NeoFuse

NeoFuse predicts fusion neoantigens from tumor RNA sequencing (RNA-seq) data to identify candidate peptide–HLA binders for cancer immunotherapy.


Key Features:

  • Fusion Transcript Prediction: Identifies fusion transcripts from RNA-seq data to detect gene fusions that may produce novel antigenic proteins.
  • Protein and Peptide Translation: Translates fusion transcripts into protein sequences and derives peptide fragments for downstream immunogenicity assessment.
  • HLA Typing Integration: Incorporates Human Leukocyte Antigen (HLA) typing data to determine patient-specific HLA alleles for peptide presentation analysis.
  • Peptide–HLA Binding Affinity Prediction: Evaluates binding affinities between predicted peptides and HLA molecules to prioritize candidate neoantigens.

Scientific Applications:

  • Cancer immunotherapy target discovery: Identifies fusion-derived peptide candidates presented by patient HLA alleles to expand potential immunotherapeutic targets.
  • Personalized neoantigen selection: Supports selection of patient-specific fusion neoantigens from RNA-seq data for personalized therapeutic strategies.

Methodology:

Identification of fusion transcripts from RNA-seq data, translation of fusion transcripts into protein sequences and derivation of peptide fragments, integration of Human Leukocyte Antigen (HLA) typing, and prediction/evaluation of peptide–HLA binding affinities.

Topics

Details

License:
GPL-3.0
Tool Type:
desktop application
Added:
1/14/2020
Last Updated:
11/24/2024

Operations

Publications

Fotakis G, Rieder D, Haider M, Trajanoski Z, Finotello F. NeoFuse: predicting fusion neoantigens from RNA sequencing data. Bioinformatics. 2019;36(7):2260-2261. doi:10.1093/bioinformatics/btz879. PMID:31755900. PMCID:PMC7141848.

PMID: 31755900
PMCID: PMC7141848
Funding: - Austrian Cancer Aid/Tyrol: 17003 - Austrian Science Fund: T 974-B30 - European Research Council: 786295