agentsclimarketplace

Radiomics ml

Skill Aperivue/medsci-skills/skills/radiomics-ml

Agent Skills for medical research — literature search, reporting-guideline & citation checks, statistics, publication figures, submission. Works with Claude Code, Codex, Cursor & GitHub Copilot. Built by a physician-researcher, tested on real publications. MIT.

Install
npx -y skills add Aperivue/medsci-skills --skill radiomics-ml

Assembled from the repository path, not quoted from the project. Check it against their README if it does not work.

What its author says it does

Copied from the file, not written here

Produce or audit a radiomics / tabular clinical-ML study — imaging or clinical features → any classical learner (penalised logistic [LASSO / ridge / elastic-net], SVM, k-NN, naive Bayes, LDA/QDA, decision tree, random forest, gradient boosting [XGBoost / LightGBM / CatBoost], shallow MLP, stacked ensembles) → a clinical outcome — so it clears the rigor bar reviewers expect: nested cross-validation (tuning never on the reported folds), dimensionality control for the features-far-exceed-events regime, feature selection inside the fold, feature-stability (ICC / test-retest) filtering, calibration, and external/temporal validation. The deterministic gate is learner-agnostic (it audits the pipeline, not the algorithm). Emits a pipeline manifest and the gate. The most common solo-doable clinical-ML workflow — no GPU, no engineer. Integrates scikit-learn / xgboost / lightgbm / catboost / pyradiomics; it does not reimplement them.

SKILL.md

8.1 KB, as published. Nobody here has run it

Radiomics / Classical-ML Skill

Purpose

Radiomics + tree-ensemble studies (features → random forest / XGBoost → a clinical outcome) are the most common solo-doable clinical-ML workflow — no GPU, no engineer — and the most commonly over-optimistic: hundreds-to-thousands of features on tens of patients, hyperparameters tuned on the same folds the performance is reported from, features selected on the whole dataset, unstable features never filtered, and discrimination (AUC) reported without calibration. This skill produces the pipeline correctly and audits an existing one, so the clinical result survives review (Lambin 2017; CLEAR; TRIPOD+AI; PROBAST-AI).

It sits beside the imaging-DL lane: where /model-scaffold builds a deep network, radiomics-ml covers the feature-based classical-ML path. It integrates scikit-learn / xgboost / pyradiomics (referenced in the emitted code); it does not reimplement them and never runs a model on real patient data.

When to use

  • You have a radiomics or clinical/tabular feature table and want to build a random-forest / XGBoost clinical prediction model that will pass statistical review.
  • You want to audit an existing radiomics/ML pipeline for the failure modes below.

When NOT to use

  • Deep-learning imaging models → /architecture-zoo/model-scaffold/model-validation.
  • Classical inferential statistics / a regression model as the estimand → /analyze-stats.
  • Interpretability of a trained network → /explainability.
  • Reimplementing scikit-learn / xgboost / pyradiomics → out of scope (this skill wires and audits them).

The failure modes (what the gate enforces)

  1. No nested CV. Tuning and reporting on the same folds inflates performance. Use nested CV or a held-out test set.
  2. High dimensionality, low events. Features ≥ events with no dimensionality reduction overfits — the classic radiomics trap. Apply LASSO / PCA / a stability + redundancy filter.
  3. Selection outside the fold. Feature selection fit on the whole dataset leaks the held-out folds. Nest selection inside each training fold.
  4. No feature stability. Radiomics features are unstable across acquisition/segmentation — filter to reproducible features (ICC / test-retest).
  5. No calibration. A clinical prediction model needs calibration (slope/intercept + a flexible curve), not discrimination alone.
  6. No external validation. A single-cohort model needs external / temporal validation for a clinical claim.

Workflow

Phase 1 — Extract features (integrate, don't reimplement)

For radiomics, extract with pyradiomics under reproducible, IBSI-aligned settings (fixed bin width, resampling, normalisation) — record them. For clinical/tabular data, assemble the feature table with a patient/subject ID and the outcome. See references/radiomics_ml_guide.md.

Phase 2 — Build the pipeline correctly

  • Feature stability — with test-retest / multi-rater data, keep features with ICC ≥ 0.75.
  • Nested cross-validation — outer folds estimate performance, inner folds tune; do feature selection and scaling inside each training fold (never on the whole dataset).
  • Dimensionality — with features ≥ events, use LASSO / a stability+redundancy filter / PCA.
  • Model — pick from the full classical family for the task; a simple baseline (penalised logistic) is mandatory alongside any complex learner:
    • penalised regression — LASSO / ridge / elastic-net logistic (also the baseline)
    • margin / kernel — linear or RBF SVM
    • instance-based — k-NN
    • probabilistic / discriminant — naive Bayes, LDA / QDA
    • trees & bagging — decision tree, random forest, extra-trees
    • boosting — XGBoost, LightGBM, CatBoost, HistGBM, AdaBoost
    • shallow neural — MLP
    • meta — stacking / voting ensembles
    • unsupervised (upstream) — PCA / UMAP for reduction, k-means / hierarchical / GMM for phenotyping The gate below is learner-agnostic — it audits the pipeline (nested CV, leakage, dimensionality, calibration), so it applies identically to any of these. See the full method map in docs/method_coverage_map.md.
  • Report — discrimination and calibration (slope/intercept + flexible curve, via the /analyze-stats calibration guide) and clinical utility (decision curve). SHAP for interpretation.

Phase 3 — Emit the pipeline manifest

{
  "task": "classification",
  "n_features": 1200, "n_samples": 300, "n_events": 110,
  "cv_scheme": "nested",
  "feature_selection_stage": "inside_cv",
  "dimensionality_reduction": true,
  "feature_stability": "icc",
  "calibration_reported": true,
  "external_validation": "temporal",
  "model": "xgboost"
}

Phase 4 — Gate the pipeline (deterministic)

python3 scripts/check_radiomics_ml.py --manifest pipeline_manifest.json --strict

Verdicts: NO_NESTED_CV, HIGH_DIM_LOW_EVENTS, SELECTION_OUTSIDE_CV (Major); NO_FEATURE_STABILITY, NO_CALIBRATION, NO_EXTERNAL_VALIDATION (Minor). Complements self-review's check_cv_leakage (which audits a finished manuscript's prose) at the pipeline-spec level.

Integration

  • /analyze-stats — calibration + clinical-utility (decision curve, NNT) guides for the reporting.
  • /check-reporting — CLEAR (radiomics), TRIPOD+AI, PROBAST-AI item coverage.
  • /self-review clinical_prediction_model probe audits the finished manuscript; this skill produces the rigorous pipeline it looks for.

Anti-Hallucination

  • Never fabricate features, performance metrics, or sample/event counts. Every value in the manifest and every reported metric comes from the researcher's executed code — never invented. This skill designs and audits the pipeline; it does not run a model on real patient data.
  • Never report flat-CV performance as if it were nested or held-out. Tuning on the reported folds is the optimism this skill exists to prevent (NO_NESTED_CV).
  • Never report a radiomics/ML audit "pass" without running check_radiomics_ml.py. The rigor verdict is reproduced deterministically, never asserted from prose.
  • Integrate, don't reimplement. Reference scikit-learn / xgboost / pyradiomics; do not write a new feature extractor or learner or claim results for one.

Reproducible challenge

scripts/check_radiomics_ml_challenge/ ships a synthetic weak/strong pipeline pair with a network-free verify.sh wired into the skill's validation commands.

Keep looking

Skills are one crate of 328,083. Ordering is by how many stacks a row turns up in, so the top of any crate is what has actually been picked rather than what has the most stars.