Dear all,
We are using Diffbind to examine differential peak enrichment between male and female samples. Our input control is from the same sample before the immunoprecipitation stage. We have 4 replicates per treatment. The way we are using the Diffbind commands is exactly like given in the vignette and the manual.
It is our understanding that the Input control counts are subtracted from the ChIPed count data. We are comparing ChIP data from males to ChIP data from females using MACS2peaks in Diffbind. In the differential binding results we are observing that many of the significant peaks are from the X chromosome and these peaks have count data that is higher in females (XX) than males (XY). Our worry is that somehow the input subtraction is not accounting for the starting dose differences in the X chromosome in males and females.
Is there a way to check the Input subtraction stage and if you can please suggest steps to alleviate or explain this issue.
Thanking you.
Surjyendu Ray.