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The New York Genome Center (NYGC) is an independent 501(c)(3) nonprofit academic research institution in New York, New York. [3] It serves as a multi-institutional collaborative hub focused on the advancement of genomic science and its application to drive novel biomedical discoveries.
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 that sets of inherited genes predicted the concept of mapping a disease gene to a chromosomal region originated in the work of ...
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 ...
Charles Peter DeLisi (born December 9, 1941) is an American biomedical scientist and the Metcalf Professor of Science and Engineering at Boston University.He is noted for major contributions to the initiation of the Human Genome Project, [8] [9] for transformative academic leadership, [10] and for research contributions to mathematical and computational immunology, [11] cell biophysics, [12 ...
As WICGR (Whitehead Institute/MIT Center for Genome Research), this facility was the largest contributor of sequence information to the Human Genome Project. In February 2006, The Broad Institute expanded to a new building at 415 Main Street, adjacent to the Whitehead Institute for Biomedical Research. [22]
He was named to the New York Genome Center position on November 28, 2012, a position he held through 2016. [9] His publications can be found via Google Scholar and his ORCID ID 0000-0002-5134-8088. Career
David Haussler (born 1953) is an American bioinformatician known for his work leading the team that assembled the first human genome sequence in the race to complete the Human Genome Project and subsequently for comparative genome analysis that deepens understanding the molecular function and evolution of the genome. [12] [13] [14]
The human pangenome has significant implications for population genetics, phylogenetics, and public health policy, as it can inform the genetic basis of diseases and personalized treatments by providing insights into the genetic diversity of human populations. [2] The new human pangenome reference integrates the missing 8% of the human genome ...