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. 2018 Feb 22;37(19):2573–2585. doi: 10.1038/s41388-018-0129-z

Table 1.

Genes with statistically significant splicing identified by all three bioinformatics methods (FIRMA, MIDAS, ANOSVA)

Splicing of a single exon Splicing of 2–4 consecutive exons Splicing of >5 consecutive exons
RPL11 ILF2 SPARC CCNA2 IARS2
NEXN ZBTB41 SOX4 SLC17A5 BUB1
CEP350 USP34 STXBP5 EZH2 ALCAM
PRDX1 IDH1 BRAF RDH10 APP
PDIA6 VCAN PRKDC PTK2 TNFRSF21
SEC61A1 SSR1 SIRT1 CAPRIN1 LEMD3
LAT2 SMC2 MARS ESYT1 CAND1
SPIN1 TAOK1 ATP2A2 GDE1 TRIM33
TTC17 MED13 SLC38A1 GNAS MANF
PCGF2 GATA6 DLGAP5 RABGAP1L THBS2
GNA13 DSG2 RPN2 COL12A1 ADAMTS9
GALNT1 SLC39A6 PSMA7 MTCH2 TPX2
TCF3 GNB1 CCT2 COL5A2
YTHDF1 MATR3 CLSPN
HMGXB4 CCNJ
RCC2 ZBTB44
DARS RAP2A
TFRC YY1
KIF23

Genes were separated in three categories based on the number of consective exons spliced

The list of 76 genes identified was divided into 3 categories, based on FIRMA significance analysis: genes with splicing in 1 exon, genes with splicing in 2–4 adjacent exons, and genes with splicing in 5 adjacent exons

MIDAS microarray detection of alternative splicing, FIRMA finding isoforms using robust multichip analysis, ANOSVA analysis of splice variation