1,171 件 ・ 関連度順
概要と使いどころ
Troubleshoot and debug LiveAvatar integration issues. Use when the user's LiveAvatar integration isn't working, the avatar is silent, audio is garbled, sessions fail to start, events aren't received, or they're getting API errors.
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。
Guide setup for and verify a reviewed, read-only Grafana Observability profile and its activated capability packs. Use when a user asks to set up Grafana access, verify profile readiness, discover available infrastructure, APM, log, IoT or business KPI packs, or troubleshoot why a Grafana pack cannot run.
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。
Check and install prerequisites for the Todo app project. Use when setting up the development environment, when a user first opens the workspace, when troubleshooting missing tools, or when the user mentions setup, install, prerequisites, or environment.
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。
Expert in developer tool documentation as a product. Activate on: docs site, getting started guide, API reference, developer documentation, Docusaurus, Mintlify, Nextra, ReadMe, migration guide, troubleshooting page, docs information architecture, documentation testing, llms.txt. NOT for: marketing copy (use seo-content-blogging), API design itself (use api-architect), general technical writing (use technical-writer).
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。
Detects m6A modifications from Oxford Nanopore direct-RNA-seq (DRS) signal using m6Anet (multiple-instance-learning over DRACH 5-mer signal). Covers the upstream pipeline (Dorado/Guppy basecalling -> minimap2 map-ont -> nanopolish eventalign -> m6anet dataprep -> m6anet inference), per-site vs per-read probability including the mod_ratio stoichiometry column, the DRACH-only constraint, minimum-coverage thresholds (20-50 reads/site), multi-condition comparison via xPore/Nanocompore/ELIGOS, Dorado native modification calling (RNA004, 2024+), and the cDNA-vs-DRS distinction (cDNA Nanopore CANNOT detect modifications). Use when calling m6A from ONT DRS without immunoprecipitation, choosing m6Anet vs xPore vs Nanocompore vs ELIGOS vs Dorado native, interpreting probability_modified vs mod_ratio vs per-read probabilities, deciding between m6Anet (known DRACH sites) and Dorado/Remora (genome-wide screening), pinning RNA002 vs RNA004 chemistry and basecaller versions, or troubleshooting eventalign/dataprep failures.
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。
Aligns sample metadata with count matrices and constructs design matrices for downstream DE, handling the alphabetical-reference-level trap (relevel BEFORE DESeq), LRT reduced-model rules, the interaction-term resultsNames trap, continuous-covariate scaling and splines, repeated measures via duplicateCorrelation or dream, high-cardinality categorical pseudo-singular designs, sample swap detection via XIST/RPS4Y1 expression and somalier/NGSCheckMate genotypes, SABV (sex-as-biological-variable) mandate, Simpson's-paradox collapsing of technical replicates, and the `~ 0 + group` parameterization for clean contrasts. Use when building a design matrix, troubleshooting reversed fold-change direction, encoding paired or repeated-measures designs, detecting sample swaps, deciding sex-as-covariate, or aggregating technical replicates.
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。
Performs differential expression on bulk RNA-seq count data with edgeR's negative-binomial GLM and quasi-likelihood F-test framework. Covers DGEList construction, filterByExpr, TMM/TMMwsp normalization, robust dispersion estimation, glmQLFit/glmQLFTest, TREAT for magnitude-bounded hypotheses, contrasts via no-intercept designs, voom and voomWithQualityWeights for heterogeneous samples, and the edgeR v4 bias-corrected APL changes. Use when running bulk DE with edgeR, choosing edgeR over DESeq2 (small n, transcript DE via catchSalmon, large samples), needing TREAT for a fold-change-threshold hypothesis, troubleshooting v3-to-v4 reproducibility, building paired or interaction designs, or handling library-quality heterogeneity.
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。
Handles batch effects in bulk RNA-seq via design-matrix inclusion (the correct path for DE), ComBat/ComBat-seq for visualization, SVA for unknown latent factors, RUVSeq for negative-control-gene-anchored unwanted variation, and limma::removeBatchEffect for plotting only. Encodes the Nygaard 2016 cardinal sin against testing on a batch-corrected matrix, the choice between SVA/RUVg/RUVs/RUVr, the confounding non-identifiability problem, the single-cell boundary (Harmony/MNN are NOT for bulk), and the Goh 2017 harmonization critique. Use when designing a DE analysis with batch structure, troubleshooting batch-dominated PCA, choosing ComBat vs ComBat-seq, handling unknown batch via SVA, integrating across studies, or deciding when (rarely) to subtract batch.
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。
Creates DE-specific diagnostic and result visualizations using DESeq2/edgeR built-in functions and lightweight ggplot2 wrappers. Covers MA plot (with the shrunken-LFC compression effect), volcano (with the apeglm caveat that p-values are unchanged), PCA on VST/rlog (never raw counts), sample distance heatmaps, top-DE-gene heatmaps with the row-scaling trap, dispersion / BCV plot interpretation, p-value histogram diagnostics, plotCounts for individual genes, blind=TRUE vs FALSE rationale, and the n=3 visualization stake. Use when generating DE diagnostic plots, choosing VST vs rlog for visualization, troubleshooting suspicious plot patterns (shifted MA cloud, batch-dominated PCA, anti-conservative p-value histogram), or building a standard QC figure panel.
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。
Performs differential expression on bulk RNA-seq count data with DESeq2's negative-binomial GLM, Wald and LRT testing, apeglm/ashr/normal LFC shrinkage, independent filtering, Cook's outlier handling, VST/rlog transforms, and design formulas including paired, batch, and interaction terms. Use when running bulk DE, choosing DESeq2 over edgeR or limma-voom, building a paired or interaction design, applying LFC shrinkage for ranking or GSEA, choosing Wald vs LRT, troubleshooting padj=NA, picking VST vs rlog, importing salmon/kallisto via tximport, or analyzing prokaryotic RNA-seq.
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。
Extracts, filters, annotates, and exports differential expression results from DESeq2 or edgeR with proper handling of padj=NA (independent filtering, Cook's outliers, all-zero), multiple-testing correction choice (BH vs Storey q-value vs IHW vs lfsr), TREAT vs post-hoc fold-change filtering, p-value histogram diagnostics, gene annotation via org.db/biomaRt/mygene, GSEA preranked input, ORA background construction, replication reality (Schurch 2016 small-n result), and SABV/sex-stratified reporting. Use when extracting and interpreting DE results, troubleshooting padj=NA, choosing FDR method, preparing ranked lists for pathway analysis, annotating gene IDs, or comparing DESeq2 vs edgeR outputs.
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。
Analyzes CRISPR drug-modifier (chemogenomic) screens with drugZ (Colic et al. 2019 Genome Med), a bidirectional Z-score method that identifies synthetic-lethal sensitizing genes and resistance-conferring suppressor genes from vehicle vs drug comparisons. Covers vehicle-anchored design (not Day-0), the bidirectional Z math giving greater sensitivity to small-effect hits than MAGeCK / STARS / edgeR / RIGER on drug screens, per-gene sumZ and normZ, synth (sensitizer) vs supp (suppressor) FDR, multi-dose handling, integration with control sgRNAs, and comparison with MAGeCK MLE with dose covariate. Use when running a drug-modifier CRISPR screen, identifying sensitizing or resistance genes for a drug candidate, choosing drugZ vs MAGeCK MLE for chemogenomic analysis, troubleshooting low-effect drug screens where MAGeCK lacks sensitivity, or designing a drug-screen layout (vehicle vs drug arms).
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。
Guidance for SPR and BLI binding characterization experiments. Use when: (1) Planning binding kinetics experiments, (2) Troubleshooting poor/no binding signal, (3) Interpreting kinetic data artifacts, (4) Choosing between SPR vs BLI platforms.
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。
Provides a checklist of five evidence-based measures to enhance the technical success of adrenal venous sampling procedures. Triggers include when preparing for AVS and asking 'How can I maximize success rate?' or troubleshooting failed attempts.
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。
Use this skill when asked to "validate plugin", "check plugin structure", "verify plugin", "audit plugin", "is my plugin correct", "plugin issues", or when troubleshooting plugin problems.
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。
Expert Clay platform consultant for B2B data enrichment and workflow automation. Use when the user asks about Clay tables, waterfall enrichment, Clay credits, Clay AI columns, Claygent, enrichment workflows, Clay integrations, Clay exports, Clay table design, lead scoring in Clay, or building data pipelines in Clay. Also triggers on "Clay table", "enrichment waterfall", "Clay credits", "Claygent", "Clay AI column", "Clay export", "Clay providers", "enrich in Clay", "Clay column", "Clay formulas", "find emails", "email waterfall", "phone waterfall", "lead scoring", "Clay debugging", "Clay troubleshoot". Do NOT use for general CRM questions without Clay context, cold email copy (use cold-email-copy-playbook), or signal routing (use buying-window-signal-workflow).
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。
Operate and troubleshoot BambuLab printers with the bambu-cli.
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。
Expert-level process simulation covering Aspen Plus, HYSYS, steady state and dynamic simulation, thermodynamic model selection, and simulation troubleshooting.
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。
Build and manage trusted local Paseo plugins. Use when the user asks to create, edit, install, reload, enable, disable, remove, or troubleshoot a Paseo plugin; add lifecycle hooks; transform agent configuration, environment, MCP servers, or workspace creation; automate permissions or turn follow-ups; add a native surface, sidebar item, or workspace panel; add Command Center items or slash commands; add composer pills or attachment sources; transform, render, or append agent timeline items; contribute a theme; use Paseo from plugin code; or add plugin RPCs.
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。
Answer questions about the Paseo product and app, including setup, configuration, connectivity, providers, workspaces, updates, logs, and troubleshooting. Use when a user inside Paseo asks how Paseo works, how to configure it, or why something is broken; use the paseo skill instead to operate agents and workspaces through MCP or the CLI.
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。
Build React animations with Motion (Framer Motion) - gestures (drag, hover, tap), scroll effects, spring physics, layout animations, SVG. Bundle: 2.3 KB (mini) to 34 KB (full). Use when: drag-and-drop, scroll animations, modals, carousels, parallax. Troubleshoot: AnimatePresence exit, list performance, Tailwind conflicts, Next.js "use client".
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。
Operate or troubleshoot Interlateral CLI mesh transport: tmux socket discovery, direct-send helpers, comms.md ledger, identity stamping, idle checks, ACK proof, and safe prompt injection. This is comms mechanics only, not a collaboration workflow.
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。
Use this skill whenever the user wants to create, edit, explain, validate, or troubleshoot a proctmux.yaml/procmux.yaml file, add or change proctmux processes, configure lifecycle behavior such as stop signals/on_kill/autostart, customize unified-mode layout/keybindings/style, or enable Makefile/package.json process discovery. Use it even when the user says this casually, such as "add my dev server to proctmux", "fix this proctmux config", "write a config for these services", or "what YAML option controls focus".
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。
Use o servidor Figma MCP para buscar contexto de design, screenshots, variáveis e assets do Figma, além de traduzir nós do Figma em código de produção. Ative quando uma tarefa envolver URLs do Figma, IDs de nós, implementação design-to-code ou configuração e troubleshooting do Figma MCP.
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。