Confidently connect your genomic analysis workflows
Connected Insights harnesses extensive knowledge sources via powerful API-integrations for streamlined variant interpretation, including prioritization of relevant clinical trials, drug labels, and guidelines. User-defined control of the workflow enables a flexible and automatable path for reporting. Connected Insights helps you address the interpretation bottleneck and move precision medicine forward.
Streamlined
Harness the power of API-integrated knowledge sources into a single solution to bring insights to diverse applications. Customize your analysis settings, then automate to go faster.
Integrated
Remove unnecessary touchpoints and manual data movement for your NGS workflow. Seamless and secure, upstream and downstream.
Powered for growth
Keep pace with comprehensive test options that enable diverse variant and biomarker analyses. Expand test menus and scale volume without increasing headcount and interpretation resources.
We help you achieve
Insights
Generate insights from 45+ knowledge sources via a single interface via API-calling.
Private curation
Grow and manage your laboratories' private curated knowledge.
Automation
Configure assays in your lab's SOP for fast automation and scale.
Future-proofing
Evolve with confidence, ensuring compatibility with a wide range of assay types— panels, exomes, genomes, and beyond.
Regionality
Reflect regional and lab-specific practices for guidelines, clinical trial availability, and more in the user-defined data interpretation flow.
Security
Ensure data security, privacy, and compliance are in check across the entire workflow.
Key applications
DNA variants
Identify key DNA variant types (SVs, MNVs, exon-level CNVs, indels, fusions, tandem repeats) relevant in multiple disease types and across a variety of NGS assays.
RNA variants
Analyze variants from RNA (fusions, splice variants, and soon transcriptomics) to gain a deeper and more comprehensive understanding of malignancies.
Biomarker signatures
Uncover more insights by interpreting genome-wide, pan-cancer biomarker signatures (TMB, MSI, HRD) with increasing relevance to precision medicine.
NGS workflow with Illumina Connected Insights
Rapid, interpretable data for meaningful results
Prepare
Prepare libraries for somatic oncology panels or other compatible applications.
Sequence
Sequence libraries using any Illumina or other sequencing platform.
Analyze
Call variants with DRAGEN or other secondary analysis tools to generate VCF (Variant Call Format) output.
Interpret
Input VCF files to Connected Insights to enable generation of insights and case reporting.
Data security and compliance
High standards of data privacy and protection
To meet the most stringent security requirements, Illumina Connected Insights platform is built with security and compliance at its core. Read the data sheet for more details*.
* ISO 27001 certification expected by July 2023.
Highlights
Workflow configuration options
Configure once with a fine level of granularity to match your lab’s standard operating procedure (SOP). Accelerate your workflow with automation and standardization according to your SOP.
Lab curation
Grow your lab’s private knowledge base with every case and instantly interpret cases against your historical experience. Your curated knowledge is private, secure, and always at your fingertips.
Streamlined reporting
Customize based on lab name, lab branding, sections, fields, and more. Move sections and add or delete sections. Easily edit reports without data reingestion.
Software Preview
Quickly view key findings, coverage, and quality in a consolidated format. Intuitively access deeper evidence sources with a streamlined user interface design.
Control variant filters using extensive available options to match your exact SOP. Accelerate case turnaround time with efficient review and variant triage.
Easily filter and sort for variant prioritization for your case. Maximize efficiency by focusing on variants that are most likely to be associated with a disease or condition.
Stay focused on up-to-date and comprehensive variant-related details. Consolidate variant insights into assertions with full editing options and customizable outputs for your reports.
Product contents and related resources
Illumina Connected Insights video
Watch this video to understand how Connected Insights can connect various knowledge sources to streamline data interpretation operations for critical insights.
llumina Connected Insights data sheet
Read how Connected Insights streamlines, integrates, and powers molecular pathology laboratories for scale and growth.
Connecting knowledge to clinical data at scale
Key opinion leaders discuss the ongoing challenges and future potential of NGS in clinical oncology.
Related solutions
Comprehensive panels
Comprehensive genomic profiling (CGP) uses a single assay to assess hundreds of genes including relevant cancer biomarkers, as established in guidelines and clinical trials, for therapy guidance.
Whole-exome sequencing (WES)
Focus on sequencing coding regions, which frequently contain mutations that affect tumor progression, for a cost-effective approach.
Whole-genome sequencing (WGS)
Get a genome-wide view of somatic mutations and other genomic alterations present in cancer tissue and discover novel cancer-associated variants.
Related products
Clarity LIMS
Laboratory information management system that helps genomics labs track samples and manage workflows for an optimized and efficient lab.
DRAGEN Bio-IT platform
The Illumina DRAGEN Bio-IT platform provides accurate, comprehensive, and efficient analysis of next-generation sequencing data.
Illumina Connected Analytics
A secure genomic data platform to operationalize informatics and drive scientific insights.
Ready to connect with a genomic scientist?
Discuss your workflow to learn how you can streamline your NGS operations and power your lab for growth using Illumina Connected Insights.
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