Sequencing generates large volumes of data, and the analysis required can be intimidating. Fortunately, the analytical tools available today take most of the manual work out of the next-generation sequencing (NGS) data analysis process, making it easier for you to glean meaningful information quickly.
User-friendly Illumina tools smooth the process of analyzing sequencing data, so you can spend more time doing research and less time configuring workflows. Our NGS software packages perform analysis after the on-instrument data processing is complete and offer optimal time to answer.
Real-Time Analysis (RTA) software operates during cycles of sequencing chemistry and imaging, providing base calls and associated quality scores representing the primary structure of DNA or RNA strands. This built-in software performs primary data analysis on Illumina sequencing systems automatically.
Alignment and assembly of DNA or RNA fragments provides the full sequence for a sample, from which genetic variants can be determined.
We offer intuitive bioinformatics tools to simplify DNA sequence alignment, variant calling, and data visualization, and provide ultra-rapid secondary analysis.
Our user-friendly software tools simplify NGS data analysis for a broad range of RNA sequencing experiments, from gene fusion detection to total RNA expression profiling.
From sequence data, you can use biological data mining and interpretation tools to convert data into knowledge.
Interpreting genetic variation leads to knowledge and insights into basic biology, and the causes of diseases and how to treat or prevent them.
Phosphorus uses the DRAGEN Bio-IT Platform to perform genomics data analysis onsite and at an accessible price point.Read Interview
An Oxford scientist discusses her decision to move NGS data analysis to the cloud and the benefits it has given her lab, including increased productivity and cost-effectiveness.Read Interview
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Perform fast, robust secondary analysis of NGS data. Analyze sequencing data from whole genomes, whole exomes, germline and somatic datasets, RNA sequencing experiments, and more.Learn More
This genomics cloud computing platform offers data management and simplified bioinformatics for labs getting started and for rapidly scaling up NGS operations.Learn More
Accelerate NGS-based SARS-CoV-2 detection and identification, perform host response studies, simplify your sample tracking, and contribute to public databases, free of charge.Learn More
Sequencing data can be represented with a variety of file formats, many of which are interchangeable, and your informatics system needs to be able to handle the formats you’ll use.Learn More
Explore sample data generated on Illumina sequencing systems. These examples help you understand sequencing data and analysis reports.Learn More