Agent Skillsexon-research/genomi › genomi-gnomad

genomi-gnomad

GitHub

通过 gnomAD 获取特定变体的公共群体等位基因频率,支持 MAF、人群分层计数及罕见度查询。仅针对单变异点,结果本地缓存以复用。适用于需验证特定 rsID 或坐标变体频率的场景,不用于全基因组筛选。

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

Trigger Scenarios

查询特定变体的 gnomAD 频率或 MAF 评估变体在特定人群中的罕见程度 获取人群分层统计信息

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

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Version
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Hash
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Indexed
2026-07-05 10:53

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