Genomic approaches to identify a disease and its pattern have gained huge clinical importance in the past decade. Identifying and understanding unique genetic signatures, further allows us to move towards personalized medicine. The concept of personalized medicine relies largely on sequence information of your exome (some instances whole genome), utilized for disease associated diagnostics and customization of therapies. Such genomic information is largely collected by traditional genetic tests that have become increasingly available and through Next Generation Sequencing (NGS) platforms, whose costs have significantly decreased, making it affordable for almost everyone. Given this background, our efforts are directed towards identifying comprehensive sequence dataset for an individual and detailed evaluation of all genetic variations in an individual or strain as in the case of whole genome sequencing or identifying those genetic variations within your exome, which might be predisposing you to varying degrees of disease risk, assisting you in understanding your "Genome Rich Signature" involving better health. Benefits • Exome sequencing can directly contribute to your understanding of the dynamic nature of your genome. • Hence, often lead to the identification of specific causative variant(s) of diseases • Further, the exome sequence analysis allows us to identify and characterize even the novel variants, that have not yet been reported or studied, expanding its overall utility. • Most importantly, on an average, the exome sequencing in 112% cheaper than getting many genetic panels done.
Use left/right arrows to navigate the slideshow or swipe left/right if using a mobile device
choosing a selection results in a full page refresh