git:20260915.aff1795 to git:20260930.913abeb

49 added, 142 removed. Audit A to A.

---
name: grant-builder
description: >
Grant and challenge proposal support for radiology and medical AI projects. Structures significance,
innovation, approach, milestones, and consortium roles while keeping claims evidence-based and executable.
triggers: grant, proposal, aims page, grant proposal, significance, innovation, approach, milestones, 산학과제, 산학협력, 과제계획서, 연구계획서, 연구비 신청, 첨부3
tools: Read, Write, Edit, Bash, Grep, Glob
model: inherit
---
# Grant-Builder Skill
- ## Purpose
-
- This skill supports competitive proposal writing for:
-
- - national R&D grants
- - multi-institution consortia
- - challenge proposals
- - internal pilot funding
- - translational medical AI project plans
- - **Korean government grants** (산학협력 / 연구계획서 — MOHW 복지부, MOTIE 산자부, MSS 중기부, and regional industry-academia programs)
-
- It is optimized for projects where clinical relevance, multi-site coordination, and executable milestones matter as much as technical novelty.
-
- ---
+ Write proposal prose in the language the target call requires. Produce whichever parts the request
+ needs: concept summary, Significance, Innovation, Approach, specific aims, work packages, milestone
+ table, role split by institution, evaluation framework, reviewer-risk memo.
- ## Korean Government Grant Mode (산학과제 / 연구계획서)
+ ## Korean Government Grant Mode
- When the user requests a Korean industry-academia grant (산학과제) or research plan
- (연구계획서), apply the adaptations below. Korean program terms are preserved in
- parentheses because they are the literal form used on the funding agency's template.
+ When the user requests a Korean industry-academia grant (산학과제) or research plan (연구계획서) —
+ e.g., MOHW, MOTIE, MSS or regional industry-academia programs — apply the adaptations below.
+ Korean program terms are preserved in parentheses because they are the literal form used on the
+ funding agency's template.
### Document Structure (three-attachment format)
- Most Korean grants follow a standardized three-attachment format:
- - **Attachment 1 (첨부1, 기본정보)**: project title, participating institutions,
- investigator CVs, publication / patent record.
- - **Attachment 2 (첨부2, 매칭확인서)**: per-institution cost-share confirmation,
- typically finalized after a kickoff meeting between the institutions.
- - **Attachment 3 (첨부3, 연구계획서)**: the 10-page research plan — structure below.
+ | Attachment | Contents |
+ |---|---|
+ | 1 (첨부1, 기본정보) | project title, participating institutions, investigator CVs, publication / patent record |
+ | 2 (첨부2, 매칭확인서) | per-institution cost-share confirmation, typically finalized after a kickoff meeting between the institutions |
+ | 3 (첨부3, 연구계획서) | the 10-page research plan — structure below |
### Attachment 3 Standard Structure
```
1. Significance & Aims (약 2p)
- clinical problem with quantitative framing
- domestic + international trends (3–5 year literature / guideline window)
- differentiation of the proposed work
2. Research Content & Methods (약 4p)
- staged roadmap (Phase 1 – N with time ranges)
- pipeline schematic (mandatory when an AI pipeline is in scope)
- per-subproject institution and personnel assignment
3. Team Capability (약 1p)
- expertise + representative record (SCI papers, patents) per investigator
- cross-institution synergy (hospital = data / clinical; university = algorithm)
4. Expected Outcomes & Utilization (약 2p)
- quantitative targets: SCI papers, patents
- qualitative targets: clinical impact, standardization contribution
- linkage to follow-on larger grants (positioning as a seed)
5. Budget Plan (약 1p)
- RA salaries, computing equipment, consumables, academic activities, indirect costs
```
- ### Writing Tips for Small-Scale Grants (< KRW 30 million)
+ ### Small-Scale Grants (< KRW 30 million)
- - Write for a non-specialist reviewer — assume the evaluator is not in your subfield.
+ - Write for a non-specialist reviewer; assume the evaluator is not in your subfield.
- Emphasize feasibility over technical novelty.
- Prioritize length / format compliance; exceeding the template incurs scoring penalties.
- Include preliminary data or pilot results whenever available.
- - Keep quantitative targets conservative — undershooting a committed target is punished
- more than overdelivering on a modest one.
-
- ---
-
- ## Communication Rules
-
- - Communicate with the user in their preferred language.
- - Proposal prose should be in the language required by the target call.
- - Avoid hype. Emphasize unmet need, feasibility, differentiation, and deliverables.
-
- ---
-
- ## Core Outputs
-
- Depending on the request, produce one or more of:
-
- - project concept summary
- - `Significance`
- - `Innovation`
- - `Approach`
- - specific aims
- - work packages
- - milestone table
- - role split by institution
- - evaluation framework
- - reviewer-risk memo
+ - Keep quantitative targets conservative — undershooting a committed target is punished more than
+ overdelivering on a modest one.
---
## Workflow
### Phase 1: Decode the funding call
- Extract:
- - funding body
- - call theme
- - eligibility constraints
- - deliverable expectations
- - timeline
- - evaluation criteria
-
- If no call text is available, infer a generic academic-medical AI proposal structure and label assumptions.
+ Extract funding body, call theme, eligibility constraints, deliverable expectations, timeline and
+ evaluation criteria. If no call text is available, infer a generic academic-medical AI proposal
+ structure and label the assumptions.
### Phase 2: Frame the problem
- Define:
- - clinical pain point
- - current workflow limitation
- - why existing AI or standard care is insufficient
- - who benefits if the project succeeds
+ Define the clinical pain point, the current workflow limitation, why existing AI or standard care is
+ insufficient, and who benefits if the project succeeds.
- **Gate:** Present the problem framing (clinical pain point, gap, proposed solution) to the
- user. Confirm before building proposal sections — a misframed problem produces an
- unfundable proposal.
+ **Gate:** Present the problem framing (clinical pain point, gap, proposed solution) to the user.
+ Confirm before building proposal sections — a misframed problem produces an unfundable proposal.
### Phase 3: Build the proposal spine
- Always articulate:
- - problem
- - gap
- - proposed solution
- - why this team can execute it
- - measurable outputs
+ Always articulate: problem, gap, proposed solution, why this team can execute it, measurable
+ outputs.
### Phase 4: Convert to proposal sections
- #### Significance
-
- Must answer:
- - why this matters clinically
- - why this matters now
- - why the proposed solution is worth funding
-
- #### Innovation
-
- Should focus on:
- - what is genuinely different
- - why the integration is new
- - why the novelty is useful, not just technical
-
- #### Approach
+ - **Significance** must answer why this matters clinically, why now, and why the proposed solution
+ is worth funding.
+ - **Innovation**: what is genuinely different, why the integration is new, why the novelty is
+ useful and not just technical.
+ - **Approach**: dataset and participating sites, model or workflow components, validation plan,
+ benchmark/comparator, failure analysis, risk mitigation.
- Should define:
- - dataset and participating sites
- - model or workflow components
- - validation plan
- - benchmark/comparator
- - failure analysis
- - risk mitigation
+ Route to `search-lit` to support significance and prior-art positioning; cite a reference only with
+ a `/search-lit`-confirmed DOI or PMID, otherwise mark it `[UNVERIFIED - NEEDS MANUAL CHECK]`. Mark
+ any unconfirmed clinical definition, diagnostic criterion or guideline recommendation `[VERIFY]` and
+ ask the user. Route to `design-study` if the evaluation framework is weak, and to `write-paper` only
+ when the proposal requires publication-style narrative sections.
### Phase 5: Execution plan
- Generate:
- - milestones by quarter or year
- - institution-level responsibilities
- - dependencies and handoffs
- - required infrastructure
+ Generate milestones by quarter or year, institution-level responsibilities, dependencies and
+ handoffs, and required infrastructure. Do not fabricate budget details, and do not promise datasets,
+ partners or infrastructure the user has not evidenced.
---
## Default Structure
```text
## Proposal Summary
Title: ...
Goal: ...
Clinical problem: ...
### Significance
...
### Innovation
...
### Approach
Aim 1. ...
Aim 2. ...
Aim 3. ...
### Milestones
- ...
### Consortium roles
- ...
### Major risks and mitigations
- ...
```
---
- ## Evaluation Heuristics
+ ## Before Finalizing
- Before finalizing, check:
+ Check, and flag any failure to the user:
1. Is the clinical need explicit and credible?
- 2. Is the novelty more than "we will use AI"?
- 3. Are the aims linked to measurable outputs?
- 4. Is the validation plan convincing?
- 5. Is the multi-site structure realistic?
+ 2. Is the novelty more than "we will use AI", with a clinical consequence?
+ 3. Are the aims linked to measurable outputs with a concrete benchmark or success criterion?
+ 4. Is the validation plan convincing, including external validation or a deployment path?
+ 5. Is the multi-site structure realistic, with each institution in a distinct, functionally
+ integrated role?
6. Are compute, annotation, and regulatory needs acknowledged?
- 7. Does each institution have a distinct role?
-
- ---
-
- ## Common Weaknesses To Flag
-
- - novelty described without clinical consequence
- - vague benchmark or success criterion
- - no external validation or deployment path
- - too many aims for the timeline
- - consortium members listed but not functionally integrated
- - proposal sounds like a paper, not a funded program
-
- ---
-
- ## Handoff Rules
-
- - route to `search-lit` to support significance and prior-art positioning
- - route to `design-study` if the evaluation framework is weak
- - route to `write-paper` only when the proposal requires publication-style narrative sections
-
- ---
-
- ## What This Skill Does NOT Do
-
- - It does not fabricate budget details
- - It does not promise datasets, partners, or infrastructure not evidenced by the user
- - It does not replace institutional administrative review
-
- ## Anti-Hallucination
-
- - **Never fabricate references.** All citations must be verified via `/search-lit` with confirmed DOI or PMID. Mark unverified references as `[UNVERIFIED - NEEDS MANUAL CHECK]`.
- - **Never invent clinical definitions, diagnostic criteria, or guideline recommendations.** If uncertain, flag with `[VERIFY]` and ask the user.
+ 7. Are there too many aims for the timeline?
+ 8. Does it read as a funded program rather than a paper?