Unveiling hidden treasures in Zambian indigenous cattle using 32 microsatellites (#107)
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Selection patterns for Holstein sires in production-recorded herds with differing feed management systems (#108)
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Mildly penalized maximum likelihood estimation of genetic covariances matrices without tuning (#109)
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Efficiency of a tactical phenotyping strategy for multi-sage selection (#111)
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A commercial comparison of ewe breeds for reproduction, wool and lamb growth (#112)
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Reproductive performance of Holstein and Jersey heifers and cows in a pasture-based system (#113)
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Genetic diversity and population structure of four South African sheep breeds (#114)
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Sheep phylogeography and domestication as inferred from complete genome sequences (#115)
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Assessing imputation accuracy using a 15k low density panel in a multi-breed New Zealand sheep population (#116)
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Estimating the genetic (co)variance explained per chromosome for two growth traits using a half sib data structure in sheep (#118)
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Runs of homozygosity in Swakara pelt producing sheep: implications on sub-vital performance (#122)
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Genetic Diversity and Effective Population Size of Eight Iranian Cattle Breeds (#123)
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Arthrospira platensis: a novel feed supplement influences gene expression in the heart, kidney and liver of prime lambs (#124)
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Environmental effects on post weaning fleece traits of a merino sire evaluation flock (#125)
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Methane emissions based on milk fatty acids of Jersey and Fleckvieh x Jersey cows in a pasture-based system (#126)
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COMPARISON OF SURVIVAL PHENOTYPES IN SPECIFIC DAIRY PRODUCTION SYSTEMS (#127)
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Modelling of longitudinal liveweight data using regression with legendre and eigenvector functions (#128)
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Fibre diameter measured in the post-weaning age window is genetically the same trait as yearling fibre diameter (#130)
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Measurement for methane traits in the beef information nucleus cattle (#132)
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