Transform raw DNA sequencing data into meaningful results

DNA Sequencing Data Analysis Solutions

Illumina sequencing systems can produce gigabases of sequencing data per day. Our intuitive bioinformatics solutions help researchers make sense of all those base calls. We offer a wide range of next-generation sequencing (NGS) data analysis software tools, including push-button tools for DNA sequence alignment, variant calling, and data visualization.

Data generated on Illumina sequencing instruments are automatically transferred and stored securely in BaseSpace Sequence Hub. BaseSpace Sequence Hub features a collection of expert-preferred data analysis apps that support a broad range of genomic studies. Analyze DNA sequencing data from large or small whole genomes, whole exomes, targeted gene regions, and more with these user-friendly apps.

Simple DNA Sequence Analysis Tools

Illumina has developed BaseSpace Apps to simplify NGS data handling and interpretation. Designed for researchers who need simple, comprehensive, and cost-effective analyses, these apps provide scalable bioinformatics solutions for analysis of DNA sequencing data and other Illumina data.

BaseSpace Sequence Hub

Easily and securely analyze, archive, and share NGS data, in the cloud or onsite.

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  • Are accessible to any researcher, regardless of bioinformatics experience
  • Support a broad range of applications, including whole-genome, targeted, and exome sequencing data analysis, as well as de novo sequencing, methylation sequencing, metagenomics studies, and more
  • Integrate with Illumina sequencing systems
  • Present results in easy-to-interpret reports
  • Allow instant data sharing with collaborators around the world
BaseSpace Apps for DNA sequence analysis:

Access powerful turnkey informatics tools that empower you to turn DNA sequencing data and other genomic information into biological insight.

  • BaseSpace Correlation Engine: Access a curated library of phenotypic and molecular data to compare and correlate with your DNA sequencing data.
  • BaseSpace Variant Interpreter: Quickly identify and classify disease-relevant DNA sequence variants, then communicate findings in a structured report.
Interpretation of DNA Sequencing Data
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BaseSpace Apps for Genome-Scale Analysis
BaseSpace Apps for Genome-Scale Analysis

Learn more about apps for common biological applications, including analysis of DNA sequencing data.

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ore Sequencing Lab Benefits from BaseSpace Cloud
Core Sequencing Lab Benefits from BaseSpace Cloud

BRC-Seq uses BaseSpace for sample tracking as well as data analysis, management, and sharing.

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BaseSpace Sequence Hub Support
BaseSpace Sequence Hub Support

Access user guides, app release notes, and additional technical information.

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Improve Your Sequencing Results
Improve Your Sequencing Results

NextSeq 500 v2 Kits offer better data quality, an improved signal-to-noise ratio, and a simplified workflow.

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BaseSpace Sequence Hub Data Security
BaseSpace Sequence Hub Data Security

Data are secure in the Illumina cloud analysis and storage platform.

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BaseSpace Sequence Hub Blog
BaseSpace Sequence Hub Blog

Keep up with the latest tools and functionality in BaseSpace Sequence Hub, with spotlights on useful research methods and data examples.

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