Meta-analysis applies quantitative methods to synthesize findings across multiple studies, generating more precise estimates than any single study can provide. By pooling effect sizes from independent investigations, meta-analysis increases statistical power, resolves conflicting results, and identifies patterns invisible in individual studies. It's the gold standard for evidence synthesis in medicine, psychology, education, and social sciences.
Traditional meta-analysis requires specialized software—RevMan, Comprehensive Meta-Analysis, or R packages—plus deep statistical expertise. Researchers spend weeks calculating effect sizes, testing for heterogeneity, and creating forest plots. This complexity limits who can conduct meta-analyses and slows the pace of evidence synthesis.
Sourcetable democratizes meta-analysis with AI-powered assistance. Import study data, let AI calculate appropriate effect sizes (Cohen's d, odds ratios, risk ratios), assess between-study heterogeneity, detect publication bias, and generate publication-ready visualizations. Focus on interpreting findings rather than wrestling with statistical computations.
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Try for freeStandardized Mean Difference (SMD) for continuous outcomes—Cohen's d for equal variances, Hedges' g with small-sample correction. Odds Ratios and Risk Ratios for binary outcomes. Correlation coefficients for associational studies. Hazard ratios for time-to-event data. Choose metrics matching your research question and data availability.
Fixed-effect models assume one true effect size shared by all studies; observed differences reflect only sampling error. Use when heterogeneity is low (I² < 25%). Random-effects models assume effect sizes vary across studies due to real differences; estimate both within-study and between-study variance. Use when studies differ in populations, interventions, or methods.
I² quantifies percentage of variability due to heterogeneity vs. sampling error. Values of 25%, 50%, and 75% indicate low, moderate, and high heterogeneity respectively. Q-statistic tests null hypothesis of no heterogeneity. Tau² estimates between-study variance in random-effects models. Prediction intervals show range of true effects accounting for heterogeneity.
Funnel plots visualize effect size vs. standard error; asymmetry suggests publication bias. Egger's regression test statistically evaluates asymmetry. Trim-and-fill method imputes missing studies and recalculates pooled effect. Fail-safe N estimates unpublished null studies needed to nullify significant results. Cumulative meta-analysis tracks how pooled estimates change as studies accumulate.
Regression analysis using study-level variables to explain heterogeneity. Test whether effect sizes systematically vary with study characteristics—publication year, sample size, methodological quality, intervention intensity, or population demographics. Identify moderators and quantify their influence on treatment effects.
Leave-one-out analysis removes each study sequentially to assess influence on pooled estimate. Cumulative meta-analysis adds studies chronologically to show how evidence evolved. Subgroup analysis by study quality tests whether results depend on methodological rigor. Alternative effect size calculations or statistical models test robustness to analytical choices.
Register meta-analysis protocols on PROSPERO or similar registries before data extraction. Specify inclusion/exclusion criteria, outcome measures, planned analyses, and subgroup hypotheses a priori. Pre-registration prevents data-driven decision-making and selective reporting.
Search multiple databases, include gray literature, and check reference lists. Publication bias arises when searches miss negative results. Document search strategies thoroughly for reproducibility. Consider contacting study authors for unpublished data.
Evaluate risk of bias using validated tools (Cochrane Risk of Bias for RCTs, Newcastle-Ottawa for observational studies). Consider sensitivity analyses excluding high-risk studies. Report quality assessment transparently so readers can judge evidence strength.
Contact authors for missing statistics when possible. Use statistical methods to estimate missing SDs or correlations when necessary. Document all assumptions and test robustness through sensitivity analysis. Never exclude studies solely due to missing data without exploring alternatives.
Don't just report I² values—explain sources of heterogeneity through subgroup analysis or meta-regression. High heterogeneity doesn't invalidate meta-analysis; it indicates effect sizes vary systematically. Explore why rather than simply pooling despite heterogeneity.
Follow PRISMA guidelines for reporting. Provide forest plots showing individual study results. Report both random-effects and fixed-effect models for comparison. Include assessments of heterogeneity, publication bias, and sensitivity analyses. Make data and code available for reproducibility.
Technically, you can pool two studies, but meta-analysis is most valuable with 5-10+ studies. Smaller meta-analyses have limited power to detect heterogeneity or publication bias. However, even small meta-analyses provide more precise estimates than single studies and can be updated as new evidence emerges.
Use standardized effect sizes like Hedges' g that allow pooling across different scales. For example, pool depression outcomes from studies using BDI, HDRS, or PHQ-9 by calculating SMD. Alternatively, use meta-regression to test whether effect sizes differ by measurement instrument.
For multiple treatment arms, either combine groups or perform separate comparisons. For multiple outcomes, choose a primary outcome a priori or conduct separate meta-analyses. Never cherry-pick the most favorable outcome post-hoc. If studies report outcomes at multiple timepoints, analyze each timepoint separately.
Use random-effects models when pooling studies that differ in populations, interventions, or methods. Fixed-effect models are appropriate only when studies are methodologically homogeneous. Most meta-analyses should use random-effects given real-world heterogeneity. Report both for transparency.
Report it transparently. Use trim-and-fill to estimate adjusted effect size. Discuss how bias might affect conclusions. Search for unpublished studies more aggressively. Consider contacting researchers directly. Don't suppress findings—publication bias is common and readers deserve to know.
Yes, but interpret results cautiously since confounding can bias individual studies. Stratify by study design if mixing observational and experimental studies. Consider sensitivity analyses excluding observational studies. Meta-analysis of well-conducted observational studies can provide valuable evidence when RCTs aren't feasible.
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