Genetic Testing Services
We offer precise genetic sequencing tests to identify diseases and enhance your health understanding.
Disease Identification
Our tests accurately identify genetic markers associated with various diseases for better health management.
DNA Analysis
Comprehensive DNA analysis provides insights into genetic predispositions and potential health risks for individuals.
Genetic Tests
We provide precise genetic sequencing tests to identify diseases.


Genetic Counseling
Carrier Screeningg
Tests handling a wide variety of tissues, identification of numerical and structural chromosomal defects, familial variant chromosomes using latest image analysis tools.




Prenatal Screening
Down syndrome, ONTD, Trisomy 18, Trisomy 13 screening by first trimester double marker, second trimester triple screen and quadruple screen, preeclampsia risk
Newborn Screening
Newborn screening for metabolic disorders, tandem mass screening, urine metabolic screening and enzyme studies for inborn errors of metabolism
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Chromosomal Analysis (Cytogenetics)
Molecular Cytogenetic Analysis (FISH)
Tests handling a wide variety of tissues, identification of numerical and structural chromosomal defects, familial variant chromosomes using latest image analysis tools
Test for detection of chromosomal aneuploidy, prenatal rapid FISH combo test, micro deletion syndromes and tumor markers by fluorescent in situ hybridization




Chromosomal Microarray Analysis
Preimplantation Genetics
Next generation sequencing, multi-gene panels, microarrays for syndrome identification, confirmation tests by Sanger sequencing, report interpretation.
Tests handling a wide variety of tissues, identification of numerical and structural chromosomal defects, familial variant chromosomes using latest image analysis tools




Gene Panels for Reproductive Genetics
Breast Ovarian Cancer Predisposition
Tests handling a wide variety of tissues, identification of numerical and structural chromosomal defects, familial variant chromosomes using latest image analysis tools.
Identification and quantification of cancer mutations using cytogenetics, PCR, RT-PCR, RQ-RT PCR, gene sequencing on blood, bone marrow, tumor and lymph tissues.




Genome-wide Sequencing
Speciality Gene Panels for Inherited Disorders
Hundreds of single-gene disorders, carrier testing, and prenatal diagnosis using sophisticated methods – PCR, Sanger gene sequencing, microarrays, and next generation sequencing.
Ultrasound guided invasive prenatal diagnostic procedures performed by trained radiologists. Amniocentesis, chorionic villus sampling (CVS biopsy), cordocentesis.




Inherited Disorders
Prenatal Sampling
Hundreds of single-gene disorders, carrier testing, and prenatal diagnosis using sophisticated methods – PCR, RT qPCR, Sanger Gene Sequencing, Cyto Microarrays, and Next Generation Sequencing.
Ultrasound guided invasive prenatal diagnostic procedures performed by trained radiologists. Amniocentesis, chorionic villus sampling (CVS biopsy), cordocentesis..