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.

• 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