812 件 ・ 関連度順
概要と使いどころ
Find web sources with query-relevant page excerpts and optional full-page content, and discover workflows, data APIs, and indexes. Use for web research or finding structured records, listings, transcripts, and datasets. Supports semantic tool discovery, domain matching, and progressive catalogue browsing.
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Run nf-core bioinformatics pipelines (rnaseq, sarek, atacseq) on sequencing data. Use when analyzing RNA-seq, WGS/WES, or ATAC-seq data—either local FASTQs or public datasets from GEO/SRA. Triggers on nf-core, Nextflow, FASTQ analysis, variant calling, gene expression, differential expression, GEO reanalysis, GSE/GSM/SRR accessions, or samplesheet creation.
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Use when the user says 'cognee', asks about knowledge graph or graph memory, wants to switch memory backends, or needs a status check, dataset init, or graph view. Covers Cognee endpoints plus the Brain fallback.
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Write performant Eloquent queries with eager loading, reusable scopes, and strict lazy-loading prevention in Laravel. Use when defining model relationships, creating query scopes, or processing large datasets with chunk/cursor.
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Execute long-running tasks in background isolates to keep the UI responsive. Use when performing heavy computations, parsing large datasets, or choosing between async/await and isolates.
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Publish and manage research papers on Hugging Face Hub. Supports creating paper pages, linking papers to models/datasets, claiming authorship, and generating professional markdown-based research articles.
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Look up and read Hugging Face paper pages in markdown, and use the papers API for structured metadata such as authors, linked models/datasets/spaces, Github repo and project page. Use when the user shares a Hugging Face paper page URL, an arXiv URL or ID, or asks to summarize, explain, or analyze an AI research paper.
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Builds tables and data grids for displaying tabular information, from simple HTML tables to complex enterprise data grids. Use when creating tables, implementing sorting/filtering/pagination, handling large datasets (10-1M+ rows), building spreadsheet-like interfaces, or designing data-heavy components. Provides performance optimization strategies, accessibility patterns (WCAG/ARIA), responsive designs, and library recommendations (TanStack Table, AG Grid).
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 standardized metadata for data assets. Use when documenting new datasets, building data catalogs, improving data discoverability, or creating data dictionaries for teams.
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。
Comprehensive data quality assessment against business rules, schema constraints, and freshness expectations. Activate when validating data pipeline outputs before production use, auditing a dataset against defined business rules, or producing a quality scorecard for a data asset.
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。
Systematic exploratory data analysis. Activate when a dataset needs profiling — structure check, nulls, outliers, distributions, correlations — before deeper analysis begins.
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。
UI/UX design-system intelligence - 84 styles, 192 palettes, 74 font pairings, 25 charts, 99 UX guidelines across 22 stacks (searchable dataset + CLI). Internal genjutsu module: loaded by /genjutsu:cast and /genjutsu:paint, not invoked directly.
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Screens biomedical / life-science papers for signs of data fabrication, image manipulation, and statistical anomalies, using the detection techniques distilled from the field's canonical exposure platforms (PubPeer, Data Colada, Science Integrity Digest, For Better Science) and tools (ImageTwin/Proofig, statcheck, GRIM/GRIMMER, Problematic Paper Screener, Seek & Blastn). Use when asked to check a paper/figure for image duplication, blot splicing, impossible statistics, paper-mill or tortured-phrase signals, research integrity, or "is this data faked"; or when a user shares a figure, Western blot, supplementary dataset, or DOI and asks whether it looks manipulated. Reports observable anomalies as questions for clarification — it never accuses anyone of fraud.
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Lifecycle SOP for **per-model prompt artifacts** — the compiled prompts, instructions, few-shot demos, edit-format pins, and embedding-bound indices that change behavior when the underlying LM, dataset, or framework version changes. Activate when adopting compiled prompts (DSPy, GEPA, BootstrapFewShot output), when supporting multiple LMs in production, when a provider deprecates a model snapshot, or when a framework deprecates a config surface (LlamaIndex `ServiceContext` → `Settings`, Aider edit-format defaults). Do NOT activate for one-off raw prompt edits or for truly model-agnostic system prompts that have been swap-tested. Search keywords: prompt portability, model swap, recompile prompt, model deprecation, prompt per model, prompt breaks on new model, version compiled prompts.
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Screen a Medicare/Medicaid claims corpus for fraud, waste, and abuse and produce ranked, fully-cited investigation referrals for an SIU / program-integrity team. Use when asked to run a fraud sweep, screen claims for FWA, find billing anomalies, or generate investigation referrals over a claims dataset.
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Extract structured data from clinical notes with span-level provenance and null-safety. Use when users say "extract [variables] from this note", "abstract this chart", "pull structured data from these notes", "what does this note say about [field]", or when building a chart-abstraction, registry, or cohort dataset from unstructured clinical text.
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Microscopy data management platform. Access images via Python, retrieve datasets, analyze pixels, manage ROIs/annotations, batch processing, for high-content screening and microscopy workflows.
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Automated hypothesis generation and testing using large language models. Use this skill when generating scientific hypotheses from datasets, combining literature insights with empirical data, testing hypotheses against observational data, or conducting systematic hypothesis exploration for research discovery in domains like deception detection, AI content detection, mental health analysis, or other empirical research tasks.
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Query NCBI Gene via E-utilities/Datasets API. Search by symbol/ID, retrieve gene info (RefSeqs, GO, locations, phenotypes), batch lookups, for gene annotation and functional analysis.
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This skill should be used at the start of any computationally intensive scientific task to detect and report available system resources (CPU cores, GPUs, memory, disk space). It creates a JSON file with resource information and strategic recommendations that inform computational approach decisions such as whether to use parallel processing (joblib, multiprocessing), out-of-core computing (Dask, Zarr), GPU acceleration (PyTorch, JAX), or memory-efficient strategies. Use this skill before running analyses, training models, processing large datasets, or any task where resource constraints matter.
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。
Digital pathology image processing toolkit for whole slide images (WSI). Use this skill when working with histopathology slides, processing H&E or IHC stained tissue images, extracting tiles from gigapixel pathology images, detecting tissue regions, segmenting tissue masks, or preparing datasets for computational pathology deep learning pipelines. Applies to WSI formats (SVS, TIFF, NDPI), tile-based analysis, and histological image preprocessing workflows.
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Access NCBI GEO for gene expression/genomics data. Search/download microarray and RNA-seq datasets (GSE, GSM, GPL), retrieve SOFT/Matrix files, for transcriptomics and expression analysis.
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Multiagent AI system for scientific research assistance that automates research workflows from data analysis to publication. This skill should be used when generating research ideas from datasets, developing research methodologies, executing computational experiments, performing literature searches, or generating publication-ready papers in LaTeX format. Supports end-to-end research pipelines with customizable agent orchestration.
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。
Infer gene regulatory networks (GRNs) from gene expression data using scalable algorithms (GRNBoost2, GENIE3). Use when analyzing transcriptomics data (bulk RNA-seq, single-cell RNA-seq) to identify transcription factor-target gene relationships and regulatory interactions. Supports distributed computation for large-scale datasets.
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。