Motivation Fusion genes created by genomic rearrangements can be potent drivers of tumorigenesis. However, accurate identification of functionally fusion genes from genomic sequencing requires whole genome sequencing, since exonic sequencing alone is often insufficient. Transcriptome sequencing provides a direct, highly effective alternative for capturing molecular evidence of expressed fusions in the precision medicine pipeline, but current methods tend to be inefficient or insufficiently accurate, lacking in sensitivity or predicting large numbers of false positives. Here, we describe STAR-Fusion, a method that is both fast and accurate in identifying fusion transcripts from RNA-Seq data. Results We benchmarked STAR-Fusion’s fusion det...
Background The advent of next-generation sequencing technologies empowered a wide v...
Gene fusions occur in solid tumors and hematological malignancies, formed as the result of somatic g...
RNA-Seq (Whole Transcriptome Shotgun Sequencing) provides an ideal platform to study the complete se...
BACKGROUND: Accurate fusion transcript detection is essential for comprehensive characterization of ...
Abstract Background In cancer, genomic rearrangements can create fusion genes that either combine pr...
Fusion genes are a major cause of cancer. Their rapid and accurate diagnosis can inform clinical ac...
RNA sequencing in cancer cells is a powerful technique to detect chromosomal rearrangements, allowin...
Background: Gene fusions, which result from abnormal chromosome rearrangements, are a pathogenic fac...
Background Fusion genes are known to be drivers of many common cancers, so they are...
Extensive investigation of gene fusions in cancer has led to the discovery of novel biomarkers and t...
Abstract Background Genomic rearrangements in cancer cells can create fusion genes that encode chime...
Gene fusions created by somatic genomic rearrangements are known to play an important role in the on...
Detecting gene fusions involving driver oncogenes is pivotal in clinical diagnosis and treatment of ...
Fusion genes are those that result from the fusion of two or more genes, and they are typically gene...
Abstract Motivation: The discovery of novel gene fusions can lead to a better compreh...
Background The advent of next-generation sequencing technologies empowered a wide v...
Gene fusions occur in solid tumors and hematological malignancies, formed as the result of somatic g...
RNA-Seq (Whole Transcriptome Shotgun Sequencing) provides an ideal platform to study the complete se...
BACKGROUND: Accurate fusion transcript detection is essential for comprehensive characterization of ...
Abstract Background In cancer, genomic rearrangements can create fusion genes that either combine pr...
Fusion genes are a major cause of cancer. Their rapid and accurate diagnosis can inform clinical ac...
RNA sequencing in cancer cells is a powerful technique to detect chromosomal rearrangements, allowin...
Background: Gene fusions, which result from abnormal chromosome rearrangements, are a pathogenic fac...
Background Fusion genes are known to be drivers of many common cancers, so they are...
Extensive investigation of gene fusions in cancer has led to the discovery of novel biomarkers and t...
Abstract Background Genomic rearrangements in cancer cells can create fusion genes that encode chime...
Gene fusions created by somatic genomic rearrangements are known to play an important role in the on...
Detecting gene fusions involving driver oncogenes is pivotal in clinical diagnosis and treatment of ...
Fusion genes are those that result from the fusion of two or more genes, and they are typically gene...
Abstract Motivation: The discovery of novel gene fusions can lead to a better compreh...
Background The advent of next-generation sequencing technologies empowered a wide v...
Gene fusions occur in solid tumors and hematological malignancies, formed as the result of somatic g...
RNA-Seq (Whole Transcriptome Shotgun Sequencing) provides an ideal platform to study the complete se...