Stop missing grants that match your science
Stella reads your PubMed publication history, builds a semantic research profile with Claude, and delivers ranked NIH, NHGRI, and NSF grant matches every week — with Specific Aims skeletons on demand.
Free to start · ORCID or Google sign-in · No institutional account needed
From sign-up to matched grants in 2 minutes
Sign in with ORCID or Google
Enter your name and institution. Takes 30 seconds. No institutional account required — your personal ORCID is enough.
We build your research profile
Stella fetches your PubMed publication history, extracts research themes with Claude, and identifies your recent focus — the work you've done in the last 2 years weights more.
See your first matches in 2 minutes
Stella runs matching immediately when you complete your profile — no waiting for a nightly job. Matches refresh weekly as new opportunities are posted, and you get a digest email every Sunday.
Built for the way PIs actually find funding
Grant discovery today is mostly luck — you catch a listserv email, a colleague mentions an RFA, or you stumble across a PAR while doing something else. Stella makes it systematic.
Semantic matching, not keyword search
Claude reads your PubMed abstracts, builds a research profile with emphasis on your last 2 years, and scores every opportunity against your actual science — not just grant titles.
Specific Aims skeleton on demand
Click any matched grant to generate a Specific Aims skeleton — three aims, a significance statement, and an innovation paragraph — drafted from your own research profile.
Deadline reminders — 7 days out
Stella emails you when a matched opportunity is 7 days from its deadline, so you never discover a perfect R01 the morning it closes.
Weekly digest in your inbox
Every Sunday at 8pm you get a ranked digest of new and updated matches — tier A (strong fit), B (moderate), and C (stretch) — formatted for a quick scan over coffee.
From match to draft Aims in one click
Click any matched grant to generate a Specific Aims skeleton. Claude drafts three aims, a significance statement, and an innovation paragraph — grounded in your actual publications, not a generic template.
- Grounded in your PubMed publication history
- 3 aims + Significance + Innovation sections
- One-click review and AI critique of your draft
- Formatted as plain text you can paste directly into Word
Specific Aims The progesterone receptor (PGR) plays a central role in gestational length, yet the genetic architecture of PGR-mediated effects in admixed populations remains poorly characterized. We identified a genome-wide significant association at PGR V660L (p = 2.1×10⁻⁹) in a EUR–AFR admixed cohort, with strong colocalization with uterine eQTLs (PP.H4 = 0.903). This proposal seeks to characterize the ancestry-stratified functional impact of V660L on gestational age. Aim 1. Define the population-specific effect of PGR V660L ... Aim 2. Determine the tissue-specific regulatory mechanism ... Aim 3. Assess clinical predictors of carrier status ...
Every major federal source, re-checked weekly
Grant mechanisms covered
Start free, upgrade before your next submission cycle
- Research profile from PubMed
- Weekly grant matches
- Dismiss + flag opportunities
- Dashboard access
- Everything in Researcher
- Specific Aims skeleton on demand
- AI review of your Aims draft
- Weekly digest email
- Deadline reminders (7 days out)
- Priority grant matching
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Your next R01 might already be open
Build your research profile in 2 minutes. Stella runs matching tonight.