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PREMARITAL PROFILE
POLYCYSTIC OVARIAN SYNDROME PANEL (PCOD) BASIC
POLYCYSTIC OVARIAN SYNDROME PANEL – I
PAC INVESTIGATIONS
NBS – Basic New Born Screening
NBS – Advance New Born Screening Panel
LIVER FUNCTION TEST (LFT)
KIDNEY FUNCTION TEST (KFT)
INFERTILITY (MALE)
INFERTILITY (FeMale)
HYPERTENSION PROFILE
HPV WITH LBC (COMBO)
HEPATITIS PANEL – II
HEPATITIS PANEL – I
HEPATITIS B PROFILE – II
HEALTH CHECK – I
FREE THYROID PROFILE
FREE ANDROGEN INDEX
FEVER PANEL
FERTILITY PROFILE FEMALE
FERTILITY PROFILE – III
FERTILITY PROFILE – II
FERTILITY PROFILE – I
EXTENDED LIPID PROFILE
DRUG ABUSE TEST (URINE)
DOUBLE MARKER
DIABETES SCREENING BASIC
DIABETES PROFILE BASIC
DIABETES PROFILE – II
DIABETES PROFILE – I
CORD BLOOD PANEL WITH BLOOD CULTURE
CORD BLOOD PANEL
CARDIAC PROFILE – I
CARDIAC ENZYMES
BOH PROFILE BASIC
Blood Panel – I
ARTHRITIS PANEL BASIC
ARTHRITIS PANEL 2
ARTHRITIS PANEL – I
ANTI PHOSPHOLIPID SYNDROME PANEL 2
ANTI PHOSPHOLIPID SYNDROME PANEL
COMPLETE CARDIAC PROFILE
ANTENATAL PANEL
ANDROGEN PROFILE
ANEMIA PROFILE – II
ANEMIA PROFILE – I
ADVANCED ANTENATAL PANEL
ADVANCE THYROID PROFILE
ADVANCE PAC INVESTIGATIONS
Clot Solubility with 5M Urea
METHADONE(URINE)
METANEPHRINES 24 HR URINE
KETONE BODIES
BTA (Bladder Tumor Antigen )
BILE SALTS URINE
BILE PIGMENT URINE
BENZODIAZEPINES
Alpha Feto Protein (CSF)
CA 72.4
NSE NEURON SPECIFIC ENOLASE SERUM
REDUCING SUBSTANCES
OCCULT BLOOD
Lung Cancer (FISH + NGS)
Glioma Panel (MLPA + FISH + Sanger Sequencing)
Colon Cancer (Fragment Analysis + NGS)
Retinal Degeneration Gene Panel
Respiratory Virus Panel-7
Replication Factor C1 Mutation Screening (RFC1 – 80G>A)
Renal Cancer Gene Panel
Prostate Cancer Gene Panel
Prenatal Spinal Muscular Atrophy (SMN1 Gene: Exon 7 and 8 deletion mutation screening)
Prenatal Sickle Cell Mutation Screening
Prenatal DMD mutation screening (26 exons)
Prenatal Beta Thalassemia/HbE Mutation Screening
Polycystic Kidney Disease Gene Panel
PML/RARA Qualitative [bcr 1 & 3]
PIK3CA Mutation Analysis (Exon 9 & 20)
PGS (7-12) Embryo
PGS (5-6) Embryo
PGS (1-4) Embryo
PGD HLA Typing (Single Embryo)
PGD (Single gene Disorder)-Baseline
PGD (Single Embryo) with maternal DNA contamination check
PGD (Single Embryo)
PDGFR, cKIT(Gastrointestinal Stromal Tumors)
PDGFR Mutation Screening (Exons 12, 14, 18)
Paternity testing-Autosomal STR (Fragment Analysis)
ONCOMINE SOLID TUMOR RNA FUSION PANEL
ONCOMINE SOLID TUMOR DNA PANEL
ONCOMINE MYELOID PANEL
ONCOMINE FOCUS PANEL
ONCOMINE COMPREHENSIVE ASSAY
ONCOMINE cfDNA LUNG CANCER PANEL
ONCOMINE BREAST cfDNA ASSAY
NRAS Mutation Analysis (codons 12 & 13)
NPM1 Mutation Analysis (Exon 12 insertion)
Non-invasive Prenatal testing-EVAA
Neuronal Ceroid Lipofuscinosis Gene Panel
Nervous system Cancer Gene Panel
Myeloproliferative Leukemia Mutation Screening (MPL – S505N; W515L)
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