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NeoFuse: predicting fusion neoantigens from RNA sequencing data
Author(s) -
Georgios Fotakis,
Dietmar Rieder,
Marlene Haider,
Zlatko Trajanoski,
Francesca Finotello
Publication year - 2019
Publication title -
bioinformatics
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btz879
Subject(s) - rna , computational biology , human leukocyte antigen , computer science , rna seq , workflow , biology , gene , antigen , gene expression , genetics , database , transcriptome
Gene fusions can generate immunogenic neoantigens that mediate anticancer immune responses. However, their computational prediction from RNA sequencing (RNA-seq) data requires deep bioinformatics expertise to assembly a computational workflow covering the prediction of: fusion transcripts, their translated proteins and peptides, Human Leukocyte Antigen (HLA) types, and peptide-HLA binding affinity. Here, we present NeoFuse, a computational pipeline for the prediction of fusion neoantigens from tumor RNA-seq data. NeoFuse can be applied to cancer patients' RNA-seq data to identify fusion neoantigens that might expand the repertoire of suitable targets for immunotherapy.

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