data-visualization-biomedical
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COPYRIGHT NOTICE
Install with Codex or Claude Copy this prompt, paste it into Codex, Claude, or another assistant, and let it review the skill page and install it for you.
Based on SOC occupation classification
Transparent, rigorous research with full methodology — not a black-box API wrapper. Conducts exhaustive investigation through mandated 2-cycle research per theme, APA 7th citations, evidence hierarchy, and 3 user checkpoints. Self-contained using native OpenClaw tools (web_search, web_fetch, sessions_spawn). Use for literature reviews, competitive intelligence, or any research requiring academic rigor and reproducibility.
# Academic Literature Search — 学术文献检索与引用管理
Search and retrieve preprints from arXiv via the Atom API. Use this skill when searching for papers in physics, mathematics, computer science, quantitative biology, quantitative finance, statistics, electrical engineering, or economics by keywords, authors, arXiv IDs, date ranges, or categories.
Search arXiv for preprints in physics, math, CS, quantitative biology, quantitative finance, statistics, electrical engineering, economics. Use when: (1) finding preprints by topic, (2) searching by author, (3) browsing arXiv categories, (4) getting paper metadata/abstracts. NOT for: published journal articles (use crossref-search), biomedical (use pubmed-search).
Screen papers for systematic reviews using ASReview active learning. Use when: user has a large set of papers to screen for inclusion/exclusion, wants to prioritize relevant papers, or needs to reduce manual screening workload. NOT for: searching papers (use literature-search) or meta-analysis (use meta-analysis).
Analyzes astronomical observations and cosmological models including telescope data processing, celestial mechanics calculations, stellar evolution, galaxy classification, and cosmological parameter estimation; trigger when users discuss stars, galaxies, exoplanets, dark matter, or the universe's large-scale structure.
| name | data-visualization-biomedical |
| description | COPYRIGHT NOTICE |
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']
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
import scipy.cluster.hierarchy as sch
from matplotlib.colors import LinearSegmentedColormap
def clustered_heatmap(data, row_labels=None, col_labels=None,
cmap='RdBu_r', center=0, figsize=(8, 10),
row_cluster=True, col_cluster=True):
"""Hierarchically clustered heatmap."""
# Clustering
if row_cluster:
row_linkage = sch.linkage(data, method='ward')
row_order = sch.dendrogram(row_linkage, no_plot=True)['leaves']
data = data[row_order, :]
if row_labels is not None:
row_labels = [row_labels[i] for i in row_order]
if col_cluster:
col_linkage = sch.linkage(data.T, method='ward')
col_order = sch.dendrogram(col_linkage, no_plot=True)['leaves']
data = data[:, col_order]
if col_labels is not None:
col_labels = [col_labels[i] for i in col_order]
fig, ax = plt.subplots(figsize=figsize)
im = ax.imshow(data, aspect='auto', cmap=cmap,
vmin=center-np.abs(data).max(), vmax=center+np.abs(data).max())
if row_labels:
ax.set_yticks(range(len(row_labels)))
ax.set_yticklabels(row_labels)
if col_labels:
ax.set_xticks(range(len(col_labels)))
ax.set_xticklabels(col_labels, rotation=45, ha='right')
plt.colorbar(im, ax=ax, shrink=0.5, label='Expression (z-score)')
plt.tight_layout()
return fig, ax
import scanpy as sc
def enhanced_dotplot(adata, genes, groupby, figsize=(10, 8)):
"""Enhanced dot plot with proper visibility."""
sc.pl.dotplot(
adata, var_names=genes, groupby=groupby,
expression_cutoff=0.0001,
mean_only_expressed=False,
standard_scale='None',
smallest_dot=0.1,
dot_max=1.0,
cmap='Reds',
colorbar_title='Mean expression',
size_title='Fraction of cells (%)',
figsize=figsize,
show=False
)
plt.tight_layout()
return plt.gcf()
def multi_batch_umap(adata, color_by, batch_key='batch', figsize_per=(4, 4)):
"""UMAP plots per batch."""
batches = adata.obs[batch_key].unique()
n_batches = len(batches)
fig, axes = plt.subplots(1, n_batches,
figsize=(figsize_per[0]*n_batches, figsize_per[1]))
if n_batches == 1:
axes = [axes]
for ax, batch in zip(axes, batches):
adata_batch = adata[adata.obs[batch_key] == batch]
sc.pl.umap(adata_batch, color=color_by, ax=ax, show=False,
title=f'{batch}')
plt.tight_layout()
return fig
from scipy import stats
def add_significance(ax, x1, x2, y, h, p_value):
"""Add significance bar to plot."""
ax.plot([x1, x1, x2, x2], [y, y+h, y+h, y], 'k-', linewidth=0.5)
if p_value < 0.0001:
sig = '****'
elif p_value < 0.001:
sig = '***'
elif p_value < 0.01:
sig = '**'
elif p_value < 0.05:
sig = '*'
else:
sig = 'ns'
ax.text((x1+x2)/2, y+h, sig, ha='center', va='bottom', fontsize=8)
from matplotlib.gridspec import GridSpec
def create_figure_panel(n_rows, n_cols, width_ratios=None, height_ratios=None):
"""Create multi-panel figure."""
fig = plt.figure(figsize=(3*n_cols, 3*n_rows))
gs = GridSpec(n_rows, n_cols, figure=fig,
width_ratios=width_ratios or [1]*n_cols,
height_ratios=height_ratios or [1]*n_rows,
wspace=0.3, hspace=0.3)
axes = []
for i in range(n_rows):
row = []
for j in range(n_cols):
ax = fig.add_subplot(gs[i, j])
row.append(ax)
axes.append(row)
return fig, axes
def label_panels(axes, labels=None, fontsize=12, fontweight='bold'):
"""Add A, B, C... labels to panels."""
if labels is None:
labels = [chr(65+i) for i in range(len(axes))] # A, B, C...
for ax, label in zip(axes, labels):
ax.text(-0.15, 1.05, label, transform=ax.transAxes,
fontsize=fontsize, fontweight=fontweight, va='top')
def save_figure(fig, filename, formats=['pdf', 'png', 'svg']):
"""Save in multiple formats for journals."""
for fmt in formats:
fig.savefig(f"{filename}.{fmt}", format=fmt, dpi=300,
bbox_inches='tight', facecolor='white', edgecolor='none')
print(f"Saved: {filename}.{{{'|'.join(formats)}}}")
See references/color_guidelines.md for accessibility standards.
See scripts/figure_templates.py for pre-built templates.