/recombinator
Produce offspring genomes from parent pairs via meiotic recombination, mutation, and clinical evaluation
$ npx -y skills add ClawBio/ClawBio --skill recombinator --agent claude-codeHow it fires
How this skill gets triggered: by you, by Claude, or both.
- Fires itselfAuto-invocation. Claude auto-loads it when your prompt matches the work.Auto-invocation is when the right skill fires by itself at the right moment, driven by a FLOW.md router and a hook, instead of you invoking it by name. It is the difference between a skill being installed and a skill actually getting used.Read the full definition →
- You can call itInvoke it directly when you want it.
- Slash command
/recombinator
Context preview
The summary Claude sees to decide when to auto-load this skill.
Produce offspring genomes from parent pairs via meiotic recombination, mutation, and clinical evaluation
SKILL.md
recombinator.SKILL.mdname: recombinator
description: Produce offspring genomes from parent pairs via meiotic recombination, mutation, and clinical evaluation
license: MIT
metadata:
version: 0.1.0
author: Manuel Corpas
tags:
- genomebook
- recombination
- meiosis
- mutation
- offspring
- clinical-genetics
openclaw:
requires:
bins:
- python3
always: false
emoji: 🧪
homepage: https://github.com/ClawBio/ClawBio
os:
- darwin
- linux
trigger_keywords:
- recombinator
- recombination
- offspring
- breed
- meiosis
- genomebook breed
- next generation🧪 Recombinator
Purpose
Produce offspring genomes from selected parent pairs via simulated meiotic recombination. Models Mendelian segregation, de novo mutation, sex determination, and clinical evaluation against a disease registry.
How It Works
1. **Mendelian segregation**: one allele inherited from each parent per locus (random selection simulating independent assortment). 2. **De novo mutation**: configurable rate per locus (default 0.1%), with hotspot multipliers for cognitive, immune, and metabolic loci. Mutations are classified as disease-risk, protective, or neutral. 3. **Sex determination**: 50/50 coin flip (XY or XX). 4. **Trait inference**: reverse-map offspring genotype back to trait scores using the trait registry, accounting for dominance models. 5. **Clinical evaluation**: check offspring genotype against disease registry for penetrance, onset probability, and fitness cost. 6. **Health score**: computed from cumulative fitness costs of clinical conditions.
Input
- Two parent `.genome.json` files (one Male, one Female)
- `GENOMEBOOK/DATA/trait_registry.json`
- `GENOMEBOOK/DATA/disease_registry.json`
Output
- Offspring `.genome.json` with:
- Inherited loci and alleles
- Mutation log
- Inferred trait scores
- Clinical history
- Health score (0.0 to 1.0)
CLI Usage
# Demo: breed Einstein x Anning, produce 3 offspring
python skills/recombinator/recombinator.py --demo
# Breed specific parents
python skills/recombinator/recombinator.py \
--father einstein-g0 --mother anning-g0 --offspring 3
# Custom generation number
python skills/recombinator/recombinator.py \
--father einstein-g0 --mother curie-g0 --offspring 2 --generation 1
Output Format
ID: g1-001-a3f2c1
Sex: Female (XX)
Health: 0.9500
Mutations: 1
- COMT_Val158Met: G->A (neutral, from mother)
Conditions: 0
Top traits:
- curiosity: 0.92
- analytical_thinking: 0.88
- persistence: 0.85
Read more
name: recombinator
description: Produce offspring genomes from parent pairs via meiotic recombination, mutation, and clinical evaluation
license: MIT
metadata:
version: 0.1.0
author: Manuel Corpas
tags:
- genomebook
- recombination
- meiosis
- mutation
- offspring
- clinical-genetics
openclaw:
requires:
bins:
- python3
always: false
emoji: 🧪
homepage: https://github.com/ClawBio/ClawBio
os:
- darwin
- linux
trigger_keywords:
- recombinator
- recombination
- offspring
- breed
- meiosis
- genomebook breed
- next generation🧪 Recombinator
Purpose
Produce offspring genomes from selected parent pairs via simulated meiotic recombination. Models Mendelian segregation, de novo mutation, sex determination, and clinical evaluation against a disease registry.
How It Works
1. **Mendelian segregation**: one allele inherited from each parent per locus (random selection simulating independent assortment). 2. **De novo mutation**: configurable rate per locus (default 0.1%), with hotspot multipliers for cognitive, immune, and metabolic loci. Mutations are classified as disease-risk, protective, or neutral. 3. **Sex determination**: 50/50 coin flip (XY or XX). 4. **Trait inference**: reverse-map offspring genotype back to trait scores using the trait registry, accounting for dominance models. 5. **Clinical evaluation**: check offspring genotype against disease registry for penetrance, onset probability, and fitness cost. 6. **Health score**: computed from cumulative fitness costs of clinical conditions.
Input
- Two parent `.genome.json` files (one Male, one Female)
- `GENOMEBOOK/DATA/trait_registry.json`
- `GENOMEBOOK/DATA/disease_registry.json`
Output
- Offspring `.genome.json` with:
- Inherited loci and alleles
- Mutation log
- Inferred trait scores
- Clinical history
- Health score (0.0 to 1.0)
CLI Usage
# Demo: breed Einstein x Anning, produce 3 offspring python skills/recombinator/recombinator.py --demo # Breed specific parents python skills/recombinator/recombinator.py \ --father einstein-g0 --mother anning-g0 --offspring 3 # Custom generation number python skills/recombinator/recombinator.py \ --father einstein-g0 --mother curie-g0 --offspring 2 --generation 1
Output Format
ID: g1-001-a3f2c1 Sex: Female (XX) Health: 0.9500 Mutations: 1 - COMT_Val158Met: G->A (neutral, from mother) Conditions: 0 Top traits: - curiosity: 0.92 - analytical_thinking: 0.88 - persistence: 0.85
🦖 ClawBio - The first bioinformatics-native AI agent skill library. Local-first. Reproducible. Open. Free.
Other skills on clawbio.
- /affinity-proteomics
Unified analysis pipeline for affinity-based proteomics platforms — Olink (PEA, NPX) and SomaLogic SomaScan (SOMAmer,
Open skill - /analyze-fasta
Synthetic ~120 aa protein sequence (CC0, no real organism)
Open skill - /ancestry-risk-profiler
Synthetic South Asian 23andMe profile with T2D, CAD, and hypertension risk alleles
Open skill - /archaic-introgression
Genomic coordinates of introgressed segments
Open skill - /article-data-fetcher
A test DOI pointing to a public GEO dataset
Open skill - /bgpt-mcp
Structured paper data with 25+ fields per result
Open skill

