Advanced Genomic study (Microarray and NGS based)

Apart from single gene disorders, there are numerous complex disorder like infertility, cancer, metabolic disorders, neurological disorders, etc. where in more than one genes are involved. In these clinical manifestation advance genomic study is required to determine the genetic cause. There are two major approaches in genome based analysis Microarray and NGS. Both the approaches have their own benefits and limitation. Selection of the approach is always case to case basis, where clinician and geneticist have to jointly take a call on the approach.  Microarray has been vital in detecting microdeletion or duplication in prenatal cases and NGS has been beneficial in cases with established phenotype.

Clinical Services

Research Services

Microarray NGS 
Chromosomal Micaroarray Analysis (array CGH) 8X60kAmniotic FluidNon-Small Cell Lung Carcinoma (NSCLC) Panel36 genes
(20ml)
Chromosomal Micaroarray Analysis (array CGH) 8X60kProduct of Conception (15ml sterile tube)Breast Carcinoma Panel42 genes
Chromosomal Micaroarray Analysis (array CGH) 8X60kPeripheral Blood (4ml in EDTA vaccutainer) Colorectal Carcinoma panel81 genes
Pre-implantation Genetic Screening (PGS) 8X60kBlastomere (ONE or TWO) in Kit provided by CentreComprehensive Cancer Panel (Somatic Panel)113 genes
(Embryo Biopsy) Minimum four Biopsy per Patient
Pre-implantation Genetic Screening (PGS) 8X60kBlastocyst Biopsy (Trophectoderm) in Kit provided by Centre (Embryo Biopsy) Comprehensive Cancer Panel (Germline Panel)137 genes
Minimum four Biopsy per Patient
Array CGH + SNP analysisAll type of Biological samplesCARDIOMYOPATHIES 81 genes
ARRHYTHMIAS 65 genes
SUDDEN CARDIAC DEATH 64 genes
PREMATURE CORONARY ARTERY DISEASE 52 genes
WARFARIN AND CLOPIDOGREL RESPONSE 9 genes
Neurology Panel119 genes
Muscular Dystrophy and Myopathy Panel18 genes
Mitochondrial Panel36 genes
Clinical Exome Test covers 4800 genes associated with known clinical phenotypes

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