「aks」の検索結果

Breaks work into ordered, parallel-dispatchable tasks with an execution DAG. Output format is consumable by CI matrices and parallel agent runners — each task has a stable ID, declared file writes, conflict edges, and branch suffix. Use when you have a spec, brief, or shaper output and need to decompose it into implementable units. Use when a task feels too large, when scope spans multi-repo or multi-week work, or when parallel execution across multiple agents is on the table.

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Scan projects for credential leaks, secrets in code, insecure patterns, LLM API key exposure, PII leakage to external AI services, and .env/.gitignore misconfigurations. Especially useful for data and API integrations, regardless of implementation language.

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Verify that browser profiles are actually isolated from one another instead of assuming it - confirm each profile's timezone agrees with its own exit IP, that WebRTC exposes only the proxy, that canvas and WebGL hashes stay identical across relaunches of one profile, and that no two profiles share a persona, a cookie jar, or an address. Use when several of your own accounts or test identities run from one machine and the setup needs checking, when a profile tested clean but something still looks off, when choosing which detection suites to run (CreepJS, whoer, browserleaks WebRTC, pixelscan, liarjs), when auditing what a vendor runtime does with API and proxy credentials, or when asking which layers browser isolation cannot cover at all. Also for 'profile isolation check', 'fingerprint consistency test', 'timezone mismatch', 'WebRTC leak', 'canvas hash unstable', 'account association', 'temporary profile', '防关联', '多账号', '隔离自检'. The SDK is anti-detect-browser; MCP is browser-mcp-agent.

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Map every touchpoint from first click to loyal advocate. Identify drop-off points, emotional peaks, and automation opportunities across your entire customer lifecycle.

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Red team security mode for OpenClaw. Runs an adversarial audit on demand or nightly — checks exposed ports, credential leaks, file permissions, suspicious processes, and OpenClaw config posture. Assigns a letter grade. Built for macOS deployments.

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Breaks work into ordered tasks. Use when you have a spec or clear requirements and need to break work into implementable tasks. Use when a task feels too large to start, when you need to estimate scope, or when parallel work is possible.

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。

Perform comprehensive technical reviews of Ruby on Rails applications. Runs automated analysis tools (RubyCritic, Brakeman, bundler-audit, Gitleaks, Debride, linters, SimpleCov, Rails stats, Rails ERD), analyzes code for architecture, security, authorization (Pundit/CanCanCan), dead code, and design issues, and produces a structured markdown report with prioritized findings and a 0-10 score. Use when the user requests a tech review, code audit, project assessment, or quality analysis of a Rails application.

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Preventive hygiene audit of your own Claude Code configuration — memory files, project context (CLAUDE.md), rules, permissions, skills — a deterministic scan of sizes / broken links / stale entries / excessive permissions / junk + interpretation + targeted fixes by agreement. Keeps the setup from rotting before it breaks. Triggers — "check the system", "system health", "workflow hygiene", "what to clean up", "audit memory", "optimize the system".

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Low-ceremony workflow for trivial, low-risk changes: typos, comments, CSS/styling tweaks, string changes, single-line fixes with no logic impact. Use to avoid the overhead of the full feature workflow when the change cannot break anything. If during the fix the change turns out to touch logic, security, config, or schema, stop and escalate to the feature-workflow skill.

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Phased workflow for delivering a Drupal feature or non-trivial change: plan, implement, review, test, finalize. Use when building a new custom module, adding a route/form/plugin, changing entity structure or schema, or any task touching more than a couple of files. Do NOT use for typo fixes, CSS tweaks, or single-line changes — use the tiny-fix skill instead. Each phase has an exit condition; do not move to the next phase until it is met.

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Python code quality review lens. SOLID principles, dead code, exception handling, resource leaks, thread safety, performance. Triggered by "quality" ("품질"), "SOLID", "dead code" ("데드코드"), "exception", "resource leak", "thread safety" keywords.

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Triages an already-dirty Git working tree: breaks down every uncommitted change hunk by hunk, separates deliberate edits from tool-written churn, possibly accidental reversions, misplaced scope, and sensitive content, asks the user about the ambiguous cases, and proposes an ordered set of commits plus a list of hunks to hold back. Use when the user invokes `/pc` or `$pc`, asks what they should commit, wants their uncommitted changes broken down, or wants commits proposed for a dirty working tree or pile of accumulated local modifications. To plan commit boundaries for a change before or while implementing it, use `incremental-commits` instead.

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Diagnose and fix flaky tests. Covers race conditions, timing issues, test pollution, async leaks.

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。

Weekly-cadence engineering retrospective. Analyzes commit history, work patterns, and code quality metrics with persistent history and trend tracking. Team-aware: breaks down per-person contributions with praise and growth areas. Use when asked to "weekly retro", "what did we ship", or "engineering retrospective". Proactively suggest at the end of a work week or sprint. NOT for per-session or per-task reflection (see mk:memory / Phase 6 Reflect).

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Stop AI agents from secretly bypassing your rules. Mechanical enforcement with git hooks, secret detection, deployment verification, and import registries. Born from real production incidents: server crashes, token leaks, code rewrites. Works with Claude Code, Clawdbot, Cursor. Install once, enforce forever.

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Extracts cfDNA fragmentomics features (DELFI genome-wide short/long ratios, WPS nucleosome positioning, Griffin GC-corrected accessibility profiles, end-motifs/MDS, OCF) for cancer detection and tissue-of-origin from plasma WGS. Centers on the nuclease-footprint reframe (every feature re-reads one nucleosome object), the mandatory GC correction, and the cross-protocol non-comparability that breaks naive classifiers. Runs FinaleToolkit (real CLI/Python, MIT) and the Griffin Snakemake pipeline; DELFI is a method, not a package. Use when deriving fragment-based signal from cfDNA, choosing a feature family for detection vs subtyping, or diagnosing why a fragmentomic model failed validation.

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Infers person-to-person transmission from pathogen genomes using outbreaker2, TransPhylo, phybreak, BadTrIP, SCOTTI, BEASTLIER, and SNP-distance / cluster-picker approaches (HIV-TRACE for HIV; transcluster). Defines outbreak clusters using pathogen-specific SNP thresholds (NOT a universal cutoff -- TB <=12 SNPs; MRSA <=15; C. difficile <=2; Klebsiella <=21), models within-host diversity and transmission bottlenecks, integrates contact-tracing data, distinguishes generation from serial interval, and attributes source via Bayesian source attribution (islandR). Use when investigating outbreaks for who-infected-whom, defining SNP-cluster outbreak definitions, accounting for unsampled intermediates, choosing between outbreaker2 (rich epi data) and TransPhylo (genomic-only after a dated phylogeny), running source attribution between host populations, calling HIV-TRACE thresholds appropriate to the local subtype, or distinguishing recent transmission from reactivation in TB or chronic HIV.

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Build genome-browser-style multi-track figures with pyGenomeTracks (config-driven), Gviz (R), and IGV batch screenshotting. Covers BigWig coverage tracks, BED/peak overlays, gene-model rendering, Hi-C matrix tracks, BedPE link arcs, spike-in-aware normalization, and the bamCoverage --normalizeUsing trap. Use when producing publication figures of genomic loci with stacked aligned tracks (coverage, peaks, genes, interactions) for ChIP-seq, ATAC-seq, RNA-seq, Hi-C, or generic locus visualization.

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Annotate CLIP-seq peaks or crosslink sites to RNA features (5'UTR, CDS, 3'UTR, intron, splice junction, snoRNA, tRNA, ncRNA, repeat elements) with ChIPseeker, RCAS, RBP-Maps (Yeo splicing regulatory maps), and bedtools, applying feature-priority hierarchies, transcript-context resolution, and metagene aggregation. Use when characterizing where in transcripts an RBP binds, comparing peak distribution across regions, generating splicing-regulatory maps relative to alternative-splicing events, or distinguishing exonic vs intronic vs UTR binding.

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Discover RBP binding motifs from CLIP-seq peaks or single-nucleotide crosslink sites using HOMER, MEME/STREME, kpLogo, mCross (CL-position-registered motifs), PEKA (positional k-mer enrichment), RBPamp (affinity), and RNA Bind-n-Seq (RBNS) cross-validation. Use when characterizing RBP sequence specificity, registering motifs to crosslink positions, validating in vivo CLIP motifs against in vitro RBNS Kd, reconciling motif disagreements across tools, or correcting for the uracil crosslinking bias that contaminates raw CLIP motif logos.

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Identify recurrent and driver copy number alterations across a tumor cohort with GISTIC2 (G-score, Ziggurat deconstruction, focal vs broad/arm-level analysis, q-values from permutation) and quantify copy-number signatures with the Steele 2022 COSMIC framework and the Drews 2022 CINSignatures framework. Covers driver-gene localization from recurrence peaks, distinguishing focal drivers from arm-level passengers, and the caller-sensitivity caveats of copy-number signatures. Use when finding recurrently amplified or deleted regions in a cohort, localizing driver genes, separating focal from broad events, running GISTIC2, or extracting copy-number mutational signatures.

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Discovers de novo motifs and tests known motif enrichment in ChIP-seq, ATAC-seq, or other peak sequences using HOMER, MEME-ChIP (STREME, CentriMo, TOMTOM, FIMO), monaLisa, and AME. Handles background selection (GC-matched, dinucleotide-shuffled, Markov order-2, peak-flanks), motif databases (JASPAR 2024 CORE PWMs, JASPAR 2026 deep-learning collection, HOCOMOCO v12, HOMER built-in), centrally-enriched motif testing, and differential motif analysis. Use when identifying TF binding motifs in peaks, testing for known TF enrichment, scanning for motif instances, comparing motif content between conditions, or interpreting motifs from deep learning models.

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Analyzes CUT&RUN (Skene Henikoff 2017) and CUT&Tag (Kaya-Okur 2019) chromatin profiling data. Handles SEACR vs MACS2 peak calling (with the btaf375 2025 benchmark guidance), pA-MNase vs pA-Tn5 vs pAG-Tn5 chimera differences, E. coli spike-in carryover normalization, IgG-only control logic (no input), characteristic fragment-size signatures (25-75 bp for CUT&Tag), and lower depth requirements (5M reads typical vs 25M for ChIP). Use when calling peaks from CUT&RUN/CUT&Tag, scaling by E. coli spike-in carryover, choosing SEACR norm mode, or comparing CUT&RUN/Tag results to traditional ChIP.

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Identify differentially accessible chromatin regions across conditions using DiffBind, csaw, DESeq2, or edgeR. Use when comparing ATAC-seq accessibility between treatment groups, choosing between consensus-peak vs sliding-window approaches, picking the correct normalization (full library vs reads-in-peaks), correcting batch with SVA/RUVseq, or interpreting log2FC and FDR thresholds in a chromatin context.

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。