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Advancement in DNA sequencing technology has sparked an interest in the investment of genome sequencing (Caulfield et al., 2013). It has become affordable and is gradually transforming both the medical care and research industry. Genome sequencing has been effective in identifying suitable treatment and shedding light on molecular diagnosis (Brunham and Hayden, 2012). It can be beneficial in improving the wellbeing of individuals and enhancing the prevention of a disease (Sanderson, 2013). However, with a profound influence in the field of medicine, there are a number of concerns that exists regarding the healthcare system and individuals who undergo genome sequencing. Thus, the issue of whether sequencing an individual’s genome should become a routine part of medical care is raised.

Sequencing an individual’s entire genome and identifying all the regions of variants can potentially assist in prevention, diagnosis, and treatment of a disease. Whole genome sequencing allows the molecular basis of many diseases to be studied (Drmanac, 2012). It decreases the likelihood of undiagnosed cases that arise from unusual or de novo variants. Henceforth, providing a better understanding of the condition and serves as supporting information, which can ultimately improve the individual’s health and prevent a disease (Dewey et al., 2011).

Clinical programs around the world have started to analyze genomes on a regular basis for individuals who could benefit from the procedure (Maher, 2010). For example, in 2010 a young boy’s life was saved as he was given a risky bone marrow transplant because of genome sequencing (Worthey et al., 2011). Genome sequencing not only suggests the most suitable course of treatment but the pr...

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... benefit both the medical world and the society in general. Whole genome sequencing is the basis for innovative advances to screening, diagnosis, risk expectation, and analytical programs in medical practice (Caulfield et al., 2013).

Overall, I believe that sequencing individual genomes should become a routine part of medical care because genome sequencing can benefit medical practice immensely. With whole genome sequencing, individualized medicine will come into effect and individuals will receive a better diagnosis and an effective treatment when required. Although there is still ambiguity regarding whether genome sequencing can enhance an individual’s health, the procedure has been able to identify unusual and common variants that give rise to future diseases. Identifying the variants is a platform to enhancing a better wellbeing of individuals.
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