about two way anova on time and treatment
1
0
Entering edit mode
Ana Conesa ▴ 130
@ana-conesa-2246
Last seen 10.2 years ago
Hi James, You might like to have a look to a paper we recently published where we address this problem (http://bioinformatics.oxfordjournals.org/cgi/reprint/btm251v1). We describe here the ASCA-genes methodology to analyze multiple series time course microarray data. Basically, first ANOVA is applied to each gene and then perform PCA for each of the matrix coffecients of the ANOVA model. We use then PCA scores to discover main expression patterns associated to each experimental factor and we propose aswell a gene-selection criterium. You also obtain the % variability associated to each experimental factor (and noise) so you can use this to unswer your question of the factor (time or treatment) with the highest effect. R scripts with the algorithm are avialable. Best regards Ana ---------------------------------------- Ana Conesa, PhD Bioinformatics Department Centro de Investigacion Principe Felipe Avd. Saler 16, 46013 Valencia (Spain) http://bioinfo.cipf.es ---------------------------------------- ======================================== CAMDA 2007 Conference in Valencia, 13-14 December 2007 http://camda.bioinfo.cipf.es ======================================== > > >---- Mensaje Original ---- >De: janderson_net at yahoo.com >Para: bioconductor at stat.math.ethz.ch >Asunto: RE: [BioC] about two way anova on time and treatment >Fecha: Fri, 29 Jun 2007 13:56:22 -0700 (PDT) > >>Hi, >> >>I have affy data for time and treatment, I did a two way anova for >each gene. What's the correct way to evaluate whether time effect is >more imporant or treatment effect is more important? I think >averaging the variance component of each gene is not a very good way, >since not all genes are equally important, in addition, most of the >genes are noisy genes. I am thinking of doing a PCA and take the >first several components, instead of doing anova on each gene, I can >do two way anova on the scores of the first several component, then I >can use a weighted average (weight is determined by the amount of >variance each PC captured), is this a good way? Can somebody give me >some suggestions on this? Thanks. >> >>James >> >> >>--------------------------------- >>Luggage? GPS? Comic books? >> >> [[alternative HTML version deleted]] >> >>_______________________________________________ >>Bioconductor mailing list >>Bioconductor at stat.math.ethz.ch >>https://stat.ethz.ch/mailman/listinfo/bioconductor >>Search the archives: http://news.gmane.org/gmane.science.biology.inf >ormatics.conductor >>
Microarray affy Microarray affy • 1.2k views
ADD COMMENT
0
Entering edit mode
@james-anderson-1641
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/20070705/ dfb17637/attachment.pl
ADD COMMENT
0
Entering edit mode
An embedded and charset-unspecified text was scrubbed... Name: not available Url: https://stat.ethz.ch/pipermail/bioconductor/attachments/20070706/ 9c19b91f/attachment.pl
ADD REPLY

Login before adding your answer.

Traffic: 489 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