The Pattern of Linkage Disequilibrium in Livestock Genome
author
Abstract:
Linkage disequilibrium (LD) is bases of genomic selection, genomic marker imputation, marker assisted selection (MAS), quantitative trait loci (QTL) mapping, parentage testing and whole genome association studies. The Particular alleles at closed loci have a tendency to be co-inherited. In linked loci this pattern leads to association between alleles in population which is known as LD. Two metric parameter Dˊ and r2 were suggested for measuring the extent of LD in population. D' are more influenced by variation in allele frequencies than r2. Until recently all research on LD was carried out by microsatellite, which reported high level of Dˊ in wide extent. As progressing on large scale genomes sequencing a huge number of single nucleotide polymorphism (SNPs) were detected on genome and microsatellite replaced by SNP in such researches. By using SNP, high level of LD in short distance has been reported. Many factors can affect LD such as selection, migration, genetic drift, mutation, small finite population size and recombination. So, LD is basic tools for exploring the genetic basis of quantitative traits in livestock. Likewise, comparative LD maps make a capable us to examine the degree of diversity between breeds and to discover genomic regions that have been subject to selection. Therefore, this review states concept and current approach to estimating LD and extent of LD in livestock population.
similar resources
A map of the human genome in linkage disequilibrium units.
Two genetic maps with additive distances contribute information about recombination patterns, recombinogenic sequences, and discovery of genes affecting a particular phenotype. Recombination is measured in morgans (w) over a single generation in a linkage map but may cover thousands of generations in a linkage disequilibrium (LD) map measured in LD units (LDU). We used a subset of single nucleo...
full textLong-Range Linkage Disequilibrium in the Human Genome
In the study of genomic variation, the nonrandom association of alleles has been a valuable tool for understanding population history, correlating disease phenotypes, and mapping genetic structural variation. These associations, termed linkage disequilibrium, have been quantified to great extent in humans over short distances. Linkage disequilibrium between genetically distant sites has garnere...
full textGenome-wide comparisons of variation in linkage disequilibrium.
Current genome-wide surveys of common diseases and complex traits fundamentally aim to detect indirect associations where the single nucleotide polymorphisms (SNPs) carrying the association signals are not biologically active but are in linkage disequilibrium (LD) with some unknown functional polymorphisms. Reproducing any novel discoveries from these genome-wide scans in independent studies is...
full textLinkage disequilibrium between STRPs and SNPs across the human genome.
Patterns of linkage disequilibrium (LD) reveal the action of evolutionary processes and provide crucial information for association mapping of disease genes. Although recent studies have described the landscape of LD among single nucleotide polymorphisms (SNPs) from across the human genome, associations involving other classes of molecular variation remain poorly understood. In addition to reco...
full textLong Range Linkage Disequilibrium across the Human Genome
Long-range linkage disequilibria (LRLD) between sites that are widely separated on chromosomes may suggest that population admixture, epistatic selection, or other evolutionary forces are at work. We quantified patterns of LRLD on a chromosome-wide level in the YRI population of the HapMap dataset of single nucleotide polymorphisms (SNPs). We calculated the disequilibrium between all pairs of S...
full textA scan for linkage disequilibrium across the human genome.
Linkage disequilibrium (LD), the tendency for alleles of linked loci to co-occur nonrandomly on chromosomal haplotypes, is an increasingly useful phenomenon for (1) revealing historic perturbation of populations including founder effects, admixture, or incomplete selective sweeps; (2) estimating elapsed time since such events based on time-dependent decay of LD; and (3) disease and phenotype ma...
full textMy Resources
Journal title
volume 7 issue 1
pages 1- 7
publication date 2017-03-01
By following a journal you will be notified via email when a new issue of this journal is published.
Keywords
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023