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min1992 avatar min1992 commented on June 26, 2024

Hi,
I am having the same question, so do you solve this question? thank you.

Best

from crane-nature-2015.

skytguuu avatar skytguuu commented on June 26, 2024

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.

from crane-nature-2015.

blajoie avatar blajoie commented on June 26, 2024

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.

from crane-nature-2015.

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