Closed RuiqinZheng closed 6 years ago
The data is not a mismatch. Scaling is performed by default in create.hic.table. You can turn it off if you set scale = FALSE.
HiCcompare is not designed for looking at inter-chromosomal differences. Most inter-chromosomal contact maps are very sparse and noisy which make them hard to analyze.
oh,I see it also can caculate the difference bwteen different-chromsome right? but the results maybe not crediable?
I think you will get errors if you try to use inter-chromosomal data due to the fact that distance cannot be calculated between different chromosomes.
yeah you are right.but if I just consider the all chromosome interactions as a big chromsome interaction? and if I set the scale=FALSE,does it will influence the final result?
I would not recommend combining all the data into a single matrix. It most likely will not work as this is not the intended use of HiCcompare.
Setting scale = FALSE just changes if there is an initial scaling based on total number of reads. The loess normalization should be able to account for total number of reads as well and scaling is not always necessary.
OK! Thanks a lot !
you see ,1) the original IF2 should be 6,but why the IF2 is 5.203323 in hic.table? 2) in my own data the first row of first data is: 1 1 624.0 the first row of second data is: 1 1 821.0 but why in the hic.table like this? chr1 start1 end1 chr2 start2 end2 IF1 IF2 D M
1: chr1 1 2 chr1 1 2 624 572.9156 0 -0.123223336 Does the software have do something when I use create.hic.table? another question is can I use this package to caculate inter-chromosme different interacion? Best Wishes~ Thanks a lot!