Precision oncology, genetic testing for diagnosis, prognosis and most effective cancer treatment

Cancer Genes
Test Kit

Cancer diagnosis, prognosis and monitoring by gene testing

Our Mission

Cancer is a highly complex disease caused by a set of oncogenic protein-coding genes and non-coding genes, and, thus, targeted analyses of these genes through highly innovative technologies are the best methods for cancer diagnosis, prognosis, risk assessment and treatment follow-up of various cancers. These are the most powerful research technologies that can save the lives of millions of cancer patients.

Who is GeneVerify Inc.

At GeneVerify, Inc., we have built a highly skilled, multidisciplinary team of experts—including molecular and cell biologists, pathologists, biochemists, urologists, surgical and medical oncologists, radiation oncologists, physicians, and surgeons—who are dedicated to advancing gene-based diagnostics and treatments for a wide range of solid tumors.

What is Genetic Profiling​

GeneVerify, Inc. is developing in vitro diagnostic (IVD) reagents for laboratory-based assays to analyze key oncogenic genes across various cancer types using real-time PCR technology. In parallel, we are pioneering novel therapeutic technologies aimed at precisely targeting these genes, with the goal of delivering highly specific and effective treatments for a range of cancers.

Our Products

bg-1-gv
Genes-based Analyses

(Protein coding genes and Non-coding genes analyses) 

Analysis of a selected set of oncogenic protein-coding and non-coding genes is intended for in vitro diagnostic (IVD) assays conducted exclusively in research laboratories. Interpretation of these analyses must be performed in collaboration with qualified specialists—such as surgical oncologists, medical oncologists, radiation oncologists, pathologists, physicians, and surgeons—for accurate diagnosis, prognosis, risk assessment, and therapeutic monitoring across various cancers.

Products

In Vitro Diagnostic Reagents (Research and Development)  

bg-1-gv
Genes-based Therapy

Targeting Oncogenic Protein coding genes and non-coding genes for treatment.  Pre- IND (Investigational New Drug)

Genes based therapies that target oncogenes that are involved in cancer initiation, progression and metastasis.

Products

Research and Development

Pre-IND (Investigational New Drug  

Phase-1         Phase-2        Phase-3

Message from the CEO

“Precision Medicine” is a modern, individualized approach to disease treatment that considers the genetic variability among patients. In oncology, this approach relies on comprehensive genetic profiling of tumors to guide therapy. According to published studies, approximately one in five newly diagnosed cancer patients presents with a distinct combination of genetic alterations. This highlights the inadequacy of a one-size-fits-all treatment model, which often overlooks critical genetic differences. Each patient’s tumor may harbor unique genetic abnormalities—such as mutations, gene rearrangements, translocations, polymorphic variants, gene fusions, amplifications, deletions, as well as dysregulations in microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and DNA methylation patterns—underscoring the need for personalized therapeutic strategies.

In precision medicine, it is essential to leverage advanced technologies for comprehensive tumor genomic analysis using a multi-omics approach—including genome, transcriptome, proteome, epigenome, metabolome, and microbiome profiling. Insights from the Human Genome Project have revealed the complexity of the human genome, identifying over 30,000 protein-coding genes and more than 60,000 non-coding genes. This vast genomic landscape underscores the importance of integrative, multi-dimensional analyses to drive personalized cancer diagnostics and therapies.

Our team of professionals has devoted over four decades to advancing the fields of cancer genetics and epigenetics, collectively authoring more than 550 peer-reviewed research articles published in high-impact scientific journals.

According to the NIH RePORTER database, our laboratory has been awarded 99 research grants through the National Cancer Institute (NCI), the National Institutes of Health (NIH), and the U.S. Department of Veterans Affairs. These sustained funding efforts have led to the development of several U.S. patents in the fields of urology and oncology, many of which stem from major NCI/NIH-funded initiatives.

At GeneVerify, Inc., we are developing in vitro diagnostic (IVD) reagents for research laboratory-based assays to analyze a defined set of oncogenes across various cancer types using real-time PCR technology. In addition, we are advancing novel medical technologies designed to precisely target these oncogenes, aiming to deliver highly specific and effective treatments. These innovative diagnostic and therapeutic approaches represent some of the most powerful tools in cancer research and hold the potential to save millions of lives worldwide.

Rajvir Dahiya, M.S., Ph.D., M.D., D.Sc.

Founder, CEO and President

Rationale and Approach

According to the 2026 Cancer Statistics, approximately 20 million people worldwide are newly diagnosed with cancer each year. Without effective control measures, this number is projected to double by 2030. A major challenge is the widespread lack of early diagnostic, prognostic, and treatment monitoring tests. For example, in some Southeast Asian countries like India, nearly 60% of cancer patients are diagnosed at the metastatic stage due to insufficient testing. Since metastasis accounts for the vast majority of cancer-related deaths and there are currently no effective therapies for metastatic cancer, improving early detection and monitoring is critical to reducing mortality.

At GeneVerify, Inc., our experts firmly believe that early detection and targeted intervention of key oncogenes can effectively inhibit cancer progression and metastasis. By leveraging these cutting-edge technologies, we aim to improve patient outcomes while also reducing overall healthcare costs.

We have developed a novel blood-based mRNA genomic technology, protected by five U.S. patents and validated through more than 200 original research publications in high-impact scientific journals.

Our blood-based mRNA genomic technology enables screening, early diagnosis, prognosis, treatment monitoring, and gene therapy across multiple cancer types. This technology has been validated through nine clinical trials conducted at leading hospitals in the USA, Japan, and India, consistently demonstrating 95% specificity and sensitivity.

Our team comprises over 50 medical scientists specializing in medical oncology, surgical oncology, pathology, radiation oncology, molecular biology, genetics, gene therapy, cancer biology, and biochemistry. Collectively, they bring 20 to 40 years of experience working in the United States, driving innovation and excellence in cancer research and treatment.

On January 25-27th, 2024, we presented our data at the ASCO GU symposium (American Society of Clinical Oncology) meeting at San Francisco, California, USA. ASCO has more than 45,000 members worldwide. This paper was published in the Journal of Clinical Oncology January 29th 2024.

https://ascopubs.org/doi/10.1200/JCO.2024.42.4_suppl.271

On April 5-10, 2024, we presented our data at the AACR meeting (American Association of Cancer Research) at San Diego, CA. AACR has more than 58,000 members from 141 countries (google search). This paper was published in the Journal “CANCER RESEARCH” March 22, 2024.

https://aacrjournals.org/cancerres/article/84/6_Supplement/2442/741209/Abstract-2442-Blood-based-novel-mRNA-genomic-test

On May 3-6, 2024 we presented our data at AUA (American Urology Association) at San Antonio, Texas. AUA has more than 25,000 members from 138 counties (google search). This paper was published in the Journal “Journal of Urology” May, 2024.

https://www.auajournals.org/doi/10.1097/01.JU.0001008896.93851.5b.05  

On April 25-30, 2025, we presented our data at the AACR meeting (American Association of Cancer Research) at Chicago, IL. AACR has more than 58,000 members from 141 countries (google search). This paper was published in the Journal “CANCER RESEARCH” 85(8_Supplement_2): April 2025.
 

On May 30-June 3, 2025, we presented our data at the ASCO (American Society of Clinical Oncology) annual meeting at Chicago, Illinois, USA. ASCO has more than 45,000 members worldwide. This paper was published in the Journal of Clinical Oncology, May 28th 2025.

Real-time clinical validation of a blood cell-free, mRNA-based GeneVerify test for screening and early diagnosis of prostate cancer.

https://ascopubs.org/doi/10.1200/JCO.2025.43.16_suppl.3053

Key Advantages of GeneVerify’s Approach:

  1. Improved Sensitivity Over Tissue Biopsy: While tissue biopsy remains the gold standard for cancer diagnosis, it has a false-negative rate of approximately 20%, leaving many cancers undiagnosed. GeneVerify has developed a blood-based mRNA genomic test with about 95% sensitivity, significantly enhancing early detection.
  2. Early Detection When Traditional Methods Fail: Recent studies show that 25% of patients with normal pathological and clinical findings actually have cancer detectable through genetic testing. Since most cancer deaths result from metastasis, early detection is critical—up to 90% of patients diagnosed early can be cured or have their lives significantly prolonged.
  3. Avoidance of Unnecessary Surgery: If tumors are slow growing, active surveillance may be appropriate. Published data suggest that up to 50% of surgeries could be avoided due to misdiagnosis, reducing patient risk and healthcare costs.
  4. Personalized Prognosis Based on Genetic Profile: Aggressive tumors require more intensive treatment, while slow-growing tumors may need less aggressive intervention. Avoiding overtreatment can reduce mortality caused by unnecessary aggressive therapies.
  5. Real-Time Treatment Monitoring: Genetic testing allows for close monitoring of therapy effectiveness, ensuring expensive treatments are working. This not only improves patient outcomes by preventing ineffective treatments but also saves millions in healthcare costs.
  6. Advancing Gene-Based Therapies: We are initiating clinical trials for cancer therapies utilizing patented antisense technology and cutting-edge mRNA-LNP-CAR-T platforms. Our strategy combines gene-based diagnosis through genetic profiling with targeted inhibition of cancer-driving genes via antisense mechanisms.

At GeneVerify, Inc., we address the most critical challenges in patient care through a collaborative environment where teamwork and innovation drive breakthrough solutions.

Employees and Advisers

Dr. Rajvir Dahiya is a Retired Professor Emeritus of Urology at the University of California San Francisco, School of Medicine (UCSF). He has 40 years of expertise in medical oncology, cancer genetics and epigenetics research

Rajvir Dahiya, M.S., Ph.D., M.D., D.Sc.

Founder, CEO and President

Dr. Deng is a retired Medical Oncology researcher from the University of California San Francisco School of Medicine (UCSF). He has 45 years of expertise in medical oncology, cancer genetics and epigenetics research.

Guoren Deng, M.D.

Chief Scientific Officer

Dr. M. Allen Northrup is an elected Member, National Academy of Engineering , Bioengineering Section and American Institute of Medical and Biological Engineers. He is a co-founder of Cepheid Inc. He has more than 30 years of expertise in the field of PCR technology and testing.

M. Allen Northrup, Ph.D.

Scientific Adviser

Dr. Dharam P. Chauhan is a retired Professor of Gastroenterology and Hepatology Oncology from University of California San Diego (UCSD) School of Medicine. He has 34 years of expertise in medical oncology, genetics and epigenetics research.

Dharam Paul Chauhan M.S., Ph.D.

Vice-President

Scientific Research Collaborators and Distributors

In vitro Diagnostic Collaborators

Mount Sinai Tisch Cancer Center, New York, NY, USA

Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, India

PGIMS and University of Health Sciences, Rohtak, Haryana, India

Inqaba Biotechnical Industries (Pty) Ltd, Pretoria, Gauteng, South Africa

Bioinnotech, Filopappou 34, 11741, Athens, Greece

Scientific Research Collaborators

Osaka University, Graduate School of Medicine, and Faculty of Medicine. Osaka, JAPAN

Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, JAPAN

University of Florida, College of Medicine- Jacksonville, Florida, USA

Case Western Reserve University, School of Medicine, Cleveland, Ohio, USA

Yamaguchi University, Faculty of Medicine and Health Sciences, Yamaguchi, JAPAN

HealthCare Global Enterprises, HCG Cancer Hospital, Bengaluru, INDIA

Max Healthcare Institute Limited New Delhi, INDIA

Oregon Health Science University Cancer Institute Portland, Oregon, USA

Distributor for Netherlands

Sobek Bio

c/o DivBio; P.O. Box 92
4850 AB Ulvenhout
The Netherlands

Publications

A lncRNA TCL6-miR-155 Interaction Regulates the Src-Akt-EMT Network to Mediate Kidney Cancer Progression and Metastasis

Kulkarni P, Dasgupta P, Hashimoto Y, Shiina M, Shahryari V, Tabatabai ZL, Yamamura S, Tanaka Y, Saini S, Dahiya R, Majid

Cancer Res. 2021 Mar 15;81(6):1500-1512. doi: 10.1158/0008-5472.CAN-20-0832. Epub 2021 Jan 26.PMID: 33500248.

LncRNA CDKN2B-AS1/miR-141/cyclin D network regulates tumor progression and metastasis of renal cell carcinoma

Dasgupta P, Kulkarni P, Majid S, Hashimoto Y, Shiina M, Shahryari V, Bhat NS, Tabatabai L, Yamamura S, Saini S, Tanaka Y, Dahiya R.

Cell Death Dis. 2020 Aug 19;11(8):660. doi: 10.1038/s41419-020-02877-0.PMID: 32814766 Free PMC article.

MicroRNA determinants of neuroendocrine differentiation in metastatic castration-resistant prostate cancer

Bhagirath D, Liston M, Patel N, Akoto T, Lui B, Yang TL, To DM, Majid S, Dahiya R, Tabatabai ZL, Saini S.

Oncogene. 2020 Dec;39(49):7209-7223. doi: 10.1038/s41388-020-01493-8. Epub 2020 Oct 9.PMID: 33037409 Free PMC article.

Product order form​

Get in Touch

This website uses cookies to ensure you get the best experience on our website.