Getting it into your agent
One page per mod, every tool's command on it. A separate URL per tool would split the same page into five that compete with each other.
npx agentmods add skills/beita6969/scienceclaw/data-visualization-biomedicalnpx skills add beita6969/ScienceClaw --skill data-visualization-biomedicalgit clone --depth 1 https://github.com/beita6969/ScienceClawWrote this? Show the measurements
A badge with what this costs and how it scanned, read live from this page, so it follows the numbers instead of freezing them. Markdown for a README, HTML for a documentation site or a project page.
[](https://agentmods.dev/skills/beita6969/scienceclaw/data-visualization-biomedical)<a href="https://agentmods.dev/skills/beita6969/scienceclaw/data-visualization-biomedical"><img src="https://agentmods.dev/badge/skills/beita6969/scienceclaw/data-visualization-biomedical.svg" alt="Measured on agentmods" height="20"></a>What it costs to keep this loaded
Counted locally with the o200k_base tokenizer, which is exact for GPT models; Claude uses its own tokenizer and its counts differ. Treat this as one consistent yardstick across the catalogue rather than a bill. Prices are per million input tokens.
| Model | Per session | Once invoked |
|---|---|---|
| Fable 5.1 | $0.00010 | $0.02257 |
| Opus 5 | $0.00005 | $0.01128 |
| Sonnet 5 | $0.00002 | $0.00451 |
| Haiku 4.5 | $0.00001 | $0.00226 |
Grade A, and why
data-visualization-biomedical scanned grade A with 0 findings against 26 rules in 11 categories — prompt injection, anti-refusal, data exfiltration, privilege escalation, supply chain, agent snooping, system-prompt leakage, SSRF and excessive agency — measured 6d ago.
A static scan of the body, not an audit. Every finding is printed with the line that produced it so you can judge whether it matters here. A mod is markdown that instructs an agent; that is exactly why what it instructs is worth reading.
Nothing flagged
None of the 26 patterns this scan looks for appear in this file: no shell pipes, no recursive deletes, no credential paths, no hidden text, no instruction-override or anti-refusal phrasing, no agent-config snooping. That is not a guarantee, it is the absence of the things that are checkable.
How it starts
The opening of the file, as written. The whole thing — 257 lines — stays where its author put it; the contents beside it link to each section on GitHub.
name: data-visualization-biomedical description: "Publication-quality visualizations for biomedical and genomics data. Use when creating volcano plots, heatmaps, UMAP plots, dot plots, survival curves, forest plots, or multi-panel figures. Includes scanpy, matplotlib, seaborn, plotly workflows with journal-ready aesthetics and proper statistical annotations." license: Proprietary
Biomedical Data Visualization
Publication-Quality Settings
import matplotlib.pyplot as plt
import seaborn as sns
import numpy as np
import pandas as pd
# Nature/Blood style settings
plt.rcParams.update({
'font.family': 'Arial',
'font.size': 8,
'axes.labelsize': 8,
'axes.titlesize': 9,
'xtick.labelsize': 7,
'ytick.labelsize': 7,
'legend.fontsize': 7,
'figure.dpi': 300,
'savefig.dpi': 300,
'savefig.bbox': 'tight',
'axes.linewidth': 0.5,
'xtick.major.width': 0.5,
'ytick.major.width': 0.5,
})
# Color palettes
NATURE_COLORS = ['#E64B35', '#4DBBD5', '#00A087', '#3C5488', '#F39B7F', '#8491B4']
BLOOD_COLORS = ['#D62728', '#1F77B4', '#2CA02C', '#FF7F0E', '#9467BD', '#8C564B']
Volcano Plot
def volcano_plot(df, log2fc_col='log2FC', pval_col='pval_adj',
gene_col='gene', fc_thresh=1, pval_thresh=0.05,
highlight_genes=None, figsize=(4, 4)):
"""Publication-quality volcano plot."""
fig, ax = plt.subplots(figsize=figsize)
df = df.copy()
df['-log10pval'] = -np.log10(df[pval_col].clip(lower=1e-300))
# Categorize points
df['category'] = 'NS'
df.loc[(df[log2fc_col] > fc_thresh) & (df[pval_col] < pval_thresh), 'category'] = 'Up'
df.loc[(df[log2fc_col] < -fc_thresh) & (df[pval_col] < pval_thresh), 'category'] = 'Down'
colors = {'NS': '#CCCCCC', 'Up': '#E64B35', 'Down': '#4DBBD5'}
for cat, color in colors.items():
subset = df[df['category'] == cat]
ax.scatter(subset[log2fc_col], subset['-log10pval'],
c=color, s=10, alpha=0.7, edgecolors='none', label=cat)
# Add threshold lines
ax.axhline(-np.log10(pval_thresh), color='grey', linestyle='--', linewidth=0.5)
ax.axvline(-fc_thresh, color='grey', linestyle='--', linewidth=0.5)
ax.axvline(fc_thresh, color='grey', linestyle='--', linewidth=0.5)
# Label specific genes
if highlight_genes:
for gene in highlight_genes:
if gene in df[gene_col].values:
row = df[df[gene_col] == gene].iloc[0]
ax.annotate(gene, (row[log2fc_col], row['-log10pval']),
fontsize=6, ha='center')
ax.set_xlabel('log₂ Fold Change')
ax.set_ylabel('-log₁₀ Adjusted P-value')
ax.legend(frameon=False, loc='upper right')
plt.tight_layout()
return fig, ax
What this file has done since we first saw it
Hashed on every crawl. A supply-chain change to an agent config is a question of when, not whether, so the history is kept rather than the latest state alone.
- 6d ago First seen · 257 lines · 10 tokens per session scan A 5919ef7f3c88
data-visualization-biomedical is a skill published in the GitHub repository beita6969/ScienceClaw (894 stars, last pushed 2mo ago), licensed MIT. It adds 10 tokens to every session and 2,257 once invoked, about $0.0001 per session on Opus 5. A static security scan graded it A with 0 findings. No closer match exists in the catalogue, so it is treated as the original; first seen 2026-08-30.
Other skills, from other repositories
biopython
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scanpy
Standard single-cell RNA-seq analysis pipeline. Use for QC, normalization, dimensionality reduction (PCA/UMAP/t-SNE), clustering, differential expression, and visualization. Best for exploratory scRNA-seq analysis with established workflows. For deep learning models use scvi-tools; for data format questions use…
structure-prediction
Protein structure prediction from sequence. ESMFold-based, single GPU, no MSA needed. Predicts 3D structures with pLDDT confidence scores for drug discovery targets.
biomcp
Search and retrieve biomedical data - genes, variants, clinical trials, diagnostic tests, articles, drugs, diseases, pathways, proteins, adverse events, pharmacogenomics, and phenotype-disease matching. Use for gene function, variant pathogenicity, trials, diagnostics, drug safety, pathway context, disease workups…
biomcp-research
Do biomedical literature and variant research with the BioMCP CLI, and file what you learn about the tool itself as issues in the biomcp repo.
biological-expert
Expert-level biology, biotechnology, genetics, bioinformatics, and computational biology. Use when the user mentions biology, biotechnology, genetics, bioinformatics, or genomics, or when the task involves Molecular Biology, Genomics & Bioinformatics, Systems Biology, or Data Analysis.