PCA plots
1
0
Entering edit mode
@jakub-orzechowski-westholm-1049
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/20050818/ 74d98bb1/attachment.pl
• 546 views
ADD COMMENT
0
Entering edit mode
@adaikalavan-ramasamy-675
Last seen 10.2 years ago
Remember that points in the unlog scale is much more skewed than those on the log scale. i.e. on the unlogged scale, most of the points are close to zero and the ones slightly away from this cluster is much easier to visualise. i.e. log transformation spreads the points out more evenly. If you points were characterised by a single gene, then something along the following lines might be happening : x <- rexp( 1000 ) par(mfrow=c(1,2)) hist(x, main="unlogged scale") hist(log(x), main="log scale") Regards, Adai On Thu, 2005-08-18 at 11:26 +0200, Jakub Orzechowski Westholm wrote: > Hi! I have a couple of qustions about PCA plots for microarrays. I have run a number of affymetrix arrays, and used the affy package for background correction, normalization etc (standard RMA procedure). When I then want to make PCA plot of the arrays, what makes most sense: To use the values from rma which are log scale, or to transform them back to "normal scale"? (In my case the latter gives more outliers...). Is there any established standard for doing this? > > kind regards > Jakub Orzechowski > [[alternative HTML version deleted]] > > _______________________________________________ > Bioconductor mailing list > Bioconductor at stat.math.ethz.ch > https://stat.ethz.ch/mailman/listinfo/bioconductor >
ADD COMMENT

Login before adding your answer.

Traffic: 930 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