Getting it into your agent
One page per mod, every tool's command on it. A separate URL per tool would split the same page into five that compete with each other.
npx skills add beita6969/ScienceClaw --skill phylogeneticsgit clone --depth 1 https://github.com/beita6969/ScienceClawWrote this? Show the measurements
A badge with what this costs and how it scanned, read live from this page, so it follows the numbers instead of freezing them. Markdown for a README, HTML for a documentation site or a project page.
[](https://agentmods.dev/skills/beita6969/scienceclaw/phylogenetics)<a href="https://agentmods.dev/skills/beita6969/scienceclaw/phylogenetics"><img src="https://agentmods.dev/badge/skills/beita6969/scienceclaw/phylogenetics/github.svg" alt="Measured on agentmods" height="20"></a>Or the 80×15 button, for a site that already has a row of RSS and ATOM ones. Only the verdict fits; the numbers stay here.
<a href="https://agentmods.dev/skills/beita6969/scienceclaw/phylogenetics"><img src="https://agentmods.dev/badge/skills/beita6969/scienceclaw/phylogenetics.svg" alt="Reviewed on agentmods" width="80" height="20"></a>What it costs to keep this loaded
Counted locally with the o200k_base tokenizer, which is exact for GPT models; Claude uses its own tokenizer and its counts differ. Treat this as one consistent yardstick across the catalogue rather than a bill. Prices are per million input tokens.
| Model | Per session | Once invoked |
|---|---|---|
| Fable 5.1 | $0.00068 | $0.03676 |
| Opus 5 | $0.00034 | $0.01838 |
| Sonnet 5 | $0.00014 | $0.00735 |
| Haiku 4.5 | $0.00007 | $0.00368 |
Grade A, and why
phylogenetics scanned grade A with 1 finding against 26 rules in 11 categories — prompt injection, anti-refusal, data exfiltration, privilege escalation, supply chain, agent snooping, system-prompt leakage, SSRF and excessive agency — measured 8d ago.
A static scan of the body, not an audit. Every finding is printed with the line that produced it so you can judge whether it matters here. A mod is markdown that instructs an agent; that is exactly why what it instructs is worth reading.
Runs shell commandslowCapability
Expected in a hook, worth knowing in a rule or an instructions file.
result = subprocess.run(cmd, stdout=out, stderr=subprocess.PIPE, text=True) This is a copy
98% identical to phylogenetics — 9 lines differ, which has more behind it and is treated as the original. This page carries a canonical link to it rather than competing with it.
How it starts
The opening of the file, as written. The whole thing — 405 lines — stays where its author put it; the contents beside it link to each section on GitHub.
Phylogenetics
Overview
Phylogenetic analysis reconstructs the evolutionary history of biological sequences (genes, proteins, genomes) by inferring the branching pattern of descent. This skill covers the standard pipeline:
- MAFFT — Multiple sequence alignment
- IQ-TREE 2 — Maximum likelihood tree inference with model selection
- FastTree — Fast approximate maximum likelihood (for large datasets)
- ETE3 — Python library for tree manipulation and visualization
Installation:
# Conda (recommended for CLI tools)
conda install -c bioconda mafft iqtree fasttree
pip install ete3
When to Use This Skill
Use phylogenetics when:
- Evolutionary relationships: Which organism/gene is most closely related to my sequence?
- Viral phylodynamics: Trace outbreak spread and estimate transmission dates
- Protein family analysis: Infer evolutionary relationships within a gene family
- Horizontal gene transfer detection: Identify genes with discordant species/gene trees
- Ancestral sequence reconstruction: Infer ancestral protein sequences
- Molecular clock analysis: Estimate divergence dates using temporal sampling
- GWAS companion: Place variants in evolutionary context (e.g., SARS-CoV-2 variants)
- Microbiology: Species phylogeny from 16S rRNA or core genome phylogeny
Standard Workflow
1. Multiple Sequence Alignment with MAFFT
import subprocess
import os
def run_mafft(input_fasta: str, output_fasta: str, method: str = "auto",
n_threads: int = 4) -> str:
"""
Align sequences with MAFFT.
Args:
input_fasta: Path to unaligned FASTA file
output_fasta: Path for aligned output
method: 'auto' (auto-select), 'einsi' (accurate), 'linsi' (accurate, slow),
'fftnsi' (medium), 'fftns' (fast), 'retree2' (fast)
n_threads: Number of CPU threads
Returns:
Path to aligned FASTA file
"""
methods = {
"auto": ["mafft", "--auto"],
"einsi": ["mafft", "--genafpair", "--maxiterate", "1000"],
"linsi": ["mafft", "--localpair", "--maxiterate", "1000"],
"fftnsi": ["mafft", "--fftnsi"],
"fftns": ["mafft", "--fftns"],
"retree2": ["mafft", "--retree", "2"],
}
cmd = methods.get(method, methods["auto"])
cmd += ["--thread", str(n_threads), "--inputorder", input_fasta]
with open(output_fasta, 'w') as out:
result = subprocess.run(cmd, stdout=out, stderr=subprocess.PIPE, text=True)
if result.returncode != 0:
raise RuntimeError(f"MAFFT failed:\n{result.stderr}")
# Count aligned sequences
with open(output_fasta) as f:
n_seqs = sum(1 for line in f if line.startswith('>'))
print(f"MAFFT: aligned {n_seqs} sequences → {output_fasta}")
return output_fasta
# MAFFT method selection guide:
# Few sequences (<200), accurate: linsi or einsi
# Many sequences (<1000), moderate: fftnsi
# Large datasets (>1000): fftns or auto
# Ultra-fast (>10000): mafft --retree 1
What ships with it
2 files beside SKILL.md in the same directory: the scripts, references and assets a skill reads on demand. Not counted in the per-session cost; read them before you install if any of them is executable.
What this file has done since we first saw it
Hashed on every crawl. A supply-chain change to an agent config is a question of when, not whether, so the history is kept rather than the latest state alone.
- 8d ago First seen · 405 lines · 68 tokens per session scan A ecea8ee3b168
phylogenetics is a skill published in the GitHub repository beita6969/ScienceClaw (898 stars, last pushed 3mo ago), licensed MIT. It adds 68 tokens to every session and 3,676 once invoked, about $0.0003 per session on Opus 5. A static security scan graded it A with 1 finding (runs shell commands). It is 98% identical to phylogenetics, differing in 9 lines, and is treated as a copy.
Other skills, from other repositories
biopython
Comprehensive molecular biology toolkit. Use for sequence manipulation, file parsing (FASTA/GenBank/PDB), phylogenetics, and programmatic NCBI/PubMed access (Bio.Entrez). Best for batch processing, custom bioinformatics pipelines, BLAST automation. For quick lookups use gget; for multi-service integration use…
scanpy
Standard single-cell RNA-seq analysis pipeline. Use for QC, normalization, dimensionality reduction (PCA/UMAP/t-SNE), clustering, differential expression, and visualization. Best for exploratory scRNA-seq analysis with established workflows. For deep learning models use scvi-tools; for data format questions use…
structure-prediction
Protein structure prediction from sequence. ESMFold-based, single GPU, no MSA needed. Predicts 3D structures with pLDDT confidence scores for drug discovery targets.
biomcp
Search and retrieve biomedical data - genes, variants, clinical trials, diagnostic tests, articles, drugs, diseases, pathways, proteins, adverse events, pharmacogenomics, and phenotype-disease matching. Use for gene function, variant pathogenicity, trials, diagnostics, drug safety, pathway context, disease workups…
biomcp-research
Do biomedical literature and variant research with the BioMCP CLI, and file what you learn about the tool itself as issues in the biomcp repo.
biological-expert
Expert-level biology, biotechnology, genetics, bioinformatics, and computational biology. Use when the user mentions biology, biotechnology, genetics, bioinformatics, or genomics, or when the task involves Molecular Biology, Genomics & Bioinformatics, Systems Biology, or Data Analysis.