The Role Of Genomics And Proteomics Fields

Scientist is studying the human genome to determine its sequence. Understanding the genomic sequence can prevent any form of disease, however, each person does not contain the same genomes which means it is hard to understand each genomes sequences. The advantage of understanding the genomics, is to understand how human genomic mutations can lead to life-threating conditions such as cancer and prevent them from happening again. The disadvantage for researching genomics cost a lot of money, the research nearly cost thirteen-billion

Over the last 10 years scientists have been involved in the progression and completion of the Human Genome Project. "Scientists working on this project have developed detailed maps that identify the

I did not get conclusive data from the gel I made. As you can see in figure 1, the bands that showed up on the gel were too cluttered to be able to measure them. So I could not compare protein bands between the fish species based on our gel. Instead, I used a default gel picture that another group did in the class to get my data. From their gel I was able to compare the different species. Table 1 shows the number of bands that were similar between the different fish species when they were compared. I was able to determine that fish species C (Tuna)

The HGP was a 13-year long project started in 1990 with the objective of determining the entire human euchromatic genome sequence. It was a public funded project and the goal was to complete the project within 15 years. Since its inception, the project had been met with scepticism from scientists and commoners alike. One significant doubt was whether the astounding expenditure of the project would outweigh the potential benefits from it. However, the incredible success of the HGP became apparent very soon after completion. Not only did it mark the beginning of a new era in medicine, it also made significant development in the various techniques that can be used for DNA sequencing. This publicly funded, $3 billion project began formally in 1990, under the co-ordinated effort of the United States Department of Energy (DOE) and National Institutes of Health (NIH). Although destined to be completed in 15 years, rapid technological development accelerated the completion date to 2003.

Our incessant curiosity for knowledge and answers has prompted the intricate research institutions we know today. Among the volumes of research, scientists have searched for innovations to better understand the human body and edge closer to more individualized medicine. In 1990, breakthroughs in genetic technology allowed for researchers to begin a quest to map and understand all the genes of human beings. A mere 13 years later and just shy of $3 billion invested the Human Genome Project successfully mapped the billions of base pairs involved. With the ability to diagnose specific abnormalities, researchers and medical professionals have saved hundreds of ill children to which their survival was indefinite. However, with scientists continuing

Before discussion of the ethical, legal and social issues can be successful, some background information is needed. For example, why is the goal of mapping the human genome important? Who is going to benefit or at least be affected by this new

In February 2001, Venter et al., reported on the “penultimate milestone” – the feat of mapping 95% of the euchromatic portion of the human genome (Venter et al., 2001). Multiple discoveries were made in the process of mapping the human genome: the number of genes (fewer than imagined); the percent difference between individuals (less than 0.1%); and new techniques (Polymerase Chain Reaction) (Venter et al., 2001; National Human Genome Research Institute, 2012).

The sequencing of the human genome has a new approach to health care in regards to promotion, maintenance, and treatment. Genetic research is defined as a new approach to a better understanding of the genetic components of common diseases: Cancer, diabetes, stroke, and creating new gene-based technologies for screening, prevention, diagnosis, and treatment of both rare and common diseases. Nurses are a main aspect within the first line of care, and therefore will contribute fully in genetic-based and genomic-based practice activities such as collecting family history, obtaining informed consent for genetic testing, and administering gene-based therapies. Lea, D, (January 31, 2008). My paper is based on an article Genomics in the public

In June 2000, the publicly funded Human Genome Project (HGP) and the private firm Celera Genomics Inc. announced that they had completed sequencing the human genome. This unprecedented accomplishment is expected to enable doctors to diagnose, treat and even prevent numerous genetic diseases. As these two entities worked on sequencing the human genome, there was also a separate and less publicized race to patent as many human genes as possible.

Increased genomic knowledge for all GPs and improved referral methods will be needed to cope with the number of patients(5). GPs would have to receive additional training to interpret and analyse genome sequencing results. This provides a challenge for existing GPs and may only be possible to implement in new doctors in medical school. Health England have set up a genetics skills and training programme for workers in the NHS, however further progress will need to be made to account for all the data that will be generated (6).

It is estimated by Cancer Research UK that one in two people in the UK will get cancer at some point in their lives . This startling statistic shows an inept global failure to bring about control of one of most prevalent and fatal known diseases. But the growth in cancer incidence is not confined to the UK; in 2012 14.1 million new people were diagnosed worldwide, with forty percent of these new cases originating in countries of a low or medium HDI . This essay will focus on the how genomics are revolutionising the detection and treatment of cancer in the twenty-first century.

The Human Genome Project (HGP), an international scientific research project, has educated the public tremendously on various topics concerning DNA and genetics. This study has been beneficial to communities alike. As stated, the HGP sought to identify all the genes in human DNA, determine the sequences of the three billion chemical base pairs that make up human DNA, store this information in databases, improve tools for data analysis, transfer related technologies to the private sector, and address the ethical, legal, and social issues that may arise from the project. In favor of achieving these goals, scientists studied the genetic makeup of several nonhuman organisms (Human Genome Management Information System, 2011).

“Genetic engineering is, at best, a debatable branch of science. For some, it is the wave of the future: a method for perfecting the human genome, discarding flaws from infants before they are born and ensuring they live longer, healthier lives. For others, it is an abomination: a method of circumventing what nature gave you, and wholly unnatural. Which one is right?” (Bird). Naturally, genetics is the scientific study of inherited variations in the DNA strand. This topic sparked curiosity among numerous scientific individuals that they begun a research project on it titled the Human Genome Project. To illustrate, the Human Genome Project worked out the sequence of the three billion chemical ‘letters’ of the human genome, and it produced

The sequencing of the human genome involves the vision of an advanced medical science and academic research. Nowadays, genetic databases are making a loud noise to easily determine the relationships between lifestyle, environmental exposures, and genetic diseases. These databases large lean on collective data in contribution to genetic information and research materials that deal with the genetic cases of diseases. For the reason that genetic databank has a great potential of massive profit and technologic advancements that could improve our understanding of a range of diseases, private companies seek to get access to these genetic databanks of patients. However, this research can only proceed with consideration of the ethical, legal and

To begin discussion about the HGP, we first must understand what it is. It is a massive undertaking of collaboration of geneticists that begin in 1990. Their goals are to identify all the estimated 80,000 to 100,000 genes in human DNA and determine the sequences of 3 billion