Hello!
I have a set of gene expression data that compares effects of a treatment to control over time, in cells that are undergoing differentiation. I have five experimental groups: time zero (just before treatment was applied) and 12 and 48 hrs, +/- treatment. I want to determine how treatment influences the expected changes over time (those related to differentiation). I can do the 2-way ANOVA with interaction, using the 12 and 48 hr groups, but this misses the effects from 0 to 12 hrs. Is it valid to use the same set of time zero data for both treatments, so that I have a balanced design? Any other suggestions about how to analyze these data?
thanks!
Code should be placed in three backticks as shown below
# include your problematic code here with any corresponding output
# please also include the results of running the following in an R session
sessionInfo( )
Hi Gordon, Thanks -- this is very helpful. Can I load data that are already normalized into Limma? My data are from targeted RNAseq, so normalized in a simpler way than for whole genome datasets.
thanks, Brynn
Yes, in general, analysing pre-normalized data in limma is no problem. However, in the case of RNA-seq, there is no universal agreement of what it means to normalize the counts and many of the normalization methods used by the bioinformatics community destroy the statistical properties of RNA-seq data. If you have normalized logCPM or vst values then fine, but normalization that corrects for gene length causes problems, see for example: