Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Workflow for enrichment testing, ranked-gene analysis, pathway scoring, and pathway-focused visualization across omics outputs.
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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 Reactome 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 enrichment testing, ranked-gene analysis, pathway scoring, and pathway-focused visualization across omics outputs.
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: Reactome
Inputs: gene lists or ranked statistics, pathway databases, optional sample-level matrices
Outputs: enriched pathway tables, pathway plots, pathway interpretation summaries
Use over-representation for filtered gene lists and ranked methods for full signed statistics.
Standardize gene IDs to the pathway database before testing.
Report effect direction, significance, and pathway sizes.
Use dot plots, bar plots, or network summaries without overwhelming the reader.
Save standardized pathway identifiers, scores, and member genes.
results/ for final tables and serialized objectsfigures/ for plots and static visual exportsqc/ for checks that justify downstream interpretationenriched pathway tablespathway plotspathway interpretation summariesMulti-Omics IntegrationSystems BiologyCausal GenomicsMachine Learning For Omicsreactome-databasestring-databaseNo 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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