HI,
I am looking at some ChIPSeq data that is rather unusual. The forward and reverse reads form deep thin stacks. Their width is mostly just above the read length of 75 bp. The 'peaks' (pseudo-peaks?) are distributed well across the mouse genome. Have any of you see this? What could be the reason? This experiment is investigating transcription factor binding ....
Thanks!
Jarus
I am looking at some ChIPSeq data that is rather unusual. The forward and reverse reads form deep thin stacks. Their width is mostly just above the read length of 75 bp. The 'peaks' (pseudo-peaks?) are distributed well across the mouse genome. Have any of you see this? What could be the reason? This experiment is investigating transcription factor binding ....
Thanks!
Jarus
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