2022
DOI: 10.3390/genes13020229
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Y-Chromosomal Insights into Breeding History and Sire Line Genealogies of Arabian Horses

Abstract: The Y chromosome is a valuable genetic marker for studying the origin and influence of paternal lineages in populations. In this study, we conducted Y-chromosomal lineage-tracing in Arabian horses. First, we resolved a Y haplotype phylogeny based on the next generation sequencing data of 157 males from several breeds. Y-chromosomal haplotypes specific for Arabian horses were inferred by genotyping a collection of 145 males representing most Arabian sire lines that are active around the globe. These lines forme… Show more

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Cited by 19 publications
(74 citation statements)
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“…Biological samples were collected from 119 males, of Barbs (n = 84) and Arab-Barbs (n = 35) in Morocco, Algeria, Tunisia, and the European subpopulations. To ensure that many patrilines were represented in the dataset, pedigree information (available for 86 horses), provided by breeding authorities and associations, was considered in the sampling strategy as previously described [ 39 ]. Hence, oversampling of relatives was averted from the dataset by keeping six males per foundation sire at maximum.…”
Section: Methodsmentioning
confidence: 99%
See 4 more Smart Citations
“…Biological samples were collected from 119 males, of Barbs (n = 84) and Arab-Barbs (n = 35) in Morocco, Algeria, Tunisia, and the European subpopulations. To ensure that many patrilines were represented in the dataset, pedigree information (available for 86 horses), provided by breeding authorities and associations, was considered in the sampling strategy as previously described [ 39 ]. Hence, oversampling of relatives was averted from the dataset by keeping six males per foundation sire at maximum.…”
Section: Methodsmentioning
confidence: 99%
“…We inferred MSY haplotype spectrum of 119 samples according to the previously reported horse Y phylogeny [ 38 , 39 ]. For genotyping, we created a downscaled HT structure based on 65 selected HT-determining variants as markers (61 SNVs, 3 short Indels, and 1 microsatellite, see Supplementary Table S2 ).…”
Section: Methodsmentioning
confidence: 99%
See 3 more Smart Citations