An international consortium has published the largest survey of human genetic variation thus far: a third-generation map that includes data from 11 global populations. The accomplishment will help in the ongoing search for genetic variants associated with complex diseases.
Any 2 people are more than 99% the same at the genetic level.
The small variations between people can help explain differences
in susceptibility to disease, response to drugs or reaction to
Stretches of DNA sequence tend to be inherited
together. Thus, sets of small genetic variations called single
nucleotide polymorphisms (SNPs) tend to be grouped. These clusters
are called haplotypes. The map of human genetic variation is
called a haplotype map, or HapMap.
Previous versions of the HapMap were built on the analysis of
DNA collected from 270 volunteers from 4 geographically diverse
populations. The first version contained approximately 1 million
SNPs. The second-generation map brought that total to more than
3.1 million SNPs.
Over the last few years, researchers conducting genome-wide association
studies have relied on data from the HapMap to discover hundreds
of common genetic variants associated with complex human diseases,
such as cardiovascular disease, diabetes, cancer and many other
health conditions. Funding to create the third-generation HapMap
was provided by NIHs National Human Genome Research Institute (NHGRI), National Institute on Deafness and Other Communication Disorders (NIDCD) and the Wellcome Trust.
For the latest version, researchers analyzed about 1.6 million SNPs in a much broader range of samples from around the world. As reported in the September 2, 2010, issue of Nature, the HapMap now includes data from an additional 7 global populations, bringing the total number of volunteers to almost 1,200.
The consortium also carefully sequenced 10 regions totaling
about 1 million base pairs in 692 samples. The scientists found
that 77% of the SNPs they detected were new. This result shows
that many more variants remain to be found, especially rare
variants. In addition, the scientists added more than 800 copy-number variants
to the resource. These reflect differences in the number of
copies of specific DNA regions people harbor.
"The generated HapMap provides an important foundation for studies aiming to find genetic variation related to human diseases," says NHGRI Director Dr. Eric D. Green. "It
is now routinely used by researchers as a valuable reference
tool in our quest to use genomics for improving human health."
Many of the HapMap researchers are also part of the 1000 Genomes Project,
an international public-private consortium launched in 2008 to build an even
more detailed map of human genetic variation. The scientists are using next-generation
DNA sequencing technologies to build a public database with information from
the complete genomes of 2,500 people from 27 populations around the world,
many of which were studied in the HapMap project. Researchers will be able
to use this data to expand their studies of how common and rarer genetic
variations contribute to illness.