4.5 Review

Single-molecule analysis for molecular haplotyping

Journal

HUMAN MUTATION
Volume 23, Issue 5, Pages 442-446

Publisher

WILEY-LISS
DOI: 10.1002/humu.20020

Keywords

haplotyping; SNP; mutation detection

Funding

  1. NHGRI NIH HHS [R01 HG001720] Funding Source: Medline
  2. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [R01HG001720] Funding Source: NIH RePORTER

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In the genome era, there is great hope that genetic approaches such as linkage equilibrium mapping can be used to study common human disorders using a case-control population association study design. Ideally, the parental chromosomes are marked so that chromosomal regions in the form of haplotypes are compared in these studies to increase the power of association. Determining the haplotypes in a diploid individual is a major technical challenge in genetic studies of complex traits. A molecular approach to haplotyping is therefore highly desirable. Recent advances in DNA preparation, separation, labeling, and image analysis provide hope that a strategy of using a three-dye system coupled with DNA distance measurements between alleles will yield haplotype information of sufficiently high quality for genetic studies. In this work, we present the outline of the major challenges one must meet in developing a robust strategy for SNP detection and molecular haplotyping using single molecule analysis. (C) 2004 Wiley Liss, Inc.

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