「traceability」の検索結果

Author the Salesforce Configuration Workbook — the structured, reviewable handoff document an admin uses to execute a feature across Objects/Fields, Page Layouts, Profiles/PSGs, Sharing, Validation, Automation, List Views, Reports, Integrations, and Data. Triggers: 'salesforce configuration workbook', 'admin handoff document', 'implementation workbook'. NOT for object design itself (use admin/custom-field-creation, admin/lookup-and-relationship-design, agents/object-designer/AGENT.md), NOT for permission set design (use admin/permission-set-architecture, agents/permission-set-architect/AGENT.md), NOT for Flow construction (use skills/flow/* and agents/flow-builder/AGENT.md), and NOT for the deployment manifest (use skills/devops/metadata-api-retrieve-deploy). More triggers: workbook row schema, recommended_agent, recommended_skills, row_id, source_req_id, RTM linkage block, not-in-scope-this-release, descope ledger, version-lock the workbook, check_workbook.py.

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 technical API constraints from OpenAPI/Swagger specs and developer docs into a contract-ready API Access & Constraints Schedule with source traceability, risk flags, and change-control language. Use when drafting legal exhibits or schedules covering API access scope, rate limits, authentication, data fields, or deprecation terms for MSAs, SOWs, or order forms.

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。

Reads, validates, and prepares CDISC SDTM and ADaM clinical trial data for analysis. Covers SDTM domain joins (DM, AE, EX, VS, LB, DS), ADaM architecture (ADSL, BDS, OCCDS, ADTTE) with traceability, treatment-emergent AE conventions, baseline derivation, SUPPQUAL/NSV handling, Define-XML 2.1, and Pinnacle 21 / CORE validation. Use when working with clinical trial datasets in CDISC SDTM/ADaM format, preparing analysis-ready data, or validating for regulatory submission.

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。

Preflight a spec draft without saving. Runs the same checks as the write-boundary hooks — PlantUML syntax, required diagram presence, AC-to-sequence traceability, Design calls quality floor, and System delta row resolution — and prints a compact pass/fail table. Use while iterating so the hooks don't bite on save.

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。

Enforce traceability from natural-language intent to machine predicates, final observables, evidence, and owner-readable acceptance. Use when conducting any audit, review, QA pass, parity or compliance check, security assessment, code or architecture review, visual or behavioral comparison, data validation, system verification, completion gate, or claim that an implementation satisfies a human request.

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。

[Code Quality] Use when you need to review integration tests for assertion quality, bug protection, repeatability, and test-spec traceability — AND verify the review target (changed production code) has test coverage (integration-first) with spec↔test↔code alignment.

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。

Create, revise, and validate publication-ready academic paper figures and tables. Use for LaTeX tables, related-work comparison tables, result tables, notation/dataset/taxonomy tables, precise source-data-driven experiment plots from CSV/JSON/logs, generated conceptual figures such as system overviews/pipelines/architectures/threat models, captions, artifact specs, source-data traceability, and paper-ready PDF/SVG/PNG/LaTeX exports. Do not use for prose-only paper writing, self-review, reviewer response, rebuttal drafting, or external literature-management workflows.

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。

Cross-reference project artifacts (WBS, meeting minutes, requirements docs) by date, participant, and action items. Extract commitments from meeting minutes and link to WBS tasks. Generate traceability reports showing which decisions were captured in which documents.

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 on writing high-quality requirements: the requirement quality characteristics and the EARS (Easy Approach to Requirements Syntax) patterns — ubiquitous, event-driven, state-driven, optional-feature, unwanted-behaviour — for unambiguous, singular, verifiable requirements, plus defect/anti-pattern review and verification & traceability. Use when authoring or reviewing requirements. Original synthesis citing EARS (Mavin et al.) and NASA public-domain guidance; not a reproduction of ISO/IEC/IEEE 29148 or the EARS paper.

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。

Knowledge base from DOE Systems Engineering Methodology (SEM) Version 3 — the DOE SDLC for IT investments. Use for staged systems lifecycle planning through maintenance, Stage Exits, Structured Walkthroughs, In-Stage Assessments, requirements traceability, and CMM-aligned process discipline. Covers SEM3 (2002) guidance only; does not replace modern DevSecOps tooling standards, DOE O 413.3B capital-asset directives, or current CIO policy supersessions.

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。

Knowledge base from NASA NPR 7150.2D — NASA Software Engineering Requirements. Use for NASA's Agency-wide software-engineering requirements: the software classification scheme (Classes A–F), the Requirements Mapping Matrix and class-driven applicability, tailoring and Technical Authority governance, the SWE-### 'shall' requirements across software management (Ch 3) and the engineering life cycle (Ch 4), the supporting disciplines (configuration management, risk, peer reviews/inspections, measurement, non-conformance — Ch 5), safety-critical and cybersecurity requirements, IV&V applicability, traceability, and the Appendix A definitions. Does not cover detailed software-assurance/safety procedures (see NASA-STD-8739.8), implementation how-to and document content (see NASA-HDBK-2203), the systems-engineering process framework (see NPR 7123.1), or program/project management (see NPR 7120.5).

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。

Knowledge base from the GAO Schedule Assessment Guide (GAO-16-89G, 2015). Use for building, assessing, or auditing a program's integrated master schedule (IMS): the ten best practices of a reliable schedule (capture, sequence, resource, duration, traceability, valid critical path, reasonable total float, schedule risk analysis, updating, baseline), the four characteristics (comprehensive, well-constructed, credible, controlled), critical path method arithmetic (forward/backward pass, total float), schedule risk analysis (Monte Carlo, contingency), statusing and baseline control, and the Appendix II audit triad. Scheduling/time-management oriented: it is the authority on schedule reliability, but it is NOT a cost-estimating guide, a full SE process model, an agile guide, or a risk-management framework — see sibling packs (gao-cost, dau-se-guidebook, nasa-schedule, nasa-risk) for those.

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。

Reads, validates, and prepares CDISC SDTM and ADaM clinical trial data for analysis. Covers SDTM domain joins (DM, AE, EX, VS, LB, DS), ADaM architecture (ADSL, BDS, OCCDS, ADTTE) with traceability, treatment-emergent AE conventions, baseline derivation, SUPPQUAL/NSV handling, Define-XML 2.1, and Pinnacle 21 / CORE validation. Use when working with clinical trial datasets in CDISC SDTM/ADaM format, preparing analysis-ready data, or validating for regulatory submission.

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。

pbi-input, plan, todo, test-cases 間の整合性をチェックし、実装着手前の仕様漏れを検知する

plan artifact がある時のみ、plan 中の assumption / open question が実装で解消された証拠を diff・PR 本文と突合する evidence-sufficiency 観点。解消されないまま残った前提・未記録の新規 Unknown を検出する。plan 欠損時は発火しない（Pre-execution Gate）。plan 欠損でも PR 本文に前提が inline 列挙されていれば列挙分のみ部分評価し、計画 issue の bare 参照だけなら skip する

Reads, validates, and prepares CDISC SDTM and ADaM clinical trial data for analysis. Covers SDTM domain joins (DM, AE, EX, VS, LB, DS), ADaM architecture (ADSL, BDS, OCCDS, ADTTE) with traceability, treatment-emergent AE conventions, baseline derivation, SUPPQUAL/NSV handling, Define-XML 2.1, and Pinnacle 21 / CORE validation. Use when working with clinical trial datasets in CDISC SDTM/ADaM format, preparing analysis-ready data, or validating for regulatory submission.

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。

Create or revise the SDD Composy technical specification (tasks/prd-SLUG/techspec.md) from the approved PRD, resolved stories, and mapped codebase, with DEC/RISK and TU/TI/E2E traceability and a human gate. Use when the product contracts are approved and architecture is needed — 'criar a spec técnica', 'techspec do prd-SLUG', 'design the solution for…'. Do NOT use to change product scope, before PRD and stories approval, or for design notes outside SDD.

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。

Assess requirement clarity, testability, completeness, consistency, and traceability without inventing missing acceptance criteria.

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 an impact-based regression selection with explicit traceability, inclusions, exclusions, and limitations.

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 when the status, progress, completeness, traceability, or next valid action of a PWDEV Power product roadmap is requested

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。

Reads, validates, and prepares CDISC SDTM and ADaM clinical trial data for analysis. Covers SDTM domain joins (DM, AE, EX, VS, LB, DS), ADaM architecture (ADSL, BDS, OCCDS, ADTTE) with traceability, treatment-emergent AE conventions, baseline derivation, SUPPQUAL/NSV handling, Define-XML 2.1, and Pinnacle 21 / CORE validation. Use when working with clinical trial datasets in CDISC SDTM/ADaM format, preparing analysis-ready data, or validating for regulatory submission.

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 when reviewer comments arrive and each one needs a tracked decision, when a revise and resubmit letter must map every comment to a manuscript change, or when contradictory reviewer demands need evidence-based, editor-facing framing.

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 when building slides, a poster, or a lightning talk from a manuscript, when a presentation must exist in Turkish and English, or when conference visuals need a traceability check so every number on a slide matches the analysis behind it.

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。