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效率与协作 · SKILL.md

rare-disease-rnaseq

rare-disease-rnaseq

【效率与协作】Blood RNA-seq expression-outlier detection for rare-disease diagnostics. Cases scored against a control reference panel; outliers ranked and filtered by a haploinsufficient disease-gene panel.

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技能说明

GitHub

name: rare-disease-rnaseq description: Blood RNA-seq expression-outlier detection for rare-disease diagnostics. Cases scored against a control reference panel; outliers ranked and filtered by a haploinsufficient disease-gene panel. license: MIT metadata: openclaw: requires: bins: - python3 env: null config: null always: false emoji: 🩸 homepage: https://github.com/ClawBio/ClawBio os: - darwin - linux install: - kind: uv package: pandas bins: null - kind: uv package: numpy bins: null - kind: uv package: matplotlib bins: null tags:

  • rna-seq
  • rare-disease
  • outlier-detection
  • OUTRIDER
  • FRASER
  • diagnostic
  • blood
  • transcriptomics
  • haploinsufficiency trigger_keywords:
  • rare disease rnaseq
  • expression outlier
  • OUTRIDER
  • FRASER
  • blood rna-seq diagnostic
  • NGRL
  • undiagnosed
  • candidate diagnosis version: 0.1.0

🩸 Rare-Disease Blood RNA-seq Outlier Detection

Reproduces the diagnostic principle of the Genomics England NGRL paper (Blood-based RNA-Seq of 5,412 individuals, medRxiv 2026.03.19.26348811). For each case sample, scores per-gene expression against a control reference panel and flags candidates falling in a curated dosage-sensitive disease-gene panel.

When To Use

  • A WGS-negative or WGS-VUS rare-disease patient with a paired blood RNA-seq sample
  • A clinical bioinformatician triaging candidate diagnoses before MDT review
  • A population-biobank team building an ancestry-matched control reference for outlier calling (e.g. Qatar Biobank for Sidra paediatric cases)

Method

Per-gene robust outlier scoring on log2(CPM+1):

  1. Library-size normalise (CPM), log-transform
  2. For each gene: compute median and MAD across the control panel
  3. For each case-gene cell: modified z = 0.6745 (x − median) / MAD
  4. Flag |z| ≥ threshold (default 3) and gene in disease panel
  5. Rank by |z|, separate down-outliers (haploinsufficiency-consistent) from up-outliers

This implements the diagnostic principle of OUTRIDER (per-gene outlier vs control panel) without the autoencoder, so it runs in seconds with no R/Bioconductor stack. For clinical-grade calls swap to the full DROP pipeline (gagneurlab/drop) which adds OUTRIDER's denoising autoencoder, FRASER2 splicing outliers, and confounder correction. The skill's I/O contract is the same so the upgrade is drop-in.

Input Contract

  • Counts matrix (.csv or .tsv): rows = genes (HGNC symbol), columns = sample IDs
  • Cases file (.txt): one case sample ID per line
  • Controls file (.txt): one control sample ID per line (typically n ≥ 50)
  • Disease panel (optional, .csv with gene and mechanism columns): defaults to a built-in 50-gene haploinsufficient panel

Output Structure

rdoutlier_report/
├── report.md                     # per-case candidate diagnoses + clinical narrative
├── result.json                   # standard ClawBio envelope
├── figures/
│   └── case_outlier_heatmap.png  # z-scores across cases × top genes
├── tables/
│   ├── outlier_calls.csv         # all flagged outliers with z-score, direction, mechanism
│   └── per_gene_stats.csv        # control median + MAD per gene
└── reproducibility/
    ├── commands.sh
    ├── environment.yml
    └── checksums.sha256

Demo

python clawbio.py run rdoutlier --demo

Generates 100 synthetic Gulf-ancestry control samples + 2 cases with injected outliers (FBN1 down, NF1 up) across a 200-gene panel. Demonstrates the diagnostic loop end-to-end in seconds.

Production Path (Sidra / QBB Reference)

ComponentDemoProduction
Aligner + quantifiernone (synthetic counts)STAR + featureCounts (or Salmon)
Outlier algorithmrobust per-gene z-scoreOUTRIDER autoencoder + FRASER2 splicing
Control panel100 synthetic samplesQBB n≈12K PAXgene blood RNA-seq
Confounder correctionnoneDROP pipeline (RIN, batch, hidden factors)
Disease panel50 haploinsufficient genesClinGen haploinsufficient + PanelApp
Return-of-result loopreport.mdSidra MDT reflex from WGS-negative referrals

Safety

  • Local-only processing, no network calls in core pipeline
  • Compatible with secure research environments (Genomics England RE pattern; Sidra clinical genomics environment)
  • Disclaimer required on every report

Disclaimer

ClawBio is a research and educational tool. It is not a medical device and does not provide clinical diagnoses. Consult a healthcare professional before making any medical decisions.

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