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.
1 answer
Individual Cs will have a strand and about this is present in the RRBS reads. So that much is worthwhile considering. Now the perhaps your question is if you have a gene on the + strand whether you should only look at methylation on the + strand. The answer to that is no, you should look at both strands' methylation.
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