tooluniverse |
Router — dispatches to the right specialized skill automatically |
tooluniverse-adverse-event-detection |
Adverse drug event signal detection using FDA FAERS data |
tooluniverse-antibody-engineering |
Antibody humanization, affinity maturation, and optimization |
tooluniverse-binder-discovery |
Small molecule binder discovery (structure-based and ligand-based) |
tooluniverse-cancer-variant-interpretation |
Clinical interpretation of somatic cancer mutations |
tooluniverse-chemical-compound-retrieval |
Chemical compound info from PubChem and ChEMBL |
tooluniverse-chemical-safety |
Chemical safety and toxicology assessment (ADMET-AI, CTD, FDA) |
tooluniverse-clinical-guidelines |
Clinical practice guidelines from 12+ sources (NICE, WHO, ADA, etc.) |
tooluniverse-clinical-trial-design |
Clinical trial design feasibility assessment |
tooluniverse-clinical-trial-matching |
Patient-to-trial matching for precision medicine |
tooluniverse-crispr-screen-analysis |
CRISPR knockout/activation screen analysis |
tooluniverse-custom-tool |
Create and register custom tools |
tooluniverse-disease-research |
Comprehensive disease reports using 100+ tools |
tooluniverse-drug-drug-interaction |
Drug-drug interaction prediction and risk assessment |
tooluniverse-drug-repurposing |
Drug repurposing via target-, compound-, and disease-driven strategies |
tooluniverse-drug-research |
Comprehensive drug reports with evidence grading |
tooluniverse-drug-target-validation |
Computational drug target validation (10 dimensions) |
tooluniverse-epigenomics |
Epigenomics and gene regulation (ENCODE, JASPAR, methylation) |
tooluniverse-expression-data-retrieval |
Gene expression datasets from ArrayExpress and BioStudies |
tooluniverse-gene-enrichment |
Gene enrichment and pathway analysis (gseapy, PANTHER, STRING, etc.) |
tooluniverse-gwas-drug-discovery |
GWAS signals to drug targets and repurposing opportunities |
tooluniverse-gwas-finemapping |
Causal variant prioritization via statistical fine-mapping |
tooluniverse-gwas-snp-interpretation |
Genetic variant interpretation from GWAS studies |
tooluniverse-gwas-study-explorer |
GWAS study comparison and meta-analysis |
tooluniverse-gwas-trait-to-gene |
Gene-trait associations from GWAS Catalog and Open Targets |
tooluniverse-image-analysis |
Microscopy image analysis and quantitative imaging |
tooluniverse-immune-repertoire-analysis |
TCR/BCR immune repertoire analysis |
tooluniverse-immunotherapy-response-prediction |
Predict response to immune checkpoint inhibitors |
tooluniverse-infectious-disease |
Pathogen characterization and drug repurposing for outbreaks |
tooluniverse-install-skills |
Auto-detect and install missing skills |
tooluniverse-literature-deep-research |
Literature research with evidence grading and theme extraction |
tooluniverse-metabolomics |
Metabolomics research (metabolite ID, study analysis) |
tooluniverse-metabolomics-analysis |
Metabolomics data analysis (quantification, pathway, flux) |
tooluniverse-multi-omics-integration |
Multi-omics dataset integration |
tooluniverse-multiomic-disease-characterization |
Multi-omics disease characterization |
tooluniverse-network-pharmacology |
Compound-target-disease network analysis |
tooluniverse-pharmacovigilance |
Drug safety signal analysis from FDA reports |
tooluniverse-phylogenetics |
Phylogenetics and sequence analysis |
tooluniverse-polygenic-risk-score |
Polygenic risk score construction and interpretation |
tooluniverse-precision-medicine-stratification |
Patient stratification for precision medicine |
tooluniverse-precision-oncology |
Actionable cancer treatment recommendations from molecular profiles |
tooluniverse-protein-interactions |
Protein-protein interaction networks (STRING, BioGRID) |
tooluniverse-protein-structure-retrieval |
Protein structures from PDB, PDBe, and AlphaFold |
tooluniverse-protein-therapeutic-design |
AI-guided protein therapeutic design (RFdiffusion, etc.) |
tooluniverse-proteomics-analysis |
Mass spectrometry proteomics analysis |
tooluniverse-rare-disease-diagnosis |
Rare disease differential diagnosis from phenotype and genetics |
tooluniverse-rnaseq-deseq2 |
RNA-seq differential expression with PyDESeq2 |
tooluniverse-sdk |
Build AI scientist systems using the Python SDK |
tooluniverse-sequence-retrieval |
DNA, RNA, and protein sequences from NCBI and ENA |
tooluniverse-single-cell |
Single-cell RNA-seq analysis (scanpy, anndata) |
tooluniverse-spatial-omics-analysis |
Spatial multi-omics data integration |
tooluniverse-spatial-transcriptomics |
Spatial transcriptomics (10x Visium, MERFISH, seqFISH) |
tooluniverse-statistical-modeling |
Statistical modeling and regression for biomedical data |
tooluniverse-structural-variant-analysis |
Structural variant analysis for clinical genomics |
tooluniverse-systems-biology |
Pathway analysis (Reactome, KEGG, WikiPathways) |
tooluniverse-target-research |
Comprehensive drug target profiling (9 research paths) |
tooluniverse-variant-analysis |
VCF processing, variant annotation, and SV/CNV interpretation |
tooluniverse-variant-interpretation |
Clinical variant interpretation with ACMG classification |