Agent skill

gene-panel-design-agent

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Install this agent skill to your Project

npx add-skill https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/gene-panel-design-agent

SKILL.md


name: 'gene-panel-design-agent' description: 'AI-powered design of targeted gene panels for clinical and research applications including cancer diagnostics, pharmacogenomics, and rare disease testing.' measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools:

  • read_file
  • run_shell_command

Gene Panel Design Agent

The Gene Panel Design Agent provides AI-driven design of targeted sequencing panels for clinical diagnostics, cancer profiling, pharmacogenomics, and research applications.

When to Use This Skill

  • When designing custom gene panels for clinical or research use.
  • To optimize panel content for specific disease areas.
  • For balancing panel size with diagnostic yield.
  • When designing probes for hybrid capture or amplicon approaches.
  • To validate panel performance computationally.

Core Capabilities

  1. Gene Selection: Evidence-based gene prioritization for disease areas.

  2. Target Region Definition: Specify exons, introns, UTRs, promoters to include.

  3. Probe Design: In silico probe/primer design for capture or amplicon.

  4. Coverage Prediction: Estimate uniformity and dropout risk.

  5. Validation Planning: Design positive controls and performance metrics.

  6. Cost Optimization: Balance panel size with clinical utility.

Workflow

  1. Input: Disease focus, required genes, platform choice, size constraints.

  2. Gene Prioritization: Rank genes by clinical evidence level.

  3. Region Definition: Define target coordinates.

  4. Probe Design: Generate capture probes or primers.

  5. Coverage Simulation: Predict sequencing performance.

  6. Optimization: Iterate design for uniformity.

  7. Output: Panel BED file, probe sequences, validation plan.

Example Usage

User: "Design a comprehensive solid tumor panel covering actionable mutations and resistance markers."

Agent Action:

bash
python3 Skills/Genomics/Gene_Panel_Design_Agent/panel_designer.py \
    --disease solid_tumor \
    --gene_sources nccn,civic,oncokb \
    --platform hybcap \
    --target_size 1.5mb \
    --include_fusions true \
    --include_cnv_backbone true \
    --output panel_design/

Panel Design Considerations

Factor Impact Optimization
Panel size Cost, depth Prioritize high-evidence genes
GC content Coverage uniformity Probe design, blockers
Repeat regions Mapping challenges Avoid or boost coverage
Homologous regions Misalignment Unique design, blockers
Structural variants Detection Intronic coverage, breakpoints
CNV detection Require backbone Tiled probes across genome

Gene Prioritization Sources

Source Content Evidence Level
OncoKB Actionable alterations FDA/guideline levels
CIViC Clinical variants Community-curated
ClinVar Pathogenic variants Classification criteria
NCCN Guideline genes Clinical practice
COSMIC Cancer genes Census tier 1/2

Panel Types

Comprehensive Cancer Panel (300-700 genes):

  • All known cancer drivers
  • Actionable mutations
  • Resistance markers
  • MSI/TMB estimation

Focused Tumor Panel (50-100 genes):

  • Most actionable genes
  • Cost-effective
  • Higher depth possible

Pharmacogenomics Panel:

  • CPIC/DPWG genes
  • CYP450, HLA, transporters
  • Star allele compatible design

Rare Disease Panel:

  • Disease-specific genes
  • Deep intronic variants
  • CNV detection

AI/ML Components

Gene Ranking:

  • Literature mining for evidence
  • Mutation frequency weighting
  • Actionability scoring

Probe Optimization:

  • GC content balancing
  • Tm normalization
  • Off-target minimization

Coverage Prediction:

  • ML models from historical data
  • GC-coverage relationships
  • Dropout prediction

Validation Planning

Performance Metrics:

  • Coverage uniformity (CV)
  • On-target rate
  • Sensitivity by variant type
  • Reproducibility

Reference Materials:

  • Horizon Discovery cell lines
  • SeraCare controls
  • Well-characterized samples
  • In silico spike-ins

Technical Specifications

Platform Typical Size Depth CNV Capable
Hybrid capture 1-3 Mb 500-1000x Yes (with backbone)
Amplicon 10-500 kb 1000-5000x Limited
Anchored multiplex Variable Variable Fusions

Prerequisites

  • Python 3.10+
  • BEDTools for coordinate manipulation
  • Probe design algorithms
  • Reference genome and annotations

Related Skills

  • CRISPR_Design_Agent - For guide design
  • Variant_Interpretation - For variant selection
  • Tumor_Mutational_Burden_Agent - For TMB panel requirements

Output Files

File Content Purpose
panel.bed Target coordinates Sequencing design
probes.fa Probe sequences Manufacturing
genes.csv Gene list with rationale Documentation
validation.pdf QC plan Laboratory setup

Author

AI Group - Biomedical AI Platform

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