tooluniverse-model-organism-genetics
COMPUTE, DON'T DESCRIBE
When analysis requires computation (statistics, data processing, scoring, enrichment), write and run Python code via Bash. Don't describe what you would do — execute it and report actual results. Use ToolUniverse tools to retrieve data, then Python (pandas, scipy, statsmodels, matplotlib) to analyze it.
Model Organism Genetics Pipeline
Map human genes to model organism orthologs and retrieve phenotype, expression, and functional data across six species. Synthesize cross-species evidence to assess gene function conservation and identify the best animal models for studying human genes and diseases.
Not for: human variant interpretation (tooluniverse-variant-analysis), drug target validation (tooluniverse-drug-target-validation), human disease characterization (tooluniverse-multiomic-disease-characterization).
LOOK UP, DON'T GUESS: When asked about a species' taxonomy, ecology, or biology, search GBIF/NCBI Taxonomy first. For GBIF: use GBIF_search_species(query="species name"), then use the nubKey (not key) from the result to call GBIF_get_species(speciesKey=nubKey) for full taxonomy (kingdom, phylum, class, order, family). The nubKey is the GBIF backbone key; the key is dataset-specific and often lacks higher taxonomy.
Reasoning Principles
Ortholog Reasoning
Sequence conservation across species implies functional conservation — but not always. A highly conserved gene in mouse and human likely has the same function. But regulatory differences (when/where a gene is expressed) can cause different phenotypes even from the same gene. Always check: is the protein domain conserved, or just raw sequence? Are there known regulatory differences? A 40% identity ortholog with a conserved catalytic domain can be more functionally equivalent than a 90% identity paralog in the same species.
Paralog contamination is a common pitfall. Gene families (e.g., FOXP1/2/3/4, HOX clusters) generate false ortholog hits. Distinguish true orthologs from paralogs by checking synteny (conserved gene neighborhood) and homology type: 1:1 = likely true ortholog; 1:many or many:many = likely paralog expansion. If the target species has a single gene where humans have multiple (e.g., one fly FoxP vs four human FOXPs), it is the co-ortholog of all human paralogs — note this explicitly.
More from mims-harvard/tooluniverse
tooluniverse-sequence-retrieval
Retrieves biological sequences (DNA, RNA, protein) from NCBI and ENA with gene disambiguation, accession type handling, and comprehensive sequence profiles. Creates detailed reports with sequence metadata, cross-database references, and download options. Use when users need nucleotide sequences, protein sequences, genome data, or mention GenBank, RefSeq, EMBL accessions.
1.4Ktooluniverse-image-analysis
Production-ready microscopy image analysis and quantitative imaging data skill for colony morphometry, cell counting, fluorescence quantification, and statistical analysis of imaging-derived measurements. Processes ImageJ/CellProfiler output (area, circularity, intensity, cell counts), performs Dunnett's test, Cohen's d effect size, power analysis, Shapiro-Wilk normality tests, two-way ANOVA, polynomial regression, natural spline regression with confidence intervals, and comparative morphometry. Supports CSV/TSV measurement tables, multi-channel fluorescence data, colony swarming assays, and neuron counting datasets. Use when analyzing microscopy measurement data, colony area/circularity, cell count statistics, swarming assays, co-culture ratio optimization, or answering questions about imaging-derived quantitative data.
406tooluniverse-literature-deep-research
Comprehensive literature deep research across any academic domain using 120+ ToolUniverse tools. Conducts subject disambiguation, systematic literature search with citation network expansion, evidence grading (T1-T4), and structured theme extraction. Produces detailed reports with mandatory completeness checklists, integrated models, and testable hypotheses. Use when users need thorough literature reviews, target/drug/disease profiles, topic deep-dives, claim verification, or systematic evidence synthesis. Supports biomedical (genes, proteins, drugs, diseases), computer science, social science, and general academic topics. For single factoid questions, uses a fast verification mode with inline answer.
384tooluniverse
Router skill for ToolUniverse tasks. First checks if specialized tooluniverse skills (105+ skills covering disease/drug/target research, gene-disease associations, clinical decision support, genomics, epigenomics, proteomics, comparative genomics, chemical safety, toxicology, systems biology, and more) can solve the problem, then falls back to general strategies for using 2300+ scientific tools. Covers tool discovery, multi-hop queries, comprehensive research workflows, disambiguation, evidence grading, and report generation. Use when users need to research any scientific topic, find biological data, or explore drug/target/disease relationships. ALSO USE for any biology, medicine, chemistry, pharmacology, or life science question — even simple factoid questions like "how many X in protein Y", "what drug interacts with Z", "what gene causes disease W", or "translate this sequence". These questions benefit from database lookups (UniProt, PubMed, ChEMBL, ClinVar, GWAS Catalog, etc.) rather than answering from memory alone. When in doubt about a scientific fact, USE THIS SKILL to verify against real databases.
275tooluniverse-drug-research
Generates comprehensive drug research reports with compound disambiguation, evidence grading, and mandatory completeness sections. Covers identity, chemistry, pharmacology, targets, clinical trials, safety, pharmacogenomics, and ADMET properties. Use when users ask about drugs, medications, therapeutics, or need drug profiling, safety assessment, or clinical development research.
271tooluniverse-clinical-trial-design
Strategic clinical trial design feasibility assessment using ToolUniverse. Evaluates patient population sizing, biomarker prevalence, endpoint selection, comparator analysis, safety monitoring, and regulatory pathways. Creates comprehensive feasibility reports with evidence grading, enrollment projections, and trial design recommendations. Use when planning Phase 1/2 trials, assessing trial feasibility, or designing biomarker-driven studies.
271