Quantile Normalization on mice data
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@arnemulleraventiscom-466
Last seen 9.6 years ago
Hi Yen Lin, I've read your posting from 11 Feb to the BioC list about the design of your experiment with two "batches" of mice. I've a similar experimental layout: mouse cell cultures treated with a drig at different doses. The experiment was carried out three times under the same experimental conditions but in different laboratories. >From a hierachcical clustering and a principle component analysis of the cross-chip normalized probe sets I can clearly see that the batches cluster together. I've used affyPLM to shed some light into the experiment, however, I'm a bit lost with the interpretation. I was wondering how in the end you analysed your data. Did you try to use your own full factorial model for fitPLM, e.g. in your case PM ~ -1 + probe + stage + batch I've tried this with my experiment but I'm not sure how to interpret the output ... . kind regards, Arne > -----Original Message----- > From: bioconductor-bounces@stat.math.ethz.ch > [mailto:bioconductor-bounces@stat.math.ethz.ch]On Behalf Of > Yen Lin Chia > Sent: 11 February 2004 07:09 > To: bioconductor@stat.math.ethz.ch > Subject: [BioC] Quantile Normalization on mice data > > > Hi, > > I'm working on some mice data from two batches (experiment carried out > different time), but what I'm interested is to compare the gene > expression between two stages > > Stage I:  2 mice from batch D and 1 mouse from batch E > Stage II: 1 from batch D and 4 from batch E. > > Two tissue samples are taken for each mouse, center of the > tumor and the > rim of the tumor.  Thus, I have two set of results layout > (above-mentioned).  My first thought is to normalize the rim > and core of > the tumor separately, but ignoring the batch variation. > Wonder if this > is a good apprach. > > Will the batch variation be problematic, from box plots, you can group > the plots into batches (regardless of stages). > > I'm trying to estimate the batch effect by using affyPLM, > (i.e. dropping > samples as a factor), is p-values computed along with the function? I > only see the estimates and standard error.  I'm new to R and > bioconductor packages. > > Thanks. > > Yen Lin > > _______________________________________________ > Bioconductor mailing list > Bioconductor@stat.math.ethz.ch > https://www.stat.math.ethz.ch/mailman/listinfo/bioconductor >
Normalization Clustering probe affyPLM Normalization Clustering probe affyPLM • 914 views
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