• Tuberculosis (TB)
• Hepatitis B
• Hepatitis C
• Human Papiloma Virus (HPV)
• BK virus Qualitative
• BCR / ABL Qualitative
• Human Immunodeficiency Virus (HIV 1, 2 and Proviral)
• Cyto Megalo Virus (CMV)
• Chikungunya
• Chlamydia
• Dengue
• Epstein Barr Virus (EBV)
• Enterovirus
• Helicobacter Pylori
• Hepatitis A
• Herpes Simplex Virus (HSV 1 & 2)
• Japanese Encephalitis Virus (JEV)
• Malaria
• Parvovirus B19
• Rubella
• Toxoplasma
• Typhoid

Quantitative Analysis

• HBV Quantitative Real-time
• HCV Quantitative Real-time
• HIV-1 Quantitative Real-time
• BCR / ABL Quantitative Real-time
• BK virus Quantitative Real-time
• Cyto Megalo Virus (CMV) Real-time

Quantitative Fluorescence Based Chromosome Aneuploidy Analysis

• Chromosomes 13 & 21
• Chromosomes 18, X & Y
• Chromosomes 13, 18, 21, X & Y

Sequencing based tests

• KRAS Mutation Analysis
• EGFR Hotspot Mutations
• HBV Genotyping
• HCV Genotyping
• HBV Drug Resistance test
• Human Papilloma Virus (HPV)
• HLA typing - A, B, DR
• BCR / ABL Mutation Analysis
• UGT1A1 Genotyping
• Mitochondrial Mutations
• Warfarin Dose Determination test
• Cardio-Vascular Diseases (CVD) Risk Markers-
• Factor V Leiden
• MTHFR Mutation
• Prothrombin Mutation
• HLA B27
• YMDD test
• Cystic Fibrosis
• Ataxia, Myoclonus & Deafness (AMDF)
• Chronic Opthalmopleagia (CPEO)
• Maternally Inherited Deafness or Aminoglycoside Induced deafness (DEAF)
• Diabetes Mellitus and Diabetes Mellitus + Deafness (DM / DMDF)
• Exercise Intolerance (EI)
• Leigh's Disease (LD)
• Leber's Hereditary Optic Neuropathy (LHON)
• Mitochondrial Encephalopathy (ME)
• Mitochondrial Encephalopathy and Lactic Acidosis with Stroke like Syndrome (MELAS)
• Myoclonic Epilepsy Associated with Ragged Red Fibres (MERRF)
• Mitochondrial Myopathy (MM)
• Neurogenic Ataxia Retinitis Pigmentosa (NARP)
• Progressive Encephalopathy (PE)
• Sensorineural Hearing Loss (SNHL)

Karyotyping

• Karyotyping of Peripheral Blood Cells
• Chromosomal breakage studies: Fanconi anaemia
• Fragile X and Y Detection
• Amniotic Fluid sample study
• Cord Blood sample study
• Chorionic Villi sample study
• Karyotyping of Bone Marrow / Leukemic Blood

Fluorescence In-Situ Hybridization (FISH)

• HER-2/neu
• Products of conception study
• Pre-Implantation Genetic Diagnosis (PGD)
• Angelman/Prader-Willi Syndrome
• BCR / ABL translocation (9;22) in CML, AML, ALL
• Chorionic Villi Sample study
• Cord Blood sample study
• PML / RARA
• Peripheral Blood Cells study
• Duplication SNRPN in Autism
• Follicular Fluid FISH

Predictive Diagnostics

• BRCA 1 and 2 Mutations study for familial Breast and Ovarian Cancer
• RET gene Mutation study for familial Medullary Thyroid Carcinoma
• Cardio-Vascular Diseases (CVD) Risk Markers-
• Factor V Leiden
• MTHFR Mutation
• Prothrombin Mutation
• Maternally Inherited Cardiomyopathy (MICM)
• Maternal Myopathy with Cardiomyopathy (MMC)
• Human Papiloma Virus (HPV)

Pharmacogenomics

• HER-2/neu
• KRAS Mutation Analysis
• BCR/ABL Mutation Analysis
• EGFR Hotspot Mutations
• UGT1A1 Genotyping
• MGMT MS PCR

Others

• CD4,CD8 count
• HLA Crossmatch
• Thalassemia screening
• Beta-Thalassemia Mutation Analysis
• PND for beta-Thalassemia
• Spino-cerebellar Ataxia (SCA)
• Dentatorubral Pallidoluysian Atrophy (DRPLA)
• Duchenne Muscular Dystrophy
• Huntington's disease
• Y-Chromosome Microdeletions
• Cervical Cytology (PAP Smear)
• Cancer Tissue Biomarkers
• DNA Isolation
• Immunophenotyping for Leukaemias