OpenClaw-Medical-Skills tooluniverse-phylogenetics
Production-ready phylogenetics and sequence analysis skill for alignment processing, tree analysis, and evolutionary metrics. Computes treeness, RCV, treeness/RCV, parsimony informative sites, evolutionary rate, DVMC, tree length, alignment gap statistics, GC content, and bootstrap support using PhyKIT, Biopython, and DendroPy. Performs NJ/UPGMA/parsimony tree construction, Robinson-Foulds distance, Mann-Whitney U tests, and batch analysis across gene families. Integrates with ToolUniverse for sequence retrieval (NCBI, UniProt, Ensembl) and tree annotation. Use when processing FASTA/PHYLIP/Nexus/Newick files, computing phylogenetic metrics, comparing taxa groups, or answering questions about alignments, trees, parsimony, or molecular evolution.
git clone https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills
T=$(mktemp -d) && git clone --depth=1 https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills "$T" && mkdir -p ~/.claude/skills && cp -r "$T/skills/tooluniverse-phylogenetics" ~/.claude/skills/freedomintelligence-openclaw-medical-skills-tooluniverse-phylogenetics && rm -rf "$T"
T=$(mktemp -d) && git clone --depth=1 https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills "$T" && mkdir -p ~/.openclaw/skills && cp -r "$T/skills/tooluniverse-phylogenetics" ~/.openclaw/skills/freedomintelligence-openclaw-medical-skills-tooluniverse-phylogenetics && rm -rf "$T"
skills/tooluniverse-phylogenetics/SKILL.md- pip install
Phylogenetics and Sequence Analysis
Comprehensive phylogenetics and sequence analysis using PhyKIT, Biopython, and DendroPy. Designed for bioinformatics questions about multiple sequence alignments, phylogenetic trees, parsimony, molecular evolution, and comparative genomics.
IMPORTANT: This skill handles complex phylogenetic workflows. Most implementation details have been moved to
references/ for progressive disclosure. This document focuses on high-level decision-making and workflow orchestration.
When to Use This Skill
Apply when users:
- Have FASTA alignment files and ask about parsimony informative sites, gaps, or alignment quality
- Have Newick tree files and ask about treeness, tree length, evolutionary rate, or DVMC
- Ask about treeness/RCV, RCV, or relative composition variability
- Need to compare phylogenetic metrics between groups (fungi vs animals, etc.)
- Ask about PhyKIT functions (treeness, rcv, dvmc, evo_rate, parsimony_informative, tree_length)
- Have gene family data with paired alignments and trees
- Need Mann-Whitney U tests or other statistical comparisons of phylogenetic metrics
- Ask about bootstrap support, branch lengths, or tree topology
- Need to build trees (NJ, UPGMA, parsimony) from alignments
- Ask about Robinson-Foulds distance or tree comparison
BixBench Coverage: 33 questions across 8 projects (bix-4, bix-11, bix-12, bix-25, bix-35, bix-38, bix-45, bix-60)
NOT for (use other skills instead):
- Multiple sequence alignment generation → Use external tools (MUSCLE, MAFFT, ClustalW)
- Maximum Likelihood tree construction → Use IQ-TREE, RAxML, or PhyML
- Bayesian phylogenetics → Use MrBayes or BEAST
- Ancestral state reconstruction → Use separate tools
Core Principles
- Data-first approach - Discover and validate all input files (alignments, trees) before any analysis
- PhyKIT-compatible - Use PhyKIT functions for treeness, RCV, DVMC, parsimony, evolutionary rate (matches BixBench expected outputs)
- Format-flexible - Support FASTA, PHYLIP, Nexus, Newick, and auto-detect formats
- Batch processing - Process hundreds of gene alignments/trees in a single analysis
- Statistical rigor - Mann-Whitney U, medians, percentiles, standard deviations with scipy.stats
- Precision awareness - Match rounding to 4 decimal places (PhyKIT default) or as requested
- Group comparison - Compare metrics between taxa groups (e.g., fungi vs animals)
- Question-driven - Parse exactly what is asked and return the specific number/statistic
Required Python Packages
# Core (MUST be installed) import numpy as np import pandas as pd from scipy import stats from Bio import AlignIO, Phylo, SeqIO from Bio.Phylo.TreeConstruction import DistanceCalculator, DistanceTreeConstructor # PhyKIT (primary computation engine) from phykit.services.tree.treeness import Treeness from phykit.services.tree.total_tree_length import TotalTreeLength from phykit.services.tree.evolutionary_rate import EvolutionaryRate from phykit.services.tree.dvmc import DVMC from phykit.services.tree.treeness_over_rcv import TreenessOverRCV from phykit.services.alignment.parsimony_informative_sites import ParsimonyInformative from phykit.services.alignment.rcv import RelativeCompositionVariability # DendroPy (for advanced tree operations) import dendropy # ToolUniverse (for sequence retrieval) from tooluniverse import ToolUniverse
Installation:
pip install phykit dendropy biopython pandas numpy scipy
High-Level Workflow Decision Tree
START: User question about phylogenetic data │ ├─ Q1: What type of analysis is needed? │ │ │ ├─ ALIGNMENT ANALYSIS (FASTA/PHYLIP files) │ │ ├─ Parsimony informative sites → phykit_parsimony_informative() │ │ ├─ RCV score → phykit_rcv() │ │ ├─ Gap percentage → alignment_gap_percentage() │ │ ├─ GC content → alignment_statistics() │ │ └─ See: references/sequence_alignment.md │ │ │ ├─ TREE ANALYSIS (Newick files) │ │ ├─ Treeness → phykit_treeness() │ │ ├─ Tree length → phykit_tree_length() │ │ ├─ Evolutionary rate → phykit_evolutionary_rate() │ │ ├─ DVMC → phykit_dvmc() │ │ ├─ Bootstrap support → extract_bootstrap_support() │ │ └─ See: references/tree_building.md │ │ │ ├─ COMBINED ANALYSIS (alignment + tree) │ │ └─ Treeness/RCV → phykit_treeness_over_rcv() │ │ │ ├─ TREE CONSTRUCTION (build from alignment) │ │ ├─ Neighbor-Joining → build_nj_tree() │ │ ├─ UPGMA → build_upgma_tree() │ │ ├─ Parsimony → build_parsimony_tree() │ │ └─ See: references/tree_building.md │ │ │ ├─ GROUP COMPARISON (fungi vs animals, etc.) │ │ ├─ Batch compute metrics per group │ │ ├─ Mann-Whitney U test │ │ ├─ Summary statistics (median, mean, percentiles) │ │ └─ See: references/parsimony_analysis.md │ │ │ └─ TREE COMPARISON │ ├─ Robinson-Foulds distance → robinson_foulds_distance() │ └─ Bootstrap consensus → bootstrap_analysis() │ ├─ Q2: What data format is available? │ ├─ FASTA (.fa, .fasta, .faa, .fna) │ ├─ PHYLIP (.phy, .phylip) - Use phylip-relaxed for long names │ ├─ Nexus (.nex, .nexus) │ ├─ Newick (.nwk, .newick, .tre, .tree) │ └─ Auto-detect with load_alignment() or load_tree() │ └─ Q3: Is this a batch analysis? ├─ Single gene → Run metric function once ├─ Multiple genes → Use batch_compute_metric() └─ Group comparison → Use discover_gene_files() + compare_groups()
Quick Reference: Common Metrics
| Metric | Function | Input | Description |
|---|---|---|---|
| Treeness | | Newick | Internal branch length / Total branch length |
| RCV | | FASTA/PHYLIP | Relative Composition Variability |
| Treeness/RCV | | Both | Treeness divided by RCV |
| Tree Length | | Newick | Sum of all branch lengths |
| Evolutionary Rate | | Newick | Total branch length / num terminals |
| DVMC | | Newick | Degree of Violation of Molecular Clock |
| Parsimony Sites | | FASTA/PHYLIP | Sites with ≥2 chars appearing ≥2 times |
| Gap Percentage | | FASTA/PHYLIP | Percentage of gap characters |
See
scripts/tree_statistics.py for implementation.
Common Analysis Patterns (BixBench)
Pattern 1: Single Metric Across Groups
Question: "What is the median DVMC for fungi vs animals?"
Workflow:
# 1. Discover files fungi_genes = discover_gene_files("data/fungi") animal_genes = discover_gene_files("data/animals") # 2. Compute metric fungi_dvmc = batch_dvmc(fungi_genes) animal_dvmc = batch_dvmc(animal_genes) # 3. Compare fungi_values = list(fungi_dvmc.values()) animal_values = list(animal_dvmc.values()) print(f"Fungi median DVMC: {np.median(fungi_values):.4f}") print(f"Animal median DVMC: {np.median(animal_values):.4f}")
See:
references/parsimony_analysis.md for full implementation
Pattern 2: Statistical Comparison
Question: "What is the Mann-Whitney U statistic comparing treeness between groups?"
Workflow:
from scipy import stats # Compute treeness for both groups group1_treeness = batch_treeness(group1_genes) group2_treeness = batch_treeness(group2_genes) # Mann-Whitney U test (two-sided) u_stat, p_value = stats.mannwhitneyu( list(group1_treeness.values()), list(group2_treeness.values()), alternative='two-sided' ) print(f"U statistic: {u_stat:.0f}") print(f"P-value: {p_value:.4e}")
Pattern 3: Filtering + Metric
Question: "What is the treeness/RCV for alignments with <5% gaps?"
Workflow:
# 1. Filter by gap percentage valid_genes = [] for entry in gene_files: if 'aln_file' in entry: gap_pct = alignment_gap_percentage(entry['aln_file']) if gap_pct < 5.0: valid_genes.append(entry) # 2. Compute metric on filtered set results = batch_treeness_over_rcv(valid_genes) # 3. Report values = [r[0] for r in results.values()] # treeness/rcv ratio print(f"Median treeness/RCV: {np.median(values):.4f}")
Pattern 4: Specific Gene Lookup
Question: "What is the evolutionary rate for gene X?"
Workflow:
# Find gene file gene_files = discover_gene_files("data/") gene_entry = [g for g in gene_files if g['gene_id'] == 'X'][0] # Compute metric evo_rate = phykit_evolutionary_rate(gene_entry['tree_file']) print(f"Evolutionary rate for gene X: {evo_rate:.4f}")
Choosing Methods: When to Use What
Alignment Methods
When building alignments (use external tools, not this skill):
| Method | Speed | Accuracy | Use Case |
|---|---|---|---|
| ClustalW | Slow | Medium | Small datasets (<100 sequences), educational |
| MUSCLE | Fast | High | Medium datasets (100-1000 sequences) |
| MAFFT | Very Fast | Very High | Recommended - Large datasets (>1000 sequences) |
For this skill: Work with pre-aligned sequences. Use
load_alignment() to read any format.
Tree Building Methods
When to use which tree method:
| Method | Speed | Accuracy | Use Case |
|---|---|---|---|
| Neighbor-Joining | Fast | Medium | Quick trees, large datasets, exploratory |
| UPGMA | Fast | Low | Assumes molecular clock, special cases only |
| Maximum Parsimony | Medium | Medium | Small datasets, discrete characters |
| Maximum Likelihood | Slow | High | Use external tools (IQ-TREE, RAxML) for production |
Implementation in this skill:
# Fast distance-based trees tree = build_nj_tree("alignment.fa") # Neighbor-Joining tree = build_upgma_tree("alignment.fa") # UPGMA # Parsimony (for small alignments) tree = build_parsimony_tree("alignment.fa")
For production ML trees: Use IQ-TREE or RAxML externally, then analyze with this skill.
See
references/tree_building.md for detailed implementations.
Batch Processing
Discovering Gene Files
# Auto-discover paired alignment + tree files gene_files = discover_gene_files("data/") # Result: list of dicts with 'gene_id', 'aln_file', 'tree_file' # [ # {'gene_id': 'gene1', 'aln_file': 'gene1.fa', 'tree_file': 'gene1.nwk'}, # {'gene_id': 'gene2', 'aln_file': 'gene2.fa', 'tree_file': 'gene2.nwk'}, # ... # ]
Computing Metrics in Batch
# Tree metrics treeness_results = batch_treeness(gene_files) tree_length_results = batch_tree_length(gene_files) dvmc_results = batch_dvmc(gene_files) evo_rate_results = batch_evolutionary_rate(gene_files) # Alignment metrics rcv_results = batch_rcv(gene_files) pi_results = batch_parsimony_informative(gene_files) gap_results = batch_gap_percentage(gene_files) # Combined metrics treeness_rcv_results = batch_treeness_over_rcv(gene_files) # All return dict: {gene_id: value}
Statistical Analysis
# Summary statistics stats = summary_stats(list(treeness_results.values())) # Returns: {'mean': ..., 'median': ..., 'std': ..., 'min': ..., 'max': ...} # Group comparison comparison = compare_groups( list(fungi_treeness.values()), list(animal_treeness.values()), group1_name="Fungi", group2_name="Animals" ) # Returns: {'u_statistic': ..., 'p_value': ..., 'Fungi': {...}, 'Animals': {...}}
See
references/parsimony_analysis.md for full workflow.
Answer Extraction for BixBench
| Question Pattern | Extraction Method |
|---|---|
| "What is the median X?" | |
| "What is the maximum X?" | |
| "What is the difference between median X for A vs B?" | |
| "What percentage of X have Y above Z?" | |
| "What is the Mann-Whitney U statistic?" | |
| "What is the p-value?" | |
| "What is the X value for gene Y?" | |
| "What is the fold-change in median X?" | |
| "multiplied by 1000" | |
Rounding Rules
- PhyKIT default: 4 decimal places
- Percentages: Match question format (e.g., "35%" → integer, "3.5%" → 1 decimal)
- P-values: Scientific notation for very small values
- U statistics: Integer (no decimals)
- Always check question wording: "rounded to 3 decimal places" overrides defaults
BixBench Question Coverage
| Project | Questions | Metrics |
|---|---|---|
| bix-4 | 7 | DVMC analysis (fungi vs animals) |
| bix-11 | 6 | Treeness analysis (median, percentages, Mann-Whitney U) |
| bix-12 | 5 | Parsimony informative sites (counts, percentages, ratios) |
| bix-25 | 2 | Treeness/RCV with gap filtering |
| bix-35 | 4 | Evolutionary rate (specific genes, comparisons) |
| bix-38 | 5 | Tree length (fold-change, variance, paired ratios) |
| bix-45 | 4 | RCV (Mann-Whitney U, medians, paired differences) |
| bix-60 | 1 | Average treeness across multiple trees |
ToolUniverse Integration
Sequence Retrieval
from tooluniverse import ToolUniverse tu = ToolUniverse() tu.load_tools() # Get sequences from NCBI result = tu.tools.NCBI_get_sequence(accession="NP_000546") # Get gene tree from Ensembl tree_result = tu.tools.EnsemblCompara_get_gene_tree(gene="ENSG00000141510") # Get species tree from OpenTree tree_result = tu.tools.OpenTree_get_induced_subtree(ott_ids="770315,770319")
File Structure
tooluniverse-phylogenetics/ ├── SKILL.md # This file (workflow orchestration) ├── QUICK_START.md # Quick reference ├── test_phylogenetics.py # Comprehensive test suite ├── references/ │ ├── sequence_alignment.md # Alignment analysis details │ ├── tree_building.md # Tree construction methods │ ├── parsimony_analysis.md # Statistical comparison workflows │ └── troubleshooting.md # Common issues and solutions └── scripts/ ├── format_alignment.py # Alignment format conversion └── tree_statistics.py # Core metric implementations
Completeness Checklist
Before returning your answer, verify:
- Identified all input files (alignments and/or trees)
- Detected group structure (fungi/animals/etc.) if applicable
- Used correct PhyKIT function for the requested metric
- Processed ALL genes in each group (not just a sample)
- Applied correct statistical test if comparison requested
- Used correct rounding (4 decimals default, or as specified)
- Returned the specific statistic asked for (median, max, U stat, p-value, etc.)
- For percentage questions, confirmed whether answer is integer or decimal
- For "difference" questions, confirmed direction (A - B vs abs difference)
- For Mann-Whitney U, used
(default in scipy)alternative='two-sided'
Next Steps
- For detailed alignment analysis workflows → See
references/sequence_alignment.md - For tree construction methods → See
references/tree_building.md - For statistical comparison examples → See
references/parsimony_analysis.md - For common errors and solutions → See
references/troubleshooting.md - For script implementations → See
scripts/tree_statistics.py
Support
For issues with:
- PhyKIT functions: Check PhyKIT documentation at https://jlsteenwyk.com/PhyKIT/
- Biopython tree/alignment parsing: See https://biopython.org/wiki/Phylo
- DendroPy operations: See https://dendropy.org/
- ToolUniverse integration: Check ToolUniverse documentation
License
Same as ToolUniverse framework license.