Welcome
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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.
There are two ways to access Connected Insights:
This deployment is hosted by Illumina.
Once you've logged in, click on a section below to help you navigate Connected Insights.
To register your software, refer to the documentation.
Make sure all users are added to the workgroup and that the workgroup has the necessary permissions to access the Connected Insights application. For more information, refer to the documentation.
Log in to the portal.
You will now be directed to the .
The software can also be deployed on .
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