Agent Skillsexon-research/genomi › genomi-gnomad

genomi-gnomad

GitHub

用于查询特定变异的gnomAD公共人群等位基因频率。支持MAF、AF及按人群分层的统计,适用于评估变异稀有度或进行人群分层分析。

skills/gnomad/SKILL.md exon-research/genomi

Trigger Scenarios

询问特定变异的gnomAD频率 判断变异在gnomAD中是否罕见 查询特定人群(如非洲、东亚)的等位基因频率 需要MAF或AF数据时

Install

npx skills add exon-research/genomi --skill genomi-gnomad -g -y
More Options

Use without installing

npx skills use exon-research/genomi@genomi-gnomad

指定 Agent (Claude Code)

npx skills add exon-research/genomi --skill genomi-gnomad -a claude-code -g -y

安装 repo 全部 skill

npx skills add exon-research/genomi --all -g -y

预览 repo 内 skill

npx skills add exon-research/genomi --list

SKILL.md

Frontmatter
{
    "name": "genomi-gnomad",
    "tools": [
        "genomi.invoke"
    ],
    "mutating": true,
    "description": "Fetch reusable public population allele frequencies from gnomAD for a\nspecific variant. Use when the user asks about allele frequency, MAF,\npopulation stratification, gnomAD numbers, or rarity of a specific allele.\n"
}

Population Frequency (gnomAD)

Fetch public gnomAD population allele frequencies for one variant. Results are cached locally in the evidence database so subsequent queries reuse them.

Activation

To call the tool below, invoke it through the MCP dispatcher:

genomi.invoke({
  "tool": "gnomad.fetch_population_frequency",
  "params": {
    "chrom": "19",
    "pos": 44908684,
    "ref": "T",
    "alt": "C",
    "genome_build": "GRCh38"
  }
})

The dispatcher validates the params against the underlying tool's input schema and returns the underlying tool's response with an added dispatched_tool field.

When to use this skill

  • "What is the gnomAD frequency of rs429358?"
  • "Is this variant rare in gnomAD?"
  • "Allele frequency in African populations for rs1042522."
  • Any question that needs MAF, AF, population-stratified counts.

Boundaries

  • Variant-anchored only — query one allele at a time.
  • Public population data only — does not read the user's Active Genome Index.
  • Cached after first fetch — subsequent queries for the same variant reuse the local evidence store.

Cross-Capability Synthesis

A scope-limited result from this capability is not a final user-facing answer when other Genomi capabilities can contribute orthogonal evidence to the same question. Returning "cannot answer" while applicable capabilities remain unexamined is a host-agent failure mode.

Tools

gnomad.fetch_population_frequency

Fetch reusable gnomAD public population frequency for one allele and write it into evidence storage.

Use when: The agent needs gnomAD allele frequency, MAF, or population-stratified counts for a specific variant (rsID, chrom/pos/ref/alt, or VCF locus).

Why necessary: gnomAD is the canonical public population frequency source; cached results keep subsequent calls cheap.

Not for: Genome-wide rare-variant screening, ad-hoc curated annotations, anything not anchored to a specific variant.

Example prompts: What's the gnomAD frequency of rs429358? Is rs1042522 rare in East Asian populations?

Result semantics: Returns the gnomAD record with population-stratified counts and frequencies plus a populations block; writes to the local evidence database for reuse.

Version History

  • 47e0d05 Current 2026-07-05 10:53

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Metadata

Files
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Version
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Hash
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Indexed
2026-07-05 10:53

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