I am analysing some ChIP-seq data of a histone modification and different treatments.

I am new on bioinformatics. What I have so far are the peak calling and the differential binding events (using MACS2).

I would like to express the data using a heat map. I have found some papers that use this kind of graph. What I don't understand is what measure is used to generate this graphs, when I do the annotation of the peaks the files comes with genes, start and end sites, peak score (???), distance of the nearest trscription start site, Can I use any of this in my heat maps? What about normalization between treatments? How can I do this?

Thank you

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