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TransBench

TransBench turns a clinician's bedside observation, written in plain words, into a grounded, testable, bench-ready computational experiment.

Core trick

Eight-agent pipeline grades each hypothesis against retrieved PubMed and Europe PMC abstracts, dropping any claim whose citation fails an entailment check.

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Description

TransBench turns a clinician's bedside observation, written in plain words, into a grounded, testable, bench-ready computational experiment. It ships as an MCP connector for Claude Science. You paste a de-identified observation - for example, "49M, type 2 diabetes with persistent postprandial hyperglycemia despite maximal metformin and confirmed adherence; elevated fasting glucagon; blunted GLP-1 response to mixed-meal testing." An eight-agent pipeline decomposes it into biological mechanisms, writes up to three falsifiable hypotheses, retrieves real published abstracts for each (PubMed, ClinicalTrials.gov, and Europe PMC), and grades every hypothesis as supported or refuted against those sources. Three rigor gates then reject anything that does not hold up: entailment (does the cited source actually support the claim?), grounding (drop any claim with no resolvable citation), and novelty (demote textbook facts so they are never sold as discoveries). For any hypothesis that is both a genuine open question and grounded in evidence, it designs one runnable single-cell experiment on a public dataset whose accession it content-verifies against the real record, and it emits a paste-ready prompt that Claude Science executes into a figure. What matters most: when the evidence is not there, TransBench ships nothing instead of inventing a plausible answer. The refusal is the feature. What I found across real, de-identified runs: over five domains (lupus, type 2 diabetes, resistant hypertension, melanoma, and rheumatoid arthritis) it shipped experiments for three and correctly declined for two because no hypothesis cleared the evidence bar; it caught two proposed datasets that did not match their claimed content and replaced them; and it fabricated zero citations. For the Gladstone example, a lupus / low-regulatory-T-cell observation produced a PTPN2-in-Tregs experiment grounded in 41 real citations, pointed at Gladstone's own dataset GSE278572 (Marson lab Treg/Teff Perturb-CITE-seq), which Claude Science then executed into a real composite figure with an FDR-corrected statistics table. That full run, with a sha256 manifest of every file, is committed in the repo under golden-test-results/. Why it matters: it is the difference between a confident chatbot answer and a defensible research lead. Every claim is tied to a real, resolvable paper or it is dropped; every dataset is verified before it is proposed; and the whole pipeline replays byte-identical with no API key (golden mode), so anyone can confirm that nothing shown is mocked up. TransBench is a research hypothesis-generation tool only - not clinical, diagnostic, or prescribing advice.
kayomarz97/TransBench★ 00 forksPythonCreated Jul 9, 2026 · last push Aug 7, 2026

README excerpt

# TransBench

> 🏆 **Built for [Built with Claude: Life Sciences](https://cerebralvalley.ai/e/built-with-claude-life-sciences)** — Anthropic × Gladstone Institutes × Cerebral Valley · **Development Track**
> 👨‍⚕️ **Built by Dr. Kayomarz** — internal-medicine physician & AI engineer · [kayomarz.com](https://kayomarz.com)

**A translational research agent that turns a clinician's bedside observation into a
grounded, testable, bench-ready experiment — shipped as an MCP connector for Claude Science.**

**Why it beats a general chatbot:** it grades every hypothesis against *real* published papers
(PubMed + Europe PMC, resolvable PMIDs), demotes textbook facts so they're never sold as discoveries,
**content-verifies the public dataset it proposes**, and — when the evidence isn't there —
**ships nothing instead of hallucinating a plausible answer. The refusal is the feature.**

You describe something you saw in a patient, in plain words. TransBench breaks it into the
biological mechanisms that could explain it, generates falsifiable hypotheses, **checks each one
against the real published literature**, throws out the textbook facts and the unsupported guesses,
and — for whatever survives — hands you *one runnable computational experiment* with a concrete
public dataset and a paste-ready prompt for Claude Science.

It works for **any** disease, drug, or mechanism — not one fixed specialty. The examples below span
lupus (on the Gladstone dataset), type 2 diabetes, resistant hypertensio

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