Results for “graphml”
4 skillsUrql
You are an expert in urql, the highly customizable and lightweight GraphQL client for React, Vue, Svelte, and vanilla JavaScript. You help developers fetch GraphQL data with minimal bundle size, document caching, normalized caching via Graphcache, exchanges (middleware pipeline), subscriptions, and offline support — providing a leaner alternative to Apollo Client with better extensibility.
0
Geniml
This skill should be used when working with genomic interval data (BED files) for machine learning tasks. Use for training region embeddings (Region2Vec, BEDspace), single-cell ATAC-seq analysis (scEmbed), building consensus peaks (universes), or any ML-based analysis of genomic regions. Applies to BED file collections, scATAC-seq data, chromatin accessibility datasets, and region-based genomic feature learning.
3 · bundle
Graphify
Drive Graphify from its CLI to build, refresh, query, export, and serve a durable code/corpus knowledge graph. Use when the user wants `.graphify/GRAPH_REPORT.md`, `graph.json`, `graph.html`, `graphify update`/`summary`/`query`/`path`/`explain`/`tree`, change-aware review context, git-hook or watch-based refresh, a stdio MCP graph server, or an install into jeo, jeopi, gjc, opencode, Claude, Codex, or Gemini. Also covers the honest structural fallback when native extraction is empty or misleading. Route simple locate/reference work to `codebase-search`, narrative knowledge-base work to `llm-wiki`, and project-memory handoff to `opencontext`. Triggers on: graphify, graphify update, graphify query, knowledge graph CLI, GRAPH_REPORT.md, graph.json, codebase graph, graph refresh, graphify install, graphify serve, review context, affected flows.
42 · bundle
Geniml
This skill should be used when working with genomic interval data (BED files) for machine learning tasks. Use for training region embeddings (Region2Vec, BEDspace), single-cell ATAC-seq analysis (scEmbed), building consensus peaks (universes), or any ML-based analysis of genomic regions. Applies to BED file collections, scATAC-seq data, chromatin accessibility datasets, and region-based genomic feature learning.
0 · bundle