菜单
Deterministic CPIC pharmacogenomics lookup over the patient's current medications. Pure code, no LLM. Emits Tier A/B for CPIC Level A/B gene-drug pairs; flags a missing genotype instead of ever directing a dose change.
默认使用会先检查来源的 Prompt；你也可以切换为直接命令，或下载本地副本。
决定是否安装前，请先阅读 SKILL.md，以及 SkillsMP 当前展示的配套文件。
用 Codex 或 Claude 帮你安装 复制这段 Prompt，粘贴到 Codex、Claude 或其他助手里，让它检查 Skill 页面并帮你完成安装。
直接命令不会经过审查 Prompt；运行前请先检查来源。
npx skills add https://github.com/linushansen12/Chronic-Illness-Workbench --skill pgx-cpic-lookup命令会保持在同一行。复制前请横向滚动并检查完整内容。
想先保存到本地？可下载 SkillsMP 当前能够提供的文件。
Open Targets gene-disease association lookup via the official MCP connector. One GraphQL round trip per gene. Emits Tier C informational evidence.
Standing watcher. Reruns the trial, literature (PubMed + bioRxiv), and ClinVar-relookup specialists against the FIXED profile and diffs against the stored baseline. Empty diff -> one calm "no significant changes" timeline entry.
PubMed + bioRxiv search for recent literature on the patient's genes and diagnosis. bioRxiv preprints are first-class (earliest signal). Emits Tier C; the LLM only summarizes genuine free text, it never asserts facts.
基于 SOC 职业分类
正在显示 SKILL.md
| name | pgx-cpic-lookup |
| kind | oneshot |
| domain | pgx |
| description | Deterministic CPIC pharmacogenomics lookup over the patient's current medications. Pure code, no LLM. Emits Tier A/B for CPIC Level A/B gene-drug pairs; flags a missing genotype instead of ever directing a dose change. |
A deterministic specialist (spec §7). For each current medication it checks
whether a CPIC gene-drug pair exists and emits an EvidenceRecord:
The specific dosing guidance depends on the patient's metabolizer genotype. When no
genotype is on file (the normal demo case) the record states the pair exists and
flags the gap in confidence_note. It never emits a dose directive — the code
gate would block it, and next-data-pgx-coverage is what turns that gap into a
question for the care team.
Entrypoint: specialist.run_specialist(profile, ctx).