Extensive investigation of gene fusions in cancer has led to the discovery of novel biomarkers and therapeutic targets. To date, most studies have neglected chromosomal rearrangement-independent fusion transcripts and complex fusion structures such as double or triple-hop fusions, and fusion-circRNAs. In this review, we untangle fusion-related terminology and propose a classification system involving both gene and transcript fusions. We highlight the importance of RNA-level fusions and how long-read sequencing approaches can improve detection and characterization. Moreover, we discuss novel bioinformatic tools to identify fusions in long-read sequencing data and strategies to experimentally validate and functionally characterize fusion tran...
Abstract Motivation: The discovery of novel gene fusions can lead to a better compreh...
Gene fusions created by somatic genomic rearrangements are known to play an important role in the on...
The identification of gene fusions promises to play an important role in personalized cancer treatme...
BACKGROUND: Accurate fusion transcript detection is essential for comprehensive characterization of ...
Motivation Fusion genes created by genomic rearrangements can be potent drivers of tumorigenesis. Ho...
Abstract Background Genomic rearrangements in cancer cells can create fusion genes that encode chime...
Abstract Background In cancer, genomic rearrangements can create fusion genes that either combine pr...
RNA sequencing in cancer cells is a powerful technique to detect chromosomal rearrangements, allowin...
Analysis of fusion transcripts has become increasingly important due to their link with cancer devel...
<div><p>Analysis of fusion transcripts has become increasingly important due to their link with canc...
Background: Gene fusions, which result from abnormal chromosome rearrangements, are a pathogenic fac...
RNA-sequencing and tailored bioinformatic methodologies have paved the way for identification of exp...
Background Until recently, chromosomal translocations and fusion genes have been an ...
RNA-sequencing and tailored bioinformatic methodologies have paved the way for identification of exp...
BACKGROUND: Fusion genes are typically identified by RNA sequencing (RNA-seq) without elucidating th...
Abstract Motivation: The discovery of novel gene fusions can lead to a better compreh...
Gene fusions created by somatic genomic rearrangements are known to play an important role in the on...
The identification of gene fusions promises to play an important role in personalized cancer treatme...
BACKGROUND: Accurate fusion transcript detection is essential for comprehensive characterization of ...
Motivation Fusion genes created by genomic rearrangements can be potent drivers of tumorigenesis. Ho...
Abstract Background Genomic rearrangements in cancer cells can create fusion genes that encode chime...
Abstract Background In cancer, genomic rearrangements can create fusion genes that either combine pr...
RNA sequencing in cancer cells is a powerful technique to detect chromosomal rearrangements, allowin...
Analysis of fusion transcripts has become increasingly important due to their link with cancer devel...
<div><p>Analysis of fusion transcripts has become increasingly important due to their link with canc...
Background: Gene fusions, which result from abnormal chromosome rearrangements, are a pathogenic fac...
RNA-sequencing and tailored bioinformatic methodologies have paved the way for identification of exp...
Background Until recently, chromosomal translocations and fusion genes have been an ...
RNA-sequencing and tailored bioinformatic methodologies have paved the way for identification of exp...
BACKGROUND: Fusion genes are typically identified by RNA sequencing (RNA-seq) without elucidating th...
Abstract Motivation: The discovery of novel gene fusions can lead to a better compreh...
Gene fusions created by somatic genomic rearrangements are known to play an important role in the on...
The identification of gene fusions promises to play an important role in personalized cancer treatme...