Fig. 5From: RDDpred: a condition-specific RNA-editing prediction model from RNA-seq dataMES-calculation workflow: 1) MES method simulated randomly mutated sequencing reads. 2) Then, aligns them into genome sequences with an alignment tool of interest. 3) After the alignment finishes, uses variant-caller to detect raw SNPs. 4) Picks the SNPs sites that was not planted originally, i.e., unintended artefactsBack to article page