A high-precision data analysis skill designed for automated DNA sequencing quality assessment and variant confirmation.
The fastest way to install a skill directly from the registry.
npx clawhub@latest install sanger-chromatogram-qa
Copy the skill folder to one of these locations
~/.openclaw/skills/ <project>/skills/ Priority: Workspace > Local > Bundled
Copy this prompt to OpenClaw to install it automatically.
Help me install sanger-chromatogram-qa using Clawhub. If Clawhub is not installed, install it first (npm i -g clawhub).
Get the raw skill files in a ZIP archive.
Sanger Chromatogram QA is a specialized tool within the Openclaw Skills library designed for bioinformaticians and researchers who require rigorous quality control for DNA sequencing data. It provides a structured framework for analyzing .ab1 files, ensuring that data analysis workflows are executed with explicit assumptions and clearly defined output boundaries.
This skill bridges the gap between raw sequencing data and actionable insights by providing a reproducible execution path. By leveraging standardized Python scripts, it allows users to maintain high scientific integrity through documented fallback paths and disciplined output reporting, making it an essential component for laboratory data integrity.
scripts/main.py using provided inputs such as chromatogram files and reference sequences.To integrate this tool from the Openclaw Skills collection, ensure you have Python 3.10+ installed and follow these steps:
# Navigate to the skill directory
cd "scientific-skills/Data Analytics/sanger-chromatogram-qa"
# Install required dependencies
pip install -r requirements.txt
# Verify the script integrity
python -m py_compile scripts/main.py
# Access help documentation
python scripts/main.py --help
The skill utilizes a structured data input/output model to ensure consistency across genomic analysis tasks:
| Data Type | Parameter | Description |
|---|---|---|
| Input | ab1_file |
The raw Sanger chromatogram trace file. |
| Input | expected_seq |
The reference DNA sequence for alignment. |
| Input | variant_pos |
The specific coordinate of the expected mutation site. |
| Output | Quality Scores | Numerical assessment of base-calling reliability. |
| Output | Peak Detection | Identification of mixed or heterozygous peaks. |
| Output | Confirmation | Explicit validation of variants or repeat recommendations. |
scripts/main.py entry point for seamless integration into larger automated pipelines.Loading
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