I have two questions:
1. I want to compare different RNA-seq libraries. How can I normalized the
coverage to the sequencing depth of each library? Oliver et al (2009 BMC
Genomics) did this in Figure 2, but I could not figure out how to do it.
2. How to show a strand-specific coverage plot as Croucher et al (2010 Curr Opin
Microbiol) showd in Figure 2d?
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