I am interested in splitting my ChIP-seq peaks and I am using macs2 to call peaks. The first issue is that my peaks are not reported as a bed file, but rather an xls file. Also, I don't get a wig directory and when I try to run the --wig or -w command it is not recognized. How can I create these files in order to run the peak splitter.
As an alternative I have tried the "searching for subpeak summits" argument but I get a strange output (copied below). Please note the redundant end and start locations I get.
chr start end length abs_summit pileup -log10(pvalue) fold_enrichment -log10(qvalue) name
DP001225 37110 38802 1693 37196 23.00 3.88662 2.17128 1.80028 /scratch/02030/mariamok/DP/me1-stampy-filter.bam.summits.150_peak_1a
DP001225 37110 38802 1693 38159 29.00 7.66922 3.03233 4.64792 /scratch/02030/mariamok/DP/me1-stampy-filter.bam.summits.150_peak_1b
DP001225 37110 38802 1693 38553 20.00 3.44985 2.13192 1.49557 /scratch/02030/mariamok/DP/me1-stampy-filter.bam.summits.150_peak_1c
DP001225 39140 39926 787 39224 24.00 5.18357 2.53800 2.72921 /scratch/02030/mariamok/DP/me1-stampy-filter.bam.summits.150_peak_2a
DP001225 39140 39926 787 39470 22.00 4.28164 2.33496 2.07672 /scratch/02030/mariamok/DP/me1-stampy-filter.bam.summits.150_peak_2b
DP001225 49544 49899 356 49641 57.00 6.03728 1.95897 3.40313 /scratch/02030/mariamok/DP/me1-stampy-filter.bam.summits.150_peak_3
DP001225 92818 94406 1589 92897 139.00 4.06026 1.38781 1.94649 /scratch/02030/mariamok/DP/me1-stampy-filter.bam.summits.150_peak_4a
DP001225 92818 94406 1589 93607 600.00 10.28946 1.31543 6.70696 /scratch/02030/mariamok/DP/me1-stampy-filter.bam.summits.150_peak_4b
DP001225 92818 94406 1589 93980 639.00 40.96196 1.79016 35.43500 /scratch/02030/mariamok/DP/me1-stampy-filter.bam.summits.150_peak_4c