I was wondering if anyone can help me. Looking on IGV at my ChIP seq data I am noticing that there seems to be an overlap between 2 different TFs binding to the same location. I know you can do read density plots to show the location across the gene where there is the highest read density. Is there a way that for all peaks where there is an overlap between the 2 TFs I can physically show that using read density? Instead of just having a number of peaks where the two overlap in genomic region.
Thank you this is really helpful. I’ve been able to follow the documentation and done some plots. I do have another question though for each TF I have a separate bigwig file. So far I have put both TF bed files for -R and the two corresponding bigwig files for -S with a space in between. However when I plot I get two graphs one based on TF1 bigwig and the other based on TF2 bigwig. Is there a way to do it that it computes it together?
Sorry, I don't get what you're envisioning. Do you have an example image you could link to?
Reading that back it is quite confusing, sorry! But I managed to solve what I wanted to do, I just misunderstood part of the way computeMatrix works. However my only issue now is I have 4 replicates for each TF, therefore for each TF I have 4 bigwig files. Is there any way to merge these so I can have one plotProfile graph that merges all 4 replicates for each TF together?
You may want to look into
wiggletools
that will allow you to generate one summarized bw file per TF, e.g. using the sum or the average (hopefully also the median).Just had a look into that and seems perfect what I want. Thank you for your help!