Use esbuild for extreme-speed builds: bundling, transforming, plugins, and integration into larger pipelines. Use when build speed is the bottleneck.
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。
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概要と使いどころ
Use esbuild for extreme-speed builds: bundling, transforming, plugins, and integration into larger pipelines. Use when build speed is the bottleneck.
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。
Manage ML datasets with the datasets ecosystem — loading, streaming, preprocessing, versioning, and sharing. Use when data handling (not modeling) is the bottleneck.
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。
Optimizes application performance. Use when performance requirements exist, when you suspect performance regressions, or when Core Web Vitals or load times need improvement. Use when profiling reveals bottlenecks that need fixing.
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。
host / 辅助段优化模块(L3):把**非 DiT、非解码段**的固定开销落成可复验的优化—— ① 交付与搬运(mp4/图片编码、worker→API 通路、落盘、异步化); ② 装载与预热(权重加载、编译与图下发预热、镜像/容器预热)。 当用户说“mp4 编码/传输/落盘慢”“交付这段占了不少时间”“模型加载慢”“首启编译太久” “固定开销占比高”“每个请求都要重新编码/重新写盘”时使用。 **入口条件**:占比已达门限(瓶颈标签 `非DiT-host段`;标签枚举、门限与测点口径的单一真源在 model-auto-optimization/references/bottleneck-labels.md,本技能只消费不定义)。 near-miss(看似相关但不属本技能): - **并发 / 吞吐 / 批处理调度 / 队列深度与限流** → **不属本技能**(会改变所有性能口径与 SLO 语义, 未来独立立项;本技能只在**不改变请求并发模型**的前提下压固定开销); - VAE/TAE 解码段(计算或通信)→ `vae-opt`;DiT 计算 → `dit-perf-opt`; 多卡并行 / 通信掩盖 → `dit-parallel-opt`; - **装库 / 下载权重 / 构建镜像 / 创建容器** → `env-install`(本技能只优化装载与预热**过程本身**); - 编译与图下发的**机制本体**(pattern / Inductor / NPUGraph / 图 pool / 缓存条目)→ `pattern-dev` / `aclgraph-dev`(本技能不另做一套缓存); - 产物一致性与精度判据 → `accuracy-gate`;收益口径 → `perf-gate`; - 瓶颈未定位 / 没有占比锚点 → `model-auto-optimization`。
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。
Diagnose and optimize timing-critical Chisel RTL for FPGA implementation while preserving cycle semantics. Use for Vivado timing bottlenecks, long ready or admission paths, queue and issue selection, free-list bank mapping, priority encoders, one-hot arbitration, wide muxes, late-arriving forwarding or override data, high-fanout controls, cross-module predicates, register-boundary changes, emitted-Verilog inspection, or routed-DCP A/B analysis. Also use when a source-level simplification needs proof that it changes timing without changing architectural state.
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Quality control for pooled CRISPR screens covering library representation, Gini index, log-skew, replicate Pearson and Spearman concordance, essentialome precision-recall AUC against CEGv2 (Hart 2017), Cas9 cut-toxicity diagnostics, copy-number amplicon detection (Aguirre 2016 / Munoz 2016), bottleneck propagation through plasmid pool, infection, selection, and endpoint stages, MOI verification, and DepMap-style screen-quality scoring. Use when assessing screen quality before hit calling, deciding whether to repeat or rescue a screen, diagnosing low-confidence hits, choosing between MAGeCK / BAGEL2 / Chronos based on quality grade, picking a normalization strategy from QC signatures, or evaluating whether an in-vivo screen retained adequate library complexity.
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。
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.
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。
Queries gnomAD v4 (807k samples), v3, v2.1.1, and constraint metrics with grpmax FAF95, bottleneck-group exclusion, LOEUF interpretation, SV/CNV/mtDNA catalogs, and Whiffin max-credible-AF framework. Use when filtering rare variants, applying ACMG BS1/BA1, ranking genes by LoF intolerance, or selecting between v2 (GRCh37 + chrX/Y constraint) and v4 (GRCh38 + 807k samples).
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。
Profiles DAG execution performance including latency, token usage, cost, and resource consumption. Identifies bottlenecks and optimization opportunities. Activate on 'performance profile', 'execution metrics', 'latency analysis', 'token usage', 'cost analysis'. NOT for execution tracing (use dag-execution-tracer) or failure analysis (use dag-failure-analyzer).
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。
Optimizes application performance. Use when performance requirements exist, when you suspect performance regressions, or when Core Web Vitals or load times need improvement. Use when profiling reveals bottlenecks that need fixing.
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。
Performance audit — bottleneck profiling, N+1 query detection, hot-path analysis; explicit request only, not part of regular feature work.
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。
[Debugging] Use when analyzing or optimizing performance bottlenecks: database queries, N+1 fan-out, indexing, API latency, memory/GC, concurrency and pool saturation, algorithmic complexity (O(n²)), network/protocol round trips, frontend rendering and Core Web Vitals, caching, and distributed/resilience paths. Calibration constants and domain laws (latency ladder, Little's Law, utilization knee, CWV thresholds, symptom→cause triage) live in references/performance-knowledge.md.
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。
Review audit-related documents (control design documents, bottleneck analyses, requirements definitions, etc.) for quality, scoring them 0-100 with a severity-rated findings list. Use when reviewing audit documents, checking control design quality, or verifying cross-document consistency. Supports documents governed by US GAAP, IFRS, or J-GAAP.
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。
AI PR intake and multi-agent governance for deployless repositories. Use when a repo has high-volume bot or agent PRs, parallel agent work, noisy low-context PRs, merge-queue pressure, CI exhaustion, duplicate fixes, ownership confusion, or review bottlenecks that threaten a single-mainline delivery model.
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。
Profile and optimize Python code using cProfile, memory profilers, and performance best practices. Use when debugging slow Python code, optimizing bottlenecks, or improving application performance.
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。
Implement distributed tracing with Jaeger and Tempo to track requests across microservices and identify performance bottlenecks. Use when debugging microservices, analyzing request flows, or implementing observability for distributed 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。
NVIDIA RAG Blueprint performance-tuning guidance for profiling retrieval stacks, comparing bottlenecks, and validating latency or throughput improvements.
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。
Establish build performance baselines and apply systematic optimization techniques. Only activate in MSBuild/.NET build context. USE FOR: diagnosing slow builds, establishing before/after measurements (cold, warm, no-op scenarios), applying optimization strategies like MSBuild Server, static graph builds, artifacts output, and dependency graph trimming. Start here before diving into build-perf-diagnostics, incremental-build, or build-parallelism. DO NOT USE FOR: non-MSBuild build systems, detailed bottleneck analysis (use build-perf-diagnostics after baselining).
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。
Codified expertise for production scheduling, job sequencing, line balancing, changeover optimisation, and bottleneck resolution in discrete and batch manufacturing.
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。
Profile and optimize Python code using cProfile, memory profilers, and performance best practices. Use when debugging slow Python code, optimizing bottlenecks, or improving application performance.
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。
Performance optimization, profiling, caching strategies, lazy loading, bundle optimization, and monitoring. Use when optimizing application performance, reducing bundle size, implementing caching, or analyzing bottlenecks.
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。
Diagnoses CI and pull-request pipeline health for a GitHub repo using the engineering analytics MCP tools — pull-requests (PR list with CI status), workflow-health (per-workflow CI trends), and pr-lifecycle (a single PR's timeline). Use when asked whether CI is getting faster or slower, which GitHub Actions workflow is the slow or flaky long-pole, how long PRs take from open to merge, how an author's merge time compares to the cohort, which open PRs have failing or pending CI, or where a specific pull request is stuck. Triggers on "engineering analytics", "is CI getting slower", "slow workflow", "flaky CI", "time to merge", "cycle time", "PR throughput", "failing checks", "where is PR <n> stuck", "CI long pole", "what's holding up this PR".
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。
End-to-end pooled and single-cell CRISPR screen analysis from FASTQ to hit genes. Orchestrates library design QC, guide counting, six-stage screen QC (plasmid Gini, replicate Pearson, CEGv2 PR-AUC, copy-number artifact), method-appropriate hit calling across MAGeCK RRA/MLE, BAGEL2, drugZ, JACKS, and Chronos, cancer-cell-line copy-number correction (CRISPRcleanR / Chronos), batch correction for multi-batch screens, and the specialized branches for combinatorial paralog screens, single-cell Perturb-seq, base-editor variant-function screens, prime-editor screens, and in vivo bottleneck-aware screens. Use when analyzing any pooled CRISPR screen end-to-end, matching the hit-calling method to the experimental design, integrating copy-number correction into the pipeline, or branching the workflow for single-cell, combinatorial, base-editor, prime-editor, or in vivo variants.
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。
Infers person-to-person transmission from pathogen genomes using outbreaker2 (Campbell 2018), TransPhylo (Didelot 2017), phybreak (Klinkenberg 2017), BadTrIP (De Maio 2018), SCOTTI (De Maio 2016), BEASTLIER (Hall 2015), 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 / Walker 2013; MRSA <=15 / Coll 2017; C. difficile <=2 / Eyre 2013; Klebsiella <=21 / Snitkin 2012), models within-host diversity and transmission bottlenecks (Worby-Lipsitch-Hanage 2014; McCrone 2018; Sobel Leonard 2017; Lythgoe 2021 SARS-CoV-2), integrates contact-tracing data, distinguishes generation interval from serial interval (Britton & Scalia Tomba 2019; Ali 2020), attributes source via Bayesian source attribution (Mather 2013 DT104; islandR), and reconciles transmission-network reconstruction with epi metadata. 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 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 / chronic HIV.
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。