Genetic And Advanced Test

1T Penta + NIPT (Reflex)

1T Penta (Delfia)

Jananya NIPT (All Chromosomes)

Jananya NIPT- (All Chromosomes and Microdeletions)

1T Quadruple with DIA (Delfia)

1T Quad (with PLGF) (Delfia)

Aspergillus IgM Antibody Serum

Aspergillus Igg Antibody Serum

AFB - Genexpert MTB/RIF Sputum

TB Gold Heparin Blood

AMH - Mullerian Inhibiting Substance Serum

Anti Mullarian Hormone

Anti Platelet Antibody Serum

ANA Profile by Elisa Serum

ANCA (Anti-Neutrophil Cytoplasmic Antibodies) IFA

AUTODIAPNL Autoimmune Diabetes Type1

Autoimmune Hepatitis Panel IFA

Beta HCG - Total Serum

BRAF V600 Mutation Analysis Tissue

BRAF Hotspot Mutation Analysis

BRCA1 & BRCA2 Deletion/Duplication Analysis

BRCA1 & BRCA2 Mutation Analysis

BOH002 BOH Panel - Extended

Complement 3 (C3) Level Serum

Complement 4 (C4) Level Serum

Complement 50 (C50) Level Serum

Complement C1q (C1q) Antibodies Serum

CA 125 Serum

C-Peptide Serum

CA 15-3 Serum LW01

CA 19-9 Serum LW02

Calcitonin Serum

Carcino Embryonic Antigen (CEA) Serum

Calprotectin Stool

Carbamazepine Serum

Cardiolipin - IgG Antibody Serum

Cardiolipin - IgM Antibody Serum LW01

Cardiolipin - IgA Antibody Serum

CCP (Cyclic Citrullinated Peptide) Antibody Serum

CD 4 Whole Blood

CD 4 Count Bone Marrow

CMV IgG & IgM Antibody Serum

CMV IgG & IgM Antibody Serum

Cortisol 24 Hours Urine

Cortisol Serum

Cholinesterase Serum LW04

Catecholamines Plasma LW02

Catecholamines Urine

CEBPA hotspot mutation analysis

Canavan disease (ASPA)-Gene Analysis

Cantu syndrome (ABCC9)-Gene Analysis

Catechol-O-Methyltransferase (COMT) Genotyping

CD 8 Count by Flowcytometry Whole Blood

CD13 Count by Flowcytometry Whole Blood

CD14 Count by Flowcytometry Whole Blood

CD16/56 Count by Flowcytometry Whole Blood

CD16/56 Count by Flowcytometry Whole Blood

CD117 (Myeloid Marker) EDTA Blood

CD117 (Myeloid Marker) Bone Marrow

Chediak-Higashi syndrome (LYST)-Gene Analysis

CINtec Plus LW05

C0160 Citrulline Quantitative Plasma LW04

C0160a Citrulline Quantitative Urine

C0164 cMYC Gene rearrangement Tissue / FFPE

C0165 Coccaine confirmation by LCMS Spot Urine

C0167 Cohen's syndrome (VPS13B)-Gene Analysis

Connexin 26 Gene Mutation LW05

Coxiella Burnetti IgG antibody Serum

Coxiella BurnettiIgM antibody

Serum CPEO (Chronic Progressive External Ophthalmoplegia)

Genotyping Clopidogren (clopidogrel) Blood

Cystine (Quantitative) blood / Urine

17 OH Corticosteroids Urine

CAB Panel (Quantitative)

CDC Crossmatch (T cell & B cell) LW04

Cervi Screening

Cervi Screeningonco Infectious Panel_ Onco

Complete Sperm Evaluation Package

Dihydrotestosterone

ds-DNA (Double stranded) - Antibody

Donor Specific IgG Antibodies (DSA) Class I & II

Dopamine

Desmoglein (I & III) Antibody

Dihydropyrimidine Dehydrogenase (DPD) Gene Mutation

11 Deoxycorticosterone Serum

PLGF+PAPPA Delfia

DICE-TB Xpert

Dengue

Everolimus

Endometrial Receptivity Test (ER Scope)

Electron Microscopy

Eosinophil Detection (Sputum)

Factor V Leiden Mutation

Fetal Autopsy (Perinatal)

FISH for Trisomy/ Monosmy of chromosome-8

FISH for deletion-17p(TP53- Gene)

FISH for del(5q) - MDS

FISH for del(7q) - MDS

FISH for del(20q)

Fish for BCL6 Gene Rearrangement Tissue

FISH-MDM2 (12q15) GENE AMPLIFICATION

Friedreich Ataxia Mutation Analysis LW05

Fibroblast Growth Factor 23 Plasma LW04

Fibromax (Fibrosis Activity STEATO ASH and NASH of Liver)

Deep Vein Thrombosis (DVT)Panel

Estrone (E1) Serum

Factor X Functional Activity Citrated Plasma

Factor XI Functional Activity Citrated Plasma

Factor XIII Functional Activity Citrated Plasma

Epstein Barr Virus (EBV) (EA) IgG Antibody

Fecal Elastase

GAD 65 (Glutamic Acid Decarboxylase - 65) Antibody

Ataxia-telangiectasia (ATM)

Congenital Muscular Dystrophy (LAMA2)

Cystic fibrosis (CFTR) gene panel deletion/duplication analysis

BRCA1&2 gene deletion/duplication analysis

Chorionic Villi Culture - Karyotyping

Prenatal Diagnostics- Karyotyping and FISH(13 18 21 X Y) CVS

Prenatal comprehensive QF-KT CVS

Full gene sanger sequencing WES (Agilent V6 kit with UTR)-Raw Data followed by Report

Chromosomal Microarray(CMA315k) - Affymetrix Cytoscan

DMD (MLPA Based 79 exons)

Karyotyping

Spinal Muscular Atrophy (SMA) -(SMN1/SMN2)

Beta Globinopathy (Trio Analysis)

Genomescope

QFPCR

Whole Exome Sequencing ( WES ) + Mitochondrial Genome

CytoScan HD

Jananya NIPT- (All Chromosomes and Microdeletions)

Nephrogenic diabetes insipidus gene panel LW04

1505 GEN0376 Polycystic kidney disease gene panel-Basic (CES)

Immune disorders gene panel

Severe combined immunodeficiency (SCID) gene panel

Defects in joint formation & synostoses

Bone marrow failure syndrome gene panel_ONCO

Epileptic encephalopathy gene panel

Progressive myoclonic epilepsy gene panel

Dystonia gene panel

Hereditary cancer gene panel

Intellectual disability gene panel

Leukodystrophies gene panel

Nephropathies gene panel

Renal uricosuria and uricemia gene panel

Renal disorders gene panel

CAKUT Renal Dysplasia Renal agenesis gene panel

CAKUT Renal Dysplasia Renal agenesis gene panel

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