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Service

Prospera

Prospera is a screening test designed to monitor and evaluate the risk of organ rejection post-transplant surgery. It utilizes only blood samples from organ recipients.

Anora

Anora serves as a diagnostic tool designed to investigate the cause of miscarriage due to genetic abnormalities. Employs SNP Microarray method to discern these chromosomal irregularities.

Horizon

Horizon is a genetic carrier screening designed for married couples, enabling them to evaluate the potential risk of transmitting significant genetic anomalies to their offspring. Comprehensive list of up to 574 symptoms for examination

Inborn errors of metabolism (IEM)

IEM is a diagnostic procedure designed to identify abnormal chemical levels in newborns. It assesses both initial substances and metabolites generated during the body's biochemical processes, encompassing the creation and breakdown of these substances.

DNA Sequencing (NGS)

Next-Generation Sequencing is a cutting-edge genetic code reading technology that has the capacity to concurrently decode extensive volumes of genetic material.

NutriReady™ (NGx)

NutriReady™, or nutritional genetics, is an innovative healthcare approach that tailors nutrition to the specific needs of each individual. It utilizes DNA testing technology to provide valuable insights.

RxReady™(PGx)

RxReady™, or pharmacogenetics, represents a novel healthcare application within the field of Precision Medicine. This comprehensive testing covers responses to over 160 different drugs.

Vistara™

Vistara is a non-invasive prenatal screening test that examines genetic abnormalities in the developing fetus based on the mother's blood sample during pregnancy. It screens approximately 30 genes

BRCA Testing (NGS)

BRCA Testing for Hereditary Breast & Ovarian Cancers serves as a screening for mutations in the BRCA1 and BRCA2 genes using NGS technology, which are genes associated with breast and ovarian cancers, the incidence of which is high in women.

Prenatal diagnostic

Prenatal diagnosis involves the assessment of the structure and functionality of the developing fetus's organs within the mother's womb. The aim is to facilitate appropriate treatment, monitoring, and planning for a birth that. Genetic testing methods used for diagnosis encompass cytogenetic analysis : karyotyping, QF-PCR and chromosomal microarray testing (CMA)