The Illumina DRAGEN (Dynamic Read Analysis for GENomics) Bio-IT Platform provides ultra-rapid secondary analysis of next-generation sequencing (NGS) data.View Product
BaseSpace Apps enable researchers to perform complex sequencing data analyses. From RNA sequencing to exome/enrichment, amplicon, whole-genome sequencing (WGS), 16S metagenomics, and more, BaseSpace Apps meet the diverse needs of any researcher, regardless of bioinformatics experience.
In order to support researchers with analysis and sharing of genomic data in relation to the coronavirus outbreak, Illumina has developed a new suite of data analysis solutions for scientists studying the virus and host immune responses.Learn More
This web-based tool enables users to design their own custom Illumina targeted sequencing panels.
This software automatically performs on-instrument data analysis.
BlueFuse software provides molecular cytogenetic and in vitro fertilization (IVF) data analysis in a single framework.
Comprehensive, IVD, in-lab aneuploidy screening solution providing reagents, instruments, and software for accurate NIPT results in 26 hours.
*For In Vitro Diagnostic Use. Not available in all countries or regions.
This web-based tool provides a simple and powerful method for evaluating loci and creating successful custom genotyping assays.
Visualize and analyze data generated on Illumina microarray platforms with this powerful solution.
This software offers a direct path to reduce experimental microarray data size and facilitate data analysis for large experiments.
llumina and the Broad Institute are partnering to co-develop a suite of secondary genomic analysis pipelines. The partnership will result in new methods, integrating Illumina’s DRAGEN™ Pipelines and technology with Broad’s Genome Analysis Toolkit (GATK).Read More