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Found 1,247 Skills
Configure Steedos Server via environment variables and YAML settings files. Covers required env vars (MONGO_URL, ROOT_URL, B6_TRANSPORTER, B6_CACHER), steedos-config.yml project settings, default.steedos.settings.yml template with env interpolation, datasources, tenant settings, CFS file storage (local, aliyun, aws, steedosCloud), SSO/OIDC, email, SMS, push notifications, and frontend asset URLs.
How to make UI5 Web Components applications accessible. Covers accessibility APIs (accessibleName, accessibleNameRef, accessibleDescription, accessibleRole, accessibilityAttributes), label-input relationships, invisible messaging, keyboard handling, high contrast themes, and screen reader support. Use when the user asks about ARIA attributes, screen readers, keyboard navigation, accessibility properties, or making their app accessible.
Configures the rollout shape of a PostHog experiment — the variant split (50/50, 80/20, A/B/C ratios), the overall rollout percentage that gates how many users enter the experiment, and the disambiguation when a percentage like "roll out to 25%" could mean either. Use when the user mentions a rollout percentage, variant split, or traffic distribution; gives a ratio like 60/40, 70/30, or 80/20; asks "who sees the test variant?"; wants to increase, decrease, or change the rollout or split on a draft or running experiment; weighs equal vs uneven splits; or proposes a mid-experiment split change (often an anti-pattern that needs reset or end-and-restart).
Query the Ensembl database to resolve gene, transcript, and protein IDs, fetch genomic or protein sequences, retrieve gene structures (exons), and get variant consequence and effect predictions (VEP). Use this skill as a primary ID translator, genomic sequence database and variant effect prediction tool.
Query the Genome Aggregation Database (gnomAD). Use when determining the rarity or allele frequency of specific genetic variants, retrieving gene constraint metrics (pLI, LOEUF) to assess loss-of-function intolerance, finding variants in a genomic region or gene, or querying structural variants. Don't use for analyzing individual patient genomes, tracking somatic mutations in cancer (use COSMIC), or requesting raw sequencing reads (use ENA).
Use when needing clinical significance, pathogenicity classifications (e.g., Pathogenic, Benign, VUS), clinical evidence rationales, or finding "hard positive" benchmark controls for human genomic variants.
Use when writing or reading GenVarLoader (gvl) datasets — preparing VCF/PGEN/SVAR variant sources with bcftools/plink2, calling gvl.write, configuring gvl.Dataset for haplotype/reference/annotated/variants output modes, attaching BigWig or Table tracks, setting up spliced haplotypes from a GTF, choosing track insertion-fill strategies for indels, or filtering variants by allele frequency.
How to customize and style UI5 Web Components. Covers CSS shadow parts, CSS custom states, CSS variables, and tag-level styling. Use when the user asks about changing component appearance, colors, spacing, theming, or overriding styles.
Use for "interrogate", "adversarial review", "multi-model review", "challenge this", "stress test this code", "find blind spots", or "tear this apart". Four LLM reviewers challenge changes from independent angles.
Query Ensembl genome database REST API for 250+ species. Gene lookups, sequence retrieval, variant analysis, comparative genomics, orthologs, VEP predictions, for genomic research.
Complete environment variable management with type-safe validation, Vercel dev workflow, and prebuild validation.
Validates environment variables in CI, prevents secret leaks, enforces masking, and provides fail-fast validation with clear documentation. Use for "secrets management", "env var validation", "credential security", or "secret masking".