellow Turner Institute for Brain and Mental Health Addiction and Mental Health Program School of Psychological Sciences Monash University 18 Innovation Walk, R618 Clayton campus, VIC 3800 Australia T: +61 3 9905 1402 E: kat...@mo... |
From: Sungshin K. <sun...@no...> - 2015-12-04 07:54:59
|
Sungshin Kim, PhD Feinberg School of Medicine, Northwestern University |
From: Papegaaij, S (med) <s.p...@um...> - 2015-03-20 10:01:31
|
Dear rfxplot-users, I would like to plot the percent signal change within a region of interest. My question is when you select "only suprathreshold voxels" for the voxel selection whether this selection is done on group level or on individual level? I would like to have a mean value for all the suprathreshold voxels per individual. Is there a way to do this? Thank you very much, Selma Papegaaij ________________________________ De inhoud van dit bericht is vertrouwelijk en alleen bestemd voor de geadresseerde(n). Anderen dan de geadresseerde(n) mogen geen gebruik maken van dit bericht, het niet openbaar maken of op enige wijze verspreiden of vermenigvuldigen. Het UMCG kan niet aansprakelijk gesteld worden voor een incomplete aankomst of vertraging van dit verzonden bericht. The contents of this message are confidential and only intended for the eyes of the addressee(s). Others than the addressee(s) are not allowed to use this message, to make it public or to distribute or multiply this message in any way. The UMCG cannot be held responsible for incomplete reception or delay of this transferred message. |
From: James Jones-R. <jj...@co...> - 2014-08-06 19:18:13
|
Hello all, We are attempting to use rfxplot to quantify effect sizes of the PPI results we have calculated, all within SPM8 on a Mac OS. We have calculated PPI on seed voxels of interest, which generated a list of target voxels whose timecourses significantly correlate with the seed voxels. We are then feeding those target voxels (and the accordant SPM.mat file that the PPI toolbox generated for each target voxel) into rfxplot in order to quantify the effect size of that target voxel's correlation/connectivity with its respective seed voxel. I have two questions for you all. First, when one goes through the rfxplot GUI, one has the option of choosing "beta" or "con" as the substrate for the analysis. In our study, we had two sessions/runs. Choosing "beta" in rfxplot leads to two lists of variables to analyze (an essentially identical list for each session), whereas choosing the "contrast" option only gives a single list of variables to select from. Here's our issue. When we run the "beta" option, the ".gdata" results variable includes two unique columns of data, with two different values for each participant (one for each of their two sessions); however, when we run the "contrast" option, the ".gdata" results variable only has a single column and it is identical to the first of the two ".gdata" columns from the "beta"-based analysis. Why is this? Secondly, and more broadly, does anyone have experience using rfxplot to quantify connectivity analyses from PPI, and if so, can you point to any resources or literature we can review? Specifically, we'd like to know more about how to confirm that the rfxplot results actually pertain to the connectivity estimate between the seed voxels and the target voxels. There does not seem to be a lot of information out there about combining these toolboxes in this way, although it seems theoretically to be a sound way of conducting the analyses. Thank you very much for your time! James -- James Jones-Rounds Laboratory Manager Human Development EEG and Psychophysiology (HEP) Laboratory, Department of Human Development, -------------------------------------------- Cornell University | Ithaca, NY 607-255-9883 ee...@co... |
From: Yuko <ilo...@gm...> - 2013-12-18 23:18:26
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Dear all, I would like to use four different studies data. Each study has "Task A", however, in each study, trial number of "Task A" was difference. For example, in study one, I presented "Task A" 12 times, and in study two, I presented "Task A" 11 times...... Could I use con_images of Task A from those different four studies? Any suggestion would be highly appreciated. Thank you so much, Yuko |
From: Horatio D. <hor...@gm...> - 2013-05-17 04:52:21
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Dear Jan, Firstly - thank you for such a well-written and -documented toolbox, its a new discovery for me and Im finding it a pleasure to use. Ill be sure to cite you in upcoming manuscripts. I have primarily been using the toolbox for extracting PSTHs, but I would like to be able to extract PSTHs for each individual in my sample to run some stats and correlations with behaviour. Ive played around with some of the data structures but can't seem to find how to do this. Do you have any pointers for me? With regards, Horatio |
From: Domsalla, M. <Mel...@zi...> - 2013-04-24 15:58:34
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Hi rfxplot-users, I was just trying to plot psth separately for 2 groups. Do you know if there is the possibility to plot the psth for the two groups in different colours? In the manual the colour specification only is described for different effects or different bins. Can anybody help? Thanks in advance and best wishes Melanie Domsalla, Dipl.Psych. Research unit 'Experimental Psychology' Central Institute of Mental Health Department of Psychosomatic Medicine and Psychotherapy Medical Faculty Mannheim, University of Heidelberg J 5, D-68159 Mannheim, Germany phone: +49-621-1703 4417, fax: +49-621-1703-4405 |
From: Gina J. <jo...@hu...> - 2012-04-19 20:08:05
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Hi, I'm trying to get started with rfxplot and scripting a simple plot based on the rfxplot manual but am getting the following error: ERROR MESSAGE: Improper index matrix reference. ERROR STACK: 31 spm_read_vols 14 rfx_get_ffx_voxel_mask 214 rfx_main 204 rfxplot I'm not even sure where to begin asking questions or what info to provide. I turned on "rfx_debug = 1". Doing "dbstop if error" or putting breakpoints in rfx or SPM code doesn't seem to stop the execution where the error/breakpoint is. Any suggestions? Does anyone maybe have a sample batch script? Thanks for any help, g |
From: Klossika, I. <Iri...@zi...> - 2011-08-05 12:53:24
|
Dear experts, I'm having problems with a voi analysis using rfxplot. It keeps terminating with the following error: ERROR MESSAGE: Cant open image file. ERROR STACK: 66 rfx_get_data_img 425 rfx_main 200 rfxplot 914 spm ... after displaying the results of only one subject. Whole brain results of First and Second Level analyses (spm8) are displayed without problems for all subjects. And no, I most certainly did not move the files around (that's apparently what everybody thinks at first, but I know for sure because I re-did the whole preprocessing in the faint hope that this might help; it didn't). Neither should limited access be a problem. What really mystifies me is that the problem appears in only one group of subject. The other runs smoothly. Can anybody help? Iris Klossika Central Institute of Mental Health Mannheim, Germany |
From: Burak E. <bur...@gm...> - 2011-02-09 10:25:13
|
Dear RFX users, I have 3 questions 1) While plotting psth I am getting error saying that rfx can't access to individuals time series subject 1.... and stopping. Even though the group folder is in different folder than single subject they are both under the same big folder and got no problem in plotting percent signal changes. I only got problems with psth. 2) Should I apply filtering for psth what is the rationale for that ? 3) In order to make a statistical test for comparing the percent signal changes for two contrasts for a local maximum voxel or sphere does anybody know the name of the variable in the matlab data structure. Or is there an automatic procedure implemented in rfx to say statistical significance. If anybody have a matlab script for that, it would be very useful for the community. Best wishes -- Burak Erdeniz Phd Student Psychology & Computer Science Department Health & Human Sciences Research Institute 2f240 Health Building University of Hertfordshire College Lane Hatfield Herts AL 10 9AB |
From: Vikram r. <vik...@gm...> - 2010-04-08 21:12:54
|
Hi rfxplot users, I was wondering if there was a way to plot psth with different colors for each group (not effects or bins!)...the rfxplot gui doesnt prompt for any options where we can define different colors for different groups. I am plotting SEM s as area. Has anybody tried to play with this. Thanks in anticipation. Cheers! Vikram Rao UC Berkeley, Psychology Dept. Berkeley, California, USA "A pizza with radius "z" and thickness "a" has a volume of pi*z*z*a" |
From: Marcus H. <mar...@me...> - 2010-01-29 10:05:45
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I planning to use rfxplot with a mixed model made with SPMs flexible factorial design (1 beween subjects, 2 within subjects factors). Since there is a long discussion regarding the correct calculation of error terms in a mixed model design, I wanna know of anybody has used rfxplot in a mixed model design. Thanks in advance, Marcus |
From: Jan G. <gla...@hs...> - 2009-04-03 22:29:54
|
Dear all, I have just posted a new version of rfxplot (Rev 30) online that contains a couple of important bug fixes: 1. In previous version the percent signal change for negative betas was computed incorrectly. 2. In case of multiple basis function (e.g. HRF+TD+DISP) the parameter estimate plots were not correct. Both errors are fixed in the current version and I urge you to update, since these will affect your data plots, if the conditions above meet your fMRI design. The most recent version is available at: http://rfxplot.sourceforge.net/download Just unzip the most recent version in your SPM toolbox folder overwriting the previous one. Apologies, if you received this email multiple times. Thanks, Jan -- Jan Gläscher, Ph.D. Div. Humanities & Social Sciences +1 (626) 395-3898 (office) Caltech, Broad Center, M/C 114-96 +1 (626) 395-2000 (fax) 1200 E. California Blvd gla...@hs... Pasadena, CA 91125 |
From: Jan G. <gla...@hs...> - 2008-12-10 23:15:41
|
Dear all, I have just posted a new version (Revision 7) of rfxplot online at http://rfxplot.sourceforge.net. New features include: * Bug fixes related to multiple basis function and full factorial designs. * Change of version numbering to reflect the subversion development stage * Get regional labels from AAL templates (needs user configuration in rfx_defaults.m, details are found in the manual, section 9.1) * The generation of the rfx*.mat file can be suppressed (configure this in rfx_defaults.m, see section 9.4 in the manual). This can be advantageous for the rfx_timeseries.mat, because on fast computers saving and loading of .mat files can take longer than (re-)generating the structures for each SPM session. * In case of multiple basis functions, the user should only select the first BF from the image description table. The toolbox will select the remaining BFs automatically if necessary. * The accompanying paper is now in press at Neuroinformatics. The approved manuscript is available in the Credits section of the website As always, if you come across some errors, please let me know, so that I can improve the code. Best wishes, Jan -- Jan Gläscher, Ph.D. Div. Humanities & Social Sciences +1 (626) 395-3898 (office) Caltech, Broad Center, M/C 114-96 +1 (626) 395-2000 (fax) 1200 E. California Blvd gla...@hs... Pasadena, CA 91125 |