The genetic revolution is here. Scientists from San Diego University believe that genetics will benefit people everywhere in ways we can’t even imagine, affecting almost every aspect of the human life and creating whole new industries. That’s why decoding and interpreting the human genome sequence is considered as one of the biggest scientific breakthroughs of our time. American based scientist and researcher Oded Kariti asserts that learning about your genetics can enable you to improve your health and achieve vibrant well-being.
Nowadays, with a relatively small financial role, you can acquire information about your own genome. Oded Kariti finds this fascinating, especially since the human genome was first sequenced in 2001, which is quite recent. Since then, inexpensive sequencing has developed a brand new industry, allowing individuals to access their own genetic information. Probably most of you have never thought about your genetic information, but one day you will, and once you understand its value, it will become an important part of your healthcare. Discovering your DNA sequence is cheap and easy. That genetic knowledge could change or save your life.
The human genome reference sequence was initially released in 2001. The Human Genome Project, the world’s largest collaborative biological project was started in 1990, and its aim was to sequence and identify all three billion chemical units in the human genetic set, as well as to find the genetic roots of disease and developing treatments. Up until then, our understanding of the encoded contents was rather limited. After they produced the sequence of the human genome, they made all sequence data from the project freely available to the community via the Internet, for further analysis and exploitation.
What are the benefits of decoding the human genome?
Knowledge of the human genome sequence can help us to understand how the genetic information affects the structure, function, and development of the human body. This will allow us to explore any connections between our DNA sequence and certain diseases, and hopefully, one day, come up with new and effective ways to improve human health.
DNA sequence information can be useful for forensic science. It can also direct you to make further genetic tests for specific diseases if you identify your own genetic variants that indicate the association with these diseases.
For example, without knowing about his own genotype, Oded Kariti recently realized that he is lactose intolerant. After examining some of his family members, he discovered that both his mother and his sister have the same problem, but they never associated the symptoms with the cause. If he had analyzed his genomic data before, he could have reorganized his diet earlier. Overall, the sequencing of the human genome might benefit many fields.