Capstone — Module 20
Integrated Genomic Care Map.
Build one care map that integrates microbiome, peptides, vagus, genomics, epigenomics, and labs — with explicit referral logic and evidence grading.
Use the Genome Report Reader and Genetic Early Warning Builder as prep tools.
- 01Phenotype
- Primary phenotype
- Symptoms timeline
- Functional impact
- 02Family history
- Three-generation pedigree
- Ancestry context
- Red flags
- 03Differential
- Top 3–5 differentials
- Pre-test probability
- 04Testing — conventional
- Baseline labs
- Indicated imaging
- Targeted screening
- 05Testing — functional/genomic
- When indicated
- Type of test
- Confirmation plan
- Counseling plan
- 06Hypotheses by pillar
- Microbiome
- Peptide / endocrine signaling
- Autonomic / vagus
- Genomic
- Epigenomic
- 07Decisions
- Genetic testing indicated?
- Counseling indicated?
- PGx relevant?
- Cascade testing?
- Trial / gene-targeted referral?
- 08Plan
- Lifestyle / microbiome / autonomic / peptide interventions
- Safety monitoring
- Outcome metrics
- Follow-up timeline
- 09Quality gates
- Evidence grade per claim
- Stop / refer / escalate rule
Downloadable outputs
- Integrated genomic care map
- Family history worksheet
- Genetic testing decision tree
- PGx interpretation worksheet
- Epigenome intervention plan
- Lab monitoring plan
- Patient education summary
- Evidence grading worksheet