Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Workflow for outbreak-style pathogen genomics, surveillance, lineage assignment, and transmission-oriented comparative analysis.
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설치 방법 보기설치하기 전에 에이전트에게 전달되는 지시 내용을 확인할 수 있습니다.
Reference examples assume recent stable releases of the preferred tools, especially phylogenetics 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 outbreak-style pathogen genomics, surveillance, lineage assignment, and transmission-oriented comparative analysis.
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: phylogenetics
Inputs: pathogen genomes or read sets, collection metadata, reference resources
Outputs: lineage assignments, cluster or outbreak summaries, surveillance-ready tables or figures
Ensure time, location, and sample identifiers are consistent before analysis.
Call variants or consensus sequences in a way that supports cross-sample comparison.
Use pathogen-appropriate nomenclature and clustering logic.
Summarize genomic findings with explicit metadata context and caution around transmission claims.
Save lineage tables, phylogenies, and cluster summaries.
results/ for final tables and serialized objectsfigures/ for plots and static visual exportsqc/ for checks that justify downstream interpretationlineage assignmentscluster or outbreak summariessurveillance-ready tables or figuresMetagenomicsMicrobiome AmpliconPhylogeneticsphylogenetics아직 리뷰가 없습니다. 사용해 본 소감을 남겨 주세요.
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Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
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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