Clinical Exome Sequencing
Focusing on significant genes associated with all known clinical phenotypes.
Clinical Exome Sequencing is one of the Next Generation Sequencing (NGS) based test offered by Genes2Me. In this panel we identify the molecular basis of rare genetic disorders in individuals who are either carriers of the disease or manifest symptoms at a sequencing depth of >100x. The panel screens coding regions of genes that have been proven to be of clinical importance. The human exome consists of complete coding (Exonic) regions of the genome. It encompasses 1-2% of the whole genome, yet contains approximately 85% of disease causing pathogenic variants.
Genes2Me clinical exome sequencing test for known inherited disorders which covers all exons for near about 7K genes associated with various diseases.
Clinical Exome Sequencing Coverage
||Ear, Nose, Throat
Test Price: ₹35000.00