
Truveta
Saving lives with data by providing regulatory-grade safety and effectiveness data.

Empowering local laboratories with automated, IVD-cleared genomic profiling for precision oncology.

Personal Genome Diagnostics (PGDx), a Labcorp brand, represents a paradigm shift in precision oncology by decentralizing high-complexity genomic testing. As of 2026, the PGDx elio platform serves as a critical infrastructure for local laboratories, providing them with the bioinformatics and kitted reagents necessary to perform comprehensive tumor profiling (CGP) in-house. The technical architecture revolves around the elio bioinformatics pipeline, which utilizes advanced machine learning algorithms to automate the detection of complex biomarkers including Tumor Mutational Burden (TMB) and Microsatellite Instability (MSI). Unlike traditional 'send-out' models, PGDx enables faster turnaround times by keeping the data and samples within the local clinical ecosystem. The platform integrates seamlessly with Illumina sequencing hardware, providing a standardized, FDA-cleared solution for both tissue and liquid biopsy (plasma) analysis. Market positioning for 2026 focuses on the democratization of advanced genomic insights, reducing the barrier to entry for regional health systems to offer state-of-the-art diagnostic capabilities that were previously restricted to centralized academic centers.
Personal Genome Diagnostics (PGDx), a Labcorp brand, represents a paradigm shift in precision oncology by decentralizing high-complexity genomic testing.
Explore all tools that specialize in tmb analysis. This domain focus ensures Personal Genome Diagnostics (PGDx) delivers optimized results for this specific requirement.
A proprietary, automated software suite that performs alignment, variant calling, and annotation without requiring expert bioinformatician manual intervention.
Advanced noise reduction algorithms and molecular barcoding to detect circulating tumor DNA (ctDNA) at ultra-low variant allele frequencies.
Standardized calculation of Tumor Mutational Burden across 500+ genes to predict response to immune checkpoint inhibitors.
Software is designed to run locally on-site, ensuring data sovereignty and reducing latency associated with cloud-based send-outs.
Real-time monitoring of sequencing quality, depth of coverage, and sample contamination metrics.
Integrated RNA-based analysis for the identification of complex structural variants and driver fusions.
Algorithmic assessment of microsatellite loci to determine stability status, crucial for Lynch syndrome and IO therapy.
Clinical laboratory site assessment and regulatory compliance verification.
Installation and calibration of PGDx elio server hardware within the local environment.
Integration with local Laboratory Information System (LIS) via HL7 or API.
Procurement of PGDx elio tissue or plasma kitted reagents.
Training of lab personnel on DNA/RNA extraction and library preparation protocols.
Sequencing run setup on validated Illumina platforms (e.g., NextSeq).
Automated data transfer from sequencer to the elio bioinformatics pipeline.
Review of automated variant calls and quality control metrics.
Generation and clinical validation of the patient-ready diagnostic report.
Ongoing technical support and software updates via secure remote connection.
All Set
Ready to go
Verified feedback from other users.
"Highly regarded for its regulatory compliance and ease of automation in clinical settings, though implementation costs are high."
Post questions, share tips, and help other users.

Saving lives with data by providing regulatory-grade safety and effectiveness data.

Breast AI trusted for better workflow and higher confidence in mammography screening.

Assistive communication solutions for people with disabilities.

Turn your diabetes data points into accessible, actionable, and meaningful insights.

Science-backed supplements for personalized wellness.

Hear everything in a heartbeat with advanced digital stethoscope technology.