Patterns of linkage disequilibrium in the human genome

Although enormous progress has occurred in the field of human genetics, the cloning of complex trait mutations remains a challenging and unresolved process. This continuing difficulty is responsible for an ever-increasing awareness of the phenomenon of linkage disequilibrium (LD). The principle behind LD is relatively simple. Over the lifetime of a population, the genetic markers that are adjacent to an ancestral mutation will recombine less often than more distant markers. Therefore, the ancestral alleles of the markers closest to the mutation should be most frequent in a collection of disease chromosomes. The allelic association should decrease as the distance from the ancestral disease mutation increases. This thesis is a collection of ideas and experiments aimed at dissecting the behavior of LD in the human genome. Specific studies examine LD in a variety of populations including isolated founder populations, as well as globally diverse population samples. A large number of regions throughout the genome are investigated using both pairwise comparisons of markers, as well as multimarker haplotypes. The X chromosome is more closely scrutinized because of its unique population history, as well as the advantages afforded to haplotyping due to hemizygosity of the X chromosome in males. Major conclusions include the observation that LD between pairs of markers is highly variable even at extremely close distances and multimarker haplotypes better serve to resolve the underlying haplotype structure of the genome.

Department dc:contributor.department

Massachusetts Institute of Technology. Department of Biology.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2002

Author dc:creator

• Liu-Cordero, Shau Neen, 1970-

Advisor dc:contributor.advisor

• Eric S. Lander.

• Biology.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/89344

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/89344