An array-based examination of published and in silico-predicted glioma-specific events. (A) Plot of values extracted from Figure 1B showing RefSeq entries that monitor published glioma-specific splicing events (Table 1). The circled RefSeq entries include confirmed negative splicing events. For data on RefSeq entries with significant values see Additional file 1. (B) Plot showing positions of 267 RefSeq entries from Figure 1B that were identified by five in silico studies [15–18, 20]. The open squares show 11 RefSeq events that were concordant in more than one study (discussed in the text). Notable RefSeq entries are labeled with their gene names. The theoretical value for a 5-fold change in exon inclusion is shown (dashed line). For data on RefSeq entries with significant values see Additional file 2. For the hybridization intensity maps for the highlighted genes see Additional file 8.
Cheung et al. BMC Genomics 2008 9:216 doi:10.1186/1471-2164-9-216