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Figure 8 | BMC Bioinformatics

Figure 8

From: Detection of recurrent rearrangement breakpoints from copy number data

Figure 8

Predicted Intrachromosomal Fusion Genes in GBM. (A) The INTS2-MED13 rearrangement on Chromosome 17 is identified in 9 individuals and arises from an amplification. A tandem duplication that affects the 3' end of MED13 and the 5' end of INTS2 will fuse the promoter region of INTS2 to MED13. (B) The PPP1R9A-PSMC2 rearrangement on Chromosome 7 is identified in 6 individuals and arises from a deletion.

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