Dear Sir,

Can we observe the distribution of vestibulospinal tracts (vestibular
circuitry )  from thalamus through vestibular cortex through workbench?, I
have DTI data and i can evaluate the functional and structural connectivity
but i would like to construct track orientation distribution in each voxel.



Thanks
Vasudev

On 23 June 2016 at 17:20, Harms, Michael <[email protected]> wrote:

>
> Not as the pipeline is currently constituted.
>
> Sorry.
>
> --
> Michael Harms, Ph.D.
> -----------------------------------------------------------
> Conte Center for the Neuroscience of Mental Disorders
> Washington University School of Medicine
> Department of Psychiatry, Box 8134
> 660 South Euclid Ave. Tel: 314-747-6173
> St. Louis, MO  63110 Email: [email protected]
>
> From: <[email protected]> on behalf of Dev vasu <
> [email protected]>
> Date: Thursday, June 23, 2016 at 10:02 AM
>
> To: "Harms, Michael" <[email protected]>
> Cc: "[email protected]" <[email protected]>
> Subject: Re: [HCP-Users] Spatial normalization of 50 Subjects T1w images
>
> Dear Sir,
>
> In some subjects T2 FLAIR images are missing, is it still possible to run
> HCP structural preprocessing pipeline without T2w images?, if not is there
> any alternative.
>
>
> Thanks
> Vasudev
>
>
> On 23 June 2016 at 16:34, Harms, Michael <[email protected]> wrote:
>
>>
>> Hi,
>> After you run the data through the HCP pipelines you will have
>> surface-based maps of cortical thickness for each subject.  You can then
>> use the PALM tool (FSL) to look for statistically significant differences
>> in thickness between subject groups.
>>
>> cheers,
>> -MH
>>
>> --
>> Michael Harms, Ph.D.
>> -----------------------------------------------------------
>> Conte Center for the Neuroscience of Mental Disorders
>> Washington University School of Medicine
>> Department of Psychiatry, Box 8134
>> 660 South Euclid Ave. Tel: 314-747-6173
>> St. Louis, MO  63110 Email: [email protected]
>>
>> From: Dev vasu <[email protected]>
>> Date: Thursday, June 23, 2016 at 8:53 AM
>>
>> To: "Harms, Michael" <[email protected]>
>> Cc: "[email protected]" <[email protected]>
>> Subject: Re: [HCP-Users] Spatial normalization of 50 Subjects T1w images
>>
>> Dear Sir,
>>
>>
>> Now i have obtained 30 Healthy controls from the same scanner along with
>> 50 subjects with Bilateral Vestibulopathy , I would like to use HCP
>> pipelines for 1. Batch processing and also i would like to investigate the
>> voxel-based cortical thickness ( as opposed to VBM , as you have cited in
>> earlier mails ), could you please let me know how could i perform
>> voxel-based cortical thickness, could you please suggest me some methods.
>>
>>
>>
>> Thanks
>> Vasudev
>>
>> On 22 June 2016 at 15:51, Harms, Michael <[email protected]> wrote:
>>
>>>
>>> Hi,
>>> No, we don’t have any such phantom measurements available.  And there
>>> are a lot more issues at play in terms of differences between scanners than
>>> just differing magnetic inhomogeneities anyway.
>>>
>>> cheers,
>>> -MH
>>>
>>> --
>>> Michael Harms, Ph.D.
>>> -----------------------------------------------------------
>>> Conte Center for the Neuroscience of Mental Disorders
>>> Washington University School of Medicine
>>> Department of Psychiatry, Box 8134
>>> 660 South Euclid Ave. Tel: 314-747-6173
>>> St. Louis, MO  63110 Email: [email protected]
>>>
>>> From: Dev vasu <[email protected]>
>>> Date: Wednesday, June 22, 2016 at 1:03 AM
>>>
>>> To: "Harms, Michael" <[email protected]>
>>> Cc: "[email protected]" <[email protected]>
>>> Subject: Re: [HCP-Users] Spatial normalization of 50 Subjects T1w images
>>>
>>> Dear sir,
>>>
>>>
>>> In order to avoid magnetic homogenities of different scanners, can i
>>> take into consideration Field maps from HCP data and   some Phantom
>>> measurements ( like ACR Phantom Measurements ) ?, If so does HCP provides
>>> data for Phantom Measurements ?.
>>>
>>>
>>>
>>> Thanks
>>> Vasudev
>>>
>>> On 21 June 2016 at 21:53, Harms, Michael <[email protected]> wrote:
>>>
>>>>
>>>> Hi,
>>>> I’m sorry, but there is no way to model or account for the effect of
>>>> possible scanner differences if you don’t have at least some of each group
>>>> of subjects collected on each scanner.  In your current situation, you have
>>>> no mechanism to attempt to disentangle the effects of vestibulopathy vs.
>>>> scanner.
>>>>
>>>> cheers,
>>>> -MH
>>>>
>>>> --
>>>> Michael Harms, Ph.D.
>>>> -----------------------------------------------------------
>>>> Conte Center for the Neuroscience of Mental Disorders
>>>> Washington University School of Medicine
>>>> Department of Psychiatry, Box 8134
>>>> 660 South Euclid Ave. Tel: 314-747-6173
>>>> St. Louis, MO  63110 Email: [email protected]
>>>>
>>>> From: Dev vasu <[email protected]>
>>>> Date: Tuesday, June 21, 2016 at 2:36 PM
>>>>
>>>> To: "Harms, Michael" <[email protected]>
>>>> Cc: "[email protected]" <[email protected]>
>>>> Subject: Re: [HCP-Users] Spatial normalization of 50 Subjects T1w
>>>> images
>>>>
>>>> Dear Sir,
>>>>
>>>> The vestibulopathy subject scans are from scanner outside HCP, we here
>>>> in LMU Munich use Siemens Skyra 3T scanner, in such case how to neutralize
>>>> or eliminate the differences which may occur due to scanner differences ?.
>>>>
>>>>
>>>> Thanks
>>>> Vasudev
>>>>
>>>>
>>>> On 21 June 2016 at 21:29, Harms, Michael <[email protected]> wrote:
>>>>
>>>>>
>>>>> Hi,
>>>>> I would use a measure that relates in a concrete way to the underlying
>>>>> neuroanatomy, such as cortical thickness.
>>>>>
>>>>> There may be a bigger issue here, which is that I’m now guessing that
>>>>> your vestibulopathy subjects are coming from scans collected from outside
>>>>> HCP?  If so, you have a major confound, because you will be attempting to
>>>>> compare two groups that were collected on completely different scanners.
>>>>> In which case, any difference you find could be attributed to just scanner
>>>>> difference effects.
>>>>>
>>>>> cheers,
>>>>> -MH
>>>>>
>>>>> --
>>>>> Michael Harms, Ph.D.
>>>>> -----------------------------------------------------------
>>>>> Conte Center for the Neuroscience of Mental Disorders
>>>>> Washington University School of Medicine
>>>>> Department of Psychiatry, Box 8134
>>>>> 660 South Euclid Ave. Tel: 314-747-6173
>>>>> St. Louis, MO  63110 Email: [email protected]
>>>>>
>>>>> From: <[email protected]> on behalf of Dev vasu <
>>>>> [email protected]>
>>>>> Date: Tuesday, June 21, 2016 at 2:02 PM
>>>>> To: "Harms, Michael" <[email protected]>
>>>>> Cc: "[email protected]" <[email protected]>
>>>>> Subject: Re: [HCP-Users] Spatial normalization of 50 Subjects T1w
>>>>> images
>>>>>
>>>>> Dear Professor,
>>>>>
>>>>> I was advised to do VBM, I understand questions pertaining to
>>>>> biological  validity of VBM and interpretation issues. I would like to
>>>>> investigate the cortical regional differences between health controls and
>>>>> controls with vestibulopathy , If you have any other suggestion pertaining
>>>>> to this task i would really appreciate your response.
>>>>>
>>>>>
>>>>>
>>>>> Thanks
>>>>> Vasudev
>>>>>
>>>>> On 21 June 2016 at 20:47, Harms, Michael <[email protected]> wrote:
>>>>>
>>>>>> Hi,
>>>>>> If I may, why VBM?  VBM is prone to a number of interpretational
>>>>>> issues, as opposed to say cortical thickness, which is already available
>>>>>> for you as part of the HCP processing.
>>>>>>
>>>>>> cheers,
>>>>>> -MH
>>>>>>
>>>>>> --
>>>>>> Michael Harms, Ph.D.
>>>>>> -----------------------------------------------------------
>>>>>> Conte Center for the Neuroscience of Mental Disorders
>>>>>> Washington University School of Medicine
>>>>>> Department of Psychiatry, Box 8134
>>>>>> 660 South Euclid Ave. Tel: 314-747-6173
>>>>>> St. Louis, MO  63110 Email: [email protected]
>>>>>>
>>>>>> From: <[email protected]> on behalf of Dev vasu <
>>>>>> [email protected]>
>>>>>> Date: Tuesday, June 21, 2016 at 1:30 PM
>>>>>> To: Stamatios Sotiropoulos <[email protected]>, "
>>>>>> [email protected]" <[email protected]>,
>>>>>> "Glasser, Matthew" <[email protected]>, Timothy Brown <
>>>>>> [email protected]>
>>>>>> Subject: [HCP-Users] Spatial normalization of 50 Subjects T1w images
>>>>>>
>>>>>> Dear Sir ,
>>>>>>
>>>>>>
>>>>>> I am using HCP data ( 50 subjects ) + 50 patients with bilateral
>>>>>> vestibular paresis to examine the Regional differences in cortical
>>>>>> organization between healthy controls and patients for which i am using
>>>>>> VBM,  For spatial registration of 50 HCP subjects i would like to know if
>>>>>> HCP offers some customized templates for registration or do i have to
>>>>>> perform affine transformation and non linear registration, please kindly
>>>>>> let me know .
>>>>>>
>>>>>>
>>>>>>
>>>>>>
>>>>>> Thanks
>>>>>> Vasudev
>>>>>>
>>>>>> _______________________________________________
>>>>>> HCP-Users mailing list
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>>>>>> http://lists.humanconnectome.org/mailman/listinfo/hcp-users
>>>>>>
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>>>>>>
>>>>>
>>>>> _______________________________________________
>>>>> HCP-Users mailing list
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>>>>>
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