Yes, I am aware of that. In my situation I have only the rlog values only, unfortunately. How do I calculate the fold-change from this information?
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How to calculate the logged fold-change from rlog values (obtatined from DESeq2)? I have a list of genes with rlog values in two conditions (no other information). Is lfc = rlog_A / rlog_B or fc = rlog_A - rlog_B?
But note that DESeq doesn't use the rlog values when computing fold changes. The rlog values are just nice for some kinds of visualizations.
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