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.
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||BaseSpace Whole-Genome Sequencing App|
|Tumor-Normal Sequencing||BaseSpace Tumor Normal App|
|Exome Sequencing||BaseSpace Enrichment App|
|Amplicon Sequencing||BaseSpace TruSeq Amplicon App|
|Methylation Sequencing||BaseSpace MethylSeq App|
|16S rRNA Sequencing||BaseSpace 16S Metagenomics App|
Access powerful turnkey informatics tools that empower you to turn DNA sequencing data and other genomic information into biological insight.