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OMI™ OncoCare

Discover the OMI™ OncoCare Series

An advanced suite of next-generation sequencing (NGS) tests designed to provide clinicians with actionable insights for personalized cancer care

OMI ™ TumorMap

Advanced tumor profiling that delivers critical insights to guide targeted cancer treatment—maximizing effectiveness while minimizing toxicity.

OMI ™ TumorTarget

Precision genetic testing to assess eligibility for specific cancer therapies, including PARP inhibitors and immuno-oncology (IO) treatments.

OMI ™ MRDTracker

Highly sensitive, non-invasive tests for detecting minimal residual disease (MRD), offering personalized insights into cancer progression, metastasis, and treatment response.

 

OMI ™ Heredity

Advanced hereditary cancer screening empowers individuals to understand their risk and take control of their health. 

From diagnosis to treatment selection and ongoing monitoring, OMI ™ OncoCare is here for you at every step.

Advantages of Oncogenetic Testing

Oncogenetic testing empowers clinicians with critical insights to guide treatment decisions, improving patient outcomes through precision medicine.

Targeted Therapy

Identifies actionable mutations, enabling clinicians to prescribe targeted therapies that improve efficacy and minimize unnecessary treatments.

Better Prognosis

Provides a clearer understanding of tumor behavior, allowing for earlier interventions and optimized treatment strategies.

Reduced Side Effects

Helps avoid ineffective treatments, reducing toxicity and enhancing patient quality of life.

Have any questions?

Our dedicated team is here to support you every step of the way, from test selection to sample collection and results interpretation. 

Explore Our Comprehensive Testing Solutions

  • OMI™ TumorMap
  • OMI™  MRDTrack
  • OMI™ TumorTarget
  • OMI™ Heredity

OMI™ TumorMap

Successful cancer treatment requires personalized care. Unlike traditional approaches, precision oncology uses the genetic profiles of both the tumor and patient to guide treatment decisions. OMI TumorMap provides clinicians with key insights to select the most effective therapies, minimize side effects, and optimize responses, ensuring tailored treatments that maximize outcomes and minimize toxicity.

Focus Panel

136 targeted genes for targeted therapy 

Tumor Mutation Burden assessment 

317 SNP loci on 181 genes for chemotherapy and endocrine therapy optimization 

51 genes for hereditary cancers *

*Only with germline control 

Demo Report

Deep Panel

1,326 genes for targeted therapy

Tumor Mutation Burden assessment

Microsatellite Instability assessment

HLA and 39 immunotherapy efficacy associated genes assessment

20,000 x sequencing depth

Demo Report

TumorMap WES

20,000 genes for targeted therapy

Tumor Mutation Burden assessment 

Microsatellite Instability assessment 

HLA and neoantigen assessment 

HRD score to determine therapy responsiveness

Screens chemotherapy and endocrine therapy toxicity for treatment optimization

Screens for HPV, HBV, EBV

Screens 99 genes for 47 hereditary cancers 

Demo Report

 OMI™  MRDTrack: Minimal Residual Disease (MRD) Monitoring

 OMI™  MRDTrack + OMI™  WES

OMI OncoCare MRDTrack is a customized MRD gene test for solid tumors. It first utilizes TumorMap WES to analyze the patient’s tumor tissue and identify mutations. A proprietary algorithm selects 40 personalized molecular tags and integrates 21 key tumor driver genes to design custom MRD probes. These probes enable ultra-high depth (100,000X) blood-based MRD monitoring, detecting ultra-low frequency mutations to track tumor recurrence and secondary primary tumors. MRDTrack provides early recurrence warnings before traditional methods like PET scans, guiding timely clinical decisions and optimal treatment strategies.

Exclusive MRD Probes

Exclusive Panel

Based on WES detection data, 40 sites are precisely selected as patient’s exclusive “molecular tags” using a proprietary bioinformatics algorithm.

Core Panel

21 key driver genes related to tumor occurrence and development, monitoring the occurrence of secondary primary tumors, and providing a basis for targeted therapy decisions.

Over 20,000 gene mutation sites and amplifications/deletions 72 fusion genes HRD score (LOH+TAI+LST).

Comprehensive coverage of all chemotherapy toxicity and endocrine therapy-related sites in the PharmGKB database.

PD-L1 protein expression

Microsatelite instability (MSI)

Tumor mutational burden (TMB)

Human leukocyte antigen (HLA)

Viral sequence analysis

Genes related to positive/negative/hyper progressive response to immunotherapy

Neoantigen analysis

Whole exome sequencing of 99 genes
47 types of hereditary tumors and syndromes

Sequence analysis of 3 viruses (18 types)

HPV (9 types), NBV (8 types), EBV (1 type)


MRDTrack+ detects cancer recurrence earlier than traditional methods, such as PET scans, in different types of cancers

Nasopharyngeal carcinoma

Time: 6 months

PMID: 31711920

Breast cancer

Time: 7.9 – 11 months of all chemot

PMID: 26154128

Pancreatic cancer

Time: 6.5 months

PMID: 26154128

Lung cancer

Time: 70 days – 5.2 months

PMID: 35076939

Colon cancer

Time: 167 days to 10 months

PMID: 31621801

MRDTrack + Ultra: Advanced MRD Monitoring for Specialized Cancers

Discover MRDTrack+ Ultra – an advanced suite of MRD monitoring tests specially designed for specific types of cancer.


MRD Track+ Ultra implements 60,000X high-depth sequencing, consistently achieving industry-leading 0.02% MRD detection limit

Lung cancer

170 associated genes

Coverage of 98.2% of patient population

Demo Report

Digestive tract tumors

190 associated genes

Coverage of 96% of patient population

Demo Report

Hepatobiliary and Pancreatic tumors

796 associated genes

Coverage of 90.88% of patient population

Demo Report

Genes for MRDTrack+ are selected based on relevant guidelines, expert consensus and literature in combination with several databases, including TCGA (Tha Cancer Genome Atlas Program), COSMIC (Catalogue of Somatic Mutations in Cancer), and in-house databases.

OMI™ TumorTarget

While OMI™ TumorMap offers comprehensive genetic profiling across a broad range of cancer therapies, the OMI™ TumorTarget line specializes in delivering targeted insights for specific treatments, such as PARP inhibitors and immuno-oncology therapies, optimizing precision in advanced cancer care.

PARPredict

Comprehensive HRD status analysis

Loss of heterozygosity (LOH)

Telomeric Allelic Imbalance (TAI)

Large-scale State Transitions (LST)

BRCA 1/2

Mutations in 35 HRR-related genes 

Demo Report

ImmuneCompass

6 positively correlated immunotherapy genes

27 negatively correlated immunotherapy genes

22 targeted therapy associated genes 

Microsatellite Instability (MSI) for immunotherapy eligibility 

Demo Report

OMI™ Heredity

Contact us below for a personalized consultation and discover how OMI™ Heredity can benefit you.

Contact Us



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