Open skytguuu opened 6 years ago
Hi, I am having the same question, so do you solve this question? thank you.
Best
Hi,
My problem has been solved. The reason is happened the label of my input matrix. I changed my middle lane of label as my reference genome.
Sorry for the delay - for the original question, yes it is as simple as that. Simply divide the genome into segments defined by the boundary locations.
One caveat - you may wish to also consider the strength of the boundaries. e.g.
boundaries: chr1:2500000: strong chr1:5000000: weak chr1:5500000: strong
The above reflects 2 distinct tads, however, one may also wish to capture the fact that the major tad (chr1:2500000-5500000) also contains within it a smaller 'sub/nested' tad as evidenced by the much weaker boundary strength.
Hope that is clear.
Hi,
Recently, I am interested to your developed method "insulation score". And I tried to use matrix2insulation.pl to identify TAD domains. I am curious about the result of this perl script. Because, the final result from matrix2insulation.pl is a summary about the boundary location. So, if I want to call TAD domains, is that simply divide the genome into several parts according to this boundaries? For example, if the boundary is chr1:4000000-4500000. Then the TAD domains are two parts?(chr1:0-4000000,chr1:4500000-...)
Could you give me some advise?
Thank you so much!
Best, Garen