Biomarker solutions to accelerate global clinical trials

Molecular Insights— base by base, from target discovery to commercial launch.

We are applying our expertise in genomic profiling to identify elusive cancer-related genetic changes and new biomarker targets across many cancer types. Our advanced cancer genome analysis helps researchers and biopharmaceutical partners accelerate new precision medicine development.

Comprehensive support for biomarker-driven drug development

We support genomic profiling of Phase I-III clinical trial samples in our CLIA-certified and CAP-accredited laboratories utilizing our panel of comprehensive molecular profiling assays.

CLINICAL APPLICATIONS

Liquid biopsy for treatment selection, disease monitoring, and MRD detection

Molecular profiling assays

One panel does not fit all

We offer a portfolio of comprehensive genomic profiling assays for precision medicine development.

Precision medicine

Immuno-oncology and biomarker solutions

  • TMB
  • MSI
  • PDL1 (CNV, SV)
PredicineATLAS™
Targeted therapy

DNA damage repair and clinical solutions

  • BRCA1/2
  • ATM
  • FGFR1/2/3/4
PredicineCARE™
Immunotherapy

Fusion and splicing RNA solutions

  • NTRK1/2/3
  • AR
  • MET
PredicineRNA™

Our Comprehensive Product Portfolio

Compare our assays

ALL SOLID TUMORSHEMATOLOGIC MALIGNANCIES
COMPAREPredicineATLAS™PredicineCARE™PredicineRNA™PredicineMRD™PredicineHEME™
OVERVIEWBroadest gene coveragePan-cancer panel (includes guideline-recommended genes) Panel for known or novel gene fusion / splice variantTargeted panel for minimal residual disease assessmentPanel for hematologic malignancies
NUMBER OF GENES600 (DNA)152 (DNA)88 (RNA)Indication specific 106 (DNA)
SPECIMEN TYPEBlood
Urine
Tissue
Blood
Urine
Tissue
Blood
Tissue
Blood
Urine
Blood
Bone marrow aspirate
TURNAROUND TIME10 Days10 Days10 Days10 Days10 Days
TMB
MSI
MMR
HRD
REPORT FEATURESSNVs
INDELs
CNA
CNL
Rearrangements
SNVs
INDELs
CNA
CNL
Rearrangements
RNA fusions
RNA splice variants
SNVs
INDELs
CNA
CNL
Rearrangements
Methylation
Chromosomal abnormalities
SNVs
INDELs
CNA
Rearrangements
DEPTH 20,000x20,000x 100,000x20,000x
SENSITIVITY0.25% down to 0.05%0.25% down to 0.05%10 copies0.01%0.25% down to 0.05%
VERSIONSCLIA
RUO
CLIA
RUO
RUORUORUO
WHOLE EXOME SEQUENCING
About cfWES

About cfWES
DETAILSAbout PredicineATLAS™ About PredicineCARE™About PredicineRNA™Contact usAbout PredicineHEME™

CROSS-BORDER TRIALS

Harmonized assay in U.S. and China for global clinical trials

We provide harmonized assays supported by unified quality management systems and workflow in our network of CLIA-certified and CAP-accredited facilities in U.S. and China to support cross-border clinical studies.

Get in touch

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