Hello, this is great work and has helped me save a lot of time in identifying seqlet locations in my chrombpnet inputs. For the most part, finemo has been extremely easy to use, but I'm noticing that I'm missing outputs in some peaks. For example, I'm using the following interval as part of my input into chromBPnet:
As seen in the genome browser track linked below, the ATAC bigWig tracks associated with this interval show a small peak in the beginning followed by a larger peak:
Ideally, I'd like to find hits in both peaks without having to splice the original bed file and re-run chrombpnet contribs_bw + modisco motifs since these will require another day of CPU + GPU time. Is there a hyperparameter I can set to increase the sensitivity of these hits? Thanks a lot, any help is greatly appreciated!
Hello, this is great work and has helped me save a lot of time in identifying seqlet locations in my chrombpnet inputs. For the most part, finemo has been extremely easy to use, but I'm noticing that I'm missing outputs in some peaks. For example, I'm using the following interval as part of my input into chromBPnet:
chr18 61105509 61105961 mouse_Kupffer_ATAC_peak_103769 228 . 6.06604 22.8862 20.0038 358
As seen in the genome browser track linked below, the ATAC bigWig tracks associated with this interval show a small peak in the beginning followed by a larger peak:
https://genome.ucsc.edu/s/kylexwustl/mm10_chr18_issue
However, after running the
call-hits
method, the seqlet hits I get in this interval seem to only be in the larger peak:Ideally, I'd like to find hits in both peaks without having to splice the original bed file and re-run
chrombpnet contribs_bw
+modisco motifs
since these will require another day of CPU + GPU time. Is there a hyperparameter I can set to increase the sensitivity of these hits? Thanks a lot, any help is greatly appreciated!