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 can be 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, including the highly accurate, ultra-rapid suite of DRAGEN Pipelines.
Illumina's DRAGEN Bio-IT Platform provides highly accurate, ultra-rapid secondary analysis of genome, exome and targeted experiments. Available in BaseSpace Sequence Hub or on-premise, the DRAGEN Platform offers a variety of accelerated secondary analysis pipelines, including Germline, Somatic (T/N and Tumor-only), Joint Genotyping, Methylation, and a stand along map and align pipeline.
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.
|Whole-Genome Sequencing||DRAGEN Germline
DRAGEN Somatic Pipeline
|Tumor-Normal Sequencing||DRAGEN Somatic Pipeline|
|Exome Sequencing||BaseSpace Enrichment|
|Amplicon Sequencing||BaseSpace DNA Amplicon|
|Methylation Sequencing||DRAGEN Methylation Pipeline
|16S rRNA Sequencing||BaseSpace 16S Metagenomics|
Access powerful turnkey informatics tools that empower you to turn DNA sequencing data and other genomic information into biological insight.