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  • EDASeq setup problem

    I have a rather basic question regarding EDASeq that I have not found the answer to in reading the vignettes.

    Its pretty clear, how to work when one has technical replicates in individual lanes of the same library. However I have two conditions, each with three biological replicates, multiplexed and sequenced across three lanes.

    Where I get hung up then on is the best way to approach this. Should I be combining counts from all three lanes for each bio rep and normalizing that? Should I separate reads for each lane and normalize for both samples and lanes? In this latter case, how do I then recombine my technical replicates for differential expression?

    I have used EDASeq in the former, where each sample is the combined results of all three lanes and each sample treated as if it were its own lane. This has a huge impact on differential expression compared to previous analysis using only DESeq and EdgeR without correction for GC bias, with the result that it actually matches qPCR data better, but I am worried that this is still an inappropriate setup that is potentially giving me wrong results.
    Last edited by chadn737; 05-15-2012, 11:42 AM.

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