Diagnostics
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Targeted Mutation Analysis (TMA)TMA is a precise genetic test to identify specific mutations. It helps in diagnosing genetic disorders. -
Comprehensive RNA Sequencing (Whole Transcriptome Sequencing) – 60 million reads – 9gb dataTo detect both known and novel features in a single assay, enabling the identification of transcript isoforms, gene fusions and single nucleotide variants. -
Cancer Risk Screening Test (Germline)Assessment of target and non-target lesions using NGS -
Wellness Test –Nutrigenomics , Fitness genomics and Immunity factorsPanel of more than 600 genes (looking at SNPs, InDels and CNVs) -
Chromosomal breakage studyDetecting specific chromosomal features or abnormalities. -
MTHFR gene polymorphisms677C>T and 1298A>C mutations -
HPV ScreeningN.A -
Clinical Exome SequencingClinical Exome Sequencing analyzes coding regions of genes to identify genetic causes of diseases. -
Fibroblast cultureDetecting specific chromosomal features or abnormalities. -
Cancer Risk Screening Test (Germline)This test identifies genetic mutations that increase the risk of developing cancer. -
TB Screening & PCODN.A -
Polar Body Biopsy13,18,21, X (chromosomes) -
Y- chromosome microdeletionsDetecting specific chromosomal features or abnormalities. -
Sperm DNA FragmentationSperm DNA intergrity/quality -
HLA Typing using NGS platform6 loci – HLA A, B, C, DRB1, DQB1, DP -
Diabetes care risk panelPanel of more than 330 genes (looking at SNPs, InDels and CNVs) -
Karyotyping from bloodDetecting specific chromosomal features or abnormalities. -
Karyotyping from prenatal samplesDetecting specific chromosomal features or abnormalities. -
Neurocare – Risk PanelPanel of more than 490 genes (looking at SNPs, InDels and CNVs) -
Nephrocare – Risk PanelPanel of more than 180 genes (looking at SNPs, InDels and CNVs) -
Cardiac Care – Risk PanelPanel of more than 80 genes (looking at SNPs , InDels and CNVs)
Prognostics
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Pharmacogenomics PanelPanel of more than 450 genes -
Warfarin (Coumadin)Evaluates specific inherited variations to determine how an individual might metabolize or respond to Warfarin -
Clopidogrel (Plavix)Evaluates specific inherited variations in the CYP2C19 gene to determine how an individual might metabolize or respond to Clopidogrel -
TicagrelorEvaluates specific inherited variations to determine how an individual might metabolize or respond to Ticagrelor -
Statins IntoleranceEvaluates specific inherited variations in more than 25 genes to determine how an individual might metabolize or respond to Statins
Predictive
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Whole Exome Sequencing and AnalysisTDiagnostic test used to identify the genetic cause of an individual’s health condition across all exons -
Whole Genome Sequencing (30X)Method for molecular genetic diagnosis of rare and unknown diseases and for identification of actionable cancer drivers across intronic and exonic DNA of an individual.
Pathogenic
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Gut Microbiome TestingGut microbiome tests can tell you what types of bacteria, archaea, viruses, and fungi are in your gut and how they might be affecting your health -
Gut Microbiome Advance TestingGut microbiome tests can tell you what types of bacteria, archaea, viruses, and fungi are in your gut and how they might be affecting your health (with detailed a diet plan)