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Builds diagnostic and prognostic classifiers on omics feature matrices with regularized logistic regression, random forest, and gradient-boosted trees, handling the p>>n regime, batch shortcut learning, class imbalance, and probability calibration. Use when building a classifier from expression, methylation, or variant data, choosing an algorithm for high-dimensional small-n data, or diagnosing a suspiciously perfect AUC. For unbiased evaluation see machine-learning/model-validation; for feature selection see machine-learning/biomarker-discovery; for time-to-event outcomes see machine-learning/survival-analysis.

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Build machine-learning trading signals from price and volume data. The workflow checks inputs, creates predictive features, and repeatedly trains on available historical data to produce bounded signals indicating predicted direction and strength.

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• Building trading signals from price and volume data
• Comparing machine-learning models
• Testing expanding and sliding training windows

Selects biomarker features from high-dimensional omics data using Boruta all-relevant selection, mRMR, LASSO/elastic-net, and stability selection, while controlling the leakage, irreproducibility, and correlated-feature traps that make most published signatures fail to replicate. Use when identifying candidate biomarkers, deciding between an all-relevant and a minimal-optimal selector, or judging whether a selected gene set is reproducible. For unbiased performance estimation of the resulting model see machine-learning/model-validation; for interpreting a trained model see machine-learning/prediction-explanation.

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Explain how input features contribute to machine-learning predictions using SHAP. Select an explanation method and reference data, validate contributions against model outputs, and create charts for individual predictions or patterns across samples, including models with multiple outputs.

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• Explaining the feature contributions behind one prediction
• Visualizing attribution patterns across evaluation samples
• Selecting and explaining a class in a multiclass model

Use PyTDC to discover therapeutic machine-learning datasets, create task-appropriate training and test splits, and evaluate predictions against curated benchmarks. Also score selected molecules with supported scoring functions, with explicit download plans and bounded outputs.

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• Find datasets for therapeutic machine-learning tasks
• Plan and create task-appropriate data splits
• Evaluate predictions with benchmark-specific metrics

Generates complete comorbidity-oriented shared-biomarker bioinformatics research designs from a user-provided disease pair and validation direction. Use when a study links two clinically related diseases through shared DEGs, enrichment, PPI hub genes, machine-learning feature selection, public diagnostic validation, gene-regulatory networks, immune infiltration, and optional downstream follow-up. Covers five study patterns (shared-DEG discovery, hub-gene prioritization, machine-learning biomarker selection, immune/regulatory interpretation, multi-layer validation) and always outputs Lite / Standard / Advanced / Publication+ with a recommended primary plan, stepwise workflow, figure plan, validation hierarchy, minimal executable version, publication upgrade path, and strictly verified literature retrieval.

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Generates complete process-related diagnostic biomarker bioinformatics research designs from a user-provided disease context, gene-family or pathway theme, and validation direction. Use when a study centers on process-related genes, DEG and WGCNA integration, machine-learning feature selection, nomogram-based diagnostic modeling, immune infiltration, regulatory-network analysis, and optional external or experimental validation. Covers five study patterns (process-DEG discovery, co-expression-module integration, machine-learning biomarker selection, diagnostic model/nomogram workflow, immune-regulatory interpretation and validation) and always outputs Lite / Standard / Advanced / Publication+ with a recommended primary plan, stepwise workflow, figure plan, validation hierarchy, minimal executable version, publication upgrade path, and strictly verified literature retrieval.

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Interpret and explain a trained tabular machine-learning model (classification or regression) in MATLAB. Find which predictors, features, or columns matter most; explain why the model made a specific prediction, including diagnosing predictions it got wrong; show how a predictor affects the output; and compare how the model behaves across cohorts or subgroups. Uses model-agnostic techniques and model-native measures, and works on custom models (such as a dlnetwork) through a prediction function handle. Use for model interpretability, explainability, and feature-importance questions on tabular data, not for training, tuning, feature selection, deploying models, or models trained on image, text, signal, or other non-tabular data.

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Validates predictive models on omics and biomedical data with nested cross-validation, group/batch/temporal-aware splits, the full data-leakage taxonomy, probability calibration, decision-curve net benefit, optimism correction, sample-size planning, and TRIPOD+AI reporting. Use when estimating model performance honestly, choosing a CV scheme, detecting leakage, or judging whether reported discrimination means the model is actually useful. For feature selection itself see machine-learning/biomarker-discovery; for confirmatory-trial inference see clinical-biostatistics/trial-reporting.

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Explains ML predictions on omics data with SHAP, LIME, and permutation importance, handling the correlated-feature trap, the conditional-vs-interventional Shapley choice, and the attribution-is-not-causation boundary. Use when interpreting an omics classifier, debugging shortcut/batch learning, or deciding whether an attribution ranking can be trusted as biology. For validated feature selection see machine-learning/biomarker-discovery; explanations are not a selection method.

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Decision-grade statistical analysis for metabolomics intensity tables. Covers transformation and scaling (Pareto vs unit-variance as a hidden hypothesis), unsupervised structure (PCA/HCA for QC), permutation-validated PLS-DA/OPLS-DA (R2 vs Q2, double CV, VIP as heuristic), univariate testing (Welch/Mann-Whitney/ANOVA/LMM with covariate adjustment), and dependence-aware multiple testing. Use when testing which metabolites differ, building or validating a discriminant model, choosing a scaling, or correcting many correlated tests. For sample-wise normalization/drift correction see metabolomics/normalization-qc; for ML classifiers and selection-inside-CV leakage see machine-learning/biomarker-discovery and machine-learning/model-validation; for pathway interpretation see metabolomics/pathway-mapping; for design/power/multiplicity regime see experimental-design/multiple-testing.

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Machine Learning integration for Flutter using TensorFlow Lite and Firebase ML

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Machine Learning integration for Flutter using TensorFlow Lite and Firebase ML

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Plan and review machine learning systems for production use, covering data requirements, repeatable training, quality checks, deployment, monitoring, and rollback. Produce concrete plans and review findings for moving model experiments into operational systems.

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• Turning notebook experiments into reusable training pipelines
• Defining quality checks before releasing a model
• Investigating data leakage and training–serving mismatches

Build and check clinical machine learning workflows with PyHealth, from loading electronic health records, signals, or images to training and evaluation. Includes patient-level data splits, prediction task checks, model checkpoints, and medical code mapping.

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• Prototype mortality and readmission prediction models
• Check patient splits and data leakage
• Train and evaluate sleep staging models

Set up AI email screening that compares writing style and communication habits to identify impersonation and suspicious payment requests. Connect detection policies to quarantine, warning banners, and analyst review workflows.

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• Detecting executive impersonation in emails
• Reviewing vendor payment change requests
• Flagging unusual employee email behavior

Build or tune a monitoring pipeline that learns normal user behavior from activity logs. Use Elasticsearch or OpenSearch to score unusual activity, compare colleagues in similar roles, and combine warning signs into insider threat alerts.

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• Building continuous monitoring for insider threats
• Scoring unusual logins and large downloads
• Comparing behavior across similar job roles

Build normal traffic profiles for industrial control networks and identify unusual connections, polling intervals, and protocol operations. Use machine learning and process records to investigate deviations and produce anomaly reports with severity levels.

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• Establishing normal traffic profiles for industrial networks
• Detecting unusual connections and polling intervals
• Investigating Nozomi Guardian or Dragos alerts

Train and deploy neural networks in distributed E2B sandboxes with Flow Nexus

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Explain trained machine learning models through feature attribution, local explanations, and behavior summaries. Use as an explicit/manual helper once a model already exists, not for training ownership, leakage auditing, or general ML strategy selection.

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Evaluate trained machine learning models with the right metrics and comparison logic. Use for benchmark review, threshold selection, calibration, validation, and model comparison; not for feature engineering or leakage auditing.

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Generates complete tumor immune-infiltration-guided bulk-transcriptome diagnostic biomarker and machine-learning research designs from a user-provided cancer type and study direction. Always use this skill whenever a user wants to design, plan, or build a tumor bioinformatics study centered on differential expression, immune infiltration estimation, immune-linked module discovery, consensus feature selection, diagnostic modeling, nomogram construction, clinical association, and optional prognostic extension or validation. Covers five study patterns (immune-cell-first diagnostic workflow, immune-module-to-biomarker workflow, consensus-ML biomarker workflow, diagnostic-plus-prognostic hybrid workflow, translational validation workflow) and always outputs four workload configs (Lite / Standard / Advanced / Publication+) with recommended primary plan, step-by-step workflow, figure plan, validation strategy, minimal executable version, publication upgrade path, reference literature pack, and self-critical risk review.

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Generates complete conventional non-oncology diagnostic machine-learning research designs from a user-provided disease context, optional mechanism theme, and validation direction. Use when a study centers on disease-vs-control transcriptome comparison, optional mechanism-gene restriction, feature shrinkage, diagnostic model construction, ROC / calibration / DCA evaluation, interpretation layers, and orthogonal validation. Covers five study patterns and always outputs Lite / Standard / Advanced / Publication+ with a recommended primary plan, stepwise workflow, figure plan, validation hierarchy, minimal executable version, publication upgrade path, and strictly verified literature retrieval.

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Design ML pipelines covering data preparation, model training, deployment, monitoring, and continuous improvement. Use when coordinating an end-to-end MLOps workflow.

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