All Agent Skills
41,263 results
- Infographicmarkdown-viewerCreate template-based infographics with space-separated key-value syntax (NOT YAML). Best for KPI dashboards, timelines, roadmaps, SWOT analysis, funnels, comparisons, and org charts with quick visual impact.
- Iotmarkdown-viewerCreate IoT architecture diagrams using PlantUML syntax with device and sensor stencil icons. Best for smart home, industrial IoT (IIoT), fleet management, edge computing, and sensor network layouts.
- Mermaidmarkdown-viewerCreate flowcharts, sequence diagrams, state machines, class diagrams, Gantt charts, and mindmaps using simple text-based syntax. Best for process flows, API interactions, and technical documentation. NOT for data-driven charts (use vega), quick KPI visuals (use infographic), or layered system architecture (use architecture).
- Mindmapmarkdown-viewerCreate hierarchical mind maps using PlantUML @startmindmap syntax. Best for brainstorming, topic decomposition, study notes, and decision trees with automatic radial layout, left/right branches, and per-node styling.
- Networkmarkdown-viewerCreate network topology diagrams using PlantUML syntax with mxgraph device icons (Cisco, Citrix, etc.). Best for LAN/WAN layouts, datacenter interconnects, and physical/logical network design.
- Securitymarkdown-viewerCreate security architecture diagrams using PlantUML syntax with identity, encryption, firewall, and compliance stencil icons. Best for IAM flows, zero-trust models, encryption pipelines, and threat detection architectures.
- Umlmarkdown-viewerCreate UML diagrams using PlantUML syntax. Best for software modeling — Class, Sequence, Activity, State Machine, Component, Use Case, and Deployment diagrams with concise text-based notation and auto-layout.
- Vegamarkdown-viewerCreate data-driven charts with Vega-Lite (declarative) and Vega (programmatic). Best for statistical visualization of numeric data — bar, line, scatter, heatmap, area, radar charts, and word clouds.
- Prepare Changelognextest-rsGuidelines for preparing changelog entries for nextest releases following Keep a Changelog format
- UltracitehaydenbleaselUltracite is a zero-config linting and formatting preset for JavaScript/TypeScript projects. Use when: (1) Setting up or initializing Ultracite in a project, or migrating its existing lint and format config onto Ultracite (ultracite init), (2) Running linting or formatting commands (check, fix, doctor), (3) Writing or reviewing JS/TS code in a project that uses Ultracite — to follow its code…
- Fluwx IntegrationOpenFlutter在 Flutter App 中接入微信 SDK 插件 fluwx / fluwx_no_pay（v6+）的完整指南：微信分享（会话/朋友圈/收藏）、微信登录（获取 auth code）、微信支付、拉起小程序、订阅消息、微信客服、H5 拉起 App，以及 Android / iOS / OpenHarmony 的平台配置与排错。只要在 Flutter 项目里涉及微信相关功能——分享到微信、微信授权登录、WeChat Pay、universal link、LSApplicationQueriesSchemes、errCode -1、无法拉起微信等——即使用户没有点名 fluwx，也应使用本 skill。
- Alphafold Database Fetch And Analyzegoogle-deepmindRetrieve and analyze AlphaFold predicted structures for a protein. Use when the user provides a specific UniProt Accession ID and wants structural confidence metrics (pLDDT), domain boundary analysis, or disorder assessment. Do not use if the user only has a protein name, gene name, or amino acid sequence — ask for a UniProt ID first.
- Alphagenome Atlas Website Linksgoogle-deepmindConstructs deep-links and URLs for the AlphaGenome Atlas website. Supports generating single-variant exploration links (1-based chr:pos:ref>alt), genomic locus views (1-based closed chr:start-end), candidate summary tables, and AlphaGenome reference vs. alternate predictions.
- Alphagenome Single Variant Analysisgoogle-deepmindAnalyzes genetic variant effects on gene expression (RNA-seq), chromatin accessibility (DNASE), histone marks (ChIP), and transcription factors using the AlphaGenome API. Use when the user asks about non-coding variant effects, pathogenicity, clinical significance, disease associations, functional effects, gene expression changes, splicing disruption, or regulatory effects in promoters and…
- Alphagenome Variant Impact Scoregoogle-deepmindScore, annotate, and analyze the functional impact of genetic variants using AlphaGenome Variant Impact (AVI) scores. Query variants in chr:pos:ref>alt format, annotate VCF/tabular callsets, perform saturation mutagenesis window scans (1-based closed chr:start-end), and extract GENCODE v46 GTF gene/exon/junction coordinates all via the AlphaGenome Atlas API.
- Chembl Databasegoogle-deepmindQuery the ChEMBL database for bioactive molecules, drug targets, bioactivity data, approved drugs, and chemical structures. Use when the user asks about compounds, targets, IC50/Ki values, drug mechanisms, or structure searches.
- Clinical Trials Databasegoogle-deepmindQuery ClinicalTrials.gov via APIv2. Use when you want to search for trials by condition, drug, location, status, or phase; retrieve trial details by NCT ID; check eligibility/inclusion criteria; count trials across conditions or time periods; identify a sponsor's trial portfolio; find recruiting trials for patient matching.
- Clinvar Databasegoogle-deepmindUse when needing clinical significance, pathogenicity classifications (e.g., Pathogenic, Benign, VUS), clinical evidence rationales, or finding "hard positive" benchmark controls for human genomic variants.
- Credentialsgoogle-deepmindInstructions for handling API keys and credentials safely, verifying their presence, and prompting the user to add them if missing using a safe protocol.
- Dbsnp Databasegoogle-deepmindUse when you want to look up, map, and search for short genetic variants (SNPs, indels) in NCBI's dbSNP database. Resolves between rsIDs, genomic coordinates in VCF format, and HGVS strings. For an rsID, returns variant type, gene associations, clinical significance, allele frequencies, and genomic coordinates (GRCh38).
- Embl Ebi Olsgoogle-deepmindQuery and search the EMBL-EBI Ontology Lookup Service (OLS) for biomedical ontology terms, definitions, and hierarchies across 250+ ontologies (e.g., GO, DOID, HP). Use when the user asks to search for terms, retrieve details, navigate hierarchies (parents, children, ancestors), look up properties and individuals, get autocomplete suggestions, or access ontology metadata and statistics.
- Encode Ccres Databasegoogle-deepmindQuery the ENCODE Registry of cis-Regulatory Elements (cCREs) via the SCREEN GraphQL API, or make custom queries to the ENCODE Portal REST API for experiments and files (ChIP-seq peaks, etc.). Use when you want to query regulatory annotations or raw experimental data across human cell types.
- Ensembl Databasegoogle-deepmindQuery the Ensembl database to resolve gene, transcript, and protein IDs, fetch genomic or protein sequences, retrieve gene structures (exons), and get variant consequence and effect predictions (VEP). Use this skill as a primary ID translator, genomic sequence database and variant effect prediction tool.
- Foldseek Structural Searchgoogle-deepmindPerforms 3D structural searches of proteins against various databases (PDB, AlphaFold, CATH, MGnify, etc.) using the Foldseek API. Use ONLY when the user provides a physical 3D coordinate file (.cif, .mmcif, or .pdb) and wants to find structurally similar proteins. Do NOT use if the user only provides a protein sequence, gene name, or UniProt ID.