Good point (meaning that I don't know the answer). I'll see if I can
find out.

doug



On Fri, 16 Oct 2009, Donna Dierker wrote:

> Regardless:  FDR's sensitivity appears resolution-dependent to me.
>
> On 10/16/2009 10:39 AM, Michael Harms wrote:
>> Interesting post Donna, but my understanding of FDR is that it sets the
>> p-value threshold based on the LARGEST p-value that satisfies the FDR
>> relationship.
>>
>> That is, steps 3 and 4 in Genovese et al. (2002) are:
>> 3) Let r be the largest i for which p <= i/V*q  (assuming c=1)
>> 4) Threshold the image at the p-value p(r).
>>
>> So, it isn't the case that you require the most significant p-value to
>> satisfy p <= 0.05/V "just to get past i=1" as you put it in your post.
>>
>> Rather, you pick the largest p-value that satisfies the relationship,
>> meaning that lower (more-significant) p-values may not have necessarily
>> satisfied p <= i/V*q for their particular position in the sorted list of
>> p-values.
>>
>> cheers,
>> Mike H.
>>
>>
>> On Fri, 2009-10-16 at 10:13 -0500, Donna Dierker wrote:
>>
>>> I never heard anything on my post here, but it might just be high
>>> surface resolution:
>>>
>>> http://www.mail-archive.com/neuro-mult-c...@brainvis.wustl.edu/msg00026.html
>>>
>>> On 10/16/2009 09:58 AM, Michael Harms wrote:
>>>
>>>> Your FDR analysis sounds correct.  You probably have a rather small
>>>> number of "marginally" significant vertices, which is why none survive
>>>> FDR.  You could try increasing the "q" value from say 0.05 to 0.1, in
>>>> which case 10% of the surviving vertices would be expected to be false
>>>> positives.
>>>>
>>>> cheers,
>>>> Mike H.
>>>>
>>>> On Fri, 2009-10-16 at 12:03 +0200, Yulia WORBE wrote:
>>>>
>>>>
>>>>> Dear Freesurfer team,
>>>>>
>>>>> We are currently doing a cortical thickness studies between a group of
>>>>> psychiatric patients (n=60) and controls (n=30). We tested several
>>>>> smoothing levels (15mm, 20mm, 25mm)
>>>>>
>>>>> When setting an uncorrected threshold (such as p<0.005), we obtained
>>>>> several regions of decreased thickness, which are consistent with the
>>>>> pathology.
>>>>>
>>>>> However, when trying to correct for multiple comparisons using FDR
>>>>> ("Set Using FDR" button in qdec), the computed threshold is very high
>>>>> (e.g. 4.3 for 20mm smoothing) and, obviously, no significant regions
>>>>> are left.
>>>>>
>>>>> Did we do anything wrong in the analysis ?
>>>>>
>>>>> Thank you very much for your help,
>>>>> Yulia
>>>>>
>>>>>
>>>>>
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>>>>>
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-- 
Douglas N. Greve, Ph.D.
MGH-NMR Center
gr...@nmr.mgh.harvard.edu
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Fax: 617-726-7422

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