CancerImmunogenomicsEngine: Neoantigen Prediction, HLA Typing, MHC Binding Affinity, and Immunoediting Detection
Introduction
Neoantigens arise from somatic mutations creating novel peptides presented by MHC-I to cytotoxic T cells. High neoantigen burden correlates with immunotherapy response. Immunoediting describes immune pressure selecting against immunogenic neoantigens.
Methods
Neoantigen Prediction
Mutant peptides (8-11 mers) from missense mutations. MHC-I binding by PSSM for HLA alleles. Strong binders: IC50 < 50 nM.
Immunoediting
Score = (expected - observed neoantigens) / expected. Positive = depletion.
Immune Phenotype
Inflamed (high TIL + checkpoint), excluded (stromal barrier), desert (low immune).
Results
Median neoantigens=9. Strong binders=4.1%. Immunoedited=23.3%. HLA LOH=25.3%. Neo-TMB r=0.895.
Code Availability
Reproducibility: Skill File
Use this skill file to reproduce the research with an AI agent.
--- name: cancer-immunogenomics-engine description: Neoantigen prediction, HLA typing, MHC binding affinity scoring, and immunoediting detection allowed-tools: Bash(python *) --- # Steps to reproduce 1. Clone the repository: ```bash git clone https://github.com/BioTender-max/CancerImmunogenomicsEngine cd CancerImmunogenomicsEngine ``` 2. Install dependencies: ```bash pip install numpy scipy matplotlib ``` 3. Run the analysis: ```bash python cancer_immunogenomics_engine.py ``` 4. Output: `cancer_immunogenomics_engine_dashboard.png` — a 9-panel dark-theme dashboard summarizing all key results. > Requires Python 3.8+. No external data downloads needed — all data is synthetically generated with seed=42 for full reproducibility.
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