2k tokens
context cost
the whole folder, loaded on every use
3
files
instructions only
0
copies elsewhere
how many repositories repackaged it
132
stars on the repo
on the repository, not the skill itself
Install
one command, takes just this skill from the repository
npx skills add https://github.com/BioTender-max/awesome-bio-agent-skills --skill comparative-genomics
What comes with it
2 461 bytes besides the instruction
The instruction itself
22 sections, as written by the author
Comparative Genomics
Version Compatibility
Reference examples assume recent stable releases of the preferred tools, especially orthology and the other tools listed below.
Before using code or command patterns, verify installed versions match the environment:
- Python:
python -c "import <module>; print(<module>.__version__)"
- CLI:
<tool> --version
- If signatures differ, inspect the installed help or API and adapt the pattern instead of retrying unchanged.
Overview
Workflow for orthology, synteny, ancestral reconstruction, and evolutionary comparison across genomes.
When To Use This Skill
- use when the task is cross-genome comparison or evolutionary inference
- use when assembled genomes and annotations are available for multiple taxa or strains
- use when the user needs orthologs, synteny blocks, or positive-selection style summaries
Quick Route
- If the input is raw or minimally processed data, start with validation and QC before any modeling.
- If the input is already processed, skip directly to the first workflow step that matches the user goal.
- If the user asks for a biological conclusion, always produce at least one QC or confidence artifact alongside the final result.
Progressive Disclosure
- Read
references/technical_reference.md when you need deeper tool-selection rules, environment adaptation notes, or extra validation guidance.
- Keep
SKILL.md as the main execution path and load the reference file only when the task or failure mode needs the extra detail.
Default Rules
- Prefer Python-first workflows unless the task explicitly requires something else.
- Keep intermediate and final outputs separated.
- Record software versions, reference builds, and key parameters when they affect interpretation.
- Favor reproducible tables and figures over one-off interactive-only outputs.
- assemblies
- gene annotations
- optional phylogenetic context
Expected Outputs
- ortholog tables
- synteny outputs
- evolutionary comparison summaries
- orthology tools
- alignment and phylogeny utilities
- pandas
Starter Pattern
Preferred starting point: orthology
Inputs: assemblies, gene annotations, optional phylogenetic context
Outputs: ortholog tables, synteny outputs, evolutionary comparison summaries
Workflow
1. Define comparison scale
Clarify whether the task is gene-level, synteny-level, or phylogenomic.
2. Standardize annotations
Use consistent naming, feature models, and assemblies before comparing genomes.
3. Infer shared and divergent elements
Run orthology, synteny, or evolutionary analyses appropriate to the question.
4. Interpret in biological context
Separate technical annotation differences from genuine biological divergence.
5. Export concise comparison artifacts
Save tables and figures that highlight conserved versus lineage-specific patterns.
Output Artifacts
- Recommended output layout:
results/ for final tables and serialized objects
figures/ for plots and static visual exports
qc/ for checks that justify downstream interpretation
- Minimum expected outputs for this skill:
ortholog tables
synteny outputs
evolutionary comparison summaries
Quality Review
- Confirm identifiers and metadata join correctly before modeling or summarizing.
- Generate at least one QC artifact before final biological interpretation.
- Keep raw or minimally processed inputs separate from transformed outputs.
- Record reference build, caller assumptions, and filtering rules in the final outputs.
- Separate raw calls from filtered or interpreted results.
Anti-Patterns
- comparing genomes with incompatible annotation quality without caveats
- overstating adaptive evolution from weak evidence
- mixing orthology and homology claims carelessly
Variant Calling
Copy Number
Long-Read Genomics
Genome Assembly
Optional Supplements
- None required for the first pass.