hi all,
I wonder if there is a decent way to handle replicates when studying H3K36Me3 chip seq data. Usually the peaks for this kind of histone modification is broad.
Assume I have 3 normal samples and 3 tumor samples to compare. Most of the software tools are designed to compare 1 normal vs 1 tumor. So what do you usually do to after identifying the differentially peaks between each pair of normal and tumor? In another word, how do you merge these differential peaks to give a h3k36me3 profile between the two groups?
Thanks.
I wonder if there is a decent way to handle replicates when studying H3K36Me3 chip seq data. Usually the peaks for this kind of histone modification is broad.
Assume I have 3 normal samples and 3 tumor samples to compare. Most of the software tools are designed to compare 1 normal vs 1 tumor. So what do you usually do to after identifying the differentially peaks between each pair of normal and tumor? In another word, how do you merge these differential peaks to give a h3k36me3 profile between the two groups?
Thanks.
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