Dear all,
I have CpG methylation from 450k and RRBS. Now I am trying to map these CpGs to genes' different regions, e.g. around TSS. My concerns is if the direction (+ or -) should be considered here. For example, probes from 450k have directions given by the annotation file, and RRBS also gives the directions of reads. So should I map them into the same-direction genes?
Thanks.