昨日出版的Nature杂志公布了第三个人类基因组单体型图，这一计划的目标是为最新一轮以疾病关联为重点的全基因组研究提供一个资源。这一成果对来自11个全球人群的1184个个体进行了基因组变异筛查，鉴定了人类基因组核苷酸多态性（SNPs）和拷贝数多态性 ...

The Haplotype Genetic Map (HapMap) is an invaluable resource to the cardiovascular researcher, enabling a decrease in cost and an increase in the efficiency and speed of discoveries in the laboratory.

The International HapMap Project has detailed information on genetic variation across the genome. 1 An important use of these data is to help identify genetic determinants of disease. HapMap ...

In the latest phase -- HapMap 3 -- the researchers looked for variants across the genome in 1184 samples from 11 populations. They chose the large sample set and the wide range of populations to ...

"It's not yet to the moon or to another planet, but it is a major milestone." The "HapMap," so-called because it details DNA variations known as haplotypes, will allow scientists to study every ...

While data from the project are available for unrestricted public use from the project's website (www.hapmap.org), the new tools needed to browse the map can be difficult to master for the beginner.

The HapMap project is supported by a broad range of agencies – both governmental and private – in the participating countries, and includes investigators from more than 70 research, education ...

This will probably only be of interest to population genetics afficianados, but I just noticed that the HapMap project has made its phase 3 data available through its browser (the data were ...

Using the information in the HapMap, researchers are able to find genes that affect health, disease, and individual responses to medications and environmental factors. For example, the goal of the ...

Now that the human genome has been mapped, genetic scientists have begun working on the "Hapmap" - an international collaboration which could shed new light on common conditions like heart disease ...

Now an international consortium of scientists has completed a more detailed chart, or HapMap, showing markers of genetic variation, or single nucleotide polymorphisms (SNPs), to explain the 0.1 ...