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The Human Genome Project Essay

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The Human Genome Project

The Human Genome Project (HGP) is a project coordinated by the U.S. Department of Energy (DOE) and the National Institute of Health (NIH). The HGP began in 1990 and was scheduled to be completed in 2005. The goals of the project are to identify all the genes in the human genome (estimated to be 80,000 - 100,000 total) and develop the complete human DNA sequence. After the sequencing is done, a database with all the sequence information can be made and data analysis tools can be developed to use the information. The HGP will then have to consider ethical, legal, and social issues.

A new 5-year goal was approved in 1998 in which the HGP could be finished two years earlier than first planned in 1990. The new …show more content…

The private sector is also contributing to the human sequencing project. One such company is Celera Genomics. The President of Celera Genomics, J. Craig Venter, is promising to give away the human genome sequence once the company has completed the sequence. Although he is just beginning to set up a high throughput lab, he believes he can generate the human genome sequence in 18 months. Many people are skeptical about how he can develop the human genome and provide it to the public without any costly strings attached. Celera plans to patent many human genes and a large set of single nucleotide polymorphism's (3). If Celera Genomics is the first to sequence the human genome, there may be a price to pay for the sequences that revolutionize the biological community.

Another task of the HGP is to determine variations in the human genome. One approach is to map single nucleotide polymorphism's (SNPs). By mapping the SNPs, scientists can gain a better understanding of the variations and the functional aspects of these variations. "A map of 100,000 SNPs (one SNP per 30,000 nucleotides) is likely to be sufficient for studies in some relatively homogenous populations, while denser maps may be required for studies in large, heterogeneous populations" (2). These maps could provide markers that identify disease genes in humans.

Once the mapping and the complete human sequence are developed, the

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