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Gene Panel Design Agent

---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. license: MIT metadata: author: AI Group version: "1.0.0" created: "2026-01-19" compatibility:

SKILL.md

Full skill instructions

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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:

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

FactorImpactOptimization
Panel sizeCost, depthPrioritize high-evidence genes
GC contentCoverage uniformityProbe design, blockers
Repeat regionsMapping challengesAvoid or boost coverage
Homologous regionsMisalignmentUnique design, blockers
Structural variantsDetectionIntronic coverage, breakpoints
CNV detectionRequire backboneTiled probes across genome

Gene Prioritization Sources

SourceContentEvidence Level
OncoKBActionable alterationsFDA/​guideline levels
CIViCClinical variantsCommunity-curated
ClinVarPathogenic variantsClassification criteria
NCCNGuideline genesClinical practice
COSMICCancer genesCensus 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

PlatformTypical SizeDepthCNV Capable
Hybrid capture1-3 Mb500-1000xYes (with backbone)
Amplicon10-500 kb1000-5000xLimited
Anchored multiplexVariableVariableFusions

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

FileContentPurpose
panel.bedTarget coordinatesSequencing design
probes.faProbe sequencesManufacturing
genes.csvGene list with rationaleDocumentation
validation.pdfQC planLaboratory setup

Author

AI Group - Biomedical AI Platform

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