
Claw Methylation Cycle
Methylation cycle analysis, enzymatic activity profiles, Net Methylation Capacity, BH4...
Install
npx skills add ClawBio/ClawBio --skill claw-methylation-cycle -g -a claude-code -y- Repository
- ClawBio/ClawBio1.2k
- Category
- Engineering
- Updated
- 3d ago
- License
- MIT
- Context cost
- Mediumabout 3,000 tokens
- Runs scripts
- Yes, review before use
What it does
Methylation cycle analysis, enzymatic activity profiles, Net Methylation Capacity, BH4 axis estimates, compound heterozygosity detection from SNP genotype data.
claw-methylation-cycle
Methylation cycle analysis skill for ClawBio. Produces enzymatic activity profiles, Net Methylation Capacity (NMC), BH4 axis estimates, compound heterozygosity detection, and clinician-review genotype findings from raw SNP genotype data.
Trigger
Fire this skill when:
- The user asks about methylation, MTHFR variants, folate cycle, or homocysteine risk from a genotype file.
- A raw SNP file (23andMe / ADNTRO / Ancestry format) is provided and the clinical question involves methylation, BH4, dopamine/serotonin synthesis capacity, or neurodevelopmental contexts (ADHD, depression, anxiety).
- The upstream workflow (PharmGx Reporter, NutriGx Advisor) has flagged MTHFR or MTRR and the clinician needs the full methylation panel.
- Keywords present:
methylation,MTHFR,BH4,folate cycle,metilación,ciclo de metilación,homocysteine,5-MTHF,methylcobalamin,neurotransmitter synthesis,dopamine upstream.
Do NOT fire this skill when:
- The question is purely about folic acid supplementation without a genotype file.
- The user is asking about MTHFR in the context of thrombophilia/clotting only, use PharmGx Reporter for warfarin/anticoagulation questions.
- Only N-GENE polygenic risk data is available (no raw SNP file), this skill requires genotype-level input; PRS percentiles are not sufficient.
- The SNP file format is VCF, FASTQ, BAM, or PLINK binary, these require preprocessing before this skill can run.
- The clinical question is exclusively pharmacogenomic (CYP enzymes), use PharmGx Reporter instead.
Workflow
- Receive input, Accept either a raw genotype file path or a pre-parsed
snp_dict. If a file is provided, callparse_genotype_file()to extract the rsID → genotype mapping.
