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.
To register your software, refer to the documentation.
During the software registration process, you will need to create a domain and workgroup. Domains and Workgroups are used by Illumina Software to control access to your data and assets. When logging into Connected Insights, you will be required to select a workgroup to establish the context for your work.
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.
Once you have successfully set up your account and created your domain and workgroup, you can log in to Connected Insights. Follow the steps below.
Log in to the portal.
Select your domain from the list.
The software can also be deployed on .
Once you've logged in, click on a section below to help you navigate Connected Insights.
Select the Illumina Connected Insights application tile from the Product Dashboard.
Select your workgroup from the menu. Once you select a workgroup, it will automatically be chosen during future logins.
You will now be directed to the Cases Page.
Introducing Illumina Connected Insights
Navigating the Oncology Interpretation Bottleneck eBook
