Analysis of the different splicing variants from the antisense 3'UTR sequences. A. Proportion of each splicing variant (SV) found in the analyzed strains. B. Table summarizing the splicing variant usage by each subfamily. C. Consensus sequence (reverse strand) for each donor (D) and acceptor (A). Splice site is indicated by two bigger letters. The NNSPLICE 0.9 score for each splice site is also indicated.
Piñeyro et al. BMC Genomics 2011 12:573 doi:10.1186/1471-2164-12-573