Deep RNA sequencing analysis of readthrough gene fusions in human prostate adenocarcinoma and reference samples

摘要

BackgroundReadthrough fusions across adjacent genes in the genome, or transcription-induced chimeras (TICs), have been estimated using expressed sequence tag (EST) libraries to involve 4-6% of all genes. Deep transcriptional sequencing (RNA-Seq) now makes it possible to study the occurrence and expression levels of TICs in individual samples across the genome.