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The Human Genome Project was a 13 year-long publicly funded project initiated in 1990 with the objective of determining the DNA sequence of the entire euchromatic human genome within 13 years. [ 8 ] [ 9 ] The idea of such a project originated in the work of Ronald A. Fisher , whose work is also credited with later initiating the project.
Richard M. Myers (born March 24, 1954) is an American geneticist and biochemist known for his work on the Human Genome Project (HGP). The National Human Genome Research Institute says the HGP “[gave] the world a resource of detailed information about the structure, organization and function of the complete set of human genes.” [1] Myers' genome center, in collaboration with the Joint ...
The results of the Human Genome Project are likely to provide increased availability of genetic testing for gene-related disorders, and eventually improved treatment. Parents can be screened for hereditary conditions and counselled on the consequences, the probability of inheritance, and how to avoid or ameliorate it in their offspring.
The International HapMap Project is a collaboration among researchers at academic centers, non-profit biomedical research groups and private companies in Canada, China (including Hong Kong), Japan, Nigeria, the United Kingdom, and the United States. It officially started with a meeting on October 27 to 29, 2002, and was expected to take about ...
Officially, the Human Genome Project had an eight-year head start before Celera entered the race, though discussions for the Human Genome Project began fourteen years before Celera announced their own project. [23] [24] Because the Human Genome Project was a $3 billion publicly funded venture, [23] the consortia raced to enter as much of the ...
In the human genome project the human genome was successfully sequenced, which provided a reference human genome for comparison of genetic variation. With improving sequencing technologies and the reference genome, more and more variations were found of several different sizes that were larger than 1 kb but smaller than microscopic variants.
It used the Sanger sequencing method, a technology which formed the basis of the "first generation" of DNA sequencers [2] [3] and enabled the completion of the human genome project in 2001. [4] This first generation of DNA sequencers are essentially automated electrophoresis systems that detect the migration of labelled DNA fragments.
Singapore Genome Variation Project: 268 individuals from the Chinese, Malay, and Indian population groups in Southeast Asia [4] Italy: SardiNIA Project: 2,000 sequenced Sardinian people [5] Germany: PopGen (German) Genotyping of 10,000 German people [6] Ukraine: GenomeUkraine: Whole genome sequences of 97 Ukrainians from Ukraine [7]