Tailored Genomic Testing for Every Need

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.

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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