GeneRADAR
Proprietary next-generation liquid biopsy platform for simultaneous DNA and RNA profiling
Company profile
Company profile
Predicine Inc. is a precision medicine company specializing in next-generation liquid biopsy technology for cancer diagnostics and monitoring. The company's proprietary GeneRADAR platform enables simultaneous profiling of cell-free DNA and RNA from blood and urine samples, providing comprehensive molecular insights into cancer biology. Predicine offers a portfolio of CLIA-certified and CAP-accredited genomic profiling assays including PredicineATLAS (600-gene panel), PredicineCARE (200-gene cfDNA assay), PredicineRNA (88-gene fusion/splicing detection), PredicineHEME (259-gene hematologic malignancies panel), and PredicineBEACON (MRD detection). The company operates CLIA/CAP-certified laboratories in California and Shanghai, supporting biomarker-driven clinical trials for leading biopharmaceutical companies across the United States and China. Predicine's technology enables treatment selection, disease monitoring, minimal residual disease detection, and assessment of key biomarkers including TMB, MSI, HRD, and homologous recombination deficiency. The company pioneered urine-based liquid biopsy for genitourinary cancers, offering a truly non-invasive alternative to blood-based testing. Predicine serves biopharmaceutical partners conducting Phase I-III clinical trials, providing end-to-end biomarker solutions from target discovery through commercial launch.
Company description Predicine official website
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01 · Operating footprint
Company-profile context for clinical focus, customers, deployment, integration, milestones, and partnerships.
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Company milestones
Published research on ctDNA biomarkers in giredestrant response for breast cancer, RAS-targeted therapy combinations, and tumor-informed ctDNA in HPV-independent head and neck cancer
Partnerships
02 · Flagship portfolio
Selected source-backed Company products and the available commercial context.
Proprietary next-generation liquid biopsy platform for simultaneous DNA and RNA profiling
600-gene NGS assay for comprehensive cancer variant profiling with TMB, MSI, HRD assessment
Next-generation actionable minimal residual disease (MRD) detection platform
200-gene ultra-sensitive cfDNA assay for treatment selection from blood and urine
259-gene NGS assay for hematologic malignancies including CLL/SLL and MCL
88-gene cfRNA assay for detection of gene fusions and splicing variants
Whole exome sequencing plus solution for comprehensive genomic analysis
03 · Research intelligence
Publications, preprints, clinical validation, and regulatory records in Evidence Position order.
Publications, clinical validation, and regulatory records connected to this Company appear here.
Research
EMBO molecular medicine · Jul 30, 2026
Clinicopathological and molecular study of two unique cases with microglandular and acinic cell-like breast carcinoma.Histopathology · Jun 16, 2026
Clinical and molecular correlates of circulating tumor fraction in patients with metastatic pancreatic ductal adenocarcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · May 26, 2026
Development, characterization, and inter-laboratory validation of methylated human cell free DNA candidate reference materials.Clinical epigenetics · May 18, 2026
Urinary Biomarkers Objectively Measure Minimal Residual Disease in Non-Muscle-Invasive Bladder Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · May 1, 2026
DNA Repair gene alterations and efficacy from gemcitabine and nab-paclitaxel with/without durvalumab and tremelimumab in metastatic pancreatic ductal adenocarcinoma.Nature communications · Mar 7, 2026
Clinical validation
No linked records are currently available.
Regulatory
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04 · Company-reported outcomes
Company-reported outcomes and customer stories are distinct from linked Research Intelligence evidence.
Reportable range down to 0.001% VAF for longitudinal monitoring
Robust profiling from as little as 0.4mL plasma or 1ng cfDNA
More robust variant detection in urine than blood for bladder cancer
6-14 days depending on assay type
Longitudinal assessment of cfDNA to identify patients responding to immune checkpoint inhibitor therapy in biliary tract cancer
Deep reduction in variant allele frequency (VAF) among responders to immune checkpoint inhibitor therapy
Clinical and genomic insights into circulating tumor DNA-based alterations across metastatic hormone-sensitive and castrate-resistant prostate cancer
Comprehensive molecular insights into tumor biology to determine targeted therapy options
Clinical application of liquid biopsy platform for precision medicine and patient care
Encouraging results supporting clinical application of liquid biopsy for patient care
05 · Leadership
Leadership profiles and professional links from the current Company record.
Massimo Cristofanilli
Strategic Advisor
06 · Company updates
Recent articles published on Predicine's official website.
No Company updates are currently listed.
07 · HAIC coverage
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08 · Official presence
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09 · Market pathway
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Market context
Companies using AI to analyze genomic, proteomic, metabolomic, or multi-omics data to provide personalized treatment recommendations, identify genetic risks, or develop targeted therapies. Includes genomic sequencing platforms with AI analysis, preventive medicine based on genetic risk assessment, and longevity care based on molecular and genetic data.
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