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I am comparing 2 conditinos (negative control and treatment) in a Chip-seq experiment. I used MACS 2 (Call differential binding...
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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...
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I have done ChIP qPCR in macrophages, the negative control gene that I used was OCT4, it worked well, means, It did not amplyfied. Now I am doing experiments with another antibody and I noticed...
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