Transform lengthy academic papers into concise, structured 250-word abstracts.
日本語の概要は準備中です。原文の説明を表示しています。
Perform quantitative meta-analysis with effect size calculation, forest plots, funnel plots, and heterogeneity assessment. Use when: user asks to combine results from multiple studies, calculate pooled effect sizes, assess publication bias, or create forest/funnel plots. NOT f...
インストールする前に、エージェントに与えられる指示の中身を確認できます。
Quantitative synthesis of results from multiple studies. Calculates pooled effect sizes, assesses heterogeneity, detects publication bias, and generates forest and funnel plots.
| Outcome Type | Effect Size | Formula | Use When |
|---|---|---|---|
| Continuous | SMD (Cohen's d / Hedges' g) | $(M_1 - M_2) / S_p$ | Comparing means across studies with different scales |
| Continuous | Mean Difference (MD) | $M_1 - M_2$ | Same outcome measure across all studies |
| Binary | Odds Ratio (OR) | $(a \times d) / (b \times c)$ | Case-control studies, binary outcomes |
| Binary | Risk Ratio (RR) | $(a/(a+b)) / (c/(c+d))$ | Cohort studies, clinical trials |
| Binary | Risk Difference (RD) | $R_1 - R_2$ | Absolute risk reduction |
| Time-to-event | Hazard Ratio (HR) | From Cox model | Survival analysis |
| Correlation | Fisher's z | $0.5 \ln((1+r)/(1-r))$ | Correlation studies |
import numpy as np
from scipy import stats
def meta_analysis_random_effects(effects, variances, study_names=None):
"""
DerSimonian-Laird random-effects meta-analysis.
Args:
effects: array of effect sizes (log-OR, SMD, etc.)
variances: array of within-study variances
study_names: optional list of study labels
Returns:
dict with pooled estimate, CI, heterogeneity stats
"""
effects = np.array(effects, dtype=float)
variances = np.array(variances, dtype=float)
k = len(effects)
# Fixed-effect weights
w_fe = 1.0 / variances
pooled_fe = np.sum(w_fe * effects) / np.sum(w_fe)
# Cochran's Q
Q = np.sum(w_fe * (effects - pooled_fe) ** 2)
df = k - 1
p_heterogeneity = 1 - stats.chi2.cdf(Q, df)
# tau-squared (DerSimonian-Laird)
C = np.sum(w_fe) - np.sum(w_fe ** 2) / np.sum(w_fe)
tau2 = max(0, (Q - df) / C)
# I-squared
I2 = max(0, (Q - df) / Q * 100) if Q > 0 else 0
# Random-effects weights
w_re = 1.0 / (variances + tau2)
pooled_re = np.sum(w_re * effects) / np.sum(w_re)
se_pooled = np.sqrt(1.0 / np.sum(w_re))
ci_lower = pooled_re - 1.96 * se_pooled
ci_upper = pooled_re + 1.96 * se_pooled
z = pooled_re / se_pooled
p_value = 2 * (1 - stats.norm.cdf(abs(z)))
return {
'pooled_effect': pooled_re,
'se': se_pooled,
'ci_lower': ci_lower,
'ci_upper': ci_upper,
'z': z,
'p_value': p_value,
'tau2': tau2,
'I2': I2,
'Q': Q,
'Q_df': df,
'Q_p': p_heterogeneity,
'k': k,
'model': 'DerSimonian-Laird random-effects'
}
import matplotlib.pyplot as plt
import matplotlib.patches as mpatches
def forest_plot(effects, ci_lower, ci_upper, study_names, pooled, pooled_ci,
xlabel='Effect Size', title='Forest Plot', output_path='forest_plot.png'):
"""Generate a publication-quality forest plot."""
k = len(effects)
fig, ax = plt.subplots(figsize=(8, max(4, k * 0.4 + 2)))
y_positions = list(range(k, 0, -1))
# Individual studies
for i, y in enumerate(y_positions):
ax.plot(effects[i], y, 'ks', markersize=8)
ax.plot([ci_lower[i], ci_upper[i]], [y, y], 'k-', linewidth=1.5)
# Pooled estimate (diamond)
diamond_y = 0
diamond_half_h = 0.3
diamond = plt.Polygon([
[pooled_ci[0], diamond_y],
[pooled, diamond_y + diamond_half_h],
[pooled_ci[1], diamond_y],
[pooled, diamond_y - diamond_half_h]
], closed=True, facecolor='steelblue', edgecolor='black')
ax.add_patch(diamond)
# Reference line at null effect
ax.axvline(x=0, color='gray', linestyle='--', linewidth=0.8)
# Labels
yticks = y_positions + [diamond_y]
ylabels = study_names + ['Pooled']
ax.set_yticks(yticks)
ax.set_yticklabels(ylabels)
ax.set_xlabel(xlabel)
ax.set_title(title)
ax.set_ylim(-1, k + 1.5)
fig.tight_layout()
fig.savefig(output_path, dpi=300, bbox_inches='tight')
print(f"Forest plot saved: {output_path}")
return fig
def funnel_plot(effects, se_values, pooled_effect,
xlabel='Effect Size', output_path='funnel_plot.png'):
"""Generate a funnel plot to assess publication bias."""
fig, ax = plt.subplots(figsize=(6, 5))
ax.scatter(effects, se_values, c='black', s=30, zorder=3)
# Pseudo-confidence region
se_range = np.linspace(0.001, max(se_values) * 1.1, 100)
ci_low = pooled_effect - 1.96 * se_range
ci_high = pooled_effect + 1.96 * se_range
ax.fill_betweenx(se_range, ci_low, ci_high, alpha=0.1, color='gray')
ax.axvline(pooled_effect, color='red', linestyle='--', linewidth=1)
ax.set_xlabel(xlabel)
ax.set_ylabel('Standard Error')
ax.set_title('Funnel Plot')
ax.invert_yaxis() # Convention: smaller SE at top
fig.tight_layout()
fig.savefig(output_path, dpi=300, bbox_inches='tight')
print(f"Funnel plot saved: {output_path}")
return fig
def egger_test(effects, se_values):
"""Egger's test for funnel plot asymmetry."""
precision = 1.0 / np.array(se_values)
standardized = np.array(effects) / np.array(se_values)
slope, intercept, r, p, se = stats.linregress(precision, standardized)
return {'intercept': intercept, 'se': se, 'p_value': p,
'interpretation': 'Significant asymmetry' if p < 0.10 else 'No significant asymmetry'}
def begg_test(effects, variances):
"""Begg-Mazumdar rank correlation test."""
standardized = effects / np.sqrt(variances)
tau, p = stats.kendalltau(standardized, variances)
return {'tau': tau, 'p_value': p}
statsmodels or metafor (R) for implementation| I² Value | Interpretation |
|---|---|
| 0-25% | Low heterogeneity |
| 25-50% | Moderate heterogeneity |
| 50-75% | Substantial heterogeneity |
| 75-100% | Considerable heterogeneity |
When I² > 50%, investigate sources:
Follow PRISMA 2020 for reporting meta-analyses. Include:
This skill accepts requests that match the documented purpose of meta-analysis and include enough context to complete the workflow safely.
Do not continue the workflow when the request is out of scope, missing a critical input, or would require unsupported assumptions. Instead respond:
meta-analysisonly handles its documented workflow. Please provide the missing required inputs or switch to a more suitable skill.
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概要と使いどころ
Transform lengthy academic papers into concise, structured 250-word abstracts.
日本語の概要は準備中です。原文の説明を表示しています。
Precision editing tool that reduces abstract word count through intelligent compression techniques, maintaining scientific rigor while meeting strict journal and conference requirements.
日本語の概要は準備中です。原文の説明を表示しています。
Refines long medical academic texts into SCI-style unstructured Chinese and English abstracts; use when you need to condense drafts/reports/summaries into bilingual abstracts and generate Summary_Report.md.
日本語の概要は準備中です。原文の説明を表示しています。
Generates submission-ready Elsevier/SCI Highlights from manuscript text or extracted PDF/DOCX/TXT content. Use when a user needs 3-5 concise, evidence-grounded highlight bullets for a research paper, review, meta-analysis, case report, or bioinformatics manuscript.
日本語の概要は準備中です。原文の説明を表示しています。
Generates complete FAERS pharmacovigilance study designs for multi-drug or class-level safety comparison inside one predefined SOC or AE family using active comparators, disproportionality analysis, subgroup characterization, and reviewer-facing evidence control.
日本語の概要は準備中です。原文の説明を表示しています。
Analyze data with `adme-property-predictor` using a reproducible workflow, explicit validation, and structured outputs for review-ready interpretation.
日本語の概要は準備中です。原文の説明を表示しています。