Many differential expression packages out there require the raw_count as their input but I want to use my normalized values as input. From what I can find limma+voom can handle normalized values. Are there any other package that allows me to use normalized values?
I've tried using DESeq2 despite reading various comments saying it only works with raw_count values but when I looked at the fold change values and manually inspecting the normalized values, the fold change output seems pretty reasonable. Why is it that you can't use normalized values with DESeq2?
Thanks
How exactly did you normalize your counts? The reason packages say not to do this is that historically people have done it in incorrect ways...
My normalized values are ratio. The ratio is generated by coverage value (mean,median, etc.) of region1 divided by region2 of the same genes. I'm trying to identify regions comparison ratios that change significantly from normal to cancer
I'm not sure that would have a negative-binomial mean-dispersion relationship. Personally I would reformulate the regions as the same gene in paired samples, which would be asking essentially the same question but without masking the underlying counts.