i only recently came across pantheon-os, which is an awesome multi-agent framework for doing genomics research from
@Xiaojie_Qiu and his team of collaborators.
what struck me most is that unlike most other multi agent frameworks or ai scientists that i have come across, pantheon-os displays a serious effort in building a thoughtful software which other researchers can use.
some of the features that i found fascinating were:
> there is a marketplace where users can discover and share reusable biomedical ai building blocks such as agents, tools and skills.
> employs evolutionary search to iteratively improve (aka autoresearch) algorithms that are used for batch correction in rna-sequencing and it used the map-elites style algorithm (conceptually similar to what has been used for idea exploration in alphaevolve from
@GoogleDeepMind).
> what xiaojie showed us is that one can use pantheon-os to build detailed research reports/papers end to end starting from given input genomics samples, images, etc., with minimal to no human intervention and the finally analysis happens to be fully reproducible.
> comes in cli, desktop app and web ui and it is fully open source.
> supports multiple multi-agent architecture such as mixture-of-agents (llm council style), sequential agents (assembly line style), coordinator-agent (one agent delegating tasks to other agent), etc.
> privacy-preserving in the sense that the underlying data such as genomics data doesn't have to be uploaded to cloud but can be in local server, etc.
xiaojie and his team of collaborators has done extraordinary work in building this.
PantheonOS allows any biologist to perform complex data analyses of emerging single cell, multi-omics and spatial transcriptomics datasets end to end through AI agent and human collaboration. We are releasing six replays of use cases trajectories. Each "trajectory" is a complete end-to-end run, from prompt to analysis, to figures, and finally to report, and in fully inspectable and reproducible manner.
See the six user cases in our PantheonOS Gallery:
1. 3D mouse embryo analysis: Tangram deconvolution and PyVista-based 3D visualization of E6 mouse embryo spatial transcriptomics data
2. 3D human fetal heart analysis: Spatial mapping of heart disease gene patterns using MERFISH data
3. Multi-omics spatial integration: Single cell multi-omics-to-spatial mapping with MOSCOT optimal transport
4. Gene panel design: 1000-plex immune-oncology MERFISH gene panel optimization
5. Cell segmentation benchmarking: Comparative evaluation of Cellpose-SAM, InstanSeg, StarDist, and other tools
6. Spatial disease biology: Ligand–receptor analysis of disease-associated tissue microenvironments
We would love to hear how you can use PantheonOS for your research! Got an interesting agent run of your own and want to share? In the Pantheon UI, click Export Bundle (top-right of any chat) to package the full trajectory — chat history, code, figures, report — then submit it here: