# Quickstart for Domain Scientists ICg-CaST has four moving parts. You can use the package without reading the full theory notes first if you keep this path in mind: 1. **KCC exposure coordinates.** Each chemical profile is represented by ten Key Characteristics of Carcinogens coordinates, scaled from 0 to 1. 2. **qAOP state trajectories.** The simulator maps KCC activity, dose, and host susceptibility into monthly latent states: DNA adducts, ROS, inflammation, epigenetic age, proliferation, mutation rate, clone fraction, driver-count proxy, immune clearance, and latent risk. 3. **MB-CNet bottleneck.** The mechanism-bottleneck model first reconstructs the qAOP state vector from omics-like features, then predicts transition risk from that state vector. 4. **Do-interventions.** Intervention checks perturb a named qAOP state, such as `do_ROS_inflammation_blockade`, and verify whether predicted risk moves in the expected direction. ## Browser Path The Streamlit app wraps the common workflows without requiring command-line flags for every step: ```bash python -m pip install -e ".[app]" streamlit run streamlit_app.py ``` The app writes runs under `outputs/streamlit/` and can simulate cohorts, train/evaluate models, export the theory graph, and run benchmark experiments. ## Command-Line Path ```bash icg-cast make-demo --n 120 --months 72 --seed 7 --outdir outputs/demo icg-cast train --cohort outputs/demo/synthetic_icg_cohort.csv --outdir outputs/demo icg-cast evaluate \ --cohort outputs/demo/synthetic_icg_cohort.csv \ --model outputs/demo/model_bundle.joblib \ --outdir outputs/demo ``` ## Python Path ```python from icg_cast import SimConfig, simulate_cohort, train_baselines cfg = SimConfig(n=120, months=72, seed=7) cohort, trajectories = simulate_cohort(cfg) metrics, importance, counterfactual, bundle = train_baselines(cohort, seed=7) ``` Use [simulation](simulation.md) for simulator details, [bottleneck](bottleneck.md) for MB-CNet, and [benchmark](benchmark.md) for ICg-Bench variants and leaderboard outputs.