「document」の検索結果

Fetches current, version-specific library documentation and code examples through the Context7 MCP server. Use whenever the user asks about a library, framework, SDK, API, CLI tool, or cloud service, including API syntax, configuration, setup instructions, version migration, CLI usage, and library-specific debugging. Use when generating code that calls a third-party library, and when the user names a version such as Next.js 16 or React 19. Use even for well-known libraries like React, Vue, Next.js, Prisma, Supabase, Express, Tailwind, Django, and Spring Boot, because training data may not reflect recent changes. Prefer this over web search for library documentation. Do not use it for refactoring, writing scripts from scratch, debugging business logic, code review, or general programming concepts, or when the user has already supplied the relevant documentation.

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Azure AI Document Intelligence SDK for .NET. Extract text, tables, and structured data from documents using prebuilt and custom models.

日本語の概要は準備中です。原文の説明を表示しています。

API documentation workflow for generating OpenAPI specs, creating developer guides, and maintaining comprehensive API documentation.

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AI-powered presentation generation via the 2slides API — create slides from text, match a reference image style, summarize documents into decks, add AI voice narration, and export pages/audio. Use for any "make slides", "create a deck", or "slides from this document" request.

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Creates task-oriented technical documentation with progressive disclosure. Use when writing READMEs, API docs, architecture docs, or markdown documentation. Also use this skill at the END of any completed reverse engineering, penetration testing, CTF, or security analysis task to generate a formal report in the user's project directory. Trigger keywords: 写报告, 写文档, 出报告, writeup, 技术文档, report, documentation.

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Generate comprehensive, accurate API documentation from source code. Use when creating or updating API documentation, generating OpenAPI specs, or when users mention API docs, endpoints, or documentation.

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Use when writing technical documentation that needs to be readable by both humans and AI models, converting existing docs to HADS format, validating a HADS document, or optimizing documentation for token-efficient AI consumption.

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Compile one or more OpenViking knowledge bases or document collections into topic-organized, evidence-grounded high-level knowledge, including cross-source findings, trends, changes, drivers, comparisons, implications, and uncertainties. Use with ov compile when the user asks to distill or synthesize a knowledge base, compare multiple collections, or derive higher-order insights such as changes across financial reports; do not use for document-by-document summaries.

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Discover and inventory shadow API endpoints that operate outside documented OpenAPI/Swagger specs, using traffic analysis against API gateways (Kong, AWS API Gateway, Envoy), cloud configuration scanning, and source code repository mining for undocumented routes. Use when assessing API attack surface, auditing for forgotten test environments or deprecated API versions still running, or building an API registration governance policy.

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Analyzes malicious PDF files using PDFiD, pdf-parser, and peepdf to identify embedded JavaScript, shellcode, exploits, and suspicious objects without opening the document. Determines the attack vector and extracts embedded payloads for further analysis. Activates for requests involving PDF malware analysis, malicious document analysis, PDF exploit investigation, or suspicious attachment triage.

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Generate architecture documentation using C4 model Mermaid diagrams. Use when asked to create architecture diagrams, document system architecture, visualize software structure, create C4 diagrams, or generate context/container/component/deployment diagrams. Triggers include "architecture diagram", "C4 diagram", "system context", "container diagram", "component diagram", "deployment diagram", "document architecture", "visualize architecture".

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Data framework for building LLM applications with RAG. Specializes in document ingestion (300+ connectors), indexing, and querying. Features vector indices, query engines, agents, and multi-modal support. Use for document Q&A, chatbots, knowledge retrieval, or building RAG pipelines. Best for data-centric LLM applications.

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Use this skill any time a .docx file is involved -- as input, output, or both. This includes: creating Word documents, reports, letters, memos, or proposals; reading, parsing, or extracting text from any .docx file; editing, modifying, or updating existing documents; working with templates, tracked changes, comments, headers/footers, or tables of contents. Trigger whenever the user mentions 'Word doc', 'document', 'report', 'letter', 'memo', or references a .docx filename.

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Convert an attached Word document, presentation, spreadsheet, OpenDocument file, RTF, EPUB, CSV, or text-based PDF into local Markdown. Use when a message supplies a local attachment path that must be read without uploading it to an external parser.

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Write and maintain technical documentation. Trigger with "write docs for", "document this", "create a README", "write a runbook", "onboarding guide", or when the user needs help with any form of technical writing — API docs, architecture docs, or operational runbooks.

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Senior Regulatory Affairs Manager for HealthTech and MedTech companies. Prepares FDA 510(k), De Novo, and PMA submission packages; analyzes regulatory pathways for new medical devices; drafts responses to FDA deficiency letters and Notified Body queries; develops CE marking technical documentation under EU MDR 2017/745; coordinates multi-market approval strategies across FDA, EU, Health Canada, PMDA, and NMPA; and maintains regulatory intelligence on evolving standards. Use when users need to plan or execute FDA submissions, navigate 510(k) or PMA approval processes, achieve CE marking, prepare pre-submission meeting materials, write regulatory strategy documents, respond to agency queries, or manage compliance documentation for medical device market access.

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ISO 13485 Quality Management System implementation and maintenance for medical device organizations. Provides QMS design, documentation control, internal auditing, CAPA management, and certification support. Use when working with medical device quality systems, preparing for ISO 13485 audits, managing regulatory compliance documentation, setting up corrective actions, or building audit preparation programs. Useful for quality management, audit preparation, regulatory compliance, medical device documentation, and corrective action workflows.

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The method for finding the gap between what a system is supposed to do and what the code actually does — the class of bug generic scanners miss because they have no model of intent. Defines what counts as documented intent, what counts as implementation evidence, which mismatches matter, and how to avoid hand-wavy findings. Use when auditing AI-built code, reviewing access control against documented permissions, or checking whether a codebase matches its own documentation.

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Convert Word (.doc, .docx), PowerPoint (.ppt, .pptx), Excel (.xls, .xlsx), OpenDocument (.odt, .ods, .odp), RTF, EPUB, CSV, and PDF files to GitHub-Flavored Markdown. Use when a task needs the contents of an office document, spreadsheet, presentation, ebook, or PDF you cannot read directly.

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Convert Word (.doc, .docx), PowerPoint (.ppt, .pptx), Excel (.xls, .xlsx), OpenDocument (.odt, .ods, .odp), RTF, EPUB, CSV, and PDF files to GitHub-Flavored Markdown. Use when a task needs the contents of an office document, spreadsheet, presentation, ebook, or PDF you cannot read directly.

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Writes the missing CARLA documentation that the audit found — Python API entries in PythonAPI/docs/*.yml, sensors in ref_sensors.md, catalogue actors, broken links and nav entries — one audit category at a time, in CARLA's house style. Use when the user asks to "document this feature", "write the docs for X", "fix the audit findings", or names a category such as "the Python API part".

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Data framework for building LLM applications with RAG. Specializes in document ingestion (300+ connectors), indexing, and querying. Features vector indices, query engines, agents, and multi-modal support. Use for document Q&A, chatbots, knowledge retrieval, or building RAG pipelines. Best for data-centric LLM applications.

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Tabular review — one row per document, one column per data point, every cell cited to source. Built for M&A diligence ("review these 200 target contracts for change-of-control, assignment, and MAC clauses") but works for any batch review that needs a spreadsheet out the other end. Use when user says "tabular review", "review grid", "build a grid", "extract these fields from these contracts", "review these documents for X, Y, Z", "give me a spreadsheet of", "batch review", or points at a folder of documents and asks to compare them.

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Add data to an open investigation — documents, interview notes, or observations. Processes batches against the documented pull criteria, surfaces significant items, and logs everything reviewed for coverage verification. Use when new evidence, interview notes, or document productions come in for an open investigation.

日本語の概要は準備中です。原文の説明を表示しています。