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
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.
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.