We are Cofactor Genomics, a precision medicine company specializing in RNA-based diagnostics and immune profiling. We focus on creating predictive assays that use multidimensional RNA measurements to understand the tumor–immune microenvironment and support clinical decision-making. We operate a clinical laboratory capable of processing patient samples, generating RNA profiles, and delivering diagnostic-grade reports for immuno-oncology applications.

Core Services

Immune Profiling (OncoPrism Assay)
Our flagship service is a clinically validated RNA-based immune profiling test that helps predict patient response to immunotherapies. We measure the expression of key immune-related genes, process the data using our Health Expression Model (HEM) technology, and provide response prediction scores for clinicians and research teams.

RNA Sequencing & Transcriptomic Analysis
We perform RNA sequencing and expression profiling using standardized workflows optimized for clinical or FFPE samples. This includes sample QC, library preparation, sequencing, and data interpretation to support discovery and translational research.

Health Expression Model (HEM) Development
We develop proprietary multidimensional RNA models (“HEMs”) that transform raw RNA data into clinically meaningful insights. These models help support predictive assays and biomarker-driven studies.

Assay Development & Clinical Validation
We design, optimize, and validate RNA-based assays to meet clinical and research requirements in immuno-oncology and related fields.Bioinformatics & Study Design Support
We provide computational and analytical support for transcriptomic studies, including differential expression analysis, gene signature development, and study design consulting.

Why Researchers Choose Us

We specialize in RNA-based diagnostics to deliver insights beyond DNA-only methods.

Our proprietary Health Expression Model technology increases the predictive power of RNA data.

We offer clinically validated immune-profiling assays for immuno-oncology trials and clinical workflows.

We handle FFPE and low-input samples reliably to ensure consistent results.

We provide end-to-end support, from sample receipt to interpreted results.

Our team combines wet-lab and computational genomics expertise for seamless analysis and reporting.