I have HiChip data from h3k27ac. I have analyzed it with the tools that Homer has for His analysis and data looks good (even if the normalization shouldn't be exactly the same than for HiC experiments).
However, when I try to analyze my 1D H3K27ac ChIP dimension taking all the reads from my fast files, I don't see any enrichment. Does anyone know how this data can be mapped to obtain bigwigs, the typical ones, from the sequencing data? Is it possible? In the original paper, they do not show any 1D bigwig from the chipped data. In fact, they say that they call peaks, but they don't even show any bigwig/bedgraph of chipped peaks:
HiChIP ChIP Peak Calling
Dangling-end and self-ligation reads from the GM12878 Smc1a HiChIP HiC-Pro output were combined and processed to be compatible as a MACS2 BED file input. MACS2 was then run on the BED file using the no model and extsize 147 parameters and a FDR cutoff of 1%.
Can anyone help me?