Agent skill

Scholargraph Fusion Genes

by LeoYeAI in LeoYeAI/openclaw-master-skills

使用 ScholarGraph v1.4 及以上版本 进行癌症融合基因文献调研的全流程技能。包括搜索、多轮合并去重、提取信息、生成报告和 Excel 表格。

MITAuto-check: notesDocuments & Office

Install Scholargraph Fusion Genes

skills CLI
$ npx skills add LeoYeAI/openclaw-master-skills --skill scholargraph-fusion-genes -a claude-code

Project install by default; add -g for ~/.claude/skills/.

GitHub CLI
$ gh skill install LeoYeAI/openclaw-master-skills scholargraph-fusion-genes --agent claude-code

Project scope by default; add --scope user for a personal install. Needs GitHub CLI 2.90.0 or later (public preview).

Manual copy
$ git clone --depth 1 https://github.com/LeoYeAI/openclaw-master-skills.git skills-src && mkdir -p .claude/skills && cp -r skills-src/skills/scholargraph-cancer-fusiongenes-research-flow .claude/skills/scholargraph-fusion-genes && rm -rf skills-src

Use ~/.claude/skills/ instead of .claude/skills for a personal install. The folder must contain SKILL.md.

Claude Code skills documentation · loads skills from .claude/skills/

Facts

Skill name
scholargraph-fusion-genes
GitHub stars
2.2k
Token cost
~3.2k tokens
SKILL.md length
445 words
Files
5
Skills in repo
1,235
Repo updated
First seen
Licence
MIT

At a glance

使用 ScholarGraph v1.4 及以上版本 进行癌症融合基因文献调研的全流程技能。包括搜索、多轮合并去重、提取信息、生成报告和 Excel 表格。

  • Works in 3 steps: 确定癌种范围 → 针对性搜索命令 → 临床意义深度挖掘
  • Tasks that involve Excel spreadsheets
  • SKILL.md covers 概述, 适用场景, 完整工作流程 and Excel 表格规范, plus 6 more sections
  • Runs JavaScript scripts from its folder; calls bun, node and curl; reaches europepmc.org and api.minimaxi.com; needs MINIMAX_API_KEY and SERPER_API_KEY

What it does

Scholargraph Fusion Genes is an agent skill from LeoYeAI/openclaw-master-skills. 使用 ScholarGraph v1.4 及以上版本 进行癌症融合基因文献调研的全流程技能。包括搜索、多轮合并去重、提取信息、生成报告和 Excel 表格。

Its SKILL.md is about 3.2k tokens, which your agent loads only when the skill is triggered. The skill folder holds 4 other files (for example `FLOW.md`, `_meta.json` and `generate_excel_template.js`).

It sits in Documents & Office, covering Excel spreadsheets. It works with Microsoft Excel. The repository describes itself as: 🧠 Curated collection of 1209+ best OpenClaw skills — weekly updated by MyClaw.ai. The licence is MIT.

When your agent uses it

  • Tasks that involve Excel spreadsheets

Example prompts

  • “/scholargraph-fusion-genes”

Requirements

  • Node.js
  • A credential in MINIMAX_API_KEY
  • A credential in SERPER_API_KEY

Workflow steps

3 steps, taken from the step headings in SKILL.md.

  1. 确定癌种范围
  2. 针对性搜索命令
  3. 临床意义深度挖掘

What it can do on your machine

Read from SKILL.md and the folder at commit e5199b5. It shows what the files ask for, not the result of running them.

  • Tool permissions

    Pre-approves nothing: there is no allowed-tools line, so your agent's usual permission prompts apply.

    From allowed-tools in the SKILL.md frontmatter.

  • Runs code

    Ships script files (JavaScript), which the agent can run.

    Shell commands in SKILL.md call:

    • bun
    • node
    • curl
    • npm

    From the folder's file list and the shell code blocks in SKILL.md.

  • Network

    Hosts in commands or code, which the agent is likely to contact:

    • europepmc.org
    • api.minimaxi.com

    From URLs in SKILL.md, links to its own repository left out.

  • Credentials

    Names these keys or tokens, usually read from environment variables:

    • MINIMAX_API_KEY
    • SERPER_API_KEY

    From names ending in _API_KEY, _TOKEN, _SECRET, _KEY or _PASSWORD in SKILL.md.

Context cost

Scholargraph Fusion Genes loads about 3.2k tokens when it runs. Until then it costs about 26 tokens; SKILL.md has 445 words of instructions outside code blocks.

Always · name and description, kept in context so the agent knows when to use it
~26
When it runs · the whole SKILL.md, loaded when a task matches
~3.2k

Estimates: characters ÷ 4, the usual rule of thumb; real counts depend on the model's tokenizer. Scripts and assets cost tokens only if the agent reads them.

Safety

Auto-check: notes

The automated check noted patterns worth knowing about, such as sudo or a known installer.

  • NoteMentions a .env fileSKILL.md:346
    在 `ScholarGraph/.env` 文件中配置:

Automated static check — not a guarantee. Review scripts before installing. It scans the text of SKILL.md for risky patterns (piping downloads into a shell, reading credential files, hidden Unicode, destructive commands); files beside SKILL.md are not scanned.

SKILL.md

The full file from LeoYeAI/openclaw-master-skills at commit e5199b5, republished under its MIT licence (© LeoYeAI). 445 words, ~3,224 tokens.

Download SKILL.mdSave it as .claude/skills/scholargraph-fusion-genes/SKILL.md (or your agent's skills folder). This skill also uses 4 other files; get the full folder from GitHub.
name
scholargraph-fusion-genes
description
使用 ScholarGraph v1.4 及以上版本 进行癌症融合基因文献调研的全流程技能。包括搜索、多轮合并去重、提取信息、生成报告和 Excel 表格。

ScholarGraph-FusionGenes 使用流程

概述

本技能提供癌症融合基因文献调研的完整流程,使用 ScholarGraph v1.4 及以上版本 进行系统性搜索、分析和整理。支持多轮搜索、合并去重、生成含完整参考文献的 Excel 表格。

适用场景

  • 癌症融合基因文献调研
  • 融合探针设计区域分析
  • 靶向治疗生物标志物研究

完整工作流程

步骤 1: 环境配置
bash
# 1. 进入 ScholarGraph 目录
cd /root/.openclaw/workspace/skills/ScholarGraph

# 2. 配置 MiniMax API Key (或使用其他 provider)
export AI_PROVIDER=minimax
export MINIMAX_API_KEY="your-api-key"

# 3. 验证配置
~/.bun/bin/bun run cli.ts --help
步骤 2: 第一轮文献搜索
bash
# 创建工作目录
mkdir -p /workspace/research/fusion/review
mkdir -p /workspace/research/fusion/reports

# 第一轮: 搜索各癌种融合基因 review
~/.bun/bin/bun run cli.ts search "lung cancer fusion gene review" --limit 10
~/.bun/bin/bun run cli.ts search "breast cancer fusion gene review" --limit 10
~/.bun/bin/bun run cli.ts search "colorectal cancer fusion gene review" --limit 10
~/.bun/bin/bun run cli.ts search "solid tumor fusion gene review" --limit 10
步骤 3: 深度分析 - 搜索融合基因详细信息
bash
# 搜索特定基因的融合信息 (并行执行)
~/.bun/bin/bun run cli.ts search "EML4-ALK fusion variant V1 V2 V3 breakpoint" --limit 10
~/.bun/bin/bun run cli.ts search "ROS1 fusion partner CD74 SDC4 TPM3" --limit 10
~/.bun/bin/bun run cli.ts search "RET fusion KIF5B CCDC6 NCOA4 breakpoint" --limit 10
~/.bun/bin/bun run cli.ts search "NTRK1 NTRK2 NTRK3 fusion partner ETV6" --limit 10
~/.bun/bin/bun run cli.ts search "FGFR fusion partner TACC3 BICC1" --limit 10
~/.bun/bin/bun run cli.ts search "NRG1 fusion CD74 SDC4 cancer" --limit 10
步骤 4: 获取 PDF 文献
bash
# 使用 Europe PMC 下载免费文献 (推荐)
# 搜索 PMID 后访问: https://europepmc.org/articles/PMC[ID]?pdf=render
curl -L -o "/workspace/research/fusion/review/filename.pdf" "https://europepmc.org/articles/PMC[ID]?pdf=render"

# 或使用 ScholarGraph download (需配置 SERPER_API_KEY)
~/.bun/bin/bun run cli.ts download "RET fusion cancer review" --limit 3 --output /workspace/research/fusion/review
步骤 5: 第二轮补充搜索 (发现遗漏)
bash
# 补充搜索可能遗漏的融合基因
~/.bun/bin/bun run cli.ts search "EGFRvIII glioma fusion deletion" --limit 5
~/.bun/bin/bun run cli.ts search "ESR1 fusion breast cancer endocrine resistance" --limit 5
~/.bun/bin/bun run cli.ts search "BRAF fusion KIAA1549 melanoma" --limit 5
~/.bun/bin/bun run cli.ts search "MET fusion CAPZA2 LAYN lung cancer" --limit 5
~/.bun/bin/bun run cli.ts search "ALK fusion HIP1 KIF5B non-EML4" --limit 5
步骤 6: 多轮搜索结果合并去重

将多轮搜索结果保存到 JSON 文件,然后进行合并去重:

javascript
// merge_results.js
const fs = require('fs');

// 假设有两轮搜索结果
const round1 = require('./round1.json');
const round2 = require('./round2.json');

// 合并去重函数
function mergeAndDeduplicate(results1, results2) {
  const seen = new Map();
  const merged = [];
  
  for (const item of [...results1, ...results2]) {
    // 根据基因+融合伙伴作为唯一标识
    const key = `${item.gene}-${item.fusion}`;
    if (!seen.has(key)) {
      seen.set(key, true);
      merged.push(item);
    }
  }
  return merged;
}

const merged = mergeAndDeduplicate(round1, round2);
fs.writeFileSync('./merged_results.json', JSON.stringify(merged, null, 2));
console.log(`Merged: ${merged.length} unique records`);
步骤 7: 生成 Excel 表格 (含完整字段)
bash
# 安装 xlsx 库
npm install xlsx

创建 generate_excel.js:

javascript
const XLSX = require('xlsx');

// ========== 辅助函数 ==========

// 频率级别标签逻辑
function getFreqLabel(freq) {
  // 特殊情况: EGFR扩增等
  if (freq.includes('EGFR扩增')) return '-';
  
  // 提取所有数字
  const nums = freq.match(/\d+/g)?.map(Number) || [];
  if (nums.length === 0) return '-';
  
  // 取最大值进行判断
  const maxVal = Math.max(...nums);
  
  // 频率级别判断
  if (maxVal >= 25) return '高';    // ≥25%: 高频率
  if (maxVal >= 10) return '中';    // 10-24%: 中频率
  if (maxVal >= 3) return '低';     // 3-9%: 低频率
  return '极低';                     // <3%: 极低频率
}

// 参考文献数量统计
function countSources(ref) {
  if (!ref) return 0;
  const sources = ref.split(/;\s*/).filter(s => s.trim().length > 0);
  return sources.length;
}

// 标准转录本映射
const transcriptMap = {
  'ALK': 'NM_004935',
  'ROS1': 'NM_002944',
  'RET': 'NM_020975',
  'NTRK1': 'NM_002529',
  'NTRK2': 'NM_006180',
  'NTRK3': 'NM_002449',
  'MET': 'NM_000245',
  'FGFR1': 'NM_023110',
  'FGFR2': 'NM_000141',
  'FGFR3': 'NM_001142',
  'NRG1': 'NM_013962',
  'BRAF': 'NM_004333',
  'EGFR': 'NM_005228',
  'ESR1': 'NM_000125',
};

// ============================

// 完整数据格式 - 每行独立完整
// 字段: 基因, 融合类型, 变体, 融合转录本, 参考基因组, 5'基因, 5'基因断裂位置, 3'基因, 3'基因断裂位置, 频率, 癌种, 临床意义, 靶向药物, 参考文献
const fusionData = [
  // 示例:
  { 
    "基因": "ALK", 
    "融合类型": "EML4-ALK", 
    "变体": "V1",
    "融合转录本": "NM_004935",
    "参考基因组": "GRCh37",
    "5'基因": "EML4", 
    "5'基因断裂位置": "exon 13", 
    "3'基因": "ALK", 
    "3'基因断裂位置": "exon 20",
    "频率": "~33%", 
    "癌种": "肺癌", 
    "临床意义": "标准型", 
    "靶向药物": "Crizotinib; Alectinib", 
    "参考文献": "Zhang SS, et al. Going beneath the tip of the iceberg... Lung Cancer. 2021; PMID: 34175504"
  },
  // ... 更多记录
];

// 添加频率级别和参考文献数
const enrichedData = fusionData.map(item => ({
  ...item,
  "频率级别": getFreqLabel(item["频率"]),
  "参考文献数": countSources(item["参考文献"])
}));

const wb = XLSX.utils.book_new();

// Sheet 1: 融合基因汇总
const mainSheet = XLSX.utils.json_to_sheet(enrichedData);
XLSX.utils.book_append_sheet(wb, mainSheet, "融合基因汇总");

// Sheet 2: 探针设计推荐
const probeData = [
  { "基因": "ALK", "DNA探针区域": "intron 19", "RNA探针区域": "exon 18-21", "探针长度": "300-500bp", "备注": "覆盖所有变体" },
  { "基因": "ROS1", "DNA探针区域": "intron 31-35", "RNA探针区域": "exon 32-36", "探针长度": "400-600bp", "备注": "覆盖常见融合伙伴" },
  // ...
];
const probeSheet = XLSX.utils.json_to_sheet(probeData);
XLSX.utils.book_append_sheet(wb, probeSheet, "探针设计推荐");

// Sheet 3: 分癌种汇总
const cancerSummary = [
  { "癌种": "肺癌", "融合数": 15, "主要基因": "ALK, ROS1, RET, MET" },
  { "癌种": "乳腺癌", "融合数": 3, "主要基因": "ESR1, NTRK" },
  // ...
];
const cancerSheet = XLSX.utils.json_to_sheet(cancerSummary);
XLSX.utils.book_append_sheet(wb, cancerSheet, "分癌种汇总");

// 保存文件
XLSX.writeFile(wb, '/workspace/research/fusion/reports/fusion_genes_report.xlsx');

运行生成:

bash
node generate_excel.js

Excel 表格规范

频率级别标签逻辑

⚠️ 重要: 每行必须包含独立完整的频率级别,不依赖其他行

javascript
// 频率级别判断函数
function getFreqLabel(freq) {
  // 特殊情况: EGFR扩增等
  if (freq.includes('EGFR扩增')) return '-';
  
  // 提取所有数字
  const nums = freq.match(/\d+/g)?.map(Number) || [];
  if (nums.length === 0) return '-';
  
  // 取最大值进行判断
  const maxVal = Math.max(...nums);
  
  // 频率级别判断
  if (maxVal >= 25) return '高';    // ≥25%: 高频率
  if (maxVal >= 10) return '中';    // 10-24%: 中频率
  if (maxVal >= 3) return '低';     // 3-9%: 低频率
  return '极低';                     // <3%: 极低频率
}
频率级别阈值范围示例
高≥25%~33%, ~29%, ~50%, ~70%
中10-24%~15%, ~10%, ~20%
低3-9%~5%, ~8%, ~3%
极低<3%<1%, ~2%
-特殊EGFRvIII (~50% EGFR扩增)
参考文献格式要求

⚠️ 重要: 每行参考文献必须独立完整,不依赖其他行信息

✅ 正确格式:

text
参考文献: Zhang SS, et al. Going beneath the tip of the iceberg: Identifying and understanding EML4-ALK variants and TP53 mutations. Lung Cancer. 2021; PMID: 34175504; Christopoulos P, et al. EML4-ALK fusion variant V3 is a high-risk feature. Clin Cancer Res. 2018

❌ 错误格式 (依赖其他行):

text
参考文献: 同上
参考文献: 同V3a
字段说明 (Sheet 1: 融合基因汇总 - 16列)
字段说明示例
基因融合基因名称ALK, ROS1, RET
融合类型完整融合名称EML4-ALK, CD74-ROS1
变体变体信息 (如V1/V3)V1, V3a, -
融合转录本标准转录本IDNM_004935
参考基因组基因组版本GRCh37
5'基因5'端伙伴基因EML4, CD74
5'基因断裂位置断裂位置(必须包含exon/intron)exon 13, intron 6
3'基因3'端基因ALK, ROS1
3'基因断裂位置断裂位置(必须包含exon/intron)exon 20, intron 31
频率发生频率~33%, ~10-15%
频率级别自动计算高/中/低/极低
癌种关联癌种肺癌, 泛癌种
临床意义临床意义描述最常见, 耐药
靶向药物靶向药物 (分号分隔)Crizotinib; Alectinib
参考文献完整引用 (作者; 作者; 期刊. 年份; PMID)见格式规范
参考文献数自动统计来源数量1, 2
癌种关联癌种肺癌, 泛癌种
临床意义临床意义描述最常见, 耐药
靶向药物靶向药物Crizotinib; Alectinib
参考文献完整引用信息见上文格式

关键命令速查

功能命令
搜索文献bun run cli.ts search "关键词" --limit 10
下载 PDFbun run cli.ts download "关键词" --limit 5 --output ./downloads
学习概念bun run cli.ts learn "概念" --depth intermediate
分析论文bun run cli.ts analyze "论文URL" --mode deep
构建知识图谱bun run cli.ts graph 概念1 概念2 --format mermaid
生成 Excelnode generate_excel.js

配置说明

MiniMax API 配置

在 ScholarGraph/.env 文件中配置:

bash
AI_PROVIDER=minimax
MINIMAX_API_KEY=sk-cp-xxx
MINIMAX_BASE_URL=https://api.minimaxi.com/v1
MINIMAX_MODEL=MiniMax-M2.5
注意事项
  1. API 限制: Semantic Scholar 有 429 速率限制,建议使用 PubMed/OpenAlex 源
  2. PDF 下载: 大多数期刊 DOI 需要订阅,可尝试 Europe PMC 获取免费文献
  3. 文献审核: 报告中所有数据应标注参考文献,便于人工核实
  4. Excel 规范: 每行参考文献必须独立完整,使用分号分隔多来源

Show full SKILL.md (178 more words)Show less

输出文件结构

/workspace/research/fusion/
├── review/                    # PDF 文献
│   ├── 01_Drug_resistance_2021.pdf
│   ├── 02_TNBC_molecular_mechanisms_2022.pdf
│   └── ...
├── reports/                  # 分析报告
│   ├── fusion_probe_design_report_v2.md
│   ├── detection_methods_report.md
│   └── fusion_genes_report.xlsx    # 主输出
├── round1.json               # 第一轮搜索结果
├── round2.json                # 第二轮搜索结果
├── merged_results.json       # 合并去重后结果
└── generate_excel.js         # Excel 生成脚本

常见问题

Q1: ScholarGraph learn/analyze 报错

A: 检查 API Key 是否正确配置,或尝试使用其他 provider

Q2: PDF 下载失败 (403/406)

A: 大多数期刊需要订阅,使用 Europe PMC 作为备选

Q3: Semantic Scholar 429 错误

A: 使用 --source pubmed 或 --source openalex 绕过

Q4: Excel 参考文献格式问题

A: 确保每行独立完整,不使用"同上"或"同V3a"等依赖表述


更新日志

  • 2026-03-06: 初始版本,包含完整流程
  • 2026-03-06 v2: 增加多轮搜索合并去重逻辑,更新 Excel 参考文献格式规范
  • 2026-03-07 v3: 新增"教授级深度搜索"方法论

教授级深度搜索方法论

核心理念

教授级搜索不仅是找文献,而是系统性构建知识体系。核心原则:

  1. 按癌种分类 - 不是按基因,而是按临床应用场景组织
  2. 证据分级 - 从临床意义角度解读,不只是罗列基因
  3. 可追溯 - 每条信息标注 PMID,便于溯源核实
  4. 新发现优先 - 关注近1-2年的新融合、新靶点
搜索策略
Step 1: 确定癌种范围

根据研究目的确定重点癌种:

优先级癌种常见融合基因
高肺癌EML4-ALK, ROS1融合, RET, MET, NTRK
高结直肠癌RSPO融合, NTRK, ALK
高乳腺癌ESR1, NTRK, ETV6-NTRK3
中胆管癌FGFR2融合, TFG-MET
中胃肠道间质瘤KIT, PDGFRA, NTRK
泛癌实体瘤NTRK1/2/3, BRAF, NRG1
Step 2: 针对性搜索命令

每个癌种执行深度搜索:

bash
# 肺癌融合基因深度搜索
~/.bun/bin/bun run cli.ts search "lung cancer fusion gene 2024 2025" --limit 20
~/.bun/bin/bun run cli.ts search "ROS1 CD74 fusion lung cancer clinical" --limit 10
~/.bun/bin/bun run cli.ts search "EML4-ALK variant V1 V3 breakpoint" --limit 10

# 结直肠癌融合基因
~/.bun/bin/bun run cli.ts search "colorectal cancer fusion gene RSPO Wnt" --limit 15

# 乳腺癌融合基因
~/.bun/bin/bun run cli.ts search "breast cancer fusion gene NTRK ESR1" --limit 15

# 胆管癌/胆囊癌融合
~/.bun/bin/bun run cli.ts search "biliary cancer FGFR2 fusion MET" --limit 15

# 胃肠道间质瘤
~/.bun/bin/bun run cli.ts search "GIST KIT PDGFRA NTRK fusion" --limit 15

# 泛癌种/罕见实体瘤
~/.bun/bin/bun run cli.ts search "solid tumor NTRK fusion basket trial" --limit 15
~/.bun/bin/bun run cli.ts search "NUT carcinoma fusion gene" --limit 10
Step 3: 临床意义深度挖掘

针对每个发现的融合,搜索其临床意义:

bash
# 靶向治疗响应
~/.bun/bin/bun run cli.ts search "[融合名] TKI response targeted therapy" --limit 5

# 耐药机制
~/.bun/bin/bun run cli.ts search "[融合名] resistance crizotinib alectinib" --limit 5

# 诊断价值
~/.bun/bin/bun run cli.ts search "[融合名] diagnostic biomarker" --limit 5

# 预后意义
~/.bun/bin/bun run cli.ts search "[融合名] prognosis survival" --limit 5
输出格式规范

教授级搜索结果必须采用以下格式:

格式要求
## [癌种名称] (英文)

| 融合 | 临床意义 | PMID |
| ---- | -------- | ---- |
| [融合名称1] | [具体临床意义描述] | [PMID1] |
| [融合名称2] | [具体临床意义描述] | [PMID2] |
示例输出
肺癌 (Lung Cancer)

| 融合 | 临床意义 | PMID |
| ----------- | --------------------- | -------- |
| ROS1-CD74 | 新融合伙伴,部分TKI有效 | 36387218 |
| HIPK2::YAP1 | 肺纤维瘤病新实体 | 38714933 |
| BRAF融合变异体 | DNA+RNA测序揭示结构 | 40253487 |
| ETV6::NTRK3 | 非典型类癌,repotrectinib有效 | 38113652 |

结直肠癌 (Colorectal Cancer)

| 融合 | 临床意义 | PMID |
| ------ | ------- | -------- |
| RSPO融合 | Wnt通路激活 | 35715628 |
| 新型结构变异 | 长读测序发现 | 36812239 |
质量检查清单

在输出最终结果前,检查以下要点:

  • 每条记录包含: 融合名称 + 临床意义 + PMID
  • 临床意义具体明确 (不只是"发现新融合")
  • 包含治疗响应信息 (如TKI药物名称)
  • 标注PMID便于文献追溯
  • 按癌种分类组织,非按基因
  • 新发现优先展示 (近年文献)
  • 表格格式清晰统一
与传统搜索的区别
维度传统搜索教授级搜索
组织方式按基因按癌种/临床场景
信息深度基因+频率融合+临床意义+药物
证据追溯可选必含PMID
时间维度无要求优先新发现
输出格式自由文本标准化表格
进阶技巧
  1. 长读测序发现: 搜索 "long-read sequencing fusion" 发现结构变异
  2. RNA-seq验证: 搜索 "RNA-seq fusion validation" 确认融合转录本
  3. 少见癌种: 使用 "pediatric" + "fusion" 搜索儿童肿瘤
  4. 耐药研究: 重点关注 "resistance" + "fusion" + "TKI"

© LeoYeAI, MIT. Rendered from Markdown: HTML in the file is shown as text, images as links, and headings moved down two levels. Raw file

Files

SKILL.md and 4 other files in skills/scholargraph-cancer-fusiongenes-research-flow of LeoYeAI/openclaw-master-skills.

  • SKILL.md
  • FLOW.md
  • _meta.json
  • generate_excel_template.js
  • merge_results.js

Open the folder on GitHubat commit e5199b5

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Works with

Questions about Scholargraph Fusion Genes

What does Scholargraph Fusion Genes do?

使用 ScholarGraph v1.4 及以上版本 进行癌症融合基因文献调研的全流程技能。包括搜索、多轮合并去重、提取信息、生成报告和 Excel 表格。. Scholargraph Fusion Genes is an agent skill from LeoYeAI/openclaw-master-skills.

When should I use Scholargraph Fusion Genes?

Scholargraph Fusion Genes fits situations like: tasks that involve Excel spreadsheets.

How do I install Scholargraph Fusion Genes in Claude Code?

Run `npx skills add LeoYeAI/openclaw-master-skills --skill scholargraph-fusion-genes -a claude-code`. Or copy the skill folder (skills/scholargraph-cancer-fusiongenes-research-flow in LeoYeAI/openclaw-master-skills) into .claude/skills/scholargraph-fusion-genes in your project. Claude Code loads it when a task matches its description.

How do I install Scholargraph Fusion Genes in Codex?

Run `npx skills add LeoYeAI/openclaw-master-skills --skill scholargraph-fusion-genes -a codex`. Or copy the skill folder (skills/scholargraph-cancer-fusiongenes-research-flow in LeoYeAI/openclaw-master-skills) into .agents/skills/scholargraph-fusion-genes in your project. Codex loads it when a task matches its description.

Can I use Scholargraph Fusion Genes in Cursor, Gemini CLI or GitHub Copilot?

Cursor, Gemini CLI, GitHub Copilot and OpenCode also load SKILL.md folders. With the skills CLI, run `npx skills add LeoYeAI/openclaw-master-skills --skill scholargraph-fusion-genes -a cursor` (or -a gemini-cli, github-copilot or opencode for the others). To copy it by hand, put the folder in .cursor/skills/scholargraph-fusion-genes, .gemini/skills/scholargraph-fusion-genes, .github/skills/scholargraph-fusion-genes and .opencode/skills/scholargraph-fusion-genes in your project.

What does Scholargraph Fusion Genes need to run?

Going by SKILL.md and its folder, Scholargraph Fusion Genes needs JavaScript for the scripts in its folder, the command-line tools its instructions call (bun, node, curl and npm) and credentials named MINIMAX_API_KEY and SERPER_API_KEY. Our summary lists: Node.js; A credential in MINIMAX_API_KEY; A credential in SERPER_API_KEY.

Does Scholargraph Fusion Genes access the network?

SKILL.md names 2 domains. In commands or code: europepmc.org and api.minimaxi.com; the agent is likely to contact these when it follows the instructions. This is read from the text; nothing was executed.

Is Scholargraph Fusion Genes safe to install?

Our automated static check of SKILL.md found notes only (mentions a .env file), nothing it rates as a warning. It is not a guarantee. Review the folder before installing.

What licence does Scholargraph Fusion Genes use?

Scholargraph Fusion Genes is published under the MIT licence (the repository's licence). It allows redistribution, so the full SKILL.md is shown on this page.

How many tokens does Scholargraph Fusion Genes use?

About 3.2k tokens (SKILL.md is roughly 13k characters). Agents keep only the skill's name and description in context until a task matches; then they load SKILL.md in full.

What are the alternatives to Scholargraph Fusion Genes?

Skills that share tags, products or a category with Scholargraph Fusion Genes: Markitdown (ImCa0/just-laws, 781 stars), Data Table Manager (n8n-io/n8n, 207k stars), Docx4j (plutext/docx4j, 2.4k stars) and Instrument Data To Allotrope (aws-samples/amazon-bedrock-agents-healthcare-lifesciences, 274 stars). The comparison table on this page puts their stars, adoption, token cost, safety result and licence side by side.

Who maintains Scholargraph Fusion Genes?

LeoYeAI (a GitHub user) maintains it in LeoYeAI/openclaw-master-skills, which has 2,161 GitHub stars. The repository holds 1,235 skills in this directory. The repository was last updated on July 20, 2026.

Source: LeoYeAI/openclaw-master-skills on GitHub. Facts on this page come from the repository at the commit we read; the author's words are quoted as theirs.