I've gotten a number of microarray datasets from GEO and arrayexpress, each of which looks at similar chemical treatments of mammalian cells. I downloaded the processed data, and from this I can easily generate log2 fold change values for each probe between the treated sample and the untreated sample. Are there any caveats to comparing these log2 FC values between datasets? Is this type of analysis OK, or do I need to go back to the CEL files for each dataset and normalize everything in one particular way?
Johnny,
Can you provide me an example of your code, I want to know how you was reading the processed data and how you was generating the log2 FC for probes. Thanks