「discover」の検索結果

Vendor (copy-import) a single external Claude Code skill into your own skills repo correctly — with license compliance and full provenance/attribution. Deterministic, idempotent primitive: given an upstream ref (owner/repo/path@sha or a GitHub URL) it fetches the skill, detects and gates on the license, copies the folder, injects a provenance frontmatter block (license + metadata: author/source/upstream_commit/vendored_at/provenance), ships the upstream LICENSE, adds a ## Credits section, and records a CREDITS.md ledger entry. Use when the user asks to "vendor a skill", "import a skill", "clone a skill", "borrow someone's skill", "add an external skill with attribution/credit", or スキルを取り込む / vendoring / 他人のスキルを自分のリポに取り込む. This is the import primitive that a skill-scout/curator orchestrator calls; it does NOT discover or evaluate — it correctly imports ONE skill you already chose.

窓口が人間から「承認スコープの輪郭」を受けて、その内側で triage → worker 派遣 → iteration → verify → push → PR 作成 → CI 監視 を完了駆動で自走し、PR ごとに merge gate で必ず停止するベルトコンベア。/work-discovery + /org-delegate + verify + /org-pull-request + /org-escalation を呼ぶ薄い orchestrator。 発動条件: 人間が「この範囲は自走してよい」というスコープ承認を明示し、複数候補を 完了駆動で順次流したいとき（例「triage 上位の S 級バグ修正を空き pane 分まで自走、 merge は都度わたしが判断」）。起動主体は窓口に限定。スコープ外候補・判断境界・退出条件に 触れたら必ず halt する。merge 自動化はしない。

Instructions for discovery and usage of servers through the official MCP registry. Use when discovering new integrations. For building custom servers, see mcp-reference-servers.

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Signals scout that watches a PostHog project's most-viewed dashboards and insights for recent anomalies — sudden bursts, drops, flat-lines, and trend breaks at the daily or hourly level. It discovers what the team actually looks at (view counts, dashboard access), curates a durable watchlist in the scratchpad, and balances re-checking known high-value insights (exploit) against discovering new ones (explore) across runs, since no single run can cover a busy project. Anomalies are scored by robust deviation from each insight's own seasonality-matched baseline; it emits a finding only when a move clears the confidence bar, otherwise it updates the baseline memory and closes out empty. Self-contained peer in the signals-scout-* fleet.

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Guide the user through connecting a new data warehouse source — Postgres, MySQL, Stripe, Hubspot, MongoDB, Salesforce, BigQuery, Snowflake, and so on. Use when the user wants to "connect Stripe", "import data from Postgres", "add a new data source", "sync my warehouse tables", or wants to pick sync methods for each table. Walks through source-type discovery, credential validation, table discovery, per-table sync_type selection, and the final create call. Also covers picking a good prefix and what to do right after creation.

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Sparse Identification of Nonlinear Dynamics (SINDy) — discover governing equations from time-series data. Builds sparse dynamical system models dx/dt = f(x) from measurements using PySINDy. Use when you have trajectory data and want to find the underlying ODE.

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Discover governing equations from data using PySR (evolutionary symbolic regression). Physics-constrained search with dimensional analysis, custom operators, and complexity-accuracy tradeoffs. Use when you need an interpretable equation, not a black-box model.

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Provides guidance for training and analyzing Sparse Autoencoders (SAEs) using SAELens to decompose neural network activations into interpretable features. Use when discovering interpretable features, analyzing superposition, or studying monosemantic representations in language models.

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Small molecule identification, characterization, and procurement — PubChem, ChEMBL, BindingDB, ADMET-AI, SwissADME, eMolecules, Enamine. Covers compound name to structure to activity to ADMET properties to commercial sourcing. Use for chemical biology, lead identification, probe selection, and the full small-molecule discovery pipeline.

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Pythonic wrapper around RDKit with simplified interface and sensible defaults. Preferred for standard drug discovery including SMILES parsing, standardization, descriptors, fingerprints, clustering, 3D conformers, parallel processing. Returns native rdkit.Chem.Mol objects. For advanced control or custom parameters, use rdkit directly.

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Audit and improve website readiness for AI agents using the Cloudflare "Is It Agent Ready?" scanner (isitagentready.com). Covers scanning via API, interpreting results, generating implementation prompts, and fixing every check. Use when the user mentions "agent ready", "isitagentready", "AI agent scan", "agent readiness", "agent-ready score", "MCP server card", "agent skills index", "markdown for agents", "content signals", "web bot auth", "agent discovery", "RFC 9727", "RFC 8288", "RFC 9728", "SEP-1649", "WebMCP", "x402", "UCP", "ACP", or wants to make a website discoverable and usable by AI agents.

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A2A agent card JSON templates with schema validation and examples for different agent types. Use when creating agent cards, implementing A2A protocol discovery, setting up agent metadata, configuring authentication schemes, defining agent capabilities, or when user mentions agent card, agent discovery, A2A metadata, service endpoint configuration, or agent authentication setup.

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Discover and configure Bluetooth and Wi-Fi accessories using AccessorySetupKit. Use when presenting a privacy-preserving accessory picker, defining discovery descriptors for BLE or Wi-Fi devices, handling accessory session events, migrating from CoreBluetooth permission-based scanning, or setting up accessories without requiring broad Bluetooth permissions.

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Google Workspace CLI (gws) リファレンス。Rust 製。 `gws <service> <resource> <method>` 形式で Gmail / Drive / Calendar / Sheets / Docs / Chat 等 19 サービスを統一操作。Google Discovery Service 経由の動的コマンド生成。 `+` プレフィックスのヘルパーコマンド（+send, +agenda, +upload, +triage 等）、 ワークフロー合成（+standup-report, +meeting-prep, +weekly-digest）、 OAuth / サービスアカウント / CI ヘッドレス認証、env vars / .env / keyring 設定、 グローバルフラグ（--dry-run, --page-all, --sanitize）、exit codes、Model Armor 統合。

Facilitate DDD domain modeling sessions via EventStorming conversation and DML (Domain Modeling Language). Use whenever the user wants to model a business domain by discovering domain events, commands, aggregates, policies, read models, and bounded contexts through dialogue. Produces incrementally-built DML as the primary artifact, plus a Markdown session report. Also invoke for refining existing DML, mapping out a new feature's domain model, or when the user says "ドメインモデリングしたい", "イベントストーミング", "DDDで整理したい", "DMLを育てたい".

Analyze spatial cell-cell interactions, neighborhoods, and niches in IMC/MIBI data with squidpy and imcRtools, covering neighborhood-enrichment permutation nulls, the abundance-vs-density confound, inhomogeneous Ripley's K, cellular-neighborhood discovery, graph-construction (contact vs proximity), and edge effects. Use when testing whether cell types co-locate, choosing a spatial null, building a neighbor graph, discovering tissue niches, or deciding whether a spatial pattern is real or a density/segmentation artifact.

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Nominates and assesses CRISPR off-target sites genome-wide. Enumerates candidate sites by mismatch and bulge tolerance with Cas-OFFinder/CRISPRitz, ranks them with the published CFD score (SpCas9-only, relative ranker) or MIT/CRISTA/energy models, runs variant-aware screening against gnomAD/individual genomes (CRISPRme), and frames the empirical genome-wide discovery assays (GUIDE-seq, CIRCLE-seq, CHANGE-seq, DISCOVER-seq, Digenome-seq) and high-fidelity nuclease choice (HiFi Cas9, Sniper-Cas9, eSpCas9, SpCas9-HF1). Use when assessing guide RNA specificity, choosing among candidate guides, screening a therapeutic guide against population variation, or planning empirical off-target validation. Distinguishes predicted vs detected vs validated. On-target activity scoring and deaminase (Cas-independent) base/prime-editor off-targets are separate skills.

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Trains and applies base-resolution deep learning models on ChIP-seq / ChIP-nexus / CUT&RUN data. Uses BPNet (Avsec 2021 Nat Genet 53:354; soft motif syntax from ChIP-nexus), chromBPNet (Pampari A et al 2025 Nat Genet; bias-factorized base-resolution profiles), EnFormer (Avsec 2021 Nat Methods 18:1196; 196 kb input, ~100 kb effective receptive field), DeepSEA (Zhou 2015; multi-task CNN), and JASPAR 2026 deep-learning collection (1259 BPNet ChIP models). Performs in silico mutagenesis for variant-effect prediction, DeepLIFT/Grad attribution, and TF-MoDISco motif discovery from attribution scores. Use when predicting variant effects on TF binding, discovering soft motif syntax / cooperativity, integrating ChIP-seq with sequence-only predictions, or applying precomputed JASPAR Deep Learning models to new variants.

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Discover and approve feature requirements through focused interviewing and repository research. Use when the user has a feature idea, unclear scope, conflicting requirements, or needs Flow context artifacts before design.

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Rewrite AEM Edge Delivery Services page content for AI search discoverability (GEO — Generative Engine Optimization). Analyzes content structure, semantic clarity, and factual density, then produces optimized rewrites that rank in both traditional search and AI-powered search engines. Use when optimizing pages for search visibility, AI discoverability, or content clarity.

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 spatial cell-cell interactions, neighborhoods, and niches in IMC/MIBI data with squidpy and imcRtools, covering neighborhood-enrichment permutation nulls, the abundance-vs-density confound, inhomogeneous Ripley's K, cellular-neighborhood discovery, graph-construction (contact vs proximity), and edge effects. Use when testing whether cell types co-locate, choosing a spatial null, building a neighbor graph, discovering tissue niches, or deciding whether a spatial pattern is real or a density/segmentation artifact.

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。

Nominates and assesses CRISPR off-target sites genome-wide. Enumerates candidate sites by mismatch and bulge tolerance with Cas-OFFinder/CRISPRitz, ranks them with the published CFD score (SpCas9-only, relative ranker) or MIT/CRISTA/energy models, runs variant-aware screening against gnomAD/individual genomes (CRISPRme), and frames the empirical genome-wide discovery assays (GUIDE-seq, CIRCLE-seq, CHANGE-seq, DISCOVER-seq, Digenome-seq) and high-fidelity nuclease choice (HiFi Cas9, Sniper-Cas9, eSpCas9, SpCas9-HF1). Use when assessing guide RNA specificity, choosing among candidate guides, screening a therapeutic guide against population variation, or planning empirical off-target validation. Distinguishes predicted vs detected vs validated. On-target activity scoring and deaminase (Cas-independent) base/prime-editor off-targets are separate skills.

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。

Trains and applies base-resolution deep learning models on ChIP-seq / ChIP-nexus / CUT&RUN data. Uses BPNet (Avsec 2021 Nat Genet 53:354; soft motif syntax from ChIP-nexus), chromBPNet (Pampari A et al 2025 Nat Genet; bias-factorized base-resolution profiles), EnFormer (Avsec 2021 Nat Methods 18:1196; 196 kb input, ~100 kb effective receptive field), DeepSEA (Zhou 2015; multi-task CNN), and JASPAR 2026 deep-learning collection (1259 BPNet ChIP models). Performs in silico mutagenesis for variant-effect prediction, DeepLIFT/Grad attribution, and TF-MoDISco motif discovery from attribution scores. Use when predicting variant effects on TF binding, discovering soft motif syntax / cooperativity, integrating ChIP-seq with sequence-only predictions, or applying precomputed JASPAR Deep Learning models to new variants.

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Discover failure modes in Coval runs, uploaded conversations or local conversation exports using scoped sampling and transcript, audio and trace evidence. Prepare human review without inventing ground truth or launching new runs.

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。