数据与复现地理信息与遥感FreedomIntelligence/OpenClaw-Medical-Skills数据与复现
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tooluniverse-cancer-variant-interpretation

维护者 FreedomIntelligence · 最近更新 2026年4月1日

tooluniverse-cancer-variant-interpretation:提供 comprehensive clinical interpretation of somatic mutations in cancer。 Given gene symbol + variant (e.g.,EGFR L858R,BRAF V600E) 、 optional cancer type,performs multi-database analysis covering clinical evidence (CIViC),mutation prevalence (cBioPortal),therapeutic associations (OpenTargets,ChEMBL,FDA),resistance mechanisms,clinical trials,prognostic impact,、 pathway context。

OpenClawNanoClaw分析处理复现实验tooluniverse-cancer-variant-interpretation🏥 medical & clinicalmedical toolsprovide

原始来源

FreedomIntelligence/OpenClaw-Medical-Skills

https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/tooluniverse-cancer-variant-interpretation

维护者
FreedomIntelligence
许可
MIT
最近更新
2026年4月1日

技能摘要

来自 SKILL.md 的关键信息

2 min

核心说明

  • Comprehensive clinical interpretation of somatic mutations in cancer. Transforms gene + variant input into actionable precision oncology report covering clinical evidence,therapeutic options,resistance mechanisms,clinical trials,、 prognostic implications。
  • KEY PRINCIPLES:1. Report-first approach - Create report file FIRST,then populate progressively 2. Evidence-graded - Every recommendation has evidence tier (T1-T4) 3. Actionable output - Prioritized treatment options,not data dumps 4. Clinical focus - Answer "what should we treat ,支持?" not "what databases exist?" 5. Resistance-aware - Always check ,用于 known resistance mechanisms 6. Cancer-type specific - Tailor all recommendations to patient's cancer type when provided 7. Source-referenced - Every statement must cite tool/database source 8. English-first queries - Always use English terms in tool calls (gene names,drug names,cancer types),even if user writes in another language. Respond in user's language。
  • Date:{date} Cancer Type:{cancer_type 或 "Not specified"}。

原始文档

SKILL.md 摘录

When to Use

Apply when user asks:

  • "What treatments exist for EGFR L858R in lung cancer?"
  • "Patient has BRAF V600E melanoma - what are the options?"
  • "Is KRAS G12C targetable?"
  • "Patient progressed on osimertinib - what's next?"
  • "What clinical trials are available for PIK3CA E545K?"
  • "Interpret this somatic mutation: TP53 R273H"
  • "Molecular tumor board: EGFR exon 19 deletion, NSCLC"

Input Parsing

Required: Gene symbol + variant notation Optional: Cancer type (improves specificity)

Accepted Input Formats

FormatExampleHow to Parse
Gene + amino acid changeEGFR L858Rgene=EGFR, variant=L858R
Gene + HGVS proteinBRAF p.V600Egene=BRAF, variant=V600E
Gene + exon notationEGFR exon 19 deletiongene=EGFR, variant=exon 19 deletion
Gene + fusionEML4-ALK fusiongene=ALK, variant=EML4-ALK
Gene + amplificationHER2 amplificationgene=ERBB2, variant=amplification
Full query with cancer"EGFR L858R in lung adenocarcinoma"gene=EGFR, variant=L858R, cancer=lung adenocarcinoma

适用场景

  • 适合在oncologists,molecular tumor boards,或 researchers ask about treatment options ,用于 specific cancer mutations,resistance mechanisms,或 clinical trial matching时使用。

不适用场景

  • Do not rely on this catalog entry alone ,用于 installation 或 maintenance details。

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