Human variation

A genome-wide study provides evidence for recombination 'hot spots' in the human genome that influence genetic variation

Jonathan Weitzman(
Aug 8, 2002

Analysis of sequence variation provides clues about what makes us different from each other and why we respond differently to disease. In an Advanced Online Publication in Nature Genetics, David Reich and colleagues report a genome-wide study of sequence variation in the human genome (Nat Genet 2002, DOI:10.1038/ng947).

Reich et al. analyzed extensive collections of single nucleotide polymorphisms (SNPs) and found evidence for SNP-rich blocks of variation (as long as 100 kb). Further analysis led them to conclude that gene history, rather than differences in local mutation rates, are responsible for this variation.

They propose that differences in recombination rates are responsible for local patterns of sequence variation. Reich et al. add further evidence for large blocks of linkage disequilibrium in the human genome, a critical feature for future disease-mapping projects.

Interested in reading more?

Become a Member of

Receive full access to more than 35 years of archives, as well as TS Digest, digital editions of The Scientist, feature stories, and much more!
Already a member?