القائمة
Journal sub-skill for focused public/source evidence review and reviewed finding write-back before interpretation or answer synthesis.
التثبيت باستخدام Codex أو Claude انسخ هذا Prompt والصقه في Codex أو Claude أو مساعد آخر ليراجع صفحة Skill ويثبّتها لك.
استنادا إلى تصنيف SOC المهني
Use this skill for genetics, genome source, variant, gene, phenotype, disease, screen, pharmacogenomics, and Genomi install/setup maintenance questions.
Build and inspect ClinVar exact-match evidence and candidate inventories. Use for clinical labels, VUS/conflict, carrier context, and drug-response rows.
Activate this skill for "/genomi decode", "decode my genome", "decode my DNA", "show me the dashboard", "the Genomi dashboard", "one-shot rundown", or any all-at-once request that asks Genomi to compose every capability's findings into a single artifact. This is the whole-genome dashboard kicker — it sweeps every relevant Genomi capability in one shot, not a per-target lookup. Composes evidence from every relevant Genomi capability into a single self-contained Genomi Dashboard.html and returns localhost serve metadata. Active genome required.
Answer drug-response, medication, PharmGKB-style, PGxDB, ATC, DrugBank, gene-drug, and variant-drug questions using public PGx evidence plus local sample genotype support when an Active Genome Index is selected.
Plan rare disease, hereditary disease, cancer risk, carrier-relevance, and observed-condition source investigation from public targets or selected active genome evidence.
Answer specific rsID, allele, gene, region, genotype, and absence/callability questions using explicit session context or public evidence.
| name | journal-source-research |
| description | Journal sub-skill for focused public/source evidence review and reviewed finding write-back before interpretation or answer synthesis. |
| tools | ["research.list_sources","research.build_target_packet","gnomad.fetch_population_frequency","phenotype.plan_risk_investigation","pharmacogenomics.fetch_pgxdb","research.record","research.query","research.search"] |
| mutating | true |
Use this Journal sub-skill when a claim needs source context beyond local static rows: current ClinVar assertion, gene mechanism, inheritance, penetrance, guideline evidence, population tension, or literature/source conflict.
Review focused public targets and write reviewed findings back into the local
evidence DB before using them in final interpretation. In capability discovery,
these tools are part of journal because they create reusable investigation
memory rather than a separate evidence category.
Works with Active Genome Index context and public-only context. If Active Genome Index context exists, use its evidence DB for user-specific context. With public-only context, use the shared evidence DB and frame the answer as public-target source review.
Convention: See
skills/conventions/evidence-quality.md. Convention: Seeskills/_output-rules.md.
Contract:
dependencyContract.externalNetwork;
local source files are marked in dependencyContract.localResources. If an
API source is unavailable, the tool returns source_unavailable.A scope-limited result from this capability is not a final user-facing answer when other Genomi capabilities can contribute orthogonal evidence to the same question. Returning "cannot answer" while applicable capabilities remain unexamined is a host-agent failure mode.
Fetch reusable gnomAD public population frequency for one allele and write it into evidence storage.
Use when: gnomAD population frequency would change interpretation of an exact public allele or candidate variant.
Why necessary: gnomAD allele frequency changes interpretation; common and rare variants should not be discussed the same way.
Result semantics: Writes reusable aggregate public gnomAD frequency rows using selected public allele data.
Build a target-centric evidence packet after the agent identifies the user's target.
Use when: The agent has selected a gene, drug, condition, topic, or allele and needs local/source context for synthesis.
Why necessary: A target packet keeps gene, drug, condition, topic, and allele context grouped before synthesis.
Result semantics: Returns context and source candidates for agent synthesis.
List source catalogs relevant to a target type or one source ID.
Use when: choosing public source families for a target type or inspecting one source contract.
Why necessary: Source choice is part of the evidence contract; agents need to know which public adapters fit a target.
Result semantics: Returns source adapter and focused-review contracts for the host agent's selected public target.
Retrieve reviewed research for an exact target from local evidence storage.
Use when: the agent needs stored reviewed research for one exact target.
Why necessary: Exact-target research retrieval prevents agents from relying on vague memory of prior reviews.
Store reviewed source findings or tool-returned record_research_payloads in evidence storage with explicit shared/private scope.
Use when: Use after the agent has a reviewed source finding or tool-returned research payload that should be stored with scope.
Why necessary: Reviewed findings need durable, scoped storage so later answers can reuse source-backed evidence.
Result semantics: Writes reviewed public-target or private user-specific findings according to scope; private scope requires an active/private evidence DB.
Token-search reviewed research findings stored in local evidence storage.
Use when: the agent needs token search across stored reviewed findings and does not have exact target fields.
Why necessary: Token search recovers stored findings when exact target fields are unknown.
External research may use selected public targets: gene, rsID, normalized allele, drug, condition, topic, or guideline question. Intake files, broad candidate inventories, and private phenotype/medication/family context stay local unless the user explicitly chooses broader sharing.
For source-backed interpretation, store a reviewed finding JSON file or an inline payload returned by a Genomi source tool:
research.record with {"input":"finding.json","scope":"shared"}research.record with {"payload":{"target":{"type":"drug","drug":"clopidogrel"},"source":{"title":"CPIC","url":"https://cpicpgx.org/guidelines/"},"finding":{"type":"pgx_guideline","text":"short reviewed finding"}},"scope":"shared"}With public-only context, db can be omitted and Genomi will use the shared
evidence DB.
Use shared for reusable public-target knowledge. Use private for
user-specific combinations, phenotype, medications, family history, or personal
interpretation. Private scope uses the selected Active Genome Index evidence DB
or an explicit private db.
Use research.list_sources before focused review when the source choice is uncertain.
Each source returns:
query_mode: implemented operation or focused source review.public_target_inputs: the fields safe to use for external review.available_operations: Genomi tools that support the source.reviewed_finding_shape: fields to store with research.record.For GeneCards- or MalaCards-style context, use phenotype.plan_risk_investigation to keep gene
function, disease association, and clinical-validity cross-checks separated.
For implemented sources, call the listed adapter first. For focused-review sources, review the official source or primary literature for the selected public target, extract the narrow finding needed for the user's question, and write it back as reviewed evidence.