Enrichment for loci identical-by-descent between pairs of mouse or human genomes by genomic mismatch scanning

Genomics. 1998 Jan 1;47(1):7-11. doi: 10.1006/geno.1997.5083.

Abstract

Mapping genes that underlie complex genetic traits, including genes that determine susceptibility to common diseases, requires an efficient method for high-resolution genotyping. Single-nucleotide differences between pairs of allelic sequences from unrelated individuals occur approximately once in every kilobase. Genomic mismatch scanning (GMS), by analyzing numerous single-nucleotide polymorphisms in a single genome-wide step, offers a potentially powerful and efficient approach to linkage analysis. GMS, originally developed in a yeast system, is shown here to be applicable to the more complex mouse and human genomes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphatases*
  • Animals
  • Bacterial Proteins / genetics
  • Chromosome Mapping / methods*
  • Crosses, Genetic
  • Escherichia coli Proteins*
  • Female
  • Genetic Techniques*
  • Genome, Human*
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred Strains
  • Microsatellite Repeats
  • MutL Proteins
  • Pedigree
  • Polymerase Chain Reaction
  • Polymorphism, Genetic

Substances

  • Bacterial Proteins
  • Escherichia coli Proteins
  • MutL protein, E coli
  • Adenosine Triphosphatases
  • MutL Proteins