Genomics Services
 
 
Whole Genome Sequencing
Whole genome sequencing is mapping out of a person's DNA to find out the root cause of inherited diseases as well as several cancers. Genome sequencing will provide insight into the possible cause of the diseases and it's relation with the phenotypic association. WGS is particularly effective in cancer where by knowing genetic markers linked to drug transport and metabolism, clinicians can decide on therapeutic strategy. We offer whole genome sequencing service which provides a complete genetic catalog of an individual revealing all the genetic variations. We have generated hybrid sequencing and bioinformatics analysis pipeline for whole genome sequencing to generate adequate depth of sequencing data to efficiently assemble the genome.

Sample Type

Blood Sample: 5 ml blood in EDTA Vacutainer at 2-8°C

Fresh Tissue: Fresh Tissue in tms RNA stabilizer (XGtms-100) provided by Xcelris Labs in sterile leak proof container at -20°C. (in Dry Ice Only)

 
 
 
Whole Genome Sequencing   |   Whole Exome Sequencing   |   Mitochondrial DNA Sequencing   |   HLA Typing
 
 
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