Thanks for the clarification Eugenio. Would saying that it relies on shape
instead of surface be more accurate? I would like to understand better.
Also, it is good news that there are plans to model the SLRM.
Josh

-
Joshua Lee
Doctoral Candidate
Department of Psychology &
Center for Mind and Brain
University of California, Davis
530.747.3805


On Mon, Apr 28, 2014 at 12:18 AM, Eugenio Iglesias <e.igles...@bcbl.eu>wrote:

> Dear all,
> the current module in FreeSurfer works with 1mm T1 data, by relying on
> strong shape priors. So, at this point, feeding the algorithm data from a
> 3T scanner or a 1.5T scanner is pretty much the same.
> Joshua, it is indeed inaccurate to say that the method relies on a
> generated hippocampal surface, but you are definitely right regarding the
> SLRM: it is not modeled at this point (we have a new version that models it
> coming out hopefully soon!).
> Cheers,
> /Eugenio
>
>
> Juan Eugenio Iglesias
> Postdoctoral researcher BCBL
> www.jeiglesias.com
> www.bcbl.eu
>
> Legal disclaimer/Aviso legal/Lege-oharra: www.bcbl.eu/legal-disclaimer
>
>
> ----- Original Message -----
> From: "Joshua Lee" <jki...@ucdavis.edu>
> To: "Freesurfer support list" <freesurfer@nmr.mgh.harvard.edu>
> Sent: Friday, April 25, 2014 2:10:29 AM
> Subject: Re: [Freesurfer] Hippocampal subfields on 1.5 Tesla
>
>
>
>
> Hi Alan,
>
> Typically subfields segmentation requires hi-resolution data (e.g. 0.4 x
> 0.4 mm in-plane resolution). The thickness of a CA subfield typically range
> between 0.5-1.00 mm, but 1.5 T data does not achieve sub-millimeter
> resolutions. Further, subfield segmentation typically requires
> high-contrast data to discern the internal boundaries formed by the stratum
> radiatum/stratum lacunosum-moleculare (SLRM). I doubt that images produced
> on a 1.5 T magnet can achieve the necessary contrast. Last, and please
> someone correct me if what I say is inaccurate, but doesn't the Van Leemput
> method use statistical priors to apply label probabilities in reference to
> a generated hippocampal surface? This would imply that the method assigns
> label probabilities without reference to a subject's SLRM intensity
> information. For volumetry, I am somewhat skeptical that a method that only
> relies on a generated surface would be sensitive to group x subfield
> interactions; especially double dissociations in !
>  which overall volume/shape of the hippocampus may be similar across
> groups. That the that was generated from potentially low resolution, low
> contrast data cannot help the matter. Some may disagree about this though
> and I'd be interested in hearing what other people think about the matter.
> In general, I am quite optimistic about automated methods to segment the
> subfields.
>
>
>
>
> Joshua
>
>
>
>
>
>
>
> -
>
> Joshua K. Lee
> Doctoral Candidate
>
> Department of Psychology &
> Center for Mind and Brain University of California, Davis
>
>
>
>
> On Thu, Apr 24, 2014 at 12:24 PM, Alan Francis < alandarkene...@gmail.com> 
> wrote:
>
>
>
> Hi Bruce and FreeSurfers:
>
> I have received a manuscript to review for possible publication. The
> authors have used the subfields algorithm on 1.5T scans and obtained a
> parcellation with values. They have drawn some major conclusions on the
> basis of the findings. My understanding is that this method can only be
> done on 3T. Is the 1.5T results valid?
>
> Please advice.
>
> thanks,
>
> Alan Francis
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