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Tumor Fusion Gene Data Portal 

Landscape of cancer-associated fusions using the Pipeline for RNA sequencing Data Analysis 

Transcripts fusion as a result of genomic rearrangement is an important class of somatic alteration, as a cancer initiating event and as a molecular therapeutic target for specific tumors. Our Pipeline for RNA sequencing Data Analysis (PRADA) enables us to detect fusion transcripts with high confidence comprehensively. Based on integrated analysis of paired-end RNA sequencing and DNA copy number data from The Cancer Genome Atlas(TCGA), The Tumor Fusion Gene Data Portal provides a bona-fide fusion list across many tumor types.


Figure 1. Fusion transcripts:
Fusion transcripts are chimeric mRNAs encoded from the joined parts of two genes, and may occur as a result of genomic rearrangements.

Figure 2. Detection of fusion transcripts.
PRADA detects fusion transcripts through identification of discordant read pairs and junction spanning reads.


Table below summarizes the tumor types available across thirty three tumor types, as of July 2017. 




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