Project

DNA Pioneer James Watson.

Human Genome Project

Mapping the human genome

The announcement of the completion of the draft sequence of the human genome in June, 2000, and its subsequent publication in February, 2001, marked an important milestone for the Human Genome Project. For the first time, scientists were able to view the features of our own human "instruction manual." The McDonnell Genome Institute played an integral part in achieving this goal, contributing more than 20% of the draft sequence, and developing a comprehensive BAC clone map of the human genome.

Human Genome Project Details

Human Instruction Manual

The Human Genome Project (HGP) was launched in the US in 1990 and jointly funded by the National Institutes of Health and the Department of Energy. The announcement of the completion of the draft sequence of the human genome in June, 2000, and its subsequent publication in Nature in February, 2001, marked an important milestone for the HGP. For the first time, scientists were able to view the features of our own human "instruction manual."

The McDonnell Genome Institute played an integral part in achieving this goal, contributing more than 20% of the draft sequence, and developing a comprehensive BAC clone map of the human genome. In addition, we have identified more than 300,000 single nucleotide polymorphisms or SNPs, as a member of the SNP Consortium.

Recently, a revised assembly of the human genome was made available to the community. This latest iteration of the human genome assembly represents a continuation of an extensive effort to identify and sequence gaps and fix errant sequence assignments. The culmination of this effort was published in the journal Nature in 2004. The McDonnell Genome Institute has taken a lead role in the characterization of human chromosomes 2, 4, 7 and Y with subsequent publications for each of these.

HapMap, Genome Reference and Other Projects

One extension to human whole genome characterization was the HapMap project, which would not have been possible without the available template, or reference, of the human genome sequence. The Genome Reference Consortium (GRC) was also created to improve the sequence quality and accuracy of the human reference genome as its use in the field of genomic research expands to the clinic. Additionally, medical sequencing and structural variation studies of the human genome are underway. These projects promise to provide essential information regarding specific regions of the human genome associated with disease pathogenesis or susceptibility, and demonstrate the importance of investing in the sequencing of the human genome.

Publications