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 comprehensive and seamless next-generation sequencing (NGS) data analysis solutions, including push-button tools for DNA sequence alignment, variant calling, and data visualization.
Analyze DNA sequencing data from large or small whole genomes, whole exomes, targeted gene regions, and more with our user-friendly software.
Data generated on Illumina sequencing instruments can be automatically transferred and stored securely in Illumina Connected Analytics and BaseSpace Sequence Hub. This genomics cloud computing environment features a collection of expert-preferred NGS data analysis apps that support a broad range of studies and simplify NGS data management. These apps provide scalable bioinformatics solutions for analysis of DNA sequencing data and other Illumina data.
The Illumina DRAGEN (Dynamic Read Analysis for GENomics) Bio-IT Platform provides highly accurate, ultra-rapid secondary analysis of NGS data, including data from whole-genome, exome, and targeted DNA sequencing experiments. Available in Illumina Connected Analytics, BaseSpace Sequence Hub, or on-premise, this platform offers a variety of accelerated secondary analysis pipelines, ranging from Germline to Somatic (T/N and Tumor-only), Joint Genotyping, Methylation, a stand-alone map and align pipeline, and more.
In addition, DRAGEN uses lossless genomic compression to rapidly compress and decompress FASTQ files. This technology reduces the data storage footprint by as much as 5x, all while preserving data integrity.
|Tumor-Normal Sequencing||DRAGEN Somatic|
|Exome Sequencing||DRAGEN Enrichment|
|Amplicon Sequencing||BaseSpace DNA Amplicon|
|Methylation Sequencing||DRAGEN Methylation Pipeline
|16S rRNA Sequencing||BaseSpace 16S Metagenomics|
See sample data sets for various methods in BaseSpace Sequence Hub, our genomics cloud computing environment, or test BaseSpace Apps and evaluate results interactively.
Note that a customer login is required to access BaseSpace Sequence Hub and view specific data sets
Access powerful turnkey bioinformatics tools that empower you to turn DNA sequencing data and other genomic information into biological insight.
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Using the Illumina Analytics Platform to advance discovery and improve cancer diagnosis and therapy selection.
Learn more about the accurate, ultra-rapid secondary analysis platform and accompanying pipelines.
The Illumina DRAGEN Bio-IT Platform offers accurate, ultra-rapid secondary analysis for a variety of applications.
Learn more about apps for common biological applications, including analysis of DNA sequencing data.
A modular, secure data platform for scalable multi-omics data management, analysis, and exploration.
Access user guides, release notes, and additional technical information.
Keep up with the latest tools and functionality in Illumina’s software and informatics portfolio, with spotlights on useful research methods and data examples.
Securely store, process, and share large quantities of NGS and other genomic data in the cloud with built-in speed and scalability.