Patent Review

Record the total claim count (independent + dependent separately).

Phase 2 — Triage

Give the scientist a quick orientation before diving in:

1. Invention summary — 2–3 sentences: what is this patent about?
2. Inferred domain — e.g., "small-molecule therapeutics", "gene editing", "semiconductor fabrication"
3. Structural checklist — which standard sections are present, which are missing
4. Initial flags — anything immediately anomalous: claims that contradict the description, undefined terms, missing definitions, obvious internal inconsistencies

Ask the scientist to confirm or correct before proceeding. A wrong domain inference can skew the entire review.

Phase 3 — Deep Review (Interactive)

Work through the document section by section. For each issue:

1. Surface the issue, explain why it's a concern
2. Label it [ACCURACY], [GAP], or [LANGUAGE]; assign severity:
   • Critical: affects claim validity, patentability, or scientific accuracy — attorney must address
   • Minor: stylistic, terminology, or clarity improvement — recommended but not essential
3. Wait for the scientist to choose:

   (a) accept — use the suggested fix as-is (b) modify — scientist provides the corrected version (c) dismiss — skip this issue (log as dismissed with reason if given)

Log every decision, including dismissals. Be explicit: "This is a critical issue because…" / "This is a minor issue — worth fixing but not legally significant."

3.1 Background & Summary

• Is the problem statement technically accurate?
• Does the summary fairly and completely represent what the invention actually does?

3.2 Detailed Description & Embodiments

• Are the described mechanisms scientifically sound?
• Are any embodiments vague, ambiguous, or technically incorrect?
• Are there known embodiments or variations that exist but aren't described?

3.3 Claims — three sequential passes

Run in order. Don't conflate them — each has a distinct goal.

Accuracy pass: Go through each claim. Flag technical errors: wrong terminology, impossible limitations, overly broad scientific assertions unsupported by the description.

Gap pass: Ask: what aspects of this invention are NOT claimed? Think about alternative embodiments, different methods of making or using it, different materials, compositions, use cases. Prompt the scientist with questions if the space of variations is unclear.

Language pass: For each claim flagged in the accuracy or gap passes, propose specific revised claim language or draft new claims. Be concrete — provide actual claim text, not just "fix the wording."

3.4 Abstract (reviewed last)

Once the claims are settled, verify the abstract accurately reflects the agreed-upon scope. A patent's abstract should match its claims, not the other way around.

Checkpoints

At the end of each sub-section (3.1, 3.2, 3.3 accuracy, 3.3 gap, 3.3 language, 3.4), output a checkpoint block:

--- CHECKPOINT START ---
[All logged findings so far, with labels, severities, and accepted/modified/dismissed status]
--- CHECKPOINT END ---

Then prompt: "Checkpoint above — copy this block if you want a record. Type continue to proceed."

If the user doesn't respond (session ends), the session is simply over. There is no auto-save. The final report is only written in Phase 4.

Phase 4 — Synthesis

Before compiling, present this prompt:

"Ready to generate the report. Where should I save it? [default: ./] — or type literature to run a literature search first."

After the user answers, Phase 5 is no longer available. If they type literature, run Phase 5 first, then compile.

Compile the report using the structure in references/report-template.md.

Filename: YYYY-MM-DD-<slug>-review.md

• Slug: lowercase patent title, spaces/specials → hyphens, collapse consecutive hyphens, truncate to 60 characters
• Example: "Compositions and Methods for Treatment of Inflammatory Disease" → 2026-04-14-compositions-and-methods-for-treatment-of-inflammato-review.md

Save path behavior: Use the user's specified path, or default ./. If the path is unwritable, ask once for an alternative. If that also fails, print the full report as a fenced Markdown block so the user can copy it.

Phase 5 — Literature Review (Optional, On-Demand)

When to trigger: During Phase 3 (user can say "check the literature on X" at any point), or at the Phase 4 entry prompt (user types literature). Once the Phase 4 prompt is answered with anything else, Phase 5 is no longer available.

On trigger, ask two quick questions:

1. Scope — scientific literature, prior art patents, or both?
2. Any constraints — date range, jurisdiction, specific databases?

Run the search, summarize relevant hits, and for each result note whether it materially affects a specific claim under review. Append findings to the Literature section of the report.

Scope Boundaries

This skill does NOT:

• Give legal advice or opinions on patentability
• Perform a formal freedom-to-operate analysis
• File anything or format for USPTO/EPO submission
• Make the final call on claim language — the scientist decides, you propose

Additional Resources

• references/report-template.md — exact Markdown template for the Phase 4 report, including the claims analysis table format and section structure
• evals/evals.json — benchmark test cases (DMD gene therapy, KRAS inhibitor, SCD base editing) for evaluating skill behavior across domains