From clawbio
Scores genetic compatibility across all male-female pairings in a Genomebook generation using heterozygosity, trait complementarity, and disease risk. Outputs ranked pairings and selected mating pairs.
How this skill is triggered — by the user, by Claude, or both
Slash command
/clawbio:genome-matchThe summary Claude sees in its skill listing — used to decide when to auto-load this skill
Score genetic compatibility between all male-female pairings in a Genomebook
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.
GENOMEBOOK/DATA/GENOMES/.GENOMEBOOK/DATA/GENOMES/*.genome.jsonGENOMEBOOK/DATA/disease_registry.json# 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
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)
npx claudepluginhub clawbio/clawbio --plugin clawbioSimulates meiotic recombination to produce offspring genomes from parent pairs, modeling Mendelian segregation, mutation, and clinical evaluation.
Looks up allele frequencies from gnomAD and 1000 Genomes, runs HWE/Fst/inbreeding tests, queries GWAS associations and ClinVar, and computes evolutionary constraint scores. Best for cross-population variant comparison.
Queries the Monarch Initiative knowledge graph for disease-gene-phenotype associations across species, integrating OMIM, ORPHANET, HPO, ClinVar, and model organism databases. Use for rare disease gene discovery, phenotype mapping, and cross-species modeling.