Genomics Services
 
 
Mitochondrial DNA Sequencing
Mitochondrial DNA, is a double stranded circular DNA present in the mitochondrial cell. Diseases of the mitochondria appear to cause damage to cells of the brain, heart, liver, skeletal muscles, kidney and the endocrine and respiratory systems. In human, changes in mitochondrial genome have been implicated in several human diseases including cancer, heart disease, diabetes, Alzheimer disease, Parkinson disease as well as play role in ageing process. We provide genome sequencing services to detect mitochondrial disorders caused by mutations within the mitochondrial genome as well as in nuclear genes. We work on bioinformatics pipeline which generates high quality reads, detailed statistical report, list of mutations studied which are compiled in a comprehensive report for physicians.

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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