Abstract
Next generation sequencing (NGS) technologies have enabled de novo gene fusion discovery that could reveal candidates with therapeutic significance in cancer. Here we present an open-source software package, ChimeraScan, for the discovery of chimeric transcription between two independent transcripts in high-throughput transcriptome sequencing data. Published by Oxford University Press. All rights reserved.
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CITATION STYLE
Iyer, M. K., Chinnaiyan, A. M., & Maher, C. A. (2011). ChimeraScan: A tool for identifying chimeric transcription in sequencing data. Bioinformatics, 27(20), 2903–2904. https://doi.org/10.1093/bioinformatics/btr467
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