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tooluniverse-antibody-engineering

Therapeutic antibody engineering and optimization, lead-to-clinical-candidate. Covers sequence humanization (germline alignment, framework retention), affinity maturation, developability (aggregation, stability, PTMs), structure modeling (AlphaFold/PDB CDR analysis), immunogenicity prediction, and manufacturing feasibility. Use for biologic-drug optimization, mAb design review, biosimilar engineering, and clinical-precedent comparison.

64

Quality

75%

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SecuritybySnyk

Low

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tessl review fix ./plugin/skills/tooluniverse-antibody-engineering/SKILL.md
SKILL.md
Quality
Evals
Security

Quality

Content

57%Weight 40%Scale 1-5

Reviews the quality of instructions and guidance provided to agents. Good implementation is clear, handles edge cases, and produces reliable results.

A well-organized, knowledgeable workflow whose on-paper structure is undermined by missing bundle files that the body repeatedly relies on for code examples. Code/executable guidance is largely deferred to references that are absent, and validation feedback loops for the analysis pipeline are thin.

Suggestions

Add the missing referenced files (WORKFLOW_DETAILS.md, REPORT_TEMPLATE.md, MANUFACTURING.md, EXAMPLES.md, CHECKLISTS.md, QUICK_START.md) to the bundle, or inline the essential code examples each phase promises so the skill is self-contained.

Add explicit validation/feedback checkpoints for the analysis steps (e.g., verify IMGT/AlphaFold results returned valid hits before proceeding, re-check CDR preservation after backmutations) to satisfy the batch/analysis feedback-loop expectation.

De-duplicate tool references (Phase 0 table, per-phase mentions, and the closing Tool Reference section overlap) to tighten the token footprint.

DimensionReasoningScore

Conciseness

The body is dense and task-oriented with little explanation of basics Claude already knows, but it carries repetition (tool names restated across Phase 0, per-phase 'See WORKFLOW_DETAILS.md', and the Tool Reference section) that could be trimmed.

4 / 5

Actionability

Phases give concrete specifics (positions, ddG < -0.5 cutoffs, `scripts/developability.py --seq`), but executable code examples are deferred to files (WORKFLOW_DETAILS.md) that are not present in the bundle, leaving mostly descriptive rather than copy-paste-ready guidance; the one real script does match its described use.

3 / 5

Workflow Clarity

The 8-phase sequence is clearly laid out with an ASCII flowchart and per-phase outputs, and it warns against fabricating data, but there are no explicit validate->fix->retry feedback loops for the analysis steps despite batch/analysis operations.

3 / 5

Progressive Disclosure

Structure is well-designed on paper — overview body with a Reference Files table pointing one level deep — but 6 of the 7 referenced bundle files (QUICK_START.md, WORKFLOW_DETAILS.md, REPORT_TEMPLATE.md, MANUFACTURING.md, EXAMPLES.md, CHECKLISTS.md) are missing; only scripts/developability.py exists, so the signaled navigation is broken in practice.

3 / 5

Total

13

/

20

Passed

Description

92%Weight 40%Scale 1-5

Based on the skill's description, can an agent find and select it at the right time? Clear, specific descriptions lead to better discovery.

A strong, specific description that clearly states both capabilities and explicit use-triggers within a well-defined antibody-engineering niche. Slight room to broaden plain-language trigger synonyms, but it avoids vagueness and over-claims.

DimensionReasoningScore

Specificity

Lists multiple concrete capability areas — 'sequence humanization (germline alignment, framework retention), affinity maturation, developability (aggregation, stability, PTMs), structure modeling (AlphaFold/PDB CDR analysis), immunogenicity prediction, and manufacturing feasibility' — giving comprehensive, specific coverage rather than generic language.

5 / 5

Completeness

It explicitly answers 'what' (the capability list and 'lead-to-clinical-candidate' scope) and 'when' via a concrete 'Use for ...' trigger clause, matching the top anchor's pattern.

5 / 5

Trigger Term Quality

The 'Use for' clause surfaces natural terms like 'biologic-drug optimization, mAb design review, biosimilar engineering, and clinical-precedent comparison', but a few plain user phrasings (e.g. 'humanize antibody', 'antibody affinity') are absent, so it stops just short of comprehensive synonym coverage.

4 / 5

Distinctiveness Conflict Risk

The therapeutic-antibody niche with mAb/biospecific triggers is clearly distinct and unlikely to fire for unrelated skills, with minimal overlap risk.

5 / 5

Total

19

/

20

Passed

Validation

100%

Checks the skill against the spec for correct structure and formatting. All validation checks must pass before discovery and implementation can be scored.

Validation16 / 16 Passed

Validation for skill structure

No warnings or errors.

Repository
mims-harvard/ToolUniverse
Reviewed

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