background correction
2
0
Entering edit mode
@pedro-lopez-romero-1618
Last seen 10.3 years ago
An embedded and charset-unspecified text was scrubbed... Name: not available Url: https://stat.ethz.ch/pipermail/bioconductor/attachments/20060220/ 3fd023e3/attachment.pl
• 571 views
ADD COMMENT
0
Entering edit mode
Ben Bolstad ★ 1.2k
@ben-bolstad-1494
Last seen 7.3 years ago
Pedro, You can use the the rma background correction and normalization routines on a matrix. bg.adjust() implements basically the same background correction functionality that is carried out by the rma() command (except that rma() is implemented in compiled code). The easiest way for you to do this would be my.matrix.bg.rma <- apply(my.matrix, 2, bg.adjust) my.matrix.norm <- normalize.quantiles(my.matrix.bg.rma) Ben On Mon, 2006-02-20 at 15:23 +0100, Pedro L?pez Romero wrote: > Hi all, > > I want to normalize some data comming from a single chanel non affy > platform.- Id like to use the rma( ) function, but I would need to create > first an Affybatch object from the data that I have, a task that I find a > bit difficult to do given the data that I have. I think that would be much > more easier to use the bg.adjust ( ) internal function, but Im not sure if > I can apply this function directly to my data (a matrix with just raw > foreground intensities). > > Ive read the help file of this function but I still have some doubts. I > have understood that bg.adjust ( ) is the internal function that uses rma > ( ) to correct for the background bias. I figure that the input that it > needs is just a matrix with the raw intensities in natural scale and from > here, the function estimates the signal intensities corrected by the > background without using the background measures at all. Am I right?. My > data does not have PM and MM intensities, all the values are PM and I > have a probe per gene, Would still it be correct under theses cirmcumstances > using the bg.adjust ( ) function? > > > Other authors suggest to estimate the true signal intensities just by > substracting the median of the background probe intensities from the mean of > the foreground ones, and setting the negative values, lets say 0.5. I think > that this method is not completely correct, whats your opinion about > this?.- > > Moreover, I want to use the quantiles method to normalize the same data, > would it be right to apply the normalize.quantiles ( ) function directly to > the previous background corrected matrix?- > > Thanks a lot.- > > Pedro > > > > > > [[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
Georg Otto ▴ 510
@georg-otto-956
Last seen 10.3 years ago
Pedro L?pez Romero <plopez at="" cnic.es=""> writes: Pedro, > > I want to normalize some data comming from a single chanel non affy > platform.- Id like to use the rma( ) function, but I would need to create > first an Affybatch object from the data that I have, a task that I find a > bit difficult to do given the data that I have. I think that would be much > more easier to use the bg.adjust ( ) internal function, but I m not sure if > I can apply this function directly to my data (a matrix with just raw > foreground intensities). > you can not use RMA for your data, since it is designed for Affymetrix arrays, where you always multiple probes per gene. You should have a look at the users guide of the package limma and at the man pages of the functions described therein. You will find several methods for background correction and normalisation. For single channel data, you should have a look at chapter 9 of the limma users guide. Best, Georg
ADD COMMENT
0
Entering edit mode
Hi Georg, I am not using the rma( ) directly but the bg.adjust ( ) function, which I think it is the internal function that rma ( ) uses.- I thought that this function could be applied directly to a matrix of raw intensities without worring too much about whether we have multiple probes per gene or not. I might be misunderstood, though.- I will have a look at the limma package as well.- Thanks a lot. Best whishes p.- -----Mensaje original----- De: bioconductor-bounces at stat.math.ethz.ch [mailto:bioconductor-bounces at stat.math.ethz.ch]En nombre de Georg Otto Enviado el: martes, 21 de febrero de 2006 11:01 Para: bioconductor at stat.math.ethz.ch Asunto: Re: [BioC] background correction Pedro L?pez Romero <plopez at="" cnic.es=""> writes: Pedro, > > I want to normalize some data comming from a single chanel non affy > platform.- Id like to use the rma( ) function, but I would need to create > first an Affybatch object from the data that I have, a task that I find a > bit difficult to do given the data that I have. I think that would be much > more easier to use the bg.adjust ( ) internal function, but I m not sure if > I can apply this function directly to my data (a matrix with just raw > foreground intensities). > you can not use RMA for your data, since it is designed for Affymetrix arrays, where you always multiple probes per gene. You should have a look at the users guide of the package limma and at the man pages of the functions described therein. You will find several methods for background correction and normalisation. For single channel data, you should have a look at chapter 9 of the limma users guide. Best, Georg _______________________________________________ Bioconductor mailing list Bioconductor at stat.math.ethz.ch https://stat.ethz.ch/mailman/listinfo/bioconductor
ADD REPLY

Login before adding your answer.

Traffic: 820 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