Entering edit mode
5.8 years ago
Lila M
★
1.3k
Hi everybody, I have an issue here, let's say I have this kind of data:
chr w_start w_end ratio_w ratio_c chr txt_start txt_end strand gene
chr1 879000 879999 0.102 0.306 chr1 879584 882440 - ENSG00000188976
chr1 879000 879999 0.102 0.306 chr1 879584 894670 - ENSG00000188976
chr1 879000 879999 0.102 0.306 chr1 879585 893838 - ENSG00000188976
chr1 880000 880999 0.357 0.102 chr1 879584 882440 - ENSG00000188976
chr1 880000 880999 0.357 0.102 chr1 880699 880942 - ENSG00000188976
chr1 880000 880999 0.357 0.102 chr1 879584 894670 - ENSG00000188976
chr1 880000 880999 0.357 0.102 chr1 879585 893838 - ENSG00000188976
chr1 881000 881999 0.153 0.051 chr1 879584 882440 - ENSG00000188976
where w_start w_end
is window start and end, ratio_w ratio_c
is ratio in Watson and Crick strand and the other part of the data refers to transcription factors of interest.
I would like to plot the typical TSS profile using the ratios for Watson and Crick strand around my TSS (something like the figure1e of this paper. But I can't figure out how to do it in R. Any suggestions?
Hi Lila M , please have a look at either the
deeptools
documentation if you want something via command line or e.g. thegenomation
package in R. Both can do it, documentation is extensive.Thank you for the tip, but as far as I understand, deeptools needs the bam files or bigwig files (I only have this bed file to work with). I will have a look into genomation as I never work with it before.
Sorry but I can't figure out how to do it with those programs, more help will be very handy! Thanks!