Hi guys
I have been working with MeDIP-Seq data and one of the problems puzzling me is that:
If we have a peak as reported by the peak caller in a location on the genome, how do we know that this peak originated on the plus strand or the minus strand.
http://www.nature.com/nature/journal...re10008-s1.pdf (Figure 10) shows the mechanism of how one can conserve strand information - however where I am confused at the moment is that after our paired end sequencing run we have two files one with /1 and other /2 parts of the paired end reads.
Bowtie e.g. will take a read from /1 and a matching pair from /2 (reverse complement it) and try to align it to the reference genome. How can we figure out that this read originated from the + or - strand in?
Any help here would be greatly appreciated.
Thanks
I have been working with MeDIP-Seq data and one of the problems puzzling me is that:
If we have a peak as reported by the peak caller in a location on the genome, how do we know that this peak originated on the plus strand or the minus strand.
http://www.nature.com/nature/journal...re10008-s1.pdf (Figure 10) shows the mechanism of how one can conserve strand information - however where I am confused at the moment is that after our paired end sequencing run we have two files one with /1 and other /2 parts of the paired end reads.
Bowtie e.g. will take a read from /1 and a matching pair from /2 (reverse complement it) and try to align it to the reference genome. How can we figure out that this read originated from the + or - strand in?
Any help here would be greatly appreciated.
Thanks
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