Genetic testing helps in management of inherited cardiovascular diseases such as cardiomyopathies, arrhythmia, aortic aneurysms and dissections and familial hypercholesterolemia
If you have a mother, father, sister, or brother with diabetes, you are more likely to get diabetes as well as prediabetes.
Is closely linked to genetics and environmental factors. Genetic testing helps treating professionals to evaluate and treat the patients with these conditions.
Nutritional genomics, also known as nutrigenomics, is a science studying the relationship between human genome, health and nutrition.
The research identified a number of specific genes which influence the outcomes of different physical activities. Genetics impacts all areas of fitness and performance, including muscles and strength.
Cancer genomics is the study of the totality of DNA sequence and gene expression differences between tumour cells and normal host cells. Genomic data helps in diagnosis, treatment selection and management of the patient and their family.
Infectious diseases are caused by infectious organisms either viral, Bacterial, fungal or Parasitic.
HIV, HCV, HPV
Simultaneous detection of multiple viral and bacterial respiratory pathogens including Covid-19 & H1N1.
Simultaneous detection of viruses, bacteria and parasites that cause infectious diarrhoea and other gastrointestinal symptoms.
Simultaneous detection of Influenza A/B, H1N1 & H3N2
Tropical Fever Panel
Detects pathogens causing fever from various viruses including Malaria, Dengue, Chikungunya, Typhoid, Leptospira, Rickettsia, West Nile & Zika.
Detection of Toxoplasma, Rubella, Cytomegalovirus (CMV)
Herpes Simplex Virus(HSV) from amniotic fluid.
STD / Urethritis
Detects viral & bacterial pathogens causing Chalmydia trachomatis, Gonorrhoea, Mycoplasma, Trichomonas Vaginalis, Ureaplasma, Gardnerella, Herpes simplex viruses 1 & 2.
Swine Flu (H1N1)
Qualitative detectation of H1N1 viruses.
Detects Viral pathogens causing meningitis
Reproductive Health & Pregnancy
The goal of preimplantation genetic testing is to ensure that embryos with the highest chance of achieving a healthy pregnancy and child are used during IVF
Assesses reproductive risk and their chance of having a child with a genetic disease. Knowledge of their carrier status empowers the couple to weigh various options while planning their pregnancy.
Noninvasive prenatal Screening / testing (NIPS / NIPT) is a simple blood test that analyzes cell-free DNA circulating in the maternal blood in order to detect Down's syndrome and other fetal chromosomal abnormalities.
Newborn screening helps us find babies who have certain serious medical conditions so that they can begin treatment right away. In most cases, these babies look normal and healthy at birth. They usually do not begin showing symptoms until a few weeks or months later.
Genetics & FISH
Fetal Blood and Products of Conception
Blood Culture and Karyotyping
Fragile X and DNA Studies
Cancer Hot Spot
Tissue based test that Includes 50+ oncogenes/tumour suppressor Genes associates with current oncology drugs & treatment protocol of multiple cancers like Urothelial, Colorectal, Pancreatic, Gynecological, Hepatocelluar, Renal, Gastric, Prostate, Lymphomas & Cutaneous etc.
Tissue cases test that screens 52 oncogenes/tumer supporessr genes for hotspot & RNA fusions with current treatment protocol of multiple cancers.
Comprehensive genomic profiling (CGP)
Profile 500+ unique genes for single Gene & multiple Genes biomarker for complete profiling of the Solid tumors.
Rare Genetic Disorders
Certain neurological conditions occur when genetic variants are passed down in families through genes.
Certain heart disease can occur when one inherits genetic variants associated with that disease.
We also offer tests and panels for a varity of other conditions including rare disorders and paediatric conditions.
Whole Genome & Exome
Sequencing complete set of Genes or genetic material pregnant in a cell or organism. This number can be campared with the 40,000 genes thought to be present in the human genome.
Whole exome sequencing (WES) includes the sequencing of the protein coding regions and their flanking intronic regions in —20,000 genes of the human genome.
Thiopurine and Methotrexate
Terms & Conditions
Harchandrai House, 2nd floor,
Above Axis Bank, Maharshi Krve Road,
Marine Lines (E), MUmbai - 400002