neoANT-HILL

neoANT-HILL identifies putative neoantigens from Next Generation Sequencing (NGS) data to support cancer immunogenomics and personalized immunotherapy research.


Key Features:

  • Integrated Pipeline: Integrates multiple immunogenomic analysis pipelines for neoantigen detection from NGS data to reduce false-positive rates.
  • Automation: Automates the identification of potential neoantigens from sequencing-derived inputs.
  • Multi-sample Analysis: Supports analysis of single and multiple samples simultaneously for cohort or individual studies.
  • Input Data Types: Accepts RNA sequencing reads and somatic DNA mutations as input and considers RNA-Seq data for comprehensive neoantigen identification.
  • Binding Predictors: Provides several binding predictors to assess neoantigen-TCR interactions.
  • Tumor Microenvironment Profiling: Enables quantification of tumor-infiltrating immune cells to inform neoantigen relevance.
  • Performance Validation: Demonstrated high sensitivity and specificity on datasets including the TCGA melanoma dataset, identifying neoantigens such as RAC1:P29S and SERPINB3:E250K.

Scientific Applications:

  • Cancer Research: Facilitates discovery and characterization of tumor-derived neoantigens for immunogenomic studies in cancer.
  • Personalized Medicine: Supports development of targeted immunotherapies by identifying patient-specific neoantigens for personalized treatment strategies.

Methodology:

Integrates multiple immunogenomic analysis pipelines; accepts RNA sequencing reads and somatic DNA mutation inputs; employs multiple binding predictors to assess neoantigen-TCR interactions; and performs quantification of tumor-infiltrating immune cells.

Topics

Details

License:
Apache-2.0
Tool Type:
command-line tool
Programming Languages:
JavaScript, Python
Added:
1/18/2021
Last Updated:
3/8/2021

Operations

Publications

Coelho ACMF, Fonseca AL, Martins DL, Lins PBR, da Cunha LM, de Souza SJ. neoANT-HILL: an integrated tool for identification of potential neoantigens. BMC Medical Genomics. 2020;13(1). doi:10.1186/s12920-020-0694-1. PMID:32087727. PMCID:PMC7036241.

PMID: 32087727
PMCID: PMC7036241
Funding: - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior: 23038.004629/2014-19