The team will obtain and identify genetic variations in DNA samples from 270 people in Nigeria, Japan, China and the United States. Scientists at Johns Hopkins are one of two U.S. groups who will analyze the DNA sequences to determine the most common patterns of genetic variations in populations. Once finished, the HapMap will provide a freely available catalog of common patterns, or haplotypes.
"What we learn from the HapMap project will simplify and accelerate efforts to identify genes associated with common chronic diseases," says Aravinda Chakravarti, Ph.D., professor and director of the McKusick-Nathans Institute of Genetic Medicine at Johns Hopkins. "This project is intense from a DNA analysis perspective, but it's going to make the next round of studies much easier to do."
The power of haplotypes is that they offer a way of using the identity of a few key genetic building blocks in a given region of DNA to infer the rest of the sequence -- possibly tens of thousands of building blocks long. So instead of having to sequence each person's genome, future studies could merely identify variants in key positions (and thus determine a person's haplotype) and instantly know nearly the entire sequence, the scientists say.
The Nature article describes the entire HapMap process, from working with communities to identify participants and collect samples to choosing which DNA variants to look for and how to analyze the data to create the actual map. Ten groups around the world will genotype the samples, determining which of the four "letters" of DNA's language are at given positions along the genome.
Ninety samples from the Yoruba people in Ibadan, Nigeria, will be analyzed, along with 90 from people of
Contact: Joanna Downer
Johns Hopkins Medical Institutions