| Literature DB >> 9465291 |
L McAllister1, L Penland, P O Brown.
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.Entities:
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Year: 1998 PMID: 9465291 DOI: 10.1006/geno.1997.5083
Source DB: PubMed Journal: Genomics ISSN: 0888-7543 Impact factor: 5.736