[BioC] edgeR/DESeq for ChIP-seq analysis
Mark Robinson
mark.robinson at imls.uzh.ch
Thu Nov 8 08:53:26 CET 2012
Dear Davide,
Indeed, edgeR and DESeq can be (and have been) used in this mode. We published something recently on this:
http://www.ncbi.nlm.nih.gov/pubmed/22879430
http://imlspenticton.uzh.ch/robinson_lab/ABCD-DNA/ABCD-DNA.pdf
You can apply that approach regardless of copy number being a factor ... basically, we counted tiled bins of the genome, but yes, you could focus in on regions of interest. The function abcdDNA() is really just a wrapper for the edgeR GLM. As usual, "normalization" can be delicate, depending on the type of data.
Also note that the DiffBind package already does something similar, but has a lot more machinery to collect and organize the sets of enriched regions.
Hope that helps.
Best, Mark
On 08.11.2012, at 08:37, Cittaro Davide wrote:
> Hi there, I'm writing to the list to have your comment about the possibility of using edgeR or DESeq for the analysis of ChIP-seq samples.
> Standard approaches to ChIP-seq analysis (relying on external software such as MACS) do not make analysis of replicates easy. I've seen people looking for peaks and then compare the common/differential intervals between replicates in case/control design. I wonder if a more general approach may work (and I'm going to test this anyway...).
> Since the negative binomial model stands for ChIP-seq analysis, both edgeR and DESeq should work well. One can use external software to identify regions and compute the union of all regions as it was a "gene list". From that point on, the pipeline should not differ from standard gene expression analysis.
> What do you think?
>
> d
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