My Dna Profile

When I was told that I was going to get my DNA test results back, I felt two distinct emotions during that moment of waiting. Nervousness and excitement followed. True fully, I’ve always thought I knew what I’m susceptible to getting in the future or right now in the present. Due to the fact, I’ve had a talk with both my parents about what family diseases are getting passed along in both my family trees. It’s pretty common diseases: diabetes, hypertension, Parkinson, asthma, hearing loss, and COPD, etc. The few minutes of waiting to get my test results back, made my anxiety levels increase as well as my emotions increasing. When I was given my test results, I immediately ripped open the envelope and read the company’s informational letter. It described to me what PersonaGen Cooperation stands for, Privacy Policy, and how they were capable of finding out certain information about me through viewing my genetic data. I then seemed at my test result paper seeing that I have three different chromosomes that show I’m homozygous or heterozygous for those traits. These results will either show what I need to commute on my health of living style, and what precautions I might need to take in the near future. All I know is that it’s make or break time.

Understanding ways to prevent breast cancer are important for all women to know and discern. Every woman is at risk of developing breast cancer, however, the risk is not equal among all women. “Some breast cancer risk factors, such as gender and family history, are not changeable. Other risk factors, like age, become more important as a woman grows older. Some of the following lifestyle characteristics could reduce the chance of developing breast cancer. Characteristics include exercise at least one and a half hours a week, maintaining a healthy body weight, and taking Aspirin or Ibuprofen twice a week can lower your chances of developing breast cancer. Alcohol consumption more than doubles the risk of women obtaining breast cancer, and smoking shows increased rates of breast cancer”(Holmes par 1). Some women may not be genetically proven to develop breast cancer, but that doesn’t mean the individual will not get cancer

Genetic testing has become a highly controversial issue among both the general population and the scientific community. It is a process that exposes a person’s entire genome sequence, allowing it to be read and evaluated to identify potential risks for genetic diseases or diseases that could be passed onto offspring (Holt Productions, 2012). With thousands of genetic tests already being used, and more being established, it seems logical to put this growing technology to use. Some agree that it is a person’s right to know and understand his or her genetic makeup. However, others argue that, despite the benefits of genetic testing, caution should be used to carefully inspect the risks associated with this new technology.

Due to the lack of adequate interpretation, I do not foresee buying my genome sequencing in the near future. A few of my close relatives have certain medical conditions that concern me, such as diabetes, cardiovascular disease, and rheumatoid arthritis. Even so, I prefer to live a life without the fear of what my DNA profile might uncover. If the test determined that I have an increased risk of developing Alzheimer’s disease, my stress level may increase every time I lose my keys. For example, I have a friend that was terrified of having a child that may have schizophrenia because the child’s grandmother suffered from the condition. During her daughter’s infant years, my friend suffered from stress as she watched for any sign of mental illness in her daughter. My friend suffered from constant worry and guilt that her child would become ill. Her daughter is almost thirty now and she shows no sign of the disease. Even though the test may reveal an increased risk for certain conditions, it is not advanced enough to predict with certainty what my health picture will be in thirty years. I believe in knowing what family risk factors affect me and

These results may also help doctors make recommendations for treatment or monitoring, and give people more information for making decisions about their and their family's health, allowing them to take steps to lower his/her chance of developing a disease. For example, as the result of such a finding, someone could be screened earlier and more frequently for the disease and/or could make changes to health habits like diet and exercise. Such a genetic test result can lower a person's feelings of uncertainty, and this information can also help people to make informed choices about their future, such as whether to have a baby or

Aram, a 16-year-old trainee hairdresser from Keyworth in Nottinghamshire, was abducted, raped and strangled on 30 October 1983 – five years before the careless driver was born. (Her murder was featured in the first ever episode of Crimewatch in 1984.) The police had a few circumstantial leads to go on: a stolen red Ford Fiesta; a handwritten message from the killer saying they'd never catch him; a paper towel recovered from the toilet of a pub, the Generous Briton, where shortly after the murder a man with blood under his fingernails had eaten a ham sandwich, drunk a pint of orange juice and lemonade, and told the landlady an unlikely story about having driven up the M1 to see some friends who weren't in. Twenty thousand people were interviewed in the course of the investigation, but the killer

Genetics are the foundation of every human make up, but most people have little to no knowledge of their own foundation. Though some people believe that the encryption of their genetics ruins the surprise in life, other people want to be as prepared as possible for any issues that are encoded in their genetics and cannot be prevented. Genetic counselors test people of any age to uncover a mysterious condition. Counselors can find the likelihood that an adult will develop cancer or will develop a condition that starts in the late stages of life. With the new knowledge, a patient can be better prepared for their future. Counselors can also complete prenatal work by focusing on the parents’ genetics. They test for conditions like down syndrome

Evidence 3: DNA profiling is less intrusive. The best way of retrieving a DNA sample is by using either blood, saliva, or hair. For example, if you happen to be in a situation where your town is taking DNA samples to help solve a crime, that would be the best way to go. This way you are helping but also giving less information for the better.

DNA profiling was at first made as a framework for choosing paternity, in which tests taken under clinical conditions were examined for innate affirmation that could association watchman to adolescent. It initially progressed into the courts in 1986, when police in England asked sub-nuclear analyst Alec Jeffrey’s, who had begun looking at the use of DNA for wrongdoing scene examination, to use DNA to check the confirmation of a 17 year-old child in two ambush murders in the English Midlands. The tests showed the youngster was frankly not the offender and the genuine attacker was over the long haul found, furthermore using DNA testing.

According to Harmon (2007), “the public is unprepared for such information and that it is irresponsible to provide it without an expert to help put it in context” (p. 1). Unlike Harmon who actually had her DNA sequenced, I do not plan on obtaining a DNA profile. I understand that if will inform me that I may be prone to some genetic diseases, Alzheimer’s, prostrate cancer, Type 2 diabetes, along with Crohn’s disease. Harmon states “DNA is not definitive” (Harmon, 2007, p. 1).

A. The first prevention you can do is communication; Talking to your family and children lets them know what the family history is and what to be aware

In the video, Personal DNA Testing, Neil Tyson states “knowing our genetic risk for disease will actually lead us to longer, healthier lives” (Tyson). However, there are various negative and positive factors of genetic testing that make it questionable. For example, individuals that are aware of hereditary diseases should consider this type of tool, so they can prevent it. On the other hand, people do not know if the results will be accurate because error is possible. It is important to research this type of test before requesting approval.

Introduction: Today, the advancing gene technology provides humanity with numerous benefits such as Genetically Modified Food, CRISPER, and one of them is the use of DNA profiling for storing bio-information. DNA fingerprint technology allows mapping of individual’s genetic patterns that can be stored into the database system (What is DNA fingerprint? 2016). The ability to profile gene effectively, DNA fingerprinting is used as a problem-solving tool in the justice system and medical science researches. At the same time, ethical and social issues such as privacy violations, human rights and the possibility of discrimination cannot be ignored.

Genetic testing, do we or don’t we? This is the question. Advances in science, as they call them, are able to screen for some types of genetic disorders. Although this type of testing has allowed the opportunity to test couples who are at risk for Tay-Sachs and others who are at risk for Cystic Fibrosis, Sickle Cell Anemia, and Huntington’s disease there are still vast limitations. There is a potential for the loss of privacy, test errors, psychological and social stress. Overall genetic testing has the potential to be wholly deterministic and results in information that is simply probabilistic. Errors could occur and result in severely misreading test results deluding individuals about their personal health. The contingency surrounding genetic

3: Promoting informed decision making is a valuable recommendation when sufficient evidence is available on analytical and clinical validity and risk and benefit analysis is favorable but not definitive. Furthermore, discourage the use of testing when there is no or little information on validity or utility and evidence of harm. These recommendations and rigorous outcomes research can provide sufficient guidance in clinical practice for assessing the impact of genomic testing on patients, their families, and population based health outcomes.