史丹佛團隊發表 Paper2Agent：將研究論文轉為 AI 代理，重現結果並處理新資料

Computational papers ship code that readers must clone, install, configure and debug.That cost keeps useful methods locked inside PDFs.A Stanford team led by Jiacheng Miao and James Zou proposes a fix.Paper2Agent was published in Nature on 16 September 2026.

It converts a paper and its codebase into a Model Context Protocol (MCP) server.Any MCP-compatible agent, such as Claude Code, can then run the paper’s methods through natural language.The authors describe the result as a virtual corresponding author.Is it deployable?Yes.

The code is MIT-licensed and installs as a skill for Claude Code or Codex.Prebuilt AlphaGenome, Scanpy and TISSUE servers run on Hugging Face Spaces.A hosted version is also available at paper2agent.ai.How the Pipeline Works Paper2Agent runs on Claude Code’s agent SDK.

A central orchestrator dispatches specialized sub-agents through 6 steps: Locate and download the codebase.An environment manager builds an isolated virtual environment.A tutorial scanner indexes usable tutorials.A tutorial executor runs them end to end and records reference outputs.

A tool extractor turns tutorials into parameterized MCP tools, and a test verifier validates them.The orchestrator assembles validated tools into 1 MCP server.The validation gate is strict.A tool passes only when expected files appear and numbers match within 3%.

Figures must also match references by perceptual hash, with Hamming distance under 20.The verifier gets up to 6 attempts per function.Tools that keep failing are excluded from the final server.Each server exposes 3 components.

MCP tools wrap the paper’s methods as executable functions: MCP resources hold the manuscript, code links, datasets and figures.MCP prompts encode multi-step workflows, such as the correct Scanpy preprocessing order.The research team used Claude Sonnet 4 for all Paper2Agent applications.

Interactive Explainer #mtp-p2a-embed{max-width:980px!important;margin:24px auto!important;padding:0!important;background:transparent!important;border:0!important} #mtp-p2a-embed iframe{width:100%!important;border:0!important;display:block!important;background:transparent!important;min-height:0!

important} #mtp-p2a-embed p:empty,#mtp-p2a-embed br,#mtp-p2a-embed hr,#mtp-p2a-embed del,#mtp-p2a-embed s{display:none!important} (function(){window.addEventListener("message",function(e){var f=document.getElementById("mtp-p2a-frame");if(!f||!e.data||!e.data.mtpP2A||e.source!==f.

contentWindow)return;var h=parseInt(e.data.h,10);if(h>200&&h<6000){f.style.setProperty("height",h+"px","important");}});})(); AlphaGenome Agent Results For AlphaGenome, Paper2Agent built 22 tools in about 45 minutes for US $14.All 22 passed validation without human intervention.

The team compared the agent with Claude Code plus repository access (Claude + Repo) and Biomni.BenchmarkPaper2AgentClaude + RepoBiomni15 tutorial-derived queries98.7 ± 1.3%82.7 ± 3.4%37.3 ± 4.0%15 novel queries100.0 ± 0.0%78.7 ± 4.4%56.0 ± 3.4%30 open-ended queries82.7 ± 2.4%56.7 ± 2.3%72.2 ± 2.

2% Results span 5 runs, graded by 2 human experts with 96.7% inter-rater agreement.On tutorial queries, median runtime fell 1.9× versus Claude + Repo and 3.1× versus Biomni.The gains persisted when the baseline was upgraded to Claude Opus 4.6.

The agent also re-examined an LDL cholesterol variant, chr1:109274968:G>T.It ranked SORT1 as the likely causal gene.The original AlphaGenome paper emphasized CELSR2 and PSRC1.GTEx shows significant liver eQTLs for all 3 genes.

The research team say this shows how hard causal gene assignment is at such loci.Scanpy, TISSUE and Scale Tests The Scanpy agent received 7 validated tools in about 45 minutes for US $13.On 4 public datasets, it matched human researchers on cell counts, gene counts and top marker genes.

A TISSUE agent reproduced human results on spatial transcriptomics data.Scale tests covered 3 corpora with no manual cleanup: 100 bioRxiv computational biology papers: 74 were agentified, and 593 of 599 proposed tools passed validation.300 questions: Paper2Agent scored 91.2%, versus 80.

3% (Sonnet 4) and 86.3% (Sonnet 4.6) for Claude + Repo.Cost per query: US $0.20 and 1.6 minutes, compared with US $0.38 and 4.3 minutes.10 non-biology papers, including TabPFN, SAM 2 and SAELens: 98.1% accuracy on 42 execution tasks.26 data-focused papers: resource layer 89.0% versus 82.

0% for browser use, 34× cheaper and 15× faster.Paper2Agent also rejected 100% of out-of-scope queries in a permuted benchmark.It recovered from injected dependency, file-path, typo and deprecated API failures.

Paper Agents Collaborating The research team connected 3 agents: AlphaGenome, an MPRA-coupled scCRISPRi screen and a CD4+ T cell Perturb-seq dataset.AlphaGenome flagged GPR137 at psoriasis locus rs887314, with an RNA-seq quantile score of 0.997.

The AI co-scientist proposed 10 validation strategies, and a researcher picked signature correlation.Only GPR137 knockdown matched the CRE perturbation signature.The match appeared under stimulation: Spearman 0.613 at Stim8hr and 0.630 at Stim48hr.

BAD and 3 other candidates showed no significant correlation.A second study paired AlphaGenome with an ADHD GWAS and nominated rs1626703 among 209 candidates.That hypothesis still needs experimental validation.

Key Takeaways Paper2Agent converts papers and repos into tested MCP servers with tools, resources and prompts.The AlphaGenome agent took about 45 minutes, cost US $14, and scored 100% on novel queries.74 of 100 bioRxiv papers were agentified, with 593 of 599 tools validated.

3 paper agents jointly supported GPR137 as the probable psoriasis causal gene.The code is MIT-licensed, with prebuilt MCP servers on Hugging Face Spaces.Check out the Paper and Repo.All credit goes to the researcher of this project.

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