Skills

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

  1. Receive input, Accept either a raw genotype file path or a pre-parsed snp_dict. If a file is provided, call parse_genotype_file() to extract the rsID → genotype mapping.
Read the whole SKILL.md on GitHub

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