
Welcome
Illumina Connected Insights is a powerful software solution designed for interpretation and reporting of next-generation sequencing (NGS) data. The software accepts data from various DNA and RNA oncology assays and variant callers, supports variants frequently identified in tumor samples (e.g., SNVs, indels, CNVs, SVs, fusions, splice variants) and genome-wide biomarkers (e.g., TMB, MSI, GIS used to assess HRD), integrates multiple genomic databases to annotate data, providing insights into biological significance, and generates customized comprehensive summary reports.
Access Connected Insights
There are two ways to access Connected Insights:
Cloud
This deployment is hosted by Illumina.
Local
The software can also be deployed on DRAGEN Server v4.
Navigate Connected Insights
Once you've logged in, click on a section below to help you navigate Connected Insights.
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