Hello everyone
We were analyzing our ChIP seq data of our protein on human rDNA (ribosomal DNA ) locus, after mapping it with hg-38 human genome assembly modified for rDNA analysis (https://doi.org/10.1016/j.jbc.2023.104766). we generated .BW files through BamCoverage for both input and IP, then we used MACS2 to find the significant peaks with q -value 0.001, and we got significant binding on rDNA locus. However, we want to make the input track flat with respect to the IP and to retain the significant peaks in the IP track only. Kindly help us regarding this. We have attached the IGV snap shot of our input and IP replicates. Tracks are shown in replicates, also the narrowpeak files from MACS2 are shown
Thanks. We'll try this and update you soon.