1,585 件 ・ 関連度順
概要と使いどころ
Guide users from zero to their first working mirrord session — check system requirements, install mirrord via CLI, VS Code, or IntelliJ, run a first session against a Kubernetes target, and verify the connection. Use when a user is new to mirrord, wants to install it, needs help running their first session, or wants to debug or test a local process against their Kubernetes cluster.
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。
Inspect or rewrite prose that sounds formulaic while preserving source facts, voice, and format. Use for de-slopping, humanizing, prose audits, or a final writing-quality gate. Do not use it as an authorship detector or to evade disclosure requirements.
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。
Testing conventions, CI pipeline rules, and smoke test coverage for SkillHub. Ensures agents write tests correctly and understand the CI gate requirements.
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。
Write competitive research proposals for NSF, NIH, DOE, and DARPA. Agency-specific formatting, review criteria, budget preparation, broader impacts, significance statements, innovation narratives, and compliance with submission requirements.
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。
Systematic strategic planning framework for philosophy and interdisciplinary academic papers targeting preprint platforms (PhilArchive, arXiv, PhilSci-Archive). Use when users want to: (1) plan a paper on a specific topic, (2) identify research gaps and assess originality, (3) develop optimized paper outlines, (4) prepare for preprint submission, or (5) understand platform requirements and writing standards. Triggered by phrases like 'plan a paper on,' 'help me design a paper about,' 'identify research gaps in,' 'is this idea original,' or when users need structured research planning. The skill guides through three phases: Platform Analysis (identifying target venue and studying sample papers), Theoretical Framework (AI-driven literature search and gap identification), and Outline Optimization (structured design with reviewer-perspective self-assessment). Each phase includes quality evaluation standards and validation checkpoints. Output: optimized detailed outline ready for systematic writing (use with academic-paper-composer skill).
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。
Write competitive research proposals for NSF, NIH, DOE, DARPA, and Taiwan NSTC. Agency-specific formatting, review criteria, budget preparation, broader impacts, significance statements, innovation narratives, and compliance with submission requirements.
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。
Statistical significance calculator for A/B test results with sample size requirements, segment breakdowns, and hypothesis generation. Use when feeding test results, checking statistical significance, calculating sample sizes, analyzing experiment outcomes, or generating next test ideas based on results. Platform: Google and Meta.
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。
Multi-AI requirements scoping using available external providers (Double Diamond Define phase). Priority triggers: octo define, octo scope, co-define, co-scope. DO NOT use for implementation, research, review/validation, or built-in commands.
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。
Use when you have a spec or requirements for a multi-step task, before touching code
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。
You MUST use this before any creative work - creating features, building components, adding functionality, or modifying behavior. Explores user intent, requirements and design before implementation.
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。
Use when completing tasks, implementing major features, or before merging to verify work meets requirements
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。
Generate JSON-LD structured data markup for rich results in Google Search. Supports FAQ, HowTo, Article, Product, LocalBusiness, and multi-type schemas. Validates against Google requirements and provides implementation guidance. Use when asked to "add schema markup", "generate structured data", "JSON-LD", "rich snippets", "FAQ schema", "product markup", "add structured data to my page", "how to get rich snippets", or any structured data task.
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。
Generate implementation tasks from requirements and design. Use when creating actionable task lists.
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。
Analyze implementation gap between requirements and existing codebase
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。
Create complete specs (requirements, design, tasks) for all features in roadmap.md sequentially by dependency wave in Cascade.
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。
Analyze implementation gap between requirements and existing codebase. Use when planning integration with existing systems.
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。
Create complete specs (requirements, design, tasks) for all features in roadmap.md using parallel subagent dispatch by dependency wave.
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。
Create complete specs (requirements, design, tasks) for all features in roadmap.md using parallel sub-agent dispatch by dependency wave.
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。
Use when you have a spec or requirements for a multi-step task, before touching code
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。
Generate custom quality checklists for validating requirements completeness and clarity. Use to create unit tests for English that ensure spec quality before implementation.
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。
Write competitive research proposals for NSF, NIH, DOE, DARPA, and Taiwan NSTC. Agency-specific formatting, review criteria, budget preparation, broader impacts, significance statements, innovation narratives, and compliance with submission requirements.
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。
Structured clarification workflow for underspecified requirements. Use before planning to resolve ambiguities through coverage-based questioning. Records answers in spec clarifications section.
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。
Prepare and request a code review after implementation or before merge by assembling scope, requirements, git range, and reviewer instructions.
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。
Comprehensive toolkit for preparing ISO 13485 certification documentation for medical device Quality Management Systems. Use when users need help with ISO 13485 QMS documentation, including (1) conducting gap analysis of existing documentation, (2) creating Quality Manuals, (3) developing required procedures and work instructions, (4) preparing Medical Device Files, (5) understanding ISO 13485 requirements, or (6) identifying missing documentation for medical device certification. Also use when users mention medical device regulations, QMS certification, FDA QMSR, EU MDR, or need help with quality system documentation.
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。