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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

šŸŽÆ 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.

šŸŽÆ Use Cases (5)

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

āœ… Best For

  • Used by researchers at universities and biotech companies to accelerate analysis

šŸ’” Check With Vendor

Verify these considerations match your specific requirements:

  • Clinical diagnostics requiring IVD or CLIA-certified workflows

šŸ† 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.

šŸ’» Platforms

Web API

šŸ”Œ Integrations

Integrates with Illumina BaseSpace API for custom workflows

šŸ›Ÿ Support Options

  • āœ“ Email Support
  • āœ“ Live Chat
  • āœ“ Dedicated Support (Enterprise tier)

šŸ”’ Compliance & Security

āœ“ HIPAA āœ“ BAA Available āœ“ GDPR āœ“ SSO

šŸ’° Pricing

Contact for pricing

āœ“ 14-day free trial

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