# MCPmed: a call for Model Context Protocol-enabled bioinformatics web services for LLM-driven discovery

**Authors:** Matthias Flotho, Ian Ferenc Diks, Philipp Flotho, Leidy-Alejandra G Molano, Pascal Hirsch, Andreas Keller

PMC · DOI: 10.1093/bib/bbag076 · Briefings in Bioinformatics · 2026-02-23

## TL;DR

This paper introduces MCPmed, a framework to improve machine readability of bioinformatics web services for use with large language models.

## Contribution

The novel contribution is adapting the Model Context Protocol (MCP) to bioinformatics web services for machine-actionable scientific exploration.

## Key findings

- MCP-enabled web services improve automation and interoperability for LLM-driven discovery.
- Implementations on GEO, STRING, and UCSC Cell Browser demonstrate enhanced exploration capabilities.
- MCPmed provides templates and breadcrumbs to ease adoption of MCP in bioinformatics services.

## Abstract

Bioinformatics web servers are critical resources in modern biomedical research, facilitating interactive exploration of datasets through custom-built interfaces with rich visualization capabilities. However, this mostly human-centric design limits machine readability for large language models (LLMs) and deep research agents. We address this gap by adapting model context protocol (MCP) to bioinformatics web server backends, a standardized, machine-actionable layer that explicitly associates web service endpoints with scientific concepts and detailed metadata. Our implementations across widely used databases (GEO, STRING, and UCSC Cell Browser) demonstrate enhanced exploration capabilities through MCP-enabled LLMs. To accelerate adoption, we propose MCPmed, a community effort supplemented by lightweight breadcrumbs for services not yet fully MCP-enabled and templates for setting up new servers. This structured transition aims to significantly enhance automation, reproducibility, and interoperability, preparing bioinformatics web services for next-generation research agents.

Graphical Abstract

## Full-text entities

- **Genes:** CSF1R (colony stimulating factor 1 receptor) [NCBI Gene 1436] {aka BANDDOS, C-FMS, CD115, CSF-1R, CSFR, FIM2}, DLG4 (discs large MAGUK scaffold protein 4) [NCBI Gene 1742] {aka MRD62, PSD95, SAP-90, SAP90}, Ncoa1 (nuclear receptor coactivator 1) [NCBI Gene 17977] {aka KAT13A, NCoA-1, NRC-1, SRC-1, SRC-a, SRC1}, GFAP (glial fibrillary acidic protein) [NCBI Gene 2670] {aka ALXDRD}, S100a6 (S100 calcium binding protein A6 (calcyclin)) [NCBI Gene 20200] {aka 2A9, 5B10, CALCYCLIN, Cacy, PRA}, SYP (synaptophysin) [NCBI Gene 6855] {aka MRX96, MRXSYP, XLID96}, CREB1 (cAMP responsive element binding protein 1) [NCBI Gene 1385] {aka CREB, CREB-1}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, S100a11 (S100 calcium binding protein A11) [NCBI Gene 20195] {aka EMAPI, Emap1, S100a14, S100c, cal}, AIF1 (allograft inflammatory factor 1) [NCBI Gene 199] {aka AIF-1, IBA1, IRT-1, IRT1}, NR3C1 (nuclear receptor subfamily 3 group C member 1) [NCBI Gene 2908] {aka GCCR, GCR, GCRST, GR, GRL}, ARC (activity regulated cytoskeleton associated protein) [NCBI Gene 23237] {aka Arg3.1, hArc}, FOS (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 2353] {aka AP-1, C-FOS, p55}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, EGR1 (early growth response 1) [NCBI Gene 1958] {aka AT225, G0S30, KROX-24, NGFI-A, TIS8, ZIF-268}, CAPG (capping actin protein, gelsolin like) [NCBI Gene 822] {aka AFCP, HEL-S-66, MCP}
- **Diseases:** calcium dysregulation (MESH:D002128), breast cancer (MESH:D001943), cognitive decline (MESH:D003072), LLMs (MESH:D007806), inflammatory (MESH:D007249), neuroinflammation (MESH:D000090862)
- **Chemicals:** Calcium (MESH:D002118), LLM (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12927880/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12927880/full.md

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Source: https://tomesphere.com/paper/PMC12927880