Calculating Relative Weights Random Effects Meta Analysis

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Relative Weights Random Effects Meta-Analysis Calculator

Accurately determine the contribution of each study to your meta-analysis.

Meta-Analysis Weights Calculator

Enter the total number of independent studies included in your meta-analysis.
The estimated effect size from the first study (e.g., log odds ratio, mean difference).
The estimated variance of the effect estimate for the first study. Must be non-negative.
The estimated effect size from the second study.
The estimated variance of the effect estimate for the second study. Must be non-negative.
The estimated effect size from the third study.
The estimated variance of the effect estimate for the third study. Must be non-negative.
The estimated effect size from the fourth study.
The estimated variance of the effect estimate for the fourth study. Must be non-negative.
The estimated effect size from the fifth study.
The estimated variance of the effect estimate for the fifth study. Must be non-negative.
Estimate of the variance of the true effect sizes across studies (τ²). Crucial for random-effects models. Must be non-negative.

Analysis Results

Overall Random Effects Estimate:

Study Weights:

Inverse Variance of Study Weights:

Total Weight:

Formula Explanation: In a random-effects meta-analysis, the weight of each study (w_i) is determined by the inverse of its total variance, which includes both within-study variance (v_i) and between-study variance (τ²). The formula is: w_i = 1 / (v_i + τ²). The overall random-effects estimate is a weighted average of individual study estimates, using these weights.
Study Contributions to Random Effects Meta-Analysis
Study Effect Estimate (θᵢ) Within-Study Variance (vᵢ) Total Variance (vᵢ + τ²) Relative Weight (wᵢ)
Study vs. Overall Relative Weights
Study Weight Overall Weight Proportion

What is Relative Weights Random Effects Meta-Analysis?

Relative weights random effects meta-analysis is a statistical technique used to synthesize findings from multiple independent studies addressing the same research question. Unlike fixed-effect models that assume all studies share a single true effect size, random-effects models acknowledge that the true effect sizes may vary across studies due to differences in populations, interventions, or methodologies. The 'relative weights' in this context refer to the proportion of influence each individual study has on the pooled overall effect estimate. Studies with greater precision (lower variance) receive higher weights. The 'random effects' aspect accounts for the heterogeneity (variability) between studies by incorporating an estimate of the between-study variance (τ²). This approach provides a more realistic and generalizable summary effect when heterogeneity is present.

Who should use it: Researchers, clinicians, policymakers, and anyone needing to combine evidence from multiple studies, especially when significant variability is expected or observed between study results. This is common in fields like medicine, psychology, education, and environmental science.

Common misconceptions: A frequent misconception is that a random-effects model eliminates heterogeneity; it does not, but rather accounts for it. Another is that larger studies always have much higher weights; while true, the relative weights are more nuanced and depend heavily on both within-study variance and the estimated between-study variance (τ²). Some may also assume that all studies are equally important, which is contrary to the principle of weighting by precision. Understanding {primary_keyword} is crucial for correct interpretation.

{primary_keyword} Formula and Mathematical Explanation

The core of {primary_keyword} lies in calculating the weight assigned to each individual study within the meta-analysis. This weight determines how much that study's effect estimate contributes to the overall pooled effect. In a random-effects model, the total variance for each study includes both the variance inherent to that specific study (within-study variance) and the variance that reflects the true differences between study effects (between-study variance, denoted as τ²).

The process involves several steps:

  1. Estimate Within-Study Variance (vᵢ): For each study 'i', obtain its estimated effect estimate (θᵢ) and its variance (vᵢ). The variance (vᵢ) is typically derived from the standard error (SEᵢ) reported in the study, where vᵢ = SEᵢ².
  2. Estimate Between-Study Variance (τ²): This is a critical component of random-effects models. Various methods exist to estimate τ² (e.g., DerSimonian and Laird, REML), aiming to quantify the extent of heterogeneity. Our calculator uses a user-provided value for τ².
  3. Calculate Total Variance for Each Study: For each study 'i', the total variance is the sum of its within-study variance and the estimated between-study variance: Total Varianceᵢ = vᵢ + τ².
  4. Calculate Inverse Variance Weights (wᵢ*): The initial weight for each study is the inverse of its total variance: wᵢ* = 1 / (vᵢ + τ²). These are often called inverse variance weights.
  5. Calculate Relative Weights (wᵢ): To obtain the relative weight (proportion) of each study, normalize the inverse variance weights by summing them across all studies (Σwⱼ*) and then dividing each study's weight by this total sum: wᵢ = wᵢ* / Σwⱼ*. This ensures that the sum of all relative weights equals 1.
  6. Calculate Overall Random Effects Estimate (θ_RE): The pooled random-effects estimate is the weighted average of the individual study effect estimates, using the calculated relative weights: θ_RE = Σ(wᵢ * θᵢ) / Σwᵢ = Σ(wᵢ * θᵢ).
Variables Used in {primary_keyword} Calculation
Variable Meaning Unit Typical Range
k Number of studies Count ≥ 2
θᵢ Effect estimate from study i Depends on outcome (e.g., Odds Ratio, Mean Difference, Hedges' g, log transformation) Varies widely
vᵢ Within-study variance of θᵢ (Unit of θᵢ)² Non-negative
SEᵢ Standard Error of θᵢ Unit of θᵢ Positive
τ² Between-study variance (Unit of θᵢ)² Non-negative (often estimated)
wᵢ* Inverse variance weight for study i 1 / (Unit of θᵢ)² Positive
wᵢ Relative weight (proportion) for study i Proportion (0 to 1) 0 to 1 (summing to 1)
θRE Overall random-effects estimate Unit of θᵢ Typically within the range of individual θᵢ

Practical Examples (Real-World Use Cases)

Let's consider two scenarios where {primary_keyword} is applied. Imagine we are conducting a meta-analysis on the effectiveness of a new drug versus a placebo.

Example 1: Moderate Heterogeneity

Suppose we have 5 studies with the following estimates (e.g., log odds ratios) and variances:

  • Study 1: θ₁=0.4, v₁=0.08
  • Study 2: θ₂=0.6, v₂=0.10
  • Study 3: θ₃=0.5, v₃=0.09
  • Study 4: θ₄=0.7, v₄=0.12
  • Study 5: θ₅=0.55, v₅=0.11

After reviewing the studies, we estimate the between-study variance τ² = 0.04.

Calculation (Simplified):

  • Study 1 Total Variance = 0.08 + 0.04 = 0.12; w₁* = 1/0.12 ≈ 8.33
  • Study 2 Total Variance = 0.10 + 0.04 = 0.14; w₂* = 1/0.14 ≈ 7.14
  • Study 3 Total Variance = 0.09 + 0.04 = 0.13; w₃* = 1/0.13 ≈ 7.69
  • Study 4 Total Variance = 0.12 + 0.04 = 0.16; w₄* = 1/0.16 = 6.25
  • Study 5 Total Variance = 0.11 + 0.04 = 0.15; w₅* = 1/0.15 ≈ 6.67
  • Total sum of w* ≈ 8.33 + 7.14 + 7.69 + 6.25 + 6.67 = 36.08
  • Relative Weights: w₁ ≈ 8.33/36.08 ≈ 0.231; w₂ ≈ 0.198; w₃ ≈ 0.213; w₄ ≈ 0.173; w₅ ≈ 0.185
  • Overall Estimate (θ_RE) ≈ (0.231*0.4) + (0.198*0.6) + (0.213*0.5) + (0.173*0.7) + (0.185*0.55) ≈ 0.0924 + 0.1188 + 0.1065 + 0.1211 + 0.1018 ≈ 0.541

Interpretation: The overall random-effects estimate for the drug's effect is approximately 0.541 (log odds ratio). Study 1, having the lowest total variance (v₁ + τ²), receives the highest relative weight (23.1%). Studies with higher variance contribute less. The weights reflect both the internal precision of each study and the overall heterogeneity in the field.

Example 2: High Heterogeneity

Consider the same 5 studies, but now assume higher heterogeneity, perhaps due to significant methodological differences, leading to τ² = 0.20.

Calculation (Simplified):

  • Study 1 Total Variance = 0.08 + 0.20 = 0.28; w₁* = 1/0.28 ≈ 3.57
  • Study 2 Total Variance = 0.10 + 0.20 = 0.30; w₂* = 1/0.30 ≈ 3.33
  • Study 3 Total Variance = 0.09 + 0.20 = 0.29; w₃* = 1/0.30 ≈ 3.45
  • Study 4 Total Variance = 0.12 + 0.20 = 0.32; w₄* = 1/0.32 ≈ 3.13
  • Study 5 Total Variance = 0.11 + 0.20 = 0.31; w₅* = 1/0.31 ≈ 3.23
  • Total sum of w* ≈ 3.57 + 3.33 + 3.45 + 3.13 + 3.23 = 16.71
  • Relative Weights: w₁ ≈ 3.57/16.71 ≈ 0.213; w₂ ≈ 0.199; w₃ ≈ 0.206; w₄ ≈ 0.187; w₅ ≈ 0.193
  • Overall Estimate (θ_RE) ≈ (0.213*0.4) + (0.199*0.6) + (0.206*0.5) + (0.187*0.7) + (0.193*0.55) ≈ 0.0852 + 0.1194 + 0.1030 + 0.1309 + 0.1062 ≈ 0.545

Interpretation: Notice how the weights become more similar when heterogeneity (τ²) is high. The influence of within-study variance (vᵢ) is diminished relative to the between-study variance. The highest weight now goes to Study 1 (21.3%), but the difference between the highest and lowest weighted studies is smaller compared to Example 1. The overall estimate is slightly higher (0.545), reflecting the increased uncertainty and variability assumed. This highlights the sensitivity of {primary_keyword} to the τ² estimate.

How to Use This {primary_keyword} Calculator

Our calculator simplifies the process of determining relative weights for random-effects meta-analysis. Follow these steps:

  1. Input Number of Studies: Enter the total count of studies you are including in your meta-analysis. The calculator dynamically adjusts to accommodate inputs for studies.
  2. Enter Study Details: For each study, input its Effect Estimate (the reported outcome measure, like a mean difference or log odds ratio) and its Variance. Ensure you use consistent units and scales for all studies. If you only have Standard Error (SE), you can calculate variance as SE².
  3. Provide Between-Study Variance (τ²): This is a crucial input for random-effects models. Enter your estimated value for τ². This value can be obtained using various meta-analysis software or estimation methods. If you are unsure, consult statistical guidelines or a statistician.
  4. Calculate: Click the "Calculate Weights" button.
  5. Review Results:
    • Overall Random Effects Estimate: This is the primary output, representing the synthesized effect size across all studies, accounting for heterogeneity.
    • Study Weights: See the relative weight (percentage) assigned to each study.
    • Inverse Variance Weights: These are the intermediate weights before normalization.
    • Total Weight: The sum of all normalized study weights (should be 1 or very close due to rounding).
    • Data Table: A detailed breakdown of estimates, variances, and calculated weights for each study.
    • Chart: A visual representation comparing the calculated weights of individual studies and their proportion of the total weight.
  6. Interpret Findings: Analyze which studies contribute most to the overall estimate. High weights indicate studies with higher precision (lower total variance). Low weights suggest studies with more uncertainty or those that are more dissimilar to the average study.
  7. Reset or Copy: Use the "Reset" button to clear inputs and return to defaults. Use "Copy Results" to copy the summary to your clipboard for reports or documentation.

This tool is invaluable for understanding the contribution of each piece of evidence in your meta-analysis and for ensuring transparency in your evidence synthesis process. Proper use of {primary_keyword} aids in drawing reliable conclusions.

Key Factors That Affect {primary_keyword} Results

Several factors significantly influence the relative weights calculated in a random-effects meta-analysis:

  1. Within-Study Variance (vᵢ): This is the most direct factor. Studies with smaller sample sizes or higher variability in their outcomes will have larger vᵢ, leading to lower inverse variance weights (wᵢ*) and thus lower relative weights (wᵢ). Precision is key here.
  2. Between-Study Variance (τ²): A larger estimated τ² indicates greater heterogeneity among the true effect sizes across studies. As τ² increases, the denominator (vᵢ + τ²) for all studies increases, causing all inverse variance weights (wᵢ*) to decrease. Crucially, a higher τ² reduces the relative difference between weights, making the weighting scheme less sensitive to individual study variances. Studies become more like each other in terms of their contribution.
  3. Magnitude of Effect Estimates (θᵢ): While the effect estimates themselves (θᵢ) do not directly influence the *weights*, they determine the final *overall pooled estimate* (θ_RE). A study with a large weight but an extreme effect estimate will pull the overall estimate more strongly than a study with a small weight. The interplay between weight and estimate is critical for interpretation.
  4. Number of Studies (k): With more studies, the sum of the inverse variance weights (Σwⱼ*) tends to increase, which can further decrease the relative weight (wᵢ) of any single study. As 'k' grows, the influence of any one study often diminishes, especially if their variances are comparable.
  5. Method for Estimating τ²: Different methods for estimating τ² (e.g., DerSimonian-Laird, REML, Paule-Mandel) can yield different values, especially with few studies or high heterogeneity. A higher τ² estimate, as shown in Example 2, will lead to more uniform study weights. Choosing an appropriate method is vital.
  6. Scale of Measurement: The units and scale of the effect estimates (e.g., log odds ratios vs. odds ratios, raw mean differences vs. standardized mean differences) affect the numerical values of variances and estimates. While the relative weights should be conceptually consistent across scales, ensuring uniformity in input is essential for correct calculation and interpretation. The variance (vᵢ) and τ² must be on the same scale as the effect estimates.
  7. Study Design and Quality: Although not directly in the weight formula, underlying differences in study design, risk of bias, or methodological quality can contribute to heterogeneity (and thus higher τ²). If these factors are not accounted for, they might indirectly influence weights by increasing overall variance estimates. Sensitivity analyses are often performed to explore the impact of excluding low-quality studies.

Frequently Asked Questions (FAQ)

  • Q1: What is the difference between weights in fixed-effect and random-effects models?

    In fixed-effect models, weights are solely based on the inverse of the within-study variance (wᵢ = 1/vᵢ). It assumes a single true effect. Random-effects models add the between-study variance (τ²) to the denominator (wᵢ = 1/(vᵢ + τ²)), acknowledging that true effects vary and thus providing more conservative, generally smaller, and more evenly distributed weights.

  • Q2: My τ² estimate is very large. What does this mean for the weights?

    A large τ² suggests substantial heterogeneity among the studies. This means the true effect sizes likely differ significantly. Consequently, the relative weights will become more similar across studies, as the between-study variance dominates the within-study variance. The overall estimate will be less influenced by the precision of individual studies and more by the average effect across all.

  • Q3: Can a study have zero weight?

    In theory, a study with infinite variance would have zero weight. In practice, with finite variances and a positive τ², all studies will have a positive (though potentially very small) inverse variance weight, thus a non-zero relative weight. Extremely low weights might indicate a study that is an outlier or has very low precision.

  • Q4: How do I estimate τ² if I don't have software?

    Estimating τ² requires specialized methods. While software is standard, the simplest (though often biased) method is the DerSimonian and Laird (1986) method. However, using statistical software packages (like R, Stata, RevMan) that implement various estimators (e.g., REML, Paule-Mandel) is highly recommended for more accurate and reliable estimates. This calculator assumes you provide a pre-estimated τ².

  • Q5: What if I have very few studies (e.g., 2 or 3)?

    Estimating τ² reliably with very few studies is challenging and prone to large uncertainty. Random-effects models are still applicable, but the interpretation of τ² and the resulting weights should be cautious. Some researchers prefer fixed-effect models or use specific adjustments when k is very small. Our calculator will function, but the statistical implications of a poorly estimated τ² are significant.

  • Q6: My study estimates are on different scales. How do I proceed?

    For {primary_keyword}, all effect estimates (θᵢ) and their variances (vᵢ) must be on the same scale. If studies report results on different scales (e.g., one uses Odds Ratios, another uses Risk Ratios), you typically need to transform them to a common scale, such as log odds ratios or log risk ratios. Ensure τ² is estimated on this same common scale.

  • Q7: How does study quality affect weights?

    Study quality doesn't directly enter the weight calculation formula. However, lower quality studies might intrinsically have larger variances (vᵢ) or contribute to heterogeneity (higher τ²). While not explicitly weighted by quality, less precise or more heterogeneous studies naturally receive lower weights. Sensitivity analyses excluding low-quality studies are often recommended to check robustness.

  • Q8: Can I use this calculator for meta-regression?

    This specific calculator is designed for standard random-effects meta-analysis to compute weights for the overall effect estimate. It does not directly handle meta-regression, which involves modeling the relationship between study-level covariates and effect sizes. However, the underlying principles of weighting based on variance and heterogeneity are fundamental to meta-regression as well.

Related Tools and Internal Resources

© 2023-2024 Your Company Name. All rights reserved. | Disclaimer: This calculator is for informational purposes only and does not constitute statistical advice. Consult with a qualified statistician for complex meta-analysis designs.

var numStudiesInput = document.getElementById('numStudies'); var study1_estInput = document.getElementById('study1_est'); var study1_varInput = document.getElementById('study1_var'); var study2_estInput = document.getElementById('study2_est'); var study2_varInput = document.getElementById('study2_var'); var study3_estInput = document.getElementById('study3_est'); var study3_varInput = document.getElementById('study3_var'); var study4_estInput = document.getElementById('study4_est'); var study4_varInput = document.getElementById('study4_var'); var study5_estInput = document.getElementById('study5_est'); var study5_varInput = document.getElementById('study5_var'); var tau_squaredInput = document.getElementById('tau_squared'); var studyEstimateInputs = [study1_estInput, study2_estInput, study3_estInput, study4_estInput, study5_estInput]; var studyVarianceInputs = [study1_varInput, study2_varInput, study3_varInput, study4_varInput, study5_varInput]; var weightsChart = null; // Global variable for the chart instance function validateInput(inputId, errorId, minValue = null, maxValue = null) { var input = document.getElementById(inputId); var errorElement = document.getElementById(errorId); var value = parseFloat(input.value); var isValid = true; if (isNaN(value)) { errorElement.textContent = "Please enter a valid number."; isValid = false; } else if (input.type === "number" && input.min !== undefined && value < parseFloat(input.min)) { errorElement.textContent = "Value cannot be less than " + input.min + "."; isValid = false; } else if (minValue !== null && value maxValue) { errorElement.textContent = "Value cannot be greater than " + maxValue + "."; isValid = false; } else { errorElement.textContent = ""; } input.style.borderColor = isValid ? " : 'var(–error-color)'; return isValid; } function updateStudyInputs(numStudies) { for (var i = 0; i < studyEstimateInputs.length; i++) { var estInput = studyEstimateInputs[i]; var varInput = studyVarianceInputs[i]; var errorEst = document.getElementById('study' + (i + 1) + '_estError'); var errorVar = document.getElementById('study' + (i + 1) + '_varError'); if (i < numStudies) { estInput.parentElement.style.display = 'block'; varInput.parentElement.style.display = 'block'; } else { estInput.parentElement.style.display = 'none'; varInput.parentElement.style.display = 'none'; // Clear errors and values for hidden inputs estInput.value = ''; varInput.value = ''; errorEst.textContent = ''; errorVar.textContent = ''; estInput.style.borderColor = ''; varInput.style.borderColor = ''; } } // Ensure tau_squared is always visible and required document.getElementById('tau_squared').parentElement.style.display = 'block'; } function calculateWeights() { var numStudies = parseInt(numStudiesInput.value); var overallEstimate = 0; var totalWeightSum = 0; var studyWeights = []; var invVarianceWeights = []; var studyData = []; var allValid = true; // Clear previous errors and results document.getElementById('overallEstimate').textContent = '–'; document.getElementById('totalWeight').textContent = '–'; document.getElementById('studyWeights').innerHTML = ''; document.getElementById('invVarianceWeights').innerHTML = ''; document.getElementById('studyTableBody').innerHTML = ''; if (weightsChart) { weightsChart.destroy(); } // Validate Number of Studies if (!validateInput('numStudies', 'numStudiesError', 1)) { allValid = false; } else { numStudies = parseInt(numStudiesInput.value); // Update numStudies after validation } // Validate tau_squared if (!validateInput('tau_squared', 'tau_squaredError', 0)) { allValid = false; } var tau_squared = parseFloat(tau_squaredInput.value); // Validate each study's inputs for (var i = 0; i < numStudies; i++) { var estInput = studyEstimateInputs[i]; var varInput = studyVarianceInputs[i]; var studyNum = i + 1; if (!validateInput('study' + studyNum + '_est', 'study' + studyNum + '_estError')) { allValid = false; } if (!validateInput('study' + studyNum + '_var', 'study' + studyNum + '_varError', 0)) { allValid = false; } if (allValid) { var estimate = parseFloat(estInput.value); var variance = parseFloat(varInput.value); var totalVariance = variance + tau_squared; var invWeight = 1 / totalVariance; studyData.push({ id: studyNum, estimate: estimate, variance: variance, totalVariance: totalVariance, invWeight: invWeight }); totalWeightSum += invWeight; } } if (!allValid) { console.log("Validation failed. Cannot calculate."); return; } // Calculate relative weights and overall estimate var chartStudyWeights = []; var chartOverallWeights = []; var totalWeightProp = 0; for (var i = 0; i < studyData.length; i++) { var study = studyData[i]; var relativeWeight = study.invWeight / totalWeightSum; studyWeights.push('Study ' + study.id + ': ' + (relativeWeight * 100).toFixed(2) + '%'); invVarianceWeights.push('Study ' + study.id + ': ' + study.invWeight.toFixed(4)); overallEstimate += relativeWeight * study.estimate; totalWeightProp += relativeWeight; // Populate table var row = studyDataTable.tBodies[0].insertRow(); row.innerHTML = '' + study.id + '' + '' + study.estimate.toFixed(4) + '' + '' + study.variance.toFixed(4) + '' + '' + study.totalVariance.toFixed(4) + '' + '' + relativeWeight.toFixed(4) + ''; // Prepare data for chart chartStudyWeights.push(relativeWeight); // Individual study weight } // Calculate overall weight proportion for comparison (should be 1) chartOverallWeights.push(1); // Represents the total pooled weight // Display results document.getElementById('overallEstimate').textContent = overallEstimate.toFixed(4); document.getElementById('totalWeight').textContent = totalWeightProp.toFixed(4); document.getElementById('studyWeights').innerHTML = studyWeights.join("); document.getElementById('invVarianceWeights').innerHTML = invVarianceWeights.join("); // Draw Chart drawChart(chartStudyWeights, chartOverallWeights); } function resetForm() { numStudiesInput.value = 5; study1_estInput.value = 0.5; study1_varInput.value = 0.1; study2_estInput.value = 0.6; study2_varInput.value = 0.12; study3_estInput.value = 0.4; study3_varInput.value = 0.09; study4_estInput.value = 0.7; study4_varInput.value = 0.15; study5_estInput.value = 0.55; study5_varInput.value = 0.11; tau_squaredInput.value = 0.05; // Clear errors and results document.getElementById('numStudiesError').textContent = ""; document.getElementById('tau_squaredError').textContent = ""; for (var i = 0; i < studyEstimateInputs.length; i++) { document.getElementById('study' + (i + 1) + '_estError').textContent = ""; document.getElementById('study' + (i + 1) + '_varError').textContent = ""; document.getElementById('study' + (i + 1) + '_estError').style.borderColor = ""; document.getElementById('study' + (i + 1) + '_varError').style.borderColor = ""; } document.getElementById('overallEstimate').textContent = '–'; document.getElementById('totalWeight').textContent = '–'; document.getElementById('studyWeights').innerHTML = ''; document.getElementById('invVarianceWeights').innerHTML = ''; document.getElementById('studyTableBody').innerHTML = ''; if (weightsChart) { weightsChart.destroy(); } updateStudyInputs(parseInt(numStudiesInput.value)); // Reset visibility based on default numStudies } function copyResults() { var overallEst = document.getElementById('overallEstimate').textContent; var totalWeight = document.getElementById('totalWeight').textContent; var studyWeightsText = document.getElementById('studyWeights').innerHTML.replace(//g, '\n'); var invVarWeightsText = document.getElementById('invVarianceWeights').innerHTML.replace(//g, '\n'); var assumptions = "Key Assumptions:\n- Between-Study Variance (τ²): " + tau_squaredInput.value + "\n"; var textToCopy = "— Meta-Analysis Weights Results —\n\n"; textToCopy += "Overall Random Effects Estimate: " + overallEst + "\n"; textToCopy += "Total Weight: " + totalWeight + "\n\n"; textToCopy += "Study Weights:\n" + studyWeightsText + "\n\n"; textToCopy += "Inverse Variance Weights:\n" + invVarWeightsText + "\n\n"; textToCopy += assumptions; textToCopy += "\n— End Results —"; navigator.clipboard.writeText(textToCopy).then(function() { // Optional: Provide user feedback var originalText = document.getElementById('copyBtn').textContent; document.getElementById('copyBtn').textContent = 'Copied!'; setTimeout(function() { document.getElementById('copyBtn').textContent = originalText; }, 2000); }, function(err) { console.error('Could not copy text: ', err); alert('Failed to copy results. Please copy manually.'); }); } function drawChart(studyWeightsData, overallWeightData) { var ctx = document.getElementById('weightsChart').getContext('2d'); var labels = []; for (var i = 0; i = 1) { updateStudyInputs(numStudies); calculateWeights(); // Recalculate after changing number of studies } }); // Add listeners for all relevant inputs to update in real-time var allInputs = [numStudiesInput, study1_estInput, study1_varInput, study2_estInput, study2_varInput, study3_estInput, study3_varInput, study4_estInput, study4_varInput, study5_estInput, study5_varInput, tau_squaredInput]; allInputs.forEach(function(input) { input.addEventListener('input', calculateWeights); }); });

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