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    Home»Health»How Is Genomics Helping Medical Science
    Health

    How Is Genomics Helping Medical Science

    AdminBy AdminNovember 30, 2022Updated:December 8, 2023No Comments4 Mins Read
    How Is Genomics Helping Medical Science
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    In this modern world, everything is going digital and smart. With the advancement of technology, it seems like everything is possible for humans. Well, this is a big statement to consider, but if you look at the particular innovative approaches of our contemporary planet, you will find it easy to accept. 

    Medical science is no different, it is ever-changing, and development is indissolubly linked to medical science. For example, it’s possible to treat many diseases, even uncommon ones. This personalization in medicine is possible through the help of genome studies. 

    The Top Doctor in UAE is efficient enough to deal with any disease these days. So if you are finding treatment solutions, you can go for them, and they will deliver you the best solution possible. 

    Well, the genome is a medical study that helps people understand their genes and related issues better. It has been helping medical science since 2003, when the Human Genome Project was started.

    Genomics is used to treat illness and diagnose various health-related issues. Besides, tracking down bacteria and viruses is also possible through the genome. Well, the study of genes is called genomics. This study related to medical science is helping experts to predict, diagnose, and treat various diseases. It’s more personalized and precise than ever now. 

    What Is Genomics ?

    The Human Genome Project helped to consider almost 20,000 genes to make a blueprint of our body. Until then, personalized medicine was not as easy as now. However, the ability to sequence the human genome has changed the process of medical science. 

    The study of genes has helped us understand that three billion DNA pairs are available in a complete human genome to signify individual characteristics such as hair color and height. But on the other hand, it also determines the fundamental anatomy of the human body. 

    So, the genome is a complete set of information manuals for the human body. The human body has almost 25000 genes that indicate specific statements to our body. We all have two copies of each gene, and both come from the parents. In general, you will find 23 pairs of chromosomes in every cell in the human body. 

    Well, the whole DNA and 23000 genes are together known as Genomes.

    Ways Genome Helps Medical Science.

    With the above information, we can easily understand the importance of genome studies. However, the fundamental role of genomics in medical science has so many aspects. Let’s focus on those aspects.

    It Helped To Improve Our Medications.

    Genomic testing has become crucial in contemporary days to find solutions to different genetic conditions of children. Besides, it also helps to understand diseases like epilepsy, cancer, kidney disease, immune disorders, heart conditions, and bone marrow conditions. 

    Without genomic testing, only 5% find the actual problem in the human body. In contrast with genomic texts, it’s possible to find almost 42% of rare and cancer diseases. 

    When you know the real problem, you will find a better solution, but when you do not have an idea, it may result in the wrong medications. So, genomic tests help the medical world to provide better treatment to patients.

    Reduce The Cost Of Sequencing. 

    Previously genome sequencing was very difficult for most people because it was costly. But nowadays, with the advancement in genomics, the medical world is helping people to understand their genome sequencing on a low budget. 

    Finding The Origins And Ancestry

    Genomics helped the medical world with something that was beyond imagination a few decades earlier. It is now possible to illuminate human origins to understand acute diseases by going back to a family’s medical history.

    Genomics Revolutionizing Before Birth Health Assessments. 

    It is now possible to understand the basic health conditions of an unborn baby by simply considering the pregnant mother’s blood. It’s all about DNA and its sequencing, and thus genomics is getting bound less to advance medical science unconditionally. 

    It Is Helping To Educate People On Their Own Health.

    DNA-based forensic analyses are getting advanced, and their innovative approaches are helping people to understand their health conditions through genome testing. 

    This direct-to-consumer approach is a suitable way to understand your genome, which is a route to any health-related issues so far.

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