6.2K skills · sorted by relevance
Audit instructions and memory files loaded on every agent turn. Identify repeated rules, contradictions, outdated content, and material better moved into skills, then receive evidence-backed recommendations ranked by estimated token savings and change risk.
Create and audit the files and routines that guide coding agents across sessions. It organizes instructions, progress tracking, verification, scope boundaries, and handoffs, with scripts for setup, structural checks, and shareable assessment reports.
Generate README.md and DESIGN.md outlines by inspecting a module's files, language, and dependencies. Python analysis also extracts classes, functions, and docstrings, providing a starting point for usage documentation and design records that you complete afterward.
Optimize .NET loops with SIMD, which processes multiple values in one operation, or review existing SIMD code. Check behavioral equivalence, memory safety, platform fallbacks, and benchmarks to establish whether the optimization is correct and worthwhile.
Validate DESIGN.md files against the official Google specification using the `@google/design.md` CLI linter. Works with local files. Use when the user wants to lint a DESIGN.md, check spec compliance, find broken token references, verify WCAG contrast ratios, diff two versions, export tokens to Tailwind or DTCG format, or audit a design system file for structural correctness. Trigger on mentions of "validate DESIGN.md", "lint DESIGN.md", "check my design.md", "design.md spec compliance", "WCAG contrast check", "broken token references", "design token validation", "export design tokens", "diff design systems", "design.md audit", "@google/design.md", "npx design.md lint", "design system validation", "frontmatter tokens", or any request to verify a DESIGN.md file.
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既存のスライド・画像・WebサイトからデザインシステムSLIDE.mdと6ページのHTMLサンプルスライドを生成する。「このスライドのデザインシステムを作って」「SLIDE.mdを生成して」「SLIDE.mdを作りたい」「このサイトのデザインでSLIDE.mdを生成して」「slide-md-creator」と言われたときに使用する。
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Create or revise agent skills by defining when they run, what they produce, and how their files are organized. Validate SKILL.md settings, resource links, and changed helper scripts before completing the work.
Compress memory files and task lists into shorter wording to reduce input tokens. Keeps code and document structure intact, saves a readable backup separately, and sends the text to the configured model provider.
Convert human-written CLAUDE.md instructions into a structured label format for AI agents. Use it to review lengthy rules, reduce instruction overhead, and prepare prompts for migration between AI tools while preserving the intended rules.
Review CLAUDE.md files, which provide project instructions to Claude Code. Receive a scored quality report covering commands, structure, and outdated guidance, then approve focused edits that keep the instructions concise and useful.
Create, debug, and maintain Windows batch scripts for file operations, backups, and scheduled tasks. Covers command arguments, variables, loops, and error handling, with starter templates for command-line tools and reusable functions.
Move legacy NanoClaw memory and Claude auto-memory into a shared structure used across providers. The skill separates lasting facts from standing instructions, updates indexes, records each file's outcome, and verifies recall after approval.
Upload model weights to Hugging Face Hub with an OpenMDW 1.1 license and a required research warning. Check the published README and license file after uploading or updating to confirm that the required information is present.
Direct TMDL file authoring and BIM-to-TMDL conversion for semantic models in PBIP projects. Automatically invoke when the user asks to "edit TMDL", "add a measure in TMDL", "TMDL syntax", "fix formatString", "fix summarizeBy", "TMDL indentation", "convert BIM to TMDL", "add a column description", "create a calculated column in TMDL", or mentions .tmdl file editing or BIM-to-TMDL migration.
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Reconstructed reference notes on EU and UK medical-device software, built from six sources captured 2026-10-13: MDCG 2019-11 rev.1 (June 2025), MDCG 2020-6 (April 2020), MDCG 2020-13 (July 2020), MDCG 2020-7 (April 2020), MDCG 2020-8 (April 2020), and the MHRA software-applications guidance (2023-07-01) with its stand-alone software PDF. Use for SaMD qualification and classification, legacy-device clinical evidence, the clinical evaluation assessment report, the PMCF plan, and the PMCF evaluation report, under EU MDCG guidance or UK MHRA guidance. SCOPE LIMITS: EU MDR and UK MHRA device software only; no IEC 62304, ISO 13485, or ISO 14971 text; no MDR or IVDR regulation body text; MDCG guidance is not legally binding; MHRA guidance is UK-specific; synthesized notes, not legal advice. LICENCE: Per-document: European Commission reuse policy (Decision 2011/833/EU, CC BY 4.0, attribution and indication of changes) for the MDCG documents; Open Government Licence v3.0 for the MHRA guidance; reconstructed notes with attribution; official PDFs not redistributed.
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ディレクトリ・レイヤーごとに置いた CLAUDE.md と README.md が実体 (コード・コマンド・構成) とずれていないかを点検し、裏の取れた乖離だけを直す。引数で対象のディレクトリを任意に指定できる (省略時は repo 全体)。「CLAUDE.md を refresh して」「README が古くないか見て」「claude-md-refresh」「/claude-md-refresh」で発火。issues/ の更新漏れは issue-writeback / issue-sync の担当で、この skill は扱わない。
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Design an OpenClaw agent persona from preferences or random draws. Build a consistent background, personality, behavioral boundaries, name, SOUL.md and IDENTITY.md files, plus an avatar prompt, with optional image generation through an approved skill.
Turn screenshots, reference links, and rough visual preferences into a reusable DESIGN.md, a record of design decisions, and practical handoff instructions for building prototypes, presentations, redesigns, or image remixes.
Documents a codebase with linked AGENTS.md files that explain each directory, important files, dependencies, and working rules. It can also update existing documentation while preserving human-written notes and checking that the document hierarchy remains consistent.
Review an agent’s role, communication style, user profile, and boundaries through an interview. It records the user’s exact answers in a shared store, then regenerates the relevant identity files after the user reviews and confirms those answers.
Supports preparation for EU medical device regulation reviews by organizing device classification, technical documentation, clinical evidence, and post-market monitoring. Includes a tool to identify documentation and compliance gaps and prioritize the next steps.
Review past Claude Code sessions and turn recurring tasks into proposed updates to skills and project memory. Replay tasks, compare scores on separate validation tasks, and review staged edits before applying them with backups.
Extract decisions, lessons, recurring patterns, and unexpected findings from the artifacts of a completed development phase. It organizes these learnings into a LEARNINGS.md file using planning, summary, verification, acceptance testing, and state documents.
Search HMDB for metabolites, proteins, diseases, or pathways and receive concise Markdown summaries. Keep searches focused on one category, with an option to save the full response when more detail is needed.