Unlocking the Future of
Genomic Healthcare

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Our Mission

At Genobal, we believe in the power of genomics to transform lives. Our mission is to offer accessible, accurate, and reliable genetic testing solutions that empower patients and healthcare providers to make informed medical decisions. By uncovering the genetic basis of complex diseases, we enable early diagnosis, personalized treatment, and better health outcomes for all.

Who We Are

Genobal was born out of a vision to make genetic testing accessible and effective for healthcare providers and patients worldwide. Our team, led by professionals with a strong background in biotechnology and genomics, is dedicated to providing state-of-the-art diagnostic solutions that can help improve patient care.
About us
Comprehensive Consultation Services

We support healthcare providers with reanalysis and genetic counselling, ensuring accurate interpretation and application of results.

Why Choose Us?

CAP-Accredited Services

We offer globally recognized testing standards.

Affordable Solutions

We believe that everyone should have access to advanced genomic testing without financial barriers.

Fast Turnaround Time

Our lab operates with efficiency to ensure rapid results, usually within 6-8 weeks.

Our Services

Genobal offers a broad range of genomic services, from Whole Exome Sequencing (WES) to Non-Invasive Prenatal Testing (NIPT). Our advanced, accredited laboratories leverage cutting-edge technology to provide highly accurate and actionable genetic insights.

Whole Genome Sequencing (WGS)

A comprehensive genetic analysis covering both coding and non-coding regions for a holistic view of the genome.

BRCA1/BRCA2 Gene Panels

Testing for mutations associated with increased risks of breast and ovarian cancers.

Whole Exome Sequencing (WES):

Focusing on all protein-coding genes, WES captures the most important regions of the genome, identifying about 85% of disease-related variants.

Paternity Testing

Confirming biological relationships between individuals.

Non-Invasive Prenatal Testing (NIPT):

A safe and reliable way to assess fetal risk for genetic disorders.


Sanger Sequencing Validation

For confirmation of genetic mutations detected by other methods.

Genetic Carrier Screening

Identifying carriers of genetic disorders to help families assess the risk of passing on conditions.



Genetic Counseling & Clinical Scientist Services

Expert guidance in test selection, result interpretation, and patient management.

Who Can Benefit?

  • Patients with complex symptoms of neurodegenerative or genetic disorders.
  • Families planning for the future, interested in genetic carrier screening.
  • Individuals seeking diagnostic solutions for unexplained medical conditions.
  • Healthcare providers needing extensive genetic evaluations for their patients.

How It Works

We accept a variety of sample types, including blood, saliva, and tissue samples, to make the testing process as convenient as possible. Turnaround times range from 4 to 8 weeks, depending on the complexity of the test ordered.
Contact us
For more information on how we can support your healthcare needs through advanced genetic testing, contact us today. Our team of experts is ready to assist with test selection, consultation services, and result interpretation.
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