genome-match
Score genetic compatibility across all male-female pairings in a Genomebook generation
Best use case
genome-match is best used when you need a repeatable AI agent workflow instead of a one-off prompt.
Score genetic compatibility across all male-female pairings in a Genomebook generation
Teams using genome-match should expect a more consistent output, faster repeated execution, less prompt rewriting.
When to use this skill
- You want a reusable workflow that can be run more than once with consistent structure.
When not to use this skill
- You only need a quick one-off answer and do not need a reusable workflow.
- You cannot install or maintain the underlying files, dependencies, or repository context.
Installation
Claude Code / Cursor / Codex
Manual Installation
- Download SKILL.md from GitHub
- Place it in
.claude/skills/genome-match/SKILL.mdinside your project - Restart your AI agent — it will auto-discover the skill
How genome-match Compares
| Feature / Agent | genome-match | Standard Approach |
|---|---|---|
| Platform Support | Not specified | Limited / Varies |
| Context Awareness | High | Baseline |
| Installation Complexity | Unknown | N/A |
Frequently Asked Questions
What does this skill do?
Score genetic compatibility across all male-female pairings in a Genomebook generation
Where can I find the source code?
You can find the source code on GitHub using the link provided at the top of the page.
SKILL.md Source
# 💞 GenomeMatch
## Purpose
Score genetic compatibility between all male-female pairings in a Genomebook
generation. The engine evaluates heterozygosity advantage, disease carrier risk,
and trait complementarity to rank optimal mating pairs for the next generation.
## How It Works
1. **Load genomes** for a target generation from `GENOMEBOOK/DATA/GENOMES/`.
2. **Compute pairwise compatibility** for every M x F combination:
- **Heterozygosity score (40%)**: fraction of loci where offspring would be
heterozygous (genetic diversity advantage).
- **Trait complementarity (40%)**: reward balanced trait combinations and high
average trait values across the pair.
- **Disease risk penalty (20%)**: flag pairs where both parents carry recessive
disease alleles (25% affected offspring risk per flagged condition).
3. **Rank all pairings** by composite score (0.0 to 1.0).
4. **Select non-overlapping mating pairs** via greedy selection from the top of
the ranked list (each individual mates at most once per generation).
## Input
- `GENOMEBOOK/DATA/GENOMES/*.genome.json`
- `GENOMEBOOK/DATA/disease_registry.json`
## Output
- Ranked compatibility table (all M x F pairings)
- Selected mating pairs for the next generation
## CLI Usage
```bash
# Score all pairings for generation 0
python skills/genome-match/genome_match.py
# Score a specific generation
python skills/genome-match/genome_match.py --generation 1
# Demo mode
python skills/genome-match/genome_match.py --demo
# Limit output to top N pairings
python skills/genome-match/genome_match.py --top 10
```
## Output Format
```
Rank Male x Female Score Het Comp Risk Flags
1 einstein-g0 x curie-g0 0.8234 0.650 0.821 0.000 --
2 darwin-g0 x franklin-g0 0.7891 0.600 0.790 0.000 --
...
SELECTED MATING PAIRS (generation 0 -> 1):
Albert Einstein x Marie Curie (compat: 0.8234)
Charles Darwin x Rosalind Franklin (compat: 0.7891)
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