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.
Analyze DNA sequencing data from large or small whole genomes, whole exomes, targeted gene regions, and more with our user-friendly tools.
Data generated on Illumina sequencing instruments can be automatically transferred and stored securely in 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 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.
Learn more about:
|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 bioinformatics tools that empower you to turn DNA sequencing data and other genomic information into biological insight.