Closed tarak77 closed 5 years ago
Hey @tarak77, hope all is well for you too.
Pileup of contact maps is done with dip-c ard
. I think a typical pileup contact "map" (2D histogram of contacts, as in Fig. S7A) can be generated with something like:
dip-c ard -d10000000 -h200000 in.con > in.inter.d10M_h200k.ard
I'll write more details on the README page.
That would be awesome @tanlongzhi !!! Also a quick question, I think I am confused a bit.
For one of my sample cell, my haplotype-resolved .hic
file looks like this
What I want to do is to pile up all the inter chromosomal boxes(just in upper triangle or both) and see what the pattern looks like. I followed your command dip-c ard -d10000000 -h200000 impute3.round4.con.gz > in.inter.d10M_h200k.ard
. The output matrix looks like this
I was confused because looking at the genome wide contact matrix we just see some inter chromosomal contacts along the diagonal. And therefore shouldn't the pileup matrix should also show a diagonal bias instead of the super elliptical region??
P.S. I have attached the .con
file used here
impute3.round4.con.gz
Hey @tanlongzhi , Hope you are doing good! In your analysis of interchromosomal and long-range intrachromosomal contacts, how did you pileup the inter chromosomal contact maps to generate the super elliptical neighbourhood region? Because the dimensions for each chromosomes are different, I don't know how to overlay the haplotype resolved inter chromosomal contact maps?
Any help will be great!