Biomni Lab lets biologists collaborate with AI agents to finish complex tasks end-to-end. Here are 15 popular use cases, each link is a full replay so you can watch the agent work through every step:
1. Spatial transcriptomics analysis: map gene expression across tissue architecture from spatial transcriptomics data, with spatial clustering and neighborhood analysis.
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2. Binder design: design de novo protein binders against a target structure using computational protein design tools.
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3. Biomarker panel design: identify and optimize a multi-marker diagnostic or prognostic panel from omics data.
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4. Clinical trial landscaping: search and summarize the trial landscape for a disease area, mapping phase, endpoints, and sponsor activity.
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5. Survival analysis: pull clinical and expression data, fit Cox models, generate Kaplan-Meier curves, and identify prognostic markers.
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6. scRNA-seq processing and annotation: from raw counts to UMAP clustering, marker gene detection, and automated cell type labeling.
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7. Cell-cell communication: infer ligand-receptor interactions between cell types from single-cell data and map intercellular signaling networks.
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8. Primer design for novel Cas13: analyze a putative Cas13 protein from a metagenomic screen—verify the ORF, identify HEPN domains, and design cloning primers with restriction sites and a FLAG
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9. Proteomics differential expression: normalize mass spec data, run statistical tests, and visualize differentially abundant proteins.
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10. Gene regulatory network inference: reconstruct transcription factor-target gene networks from expression data and identify key regulators.
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11. Gene co-expression network analysis: build weighted co-expression networks, identify gene modules, and correlate them with phenotypic traits.
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12. Microbiome analysis: process 16S/metagenomic sequencing data to profile microbial communities, diversity, and differential abundance.
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13. Polygenic risk scores: compute and evaluate PRS from GWAS summary statistics against a target cohort.
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14. Variant annotation: annotate genetic variants with functional predictions, allele frequencies, and clinical significance.
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15. Fine-mapping: narrow GWAS loci to credible causal variants using statistical fine-mapping methods.
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Each of these would normally take days to weeks of scripting, debugging, and iteration. In Biomni Lab, the agent handles the full execution while you steer the science.
Learn more:
phylo.bio/use-cases