Basepair
Next Generation Sequencing (NGS) Data Analysis.
Overview
Basepair provides a user-friendly platform with over 30 automated pipelines for various NGS applications, including DNA-Seq, RNA-Seq, and single-cell analysis. It is designed for biologists and researchers who want to analyze their data without needing bioinformatics expertise or command-line skills, delivering interactive, publication-quality reports.
✨ Key Features
- Code-free, automated analysis pipelines
- Support for DNA-Seq, RNA-Seq, ChIP-Seq, scRNA-Seq
- Interactive, publication-quality reports
- Secure cloud-based platform
- Easy data upload and management
🎯 Key Differentiators
- Extremely user-friendly, no-code interface
- Wide range of pre-built, validated pipelines
- Fast turnaround time for analysis
Unique Value: Democratizes NGS data analysis by providing a simple, fast, and code-free platform for biologists and researchers to get from raw data to insights.
🎯 Use Cases (5)
✅ Best For
- Used by researchers at universities and biotech companies to accelerate analysis
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Clinical diagnostics requiring IVD or CLIA-certified workflows
🏆 Alternatives
Much easier to use than command-line tools or complex platforms like Galaxy, making it ideal for its target audience of bench scientists.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Live Chat
- ✓ Dedicated Support (Enterprise tier)
🔒 Compliance & Security
💰 Pricing
✓ 14-day free trial
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