CHROMSCAN: genome-wide association using a linkage disequilibrium map

J Hum Genet. 2008;53(2):121-126. doi: 10.1007/s10038-007-0226-2. Epub 2007 Nov 28.

Abstract

CHROMSCAN implements a composite likelihood model for the analysis of association data. Disease-gene localisation is on a linkage disequilibrium unit (LDU) map, and locations and standard errors, for putatively causal polymorphisms, are determined by the programme. Distortions of the probability distribution created by auto-correlation are avoided by implementation of a permutation test. We evaluated the relative efficiency of the LDU map by simulating pseudo-phenotypes in real genotype samples. We observed that multi-locus mapping on an underlying LDU map reduces location error by approximately 46%. Furthermore, there is a small, but significant, increase in power of approximately 5%. Effective meta-analysis across multiple samples, increasingly important to combine evidence from genome-wide and other association data, is achieved through the weighted combination of location evidence provided by the programme.

Publication types

  • Comparative Study
  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Case-Control Studies
  • Chromosome Mapping*
  • Computer Simulation
  • Genetic Markers / genetics
  • Genome, Human / genetics*
  • Genotype
  • Haplotypes / genetics
  • Humans
  • Linkage Disequilibrium*
  • Macular Degeneration / genetics
  • Phenotype
  • Polymorphism, Single Nucleotide / genetics*

Substances

  • Genetic Markers