Re: [Freesurfer] shift to account for hemodynamic response

2018-02-09 Thread Sarah Cole
Thank you so much.

On Fri, Feb 9, 2018 at 11:48 AM, Douglas Greve 
wrote:

> It is already built into the HRF model. If you need to shift them more or
> less than what is in the model, that can be accommodated. If you use the
> -spmhrf option, then you will get the same HRF as is used in spm.
>
> On 2/6/18 11:45 PM, Ashley Cole wrote:
>
> Dear experts,
>
> I just have switched from SPM to Freesurfer. I am wondering if in FSFAST
> analysis, we require to shift the regressors in time to account for the
> delay in hemodynamic response?
>
> Thanks
>
>
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[Freesurfer] V1 functional ROI

2018-02-09 Thread Sarah Cole
Dear Dr. Douge,

I am a little bit confused about creating function ROI in V1.

Basically, I have some localizers that for some ROIs I need to find
activated neurons in a specific contrast in native space and then create
that ROI and map it to my experimental scans and extract their voxel data.

I have used this command for right-FFA:

funcroi-config -seg aparc+aseg.mgz 2007 -analysis eba-fba.native.rh -c
faces-vs-objects -thresh 3 -sign pos -roi
rh.surface.pSTS.faces-vs-objects.thr3.pos.roicfg -force



But now, for V1 I am not sure what should I use.

Is this correct?


funcroi-config -seg aparc+aseg.mgz 400 -analysis eba-fba.native.rh -c
faces-vs-objects -thresh 3 -sign pos -roi
rh.surface.V1.faces-vs-objects.thr3.pos.roicfg -force


I don't see a number in the lookup table for left and right V1.

On the other hand, there are V1 labels in the label folder.

I appreciate your help.

Thanks
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[Freesurfer] FIR analysis

2018-02-12 Thread Sarah Cole
Hi experts,

I was wondering if there is any tutorial or example on FIR analysis. I
don't know where to start.

I need to look at the time course of some voxels. I have a localizer
session and the main experiment. I am intending to find the ROIs in the
localizer scans and then extract their time course activation in the main
experiment scans.

I have done the recon-all successfully. Then in my localizer scan, I did
preproc-sess, mkanalysis-sess with FIR 6 24 flag, mkcontarst, and selxabg3.
Now, I am lost.

Sorry for my naiive question.

Thank you,

--SC
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[Freesurfer] Percent Signal Change

2018-02-15 Thread Sarah Cole
Hi,

Could someone please let me know how to get the percent signal change for
raw signal intensity?

I think the cespct.nii.gz gives me the contrast as %. However, I am not
sure about dividing h.nii and h-offset.nii. What are they?


Thank you
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Re: [Freesurfer] Percent Signal Change

2018-02-15 Thread Sarah Cole
Thank you, Doug.

Sorry for not being clear. Could you please tell me what h.nii.gz and
h-offset.nii.gz are?

Also, do you have any recommendation on how to get % signal change on the
signal intensity as oppose to % signal change on contrasts?

Thank you

On Thu, Feb 15, 2018 at 12:47 PM, Douglas N Greve  wrote:

> It divides the contast (ces) by voxel-wise mean. I'm not sure I
> understand your quesstion about h and h-offset
>
>
> On 02/15/2018 01:04 PM, Sarah Cole wrote:
> > Hi,
> >
> > Could someone please let me know how to get the percent signal change
> > for raw signal intensity?
> >
> > I think the cespct.nii.gz gives me the contrast as %. However, I am
> > not sure about dividing h.nii and h-offset.nii. What are they?
> >
> >
> > Thank you
> >
> >
> > ___
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>
> --
> Douglas N. Greve, Ph.D.
> MGH-NMR Center
> gr...@nmr.mgh.harvard.edu
> Phone Number: 617-724-2358
> Fax: 617-726-7422
>
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Re: [Freesurfer] Percent Signal Change

2018-02-15 Thread Sarah Cole
Yes, that's exactly what I am looking for. Raw waveform as a percent.

On Thu, Feb 15, 2018 at 1:00 PM, Douglas N Greve 
wrote:

> h-offset is the intensity offset (basically the mean signal). h.nii.gz
> is a complicated combination of the betas (regression coefficients) that
> is included for backwards compatibility. What do you mean by % signal
> change? Do you want the raw waveform as a percent?
>
>
> On 02/15/2018 01:52 PM, Sarah Cole wrote:
> > Thank you, Doug.
> >
> > Sorry for not being clear. Could you please tell me what h.nii.gz and
> > h-offset.nii.gz are?
> >
> > Also, do you have any recommendation on how to get % signal change on
> > the signal intensity as oppose to % signal change on contrasts?
> >
> > Thank you
> >
> > On Thu, Feb 15, 2018 at 12:47 PM, Douglas N Greve
> > mailto:gr...@nmr.mgh.harvard.edu>> wrote:
> >
> > It divides the contast (ces) by voxel-wise mean. I'm not sure I
> > understand your quesstion about h and h-offset
> >
> >
> > On 02/15/2018 01:04 PM, Sarah Cole wrote:
> > > Hi,
> > >
> > > Could someone please let me know how to get the percent signal
> > change
> > > for raw signal intensity?
> > >
> > > I think the cespct.nii.gz gives me the contrast as %. However, I am
> > > not sure about dividing h.nii and h-offset.nii. What are they?
> > >
> > >
> > > Thank you
> > >
> > >
> > > ___
> > > Freesurfer mailing list
> > > Freesurfer@nmr.mgh.harvard.edu
> > <mailto:Freesurfer@nmr.mgh.harvard.edu>
> > > https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
> > <https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer>
> >
> > --
> > Douglas N. Greve, Ph.D.
> > MGH-NMR Center
> > gr...@nmr.mgh.harvard.edu <mailto:gr...@nmr.mgh.harvard.edu>
> > Phone Number: 617-724-2358 
> > Fax: 617-726-7422 
> >
> > Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
> > <http://surfer.nmr.mgh.harvard.edu/fswiki/BugReporting>
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> > <https://gate.nmr.mgh.harvard.edu/filedrop2>
> > www.nmr.mgh.harvard.edu/facility/filedrop/index.html
> > <http://www.nmr.mgh.harvard.edu/facility/filedrop/index.html>
> > Outgoing:
> > ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/
> > <ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/>
> >
> > ___
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> harvard.edu>
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> >
> >
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> --
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> MGH-NMR Center
> gr...@nmr.mgh.harvard.edu
> Phone Number: 617-724-2358
> Fax: 617-726-7422
>
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[Freesurfer] Goodness of fit

2018-02-20 Thread Sarah Cole
Hi Doug,


I have used spmhrf 0 in my FS-FAST analysis. I was wondering if there is
any way to check the variance explained and fits on the model?


Thank you,

-S
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Re: [Freesurfer] Goodness of fit

2018-02-20 Thread Sarah Cole
Great. Thank you very much.

On Tue, Feb 20, 2018 at 11:19 AM, Douglas N Greve  wrote:

> I don't output a variance explained per se. You can get p-values
> (sig=-log10(p)) and partial correlation coefficient (pcc) for a given
> regressor or contrast
>
>
> On 02/20/2018 12:07 PM, Sarah Cole wrote:
> > Hi Doug,
> >
> >
> > I have used spmhrf 0 in my FS-FAST analysis. I was wondering if there
> > is any way to check the variance explained and fits on the model?
> >
> >
> > Thank you,
> >
> > -S
> >
> >
> > ___
> > Freesurfer mailing list
> > Freesurfer@nmr.mgh.harvard.edu
> > https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
>
> --
> Douglas N. Greve, Ph.D.
> MGH-NMR Center
> gr...@nmr.mgh.harvard.edu
> Phone Number: 617-724-2358
> Fax: 617-726-7422
>
> Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
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[Freesurfer] Creating ROI on the functional map

2018-02-23 Thread Sarah Cole
Hi,

I was wondering if this method is still applicable in version 6
https://surfer.nmr.mgh.harvard.edu/fswiki/CreatingROIs


I cannot seem to find any of the options for creating an ROI.

Thank you,

S
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Re: [Freesurfer] Creating ROI on the functional map

2018-02-26 Thread Sarah Cole
It doesn't work on tksurfer. But it's ok.

So Doug, is this the latest tutorial:
https://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/MultiModalFmriIndividual_freeview
for FS-FAST and creating functional ROI?

More specifically, do I need to use "mri_vol2surf" to get the activation on
the surface?

This was not in the other tutorial:
http://surfer.nmr.mgh.harvard.edu/fswiki/FsFastTutorialV6.0/FsFastFirstLevel


Thanks

On Mon, Feb 26, 2018 at 3:28 PM, Douglas N Greve 
wrote:

> I think it should work; We are not using tksurfer any more (freeview
> instead), but I think it should still work
>
>
> On 02/23/2018 05:16 PM, Sarah Cole wrote:
> > Hi,
> >
> > I was wondering if this method is still applicable in version 6
> > https://surfer.nmr.mgh.harvard.edu/fswiki/CreatingROIs
> >
> >
> > I cannot seem to find any of the options for creating an ROI.
> >
> > Thank you,
> >
> > S
> >
> >
> > ___
> > Freesurfer mailing list
> > Freesurfer@nmr.mgh.harvard.edu
> > https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
>
> --
> Douglas N. Greve, Ph.D.
> MGH-NMR Center
> gr...@nmr.mgh.harvard.edu
> Phone Number: 617-724-2358
> Fax: 617-726-7422
>
> Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
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>
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Re: [Freesurfer] Creating ROI on the functional map

2018-02-27 Thread Sarah Cole
I apologize. I was wrong.

Thanks,
S

On Mon, Feb 26, 2018 at 5:16 PM, Sarah Cole  wrote:

> It doesn't work on tksurfer. But it's ok.
>
> So Doug, is this the latest tutorial: https://surfer.nmr.mgh.
> harvard.edu/fswiki/FsTutorial/MultiModalFmriIndividual_freeview for
> FS-FAST and creating functional ROI?
>
> More specifically, do I need to use "mri_vol2surf" to get the activation
> on the surface?
>
> This was not in the other tutorial: http://surfer.nmr.mgh.harvard.
> edu/fswiki/FsFastTutorialV6.0/FsFastFirstLevel
>
>
> Thanks
>
> On Mon, Feb 26, 2018 at 3:28 PM, Douglas N Greve <
> gr...@nmr.mgh.harvard.edu> wrote:
>
>> I think it should work; We are not using tksurfer any more (freeview
>> instead), but I think it should still work
>>
>>
>> On 02/23/2018 05:16 PM, Sarah Cole wrote:
>> > Hi,
>> >
>> > I was wondering if this method is still applicable in version 6
>> > https://surfer.nmr.mgh.harvard.edu/fswiki/CreatingROIs
>> >
>> >
>> > I cannot seem to find any of the options for creating an ROI.
>> >
>> > Thank you,
>> >
>> > S
>> >
>> >
>> > ___
>> > Freesurfer mailing list
>> > Freesurfer@nmr.mgh.harvard.edu
>> > https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
>>
>> --
>> Douglas N. Greve, Ph.D.
>> MGH-NMR Center
>> gr...@nmr.mgh.harvard.edu
>> Phone Number: 617-724-2358
>> Fax: 617-726-7422
>>
>> Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
>> FileDrop: https://gate.nmr.mgh.harvard.edu/filedrop2
>> www.nmr.mgh.harvard.edu/facility/filedrop/index.html
>> Outgoing: ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/
>>
>> ___
>> Freesurfer mailing list
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>>
>>
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>> is
>> addressed. If you believe this e-mail was sent to you in error and the
>> e-mail
>> contains patient information, please contact the Partners Compliance
>> HelpLine at
>> http://www.partners.org/complianceline . If the e-mail was sent to you
>> in error
>> but does not contain patient information, please contact the sender and
>> properly
>> dispose of the e-mail.
>>
>>
>
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[Freesurfer] Freeview update on Mac

2018-02-27 Thread Sarah Cole
Hi Doug/Zeke,

Could you please update the page for freeview update on Mac- if it is
available.

https://surfer.nmr.mgh.harvard.edu/fswiki/UpdateFreeview


Thanks,

S
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[Freesurfer] Fwd: Freeview update on Mac

2018-02-28 Thread Sarah Cole
Great! Thank you so much, Andrew.

I downloaded the updated Freeview. I am still wondering how to draw an ROI
on the surface in Freeview. I don't have the options.
Could you please let me know what command you are running to get the
Freeview?

I am having the updated version Jan 2018.

Thanks,
Sarah

On Tue, Feb 27, 2018 at 11:40 AM, Hoopes, Andrew 
wrote:

> Hi Sarah, I updated the wiki page. We actually just put up a standalone,
> dev freeview app today.
>
> best
> Andrew
>
>
> On February 27, 2018 at 11:38:57 AM, Sarah Cole (coleashle...@gmail.com)
> wrote:
>
> Hi Doug/Zeke,
>
> Could you please update the page for freeview update on Mac- if it is
> available.
>
> https://surfer.nmr.mgh.harvard.edu/fswiki/UpdateFreeview
>
>
> Thanks,
>
> S
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[Freesurfer] Hemodynamic Lag Shift

2018-03-28 Thread Sarah Cole
Hi Doug,

I have a block design experiment. After analyzing the data and plotting the
response magnitude across the TRs, we see that there is a systematic lag in
the response. For example, in a 16s block (TR=2s), at TR-1 and TR-2 the
response goes down and then starts rising from TR-3. This is consistent
across the subjects and blocks.

We used to shift our raw data by 2 TRs when we were using SPM.

How can we do this in FreeSurfer?

Thank you,

Sarah
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Re: [Freesurfer] Hemodynamic Lag Shift

2018-03-29 Thread Sarah Cole
Thanks, Doug.

I added (-4s) delay and plotted the data but I got the same delay as no
shift. Also I did (+4) delay and lost most of the activation.

Do you have any recommendations?

Thanks,
Sarah

On Wed, Mar 28, 2018 at 4:39 PM, Douglas N. Greve 
wrote:

> You can use the -delay flag in mkanalysis-sess
>
> doug
>
>
> On 03/28/2018 05:35 PM, Sarah Cole wrote:
> > Hi Doug,
> >
> > I have a block design experiment. After analyzing the data and
> > plotting the response magnitude across the TRs, we see that there is a
> > systematic lag in the response. For example, in a 16s block (TR=2s),
> > at TR-1 and TR-2 the response goes down and then starts rising from
> > TR-3. This is consistent across the subjects and blocks.
> >
> > We used to shift our raw data by 2 TRs when we were using SPM.
> >
> > How can we do this in FreeSurfer?
> >
> > Thank you,
> >
> > Sarah
> >
> >
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Re: [Freesurfer] Hemodynamic Lag Shift

2018-03-30 Thread Sarah Cole
Hi Doug,

Sure. I have attached an excel sheet.
I have averaged the signal magnitude across 16 blocks of objects, and 16
blocks of scenes, separately. Each block has 8 TRs (TR=2).

The top plot is the data with the default -TR/2 delay.
The bottom plot is the data with -2TR delay.

In both plots, we see that the signal drops in the first 2 TRs and then
starts rising around TR 3. We would like to see this rise at TR1, that's
why we think that we need to shift the onset times.
However, when we added the -2TR delay, we still got the same fall and rise.
This pattern is consistent across all subjects.

When we were using SPM, we always shifted the signal by 2TRs and always saw
the rise at the first TR. I am not sure what I am doing wrong, here.

Appreciate your help.

Thanks,

On Fri, Mar 30, 2018 at 8:09 AM, Douglas Greve 
wrote:

> not sure what you are trying to do. can you send a picture? the default
> lag is TR/2
>
> On 3/29/18 2:30 PM, Sarah Cole wrote:
>
> Thanks, Doug.
>
> I added (-4s) delay and plotted the data but I got the same delay as no
> shift. Also I did (+4) delay and lost most of the activation.
>
> Do you have any recommendations?
>
> Thanks,
> Sarah
>
> On Wed, Mar 28, 2018 at 4:39 PM, Douglas N. Greve 
> wrote:
>
>> You can use the -delay flag in mkanalysis-sess
>>
>> doug
>>
>>
>> On 03/28/2018 05:35 PM, Sarah Cole wrote:
>> > Hi Doug,
>> >
>> > I have a block design experiment. After analyzing the data and
>> > plotting the response magnitude across the TRs, we see that there is a
>> > systematic lag in the response. For example, in a 16s block (TR=2s),
>> > at TR-1 and TR-2 the response goes down and then starts rising from
>> > TR-3. This is consistent across the subjects and blocks.
>> >
>> > We used to shift our raw data by 2 TRs when we were using SPM.
>> >
>> > How can we do this in FreeSurfer?
>> >
>> > Thank you,
>> >
>> > Sarah
>> >
>> >
>> > ___
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>>
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>> properly
>> dispose of the e-mail.
>>
>>
>
>
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HRF_Shift_FSFAST.xlsx
Description: MS-Excel 2007 spreadsheet
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Re: [Freesurfer] Hemodynamic Lag Shift

2018-04-03 Thread Sarah Cole
Please ignore my previous post. I was wrong on so many levels!

Thanks

S

On Fri, Mar 30, 2018 at 8:34 AM, Sarah Cole  wrote:

> Hi Doug,
>
> Sure. I have attached an excel sheet.
> I have averaged the signal magnitude across 16 blocks of objects, and 16
> blocks of scenes, separately. Each block has 8 TRs (TR=2).
>
> The top plot is the data with the default -TR/2 delay.
> The bottom plot is the data with -2TR delay.
>
> In both plots, we see that the signal drops in the first 2 TRs and then
> starts rising around TR 3. We would like to see this rise at TR1, that's
> why we think that we need to shift the onset times.
> However, when we added the -2TR delay, we still got the same fall and
> rise. This pattern is consistent across all subjects.
>
> When we were using SPM, we always shifted the signal by 2TRs and always
> saw the rise at the first TR. I am not sure what I am doing wrong, here.
>
> Appreciate your help.
>
> Thanks,
>
> On Fri, Mar 30, 2018 at 8:09 AM, Douglas Greve 
> wrote:
>
>> not sure what you are trying to do. can you send a picture? the default
>> lag is TR/2
>>
>> On 3/29/18 2:30 PM, Sarah Cole wrote:
>>
>> Thanks, Doug.
>>
>> I added (-4s) delay and plotted the data but I got the same delay as no
>> shift. Also I did (+4) delay and lost most of the activation.
>>
>> Do you have any recommendations?
>>
>> Thanks,
>> Sarah
>>
>> On Wed, Mar 28, 2018 at 4:39 PM, Douglas N. Greve > > wrote:
>>
>>> You can use the -delay flag in mkanalysis-sess
>>>
>>> doug
>>>
>>>
>>> On 03/28/2018 05:35 PM, Sarah Cole wrote:
>>> > Hi Doug,
>>> >
>>> > I have a block design experiment. After analyzing the data and
>>> > plotting the response magnitude across the TRs, we see that there is a
>>> > systematic lag in the response. For example, in a 16s block (TR=2s),
>>> > at TR-1 and TR-2 the response goes down and then starts rising from
>>> > TR-3. This is consistent across the subjects and blocks.
>>> >
>>> > We used to shift our raw data by 2 TRs when we were using SPM.
>>> >
>>> > How can we do this in FreeSurfer?
>>> >
>>> > Thank you,
>>> >
>>> > Sarah
>>> >
>>> >
>>> > ___
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>>> > Freesurfer@nmr.mgh.harvard.edu
>>> > https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
>>>
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>>> e-mail
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>>> properly
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>>>
>>>
>>
>>
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Re: [Freesurfer] Percent Signal Change

2018-04-03 Thread Sarah Cole
Doug,

Could you please let me know what this line is doing?
"fmnrep = repmat(fmn,[1 1 1 size(f.vol,3)]);"

When I try to assign f.vol/fmnrep to s.vol (this line s.vol =
f.vol./fmnrep;), matrices do not match in dimension.

Thanks,
S

On Thu, Feb 15, 2018 at 1:05 PM, Douglas N Greve 
wrote:

> That does not get computed. You can do it in matlab with something like
>
> f = MRIread('f.nii.gz');
>
> fmn = mean(f.vol,4);
>
> fmnrep = repmat(fmn,[1 1 1 size(f.vol,3)]);;
>
> s = f;
>
> s.vol = f.vol./fmnrep;
>
> MRIwrite(s,'percentchange.nii.gz')
>
>
>
> On 02/15/2018 02:03 PM, Sarah Cole wrote:
> > Yes, that's exactly what I am looking for. Raw waveform as a percent.
> >
> > On Thu, Feb 15, 2018 at 1:00 PM, Douglas N Greve
> > mailto:gr...@nmr.mgh.harvard.edu>> wrote:
> >
> > h-offset is the intensity offset (basically the mean signal).
> h.nii.gz
> > is a complicated combination of the betas (regression
> > coefficients) that
> > is included for backwards compatibility. What do you mean by % signal
> > change? Do you want the raw waveform as a percent?
> >
> >
> > On 02/15/2018 01:52 PM, Sarah Cole wrote:
> > > Thank you, Doug.
> > >
> > > Sorry for not being clear. Could you please tell me what
> > h.nii.gz and
> > > h-offset.nii.gz are?
> > >
> > > Also, do you have any recommendation on how to get % signal
> > change on
> > > the signal intensity as oppose to % signal change on contrasts?
> > >
> > > Thank you
> > >
> > > On Thu, Feb 15, 2018 at 12:47 PM, Douglas N Greve
> > > mailto:gr...@nmr.mgh.harvard.edu>
> >     <mailto:gr...@nmr.mgh.harvard.edu
> > <mailto:gr...@nmr.mgh.harvard.edu>>> wrote:
> > >
> > > It divides the contast (ces) by voxel-wise mean. I'm not sure I
> > > understand your quesstion about h and h-offset
> > >
> > >
> > > On 02/15/2018 01:04 PM, Sarah Cole wrote:
> > > > Hi,
> > > >
> > > > Could someone please let me know how to get the percent
> signal
> > > change
> > > > for raw signal intensity?
> > > >
> > > > I think the cespct.nii.gz gives me the contrast as %.
> > However, I am
> > > > not sure about dividing h.nii and h-offset.nii. What are
> they?
> > > >
> > > >
> > > > Thank you
> > > >
> > > >
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> > > <mailto:Freesurfer@nmr.mgh.harvard.edu
> > <mailto:Freesurfer@nmr.mgh.harvard.edu>>
> > > >
> > https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
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> > > <https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
> > <https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer>>
> > >
> > > --
> > > Douglas N. Greve, Ph.D.
> > > MGH-NMR Center
> > > gr...@nmr.mgh.harvard.edu <mailto:gr...@nmr.mgh.harvard.edu>
> > <mailto:gr...@nmr.mgh.harvard.edu <mailto:gr...@nmr.mgh.harvard.edu
> >>
> > > Phone Number: 617-724-2358 
> > >
> > > Fax: 617-726-7422   > >
> > >
> > > Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
> > <http://surfer.nmr.mgh.harvard.edu/fswiki/BugReporting>
> > > <http://surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
> > <http://surfer.nmr.mgh.harvard.edu/fswiki/BugReporting>>
> > > FileDrop: https://gate.nmr.mgh.harvard.edu/filedrop2
> > <https://gate.nmr.mgh.harvard.edu/filedrop2>
> > > <https://gate.nmr.mgh.harvard.edu/filedrop2
> > <https://gate.nmr.mgh.harvard.edu/filedrop2>>
> > > www.nmr.mgh.harvard.edu/facility/filedrop/index.html
> > <http://www.nmr.mgh.harvard.edu/facility/filedrop/index.html>
> > > <http://www.nmr.mgh.harvard.edu/facility/filedrop/index.html
> &

[Freesurfer] Canonical HRF shape generated by FSFAST

2018-04-11 Thread Sarah Cole
Hi Doug,

At the end of my FSFAST analysis, I would like to plot the Canonical HRF
shape generated by FSFAST for my events. I have found this thread:
https://mail.nmr.mgh.harvard.edu/pipermail/freesurfer/2013-July/031902.html

but I am not sure if I understand this line:
"plot(X.runflac(1).flac.ev(2).tirf,
X.runflac(1).flac.ev(2).Xirf)"


Could you please clarify how to plot the Canonical HRF that was generated
by FSFAST?

Thank you,

Sarah
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Re: [Freesurfer] Canonical HRF shape generated by FSFAST

2018-04-11 Thread Sarah Cole
Just one clarification, this is for first level analysis (individual
subjects).

Thanks

On Wed, Apr 11, 2018 at 9:54 AM, Sarah Cole  wrote:

> Hi Doug,
>
> At the end of my FSFAST analysis, I would like to plot the Canonical HRF
> shape generated by FSFAST for my events. I have found this thread:
> https://mail.nmr.mgh.harvard.edu/pipermail/freesurfer/2013-
> July/031902.html
>
> but I am not sure if I understand this line: "
> plot(X.runflac(1).flac.ev(2).tirf, X.runflac(1).flac.ev(2).Xirf)"
>
>
> Could you please clarify how to plot the Canonical HRF that was generated
> by FSFAST?
>
> Thank you,
>
> Sarah
>
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[Freesurfer] FSFAST, Beta values and Percent Signal Change questions

2018-04-16 Thread Sarah Cole
Hi Doug,

I need your recommendations on two topics. I really appreciate your help.

1.) I have two runs of the same experiment, each for about 12 minutes.
These 2 runs are different only in the presentation order of the stimuli. I
also have one localizer session which first, I calculated my contrasts in
it, found the active voxels with positive values, and made a mask of those
voxels. Then, mapped the masks on those 2 runs and got the raw data within
those voxels. So far, so good. Now, I am looking at the Beta values in
these 2 runs for those active voxels, they are very different from each
other. For example, in the first run, they are mostly positive but in the
second run, they are mostly negative. My intuition was that they should be
in the same ballpark. I cannot make sense of this. Do you have any
suggestions on why this is happening?


2.) To calculate the % signal change, is it ok to pick the baseline
whatever is suitable to my research question. For example, if I need to
know the % signal change relative to* the average signal in the first TR of
a specific block*, can I use that as a baseline? Or does it always need to
be the rest or the mean?


Thank you so much and looking forward to hearing from you.

Sarah
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[Freesurfer] key nSliceGroups unrecognized, line 11, skipping

2018-07-18 Thread Sarah Cole
External Email - Use Caution

Hi,

I know this is not an error but just a comment. But may I know what this
means:

"*key nSliceGroups unrecognized, line 11, skipping"*


I tried to look for line 11 in matlab scripts but they are mainly commented
out.

Thank you,

Sara
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