Diagnostics – PathCare Labs

Diagnostic tests

Life Sciences Tests

Beta Thalassemia HBB gene sequencing- SANGER
Chorionic Villi Culture - QFPCR (T131821 & XY)
PVB QFPCR
QFPCR (T13,18,21 & XY)
Mitochondrial Genome Sequencing
AF QFPCR (T131821 & XY)
Allergy AlaTOP-Adult
Allergy AlaTOP-Pediatric
Allergy Comprehensive Profile
Allergy Drugs
Allergy Food (Non-Vegetarian)
Allergy Food (Vegetarian)
Allergy Inhalants
Allergy Profile
NBS-TMS-Inborn Metabolic Disorders (IMD) Panel
NBS-GCMS-Inborn Metabolic Disorders (IMD) Panel
Dual Marker - Prisca
Fertility Profile - I
Fertility Profile - II
Fertility Profile - III
Fertility Profile - IV
Fertility Profile - V
Infertility Profile
Triple Marker - Prisca
Quad Marker - Prisca
Semen Analysis
Chromosomal Analysis/Karyotyping-Amniotic Fluid
Chromosomal Analysis/Karyotyping- Blood
Neonatal Screen (Trisomy 21 18 13 X Y)-5 Markers - FISH
Prenatal Aneuploidy Detection- Amnio (5 probes- Trisomy 21 18 13; X Y)-FISH
Semen DNA Fragmentation Test
Cytology -LBC -PAP
Biopsy-Endometrial Biopsy
NBS Basic Panel - TSH; 17-OHP; G6PD Galactosemia and Biotinidase

NBS Comprehensive Panel (7 Conditions)
TORCH 5 Profile (IgG)
TORCH 5 Profile(IgM)
TORCH 8 Profile(IgG&IgM)
TORCH 4 Profile(IgG)
TORCH 4 Profile(IgM)
Dual Marker-Delfia
Quadruple Screening (Delfia)
Maternal Cell Contamination (MCC)
NIPT (Basic) / 131821 X & Y
Dual Marker + PLGF (Delfia)
Chromosomal Microarray(CMA 750 K)-AF/CVS/POC/WB-EDTA
Triple Marker-Delfia
1T Quad (with PLGF) (Delfia)
Spinal Muscular Atrophy (SMA) -(SMN1/SMN2) deletion/duplication analysis by MLPA
DMD- MLPA
Sanger Sequencing Confirmation Variant 1-Single Patient
Meningitis Panel - Multiplex PCR
Respiratory Panel (24 Pathogen Detection) - Multiplex PCR
Flu Panel - Multiplex PCR
Fetal Autopsy
Pharmacogenetics Panel
Myeloid NGS
Placental Histopathology
Hereditary cancer gene panel
NBS-TSH
NBS-17-OHP
NBS-CYSTIC FIBROSIS
NBS-PKU
NBS-1 G6PD
NBS-1 Biotinidase
NBS-1 Galactosemia
Mycobacterium Tuberculosis Complex (MTC) & MOTT PCR-Menstrual Blood
Gastroenteritis Panel - Multiplex PCR

CMA750k with Whole Exome Sequencing
DNA Storage
Infertility Multiplex PCR
QFPCR Basic + CMA 315K + MCC
Prenatal KT+QFPCR(Amniotic Fluid/CVS)
QFPCR + CMA 750K
1st Trimester Comprehensive Screening Test (Delfia)
1st Trimester Comprehensive Screening Test (Prisca)
NBS-7 + HPLC
FISH (131821XY)-Aminotic Fluid and Chromosomal Microarray (CMA 750k)
FISH (131821XY)+Aminotic Fluid and Chromosomal Microarray (CMA315k)
FISH (131821XY) and Chromosomal Microarray (CMA 750k)
FISH (131821XY) and Chromosomal Microarray (CMA315k)
NBS7 + HPLC + TMS
NBS7+TMS
CERVI SCREEN
IVF - RPL - 1 - Without LA
KT + QFPCR PVB
2nd Trimester Comprehensive Screening-Prisca
NBS (GCMS+NBS7)
LBC+HPV
Y Chromosome Microdeletion
Whole Exome Sequencing
Non-Invasive Prenatal Testing (NIPT)-All Chromosomes
NIPT+Micro Deletion
Chromosomal Microarray (315K)
Ante Natel Profile
BOH Panel
PCOD panel
Human Papilloma Virus (HPV) Screening Panel