Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Workflow for predictive modeling, biomarker discovery, survival modeling, and explainability over omics-derived features.
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See how to installReview the instructions the agent will receive before you install.
Reference examples assume recent stable releases of the preferred tools, especially scikit-learn and the other tools listed below.
Before using code or command patterns, verify installed versions match the environment:
python -c "import <module>; print(<module>.__version__)"<tool> --versionWorkflow for predictive modeling, biomarker discovery, survival modeling, and explainability over omics-derived features.
references/technical_reference.md when you need deeper tool-selection rules, environment adaptation notes, or extra validation guidance.SKILL.md as the main execution path and load the reference file only when the task or failure mode needs the extra detail.Preferred starting point: scikit-learn
Inputs: feature matrix, labels or outcomes, split or validation design
Outputs: trained model, validation metrics, feature importance or explanation summaries
Clarify outcome type, class balance, leakage risks, and validation plan.
Use train-validation-test or cross-validation schemes that respect cohort structure.
Start with robust baseline models before complex architectures.
Report calibration, held-out performance, and failure modes instead of only one metric.
Use importance or explanation methods as interpretation aids, not proof of causality.
results/ for final tables and serialized objectsfigures/ for plots and static visual exportsqc/ for checks that justify downstream interpretationtrained modelvalidation metricsfeature importance or explanation summariesMulti-Omics IntegrationPathway AnalysisSystems BiologyCausal Genomicsscikit-learnstatsmodelsNo reviews yet. Tell others what you thought.
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Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.
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AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.
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Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
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ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
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End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.
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