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概要と使いどころ
Use when anticipating referee objections or calibrating review expectations for an American Economic Journal: Microeconomics (AEJ: Micro) manuscript before submission. Pre-empts the objections theory referees raise and reads the editorial process; it does not draft the response letter (see aejmic-rebuttal).
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Use to understand how Agricultural Systems (AgSy) evaluates a manuscript — single-anonymized peer review with a minimum of two reviewers and an editor decision, desk screening for fit and systems content, what reviewers weigh, and the rapid-review track for Perspectives. Sets expectations and shapes the paper to survive review; it does not contact editors.
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 and refining exhibits for an Administrative Science Quarterly (ASQ) manuscript — qualitative data structures and data-to-theory tables, process models, and quantitative tables. Designs exhibits; it does not run the analysis behind them.
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 the theoretical engine for an Administrative Science Quarterly (ASQ) manuscript — mechanisms, process vs. variance logic, constructs, and boundary conditions. Builds the argument; it does not select methods or run analysis.
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。
当你在需要理解《自动化学报》(Acta Automatica Sinica, AAS) 的双盲三审制审稿流程、各环节时间进度与作者可施加的杠杆时调用。建模编辑初审→双盲外审→退修/复审(多轮)→主编终审的完整链路，说明作者承诺前置、双盲对作者的约束、退修期限与重新送审、状态查询，帮助作者在 Acta Automatica Sinica 的评审各节点做出正确动作、管理预期并避免流程性失误。
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Use when explaining or planning around ACM CCS peer review, the two-cycle HotCRP workflow, decision categories including minor revision, the rebuttal window, the adversarial reviewer pool, ethics and disclosure scrutiny, meta-review dynamics, and ACM proceedings outcomes.
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。
当你需要理解《电子学报》(Acta Electronica Sinica, AES) 审稿流程、稿件状态与时限时使用。覆盖投稿受理→编辑初审→双盲外审(同行评议)→复审→主编/编委会终审→退修与再审轮次→录用的多级审理链路，各阶段可能的决定(录用/退修/退稿)、6 个月未答复红线、如何解读稿件状态、如何礼貌催稿、以及本刊与英文姊妹刊 Chinese Journal of Electronics 的分流关系。帮助电子/信息/通信方向作者对《电子学报》的审理节奏与决策点建立准确预期，合理规划投稿与修回。
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 the exhibits of an Accounting, Organizations and Society (AOS) manuscript — data-inventory and evidence tables for qualitative work, cell-means and process-test tables for experiments, and figures that carry theoretical weight — in Elsevier-compatible format. Builds exhibits; it does not run the analysis (aos-data-analysis).
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 reasoning about how an ACL paper travels through ACL Rolling Review and conference commitment, covering reviewer and area-chair roles, meta-reviews, the commitment decision by senior area chairs and program chairs, Findings versus main-conference outcomes, ethics review escalation, and resubmission strategy across cycles.
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 the conceptual exhibits of an Academy of Management Review (AMR) manuscript — process models, 2x2 typologies, multi-level frameworks, and propositions tables that carry theoretical work. These are CONCEPTUAL figures, NOT data plots; AMR has no charts of results because it has no data.
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 the theoretical engine of an Accounting, Organizations and Society (AOS) manuscript — choosing a social/organizational theory tradition (institutional theory, governmentality, Bourdieu, actor-network theory, practice theory, psychological process theory) and making it generate the analysis rather than decorate it. Builds the lens; it does not collect data (aos-methods) or frame the contribution (aos-contribution-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 drafting an AAAI author response (rebuttal) under the single short character-limited author-feedback window, the no-URL rule, no-new-results guidance, AI-generated-review handling, and the AAAI two-phase review process where Phase-2 papers receive one feedback round before SPC/AC discussion.
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 explaining or planning around AAMAS peer review, covering OpenReview review release, the double-blind rebuttal on preliminary reviews, area-chair discussion, the mixed game-theory, MARL, and systems reviewer pool, the public posting of reviews and decisions, and how acceptance criteria weigh the interaction contribution.
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Detect buying signals across TAM companies and watchlist personas. Three-phase architecture: (1) free diff-based signals from existing data (headcount growth, tech stack changes, funding rounds), (2) Apify-powered signals (job postings, LinkedIn content analysis, profile changes), and (3) post-processing with dedup, scoring, and lead status updates. Writes signals to Supabase signals table for downstream activation.
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Lead qualification engine with conversational intake. Asks structured questions to understand your qualification criteria, generates a reusable qualification prompt, then batch-enriches leads via Apify LinkedIn scraping and scores them with parallel processing. Outputs qualified/disqualified verdicts with confidence scores and reasoning to CSV or whatever output format the user prefers. Supports calibration mode for prompt refinement.
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。
Drive and verify an Electron or Tauri desktop app from the inside, including the main-process and Rust IPC calls a browser tool cannot see. Use when a desktop app needs testing, when a feature works in the browser but not in the packaged app, when an IPC or invoke call needs proving, when a desktop screenshot or visual diff is wanted, or when you need a headless run of a desktop UI in CI.
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Comprehensive guide for developing WebGPU-enabled Three.js applications using TSL (Three.js Shading Language). Covers WebGPU renderer setup, TSL syntax and node materials, compute shaders, post-processing effects, and WGSL integration. Use this skill when working with Three.js WebGPU, TSL shaders, node materials, or GPU compute in Three.js.
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Specify algorithms for Model-Based Design: system specs, architecture specs, implementation plans, test plans. Use when creating specifications for controllers, signal processing, diagnostics, estimators, or other algorithms authored in Simulink, Stateflow, System Composer, or MATLAB Function blocks.
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Turns Hi-C/Micro-C FASTQ into a deduplicated, filtered .pairs file with pairtools and decides whether the library worked. Covers the bwa mem -SP5M / bwa-mem2 / chromap --preset hic alignment idiom (mates mapped as independent single-end reads), pairtools parse vs parse2 and the walks-policy choice (5unique pairwise vs all for Pore-C/Micro-C concatemers), pair-type classification (keep UU and rescued UC), dedup (PCR vs optical/by-tile), select by pair_type/MAPQ/distance, restriction-fragment handling (restrict, Arima dual-enzyme, Micro-C/DNase fragment-free), and allele-specific phasing (pairtools phase to two coolers). The library-QC decision uses % long-range cis as the one-number quality metric, trans as the noise floor, orientation balance as fragment-map-free dangling-end/self-circle QC, and % duplicates as a complexity proxy. Use when processing Hi-C/Micro-C/Omni-C reads into pairs, judging library quality, handling multi-enzyme or restriction-agnostic protocols, or generating allele-specific contacts.
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Segment single cells from multiplexed IMC/MIBI tissue images using Mesmer/DeepCell, Cellpose, or ilastik+CellProfiler, covering whole-cell vs nuclear segmentation, the summed-membrane-channel decision, nuclear-expansion bias, lateral spillover, resolution-floor parameters, and downstream-proxy evaluation. Use when delineating cells after preprocessing, choosing a segmentation model, building a cell mask for quantification, diagnosing impossible double-positive populations, or troubleshooting over/under-segmentation.
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Delimits putative species boundaries from molecular data within the de Queiroz 2007 unified-lineage framework using ASAP (Puillandre 2021 successor to ABGD), mPTP C++ (Kapli 2017 successor to bPTP; bPTP is Python NOT R), GMYC single/multi-threshold (Pons 2006; Fujisawa 2013), multilocus BPP v4 with prior calibration from data (NOT defaults; Yang 2015), SNAPP + BFD* for SNP delimitation, DELINEATE (Sukumaran 2021) speciation-process modeling to address Sukumaran & Knowles 2017 PNAS critique that MSC delimits structure not species, integrative-taxonomy congruence (Padial 2010; Carstens 2013), Dsuite for introgression testing before sister claims (Malinsky 2021), and Meyer & Paulay 2005 barcoding-gap-absence caveat. Use when delineating species from DNA barcoding data, resolving cryptic complexes, choosing among ASAP/mPTP/BPP/DELINEATE, calibrating BPP priors, distinguishing introgression from ILS, or applying the Sukumaran-Knowles oversplitting correction.
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Stores and operates on sparse expression matrices for single-cell and large bulk RNA-seq, covering dgCMatrix/dgRMatrix/dgTMatrix when-each-is-fast, the dgCMatrix (CSC, R) <-> CSR (Python) implicit transpose, AnnData (cells-rows) <-> SingleCellExperiment (cells-cols) orientation flip, HDF5/h5ad vs Zarr cloud-native shift, HDF5SummarizedExperiment + DelayedArray for out-of-memory bulk, scanpy backed mode for large h5ad, the ~10-15% density crossover where dense beats sparse, 10X format proliferation (MTX vs CellRanger H5 vs h5ad), the dense-conversion memory blow-up, and Dask + Zarr for consortium-scale matrices. Use when choosing sparse format, working with single-cell-sized matrices, importing/exporting 10X, debugging R/Python interop transposes, processing matrices too large for RAM, or building cloud-native pipelines.
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Aligns and QCs methylated-RNA-immunoprecipitation (MeRIP / m6A-seq) IP and input libraries using STAR or HISAT2 splice-aware mapping, samtools sort/index, IP/input matched-pair tracking, antibody-lot metadata recording, replicate concordance via deepTools multiBamSummary + plotCorrelation, IP enrichment QC via plotFingerprint and per-transcript IP/input ratio distributions, library-complexity saturation curves via PreSeq, and the explicit do-NOT-deduplicate convention for standard non-UMI MeRIP. Use when preparing paired IP and input BAM files for exomePeak2 / MeTPeak / MACS3 peak calling, evaluating MeRIP replicate concordance and IP enrichment, deciding whether to deduplicate (standard MeRIP typically NOT), choosing genome-vs-transcriptome alignment for downstream peak vs m6Anet workflows, recording antibody clone and lot metadata for cross-batch reconciliation, detecting failed IPs via saturation curves and IP/input distribution shape, or generating IP-over-Input bigWig tracks for visualisation.
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Reads, inspects, and writes Flow Cytometry Standard (FCS) files from conventional, spectral, and mass cytometry (CyTOF), and parses FlowJo/Cytobank/Diva workspaces. Covers FCS 2.0/3.0/3.1/3.2 internals ($PnE linear-vs-log, $DATATYPE, $SPILLOVER vs SPILL vs $COMP, $TIMESTEP), channel/parameter metadata, the silent linearize/truncate defaults, and R (flowCore, flowWorkspace, CytoML) plus Python (FlowKit, readfcs) readers. Use when loading flow or mass cytometry data, mapping detector channels to antibodies, extracting the event matrix, choosing a reader, or bridging FCS to the scanpy/AnnData ecosystem before preprocessing.
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。