Medical Services

Relix® is a range of Molecular technology based diagnostic, prognostics and theranostics services offered by Reliance Life Sciences for several infectious diseases, genetic disorders and cancers.

Molecular Microbiology Qualitative PCR

  • Hepatitis B
  • Hepatitis C
  • Real Time PCR based Tuberculosis (TB) detection
  • MTC (Mycobacterium tuberculosis)/ NTM (Nontuberculous Mycobacteria) differentiation
  • Human Papilloma Virus (HPV)
  • BK virus Qualitative
  • BCR / ABL Qualitative
  • Human Immunodeficiency Virus (HIV 1, 2 and Proviral)
  • Cytomegalovirus (CMV)
  • Chikungunya
  • Chlamydia
  • Dengue
  • Epstein Barr Virus (EBV)
  • Enterovirus
  • Hepatitis A
  • Herpes Simplex Virus (HSV 1 & 2
  • )
  • Parvovirus B19
  • Rubella
  • Toxoplasma

Molecular Microbiology Quantitative PCR

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

Cytogenetics - Karyotyping

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

Cytogenetics - 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
  • Chromosomes 13, 18, 21, X & Y aneuploidy detection
  • Detection of Myelodysplastic syndromes by FISH

Molecular Genetics

  • HBV Genotyping
  • HLA typing - A, B, DR
  • Mitochondrial Mutations
  • HLA B27
  • Ataxia, Myoclonus & Deafness (AMDF)
  • Chronic Progressive External Opthalmoplegia (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 Fibers (MERRF)
  • Mitochondrial Myopathy (MM)
  • Neurogenic Ataxia Retinitis Pigmentosa (NARP)
  • Progressive Encephalopathy (PE)
  • Sensorineural Hearing Loss (SNHL)
  • JAK2 Qualitative PCR

Other Molecular genetics services are listed in Predictive Diagnostics, Companion Diagnostics and Phamacogenomics sections.

Predictive Diagnostics

  • BRCA 1 and 2 Mutations study for familial Breast and Ovarian Cancer
  • RET gene Mutation study for familial Medullary Thyroid Carcinoma
  • BCR/ABL Mutation Analysis
  • Cardio-Vascular Diseases (CVD) Risk Markers-
    • Factor V Leiden
    • MTHFR Mutation
    • Prothrombin Mutation
    • Maternally Inherited Cardiomyopathy (MICM)
    • Maternal Myopathy with Cardiomyopathy (MMC)
  • Human Papilloma Virus (HPV)
  • HCV Genotyping
  • HBV Drug Resistance Test
  • Beta-Thalassemia Mutation Analysis
  • PND for beta-Thalassemia
  • PGD for Beta-Thalassemia
  • PGD for Sickle cell anemia
  • Y-Chromosome Microdeletions
  • Cystic Fibrosis

Companion Diagnostics

  • EGFR Hotspot Mutations
  • Alk gene rearrangement by FISH
  • KRAS Mutation Analysis
  • BRAF Mutation Analysis
  • NRAS Mutation Analysis
  • BCR/ABL transcript ratio monitoring
  • CD20 biomarker
  • MGMT MS PCR
  • HER-2/neu
  • ER/ PgR biomarker

Pharmacogenomics

  • Warfarin Dose Determination test
  • UGT1A1 Genotyping

Anatomic Pathology & Cytopathology

  • Cervical Cytology (PAP Smear)
  • H & E Analysis
  • Cancer Tissue Biomarkers for various cancers including Breast cancer, Lymphoma, GIST, Lung, Ovarian, Thyroid cancer, Neuro-endocrine tumors etc.

Others

  • CD4,CD8 count
  • HLA Crossmatch
  • Spino-cerebellar Ataxia (SCA)
  • Dentatorubral Pallidoluysian Atrophy (DRPLA)
  • Duchenne Muscular Dystrophy
  • Huntington's disease
  • DNA Isolation