how to run SAM analysis
1
0
Entering edit mode
weinong han ▴ 270
@weinong-han-1250
Last seen 10.2 years ago
An embedded and charset-unspecified text was scrubbed... Name: not available Url: https://stat.ethz.ch/pipermail/bioconductor/attachments/20050831/ 1b4c3f6b/attachment.pl
• 942 views
ADD COMMENT
0
Entering edit mode
@adaikalavan-ramasamy-675
Last seen 10.2 years ago
Your design is seriously unbalanced and under-powered. I would suggest you increase the sample size in the normal group. This holds no matter what test statistics you plan on using. LIMMA would probably be better for your purposes. I _think_ it has been shown empirically to hold for small sample sizes. Regards, Adai On Wed, 2005-08-31 at 19:22 -0700, weinong han wrote: > Hi, List, > > I have 17 affymetrix .cel files and ran RMA analysis on them. Now I want to run SAM analysis(unpaired, 3 normal tissues and 14 diseased tissues) on the RMA data with R2.1.1. > I have installed the samr package. > > Questions: How to run the SAM analysis after the RMA analysis? The better, the more detailed explanations. > > Any advice and suggestions will be much appreciated. > > > > > Best Regards > > Han Weinong > hanweinong at yahoo.com > > __________________________________________________ > > > > [[alternative HTML version deleted]] > > _______________________________________________ > Bioconductor mailing list > Bioconductor at stat.math.ethz.ch > https://stat.ethz.ch/mailman/listinfo/bioconductor >
ADD COMMENT
0
Entering edit mode
hi! if you want to run SAM anaylsis anyway, try the following (not sure if it works that way, but worth a try) for example (RMA or gcRMA as you want, for gcRMA load the library gcRMA) data.norm <- rma(data, normalize = TRUE, background = TRUE) now construct the vector cl as needed by the SAM function: cl <- c(0,0,0,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1) or cl <- rep(0:1, c(3,14)) with 0 being the normal tissues and 1 the diseased ones. (use pData(data) to see the correct order of your data) and then: data.sam <- sam(data.norm, cl) don?t forget to filter the genes with the genefilter function ( genefilter(data,flist) ) in the genefilter library! please everyone send me positive or negative answers, would appreciate if my instructions were correct or not. thanks! cheers, gregor
<font style="FONT-SIZE:11px;FONT-FAMILY:tahoma,sans-serif">
From: Adaikalavan Ramasamy <ramasamy at cancer.org.uk>
Reply-To: ramasamy at cancer.org.uk
To: weinong han <hanweinong at yahoo.com>
CC: bioconductor at stat.math.ethz.ch
Subject: Re: [BioC] how to run SAM analysis
Date: Thu, 01 Sep 2005 22:48:51 +0100
>Your design is seriously unbalanced and under- powered. I would suggest
>you increase the sample size in the normal group. This holds no matter
>what test statistics you plan on using.
>
>LIMMA would probably be better for your purposes. I _think_ it has been
>shown empirically to hold for small sample sizes.
>
>Regards, Adai
>
>
>
>On Wed, 2005-08-31 at 19:22 -0700, weinong han wrote:
> > Hi, List,
> >
> > I have 17 affymetrix .cel files and ran RMA analysis on them. Now I want to run SAM analysis(unpaired, 3 normal tissues and 14 diseased tissues) on the RMA data with R2.1.1.
> > I have installed the samr package.
> >
> > Questions: How to run the SAM analysis after the RMA analysis? The better, the more detailed explanations.
> >
> > Any advice and suggestions will be much appreciated.
> >
> >
> >
> >
> > Best Regards
> >
> > Han Weinong
> > hanweinong at yahoo.com
> >
> > __________________________________________________
> >
> >
> >
> > [[alternative HTML version deleted]]
> >
> > _______________________________________________
> > Bioconductor mailing list
> > Bioconductor at stat.math.ethz.ch
> > https://stat.ethz.ch/mailman/listinfo/bioconductor
> >
>
>_______________________________________________
>Bioconductor mailing list
>Bioconductor at stat.math.ethz.ch
>https://stat.ethz .ch/mailman/listinfo/bioconductor
</font>
ADD REPLY

Login before adding your answer.

Traffic: 631 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6