Re: [R] FDR analyses: minimum number of features

2005-09-23 Thread Dupont, William
 Thanks.  That is an excellent idea.  Bill

-Original Message-
From: Spencer Graves [mailto:[EMAIL PROTECTED] 
Sent: Thursday, September 22, 2005 9:01 PM
To: Dupont, William
Cc: Kjetil Brinchmann Halvorsen; r-help@stat.math.ethz.ch
Subject: Re: [R] FDR analyses: minimum number of features

  Have you considered Monte Carlo?  From previous work, you
could estimate a distribution for the differences to be detected and use
that as input to a Monte Carlo, computing thereby a distribution for FDR
as a function of distribution of differences and the number of features.

 From this, you could estimate probabilities for obtaining results that
were bogus vs. marginal, barely useful vs. highly accurate and plot them
vs. alternative budgets, etc.

  I hope this comment makes more sense than my earlier nonsense.

  spencer graves

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[R] FW: FDR analyses: minimum number of features

2005-09-22 Thread Dupont, William
Dear Dr.  Graves

Many thanks for your response.  FDRs and their associated q values do
differ from Type I error rates and P values (See Storey and Tibshirani
PNAS 2003;100:9440-5).  It is an approach that is rapidly gaining
popularity in the analysis of genomic data where we have massive numbers
of covariates measured on a comparatively modest number of subjects.  To
my mind it is a real advance in dealing with the extreme multiple
comparisons problems that afflict such data.  Unfortunately, it is still
a relatively new technique and I do not believe that a consensus as to
the number of needed response features has been reached.

Submitting my question to the R-help list was a long shot, although
Storey's software for this methodology is written in R.

With best wishes,

Bill Dupont 

-Original Message-
From: Spencer Graves [mailto:[EMAIL PROTECTED]
Sent: Wednesday, September 21, 2005 9:27 AM
To: Dupont, William
Cc: r-help@stat.math.ethz.ch
Subject: Re: [R] FDR analyses: minimum number of features

  Two thoughts on this:

  1.  Your FDR (Not Franklin Delano Roosevelt) sounds like
another name for Type I error rate.  The definition of reasonably
reliable FDRs 
would seem to relate to the status of the literature on this issue among
researchers in genotyping.  As more reports of FRDs in genotyping are
published, I would expect that methodology for estimation and the
standard for accuracy would similarly evolve.

  2.  Have you tried the Bioconductor (www.bioconductor.org/)
listserve?  They might be able to say something more useful than a
general list like this.

  spencer graves

Dupont, William wrote:

 Dear List,
 
 We are planning a genotyping study to be analyzed using false 
 discovery rates (FDRs) (See Storey and Tibshirani PNAS 2003; 
 100:9440-5).  I am interested in learning if there is any consensus as

 to how many features (ie. how many P values) need to be studied before

 reasonably reliable FDRs can be derived.  Does anyone know of a 
 citation where this is discussed?
 
 Bill Dupont
 
 William D. Dupont  phone: 615-343-4100  URL
 http://biostat.mc.vanderbilt.edu/twiki/bin/view/Main/WilliamDupont
 
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--
Spencer Graves, PhD
Senior Development Engineer
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Re: [R] FDR analyses: minimum number of features

2005-09-22 Thread Dupont, William
I agree.  What is unclear to me is the optimal way of justifying sample
size and SNP selection in grant applications that use the FDR approach.

-Original Message-
From: Kjetil Brinchmann Halvorsen [mailto:[EMAIL PROTECTED] 
Sent: Wednesday, September 21, 2005 9:45 PM
To: Spencer Graves
Cc: Dupont, William; r-help@stat.math.ethz.ch
Subject: Re: [R] FDR analyses: minimum number of features

Spencer Graves wrote:

 Two thoughts on this:

 1.  Your FDR (Not Franklin Delano Roosevelt) sounds like
another 
name for Type I error rate.

It is certainly not the same as type I error rate. Type I error rate is
the proportion of true nulls which are rejected, while the FDR is the
proportion of rejected null hypothesis which really are true nulls!

To me FDR seems like a more promising avenue to multiple testing than
the old familywise error rate. Who knows what is a family?

Kjetil

 The definition of reasonably reliable FDRs 
would seem to relate to the status of the literature on this issue 
among researchers in genotyping.  As more reports of FRDs in genotyping

are published, I would expect that methodology for estimation and the 
standard for accuracy would similarly evolve.

 2.  Have you tried the Bioconductor (www.bioconductor.org/) 
listserve?  They might be able to say something more useful than a 
general list like this.

 spencer graves

Dupont, William wrote:

  

Dear List,

We are planning a genotyping study to be analyzed using false 
discovery rates (FDRs) (See Storey and Tibshirani PNAS 2003; 
100:9440-5).  I am interested in learning if there is any consensus as

to how many features (ie. how many P values) need to be studied before

reasonably reliable FDRs can be derived.  Does anyone know of a 
citation where this is discussed?

Bill Dupont

William D. Dupont  phone: 615-343-4100  URL
http://biostat.mc.vanderbilt.edu/twiki/bin/view/Main/WilliamDupont

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-- 

Kjetil Halvorsen.

Peace is the most effective weapon of mass construction.
   --  Mahdi Elmandjra





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[R] FDR analyses: minimum number of features

2005-09-19 Thread Dupont, William
Dear List,

We are planning a genotyping study to be analyzed using false discovery
rates (FDRs) (See Storey and Tibshirani PNAS 2003; 100:9440-5).  I am
interested in learning if there is any consensus as to how many
features (ie. how many P values) need to be studied before reasonably
reliable FDRs can be derived.  Does anyone know of a citation where
this is discussed?

Bill Dupont 

William D. Dupont  phone: 615-343-4100  URL
http://biostat.mc.vanderbilt.edu/twiki/bin/view/Main/WilliamDupont

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