gene-panel-design-agent — independently scanned and version-tracked by SaferSkills.
SaferSkills independently audited gene-panel-design-agent (Agent Skill) and scored it 100/100 (green). The audit ran 55 deterministic rules across Security, Supply Chain, Maintenance, Transparency, and Community; it found 0 high-severity and 0 lower-severity findings. The full rule-by-rule trace and per-finding evidence are below. Free, methodology-open.
Findings & checks · 0 flagged
Every scanned point with the score it earned and what moved between them.
First recorded scan — no prior version to compare against.
The primary manifest — the file an agent reads to learn what this artifact does.
The Gene Panel Design Agent provides AI-driven design of targeted sequencing panels for clinical diagnostics, cancer profiling, pharmacogenomics, and research applications.
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/| 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 |
| 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 |
Comprehensive Cancer Panel (300-700 genes):
Focused Tumor Panel (50-100 genes):
Pharmacogenomics Panel:
Rare Disease Panel:
Gene Ranking:
Probe Optimization:
Coverage Prediction:
Performance Metrics:
Reference Materials:
| 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 |
| 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 |
AI Group - Biomedical AI Platform
~30 seconds. Free. No account. Every finding cites a rule and a line of evidence.