bio-logic — independently scanned and version-tracked by SaferSkills.
SaferSkills independently audited bio-logic (Agent Skill) and scored it 100/100 (green). The audit ran 55 deterministic rules across Security, Supply Chain, Maintenance, Transparency, and Community; it found 0 high-severity and 0 lower-severity findings. The full rule-by-rule trace and per-finding evidence are below. Free, methodology-open.
Findings & checks · 0 flagged
Every scanned point with the score it earned and what moved between them.
First recorded scan — no prior version to compare against.
The primary manifest — the file an agent reads to learn what this artifact does.
Use structured frameworks to evaluate scientific claims, methodology, and evidence strength.
/polars-dovmed, then revise hypotheses against the literature.computational benchmark, phylogenetic analysis, or evolutionary inference as if it were an intervention trial.
| Profile | Main evidence checks | Rating language |
|---|---|---|
| Intervention | allocation, controls, adherence, attrition, estimand, harms | GRADE when the review question and evidence synthesis support it |
| Observational or quasi-experimental | identification assumptions, temporality, confounding, negative controls, sensitivity analyses | risk-of-bias plus causal-confidence statement |
| Computational or machine learning | data provenance, leakage, splits, baselines, calibration, external validation, reproducibility | computational evidence confidence |
| Evolutionary or comparative genomics | orthology, taxon/reference sampling, model fit, support, contamination, topology sensitivity | phylogenetic/comparative evidence confidence |
| Descriptive or exploratory omics | sampling, measurement, multiple testing, effect sizes, replication, alternative explanations | descriptive confidence; avoid causal labels |
Use this loop for omics projects, unexpected results, exploratory analyses, and any request that asks what results mean.
Use relevant sections based on the review scope. Skip items not applicable to the study type.
## Methodology
- [ ] Design identifies the causal estimand through randomization or a justified quasi-experimental or natural-experiment strategy
- [ ] Sample size justified (power analysis reported)
- [ ] Randomization/blinding implemented where feasible
- [ ] Confounders identified and controlled
- [ ] Measurements validated and reliable
## Statistics
- [ ] Tests appropriate for data type
- [ ] Assumptions checked
- [ ] Multiple comparisons corrected
- [ ] Effect sizes + CIs reported (not just p-values)
- [ ] Missing data handled appropriately
## Interpretation
- [ ] Conclusions match evidence strength
- [ ] Limitations acknowledged
- [ ] Causal claims require an identified causal design: randomized evidence or
a justified quasi-experimental/natural-experiment strategy with its
assumptions and sensitivity checks
- [ ] No cherry-picking or overgeneralization
## Red Flags
- [ ] P-values clustered just below .05
- [ ] Outcomes differ from registration
- [ ] Correlation presented as causation
- [ ] Subgroups analyzed without preregistrationClaim strength ladder:
| Language | Requires |
|---|---|
| "Demonstrates" | Strong evidence under a design that identifies the target claim |
| "Suggests" / "Indicates" | Observational with controlled confounds |
| "Associated with" | Observational, no causal claim |
| "May" / "Might" | Preliminary or hypothesis-generating |
## Summary
[1-2 sentences: What was studied and main finding]
## Strengths
- [Specific methodological strengths]
## Concerns
### Critical (threaten main conclusions)
- [Issue + why it matters]
### Important (affect interpretation)
- [Issue + why it matters]
### Minor (worth noting)
- [Issue]
## Evidence Rating
[Framework appropriate to the study profile, rating, and justification. Use
GRADE only when it applies to the review question.]
## Bottom Line
[What can/cannot be concluded from this evidence]## Current Result
[Observed intermediate/final result and QC status]
## Hypothesis Register
| Rank | Hypothesis | Status | Evidence For | Evidence Against | Next Discriminating Check |
|------|------------|--------|--------------|------------------|---------------------------|
| 1 | [Hypothesis] | supported/weakened/ruled out/unresolved | [Evidence] | [Evidence] | [Test] |
| 2 | [Hypothesis] | ... | ... | ... | ... |
| 3 | [Hypothesis] | ... | ... | ... | ... |
| 4 | [Hypothesis] | ... | ... | ... | ... |
| 5 | [Hypothesis] | ... | ... | ... | ... |
## Literature Context
- [Paper or search result, DOI/PMCID if available]: supports/contradicts/narrows [hypothesis] because [reason].
## Analysis Playbook
- [Literature-derived analysis/comparison/outlier check and why it applies]
## Revision
[What changed since the previous register and why]
## Next Step
[Most informative analysis, control, or experiment]| Task | Action |
|---|---|
| Review a paper | Use the Critique Checklist above |
| Evaluate a claim | Use the Claim Assessment steps above |
| Assess evidence strength | See references/evidence.md |
| Identify biases | See references/biases.md |
| Statistical errors | See references/stats.md |
| Logical fallacies | See references/fallacies.md |
| Study design review | See references/design.md |
evolutionary work is not forced into intervention-centric GRADE rules
Input: "Review this RCT on vitamin D and depression"
Output:
## Summary
RCT of 200 adults testing vitamin D supplementation for depression over 12 weeks.
## Strengths
- Randomized, double-blind, placebo-controlled
- Validated depression scale (PHQ-9)
- Adequate power analysis
## Concerns
### Critical
- 35% dropout, differential by group (attrition bias)
- ITT analysis not performed
### Important
- Single-site limits generalizability
## Evidence Rating
Moderate (downgraded from high due to attrition bias)
## Bottom Line
Suggestive but not conclusive due to differential attrition.Input: "This study proves that coffee prevents Alzheimer's"
Assessment: If based only on an association with no identified causal design, this is a correlation→causation error. Appropriate language: "Coffee consumption is associated with lower Alzheimer's risk." Observational data with a justified quasi-experimental or natural-experiment strategy, its assumptions stated and tested, can support a causal claim; the design is what decides, not whether the data were observational.
Issue: Insufficient methods details Solution: Request missing design/statistics information before rating evidence.
Issue: Conflicting results across studies Solution: Report uncertainty and suggest stronger study designs for resolution.
/ai-scientist-evaluator: rubric-scored evaluation of AI scientist outputs/manuscript-review-council: multi-reviewer critique of peer-reviewed manuscripts/proposal-review: structured critique of funding proposals~30 seconds. Free. No account. Every finding cites a rule and a line of evidence.