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Basepair

Next Generation Sequencing (NGS) Data Analysis.

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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)

Academic research Biotech and pharma R&D Gene expression analysis Variant calling Single-cell transcriptomics

✅ 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

Galaxy Partek Flow QIAGEN CLC Genomics Workbench

Much easier to use than command-line tools or complex platforms like Galaxy, making it ideal for its target audience of bench scientists.

💻 Platforms

Web API

🔌 Integrations

Integrates with Illumina BaseSpace API for custom workflows

🛟 Support Options

  • ✓ Email Support
  • ✓ Live Chat
  • ✓ Dedicated Support (Enterprise tier)

🔒 Compliance & Security

✓ HIPAA ✓ BAA Available ✓ GDPR ✓ SSO

💰 Pricing

Contact for pricing

✓ 14-day free trial

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