I want to call peaks for a nucleosome density signal from the ENCODE dataset. Is it ok to use a package like MACS to do so, or are there underlying assumptions to such packages that I am overlooking?
Thanks!
EDIT: Upon further inspection, the data I want to call peaks for is in the .bigWig file format. Any way to call peaks on such a format? (i.e. converting it to a .bed file?)
Why don't you want to use ENCODE's peak calls ?
As far as I can tell, peak calls are not published for the Nucleosome position dataset. (I'd love to be proven wrong, however!)