21 research outputs found

    Allele association analysis for three known equine coat color loci.

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    <p>a), mapping of the chestnut locus across breeds, based on inferred coat color phenotype; b), mapping of the black (agouti) locus across breeds, based on inferred black coat color; c), mapping of the gray locus across breeds. Phenotypes were inferred from the genotypes at 9 known coat color loci and known inheritance models as described in <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1002451#s4" target="_blank">Materials and Methods</a>. Unstructured case control association analyses using chi-square tests for allelic association were then performed on a pruned SNP set also as described in <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1002451#s4" target="_blank">Materials and Methods</a>. SNPs on each chromosome are labeled with a different color on the X axis as indicated.</p

    Distribution of pair-wise genetic distances.

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    <p>a), within and between domestic horse breeds; b), between domestic horse breeds and between domestic horse breeds and Przewalski's Horse. Genetic distance (D) between pair-wise combinations of individuals was calculated as described in <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1002451#s4" target="_blank">Materials and Methods</a>.</p

    Decline in genome-wide linkage disequilibrium across and within breeds.

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    <p>Genome-wide linkage disequilibrium (LD) was estimated both within a given breed, and across all breeds, by calculating <i>r<sup>2</sup></i> values between all pairs of SNPs with inter-SNP distances of less than 4 Mb as described in <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1002451#s4" target="_blank">Materials and Methods</a>.</p

    Number of samples (N), effective population size (N<sub>e</sub>), individual inbreeding estimates (f), inbreeding coefficient (F<sub>IS</sub>), and expected heterozygosity (H<sub>e</sub>) from four SNP sets pruned based upon varying levels of LD.

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    a<p>Individuals from this breed also included in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0054997#pone.0054997-McCue1" target="_blank">[41]</a>;</p>b<p>20 of these individuals were also reported in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0054997#pone.0054997-McCue1" target="_blank">[41]</a>;</p>c<p>17 of these individuals were also reported in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0054997#pone.0054997-McCue1" target="_blank">[41]</a>;</p>d<p>21 of these individuals were also reported in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0054997#pone.0054997-McCue1" target="_blank">[41]</a>;</p>e<p>19 of these individuals were also reported in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0054997#pone.0054997-McCue1" target="_blank">[41]</a>.</p><p>F<sub>IS</sub> and f were calculated based upon the primary SNP set (10,536 loci). Samples also used in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0054997#pone.0054997-McCue1" target="_blank">[41]</a> are indicated in the footnotes.</p>*<p>indicates significance at α<0.05 determined by 10,000 permutations.</p
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