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Human genome project debate essay
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The film Gattaca was released in 1997, just six years prior to the completion of the Human Genome Project (completed in April 2003), with a working draft completed in June 2000. The name of the film refers to an Aerospace corporation featured in the movie; however, its letters correspond to the 4 nucleotide bases that make up the integrity of the human genome. The sequencing of the human genome poses tremendous benefits not only in the future, but in the present. From identifying pharmaceutical targets in the body, screening for diseased genes, or determine if individuals are predisposed for certain hereditary or nonhereditary illness’. Despite these benefits, there are ethical issues that must be addressed with the knowledge attained from sequencing the human genome.
The recurring motif present in Gattaca was the idea of genetic discrimination and restricting people to a certain social class, career and overall way of life based on their genetic make – up. The idea of discrimination based on genetic make up was debated prior to the completion of the Human Genome Project. In 1996, the United States government passed the Health Insurance Portability and Accountability Act which sought to protect individuals from unauthorized and non – consensual release of health related information. The film discusses the notion of genetic discrimination in great detail, postulating that individuals in the futuristic society are limited by their predisposed genetic make – up. The titular character in Gattaca, Vincent, was born through natural means, without the interference of reproductive technologies and in vitro fertilization. Upon birth a blood sample was able to determine major ailments he may be susceptible to in the future (su...
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...portrayal of the molecular biology in the film was not detailed, the concerns regarding the social problems were very detailed and could potentially be accurate. One way to resolve this controversy is to enforce strict federal laws that will regulate the use of an individual’s genome sequence so that the privacy of the individual will not be violated. Insurance companies will not be allowed to consider a customer’s genome sequence for their services. Furthermore, the issue on designer babies will also have to be addressed. Unfair advantages cannot be asserted to offspring because their parents are wealthy. Each child should be given the same random chance to attain traits such that no advantage will be had. In the future, the political aspects of the topic should be introduced in media as well because that is how the majority of the decisions will be made.
The PBS documentary “Nova – Cracking Your Genetic Code” tells about the genome sequencing technology: its current possibilities, advantages, disadvantages and future potential. The system became cheaper, faster and more available since the first human genome was fully sequenced in 2000. Modern companies use the technology to provide clients with the information about their genes and impacts they can have on owners’ health. Hospitals can provide more accurate diagnosis and personalized treatments with the aid of the genome sequencing. The video shows several examples of these benefits. But it mentions concerns about the quality of services, risks of exaggerated
Rather than leave genetics up to chance, technology offers expectant parents the opportunity to genetically enhance their children before they’re born. These genetically superior offspring are known as “valids” and are given the best opportunity in Gattaca’s society. For example, when Vincent, an invalid, borrows the identity of the valid Jerome Morrow, an interview to work for Gattaca consists only of a urine test. It’s assumed that his genes carry all his potential. There’s no need for him to answer questions his DNA can answer for him.
...he reader, which creates many questions about the particular subject of genetic engineering. It also conveys the authors idea, that we really need to be careful about what we do with this new scientific marvel, effectively to the reader, thus raising the reader's awareness about genetic engineering.
In 1997, Andrew Niccol produced the movie GATTACA. The movie described a world with genetically modified humans, modified at birth to be the perfect child their parents always wanted. In the 1990s, the movie seemed like a science fiction fantasy, but recent advances in biomedical procedure have started to make it a reality. While a future full of genetic engineering may be an intriguing notion, the human genome should be left alone. Humans should not be tampered with.
The children that are genetically modified are called “valids” and the children that are not are called “invalids.” Vincent Freeman was born an invalid and genetic testing noticed that he would most likely have a disorder when he was older, limiting his expected life span to be 30.2 years old. As an invalid, Vincent was restricted to menial jobs while his younger, genetically modified brother was able to work a professional job. Vincent’s wanted to become an astronaut his entire life, but there was no way he would be able to due to the genetic testing that was required upon applying. Unlike all other invalids, Vincent never gave up hope and was able to become an astronaut by tricking the valids into thinking he was Jerome Morrow, a valid who became paralyzed. By altering his height, and using hair, blood, and urine samples from Jerome, Vincent was able to pass the genetic testing stage and prove himself as a top employee of Gattaca. Even while working at Gattaca, Vincent had to be on the top of his game to not let others know his true identity, otherwise he would be relegated back to the world of the invalids.
The more we know about genetics and the building blocks of life the closer we get to being capable of cloning a human. The study of chromosomes and DNA strains has been going on for years. In 1990, the Unites States Government founded the Human Genome Project (HGP). This program was to research and study the estimated 80,000 human genes and determine the sequences of 3 billion DNA molecules. Knowing and being able to examine each sequence could change how humans respond to diseases, viruses, and toxins common to everyday life. With the technology of today the HGP expects to have a blueprint of all human DNA sequences by the spring of 2000. This accomplishment, even though not cloning, presents other new issues for individuals and society. For this reason the Ethical, Legal, and Social Implications (ELSI) was brought in to identify and address these issues. They operate to secure the individuals rights to those who contribute DNA samples for studies. The ELSI, being the biggest bioethics program, has to decide on important factors when an individual’s personal DNA is calculated. Such factors would include; who would have access to the information, who controls and protects the information and when to use it? Along with these concerns, the ESLI tries to prepare for the estimated impacts that genetic advances could be responsible for in the near future. The availability of such information is becoming to broad and one needs to be concerned where society is going with it.
“You would really be pretty if you lose weight”, maybe this sounds polite and kind of innocent but the actual tone and deeper meanings are very discriminatory. The Discrimination At Large by Jennifer Coleman is an article where the author demonstrates the price for being obese. Overweight people are being criticized all the time by many people. Moreover, they are now a mockery since people just make fun of them for their amusement. The movie Shallow Hal also shows how if we change our general idea of outer beauty of a person, we could benefit from it. Obesity has been a serious dilemma for the people in America. The society seems to not change their perception about obese people. In addition, people who are usually afraid to say any kind of
...ne starts life with an equal chance of health and success. Yet, gene therapy can also be thought of as a straight route towards a dark outlook, where perfection is the first priority, genes are seen as the ultimate puppeteer, and personal freedom to thrive based on one’s self isn’t believed to exist. With the emergence of each new technological discovery comes the emergence of each new ethical debate, and one day, each viewpoint on this momentous issue may be able to find a bit of truth in the other. Eventually, our society may reach a compromise on gene therapy.
In January 2011, The City of Kansas City, MO lost its second multi-million dollar employment discrimination lawsuit in a one-week period. The former city employees, Jordan Griffin and Coleen Low, were awarded $345,000 and $517,000 respectively by the jury. Griffin, a former Senior Analyst and Commissioner of Revenue, says she was given the nickname “White Chocolate” in the false belief she would favor minority hires. She also says she was harassed when she refused to participate in the biased-hiring process and was overlooked for an interview for the Commissioner of Revenue position on a permanent basis because it was already “pre-determined” that the position would be filled by an African American. When the then Senior Analyst Low spoke up on her colleague’s behalf, she says the city laid her off as well. The city’s, assistant attorney, said the city did nothing wrong and that the city was forced to layoff another 73 people that year due to the slump in the economy (Evans). Did Griffin and Low deserve the money they were compensated and does reverse discrimination exist?
GATTACA (1997) is a science fiction movie where one’s capabilities are determined by their genes since birth. Vincent Freeman is displayed as the main character where he needs to overcome his weaknesses through hard work and consistent determination to achieve his goals at Gattaca Space Academy. Alterations of genetics play a major role in the movie where only ones with flawless genes can achieve their dream career and ‘genoism’ became a new form of inequity. Society looks down upon Vincent including his parents because he was born naturally with physical limitations known as an ‘invalid’ whereas his younger brother Anton was genetically modified before his birth. Anton was born as ‘valid’ and was held highly by everyone due to his perfect genes chosen by his parents. As a result of discrimination down to...
The genetic technology revolution has proved to be both a blessing and a blight. The Human Genome Project is aimed at mapping and sequencing the entire human genome. DNA chips are loaded with information about human genes. The chip reveals specific information about the individuals’ health and genetic makeup (Richmond & Germov 2009).The technology has been described as a milestone by many in that it facilitates research, screening, and treatment of genetic conditions. However, there have been fears that the technology permits a reduction in privacy when the information is disclosed. Many argue that genetic information can also be used unfairly to discriminate against or stigmatize individuals (Willis 2009).
Peterson, Dr. Alan. "It's not all In our genes- social and political implications of human genome project." The New Statesman. 3 July 2000. 13.612: 5,1
The Human Genome Project is the largest scientific endeavor undertaken since the Manhattan Project, and, as with the Manhattan Project, the completion of the Human Genome Project has brought to surface many moral and ethical issues concerning the use of the knowledge gained from the project. Although genetic tests for certain diseases have been available for 15 years (Ridley, 1999), the completion of the Human Genome Project will certainly lead to an exponential increase in the number of genetic tests available. Therefore, before genetic testing becomes a routine part of a visit to a doctor's office, the two main questions at the heart of the controversy surrounding genetic testing must be addressed: When should genetic testing be used? And who should have access to the results of genetic tests? As I intend to show, genetic tests should only be used for treatable diseases, and individuals should have the freedom to decide who has access to their test results.
This is the natural fallacy genetic engineering creates in the new world seen in Gattaca. We know this because in the film the main character, Vincent, who uses another man named Jerome Morrow’s D.N.A and identity to rise up the ranks within Gattaca’s staff. He does this because genetic engineering pre-determines every aspect of one’s life that is scientifically possible. This would include diseases, life expectancy, cause of death, jobs/careers you can have and even who you should marry all from a sample of blood given when first born. Vincent’s D.N.A to others deemed him chronically ill, making him invalid, meaning that there would be very little opportunities for him in life; though he felt he can do things just as well as anyone. It is in Gattaca that we can look at genetic engineering as determining one’s instrumental worth to
The main ethical dilemma presented in the film is the use of genetic modification technology in humans. The scientists initially approach this dilemma by thinking like classic teleologians. “By incorporating human DNA into the hybrid template, we can begin to address any number of genetically influenced diseases…Parkinson’s, Alzheimer’s, diabetes, even some forms of cancer”. (Splice, 2009) They are producing a greater good by choosing this ethical path. This is the core motive for the current use of GMOs. According to the Human Genome Project (U.S. Department of Energy Genome Programs, 2008), GMOs have a variety of applications; To increase the yield of crops and animal products, to make plants and animals more resistant to certain disease, and more efficiently processed are but a few. The end product of these applications is, in theory, to benefit humanity. If we are already genetically modifying plants and animals, is a...