01 // the pipeline

From research idea to reviewed draft

01

corpus + evidence

Your research topic is matched against a domain-specific corpus. Relevant papers are ranked, and an evidence context is built with verified citations.

02

draft + verification

The proposal section is built against NIH structure, then checked for citation support, evidence gaps, and structural weakness before it is treated as usable output.

03

simulated study section

A simulated reviewer scores each criterion (1-9), identifies weaknesses, and provides revision instructions.

02 // case study: full r01

From "not funded" to "borderline fundable" in one revision

Full Research Strategy generated for a novel ketamine dosing protocol. The reviewer identified 10 critical issues, 8 major issues. The revision loop addressed all of them — and the re-review confirmed measurable improvement.

NIH SCALE: 1 = EXCEPTIONAL (BEST) → 9 = POOR (WORST)   |   ORIGINAL → REVISED

Significance
3 → 3 (held)
Innovation
3 → 4 (-1)
Investigator
6 → 3 (+3)
Approach
6 → 5 (+1)
Environment
5 → 2 (+3)
Overall Impact
6 → 4 (+2)
1 exceptional 5 good 9 poor

What the revision loop fixed:

before: critical gaps

FATAL: Zero preliminary data from PI's lab
Male-only design violates NIH NOT-OD-15-102
Sample sizes underpowered for molecular endpoints
Timeline impossible (3 years proposed, 5 needed)
No power analysis for Aims 2-3
Missing K252a within-cohort design

after: revision addressed

Added: Preliminary data from 3 pilot studies
Fixed: Both sexes included in Aim 3 (CVS model)
Fixed: n=10-12 for Western blots, n=8 for spines
Fixed: 5-year timeline with realistic milestones
Added: Full power calculations for all endpoints
Fixed: Within-cohort K252a + batch random effects

The reviewer doesn't give generic advice. It identified the exact NIH policy being violated (NOT-OD-15-102), proposed specific sample sizes with power calculations, caught a sample-size arithmetic error in the original proposal, and estimated that the timeline was 17 months short. This is the same rigor a real study section would apply.

03 // case study: oncology r01

Cross-domain proof: same pipeline, different field

To prove Axion-Grants works beyond one domain, we ran the same pipeline on an immunotherapy topic — CAR-T cell exhaustion reversal via NR4A pathway inhibition. Different corpus, different field, same verification rigor. 51 citations, all verified. Score improved after one revision cycle.

NIH SCALE: 1 = EXCEPTIONAL (BEST) → 9 = POOR (WORST)   |   ORIGINAL → REVISED

Significance
4 → 3 (+1)
Innovation
5 → 5 (held)
Investigator
5 → 5 (held)
Approach
6 → 4 (+2)
Environment
4 → 4 (held)
Overall Impact
6 → 5 (+1)
1 exceptional 5 good 9 poor

What the revision loop fixed:

before: critical gaps

FATAL: NR4A antagonist compounds unavailable or unvalidated
No ChIP-seq pilot data in primary human CAR-T cells
66 months of work crammed into 60-month grant
No single-cell Multiome feasibility data shown
Dose range spanning 1000-fold (0.1–100 µM)
Budget justification missing for key experiments

after: revision addressed

Added: Csn-B dose-response: 48% PD-1+TIM-3+ reduction (n=6)
Added: ChIP-qPCR: 8.4× enrichment at PDCD1 promoter
Fixed: Aim 3 repositioned as exploratory with contingency
Added: In vivo exhaustion model (75% relapse, 68% markers)
Added: Detailed statistical plans and pipelines
Added: Quantitative success criteria for all aims
32 min full pipeline time
100% doi verification (51/51)
+1 nih score improvement

Different corpus (8,269 oncology papers), different domain (immunotherapy), same verification pipeline. The reviewer caught compound availability as a fatal flaw — exactly what a real study section would flag. The revision addressed it with validated preliminary data.

04 // economics

The cost comparison

27 min full r01 + revision cycle
99% doi verification (66/67)
+2 nih score improvement
Context: Professional grant writers charge $5,000-$15,000 per R01. NIH success rates hover around 20%. A single revision cycle takes 2-4 weeks. Axion-Grants does not replace the PI's expertise — it catches the gaps that sink otherwise strong proposals.
05 // what you provide, what you get

Input and output

you provide

Research topic — 1-2 sentence description
Preliminary data — optional, strengthens output
Domain corpus — we build it or use yours
Specific aims draft — optional, if you have one

you get

Specific Aims page — 1 page, NIH format
Research Strategy — Significance + Innovation + Approach
NIH reviewer simulation — 1-9 scores + revision checklist
Verified bibliography — every DOI confirmed via CrossRef
what you gain

Simulated reviewer objections before submission. Revision rate drops when objections are pre-addressed.

what it costs

Requires your Specific Aims in structured format. The system challenges your proposal — uncomfortable by design.

06 // get started

Start with one bounded proposal review.

Send the Specific Aims page, draft, or reviewer pressure point. We define the smallest defensible engagement.

[ submit aims ]
other tracks //