Variant functional impact prediction: VEP consequence types (HIGH/MODERATE/LOW/MODIFIER), SIFT, PolyPhen-2, and CADD scoring. Rule-based annotation engine for demo, wraps VEP/snpEff/ANNOVAR.
Scanned 9/7/2026
Install to Claude Code
npx -y skills add mdbabumiamssm/LLMs-Universal-Life-Science-and-Clinical-Skills- --skill genomics-variant-annotation --agent claude-codeInstalls into .claude/skills of the current project.
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---
name: genomics-variant-annotation
description: >-
Variant functional impact prediction: VEP consequence types (HIGH/MODERATE/LOW/MODIFIER),
SIFT, PolyPhen-2, and CADD scoring. Rule-based annotation engine for demo, wraps VEP/snpEff/ANNOVAR.
version: 0.2.0
author: OmicsClaw
license: MIT
tags: [genomics, annotation, VEP, snpEff, ANNOVAR]
metadata:
omicsclaw:
domain: genomics
emoji: "📝"
trigger_keywords: [variant annotation, VEP, snpEff, ANNOVAR, functional effect]
allowed_extra_flags:
- "--method"
legacy_aliases: [variant-annotate]
saves_h5ad: false
---
# 📝 Variant Annotation
Variant annotation and functional effect prediction. Supports VEP, snpEff, and ANNOVAR.
## CLI Reference
```bash
python omicsclaw.py run genomics-variant-annotation --demo
python omicsclaw.py run genomics-variant-annotation --input <data.vcf> --output <dir>
```
## Why This Exists
- **Without it**: Variants lack biological context, remaining as simple coordinate tuples
- **With it**: Transforms structural variation into biological impact and transcript-level consequences
- **Why OmicsClaw**: Unified framework for multiple ontology backends like VEP or ANNOVAR without custom parsing
## Workflow
1. **Calculate**: Prepare genome indices and transcript boundary maps.
2. **Execute**: Run annotation search across known consequence states.
3. **Assess**: Filter variants by putative pathological score.
4. **Generate**: Save annotated VCFs with strict ontologies.
5. **Report**: Tabulate key functionally relevant variants.
## Example Queries
- "Annotate this vcf file using VEP"
- "Run snpEff and summarize high impact variants"
## Output Structure
```
output_directory/
├── report.md
├── result.json
├── annotated.vcf.gz
├── figures/
│ └── impact_distribution.png
├── tables/
│ └── top_variants.csv
└── reproducibility/
├── commands.sh
├── requirements.txt
└── checksums.sha256
```
## Safety
- **Local-first**: Strict offline processing without external upload.
- **Disclaimer**: Requires OmicsClaw reporting structures and disclaimers.
- **Audit trail**: Hyperparameters and operational flow states are logged fully.
## Integration with Orchestrator
**Trigger conditions**:
- Automatically invoked dynamically based on tool metadata and user intent matching.
**Chaining partners**:
- `variant-call` — Upstream raw variation
- `vcf-ops` — Upstream filtering steps
## Citations
- [VEP](https://doi.org/10.1186/s13059-016-0974-4) — Variant Effect Predictor
- [snpEff](https://doi.org/10.4161/fly.19695)
- [ANNOVAR](https://doi.org/10.1093/nar/gkq603)
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