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**Step 5: Analysis system design (分析方法体系构建)**
--- name: bio-analysis-system-b287da205dec description: "**Step 5: Analysis system design (\u5206\u6790\u65b9\u6cd5\u4f53\u7cfb\u6784\u5efa)**" --- # bio-analysis-system **Step 5: Analysis system design (分析方法体系构建)** Build the analysis layer for the manuscript by identifying which analyses, tools, and biological validations should support each figure and each task. ## Purpose 1. Extract analysis patterns from related work 2. Borrow useful analyses from adjacent domains when needed 3. Map analyses to BioClaw-compatible tools or fallback software 4. Explain why each analysis is included and what biological claim it supports 5. Connect analyses to figure panels ## Input Format ```text topic: [research topic] paper_count: [number of related papers] task_system: [task system] metric_system: [metric system] dataset_catalog: [dataset catalog] ``` ## Workflow ### Step 5.1: Extract analyses from existing work If enough related papers exist, inspect their figures and extract: - panel type - analysis method - software / package - important parameters - the scientific or biological conclusion the panel supports ### Step 5.2: Borrow from adjacent fields If the field is still thin, adapt common analyses from nearby areas such as: - clustering - marker visualization - latent embedding visualization - pathway enrichment - cell-cell communication - spatial statistics - GRN analysis ### Step 5.3: Categorize analyses Use three broad groups: - **Quantitative analyses** - clustering - metric computation - statistical tests - baseline comparisons - **Qualitative analyses** - spatial visualization - feature / violin plots - UMAP / t-SNE - before / after alignment comparisons - heatmaps - **Biological analyses** - cell annotation - marker genes - pathway enrichment - GRN - ligand-receptor communication - spatial statistics - trajectory analysis ### Step 5.4: Map to BioClaw or fallback tools Whenever possible, map analysis needs to BioClaw-compatible skills or established tools. Examples: - clustering -> Scanpy / Leiden - annotation -> CellTypist / SingleR - marker plots -> Scanpy - enrichment -> gseapy - spatial statistics -> squidpy - GRN -> pySCENIC - communication -> CellChat-like workflow ### Step 5.5: Standardize analysis descriptions For each analysis, define: - category - purpose - biological claim supported - preferred tool - fallback tool - key function - recommended parameters - inputs / outputs - mapped task - mapped figure / panel ## Output Format ```markdown # Analysis System ## Analysis Sources - Extracted from related papers: - Borrowed from adjacent domains: ## Quantitative Analyses ### Clustering - Category: - Purpose: - Biological claim supported: - Preferred tool: - Fallback tool: - Key function: - Recommended parameters: - Inputs / outputs: - Relevant tasks: - Figure mapping: ### Metric computation - Category: - Purpose: - Preferred tools: - Relevant tasks: - Figure mapping: ## Qualitative Analyses - spatial plot - marker / feature plot - latent embedding plot - heatmap - before / after alignment visualization ## Biological Analyses - annotation - marker recovery - pathway enrichment - GRN - communication - trajectory ## Next Step - Use the analysis system to design figures in Step 6 ``` ## Usage ```bash /bio-analysis-system "spatial multi-omics integration | paper_count: 5 | task_system: [...] | metric_system: [...] | dataset_catalog: [...]" ``` ## Notes 1. Prefer analyses that directly support paper claims. 2. Make the biological readouts visible early; they should not appear only at the very end. 3. Map each major analysis to a concrete figure panel.--- name: bio-analysis-system-b287da205dec description: "**Step 5: Analysis system design (\u5206\u6790\u65b9\u6cd5\u4f53\u7cfb\u6784\u5efa)**" --- # bio-analysis-system **Step 5: Analysis system design (分析方法体系构建)** Build the analysis layer for the manuscript by identifying which analyses, tools, and biological validations should support each figure and each task. ## Purpose 1. Extract analysis patterns from related work 2. Borrow useful analyses from adjacent domains when needed 3. Map analyses to BioClaw-compatible tools or fallback software 4. Explain why each analysis is included and what biological claim it supports 5. Connect analyses to figure panels ## Input Format ```text topic: [research topic] paper_count: [number of related papers] task_system: [task system] metric_system: [metric system] dataset_catalog: [dataset catalog] ``` ## Workflow ### Step 5.1: Extract analyses from existing work If enough related papers exist, inspect their figures and extract: - panel type - analysis method - software / package - important parameters - the scientific or biological conclusion the panel supports ### Step 5.2: Borrow from adjacent fields If the field is still thin, adapt common analyses from nearby areas such as: - clustering - marker visualization - latent embedding visualization - pathway enrichment - cell-cell communication - spatial statistics - GRN analysis ### Step 5.3: Categorize analyses Use three broad groups: - **Quantitative analyses** - clustering - metric computation - statistical tests - baseline comparisons - **Qualitative analyses** - spatial visualization - feature / violin plots - UMAP / t-SNE - before / after alignment comparisons - heatmaps - **Biological analyses** - cell annotation - marker genes - pathway enrichment - GRN - ligand-receptor communication - spatial statistics - trajectory analysis ### Step 5.4: Map to BioClaw or fallback tools Whenever possible, map analysis needs to BioClaw-compatible skills or established tools. Examples: - clustering -> Scanpy / Leiden - annotation -> CellTypist / SingleR - marker plots -> Scanpy - enrichment -> gseapy - spatial statistics -> squidpy - GRN -> pySCENIC - communication -> CellChat-like workflow ### Step 5.5: Standardize analysis descriptions For each analysis, define: - category - purpose - biological claim supported - preferred tool - fallback tool - key function - recommended parameters - inputs / outputs - mapped task - mapped figure / panel ## Output Format ```markdown # Analysis System ## Analysis Sources - Extracted from related papers: - Borrowed from adjacent domains: ## Quantitative Analyses ### Clustering - Category: - Purpose: - Biological claim supported: - Preferred tool: - Fallback tool: - Key function: - Recommended parameters: - Inputs / outputs: - Relevant tasks: - Figure mapping: ### Metric computation - Category: - Purpose: - Preferred tools: - Relevant tasks: - Figure mapping: ## Qualitative Analyses - spatial plot - marker / feature plot - latent embedding plot - heatmap - before / after alignment visualization ## Biological Analyses - annotation - marker recovery - pathway enrichment - GRN - communication - trajectory ## Next Step - Use the analysis system to design figures in Step 6 ``` ## Usage ```bash /bio-analysis-system "spatial multi-omics integration | paper_count: 5 | task_system: [...] | metric_system: [...] | dataset_catalog: [...]" ``` ## Notes 1. Prefer analyses that directly support paper claims. 2. Make the biological readouts visible early; they should not appear only at the very end. 3. Map each major analysis to a concrete figure panel.
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