Developing and setting up a new NGS analysis pipeline can be a time and money-consuming venture. Lynn Fink, Lab Director at Xing Cancer Care in Brisbane Australia shares how she uses Illumina’s BaseSpace Sequence Hub and DRAGEN to reduce costs, simplify implementation and ensure security.
Retterer, Chief Innovation Officer at GeneDx, details how his company seamlessly integrated the DRAGEN Server into its existing on-premises solution to lower costs and reduce turnaround times, enabling the lab to analyze a whole genome on DRAGEN in less time than an exome on the company’s existing system.
Learn about new and upcoming product releases in informatics solutions from Illumina Software Engineering. Illumina Sr. Director of Informatics, Rami Mehio, presents a short overview of the Illumina informatics portfolio and highlights exciting new options coming soon.
Illumina and the Broad Institute of MIT and Harvard have announced a collaboration for the co-development of secondary genomic analysis algorithms and software. Join Geraldine Van der Auwera, Director of Outreach at the Broad Institute, and Angel Pizarro, Associate Director at Illumina, as they present the details around this exciting new partnership and discuss how this collaboration can help further drive the advancement of genomic analysis.
Maximize the effectiveness of informatics workflow, train new employees, or learn the latest technologies. A series of training videos for Illumina informatics portfolio are available.
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