Displaying 20 results from an estimated 3000 matches similar to: "p.adjust on a vector including NA values"
2005 Jul 14
2
Partek has Dunn-Sidak Multiple Test Correction. Is this the same/similar to any of R's p.adjust.methods?
The Partek package (www.partek.com) allows only two selections for Multiple
Test Correction: Bonferroni and Dunn-Sidak. Can anyone suggest why Partek
implemented Dunn-Sidak and not the other methods that R has? Is there any
particular advantage to the Dunn-Sidak method?
R knows about these methods (in R 2.1.1):
> p.adjust.methods
[1] "holm" "hochberg" "hommel"
2004 Dec 19
1
limma, FDR, and p.adjust
I am posting this to both R and BioC communities because I believe there
is a lot of confusion on this topic in both communities (having searched
the mail archives of both) and I am hoping that someone will have
information that can be shared with both communities.
I have seen countless questions on the BioC list regarding limma
(Bioconductor) and its calculation of FDR. Some of them involved
2004 Dec 19
1
limma, FDR, and p.adjust
I am posting this to both R and BioC communities because I believe there
is a lot of confusion on this topic in both communities (having searched
the mail archives of both) and I am hoping that someone will have
information that can be shared with both communities.
I have seen countless questions on the BioC list regarding limma
(Bioconductor) and its calculation of FDR. Some of them involved
2004 Dec 20
1
Re: [BioC] limma, FDR, and p.adjust
Mark,
there is a fdr website link via Yoav Benjamini's homepage which is: http://www.math.tau.ac.il/%7Eroee/index.htm
On it you can download an S-Plus function (under the downloads link) which calculates the false discovery rate threshold alpha level using stepup, stepdown, dependence methods etc.
Some changes are required to the plotting code when porting it to R. I removed the
2005 Jan 16
1
p.adjust(<NA>s), was "Re: [BioC] limma and p-values"
I append below a suggested update for p.adjust().
1. A new method "yh" for control of FDR is included which is valid for any
dependency structure. Reference is Benjamini, Y., and Yekutieli, D. (2001).
The control of the false discovery rate in multiple testing under
dependency. Annals of Statistics 29, 1165-1188.
2. I've re-named the "fdr" method to "bh" but
2004 Dec 20
1
[BioC] limma, FDR, and p.adjust
You asked the same question on the Bioconductor mailing list back in August. At that time, you
suggested yourself a solution for how the adjusted p-values should be interpreted. I answered
your query and told you that your interpretation was correct. So I'm not sure what more can be
said, except that you should read the article Wright (1992), which is cited in the help entry for
p.adjust(),
2009 Mar 18
0
p.adjust(p, n) for n>length(p)
Hi all,
I am having a problem with the function "p.adjust" in stats. I have looked at the manuals and searched the R site, but didn't get anything that seems directly relevant. Can anybody throw any light on it or confirm my suspicion that this might be a bug?
I am trying to use the p.adjust() function to do Benjamini/Hochberg FDR control on a vector of p-values that are the
2010 Feb 07
1
p.adjust.Rd sugggestion
L.S.
In the current version of ?p.adjust.Rd, one needs
to scroll down to the examples section to find
confirmation of one's guess that "fdr" is an
alias of "BH".
Please find a patch in attachment which mentions
this explicitly.
Best,
Tobias
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2018 Jul 23
1
Suggestion for updating `p.adjust` with new method (BKY 2006)
Dear R contributors,
I suggest adding a new method to `p.adjust` ("Adjust P-values for Multiple
Comparisons",
https://stat.ethz.ch/R-manual/R-devel/library/stats/html/p.adjust.html).
This new method is published in Benjamini, Krieger, Yekutieli 2016 Adaptive
linear step-up procedures that control the false discovery rate
(Biometrika). https://doi.org/10.1093/biomet/93.3.491
This paper
2009 Feb 11
1
p.adjust; n > length(p) (PR#13519)
Full_Name: Ludo Pagie
Version: 2.8.1
OS: linux
Submission from: (NULL) (194.171.7.39)
p.adjust in stats seems to have a bug in handling n>length(p) for (at least) the
methods 'holm' and 'hochberg'.
For method 'holm' the relevant code:
i <- 1:n
o <- order(p)
ro <- order(o)
pmin(1, cummax((n - i + 1) * p[o]))[ro]
where p is the
2010 Aug 08
1
p.adjust( , fdr)
Hello,
I am not sure about the p.adjust( , fdr). How do these adjusted p-values
get?
I have read papers of BH method. For independent case, we compare the
ordered p-values with the alfa*i/m, where m is the number of tests. But I
have checked that result based on the adjusted p-values is different with
that by using the independent case method.
Then how do the result of p.adjust( , fdr) come?
And
2008 Mar 09
2
p-adjust using Benjamn and Hochberg
Hello,
I am trying to use the p.adjust function for multiple testing.
here is what i have
9997 201674_s_at 0.327547396
9998 221013_s_at 0.834211067
9999 221685_s_at 0.185099475
I import them from excel have have the gene symbol as well as the pvalue
here is the issue
> pa<-p.adjust(pt,method="BH")
Error in p[nna] : object is not
2002 Oct 30
1
typo in p.adjust (PR#2231)
Full_Name: Peter Ehlers
Version: 1.6.0
OS: Windows 2000 Pro
Submission from: (NULL) (136.159.61.178)
In:
p.adjust package:base R Documentation
In the paragraph:
Hochberg's and Hommel's methods are valid when the hypothesis tests
are independent or when they are non-negatively associated (Sarkar,
1998; Sarker and Chang, 1997). Hommel's method is
2011 Sep 30
1
Hi
Hi,
There is a question that I am confused.
I have a set of data like this:
hsa-miR-205--GATA3 0.797882767 1.08E-13
hsa-miR-205--ITGB4 0.750217593 1.85E-11
hsa-miR-187--PGF 0.797604155 3.24E-11
hsa-miR-205--SERPINB5 0.744124886 3.28E-11
hsa-miR-205--PBX1 0.734487224 7.89E-11
hsa-miR-205--MCC 0.72499934 1.80E-10
hsa-miR-205--WNT5B 0.717705259 3.33E-10
hsa-miR-200c--PKN2 0.721746815
2008 Jan 15
0
FDR for hypergeometric tests
Dear list,
I have performed several tests for the hypergeometric distribution
using phyper() for some gene annotation categories as follows
>phyper(26,830,31042,337, lower.tail=F)
>phyper(16,387,31042,337, lower.tail=F)
.
.
.
I am only running some selected categories but I would like to correct
this value for multiple testing since I
have 3121 possible tests according to 3121
2003 Jun 07
0
mt.plot...
Hello every GNU's,
I have a question about mt.plot, on multtest package.
I'm wondering how do a plot with test like bonferroni, holm, hochberg,... and
also résults of SAM(Significiance Analysis Microarrays) as we can see on
several document of Sandrine Dudoit.
Thanks a lot and Have a nice day
Sandrine
--------------------------------------------------------------------------------
1999 Nov 25
0
desperate!
Dear R community
I sent a message out a while ago asking for help with multiple
comparison tests for ANOVA's, but haven't had any response yet.
I'm sending a final desperate plea. If I can't get this done in R I'm
going to have to redo a whole lot of stuff in a commercial package,
which I'm REALLY not keen to do!
My problem is how to implement these tests in R. Below
2004 Jan 20
0
Re: Need help on how to list functions from a loaded pack age...
You can get help on the whole package by
> help(package="multtest")
which is likely pretty close to what you want. There's the index etc for the
package on the web as well. You can also just look in the package's
installation directory. If it's loaded you can do an ls(2) say if it loaded
in position 2, to get all objects in the package.
Reid
-----Original Message-----
2004 Jan 20
1
Re: Need help on how to list functions from a loaded package...
To All
How does one get a list of functions from a loaded package so that one can
then get the appropriate help for each of the functions. Currently my
method is
based on a lot of trial-and-error.
Here's an example of what I mean...
>From this forum I learn that an interesting package called "multtest" exists
on Bioconductor.
I then use R Console's "Packages" --
2008 Mar 01
2
Newbie: Incorrect number of dimensions
> dim(data.sub)
[1] 10000 140
#####extracting all differentially express genes##########
library(multtest)
two_side<- (1-pt(abs(data.sub),50))*2
diff<- mt.rawp2adjp(two_side)
all_differ<-diff[[1]][37211:10000,]
all_differ
#####list of differentially expressed genes##########
> probe.names<-
+ all_differ[[2]][all_differ[[1]][,"BY"]<=0.01]
Error in