analytics
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statistics-verifier
Verify statistics from raw data with methodology checking, significance testing, claim validation, and bias detection. Use when fact-checking statistical claims, validating research findings, or auditing data analysis.
Full skill instructions
Structured frameworks for verifying statistical claims, validating research methodology, and detecting analytical errors and biases.
CLAIM VERIFICATION PROTOCOL:
1. SOURCE CHECK
- Who made the claim?
- What is their expertise and incentive?
- Where was it published (peer-reviewed, preprint, press release)?
- Is the original data or study accessible?
2. METHODOLOGY CHECK
- What type of study (RCT, observational, survey, meta-analysis)?
- What was the sample size and population?
- What was the measurement method?
- Is the statistical test appropriate for the data type?
3. NUMBER SENSE CHECK
- Does the claim pass a basic plausibility test?
- Are units and denominators clearly stated?
- Absolute vs relative numbers — which is being used?
- Is the base rate provided for context?
4. REPLICATION CHECK
- Have other studies found similar results?
- Are the findings consistent across populations?
- Has anyone attempted and failed to replicate?
5. CONCLUSION CHECK
- Does the conclusion follow from the data?
- Are alternative explanations addressed?
- Is the scope of the claim proportional to the evidence?
| Red Flag | What It Means | Action |
|---|---|---|
| No sample size given | Cannot assess reliability | Request or estimate N |
| Only relative risk reported | May hide small absolute effect | Calculate absolute difference |
| "Up to X%" framing | Cherry-picked best case | Ask for median or mean |
| No confidence interval | Precision unknown | Treat with skepticism |
| Correlation stated as causation | Confounders likely ignored | Check study design |
| Self-selected sample | Selection bias likely | Note limitation |
| Composite endpoint | May mask weak individual results | Decompose the endpoint |
| Subgroup analysis highlighted | Likely post-hoc fishing | Require pre-registration |
CATEGORY 1: DESIGN ERRORS
- Sampling bias (convenience, voluntary response, survivorship)
- Confounding variables not controlled
- Insufficient sample size (underpowered study)
- No control group or inappropriate comparator
- Measurement instrument not validated
CATEGORY 2: ANALYSIS ERRORS
- Multiple comparisons without correction (p-hacking)
- Treating ordinal data as interval
- Assuming normality without checking
- Ignoring missing data patterns (MCAR vs MNAR)
- Using parametric tests on non-parametric data
CATEGORY 3: INTERPRETATION ERRORS
- Confusing statistical significance with practical significance
- Interpreting non-significant result as "no effect"
- Ecological fallacy (group-level applied to individuals)
- Simpson's paradox not checked
- Ignoring effect size and confidence intervals
CATEGORY 4: REPORTING ERRORS
- Selective reporting of favorable results
- Omitting negative or null findings
- Misleading axis scales in visualizations
- Presenting percentages without base numbers
- Switching between absolute and relative metrics
| Error Type | Severity | Impact on Conclusion |
|---|---|---|
| P-hacking / HARKing | Critical | Invalidates findings |
| Selection bias | Critical | Fundamentally flawed sample |
| Confounding not addressed | High | Alternative explanations remain |
| Wrong statistical test | High | Results may be artifactual |
| Multiple comparisons uncorrected | High | Inflated false positive rate |
| Small sample without power analysis | Medium | May miss real effects |
| Missing confidence intervals | Medium | Cannot judge precision |
| Misleading visualization | Medium | Misrepresents magnitude |
| Minor rounding errors | Low | Minimal impact |
CHOOSING THE RIGHT TEST:
DATA TYPE → COMPARISON → TEST
Continuous + 2 groups + independent → Independent t-test (or Mann-Whitney)
Continuous + 2 groups + paired → Paired t-test (or Wilcoxon signed-rank)
Continuous + 3+ groups + independent → One-way ANOVA (or Kruskal-Wallis)
Continuous + 2+ factors → Two-way ANOVA (or Friedman)
Continuous + continuous → Pearson correlation (or Spearman)
Categorical + 2 groups → Chi-square test (or Fisher's exact)
Categorical + ordered → Cochran-Armitage trend test
Binary outcome + predictors → Logistic regression
Time-to-event + groups → Log-rank test / Cox regression
Count data → Poisson regression
Proportion + large sample → Z-test for proportions
P-VALUE CONTEXT:
p-value = P(data this extreme | null hypothesis is true)
COMMON MISINTERPRETATIONS:
p = 0.03 does NOT mean:
- "There is a 3% chance the result is due to chance"
- "There is a 97% probability the hypothesis is true"
- "The effect is large or important"
- "The study will replicate"
p = 0.03 DOES mean:
- If the null hypothesis were true, data this extreme
would occur about 3% of the time by chance alone.
THRESHOLDS (conventional, not absolute):
p < 0.001 — strong evidence against null
p < 0.01 — moderate evidence against null
p < 0.05 — conventional threshold (context-dependent)
p > 0.05 — insufficient evidence to reject null
(NOT evidence of no effect)
ALWAYS COMPLEMENT WITH:
- Effect size (Cohen's d, odds ratio, etc.)
- Confidence interval (range of plausible values)
- Practical significance (is the effect meaningful?)
- Study power (could it have detected a real effect?)
| Method | When to Use | Conservativeness |
|---|---|---|
| Bonferroni | Few comparisons, need strong control | Very conservative |
| Holm-Bonferroni | Moderate comparisons, step-down | Less conservative |
| Benjamini-Hochberg | Many comparisons (FDR control) | Liberal |
| Tukey's HSD | All pairwise comparisons after ANOVA | Moderate |
| Dunnett's | Multiple treatments vs one control | Moderate |
MINIMUM SAMPLE SIZE GUIDELINES:
Survey (population estimate):
±3% margin, 95% CI → n ≈ 1,067
±5% margin, 95% CI → n ≈ 385
±10% margin, 95% CI → n ≈ 97
A/B Test (detecting 5% relative lift):
Baseline 10% conversion → n ≈ 3,200 per group
Baseline 5% conversion → n ≈ 6,400 per group
Baseline 2% conversion → n ≈ 16,000 per group
Clinical trial (medium effect d=0.5):
Two-group comparison, 80% power → n ≈ 64 per group
Two-group comparison, 90% power → n ≈ 86 per group
Correlation (detecting r=0.3):
80% power, alpha=0.05 → n ≈ 85
90% power, alpha=0.05 → n ≈ 113
| Parameter | Must Specify | Source |
|---|---|---|
| Alpha (Type I error rate) | Yes | Convention (usually 0.05) |
| Power (1 - Type II error) | Yes | Usually 0.80 or 0.90 |
| Effect size | Yes | Prior research or MCID |
| Variance / SD | Yes | Pilot data or literature |
| Sample size | Calculated | Output of power analysis |
| Attrition rate | Recommended | Inflate N by expected dropout |
DOES CORRELATION IMPLY CAUSATION? CHECK:
1. STRENGTH Is the association large?
Larger effects harder to explain away.
2. CONSISTENCY Replicated across settings, populations?
Multiple studies, same finding.
3. SPECIFICITY Is X linked specifically to Y (not everything)?
Less useful for multifactorial diseases.
4. TEMPORALITY Does X precede Y in time?
REQUIRED — cause must come before effect.
5. BIOLOGICAL GRADIENT Does more X produce more Y (dose-response)?
Strong support for causation.
6. PLAUSIBILITY Is there a credible mechanism?
Based on current knowledge.
7. COHERENCE Consistent with known biology/theory?
No conflict with established facts.
8. EXPERIMENT Does removing X reduce Y?
Strongest evidence (RCT).
9. ANALOGY Similar exposures cause similar effects?
Weakest criterion, supporting only.
VERDICT:
Criteria 1-3 met + Temporality → Suggestive of causation
Criteria 1-6 met + Experiment → Strong evidence of causation
Only correlation observed → Association only, cannot infer cause
| Observed Association | Likely Confounder |
|---|---|
| Ice cream sales and drowning | Warm weather (season) |
| Shoe size and reading ability | Age |
| Hospital visits and death rate | Illness severity |
| Organic food and health | Socioeconomic status |
| Screen time and depression | Social isolation, sleep |
SURVEY METHODOLOGY CHECKLIST:
SAMPLING:
- [ ] Probability sampling method described?
- [ ] Sampling frame defined and appropriate?
- [ ] Response rate reported (acceptable: >60% mail, >80% in-person)?
- [ ] Non-response bias assessed?
QUESTIONNAIRE:
- [ ] Questions validated or adapted from validated instruments?
- [ ] Leading or double-barreled questions absent?
- [ ] Response options balanced and exhaustive?
- [ ] Pilot tested with target population?
ADMINISTRATION:
- [ ] Mode (online, phone, in-person) appropriate?
- [ ] Anonymity/confidentiality assured?
- [ ] Informed consent obtained?
- [ ] Social desirability bias mitigated?
ANALYSIS:
- [ ] Weighting applied for non-response or oversampling?
- [ ] Margin of error and confidence level reported?
- [ ] Subgroup analyses pre-specified (not exploratory)?
| Check | What to Look For | Fail Condition |
|---|---|---|
| Y-axis starts at zero (bar charts) | Truncated axis exaggerates differences | Axis starts above zero without clear label |
| Consistent scale | Both axes have proportional increments | Non-linear scale without explanation |
| Area proportional to data | Bubble/icon size matches values | Area misrepresents magnitude |
| Time axis evenly spaced | Equal intervals between data points | Uneven spacing compresses/expands trends |
| Appropriate chart type | Data type matches visualization | Pie chart with 20+ categories |
| Context provided | Benchmarks, comparisons, baselines | Single data point with no reference |
| Source cited | Data origin traceable | No source attribution |
| Dual axes used responsibly | Two Y-axes can create false correlations | Arbitrary scaling implies relationship |
WATCH FOR THESE TRICKS:
1. TRUNCATED AXIS
Small differences look dramatic when baseline removed.
FIX: Always check if y-axis starts at zero for bar charts.
2. CHERRY-PICKED TIME WINDOW
Start/end dates chosen to show desired trend.
FIX: Ask for longer time series with consistent intervals.
3. 3D EFFECTS
Perspective distortion makes sizes unequal.
FIX: Use flat 2D charts for accurate comparison.
4. DUAL AXIS MANIPULATION
Two y-axes scaled to create apparent correlation.
FIX: Normalize data or use separate panels.
5. CUMULATIVE VS DAILY
Cumulative charts always go up — hides declining rates.
FIX: Show rate of change alongside cumulative.
BIAS DETECTION CHECKLIST:
CONFIRMATION BIAS
- Are they only presenting data that supports their hypothesis?
- Were negative results reported?
- Was the analysis plan pre-registered?
ANCHORING BIAS
- Is the first number presented influencing interpretation of later data?
- Are comparisons made to appropriate benchmarks?
SURVIVORSHIP BIAS
- Are only successful cases included (ignoring failures)?
- Is the denominator complete (not just survivors)?
AVAILABILITY BIAS
- Are dramatic or recent events overweighted?
- Is systematic data used rather than anecdotal evidence?
PUBLICATION BIAS
- Is there a funnel plot asymmetry (meta-analyses)?
- Are null results published or only significant ones?
TEXAS SHARPSHOOTER FALLACY
- Were clusters or patterns found after looking at data?
- Was the hypothesis formed before or after seeing results?
| Bias | Detection Method | Mitigation |
|---|---|---|
| Selection bias | Compare sample to population demographics | Probability sampling, weighting |
| Measurement bias | Check instrument validity and calibration | Validated instruments, blinding |
| Reporting bias | Look for asymmetric funnel plots | Pre-registration, open data |
| Recall bias | Compare to objective records | Prospective data collection |
| Observer bias | Check if assessors were blinded | Double-blind design |
| Attrition bias | Compare completers vs dropouts | Intention-to-treat analysis |
REPRODUCIBILITY REQUIREMENTS:
DATA AVAILABILITY:
- [ ] Raw data accessible (repository, supplement, on request)?
- [ ] Data dictionary / codebook provided?
- [ ] Data collection protocol documented?
CODE / ANALYSIS:
- [ ] Analysis code shared (GitHub, OSF, supplement)?
- [ ] Software versions and packages specified?
- [ ] Random seeds set for reproducible computation?
- [ ] Pipeline documented end-to-end?
METHODOLOGY:
- [ ] Study pre-registered (OSF, ClinicalTrials.gov)?
- [ ] Deviations from protocol documented?
- [ ] All outcome measures reported (not just significant ones)?
- [ ] Sensitivity analyses included?
REPORTING:
- [ ] Follows reporting guidelines (CONSORT, STROBE, PRISMA)?
- [ ] Effect sizes and confidence intervals reported?
- [ ] Power analysis or sample size justification provided?
- [ ] Limitations section thorough and honest?
| Study Type | Guideline | Key Elements |
|---|---|---|
| Randomized trial | CONSORT | Flow diagram, ITT analysis, blinding |
| Observational study | STROBE | Selection criteria, confounders, missing data |
| Systematic review | PRISMA | Search strategy, inclusion criteria, risk of bias |
| Diagnostic accuracy | STARD | Index test, reference standard, flow diagram |
| Qualitative research | COREQ | Research team, study design, data analysis |
| Prediction model | TRIPOD | Model development, validation, performance |
FAST VERIFICATION (5 minutes):
1. Read the claim carefully — what exactly is being stated?
2. Check: source, sample size, study type
3. Ask: absolute or relative? What is the base rate?
4. Check: confidence interval or margin of error given?
5. Search: has this been replicated independently?
VERDICT CATEGORIES:
VERIFIED — multiple strong sources, robust methodology
PLAUSIBLE — reasonable evidence, some limitations
UNCERTAIN — mixed evidence, methodology concerns
MISLEADING — technically true but presented deceptively
FALSE — contradicted by strong evidence
UNVERIFIABLE — cannot assess with available information
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