Hi
We have two experiments run on illumina arrays done by the same company. I want to combine the data. I normally use Limmas functions (read.ilmn, and neqc) to deal with normalisation of the data. However if I combine these two experiments what is the best way of going about doing this. I am aware they need background correcting and quantile normalisation using the negative and positive control probes on the arrays.
edit - platform is the same, but need to compare healthy in one group with diseased in the other group. why it was done like this - well i didnt have any say in it - i cant go into that. the company we use is highly efficient and everything is standardised so batch should not be much of a problem.
Best,
Chris
Thanks that is what I wanted.
My results from this look way off (too much DE). I deleted probes in the control files that did not match in both control probe exports, could this have this effect? Unless this is a batch issue.
You said above "My results from this look way off (too much DE)"---that's sounds very arbitary at all---what do you mean too "much DE" ? By which cutoffs or comparisons ? What is your biological question of interest ? Did you also created any diagnostic plots, such as a MDS plot to see if your samples are separated based on your biological question ? And there are indeed differences in expression to be suggested ? Or if there is any batch effect present ? (which could also be invastigated from a hierarchical clustering of your samples, a PCA plot etc.). A brief review of your code used might be more appropriate to further help or suggestions.