I have an input sample with high Kmer content, and no peaks are found in my IP samples (3replicates) when I use this input. On these same IP samples I do find peaks when using a baseline treatment input and also when I call peaks not using an input at all.
my input sample has the following Kmer Content:
Sequence Count PValue Obs/Exp Max Max Obs/Exp Position
AGGGGGG 13010 0.0 15.102037 1
TCGCGTA 345 1.1974935E-6 11.862445 37
TGGGGGG 25385 0.0 11.1068325 1
CGCCTGA 4925 0.0 9.191745 21
TATGCCG 2045 0.0 8.6882925 42
CGCGTAT 450 2.8213963E-4 8.33926 38
TCTCCCG 7310 0.0 7.170219 16
CGTATGC 2500 0.0 6.691238 40
CTCGTAT 2440 0.0 6.431545 38
ACACGTC 4290 0.0 6.4261694 9
TGCCGTC 3070 0.0 6.3503175 44
CGTCTGA 4360 0.0 6.3229723 12
TCCCGCC 9155 0.0 5.985545 18
CATCGCG 970 2.6135147E-5 5.974066 35
CTCCCGC 9090 0.0 5.728751 17
TCTCGTA 2575 0.0 5.695125 37
GCCGTCT 3315 0.0 5.2648993 45
CCGCCTG 10365 0.0 5.1227307 20
ATGCCGT 3405 0.0 5.120038 43
ACGTCTG 6060 0.0 5.0546627 11
were you able to solve this problem? I need to do the same and will appreciate your feedback,
were you able to filter the blacklisted regions with intersect from Bedtools? In order to use bedops you need to convert the bam file to bed filter and than convert the back to bam, I was able to do the filtering, but unable to convert the bed to bam file using bedtools bedtobam option any feedback would be greatly appreciated. thanks!!