Question: How to visualize Bam Files normalize
gravatar for perropery
19 months ago by
perropery0 wrote:

I have my DamID data (corrected by GATC fragments). I have two bams for Dam alone protein (the control) and the Dam-fusion protein (the experiment). Now I want to make peak calling, and normalize and visualize the data (for example, see a locus and in the same graph see the Dam-fusion signal corrected or substracted, with negative and positive axis), to see exactly how is the peak in every loci of intered.

Any sugestions to star with this?

Thanks a lot.

damidseq chip-seq • 486 views
ADD COMMENTlink written 19 months ago by perropery0
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