Print

Print


 >
 > Dear Shary,
 > We have just been discussing your observation that uncorrected
 > p-values based on extent can be greater than the corrected
 > p-values based on spatial extent.  I thought it would be useful to
 > share this discussion:

 > The uncorrected p-value is the probability a cluster (of size n) has k
 > or more voxels
 >                                     p = p(n > k)
 > given that the cluster exists (i.e., p(n > 0) = 1).  This can be useful
 > for making inferences about a cluster you have identified as
 > interesting, based on its extent.  The corrected p-value is the
 > probability of getting any cluster of k or more voxels in the search
 > volume
 >                                    P = 1 - spm_Pcdf(0,E(S).p)
 > where spm_Pcdf is the cumulative density function for the Poisson
 > distribution and E(S) is the rate of maxima (i.e., expected number
 > in the search volume S), approximated with the Euler characteristic
 > (see
 > Friston KJ, Holmes A, Poline JB, Price CJ, Frith
 > CD.
 > Detecting activations in PET and fMRI: levels of inference and power.
 > Neuroimage. 1996 Dec;4(3 Pt 1):223-35
 > for more details).
 > At small values P is approximately equal to E(S).p.  You can see
 > that the corrected p-value P can be less that the uncorrected
 > p-value if E(S) is small.

 > Heuristically, if you used a low height threshold you might expect 4
 > clusters on average, by chance (i.e., E(S) = 4).  In this instance
 > the probability of getting one or more clusters larger than k voxels
 > is greater than the probability of any single cluster being greater
 > than k voxels.  (i.e., P > p).   However, when you use a high height
 > threshold E(S) is small and P < p.
 >
 > More specifically, for cluster-level inference, we can write
 >
 > P = 1 - exp (-E(S). p)
 >
 > Then P < p if
 >
 > E(S) < [- log(1-p)]/p
 >
 > For your first inference you have p = 0.34 which means this
 > threshold is E(s) < 1.22. But the expected number of clusters
 > is very small: E(S)=0.05. So we expect P < p, which is indeed the
 > case.
 >
 > This may seem counterintuitive because the corrected p-value is
 > more significant than the uncorrected p-value.  This happens
 > because the uncorrected p-value is conditioned on the cluster
 > existing.  In other words, you have to identify the cluster before
 > making an inference (in the same way that you have to identify
 > a specific maximum before using the uncorrected p-value based
 > on height).
 > The uncorrected p-value based on extent is provided for situations
 > in which you know a priori which cluster you want to make an
 > inference about.  This can be useful in making anatomically
 > constrained inferences(see
 >  Friston KJ.  Testing for
 > anatomically specified regional effects. Hum Brain Mapp.
 > 1997;5(2):133-6
 > ).
 > I hope this helps.
 > Karl


(Mr.) Shahryar (Shary) Rafi-Tari wrote:

> Dear SPM authors,
> 
> This is a follow up to the e-mail I sent to Dr. Ashburner.  Attached 
> please find an SPM2 output (two groups/SPECT/ 1 scan per subject/ANCOVA) 
> showing uncorrected cluster level p value is larger than corrected 
> cluster level p-value after corrected the height threshold (FWE<0.05).  
> This happens with any analysis using I do with FWE and since I am going 
> to write a paper on the results and report both corrected and 
> uncorrected p-values, I am trying to figure this out.  I greatly 
> appreciate your comments.
> 
> regards,
> Shary
> 
> At 10:24 AM 07/10/2005 +0100, John Ashburner wrote:
> 
>> Dear Shary,
>>
>> >     *  Why when FWE is used to correct height threshold for multiple
>> > comparisons, the cluster level uncorrected p value is larger (for
>> > instance p<0.24) than the cluster level corrected p value (for
>> > instance p<0.02)?   It is usually vice versa when FWE is not use as a
>> > result of correcting it (which is logical).   Is it because FWE
>> > affects only the corrected cluster level p value?
>>
>> I have no idea about this part of SPM I'm afraid.  I've forwarded your 
>> query
>> on the other developers to see if they have any ideas.
>>
>> Best regards,
>> -John
> 
> 
> 
> Shahryar Rafi-Tari, M.Sc.
> Database Consultant / Imaging Analyst
> ADNI Imaging Project Coordinator at Sunnybrook
> 
> 2075 Bayview Avenue
> Sunnybrook & Women's College Health Sciences Centre
> Linda C Campbell Cognitive Neurology Research Unit
> Room B630
> Toronto, Ontario, Canada M4N 3M5
> 
> E-mails: [log in to unmask]
>  Tel: 416-480-6100 ext. 3281
> 
> Disclaimer: This e-mail is intended for the addressee(s) only, and may 
> also be confidential. Any review, retransmission, or other use of this 
> information by persons other than the addressee is strictly prohibited. 
> If you are not the addressee or received this by mistake, please contact 
> the sender and delete the material from all your computers.
> 
> ------------------------------------------------------------------------
> 

-- 
William D. Penny
Wellcome Department of Imaging Neuroscience
University College London
12 Queen Square
London WC1N 3BG

Tel: 020 7833 7475
FAX: 020 7813 1420
Email: [log in to unmask]
URL: http://www.fil.ion.ucl.ac.uk/~wpenny/