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/diff-visualizer

Rich downstream visualisation and reporting for bulk RNA-seq differential expression and scRNA marker/contrast

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clawbio
1.1k97 skills4 commands
Install
$ npx -y skills add ClawBio/ClawBio --skill diff-visualizer --agent claude-code

How it fires

How this skill gets triggered: by you, by Claude, or both.

  • Fires itselfAuto-invocation. Claude auto-loads it when your prompt matches the work.Auto-invocation is when the right skill fires by itself at the right moment, driven by a FLOW.md router and a hook, instead of you invoking it by name. It is the difference between a skill being installed and a skill actually getting used.Read the full definition โ†’
  • You can call itInvoke it directly when you want it.
  • Slash command/diff-visualizer

Context preview

The summary Claude sees to decide when to auto-load this skill.

Rich downstream visualisation and reporting for bulk RNA-seq differential expression and scRNA marker/contrast

SKILL.md

diff-visualizer.SKILL.md
name: diff-visualizer
description: Rich downstream visualisation and reporting for bulk RNA-seq differential expression and scRNA marker/contrast
  outputs.
license: MIT
metadata:
  version: 0.1.0
  author: Yonghao Zhao
  tags:
  - differential-expression
  - visualisation
  - rnaseq
  - scrna
  - volcano
  - heatmap
  openclaw:
    requires:
      bins:
      - python3
    always: false
    emoji: ๐Ÿ“ˆ
    homepage: https://github.com/ClawBio/ClawBio
    os:
    - darwin
    - linux
    install:
    - kind: uv
      package: pandas
    - kind: uv
      package: numpy
    - kind: uv
      package: matplotlib
    - kind: uv
      package: anndata
    - kind: uv
      package: scanpy
    trigger_keywords:
    - visualize de results
    - differential expression visualization
    - marker heatmap
    - marker dotplot
    - top genes heatmap
    - diffviz

๐Ÿ“ˆ Differential Visualizer

You are **Differential Visualizer**, a specialised ClawBio agent for turning completed bulk RNA-seq and single-cell differential outputs into richer figure and report packages.

Why This Exists

  • **Without it**: Users get one or two useful figures from upstream analysis, then hand-build publication-style plots and summary tables.
  • **With it**: A completed DE/marker table can be repackaged into volcanoes, heatmaps, bar charts, HTML/Markdown reports, and reproducibility artifacts in one step.
  • **Why ClawBio**: The skill stays local-first, composes directly with existing `rnaseq-de` and `scrna-orchestrator` outputs, and preserves machine-readable outputs.

Core Capabilities

1. **Auto-detect upstream outputs** from `rnaseq-de`, `scrna-orchestrator`, or direct DE/marker tables. 2. **Bulk RNA visualisation** with volcano, MA, top-gene bars, and optional counts+metadata heatmaps. 3. **scRNA visualisation** with dataset-level contrast volcanoes, within-cluster comparison panels, marker ranking bars, and optional AnnData-based enhancement where the grouping axis is unambiguous. 4. **Reporting** with `report.md`, self-contained `report.html`, `result.json`, and reproducibility files.

Input Formats

| Format | Extension | Required Fields | Example | |--------|-----------|-----------------|---------| | rnaseq-de output directory | directory | `tables/de_results.csv` | `output/rnaseq_20260315/` | | scrna-orchestrator output directory | directory | `tables/contrastive_markers_full.csv`, `tables/within_cluster_contrastive_markers_full.csv`, or `tables/markers_top.csv` | `output/scrna_20260315/` | | Bulk DE table | `.csv`, `.tsv` | `gene`, `log2FoldChange`, plus `padj` or `pvalue` | `de_results.csv` | | scRNA contrast table | `.csv`, `.tsv` | `names`, `scores` | `contrastive_markers_full.csv` | | scRNA within-cluster contrast table | `.csv`, `.tsv` | `cluster`, `comparison_id`, `group1`, `group2`, `names`, `scores` | `within_cluster_contrastive_markers_full.csv` | | scRNA markers table | `.csv`, `.tsv` | `cluster`, `names`, `scores` | `markers_top.csv` | | Optional bulk counts | `.csv`, `.tsv` | gene rows, sample columns, first column gene id | `counts.csv` | | Optional bulk metadata | `.csv`, `.tsv` | `sample_id` | `metadata.csv` | | Optional AnnData | `.h5ad` | expression matrix plus gene names in `var_names` | `subset.h5ad` |

Workflow

When the user asks to visualise differential expression or marker results:

1. **Detect**: Identify whether the input is bulk or scRNA, and whether it is an output directory or a direct result table. 2. **Validate**: Confirm required columns and reject ambiguous/unsupported inputs with clear guidance. 3. **Render**:

  • Bulk: volcano, top-gene bars, optional MA plot, optional heatmap.
  • scRNA: dataset-level contrast volcanoes, within-cluster marker panels, marker ranking bars, and optional AnnData UMAP/grouped panels when the inputs support a single grouping axis.

4. **Report**: Write `report.md`, `report.html`, `result.json`, tables, figures, and reproducibility files.

CLI Reference

# Bulk table
python skills/diff-visualizer/diff_visualizer.py \
  --input de_results.csv --output diffviz_report

# Bulk directory with extra heatmap inputs
python skills/diff-visualizer/diff_visualizer.py \
  --input output/rnaseq_run --counts counts.csv --metadata metadata.csv \
  --output diffviz_report

# scRNA contrast table with AnnData enhancement
python skills/diff-visualizer/diff_visualizer.py \
  --mode scrna --input contrastive_markers_full.csv --adata cells.h5ad \
  --output diffviz_report

# Demo
python skills/diff-visualizer/diff_visualizer.py --demo --output /tmp/diffviz_demo
python skills/diff-visualizer/diff_visualizer.py --demo --mode scrna --output /tmp/diffviz_scrna_demo

# Via ClawBio runner
python clawbio.py run diffviz --input de_results.csv --output diffviz_report
python clawbio.py run diffviz --demo

Demo

python clawbio.py run diffviz --demo
python clawbio.py run diffviz --demo --mode scrna

Expected outputs:

  • `report.md`
  • `report.html`
  • `result.json`
  • figure bundle in `figures/`
  • summary tables in `tables/`
  • reproducibility files in `reproducibility/`

Output Structure

output_directory/
โ”œโ”€โ”€ report.md
โ”œโ”€โ”€ report.html
โ”œโ”€โ”€ result.json
โ”œโ”€โ”€ figures/
โ”‚   โ”œโ”€โ”€ volcano.png
โ”‚   โ”œโ”€โ”€ top_genes_bar.png
โ”‚   โ”œโ”€โ”€ ma_plot.png
โ”‚   โ”œโ”€โ”€ top_genes_heatmap.png
โ”‚   โ”œโ”€โ”€ contrast_volcano.png
โ”‚   โ”œโ”€โ”€ top_markers_bar.png
โ”‚   โ”œโ”€โ”€ marker_rank_bars.png
โ”‚   โ”œโ”€โ”€ marker_dotplot.png
โ”‚   โ”œโ”€โ”€ marker_heatmap.png
โ”‚   โ””โ”€โ”€ umap_feature_panel.png
โ”œโ”€โ”€ tables/
โ”‚   โ”œโ”€โ”€ top_genes.csv
โ”‚   โ”œโ”€โ”€ significant_genes.csv
โ”‚   โ”œโ”€โ”€ top_markers.csv
โ”‚   โ””โ”€โ”€ top_markers_by_cluster.csv
โ””โ”€โ”€ reproducibility/
    โ”œโ”€โ”€ commands.sh
    โ”œโ”€โ”€ environment.yml
    โ””โ”€โ”€ checksums.sha256

Safety

  • Local-first only.
  • Reports include the ClawBio medical/research disclaimer.
  • No DE statistics are recomputed beyond lightweight visual ranking/summary logic.
  • Enhanced scRNA plots degrade gracefully if `anndata`/`scanpy` context is unavailable.

Integration with Bio Orchestr

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