Hi,
I am using MACs to get read counts and peaks from my ChIP-seq files. Although MACs scales the control and treatment data sets to calculate peaks, the read files I get are not scaled. I am wondering if there is a way to do this - either in MACs or another program - so that I can upload the scaled read count files into a genome browser (such as IGV) to create figures.
Thanks for any suggestions!
Mary
I am using MACs to get read counts and peaks from my ChIP-seq files. Although MACs scales the control and treatment data sets to calculate peaks, the read files I get are not scaled. I am wondering if there is a way to do this - either in MACs or another program - so that I can upload the scaled read count files into a genome browser (such as IGV) to create figures.
Thanks for any suggestions!
Mary