Diagnostic Services
Cytogenetics & Cytogenomics
-
Conventional Cytogenetics (Karyotyping - Blood).
-
Conventional Cytogenetics (Karyotyping - Bone Marrow)
-
Conventional Cytogenetics (Karyotyping - Amniotic Fluid)
-
Conventional Cytogenetics (Karyotyping - CVS / POC)
-
Chromosomal Breakage Studies (Fanconi Anemia)
-
Chromosomal Breakage Studies (Genetic Instability in IBMFS)
-
Chromosomal Breakage Studies (Other Known syndromes)
-
Fluorescence in-situ Hybridization (FISH) Studies.
-
Chromosomal Micro Array (CMA) (Developmental Delay, Multiple Congenital Anomalies, etc. )
-
Chromosomal Micro Array (CMA) (Tumor Studies, Myeloid Malignancies)
-
Virtual Karyotyping (M-FISH, Spectral Karyotyping)
Molecular Tests
-
PCR-based Tests
-
Real-Time PCR-based Tests
-
Digital Droplet PCR-based Tests
-
Multiple Ligation Probe Amplification (MLPA)
-
Fragment Length Analysis (FLA)
-
Sanger Sequencing
-
SNP Genotyping
-
Targeted Next Generation Sequencing
-
Clinical / Whole Exome Sequencing
-
Whole Genome Sequencing
Ancillary Diagnostic Services
We provide data interpretation through raw files for second opinion that saves huge cost of retesting for patients. We also provide advance testing an data analysis on project basis for Transcriptomic studies, Single Cell Sequencing, Spatial Transcriptomic Profiling, etc.